Robert G. McArthur 1039 Growth Retardation: An Approach to Management Walter J. Duncan 1047 Childhood Cardiac Murmurs: Innocent or Not? Howard L. Rudner 1051 Differential Diagnosis of Upper Airway Disease in Children Frances Gorzalka, Jay S. Keystone 1055. Infections in Refugee Children fom Developing Countries Walter P. Bobechko 1061 Limp Affecting the Hip and Knee in Children Barry Shandling 1065 The Unusual but Benign in Pediatric Surgety Barry Zimmernan, Sasson Lavi, Alex Lozynsky, Elizabeth Weber 1071 Lifestyle 1091 Allergy in Pediatrics A CFP information section to help healthy patients stay healthy Margaret McCaffery Interview 1100 Donald Ingram Rice: The Man, The Doctor, The Official Heather E. Bryant Report 1109 Miscarriage: How to Help in the Crisis H. C. Soltan, Z. Pyatt, G. G. Hinton Family Practice 1119 Case Book Atypical Severe Muscular Dystrophy in a Male: Genetic Implications for Female Relatives Douglas P. Black, Lynn Dunikowski Academic 1161 Commentary Videotapes as Continuing Medical Education for Physicians in Isolated Communities Cover: Baby boots are like babies: dainty but durable. The boots on the cover are more than 35 years old and still going strong. Photograph by Bill Woods. The opinions expressed in articles and claims made in advertisements appearing in CANADIAN FAMILY PHYSICIAN are the opinions of the authors and advertisers respectively and do not imply endorsement by The College of Family Physicians of Canada. Published monthly by The College of Family Physicians of Canada, 4000 Leslie St., Willowdale, ON. M2K 2R9. Telephone (416) 493-7513. Montreal Office: 14, 13th Street, Roxboro, Que. Authorized second class mail-registration number 5380. Post Office Department, Ottawa and for payment of postage, paid at Oshawa. This journal is listed in CURRENT CONTENTS/CLINICAL PRACTICE and in FAMLI (Family Medicine Literature Index). IPAASlI ccppinzi NOTE: All prescription drug advertisements in CFP have been precleared by the Pharmaceutical Advertising Advisory Board. CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 891 Canadian Family Physician Editorial Director Donald I. Rice, MD Editor Margaret McCaffery Associate Editor Alison Quaggin Harkin Editorial Assistant Rosaline Chuter Secretariat Nancy Nenczyn Sonya Gordensky Art Director Bill Woods Photographic Consultant Barry E. Neubauer Director of Communications George Ackehurst Advertising Manager Jack T. Hayes Advertising Production Manager Nancy Tughan-Kent Classified Advertising/ Subscriptions Secretary Pat Backus Translation Computex Enr. Geriatrics Dr. David Skelton, Edmonton Neurology Dr. T. J. Murray, Halifax Prevention/Community Medicine Dr. Ronald E. M. Lees, Kingston Editorial Advisory Board G. R. Spooner, MD, Indian Head (Chairman) Ian Cameron, MD, Halifax Brian M. Comelson, MD, Winnipeg Edgar R. Cowtan, MD, Medicine Hat C. E. Evans, MD, Hamilton Colin Herd, MD, Toronto Verity Livingstone, MD, Vancouver W. W. Rosser, MD, Ottawa Howard Seiden, MD, Toronto Renee Turcotte, MD, Moncton Consultant Editorial Advisers Biostatistics Dr. Moira Stewart, London The Family Dr. Yves Talbot, Toronto Family Medicine Dr. Ian McWhinney, London Radiology Dr. H. F. Morrish, Calgary Research in Family Medicine Dr. Martin J. Bass, London Therapeutics Dr. John Ruedy, Vancouver Annual Subscription Rates Canada and United States: $18 All other countries: $25 Single copies: $1.50 The CFPC grants a maximum of 25 hours study credit for independent learning activities-all or part of which may come from reading CANADIAN FAMILY PHYSICIAN. 0 Information for Authors CANADIAN FAMILY PHYSICIAN is distributed to all family physicians, non-certified specialists, family practice residents and some final year medical students in Canada-a circulation of approximately 19,000. Articles on clinical, academic, research, philosophical, political or business topics ofdirect relevance to the practicing family physician are welcomed. Letters to the editor are also welcomed; they should be brief and should contain precise references to quoted material. CANADIAN FAMILY PHYSICIAN is listed in Current Contents/Clinical Practice and FAMLI. Manuscripts Material or publication is reviewed by an editorial advisory board of practicing family physicians. Manuscripts should be sent to the editor at 1200 Sheppard Ave. E., Willowdale, ON. M2K 2S5, with a covering letter. CANADIAN FAMILY PHYSICIAN accepts only original material which is not under consideration by any other publication and which may not be the consent of both the The editor reserves the right to edit manuscripts for length, reprinted without author and the editor. CAN. AM. HYSIIAN ol.-1:-MY 195 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 dlarity and conformity with the journal's style. Articles should be typed double spaced and the author shouldretain one copy, sending three to the editor. American spelling should be used, and measurements must be given in correct metric abbreviations, e.g. mg =milligrarn(s), cm = centimeter(s). Drugs should be referred to generically, with the usual trade name following in brackets. Articles may be submitted in English or French. A title page should be submitted with the article, listing the title, authors' names their current positions, an address for reprints and a 100 word summazy. Do-NOT sent first drafts. Illustrations and Tables All illustrations and tables should be included separately from the manuscript and shouldbe clearly identified in Arabic numerals, showing which is the top of the illustration if this is not obvious. Legends for illustration (which should be referred to as 'Figures') should be typed separately. Tables must supplement the text without duplicating it. They should be numbered in Arabic numerals and should include an appropriate title. Illustrations should be either black and white glossy photographs or India ink drawings. Uiless previously agreed with the editor, color illustrations can be published only at the author's expense. References References should be numbered according to their appearance in the text and should be limited to work cited in the article, rather than a bibliography of the subject. Personal communications are not acceptable as references; unpublished material should be included only if an address can be given from which a copy is available. Authors are responsible for accuracy of references, which should be in keeping with the Uniform Requirements for Manuscripts Submitted to Biomedical Journals. Proofs and Reprnts Galley proofs of the edited article will be sent to the author and should be returned within three days. Major changes cannot be made on galley proofs; proofreading should therefore bi for accuracy only. Authors will receive 50 reprints of their articles plus an order form and price list for furtfier prints. 89 893 Executive Director's Donald I. Rice My Last Hurrah! MANY MEMBERS of the College of Family Physicians of Canada and other readers of CANADIAN FAMILY PHYSICIAN will know that I have announced my retirement as the College's executive director, effective June 1, 1985. This will be my last opportunity to communicate with CFP readers through the Executive Director's Page-my last hurrah! Many changes have taken place within the College of Family Physicians of Canada, and within the discipline of general practice/family medicine during the past 21 years. It has been an exciting and mostly rewarding experience to have been a part of these changes. As one might expect, my retirement has prompted numerous interviews by representatives of the medical media. Most have followed a pattern of reflecting on major changes that have occurred during my tenure; satisfactions that I have had; disappointments that I have experienced. In some instances, I have been invited to share my thoughts on where I see the College of Family Physicians and family medicine going in the future. Certain of these reflections have been recorded in this issue of CANADIAN FAMILY PHYSICIAN (page 1100); others in the Canadian Medical Association Journal, Medical Post, and in other publications. On the eve of retirement following 21 years as the College's chief executive officer, I am entitled to reflect for a while on past events and at the same time, anticipate a degree of immunity CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 from critics should I become unduly melancholy or preoccupied with the past. I might even be entitled to a glimpse into the future. In this, my final Executive Director's Page, I would like to be somewhat more personal than I have chosen to be during the several interviews that I have mentioned. I was motivated to leave the relative security of general practice 21 years ago (August 1964) to assume the office of the College's associate executive director for several very distinct reasons. I was greatly concerned by the serious trend away from general practice by medical students who at every turn were being encouraged by their specialist teachers to become specialists, not family doctors. I was concerned that this trend could only continue and worsen as long as there were no general practitioner teachers in our medical schools, to participate in the education of medical students, and to serve as role models-not to encourage all medical students to become family doctors, but to provide students with a proper perspective that would enable them to make an unbiased selection in their future professional careers. General practice in the fifties and sixties represented a major paradox. Like many of my colleagues, I found that the demands for my kind of doctor were so great that I had real difficulty in coping with these demands, and yet no attempt was being made to train and in turn perpetuate this kind of doctor. Medical schools were preoccupied with training undifferentiated physicians with the expectation that most students would take additional residency training and become specialists; the remainder would enter practice without the benefit of residency training to become "just a GP". Little wonder that some general practitioners of my vintage developed a professional inferiority complex. A second concem was that few individuals in a position of authority, and least of all medical educators, acknowledged this need, and were prepared to do something about it. It became abundantly clear that if change was to take place, family doctors themselves would have to assume the major responsibility for influencing this change. This acknowledgment by the many concerned and committed members of the College of Family Physicians of Canada who have contributed to the evolution of present day family medicine, and to the relatively secure position of today's family physician, is an object lesson that we must always keep before us. The needs as they concern family physicians may vary, but the mechanism for response will remain essentially unchanged. To a considerable degree, the future destiny of family physicians rests with family physicians themselves. "If it's to be-it's up to me." These earlier events have substantially influenced my own philosophy, and have encouraged me to impose a similar philosophy on the policy of the 905 College during the past two decades. At this stage in my professional career, people have been most generous in their acknowledgment of the contribution that I have made to the many changes that have taken place in family medicine. While I appreciate this acknowledgment, I would be less than honest if I did not concede that much of what has happened has been the result of the College's response to a legitimate and unmet need. It has been my good fortune to have been in the right place at the right time to-influence the factors necessary to effect this balance. But history has a way of repeating itself. If one looks critically at the present climate of family practice, and in particular at several well established trends, one gets the distinct feeling that one has been there before-a different plot and different actors, but the stage is essentially unchanged. Despite the substantial improvement in the status of family medicine, and the position of family physicians in our present health care system, storm clouds are on the horizon that command early and appropriate attention. By whom? Again, by family physicians. Who else? The hospital privileges of family physicians are being eroded, frequently by family physicians themselves, many of whom are disinterested in the hospital care of patients. An increasing number of family physicians are no longer providing complete obstetrical care: many have given up deliveries, others want no part of obstetrical care in any form. The withdrawal of many family physicians from the episodic care of patients is giving rise to an increasing number of episodic care clinics-"docs in the box". Too many family physicians are developing a pattern of practice that is essentially an ambulatory practice limited to an adult population. Others are developing special interest areas in emergency medicine, geriatrics and occupational medicine, at the expense of, rather than as an integral part of family practice. And while these voluntary changes in patterns of practice are taking place, other health professionals (notably the nurse) are standing in the wings anxious to take over responsibilities in family practice being vacated by the family physician. There are certainly reasons for these changes, but are they legitimate reasons, and do they stand up to critical scrutiny? Again, the relative strength of present day family medicine is the result of concerned family physicians having acknowledged and responded to legitimate unmet needs-needs that have been largely met by improving the ratio between consulting specialists and family physicians, and ensuring that family physicians are properly trained to provide a broad spectrum of primary, continuing and comprehensive care; family physicians who are people oriented as well as disease oriented; family physicians who are as interested in keeping people well as in treating people once they become ill. From my vantage point, this need continues to exist. My closing challenge to family physicians is to hold the line, stand up and be counted, and resist many of the increasing pressures on the system that are influencing significant changes in patterns of practice-frequently for the wrong reasons. At the same time, be an integral part of necessary and appropriate change and become involved to the degree that is necessary to ensure that these changes continue to be in the best interests of patient care, and at the same time provide the family physician with the essentials that are neces- sary for professional satisfaction. And finally, this Executive Director's Page provides me with an opportunity to publicly thank the legions of College members, specialist colleagues, members of other health professions, representatives of govemment, the pharmaceutical industry, and the many others with whom I have been associated during my time as the executive director of the College of Family Physicians of Canada. We have shared both disappointing and rewarding experiences, and I am deeply grateful for the support that I have enjoyed. There have been skirmishes along the way; battles won and battles lost, but on the average, I am quite confident that the decisions we have reached together have been in everyone's mutual interest. I feel very positive about stepping down as the College's Executive Director at this time. I consider myself singularly fortunate to have been involved in the life of the College during a period that historians will almost certainly record as one of the most significant periods in the College's history. I look forward to a change in direction that will enable me to maintain an interest in selected professional activity, while at the same time enjoying more leisure time with my family-an activity that has seemed to elude me for too many years. I have great confidence in the future of family medicine in this country, and am singularly impressed with the quality of young men and women who have made a commitment to family medicine as a professional career. My message to these younger family physicians is to stand tall; take pride in being a family doctor, in the knowledge that your future, and that of family medicine is in your own hands. Goodbye-au revoir. 1---- 906 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 capsules Go PRESCRIBING INFORMATION COMPOSITION: Each 5 mL (1 tsp) of GAVISCON liquid contains sodium alginate, 250 mg; aluminum hydroxide, 100 mg. Each GAVISCON tablet contains alginic acid, 200 mg; aluminum hydroxide, 80 mg; magnesium trisillicate, 20 mg. INDICATIONS: For symptomatic treatment of heartburn and oesophagitis associated with gastric acid reflux. This often accompanies ineffective lower oesophageal sphincter tone as in hiatus hernia, or pregnancy and nasogastric intubation. DOSAGE: Adults: 10 to 20 mL (2 to 4 tsp) of GAVISCON Liquid, or 2 to 4 GAVISCON tablets, 1 to 4 times daily, after meals and on retiring. ACTION: GAVISCON liquid or GAVISCON tablets, when chewed, produce a viscous, demulcent antacid foam which floats on the stomach contents serving as a protective barrier for the oesophagus against reflux of gastric contents. The alkaline foam readily flows into the oesophagus during reflux, aiding in the neutralization of refluxed gastric acids. Gaviscon also effectively reduces the frequency of reflux episodes. ADMINISTRATION: GAVISCON liquid may be followed by a sip of water, if desired. GAVISCON tablets must be chewed thoroughly,and may befollowed bya drinkof water or milk if desired. CONTRAINDICATIONS: There are no specific contraindications for GAVISCON LIQUID and GAVISCON FOAMTABS. See "Precautions' below. PRECAUTIONS: Each 5 mL of GAVISCON liquid contains approximately 30 mg and each GAVISCON tablet contains approximately 22 mg of Na+ which should be noted for patients on severely restricted sodium diets. The divalent cations of magnesium. and aluminum interfere with the absorption of tetracycline, iron and phosphate. In addition, oral magnesium may accumulate in the plasma of patients with impaired renal function. Each 5 ml of GAVISCON liquid contains 20 mg of sodium cyclamate, an artificial sweetener. Each GAVISCON tablet contains 1.2 g of sucrose which is equivalent to 4.7 calories. ADVERSE EFFECTS: Nausea, vomiting, eructation, flatulence. OVERDOSAGE: Should overdosage occur, gastric distention may result and is best treated conservatively. PRESENTATION: GAVISCON LIQUID is a light tan-coloured, pleasantly flavoured suspension supplied in plastic boftles of 340 mL. GAVISCON FOAMTABS are round creamywhite butterscotch flavoured tablets with the name 'GAVISCON" imprinted on one side and the lefter 'W" imprinted on the opposite side. Supplied in plastic boftles of 36 and 100 tablets. STORAGE PRECAUTIONS: GAVISCON liquid should be stored in a cool place. GAVISCON tablets should be stored in a dry place. REFERENCES: 1. Goodall, J.S., Orwin, J.M. and Imrie, M.J., A Combined pH and X-Ray Study of a Liquid Alginate/Antacid Formulation Using a Novel XRay Contrast Medium. Acta Therapeutica 3:141-153, 1977. 2. Beckloff, G.L., M.D., Chapman, J.H., M.D., and Shiverdecker, P., Objective Evaluation of an Antacid with Unusual Properties. J. of Clin. Pharm. 12:11-21, 1972. 3. In Vitro experiment, data on file, Winthrop Laboratories, Aurora, Ontario. 4. Stanciu, C. and Bennet, J.R., Alginate/Antacid in the Reduction of Gastro-Oesophageal Reflux. Lancet 1:109 111, 1974. 5. McHardy, G. and Balart, L., Reflux Esophagitis in the Elderly, with Special References to Antacid Therapy. J. Amer. Ger. Soc. 20:293-304, 1972. 6. Williams, D.L., Haigh, G.G. and Redfern, J.N., The Symptomatic Treatment of Heartburn and Dyspepsia with Liquid Gaviscon: A Multicentre General Practitioner Study. J. Int Med. Res. 7, 551, 1979. 7. McHardy, G., A Multicentric, Randomized Clinical Trial of Gaviscon in Reflux Esophagitis. Southern Med. J. 71, Supp. No. 1:16-21, 1978. 8. Chevrel, B., A Comparative Crossover Study on the Treatment of Heartburn and Epigastric Pain: Liquid Gaviscon and a Magnesium-Aluminum Antacid Gel. J. Int. Med. Res. 8:300-302, 1980. Wminrop Lahoratornes*); Division of SnerIingDmsgLnd.** Aurora, Ontarno L4G 3H6 ZRegistered User Reg, Trade Mark ItVF[ :PA tP The family medicine literature is wide and varied-and not all to be found in Index Medicus. On this page, our librarian Lynn Dunikowski provides synopses of articles from the current literature, full texts of which can be obtained from the Canadian Library of Family Medicine, Medical Library, University of Western Ontario, London N6A 5C1. Alternatively, local medical libraries or hospital libraries may be able to help. Child Development Houston HL, Davis RH. Opportunistic surveillance of child development in primary care: is it feasible? J R Coll Gen Pract 1985; 35:77-9. The authors postulate that effective developmental surveillance of children, in terms of detecting abnormalities and maternal counselling, can be done during ordinary consultations to identify problems and offer advice. Results presented are part of a more detailed study in progress to compare opportunistic methods of health surveillance with the traditional method of regular age-linked examinations provided by clinical medical officers. From a retrospective analysis of the medical records of 58 one year olds who had been registered with the study practice since their birth, the authors suggest, based upon attendance rates, that opportunistic assessment of development by a family physician or health visitor is more likely to encompass children most at risk than by assessment at clinics. Cholestasis Balistreri WF. Neonatal cholestasis. J Pediatr 1985; 106:171-84. The heterogeneous nature of diseases that have neonatal cholestasis (prolonged conjugated hyperbilirubinemia) as the first symptom creates challenges in evaluation and effective management. Potential causes of cholestasis in early life are diverse, and it is important for clinicians to recognize specific treatable metabolic or infectious entities rapidly in order to begin early, appropriate, and effective management. In many patients, however, it is difficult to pinpoint the precise nature of the aberration; this subset has been termed idiopathic obstructive infantile cholangiopathy; extrahepatic biliary atresia and neonatal hepatitis comprise the majority of the cases. Uncertainty arises because the nosology and diagnostic criteria vary and there is little information about the pathophysiologic basis of specific causes of neonatal cholestasis. This review discusses new concepts about the genesis of neonatal cholestasis and the implications of current methods of evaluation and management. Continuity of Care Goldberg HI, Dietrich AJ. The continuity of care provided to primary care patients. Med Care 1985; 3:63-73. The authors compared the continuity of care that family physicians, general internists, and medical subspecialists gave to their adult primary care patients. The 40 physicians in the study came from large, private, multispecialty practices in the San Francisco Bay area. The three types of physicians did not differ significantly in the degree of continuity provided, measured by the proportion of total visits to a patient's primary provider, each type providing about 80% of its primary care patients' visits. In contrast, the continuity scores of individual physicians ranged widely, from 57% to 98%. Proxy measures of case mix and physician expertise were found to be associated with differing scores. Detailed exploration of the subspecialists revealed that the lowest levels of continuity were given to patients with high user rates who did not carry a diagnosis in their primary physician's area of subspecialty expertise. The "generalist versus subspecialist" debate assumes that a physician' s training background is a major determinant of quality of primary care. This was not true in this study for providing CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 one aspect of quality: a high level of lihood of life-threatening intraperitoncontinuity. If factors other than spe- eal hemorrhage and may allow perforcialty or subspecialty designation are mance of more conservative surgery. generally found to be the important determinants of continuity, isolated Hearing Disorders changes in the proportion of physi- Wiet RJ, Monsell EM, Hotaling cians receiving generalist versus sub- AJ. Hearing and balance disorders: specialty training may have relatively how to recognize, when to refer. little impact on the level of continuity Postgrad Med 1985; 77:119-30. given to adult medical patients. Disorders of hearing and balance can be devastating to patients and disDysuria tressing to their families. The primary Carlson KJ, Mulley AG. care physician is generally the first to Management of acute dysuria. Ann examine these patients, and in many Intern Med 1985; 102:244-9. cases can provide definitive treatment. A decision-analysis model was de- The goal of this article is to help physiveloped to estimate the effects and cians recognize hearing and balance costs of alternative initial management disorders, select the proper treatment, strategies for women presenting with and determine when referral is approdysuria and pyuria. The authors com- priate. pared days of morbidity and direct medical costs of single- and multiple- Hepatitis B dose regimens of amoxicillin and tri- American Academy of Pediatrics. methoprim-sulfamethoxazole, and ex- Committee on Infectious Diseases. amined the cost-effectiveness of an Prevention of hepatitis B virus initial urine culture. infections. Pediatrics 1985; Varying assumptions were used for 75:362-4. prevalence of etiologic agents, treatInfants born to mothers who are hement efficacy, frequency of side effects, and duration of symptoms. Single-dose regimens were preferable to multiple-dose regimens of either drug, and trimethoprim-sulfamethoxazole was preferable to amoxicillin. Singledose trimethoprim-sulfamethoxazole therapy resulted in the fewest expected symptom-days (2.7) and the lowest expected cost ($54). The advantage of single-dose strategies in minimizing expected symptom-days resulted largely from the 75-100% increase in side effects reported with multipledose therapy. Obtaining initial urine cultures, in all patients reduced expected symptom-days by about 10% but increased cost by about 40%. patitis B surface antigen (HBsAg) positive are frequently infected with hepatitis B virus (HBV). Many of these newborns will become chronic carriers of HBV and will subsequently develop chronic liver disease. Recent studies have demonstrated that perinatal transmission can be prevented by immunizing the newborn. Recommendations are presented for managing infants at risk. Home Care Zimmer JG, Groth-Juncker A, McCusker J. A randomized controlled study of a home health care team. Am J Public Health 1985; 75:134-41. This report describes the findings of a randomized study of a new team approach to home care for homebound chronically or terminally ill elderly. The team includes a physician, nurse practitioner, and social worker who deliver primary health care in patients' homes (including physician house calls). Weekly team conferences assure coordination of patient care and Ectopic Pregnancy Quan MA, Johnson RA, Puffer JC. The diagnosis of ectopic pregnancy. Am Fam Physician 1985; 31:201-7 Ectopic pregnancy presents a major challenge to physicians providing services to women of reproductive age and is frequently an elusive diagnosis to make. Recent developments in pregnancy testing, pelvic ultrasound, and diagnostic laparoscopy have enabled physicians to make early and accurate diagnosis. Familiarity with these diagnostic aids is critical since prompt diagnosis will reduce the likeCAN. FAM. PHYSICIAN Vol. 31: MAY 1985 SHEE ROUTIN 977 the team is available for emergency consultation through a 24-hour telephone service. The team physician attends to the patient during hospitalizations. This approach was evaluated in a randomized experimental design study measuring its impact on health care use, functional changes in patients, and patient and caretaker satisfaction. Team patients had fewer hospitalizations, nursing home admissions, and outpatient visits than controls. They were more often able to die at home, if this was their wish and, as expected, they used more in-home services. Measured in weighted cost figures, overall costs were lower than for controls, but the difference was not statistically significant. Their functional abilities were the same as the controls, but they, and especially their informal caretakers in the home, expressed significantly higher satisfaction with the care received. Most texts on malignant melanoma (MM) have concentrated on descriptions of advance lesions. The inevitable corollary of this approach has been the very poor prognosis. Over the past decade, intensive clinicopathologic studies have clearly defined pathological features of prognostic significance, which allow a high degree of accuracy of prognostication, not only for groups of patients, but also for individuals. It is clear that patients with MM diagnosed at a late stage have five-year survival rates of about 40%, while those with lesions diagnosed earlier have a significantly improved five-year survival of over 85%. This article describes and illustrates the early signs of malignant melanoma. As early diagnosis of such tumors becomes a reality, the goal of accurately identifying precursor lesions, if they exist, also assumes new significance. Types of melanocytic nevi and their natural life history are described, and the evidence linking soMedical Education called precursor lesions with malignCurry L, Woodward C. A survey of ant melanoma is presented. postgraduate training for family practice. Can Med Assoc J 1985; Preventive Medicine 132:345-9. Fowkes FG, Williams T. Preventive The results of a survey of Canadian medicine during office visits to primary care physicians for the Cana- family physicians and other dian Medical Association (CMA's) primary care specialists in the Task Force on Education for the Provi- United States. Fam Pract Research sion of Primary Care Services are re- J 1984 Winter; 4:69-78. ported. Recent Canadian medical Family physicians frequently note school graduates in primary care praca special feature of family practice that tice reported that the three major trainand continuity of care is the ability to ing routes (rotating and mixed internships and family medicine residencies) initiate preventive care at appointprepared them differently for practice. ments made for other purposes. The Graduates of two-year family medi- extent that family physicians and other cine residencies were more satisfied primary care specialists in the U.S. with their preparation than were gradu- acted on this opportunity in 1978 was ates of the other major training routes. determined from the U.S. National A two- or three-year family medicine Ambulatory Medical Care Survey. Two types of consultation were exresidency was preferred by 50% of refor general medical examined:,visits of them 33% spondents, although only and visits for certain acute amination, had actually taken one of these routes. where prevenillnesses self-limiting There was considerable agreement in as part be care was not to tive expected the postrespondents' assessments of graduate education needed for primary of normal doctor-patient interaction. care practice. Survey results were con- General medical examinations were sistent with recommendations in the common, with the equivalent of one annual examination requested per final report of the CMA's task force. seven adults in the population. For visits doctors indicated that they these Melanoma more commonly performed diagnostic tests and prescribed drugs than carried MacKie RM. Clinical features of out "significant" counseling; less than of and the role melanoma cutaneous one percent of females received family nevi as precursor lesions. Clin in planning advice. Oncol 1984; 3:439-55. 978 The results suggest that high priority was not given to health promotion and disease prevention during patient consultations in primary care in the U.S. in 1978. Research Schmitt B. Research design for family physicians. Fam Pract Research J 1984; 4:15-26. With the growth of medical science and the explosion of medical literature, both practitioners and academics are continually confronted by practical issues in research design. Is one treatment more efficacious than another for a given disease? What is the disease's prognosis if not treated? How useful is a diagnostic test for ruling in or ruling out the disease and in what situations? These questions routinely arise in clinical practice. However, the pursuit of valid answers is often frustrated by incomplete, biased, or nongeneralizable data. This article acquaints readers with important aspects of research design necessary for critiquing medical literature or for planning a research project and examines major roadblocks to validity-bias and chance. An overview of research design and individual design models are described, along with potential weaknesses making them vulnerable to bias. Women Physicians Mitchell JB. Why do women physicians work fewer hours than men physicians? Inquiry 1984; 21:361-8. Because of the large public investment in medical education, it is important to understand why women physicians work significantly fewer hours than men physicians. National survey data on office-based private practice physicians were used to estimate hours and weeks worked for men and women physicians separately. shorter work weeks for women physicians are not the result of child care responsibilities, nor would higher earnings encourage them to work longer hours. Instead, results showed significant work reductions among married women physicians (but not men), implying subordination of careers by women where combined family incomes are high. CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Calendar JUNE S M T W T F 2 3 4 5 6 7 9 10 11 12 13 14 16 17 18 19 20 21 23 24 25 26 27 28 30 S 1 8 15 22 29 Send all information on courses to Calendar, 1200 Sheppard Ave. E., #507, Willowdale, ON. M2K 2S5, at least three months before the date of the course. Readers wishing to register or get further information on courses should write to the address listed under 'Information', and NOT to CANADIAN FAMILY PHYSICIAN. Recommended Courses 3 Peace Arch Hospital Rounds. Peace Arch Hospital, 10-12 Electrocardiogram Interpretation and ArrhythWhite Rock, BC. Information: Dr. Charles D. King, mia Management. Resorts International, Atlantic City, 2781 Gordon Ave., Crescent Beach, Surrey, BC. NJ. Information: Margaret A. Kleiger, International V4A 3J5 Medical Education Corporation, 64 Inverness Drive 3-5 Helping Children Cope with Death. King's College, East, Englewood, CO. 80112, U.S.A. (13 hours) London, ON. Information: Dr. J. D. Morgan, King's 10-14 Conference for International Relief Personnel College, 266 Epworth Ave., London, ON. N6A 2M3 Working with Refugees and Displaced Communities. (20 hours) Seneca College of Applied Arts and Technology, Leslie 5 Current Therapeutics. University of British Columbia, Campus, North York, ON. Information: Mildred G. Vancouver, BC. Information: Dr. P. Grantham, Dept. of Jarvis, Seneca College, Leslie Campus, 1255 Sheppard Ave. E., North York, ON. M2K 1E2 (25 hours) Family Practice, Mather Bldg., University of British Columbia, Vancouver, BC. V6T 1W5 (4 hours) 13 Update on Thyroid Disease and Diabetes. Mount Sinai 5 Sports Medicine Program. Chedoke Hospital, Hamilton, ON. Information: Program in Continuing Medical Education, McMaster University Health Sciences Centre, Room 1M6, 1200 Main St. West, Hamilton, ON. L8S 4J9 5-9 Ninth Western Canadian Conference on Family Practice. University of British Columbia, Vancouver, BC. Information: Alix Hirabayashi, Conference Administrator, School of Social Work, The University of British Columbia, Vancouver, BC. V6T iW5 6-7 Cancer Symposium '85. University Hospital, Saskatoon, SK. Information: Continuing Medical Education Office, 408 Ellis Hall, University of Saskatchewan, Saskatoon, SK. S7N OWO 6-7 Prediction of Drug Levels and Drug Monitoring. Madison, WI. Information: Sarah Z. Aslakson, Continuing Medical Education, University of Wisconsin, 465B WARF Building, 610 Walnut St., Madison, WI. 53705, U.S.A. 7 Intervention in Child Abuse. The Doctors Hospital, Toronto, ON. Information: Dr. Jess Goodman, 895 Bloor St. West, Toronto, ON. M6H 1L2 (2 hours) 7 Neurology Update. Inn on the Park, Toronto, ON. Infor.~~~~~~~U. mation: Organizing Secretary, Neurology Update, Room E-4623, Sunnybrook Medical Centre, 2075 Bayview Ave., Toronto, ON. M4N 3M5 (6 hours) 7-8 Advanced Trauma Life Support Course. University of British Columbia Hospital, Vancouver, BC. Informa(loperamide) tion: Dr. Norman E. Hamilton, #403-145 East 13th St., North Vancouver, BC. V7L 2L4 10 Peace Arch Hospital Rounds. Peace Arch Hospital, White Rock, BC. Information: Dr. Charles D. King, PAAB iJANSSEN 11073E 'Trademark PHARMACEUTICA CJanssen 1985 2781 Gordon Ave., Crescent Beach, Surrey, BC. V4A 3J5 DON'T LEAVE HOME WITHOUT IT IMODIUM For travellers diarrhea CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 981 Hospital, Toronto, ON. Information: Ms. Carol Duncan, Dept. of Family and Community Medicine, 222 Elm St., Suite 101, Toronto, ON. M5G iK5 13-14 Child Abuse-Everyone's Concern. Royal York Hotel, Toronto, ON. Information: Ingrid Norrish, Program Manager, Professional and Management Development, Humber College, Box 1900, Rexdale, ON. M9W 5L7 14 Between Therapist and Client: Views of the Therapeutic Relationship. Kitchener-Waterloo Hospital, Kitchener, ON. Information: Dr. D. Barnes, KitchenerWaterloo Hospital, 835 King St., West, Kitchener, ON. N2G 1G3 (6½/2 hours) 15-21 Seventh Annual Conference on Sexuality: Love, Sex and Intimacy. University of Guelph, Guelph, ON. Information: Dr. E. Herold, Family Studies, University of Guelph, Guelph, ON. NIG 2W1 (11/2 hours) 16-18 New Developments in Child and Adolescent Mental Health: Clinical, Educa,ional, Socio-Legal and Research Considerations. Westin Hotel, Ottawa, ON. Information: Dr. C. Stavrakaki, Royal Ottawa Hospital, 1145 Carling Ave., Ottawa, ON. K1Z 7K4 (8 hours) 17 Peace Arch Hospital Rounds. Peace Arch Hospital, White Rock, BC. Information: Dr. Charles D. King, 2781 Gordon Ave., Crescent Beach, Surrey, BC. V4A 3J5 19-21 Childbirth Educators' Workshop. McMaster University, Hamilton, ON. Information: Program in Continuing Medical Education, McMaster University Health Sciences Centre, Room 1M6, 1200 Main St. West, Hamilton, ON. L8S 4J9 21 Disorders of Sleep and Wakefulness. University Hospital, Saskatoon, SK. Information: Continuing Medical Education Office, 408 Ellis Hall, University of Saskatchewan, Saskatoon, SK. S7N OWO 21 Medicine. York County Hospital, Newmarket, ON. Information: Dr. E. Palermo, 93 Rutledge Ave., Newmarket, ON. L3Y 5T5 (1½/2 hours) 21 Pharmacological Management of Chronic Disease Induced Depression. University of Ottawa, Ottawa, ON. Information: Education Department, Royal Ottawa Regional Rehabilitation Centre, 505 Smyth Road, Ottawa, ON. K I H 8M2 (4 hours) 23-24 Pediatric Emergencies for Emergency Physicians. The Hospital for Sick Children, Toronto, ON. Information: Dr. James C. Fallis, The Hospital for Sick Children, 555 University Ave., Toronto, ON. M5G lX8 (13/2 hours) 23-Jul 18 New Horizons: Professional Development Seminar. Gabriola Island, BC. Information: Dr. J. McKeen, PD Seminars, Davis Road, Gabriola Island, BC. VOR IXO 24 Peace Arch Hospital Rounds. Peace Arch Hospital, White Rock, BC. Information: Dr. Charles D. King, 2781 Gordon Ave., Crescent Beach, Surrey, BC. V4A 3J5 26 Inflammatory Bowel Disease. McMaster University, Hamilton, ON. Information: Program in Continuing Medical Education, McMaster University Health Sciences Centre, Room lM6, 1200 Main St. West, Hamilton, ON. L8S 4J9 28-30 Electrocardiogram Interpretation and ArrhythCAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Information: Margaret A. Kleiger, International Medical Education Corporation, 64 Inverness Drive East, Englewood, CO. 80112, U.S.A. (13 hours) Other Courses 2-5 Eighty-fifth Annual Meeting of the Canadian Lung Association and the Annual Scientific Meetings of the Canadian Nurses' Respiratory Society and the Physiotherapy Section of the Canadian Lung Association. Skyline Hotel, Ottawa, ON. Information: Mr. A. Les McDonald, Health Education Coordinator, Canadian Lung Association, 75 Albert St., Suite 908, Ottawa, ON. KIP 5E7 5 First National Advanced Life Support Competition. Westin Hotel, Ottawa, ON. Information: Advanced Coronary Treatment Foundation, 2625 Queensview Drive, Ottawa, ON. K2A 3Y4 2-8 Cancer in Children. London, U.K. Information: The Representative, The British Council, c/o British High Commission, 80 Elgin St., Ottawa, ON. KIP 5K7 3-7 Ninth Annual Occupational and Safety Workshop Program for a Better Work Environment. Sydney, NS. Information: Mr. Sheldon Maclnnes, Program Coordinator, Chair of Occupational Health and Safety, University College of Cape Breton, P.O. Box 5300, Sydney, NS. B1P 6L2 (lopemamide) For acute diarrhea I1072E CJanssen JANSSEN 1(PHARMACEUTICA rademark 983 3-8 Health Care of the Geriatric Patient. Charleston, SC. Kingston, ON. K7L 3N6 Information: Dr. Ben Goodman, Program Coordinator, 20 Critical Care and Medical Management of the Department of Family Medicine, Medical University of Cancer Patient. Roswell Park Memorial Institute, BufSouth Carolina, 171 Ashley Ave., Charleston, SC. falo, NY. Information: Gayle Bersani, RN, Coordinator 29425, U.S.A. of Continuing Education Programs, Education Depart5 Sexual Abuse of Children. Donald Gordon Centre, ment, Roswell Park Memorial Institute, 666 Elm St., Kingston, ON. Information: Office of Continuing Medical Education, Queen's University, Kingston, ON. K7L 3N6 5-7 A Practical Course in Emergency Medicine. Montreal General Hospital, Montreal, PQ. Information: Centre for Continuing Medical Education, McGill University, 1110 Pine Ave. West, Montreal, PQ. H3A 1 A3 6-8 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station Q, Toronto, ON. M4T 2M1 6-8 Annual Scientific Assembly of the Canadian Association of Emergency Physicians. Westin Hotel, Ottawa, ON. Information: Dr. Anna Malawski, CAEP Assembly, Emergency Department, Ottawa General Hospital, 501 Smyth Road, Ottawa, ON. K1H 8L6 9-15 Growth Areas in Oncology. London, U.K. Information: The Representative, The British Council, c/o British High Commission, 80 Elgin St., Ottawa, ON. KlP 5K7 10-15 Family Practice Review. Estes Park, CO. Information: Office of Postgraduate Medical Education, The University of Colorado School of Medicine, 4200 East Ninth Ave., Box C-295, Denver, CO. 80262, U.S.A. 11-16 Combined European Congress of General Practice/Family Medicine, 33rd International Congress of General Practice (SIMG) and 19th German Congress of General Practice and Family Medicine (DEGAM). Maritim Park Hotel, Mannheim/Heidelberg, West Germany. Information: Dr. Hans Hamm, President, German Association of General Practice, D-2100 Hamburg 90, Alter Postweg 20, West Germany. 14-15 Advanced Trauma Life Support Instructors' Course. Universite de Sherbrooke, Sherbrooke, PQ. Information: Centre de formation continue, Faculte de medecine, Universite de Sherbrooke, 3001-12e Avenue nord, Sherbrooke, PQ. JIH 5N4 14-15 Sexual Dysfunctions. Montreal General Hospital, Montreal, PQ. Information: Centre for Continuing Medical Education, McGill University, 1110 Pine Ave. West, Montreal, PQ. H3A 1A3 16-20 International Conference on Oceans-Safety and Health: Issues Affecting Insurability. Sydney, NS. Information: Prof. Lino Polegato, Director, Division of Engineering, University College of Cape Breton, P.O. Box 5300, Sydney, NS. BIP 6L2 17-21 Symposium on the Temporomandibular Joint. Maui Mariott Hotel, Maui, Hawaii. Information: University of California, San Francisco, CA. 94143, U.S.A. 17-22 Canadian Summer School in Occupational Health. Quebec, PQ. Information: Canadian Summer School in Occupational Health, Faculte de Medecine, Universite Laval, Sainte-Foy, PQ. GiK 7P4. 19 Important Pediatric Issues in Family Medicine. Hotel Dieu Hospital, Kingston, ON. Information: Office of Continuing Medical Education, Queen's University, CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Buffalo, NY. 14263, U.S.A. 20-22 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station Q, Toronto, ON. M4T 2M1 21 Bioethics: Daily Implications for Health Care Professionals. Ottawa, ON. Information: Social Work Department, Ottawa Civic Hospital, 1053 Carling Ave., Ottawa, ON. K1Y 4E9 21-23 Advanced Cardiac Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station Q, Toronto, ON. M4T 2M1 21-23 Third Annual Symposium on Pediatric Nutrition. Montreal, PQ. Information: Dr. R. K. Chandra, Janeway Child Health Centre, St. John's, NF. AlA 1R8 23-26 Forty-Eighth Annual Meeting of the Canadian Ophthalmological Society. Harbour Castle Hilton Hotel, Toronto, ON. Information: Canadian Ophthalmological Society, 1867 Alta Vista Drive, P.O. Box 8844, Ottawa, ON. K I G 3J2 23-26 Seventeenth Annual Conference of the Canada Safety Council. Hotel Newfoundland, St. John's, NF. IMODIUM* (loperamide) For diarrhea in children I11059E CJanssen 1986 EJANSSEN PHARMACEUTICA PAAB 'rdemark 985 Information: Canada Safety Council, 1765 St. Laurent Blvd., Ottawa, ON. KIG 3V4 23-28 Twenty-First Annual Northern Michigan Summer Conference: An Update on Common Clinical Concerns. Hilton Shanty Creek, Bellaire, MI. Information: Dove Margenau, The Office of Continuing Medical Education, The Towsley Centre, Box 057, The University of Michigan Medical School, Ann Arbor, MI. 48109, U.S.A. JULY Recommended Courses 5-9 Electrocardiogram Interpretation and Arrhythmia Management. Westin Ilkai, Oahu, Hawaii. Informa1 2 3 4 5 6 tion: Margaret A. Kleiger, International Medical Education Corporation, 64 Inverness Dr. East, Englewood, 7 8 9 10 11 12 13 CO. 80112, U.S.A. (13 hours) 14 15 16 17 18 19 20 8-10 Masters Games Sports Medicine Symposium. Hil21 22 23 24 25 26 27 ton Harbour Castle Hotel, Toronto, ON. Information: Dr. Robert Brock, Ontario Medical Association, 240 St. 28 29 30 31 George St., Toronto, ON. M5R 2P4 (24 hours) 10-16 Tenth International Congress of Hypnosis and Psychosomatic Medicine. Harbour Castle Hilton, Recommended Courses ON. Information: 10th International Congress Toronto, 12-14 Electrocardiogram Interpretation and Arrhyth200 St. Clair Ave., West, Suite 402, Secretariat, mia Management. Fort Magruder Inn, Williamsburg, M4V lRl (25 hours) ON. Toronto, VA. Information: Margaret A. Kleiger, International Workshop on Stress for Physicians and 23-25 Weekend Medical Education Corporation, 64 Inverness Drive Gabriola Island, BC. InforHaven-by-the-Sea, Spouses. East, Englewood, CO. 80112, U.S.A. (13 hours) PD Seminars, Davis Road, Dr. McKeen, Jock mation: 15-26 Fundamental Concepts in Addictions. School for hours) lXO (12 VOR BC. Island, Gabriola Addiction Studies, Toronto, ON. Information: Dr. DonOther Courses ald E. Meeks, Director, School for Addiction Studies, 8 4-10 Thirty-Fourth International Congress on AlcoholMay St., Toronto, ON. M4W 2Y1 (22 hours) ism and Drug Dependency. Calgary, AB. Information: 17-18 Fifth Annual Common Emergency Care ProbTom Wispinski, Congress Secretariat, #803, 10109-106 lems. Sheraton Inn and Conference Centre, Madison, AB. T5J 3L7 Edmonton, St., WI. Information: Sarah Z. Aslakson, Continuing MediMedicine. Lake Tahoe, NV. InformaWilderness 12-16 WARF 465b of Wisconsin, cal Education, University Medical Education, M-017, Office of Continuing tion: Bldg., 610 Walnut St., Madison, WI. 53705, U.S.A. Diego School of Medicine, California, San University of ( 12 hours) S M T W T F S La Jolla, CA. 92093, U.S.A. 14-16 Second International Conference on Illness BeOther Courses havior. Roy Thomson Hall, Toronto, ON. Information: 14-19 Twenty-Sixth Annual Institute on Addiction Behavior Conference, c/o Gut Behaviour International Studies. Hamilton, ON. Information: Kathryn Irwin, Toronto Western Hospital, 399 Bathurst St., Unit, Alcohol & Drug Concerns, 11 Progress Ave., Suite 200, M5T 2S8 ON. Toronto, MIP 4S7 ON. Scarborough, 14-26 Progress in Dermatological Therapy. London, U.K. Information: The Representative, The British Council, c/o British High Commission, 80 Elgin St., Ottawa, ON. K1P 5K7 15-19 Update Course for Isolated Practitioners. Queensland, Australia. Information: The Secretary, The Royal Australian College of General Practitioners, Queensland Faculty, Private Box 3, Eildon Post Office, Windsor 4030, Australia. 26-28 The Second International Congress on Pre- and Perinatal Psychology. Town and Country Convention Centre, San Diego, CA. Information: Congress Secretariat, 9091/2 Hayes Ave., San Diego, CA. 92103, U.S.A. 986 SEPTEMBER S M T W T F S 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 4 PRESCRIBING INFORMATION > Recommended Courses 13-15 Marriage and the Stress of the Eighties. Inn on the Park, Toronto, ON. Information: Dr. Donald M. DenCOMPARATIVE SINGLE DOSE ABSORPTION DATA mark, 4078 Petrolia St., Petrolia, ON. NON IRO (9 Category/Product Peak Serum Concentrations of hours) Erythromycin Base mcg/mL Erythromycin Base 19-21 Annual Scientific Assembly and Business Meeting (Ernapslated Enteric-| ERY coated Pellets) of the Saskatchewan Chapter of The College of FamErythromnycn1 1.15 ily Physicians of Canada, Ramada Renaissance Hotel, tablets), Saskatoon, SK. Information: Mrs. Frances Maksymiw, S| t>| (Er¶teric-coated tabetS2 J 110.73 Administrative Secretary, Saskatchewan Chapter, CFPC, Box 217, Rockglen, SK. SOH 3R0 Erythromycin Salt 20 Biomechanical Analysis of the Foot and Ankle. Toronto East General and Orthopedic Hospital, Toronto, ON. Information: Susan Johnson, Director, RehabilitaErythromycin Ester tion Medicine Dept., Toronto East General and OrthopeErythomycvin dic Hospital, 825 Coxwell Ave., Toronto, ON. M4C 3E7 (6 hours) C<0.51 20-24 Annual Scientific Assembly of the British ColumReerereces. of Hospital Ptharmacy. 1203 Vo. 37, Sept 1980 Aenerican bia Chapter of The College of Family Physicians of FraserL 199 2. id 3. Physicsn Desk Reterence.ed 35. Oraddl, New Jersey. Medical Ecoremics Company, a Litton dtotson. 1 981 p. 705. Canada. Delta Mountain Inn, Whistler, BC. Informa4. bid pp 830. 5. Sande M.A., Mandell G.L. Antimicrobal agents, Giloan A.G., Goodman LS.. and Giknan A. (ofs): Goodmanand Glman's. The Pharmacolog,al Basis of Therapeutics, ed 6. New York. MacmsllBa Publisheg Co. Inc. 1980. pp 1222-1248. tion: Ms. Bev Kulyk, Administrator, British Columbia Chapter, CFPC, 1807 West 10th Ave., Vancouver, BC. Indications: The treatment of the following infections when caused by susceptible strains of micro-organisms: upper and lower respiratory tract infections; skin V6J 2A9 and soft tissue infections; gonorrhea; syphilis; Legionnaires' disease; pertussis; diphtheria; short term prophylaxis of bacterial endocarditis in patients hypersen- 21 International Symposium on the Clinical Aspects of Immunology. Parkway Inn, Cornwall, ON. Informasitive to penicillin. tion: Dr. Margaret Macaulay, 125 First St. East, CornContraindicatlons: Known hypersensitivity to erythromycin. Precautions: The possibility of superinfection caused by overgrowth of nonwall, ON. K6H 1K8 (8 hours) susceptible bacteria or fungi should be kept in mind during prolonged or repeated 21-22 Pediatrics Update. Pillar and Post Inn, Niagara-ontherapy with ERYC. In such instances, the administration of ERYC should be discontinued and appropriate treatment instituted if necessary. the-Lake, ON. Information: Program in Continuing Erythromycin is excreted principally by the liver. Caution'should be exercised when Medical Education, McMaster University Health administering ERYC to patients with impaired hepatic function. Sciences Centre, Room 1M6, 1200 Main St. West, The concomitant administration of erythromycin and high doses of theophylline may be associated with increased serum theophylline levels and possible Hamilton, ON. L8S 4J9 theophylline toxicity. The dose of theophylline may require reduction while pa- 22-25 Orthopedic Medicine-Cyriax Techniques: Part tients are receiving ERYC. C. Calgary, AB. Information: Catherine McGinley, FacThe safety of ERYC for use in pregnant patients has not been established. There is placental transfer and excretion of erythromycin in breast milk. ulty of Continuing Education, The University of CalAdverse Effects: The most frequent side effects are gastrointestinal and are dosegary, 2500 University Drive N.W., Calgary, AB. related. They include nausea, vomiting, abdominal pain, diarrhea and anorexia. T2N 1N4(14hours) Symptoms of hepatic dysfunction and/or abnormal liver function test results may 23-25 Ontario Public Health Association's Annual Meetoccur. ing-Working Together: Building Coalitions for Serious allergic reactions have been extremely Infrequent. Mild allergic reactions such as rashes with or without pruritis, urticaria, bullous eruptions Public Health. Sheraton Centre, Toronto, ON. Informaand eczema have been reported with erythromycin. tion: Dr. Trevor Hancock, 64 Merton St., Toronto, ON. Dosage: The most reliable serum levels of erythromycin are achieved when ERYC l (14 hours) M4S IA capsules are taken one hour before meals or in the fasting state. USP E RYC*Erythmmycin, Encapsulated enteric-coated pellets ER C [_ J (Film coted Estoysucate 1 (Fiim coatdlablets} 1. > Journal p. Donald G. p. 1 in Adults: The usual dose is 250 mg (one capsule) every 6 hours taken one hour before meals. If twice-a-day dosage is desired, the recommended dose is 500 mg (two 250 mg capsules) every 12 hours. Twice-a-day dosing is not recommended when doses larger than 1 g daily are administered. In the treatment of streptococcal infections, a therapeutic dosage of erythromycin should be administered for at least 10 days. In continuous prophylaxis of streptococcal infections in persons with a history of rheumatic heart disease, the dose is 250 mg twice-a-day. For the prevention of bacterial endocarditis due to alpha-hemolytic streptococci in penicillin-allergic patients with valvular heart disease who are to undergo dental procedures or surgical procedures of the upper respiratory tract, the recommended dose for adults is 500 mg 1.5 to 2 hours prior to the procedure and then 500 mg every 8 hours for at least 3 days. Primary syphilis: 2-4 grams per day for a period of 10-15 days. Intestinal ameblasis: 250 mg four times daily for 10-15 days for adults. Legionnaire's disease: Although optimum doses have not been established doses used in reported clinical data were 1 to 4 g daily in divided doses. How supplied: ERYC capsule is a two-tone clear and orange opaque capsule, each containing 250 mg erythromycin base as enteric-coated pellets. Available in bottles of 100. Store at a room temperature below 30°C. Protect from moisture and light. Full prescribing information available on request. PARKE-DAVIS Parke-Davis Canada Inc., Scarborough, Ontario 0Reg. 988 T.M. Parke, Davis & Company, Parke-Davis Canada Inc., auth. user " Other Courses 5-7 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station 'Q", Toronto, ON. M4T 2M1 8-11 Canadian Pediatric Society Annual Meeting. Hyatt Regency Hotel, Vancouver, BC. Information: Dr. Joe Clarke, Director, Genetic & Metabolic Disease Program, Hospital for Sick Children, 555 University Ave., Toronto, ON. M5G 1X8 8-12 Fourth International Congress on Medicine and Law: Hospital Laws-Procedures & Ethics. Israel. Information: Society of Medicine & Law in Israel, P.O.B. 394, Tel Aviv 61003, Israel. 9-12 Conjoint Meeting of the Royal College of Physicians and Surgeons and The Canadian Thoracic Society. Vancouver, BC. Information: Mr. A. Les McDonald, Health Education Coordinator, Canadian Lung Association, 75 Albert St., Suite 908, Ottawa, ON. K1P SE7 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 9-13 The 1985 National Conference of the Occupational Medical Association of Canada. Calgary, AB. Information: 1985 Occupational Medical Association of Canada Conference, c/o Margaret-Anne Stroh, Conference Office, Faculty of Continuing Education, University of Calgary, 2500 University Dr. N.W., Calgary, AB. T2N 1N4 16-21 Challenge '85: Joint National Convention Pacific Regional Conference of WONCA and Annual General Meeting and National Convention of the Royal Australian College of General Practitioners. Regent Hotel, Melbourne, Australia. Information: Mrs. Pat Palmer, Challenge '85, Victoria Faculty, The Royal Australian College of General Practitioners, "Trawalla", 22 Lascelles Ave., Toorak, Victoria 3142, Australia. 16-21 Thirty-Fourth International Congress on General Practice of the Societas Internationalis Medicinae Generalis. Klagenfurt, Austria. Information: Mrs. Sigrid Taupe, Secretariat of the Societas Internationalis Medicinae Generalis, A-9020 Klagenfurt, Bahnhofstrabe 22, Austria. 19-21 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station "Q", Toronto, ON. M4T 2M1 19-21 The Challenge of the Lumbar Spine. Amfac Hotel, Minneapolis, MN. Information: Devora J. Segal, Program Coordinator, The Institute for Low Back Care, 2737 Chicago Ave., Minneapolis, MN. 55407, U.S.A. 20 A Day in Family Medicine. Hotel Dieu Hospital, Kingston, ON. Information: Dr. C. Johnson, Family Medicine Centre, 220 Bagot St., P.O. Bag 8888, Kingston, ON. K7L 5E9 26-28 Seventh Annual Frontiers in Nutrition. Mariner's Inn, Hilton Head Island, SC. Information: Division of Continuing Education, Medical College of Georgia, Augusta, GA. 30912, U.S.A. 16 Annual Day in Obstetrics and Gynecology. Henderson Hospital, Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 16-20 Canadian Association of Gerontology Program. Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 24-26 Annual Scientific Assembly of the Maritime Chapters of the College of Family Physicians of Canada. Saint John, NB. Information: Mrs. Mavis Alain, Executive Secretary, New Brunswick Chapter, CFPC, New Brunswick Medical Society, Suite 209, Priestman Centre, 565 Priestman St., Fredericton, NB. E3B 5X8 30 Occupational Health Program. Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room IM6-,+Iamilton, ON. L8S 4J9 Other Courses 1-4 International Exhibition and the German Congress for Safety and Medical Care at Work. Dusseldorf, West Germany. Information: P.R. Charette Inc., 5890 Monkland Ave., Suite 206, Montreal, PQ. H4A 1G2 3-5 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station "Q", Toronto, ON. M4T 2M1 4-5 Current Psychiatric Issues in Primary Care. The Marriott Hotel, San Antonio, TX. Information: Medical School Continuing Education Services, University of Texas Health Science Centre, 7703 Floyd Curl Dr., San Antonio, TX. 78284, U.S.A. 7-11 Update Course for General Practitioners. Queensland, Australia. Information: The Secretary, The Royal Australian College of General Practitioners, Queensland Faculty, Private Box 3, Eildon Post Office, Windsor 4030, Australia. 17-19 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management ConT F T S M W S sultants Ltd., P.O. Box 224, Postal Station "Q", Toronto, ON. M4T 2M1 1 2 3 4 5 18 Stroke Rehabilitation: Present Trends and Future 6 7 8 9 10 11 12 Directions. Jewish Rehabilitation Hospital, Laval, PQ. Information: Dr. Henry Coopersmith, 3205 Place Alton 13 14 15 16 17 18 19 Goldbloom, Laval, PQ. H7V 1R2 20 21 22 23 24 25 26 20-Nov 1 Infertility. London, U.K. Information: The Representative, The British Council, c/o British High Com27 28 29 30 31 mission, 80 Elgin St., Ottawa, ON. KIP 5K7 21-22 The Immediate and Long-Term Effects of Separation and Divorce on Parents' Children: New Findings Recommended Courses and New Interventions. Westin Hotel, Toronto, ON. 9 Rheumatology Update. Stratford, ON. Information: Ms. Information: Gilda Ennis, 53 Lisa Cres., Thomhill, ON. Laurie Woltman, Program In Continuing Medical EduL4J 2N2 cation, McMaster University H.S.C., 1200 Main St. 23-24 The Immediate and Long-Term Effects of SeparaWest, Room 1M6, Hamilton, ON. L8S 4J9 tion and Divorce on Parents' Children: New Findings 12-13 Laboratory Medicine Seminar. Hamilton Convenand New Interventions. Four Seasons Hotel, Montreal, tion Centre, Hamilton, ON. Information: Ms. Laurie PQ. Information: Gilda Ennis, 53 Lisa Cres., Thornhill, Woltman, Program In Continuing Medical Education, ON. L4J 2N2 McMaster University H.S.C., 1200 Main St. West, 24-25 Living with the Reality of Diabetes: Twelfth AnRoom 1M6, Hamilton, ON. L8S 4J9 OCTOBER 990 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 nual Meeting and Workshop. Hyatt Regency Hotel, Administrative Director, Ontario Chapter, CFPC, 4000 Montreal, PQ. Information: Ms. Gilda Bastasi, ConferLeslie St., Willowdale, ON. M2K 2R9 ence Chairperson, Montreal General Hospital, 1650 Cedar Ave., Room 200A, Montreal, PQ. H3G 1A4 Other Courses 31-Nov 2 Advanced Trauma Life Support Provider 14-16 Advanced Trauma Life Support Provider Course. Course. Sunnybrook Medical Centre, Toronto, ON. InSunnybrook Medical Centre, Toronto, ON. Information: formation: Emergency Department Physicians ManageEmergency Department Physicians Management Conment Consultants Ltd., P.O. Box 224, Postal Station sultants Ltd., P.O. Box 224, Postal Station "Q', "Q", Toronto, ON. M4T 2M1 Toronto, ON. M4T 2M1 20-23 REHA 85: The International Fair and Forum on Rehabilitation Aids for the Disabled. Dusseldorf, West Germany. Information: P.R. Charette Inc., 5890 Monkland Ave., Suite 206, Montreal, PQ. H4A 1G2 28-30 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: T F S T W M S Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station "Q", 1 2 Toronto, ON. M4T 2M1 NOVEMBER 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 DECEMBER Recommended Courses 1 Colorectal Cancer. Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 2-4 Toronto Rehabilitation Centre's Third International Symposium on Ischemic Heart Disease, Exercise, and Related Topics. Royal York Hotel, Toronto, ON. Information: Dr. Terence Kavanagh, 345 Rumsey Road, Toronto, ON. M4G 1R7 (20 hours) 6 Twelfth Annual Day in Medicine. Royal Connaught Hotel, Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 7-8 Saskatchewan Medical Association Annual Meeting. Saskatoon, SK. Information: Continuing Medical Education Office, 408 Ellis Hall, University of Saskatchewan, Saskatoon, SK. S7N OWO 12-13 Computers in Medicine. Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 20 Minor Office Procedures. Hamilton, ON. Information: Ms. Laurie Woltman, Program In Continuing Medical Education, McMaster University H.S.C., 1200 Main St. West, Room 1M6, Hamilton, ON. L8S 4J9 27-30 Twenty-Third Annual Scientific and Business Meeting of the Ontario Chapter of The College of Family Physicians of Canada. Hilton Harbour Castle Hotel, Toronto, ON. Information: Mrs. Marcia Barrett, 2 992 S M 1 8 15 22 29 2 9 16 23 30 F S 3 4 5 6 10 11 12 13 17 18 19 20 24 25 26 27 31 7 14 21 28 T W T Recommended Courses 5-6 Infectious Diseases '85. University Hospital, Saskatoon, SK. Information: Continuing Medical Education Office, 408 Ellis Hall, University of Saskatchewan, Saskatoon, SK. S7N OWO 26-30 Allergy, Drugs and Drug Allergies. Royal Lahaina Resort, Kaanapali, Maui, HI. Information: Joe Harrison, Symposium Maui, Inc., P.O. Box 10185, Lahaina, Maui, HI. 96761, U.S.A. (13½/2 hours) Other Courses 12-14 Advanced Trauma Life Support Provider Course. Sunnybrook Medical Centre, Toronto, ON. Information: Emergency Department Physicians Management Consultants Ltd., P.O. Box 224, Postal Station "Q", Toronto, ON. M4T 2M1 15-19 Fourth International Congress on Medicine and Law: Drugs and Alcohol. Israel. Information: Society of Medicine and Law in Israel, P.O.B. 394, Tel Aviv 61003, Israel. _AN. FAM. PHYI -V-l. 31: MAY 198 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 PRESCRIBING INFORMATION floctafenine 200 mg tablets THERAPEUTIC CLASSIFICATION: Analgesic ACTION: IDARAC (floctafenine) is an anthranilic acid derivative which has analgesic and anti-inflammatory properties. Floctafenine has been shown to inhibit in vitro biosynthesis of prostaglandins PGE2 and PGF2a. Gastro-intestinal bleeding determined by daily fecal blood loss was shown in one clinical trial to be approximately 1.2 ml after 1600 mg/day of floctafenine compared to 10.4 ml after 2400 mg/day of acetylsalicylic acid. In normal volunteers, IDARAC was well absorbed after oral administration and peak plasma levels were attained 1-2 hours after administration and declined in a biphasic manner with an initial (0 phase) half-life of approximately 1 hour and a later (fA phase) half-life of approximately 8 hours. Floctafenine and its metabolites do not accumulate following oral administration of multiple doses. After oral and intravenous administration of 14C labelled IDARAC, urinary excretion accounted for 40% and fecal and biliary excretion accounted for 60% of the recovered radioactivity The main urinary metabolites are floctafenic acid and its conjugate with minimal amounts of free floctafenine. INDICATIONS: IDARAC (floctafenine) is indicated for short-term use in acute pain of mild and moderate severity CONTRAINDICATIONS: IDARAC (floctafenine) is contraindicated in patients with peptic ulcer or any other active inflammatory disease of the gastrointestinal tract and in patients who have demonstrated a hypersensitivity to the drug. WARNINGS: USE IN PREGNANCY: The use of IDARAC (floctafenine) in women of childbearing potential requires that the likely benefit of the drug be weighed against the possible risk to the mother and fetus. Use of the drug in women who are nursing is not recommended. USE IN CHILDREN: The safety and efficacy of IDARAC in children have not been established and therefore is not recommended. The safety and efficacy of longterm use of IDARAC have not been established. PRECAUTIONS: IDARAC (floctafenine) should be used with caution in patients with impaired renal function. In clinical trials with IDARAC, dysuria without apparent changes in renal function was reported. It has not been established whether dysuria is related to dose and or duration of drug administration. Patients taking anticoagulant medication may be given IDARAC with caution. Alterations in prothrombin time have been observed only in clinical trials where the administration of IDARAC was extended beyond two weeks. IDARAC should be used with caution in patients with a history of peptic ulcer or other gastro-intestinal lesions. ADVERSE REACTIONS: The most commonly occurring side effects reported during IDARAC (floctafenine) therapy were: CENTRAL NERVOUS SYSTEM: Drowsiness, dizziness, headache, insomnia, nervousness, irritability. GASTRO-INTESTINAL SYSTEM: Nausea, diarrhea, abdominal pain or discomfort, heartbum, constipation, abnormal liver function, gastro-intestinal bleeding. UROGENITAL SYSTEM: Dysuria, burning micturition, polyuria, strong smelling urine, urethritis and cystitis. ALLERGIC-TYPE REACTIONS: Maculopapular skin rash, pruritis, urticaria, redness and itching of the face and neck. SYMPTOMS AND TREATMENT OF OVERDOSE: No cases of overdose have been reported with IDARAC (floctafenine). In a case of overdose standard procedures to evacuate gastric contents, maintain urinary output and provide general supportive care should be employed. DOSAGE AND ADMINISTRATION: The usual adult dose of IDARAC (floctafenine) is 1 to 2 tablets (200 to 400 mg), 3 to 4 times per day as required. The maximum recommended daily dose is 1200 mg. IDARAC is recommended for short-term management of acute pain. The tablets should be taken with a glass of water IDARAC is not recommended for use in children. AVAILABILITY: Each tablet of IDARAC contains 200 mg of floctafenine. Tablets are biconvex, cylindrical, yellowish-white, scored on one side with D57 above the breakline and a distinctive logo on the reverse side. IDARAC is available in botties of 100 tablets. Store at room temperature, protected from light. IDARAC is a Schedule F (prescription) drug. Product monograph upon request. VithopterigDus.', piviio o References 1. Valdez-Dapena MA. Sudden infant death syndrome: a review of the medical literature 1974-79. Pediatr 1980; 66:597614. 2. Merritt TA. Commentary. In: Proceedings of the 17th Annual Intra-Science Symposium on Sudden Infant Death Syndrome, 1984, Santa Monica. Bethesda, MD., National Institute of Child Health and Human Development, (in press). 3. Naeye RL. Hypoxia and the sudden infant death syndrome. Science 1974; 186:837. 4. Naeye RL, Fisher R, Ryser M, et al. Carotid body in the sudden infant death syndrome. Science 1976; 191:567. 5. Winn K, et al. Medical examiner network for collection of materialfrom infants who die acutely in an accident. Baltimore, MD, National Center for the Prevention of Sudden Infant Death, Altanta, GA, American Sudden Infant Death Institute, 1985. 6. Merritt TA, Krous H, Norris G, ValdezDapena M, Brooks JG. Rebuttal statement on DPT. Landover, MD, National Sudden Infant Death Syndrome Foundation, 1985. 7. Bernier RH, Frank JA, Dondero TJ, Turner P. Diphtheria-tetanus-toxoids-pertussis vaccination and sudden infant death in Tennessee. J Pediatr 1982; 101:419- 29. 8. National Institute of Child Health and Human Development multicenter case-control study on SIDS 1980-1985. Bethesda, MD, National Institute of Health. 9. Segal S, Clogg DK, Fried C, Haworth J, Krause V, Swyer P, et al. The monitoring of an infant in the home, a commentary by the Scientific Advisory Committee, Canadian Foundation for the Study of Infant Deaths, Toronto, ON, 1982. 10. Wasserman AL. A prospective study of the impact of home monitoring on the family. Pediatr 1984; 74:323-9. 11. Deykin E, Bauman ML, Kelly DH, Hsieh C-C, Shannon D. Apnea of infancy and subsequent neurologic, cognitive, and behavioural status. Pediatr 1984, 73:63845. 12. Pamphlets and various reprints available from The Canadian Foundation for the Study of Infant Deaths, Box 190, Station R, Toronto, ON. M4G 3Z9. 13. Segal S, Fletcher M, Meekison WG. Bereaved parents-a retrospective look. Submitted to Can Med Assoc J 1985. 14. Weinstein SE, ed. Mental health issues Canadian Family Physician Coming Next Month Oncology Testis Cancer R. Brewer Auld Hodgkin's Disease 1985 Robert E. Myers Diet and Cancer Prevention Elizabeth Bright-See Gastric Cancer in Young People R. G. Chaytors Breast Self-Examintion: Available Programs and Materials Linda Del Greco Practical Cancer Chemotherapy: Venous Access and Extravasation Malcolm L. Brigden, L. N. Hughes, J. B. Barnett Cutaneous Malignant Melanoma S. T. Norvell, A. J. Bodurtha Cancer in Canada: An Epidemiological Perspective Gerry B. Hill Hypodermoclysis for Syptom Control in Terminal Care Helen Hays Carcinoma of the Prostate J. E. DeMaria, W. L. Orovan Lung Cancer: To Treat or Not To Treat? Melvyn Goldberg Nutritional Considerations for Cancer Patients Angela Chen Multiple Myeloma Ralph M. Myer In addition to this comprehensive look at current trends in cancer management, CFP's June issue will also include its regular features such as Dermacase, Radiology Rounds, and Medical Digest, as well as articles on filing reprints, in grief counselling. Summary of proceed- being a team physician, and ings, National Conference on Mental selecting practice location Health Issues Related to Sudden Infant according to training. Death Syndrome held in Baltimore, MD, 1977. Washington, DC.: Department of Health and Welfare, 1983. 15. Proceedings of the 17th annual intrascience symposium on sudden infant death syndrome. 1984, Santa Monica. Bethesda, MD., National Institute of Child Health and Human Development, (in press). defamilie Medecin Canadien doatre eitrdUe Aurora,OntanoL4U(3H6 'Kg.IraeMarlK 1030 about SIDS. The recent NICHD survey and some of the newer technology may open avenues of research leading to an understanding of the causes and prevention of SIDS. CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 arthroscopy or surgery indicated in the teenager for chondromalacia. In this age group the symptoms of chondromalacia virtually always vanish spontaneously over a couple of years. A dislocated patella, which is a distinct full lateral momentary dislocation, may at times be associated with chondromalacia but here the patient's apprehension is immediately reproduced by any attempt to slide the patella into the lateral dislocated position. In this condition the patella should be surgically tightened by tendon transfers to avoid long-term damage to the knee joint by repeated true dislocation which may occur without warning and then spontaneously reduce to normal. Osgood Schlatter's disease typically occurs in active teenage boys and is often bilateral. There is diffuse pain over the soft tissues at the patellar tendon insertion site into the tibial tubercle area. This is point tenderness. Soft tissue swelling usually occurs adjadent to the enlarged tibial tubercle area. There is a minor degree of lifting or partial avulsion of the epiphyseal projection along the upper tibial shaft. Here again the epiphyseal plate, like elsewhere, is weaker than the adjacent bones, tendon or ligaments. Fortunately the epiphyseal projection of the tibial tubercle is extra-articular; the growing athlete can be assured that his knee will not be ruined by continuing activity associated with this pain. Osgood-Schlatter's disease is an extraarticular epiphyseal inflammation: only rarely is a tensor bandage required around the knee for several weeks to minimize extremes of flexion which place the greatest stress, via the patellar tendon, on the tibial tubercle epiphysis. If a tensor bandage is used to limit knee activity, the patient should be simultaneously taught isometric quadriceps exercises to prevent otherwise rapid muscular atrophy of the thigh. The epiphyseal plate heals quickly but often in a slightly lifted position. At the end of growth, when the tibial epiphysis is permanently fused to the tibia, a small painless bump may be the only remaining evidence of boyhood Osgood Schlatter's disease. In most childhood knee complaints the history and diagnosis are easy. The management is simple-but do not forget that an X-ray is mandatory. Canadians have the vivid example of Terry Fox to remind them of osteogenic sarcoma. i CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 GROUP LIFE AND DISABILITY INSURANCE FOR MEMBERS OF THE COLLEGE OF FAMILY PHYSICIANS OF CANADA GROUP COVERAGE FEATURES * Income Replacement Plan for Members-provides up to $3,500 per month when unable to work due to sickness or accident. * Income Replacement Plan for Employees of Members-provides up to $1,500 per month when unable to work due to sickness or accident. . Term Life Insurance Plans for Members and Employees of Members-provides a choice of two plans through which benefits of up to $300,000 are available. * Family Term Life Insurance Option-provides up to $100,000 in benefits for a spouse of a member or employee of a member, and $5,000 for each dependent child. For further information write to: COLLEGE OF FAMILY PHYSICIANS OF CANADA 4000 Leslie St. Willowdale, ON. M2K 2R9 NPARAFON FORTE* C3 PRESCRIBING INFORMATION THERAPEUTIC CLASSIFICATION: Analgesic Muscle Relaxant. INDICATIONS: PARAFON FORTE CB tablets with codeine are indicated as an adjunct to rest and physical therapy for the symptomatic relief of mild to moderate pain, associated with acute painful musculoskeletal disorders and cervical and disc syndromes. CONTRAINDICATIONS: Hypersensitivity to any of the three components (chlorzoxazone, acetaminophen, codeine). WARNINGS: Drowsiness can occur with the use of PARAFON FORTE C8 tablets with codeine and may be additive to drowsiness from the concomitant use of alcohol or other central nervous system depressants. Patients should be cautioned about driving a car or operating potentially hazardous machinery if they become drowsy or show impaired mental or physical abilities while taking this medication. This product contains codeine which can produce drug dependence of the morphine type and, therefore, has the potential for being abused. PARAFON FORTE C8 tablets with codeine are not recommended during pregnancy or lactation, since safety in pregnant women or nursing mothers has not been established. Because safety and effectiveness of PARAFON FORTE C8 tablets with codeine in children have not been established, such use is not recommended. PRECAUTIONS: Use with caution in patients with known allergies or with a history of allergic reactions to drugs. PARAFON FORTE C8 tablets with codeine should be discontinued if a sensitivity reaction occurs such as urticaria, redness or itching of the skin. PARAFON FORTE C8 tablets with codeine are not recommended for patients with liver disease, and should be discontinued if any signs or symptoms suggestive of liver dysfunction occur. AOVERSE EFFECTS: Most frequently observed are central nervous system effects such as dizziness, lightheadedness, drowsiness, overstimulation, or malaise. These may be alleviated if the patient lies down. Occasionally, gastro-intestinal effects such as nausea and vomiting. Constipation may develop after long-term use. Rarely discolouration of the urine may be observed, resulting from a phenolic metabolite of chlorzoxazone. This is of no known clinical significance. Rarely allergic type skin rashes, petechia, ecchymoses. Angioneurotic edema or anaphylactic reactions are extremely rare. DRUG INTERACTIONS: None of great clinical significance. OVERDOSE SYMPTOMS: The manifestation of an overdose of PARAFON FORTE C8 tablets with codeine are those of chlorzoxazone and acetaminophen overdose, combined with an exaggeration of the adverse effects of codeine. Chlorzoxazone: Initially, gastro-intestinal disturbances, nausea, vomiting, or diarrhea together with drowsiness, dizziness, lightheadedness or headache. Then malaise or sluggishness which may be followed by loss of muscle tone and voluntary moverTient. Acetminophen: Early symptoms of acetaminophen overdose overlap the symptoms of codeine overdose and include gastro-intestinal irritability, nausea, vomiting, anorexia, diaphoresis and general malaise. Symptoms of hepatic necrosis may become evident from three to five days following ingestion. Codeine: In sufficient overdose, codeine can cause euphoria, dysphoria, miosis, a decrease in respiratory rate, cyanosis and hypotension. Death due to respiratory failure may result. TREATMENT: The stomach should be emptied promptly by lavage or induction of emesis with syrup of ipecac, followed by administration of activated charcoal. The hepatotoxic effect of acetaminophen overdose can be countered with the antidote N-acetylcysteine. Further information on the clinical course of acetaminophen overdose and its treatment with N-acetylcysteine is available from McNeil Pharmaceutical (Canada) Ltd. The respiratory depressant effect of codeine overdose can be countered with a specific narcotic antagonist such as naloxone. In the presence of hypoventilation or apnea, oxygen should be administered and respiration assisted or controlled. A patent airway must be maintained. Hypotension may be counteracted by administration of norepinephrine. Cholinergic drugs or analeptic drugs should not be used. AOULT DOSAGE: PAMFON FORTE U8 bblets with codeine: 1 or 2 tablets 4 times a day, not to exceed 8 tablets in a 24-hour period. DOSAGE FORM: PARAFON FORTE C8 tablets with codeine: Each tablet imprinted PARAFON FORTE C8 one side and "M" on the reverse, contains: chlorzoxazone 250 mg, acetaminophen 300 mg, and codeine phosphate 8 mg. COMbPLETE PRODUCT INFORMA^TION IS AVAILABLE ON rw REQUEST. McNEIL PHARMACEUTICAL (CANADA) LTD. Oniario LOH 1LO (4161 640-6900 600 Main Street Went, Stouffville, Trademark c 1085 McNEIL- I A section of CFP for readers who want to help healthy patients stay healthy In this issue: Info section: Proposal to forbid drivers to drink alcohol . . Smoking habits Running boots to limit bone stress . . . On the job noise and hypertension Stress tests for middle-aged patients Ultraviolet B and sore eyes . . . Newsletter on preventing heart disease Cushion for low back pain sufferers 1092 . ... ... ... ... CAN. FAM. PHYSICIANVol. 31: MAY1985 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 1091~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~f ~ ~- 1091 mally. The younger two sisters undertook their last three pregnancies only after genetic counselling. The ten nephews and nieces of the patient live in three different parts of Ontario. Since these relatives whom we have not seen are reported to be developing normally by their mothers, it is likely that the anxiety which might be generated by requests for neurological assessments would surpass any benefit. Medical Digest THIS MONTH * Stomach cancer risk in immunodeficient patients * Contraindication to gastric restriction surgery * Early 'pill' use and breast cancer . Heavy lifting in pregnant women * Diabetic patients' protection from migraine * Effects of parvovirus infection in pregnancy * Antihypertensive therapy in pregnancy * Treating split fingernails * Videotaping consultations * Fetal hazards from airport Conclusion screening * Effects of fluoride from toothpaste on the GI tract The principles followed in the investigations and counselling of this * Toxic shock syndrome and contraceptive sponges family have general applicability for * Anti-inflammatory drugs and bowel perforations family practice. Wherever a family * Leukemia risk from long-term chemotherapy history of suspected genetic disease is * Unemployment a cause of suicide? * Dose dumping of elicited in a patient or couple who want to have children, every possible once-a-day theophylline * To treat or not: mildly effort must be made to arrive quickly hypertensive women . Tips for helping learning disabled at an accurate and specific diagnosis of children * Susceptibility to infective endocarditis the relative's condition, whether that * Panic-ridden students relative is alive or dead. This should be followed by appropriate genetic counselling and genetic management of the problem which, in an increasing proportion of such cases, involves the Read anything in the overseas option of prenatal diagnosis or its pos- medical literature that you think is sibility in the near future. worth quoting on these pages? Send a copy along to Medical Digest. Acknowledgements This column reviews all We thank Dr. J. Gilbert for review- non-Canadian English language ing the patient's 23-year-old muscle medical journals for items of biopsy slides, Dr. S. A. Stewart for interest to the Canadian family the EMG studies and Dr. E. G. doctor. Extracts should preferably Murphy and Dr. A. J. Hudson for the be not more than one column in information about the neurological length and should be accompanied status of the patient at ages nine and 25 by the correct Index Medicus respectively. We are most grateful to reference to the journal. our deceased patient who cheerfully cooperated in our studies so that we could provide genetic counselling to his sisters and eventually to their children. immunodeficiency And Stomach Ca References 1. Gardner-Medwin D. Clinical features and classification of the muscular dystrophies. Br Med Bull 1980; 36:109-15. 2. Zatz, M. Diagnosis carrier detection and genetic c ounselling in the musc ular dystrophies. Pediatr Clin North Am 1978; 25:557-73. 3. Heych H, Laudahn G. Die progressivedystrophischen myopathien. Berlin: Springer-Verlag, 1969. ' 4. Worton R. Duchenne muscular dystrophy involving translocation of D.M.D. gene next to ribosomal RNA genes. Science 1984; 224:1447-9. 5. Kingston H, Thomas N, Pearson P, et al. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence in the short arm of the X-chromosome. J Med Genet 1983; 20.255-8. CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 " (Recent authors) have made a valuable contribution towards understanding of the role of immunodeficiency in oncogenesis by providing a denominator which allowed them to calculate the increased risk of cancer in patients with common variable immunodeficiency (CVID). Registries of primary immunodeficiency disorders such as X-linked lymphoproliferative syndrome (XLP) offer an opportunity to estimate the frequency of malignancies in immune-deficient patients: among the first 100 patients in our registry of XLP, 35% have now had B-cell lymphomas. The types of malignancies which occur in immune- deficient patients, such as B-cell lymphoma, Kaposi's sarcoma, cervical carcinoma, and hepatocellular carcinoma, are probably the result of impaired immunological surveillance of ubiquitous viruses. Data on the role of EBV in the induction of malignant Bcell lymphomas in patients with inherited or acquired immunodeficiency support this hypothesis. The authors have postulated that the increased risk of stomach cancer seen in patients with CVID could be due to synergistic activity of achlorhydria and immune impairment. There is no evidence of a virus inducing the gastric cancers and thus the hypothesis of impaired immune surveillance of virally infected gastric cells seems unlikely. An alternative, testable hypothesis is that immune-deficient patients, such as those with CVID or ataxiatelangiectasia, have defective immune regulation and recognition capabilities, so cytotoxic antibodies and other misdirected immune responses arise and could damage gastric epithelium. This would lead to cellular proliferation, which would predispose to the occurrence of genetic error in a proliferating cell and thereby possibly cancer. Patients with pernicious anemia have achlorhydria, atrophic gastritis with gastric cellular proliferation, lymphoid infiltration of the gastric mucosa, autoantibodies to gastric mucosa, and an 1125 increased risk of stomach cancer. Also lending support to our hypothesis is the finding that individuals living in areas of Venezuela who are at high risk for stomach cancer are immunodeficient. Our hypothesis requires further testing. " Purtilo DT, Merino F. Immunodeficiency and stomach cancer. Lancet 1985; L:751. Contraindication For Obesity Surgery 6 Since 1978, I have performed 160 gastric restriction procedures for weight loss at Rush-Presbyterian-St Luke's Medical Center in Chicago. Patients ranged in age from 12-62 years. All were more than 90% above their ideal weight, and those who were less than 100% above the ideal had significant weight-influenced diseases *DERMOVATE® (clobetasol propionate 0.05%) Indications: Topical therapy of recalcitrant corticosteroidresponsive dermatoses. Contraindications: Infected skin lesions if no anti-infective agent is used simultaneously; fungal, viral, and tuberculous infections of the skin; pregnancy and lactation; hypersensitivity to any of the ingredients. Warnings: Do not use in the eye. Use Dermovate for brief periods only and discontinue use after lesion has cleared. Do not use more than 50 g or mL perweek. Physiciansshould be advised of prior patient use of corticosteroids. Precautions: Use with caution on lesionsclosetotheeye.As adjunctive therapy in bacterial skin infections, discontinue Dermovate if no response is noted within one week Discontinue use if hypersensitivity reactions.occur. Dermovate is not recommended under occlusive dressings. Because the safety and effectiveness of Dermovate has not been established in children, its use is not recommended. Adverse Reactions: Local burning, irritation, itching, skin atrophy, striae, change in pigmentation, secondary infection, hypertrichosis and adrenal suppression. Dosage and Administration: Dermovate Cream and Ointment: Apply thinly to cover the affected area and rub gently into skin, two to three times daily. Dermovate Scalp Application: Apply once or twice daily to the affected areas of the scalp and rub in gently. Note: As with all alcohol based topical preparations, initial and transient stinging sensations may occur. Caution is advised particularly when applying to skin with open lesions. Availability: Dermovate Cream and Ointment are available in 15 g and 50 g tubes and 100 g jars. Dermovate Scalp Application (an alcohol solution) is available in 60 mL and 20 mL opaque bottles. Once remission is achieved with Dermovate, prescribe Eumovate for maintenance therapy. Product monograph available on request. Glaxo Glaxo Laboratories A Glaxo Canada Limited Company Montreal, Quebec Toronto, Ontario CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 [PAiI1 IP such as diabetes or arthritis. Nine patients had reversal of a jejunoileal bypass done at the same time as the gastric procedure. During this time, six patients required reversal of their gastric operations (one had her original surgery elsewhere). Reversal was done for intractable vomiting and was followed by significant weight regain. All patients who had a takedown of the surgery had at least one rehospitalization and numerous office visits. Investigation of these patients during numerous encounters with them led to an awareness that all had a complete upper dental prosthesis with a hard plastic portion occluding the hard palate. A review of the other cases in the series led to the discovery of three additional patients who had had more of a problem with emesis than usual but who, with perseverance and extreme dietary caution, had managed to avoid reversal of the procedure. No patient was found who had extreme prolonged emesis who did not have a complete upper dental prosthesis. These patients had a problem even with chopped foods such as tuna salad. During endoscopy on each of these patients, gastritis of the pouch was noted. Most gastric restriction procedures use a small proximal gastric pouch and a nine to 12-mm stoma between the pouch and the remainder of the gastrointestinal tract. The pouch retains food in the region of the gastroesophageal junction. The small stoma delays emptying to prolong the feeling of postprandian satiety resulting from a full pouch. Patients must learn to eat small amounts of food slowly and to masticate it to a state close to that of a puree before swallowing. These procedures may be considered to be a sort of externally enforced form of behavioral modification. In theory, patients who could learn to eat small amounts of normal food slowly, abstaining from high-calorie foods, should lose weight without surgery. People who have a full upper dental plate are less able to sense the state of mastication of the food bolus within their oral cavity than those who get sensory feedback from both the tongue and the hard palate. There have been many reports of persons with complete upper dental plates who have inadvertently swallowed bones and other indigestible objects. Surgeons who are performing these types of procedures need to become aware of their patients' state of dentition during the preoperative evaluation. Patients who have full upper dentures should be warned that they could have serious problems with eating solid foods after surgery. " Pomerantz MA. A new contraindication for obesity surgery. JAMA 1985; 253:44. The Pill And Breast Cancer ( Two investigations have suggested a relation between oral contraceptive use (OC) and breast cancer in young women. These studies were done in areas where OC use was established early and had become extensive. We report here the findings in a study in another such area, southern Sweden. A case-control study was done on 80 consecutive cases of breast cancer in women bom in 1939 or later and diagnosed at the age of 45 or earlier. This number constitutes 40% of all cases in the health care region of southern Sweden in 1979-83, Malmo being excluded because of screening activities for breast cancer. The cases were interviewed personally by their physician. Three healthy women, selected from the population registry, were individually matched to each case on birth year and parish. Two hundred and twenty-five controls remained after losses because some controls declined the interview and others could not be contacted. The controls were spoken to over the telephone by a female questioner. When the data were analyzed by conditional logistic regression women who had started OC use at 20-24 years of age had three times the risk of developing breast cancer before 46 years of age compared with non-users. The relative risk increased with earlier age of OC start. Because an early age of OC use was highly correlated with the duration of use, a unique effect of duration could not be found when starting age was accounted for. Women who had started OC use after their first pregnancy had a lower relative risk than others, although the different was not significant. The risk estimates were adjusted for age at menarche and age at first fullterm pregnancy. In our investigation both a low age at menarche and a high 1127 Change of Address If you plan to move, please let us know well in advance by attacthing the address label fronm youLr copy of the journial in the space provided and by filling in your new address. I f you 're a family phlysician and are not getting y our own copy of tlle journal, let us know. Stick old address label here Nanie_ New address CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 age at first full-term pregnancy were related to increased breast cancer risk (p=0l12 and p=0-06, respectively). Different brands of OC were not analyzed. To investigate the validity of using two interviewing techniques 17 healthy OC users personally interviewed about their OC use by their physician in 1980 in connection with health check-ups were interviewed again in 1984 by telephone. The reported starting age was, on average, 1 8 years lower when the interview was by telephone. This quick validity check indicates that any bias due to different interviewing techniques would affect the study in the direction of underestimation. Our results accord with those of Harris et al, Paffenberger et al, Pike et al and McPherson et al but differ from those of the Centers for Disease Control Cancer and Steroid Hormone Study. Another study, by Rosenberg et al, though reported negative, shows a significant association between early OC use and breast cancer risk in the same age groups. Our results, taken together with earlier reports linking early OC use with breast cancer, are a matter of great concern in respect of OC use by young women.... Olsson H, Landin Olsson M, Moller TR, Ranstam J, Holm P. Oral contraceptive use and breast cancer in young women in Sweden. Lancet 1985; 1:748-9. Heavy 'Labor' In Early Pregnancy ( Q: What advice should be given to a woman in early pregnancy whose job requires her to lift boxes regu- larly? A: There is no hard and fast advice to women in early pregnancy undertaking heavy manual labor: it should depend on any relevant obstetric history or at risk factors. For instance, women with a history of recurrent spontaneous abortion are best advised against continuing this type of occupation. In general, however, I would suggest that patients inform their employersf. of their pregnancy and request that they be given light duties at work. I find thiat most employers are helpful in these circumstances. Lewis GJ. Any questions? Br Med J 1985; 290:53. 1129 Prescribing Information (RANiTIDINE HC1) NZANTACO TABLETS (ranitidine hydrochloride) PHARMACOLOGICAL CLASSIFICATION Histamine H2-receptor antagonist INDICATIONS AND CLINICAL USE - Zantac Tablets are indicated for the treatment of all conditions where a controlled reduction of gastric secretion is required for the rapid relief ofpain and/or ulcer healing. These include duodenal ulcer, benign gastric ulcer and reflux ssophagitis. CONTRAINDICATIONS - There are no known contraindications to the use of Zantac (ranitidine). WARNINGS - Gastric ulcer - Treatment with a histamine H2-antagonist may mask symptoms associated with carcinoma of the stomach and therefore may delay diagnosis ofthe condition. Accordingly, where gastric ulcer is suspected the possibility of malignancy should be excluded before therapy with Zantac Tablets is instituted. PRECAUTIONS - Use in pregancy and nursing mothers -The safety ofZantac in the treatment ofconditions where a controlled reduction of gastric secretion is required during pregnancy has not been established. Reproduction studies performed in rats and rabbits have revealed no evidence of impaired fertility or harm to the foetus due to Zantac. If the administration of Zantac is considered to be necessary, its use requires that the potential benefits be weighed against possible hazards to the patient and to the foetus. Ranitidine is secreted in breast milk in lactating mothers but the clinical significance of this has not been fully evaluated. Use in impaired renal fnction - Ranitidine is excreted via the kidney and in the presence of severe renal impairment, plasma levels of ranitidine are increased and prolonged. Accordingly, in the presence of severe renal impairment, clinicians may wish to reduce the dose to a half of the usual dose taken twice daily. Children - Experience with Zantac Tablets in children is limited and such use has not been fully evaluated in clinical studies. It has however been used successfully in children aged 8-18 years in doses up to 150 mg twice daily without adverse effect. ADVERSE REACTIONS - No serious adverse effects have been reported to date in patients treated with Zantac. There has been no clinically significant interference with endocrine, gonadal or liver function, nor has the drug adversely affected the central nervous system even in elderly patients. The incidence of adverse events among Zantac-treated patients (8.1%) was very little greater than that among placebo-treated patients (7.7%). Only five adverse events, namely, tiredness (0.38%), headache (0.90%), dizziness (0.32%), diarrhea (0.52%) and skin rashes (0.52%) had a greater incidence in the ranitidine treated group than in the control group. OVERDOSAGE - Zantac is very specific in action and accordingly no particular problems are expected following overdosage with the drug. Symptomatic and supportive therapy should be given as appropriate. Ifneed be, the drug may be removed from the plasma by haemodialysis. DOSAGE AND ADMNISTRATION - Adults: Duodenal ulcer and benign gastric ulcer: 300 mg once daily, at bedtime. It is not necessary to time the dose in relation to meals. In most cases of duodenal ulcer and benign gastric ulcer, healing will occur in four weeks. In the small number of patients whose ulcers may not have fully healed, these are likely to respond to a further course of treatment. Patients who have responded to this short term therapy, particularly those with a history of recurrent ulcer, may usefully have extended maintenance treatment at a reduced dosage of one 150 mg tablet at bedtime. To help in the management ofreflux cesophagitis, the recommended course of treatment is one 150 mg tablet twice daily for up to 8 weeks. Experience with Zantac in children is limited and it has not been fully evaluated in clinical studies-see PRECAUTIONS. AVAILABILITY - Zantac Tablets are available as white film-coated tablets engraved ZANTAC 150 on one face and GLAXO on the other containing 150 mg ranitidine (as the hydrochloride), in packs of 28 & 56 tablets. REFERENCES: 1. Ireland A. et al Ranitidine: 150 mg twice daily vs 300 mg nightly in the treatment of duodenal ulcers. The Lancet, August 4, 1984 pp 274-275. 2. Brogden R.N. et al Ranitidine: A review of its Pharmacology and Therapeutic Use in Peptic Ulcer Disease and Other Allied Diseases (1982) Drugs 24: 267-303. 3. Product Monograph. 4. Gledhill T. et al (1983): Single nocturnal dose of an H2 receptor antagonist for the treatment of duodenal ulcer. Gut. 24: 904-908. 5. Dammann H.G. et al: Effects ofhistamine H2 receptor antagonists and other agents on intragastric acidity and acid secretion in Misiewicz J.J. and Wood J.R., Ranitidine Therapeutic Advances pp 126-139 Excerpta Medica 1984. 6. Colin-Jones D.G.* Comparison of ranitidine, 150 mg twice daily with ranitidine 300 mg in one evening dose, in the treatment ofduodenal ulcer in Misiewicz J.J. and Wood J.R., Ranitidine Therapeutic Advances pp 140-153 Excerpta Medica 1984. *Collaborating physicians listed at the end of the chapter. 7. Dobrilla G. et al. A single nocturnal dose ofranitidine for the short-term treatment ofduodenal ulcer: interim results of an Italian Multicentre Study in Misiewicz J.J. and Wood J.R., Ranitidine Therapeutic Advances pp 154-167 Excerpta Medica 1984. Product monograph available on request. Glaxo Glaxo Laboratories A Glaxo Canada Limited Company Montreal, Quebec Toronto, Ontario Diabetes: No Headache? - We have read with considerable interest the observation of recent authors that the prevalence of migraine in diabetic patients is less than that in the normal population. Some of our previous observations may be relevant to this fact. We have previously shown that while cerebral blood flow and its age related decrease in diabetic patients and normal subjects is similar, cerebrovascular reactivity in diabetics is abnormal. For example, cerebral blood flow increases after carbon dioxide challenge in normal subjects, whereas in over half of diabetic patients it either falls or does not increase. Carbon dioxide is the most potent dilator of cerebral blood vessels, and the absence of its dilatory effect on cerebral vasculature in diabetics indicates a fundamental fault in the ability of this vasculature to respond to enhanced metabolic requirements. Since cerebral vasodilatation is an essential component of the pathogenesis of migraine, the impaired ability of cerebral vasculature to dilate is probably important to the relative 'protection' of diabetic patients from developing migraine. The mechanism underlying the diminished vasodilatory capacity of cerebral vasculature in diabetics is probably very complex. Diminution in the secretion of prostacyclin (PGI2) in diabetes mellitus may appear to be an obvious contributory mechanism, as suggested by us previously. However, PGI2 infusion in the human has been shown to cause a fall in cerebral blood flow. Whether this PGI2-induced fall in cerebral blood flow is due to a diffuse vasodilatation which results in a 'steal' from cerebral vasculature or whether it is the direct result of a paradoxical vasoconstriction of cerebral vessels requires further elucidation. Changes in blood glucose concentrations have not hitherto been associated with altered vascular reactivity, but fatty acids and other lipids probably do contribute to alterations in the response of vascular smooth muscle to vasoactive agents. Fatty acids also inhibit the secretion of PGI2 and accelerate its degradation. The role of platelets in the pathogenesis of migraine, especially in terms of the 'protection' offered by CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 diabetes mellitus, is even more perplexing. Activation of platelets, platelet hyperaggregability, and the release of vasoactive substances from platelets have all been incriminated in the pathogenesis of migraine. Platelets are known to be hyperactive and hyperaggregable in diabetes mellitus and release more thromboxane A2, especially when macrovascular disease is concomitantly present. Yet diabetes mellitus offers protection from migraine. This would suggest that the answer to the diabetic's 'protection' from migraine lies not in platelets but in blood vessels themselves. " Dandona P, James IM, Beckett AG. Prevalence of migraine in patients with diabetes. Br Med J 1985; ceived rubella revaccination after delivery. Now that a serological test is available for parvovirus we should like to encourage our colleagues to consider this infection in the differential diagnosis of any rash developing during pregnancy. Only by identifying more cases can the true importance of parvovirus infection in pregnancy be determined. " Wright EP, Dyson AJ, Alaily A. Infection with parvovirus during pregnancy. Br Med J 1985; 290:241. Diuretics in Pregnancy with pre-eclampsia in the UK declined from 4-3 per 1,000 in 1958 (when most of the studies cited by Dr. Collins and others would have been in progress) to 0-8 per 1,000 in 1981-2. Other outcomes such as gestational age at birth, birth weight, and mother's time spent in hospital before delivery should therefore be considered. These outcomes are still important to mothers and their infants, and the use of such measures may not entail such large numbers as are clearly necessary to study perinatal mortality. For these reasons our study was primarily concerned with birth weight. However, it was obviously necessary to indicate the numbers of abortions and stillbirths, together with other characteristics of birth such as method of delivery. As indicated above, we did not expect antihypertensive therapy or its effects on blood pressure to influence the numbers of deaths. If a difference had been found our comparison of birth weights might have been biased and difficult to interpret. Accordingly, although we analyzed and described birth weight in detail no for- Perinatal mortality may not be the best indicator of outcome in trials of antihypertensive therapy in pregnancy. At the gestational age (more than 30 weeks) at which most cases present the fetus can nearly always be electively delivered and will almost certainly survive given the recent advances in perinatal care. For - (A recent) report describes a sero- example, the fetal loss rates associated logically proved infection with parvovirus possibly contributing to intrauterine death at birth. Another recent report provides an association between intrauterine parvovirus infection and hydrops fetalis. We should like to describe a case in which a parvovirus infection during pregnancy had a much happier outcome. At 14 weeks' gestation a 30-yearold para 1+0 developed a transient fine macular rash on her limbs followed by swelling, stiffness, and pain in her fingers, elbows, knees, and toes. There was no sore throat or occipital lymphadenopathy. Antenatal sSl|t clinic screening at ten weeks had PAIdC&uidpodon shown the patient to be susceptible to rubella despite previous rubella vaccination. Serum collected three weeks after the onset of the rash was compared with the stored antenatal clinic serum but showed no evidence of recent herpes simplex, varicella zoster, measles, rubella, or syphilis infection. The Paul-Bunnell and antistreptolysin 0 screening test were also negative, occasional conslI* but the antihuman parvovirus IgM rose from <0 3 to 21 g/l. The illness quickly settled and the pregnancy progressed to term, when a healthy girl weighing 3300 g was delivered. Follow up three months later confirmed a normal, healthy infant with no apparent abnormalities. The mother re- 290:467-8. Parvovirus Infection in Pregnancy |'ForGeIO CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 *13 1 133 mal analysis of deaths was presented and no p values were given. We merely observed that the groups were comparable but did not discuss the relevance or importance of this lack of difference in outcome. The authors' statement that we concluded that there was no difference in final fetal outcome because there was no difference in stillbirth rates in the treatment group was inappropriate. Our chief concern was birth weight, not perinatal mortality. In any case it was inappropriate to compare our findings with those of Rubin et al (see accompanying letter) since our studies were quite different in concept. " De Swiet M, Fayers P. Overview of randomised trials of diuretics in pregnancy. Br Med J 1985; 290:788. Splitting Nails ii Q: Why does a split fingernail commonly fail to repair? What treatment is advised? Agarol* * PRESCRIBING INFORMATION > INDICATIONS: Acute functional constipation: debilitating disorders complicated by inadequate bowel action; in post-operative cases, hypertensive or chronic cardiac disorders where forcing a stool must be avoided; in constipation of pregnancy; in bed-ridden or elderly patients. CONTRAINDICATIONS: Symptoms of appendicitis. Idiosyncrasy to phenolphthalein. PRECAUTIONS: Frequent or prolonged use of this preparation may result in dependence on laxatives. If a skin rash develops, discontinue the use of this or any other phenolphthaleincontaining preparation. DOSAGE: Adults-2 to 4 teaspoonfuls at bedtime; if necessary repeat this dosage the next morning, two hours after breakfast. Children (three to six years) - Y2 to 1 teaspoonful; (over 6 years)- 1 to 2 teaspoonfuls; (under three years)- proportionately smaller doses according to age. May be taken alone or in milk, water, fruit juice or any miscible food. SUPPLIED: Each 5 mL of creamy white, marshmallow-flavoured, calorie-free emulsion contains: mineral oil-1.60 mL, glycerin200.0 mg, phenolphthalein-65.0 mg. Also contains agar. Sodium content: 8.3 mg/5 mL. Available in 250 mL, 500 mL and 750 mL plastic bottles. Full information is available on request. PARKE-DAVIS Parke-Davis Canada Inc., Scarborough, Ontario IpAA'B 'Reg. T.M. Warner-Lambert Company ICCPP 1134 Parke-Davis Canada Inc. auth. user Q: A nail may split in various ways and the cause differs depending on the type of split. The commonest form of splitting is splitting into layers, and this is most pronounced near the tip of the nail. The condition is common in housewives and others whose hands are often in water, especially if the water is alkaline. Electronmicroscopic studies show that the nail cells have lost their adhesion and there may be 30 layers, each one cell in thickness. There is no satisfactory treatment unless the hands can be kept dry and solvents such as acetone (used to remove nail varnish) are avoided. Another form of splitting occurs lengthwise along ridges that extend from cuticle to tip. The ridges may result from poor peripheral circulation or old age and, less often, lichen planus, which may play havoc with the nails. In these cases several nails are likely to be affected and the condition is due to injury to the nail matrix. Similar but less severe splitting usually near the edge of one nail is almost certainly due to a minor injury in the past that was overlooked at the time but which has split the matrix. The failure to unite is due to the split matrix, and usually no treatment is advised except to keep the nail cut as short as possible. If the split is particularly troublesome the smaller part of the nail can be removed surgically. " Samman PD. Any questions? Br Med J 1985; 290:775. Patients On Camera - Recent authors are to be congratulated on their interesting paper concerning the reactions of patients to a video camera in the consulting room. There is no doubt that a proportion of patients prefer not to have their consultations recorded, and I suspect that many who dislike the practice are unwilling to verbalize their disapproval for fear of jeopardizing their relationship with their general practitioner. The strength of general practice lies in trust between doctor and patient in the consulting room. Personally, if I discovered that my general practitioner was using a video to record consultations, I would cancel my appointment and seek advice elsewhere. There is another objection, more subtle and more powerful than that of confidentiality. When a video is used, both doctor and patient are play-acting. Instead of honest question and answer, straightforward clinical examination restricted to essentials, and business-like management of treatment, issues tend to be fudged by consideration of what the transaction will look like to those viewing it later. The patient may disguise his real objective in seeking the consultation, and the doctor may become more concerned by what his peers will think of his practice than what is most necessary and effective in the management of his patient's problem. An element of artificiality, often amounting to humbug, is injected into the whole affair. There are, undoubtedly occasions when a doctor's personal ambitions are allowed to take precedence over his prime duty to protect and foster the interests of his patient. I suggest that all too often the use of video camera in the consulting room aids and abets undesirable objectives. " Hart C. Reactions of patients to a video camera in the consulting room. J R Coll Gen Pract 1985; 35:42. Prenatal 'Screening' At Airports - Q: What are the hazards to the fetus when the mother passes through the screening gate at airports? A: The screening gate at airports works by detecting the disturbances in a magnetic field induced by metallic objects being carried through it by passengers. There is no ionizing radiation such as X and gamma rays. There is no evidence that exposure to magnetic fields in this way is harmful to the fetus. Baggage may be examined by equipment using X-rays. The exposure used is very short and the image obtained is maintained on the screen by electronic means so as to permit detailed inspection. The radiation doses to the staff using the apparatus and to passengers in the immediate vicinity have been monitored and found to be tiny and insignificant (National Radiological Protection Board, unpublished data). Rae S. Any questions? Br Med J 1985; 290:227. CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Tagantet (ciuefidine, SK&F) Brief Prescribing Information for Adult Oral Use PHARMACOLOGICAL CLASSIFICATION Histamine H2-Receptor Antagonist ACTION Cimetidine competitively inhibits the action of histamine at the histamine H2-receptor. It inhibits daytime and nocturnal basal gastric acid secretion and also gastric acid secretion stimulated by food, histamine, pentagastrin, caffeine and insulin. Total pepsin output is reduced as a result of the decrease in volume of gastric juice. Cimetidine has rio effect on the rate of gastric emptying or lower esophageal sphincter pressure. INDICATIONS * Duodenal ulcer and prophylaxis of recurrent duodenal ulcer * Non-malignant gastric ulcer and prophylaxis * Gastroesophageal reflux disease CONTRAINDICATIONS None known. PRECAUTIONS Use in Pregnancy, Nursing Mothers: Experience in pregnant patients is limited. Animal studies have revealed no evidence of impaired fertility or harm to the fetus. TagametX crosses the placental barrier. It is secreted in human milk. Anticipated benefits should be weighed against potential risks. Tagamet, has been used in clinical trials for the prevention of acid aspiration pneumonitis in women undergoing cesarean section or vaginal delivery without harm to the fetus. In impaired renal function: Dosage should be reduced - see Product Monograph Drug Interactions: Tagamet' may reduce the hepatic metabolism of warfarin-type anticoagulants, phenytoin, propranolol, chlordiazepoxide, lidocaine, diazepam and theophylline, thereby increasing blood levels of these drugs. Benzodiazepines metabolized by other systems do not exhibit this effect. Since clinically significant effects have been reported with warfarin anticoagulants, close monitoring of prothrombin time is recommended, and adjustment of anticoagulant dose may be necessary. Use in Gastric Ulcer: Symptomatic response to Tagamet'k does not preclude the presence of a gastric malignancy ADVERSE REACTIONS Mild and transient diarrhea, tiredness, dizziness and rash have occurred in a small number of patients. A few patients have developed mild, reversible qynecomastia during prolonged treatment. A few cases of the following have been reported. decreased white blood cell counts (including agranulocytosis), thrombocytopenia, aplastic anemia; reversible confusional state.s, usually in elderly and./or severely ill patients with renal insufficiency or organic brain syndrome, fever; hepatitis; interstitilc1 nephritis; pancreatitis; small increases in plasma creatinine and serum tra nsam inases. OVERDOSAGE Oral ingestion of up to 20 grams haE caused no untoward effects. Recovery has been uneventful. Treatment: Emesis and/or gastric lavage, monitoring and supportive therapy. Assisted respiration may be of value. DOSAGE AND ADMINISTRATION ADULTS In clinical studies, Tagamet' has been used in divided doses of up to 2400 mg per day. ACTIVE DUODENAL ULCER 400 mg or 600 mg twice daily (breakfast and bedtime) or 300 mg four times daily (with meals and at bedtime) or 2 x 400 mg (at bedtime) for at least 4 weeks. NON-MALIGNANT GASTRIC ULCER 400 mg or 600 mg twice daily (breakfast and bedtime) or 300 mg four times daily (with meals and at bedtime). Continue therapy for at least six weeks. PROPHYLAXIS OF RECURRENT DUODENAL OR GASTRIC ULCER 400 mg at bedtime or 300 mg twice daily at breakfast and bedtime. Continue therapy for at least 6-12 months. GASTROESOPHAGEAL REFLUX DISEASE 600 mg twice daily (breakfast and bedtime) or 300 mg four times daily (with meals and at bedtime). Continue therapy for 8-12 weeks. Refer to Product Monograph for information on dosage adjustment for patients with impaired renal function. AVAILABILITY: Tablets: 200, 300, 400 and 600 mg cimetidine. PatientPakT: Each PatientPakT contains Tagamet` in blister-packed strips and disease-specific patient information in audiotape cassette and booklet formats. Tagamett UlcerPak.T: 28 days' supply of 300, 400, or 600 mg cimetidine tablets. Tagamet' RefluxPakT': 28 days' supply of 300 mg cimetidine tablets. TagametR PreventPak': 56 days' supply of 400 mg cimetidine tablets. Liquid: Cimetidine hydrochloride equivalent to 300 mg cimetidine per 5 mL. (Alcohol content 2.85%/ v/v.) Complete Product Monograph available to physicians and pharmacists on request. TagametP (cilmelidine, SK&F) NO SUBSTITUTION SK&F SmusthKlmnc companuj a '1i c:.l* < r' .:h} (.c-i.<'. l.ti .99 1 L(I" Sodium Fluoride Gel: GI Hazard? ( Q: A fluoride gel prescribed by dentists for some patients has 0.4% stannous fluoride. Patients are advised to brush the teeth at bedtime, to expectorate after one minute, but not to rinse; thus, some residual gel may be inadvertently swallowed during sleep. Could this be a hazard to persons with quiescent duodenal ulcer disease and a of bleeding? A: Fluoride, when taken orally in large quantities, can injure the gastrointestinal (GI) tract. The lethal dose sodium fluoride for an adult is approximately five grams. The amount of fluoride that could enter the GI tract after exposure to this particular dental product is probably quite small. The likelihood of GI mucosal injury or duodenal ulcer reactivation as a result of the use of this product is uncertain, although I believe it is probably negli- history of gible. " Feldman M. Sodium fluoride gel. JAMA 1985; 253:414. 'Sponge Shock' ii Although toxic shock syndrome (TSS) is most commonly associated with the use of vaginal tampons during menstruation, it has been recognized in association with many nonmenstrual conditions. These include surgical incisions, nonsurgical focal infections, and conditions of postpartum mothers, ifter spontaneous abortion, vaginal infections, pelvic inflammatory disease, and diaphragm use. The Centers for Disease Control has briefly reported on four cases of TSS in association with the use of the vaginal contraceptive sponge and has encouraged reporting of other cases. Currently, 13 confirmed cases of TSS with this association have been reported. We report such a case in greater detail. . . .On the first day of an expected menstrual period, an 18-year-old white, nulligravida woman was seen in the emergency department with a oneday history of yellow-green vaginal discharge accompanied by fever, chills, nausea, and severe orthostatic dizziness. There was no myalgia, frank vomiting, or diarrhea. The discharge had started shortly after the 1139 rrs TIM ORNGAM S OSS n - painful removal of a contraceptive sponge. The sponge had been in place for 20 hours. A sponge had been used five days earlier, for several hours, without difficulty. No vaginal tampons had been used. The patient was alert and cooperative. She appeared ill, but not in great distress. Her oral temperature was 38.8°C with a supine blood pressure of 150/80 mm Hg and pulse rate of 100 beats per minute. There were marked orthostatic changes on standing. Examination of the head and neck revealed moderate pharyngeal erythema with a small exudate. There was no conjunctival erythema. Pelvic examination revealed a small amount of dark blood and mucus in the vagina and a slightly erythematous vaginal mucosa. Two small excoriations were noted on the cervix and vaginal wall. Laboratory findings revealed a white blood cell count of 16,700/cu mm, with 72% polymorphonuclear cells and 23% band forms. The hemoglobin level was 15.4 g and the platelet count was estimated normal. Levels of serum electrolytes were normal, ex- cept for a bicarbonate value of 16.9 mEq/L. Total bilirubin level was 1.4 mg/dL. Values for alkaline phosphatase were 73 IU/L and for serum glutamicpyruvic transaminase, 23 IU/L. Urinalysis results were normal. Findings from a screen for 8-subunit of human chorionic gonadotropin were negative. Throat culture showed no growth of staphylococcal or streptococcal organisms. Blood cultures showed no growth, but cervical culture showed growth of Staphylococcus aureus. The patient was admitted and treated with intravenous nafcillin. Within a few hours, her oral temperature rose to 39.2°C and a fine, erythematous, maculopapular rash developed over her limbs and torso. She was discharged four days later, after a repeated cervical culture showed no growth of staphylococcal organisms and all laboratory study results had returned to normal. Desquamation involving the hands, feet, and small areas of the thighs occurred after two weeks. .. .The cases described by the Centers for Disease Control all occurred during 1983, among users of a vaginal contraceptive sponge. All four patients were white, 20-29 years old, and met the criteria for diagnosis of TSS. They also had a vaginal discharge, but none were menstruating. Vaginal cultures showed growth of S aureus. Two of these patients left the sponge in much longer than directed and another had the sponge fragment during a difficult removal. The case presented herein is similar but has notable differences. The patient was younger, left the sponge in well under the recommended time of 30 hours, and was menstruating. This case falls between the previously reported cases involving a vaginal sponge and the usual case of TSS associated with tampon usage during menstruation. The vaginal sponge is gaining acceptance as a convenient, effective contraceptive device with a predicted low incidence of complications. Evaluation to date indicates an acceptable risk-benefit ratio, but diligent reporting of further complications is essential. Physicians likely to encounter patients using the vaginal sponge should be aware of the possibility of TSS. Dart RC. Toxic shock syndrome associated with the use of the vaginal contraceptive sponge. JAMA 1985; 253:1877. Bowel Perforations From Ingestion of Anti-infiammatories f Following a recent report on the suggested relation between the ingestion of anti-inflammatory drugs and colonic or small bowel perforation or hemorrhage we would like to report our experience of a patient who developed multiple perforations after the ingestion of indomethacin. A previously fit, 38-year-old man received indomethacin 50 mg, three times a day for a painful toe. After one day he experienced generalized abdominal pain and diarrhea but continued to take the drug. Three days later his pain had become more severe and he was admitted to hospital with peritonitis. At laparotomy there was a single perforation in the sigmoid colon CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 and multiple sigmoid diverticulae. A localized sigmoid colectomy was performed, but after operation he continued to have pain and developed signs of generalized sepsis and his abdominal wound began discharging feculant fluid. He underwent a second laparotomy 13 days later, when extensive peritonitis was found, with pus and feces throughout the abdomen, and the formation of interloop abscesses. Three small perforations in the small bowel were oversewn, but there were also multiple areas of necrosis and perforation throughout the large bowel. A total colectomy was performed, the rectum was oversewn, and an ileostomy created. Four days later a third laparotomy was required, at which several small bowel perforations were again oversewn. After this his nutritional state was so poor that he was transferred to our unit for parenteral nutrition. Unfortunately he continued to drain small bowel contents from his original wound and once again developed peritonitis. At his fourth laparotomy several new perforations in the small bowel were repaired. Apart from the persistence of an enterocutaneous fistula there were no further abdominal problems. Following three months of total parenteral nutrition his fistula closed, and enteral feeding was reintroduced without any problems. A multitude of investigations, including histological examination of the resected bowel, has not provided any explanation for the spontaneous development of multiple large and small bowel perforations in this man. We suggest that ingestion of indomethacin may have been responsible. Reports of lower gastrointestinal tract lesions attributable to nonsteroidal anti-inflammatory agents are uncommon. The Committee on Safety of Medicines has recorded 12 cases of intestinal perforation (with seven deaths) attributed to indomethacin, as well as five cases (one death) of intestinal ulceration, and two cases (no deaths) of intestinal ulceration and perforation since January 1965. There has also been one report (one death) of perforated diverticula (personal communication). It is not known how many of these cases were due to conventional formulations of indomethacin and how many were due to delayed release preparations such as Osmosin.... Stewart JT, Pennimgton CR, Pringle R. Anti-inflammatory drugs and bowel perforations and hemorrhage. Br Med J 1985; 290:787-8. Leukemia From Long-term Chemotherapy non-malignant conditions. The following case emphasizes the need for accurate assessment of the magnitude of relative risks. (A) patient suffered from intractable pustular psoriasis unresponsive to a wide range of topical treatments. Methotrexate produced a modest improvement. The severity of his psoriasis prevented him working or leading any sort of normal life. A major coronary artery occlusion precluded systemic treatment with retinoids because of their hypercholesterolemic effects. Within six months of receiving oral razoxane his skin was almost normal and his life was transformed. His life expectancy must be reduced by his poor coronary history, but how does this risk relate to the risk of his developing leukemia from continuing chemotherapy? I suggest that the decision for or against chemotherapy should not be confined to whether or not the condition treated is malignant. - A (recent) leading article ... on the risk of leukemia developing in cancer patients receiving long-term chemotherapy serves as a timely reminder for us to assess accurately the risks associated with our treatments relative to the suffering caused by the disease we are treating. For most patients with cancer the alternatives are death or survival. Chemotherapeutic agents with cell cycle modulating effects are used in several non-malignant rheumatological conditions and in severe psoriasis. The recent finding of an increased incidence of acute myelomonocytic leukemia in patients with psoriasis treated with razoxane has led Griffiths WAD. Risk of leukaemia many doctors to conclude that this and associated with chemotherapy. Br similar drugs should never be used in Med J 1985; 290:555. R:iTt.gt I0 T r dtla itfr * * S purpura, thrombocytopenia, neutropenia. Others: Restlessness, fever. SYMPTOMS AND TREATMENT OF OVERDOSAGE The most common signs and symptoms to be expected from overdosage are dehydration and electrolyte imbalance. Abnormal potassium levels may cause cardiac arrythmias especially in digitalized patients. No specific antidote is available. It is not known whether the drug is dialyzable. Discontinue MODURET* and observe patient closely. Treatment is symptomatic and supportive. Suggested measures include induction of emesis and/or gastric lavage. DOSAGE AND ADMINISTRATION Optimal dosage should be established by the individual titration of the components. Maintenance doses may be lower than those required to initiate diuresis; therefore, attempt reduction in daily dosage when patient's weight is stabilized. Hepatc Cirrhosis with Ascites and Edema: Usual maintenance dose: 1 tablet once a day; dosage should not exceed 4 tablets a day in single or divided doses. Edema of Cardiac Orign: Usual maintenance dose: 1 or 2 tablets once a day or in divided doses; dosage should not exceed 4 tablets a day. Therapy may be on an intermittent basis. Hypertension: Usual maintenance dose: 1 or 2 tablets once a day or in divided doses; dosage should not exceed 4 tablets a day. AVAILABILITY Ca 9626 - Peach-coloured, diamond-shaped compressed tablets, scored on one side with MSD 917, and tradename MODURET* on the other, containing 50 mg hydrochlorothiazide and 5 mg amiloride hydrochloride. Available in bottles of 100 and 1000. FULL PRODUCT MONOGRAPH AVAILABLE ON REQUEST 1. Multicenter diuretic cooperative study group: Multiclinic comparison of amiloride, hydrochlorothiazide, and hydrochlorothiazide plus amiloride in essential hypertension, Arch Intern Med 141:482-486, March 1981. 2. Kaplan, N.M.: Our appropriate concern about hypokalemia, Am J Med 77:1-4, July 1984. PAAB MSD MEMBER MERCK PMAC SH RP 5-115 CANADA *@Trademark DORVAL, QUEBEC H9R 4P8 P.O. BOX 1005, POINTE-CLAIRE CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Unemployment And Suicide ( Recent authors report that only five out of 107 unemployed male parasuicide patients mentioned unemployment as their most important current problem. They conclude that unemployed people committing parasuicide do not see unemployment as relevant to their action, and warn of the danger of interpreting the higher risk of parasuicide among the unemployed . . . as evidence of a "causal connection". Their findings are in line with other such investigations. In only a small minority of cases is work or non-work cited as a "reason for" or "cause of" the overdose. However, attempts to elicit from individuals the reasons or motives for their behavior are fraught with methodological and conceptual problems. Colleagues such as those at the Warneford Hospital, Oxford, sought for many years to develop a valid technique for describing the subject's own perceptions and definitions of his or her overdose and its antecedents. The results of their careful studies were by no means unequivocal, and no further research along these lines is planned. Like many others, they came to realize that the concept of a "reason" is extraordinarily complex. If it is to be used at all it requires strict definition, carefully structured questioning, and precise techniques of clarification. The kind of interview method used by (the authors) would not be very helpful in this context. A second point concerns the interpretation of our epidemiological findings on the relation between unemployment and parasuicide. It is a matter of arithmetic that being unemployed raises the risk of parasuicide by a factor of about 12 and that this risk tends to increase with lengthening durations of unemployment. These are facts, not inferences. But we nowhere suggest that unemployment is a precipitant of parasuicide, and logically it would make no sense to do so, as (the authors) suggest. If it is of causal significance it is almost certainly as a predisposing or vulnerability factor. Here we refer to a recent study of 95 patients who committed parasuicide admitted also to the regional poisoning treatment centre. Using a full array of life event research techniques the researchers found that 35% had experi- 'HISMANAL: rHERAPEUTIC CLASSIFICATION iistamine Hi-antagonist kCTION Astemizole is a potent, long-acting and selective iistamine Hi-antagonist. It produces a dose-related nhibition of skin reactions to intradermal histamine. kstemizole inhibits the nose reaction to nasal challenge vith histamine and allergens. It inhibits the bronchial reiction to inhaled histamine and allergens in asthmatic atients. Astemizole has extremely weak serotonin anagonism, no anticholinergic properties, no antagonism f dopamine or other catecholamines. Astemizole has io effect on the C.N.S. and does not interact with drugs icting on the C.N.S. kstemizole is rapidly absorbed after oral administration. plasma levels are obtained within one hour. kstemizole is extensively metabolized, and plasma levels unchanged drug are low. kstemizole is completely metabolized in the liver and nainly excreted through the faeces. Two metabolites of stemizole, desmethylastemizole and norastemizole ave, orally, the same pharmacological properties as the compound. NOICATIONS HISMANAL* astemizole is indicated for he treatment of seasonal allergic rhinitis, allergic conunctivitis, chronic urticaria and other allergic 'eak If larent :onditions. :ONTRAINDICATIONS HISMANAL astemizole is conraindicated in patients with a known hypersensitivity to he drug. Use In Pregnancy Due to insufficient lata, HISMANAL astemizole should be used in pregnant vomen only when, in the opinion of the physician, the iotential benefits outweigh the possible hazards. with C.N.S. Depressants HISMANAL astemizole no potentiating effects with alcohol or other C.N.S. lepressants in clinical and laboratory studies. 1rug Interaction No drug interaction has been ound between astemizole and bronchodilators, other antihistamines, antibiotics, sulfonamides, estrogens, progestogens, oral conraceptives, diuretics, antihypertensive agents, analgeics and anti-inflammatory agents, tranquillizers and intidepressants. REACTIONS The incidence of adverse experinces during astemizole treatment was comparable to hat during placebo control treatment. uring chronic treatment, body weight tended to inThis is probably due to an increase in appetite. tatemizole had no effect on laboratory parameters. AND TREATMENT OF OVERDOSAGE In reported to date, involving oral ingestions of up to 100 mg of HISMANAL astemizole, no untoward effects iave been noted. )OSAGE AND ADMINISTRATION Adults and children hlder than 12 years of age: 1 tablet (10 mg) once a day. between 6 and 12 years of age: 1/2 tablet (5 mg) nce a day. under 6 years of age: 2 mg (1 mL suspension) ier 10 kg/day. b achieve optimal absorption, astemizole should be aken on an empty stomach. 'RECAUTIONS Jse lad iystemic :orticosteroids, hOVERSE :rease. ;YMPTOMS :ases ,hildren ,hildren iVAILABILITY ablets Each white, round scored compressed tablet :ontains 10 mg astemizole. Available in boxes containig 2 blister packs of 10 tablets each. ouspension Each mL contains 2 mg astemizole. kvailable in bottles of 30 mL. IEFERENCES Sussman, G. L: Today's Ther Trends (in press) 1985. 2. Vanden lussche, G. et al.: A Review of Woddwide literature HISMANAL Beerse, Belgium 1983. 3. Holgate, S. T.: THORAX 39 10.9 668-672 1984. 4. Smith, N. T.: SATELITrE SYMPOSIUM, Am Icad All & Immun, Chicago, 1984. 5. SeppaJa, T.: CurrTher Res 31: 38-44, 1982. 6. Laduron, P. M.: Mol Pharmocol 21: 294-300, 982. 7. Knight, A.: Cdn J Otol 1985. ;YMPOSIUM, m JANSSEN - st d m] M\SSR1£:E XH; t,1:.9<. a. .CNl (',IY X,^t, '.. 1145 enced serious unemployment, which was judged to represent a substantial threat or difficulty. Similarly, Fruensgaard et al. found that unemployment was an important causal factor in their sample of unemployed patients admitted to a psychiatry emergency department, of whom about half were admitted after parasuicide, usually in conjunction with other external factors-for example, interpersonal conflicts, housing problems, and economic difficulties-all of which are, of course, heightened by unemployment. Whether or not individuals see unemployment as being relevant to their action, outside observers and clinicians taking a longer term and more objective viewpoint have certainly seen its importance. Having established that there is a very high risk of parasuicide associated with long-term unemployment, we clearly need to elucidate the nature of this relationship. This is an urgent task, but more complex than (the authors) realize. - lif. Platt S, Kreitman N. Is unemploy- she ate two bowls of 'Cheerios' cereal ment a cause of parasuicide? Br immediately after taking her theophylMed J 1985; 290:161. line dose and later that day had a headache and mild nausea. The next morning she ate some candy from her Easter basket within 15 min of her dose. Later that day she had a severe headache and projectile vomiting, and was ( An 11-year-old girl had been tak- taken to an emergency room. Her ing a slow-release theophylline prod- serum concentration, 111/2 hours after uct ('Theo-Dur') for several months at the dose, was 41-7 ,ug/ml (analyzed a total daily dose of 700 mg (28 mg/kg twice). She was admitted to intensive daily) as three doses every eight hours. care and given intravenous anticonvulOn this regimen she had no side- sants prophylactically and activated effects, and a serum concentration was charcoal every three hours to increase reported to be 16 ug/ml. All doses the rate of elimination of the drug. were administered by her mother. Sub- Symptoms of theophylline toxicity dissequently, the theophylline prepara- appeared about six hours after admistion was changed, for increased conve- sion. This pattern of change in theophylnience, to a once-a-day product ('Theo-24', 'Pulmo-Timelets'). She line concentration is consistent with took the same dose of 700 mg daily for the results of a study in eight volunseveral weeks at 0700 hours and ate teers, where absorption was slow and breakfast at 0800 hours without ill- incomplete (71%) when the drug was effect. On the new regimen, a serum taken fasting, but half the dose was concentration of 17-3 ug/ml was re- dumped, beginning after six to eight ported. However, on April 22, 1984, hours when the dose was taken with a bacon-and-eggs breakfast. The mechanism for the dose-dumping is likely to be the pH change in the duodenum that occurs in response to food, since the coating on the beads rapidly dissolves atpH7-4. " Hendeles L, Wubbena P, Weinberger M. Food-induced dose dumping of once-a-day theophylline. Lancet 1984; 2:1471. Theophylline Dose Dumping For starting therapy: LOPRESOR 50 mg b.i.d. increased to LOPRESOR 100 mg b.i.d. if necessary For once-a-day maintenance: LOPRESOR SR 200 mg WRITE 'NO SUBSTITUTION' (metoprolol tarrrate) Geigy 1X1 Mississauga, Ontario G-4066 L5N 2W5 1146 Hypertension: Not A 'Woman's Problem'? - (A recent author) concludes "that no significant benefit of treatment of hypertension has been found in mildly hypertensive women". He is mistaken. In 1980 the management committee of the Australian trial undertook to publish a future paper analyzing the effect of treatment on the various subgroups, including by sex. This analysis was reported in April 1984 and was the subject of a leading article in another journal in June. Univariate and multivariate analysis of trial end points in women showed the treatment effect to be significant at the 5% level. The committee was unable to identify, by any covariate considered, subjects under 70 with mild hypertension sustained over a four month period of repeated blood pressure measurement CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 who might be safely spared drug treatment. Indeed, among smokers, the benefit of drug treatmedt was actually greater for women with hypertension than for men. By way of extra confusion, Dr Silman has chosen to redefine the terms "mild" and "severe" hypertension. The Australian trial and the Medical Research Council trial defined mild hypertension as a diastolic blood pressure of 95-109 and 90-109 mm Hg respectively. Yet Dr Silman states that severe hypertension is a diastolic blood pressure over 105 mm Hg, although the term is normally reserved for a diastolic blood pressure over 120 mm Hg. Whatever adjective is used, hypertension in women is a suitable, not separate, case for treatment.... Bradley N. Hypertension in women. Br Med J 1985; 290:73-4. Helping the Learning Disabled " While the leaming-disabled student generally fares worse than his or her normal peers in scholastic achievement and social success, parents may be able to enhance their child's selfesteem and sense of success in several ways. They can: * Give continuing suppoIt and encouragement * Arrange for private tutoring * Encourage participation in sports and other out-of-school activities * Foster nonacademic skills * Allow the child to have work experience during junior and senior high school So says Harry E. Hartzell, MD, clinical professor of pediatrics, Stanford University School of Medicine, Stanford, Calif., and chief of pediatrics, Palo Alto Medical Clinic, Palo Alto, Calif. In a ten-year follow-up study of 114 learning-disabled students and their normal siblings, Dr. Hartzell and Carolyn Compton, PhD, found in interviews with students and parents that -such interventions are associated positively with the learningdisabled student's sense of academic and social success. Dr. Hartzell emphasizes the need for continuing support from the family. "The learning problem doesn't go away. It continues to be a problem all the way through school. It's something CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 *Cyclomen danazol capsules U.S.P. PRESCRIBING INFORMA3nON THERAPEUTIC CLASSIFICATION: Pituitary gonadotropin inhibitor. CLNICALPHARMACOLOGY: CYCLOMEN suppresses the pituitaryovarian axis by inhibiting the output of gonadotropins from the pituitary gland. It has mild androgenic activity. Studies have established that the drug is neither estrogenic nor progestational. Recent evidence suggests a direct inhibitory effect at gonadal sites and a binding of CYCLOMEN to receptors of gonadal steroids at target organs. Generally the pituitary-suppressive action ofCYCLOMEN is reversible. Ovulation and cyclic bleeding usually return within 60 to 90 days after CYCLOMEN therapy is discontinued. INDICATIONS AND CLINICAL USE ENDOMETRIOSIS: Cyclomen is indicated for the treatment ofendometriosis characterized by dysmenorrhea, pelvic pain, infertility, induration ofthe cul-de-sac, or dyspareunia. Cyclomen is not indicated in those patients where surgery alone is considered the treatment of choice. FIBROCYSTIC BREAST DISEASE: Cyclomen is indicated for the symptomatic relief of pain and tenderness associated with fibrocystic disease of the breast. Only those patients should be selected for treatment, who are unresponsive to, or intolerant of, other therapeutic measures, or in whom such measures are otherwise inadvisable. CONTRAINDICATIONS: CYCLOMEN should not be administered in these conditions: 1. Undiagnosed abnormal genital bleeding. 2. Markedly impaired hepatic, renal or cardiac function. 3. Pregnancy. 4. Breast feeding. PRECAUTIONS: Because CYCLOMEN may cause some degree offluid retention, conditions that might be influenced by this factor, such as epilepsy, migraine, or cardiac or renal dysfunction, require careful observation. ADVERSE REACTIONS: The following androgenic effects have occurred in patients receiving CYCLOMEN: acne, edema, mild hirsutism, decrease in breast size, deepening of the voice, oiliness of the skin or hair, weight gain, and rarely, clitoral hypertrophy. Also hypoestrogenic manifestations such as flushing, sweating, vaginitis including itching, dryness, burning and vaginal bleeding, nervousness, and emotional instability have been reported. Hepatic dysfunction, as evidenced by elevated serum enzymes and/or jaundice, has been reported in patients receiving adailydosageofCYCLOMEN of400 mgor more. It is recommended that patients receiving CYGLOMEN be monitored for hepatic dysfunction by laboratory tests and clinical observation. Prolongation of prothrombin time in patients stabilized on warfarin has also been reported. Alter- ations in lipids have also been observed. Although the following reactions have also been reported a causal relationship to the administration of CYCLOMEN has neither been confirmed nor refuted: allergic: skin rashes, and rarely, nasal congestion. CN'S effects: dizziness, headache, sleep disorders, fatigue, tremor, and rarely, paresthesia in extremities, visual disturbances, anxiety, depression, changes in appetite and chills. gastrointestinal: gastroenteritis, and rarely, nausea, vomiting, constipation. musculoskeletal: muscle cramps or spasms, joint lock-up, joint swelling, and pain in back, neck or legs. genitourinary: rarely, hematuria. other: abnormal glucose tolerance testand increased insulin requirements in diabetic patients, loss ofhair, changes in libido, elevation in blood pressure, and rarely, pelvic pain. DOSAGE AND ADMINISTRATION: Therapy should begin during menstruation. Otherwise, appropriate tests should be performed to ensure that the patient is not pregnant while on CYCLOMEN therapy A non-hormonal method ofcontraception is recommended. Endometriosis: In moderate to severe disease, or in patients infertile due to endometriosis, a starting dose of 800 mg. given in two divided doses is recommended. For mild cases, an initial daily dose of 200 to 400 mg given in two divided doses is recommended and may be adjusted depending on patient response. It is essential that therapy continue uninterrupted for 3 to 6 months but may be extended to 9 months if necessary. After termination of therapy, if symptoms recur, treatment can be reinstituted. Fibrocystic Breast Disease: The total daily dosage ofCYCLOMEN for fibrocystic breast disease ranges from 100 mg to 400 mg given in two divided doses depending upon patient response. In most cases, breast pain and tenderness are significantly relieved by the first month and eliminated in 2 to 3 months. Usually elimination of nodularity requires 4 to 6 months of uninterrupted therapy. Irregular menstrual patterns may occur. Clinical studies have demonstrated that up to 50% of patients may show evidence of recurrence of symptoms within one year. In this event, treatment may be reinstated. HOW SUPPLIFD: Each capsule contains: danazol 50 mg (orange and white), 100 mg (yellow), or 200 mg (orange) in bottles of 100. Product Monograph available on request. References: 1. Aksu, M.F., Tzingounis, V.A., Greenblatt, R.B.: Treatment of Benign Breast Disease with Danazol: A Follow-up Report.J. of Reprod. Med. 21:181-184,1978. Winthrop Laboratories Division of Sterling DrugLtd.** Aurora, Ontario L4G 3H6 SRegistered User aRe,,. Trade Mark IaP I[P>] Answer to Dermacase (page 953) 4. Acne rosacea Acne rosacea is an idiopathic chronic eruption of the face. The four clinical components of the disease are erythema, telangiectasia, acneform lesions and rhinophyma. The last of these elements may cause a bulbous deformity of the nose, resulting from hyperplasia with lobulation of the sebaceous glands. Acne rosacea is more common in middle-aged women than men but rhinophyma formation, when it occurs, is seen almost exclusively in men. The changes are most apparent in the middle third of the face. The earliest manifestation of the disease is simple intermittent flushing involving the nose and cheeks. In time the erythema becomes fixed, telangiectasia develop, and acneform lesions may be seen. Although papules and pustules are common, comedones are not seen. Many patients note that alcohol, that parents need to be aware of as a cause of frustration about school." Effective family functioning was one of the two factors the study found to be most predictive of academic successthe other being high IQ. Private tutoring proved particularly helpful, in part because its anonymity bolstered the child's self-esteem. Involvement in athletics and employment during junior and senior high school resulted in positive feelings of worth by offsetting the chronic lack of academic and social success associated with a learning disability. While special education classes tailored to the needs of learning-disabled children can be vital to academic achievement, such classes were associated with low academic and social success, at least in part because the students with the greatest disabilities tended to be enrolled in them. The children in the study came primarily from upper middle-class families where the breadwinner had a high occupation level and the mother had attained a high level of educationboth factors predictive of success in the child. Additionally, learning-disabled students who had high IQs, relatively minor learning disabilities, or coffee, tea and spicy foods cause their disease to flare. Seborrheic dermatitis produces redness with scaliness of the face, especially the eyelids, eyebrow skin, and nasolabial folds. The absence of telangiectasia or acneform lesions helps to differentiate seborrheic dermatitis from acne rosacea. Lupus erythematosus may produce redness with telangiectasia of the face but acneform lesions and subaceous hyperplasia of the nose are not normally seen. Also, most patients with lupus erythematosus notice that the sun causes their skin disease to become worse, which is not usually a feature of acne rosacea. Acne vulgaris may be seen in patients this age but will lack the erythema and telangiectasia seen in acne rosacea. In acne vulgaris the lesions arise from normal rather than erythematous skin. Acne rosacea is chronic and to experience greater academic and social success. At initial evaluation, the students ranged in age from six to 12 years and all had primary diagnoses of learning disability (defined as "a discrepancy between intellectual ability and academic achievement due to a deficit in one or more psychological processes such as attention, memory, or perception"). The researchers excluded mentally retarded children and those with primary emotional disturbance. Although learning-disabled students are often spotted by educators during the first years of school, it is not uncommon for a learning disability to present as a medical dysfunction. Dr. Hartzell suggests giving a child with a school-related problem-such as vomiting, headache, stomachache, or anxiety before or after a school day-a simple reading or math test to help judge whether the problem might be linked to a learning disability. He adds that (physicians) might also find it worthwhile to seek out and evaluate services in (their) community geared toward the learning-disabled child so (they) can improve (their) effectiveness as a liaison between consultants positive personalities were more likely and the family. " 1148 indolent. Ocular complications include blepharitis, conjunctivitis, iritis and even keratitis. Treatment is difficult. The avoidance of excessive exposure to tea, coffee, hot drinks, alcoholic beverages and spicy foods is desirable, since these foodstuffs seem to aggravate acne rosacea. Hydrocortisone cream may dampen down some of the redness but has no effect on the telangiectasia, acneform lesions, and sebaceous hyperplasia. Topical fluorinated steroids may aggravate the telangiectasia and should be avoided. Tetracycline in low doses (250-500 mg per day) with topical antibiotic solutions (tetracycline, erythromycin or clindamycin) or benzoyl peroxide lotions, or gels, will control the acneform changes. When it is cosmetically offensive, the rhinophyma may be treated by dermabrasion, laser therapy, or electrosurgery . Bruni PJ. What added help can I give my learning disabled child? Patient Care 1985 Mar 15; 19:180-1. Antibiotic Prophylaxis For Electrolysis Patients CC Recent authors draw attention to the small but definite risk of infective ndocarditis associated with insertion f intrauterine contraceptive devices. Hair electrolysis is another procedure that is not generally regarded as causing appreciable bacteremia in patients at risk of infective endocarditis. A 40-year-old teacher presented with mild fever, nausea and vomiting, in the upper visual fields, and a throbbing headache of three days' duration. She had had rheumatic fever at age 11 and an episode of bacterial endocarditis at age 12. Mitral regurgitation with paroxysmal atrial fibrillation had been noted at age 26, and after increasing episodes of this she was started on warfarin at age 34. Five years later she had developed a right parieto-occipital cerebral hematoma, which was successfully removed, and she had made an excellent recovery. Qickering CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 Examination on admission was normal apart from a residual left homonymous hemianopia, mitral regurgitation, atrial fibrillation, and a temperature of 37 2°C. Blood cultures were reported the following day as containing Gram positive cocci in two out of six specimens. The organism was identified as Staphylococcus epidermidis and regarded as a probable contaminant. A computed tomogram of the brain was normal. Patenteral antibiotics were stopped, and she was allowed home taking oral penicillin on the fifth day. Four days after her discharge all six blood culture specimens had grown S epidermidis. She was therefore readmitted for a full course of intravenous antibiotics. Examination on readmission showed numerous splinter hemorrhages in the finger and toe nails. No new ones appeared after the start of intravenous antibiotics, and she made a full recovery. Exhaustive questioning regarding the source of the bacteremia was initially unhelpful. Later, the patient volunteered that three weeks before her admission she had had extensive hair electrolysis for facial hair and during that period had not received antibiotic prophylaxis. This case suggests that apparently minor 'external' procedures such as hair electrolysis may expose susceptible individuals to infective endocarditis. " Daneshmend TK. Need for antibiotic prophylaxis during hair electrolysis? Br Med J 1984; 289:1693. Examination Panic prepared and are overconcerned with THE 8 HOUR NITROGLYCERIN their work. Some students may have too great a need to perform well, fearINFORMATION ing that they will not do themselves PRESCRIBING Nitroglycerin sustained-release tablets justice and so fail to obtain that co- Therapeutic classification veted first class honors degree so nec- Anti-anginal Agent Indications essary for a postgraduate research fel- Nitrong SR Tablets are indicated for the prevention of attacks of angina pectoris associated with lowship. Their sense of reality chronic angina of effort. becomes distorted, their humor van- Contraindications ishes, and all they see is doom and Nitrong SR Tablets are contraindicated in patients severe anemia, increased intraocular presgloom. If such a student is seen just with sure, increased intracranial pressure and hypotenNitrong SR is also contraindicated in patients before taking the examination or he sion. known idiosyncrasy to organic nitrates. panics in the examination room then with Warnings immediate help can often save things. Data on the safe use of Nitrong SR during the early phase of myocardial infarction (the period during A quiet room away from the main ex- which clinical and laboratory findings are unstable) amination hall is the setting for a firm are insufficient to establish safety. use of Nitrong SR in patients with congestive friendly challenge and in most cases a The heart failure requires careful clinical and/or hemorest, a cup of coffee, and a continuing dynamic monitoring. Nitrate dependence may occur in patients with relationship with a sympathetic invigi- chronic use. To avoid possible withdrawal effects, lator will enable the student to start, or the administration of Nitrong SR should gradually be reduced over 4-6 weeks. In industry workers restart, the paper and do himself jus- continuously exposed to nitrates, chest pain, acute tice. If the potential problem is expected then deconditioning and relaxation procedures are of great benefit. Such a program might consist of writing an examination question initially under no pressure and then over some weeks being steadily forced to do more than one question until finally examination papers are done under examination conditions. This helps to make the actual examination no more than a continuation of a well established procedure. During this period relaxation techniques can be taught so that as tension occurs the student may deal with it competently and quickly. It is also necessary to check that overleaming and overworking are defused and that realistic expectations rather than false hopes are produced by the close involvement of department tutors. Centres of higher education approach these problems in various ways but all would try to offer some help. The more efficient the service the less need for medication. I have not found /8 blockers to be of great value and benzodiazepines may lead to sedation and disaster if taken on the morning of the examination. Better by far are sympathetic friends and parents, a clearly defined course, approachable tutors and competent invigilators, and a back up team of psychologists, nurse, and doctor when needed. " - Q: What advice and treatment (if any) should be given to a university student who suffers from examination panic? A: Try to understand why the student is panicking. It is unusual for a lazy student to seek medical help just before an examination, but it is possible, and needs to be excluded by checking that he has done his course work and prepared adequately. Nearly all students who suffer from examination panic are diligent, hard working, Dickinson KG. Any questions? Br conscientious people who have over- Med J 1985; 290:922. myocardial infarction and even sudden death have occurred during temporary withdrawal of nitrate exposure. Precautions Headaches or symptoms of hypotension, such as weakness or dizziness, particularly when arising suddenly from a recumbent position, may be due to overdosage. When they occur, the dose should be reduced or use of Nitrong SR discontinued. Nitroglycerin is a potent vasodilator and causes a slight decrease in mean blood pressure (approximately 10-15 mm Hg) in some patients when used in therapeutic dosages. Caution should be exercised in using the drug in patients who are prone to, or who might be affected by hypotension. Nitrong SR Tablets are not intended for immediate relief of acute attacks of angina pectoris. Sublingual nitroglycerin preparations should be used for this purpose. Tolerance to this drug and cross tolerance to other nitrates or nitrites may occur. Adverse Effects Headache is the most common side effect, especially when higher dosages of Nitrong SR are used. Headache may be treated with concomitant administration of mild analgesics. If headache is unresponsive to such treatment, the dose of Nitrong SR should be reduced or the use of the product discontinued. Less frequently, postural hypotension, an increase in heart rate, faintness, flushing, dizziness, nausea and vomiting have been reported. Symptoms and treatment of overdosage Symptoms of overdosage are primarily related to vasodilation, including cutaneous flushing, headache, nausea, dizziness and hypotension. Methemoglobinemia is also possible. No specific antidote is available. Treatment should primarily be symptomatic and supportive. Dosage and administration Adult: Recommended initial dosage is 1 tablet 3 times a day before breakfast, late afternoon before meal and before retiring. Dosage may be increased progressively up to 2 tablets 3 times a day. Availability Sustairied-Release Tablets of 2.6 mg - Bottles of 100 and 1000. References: 1. Winsor, T and Berger, H.J., Am. Heart J, Vol. 90, 611-612 (1975) 2. Hirshleifer. I., Curr Ther. Res., 15, 4, 158 (1973) 3. Gensini, G.G., et al., Chest, 60, 522 (1971) Aw Registered Trademarh PRHQtNE POULfNC CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 O,Dstribted by Rhone-Pouldenc Pharma Inc Manufactured by U S. Ethicals. Long Island City. N Y ., uA |PA took an ardent stand against the British Medical Association and recommended that all GPs embrace the service and thus "get medicine out of the market place". Support came from consultants whose names read like a role of honor in British medicine. If only he could have lived a little longer and seen what he had forecast-health visitors, district nurses, and doctors working together in health centres, and a very strong Royal College of General Practitioners with an international reputation for sound GP research and clinical audit. Those hectic months are faithfully and interestingly described by John Pemberton. The last quarter of the book catelogues the h-onors coming Pickles' way as an internationally acclaimed medical giant whose reputation is assured throughout future generations of doctors, particularly among those concerned about moral and ethical aspects of our profession. So here is the story of the life of one of my heroes. Thanks to Pemberton I admire Will even more than before I opened this book. Reviewed by John Z. Garson. Dr. Garson, a member of the College, is a retired medical officer of health, and is now a health care consultant in Gabriola, BC. Will This Book Get You Out Of a Pickle? Title: Epidemiology in Country Practice Author: William Pickles Publisher: The Royal College of General Practitioners, Publications Office, 9 Marlborough Rd., Exeter, Devon, U.K. Publication Date: 1984 Pages: 112 Price: £5.50 This remarkable book is republished in paperback with the Royal College of General Practitioners' distinctive cover, and is a photo reproduction of the sold-out, limited edition of 1972. Will Pickles of Wensleydale is probably the most famous GP researcher, and, with Ryle, a foremost medical natural historian; if his work is read with this in mind, his advanced thinking is astounding. 1158 This slim volume begins with a description of the geology and water supply of the dale; he then discusses the lines of communication taken by the infecting germs of communicable disease and describes his method of study-enlisting the aid of wife, daughter, school principal, and medical officer of health. The casual acceptance of the easy partnership and relationship between the GP and the MOH highlights the loss to both by the demise of this essential relationship. Pickles exhorted GPs 50 years ago to form groups to study the epidemiology of disease, thus presaging the British Epidemiology Observation Unit and our own NaReS. He then goes on to describe the epidemiology of the common communicable diseases. I must have read the chapters on catarrhal jaundice and epidemic myalgia at least ten times over the past 12 years, yet at each reading, I am equally enthralled. I still remember my first case of epidemic myalgia when I was a house surgeon some 40 years ago in a London, U.K. children's hospital. If only I had read Pickles, it would have saved me from a worrying night of watching a little boy sweat with pain. While it is true that his work was concerned with common infectious diseases, Pickles' scrupulous method and precise observation is still needed today for unravelling the etiologies of the myriad of illnesses presenting in family practice; a casual glance at any textbook of medicine will show that we still don't know the etiology of most illnesses apart from communicable diseases. Certainly family physicians have a role to play in unravelling some of these illnesses, and the method Pickles describes is still valid, especially now (with the formation of NaReS) that we have fulfilled his call for team work. Who should read this book? It is hard to think of any doctor who would not benefit, but perhaps it is fair to suggest that all FPs, all medical students, and all family practice and community medicine residents should read it. It should be in the library of family practice teaching units. Reviewed by John Z. Garson. Dr. Garson, a member of the College, is a retired medical officer of health, and is now a health care consultant in Gabriola, BC. Book Received Borland J, Dacks B: Cast A Thin Shadow. Toronto, McClelland & Stewart-Bantam Ltd., 1984. $4.50 Bradbear RA, Campbell CB, Powell LW: Gastroenterology Revision. New York, Churchill Livingstone Inc., 1984. $19.75 Cherniak D: A Book About Sexually Transmitted Diseases. Montreal, Montreal Press Co., 1983. $2 Epstein E: Regional Dermatology: A System of Diagnosis. Toronto, Grune & Stratton, Inc., 1985. $83.50 Feneley RCL, Blannin JP: Incontinence. New York, Churchill Livingstone Inc., 1984. $4.50 Frampton M: Agoraphobia. New York, Sterling Publishing Co., Inc., 1985. $8.95 Freudberg F, Emanuel ES: Herpes: A Complete Guide to Relief and Reassurance. Philadelphia, Running Press, 1982. $10.95 Graedon J: The New People's Pharmacy. New York, Bantam Books, Inc, 1985. $9.95 Gunatilleke G (ed): Intersectoral Linkages and Health Development: Case Studies in India (Kerala State), Jamaica, Norway, Sri Lanka, and Thailand. Geneva, World Health Organization, 1984. 5 Swiss francs Hansten PD: Drug Interactions, ed. 5. Philadelphia, Lea & Febiger, 1985. $30 Mark Farren (compiler): Infant Mortality and Health In Latin America: An Annotated Bibliography From the 1979-82 Literature. Ottawa, International Development Research Centre, 1984. Krauer B, Krauer F, Hytten F: Drug Prescribing in Pregnancy. New York, Churchill Livingstone Inc., 1984. $25.75 Kucera LS, Myvik QN: Fundamentals of Medical Virology, ed. 2. Philadelphia, Lea & Febiger, 1985. Lesnoff-Caravaglia G: The World of the Older Woman: Conflicts and Resolutions. New York, Human Sciences Press, Inc., 1985. $19.95 Meisel AD, Bullough PG: Atlas of Osteoarthritis. Philadelphia, Lea & Febiger, 1984. $39.25 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985 CHILDREN'S PANADOC acetminophen The only alcohol free, sugar free children's acetaminophen antipyretic in all dosage forms. ACTIONS: Acetaminophen is an analgesic and antipyretic. INDICATIONS: Panadol* Acetaminophen is indicated for the relief of pain and fever in various conditions including the symptomatic treatment of colds. CONTRAINDICATIONS: Hypersensitivity to acetaminophen. ADVERSE EFFECTS: In contrast to salicylates, gastrointestinal irritation rarely occurs with acetaminophen. If a rare hypersensitivity reaction occurs, discontinue the drug. Hypersensitivity is manifested by rash or urticaria. Regular use of acetaminophen has shown to produce a slight increase in prothrombin time in patients receiving oral anticoagulants, but the clinical significance of this effect is not clear. PRECAUTIONS AND TREATMENT OF OVERDOSE: The majority of patients who have ingested an overdose large enough to cause hepatic toxicity have early symptoms. However, since there are exceptions, in cases of suspected acetaminophen overdose, begin specific antidotal therapy as soon as possible. Maintain supportive treatment throughout management of overdose as indicated by the results of acetaminophen plasma levels, liver function tests and other clinical laboratory tests. N-acetylcysteine as an antidote for acetaminophen overdose is recommended and is available in oral and parenteral dosage forms. More detailed information on the treatment of acetaminophen overdose with N-acetylcysteine in its oral and parenteral dosage forms is available from the manufacturers (Mucomyst, Bristol-Myers Canada Limited trademark for its brand of oral N-acetylcysteine; Parvolex, Glaxo Canada Ltd. trademark for its brand of parenteral N-acetylcysteine), or contact your nearest Poison Control/Information Centre. DOSAGE: Children: Based on Weight 10-15 mg/kg every 4 to 6 hours, not to exceed 65 mg/kg in 24 hours. Based on Age Single Dose Age 40 mg Newborn to under 4 months 80 mg 4 months to under 12 months 120 mg 12 months to under 2 years 160 mg 2 and 3 years 4 and 5 years 240 mg 320 mg 6, 7 and 8 years 400 mg 9 and 10 years 480 mg 11 and 12 years 640 mg 13 years and older Dosage may be repeated 4 to 5 times, not to exceed 5 doses in 24 hours. SUPPLIED: Panadol* Drops: Each 0.8 mL contains 80 mg acetaminophen in a deep red liquid vehicle with a slightly bitter fruit flavoured taste. Available in amber bottles containing 15 mL t and 25 mL t and a calibrated dropper. Panadol* Elixir: Each 5 mL contains 120 mg acetaminophen in a fruit flavoured red vehicle. Available in amber bottles containing 100 mL t. Panadol* Pleasant tasting Chewable Tablets 80 mg: Each round, pink tablet scored one side and engraved Panadol* the other side, contains 80 mg acetaminophen. Available in amber bottles of 24 t tablets. Sterling Products Division of Sterling Drug Ltd., Aurora, Ontario L4G 3H6. *Trade Mark REFERENCE: American Academy of Pediatrics, Committee on Drugs: Ethanol in Liquid Preparations intended for FITH COLUMN Seen any good misprints lately? Heard any good lines from patients? We're interested-a laugh a day keeps the doctor away. Send items to The Fifth Columnist, 4000 Leslie St., Willowdale M2K 2R9. Ashes to Ashes You've probably all read about "Weedless Wednesday" -the day when the general public is advised to "choose to be smoke free" by the Canadian Council on Smoking and Health. The Council's publication "Smoking or Health Update" tells us about another Wednesday, when a shop steward successfully brought a grievance that tobacco smoke violates the Dangerous Substances Safety Standard for the civil service. The hearings began on Ash Wednesday. state, and "the chancellor of the exchequer is pushing for a benefits shake-up which will shave billions off the $38 million cost of social security." We assume that's a Conservative estimate. Metamorphosis Fifth Columnists are to be found in the most august echelons. A member of the executive committee for the College's Section of Teachers, visiting CFP's new offices recently, noted the flowchart for copy between CFP and General Printers of Oshawa. One column in particular caught his eye: "Dummy to GP". "Hmmm", he mused, "I used to be a dummy, but now I'm a GP". At least he didn't say "just a GP". General Medicine? The Birds and the Bees and the Flowers and the ... "At the lectern yesterday in the Parklawn Building in Rockville stood the general-U.S. Surgeon General C. Everett Koop-resplendent in black uniform with gold buttons and bars, -xhorting the corps to fight the good fight against the- enemies of disease and illness". Washington Post General-a word in your ear about Sexual taboos evidently don't apply to the plant kingdom. One Fifth Columnist received a brilliant azalea plant from a birthday well-wisher with this ominous warning tucked among the foliage: "Asexual Reproduction of enemies . . . This Plant Without License is Prohibited". Apparently the birds and the bees have total freedom to cross-polli- You Said It nate to their hearts' content-and they don't even need a license! But for a Nice work if you can get it-and a human to do an innocent cutting with- UBC professor of history's got it. The out going through the proper chan- Guggenheim Foundation is going to fund Richard Unger to "write a comnels? Forbidden fruit. plete history of the brewing industry in the Netherlands", according to a recent UBC press release. We've Told You Is Prof. Unger happy in his work? A Billion Times The press release quotes him as sayDon't Exaggerate ing: "One of the problems of this projis simply digesting the amount of And it was in the London Sunday Times, no less. Seems that the U.K. material that's available". cabinet is trying to reform the welfare Hic! :hose sct C'hildren. Pediatrics 73: (3) March 1984: 405-407. 1170 CAN. FAM. PHYSICIAN Vol. 31: MAY 1985
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