Treatment of Type 2 Diabetes Improving Patient Care through Evidence

Improving Patient Care through Evidence
Treatment of Type 2 Diabetes
This information is based on a comprehensive review of the
evidence for best practices in the treatment of type 2 diabetes and
is sponsored by the Agency for Health Care Research and Quality.
Improving Patient Care through Evidence: Treatment of Type 2 Diabetes
The growing epidemic of type 2 diabetes
1
• Diabetes affects over 25 million Americans.
• 27% of people over 65 have diabetes.
• Rates of stroke and death due to heart disease are 2-4 times higher in adults with diabetes.
Figure 1. Rapidly increasing rate of diabetes2
10.0
Crude
9.0
Age-Adjusted
8.0
Percentage
7.0
6.0
5.0
4.0
3.0
2.0
1.0
0.0
‘80
‘85
‘90
‘95
‘00
‘05
‘10
Year
Patients with diabetes are likely to have other important
co-morbid conditions
• Nearly 60% of adults with diabetes have hypertension.
• People with diabetes are twice as likely to suffer from depression.
• Diabetes is the leading cause of kidney failure, lower limb amputations, and blindness.
Achieving the best outcomes
For most patients with diabetes, the target for HbA1c should be below 7%. Achieving this
level of control reduces the risk of end-organ damage including renal insufficiency, visual
impairment, and neuropathy. Less strict targets may be appropriate for older patients and
other vulnerable populations.
2
Evidence-based treatment can improve outcomes
• Every 1% drop in HbA1c reduces the risk of microvascular complications by 40%,
and death by 21%.1,3
• Reducing diastolic blood pressure from 90 mmHg to 80 mmHg in people with diabetes
reduces the risk of major cardiovascular events by 50%.1
Figure 2. Death related to diabetes3
Hazard ratio
4
21% decrease
per 1% reduction
in HbA1c
p < 0.0001
1
0.5
0
5
6
7
8
9
10
11
Mean HbA1c over time
Treatment approach4,5
Successful treatment of diabetes requires a persistent approach that begins with modification
of diet and lifestyle and then, when medication is needed, adds medications in a stepwise
fashion, guided by periodic assessment of HbA1c.
The foundation: Lifestyle management 4,5
Any diabetes treatment plan starts with weight management, diet, and exercise.
• Weight loss reduces insulin resistance
––reduces the risk of developing diabetes in patients with pre-diabetes.
• Combined weight loss and exercise can result in an average HbA1c reduction of 0.3%.
Adding medication
Most patients with type 2 diabetes, even with diligent work on lifestyle management, will
ultimately have HbA1c levels above 7%, and will require medication. Guidelines from the
American Diabetes Association and other groups focus on:
• setting specific HbA1c targets,
• stepwise approach for initiation of drug therapy, and
• prompt intensification of treatment when goals are not met.
3
Improving Patient Care through Evidence: Treatment of Type 2 Diabetes
Non-insulin agents
1
STEP
Start with metformin
For patients not meeting HbA1c targets with diet and exercise, metformin (Glucophage) is the
recommended first choice medication in all major guidelines.
Why metformin?
• Well documented effectiveness for controlling glucose and preventing end-organ damage
• Best evidence for reducing long term complications of diabetes
• Most beneficial effects on lipids and body weight
• Predictable and manageable side effect profile
• Affordable for patients
GI side effects are common with initial use of metformin; these effects may be minimized by
starting with a low dose and slowly increasing it.
Metformin can increase the risk of lactic acidosis when used in patients with low creatinine clearance, but the absolute
risk is very low. Because of this risk, it should not be used in patients with renal insufficiency.
STEP
2
Add a second agent if HbA1c goal is not achieved
• Monotherapy with an oral agent will generally lower HbA1c by 1% in most patients.
• Wait no more than 3 months before stepping up the regimen if HbA1c remains above
goal (7% for most patients).
• The natural course of diabetes is a progressive loss of insulin sensitivity and production.
• Half of patients initially controlled on a single agent will require an additional drug
after 3 years.
4
Choosing a second line agent
• There are many non-insulin agents available, with differing mechanisms of action.
• A second non-insulin drug will generally reduce HbA1c by an additional 0.5–1%.
• There are no significant differences among the agents for HbA1c lowering, with the
exception of DPP4 inhibitors, which appear to produce smaller reductions in HbA1c.
• Insulin provides significantly greater reductions in HbA1c than any other alternative.
Table 1. Classes and mechanisms of action of major non-insulin agents
Class
Examples
Mechanisms of Action
biguanides
metformin (Glucophage)
Decreases hepatic glucose production
(major); increases uptake of glucose from
blood into the tissues (minor)
sulfonylureas*
glyburide (Diabeta, Micronase)
glipizide (Glucotrol)
glimepiride (Amaryl)
Increases insulin secretion
glitazones
pioglitazone (Actos)
Increases insulin-mediated glucose
uptake into adipose tissues and skeletal
muscles (major); decreases hepatic
glucose production (minor)
DDP4 inhibitors
sitagliptin (Januvia)
saxagliptin (Onglyza)
linagliptin (Tradjenta)
Increases incretin hormones, which
augments glucose-dependent insulin
secretion and decreases glucagon release
GLP-1 receptor
agonists
exenatide (Byetta)**
exenatide ER (Bydureon)**
liraglutide (Victoza)**
Mimics naturally occurring incretin
hormones, which stimulates insulin
production and the response to elevated
blood glucose; inhibits release of
glucagon after meals; slows nutrient
absorption; increases satiety
*”sulfonylureas” refers only to second generation agents and not older agents (such as chlorpropamide),
which are seldom used in current practice.
**These agents are given by subcutaneous injection.
5
Improving Patient Care through Evidence: Treatment of Type 2 Diabetes
Non-insulin agents have some important differences
Second line agents can differ with respect to side effect profile, cost, and impact on other
outcomes such as weight gain and lipids. While all are effective in reducing blood glucose
levels, most newer agents do not have the same level of evidence for reduction of actual
end-organ damage, compared to metformin, the sulfonylureas, or insulin.
• Cost: Costs for diabetes medications can vary from a few dollars to hundreds of
dollars per month.
• Experience: After metformin, the sulfonylureas have the longest track record.
• Side effect profile: The glitazones substantially increase the risk of CHF and peripheral
edema compared to other agents, as well as increase the risk of fracture in women.
Pioglitazone may increase the risk of bladder cancer.
Sulfonylureas and meglitinides increase the risk of hypoglycemia, while other classes
of agents do not.
Longer-acting sulfonylureas (e.g., glyburide) are more likely to cause prolonged
hypoglycemia than short-acting agents (e.g., glipizide).
Table 2. Summary of comparative efficacy, safety, and cost of non-insulin agents
Drug
a
em
nts
e
s
d
s
v
e
,
e
lo
d
1c
th
an
or
ia
ts
bA
ea or CV
e
n
d
H
m
r
i
f aj
fec
f
e
a
u
l
f
c
o
o
i
g
e
y
l
a
m
k
f
e
gl
ht
ro
Ris d/or
po
sid
art
nt
L
st
eig
y
I
e
o
D
n
C
W
H
H
L
G
Co
a
metformin
sulfonylureas
glitazones
a-glucosidase
inhibitors
meglitinides
DPP4 inhibitors
GLP-1 receptor
agonists
Best outcome
Intermediate
Problem
LDL = LDL cholesterol level; GI = gastrointestinal intolerance
6
Unknown
ll
era
Ov
STEP
3
Add a third-line agent
• If adequate control is not achieved after introducing a second line therapy, further
intensification is necessary.
• Insulin offers the best chance to control HbA1c when added as a third agent, though
non-insulin agents remain an option for patients unable or unwilling to use insulin.
Why insulin?
• Additional non-insulin agents are unlikely to add more than a 0.5%–1% reduction
in HbA1c, whereas insulin can do much more.
• Further delay in achieving control can allow end-organ damage to proceed unchecked.
• Prescribing three or more oral agents can make a patient’s medication regimen
more confusing and difficult to afford.
Prompt initiation of
insulin can improve
HbA1c control
7
Improving Patient Care through Evidence: Treatment of Type 2 Diabetes
Insulins
Delays in insulin initiation
The initiation of insulin therapy is often delayed unnecessarily.
• Only about 37% of patients achieve the goal of < 7% HbA1c.
• Insulin is the most effective glucose lowering medicine available.
• One study found that the average delay of initiation of insulin therapy after failure
of non-insulin therapy was 4-6 years.
Percentage of patients
Figure 3. Evolution of nephropathy in patients with type 2 diabetes treated with
intensive vs. conventional treatment6
50
Conventional treatment
40
30
20
Intensive treatment
10
0
0
1
2
3
4
5
6
7
8
Year
Choose the right time to start
• Combination therapy with oral agents and insulin can produce improved glucose control
and less weight gain than therapy with insulin alone. Insulin combined with metformin offers
the greatest synergy for clinical effect and the lowest risk of adverse events.
• If a diabetic patient has an HbA1c > 8.5% on maximal dose oral diabetic monotherapy,
or an HbA1c > 8% on two non-insulin agents, insulin therapy should generally be initiated.
Also consider insulin if HbA1c is between 7% and 8% on two non-insulin agents.
Choices for insulin treatment
Several types of insulin are available, varying mainly in their dosing and cost.
• Rapid acting: lispro (Humalog), aspart (NovoLog), glulisine (Apidra)
• Intermediate acting: NPH (Humulin N / Novolin N)
• Long acting (basal): glargine (Lantus), detemir (Levemir)
8
Figure 4. Time-activity curves for selected insulin formulations7
Premixed insulins combine rapid and
slower acting insulins.
Relative glycemic effect
Lispro, aspart, glulisine
Regular human
Long-acting insulin (e.g., glargine)
and intermediate-acting insulin (NPH) are
similarly effective for glucose control in
patients with type 2 diabetes. Longeracting insulins cause modest reductions
in overnight hypoglycemic events.
NPH
Detemir
Glargine
0
12
Hours
24
Biphasic and rapid-acting formulations
produce more hypoglycemia and are more
difficult for patients to manage.
3 Start with a basal insulin
Most patients should begin with basal insulin at night, either intermediate or long-acting
insulin. Such a regimen will be easier for patients to manage and can provide a good foundation
for improving glucose control. Insulin choices should be tailored to the needs of individual
patients, including considerations of convenience and cost for patients.
3 Intensify insulin treatment as needed
Many patients will not achieve glycemic control on their initial dose of basal insulin.
Intensification of insulin therapy should be guided by daily glucose values and periodic
checks of HbA1c levels.
Treating to target
A commonly used algorithm
for insulin intensification comes
from the Treat-to-Target study.8
This randomized controlled trial
demonstrated that most patients
inadequately controlled on one
or two oral agents (metformin,
sulfonylurea, or glitazone) could
achieve an HbA1c < 7% by following
this simple algorithm.
• Start with 10 units per day of bedtime basal insulin.
•Adjust insulin every week. To adjust, calculate the
mean self-monitored fasting plasma glucose (FPG)
values from the previous 2 days.
Mean FPG
Increase insulin by
100-120 mg/dL
2 units
120-140 mg/dL
4 units
140-180 mg/dL
6 units
≥ 180 mg/dL
8 units
9
Improving Patient Care through Evidence: Treatment of Type 2 Diabetes
Treatment of type 2 diabetes
4
Healthy eating, weight control, increased physical activity
Initial drug monotherapy: Metformin
If needed to reach individualised HbA1c target after ~3 months, proceed to
two-drug combination (order not meant to denote any specific preference):
Two-drug combinations: Metformin + one other druga
+Sulfonylureab
+Thiazolidine-
+DPP-4
+GLP-1 receptor +Insulin
dioneInhibitoragonist(usually basal)
If needed to reach individualised HbA1c target after ~3 months, proceed to
three-drug combination (order not meant to denote any specific preference):
Three-drug combinations: Metformin + two other drugs
+Sulfonylureab
+Thiazolidine-
+DPP-4
+GLP-1 receptor +Insulin
dioneInhibitoragonist(usually basal)
+
TZD
+
SUb
+
SUb
+
SUb
+
TZD
or
DPP-4 I
or
DPP-4 I
or
TZD
or
TZD
or
DPP-4 I
or
GLP-1-RA
or
GLP-1-RA
or
Insulinc
or
Insulinc
or
GLP-1-RA
or
Insulinc
or
Insulinc
If combination therapy that includes basal insulin has failed to achieve HbA1c target after
3-6 months, proceed to a more complex insulin strategy, usually in combination with
one or two non-insulin agents:
More complex insulin strategies
Insulind
(multiple daily doses)
10
a.Consider beginning at this stage in patients presenting initially with very high HbA1C (e.g., ≥ 9%).
b.Consider rapid-acting, nonsulfonylurea secretagogues (meglitinides) in patients with irregular meal schedules or who
develop late postprandial hypoglycemia on sulfonylureas.
c.Usually a basal insulin (NPH, glargine, detemir) in combination with noninsulin agents.
d.Certain noninsulin agents may be continued with insulin. Consider beginning at this stage if patient presents with
severe hyperglycemia ≥ 16.7–19.4 mmol/L [≥ 300–350 mg/dL]; HbA1C ≥ 10.0–12.0% with or without catabolic features
(weight loss, ketosis, etc.).
Careful management of lipids and blood pressure also plays a critical
role in reducing the risk of cardiovascular complications of diabetes.
Table 3. Treatment of related conditions
Condition
Identification
Goal of Therapy
Recommended Interventions
Hypertension
Check BP at
all visits
SBP ≤ 140 mmHG
DBP ≤ 80 mmHG
•Begin with lifestyle modification
•Drug therapy should include
ACEI (ARB if ACEI not tolerated)
•Add thiazide-type diuretic if
2nd agent needed
Hyperlipidemia
Check fasting
lipids
LDL < 100 mg/dL
(LDL < 70 mg/dL
if CAD)
•Treat with statin if elevated LDL
Smoking
Assess for
tobacco use
Smoking
cessation
•Nicotine replacement
•Bupropion/varenicline
•Counseling programs
References:
1.Centers for Disease Control and Prevention. National diabetes fact sheet: national estimates and general information on
diabetes and prediabetes in the United States, 2011. Atlanta, GA: U.S. Department of Health and Human Services.
2.Centers for Disease Control and Prevention. Crude and Age-Adjusted Percentage of Civilian, Noninstitutionalized Adults
with Diagnosed Diabetes, United States, 1980–2010. Accessed August 30, 2012 from http://www.cdc.gov/diabetes/statistics/
prev/national/figageadult.htm
3.Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective
observational study. BMJ. Aug 12 2000; 321:405-12.
4.Inzucchi SE, Bergenstal RM, Buse JB et al, Management of Hyperglycemia in Type 2 Diabetes: A Patient-Centered Approach.
Diabetes Care. Apr 19 2012;35(6):1264-1379.
5.Nathan DM, Buse JB, Davidson MB, et al. Medical management of hyperglycemia in type 2 diabetes: a consensus algorithm
for the initiation and adjustment of therapy: a consensus statement of the American Diabetes Association and the European
Association for the Study of Diabetes. Diabetes Care. Jan 2009;32(1):193-203.
6.American Diabetes Association, From Diabetes Care, Vol. 23, Suppl. 1, 2000; B21-B29.
7.McMahon GT, Dluhy RG. Intention to treat—initiating insulin and the 4-T study. The New England Journal of Medicine.
Oct 25 2007;357(17):1759-1761.
8.Riddle MC, Rosenstock J, Gerich J. The treat-to-target trial: randomized addition of glargine or human NPH insulin to oral
therapy of type 2 diabetic patients. Diabetes Care. Nov 2003;26(11):3080-3086.
11
Key components of the treatment of type 2 diabetes
• Aggressive treatment reduces risk of short-term and long-term health problems.
• Target HbA1c < 7% for most patients, with less strict targets for elderly and other
vulnerable patients.
• Lifestyle management should include: weight management, diet, and exercise.
• Most patients will need drug therapy in addition to lifestyle management.
• Follow a stepwise approach for drug therapy, with prompt intensification of
treatment when HbA1c goals are not met.
• Begin drug treatment with metformin, adding a second non-insulin agent if
HbA1c remains above goal for 3 months.
• Insulin should be initiated if HbA1c is > 8.5% on the maximum dose of metformin
or > 8% on two non-insulin agents.
• Using insulin as the third agent if HbA1c is between 7 and 8% on two non-insulin
agents is the most effective way to lower HbA1c further.
• Adding a third non-insulin agent is an option for patients unable or unwilling
to add insulin.
• Careful management of lipids and blood pressure, as well as smoking cessation,
improve outcomes for patients with type 2 diabetes.
This brochure was developed by NaRCAD (the National Resource Center for Academic Detailing) with support
from a grant from the Agency for Healthcare Research and Quality to the Division of Pharmacoepidemiology
and Pharmacoeconomics of the Brigham and Women’s Hospital Department of Medicine. It was adapted from
materials originally developed by the non-profit Alosa Foundation. Complete references and a longer discussion
of the evidence underlying these recommendations is provided at www.RxFacts.org. Neither NaRCAD nor Alosa
has any affiliations with any pharmaceutical company, and none of the physicians who prepared this material
accepts any personal compensation from any drug manufacturer.
These are general recommendations only; specific clinical decisions should be made by the treating physician
based on an individual patient’s clinical condition.
DoPE
© 2013 Alosa Foundation, Inc.