NOTTINGHAM UNIVERSITY HOSPITALS NHS TRUST PATIENT DATA QUALITY POLICY Documentation Control Reference Approving Body Date Approved Implementation Date Version Summary of Changes from Previous Version Supersedes Consultation Undertaken Date of Completion of Equality Impact Assessment Date of Completion of We Are Here for You Assessment Date of Environmental Impact Assessment (if applicable) Legal and/or Accreditation Implications Target Audience Review Date GG/INF/019 Directors’ Group 23 April 2103 23 April 2013 3 Update of definitions and Process Flows appendix as part of Policy review date expiring. PATIENT DATA QUALITY POLICY Version 2.0 Approved 1st February 2012 Information Governance Committee Deputy Director of Operations 8th February 2013 – see separate template attached at Appendix 3 7th February 2013 – see separate template attached at Appendix 5 N/A N/A All Trust staff who collect or process patient data April 2015 Lead Executive Director of Finance and Procurement Chief Operating Officer Author/Lead Manager Name : Steve Baxter Job title : Head of Information Extension : 62009 Further Guidance/Information Name : Jim Hatton Job title : Deputy Director of Operations Extension : 76141 Patient Data Quality Policy Version 3 April 2013 1 CONTENTS Paragraph Title 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. Introduction Executive Summary Policy Statement Definitions (including Glossary as needed) Roles and Responsibilities Policy and/or Procedural Requirements Training, Implementation and Resources Impact Assessments Monitoring Matrix Relevant Legislation, National Guidance and Associated NUH Documents Flow charts relating to section 6 Data Output Standards Equality Impact Assessment Environmental Impact Assessment Here For You Assessment Certification Of Employee Awareness Appendix (1) Appendix (2) Appendix (3) Appendix (4) Appendix (5) Appendix (6) Page 3 3 4 5 5 6 8 11 12 13 14 19 21 24 26 28 1.0 Introduction 1.1 Nottingham University Hospitals NHS Trust requires the collection, storage and management of patient data to be accurate, timely, relevant and secure in order to support the delivery of effective and efficient patient care and the achievement of the Trusts’ core business objectives and statutory obligations. Good quality data is not an optional extra; it is a fundamental requirement for the delivery of high standard services. 2.0 Executive Summary 2.1 This policy applies to the administrative and clinical patient related data contained within the Trusts’ electronic and paper based systems. Patient Data Quality Policy Version 3 April 2013 2 This policy is a statement of intent which members of staff are expected to follow and should be regarded as mandatory by all staff. Failure to follow a trust policy could result in disciplinary action being taken, up to and including dismissal. Patient data is collected and processed by many staff across the Trust. Data quality may be affected by a wide range of activities; the need for good quality data must therefore be embedded in the culture, values and actions of Trust staff. This policy compliments the following Trust policies: Health Records Management Policy Health Records Keeping Policy Information Security & Data Protection Policy Information Governance Policy Corporate Data Validation Policy 3.0 Policy Statement 3.1 The Trust will: Ensure that operational and clinical staff are aware of the importance and value of good quality patient data. Continue to identify and implement ways of achieving and sustaining improved data quality through training, technical and process developments and collaborative working between staff. Adhere to standards set out in the NHS Data Dictionary and will ensure that locally developed standards are consistent with the NHS Data Dictionary. Continue to set standards for patient data quality that are challenging and consistent with national targets. Maintain and regularly review its Information Security & Data Protection Policy to ensure that it continues to underpin data quality principles. Staff must abide by the principles contained in the Information Security & Data Protection Policy, in particular, be familiar with the principles set out in the Data Patient Data Quality Policy Version 3 April 2013 3 Protection Act (1998). Have a nominated Information Governance Manager and Caldicott Guardian. Data Custodians will be identified throughout the Trust to ensure that Data Protection and Caldicott principles are fully observed and complied with. The roles and responsibilities of these officers will be set out in the Trusts Information Security & Data Protection Policy. Ensure staff abides by the Trust policy for the communication of personal and sensitive data in the process of rectifying data quality issues. All personal and sensitive data must be transferred by either NHS Mail, or if using NUH mail systems, encrypted to NHS standards using software approved by the Trust in accordance with the Trusts E-Mail Policy. Ensure users sign a confidentiality clause and an undertaking to take reasonable steps to ensure the accuracy of information they enter on the computer system. Users will only be given access to the menus and access levels that are appropriate to their job. If a user changes their job within the hospital, access to hospital systems will be reviewed, to ensure that they do not have any inappropriate access. Systematically monitor, review and report on compliance with this policy. 4.0 Definitions 4.1 CSA – Clinical Spine Application CCG – Care Commissioning Group SUS – Secondary Uses Service HRMG – Health Records Management Group CNST – Clinical Negligence Scheme for Trusts EMIAS – East Midland Internal Audit Services 5.0 Roles and Responsibilities 5.1 Committees The Trust Board is responsible for ensuring that arrangements are in place so that it can be assured about patient data quality and compliance with this policy. Patient Data Quality Policy Version 3 April 2013 4 The Information Governance Committee is responsible for overseeing implementation of data quality improvement plans as part of the NHS Information Governance programme. 5.2 Individual Officers The Chief Operating Officer is responsible for promotion and implementation of this policy. The Director of ICT is responsible for the technical integrity of electronic systems used for recording patient data and for delivery of training in the use of these systems. The Deputy Director of Information is responsible for: providing support and advice about NHS Data Standards, their interpretation and implementation corporate monitoring, validation and reporting of patient data quality taking remedial action where patient data quality is found to be below acceptable standards monitoring, reviewing and reporting on compliance with this policy Departmental managers are responsible for monitoring patient data quality and for ensuring that their staff: are aware of the importance of good quality patient data have access to and apply local Standard Operating Procedures that set out the standards and procedures for patient data recording have sufficient training and understanding in the use of systems (paper and electronic) used for recording patient data All staff are responsible for ensuring that they record patient data promptly and accurately with reference to the latest procedures and definitions. Patient Data Quality Policy Version 3 April 2013 5 6.0 Policy and/or Procedural Requirements 6.1 System users must have up to date written departmental procedures available which include procedures for the collection, validation and entry of data. The procedures will be available to staff in all appropriate locations and will be updated in accordance with changes to guidelines and data definitions. As a minimum the following procedures will be documented: Registering a patient GP Referral to Outpatient Clinic or Test Attendance, Cancellation, DNA at outpatient clinic and outcome Add patient to Inpatient Waiting List Emergency or Elective admission Attendance in the Emergency Department All service user and associated data must be entered in accordance with defined standards. Staff who collect and enter service user data have a responsibility to ensure that its accuracy is validated with service users at every opportunity and that any necessary corrections are made promptly. Inaccurate demographics may result in important letters being mislaid, or incorrect identification of a service user. All reference tables, such as GP, Specialty and Postcodes, will be updated within a month of publication unless there are doubts about the quality of the data supplied. All data items held on Trust computer systems must be valid. Where codes are used, these must comply with national standards or map to national values. Wherever possible, computer systems will be programmed to only accept valid entries. Regular validation of compliance and processes will be undertaken on service user data to assess its accuracy. For example Waiting List validations, Duplicate Records, checks for logical errors. Internally a regular program of daily, weekly and monthly error reports from key Trust systems is produced. In addition departmental processes for data validation are outlined in Patient Data Quality Policy Version 3 April 2013 6 the Trusts ‘Corporate Data Validation Policy’. Accredited external sources of information e.g. Clinical Spine Application (CSA), will be used to assist with the validation of service user records. Internal Data Quality reports will be produced and communicated to directorates and CCG’s. These reports will be used to inform management, improve service user processes, ensure focused training, enhance documentation, and enable complete data capture on computer systems. Accredited external organisations will be used to assist in the communication of data quality assurance issues and may include the following: Secondary Uses Service (SUS) Data Quality/Completeness Reports Data Quality Audits Performance Indicators (Annual Health Check) NHS Choices Indicators Service User Queries Commissioner Complaints 7.0 Training and Implementation 7.1 Training As part of the Trusts information systems training courses for staff, the Trust requires all trainers to address the requirement for accurate data and to undertake procedures necessary to achieve this goal. Staff must attend appropriate training to ensure an adequate level of competency in the patient administration functions used in their role. Refresher training will be offered as required. All training should include evaluation of its effectiveness in terms of staff feedback forms: Appropriate staff will receive training on record keeping and management. All data entry systems should have an audit trail that is Patient Data Quality Policy Version 3 April 2013 7 activated and used. (Refer to Training and User Guides for detailed training documentation) 7.2 Implementation Health Records Management 7.2.1 There will be a Health Records Management Group (HRMG) with multi-disciplinary membership. The groups terms of reference will include achievement of Clinical Negligence Scheme for Trusts standards (CNST). 7.2.2 The Health Records Management Group will work in conjunction with partnership agencies and will determine policy for health records management and specify standards for the performance of the health records service. 7.2.3 The Health Records Management Group will review health records policies and procedures and ensure consistency in the operation and performance of the Trusts records stores. Data Quality Standards 7.2.4 The Trusts service users will expect that all data held on them will be 100% accurate. 7.2.5 Service user data held by the Trust must be ‘fit for purpose’. There are many aspects to good quality data: Completeness All mandatory data items within a data set should be completed. Use of default codes should only be used where appropriate, and not as a substitute for real data. If it is necessary to omit a data item in order to admit that patient, the missing data should be reported for immediate follow up. Consistency Data items should be internally consistent. Patients with multiple episodes should have consistent dates. Operations Patient Data Quality Policy Version 3 April 2013 8 and diagnoses will be consistent for ages and/or sex. Coverage Data must reflect all the work done by the Trust. A&E attendances, Admissions, Outpatient attendances and procedures must be recorded. Correct procedures are essential to ensure complete data capture. Spot checks and comparisons between systems will be used to identify missing data. Accuracy Data recorded in notes and on computer systems should accurately reflect what actually happened to a patient. Timeliness Recording of timely data is beneficial to the treatment of the patient. Entering test results into the computer or recording diagnoses and procedures makes that information available to all treating the patient even if they do not have access to the paper notes. All data must be recorded promptly. The accurate recording of data items must not be allowed to delay the urgent treatment of a patient. (Standards for service user data quality are contained in Appendix 2) Accountability 7.2.6 All staff are responsible for assuring the quality of data and information held on service users with whom they are in contact. Managers are accountable for the data quality within the services that they provide. 7.2.7 The lead director reporting to the Trust Board on data quality is the Chief Operating Officer. Audit & Monitoring 7.2.8 The Trust will undertake audits and data quality checks. These will include: External clinical coding audits Internal audits (topics to be agreed) Patient Data Quality Policy Version 3 April 2013 9 Accuracy checks Completeness and validity checks Compliance checks The Trust has undertaken a review of integrated performance reporting with the East Midland Internal Audit Services (EMIAS), the results of which gave ‘significant assurance’ regarding data quality processes. The reports are available from the NUH Information Services website: http://nuhnet/operations/info_services/dataquality/reports/ ReportsLibrary/Forms/current.aspx 7.2.9 Additionally the Trust will use available external reports to monitor data quality and rectify issues identified wherever possible. Information Services will produce and monitor progress against an annual data quality work programme, reporting progress and issues to the Information Governance Committee. Communication on data quality issues to all staff will be maintained through the Trusts Data Quality Newsletter and through the Trusts team brief mechanisms. 7.3 Resources No additional resources needed 8.0 Trust Impact Assessments 8.1 Equality Impact Assessment An equality impact assessment has been undertaken on this draft and has not indicated that any additional considerations are necessary. 8.2 Environmental Impact Assessment An environmental impact assessment has been undertaken on this draft and has not indicated that any additional considerations are Patient Data Quality Policy Version 3 April 2013 10 necessary. 8.3 Here For You Assessment A Here For You assessment has been undertaken on this document and has indicated the need for additional considerations which have been duly incorporated. Patient Data Quality Policy Version 3 April 2013 11 9.0 Policy / Procedure Monitoring Matrix Minimum requirement to be monitored Responsible individual/ group/ committee Process for monitoring e.g. audit Frequency of monitoring Responsible individual/ group/ committee for review of results Daily, Weekly and Monthly Validation reports Directorate Managers Error Reports, Audit of Casenotes Daily, Weekly and Monthly Relevant staff members and Directorate Managers Patient Data Quality Policy Version 3 April 2013 Responsible individual/ group/ committee for development of action plan Directorate Governance Forums Responsible individual/ group/ committee for monitoring of action plan Directorate Governance Forums 12 10.0 Relevant Legislation, National Guidance and Associated NUH Documents 10.1 Equal Pay Act (1970 and amended 1983) Sex Discrimination Act (1975 amended 1986) Race Relations (Amendment) Act 2000 Disability Discrimination Act (1995) Employment Relations Act (1999) Rehabilitation of Offenders Act (1974) Human Rights Act (1998) Trade Union and Labour Relations (Consolidation) Act 1999 Code of Practice on Age Diversity in Employment (1999) Part Time Workers - Prevention of Less Favourable Treatment Regulations (2000) Civil Partnership Act 2004 Fixed Term Employees - Prevention of Less Favourable Treatment Regulations (2001) Employment Equality (Sexual Orientation) Regulations 2003 Employment Equality (Religion or Belief) Regulations 2003 Employment Equality (Age) Regulations 2006 Equality Act (Sexual Orientation) Regulations 2007 Patient Data Quality Policy Version 3 April 2013 13 APPENDIX 1 Patient Data Quality Policy Version 3 April 2013 14 Patient Data Quality Policy Version 3 April 2013 15 Patient Data Quality Policy Version 3 April 2013 16 Patient Data Quality Policy Version 3 April 2013 17 Patient Data Quality Policy Version 3 April 2013 18 APPENDIX 2 Data Output Standards Admitted Patient Care NHS Number Patient Pathway (PPI) Postcode of Usual Address Ethnic Category GP Practice (registered) Date of Birth Sex Source of Admission Method of Admission Admission date Discharge Destination Discharge Method Discharge Date Episode Start Date Episode End Date Intended management Consultant Code Treatment Specialty Primary Diagnosis Healthcare Resource Group Code (HRG) Percentage Complete & Valid 98 100 100 95 99 99 100 99 99 99 99 99 99 99 99 98 100 100 99 99 Outpatients NHS Number Patient Pathway (PPI) Postcode of Usual Address GP Practice (registered) Date of Birth Sex Source of Referral Referral Request Received date Attended or Did Not Attend First Attendance Outcome of Attendance Attendance Date Consultant Code Treatment Specialty Patient Data Quality Policy Version 3 April 2013 98 100 100 99 99 99 99 99 99 99 99 99 100 100 19 Emergency Department NHS Number Postcode of Usual Address GP Practice (registered) Date of Birth Sex Ethnic Group Source of Referral Discharge Destination Primary Diagnosis First Investigation First Treatment Attendance Date Departure Time Patient Data Quality Policy Version 3 April 2013 Percentage Complete & Valid 98 100 99 99 99 99 99 99 99 99 99 100 100 20 APPENDIX 3 Equality Impact Assessment (EQIA) Form (Please complete all sections) Q1. Date of Assessment: 8th February 2013 Q2. For the policy and its implementation answer the questions a – c below against each characteristic (if relevant consider breaking the policy or implementation down into areas) a) Using data and supporting b) What is already in place in c) Please state any Protected information, what issues, the policy or its barriers that still need to Characteristic needs or barriers could the implementation to address be addressed and any protected characteristic any inequalities or barriers to proposed actions to groups experience? i.e. are access including under eliminate inequality there any known health representation at clinics, inequality or access issues to screening consider? The area of policy or its implementation being assessed: Race and No Impact Identified Ethnicity Gender No Impact Identified Age Religion Disability Sexuality Patient Data Quality Policy Version 3 April 2013 No Impact Identified No Impact Identified No Impact Identified No Impact Identified 21 Pregnancy and Maternity Gender Reassignment Marriage and Civil Partnership Socio-Economic Factors (i.e. living in a poorer neighbour hood / social deprivation) No Impact Identified No Impact Identified No Impact Identified No Impact Identified Area of service/strategy/function Q3. What consultation with protected characteristic groups inc. patient groups have you carried out? Following the above initial assessment, this policy does not have an impact either positively or negatively on any of the above strands of equality as the policy sets out the importance of the quality of data collection, for example the appropriateness on the electronic systems used to collect and record patient data not what data is actually being collected. Q4. What data or information did you use in support of this EQIA? Not Applicable Q.5 As far as you are aware are there any Human Rights issues be taken into account such as arising from surveys, questionnaires, comments, concerns, complaints or compliments? None Q.6 What future actions needed to be undertaken to meet the needs and overcome barriers of the groups identified or to create confidence that the policy and its implementation is not discriminating against any groups Not Applicable Patient Data Quality Policy Version 3 April 2013 22 What By Whom By When Resources required Q7. Review date Patient Data Quality Policy Version 3 April 2013 23 APPENDIX 4 Environmental Impact Assessment The purpose of an environmental impact assessment is to identify the environmental impact of policies, assess the significance of the consequences and, if required, reduce and mitigate the effect by either, a) amend the policy b) implement mitigating actions. Area of Environmental Risk/Impacts to consider impact Waste and Is the policy encouraging using more materials/supplies? materials Is the policy likely to increase the waste produced? Does the policy fail to utilise opportunities for introduction/replacement of materials that can be recycled? Soil/Land Is the policy likely to promote the use of substances dangerous to the land if released (e.g. lubricants, liquid chemicals) Does the policy fail to consider the need to provide adequate containment for these substances? (e.g. bunded containers, etc.) Water Is the policy likely to result in an increase of water usage? (estimate quantities) Is the policy likely to result in water being polluted? (e.g. dangerous chemicals being introduced in the water) Does the policy fail to include a mitigating procedure? (e.g. modify procedure to prevent water from being polluted; polluted water containment for adequate disposal) Air Is the policy likely to result in the introduction of procedures Patient Data Quality Policy Version 3 April 2013 Action Taken (where necessary) Not Applicable Not Applicable Not Applicable Not Applicable 24 Energy Nuisances Patient Data Quality Policy Version 3 April 2013 and equipment with resulting emissions to air? (e.g. use of a furnaces; combustion of fuels, emission or particles to the atmosphere, etc.) Does the policy fail to include a procedure to mitigate the effects? Does the policy fail to require compliance with the limits of emission imposed by the relevant regulations? Does the policy result in an increase in energy consumption levels in the Trust? (estimate quantities) Would the policy result in the creation of nuisances such as noise or odour (for staff, patients, visitors, neighbours and other relevant stakeholders)? Not Applicable Not Applicable 25 APPENDIX 5 We Are Here For You Policy and Trust-wide Procedure Compliance Toolkit The We Are Here For You service standards have been developed together with more than 1,000 staff and patients. They can help us to be more consistent in what we do and say to help people to feel cared for, safe and confident in their treatment. The standards apply to how we behave not only with patients and visitors, but with all of our colleagues too. They apply to all of us, every day, in everything that we do. Therefore, their inclusion in Policies and Trust-wide Procedures is essential to embed them in our organization. Please rate each value from 1 – 3 (1being not at all, 2 being affected and 3 being very affected) Value 1. Polite and Respectful Whatever our role we are polite, welcoming and positive in the face of adversity, and are always respectful of people’s individuality, privacy and dignity. 2. Communicate and Listen We take the time to listen, asking open questions, to hear what people say; and keep people informed of what’s happening; providing smooth handovers. 3. Helpful and Kind All of us keep our ‘eyes open’ for (and don’t ‘avoid’) people who need help; we take ownership of delivering the help and can be relied on. 4. Vigilant (patients are safe) Every one of us is vigilant across all aspects of safety, practices hand hygiene & demonstrates attention to detail for a clean and tidy environment everywhere. Patient Data Quality Policy Version 3 April 2013 Score (1-3) 3 3 2 2 26 5. On Stage (patients feel safe) We imagine anywhere that patients could see or hear us as a ‘stage’. Whenever we are ‘on stage’ we look and behave professionally, acting as an ambassador for the Trust, so patients, families and carers feel safe, and are never unduly worried. 6. Speak Up (patients stay safe) We are confident to speak up if colleagues don’t meet these standards, we are appreciative when they do, and are open to ‘positive challenge’ by colleagues 7. Informative We involve people as partners in their own care, helping them to be clear about their condition, choices, care plan and how they might feel. We answer their questions without jargon. We do the same when delivering services to colleagues. 8. Timely We appreciate that other people’s time is valuable, and offer a responsive service, to keep waiting to a minimum, with convenient appointments, helping patients get better quicker and spend only appropriate time in hospital. 9. Compassionate We understand the important role that patients’ and family’s feelings play in helping them feel better. We are considerate of patients’ pain, and compassionate, gentle and reassuring with patients and colleagues. 10. Accountable Take responsibility for our own actions and results 11. Best Use of Time and Resources Simplify processes and eliminate waste, while improving quality 12. Improve Our best gets better. Working in teams to innovate and to solve patient frustrations TOTAL Patient Data Quality Policy Version 3 April 2013 2 2 1 3 3 3 3 3 30 27 APPENDIX 6 CERTIFICATION OF EMPLOYEE AWARENESS Document Title Version (number) Version (date) Patient Data Quality Policy 3 23 April 2013 I hereby certify that I have: Identified (by reference to the document control sheet of the above policy/ procedure) the staff groups within my area of responsibility to whom this policy / procedure applies. Made arrangements to ensure that such members of staff have the opportunity to be aware of the existence of this document and have the means to access, read and understand it. Signature Print name Date Directorate/ Department The manager completing this certification should retain it for audit and/or other purposes for a period of six years (even if subsequent versions of the document are implemented). The suggested level of certification is; Clinical directorates - general manager Non clinical directorates - deputy director or equivalent. The manager may, at their discretion, also require that subordinate levels of their directorate / department utilize this form in a similar way, but this would always be an additional (not replacement) action. Patient Data Quality Policy Version 3 April 2013 28
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