Intended for healthcare professionals

Education And Debate

Measuring “goodness” in individuals and healthcare systems

BMJ 2002; 325 doi: https://doi.org/10.1136/bmj.325.7366.704 (Published 28 September 2002) Cite this as: BMJ 2002;325:704
  1. Mike Pringle (mike.pringle{at}nottingham.ac.uk), professora,
  2. Tim Wilson, directorb,
  3. Richard Grol, professorc
  1. aDivision of General Practice, University of Nottingham, Nottingham NG7 2RD
  2. bQuality Unit, Royal College of General Practitioners, London SW7 1PU
  3. cDirector's Centre for Quality of Care Research (WOK), Nijmegen University, Netherlands PO Box 9101, 6500 HB Nijmegen, Netherlands
  1. Correspondence to: M Pringle

    All agree that we need to measure the quality of health care, including the care given by individual doctors. Measuring “goodness” requires accurate data used appropriately, and it must be done without demoralising and demotivating staff. Do current measures fulfil these requirements, and if not, what measures should be used?

    In the recent Reith lectures (broadcast annually by BBC radio on issues of contemporary interest), Onora O'Neill explored the new age of accountability. She concluded that increasing reliance on measurement reduced trust in health (and other public) services and that professionals and public servants should be free to serve the public.'1 This will ring true with many.

    However, patients, funders, commissioners, provider organisations, and health professionals legitimately want to know just how “good” are individual doctors, teams, and healthcare providing organisations. The traditionally qualitative, anecdotal approach, supplemented by trust, is being increasingly replaced by data on effectiveness, safety, acceptability, and efficiency.

    Measurement is crucial for a range of purposes—learning, quality improvement, accountability, and regulation—but must be used appropriately. We contend that measurement can be used to reinforce the natural desire of healthcare staff to improve care at the same time as understanding the quality of the service delivered.

    However, creating meaningful information from accurate data to facilitate rational choices is a real challenge. It must be done without distorting staff behaviour or demoralising and demotivating health professionals (including managers), and it must offer true comparisons.

    Summary points

    • Individuals and organisations constantly strive to define and measure quality of health care

    • Good data on quality of care are needed to achieve understanding and effective change

    • Data are often used out of context and without taking account of natural variation

    • A good measure of quality of care is appropriate to that task and is used appropriately

    • Twelve attributes can be ascribed to quality measureshelpful when choosing indicators

    Background

    Recently the Institute of Medicine in the United States concluded that “between health care we have and the care we could have is not just a gap but a chasm.”2 An evaluation in a large sample of general practitioners of the use of 29 national (evidence based) guidelines and 282 indicators for primary care in the Netherlands showed that on average 67% of the recommended care was provided to patients.3 Patients' evaluations of primary care collected in 16 countries in Europe with an internationally standardised questionnaire showed that 30-40% of the patients thought that the organisation of services could be better (50% in the United Kingdom).4

    These findings support the action of societies, governments, and healthcare organisations in their monitoring of health care for expenditure, value for money, and safety. Doctors, nurses, and other health professionals need to compare themselves with their peers and against external and self generated standards in order to improve care. And crucially, patients need information to make rational choices—is their doctor competent, is their hospital safe, is their treatment optimal?

    In particular, both the public and managers want to know which the “good” doctors, teams, and institutions are. They want to protect themselves from the bad and incompetent. Of course, there are many definitions and therefore assessments of good, and any one doctor may be very good in some aspects of care but “poor” in others.

    How is “goodness” currently measured?

    The Institute of Medicine has recommended improvements in the way that the healthcare system is measured2 as standards, performance, and changes cannot be monitored effectively without secure measures. However, inappropriate measures (and there is no such thing as the perfect or right measure) can result in perverse incentives or justification for data manipulation. If the person or organisation whose performance is being measured feels powerless to influence the indicator, inappropriate measurement can also lead to demotivation, dysfunction, and crisis. Currently, the selection of quality measures is often driven by what can be measured3 rather than by a definition of “goodness” followed by the derivation of an appropriate measure.

    Many quality measures, such as revalidation, consultation satisfaction rating, or the “fellowship by assessment” quality assurance programme of the Royal College of General Practitioners, relate to individual health professionals. Others more clearly relate to teams or whole organisations. These include star ratings, assessments by the Commission for Health Improvement, or satisfaction with services.

    Examples of measures from the United States include a comprehensive set of quality indicators (developed by researchers at Rand, California), tested for validity and feasibility, that cover many aspects of health care,5 and a set of complex assessments to accredit care—used by the Joint Commission for Accreditation of Health Organisations and the National Committee for Quality Assurance. Other international examples can be found in box B1 on the BMJ ‘s website (bmj.com).

    Official bodies and outside commercial organisations have begun placing data derived from health service self reporting sources in the public domain in ways that make it accessible to patients, managers, researchers, and clinicians. For example, the 60 US hospitals with lowest mortality within 30 days after a myocardial infarction scored lower on patient evaluations of care.6 The hope is that public access to such data will lead to better data, choices, and care, although its impact is still unproved and use by the target groups (patients, other providers, and commissioners) is still limited. 7 8

    Even though choices are often severely constrained, people can look at local comparisons and in many cases add their own vital contextual understanding in making their choice. Prospective patients must weigh comparative information, such as waiting times and outcomes, keeping in mind their own previous experience and the experience of family, friends, and advisers.

    We aspire to a world in which patients are protected by measures of competency; failing teams and organisations can be identified and remedial action taken; patients and their advisers, especially family doctors, can make informed choices of services to use; and service commissioners can deploy resources most efficiently to achieve best care. Finally, the treasury can monitor improvements in care and be held to account by the electorate. This world is currently far from reality.

    How should health care be measured?

    Data on their own are of limited value. Information that compares data with others or against standards is more useful, but without context—and thus understanding—it cannot be applied effectively (figure). Ideally comparisons would be “like with like,” but this rarely happens. Local health needs, service configurations, and case mix all influence data, and this is what is meant by “context.” The easiest way to get good surgical outcomes is to admit only low risk cases; high immunisation rates are much more difficult to achieve in deprived areas.

    Figure1

    Using data for quality improvement and the levels at which they are applied

    In the table we suggest 12 attributes to use when appraising quality measures—with examples of current quality measures in the United Kingdom that we believe have or do not have these attributes. For example, surgical waiting times have good face validity, are usually available, and offer a comparison between teams and organisations. They fall down on effectiveness: they measure only part of the patient's experience, such as time on the waiting list for surgery; their reliability is compromised by manipulation; they are usually not adjusted for the context; and it is never clear whether a long waiting list is due to inefficient surgical teams, poor management, or lack of capacity—so, it is unclear if and how the problem can be resolved.

    Twelve attributes and ideal descriptions of quality measures, with examples from United Kingdom

    View this table:

    If poor quality measures as defined against the attributes in the table are applied, then perverse incentives and demoralisation of managers and health professionals become a real possibility. One major English trust—the Royal United Hospitals, Bath—had manipulated the number it reported for patients waiting over 15 months for surgery. This is precisely the outcome to be avoided. Another powerful lesson from recent experience with performance indicators is that variation occurs in all systems and that detecting unacceptable or dangerous variation is the key task.9 Not all differences are meaningful.

    Lastly, the involvement of service users and the public in developing quality measures is an essential aspect of quality improvement. Although some measures will continue to be technical, there is a shortage of good measures of dimensions of care that are directly relevant to service users and which meet the attributes in the table.

    Right tool for the job

    Measurement can be used for learning and developing, quality improvement, making informed choices, accountability, contracting, and regulation. In choosing a measure, the purpose must be explicit, alternative measures appraised, and the limitations of the chosen measure openly acknowledged.

    In regulation, for example, definitive judgments are needed—a doctor cannot be “slightly” fit to practise—and this requires high face validity, reliability of data (or evidence), and attribution to an individual. Context and interpretation may be used in mitigation, but the key decision is a bipolar judgment: is this behaviour acceptable or unacceptable?

    However, many measures of quality are for feeding into the quality improvement cycle (see box B2 on bmj.com). In this setting, it is much more important that the data are understood and are interpreted within the context of the performance. If a town has a high rate of ischaemic heart disease owing to local deprivation, ethnic mix, or population behaviour, its appearance at the bottom of league tables is more likely to create poor morale and apathy than improvement. If, however, the same data are used to measure “health gain”—the level of care or outcome adjusted for the context—teams will understand the context and use them wisely. As the second of Langland's rules states that “measurement for improvement is not measurement for judgment.”10

    Teams and individuals are increasingly committed to improving the quality of their care as part of their professional imperative and culture.11 The adoption of clinical audit and reflective practice has been slow,12 but the evidence of its effectiveness is mounting, particularly when the audit is integrated in a more comprehensive approach to improving patient care.13 One cornerstone of healthcare improvement is continual measurement as a tool for understanding systems and determining whether changes are effective.

    The way in which data are used (as in figure) is important. At one extreme, simply sending people data on their performance does not create quality improvement. We know that “facilitated feedback” (or “academic detailing”)—that is, using someone trained in interpreting the data to give the feedback—is the most effective way of giving people feedback, but it has to be supported with leadership and resources.

    Conclusions

    It is right that the public, health professionals, and health service managers want to measure absolute and relative performance—or “goodness”—as a means to improve care and support informed choices. The measures used will meet the ideal attributes to a greater or lesser degree and require value judgments in arriving at a conclusion.

    Data should be accurate, measures appropriate, context adjusted for, and interpretation responsible and cautious. That way, stakeholders in health care, especially service users, will be able to make informed choices; good care will be identified and rewarded; and safety will be improved. If healthcare regulators are serious about promoting quality then they must ensure that measures of quality are not misapplied and abused,14 that natural variations in systems are recognised, and that measures are not perceived as capricious tools for shifting responsibility and blame.

    Footnotes

    • Conflict of interest Competing interests: MP is the strategic director of Primary Care Information services (PRIMIS) and is a paid adviser to Dr Foster home.drfoster.co.uk,a guide to local NHS and private healthcare services. TW has been paid for talks and workshops on measurement.


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      More examples of quality measures can be found on bmj.com

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