Routine health outcomes measurement
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- 1 Definition of health outcomes
- 2 Health outcomes measurement and evidence-based practice
- 3 History of routine health outcomes measurement
- 4 Mortality as an outcome measure
- 5 Principles of routine health outcomes measurement
- 6 Current status of routine health outcomes measurement
- 7 Benefits of routine health outcomes measurement
- 8 Risks of routine health outcomes measurement
- 9 Practical issues in routine health outcomes measurement
- 10 References
- 11 See also
Definition of health outcomes
Routine health outcomes measurement is the process of examining whether or not interventions are associated with change (for better or worse) in the patient's health status. This change can be directly measured (e.g. by rating scales used by the clinician or patient) or assumed by the use of proxy measurement (e.g. a blood test result). Interventions can be direct (e.g. medication) or indirect (e.g. change in the process of health care like integration care by different specialists). Some definitions of health outcomes measurement stipulate that the population or group has to be defined (different outcomes are expected for different people & conditions). A strong example is that of Australia’s New South Wales Health Department: health outcome is
"change in the health of an individual, group of people or population which is attributable to an intervention or series of interventions"
In its purest form, measurement of health outcomes implies identifying the context (diagnosis, demographics etc.), measuring health status before an intervention is carried out, measuring the intervention, measuring health status again and then plausibly relating the change to the intervention.
Health outcomes measurement and evidence-based practice
Evidence-based practice describes a healthcare system in which evidence from published studies, often mediated by systematic reviews or processed into medical guidelines is incorporated into clinical practice. The flow of information is one way; from research to practice. However many interventions by health systems and treatments by their staff have never been, or cannot easily be, subject to research study. Of the rest, quite a lot is from research that is graded as low quality. All health staff intervene in their patients on the basis of both information from research evidence and from their own experience. The latter is personal, subjective and strongly influenced by stark instances which may not be representative. However, when information on these interventions and their outcomes are collected systematically it becomes "practice-based evidence" and can complement that from academic research. To date, such initiatives have been largely confined to primary care and rheumatology. An example of practice-based evidence is found in the evaluation of a simple intervention like a medication. Efficacy is the degree with which it can improve patients in randomised controlled trials– the epitome of evidence-based practice. Effectiveness is the degree with which the same drug improves patients in the uncontrolled hurly-burly of everyday practice; data which are much more difficult to come by. Routine health outcomes measurement has the potential to provide such evidence.
The information required for practice-based evidence is of three sorts: context (e.g. case mix), intervention (treatment) and outcomes (change). Some mental health services are developing a practice-based evidence culture with the routine measurement of clinical outcomes and creating behavioral health outcomes management programs.
History of routine health outcomes measurement
An early example of a routine clinical outcomes system was set up by Florence Nightingale in the Crimean War. The outcome under study was death. The context was the season and the cause of death– wounds, infections and any other cause. The interventions were nursing and administrative. She arrived just before the barracks in Scutari were accepting the first soldiers wounded at the battle of Inkerman in November 1854, and mortality was already high. She was appalled at the disorganisation and standards of hygiene and set about cleaning and reorganisation. However, mortality continued to rise. It was only after the sewers were cleared and ventilation improved in March 1856 that mortality fell. On return to the UK she reflected on these data and produced new sorts of chart (she had trained in mathematics rather than "worsted work and practising quadrilles") to show that it was most likely that these excess deaths were caused by living conditions rather than, as she initially believed, poor nutrition. She also showed that soldiers in peacetime also had an excess mortality over other young men, presumably from the same causes. Her reputation was damaged, however, when she and William Farr, Registrar General, collaborated in producing a table which appeared to show a mortality in London hospitals of over 90% compared with less than 13% in Margate. They had made an elementary error in the denominator; the true rate for London hospitals was actually 9% for admitted patients. She was never too keen on hospital mortality figures as outcome measures anyway:
"If the function of a hospital were to kill the sick, statistical comparisons of this nature would be admissible. As, however, its proper function is to restore the sick to health as speedily as possible, the elements which really give information as to whether this is done or not, are those which show the proportion of sick restored to health, and the average time which has been required for this object…"
Here she presaged the next key figure in the development of routine outcomes measurement
Ernest Amory Codman
Codman was a Boston orthopaedic surgeon who developed the "end result idea". At its core was
"The common sense notion that every hospital should follow every patient it treats, long enough to determine whether or not the treatment has been successful, and then to inquire 'if not, why not?' with a view of preventing similar failures in the future."
He is said to have first articulated this idea to his gynaecologist colleague and Chicagoan Franklin H Martin, who later founded the American College of Surgeons, in a Hansom Cab journey from Frimley Park, Surrey, UK in the summer of 1910. He put this idea into practice in Massachusetts General Hospital.
"Each patient who entered the operating room was provided with a 5-inch by 8-inch card on which the operating surgeon filled out the details of the case before and after surgery. This card was brought up 1 year later, the patient was examined, and the previous years' treatment was then evaluated based on the patient's condition. This system enabled the hospital and the public to evaluate the results of treatments and to provide comparisons among individual surgeons and different hospitals"
He was able to demonstrate his own patients’ outcomes and those of some of his colleagues but unaccountably this system was not embraced by his colleagues. Frustrated by their resistance, he provoked an uproar at a public meeting and thus fell dramatically from favour in the hospital and at Harvard, where he held a teaching post, and he was only able to fully realize the idea in his own, struggling small private hospital although some colleagues continued with it at the larger hospitals. He died in 1940 disappointed that his dream of publicly available outcomes data was not even on the horizon, but hoped that posterity would vindicate him.
In a classic 1966 paper, Avedis Donabedian, the renowned public health pioneer, described three distinct aspects of quality in health care: outcome, process and structure (in that order in the original paper). He had misgivings about solely using outcomes as a measure of quality, but concluded that:
"Outcomes, by and large, remain the ultimate validation of the effectiveness and quality of medical care."
He may have muddied the waters a bit when discussing patient satisfaction with treatment (usually regarded as a measure of process) as an outcome, but more importantly it has become apparent that his three-aspect model has been subverted into what is called the "structure-process-outcomes" model, a directional, putatively causal chain that he never originally described. This subversion has been the justification for repeated attempts to improve process and thus outcomes by reorganizing the structure of health care, wittily described by Oxman et al. Donabedian himself cautioned that outcomes measurement cannot distinguish efficacy from effectiveness: (outcomes may be poor because the right treatment is badly applied or the wrong treatment is carried out well), that outcomes measurement must always take into account context (factors other than the intervention may be very important in determining outcomes), and also that the most important outcomes may be the least easy to measure, so easily measured but irrelevant outcomes are chosen (e.g. mortality instead of disability).
Mortality as an outcome measure
Perhaps because of instances of scandalously poor care (for example at the Bristol Royal Infirmary 1984-1995) mortality data have become more and more openly available as a proxy for other health outcomes in hospitals, and even for individual surgeons. However Florence Nightingale’s astringent judgement and Donabedian’s reservations retain their full force for most health services, where routine non-mortal health outcomes measurement remains the most appropriate method.
Principles of routine health outcomes measurement
- All three dimensions (context, intervention as well as outcomes) must be measured. It is not possible to understand outcomes data without all three of these.
- Different perspectives on outcomes need to be acknowledged. For instance, patients, carers and clinical staff may have different views of what outcomes are important, how you would measure them, and even which were desirable
- Prospective and repeated measurement of health status is superior to retrospective measurement of change such as Clinical Global Impressions. The latter relies on memory and may not be possible if the rater changes.
- The reliability (statistics) and validity (statistics) of any measure of health status must be known so that their impact on the assessment of health outcomes can be taken into account. In mental health services these values may be quite low, especially when carried out routinely by staff rather than by trained researchers, and when using short measures that are feasible in everyday practice.
- Data collected must be fed back to them to maximize data quality, reliability and validity. Feedback should be of content (e.g. relationship of outcomes to context and interventions) and of process (data quality of all three dimensions)
Current status of routine health outcomes measurement
Why is routine health outcomes measurement so rare? One can find reports of routine health outcomes measurement in many medical specialties and in many countries. However, the vast majority of these reports are by or about enthusiasts who have set up essentially local systems, with little connection with other similar systems elsewhere, even down the street. In order to realise the full benefits of an outcomes measurement system we need large-scale implementation using standardised methods with data from high proportions of suitable healthcare episodes being trapped. In order to analyse change in health status (health outcomes) we also need data on context, as recommended by Donabedian and others, and data on the interventions being used, all in a standardised manner. Such large-scale systems are only at present evident in the field of mental health services, and only well developed in two locations: Ohio and Australia, even though in both of these data on context and interventions are much less prominent than data on outcomes. The major challenge for health outcomes measurement is now the development of usable and discriminatory categories of interventions and treatments, especially in the field of mental health.
Benefits of routine health outcomes measurement
Aspirations include the following benefits
- Aggregated data
- Can form the basis of effectiveness data that complement efficacy data. This could show the actual benefits in everyday clinical practice of interventions previously tested by randomised clinical trials, or the benefits of interventions that have not been or cannot be tested in Randomized Controlled Trials and systematic reviews
- Can identify hazardous interventions that are only apparent in large datasets
- Can be used to show differences between clinical services with similar case mix and thus stimulate search for testable hypotheses that might explain these differences and lead to improvements in treatment or management
- Can be used to compare the outcomes of treatment and care from different perspectives– e.g. clinical staff and patient
- Data about individual patients
- Can be used to track changes during treatment over periods of time too long to be amenable to memory by an individual patient or clinician, and especially when more than one clinician or team is involved
- Can, especially when different perspectives are available, be used in discussions between patients, clinicians and carers about progress
- Can be used to speed up and crispen clinical meetings
Risks of routine health outcomes measurement
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- If attempts are made to purchase or commission health services using outcomes data, bias may be introduced that will negate the benefits, especially in the service provider produces the outcomes measurement. See Goodhart's Law
- Inadequate attention may be paid to the analysis of context data, such as case mix, leading to dubious conclusions.
- If data are not fed back to clinicians participating then data quality (and quantity) is likely to fall below the thresholds necessary for reasonable interpretation.
- If only a small proportion of episodes of health care have completed outcomes data, then these data may not be representative of all episodes, although the threshold for this effect will vary from service to service, measure to measure.
- Some risks of bias, widely foretold, are proving to be insubstantial but need guarding against
Practical issues in routine health outcomes measurement
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Experience suggests that the following factors are necessary for routine health outcomes measurement
- an electronic patient record system with easy extraction from data warehouse. Entry of outcomes data can then become part of the everyday entry of clinical data. Without this, aggregate data analysis and feedback is very difficult indeed.
- resources and staff time set aside for training and receiving feedback
- resources and personnel to extract, analyse and proactively present outcomes, casemix and, where available, intervention data to clinical teams
- regular reports on data quality as part of a performance management process by senior managers can supplement, but not replace, feedback
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