Prognosis research strategy (PROGRESS) 1: A framework for researching clinical outcomes

BMJ 2013; 346 doi: http://dx.doi.org/10.1136/bmj.e5595 (Published 5 February 2013)
Cite this as: BMJ 2013;346:e5595
  1. Harry Hemingway, professor of clinical epidemiology1,
  2. Peter Croft, professor of epidemiology2,
  3. Pablo Perel, clinical senior lecturer3,
  4. Jill A Hayden, assistant professor4,
  5. Keith Abrams, professor of medical statistics5,
  6. Adam Timmis, professor of clinical cardiology6,
  7. Andrew Briggs, Lindsay chair in health policy & economic evaluation7,
  8. Ruzan Udumyan, research assistant1,
  9. Karel G M Moons, professor of clinical epidemiology8,
  10. Ewout W Steyerberg, professor of medical decision making9,
  11. Ian Roberts, professor of epidemiology and public health3,
  12. Sara Schroter, senior researcher10,
  13. Douglas G Altman, professor of statistics in medicine11,
  14. Richard D Riley, senior lecturer in medical statistics12
  15. for the PROGRESS Group
  1. 1Department of Epidemiology and Public Health, University College London, London WC1E 7HB, UK
  2. 2Arthritis Research UK Primary Care Centre, Keele University, Keele ST5 5BG, UK
  3. 3London School of Hygiene & Tropical Medicine, London WC1E 7HT
  4. 4Department of Community Health and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada B3H 1V7
  5. 5Centre for Biostatistics & Genetic Epidemiology, Department of Health Sciences, School of Medicine, University of Leicester, Leicester LE1 7RH, UK
  6. 6London Chest Hospital, London E2 9JX
  7. 7Health Economics & Health Technology Assessment, Centre for Population & Health Sciences, University of Glasgow, Glasgow G12 8RZ, UK
  8. 8Julius Center for Health Sciences and Primary Care, UMC Utrecht, Utrecht, Netherlands
  9. 9Department of Public Health, Erasmus MC, Rotterdam, Netherlands
  10. 10BMJ, BMA House, London WC1H 9JR
  11. 11Centre for Statistics in Medicine, University of Oxford, Oxford OX2 6UD, UK
  12. 12School of Health and Population Sciences, University of Birmingham, Birmingham B15 2TT, UK
  1. Correspondence to: H Hemingway h.hemingway{at}ucl.ac.uk
  • Accepted 29 July 2012

Understanding and improving the prognosis of a disease or health condition is a priority in clinical research and practice. In this article, the authors introduce a framework of four interrelated themes in prognosis research, describe the importance of the first of these themes (understanding future outcomes in relation to current diagnostic and treatment practices), and introduce recommendations for the field of prognosis research

In clinical medicine, the term prognosis refers to the risk of future health outcomes in people with a given disease or health condition. Prognosis research is thus the investigation of the relations between future outcomes (endpoints) among people with a given baseline health state (startpoint) in order to improve health (see supplementary figure on bmj.com). The study of prognosis has never been more important, as globally more people are living with one or more disease or health impairing condition than at any previous time.1 For this reason, governments across the world are increasing their interest in the outcomes of healthcare currently provided for people with disease.2 Similarly, research funders and researchers are increasingly focused on translating new interventions and technologies from the laboratory to clinical practice and then healthcare policy in order to establish and implement new standards of high quality care and improve patient outcomes.

Prognosis research findings should thus be integral to clinical decision making, healthcare policy, and discovering and evaluating new approaches to patient management. However, there is a concerning gap between the potential and actual impact of prognosis research on health. Prognosis research studies too often fall a long way short of the high standards required in other fields, such as therapeutic trials and genetic epidemiology.

In the PROGnosis RESearch Strategy (PROGRESS) series (www.progress-partnership.org), we propose a framework of four distinct but inter-related prognosis research themes:

  • (1) The course of health related conditions in the context of the nature and quality of current care (fundamental prognosis research)

  • (2) Specific factors (such as biomarkers) that are associated with prognosis (prognostic factor research)3

  • (3) The development, validation, and impact of statistical models that predict individual risk of a future outcome (prognostic model research)4

  • (4) The use of prognostic information to help tailor treatment decisions to an individual or group of individuals with similar characteristics (stratified medicine research).5

Figure 1 illustrates these four prognosis research areas for women with breast cancer (startpoint) and the endpoint of death or disease-free survival. Part (a) shows country variations in age adjusted, five year survival (fundamental prognosis research)6; part (b) shows survival curves according to the value of extracellular domain of human epidermal growth factor receptor 2 (HER2 ECD), which is identified to be prognostic of disease outcome (prognostic factor research)7; part (c) shows the use of multiple clinical variables within a statistical model to estimate individual risk of a particular endpoint (prognostic model research)8; and part (d) shows why a positive oestrogen receptor status is used to identify those who will benefit from tamoxifen therapy (stratified medicine research).9

Fig 1 Framework of four different types of prognosis research question, illustrated for breast cancer. a) Fundamental prognosis research: variations between countries in age adjusted, five year survival (with permission from Cancer Research UK6). b) Prognostic factor research: survival curves showing that patients with “positive” values (>8.9 ng/mL) of the extracellular domain of human epidermal growth factor receptor 2 (HER2 ECD) have a worse survival than those with negative values (≤8.9 ng/mL), and thus HER ECD is a potential prognostic factor (from Tsai et al7). c) Prognostic model research: use of multiple clinical variables in a model to estimate risk of endpoint, and then combined with evidence of treatment effectiveness to inform clinical decisions (ER=oestrogen receptor) (from Adjuvant! Online8). d) Stratified medicine research: predictors of differential treatment response identified in randomised trials, showing that the benefit of tamoxifen is confined to those with positive oestrogen receptor (ER) status (based on data from Early Breast Cancer Trialists Collaborative Group9)

The overarching aim of the PROGRESS series is to explain how each of these four prognosis research themes provides important evidence that can be used at multiple (translational) pathways toward improving clinical outcomes—from the discovery of new interventions, through to their evaluation and implementation in the clinical management of individual patients, and to examining the impact of interventions and healthcare policies on patient outcomes. This contrasts with previous reviews of prognosis research which consider impact at one end of the translational spectrum (such as clinical decision making) or on just one type of prognosis question (such as prognostic models10). Whereas previous reviews focus on one specific disease area (such as cancer),11 12 we include examples from cancer, cardiovascular disease, musculoskeletal disorders, trauma, and other conditions. Our series describes the current challenges and opportunities in the field and makes recommendations for necessary improvements to move toward a clearer map for prognosis research that ultimately improves patient outcomes (summarised in supplementary table 1 on bmj.com).

An important place to start is with research that aims to examine the outcomes of a disease or health condition in the context of current clinical practice, and this we term fundamental prognosis research. In this first article we consider what this entails, explain its importance in pathways toward improving patient outcomes, and outline a set of recommendations with the aim of improving the quality and impact across all of the inter-related themes in prognosis research and which will be expanded in the other articles in our series.

What is fundamental prognosis research?

Before carrying out research into novel prognostic factors, prognostic models, or stratified medicine it is necessary to carry out research describing and explaining future outcomes in people with a disease or health condition in relation to current diagnostic and treatment practices. There is a close relation between the questions “What is the prognosis of people with this condition?” and “What are the outcomes of the care which people receive for this condition?” In order to improve the quality of healthcare, evidence is required on how the specific patterns of care received (such as investigation, treatment, support), and their variations (such as underuse, overuse, misuse) have an impact on future endpoints.13 Such research has a broad remit. It spans, for example, investigations into societal influences (inequitable variations in care and outcome among older people, women, the socially disadvantaged, and ethnic minorities), patient safety,14 15 unanticipated harms and benefits from treatments, and screening research. Prognosis in the absence of care—which is sometimes termed natural history—is an important parameter for judging the potential impact of screening for asymptomatic disease (such as mammography for breast cancer), as well as for case detection of symptomatic undiagnosed or unpresented conditions such as back pain or angina.16 17

These relations may be expressed as an absolute risk (or rate) of one or more type of endpoint among groups of people who share demographic and clinical characteristics; some refer to this as an average prognosis in a particular group of interest, or as a baseline risk. Here the research provides initial answers to the question “What is the prognosis of people with a given disease?” For example, on average about 15% of people aged 65 years or older, admitted in 2006 in the US died within 30 days of admission to hospital with a heart attack compared with an average of 19% in 1995.18 Such a change in the average mortality rate is illustrated in figure 2. This shows the decreasing prognostic burden of heart attack and motivates inquiry into new approaches to understand and reduce this risk further. This clinical scenario also exemplifies that “the prognosis” of a disease or condition is a somewhat misleading expression: what is observed is prognosis of people in particular clinical contexts, defined by current clinical approaches in diagnosing, characterising, and managing patients with a symptom or disease.

Fig 2 Example of use of fundamental prognosis research to examine variations in outcomes from medical care: inter-hospital variation in mortality per 100 population within 30 days of admission with acute myocardial infarction (created using fictional data for illustration purposes, but based on the findings of Krumholz et al18)

Such prognosis research is also concerned with describing and understanding the variations around the average course.19 20 These variations may occur between individual patients or between patients clustered, for example, within surgeons, hospitals, or regions. The acute myocardial infarction example above demonstrates striking variations between hospitals in prognosis, and similar variations are seen in traumatic brain injury and other conditions.18 21 Indeed, for most hospitals the national average is a poor guide to the mortality of their patients (fig 2).

Stephen J Gould, the evolutionary biologist, having survived 20 years after being told the median survival of his abdominal mesothelioma was eight months, famously remarked, “the median isn’t the message.”22 Describing and explaining the sources of variability in prognosis is a theme throughout our PROGRESS framework.3 4 5 Fundamental prognosis research may help explain Gould’s long survival in terms of the demographic and clinical context (for example, his high educational status and the quality of care received), whereas research into emerging prognostic factors may examine psychological, behavioural, or biomarker factors associated with improved outcome (see paper 2 in our series3), or the extent to which his survival was predictable from statistical models of individual risk prediction (paper 3 in our series4), or whether particular treatments had a larger beneficial effect for him than for others (paper 4 in our series5).

Importance of fundamental prognosis research in the pathways toward improved health outcomes

Healthcare professionals, people with a disease or health condition, funders, and policy makers require valid, reliable evidence about the outcomes of diseases and health conditions in order to make decisions. Here we review the potential impact of such evidence across translational pathways in healthcare, starting from the applied, healthcare delivery end (far right of pathways schema shown at bottom of figs 2, 3, and 4) and working back to discovery and new approaches (far left of schema).

Importance for public health policy

Public health policy makers need estimates of average prognosis to model the population burden of diseases and assess the relative contribution of healthcare delivery among those with disease (secondary prevention) and without disease (primary prevention). For example, the public health objective of reducing overall coronary heart disease mortality (a conflation of incidence of non-fatal coronary disease and subsequent death) has been helped by modelling the impact of population interventions aimed at early detection and primary and secondary prevention.23 24 25 Such models use an average prognosis of heart attack survival from the date of diagnosis among age and sex strata to attribute quality adjusted life years (and health service costs of managing the disease) which would be saved with successful prevention.

By contrast with the improvements over time in the prognosis of coronary disease, for people with low back pain there is little evidence that the average prognosis (based on symptom relief 26 27) has changed over the past 20 years, nor does it differ between countries with different healthcare systems.28 This suggests that healthcare itself is not a major influence on average symptomatic outcome in people with back pain. However, when considering the outcome of sickness absence, there are dramatic variations over time and between countries—suggesting the importance of the broader public health context of working patterns and benefit payments for chronic illness.29

Importance for comparative effectiveness and health services research

Insights into health and healthcare policy may come from comparing the prognosis of specific conditions over time and place in order to assess the comparative effectiveness of systems of care.30 31 For example, figure 1 shows that the five year survival from breast cancer in 2000-03 varies widely from country to country (from about 70% in the Czech Republic to 90% in Iceland). The UK seems to have worse cancer survival than most other European countries,32 and the latter have worse survival for some cancers than the US. Such international comparisons of average prognosis provide a motivation for researchers to uncover explanations and for healthcare policy makers to improve the quality of care and deliver better health outcomes.2 Policy makers seeking to improve national cancer outcomes may consider a range of interventions, including: early detection (such as mammography screening), population-wide guidance (such as encouraging self examination),33 34 centralisation of services, and systematic implementation of cost effective therapies. Ecological comparisons of country-level factors (such as smoking prevalence or number of specialists per capita population) can be related to outcomes. Such research may generate hypotheses for prognostic factor research (see paper 2 in our series3) as well as helping to formulate service and policy development.

Fundamental prognosis research is vital in addressing the “second gap” in translation,35 in which evidence from randomised trials of effective treatments may fail to be implemented in usual clinical practice (far right of translational pathway toward improved clinical outcomes). For example, the between hospital variations in outcome from acute myocardial infarction (fig 2) may, in part, stem from differing use of evidence based therapies. These findings have profound implications for healthcare policy. It demonstrates a “normal distribution” of mortality between hospitals; over time the whole distribution of hospital mortality improves and shifts to the left and the variation between hospitals in outcomes narrows. The policy implication is that improvements in the quality of care in the population of all hospitals may have contributed to the observed shift in the average prognosis. Thus the evidence did not support a contrasting policy alternative of focusing on the identification of, and remedial action in, outlying poor performers.36 Here prognosis research is contributing evidence about health services and is managing knowledge generated from electronic health records. Such evidence35 informs policy choices which are themselves highly unlikely to be subjected to randomised trials.37

Importance for health technology assessment of imaging and other tests

A key target for translational research is the development of new clinical imaging and molecular markers which may identify patient phenotypes in such a way as to lead to improved outcomes. Such new technologies may change the spectrum of diagnosed disease, and the question is whether prognosis is the same as with the use of standard tests and whether the balance of benefit and harm of treatment remains the same. For example, for decades exercise electrocardiography has been used in the characterisation of patients with stable chest pain, and recent guidelines recommend the use of an emerging technology, non-invasive computed tomographic coronary angiography, in some patients.38 Since event powered randomised trials of imaging remain rare, fundamental prognosis research provides an important method of health technology assessment.39

Importance for trials and decision models

Estimates of average prognosis are also crucial for the rationale, design, interpretation, and impact modelling of trials of an intervention to improve prognosis. For example, prognosis research among people with angina shows that 50% of people with existing therapies have recurrent or persistent symptoms,40 suggesting the need for trials of new interventions. Reliable estimates of prognosis inform the estimates of likely accrual of endpoints in the trial arms (such as expected proportion experiencing an event by a particular time), and hence facilitate statistical sample size calculations. They also contribute to the interpretation in terms of generalisability of clinical trial results, as one can compare the average prognosis of patients in the trial without treatment with the average prognosis in particular populations.

Importantly, in order to translate relative treatment effects (such as relative risks or hazard ratios) back to the absolute scale, one needs to know the average prognosis (baseline risk) in the untreated group. One can then talk in terms of the reduction in probability of a poor outcome (risk difference), which leads to clinically informative measures such as the number needed to treat in order to save one patient from a particular poor outcome. Absolute effects are used within decision models and cost effectiveness analyses, which are highly influential to decision makers such as the National Institute of Health and Clinical Excellence (NICE). Such models combine parameters of average prognosis along with estimates of treatment effects and costs. Conclusions from these models are often particularly sensitive to the accuracy of the data on average prognosis among those without the specific treatment of interest.

Importance for new approaches, mechanisms, and targets for trials

Fundamental prognosis research may provide insights beyond evaluating the status quo of clinical care. Estimating the prospective associations between two diseases has led to startling discoveries that have stimulated the development of new interventions and new clinical trials that have ultimately changed clinical practice. For example, few foresaw that a prognostic consequence of Helicobacter pylori infection was peptic ulcer before the Nobel prize winning work that established the link and subsequent antibiotic trials.41 Importantly, the outcomes of uncommon conditions may give insights into disease mechanisms of common conditions. For example, the increased risk of coronary outcomes among people with familial hypercholesterolaemia focused interest on the low density lipoprotein cholesterol pathways which are important in coronary disease experienced by people without this genetic disorder and contributed to the development of lipid lowering therapy.

Taking a broad view of prognostic outcomes may generate new knowledge at the start of translational pathways with (as yet) unknown implications for developing new interventions. Consider the example of following up people with Parkinson’s disease. The risk of cancer is not an endpoint that would conventionally be considered. However, a meta-analysis found that the risk of cancer was significantly reduced compared with people without Parkinson’s disease (fig 3).42 This raises the question whether specific characteristics of Parkinson’s disease that explain this apparent protective effect can be identified, and whether this might lead to new intervention targets. There are probably many prognostic associations between two or more diseases that have yet to be uncovered. Some have proposed that approaches using all available clinical data (so called phenome-wide scans), agnostic to any prior theories about mechanism, might identify new associations between conditions.43

Fig 3 Example of use of fundamental prognosis research to discover new associations between diseases: cancer among non-smoking people with Parkinson’s disease (drawn using data from Bajaj et al42). Path element adapted from chart 7.1 in the Cooksey report (2006) http://bit.ly/Ro27rL (made available for use through the Open Government License)

Importance for overcoming the limitations of diagnosis

The understanding of future outcome risk (prognosis) may be a more useful way of formulating clinical problems than pursuing diagnosis for several reasons. First, subjectively reported illness such as mental health problems and pain syndromes is often managed more with prognostic than diagnostic labels.44 For example, a physician may reasonably say to a person presenting with back pain, “I do not know what is wrong, but I do know that this is the sort of back pain that is very likely to get better quickly.” Evidence from prognosis research has helped to redefine low back pain. Spinal radiography and magnetic resonance imaging contribute little to understanding the average prognosis of most back pain,16 45 but the duration of symptoms at presentation in primary care is strongly related to outcome. Figure 4 shows that the chance of reduced disability at one year is about 70% in those with a shorter duration (<3 years) of symptoms at presentation versus 40% in those with a longer duration.26 29 46 Clinical practice guideline recommendations use symptom duration to guide management decisions.47 Symptom duration is associated with clinical outcome and is thus a prognostic factor (see paper 2 in our series3), which has resulted in it being a standard component of the clinical evaluation of back pain.

Fig 4 Example of use of fundamental prognosis research to define clinically relevant subgroups: duration of low back pain at presentation (<3 or ≥3 years) and the time to improvement of disability disease (drawn using data from Dunn et al46). Path element adapted from chart 7.1 in the Cooksey report (2006) http://bit.ly/Ro27rL (made available for use through the Open Government License)

Second, fundamental prognosis research can take a holistic view of all comorbidities that a person experiences, whereas diagnosis implies a focus on a single organ system or pathology. The prognosis of some cancers, traumatic brain injury, and back pain are importantly influenced by conditions not related to the tumour, brain, and spine respectively. Third, diagnosis implies a dichotomy (case v not at a single point in time), which may be a misleading basis for clinical decision making. For example, in many countries the decision to lower blood cholesterol is not based on a diagnosis of hypercholesterolaemia but on thresholds of continuous risk, determined by age, sex, smoking, blood pressure, and lipids (see paper 3 in our series4). Such observations have led to the radical proposition that the dichotomous, cross sectional snapshot of diagnostic practice may become redundant, as clinicians increasingly have access to continuous measures of future risk.48 49

Importance for discovering new diseases

Fundamental prognosis research drives definitions of the diseases for which interventions are sought.50 Such research helps define our current view of what distinct clinical conditions exist and what role new clinical tests might have in changing our classification of disease entities (nosology). The question “what is the prognosis of this condition?” is intimately related to the question “what is this condition?” For example, the entity of non-fatal myocardial infarction was identified only after many decades of clinical prognostic observation that symptoms of chest pain may precede death, replacing the view that the disease of myocardial infarction was inevitably and instantly fatal. More recently, prognosis research has helped to redefine non-fatal acute myocardial infarctions51 based on the presence or absence of ST elevation, a predictor of differential response to therapy, and serum troponin measurement. Figure 5 shows that examination of survival patterns differentiates clinical phenotypes among people admitted with suspected non-fatal myocardial infarction. An example of a newly recognised genetic disorder discovered through prognostic observation is Brugada syndrome in which an ST elevation pattern on resting electrocardiogram is associated with sudden death.52

Fig 5 Example of use of fundamental prognosis research to distinguish clinically relevant groups: people admitted with suspected acute myocardial infarction (results based on an analysis of 180 000 patients in the Myocardial Ischaemia National Audit Project, A Timmis and H Hemingway personal communication)

Recommendations for improving the quality and impact of prognosis research

For each of the four themes of prognosis research to achieve its potential for improving clinical outcomes, important challenges need to be addressed and opportunities seized in prognosis research as a whole. The research community needs to address serious flaws in the design, conduct, and reporting of prognosis studies and to recognise the clinical value of reliable prognostic evidence. In the PROGRESS series we thus make recommendations for progress in the field, and these are summarised in supplementary table 1 on bmj.com. Here we introduce recommendations that cut across the different research themes. In papers 2–4 in the PROGRESS series,3 4 5 we discuss the other recommendations from supplementary table 1. These recommendations add to, and further specify, those which we have previously made in the BMJ.53

Fuelling changes in medicine and healthcare

As shown in the examples above, improvements in electronic health records, clinical imaging, and “omic” technologies (genotyping and phenotyping) are beginning to challenge current disease taxonomy, the focus of much healthcare policy on process (rather than clinical outcomes), and the clinical preoccupation with diagnosis (rather than risk). There should be a formative shift in clinical practice, healthcare policy, and translational research based on evidence from prognosis research—that is, the prospective relationships between the phenotypic, genomic, and environmental assessment of people with a given startpoint and subsequent endpoints (recommendation 1 in supplementary table 1). Over their life course, individuals develop multiple diseases (both distinct and related) that often do not respect the current organisation of medical research or practice. There should be new programmes of prognosis research that bridge multiple clinical specialties, health systems, pathological mechanisms, and biological systems and that put the whole patient across his or her “journey” as the central unit of concern (recommendation 2).

Electronic health records

The scope and impact of prognosis research and electronic health records research (in primary and secondary care, and in disease and procedure registries) are intimately related. There is increasing availability of electronic health records in primary54 and secondary care, and disease and procedure registries. Particularly where such sources can be linked,55 there is the possibility of examining the “patient journey” with repeated measures of risk and care in larger populations than are feasible with bespoke, investigator led studies. Population coverage, data quality, and the extent of blood, imaging, and other diagnostic data are all improving. But concerted efforts are required to harmonise data on startpoints, endpoints, and populations of interest in order to make temporal and international comparisons in prognosis. There should be new programmes of methodological and empirical prognosis research exploiting electronic health records to define, phenotype, and follow up people with different health related conditions (recommendation 3).

Visibility of the field

Prognosis research is currently fragmented and not visible as a distinct entity. Prognosis research should be recognised as a field of inquiry important in translational research and intrinsic to the practice of clinical medicine and development of healthcare policy (recommendation 4). Efforts should be made to establish prognosis research as a distinct branch of knowledge, with a set of scientific methods aimed at understanding and improving health. Evidence about prognosis is somewhat neglected; such as in medical textbooks, where the focus is on the effectiveness of therapies, with only brief details given on average prognosis,56 sometimes as if therapies can be divorced from the context of clinical care.57 58

Fundamental prognosis research should compare the prognosis of clinical cohorts with that of the healthy population (recommendation 5). Relative survival methods are commonly applied in cancer, but less often in other disease areas. Relative survival methods model the survival probability of people with a condition relative to the expected survival without the condition (obtained from national population life tables stratified by age, sex, calender year, and other covariates). By comparing the observed and expected survival, one can estimate the added risk of mortality due to having the condition rather than not having it (that is, measure how prognosis is modified by onset of a disease). Such methods help prognosis research prioritise which clinical cohorts require the most attention and most translational research (that is, identify those cohorts whose prognosis is most changed by disease onset).

The situation for cancer, where estimates of survival are readily available (such as Surveillance Epidemiology and End Results, SEER59) is exceptional. Knowledge management in prognosis seems somewhat chaotic in generation, dissemination, and accessibility. Difficulties in identifying and accessing information about prognosis, and evidence from prognosis research studies, hamper efforts to inform patients and evaluate the impact of translational efforts to improve outcomes. Evidence from prognosis research and information about prognosis should be systematically collated, made easily accessible, and updated (recommendation 6).

Teaching and training

Undergraduate and postgraduate training do not currently provide instruction in how to generate or use evidence from prognosis research. All healthcare professionals should be trained in the generation and use of prognosis research evidence; there should be an expansion of training and education opportunities for those interested in methodological aspects of prognosis research (recommendation 7).

Patient and public involvement

Questions of prognosis are among the most important to patients, but the level of patient and public involvement in prognosis research is low. Patient reported outcomes are important to clinical decision and policy making but are understudied. For example, people with angina might reasonably ask “will my symptoms get better?” yet a recent systematic review of 83 studies found none that reported symptomatic status as an endpoint (favouring acute coronary events instead).60 Symptom status is acknowledged as a major determinant of the clinical decision to recommend revascularisation.61 Prognosis research using person focused endpoints may yield unanticipated results. For example, people with rheumatoid arthritis may care more about fatigue than about the joint pain, on which doctors tend to focus.62 Patients and the wider public should be more engaged in the goals and value of prognosis research, appropriate use of their clinical data, and better integration of patient reported outcome measures (recommendation 8).

Conclusion

In this first article in the PROGRESS series, we have introduced a framework of four themes in prognosis research, and outlined the importance of initial, fundamental prognosis research. This first theme is central to the practice of medicine; from basic understanding of the categories we choose to call disease through to understanding how variations in healthcare influence the risk of endpoints. As such, it has a broad array of uses for policy makers, patients, and clinical decision making and should be considered a core component of prognosis research. To maximise the impact of each interrelated theme of prognosis research,3 4 5 we have begun outlining a set of recommendations to enhance the prognosis field, including better use of electronic health records, greater training and public involvement, and a wider appreciation of the clinical value of prognosis research findings.

Summary points

  • The PROGRESS series (www.progress-partnership.org) sets out a framework of four interlinked prognosis research themes and provides examples from several disease fields to show why evidence from prognosis research is crucial to inform all points in the translation of biomedical and health related research into better patient outcomes. Recommendations are made in each of the four papers to improve current research standards

  • What is prognosis research? Prognosis research seeks to understand and improve future outcomes in people with a given disease or health condition. However, there is increasing evidence that prognosis research standards need to be improved

  • Why is prognosis research important? More people now live with disease and conditions that impair health than at any other time in history; prognosis research provides crucial evidence for translating findings from the laboratory to humans, and from clinical research to clinical practice

  • This first article introduces the framework of four interlinked prognosis research themes and then focuses on the first of the themes—fundamental prognosis research, studies that aim to describe and explain future outcomes in relation to current diagnostic and treatment practices, often in relation to quality of care

  • Fundamental prognosis research provides evidence informing healthcare and public health policy, the design and interpretation of randomised trials, and the impact of diagnostic tests on future outcome. It can inform new definitions of disease, may identify unanticipated benefits or harms of interventions, and clarify where new interventions are required to improve prognosis

  • The other papers in the series are:

Notes

Cite this as: BMJ 2013;346:e5595

Footnotes

  • We thank John Scadding, emeritus dean at the Royal Society of Medicine, for his support of the PROGRESS Group, contributions to discussions, and helpful comments on drafts of the manuscripts. We thank Ruzan Udumyan for assistance in drawing figures and preparing manuscripts. We thank Virginia Barbour and Trish Groves for contributing to the workshops and their support for the series. We thank Lucy Chappell (King’s College London) for her valuable help as guest editor on the PROGRESS series.

  • Contributors: HH, RDR, SS, and DGA initiated the PROGRESS Group, organised the three workshops, coordinated the writing groups, and were the scientific writing editors for all the papers in the PROGRESS series. HH, RDR, and DGA are the guarantors for this paper. HH wrote the first version, and PC, PP, JAH, KA, AT, AB, KGMM, EWS, IR, SS, DGA, and RDR contributed to the conception of the paper and to the revising of draft versions and approved the final version. All members of PROGRESS Group contributed through workshops and discussions to the development of the article series.

  • Members of the PROGRESS Group: Keith Abrams (UK), Doug Altman (UK), Andrew Briggs (UK), Nils Brunner (Denmark), Peter Croft (UK), Jill Hayden (Canada), Aroon D Hingorani (UK), Harry Hemingway (UK), Panayiotis Kyzas (UK), Núria Malats (Spain), Karel Moons (Netherlands), George Peat (UK), Pablo Perel (UK), Richard Riley (UK), Ian Roberts (UK), Willi Sauerbrei (Germany), Sara Schroter (UK), Ewout Steyerberg (Netherlands), Adam Timmis (UK), Daniëlle van der Windt (UK).

  • Funding: This series had no explicit funding, but some of the authors were supported by research grants: PROGRESS is supported by a Partnership grant from the Medical Research Council (G0902393), involving University College London (HH, AH), Oxford University (DGA), Birmingham University (RDR), London School of Hygiene and Tropical Medicine (IR, PP), Keele University (PC, D van der Windt), and Queen Mary University London (ADT). DGA is supported by a programme grant from Cancer Research UK (C5529). HH is supported by grants from the UK National Institute for Health Research (RP-PG-0407-10314) and the Wellcome Trust (086091/Z/08/Z). The work of HH and AT is supported by the Health eResearch Centre Network (HERC-UK), funded by the Medical Research Council in partnership with Arthritis Research UK, the British Heart Foundation, Cancer Research UK, the Economic and Social Research Council, the Engineering and Physical Sciences Research Council, the National Institute of Health Research, the National Institute for Social Care and Health Research (Welsh Assembly Government), the Chief Scientist Office (Scottish Government Health Directorates) and the Wellcome Trust (the views expressed in this paper are those of the authors and not necessarily those of the NHS, the NIHR, or the Department of Health). RDR is supported by the MRC Midlands Hub for Trials Methodology Research. JAH is supported by a New Investigator Award from the Canadian Institutes of Health Research and a grant from the Nova Scotia Health Research Foundation, and holds a Dalhousie University/CCRF research professorship. KGMM is supported by The Netherlands Organization for Scientific Research (ZON-MW 918.10.615 and 9120.8004). EWS was supported by The Netherlands Organization for Scientific Research (grant 9120.8004). PC holds a UK National Institute of Health Research Senior Investigator Award (NI-SI-0509-10183). KA holds a UK National Institute of Health Research Senior Investigator Award (NI-SI-0508-10061).

  • Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare: no support from any organisation for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years, no other relationships or activities that could appear to have influenced the submitted work. SS is a full time employee of the BMJ Group but is not involved in deciding which manuscripts are accepted for publication.

  • Provenance and peer review: Not commissioned; externally peer reviewed. In order to disseminate the output widely, these papers are being published jointly between BMJ (PROGRESS papers 1 and 4) and PLoS Medicine (PROGRESS papers 2 and 3). As one of the authors is a member of staff at BMJ Group, the handling editor at the BMJ for the manuscripts was an external guest editor, Lucy Chappell (King’s College London).

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.

References

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