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      A Systematic Review of Predictions of Survival in Palliative Care: How Accurate Are Clinicians and Who Are the Experts?

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          Abstract

          Background

          Prognostic accuracy in palliative care is valued by patients, carers, and healthcare professionals. Previous reviews suggest clinicians are inaccurate at survival estimates, but have only reported the accuracy of estimates on patients with a cancer diagnosis.

          Objectives

          To examine the accuracy of clinicians’ estimates of survival and to determine if any clinical profession is better at doing so than another.

          Data Sources

          MEDLINE, Embase, CINAHL, and the Cochrane Database of Systematic Reviews and Trials. All databases were searched from the start of the database up to June 2015. Reference lists of eligible articles were also checked.

          Eligibility Criteria

          Inclusion criteria: patients over 18, palliative population and setting, quantifiable estimate based on real patients, full publication written in English. Exclusion criteria: if the estimate was following an intervention, such as surgery, or the patient was artificially ventilated or in intensive care.

          Study Appraisal and Synthesis Methods

          A quality assessment was completed with the QUIPS tool. Data on the reported accuracy of estimates and information about the clinicians were extracted. Studies were grouped by type of estimate: categorical (the clinician had a predetermined list of outcomes to choose from), continuous (open-ended estimate), or probabilistic (likelihood of surviving a particular time frame).

          Results

          4,642 records were identified; 42 studies fully met the review criteria. Wide variation was shown with categorical estimates (range 23% to 78%) and continuous estimates ranged between an underestimate of 86 days to an overestimate of 93 days. The four papers which used probabilistic estimates tended to show greater accuracy (c-statistics of 0.74–0.78). Information available about the clinicians providing the estimates was limited. Overall, there was no clear “expert” subgroup of clinicians identified.

          Limitations

          High heterogeneity limited the analyses possible and prevented an overall accuracy being reported. Data were extracted using a standardised tool, by one reviewer, which could have introduced bias. Devising search terms for prognostic studies is challenging. Every attempt was made to devise search terms that were sufficiently sensitive to detect all prognostic studies; however, it remains possible that some studies were not identified.

          Conclusion

          Studies of prognostic accuracy in palliative care are heterogeneous, but the evidence suggests that clinicians’ predictions are frequently inaccurate. No sub-group of clinicians was consistently shown to be more accurate than any other.

          Implications of Key Findings

          Further research is needed to understand how clinical predictions are formulated and how their accuracy can be improved.

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          Most cited references72

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          Assessing bias in studies of prognostic factors.

          Previous work has identified 6 important areas to consider when evaluating validity and bias in studies of prognostic factors: participation, attrition, prognostic factor measurement, confounding measurement and account, outcome measurement, and analysis and reporting. This article describes the Quality In Prognosis Studies tool, which includes questions related to these areas that can inform judgments of risk of bias in prognostic research.A working group comprising epidemiologists, statisticians, and clinicians developed the tool as they considered prognosis studies of low back pain. Forty-three groups reviewing studies addressing prognosis in other topic areas used the tool and provided feedback. Most reviewers (74%) reported that reaching consensus on judgments was easy. Median completion time per study was 20 minutes; interrater agreement (κ statistic) reported by 9 review teams varied from 0.56 to 0.82 (median, 0.75). Some reviewers reported challenges making judgments across prompting items, which were addressed by providing comprehensive guidance and examples. The refined Quality In Prognosis Studies tool may be useful to assess the risk of bias in studies of prognostic factors.
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            Factors considered important at the end of life by patients, family, physicians, and other care providers.

            A clear understanding of what patients, families, and health care practitioners view as important at the end of life is integral to the success of improving care of dying patients. Empirical evidence defining such factors, however, is lacking. To determine the factors considered important at the end of life by patients, their families, physicians, and other care providers. Cross-sectional, stratified random national survey conducted in March-August 1999. Seriously ill patients (n = 340), recently bereaved family (n = 332), physicians (n = 361), and other care providers (nurses, social workers, chaplains, and hospice volunteers; n = 429). Importance of 44 attributes of quality at the end of life (5-point scale) and rankings of 9 major attributes, compared in the 4 groups. Twenty-six items consistently were rated as being important (>70% responding that item is important) across all 4 groups, including pain and symptom management, preparation for death, achieving a sense of completion, decisions about treatment preferences, and being treated as a "whole person." Eight items received strong importance ratings from patients but less from physicians (P<.001), including being mentally aware, having funeral arrangements planned, not being a burden, helping others, and coming to peace with God. Ten items had broad variation within as well as among the 4 groups, including decisions about life-sustaining treatments, dying at home, and talking about the meaning of death. Participants ranked freedom from pain most important and dying at home least important among 9 major attributes. Although pain and symptom management, communication with one's physician, preparation for death, and the opportunity to achieve a sense of completion are important to most, other factors important to quality at the end of life differ by role and by individual. Efforts to evaluate and improve patients' and families' experiences at the end of life must account for diverse perceptions of quality. JAMA. 2000;284:2476-2482.
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              Systematic reviews of evaluations of prognostic variables.

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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                25 August 2016
                2016
                : 11
                : 8
                : e0161407
                Affiliations
                [1 ]Marie Curie Palliative Care Research Department, Division of Psychiatry, University College London, London, United Kingdom
                [2 ]Department of Primary Care & Public Health Sciences, King’s College London, London, United Kingdom
                [3 ]Department of Experimental Psychology, University College London, London, United Kingdom
                [4 ]Department of Clinical Sciences, Brunel University London, London, United Kingdom
                University of Exeter, UNITED KINGDOM
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: NW FR PS.

                • Data curation: NW FR PS PH AH.

                • Formal analysis: NW FR PS.

                • Funding acquisition: PS.

                • Investigation: NW PS.

                • Methodology: NW FR PS.

                • Project administration: NW FR PS PH AH.

                • Resources: NW FR PS.

                • Supervision: PH AH PS.

                • Validation: NW FR PS.

                • Visualization: NW FR PS PH AH.

                • Writing – original draft: NW FR PS PH AH.

                • Writing – review & editing: NW FR PS PH AH.

                ‡ These authors also contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-7438-0072
                http://orcid.org/0000-0002-0762-8111
                http://orcid.org/0000-0002-5765-9047
                Article
                PONE-D-16-19692
                10.1371/journal.pone.0161407
                4999179
                27560380
                cbf9834f-22c8-4e18-b167-e8ee88f751f4
                © 2016 White et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 18 May 2016
                : 4 August 2016
                Page count
                Figures: 3, Tables: 4, Pages: 20
                Funding
                This review was completed as part of a PhD studentship awarded from University College London (UCL). Data collection, analysis, interpretation, and writing of the report were done independently by the authors. All authors had full access to the study data and had the final responsibility for the decision to submit the paper for publication.
                Categories
                Research Article
                Medicine and Health Sciences
                Health Care
                Health Care Providers
                Nurses
                People and Places
                Population Groupings
                Professions
                Nurses
                Medicine and Health Sciences
                Diagnostic Medicine
                Prognosis
                Medicine and Health Sciences
                Oncology
                Medicine and Health Sciences
                Health Care
                Palliative Care
                Research and Analysis Methods
                Research Assessment
                Systematic Reviews
                Research and Analysis Methods
                Database and Informatics Methods
                Database Searching
                Medicine and Health Sciences
                Health Care
                Health Care Providers
                Medical Doctors
                People and Places
                Population Groupings
                Professions
                Medical Doctors
                Social Sciences
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                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

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