Patient-Reported Morbidity Instruments: A Systematic Review.


Journal

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
ISSN: 1524-4733
Titre abrégé: Value Health
Pays: United States
ID NLM: 100883818

Informations de publication

Date de publication:
06 2020
Historique:
received: 10 09 2019
revised: 27 01 2020
accepted: 26 02 2020
entrez: 17 6 2020
pubmed: 17 6 2020
medline: 4 9 2020
Statut: ppublish

Résumé

Although comorbidities play an essential role in risk adjustment and outcomes measurement, there is little consensus regarding the best source of this data. The aim of this study was to identify general patient-reported morbidity instruments and their measurement properties. A systematic review was conducted using multiple electronic databases (Embase, Medline, Cochrane Central, and Web of Science) from inception to March 2018. Articles focusing primarily on the development or subsequent validation of a patient-reported morbidity instrument were included. After including relevant articles, the measurement properties of each morbidity instrument were extracted by 2 investigators for narrative synthesis. A total of 1005 articles were screened, of which 34 eligible articles were ultimately included. The most widely assessed instruments were the Self-Reported Charlson Comorbidity Index (n = 7), the Self-Administered Comorbidity Questionnaire (n = 3), and the Disease Burden Morbidity Assessment (n = 3). The most commonly included conditions were diabetes, hypertension, and myocardial infarction. Studies demonstrated substantial variability in item-level reliability versus the gold standard medical record review (κ range 0.66-0.86), meaning that the accuracy of the self-reported comorbidity data is dependent on the selected morbidity. The Self-Reported Charlson Comorbidity Index and the Self-Administered Comorbidity Questionnaire were the most frequently cited instruments. Significant variability was observed in reliability per comorbid condition of patient-reported morbidity questionnaires. Further research is needed to determine whether patient-reported morbidity data should be used to bolster medical records data or serve as a stand-alone entity when risk adjusting observational outcomes data.

Identifiants

pubmed: 32540238
pii: S1098-3015(20)30132-7
doi: 10.1016/j.jval.2020.02.006
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

791-811

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Arvind Oemrawsingh (A)

Department of Public Health, Erasmus University Medical Center, Rotterdam, The Netherlands. Electronic address: a.oemrawsingh@erasmusmc.nl.

Nishwant Swami (N)

University of Massachusetts Medical School, Worcester, MA, USA.

José M Valderas (JM)

International Society for Quality of Life Research, Health Services & Policy Research, University of Exeter Medical School, Exeter, England, UK.

Jan A Hazelzet (JA)

Department of Public Health, Erasmus University Medical Center, Rotterdam, The Netherlands.

Andrea L Pusic (AL)

Division of Plastic and Reconstructive Surgery, Patient Reported Outcomes, Value, and Experience Center, Brigham and Women's Hospital, Boston, MA, USA.

Richard E Gliklich (RE)

Department of Otolaryngology - Head and Neck Surgery, Harvard Medical School, Boston, MA, USA.

Regan W Bergmark (RW)

Department of Otolaryngology - Head and Neck Surgery, Harvard Medical School, Boston, MA, USA; Center for Surgery and Public Health, Patient Reported Outcomes, Value and Experience Center, Brigham and Women's Hospital, Boston, MA, USA.

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Classifications MeSH