Patient-reported outcome measures for life participation in kidney transplantation: A systematic review.

clinical research/practice health services and outcomes research kidney disease kidney transplantation/nephrology quality of life (QOL) social sciences

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
08 2019
Historique:
received: 11 11 2018
revised: 07 01 2019
accepted: 13 01 2019
pubmed: 22 1 2019
medline: 1 9 2020
entrez: 22 1 2019
Statut: ppublish

Résumé

For many patients with end-stage kidney disease, transplantation improves survival and quality of life compared with dialysis. However, complications and side effects in kidney transplant recipients can limit their ability to participate in activities of daily living including work, study, and recreational activities. The aim of this study was to identify the characteristics, content, and psychometric properties of the outcome measures used to assess life participation in kidney transplant recipients. We searched MEDLINE, Embase, PsycINFO, and CINAHL from inception to July 2018 for all studies that reported life participation in kidney transplant recipients. Two authors identified instruments measuring life participation and reviewed for characteristics. In total, 230 studies were included: 19 (8%) randomized trials, 17 (7%) nonrandomized trials, and 194 (85%) observational studies. Across these studies, we identified 29 different measures that were used to assess life participation. Twelve (41%) measures specifically assessed aspects of life participation (eg, disability assessment, daily activities of living), while 17 (59%) assessed other constructs (eg, quality of life) that included questions on life participation. Validation data to support the use of these measures in kidney transplant recipients were available for only 7 measures. A wide range of measures have been used to assess life participation in kidney transplant recipients, but validation data supporting the use of these measures in this population are sparse. A content relevant and validated measure to improve the consistency and accuracy of measuring life participation in research may inform strategies for transplant recipients to be better able to engage in their life activities.

Identifiants

pubmed: 30664327
doi: 10.1111/ajt.15267
pii: S1600-6135(22)09196-1
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2306-2317

Informations de copyright

© 2019 The American Society of Transplantation and the American Society of Transplant Surgeons.

Auteurs

Angela Ju (A)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.

Bi Yang Chow (BY)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.

Angelique F Ralph (AF)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.

Martin Howell (M)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.

Michelle A Josephson (MA)

Department of Medicine, University of Chicago, Chicago, Illinois.

Curie Ahn (C)

Transplantation Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Transplantation Center, Seoul National University Hospital, Seoul, Republic of Korea.

Zeeshan Butt (Z)

Departments of Medical Social Sciences and Surgery (Division of Organ Transplantation), Northwestern University, Chicago, Illinois.

Fabienne Dobbels (F)

Department of Public Health, KU Leuven, Leuven, Belgium.

Kevin Fowler (K)

Kidney Health Initiative, Patient Family Partnership Council, The Voice of the Patient, Elmhurst, Illinois.

Sheila Jowsey-Gregoire (S)

Department of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.

Vivekanand Jha (V)

George Institute for Global Health, New Delhi, India.

Jayme E Locke (JE)

University of Alabama at Birmingham, Birmingham, Alabama.

Jane C Tan (JC)

Department of Medicine, Stanford University, Stanford, California.

Quinetta Taylor (Q)

Patient Partner, Chicago, Illinois.

Claudia Rutherford (C)

School of Psychology, University of Sydney, Sydney, New South Wales, Australia.
Sydney Nursing School, University of Sydney, Sydney, New South Wales, Australia.

Jonathan C Craig (JC)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.

Allison Tong (A)

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.

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Classifications MeSH