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JACC. Heart failure · Oct 2016
Patient-Reported Outcomes in Chronic Heart Failure: Applicability for Regulatory Approval.
- Mitchell A Psotka, Robyn von Maltzahn, Milena Anatchkova, Irene Agodoa, Dina Chau, Fady I Malik, Donald L Patrick, John A Spertus, Ingela Wiklund, and John R Teerlink.
- School of Medicine, University of California San Francisco and Section of Cardiology, San Francisco Veterans Affairs Medical Center, San Francisco, California.
- JACC Heart Fail. 2016 Oct 1; 4 (10): 791-804.
ObjectivesThe study sought to review the characteristics of existing patient-reported outcome (PRO) instruments used with chronic heart failure (HF) patients and evaluate their potential to support an approved U.S. Food and Drug Administration (FDA) product label claim.BackgroundPROs, including symptoms and their associated functional limitations, contribute substantially to HF patient morbidity. PRO measurements capture the patient perspective and can be systematically assessed with structured questionnaires, however rigorous recommendations have been set by the FDA regarding the acceptability of PRO measures as a basis for product label claims.MethodsExtensive searches of databases and specialty guidelines identified PRO instruments used in patients with chronic HF. Information on critical properties recommended by the FDA guidance were systematically extracted and used to evaluate the selected PRO instruments.ResultsNineteen PRO instruments used with chronic HF patients were identified. The Kansas City Cardiomyopathy Questionnaire and Minnesota Living with Heart Failure Questionnaire were the most extensively evaluated and validated in studies of this population. However, judged by criteria listed in the FDA PRO guidance, no existing PRO measure met all of the criteria to support a product label claim in the United States.ConclusionsCurrently available chronic HF PRO measures do not fulfill all the recommendations provided in the FDA PRO guidance and therefore may not support an FDA-approved product label claim. Future investigations are merited to develop a PRO measure for use in patients with chronic HF in accordance with the FDA guidance.Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
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