Cargando…

Patients’ preferences for selection of endpoints in cardiovascular clinical trials

BACKGROUND: To reduce the duration and overall costs of cardiovascular trials, use of the combined endpoints in trial design has become commonplace. Though this methodology may serve the needs of investigators and trial sponsors, the preferences of patients or potential trial subjects in the trial d...

Descripción completa

Detalles Bibliográficos
Autores principales: Chow, Robert D., Wankhedkar, Kashmira P., Mete, Mihriye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937559/
https://www.ncbi.nlm.nih.gov/pubmed/24596645
http://dx.doi.org/10.3402/jchimp.v4.22643
_version_ 1782305518005518336
author Chow, Robert D.
Wankhedkar, Kashmira P.
Mete, Mihriye
author_facet Chow, Robert D.
Wankhedkar, Kashmira P.
Mete, Mihriye
author_sort Chow, Robert D.
collection PubMed
description BACKGROUND: To reduce the duration and overall costs of cardiovascular trials, use of the combined endpoints in trial design has become commonplace. Though this methodology may serve the needs of investigators and trial sponsors, the preferences of patients or potential trial subjects in the trial design process has not been studied. OBJECTIVE: To determine the preferences of patients in the design of cardiovascular trials. DESIGN: Participants were surveyed in a pilot study regarding preferences among various single endpoints commonly used in cardiovascular trials, preference for single vs. composite endpoints, and the likelihood of compliance with a heart medication if patients similar to them participated in the trial design process. PARTICIPANTS: One hundred adult English-speaking patients, 38% male, from a primary care ambulatory practice located in an urban setting. KEY RESULTS: Among single endpoints, participants rated heart attack as significantly more important than death from other causes (4.53 vs. 3.69, p=0.004) on a scale of 1–6. Death from heart disease was rated as significantly more important than chest pain (4.73 vs. 2.47, p<0.001), angioplasty/PCI/CABG (4.73 vs. 2.43, p<0.001), and stroke (4.73 vs. 2.43, p<0.001). Participants also expressed a slight preference for combined endpoints over single endpoint (43% vs. 57%), incorporation of the opinions of the study patient population into the design of trials (48% vs. 41% for researchers), and a greater likelihood of medication compliance if patient preferences were considered during trial design (67% indicated a significant to major effect). CONCLUSIONS: Patients are able to make judgments and express preferences regarding trial design. They prefer that the opinions of the study population rather than the general population be incorporated into the design of the study. This novel approach to study design would not only incorporate patient preferences into medical decision making, but it also has the potential to improve compliance with cardiovascular medications.
format Online
Article
Text
id pubmed-3937559
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Co-Action Publishing
record_format MEDLINE/PubMed
spelling pubmed-39375592014-03-04 Patients’ preferences for selection of endpoints in cardiovascular clinical trials Chow, Robert D. Wankhedkar, Kashmira P. Mete, Mihriye J Community Hosp Intern Med Perspect Research Article BACKGROUND: To reduce the duration and overall costs of cardiovascular trials, use of the combined endpoints in trial design has become commonplace. Though this methodology may serve the needs of investigators and trial sponsors, the preferences of patients or potential trial subjects in the trial design process has not been studied. OBJECTIVE: To determine the preferences of patients in the design of cardiovascular trials. DESIGN: Participants were surveyed in a pilot study regarding preferences among various single endpoints commonly used in cardiovascular trials, preference for single vs. composite endpoints, and the likelihood of compliance with a heart medication if patients similar to them participated in the trial design process. PARTICIPANTS: One hundred adult English-speaking patients, 38% male, from a primary care ambulatory practice located in an urban setting. KEY RESULTS: Among single endpoints, participants rated heart attack as significantly more important than death from other causes (4.53 vs. 3.69, p=0.004) on a scale of 1–6. Death from heart disease was rated as significantly more important than chest pain (4.73 vs. 2.47, p<0.001), angioplasty/PCI/CABG (4.73 vs. 2.43, p<0.001), and stroke (4.73 vs. 2.43, p<0.001). Participants also expressed a slight preference for combined endpoints over single endpoint (43% vs. 57%), incorporation of the opinions of the study patient population into the design of trials (48% vs. 41% for researchers), and a greater likelihood of medication compliance if patient preferences were considered during trial design (67% indicated a significant to major effect). CONCLUSIONS: Patients are able to make judgments and express preferences regarding trial design. They prefer that the opinions of the study population rather than the general population be incorporated into the design of the study. This novel approach to study design would not only incorporate patient preferences into medical decision making, but it also has the potential to improve compliance with cardiovascular medications. Co-Action Publishing 2014-02-17 /pmc/articles/PMC3937559/ /pubmed/24596645 http://dx.doi.org/10.3402/jchimp.v4.22643 Text en © 2014 Robert D. Chow et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chow, Robert D.
Wankhedkar, Kashmira P.
Mete, Mihriye
Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title_full Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title_fullStr Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title_full_unstemmed Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title_short Patients’ preferences for selection of endpoints in cardiovascular clinical trials
title_sort patients’ preferences for selection of endpoints in cardiovascular clinical trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937559/
https://www.ncbi.nlm.nih.gov/pubmed/24596645
http://dx.doi.org/10.3402/jchimp.v4.22643
work_keys_str_mv AT chowrobertd patientspreferencesforselectionofendpointsincardiovascularclinicaltrials
AT wankhedkarkashmirap patientspreferencesforselectionofendpointsincardiovascularclinicaltrials
AT metemihriye patientspreferencesforselectionofendpointsincardiovascularclinicaltrials