From Evidence to Effectiveness: Implications of the Randomized Trial to Prevent Vascular Events in HIV Study for People With Human Immunodeficiency Virus in Low- and Middle-Income Settings.
HIV
cardiovascular disease
integrated care
Journal
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213
Informations de publication
Date de publication:
08 Dec 2023
08 Dec 2023
Historique:
received:
19
08
2023
medline:
9
12
2023
pubmed:
9
12
2023
entrez:
9
12
2023
Statut:
aheadofprint
Résumé
The Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) study found a 35% reduction in major adverse cardiovascular events for people with human immunodeficiency virus who received daily pitavastatin. However, how this evidence will change practice is far from certain. Here, we outline evidence gaps and political and healthcare delivery challenges that will need to be addressed for REPRIEVE to offer public health benefits in low- and middle-income countries.
Identifiants
pubmed: 38066673
pii: 7463998
doi: 10.1093/cid/ciad702
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIDDK NIH HHS
ID : K23 DK125162
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG3 HL156388
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG3HL156388
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23125162
Pays : United States
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Déclaration de conflit d'intérêts
Potential conflicts of interest. J. M.-G. reports grants or contracts from GSK Pharmaceuticals and Regeneron Pharmaceuticals and consulting fees from the World Health Organization (WHO). V. C. M. reports grants or contracts from Gilead for ACTT2, ACTT3, and ACTT4, from ViiV for DISCO and ASPIRE, and from CDC/NIH/VA for other studies; participation on a data and safety monitoring board or advisory board for IL-1b inhibitor study, CLEAR HIV, VB201, Outsmart, and ECLIPSE; and a role as study section chair for NIH. M. K. A. reports personal fees outside the scope of this work from Eli Lilly. D. F. reports consulting fees (to institution) as a diabetes consultant for the WHO; career development funding on implementation science for cardiovascular disease prevention (award K23HL161271) from NIH; and service as an unpaid staff physician for the Maya Health Alliance and GlucoSalud (nongovernmental health organizations in Guatemala). W. D. F. V. reports grants or contracts unrelated to this work from the Bill and Melinda Gates Foundation, US Agency for International Development, Unitaid, SA Medical Research Council, Foundation for Innovative New Diagnostics, Children's Investment Fund Foundation, Gilead, ViiV, Mylan, Merck, Adcock-Ingram, Aspen, Abbott, Roche, Johnson & Johnson, Sanofi, Virology Education, SA HIV Clinicians Society, and Dira Sengwe. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.