Treatment of early hypertension among persons living with HIV in Haiti: Protocol for a randomized controlled trial.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 28 05 2021
accepted: 02 06 2021
entrez: 5 8 2021
pubmed: 6 8 2021
medline: 24 11 2021
Statut: epublish

Résumé

People living with HIV (PLWH) are at increased risk of cardiovascular disease (CVD) and death, with greater burdens of both HIV and CVD in lower-middle income countries. Treating prehypertension in PLWH may reduce progression to hypertension, CVD risk and potentially mortality. However, no trial has evaluated earlier blood pressure treatment for PLWH. We propose a randomized controlled trial to assess the feasibility, benefits, and risks of initiating antihypertensive treatment among PLWH with prehypertension, comparing prehypertension treatment to standard of care following current WHO guidelines. A total of 250 adults 18-65 years and living with HIV (PLWH) with viral suppression in the past 12 months, who have prehypertension will be randomized to prehypertension treatment versus standard of care. Prehypertension is defined as having a systolic blood pressure (SBP) 120-139 mmHg or diastolic blood pressure (DBP) 80-89 mmHg. In the prehypertension treatment arm, participants will initiate amlodipine 5 mg daily immediately. In the standard of care arm, participants will initiate amlodipine only if they develop hypertension defined as SBP ≥ 140 mmHg or DBP ≥ 90 mmHg. The primary outcome is the difference in mean change of SBP from enrollment to 12 months. Secondary outcomes include feasibility, acceptability, adverse effects, HIV viral suppression, and medication adherence. Qualitative in-depth interviews with providers and participants will explore attitudes about initiating amlodipine, satisfaction, perceived CVD risk, and implementation challenges. PLWH have a higher CVD risk and may benefit from a lower BP threshold for initiation of antihypertensive treatment. Clinicaltrials.gov registration number NCT04692467, registration date December 15, 2020, protocol ID 20-03021735.

Sections du résumé

BACKGROUND
People living with HIV (PLWH) are at increased risk of cardiovascular disease (CVD) and death, with greater burdens of both HIV and CVD in lower-middle income countries. Treating prehypertension in PLWH may reduce progression to hypertension, CVD risk and potentially mortality. However, no trial has evaluated earlier blood pressure treatment for PLWH. We propose a randomized controlled trial to assess the feasibility, benefits, and risks of initiating antihypertensive treatment among PLWH with prehypertension, comparing prehypertension treatment to standard of care following current WHO guidelines.
METHODS
A total of 250 adults 18-65 years and living with HIV (PLWH) with viral suppression in the past 12 months, who have prehypertension will be randomized to prehypertension treatment versus standard of care. Prehypertension is defined as having a systolic blood pressure (SBP) 120-139 mmHg or diastolic blood pressure (DBP) 80-89 mmHg. In the prehypertension treatment arm, participants will initiate amlodipine 5 mg daily immediately. In the standard of care arm, participants will initiate amlodipine only if they develop hypertension defined as SBP ≥ 140 mmHg or DBP ≥ 90 mmHg. The primary outcome is the difference in mean change of SBP from enrollment to 12 months. Secondary outcomes include feasibility, acceptability, adverse effects, HIV viral suppression, and medication adherence. Qualitative in-depth interviews with providers and participants will explore attitudes about initiating amlodipine, satisfaction, perceived CVD risk, and implementation challenges.
DISCUSSION
PLWH have a higher CVD risk and may benefit from a lower BP threshold for initiation of antihypertensive treatment.
TRIAL REGISTRATION
Clinicaltrials.gov registration number NCT04692467, registration date December 15, 2020, protocol ID 20-03021735.

Identifiants

pubmed: 34351939
doi: 10.1371/journal.pone.0254740
pii: PONE-D-21-17453
pmc: PMC8341523
doi:

Banques de données

ClinicalTrials.gov
['NCT04692467']

Types de publication

Clinical Trial Protocol Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0254740

Subventions

Organisme : FIC NIH HHS
ID : D43 TW011972
Pays : United States
Organisme : FIC NIH HHS
ID : R21 TW011693
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069421
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069421
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL143788
Pays : United States

Déclaration de conflit d'intérêts

VR, JWP, MLM report a grant from the Fogarty International Center, grant number R21 TW011693. The remaining authors declare they have no conflicts of interest.

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Auteurs

Lily D Yan (LD)

Division of General Internal Medicine, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Center for Global Health, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Vanessa Rouzier (V)

Center for Global Health, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Eliezer Dade (E)

Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Collette Guiteau (C)

Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Jean Lookens Pierre (JL)

Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Stephano St-Preux (S)

Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Miranda Metz (M)

Center for Global Health, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.

Suzanne Oparil (S)

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.

Jean William Pape (JW)

Center for Global Health, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

Margaret McNairy (M)

Division of General Internal Medicine, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Center for Global Health, Department of Medicine, Weill Cornell Medicine, New York, New York, United States of America.
Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.

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