Kidney, Cardiac, and Safety Outcomes Associated With α-Blockers in Patients With CKD: A Population-Based Cohort Study.


Journal

American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075

Informations de publication

Date de publication:
02 2021
Historique:
received: 08 10 2019
accepted: 04 07 2020
pubmed: 14 9 2020
medline: 20 2 2021
entrez: 13 9 2020
Statut: ppublish

Résumé

Alpha-blockers (ABs) are commonly prescribed for control of resistant or refractory hypertension in patients with and without chronic kidney disease (CKD). The association between AB use and kidney, cardiac, mortality, and safety-related outcomes in CKD remains unknown. Population-based retrospective cohort study. Ontario (Canada) residents 66 years and older treated for hypertension in 2007 to 2015 without a prior prescription for an AB. New use of an AB versus new use of a non-AB blood pressure (BP)-lowering medication. 30% or greater estimated glomerular filtration rate (eGFR) decline; dialysis initiation or kidney transplantation (kidney replacement therapy); composite of acute myocardial infarction, coronary revascularization, congestive heart failure, or atrial fibrillation; safety (hypotension, syncope, falls, and fractures) events; and mortality. New users of ABs (doxazosin, terazosin, and prazosin) were matched to new users of non-ABs by a high dimensional propensity score. Cox proportional hazards and Fine and Gray models were used to examine the association of AB use with kidney, cardiac, mortality, and safety outcomes. Interactions by eGFR categories (≥90, 60-89, 30-59, and<30mL/min/1.73m Among 381,120 eligible individuals, 16,088 were dispensed ABs and matched 1:1 to non-AB users. AB use was associated with higher risk for≥30% eGFR decline (HR, 1.14; 95% CI, 1.08-1.21) and need for kidney replacement therapy (HR, 1.28; 95% CI, 1.13-1.44). eGFR level did not modify these associations, P interaction=0.3and 0.3, respectively. Conversely, AB use was associated with lower risk for cardiac events, which was also consistent across eGFR categories (HR, 0.92; 95% CI, 0.89-0.95; P interaction=0.1). AB use was also associated with lower mortality risk, but only among those with eGFR<60mL/min/1.73m Observational design, BP measurement data unavailable. AB use in CKD is associated with higher risk for kidney disease progression but lower risk for cardiac events and mortality compared with alternative BP-lowering medications.

Identifiants

pubmed: 32920153
pii: S0272-6386(20)30937-9
doi: 10.1053/j.ajkd.2020.07.018
pii:
doi:

Substances chimiques

Adrenergic alpha-Antagonists 0
Antihypertensive Agents 0
Terazosin 8L5014XET7
Doxazosin NW1291F1W8
Prazosin XM03YJ541D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

178-189.e1

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Gregory L Hundemer (GL)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada. Electronic address: ghundemer@toh.ca.

Greg A Knoll (GA)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

William Petrcich (W)

The Institute of Clinical Evaluative Sciences, Ontario, Canada.

Swapnil Hiremath (S)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Marcel Ruzicka (M)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Kevin D Burns (KD)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada; Kidney Research Centre, University of Ottawa, Ottawa, Canada.

Cedric Edwards (C)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Ann Bugeja (A)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Emily Rhodes (E)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Manish M Sood (MM)

Department of Medicine (Division of Nephrology) and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada; The Institute of Clinical Evaluative Sciences, Ontario, Canada.

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Classifications MeSH