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Angiotensin-Converting Enzyme Inhibitors or Angiotensin Receptor Blockers After Transcatheter Aortic Valve Replacement: A Meta-Analysis.
Bhat, Vivek; Kumar, Ashish; Kalra, Ankur.
Afiliação
  • Bhat V; Department of Internal Medicine, St. John's Medical College, Bangalore, India.
  • Kumar A; Department of Internal Medicine, Cleveland Clinic Akron General, Akron, Ohio, USA.
  • Kalra A; Franciscan Health, Lafayette, Indiana, USA.
JACC Adv ; 3(5): 100927, 2024 May.
Article em En | MEDLINE | ID: mdl-38939627
ABSTRACT

Background:

Persistent left ventricular hypertrophy after transcatheter aortic valve replacement (TAVR) has been associated with poor outcomes. Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs), due to their favorable effects on ventricular remodeling, have been hypothesized to improve outcomes post-TAVR, yet there are no recommendations regarding their use.

Objectives:

This study aimed to compare the outcomes of patients receiving ACEIs/ARBs with those not receiving ACEIs/ARBs after TAVR.

Methods:

We performed a literature search on PubMed and Cochrane Library until June 14, 2023, and included all studies comparing clinical outcomes between patients given ACEIs/ARBs and those not given ACEIs/ARBs after TAVR. All-cause mortality was the primary outcome. We used a random effects model with appropriate corrections to calculate relative risk (RR) and CIs, with all analyses carried out using R v4.0.3.

Results:

We included ten studies on the use of ACEIs/ARBs post-TAVR. Patients on ACEIs/ARBs had lower risk of all-cause mortality (RR 0.74, 95% CI 0.65-0.86, I2 = 62%, chi-square P < 0.01), cardiovascular mortality (RR 0.70, 95% CI 0.56-0.88, I2 = 0%, chi-square P = 0.54), and new-onset atrial fibrillation (RR 0.71, 95% CI 0.52-0.96, I2 = 0%, chi-square P = 0.59). Patients on ACEIs/ARBs had a similar risk of myocardial infarction, heart failure, stroke, new permanent pacemaker implantation, acute kidney injury, major bleeding, vascular complications, aortic regurgitation, and mitral regurgitation.

Conclusions:

We found that patients receiving ACEIs/ARBs had a lower risk of all-cause mortality, cardiovascular mortality, and new-onset atrial fibrillation. Risk of other outcomes was similar to patients not receiving ACEIs/ARBs. Randomized clinical trials are needed to explore the benefits of ACEIs/ARBs post-TAVR, so that definitive guidelines can be developed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACC Adv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACC Adv Ano de publicação: 2024 Tipo de documento: Article