Angiotensin-Converting Enzyme Inhibitors or Angiotensin Receptor Blockers After Transcatheter Aortic Valve Replacement: A Meta-Analysis
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Published on: June 3, 2018
Vivek Bhat1, Ashish Kumar2, Ankur Kalra3,4
1Department of Internal Medicine, St. John's Medical College, Bangalore, India.
Insights
Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) use after transcatheter aortic valve replacement (TAVR) is associated with reduced all-cause mortality and new-onset atrial fibrillation. Further randomized trials are needed to establish definitive guidelines for ACEIs/ARBs post-TAVR.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Persistent left ventricular hypertrophy post-transcatheter aortic valve replacement (TAVR) is linked to adverse outcomes.
- Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) may improve ventricular remodeling and outcomes after TAVR.
- Current guidelines lack recommendations on ACEI/ARB use post-TAVR.
Purpose of the Study:
- To compare clinical outcomes in patients receiving ACEIs/ARBs versus those not receiving them after TAVR.
- To evaluate the impact of ACEIs/ARBs on mortality and other adverse events post-TAVR.
Main Methods:
- A systematic literature search was conducted on PubMed and Cochrane Library up to June 14, 2023.
- Included studies compared clinical outcomes between patients on ACEIs/ARBs and those not on these medications post-TAVR.
- All-cause mortality was the primary outcome, analyzed using a random effects model.
Main Results:
- Ten studies were included. Patients on ACEIs/ARBs showed a significantly lower risk of all-cause mortality (RR: 0.74) and cardiovascular mortality (RR: 0.70).
- A reduced risk of new-onset atrial fibrillation was observed in patients taking ACEIs/ARBs (RR: 0.71).
- No significant differences were found in risks of myocardial infarction, heart failure, stroke, pacemaker implantation, acute kidney injury, bleeding, vascular complications, or valvular regurgitation.
Conclusions:
- ACEI/ARB use post-TAVR is associated with improved survival and reduced incidence of new-onset atrial fibrillation.
- The risk of other major adverse events remains comparable between groups.
- Randomized clinical trials are warranted to confirm these findings and inform guideline development for ACEI/ARB therapy post-TAVR.
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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