Impact of Angiotensin Receptor Blockers (ARB) versus Other Antihypertensive Medication on Blood Pressure in Patients

Karthika Devi D S1, J Jenifer Florence Mary2, Reenaa Mohan1

  • 1Department of Community Medicine, Sri Manakula Vinayagar Medical College and Hospital, Puducherry, India.

PubMed

Insights

Angiotensin-II receptor blockers (ARBs) and other antihypertensive drugs show similar effectiveness in managing hypertension for dialysis patients. This meta-analysis found no significant difference in blood pressure reduction or adverse events between ARBs and other agents.

Area of Science:

  • Nephrology
  • Cardiology
  • Pharmacology

Background:

  • Hypertension is a major cause of mortality in dialysis patients.
  • Angiotensin-II receptor blockers (ARBs) are effective antihypertensives with fewer side effects than ACE inhibitors.

Purpose of the Study:

  • To systematically review and meta-analyze the efficacy and safety of ARBs compared to other antihypertensive agents in adult dialysis patients with hypertension.

Main Methods:

  • A systematic search of multiple databases (PubMed, MEDLINE, SCOPUS, etc.) was conducted until February 2023.
  • Included studies involved adult dialysis patients (≥18 years) and compared ARBs with other antihypertensives.
  • Data on systolic and diastolic blood pressure changes and adverse events were pooled using a random-effects model.

Main Results:

  • The meta-analysis included 13 studies with 1,462 patients.
  • No statistically significant differences were found in pre- or post-dialysis systolic or diastolic blood pressure reduction between ARBs and other antihypertensive agents.
  • Adverse events were not significantly different between ARB and other antihypertensive groups.

Conclusions:

  • ARBs and other antihypertensive medications demonstrate comparable efficacy in treating hypertension among dialysis patients.
  • The findings suggest that ARBs are a viable alternative to other antihypertensives in this population, with similar safety profiles.
Abstract

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