SAIMSARA Journal

Machine-Readable Science • ISSN 3054-3991

Ramipril vs Candesartan: Scoping Review with ☸️SAIMSARA.

Cardiac & Vascular Health icon

Cardiac & Vascular Health

Issue 1, Volume 1, 2026

DOI: 10.62487/saimsarae1a78e09

Editorial note
• Last update: 2026-06-02 22:03:19
What is this paper about
This review shows that ramipril and candesartan are not simply interchangeable RAAS drugs: blood-pressure control is broadly comparable, but the evidence separates them by exercise BP response, tolerability, diastolic function, anti-fibrotic signals, and perioperative fibrinolytic effects. The full read maps 37 references across 33 original studies and 399,243 observations, clarifying where candesartan, ramipril, or single-pill combinations may offer the more rational clinical choice.
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Abstract: The aim of this scoping review is to systematically synthesize and evaluate the comparative efficacy, safety, tolerability, and physiological impacts of ramipril versus candesartan across experimental animal models, laboratory biological systems, and clinical cohorts. The review uses 37 references and builds its evidence map from 33 original studies with 399243 total participants/sample observations (topic-deduplicated ΣN). This scoping review suggests that ramipril and candesartan offer broadly comparable blood-pressure control but diverge meaningfully in tolerability and selected target-organ effects, with candesartan associated with superior exercise blood-pressure reduction in a small crossover study reported across related records, diastolic function improvement, and sustained anti-fibrotic activity, and ramipril showing distinct perioperative bradykinin and fibrinolytic effects during cardiopulmonary bypass. Single-pill combinations of either agent with amlodipine were associated with improved persistence and lower cardiovascular event or mortality risk (HR 0.77 and 0.80) compared with multi-pill regimens. Tolerability signals, including cough and rare bronchial cast formation with ramipril, support individualized switching when class-specific adverse effects emerge. Given the heterogeneous and largely non-pooled evidence base, future head-to-head trials should clarify which patient phenotypes—defined by sex, comorbidity, or exercise exposure—derive the greatest differential benefit from each agent.
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Keywords: Ramipril; Candesartan; Angiotensin-converting enzyme inhibitors; Angiotensin receptor blockers; Hypertension; Antihypertensive therapy; Cardioprotection; Endothelial function; Blood pressure regulation; Adverse drug events

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Reference Index (37)

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