Ramipril and Cardiovascular Outcomes in Patients on Maintenance Hemodialysis

Author:

Ruggenenti Piero,Podestà Manuel AlfredoORCID,Trillini Matias,Perna Annalisa,Peracchi Tobia,Rubis Nadia,Villa Davide,Martinetti DavideORCID,Cortinovis Monica,Ondei Patrizia,Condemi Carmela Giuseppina,Guastoni Carlo Maria,Meterangelis Agnese,Granata Antonio,Mambelli Emanuele,Pasquali Sonia,Genovesi Simonetta,Pieruzzi Federico,Bertoli Silvio Volmer,Del Rosso Goffredo,Garozzo Maurizio,Rigotti Angelo,Pozzi Claudio,David Salvatore,Daidone Giuseppe,Mingardi Giulio,Mosconi Giovanni,Galfré Andrea,Romei Longhena Giorgio,Pacitti Alfonso,Pani Antonello,Hidalgo Godoy Jorge,Anders Hans-Joachim,Remuzzi Giuseppe,

Abstract

Background and objectivesRenin-angiotensin system (RAS) inhibitors reduce cardiovascular morbidity and mortality in patients with CKD. We evaluated the cardioprotective effects of the angiotensin-converting enzyme inhibitor ramipril in patients on maintenance hemodialysis.Design, setting, participants, & measurementsIn this phase 3, prospective, randomized, open-label, blinded end point, parallel, multicenter trial, we recruited patients on maintenance hemodialysis with hypertension and/or left ventricular hypertrophy from 28 Italian centers. Between July 2009 and February 2014, 140 participants were randomized to ramipril (1.25–10 mg/d) and 129 participants were allocated to non-RAS inhibition therapy, both titrated up to the maximally tolerated dose to achieve predefined target BP values. The primary efficacy end point was a composite of cardiovascular death, myocardial infarction, or stroke. Secondary end points included the single components of the primary end point, new-onset or recurrence of atrial fibrillation, hospitalizations for symptomatic fluid overload, thrombosis or stenosis of the arteriovenous fistula, and changes in cardiac mass index. All outcomes were evaluated up to 42 months after randomization.ResultsAt comparable BP control, 23 participants on ramipril (16%) and 24 on non-RAS inhibitor therapy (19%) reached the primary composite end point (hazard ratio, 0.93; 95% confidence interval, 0.52 to 1.64; P=0.80). Ramipril reduced cardiac mass index at 1 year of follow-up (between-group difference in change from baseline: −16.3 g/m2; 95% confidence interval, −29.4 to −3.1), but did not significantly affect the other secondary outcomes. Hypotensive episodes were more frequent in participants allocated to ramipril than controls (41% versus 12%). Twenty participants on ramipril and nine controls developed cancer, including six gastrointestinal malignancies on ramipril (four were fatal), compared with none in controls.ConclusionsRamipril did not reduce the risk of major cardiovascular events in patients on maintenance hemodialysis.Clinical Trial registry name and registration number:ARCADIA, NCT00985322 and European Union Drug Regulating Authorities Clinical Trials Database number 2008–003529–17.

Funder

Agenzia Italiana del Farmaco, Ministero della Salute

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

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