医学
内科学
随机对照试验
血液透析
透析
肾脏疾病
心脏病学
危险系数
临床终点
不利影响
安慰剂
置信区间
心力衰竭
外科
血管紧张素转换酶抑制剂
雷米普利
作者
Piero Ruggenenti,Manuel Alfredo Podestà,Matias Trillini,Annalisa Perna,Tobia Peracchi,Nadia Rubis,Davide Villa,Davide Martinetti,Monica Cortinovis,Patrizia Ondei,Carmela Giuseppina Condemi,Carlo Guastoni,Agnese Meterange-Lis,Antonio Granata,E. Mambelli,Sonia Pasquali,Simonetta Genovesi,Federico Pieruzzi,Silvio Bertoli,Goffredo Del Rosso,Maurizio Garozzo,Angelo Rigotti,Claudio Pozzi,Salvatore David,Giuseppe Daidone,Giulio Mingardi,Giovanni Mosconi,Andrea Galfré,Giorgio Romei Longhena,Alfonso Pacitti,Antonello Pani,Jorge Hidalgo Godoy,Hans-Joachim Anders,Giuseppe Remuzzi
出处
期刊:Clinical Journal of The American Society of Nephrology
[American Society of Nephrology]
日期:2021-03-29
卷期号:16 (4): 575-587
被引量:1
摘要
Background and objectives Renin-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, & measurements In 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. Results At 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. Conclusions Ramipril 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.