The Aldosterone Blockade for Health Improvement Evaluation in End-Stage Renal Disease (ACHIEVE) Trial: Rationale and Clinical Research Protocol.

IF 1.6 Q3 UROLOGY & NEPHROLOGY
Canadian Journal of Kidney Health and Disease Pub Date : 2025-06-03 eCollection Date: 2025-01-01 DOI:10.1177/20543581251348187
Michael Walsh, David Collister, Martin Gallagher, Patrick B Mark, Janak R de Zoysa, Jessica Tyrwhitt, Karthik Tennankore, Laura Sola, Gilmar Reis, Denis Xavier, Russell Villanueva, Wen J Liu, Camilo Félix, Li Zuo, Mustafa Arici, Vivekanand Jha, Ron Wald, Amanda Y Wang, Atiya R Faruqui, Fei Yuan, Shun Fu Lee, Alena Kuptsova, Courtney Christou, P J Devereaux
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引用次数: 0

Abstract

Background: The mineralocorticoid aldosterone may contribute to the risk of cardiovascular morbidity and mortality in patients receiving maintenance dialysis. Whether spironolactone, a mineralocorticoid receptor antagonist, improves outcomes for patients receiving maintenance dialysis is unclear.

Objective: To assess the efficacy and safety of spironolactone in patients receiving maintenance dialysis.

Design: Placebo-controlled, randomized controlled trial.

Setting: Dialysis units.

Patients: Patients receiving maintenance dialysis who are adherent to and able to tolerate spironolactone 25 mg daily during an open-label run-in period of at least 49 days were randomized to spironolactone 25 mg daily or matching placebo.

Measurements: Randomized participants were followed for the primary outcome of cardiovascular death or hospitalization due to heart failure. Secondary outcomes include cause specific deaths, hospitalization due to heart failure, all-cause death, all-cause hospitalizations, and severe hyperkalemia. All deaths and possible hospitalizations for heart failure were adjudicated.

Methods: Eligible participants received open-label spironolactone 25 mg daily for at least 7 weeks during a run-in period. Participants who tolerated and adhered to treatment were randomly allocated to continue spironolactone 25 mg daily or a matching placebo. We followed participants until trial close.

Results: The trial began recruitment in 2018 and concluded recruitment in December 2024. Despite a reduced rate of recruitment during the global COVID-19 pandemic 3565 eligible participants were enrolled of whom 2538 were randomized to spironolactone or placebo from 143 dialysis programs.

Limitations: Limited funding and the trial was stopped early due to futility to demonstrate an effect.

Conclusions: ACHIEVE was designed as a large, simple trial to determine if spironolactone 25 mg daily prevents cardiovascular mortality and heart failure hospitalizations in patients with kidney failure receiving maintenance dialysis. ACHIEVE demonstrates the possibility of conducting large, international, investigator initiated randomized controlled trials for patients with kidney failure receiving dialysis.NCT03020303.

醛固酮阻断剂对终末期肾病患者健康改善评价(ACHIEVE)试验:基本原理和临床研究方案。
背景:矿化皮质激素醛固酮可能增加维持性透析患者心血管发病率和死亡率的风险。螺内酯(一种矿皮质激素受体拮抗剂)是否能改善维持性透析患者的预后尚不清楚。目的:评价螺内酯在维持性透析患者中的疗效和安全性。设计:安慰剂对照,随机对照试验。设置:透析装置。患者:接受维持性透析的患者在至少49天的开放标签磨合期内坚持并能够耐受每天25mg的螺内酯,随机分配到每天25mg的螺内酯组或匹配的安慰剂组。测量方法:随机随访参与者的主要结局是心血管死亡或因心力衰竭住院。次要结局包括因特定原因死亡、因心力衰竭住院、全因死亡、全因住院和严重高钾血症。所有因心力衰竭而死亡和可能住院的病例均被确认。方法:符合条件的参与者在磨合期接受开放标签的螺内酯25mg,每天至少7周。耐受并坚持治疗的参与者被随机分配继续服用每日25mg的螺内酯或相应的安慰剂。我们跟踪参与者直到试验结束。结果:试验于2018年开始招募,2024年12月结束招募。尽管在全球COVID-19大流行期间招募率有所下降,但仍招募了3565名符合条件的参与者,其中2538人从143个透析项目中随机分配到螺内酯或安慰剂组。限制:资金有限,试验因无法证明效果而提前停止。结论:ACHIEVE是一项大型、简单的试验,旨在确定每天25mg螺内酯是否能预防接受维持性透析的肾衰竭患者的心血管死亡率和心力衰竭住院。ACHIEVE证明了在接受透析的肾衰竭患者中开展大型、国际性、研究者发起的随机对照试验的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.00
自引率
5.90%
发文量
84
审稿时长
12 weeks
期刊介绍: Canadian Journal of Kidney Health and Disease, the official journal of the Canadian Society of Nephrology, is an open access, peer-reviewed online journal that encourages high quality submissions focused on clinical, translational and health services delivery research in the field of chronic kidney disease, dialysis, kidney transplantation and organ donation. Our mandate is to promote and advocate for kidney health as it impacts national and international communities. Basic science, translational studies and clinical studies will be peer reviewed and processed by an Editorial Board comprised of geographically diverse Canadian and international nephrologists, internists and allied health professionals; this Editorial Board is mandated to ensure highest quality publications.
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