Lund Lars H, James Stefan, DeVore Adam D, Anstrom Kevin J, Fudim Marat, Aaronson Keith D, Dahlström Ulf, Desvigne-Nickens Patrice, Fleg Jerome L, Yang Song, Fu Michael, Hage Camilla, Held Claes, Karlström Patric, Nygren Magnus, Peterson Eric D, Pol Tymon, Sapp Shelly, Sundström Johan, Östlund Ollie, Oldgren Jonas, Pitt Bertram
Department of Medicine, Karolinska Institutet, Sweden.
Department of Cardiology, Karolinska University Hospital, Stockholm, Sweden.
Eur J Heart Fail. 2024 Nov;26(11):2453-2463. doi: 10.1002/ejhf.3453. Epub 2024 Sep 16.
Benefits of mineralocorticoid receptor antagonists (MRAs) in heart failure with preserved and mildly reduced ejection fraction (HFpEF/HFmrEF) have not been established. Conventional randomized controlled trials are complex and expensive. The Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure with Preserved Ejection Fraction (SPIRRIT-HFpEF) is a unique pragmatic registry-based randomized controlled trial.
SPIRRIT-HFpEF is a multicentre, prospective, randomized, open-label, blinded endpoint trial conducted on platforms in the Swedish Heart Failure Registry (SwedeHF) and the United States (US) Trial Innovation Network. Patients with HFpEF/HFmrEF are randomized 1:1 to spironolactone (or eplerenone) in addition to usual care, versus usual care alone. The primary outcome is total number of cardiovascular deaths and hospitalizations for heart failure. Outcomes are collected from Swedish administrative complete coverage registries and a US call centre and subsequently adjudicated. Simple eligibility criteria were based on data available in SwedeHF: heart failure as outpatient or at discharge from hospital, left ventricular ejection fraction ≥40%, N-terminal pro-B-type natriuretic peptide >300 ng/L (in sinus rhythm) or >750 ng/L (in atrial fibrillation), with pre-specified adjustment for elevated body mass index, and chronic loop diuretic use. Power and sample size assessments were based on an event-driven design allowing enrolment over approximately 6 years, and application of hazard ratios from the TOPCAT trial, Americas subset. The final sample size is expected to be approximately 2400 patients.
SPIRRIT-HFpEF will be informative on the effectiveness of generic MRAs in HFpEF and HFmrEF, and on the feasibility of conducting pragmatic and registry-based trials in heart failure and other chronic conditions.
盐皮质激素受体拮抗剂(MRAs)在射血分数保留和轻度降低的心力衰竭(HFpEF/HFmrEF)中的益处尚未确定。传统的随机对照试验复杂且昂贵。射血分数保留的心力衰竭螺内酯起始登记随机干预试验(SPIRRIT-HFpEF)是一项独特的基于实用登记的随机对照试验。
SPIRRIT-HFpEF是一项多中心、前瞻性、随机、开放标签、盲终点试验,在瑞典心力衰竭登记处(SwedeHF)和美国试验创新网络的平台上进行。HFpEF/HFmrEF患者被1:1随机分配,除常规治疗外,加用螺内酯(或依普利酮),与单纯常规治疗进行对比。主要结局是心血管死亡和因心力衰竭住院的总数。结局数据从瑞典行政全覆盖登记处和美国呼叫中心收集,随后进行判定。简单的纳入标准基于SwedeHF中可用的数据:门诊或出院时的心力衰竭、左心室射血分数≥40%、N末端B型利钠肽原>300 ng/L(窦性心律时)或>750 ng/L(心房颤动时),并对体重指数升高和长期使用袢利尿剂进行预先指定的调整。效能和样本量评估基于事件驱动设计,允许在约6年的时间内入组,并应用TOPCAT试验美洲亚组的风险比。最终样本量预计约为2400例患者。
SPIRRIT-HFpEF将为通用MRAs在HFpEF和HFmrEF中的有效性,以及在心力衰竭和其他慢性病中开展实用的基于登记的试验的可行性提供信息。