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DOI 10.1002/ejhf.3453

Медицинская библиотека · European journal of heart failure · 2024

The Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure with Preserved Ejection Fraction (SPIRRIT-HFpEF): Rationale and design.

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

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Аннотация

AIMS: 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.

METHODS

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.

CONCLUSION

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.

Для цитирования: 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. The Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure with Preserved Ejection Fraction (SPIRRIT-HFpEF): Rationale and design.. European journal of heart failure. 2024. DOI: 10.1002/ejhf.3453.

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