Vaishnav Joban, Yanek Lisa R, Hahn Virginia S, Yang Eunice, Trivedi Rishi, Kass David A, Sharma Kavita
Department of Medicine, Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
J Card Fail. 2022 May;28(5):723-731. doi: 10.1016/j.cardfail.2021.12.007. Epub 2021 Dec 18.
Therapy for heart failure with preserved ejection fraction (HFpEF) remains an unmet need with lack of a consensus definition of HFpEF for inclusion into clinical trials. We evaluated whether hemodynamically characterized patients from a HFpEF referral center met inclusion criteria for 4 major HFpEF trials.
Patients were assessed for theoretical inclusion into 4 major clinical trials (I-PRESERVE, RELAX, TOPCAT, and PARAGON-HF). Clinical, echocardiographic and hemodynamic characteristics and cardiovascular outcomes were compared between patients who met the inclusion criteria vs those who did not for each trial. Of 131 patients with HFpEF, 23% of patients met the enrollment criteria for I-PRESERVE, 38% for RELAX, 18% for TOPCAT, and 13% for PARAGON-HF. The top criteria that excluded patients included low natriuretic peptide level, obesity, uncontrolled hypertension, young age, and low hemoglobin. There was no difference in the probability of HF hospitalization or death in patients included or excluded into each clinical trial.
In a cohort with hemodynamic evidence of HFpEF, a low proportion of patients met inclusion criteria for major HFpEF clinical trials, with no difference in outcomes in patients who did or did not meet inclusion criteria. Given relative the lack of proven therapies in HFpEF, consideration should be given to modifying clinical trial enrollment criteria to better represent contemporary patients with HFpEF in future clinical trials.
射血分数保留的心力衰竭(HFpEF)治疗仍是未满足的需求,缺乏纳入临床试验的HFpEF共识定义。我们评估了来自HFpEF转诊中心的血流动力学特征明确的患者是否符合4项主要HFpEF试验的纳入标准。
评估患者理论上是否可纳入4项主要临床试验(I-PRESERVE、RELAX、TOPCAT和PARAGON-HF)。比较了每项试验中符合纳入标准的患者与不符合纳入标准的患者的临床、超声心动图和血流动力学特征及心血管结局。在131例HFpEF患者中,23%的患者符合I-PRESERVE的入组标准,38%符合RELAX的标准,18%符合TOPCAT的标准,13%符合PARAGON-HF的标准。排除患者的首要标准包括利钠肽水平低、肥胖、未控制的高血压、年轻和血红蛋白水平低。各临床试验中纳入或排除的患者发生心力衰竭住院或死亡的概率无差异。
在有HFpEF血流动力学证据的队列中,只有一小部分患者符合HFpEF主要临床试验的纳入标准,符合或不符合纳入标准的患者结局无差异。鉴于HFpEF缺乏经证实的治疗方法,未来临床试验应考虑修改临床试验入组标准,以更好地代表当代HFpEF患者。