Department of Cardiology, Zhengzhou University People's Hospital, Zhengzhou, 450003, Henan, China.
Department of Cardiology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Cardiovasc Drugs Ther. 2018 Dec;32(6):577-580. doi: 10.1007/s10557-018-6827-5.
Previous studies have evaluated intra-study heterogeneities of heart failure with preserved ejection fraction (HFpEF), but inter-study heterogeneities remain poorly understood. We investigate the heterogeneities of outcomes among control groups of HFpEF trials.
We included randomized controlled trials recruiting HFpEF patients with ejection fraction ≥ 40% and reporting Kaplan-Meier curves for at least 36 months. The Kaplan-Meier curves of control groups were extracted and calculated for hazard ratios and 95% confidence intervals. Two virtual trials were developed to validate the reliability and accuracy of our method.
Of 4161 studies, we included six trials containing 7682 HFpEF patients in control groups. The DIG trial had the highest all-cause mortality, cardiovascular mortality, heart failure mortality, and composite endpoints of cardiovascular mortality and heart failure hospitalization (all p < 0.001). The TOPCAT trial had the lowest all-cause mortality, cardiovascular mortality, heart failure hospitalization, and composite of cardiovascular mortality and heart failure hospitalization (all p < 0.001). Adoption of different ejection fraction cut-off values for HFpEF diagnosis did not significantly change the outcomes of control groups in the DIG trial (45% vs. 50%: hazard ratio, 1.05, 95% confidence interval, 0.97-1.13, p = 0.271), or in the CHARM-Preserved trial (40% vs. 50%: hazard ratio, 1.01, 95% confidence interval, 0.93-1.09, p = 0.864) during 36-month follow-up.
The control groups of HFpEF trials have heterogeneous outcomes. Future trials should consider these heterogeneities when designing protocols.
先前的研究已经评估了射血分数保留型心力衰竭(HFpEF)的研究内异质性,但研究间的异质性仍知之甚少。我们研究了 HFpEF 试验对照组结果的异质性。
我们纳入了招募射血分数≥40%的 HFpEF 患者且报告至少 36 个月 Kaplan-Meier 曲线的随机对照试验。提取对照组的 Kaplan-Meier 曲线,并计算风险比和 95%置信区间。设计了两个虚拟试验来验证我们方法的可靠性和准确性。
在 4161 项研究中,我们纳入了包含 7682 例 HFpEF 患者对照组的 6 项试验。DIG 试验的全因死亡率、心血管死亡率、心力衰竭死亡率和心血管死亡率和心力衰竭住院的复合终点最高(均 p<0.001)。TOPCAT 试验的全因死亡率、心血管死亡率、心力衰竭住院率和心血管死亡率和心力衰竭住院的复合终点最低(均 p<0.001)。采用不同的 HFpEF 诊断射血分数截断值不会显著改变 DIG 试验对照组的结果(45%与 50%:风险比,1.05,95%置信区间,0.97-1.13,p=0.271),或 CHARM-Preserved 试验(40%与 50%:风险比,1.01,95%置信区间,0.93-1.09,p=0.864)在 36 个月的随访期间。
HFpEF 试验的对照组结果存在异质性。未来的试验在设计方案时应考虑这些异质性。