在心力衰竭临床试验中利用生活质量调整后的存活和出院天数

Pishoy Gouda, Sarah Rathwell, Eloisa Colin-Ramirez, G. Michael Felker, Heather Ross, Jorge Escobedo, Peter Macdonald, Richard W. Troughton, Christopher M. O’Connor, Justin A. Ezekowitz
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摘要

背景:在心力衰竭(HF)试验中,人们一直在强调使用更多的以患者为中心的结果,包括生活质量(QoL)、存活天数和出院天数。方法:我们利用两项心力衰竭试验(心力衰竭生物标记物强化治疗指导循证疗法[GUIDE-IT]和心力衰竭100毫摩尔以下饮食干预研究[SODIUM-HF])的数据,以18个月时根据QoL调整的存活和出院天数百分比(%DAOH)作为主要结果,确定治疗差异。每位参与者的存活和出院天数百分比计算为存活和出院天数与总随访天数之比。结果:在 GUIDE-IT 试验中,847 名参与者的基线堪萨斯城心肌病问卷总分中位数为 59.0(四分位间范围为 40.8-74.3),在 18 个月内没有变化。生物标志物指导组的DAOH%为90.76%±22.09%,常规治疗组为88.56%±25.27%。调整后的 QoL %DAOH 无明显差异(1.09% [95% CI, -1.57% to 3.97%])。在 SODIUM-HF 试验中,796 名参与者的基线堪萨斯城心肌病问卷总体汇总得分中位数为 69.8(四分位间范围为 49.3-84.3),18 个月内没有变化。低钠治疗组的脱氧血症发生率为 95.69%±16.31%,常规治疗组的脱氧血症发生率为 95.95%±14.76%。结论:在两项大型 HF 临床试验中,根据 QoL 调整 %DAOH 是可行的,可为临床试验中的治疗效果提供补充信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utilizing Quality of Life Adjusted Days Alive and Out of Hospital in Heart Failure Clinical Trials
BACKGROUND:In heart failure (HF) trials, there has been an emphasis on utilizing more patient-centered outcomes, including quality of life (QoL) and days alive and out of hospital. We aimed to explore the impact of QoL adjusted days alive and out of hospital as an outcome in 2 HF clinical trials.METHODS:Using data from 2 trials in HF (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment in Heart Failure [GUIDE-IT] and Study of Dietary Intervention under 100 mmol in Heart Failure [SODIUM-HF]), we determined treatment differences using percentage days alive and out of hospital (%DAOH) adjusted for QoL at 18 months as the primary outcome. For each participant, %DAOH was calculated as a ratio between days alive and out of hospital/total follow-up. Using a regression model, %DAOH was subsequently adjusted for QoL measured by the Kansas City Cardiomyopathy Questionnaire Overall Summary Score.RESULTS:In the GUIDE-IT trial, 847 participants had a median baseline Kansas City Cardiomyopathy Questionnaire Overall Summary Score of 59.0 (interquartile range, 40.8–74.3), which did not change over 18 months. %DAOH was 90.76%±22.09% in the biomarker-guided arm and 88.56%±25.27% in the usual care arm. No significant difference in QoL adjusted %DAOH was observed (1.09% [95% CI, −1.57% to 3.97%]). In the SODIUM-HF trial, 796 participants had a median baseline Kansas City Cardiomyopathy Questionnaire Overall Summary Score of 69.8 (interquartile range, 49.3–84.3), which did not change over 18 months. %DAOH was 95.69%±16.31% in the low-sodium arm and 95.95%±14.76% in the usual care arm. No significant difference was observed (1.91% [95% CI, −0.85% to 4.77%]).CONCLUSIONs:In 2 large HF clinical trials, adjusting %DAOH for QoL was feasible and may provide complementary information on treatment effects in clinical trials.
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