Hanberg Jennifer S, Tang W H Wilson, Wilson F Perry, Coca Steven G, Ahmad Tariq, Brisco Meredith A, Testani Jeffrey M
Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
Section of Heart Failure and Cardiac Transplantation, The Cleveland Clinic, Cleveland, OH, United States.
Int J Cardiol. 2017 Aug 15;241:277-282. doi: 10.1016/j.ijcard.2017.03.114. Epub 2017 Mar 27.
Effective decongestion of heart failure patients predicts improved outcomes, but high dose loop diuretics (HDLD) used to achieve diuresis predict adverse outcomes. In the DOSE trial, randomization to a HDLD intensification strategy (HDLD-strategy) improved diuresis but not outcomes. Our objective was to determine if potential beneficial effects of more aggressive decongestion may have been offset by adverse effects of the HDLD used to achieve diuresis.
A post hoc analysis of the DOSE trial (n=308) was conducted to determine the influence of post-randomization diuretic dose and fluid output on the rate of death, rehospitalization or emergency department visitation associated with the HDLD-strategy. Net fluid output was used as a surrogate for beneficial decongestive effects and cumulative loop diuretic dose for the dose-related adverse effects of the HDLD-strategy. Randomization to the HDLD-strategy resulted in increased fluid output, even after adjusting for cumulative diuretic dose (p=0.006). Unadjusted, the HDLD-strategy did not improve outcomes (p=0.28). However, following adjustment for cumulative diuretic dose, significant benefit emerged (HR=0.64, 95% CI 0.43-0.95, p=0.028). Adjusting for net fluid balance eliminated the benefit (HR=0.95, 95% CI 0.67-1.4, p=0.79).
A clinically meaningful benefit from a randomized aggressive decongestion strategy became apparent after accounting for the quantity of loop diuretic administered. Adjusting for the diuresis resulting from this strategy eliminated the benefit. These hypothesis-generating observations may suggest a role for aggressive decongestion in improved outcomes.
心力衰竭患者有效的消肿治疗预示着预后改善,但用于实现利尿的高剂量袢利尿剂(HDLD)却预示着不良预后。在剂量试验中,随机分组至HDLD强化策略(HDLD策略)可改善利尿情况,但并未改善预后。我们的目的是确定更积极的消肿治疗的潜在有益效果是否可能被用于实现利尿的HDLD的不良反应所抵消。
对剂量试验(n = 308)进行事后分析,以确定随机分组后利尿剂剂量和液体排出量对与HDLD策略相关的死亡、再次住院或急诊就诊率的影响。净液体排出量用作有益消肿效果的替代指标,累积袢利尿剂剂量用作HDLD策略剂量相关不良反应的指标。随机分组至HDLD策略导致液体排出量增加,即使在调整累积利尿剂剂量后也是如此(p = 0.006)。未经调整时,HDLD策略并未改善预后(p = 0.28)。然而,在调整累积利尿剂剂量后,出现了显著益处(HR = 0.64,95%CI 0.43 - 0.95,p = 0.028)。调整净液体平衡后消除了这种益处(HR = 0.95,95%CI 0.67 - 1.4,p = 0.79)。
在考虑袢利尿剂给药量后,随机积极消肿策略的临床显著益处变得明显。调整该策略产生的利尿作用后消除了这种益处。这些产生假设的观察结果可能提示积极消肿在改善预后方面的作用。