CHRU Nancy Hôpitaux de Brabois, INSERM, CIC, Epidémiologie Clinique, Université de Lorraine, 9 Allée du Morvan, 54000, Vandœuvre-lès-Nancy, Nancy, France.
APEMAC, Université de Lorraine, 54500, Nancy, France.
Crit Care. 2023 Nov 6;27(1):426. doi: 10.1186/s13054-023-04701-5.
Intention-to-treat analyses of POINCARE-2 trial led to inconclusive results regarding the effect of a conservative fluid balance strategy on mortality in critically ill patients. The present as-treated analysis aimed to assess the effectiveness of actual exposure to POINCARE-2 strategy on 60-day mortality in critically ill patients.
POINCARE‑2 was a stepped wedge randomized controlled trial. Eligible patients were ≥ 18 years old, under mechanical ventilation and had an expected length of stay in ICU > 24 h. POINCARE-2 strategy consisted of daily weighing over 14 days, and subsequent restriction of fluid intake, administration of diuretics, and/or ultrafiltration. We computed a score of exposure to the strategy based on deviations from the strategy algorithm. We considered patients with a score ≥ 75 as exposed to the strategy. We used logistic regression adjusted for confounders (ALR) or for an instrumental variable (IVLR). We handled missing data using multiple imputations.
A total of 1361 patients were included. Overall, 24.8% of patients in the control group and 69.4% of patients in the strategy group had a score of exposure ≥ 75. Exposure to the POINCARE-2 strategy was not associated with 60-day all-cause mortality (ALR: OR 1.2, 95% CI 0.85-1.55; IVLR: OR 1.0, 95% CI 0.76-1.33).
Actual exposure to POINCARE-2 conservative strategy was not associated with reduced mortality in critically ill patients. Trial registration POINCARE-2 trial is registered at ClinicalTrials.gov (NCT02765009). Registered 29 April 2016.
POINCARE-2 试验的意向治疗分析得出了关于保守液体平衡策略对危重症患者死亡率影响的不确定结果。本研究旨在评估实际暴露于 POINCARE-2 策略对危重症患者 60 天死亡率的有效性。
POINCARE-2 是一项阶梯式楔形随机对照试验。纳入标准为年龄≥18 岁,接受机械通气,预计 ICU 住院时间超过 24 小时。POINCARE-2 策略包括 14 天内每天称重,随后限制液体摄入、使用利尿剂和/或超滤。我们根据策略算法的偏差计算了暴露于策略的评分。我们将得分≥75 分的患者视为暴露于策略。我们使用调整混杂因素(ALR)或工具变量(IVLR)的逻辑回归进行分析。我们使用多重插补处理缺失数据。
共纳入 1361 例患者。对照组中 24.8%的患者和策略组中 69.4%的患者得分≥75。暴露于 POINCARE-2 策略与 60 天全因死亡率无关(ALR:OR 1.2,95%CI 0.85-1.55;IVLR:OR 1.0,95%CI 0.76-1.33)。
实际暴露于 POINCARE-2 保守策略与危重症患者死亡率降低无关。试验注册 POINCARE-2 试验在 ClinicalTrials.gov 注册(NCT02765009)。2016 年 4 月 29 日注册。