Department of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Department of Cardiovascular Anesthesia and Intensive Care, Fondazione Cardiocentro Ticino, Lugano, Switzerland.
PLoS One. 2018 Apr 24;13(4):e0196088. doi: 10.1371/journal.pone.0196088. eCollection 2018.
Furosemide is the most common loop diuretic used worldwide. The off-label administration of furosemide bolus(es) for the prevention or to reverse acute kidney injury (AKI) is widespread but not supported by available evidence. We conducted a meta-analysis of randomized trials (RCTs) to investigate whether bolus furosemide to prevent or treat AKI is detrimental on patients' survival.
Electronic databases were searched through October 2017 for RCTs comparing bolus furosemide administration versus any comparator in patients with or at risk for AKI. The primary endpoint was all-cause longest follow-up mortality. Secondary endpoints included new or worsening AKI, receipt of renal replacement therapy, length of hospital stay, and peak serum creatinine after randomization.
A total of 28 studies randomizing 3,228 patients were included in the analysis. We found no difference in mortality between the two groups (143/892 [16%] in the furosemide group versus 141/881 [16%] in the control group; odds ratio [OR], 0.84; 95% confidence interval [CI], 0.63 to 1.13; p = 0.25). No significant differences in secondary outcomes were found. A significant improvement in survival was found in the subgroup of patients receiving furosemide bolus(es) as a preventive measure (43/613 [7.0%] versus 67/619 [10.8%], OR 0.62; 95% CI, 0.41 to 0.94; p = 0.03).
Intermittent furosemide administration is not associated with an increased mortality in patients with or at risk for AKI, although it may reduce mortality when used as a preventive measure. Future high-quality RCTs are needed to define the role of loop diuretics in AKI prevention and management.
The study protocol was registered on PROSPERO database for systematic reviews (Registration no. CRD42017078607 - http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017078607).
呋塞米是世界范围内最常用的袢利尿剂。非适应证下使用呋塞米推注以预防或逆转急性肾损伤(AKI)的情况非常普遍,但尚无证据支持这种用法。我们进行了一项随机对照试验(RCT)的荟萃分析,旨在探讨推注呋塞米预防或治疗 AKI 是否会对患者的生存造成危害。
通过电子数据库检索 2017 年 10 月前发表的比较 AKI 患者或 AKI 高危患者使用呋塞米推注与任何对照治疗的 RCT。主要终点是全因最长随访死亡率。次要终点包括新发或恶化 AKI、接受肾脏替代治疗、住院时间和随机分组后血清肌酐峰值。
共纳入 28 项随机分配 3228 名患者的研究。我们发现两组死亡率无差异(呋塞米组 143/892[16%]与对照组 141/881[16%];比值比[OR],0.84;95%置信区间[CI],0.63 至 1.13;p=0.25)。次要结局也无显著差异。接受呋塞米推注作为预防措施的亚组患者生存情况显著改善(43/613[7.0%]与 67/619[10.8%],OR 0.62;95%CI,0.41 至 0.94;p=0.03)。
间歇使用呋塞米与 AKI 患者或 AKI 高危患者的死亡率增加无关,但作为预防措施时可能会降低死亡率。需要未来开展高质量的 RCT 来明确袢利尿剂在 AKI 预防和管理中的作用。
研究方案在 PROSPERO 数据库(系统评价登记号:CRD42017078607 - http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017078607)进行了注册。