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利尿剂匹配与标准水化在经皮心血管介入治疗患者中的比较:随机临床试验的荟萃分析。

Diuresis-matched versus standard hydration in patients undergoing percutaneous cardiovascular procedures: meta-analysis of randomized clinical trials.

机构信息

Division of Cardiology, Azienda Ospedaliero-Universitaria Policlinico G. Rodolico-San Marco, University of Catania, Catania, Italy.

Division of Cardiology, Azienda Ospedaliero-Universitaria Policlinico G. Rodolico-San Marco, University of Catania, Catania, Italy.

出版信息

Rev Esp Cardiol (Engl Ed). 2023 Oct;76(10):759-766. doi: 10.1016/j.rec.2023.02.001. Epub 2023 Feb 16.

DOI:10.1016/j.rec.2023.02.001
PMID:36801376
Abstract

INTRODUCTION AND OBJECTIVES

Contrast-associated acute kidney injury (CA-AKI) is a potential complication of procedures requiring administration of iodinated contrast medium. RenalGuard, which provides real-time matching of intravenous hydration with furosemide-induced diuresis, is an alternative to standard periprocedural hydration strategies. The evidence on RenalGuard in patients undergoing percutaneous cardiovascular procedures is sparse. We used a Bayesian framework to perform a meta-analysis of RenalGuard as a CA-AKI preventive strategy.

METHODS

We searched Medline, Cochrane Library and Web of Science for randomized trials of RenalGuard vs standard periprocedural hydration strategies. The primary outcome was CA-AKI. Secondary outcomes were all-cause death, cardiogenic shock, acute pulmonary edema, and renal failure requiring renal replacement therapy. A Bayesian random-effect risk ratio (RR) with corresponding 95% credibility interval (95%CrI) was calculated for each outcome. PROSPERO database number CRD42022378489.

RESULTS

Six studies were included. RenalGuard was associated with a significant relative reduction in CA-AKI (median RR, 0.54; 95%CrI, 0.31-0.86) and acute pulmonary edema (median RR, 0.35; 95%CrI, 0.12-0.87). No significant differences were observed for the other secondary endpoints [all-cause death (RR, 0.49; 95%CrI, 0.13-1.08), cardiogenic shock (RR, 0.06; 95%CrI, 0.00-1.91), and renal replacement therapy (RR, 0.52; 95%CrI, 0.18-1.18)]. The Bayesian analysis also showed that RenalGuard had a high probability of ranking first for all the secondary outcomes. These results were consistent in multiple sensitivity analyses.

CONCLUSIONS

In patients undergoing percutaneous cardiovascular procedures, RenalGuard was associated with a reduced risk of CA-AKI and acute pulmonary edema compared with standard periprocedural hydration strategies.

摘要

介绍和目的

对比剂相关急性肾损伤(CA-AKI)是需要使用碘造影剂的介入程序的潜在并发症。RenalGuard 通过实时匹配静脉补液和速尿诱导的利尿,是标准围手术期补液策略的替代方案。在接受经皮心血管介入程序的患者中,RenalGuard 的证据很少。我们使用贝叶斯框架对 RenalGuard 作为 CA-AKI 预防策略进行了荟萃分析。

方法

我们在 Medline、Cochrane 图书馆和 Web of Science 中搜索了 RenalGuard 与标准围手术期补液策略的随机试验。主要结局是 CA-AKI。次要结局为全因死亡、心源性休克、急性肺水肿和需要肾脏替代治疗的肾衰竭。计算了每个结局的贝叶斯随机效应风险比(RR)及其对应的 95%可信度区间(95%CrI)。PROSPERO 数据库编号 CRD42022378489。

结果

纳入了 6 项研究。RenalGuard 与 CA-AKI(中位数 RR,0.54;95%CrI,0.31-0.86)和急性肺水肿(中位数 RR,0.35;95%CrI,0.12-0.87)的相对减少显著相关。对于其他次要终点,没有观察到显著差异[全因死亡(RR,0.49;95%CrI,0.13-1.08)、心源性休克(RR,0.06;95%CrI,0.00-1.91)和肾脏替代治疗(RR,0.52;95%CrI,0.18-1.18)]。贝叶斯分析还表明,RenalGuard 在所有次要结局中都有很大可能排名第一。这些结果在多次敏感性分析中是一致的。

结论

在接受经皮心血管介入程序的患者中,与标准围手术期补液策略相比,RenalGuard 与 CA-AKI 和急性肺水肿的风险降低相关。

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