Tarantini Giuseppe, Prasad Anand, Rathore Sudhir, Bansal Shweta, Gottfried Regine, Rosenkranz Alexander R, Briguori Carlo, Yaghoubi Mohsen, Mashayekhi Atefeh, Javanbakht Mehdi, Moloney Eoin
Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova, Padua, Italy.
Department of Medicine, Division of Cardiology, University of Texas Health Science Center, San Antonio, TX, United States.
Front Med (Lausanne). 2022 Apr 25;9:841876. doi: 10.3389/fmed.2022.841876. eCollection 2022.
Contrast-associated acute kidney injury (CA-AKI) is an important adverse effect associated with injecting iodinated intra-arterial contrast media (CM) during coronary angiography. The DyeVert™ Contrast Reduction System is a medical device intended to reduce the intra-arterial CM volume (CMV) administered. The aim of this study was to assess DyeVert System clinical effectiveness and safety by implementing a systematic review and meta-analysis of existing evidence.
Systematic electronic literature searches were conducted in MEDLINE, Embase, the Cochrane Database of Systematic Reviews, ClinicalTrials.gov, and the International Clinical Trials Registry Platform database. Relevant data were extracted from included studies and meta-analyses were performed to synthesize evidence across studies.
The review included 17 eligible studies involving 1,731 DyeVert System cases and 1,387 control cases (without the use of DyeVert). Meta-analyses demonstrated use of the DyeVert System reduced CMV delivered to the patient by 39.27% (95% CI, 36.10-42.48%, < 0.001), reduced CMV/baseline renal function ratios (Hedges's g, -0.56; 95% CI, -0.70 to -0.42, < 0.001) and percentage of cases exceeding the maximum CMV threshold (risk difference -0.31, 95% CI, -0.48 to -0.13, < 0.001) while maintaining adequate image quality in 98% of cases. DyeVert System cases demonstrated lower CA-AKI incidence vs. controls (absolute risk reduction 5.00% (95% CI, 0.40-9.80%; = 0.03), relative risk 0.60 (95% CI, 0.40-0.90; = 0.01) with a pooled estimate of the number needed to treat with the DyeVert System to avoid 1 CA-AKI event of 20.
DyeVert System use significantly reduces CMV delivered to the patient, CMV/baseline renal function ratios, and CA-AKI incidence while maintaining image quality. Accordingly, the device may serve as an adjunctive, procedure-based strategy to prevent CA-AKI. Future multi-center studies are needed to further assess effects of minimizing CMV on endpoints such as CA-AKI prevention, incidence of adverse cardiac and renal events, and health care costs.
对比剂相关急性肾损伤(CA-AKI)是冠状动脉造影期间注射碘化动脉内造影剂(CM)相关的重要不良反应。DyeVert™对比剂减量系统是一种旨在减少动脉内注射造影剂体积(CMV)的医疗设备。本研究的目的是通过对现有证据进行系统评价和荟萃分析,评估DyeVert系统的临床有效性和安全性。
在MEDLINE、Embase、Cochrane系统评价数据库、ClinicalTrials.gov和国际临床试验注册平台数据库中进行系统的电子文献检索。从纳入研究中提取相关数据,并进行荟萃分析以综合各研究的证据。
该评价纳入了17项符合条件的研究,涉及1731例使用DyeVert系统的病例和1387例对照病例(未使用DyeVert)。荟萃分析表明,使用DyeVert系统可使输送给患者的CMV降低39.27%(95%CI,36.10-42.48%,P<0.001),降低CMV/基线肾功能比值(Hedges's g,-0.56;95%CI,-0.70至-0.42,P<0.001)以及超过最大CMV阈值的病例百分比(风险差异-0.31,95%CI,-0.48至-0.13,P<0.001),同时98%的病例维持了足够的图像质量。与对照组相比,使用DyeVert系统的病例CA-AKI发生率较低(绝对风险降低5.00%(95%CI,0.40-9.80%;P=0.03),相对风险0.60(95%CI,0.40-0.90;P=0.01),使用DyeVert系统避免1例CA-AKI事件所需治疗人数的合并估计值为20。
使用DyeVert系统可显著降低输送给患者的CMV、CMV/基线肾功能比值和CA-AKI发生率,同时维持图像质量。因此,该设备可作为预防CA-AKI的基于操作的辅助策略。未来需要进行多中心研究,以进一步评估最小化CMV对诸如预防CA-AKI、不良心脏和肾脏事件发生率以及医疗保健成本等终点的影响。