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在所有患者登记研究中,超低剂量和零对比 PCI 的安全性、可行性和增量价值。

Safety, feasibility, and incremental value of ultralow and zero contrast PCI in an all-comers registry.

机构信息

Chandler Regional Medical Center, Chandler, Arizona, USA.

出版信息

Catheter Cardiovasc Interv. 2024 Oct;104(4):648-654. doi: 10.1002/ccd.31214. Epub 2024 Sep 2.

DOI:10.1002/ccd.31214
PMID:39219453
Abstract

BACKGROUND

Patients with chronic kidney disease and CAD have been denied revascularization because of fear of precipitating acute renal failure from contrast exposure. Skepticism on whether Ultra-Low contrast percutaneous coronary intervention (PCI) or Zero contrast PCI (ULC/ZC PCI) can be safely performed has limited its adoption.

METHODS

This observational registry enrolled 200 consecutive patients referred for elective PCI at a single center from June 2021 to December 2022. The study investigated whether the clinical outcomes of PCI performed with UL/ZC-PCI (n-48) were comparable to outcomes following standard PCI (n-152).

RESULTS

Both groups were well matched in baseline and procedural characteristics. The groups had a highly statistical difference in the use of CV. Mean CV was 19.17 ± 7.29 cc in the ULC/ZC-group and 147.14 ± 73.55 cc in the control arm. The principal findings of the study were that the incidence of ontrast-induced acute kidney injury (AKI) was eightfold lower in patients receiving UL/ZC compared to the control group that received standard PCI. The incidence of all-cause mortality, myocardial infarction and major bleeding were similar in both groups. At 6 months, the decrement in renal function was lower in the group that received lower volumes of contrast.

CONCLUSIONS

This single center observational registry demonstrated that UL-C/ZC-PCI is safe and effective in a broad spectrum of complex lesions. The skillsets needed to perform this are teachable, widely applicable and do not require a large upgrade of capital equipment. AKI rates and decrement in renal function at 6 months were both significantly lower in the UL-ZC group.

摘要

背景

由于担心对比剂暴露会引发急性肾衰竭,患有慢性肾脏病和 CAD 的患者被拒绝血运重建。对于是否可以安全进行超低对比经皮冠状动脉介入治疗(PCI)或零对比 PCI(ULC/ZC PCI)存在怀疑,这限制了其应用。

方法

这项观察性注册研究纳入了 2021 年 6 月至 2022 年 12 月期间在一家单中心因择期 PCI 而就诊的 200 例连续患者。本研究调查了使用 UL/ZC-PCI(n=48)进行 PCI 的临床结局是否与标准 PCI(n=152)的结局相当。

结果

两组在基线和手术特征方面均匹配良好。两组在 CV 的使用方面存在高度统计学差异。ULC/ZC 组的平均 CV 为 19.17±7.29 cc,对照组为 147.14±73.55 cc。该研究的主要发现是,与接受标准 PCI 的对照组相比,接受 UL/ZC 的患者发生对比剂诱导的急性肾损伤(AKI)的发生率低 8 倍。两组的全因死亡率、心肌梗死和主要出血发生率相似。在 6 个月时,接受较低剂量对比剂的组肾功能下降幅度较低。

结论

这项单中心观察性注册研究表明,在广泛的复杂病变中,ULC/ZC-PCI 是安全有效的。进行这项技术所需的技能是可教的、广泛适用的,并且不需要大量升级资本设备。UL-ZC 组的 AKI 发生率和 6 个月时肾功能下降幅度均显著降低。

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