Stone Gregg W, Christiansen Evald H, Ali Ziad A, Andreasen Lene N, Maehara Akiko, Ahmad Yousif, Landmesser Ulf, Holm Niels R
The Zena and Michael A Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Aarhus University Hospital, Aarhus, Denmark.
Lancet. 2024 Mar 2;403(10429):824-837. doi: 10.1016/S0140-6736(23)02454-6. Epub 2024 Feb 21.
Previous meta-analyses have shown reduced risks of composite adverse events with intravascular imaging-guided percutaneous coronary intervention (PCI) compared with angiography guidance alone. However, these studies have been insufficiently powered to show whether all-cause death or all myocardial infarction are reduced with intravascular imaging guidance, and most previous intravascular imaging studies were done with intravascular ultrasound rather than optical coherence tomography (OCT), a newer imaging modality. We aimed to assess the comparative performance of intravascular imaging-guided PCI and angiography-guided PCI with drug-eluting stents.
For this systematic review and updated meta-analysis, we searched the MEDLINE, Embase, and Cochrane databases from inception to Aug 30, 2023, for studies that randomly assigned patients undergoing PCI with drug-eluting stents either to intravascular ultrasound or OCT, or both, or to angiography alone to guide the intervention. The searches were done and study-level data were extracted independently by two investigators. The primary endpoint was target lesion failure, defined as the composite of cardiac death, target vessel-myocardial infarction (TV-MI), or target lesion revascularisation, assessed in patients randomly assigned to intravascular imaging guidance (intravascular ultrasound or OCT) versus angiography guidance. We did a standard frequentist meta-analysis to generate direct data, and a network meta-analysis to generate indirect data and overall treatment effects. Outcomes were expressed as relative risks (RRs) with 95% CIs at the longest reported follow-up duration. This study was registered with the international prospective register of systematic reviews (PROSPERO, number CRD42023455662).
22 trials were identified in which 15 964 patients were randomised and followed for a weighted mean duration of 24·7 months (longest duration of follow-up in each study ranging from 6 to 60 months). Compared with angiography-guided PCI, intravascular imaging-guided PCI resulted in a decreased risk of target lesion failure (RR 0·71 [95% CI 0·63-0·80]; p<0·0001), driven by reductions in the risks of cardiac death (RR 0·55 [95% CI 0·41-0·75]; p=0·0001), TV-MI (RR 0·82 [95% CI 0·68-0·98]; p=0·030), and target lesion revascularisation (RR 0·72 [95% CI 0·60-0·86]; p=0·0002). Intravascular imaging guidance also reduced the risks of stent thrombosis (RR 0·52 [95% CI 0·34-0·81]; p=0·0036), all myocardial infarction (RR 0·83 [95% CI 0·71-0·99]; p=0·033), and all-cause death (RR 0·75 [95% CI 0·60-0·93]; p=0·0091). Outcomes were similar for OCT-guided and intravascular ultrasound-guided PCI.
Compared with angiography guidance, intravascular imaging guidance of coronary stent implantation with OCT or intravascular ultrasound enhances both the safety and effectiveness of PCI, reducing the risks of death, myocardial infarction, repeat revascularisation, and stent thrombosis.
Abbott.
既往的荟萃分析表明,与单纯血管造影引导相比,血管内成像引导的经皮冠状动脉介入治疗(PCI)可降低复合不良事件的风险。然而,这些研究的样本量不足以显示血管内成像引导是否能降低全因死亡或所有心肌梗死的风险,并且既往大多数血管内成像研究使用的是血管内超声而非光学相干断层扫描(OCT)这种更新的成像方式。我们旨在评估血管内成像引导的PCI与血管造影引导的药物洗脱支架PCI的对比性能。
对于这项系统评价和更新的荟萃分析,我们检索了MEDLINE、Embase和Cochrane数据库,检索时间从数据库建立至2023年8月30日,以查找将接受药物洗脱支架PCI的患者随机分配至血管内超声或OCT或两者,或仅接受血管造影以指导干预的研究。检索工作由两名研究人员独立完成,并提取研究水平的数据。主要终点是靶病变失败,定义为心源性死亡、靶血管心肌梗死(TV-MI)或靶病变血运重建的复合事件,在随机分配至血管内成像引导(血管内超声或OCT)与血管造影引导的患者中进行评估。我们进行了标准的频率学派荟萃分析以生成直接数据,并进行了网状荟萃分析以生成间接数据和总体治疗效果。结局以最长报告随访期的相对风险(RR)及95%可信区间(CI)表示。本研究已在国际前瞻性系统评价注册库(PROSPERO,编号CRD42023455662)注册。
共纳入22项试验,15964例患者被随机分组,加权平均随访时间为24.7个月(每项研究的最长随访时间为6至60个月)。与血管造影引导的PCI相比,血管内成像引导的PCI降低了靶病变失败的风险(RR 0.71 [95%CI 0.63-0.80];p<0.0001),其中心源性死亡风险降低(RR 0.55 [95%CI 0.41-0.75];p=0.0001)、TV-MI风险降低(RR 0.82 [95%CI 0.68-0.98];p=0.