Yamamoto Ko, Shiomi Hiroki, Nishikawa Ryusuke, Morimoto Takeshi, Miyazawa Akiyoshi, Naganuma Toru, Suwa Satoru, Fujita Takanari, Domei Takenori, Tatsushima Shojiro, Hamaguchi Yukihiro, Nishimoto Yuji, Matsuda Kensho, Takayama Yohei, Kuribara Jun, Kirigaya Hidekuni, Yoneda Kohei, Shigetoshi Masataka, Yokomatsu Takafumi, Kadota Kazushige, Ando Kenji, Hibi Kiyoshi, Ono Koh, Kimura Takeshi
Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Am J Cardiol. 2025 Mar 15;239:20-27. doi: 10.1016/j.amjcard.2024.12.020. Epub 2024 Dec 17.
There is a scarcity of data on clinical outcomes after intravascular ultrasound (IVUS)-guided percutaneous coronary intervention (PCI) in patients with multivessel disease and chronic kidney disease (CKD). The Optimal Intravascular Ultrasound (OPTIVUS)-Complex PCI study multivessel cohort was a prospective multicenter single-arm trial enrolling 1,015 patients who underwent multivessel IVUS-guided PCI including left anterior descending coronary artery target with an intention to meet the prespecified OPTIVUS criteria for optimal stent expansion. We compared the clinical outcomes between patients with and without CKD. The primary end point was a composite of death, myocardial infarction, stroke, or any coronary revascularization. There were 528 patients (52.0%) without CKD (estimated glomerular filtration rate [eGFR] ≥60 ml/min/1.73 m), 391 patients (38.5%) with moderate CKD (60 >eGFR ≥30 ml/min/1.73 m), and 96 patients (9.5%) with severe CKD (eGFR <30 ml/min/1.73 m or hemodialysis). The rate of meeting OPTIVUS criteria was not different across the 3 groups. The cumulative 1-year incidence of the primary end point was 9.1%, 9.0%, and 22.1% in patients without CKD, with moderate CKD, and with severe CKD, respectively (log-rank p <0.001). After adjusting confounders, the higher risk of severe CKD relative to no CKD remained significant for the primary end point (hazard ratio 2.42, 95% confidence interval 1.30 to 4.25, p = 0.01), whereas the risk of moderate CKD relative to no CKD was not significant for the primary end point (hazard ratio 0.97, 95% confidence interval 0.61 to 1.53, p = 0.88). In conclusion, in patients who underwent multivessel IVUS-guided PCI, and were managed with contemporary clinical practice, 1-year clinical outcomes were worse in patients with severe CKD, whereas 1-year clinical outcomes were not different between patients without CKD and with moderate CKD.
关于多支血管病变和慢性肾脏病(CKD)患者在血管内超声(IVUS)引导下经皮冠状动脉介入治疗(PCI)后的临床结局,相关数据较为匮乏。优化血管内超声(OPTIVUS)-复杂PCI研究的多支血管队列是一项前瞻性多中心单臂试验,纳入了1015例接受多支血管IVUS引导下PCI的患者,其中包括以达到预设的OPTIVUS最佳支架扩张标准为目标的左前降支冠状动脉病变。我们比较了有和没有CKD患者的临床结局。主要终点是死亡、心肌梗死、中风或任何冠状动脉血运重建的复合终点。共有528例(52.0%)患者无CKD(估计肾小球滤过率[eGFR]≥60 ml/min/1.73 m²),391例(38.5%)患者有中度CKD(60>eGFR≥30 ml/min/1.73 m²),96例(9.5%)患者有重度CKD(eGFR<30 ml/min/1.73 m²或接受血液透析)。三组达到OPTIVUS标准的比例没有差异。无CKD、中度CKD和重度CKD患者的主要终点1年累积发生率分别为9.1%、9.0%和22.1%(对数秩检验p<0.001)。在调整混杂因素后,相对于无CKD,重度CKD患者发生主要终点的较高风险仍然显著(风险比2.42,95%置信区间1.30至4.25,p = 0.01),而相对于无CKD,中度CKD患者发生主要终点的风险不显著(风险比0.97,95%置信区间0.61至1.53,p = 0.88)。总之,在接受多支血管IVUS引导下PCI且采用当代临床实践管理的患者中,重度CKD患者的1年临床结局较差,而无CKD和中度CKD患者的1年临床结局没有差异。