Hu Xinyang, Zhang Jinlong, Yang Seokhun, Jiang Jun, Peng Xiaoping, Lu Dongsheng, Pan Yibin, Guo Lijun, Li Jilin, He Wenming, Zhou Hao, Pu Jun, Huang Jinyu, Jiang Fan, Liu Qiang, Song Daqing, Lu Liang, Cheng Zhenfeng, Yang Bin, Ma Jianliang, Chen Peng, Li Shiqiang, Meng Zhaohui, Tang Lijiang, Fan Yongzhen, Shin Eun-Seok, Tu Shengxian, Nam Chang-Wook, Fearon William F, Koo Bon-Kwon, Wang Jian'an
Department of Cardiology, the Second Affiliated Hospital of Zhejiang University School of Medicine, State Key Laboratory of Transvascular Implantation Devices, Heart Regeneration and Repair Key Laboratory of Zhejiang Province, Transvascular Implantation Devices Research Institute, Hangzhou, China.
Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Lancet. 2025 Apr 26;405(10488):1491-1504. doi: 10.1016/S0140-6736(25)00504-5. Epub 2025 Mar 30.
Revascularisation decisions based on angiography-derived fractional flow reserve (FFR) or optimisation of stent implantation with intravascular ultrasound yield superior clinical outcomes compared with percutaneous coronary intervention (PCI) guided by angiography alone. However, the differences in outcomes when a single approach is used for both purposes remain unclear. We aimed to assess the non-inferiority of angiography-derived FFR versus intravascular ultrasound guidance in terms of clinical outcomes at 12 months in patients with angiographically significant stenosis.
This investigator-initiated, open-label, multicentre, randomised, non-inferiority trial, which was done in 22 centres in China, enrolled patients aged 18 years or older with suspected ischaemic heart disease and with at least 50% stenosis in epicardial coronary arteries measuring at least 2·5 mm by visual estimation on coronary angiography. Patients were randomly assigned (1:1) to undergo PCI guided by either angiography-derived FFR or intravascular ultrasound, including revascularisation decisions and optimisation of the stent implantations based on prespecified PCI criteria and optimal PCI goals. Use of both modalities simultaneously was not permitted. Randomisation as performed using a web-based program and stratified based on the trial centre and the presence or absence of diabetes. The primary outcome was a composite of death, myocardial infarction, or revascularisation at 12 months in the intention-to-treat population, and the non-inferiority margin was 2·5 percentage points. This trial is registered with ClinicalTrials.gov, NCT04397211; long-term follow-up is ongoing.
Between May 29, 2020, and Sept 20, 2023, 1872 patients were enrolled. After 33 patients withdrew, 923 patients were randomly assigned to the angiography-derived FFR group and 916 to the intravascular ultrasound group. Median age of the study population was 66·0 years (IQR 58·0-72·0), and 1248 (67·9%) patients were male and 591 (32·1%) were female. Revascularisation was performed in 688 (69·5%) of 990 target vessels in the angiography-derived FFR group and 797 (81·0%) of 984 target vessels in the intravascular ultrasound group. At a median follow-up of 12 months (IQR 12-12), the primary outcome event occurred in 56 patients in the angiography-derived FFR group and 54 patients in the intravascular ultrasound group (6·3% vs 6·0%, absolute difference 0·2 percentage points [upper boundary of one-sided 97·5% CI 2·4], p=0·022; hazard ratio 1·04 [95% CI 0·71 to 1·51]). Mortality did not differ between the two groups (1·8% in the angiography-derived FFR group vs 1·3% in the intravascular ultrasound group, absolute difference 0·4 percentage points [95% CI -0·7 to 1·6]; hazard ratio 1·34 [0·63 to 2·83], p=0·45). The incidence of recurrent angina was low in both groups: 26 (2·8%) of 923 patients in the angiography-derived FFR group and 35 (3·8%) of 916 patients in the intravascular ultrasound group.
The angiography-derived FFR-guided comprehensive PCI strategy, encompassing revascularisation decision making and stent optimisation, was non-inferior to intravascular ultrasound guidance. This finding might have implications for future guidelines on its role and application.
National Natural Science Foundation of China, The Key R & D Projects of Zhejiang Province, and the RCT Program from The Second Affiliated Hospital of Zhejiang University School of Medicine.
与单纯血管造影引导的经皮冠状动脉介入治疗(PCI)相比,基于血管造影衍生的血流储备分数(FFR)进行血运重建决策或使用血管内超声优化支架植入可产生更好的临床结果。然而,当单一方法用于这两个目的时,结果的差异仍不明确。我们旨在评估在血管造影显示有明显狭窄的患者中,血管造影衍生的FFR与血管内超声引导在12个月临床结果方面的非劣效性。
这项由研究者发起的、开放标签、多中心、随机、非劣效性试验在中国的22个中心进行,纳入年龄在18岁及以上、疑似缺血性心脏病且在冠状动脉造影上目测至少有50%狭窄、心外膜冠状动脉直径至少2.5 mm的患者。患者被随机分配(1:1)接受基于血管造影衍生的FFR或血管内超声引导的PCI,包括根据预先指定的PCI标准和最佳PCI目标进行血运重建决策和支架植入优化。不允许同时使用这两种方式。使用基于网络的程序进行随机分组,并根据试验中心和是否患有糖尿病进行分层。主要结局是在意向性治疗人群中12个月时的死亡、心肌梗死或血运重建的复合结局,非劣效性界值为2.5个百分点。本试验已在ClinicalTrials.gov注册,NCT04397211;长期随访正在进行。
在2020年5月29日至2023年9月20日期间,共纳入1872例患者。33例患者退出后,923例患者被随机分配至血管造影衍生的FFR组,916例患者被随机分配至血管内超声组。研究人群的中位年龄为66.0岁(四分位间距58.0 - 72.0),男性1248例(67.9%),女性591例(32.1%)。血管造影衍生的FFR组990个靶血管中有688个(69.5%)进行了血运重建,血管内超声组984个靶血管中有797个(81.0%)进行了血运重建。在中位随访12个月(四分位间距12 - 12)时,血管造影衍生的FFR组有56例患者发生主要结局事件,血管内超声组有54例患者发生主要结局事件(6.3%对6.0%,绝对差异0.2个百分点[单侧97.5%CI的上界2.4],p = 0.022;风险比1.04[95%CI 0.71至1.51])。两组之间的死亡率无差异(血管造影衍生的FFR组为1.8%,血管内超声组为1.3%,绝对差异0.4个百分点[95%CI -0.7至1.6];风险比1.34[0.63至2.83],p = 0.45)。两组复发性心绞痛的发生率均较低:血管造影衍生的FFR组923例患者中有26例(2.8%),血管内超声组916例患者中有35例(3.8%)。
基于血管造影衍生的FFR引导的综合PCI策略,包括血运重建决策和支架优化,不劣于血管内超声引导。这一发现可能对其作用和应用的未来指南有影响。
国家自然科学基金、浙江省重点研发项目以及浙江大学医学院附属第二医院的随机对照试验项目。