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Impact of Sex on Residual Angina After Percutaneous Coronary Interventions

医学 心脏病学 经皮 内科学 心理干预 心绞痛 经皮冠状动脉介入治疗 稳定型心绞痛 冠心病 残余物 梅德林 不稳定型心绞痛 介入心脏病学 外科 传统PCI 冠心病
作者
Masahiro Hada,Takuya Mizukami,Kazumasa Ikeda,Daniel Munhoz,Sofie Brouwers,Jeroen Sonck,Hitoshi Matsuo,Toshiro Shinke,Hirohiko Ando,Brian Ko,Simone Biscaglia,Fernando Rivero,Thomas Engstrøm,Ketina Arslani,Antonio Maria Leone,Domenico Galante,Lokien X. van Nunen,William F. Fearon,Evald Høj Christiansen,Stéphane Fournier
出处
期刊:Catheterization and Cardiovascular Interventions [Wiley]
卷期号:107 (4): 987-996
标识
DOI:10.1002/ccd.70419
摘要

BACKGROUND: Sex-related differences in the clinical presentation of coronary artery disease (CAD) are well recognized. The pullback pressure gradient (PPG) characterizes pathophysiological CAD patterns as focal or diffuse. OBJECTIVES: To evaluate the influence of sex on residual angina at one year after percutaneous coronary intervention (PCI), stratified by PPG. METHODS: We performed a sub-analysis of PPG Global, a multicenter, prospective, single-arm study. All patients had hemodynamically significant CAD (fractional flow reserve [FFR] ≤ 0.80) and underwent a manual FFR pullbacks to calculate PPG before PCI. Patient-reported outcomes were collected using the 7-item Seattle Angina Questionnaire (SAQ-7) at baseline and 1-year follow-up. RESULTS: We included 814 patients (205 [25.2%] women and 609 [74.8%] men). Women were significantly older than men (70 ± 10 years vs. 67 ± 10 years p < 0.001). Baseline FFR were comparable between sexes (0.68 ± 0.13 vs. 0.66 ± 0.12, p = 0.098), but women had a more focal CAD compared to men (PPG 0.66 ± 0.15 vs. 0.63 ± 0.15, p = 0.047). Post PCI-FFR was higher in women than men (0.88 ± 0.07 vs. 0.87 ± 0.07, p = 0.041); however, angina at 1 year was more frequent in women (SAQ angina frequency score 94 ± 12 vs. 96 ± 10, p = 0.041). CONCLUSION: Despite having a more focal CAD pattern and achieving higher post-PCI FFR, women report more residual angina than men at 1-year follow-up. TRIAL REGISTRATION: ClinicalTrials.gov NCT04789317.
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