Department of Invasive Cardiology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Department of Internal Medicine, Hypertension and Angiology, Warsaw Medical University, Warsaw, Poland.
Transl Res. 2021 May;231:64-75. doi: 10.1016/j.trsl.2020.11.009. Epub 2020 Nov 21.
This study aimed to assess the angiographic characteristics, feasibility and safety of the provocative test with acetylcholine (AChT), and the influence on further treatment and prognosis of Middle European patients in 5-year follow-up, especially focusing on those with a history of myocardial infarction (MI) with nonobstructive coronary arteries (MINOCA). The AChPOL Registry was an ongoing prospective single-center registry that included patients undergoing AChT from December 2010 to March 2013 for further diagnostic evaluation of a suspicious variant angina or coronary microvascular spasm, based on the COVADIS criteria. AChT was injected in incremental doses of 25, 50, and 75µg into the right coronary artery and 25, 50, and 100 µg into the left coronary artery, and the patients were followed up for 5 years. We enrolled 211 patients in the AChPOL Registry. Their mean age was 60.5 ± 7.8 years, with women accounting for 67.8%. The median follow-up was 56 months. AChT revealed variant angina in 99 patients (46.9%) and coronary microvascular spasm in the remaining 72 patients (34.1%). In patients with variant angina, spasm was most frequently observed in the left anterior descending artery (89.9%) and was most frequently diffuse (61.6%). In the microvascular spasm subgroup, there was a significantly higher rate of recurrent chest pain requiring hospitalization in the follow-up than in AChT negative patients. Interestingly, patients with a history of MINOCA had higher rates of MI and recurrent chest pain requiring hospitalization in the follow-up. We showed that AChT was safe in Middle European patients. In the follow-up patients with microvascular spasm and a history of MINOCA had the highest risk of MI and recurrent chest pain requiring hospitalization.
这项研究旨在评估乙酰胆碱激发试验(AChT)的血管造影特征、可行性和安全性,以及对 5 年随访期间中东欧患者进一步治疗和预后的影响,尤其关注伴有非阻塞性冠状动脉的心肌梗死(MINOCA)病史的患者。AChPOL 登记研究是一项正在进行的前瞻性单中心登记研究,纳入了 2010 年 12 月至 2013 年 3 月期间因可疑变异型心绞痛或冠状动脉微血管痉挛而接受 AChT 进一步诊断评估的患者,这些患者符合 COVADIS 标准。AChT 以 25、50 和 75μg 的增量剂量注入右冠状动脉,以 25、50 和 100μg 的增量剂量注入左冠状动脉,患者随访 5 年。我们共纳入了 211 名 AChPOL 登记研究的患者。他们的平均年龄为 60.5±7.8 岁,女性占 67.8%。中位随访时间为 56 个月。AChT 显示 99 名患者(46.9%)存在变异型心绞痛,其余 72 名患者(34.1%)存在冠状动脉微血管痉挛。在变异型心绞痛患者中,痉挛最常发生在前降支(89.9%),且最常呈弥漫性(61.6%)。在微血管痉挛亚组中,随访期间因胸痛复发需要住院的患者比例明显高于 AChT 阴性患者。有趣的是,MINOCA 病史患者的 MI 和随访期间因胸痛复发需要住院的风险更高。我们表明,AChT 在中东欧患者中是安全的。在随访期间,有微血管痉挛和 MINOCA 病史的患者发生 MI 和因胸痛复发需要住院的风险最高。