医学
传统PCI
心脏病学
内科学
四分位间距
心肌梗塞
经皮冠状动脉介入治疗
溶栓
罪魁祸首
蒂米
血管造影
作者
Doosup Shin,Ju‐Won Kim,Ki Hong Choi,Neng Dai,Yinliang Li,Seung Hun Lee,Hyun Sung Joh,Hyun Kuk Kim,Sung Mok Kim,Sang Jin Ha,Mi Ja Jang,Taek Kyu Park,Jeong Hoon Yang,Young Bin Song,Joo‐Yong Hahn,Seung‐Hyuk Choi,Yeon Hyeon Choe,Hyeon‐Cheol Gwon,Joo Myung Lee
标识
DOI:10.1016/j.rec.2022.01.004
摘要
The index of microcirculatory resistance (IMR) measured after primary percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI) is associated with microvascular obstruction (MVO) and adverse clinical events. To evaluate MVO after successful primary PCI for STEMI without pressure wires or hyperemic agents, we investigated the feasibility and usefulness of functional angiography-derived IMR (angio-IMR).The current study included a total of 285 STEMI patients who underwent primary PCI and cardiac magnetic resonance (CMR). Angio-IMR of the culprit vessel after successful primary PCI was calculated using commercial software. MVO, infarct size, and myocardial salvage index were assessed using CMR, which was obtained a median of 3.0 days [interquartile range, 3.0-5.0] after primary PCI.Among the total population, 154 patients (54.0%) showed elevated angio-IMR (> 40 U) in the culprit vessel. MVO was significantly more prevalent in patients with angio-IMR> 40 U than in those with angio-IMR ≤ 40 U (88.3% vs 32.1%, P <.001). Infarct size, extent of MVO, and area at risk were significantly larger in patients with angio-IMR> 40 U than in those with angio-IMR ≤ 40 U (P <.001 for all). Angio-IMR showed a significantly higher discriminatory ability for the presence of MVO than thrombolysis in myocardial infarction flow grade or myocardial blush grade (area under the curve: 0.821, 0.504, and 0.496, respectively, P <.001).Angio-IMR was significantly associated with CMR-derived infarct size, extent of MVO, and area at risk. An elevated angio-IMR (> 40 U) after primary PCI for STEMI was highly predictive of the presence of MVO in CMR. This trial was registered at ClnicalTrialsgov (Identifier: NCT04828681).
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