Horie Tomoki, Hamaya Rikuta, Sugiyama Tomoyo, Hirano Hidenori, Hoshino Masahiro, Kanaji Yoshihisa, Lee Tetsumin, Yonetsu Taishi, Sasano Tetsuo, Kakuta Tsunekazu
Department of Cardiology, Tsuchiura Kyodo General Hospital, Tsuchiura, Japan.
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Cardiol Res Pract. 2022 Aug 17;2022:9582174. doi: 10.1155/2022/9582174. eCollection 2022.
To assess the clinical utility of synthesized V7-V9 ST-segment elevation (sV7-9 STE) in patients with 12-lead-electrocardiogram (ECG)-based non-STE myocardial infarction (NSTEMI) in diagnosing left circumflex artery (LCx) STEMI-equivalent acute coronary syndrome (ACS).
The 12-lead-ECG is insufficient for diagnosing patients with ACS, especially those with an LCx culprit.
We retrospectively examined 219 patients with NSTEMI who underwent synthesized 18-lead ECG acquisition on admission and urgent catheterization. Associations between baseline variables, including sV7-9 STE and LCx STEMI-equivalent ACS, were analyzed using logistic regression models and receiver operating characteristics. LCx-culprit ACS was defined as thrombolysis in myocardial infarction (TIMI) 0-1 flow. The association between sV7-9 STE and myocardial damage was also assessed.
The mean (SD) age of the population was 68.8 (12.0) years, and 81.7% were men. LCx-culprit NSTEMI occurred in 58 (26.5%) patients and 15 (6.8%) were LCx STEMI-equivalent. SV7-9 STE was observed in 16 patients (7.9%). SV7-9 STE was the sole significant predictor of LCx STEMI-equivalent ACS with an odds ratio of 19.0 (95% CI: 5.6-63.9, < 0.001), area under the curve of 0.71 (95% CI: 0.58-0.84), sensitivity of 46.7%, and specificity of 95.6%. After adjustment for confounders, sV7-9 STE was significantly associated with a 308% (95% CI: 78-834%) increase in peak high-sensitivity cardiac troponin I (=0.001).
SV7-9 STE had sole preprocedural diagnostic utility in detecting LCx STEMI-equivalent ACS with greater myocardial damage among patients with 12 ECG-based NSTEMI. The use of synthesized extra leads on admission may help identify patients with NSTEMI requiring primary revascularization.
评估基于12导联心电图(ECG)的非ST段抬高型心肌梗死(NSTEMI)患者中合成的V7 - V9 ST段抬高(sV7 - 9 STE)在诊断左旋支动脉(LCx)ST段抬高型心肌梗死等效急性冠状动脉综合征(ACS)中的临床应用价值。
12导联ECG对ACS患者的诊断不足,尤其是那些以LCx为罪犯血管的患者。
我们回顾性研究了219例NSTEMI患者,这些患者入院时接受了合成18导联ECG采集并进行了紧急导管插入术。使用逻辑回归模型和受试者工作特征分析基线变量之间的关联,包括sV7 - 9 STE与LCx ST段抬高型心肌梗死等效ACS。LCx罪犯血管ACS定义为心肌梗死溶栓(TIMI)0 - 1级血流。还评估了sV7 - 9 STE与心肌损伤之间的关联。
研究人群的平均(标准差)年龄为68.8(12.0)岁,男性占81.7%。58例(26.5%)患者发生LCx罪犯血管NSTEMI,15例(6.8%)为LCx ST段抬高型心肌梗死等效。16例患者(7.9%)观察到sV7 - 9 STE。sV7 - 9 STE是LCx ST段抬高型心肌梗死等效ACS的唯一显著预测因子,比值比为19.0(95%置信区间:5.6 - 63.9,P < 0.001),曲线下面积为0.71(95%置信区间:0.58 - �.84),敏感性为46.7%,特异性为95.6%。在调整混杂因素后,sV7 - 9 STE与高敏心肌肌钙蛋白I峰值显著增加308%(95%置信区间:78 - 834%)相关(P = 0.001)。
sV7 - 9 STE在基于12导联ECG的NSTEMI患者中对检测具有更大心肌损伤的LCx ST段抬高型心肌梗死等效ACS具有唯一的术前诊断价值。入院时使用合成额外导联可能有助于识别需要进行直接血运重建的NSTEMI患者。