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评估首次ST段抬高型心肌梗死后选定的基线和PCI术后心电图参数作为左心室收缩功能障碍预测指标的研究

Assessment of Selected Baseline and Post-PCI Electrocardiographic Parameters as Predictors of Left Ventricular Systolic Dysfunction after a First ST-Segment Elevation Myocardial Infarction.

作者信息

Fabiszak Tomasz, Kasprzak Michał, Koziński Marek, Kubica Jacek

机构信息

Department of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, ul. Skłodowskiej-Curie 9, 85-094 Bydgoszcz, Poland.

Department of Cardiology and Internal Medicine, Medical University of Gdańsk, ul. Powstania Styczniowego 9B, 81-519 Gdynia, Poland.

出版信息

J Clin Med. 2021 Nov 22;10(22):5445. doi: 10.3390/jcm10225445.

DOI:10.3390/jcm10225445
PMID:34830726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8619668/
Abstract

OBJECTIVE

To assess the performance of ten electrocardiographic (ECG) parameters regarding the prediction of left ventricular systolic dysfunction (LVSD) after a first ST-segment-elevation myocardial infarction (STEMI).

METHODS

We analyzed 249 patients (74.7% males) treated with primary percutaneous coronary intervention (PCI) included into a single-center cohort study. We sought associations between baseline and post-PCI ECG parameters and the presence of LVSD (defined as left ventricular ejection fraction [LVEF] ≤ 40% on echocardiography) 6 months after STEMI.

RESULTS

Patients presenting with LVSD ( = 52) had significantly higher values of heart rate, number of leads with ST-segment elevation and pathological Q-waves, as well as total and maximal ST-segment elevation at baseline and directly after PCI compared with patients without LVSD. They also showed a significantly higher prevalence of anterior STEMI and considerably wider QRS complex after PCI, while QRS duration measurement at baseline showed no significant difference. Additionally, patients presenting with LVSD after 6 months showed markedly more severe ischemia on admission, as assessed with the Sclarovsky-Birnbaum ischemia score, smaller reciprocal ST-segment depression at baseline and less profound ST-segment resolution post PCI. In multivariate regression analysis adjusted for demographic, clinical, biochemical and angiographic variables, anterior location of STEMI (OR 17.78; 95% CI 6.45-48.96; < 0.001), post-PCI QRS duration (OR 1.56; 95% CI 1.22-2.00; < 0.001) expressed per increments of 10 ms and impaired post-PCI flow in the infarct-related artery (IRA; TIMI 3 vs. <3; OR 0.14; 95% CI 0.04-0.46; = 0.001) were identified as independent predictors of LVSD (Nagelkerke's pseudo R for the logistic regression model = 0.462). Similarly, in multiple regression analysis, anterior location of STEMI, wider post-PCI QRS, higher baseline number of pathological Q-waves and a higher baseline Sclarovsky-Birnbaum ischemia score, together with impaired post-PCI flow in the IRA, higher values of body mass index and glucose concentration on admission were independently associated with lower values of LVEF at 6 months (corrected R = 0.448; < 0.00001).

CONCLUSIONS

According to our study, baseline and post-PCI ECG parameters are of modest value for the prediction of LVSD occurrence 6 months after a first STEMI.

摘要

目的

评估十个心电图(ECG)参数对首次ST段抬高型心肌梗死(STEMI)后左心室收缩功能障碍(LVSD)的预测性能。

方法

我们分析了纳入单中心队列研究的249例接受直接经皮冠状动脉介入治疗(PCI)的患者(男性占74.7%)。我们探寻STEMI后6个月时基线和PCI后ECG参数与LVSD(定义为超声心动图显示左心室射血分数[LVEF]≤40%)存在之间的关联。

结果

与无LVSD的患者相比,出现LVSD的患者(n = 52)在基线时以及PCI后即刻的心率、ST段抬高导联数和病理性Q波数量,以及ST段总抬高和最大抬高值均显著更高。他们还显示前壁STEMI的患病率显著更高,且PCI后QRS波群明显更宽,而基线时QRS时限测量无显著差异。此外,6个月后出现LVSD的患者入院时缺血明显更严重,这通过Sclarovsky-Birnbaum缺血评分评估,基线时镜像ST段压低更小,PCI后ST段回落程度更低。在对人口统计学、临床、生化和血管造影变量进行校正的多变量回归分析中,STEMI的前壁位置(比值比[OR] 17.78;95%置信区间[CI] 6.45 - 48.96;P < 0.001)、PCI后QRS时限(OR 1.56;95% CI 1.22 - 2.00;P < 0.001,每增加10毫秒表示)以及梗死相关动脉(IRA)PCI后血流受损(TIMI 3级与<3级相比;OR 0.14;95% CI 0.04 - 0.46;P = 0.001)被确定为LVSD的独立预测因素(逻辑回归模型的Nagelkerke伪R² = 0.462)。同样,在多元回归分析中,STEMI的前壁位置、PCI后更宽的QRS波、更高的基线病理性Q波数量和更高的基线Sclarovsky-Birnbaum缺血评分,以及IRA的PCI后血流受损、入院时更高的体重指数和血糖浓度与6个月时更低的LVEF值独立相关(校正R² = 0.448;P < 0.00001)。

结论

根据我们的研究,基线和PCI后ECG参数对首次STEMI后6个月LVSD发生的预测价值有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/94cb6ad3bb40/jcm-10-05445-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/9325f828d082/jcm-10-05445-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/4d07cd8faf30/jcm-10-05445-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/94cb6ad3bb40/jcm-10-05445-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/9325f828d082/jcm-10-05445-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/4d07cd8faf30/jcm-10-05445-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9385/8619668/94cb6ad3bb40/jcm-10-05445-g003.jpg

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