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心率变异性和整体纵向应变在保守治疗的心肌梗死患者预后评估及恢复评估中的应用

Heart Rate Variability and Global Longitudinal Strain for Prognostic Evaluation and Recovery Assessment in Conservatively Managed Post-Myocardial Infarction Patients.

作者信息

Bogdan Carina, Apostol Adrian, Ivan Viviana Mihaela, Sandu Oana Elena, Petre Ion, Suciu Oana, Marc Luciana-Elena, Maralescu Felix-Mihai, Lighezan Daniel Florin

机构信息

Department VII, Internal Medicine II, Discipline of Cardiology, "Victor Babeş" University of Medicine and Pharmacy, Eftimie Murgu Sq. No. 2, 300041 Timişoara, Romania.

Centre for Molecular Research in Nephrology and Vascular Disease, Faculty of Medicine "Victor Babeş", 300041 Timișoara, Romania.

出版信息

J Clin Med. 2024 Sep 13;13(18):5435. doi: 10.3390/jcm13185435.

DOI:10.3390/jcm13185435
PMID:39336923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11432728/
Abstract

: Heart rate variability (HRV) is the fluctuation in the time intervals between adjacent heartbeats. HRV is a measure of neurocardiac function that is produced by dynamic autonomic nervous system (ANS) processes and is a simple measure that estimates cardiac autonomic modulation. : The study included 108 patients admitted to the Coronary Intensive Care Unit with acute myocardial infarction (AMI) who did not undergo primary percutaneous transluminal coronary angioplasty (PTCA) or systemic thrombolysis and followed conservative management. All patients underwent detailed clinical, biological, and paraclinical assessments, including evaluation of HRV parameters and echocardiographic measurements. The analysis of RR variability in both time and frequency domains indicates that the negative prognosis of patients with AMI is associated with an overall imbalance in the neuro-vegetative system. The HRV parameters were acquired using continuous 24 h electrocardiogram (ECG) monitoring at a baseline, after 1 month, and 6 months. : Our analysis reveals correlations between alterations in HRV parameters and the increased risk of adverse events and mortality after AMI. The study found a significant improvement in HRV parameters over time, indicating better autonomic regulation post-AMI. The standard deviation of all RR intervals (SDNN) increased significantly from baseline (median 75.3 ms, IQR 48.2-100) to 1 month (median 87 ms, IQR 55.7-111) and further to 6 months (median 94.2 ms, IQR 67.6-118) ( < 0.001 for both comparisons). The root mean square of successive difference of RR (RMSSD) also showed significant increases at each time point, from baseline (median 27 ms, IQR 22-33) to 1 month (median 30.5 ms, IQR 27-38) and from 1 month to 6 months (median 35 ms, IQR 30-42) ( < 0.001 for all comparisons), indicating enhanced parasympathetic activity. Moreover, changes in HRV parameters have been associated with impaired left ventricle ejection fraction (LVEF) and global longitudinal strain (GLS), indicating a relationship between autonomic dysfunction and myocardial deformation. GLS values improved from a baseline median of -11% (IQR 5%) to -13% (IQR 4%) at 6 months ( < 0.001), reflecting better myocardial function. : HRV parameters and cardiac performance analysis, especially using GLS, offer a solid framework for evaluating recovery and predicting adverse outcomes post-MI.

摘要

心率变异性(HRV)是相邻心跳之间时间间隔的波动。HRV是一种神经心脏功能的测量指标,由动态自主神经系统(ANS)过程产生,是一种估计心脏自主神经调节的简单测量方法。

该研究纳入了108例入住冠心病重症监护病房的急性心肌梗死(AMI)患者,这些患者未接受直接经皮冠状动脉腔内血管成形术(PTCA)或全身溶栓治疗,而是采用保守治疗。所有患者均接受了详细的临床、生物学和辅助检查评估,包括HRV参数评估和超声心动图测量。对RR变异性在时域和频域的分析表明,AMI患者的不良预后与神经植物神经系统的整体失衡有关。HRV参数是在基线、1个月和6个月时通过连续24小时心电图(ECG)监测获得的。

我们的分析揭示了HRV参数改变与AMI后不良事件和死亡风险增加之间的相关性。研究发现,随着时间的推移,HRV参数有显著改善,表明AMI后自主神经调节更好。所有RR间期的标准差(SDNN)从基线(中位数75.3毫秒,四分位间距48.2 - 100)显著增加到1个月时(中位数87毫秒,四分位间距55.7 - 111),并进一步增加到6个月时(中位数94.2毫秒,四分位间距67.6 - 118)(两次比较均<0.001)。RR间期连续差值的均方根(RMSSD)在每个时间点也显示出显著增加,从基线(中位数27毫秒,四分位间距22 - 33)到1个月时(中位数30.5毫秒,四分位间距27 - 38),以及从1个月到6个月时(中位数35毫秒,四分位间距30 - 42)(所有比较均<0.001),表明副交感神经活动增强。此外,HRV参数的变化与左心室射血分数(LVEF)和整体纵向应变(GLS)受损有关,表明自主神经功能障碍与心肌变形之间存在关联。GLS值从基线中位数-11%(四分位间距5%)改善到6个月时的-13%(四分位间距4%)(<0.001),反映出心肌功能更好。

HRV参数和心脏性能分析,特别是使用GLS,为评估心肌梗死后的恢复情况和预测不良结局提供了坚实的框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/cd5766482423/jcm-13-05435-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/703153d18707/jcm-13-05435-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/e73e765387f3/jcm-13-05435-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/1bd23f4020b2/jcm-13-05435-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/cd5766482423/jcm-13-05435-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/703153d18707/jcm-13-05435-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/e73e765387f3/jcm-13-05435-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/1bd23f4020b2/jcm-13-05435-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3896/11432728/cd5766482423/jcm-13-05435-g004.jpg

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