Factors predicting resolution of left ventricular thrombus in different time windows after myocardial infarction.


Journal

BMC cardiovascular disorders
ISSN: 1471-2261
Titre abrégé: BMC Cardiovasc Disord
Pays: England
ID NLM: 100968539

Informations de publication

Date de publication:
29 May 2024
Historique:
received: 12 11 2023
accepted: 23 04 2024
medline: 30 5 2024
pubmed: 30 5 2024
entrez: 29 5 2024
Statut: epublish

Résumé

Left ventricular thrombus (LVT) is a serious complication after myocardial infarction. However, due to its asymptomatic nature, early detection is challenging. We aimed to explore the differences in clinical correlates of LVT found in acute to subacute and chronic phases of myocardial infarction. We collected data from 153 patients who were diagnosed with LVT after myocardial infarction at the Affiliated Hospital of Qingdao University from January 2013 to December 2022. Baseline information, inflammatory markers, transthoracic echocardiograph (TTE) data and other clinical correlates were collected. Patients were categorized into acute to subacute phase group (< 30 days) and chronic phase group (30 days and after) according to the time at which echocardiograph was performed. The resolution of thrombus within 90 days is regarded as the primary endpoint event. We fitted logistic regression models to relating clinical correlates with phase-specific thrombus resolution. For acute to subacute phase thrombus patients: C-reactive protein levels (OR: 0.95, 95% CI: 0.918-0.983, p = 0.003) were significantly associated with thrombus resolution. For chronic phase thrombus patients: anticoagulant treatment was associated with 5.717-fold odds of thrombus resolution (OR: 5.717, 95% CI: 1.543-21.18, p = 0.009). Higher levels of CRP were associated with lower likelihood of LVT resolution in acute phase myocardial infarction; Anticoagulant therapy is still needed for thrombus in the chronic stage of myocardial infarction.

Sections du résumé

BACKGROUND BACKGROUND
Left ventricular thrombus (LVT) is a serious complication after myocardial infarction. However, due to its asymptomatic nature, early detection is challenging. We aimed to explore the differences in clinical correlates of LVT found in acute to subacute and chronic phases of myocardial infarction.
METHODS METHODS
We collected data from 153 patients who were diagnosed with LVT after myocardial infarction at the Affiliated Hospital of Qingdao University from January 2013 to December 2022. Baseline information, inflammatory markers, transthoracic echocardiograph (TTE) data and other clinical correlates were collected. Patients were categorized into acute to subacute phase group (< 30 days) and chronic phase group (30 days and after) according to the time at which echocardiograph was performed. The resolution of thrombus within 90 days is regarded as the primary endpoint event. We fitted logistic regression models to relating clinical correlates with phase-specific thrombus resolution.
RESULTS RESULTS
For acute to subacute phase thrombus patients: C-reactive protein levels (OR: 0.95, 95% CI: 0.918-0.983, p = 0.003) were significantly associated with thrombus resolution. For chronic phase thrombus patients: anticoagulant treatment was associated with 5.717-fold odds of thrombus resolution (OR: 5.717, 95% CI: 1.543-21.18, p = 0.009).
CONCLUSIONS CONCLUSIONS
Higher levels of CRP were associated with lower likelihood of LVT resolution in acute phase myocardial infarction; Anticoagulant therapy is still needed for thrombus in the chronic stage of myocardial infarction.

Identifiants

pubmed: 38811882
doi: 10.1186/s12872-024-03898-9
pii: 10.1186/s12872-024-03898-9
doi:

Substances chimiques

Anticoagulants 0
C-Reactive Protein 9007-41-4
Biomarkers 0

Types de publication

Journal Article Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

278

Subventions

Organisme : the Shandong Provincial Natural Science Foundation
ID : ZR2023MH337

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Zhen Lu (Z)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao University, Qingdao Medical College, Qingdao, China.

Bingxue Song (B)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China.

Xin Liu (X)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China.

Ning Zhang (N)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China.

Fuhai Li (F)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China.

Fengqiang Xu (F)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China.

Zhexun Lian (Z)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China. lianzx566@163.com.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China. lianzx566@163.com.

Junjie Guo (J)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China. guojunjie@qdu.edu.cn.
Qingdao Municipal Key Laboratory of Hypertension (Key Laboratory of Cardiovascular Medicine), Qingdao, Shandong, China. guojunjie@qdu.edu.cn.

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