High on-treatment platelet reactivity is associated with poor outcomes after ischemic stroke: A meta-analysis

被引:8
|
作者
Zhou, Kun [1 ,2 ]
Yu, Shiyuan [3 ]
Li, Jingjing [1 ,2 ]
Tan, Yan [1 ,2 ]
Xing, Shihui [1 ,2 ]
Chen, Yicong [1 ,2 ]
Ouyang, Fubing [1 ,2 ]
Zeng, Jinsheng [1 ,2 ]
Zhang, Jian [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Guangdong Prov Key Lab Diag & Treatment Major Neu, Natl Key Clin Dept, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Key Discipline Neurol, Guangzhou, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Med Coll, Guangzhou, Peoples R China
来源
ACTA NEUROLOGICA SCANDINAVICA | 2022年 / 146卷 / 03期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
high on-treatment platelet reactivity; HTPR; ischemic stroke; meta-analysis; platelet function; activity; transient ischemic attack; EARLY NEUROLOGICAL DETERIORATION; ASPIRIN RESISTANCE; ANTIPLATELET THERAPY; GENETIC POLYMORPHISMS; CLINICAL-OUTCOMES; RECURRENT STROKE; MINOR STROKE; CLOPIDOGREL; SEVERITY; EVENTS;
D O I
10.1111/ane.13655
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives High on-treatment platelet reactivity (HTPR) determined by platelet function assays is present in certain patients with ischemic stroke or transient ischemic attack (TIA). However, it is unclear whether HTPR is associated with poor clinical outcomes. Our study aimed to investigate the relationship of HTPR with recurrent vascular events in ischemic stroke or TIA. Methods Pubmed (MEDLINE), EMBASE, and Cochrane Library were searched for eligible studies from inception to January 1, 2022. Stata 17.0 software was used to calculate the risk ratio (RR). Subgroup and sensitivity analyses were conducted to assess the source of heterogeneity. A random-effects model was used when heterogeneity was present. Primary endpoint of the meta-analysis was the risk ratio of recurrent vascular events in HTPR Patients. While stroke and TIA, all-cause death, early neurological deterioration, early new ischemic lesions, and stroke severity measured by National Institute of Health Stroke Scale (NIHSS) scores at admission were also pooled. Results Thirty articles (7995 patients) were eligible including 28 cohort studies and 2 prospective case-control studies. The prevalence of HTPR varied from 5.9% to 60%. HTPR was associated with an increased risk of recurrent vascular events (RR = 2.94, 95% CI 2.04-4.23), stroke recurrence (RR = 2.05; 95% CI 1.43-2.95), and all-cause mortality (RR = 2.43; 95% CI 1.83-3.22). Subgroup analysis showed that HTPR determined by optical aggregometry, Verify-Now system and 11dh TXB2 is related to a higher risk of recurrent vascular events (RR = 3.53, 95% CI 1.51-9.40; RR = 2.16, 95% CI 1.02-4.56; RR = 3.76, 95% CI 1.51-9.40, respectively). Moreover, patients with HTPR had an increased incidence of early neurological deterioration (RR = 2.75; 95% CI 1.76-4.30) and higher NIHSS scores at admission (Mean difference 0.19, 95% CI 0.01-0.36). Conclusions This meta-analysis demonstrates HTPR is associated with higher risk of recurrent vascular events, early neurological deterioration and increased severity in patients with ischemic stroke and TIA. HTPR measured by platelet function assays may guide the use of antiplatelet agents in ischemic stroke and TIA.
引用
收藏
页码:205 / 224
页数:20
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