免疫性血小板减少性紫癜和免疫性血栓性血小板减少性紫癜患者急性缺血性卒中和颅内出血的患病率和特征:一项系统综述和荟萃分析

Q2 Medicine
Syed Ameen Ahmad, Olivia Liu, Amy Feng, Andrew Kalra, Apurva Dev, Marcus Spann, Aaron M Gusdon, Shruti Chaturvedi, Sung-Min Cho
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引用次数: 0

摘要

背景:人们对免疫性血小板减少性紫癜(ITP)和免疫性血栓性血小板减少性紫癜(iTTP)患者卒中风险增加有了新的认识。我们旨在通过系统回顾和荟萃分析确定ITP和iTTP患者的急性缺血性卒中(AIS)和颅内出血(ICH)的患病率和特征。方法:我们使用PubMed、Embase、Cochrane、Web of Science和Scopus检索从成立到2023年3月11日与ITP、iTTP、卒中、AIS和ICH相关的文本。我们的主要结局是确定ITP或iTTP患者队列中AIS和/或ICH的患病率(年龄在18岁至18岁之间)。我们的次要结局是确定ITP患者与血小板生成素受体激动剂(TPO-RAs)相关的卒中类型,以及ITP和iTTP患者与卒中相关的危险因素。结果:我们纳入了42项研究,118,019例患者(平均年龄为50岁,45%为女性)。其中,27项研究(n = 116,334)调查了ITP患者的卒中,15项研究(n = 1,685)调查了iTTP患者的卒中。在所有ITP患者中,AIS和ICH的患病率分别为2.1%[95%可信区间(CI) 0.8-4.0%]和1.5% (95% CI 0.9%-2.1%)。作为TPO-RAs不良事件(AE)经历卒中的ITP患者,AIS患病率为1.8% (95% CI 0.6 -3.4%), ICH患病率为2.0% (95% CI 0.2%-5.3%)。卒中患病率在所有ITP患者和接受TPO-RAs治疗的患者之间没有显著差异。iTTP患者的AIS和ICH患病率分别为13.9% (95% CI 10.2%-18.1%)和3.9% (95% CI 0.2%-10.4%)。亚组分析显示,与所有ITP患者相比,iTTP患者AIS和ICH的患病率更高(p)。结论:所有ITP患者不同脑卒中类型的患病率均低于iTTP患者。此外,ITP患者卒中患病率相似,无论他们是否被明确标记为TPO-RAs治疗,支持TPO-RAs在治疗中的继续使用。中风的危险因素尚不清楚,未来的研究应继续调查这种关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence and characteristics of acute ischemic stroke and intracranial hemorrhage in patients with immune thrombocytopenic purpura and immune thrombotic thrombocytopenic purpura: a systematic review and meta-analysis.

Background: There is an emerging understanding of the increased risk of stroke in patients with immune thrombocytopenic purpura (ITP) and immune thrombotic thrombocytopenic purpura (iTTP). We aimed to determine the prevalence and characteristics of acute ischemic stroke (AIS) and intracranial hemorrhage (ICH) in patients with ITP and iTTP in a systematic review and meta-analysis.

Methods: We used PubMed, Embase, Cochrane, Web of Science, and Scopus using text related to ITP, iTTP, stroke, AIS, and ICH from inception to 11/3/2023. Our primary outcome was to determine prevalence of AIS and/or ICH in a cohort of ITP or iTTP patients (age > 18). Our secondary outcomes were to determine stroke type associated with thrombopoietin receptor agonists (TPO-RAs) in ITP patients, as well as risk factors associated with stroke in ITP and iTTP patients.

Results: We included 42 studies with 118,019 patients (mean age = 50 years, 45% female). Of those, 27 studies (n = 116,334) investigated stroke in ITP patients, and 15 studies (n = 1,685) investigated stroke in iTTP patients. In all ITP patients, the prevalence of AIS and ICH was 2.1% [95% Confidence Interval (CI) 0.8-4.0%] and 1.5% (95% CI 0.9%-2.1%), respectively. ITP patients who experienced stroke as an adverse event (AE) from TPO-RAs had an AIS prevalence of 1.8% (95% CI 0.6%-3.4%) and an ICH prevalence of 2.0% (95% CI 0.2%-5.3%). Prevalence of stroke did not significantly differ between all ITP patients and those treated with TPO-RAs. iTTP patients had a prevalence of AIS and ICH of 13.9% (95% CI 10.2%-18.1%) and 3.9% (95% CI 0.2%-10.4%), respectively. Subgroup analysis revealed the prevalence of AIS and ICH was greater in iTTP patients vs. all ITP patients (p < 0.01 and p = 0.02, respectively). Meta-regression analysis revealed none of the collected variables (age, sex, history of diabetes or hypertension) were risk factors for stroke in all ITP patients, although there were high levels of data missingness.

Conclusions: Prevalence of different stroke types was lower in all ITP patients vs. iTTP patients. Additionally, ITP patients experienced a similar prevalence of stroke regardless of if they were specifically denoted to have been treated with TPO-RAs or not, supporting the continued use of TPO-RAs in management. Risk factors for stroke remain unclear, and future studies should continue to investigate this relationship.

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