Mohamed Elsaid, Arvind Nune, Aml M Brakat, Ayush Anand, Mahmoud Alashwah, Ahmed Maher, Nitu Lama, Criselle Angeline C Peñamante
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引用次数: 0
Abstract
Background: The American Society of Haematology defines immune thrombocytopenic purpura (ITP) as a common hematologic disorder characterized by a transient or long-term decrease in platelet counts (< 100 × 109/L.), purpura, and haemorrhagic episodes caused by antiplatelet autoantibodies, with the exclusion of other clinical conditions. We aimed to systematically determine the incidence of ITP in adults and children following influenza vaccination, the duration between vaccination and the occurrence of ITP, and to identify predictors of ITP after the vaccine.
Methods: We searched PubMed, Cochrane Library, Google Scholar, Web of Science, Scopus, and Science Direct. We included primary studies that assessed the occurrence of immune thrombocytopenia in individuals who had received any influenza vaccine (primary or booster dose), regardless of the dosage, preparation, time of administration, or age of the participants. We excluded studies that were (a) Narrative, scoping, and umbrella reviews ;(b) studies with no accessible full text, abstract-only studies, or (c) Overlapping or unreliable data. The risk of bias in the included studies was assessed using the Joanna Briggs Institute (JBI) tool. We categorized studies for qualitative analysis based on study design. Descriptive statistics were used to summarize quantitative data, including the incidence of ITP after influenza vaccination.
Results: Out of 729 articles retrieved from the database search, we included 24 studies. All patients identified and included in this systematic review presented with immune thrombocytopenia, determined by their platelet count. The period between vaccination and the occurrence of ITP ranged from (2:35 days). The mean duration was 13.5 days. The analysis revealed a statistically significant incidence rate ratio (IRR) = 1.85,95% CI [1.03-3.32] of ITP occurrence after 42 days.
Conclusions: Influenza-associated ITP is uncommon, self-limiting, non-life-threatening, and curable. None of the patients reported having severe adverse events or death. Further studies are required to confirm the exact incidence of the ITP to better understand the pathophysiology of ITP development post-influenza vaccination.
背景:美国血液学学会将免疫性血小板减减性紫癜(ITP)定义为一种常见的血液学疾病,其特征是血小板计数短暂或长期下降(方法:我们检索了PubMed, Cochrane Library, Google Scholar, Web of Science, Scopus和Science Direct。我们纳入了评估接种任何流感疫苗(初级或加强剂量)的个体发生免疫性血小板减少症的初步研究,而不考虑剂量、制备、给药时间或参与者的年龄。我们排除了以下研究:(a)叙述性、范围界定性和总括性综述;(b)没有可获得的全文研究、只有摘要的研究;或(c)重叠或不可靠的数据。纳入研究的偏倚风险使用乔安娜布里格斯研究所(JBI)工具进行评估。我们根据研究设计对研究进行分类进行定性分析。描述性统计用于总结定量数据,包括流感疫苗接种后ITP的发生率。结果:在数据库检索到的729篇文章中,我们纳入了24篇研究。本系统综述中确定并纳入的所有患者均表现为免疫性血小板减少症,由血小板计数决定。从接种疫苗到ITP发生之间的时间为(2:35天)。平均持续时间为13.5 d。分析显示,42 d后ITP的发生率比(IRR) = 1.85,95% CI[1.03-3.32]具有统计学意义。结论:流感相关的ITP是罕见的、自限性的、不危及生命的、可治愈的。没有患者报告发生严重不良事件或死亡。需要进一步的研究来确认ITP的确切发病率,以更好地了解流感疫苗接种后ITP发展的病理生理学。
期刊介绍:
Tropical Diseases, Travel Medicine and Vaccines is an open access journal that considers basic, translational and applied research, as well as reviews and commentary, related to the prevention and management of healthcare and diseases in international travelers. Given the changes in demographic trends of travelers globally, as well as the epidemiological transitions which many countries are experiencing, the journal considers non-infectious problems including chronic disease among target populations of interest as well as infectious diseases.