Risk Factors Associated With Thrombocytopenia Induced by Intravenous Immunoglobulin Formulations: An Analysis Using the JADER database.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-07-01 DOI:10.21873/invivo.14028
Yoshihiro Nishita, Natsuko Ishida, Hirofumi Nagai, Togen Masauji, Junko Ishizaki
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引用次数: 0

Abstract

Background/aim: Thrombocytopenia is a serious adverse event observed with intravenous immunoglobulin formulations (IVIg). There have been some individual case reports of such events, but to our knowledge, no epidemiological studies have been reported. In this study, the risk of IVIg-induced thrombocytopenia and factors associated with IVIg-induced thrombocytopenia were examined using the Japanese Adverse Drug Event Report database.

Patients and methods: Data spanning from April 2004 to August 2024 were used. The association between IVIg and thrombocytopenia was evaluated using the reporting odds ratio (ROR). The reports of IVIg-induced thrombocytopenia events were evaluated by disease and aggregated by disease group. Factors associated with IVIg-induced thrombocytopenia were detected using multiple logistic regression with age, sex, formulation method, and disease group as explanatory variables and adjusted RORs were calculated.

Results: The IVIgs examined were significantly associated with thrombocytopenia. Pemphigoid was the most frequently reported disease, followed by Kawasaki disease and polymyositis/dermatomyositis. Immune-mediated skin diseases were the most frequently reported disease group, followed by Kawasaki disease, immune-mediated neurological diseases, and immune-mediated muscular diseases. Multiple logistic regression analysis showed that at age 60 years or older, immune-mediated skin diseases and immune-mediated muscular diseases were independently associated with significantly increased RORs.

Conclusion: This study suggests that IVIg can induce thrombocytopenia and that thrombocytopenia should be assessed in patients with immune-mediated skin diseases, immune-mediated muscular diseases and in the elderly.

与静脉注射免疫球蛋白制剂引起的血小板减少相关的危险因素:使用JADER数据库的分析。
背景/目的:血小板减少症是静脉注射免疫球蛋白制剂(IVIg)的严重不良事件。有一些此类事件的个案报告,但据我们所知,没有流行病学研究报告。在这项研究中,使用日本不良药物事件报告数据库检查了ivig诱导的血小板减少的风险和与ivig诱导的血小板减少相关的因素。患者和方法:2004年4月至2024年8月的数据。使用报告优势比(ROR)评估IVIg和血小板减少症之间的关联。ivig诱导的血小板减少事件报告按疾病进行评估,并按疾病组进行汇总。以年龄、性别、配方方法和疾病组为解释变量,采用多元logistic回归检测与ivig诱导的血小板减少相关的因素,并计算调整后的ror。结果:所检查的ivig与血小板减少有显著相关性。类天疱疮是最常见的疾病,其次是川崎病和多发性肌炎/皮肌炎。免疫介导的皮肤病是最常见的疾病组,其次是川崎病、免疫介导的神经系统疾病和免疫介导的肌肉疾病。多元logistic回归分析显示,在60岁及以上年龄,免疫介导的皮肤病和免疫介导的肌肉疾病与RORs显著升高独立相关。结论:本研究提示IVIg可诱导血小板减少,应在免疫介导性皮肤病、免疫介导性肌肉疾病患者和老年人中评估血小板减少情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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