Nishita Yoshihiro, Ishida Natsuko, Nagai Hirofumi, Masauji Togen, Ishizaki Junko
Clinical Pharmacy and Healthcare Science, Kanazawa University, Kanazawa, Japan;
Department of Pharmacy, Kanazawa Medical University Hospital, Kanazawa, Japan.
In Vivo. 2025 Jul-Aug;39(4):2320-2327. doi: 10.21873/invivo.14028.
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.
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.
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.
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.
背景/目的:血小板减少症是静脉注射免疫球蛋白制剂(IVIg)时观察到的一种严重不良事件。已有一些关于此类事件的个别病例报告,但据我们所知,尚无流行病学研究报告。在本研究中,使用日本药品不良事件报告数据库研究了IVIg诱导的血小板减少症的风险以及与IVIg诱导的血小板减少症相关的因素。
使用了2004年4月至2024年8月的数据。使用报告比值比(ROR)评估IVIg与血小板减少症之间的关联。对IVIg诱导的血小板减少症事件的报告按疾病进行评估,并按疾病组进行汇总。以年龄、性别、制剂方法和疾病组作为解释变量,通过多元逻辑回归检测与IVIg诱导的血小板减少症相关的因素,并计算调整后的ROR。
所检测的IVIg与血小板减少症显著相关。类天疱疮是报告最频繁的疾病,其次是川崎病和多发性肌炎/皮肌炎。免疫介导的皮肤病是报告最频繁的疾病组,其次是川崎病、免疫介导的神经疾病和免疫介导的肌肉疾病。多元逻辑回归分析表明,60岁及以上、免疫介导的皮肤病和免疫介导的肌肉疾病与ROR显著增加独立相关。
本研究表明IVIg可诱导血小板减少症,对于免疫介导的皮肤病、免疫介导的肌肉疾病患者及老年人,应评估血小板减少症情况。