药物引起的自发性胃肠道血肿:现实世界的药物警戒分析。

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Pharmacology Pub Date : 2024-12-31 DOI:10.1097/FJC.0000000000001662
Xuehong Wang, Min Luo, Wenyu Li, Yuqian Zhou
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引用次数: 0

摘要

目前尚不清楚华法林以外的药物是否可引起自发性胃肠道腔内血肿(SGIH)。本研究旨在根据FDA不良事件报告系统(FAERS)的数据,探讨引起SGIH的药物。进行回顾性药物警戒研究。对2004年第一季度至2023年第四季度的药物性SGIH报告进行歧化分析。采用logistic回归分析探讨药物相关的SGIH危险因素。SGIH发病时间采用威布尔分布。FAERS数据库中共报道了116种与SGIH相关的药物。在去除重复后,确定了88种独特药物,涉及210名患者。这些药物大致可分为四类:(1)抗凝血药;(2)新型直接口服抗凝血药;(3)抗血小板药;(4)其他药物。第一组以华法林为主(59/210),第二组利伐沙班占比最大(9/210)。第三组以阿司匹林为主(16/210),第四组以引起血小板减少的药物为主。报告病例的中位数为每年11.5例,占所有与靶向药物相关的不良事件的中位数百分比为0.0094%。与药物相关的SGIH发病的中位时间为12.5天(四分位数范围为1-220.25天)。当使用相关药物的患者出现相应的腹部症状时,尽管SGIH的发病率很低,但仍应考虑鉴别诊断。
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Drug-induced Spontaneous intramural hematoma of the gastrointestinal tract: A real-world pharmacovigilance analysis.

It is unclear whether drugs other than warfarin can cause spontaneous gastrointestinal intraluminal hematomas (SGIH). This study aimed to investigate the drugs that induced SGIH based on the FDA Adverse Event Reporting System (FAERS) data. A retrospective pharmacovigilance study was conducted. The disproportionality analysis was performed to assess the reports of drug-induced SGIH from the first quarter of 2004 to the fourth quarter of 2023. Logistics regression analysis was used to explore drug-related SGIH risk factors. Weibull distribution was applied for the onset time of SGIH. A total of 116 drugs associated with SGIH have been reported in the FAERS database. After removing duplicates, 88 unique drugs involving 210 patients were identified. These drugs can be broadly classified into four categories: (1) anticoagulants, (2) new direct oral anticoagulants, (3) antiplatelet agents, and (4) others. The first group is dominated by warfarin (59/210), while the second group, rivaroxaban, accounts for the most significant proportion (9/210). As for the third group, aspirin is the dominant drug (16/210), and for the fourth group, drugs that cause thrombocytopenia are dominant. The median number of reported cases was 11.5 per year, accounting for a median percentage of 0.0094% of all adverse events related to target drugs. The median time to drug-related SGIH onset was 12.5 days (interquartile range 1-220.25 days). When patients on the related drugs present with corresponding abdominal symptoms, it is crucial to consider the differential diagnosis of SGIH despite its low incidence.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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