Retrospective Analysis of Risk Factors for Cefoperazone/Sulbactam-Induced Thrombocytopenia in Adult Chinese Patients: A Six-Year Real-World Study

IF 2.9 3区 医学 Q2 INFECTIOUS DISEASES Infection and Drug Resistance Pub Date : 2024-09-05 DOI:10.2147/idr.s475590
Bolin Zhu, Pengfei Jin, Jianchun Li, Yuanchao Zhu
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Abstract

Background: Drug-induced thrombocytopenia is a rare adverse reaction of drug therapy and usually underdiagnosed. Cefoperazone/sulbactam is a compound preparation composed of the third generation of cephalosporin and β-lactamase inhibitor, of which thrombocytopenia is an uncommon but serious adverse reaction. However, the existing literature on cefoperazone/sulbactam-induced thrombocytopenia remains limited, and the specific risk factors associated with this adverse effect have not been thoroughly elucidated. Consequently, this study aims to investigate the clinical characteristics and identify the risk factors for thrombocytopenia in adult patients undergoing cefoperazone/sulbactam therapy.
Methods: In this retrospective study, we reviewed patients treated with cefoperazone/sulbactam at Beijing Hospital between January 2017 and June 2023. Patients were categorized into two groups based on the presence or absence of thrombocytopenia: the thrombocytopenia group and the non-thrombocytopenia group. We collected data on demographic features, clinical characteristics, laboratory parameters, treatments, and outcomes. Subsequently, univariate and multivariate logistic regression analyses were performed to identify potential risk factors for cefoperazone/sulbactam-induced thrombocytopenia.
Results: In total, 6489 patients were included in this study, and 2.4% (155/6489) developed thrombocytopenia. The results of multivariate analysis showed that cefoperazone/sulbactam therapy duration (d) > 14, PLT (109/L) < 200, daily dose of cefoperazone/sulbactam (g) ≥ 6, TBil (μmoL/L) > 21, AST (U/L) > 35, and use of non-invasive ventilator were risk factors for cefoperazone/sulbactam-induced thrombocytopenia.
Conclusion: Despite the low incidence (2.4%), cefoperazone/sulbactam could cause serious thrombocytopenia sometimes accompanied with hemorrhage. In clinical therapy, clinicians should be vigilant in monitoring platelet count, especially for patients with risk factors of cefoperazone/sulbactam-induced thrombocytopenia.

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中国成年患者中头孢哌酮/舒巴坦诱发血小板减少症风险因素的回顾性分析:一项为期六年的真实世界研究
背景:药物诱发的血小板减少症是一种罕见的药物治疗不良反应,通常诊断不足。头孢哌酮/舒巴坦是由第三代头孢菌素和β-内酰胺酶抑制剂组成的复方制剂,其中血小板减少是一种不常见但严重的不良反应。然而,关于头孢哌酮/舒巴坦诱发血小板减少症的现有文献仍然有限,与这一不良反应相关的具体风险因素尚未得到彻底阐明。因此,本研究旨在调查接受头孢哌酮/舒巴坦治疗的成人患者血小板减少的临床特征并确定其风险因素:在这项回顾性研究中,我们回顾了 2017 年 1 月至 2023 年 6 月期间在北京医院接受头孢哌酮/舒巴坦治疗的患者。根据是否存在血小板减少症将患者分为两组:血小板减少症组和非血小板减少症组。我们收集了有关人口统计学特征、临床特征、实验室参数、治疗方法和结果的数据。随后,我们进行了单变量和多变量逻辑回归分析,以确定头孢哌酮/舒巴坦诱发血小板减少症的潜在风险因素:本研究共纳入 6489 例患者,2.4%(155/6489)的患者出现血小板减少。多变量分析结果显示,头孢哌酮/舒巴坦治疗持续时间(d)> 14、PLT(109/L)< 200、头孢哌酮/舒巴坦日剂量(g)≥6、TBil(μmoL/L)> 21、AST(U/L)> 35、使用无创呼吸机是头孢哌酮/舒巴坦诱发血小板减少的危险因素:尽管发病率较低(2.4%),但头孢哌酮/舒巴坦可导致严重的血小板减少,有时还伴有出血。在临床治疗中,临床医生应警惕监测血小板计数,尤其是对有头孢哌酮/舒巴坦诱发血小板减少危险因素的患者。
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
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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