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氟喹诺酮类药物短期治疗单纯性尿路感染患者发生胶原相关疾病和神经事件的风险:一项队列研究

Risk of collagen-related disorders and neurological events among patients with uncomplicated urinary tract infection following short treatment with fluoroquinolones: a cohort study.

作者信息

Mitrani-Gold Fanny S, Ju Shinyoung, Drysdale Myriam, Schultze Anna, Mu George, Logie John

机构信息

GSK, Collegeville, Pennsylvania, USA.

GSK, London, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2024 Dec 5;68(12):e0069024. doi: 10.1128/aac.00690-24. Epub 2024 Oct 29.

Abstract

Studies of fluoroquinolone (FQ) safety across indications show increased collagen/neurological adverse event (AE) risk, yet patients still receive FQs for uncomplicated urinary tract infections (uUTIs). This retrospective, cohort study investigated the risk of collagen/neurological AEs of special interest (AESIs) with short-term FQ use versus standard-of-care antibiotics (trimethoprim-sulfamethoxazole [SXT], nitrofurantoin [NTF]) among female outpatients with uUTIs. This study was conducted between December 2009 and 2019 using Optum's de-identified Clinformatics Data Mart Database. Adjusted absolute risks were calculated for composite/collagen/neurological AESIs (Kaplan-Meier cumulative hazards, after applying stabilized inverse probability of treatment weighting [sIPTW]). Adjusted hazard ratios were generated (sIPTW Cox proportional hazard modeling). Overall, 954,777 patients were included: FQ ( = 386,537 [40.5%]); SXT ( = 237,120 [24.8%]); NTF ( = 314,585 [32.9%]). Adjusted absolute risk range for collagen/neurological AESIs was <1%-4.5%. The hazard (95% CI) of tendon rupture was 25% higher with FQ versus SXT (1.25 [1.00-1.57]; = 0.0497). Patients receiving FQ had lower hazard of neurological (0.95 [0.93-0.97]; < 0.0001), central nervous system (0.85 [0.80-0.89]; < 0.0001), and peripheral nervous system (0.96 [0.93-0.98]; = 0.0016) AESIs versus NTF. Following a short treatment duration, FQs were associated with increased risk of tendon rupture versus SXT and reduced risk (adjusted hazard ratios) of neurological AESI versus NTF. Individual patient risk and consequences for known uncommon, yet serious, AEs need to inform appropriate antibiotic choice in treating uUTIs. Patient profile, efficacy, microbiome impact, safety, and surveillance should inform antibiotic selection for uUTI management, in accordance with guidelines.

摘要

针对不同适应症的氟喹诺酮(FQ)安全性研究表明,其导致胶原蛋白/神经学不良事件(AE)的风险增加,但患者仍在因单纯性尿路感染(uUTI)而接受FQ治疗。这项回顾性队列研究调查了患有uUTI的女性门诊患者短期使用FQ与标准护理抗生素(甲氧苄啶-磺胺甲恶唑[SXT]、呋喃妥因[NTF])相比,发生特定胶原蛋白/神经学严重不良事件(AESI)的风险。本研究于2009年12月至2019年期间使用Optum的去识别化临床信息数据集市数据库进行。计算了复合/胶原蛋白/神经学AESI的调整后绝对风险(应用稳定化治疗权重逆概率[sIPTW]后采用Kaplan-Meier累积风险)。生成了调整后风险比(sIPTW Cox比例风险模型)。总体而言,共纳入954,777例患者:FQ组(n = 386,537 [40.5%]);SXT组(n = 237,120 [24.8%]);NTF组(n = 314,585 [32.9%])。胶原蛋白/神经学AESI的调整后绝对风险范围为<1%-4.5%。与SXT相比,FQ导致肌腱断裂的风险(95%CI)高25%(1.25 [1.00 - 1.57];P = 0.0497)。与NTF相比,接受FQ治疗的患者发生神经学(0.95 [0.93 - 0.97];P < 0.0001)、中枢神经系统(0.85 [0.80 - 0.89];P < 0.0001)和外周神经系统(0.96 [0.93 - 0.98];P = 0.0016)AESI的风险较低。在短疗程治疗后,与SXT相比,FQ与肌腱断裂风险增加相关,与NTF相比,神经学AESI的风险(调整后风险比)降低。个体患者的风险以及已知罕见但严重的AE的后果需要为治疗uUTI时选择合适的抗生素提供依据。患者概况、疗效、对微生物群的影响、安全性和监测应根据指南为uUTI管理中的抗生素选择提供依据。

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