无并发症尿路感染患者在接受氟喹诺酮类药物短期治疗后发生胶原相关疾病和神经系统事件的风险:一项队列研究。

IF 4.1 2区 医学 Q2 MICROBIOLOGY
Antimicrobial Agents and Chemotherapy Pub Date : 2024-12-05 Epub Date: 2024-10-29 DOI:10.1128/aac.00690-24
Fanny S Mitrani-Gold, Shinyoung Ju, Myriam Drysdale, Anna Schultze, George Mu, John Logie
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引用次数: 0

摘要

对氟喹诺酮(FQ)各适应症安全性的研究显示,胶原蛋白/神经系统不良事件(AE)风险增加,但患者仍在接受氟喹诺酮治疗非复杂性尿路感染(UTI)。这项回顾性队列研究调查了尿路感染女性门诊患者短期使用 FQ 与标准抗生素(三甲双氨-磺胺甲噁唑 [SXT]、硝基呋喃妥因 [NTF])相比发生胶原蛋白/神经系统特异性不良事件 (AESI) 的风险。这项研究是在 2009 年 12 月至 2019 年期间利用 Optum 的去标识化临床信息学数据集市数据库进行的。计算了复合/胶原/神经系统 AESI 的调整后绝对风险(卡普兰-梅耶累积危险度,应用稳定的逆治疗概率加权法 [sIPTW])。得出调整后的危险比(sIPTW 考克斯比例危险模型)。共纳入 954 777 名患者:FQ(n = 386,537 [40.5%]);SXT(n = 237,120 [24.8%]);NTF(n = 314,585 [32.9%])。胶原蛋白/神经系统 AESI 的调整后绝对风险范围为 P = 0.0497)。与NTF相比,接受FQ治疗的患者发生神经系统(0.95 [0.93-0.97];P < 0.0001)、中枢神经系统(0.85 [0.80-0.89];P < 0.0001)和周围神经系统(0.96 [0.93-0.98];P = 0.0016)AESI的风险较低。在短疗程治疗后,FQs 与 SXT 相比增加了肌腱断裂的风险,而与 NTF 相比降低了神经系统 AESI 的风险(调整后危险比)。在治疗尿路感染时,需要根据患者的个体风险和已知不常见但严重的 AEs 后果选择适当的抗生素。在治疗尿路感染时,应根据指南对患者情况、疗效、微生物组的影响、安全性和监测情况进行抗生素选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of collagen-related disorders and neurological events among patients with uncomplicated urinary tract infection following short treatment with fluoroquinolones: a cohort study.

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 (n = 386,537 [40.5%]); SXT (n = 237,120 [24.8%]); NTF (n = 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]; P = 0.0497). Patients receiving FQ had lower hazard of neurological (0.95 [0.93-0.97]; P < 0.0001), central nervous system (0.85 [0.80-0.89]; P < 0.0001), and peripheral nervous system (0.96 [0.93-0.98]; P = 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.

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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
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