头孢他啶/阿维巴坦与其他积极治疗台湾产oxacillinase -48耐碳青霉烯肺炎克雷伯菌血症的疗效比较

IF 5.3 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-09-01 Epub Date: 2025-08-08 DOI:10.1007/s40121-025-01210-6
Szu-Yu Liu, Chien Chuang, Chih-Han Juan, Yu-Chien Ho, Sheng-Hua Chou, Yi-Ru Huang, Wan Chin, Hsiang-Ling Ho, Yi-Tsung Lin
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引用次数: 0

摘要

简介:产Oxacillinase-48 (OXA-48)的耐碳青霉烯肺炎克雷伯菌(CRKP)感染在台湾越来越多的报道。关于这些感染的有效治疗的实际研究有限,国际指南的建议也存在争议。本研究的目的是比较头孢他啶/阿维巴坦(CZA)治疗和接受其他积极治疗的患者产生oxa -48的CRKP菌血症的临床结果。方法:纳入2017年6月至2024年12月在台北退伍军人总医院接受CZA或其他体外治疗至少3天的oxa -48产生CRKP菌血症的独特成人患者。比较两组患者的临床特点和治疗结果。采用聚合酶链反应(PCR)和Sanger测序法检测OXA-48菌株。结果:本研究纳入的45例患者中,18例患者接受CZA治疗,27例患者接受其他积极治疗。4例患者接受联合治疗。大多数菌株为OXA-48产生菌(n = 42),其余菌株为OXA-181产生菌(n = 42)。治疗组间30天死亡率无显著差异(22.2%对33.3%,p = 0.420),甚至在危重患者中也无显著差异(28.6%对43.8%,p = 0.389)。急性生理和慢性健康评估II (APACHE II)评分(风险比[HR] 1.07, 95%可信区间[CI] 1.01-1.15, p = 0.028)是30天死亡率的独立危险因素,基于粘菌素的治疗(风险比[HR] 3.02, 95% CI 1.00-9.13, p = 0.050)与30天死亡率具有边际显著性。CZA的使用与30天死亡率无关。结论:我们的研究结果显示,CZA和其他积极疗法的结果相似,但应谨慎使用以粘菌素为基础的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of Effectiveness between Ceftazidime/Avibactam and Other Active Therapies for Oxacillinase-48-Producing Carbapenem-Resistant Klebsiella pneumoniae Bacteremia in Taiwan.

Comparison of Effectiveness between Ceftazidime/Avibactam and Other Active Therapies for Oxacillinase-48-Producing Carbapenem-Resistant Klebsiella pneumoniae Bacteremia in Taiwan.

Introduction: Oxacillinase-48 (OXA-48)-producing carbapenem-resistant Klebsiella pneumoniae (CRKP) infections have been increasingly reported in Taiwan. Real-world studies regarding effective treatments for these infections are limited, and recommendations from international guidelines are controversial. The aim of this study was to compare clinical outcomes of OXA-48-producing CRKP bacteremia between patients treated with ceftazidime/avibactam (CZA) and those receiving other active therapies.

Methods: Unique adult patients with OXA-48-producing CRKP bacteremia who received CZA or other therapies in vitro for at least 3 days between June 2017 and December 2024 at Taipei Veterans General Hospital were enrolled. Clinical characteristics and outcomes were compared among the treatment groups. OXA-48 strains were detected using polymerase chain reaction (PCR) followed by Sanger sequencing.

Results: Of 45 patients included in this study, 18 were treated with CZA, and 27 were treated with other active therapies. Four patients received combination therapy. Most strains were OXA-48 producers (n = 42), and the rest were OXA-181 producers. No significant difference in 30-day mortality rate was observed between the treatment groups (22.2% versus 33.3%, p = 0.420), and even in critically ill patients (28.6% versus 43.8%, p = 0.389). Acute Physiology and Chronic Health Evaluation II (APACHE II) score (hazard ratio [HR] 1.07, 95% confidence interval [CI] 1.01-1.15, p = 0.028) was an independent risk factor for 30-day mortality, and colistin-based therapy (HR 3.02, 95% CI 1.00-9.13, p = 0.050) showed marginal significance with 30-day mortality. CZA use was not associated with 30-day mortality.

Conclusions: Our findings revealed that CZA and other active therapies showed similar outcomes, but colistin-based regimens should be used cautiously.

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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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