微生物检测对瑞士军团病抗生素处方的测试和治疗影响:多中心SwissLEGIO研究结果

IF 6.2 Q1 RESPIRATORY SYSTEM
Melina Bigler, Florian Zacher, Sarah Dräger, Werner C Albrich, Daniel Mäusezahl
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引用次数: 0

摘要

背景:军团病(LD)是一种严重的主要是社区获得性肺炎(CAP)。为确认军团菌感染,需要进行微生物检测。瑞士和欧洲的指南建议对所有住院的CAP患者进行LD检测。然而,这种常规检测的低阳性率(1.5-3%)引起了人们对其成本效益和临床实用性的担忧。在推荐常规检测的环境下,这项多中心研究评估了LD检测对感染临床管理和抗菌药物处方的影响。方法:对瑞士20家医院(2022年8月- 2024年3月)195例社区获得性LD (CALD)患者的病历资料进行分析。我们评估了CALD的临床管理,重点关注微生物检测对抗生素处方的影响。使用标准化途径分析方法评估抗生素选择的适宜性和治疗时间。使用混合效应logistic回归分析评估与无证据支持的抗生素处方相关的因素。结果:及时开展微生物检测,85.1%的患者在入院后24小时内获得结果,92.3%的患者在48小时内获得结果。88.2%的患者在入院24小时内开始使用军团菌覆盖的抗生素。军团菌检测阳性影响抗生素处方:97.9%的患者接受了对军团菌有活性的抗生素治疗,79.6%的患者在收到检测结果后24小时内接受了适当的靶向单药治疗。总体而言,35.4%的患者接受抗生素治疗的时间中位数比指南推荐的时间长4天(IQR 3-4天)(免疫功能正常的患者定义为> 10天,免疫功能低下的患者定义为> 21天)。延长治疗时间与CALD严重程度和出院后2天的抗生素使用相关(代表达到临床稳定)。38.5%的肾功能受损患者接受左氧氟沙星次优负荷剂量。结论:LD的常规病原学检测有助于快速发现CALD病例,及时启动适当的靶向抗生素治疗,改善了CALD的临床管理。未来的抗菌药物管理工作应使医生意识到,根据最新的瑞士CAP指南,较短的5至7天的CALD抗生素治疗时间是足够和安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Test and treat-impact of microbiological testing on antibiotic prescribing for Legionnaires' disease in Switzerland: results of the multicentre SwissLEGIO study.

Test and treat-impact of microbiological testing on antibiotic prescribing for Legionnaires' disease in Switzerland: results of the multicentre SwissLEGIO study.

Test and treat-impact of microbiological testing on antibiotic prescribing for Legionnaires' disease in Switzerland: results of the multicentre SwissLEGIO study.

Background: Legionnaires' disease (LD) is a severe form of primarily community-acquired pneumonia (CAP). To confirm a Legionella infection, microbiological testing is required. The Swiss and European guidelines recommend LD testing for all hospitalised CAP patients. However, the low positivity rate of such routine testing (1.5-3%) raises concerns about its cost-effectiveness and clinical utility. In a setting where routine testing is recommended, this multicentre study evaluated the impact of LD testing on the clinical management of the infection and antimicrobial prescribing.

Methods: Data from medical records of 195 community-acquired LD (CALD) patients from 20 Swiss hospitals (August 2022-March 2024) were analysed. We assessed the clinical management of CALD, focusing on the impact of microbiological testing on antibiotic prescribing. The appropriateness of antibiotic choice and duration of treatment was assessed using a standardised pathway analysis approach. Factors associated with unsupported antibiotic prescribing were assessed using mixed-effects logistic regression analysis.

Results: Microbiological testing was initiated promptly, with results available within 24 h after presenting to the hospital for 85.1% and within 48 h for 92.3% of patients. Antibiotics with Legionella coverage were initiated in 88.2% of patients within 24 h of admission. A positive Legionella test influenced antibiotic prescribing: 97.9% of patients received antibiotics active against Legionella spp., and 79.6% were prescribed appropriate and targeted monotherapy within 24 h of receiving the test result. Overall, 35.4% of patients were treated with antibiotics for a median of 4 days (IQR 3-4 days) longer than guidelines recommend (defined as > 10 days for immunocompetent or > 21 days for immunocompromised patients). Prolonged treatment was associated with CALD severity and antibiotic use > 2 days postdischarge (proxy for clinical stability reached). 38.5% of patients with impaired renal function received a suboptimal loading dose of levofloxacin.

Conclusion: Routine aetiological testing for LD has improved the clinical management of CALD by facilitating rapid detection of CALD cases and timely initiation of appropriate and targeted antibiotic therapy. Future antimicrobial stewardship efforts should sensitise physicians that a shorter duration of antibiotic treatment for CALD of 5 to 7 days according to the latest Swiss CAP guidelines is sufficient and safe.

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Pneumonia
Pneumonia RESPIRATORY SYSTEM-
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