Clinical Impact of Implementing a Specific Clinical Pathway for the Management of Clostridioides difficile Infection.

IF 5.3 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2026-01-01 Epub Date: 2025-11-07 DOI:10.1007/s40121-025-01261-9
Miguel Rodríguez-Fernández, Rocio Herrero, Pilar González-De-La-Aleja, María Dolores Valverde-Fredet, María-Paz Ventero, Marta Trigo-Rodríguez, Livia Giner, Ana Isabel Aller-García, Héctor Pinargote-Celorio, Reinaldo Espíndola-Gómez, Mónica Parra, Pedro Martínez Pérez-Crespo, José-Manuel Ramos-Rincón, Antonio Fernández-Pevida, Joaquín Lanz-García, Eva León, Lucía Valiente-De-Santis, Juan E Corzo, Juan-Carlos Rodríguez, Esperanza Merino, Nicolás Merchante
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引用次数: 0

Abstract

Introduction: Despite Clostridioides difficile infection (CDI) being a leading healthcare-associated infection with high morbimortality, there is little evidence on specific antimicrobial stewardship program (ASP) interventions for CDI. The objective of this study was to assess the clinical impact of implementing a specific clinical pathway for CDI management at two Spanish hospitals.

Methods: This was a quasi-experimental pre-post intervention study, and three periods were evaluated: historical (2014-2017), educational-ASP (2018-2020), and intervention (2021-2023), after implementation of a CDI-specific measures bundle. Key measures included: (1) updated local CDI guidelines; (2) 24/7 diagnostic testing and real-time positive results notification to ASP-CDI team; (3) systematic evaluation of new cases; (4) optimizing CDI antibiotic treatment and overall management; and (5) structured follow-up until 8 weeks post-treatment. Primary outcome was first CDI recurrence, and secondary outcomes were readmissions during recurrent CDI episodes and 30-day all-cause mortality.

Results: In total, there were 1435 patients with CDI included: 370 in the historical period (2014-2017), 537 in the educational-ASP period (2018-2020), and 528 in the CDI-specific clinical pathway period (2021-2023). First CDI recurrence rates significantly declined across periods in high-risk groups: immunocompromised patients, 29% in 2014-2017, 22% in 2018-2020, and 15% in 2021-2023 (p = 0.038); those with severe/fulminant initial CDI, from 38% to 34% to 24% (p = 0.027); and patients aged 65-79 years, from 29% to 31% to 13% (p = 0.003). Hospitalization during recurrent CDI episodes and mortality were significantly reduced in the CDI-specific clinical pathway period: readmissions, 11% (2014-2017), 13% (2018-2020), and 6% (2021-2023) (p = 0.017); mortality, 7%, 6%, and 4% (p = 0.023).

Conclusions: The implementation of a structured, multifaceted clinical pathway specifically designed for CDI management had significant clinical benefits, including a reduction of recurrences in high-risk groups, readmissions, and mortality.

Trial registration: ClinicalTrials.gov identifier NCT04801862.

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实施特定临床途径管理艰难梭菌感染的临床影响。
导语:尽管艰难梭菌感染(CDI)是一种高死亡率的主要卫生保健相关感染,但关于CDI的特定抗菌药物管理计划(ASP)干预措施的证据很少。本研究的目的是评估在两家西班牙医院实施CDI管理的特定临床途径的临床影响。方法:这是一项准实验的干预前后研究,在实施cdi特定措施包后,评估了三个阶段:历史(2014-2017)、教育- asp(2018-2020)和干预(2021-2023)。主要措施包括:(1)更新本地CDI指南;(2)全天候诊断检测,实时向ASP-CDI团队通报阳性结果;(3)对新病例进行系统评价;(4)优化CDI抗生素治疗及整体管理;(5)随访至治疗后8周。主要结局是首次CDI复发,次要结局是CDI复发期间再入院和30天全因死亡率。结果:共纳入1435例CDI患者:历史期(2014-2017年)370例,教育- asp期(2018-2020年)537例,CDI特异性临床途径期(2021-2023年)528例。高危人群的首次CDI复发率在各时期均显著下降:免疫功能低下患者,2014-2017年为29%,2018-2020年为22%,2021-2023年为15% (p = 0.038);重度/暴发性首发CDI患者,从38% ~ 34% ~ 24% (p = 0.027);65 ~ 79岁患者,从29%降至31%至13% (p = 0.003)。复发性CDI发作期间的住院率和死亡率在CDI特异性临床通路期间显著降低:再入院率为11%(2014-2017年)、13%(2018-2020年)和6%(2021-2023年)(p = 0.017);死亡率分别为7%、6%和4% (p = 0.023)。结论:实施专门为CDI管理设计的结构化、多方面的临床途径具有显著的临床益处,包括减少高危人群的复发率、再入院率和死亡率。试验注册:ClinicalTrials.gov标识符NCT04801862。
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
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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