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[艰难梭菌——新见解与治疗建议]

[Clostridioides difficile - New Insights and Therapy Recommendations].

作者信息

Schönherr Sebastian, Jung Laura, Lübbert Christoph

机构信息

Bereich Infektiologie und Tropenmedizin, Klinik und Poliklinik für Hämatologie, Zelltherapie, Hämostaseologie und Infektiologie, Universitätsklinikum Leipzig, Leipzig.

Interdisziplinäres Zentrum für Infektionsmedizin, Universitätsklinikum Leipzig, Leipzig.

出版信息

Dtsch Med Wochenschr. 2023 Jun;148(12):752-758. doi: 10.1055/a-1970-9211. Epub 2023 May 31.

DOI:10.1055/a-1970-9211
PMID:37257477
Abstract

After an increase in infections (CDI) until 2013 due to epidemic ribotypes such as 027 and 078, CDI incidence in Germany is now declining, as confirmed by recent epidemiological data. Despite this success through antimicrobial stewardship and hospital hygiene, the burden of disease remains high, especially in older patients (>65 years) with comorbidities. The main risk factor for CDI is the use of broad-spectrum antibiotics, which disrupt the gut microbiota, allowing colonization. Coinfection with other intestinal pathogens such as enterococci can further increase the virulence of . The updated 2021 ESCMID guidelines recommend fidaxomicin instead of vancomycin as the antibiotic of choice for the treatment of CDI because of its lower recurrence rate. Vancomycin remains a good alternative; however, metronidazole should only be used if neither antibiotic is available. In the future, ridinilazole may be available as another therapeutic option that has a narrow spectrum of activity and low intestinal absorption. For the treatment of recurrent CDI, the new guidelines also include the use of the monoclonal antibody bezlotoxumab. In addition, a new oral microbiome therapy, SER-109 (capsules containing purified Firmicutes spores), which showed promising results in a phase 3 study, may provide an easy-to-administer alternative to fecal microbiota transplantation. Hopes for a well-performing toxoid vaccine for primary and secondary prevention of CDI have unfortunately not been fulfilled in the CLOVER trial.

摘要

在2013年之前,由于027和078等流行核糖型导致艰难梭菌感染(CDI)增加,而近期的流行病学数据证实,德国的CDI发病率目前正在下降。尽管通过抗菌药物管理和医院卫生措施取得了这一成效,但疾病负担仍然很高,尤其是在患有合并症的老年患者(>65岁)中。CDI的主要危险因素是使用广谱抗生素,这会破坏肠道微生物群,从而使艰难梭菌得以定植。与其他肠道病原体如肠球菌的合并感染会进一步增加艰难梭菌的毒力。2021年更新的欧洲临床微生物学和传染病学会(ESCMID)指南推荐非达霉素而非万古霉素作为治疗CDI的首选抗生素,因为其复发率较低。万古霉素仍然是一个不错的替代选择;然而,仅在两种抗生素均无法获得时才应使用甲硝唑。未来,利迪尼唑可能作为另一种治疗选择上市,其活性谱窄且肠道吸收低。对于复发性CDI的治疗,新指南还包括使用单克隆抗体贝佐妥单抗。此外,一种新的口服微生物组疗法SER-109(含有纯化厚壁菌门孢子的胶囊)在一项3期研究中显示出了有前景的结果,可能为粪便微生物群移植提供一种易于给药的替代方法。遗憾的是,在CLOVER试验中,用于CDI一级和二级预防的高效类毒素疫苗的希望尚未实现。

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