艰难梭菌感染:最新进展。

Le infezioni in medicina Pub Date : 2024-09-01 eCollection Date: 2024-01-01 DOI:10.53854/liim-3203-3
Federica Salvati, Francesca Catania, Rita Murri, Massimo Fantoni, Carlo Torti
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引用次数: 0

摘要

艰难梭菌(C. difficile)是一种革兰氏阳性厌氧芽孢杆菌,是全球腹泻的主要病因。艰难梭菌感染(CDI)对医疗系统的影响令人担忧,因为治疗成本高昂,住院时间延长。CDI 的发病率受到 027 核型等高毒力菌株的影响,这些菌株是北美和欧洲重大疫情爆发的罪魁祸首。CDI 的流行病学也在发生变化,除了传统的医院感染病例外,社区获得性病例也在增加。死亡率居高不下,反复感染进一步增加了风险。艰难梭菌主要通过孢子传播,孢子在医疗机构中存活并在传播中发挥关键作用。不仅医护人员,食物链也会对感染传播产生重大影响,不过目前还没有经食物传播的确诊病例。艰难梭菌的致病性涉及孢子发芽和毒素产生。毒素 A 和毒素 B 可对宿主造成细胞损伤和炎症反应,导致结肠炎。临床表现可从轻微腹泻到伴有中毒性巨结肠和肠穿孔的暴发性结肠炎。CDI 的风险因素包括抗生素暴露、高龄、住院和使用质子泵抑制剂。接受过腹部手术的患者或患有炎症性肠病(IBD)的患者由于肠道微生物群受损而特别容易感染。CDI 的治疗方法也在不断发展,对于初次感染和复发感染,菲达霉素因其可降低复发率而成为优于万古霉素的治疗选择。粪便微生物群移植(FMT)可有效治疗复发性 CDI,恢复肠道生态平衡。针对艰难梭菌毒素 B 的单克隆抗体 Bezlotoxumab 有望降低复发率。严重的 CDI 病例可能需要手术治疗,尤其是在中毒性巨结肠或肠穿孔的情况下。总之,CDI 仍然是一个重要的临床实体。要改善患者的治疗效果并减轻医疗系统的负担,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clostridioides difficile infection: an update.

Clostridioides difficile (C. difficile) is a Gram-positive, spore-forming anaerobic bacterium emerged as a leading cause of diarrhea globally. CDI's (Clostridioides difficile infection) impact on healthcare systems is concerning due to high treatment cost and increased hospitalisation time. The incidence of CDI has been influenced by hypervirulent strains such as the 027 ribotype, responsible for significant outbreaks in North America and Europe. CDI's epidemiology has evolved, showing increased community-acquired cases alongside traditional hospital-acquired infections. Mortality rates remain high, with recurrent infections further elevating the risk. Transmission of C. difficile primarily occurs via spores, which survive in healthcare settings and play a pivotal role in transmission. Not only health workers, but also the food chain could have a significant impact on the transmission of infection, although no confirmed foodborne cases have been documented. Pathogenicity of C. difficile involves spore germination and toxin production. Toxins A and B can cause cellular damage and inflammatory responses in the host, leading to colitis. Clinical picture can range from mild diarrhea to fulminant colitis with toxic megacolon, and bowel perforation. Risk factors for CDI include antibiotic exposure, advanced age, hospitalization, and use of proton pump inhibitors. Patients who experience abdominal surgery or patients with inflammatory bowel disease (IBD) are particularly susceptible due to their compromised gut microbiota. Management of CDI has evolved, with fidaxomicin emerging as a superior treatment option over vancomycin for initial and recurrent infections due to its reduction of recurrence rate. Faecal microbiota transplantation (FMT) is effective for recurrent CDI, restoring gut eubiosis. Bezlotoxumab, a monoclonal antibody against C. difficile toxin B, has shown promise in reducing recurrence rates. Severe cases of CDI may require surgical intervention, particularly in instances of toxic megacolon or bowel perforation. In conclusion, CDI remains a significant clinical entity. Further research are needed to improve patients' outcome and reduce the burden on healthcare systems.

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