Tucker Emily C, Angelica Bianca, Mathias Ryan M, Edwards Louisa, Bryant Robert V, Costello Samuel P
Infectious Diseases Unit, Central Adelaide Local Health Network, Adelaide, Australia.
School of Medicine, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
Open Forum Infect Dis. 2025 Mar 13;12(4):ofaf149. doi: 10.1093/ofid/ofaf149. eCollection 2025 Apr.
Fecal microbiota transplantation (FMT) sourced from a bank of prescreened anaerobically processed frozen donor stool has been available in South Australia since 2013. This study aimed to evaluate the real-world clinical and safety outcomes of FMT for recurrent, refractory, and/or severe or fulminant infection (CDI) facilitated via this centralized facility.
Donor screening test data were prospectively collected on all donors who passed prescreening evaluations between April 2013 and August 2023. The South Australian FMT for CDI database prospectively recorded outcomes for consecutive patients who underwent FMT for CDI from August 2013 to May 2023 in South Australia.
An overall 98 potential donors passed prescreening assessments and underwent laboratory screening tests: 32 (33%) had tests that failed, 5 (5%) had incomplete screening, and 61 (62%) passed. Detection of an extended-spectrum β-lactamase-producing organism (9/65, 14%) was the common reason for ineligibility following completion of screening tests. In total 220 cases of CDI were recorded, and follow-up data were available in 216. Primary cure occurred in 84% of cases (182/216): 88% (132/150) for recurrent CDI, 76% (50/66) for refractory CDI, 85% (51/60) for severe disease, and 65% (17/26) for fulminant disease. Repeat FMT was delivered in 23 of 34 cases (68%), with secondary cure in 74% (17/23 cases). Serious adverse events were observed in 6 patients overall (3%). No deaths were directly attributable to FMT.
FMT was safe and efficacious for management of recurrent and refractory CDI over a 10-year period in a real-world prospective Australian cohort. Further studies to optimize the use of FMT for severe and fulminant CDI are warranted.
自2013年以来,南澳大利亚州已有来自经过预先筛选的厌氧处理冷冻供体粪便库的粪便微生物群移植(FMT)。本研究旨在评估通过该集中设施进行的FMT治疗复发性、难治性和/或严重或暴发性艰难梭菌感染(CDI)的真实世界临床和安全性结果。
前瞻性收集2013年4月至2023年8月间通过预筛选评估的所有供体的筛查测试数据。南澳大利亚州CDI的FMT数据库前瞻性记录了2013年8月至2023年5月在南澳大利亚州接受FMT治疗CDI的连续患者的结果。
共有98名潜在供体通过了预筛选评估并接受了实验室筛查测试:32名(33%)测试不合格,5名(5%)筛查不完整,61名(62%)通过。筛查测试完成后,检测到产超广谱β-内酰胺酶的生物体(9/65,14%)是不符合条件的常见原因。总共记录了220例CDI病例,其中216例有随访数据。84%的病例(182/216)实现了初次治愈:复发性CDI为88%(132/150),难治性CDI为76%(50/66),重症疾病为85%(51/60),暴发性疾病为65%(17/26)。34例中有23例(68%)进行了重复FMT,其中74%(17/23例)实现了二次治愈。总体上6名患者(3%)观察到严重不良事件。没有死亡直接归因于FMT。
在澳大利亚一个真实世界的前瞻性队列中,FMT在10年期间治疗复发性和难治性CDI是安全有效的。有必要进一步研究优化FMT用于重症和暴发性CDI的使用。