用于复发性艰难梭菌感染的口服、冷冻粪便微生物群移植(FMT)胶囊。

Oral, frozen fecal microbiota transplant (FMT) capsules for recurrent Clostridium difficile infection.

作者信息

Youngster Ilan, Mahabamunuge Jasmin, Systrom Hannah K, Sauk Jenny, Khalili Hamed, Levin Joanne, Kaplan Jess L, Hohmann Elizabeth L

机构信息

Divisions of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.

Division of Infectious Diseases, Boston Children's Hospital, 300 Longood Ave, Boston, MA, 02115, USA.

出版信息

BMC Med. 2016 Sep 9;14(1):134. doi: 10.1186/s12916-016-0680-9.

Abstract

BACKGROUND

Fecal microbiota transplantation (FMT) has been shown to be safe and effective in treating refractory or relapsing C. difficile infection (CDI), but its use has been limited by practical barriers. We recently reported a small preliminary feasibility study using orally administered frozen fecal capsules. Following these early results, we now report our clinical experience in a large cohort with structured follow-up.

METHODS

We prospectively followed a cohort of patients with recurrent or refractory CDI who were treated with frozen, encapsulated FMT at our institution. The primary endpoint was defined as clinical resolution whilst off antibiotics for CDI at 8 weeks after last capsule ingestion. Safety was defined as any FMT-related adverse event grade 2 or above.

RESULTS

Overall, 180 patients aged 7-95 years with a minimal follow-up of 8 weeks were included in the analysis. CDI resolved in 82 % of patients after a single treatment, rising to a 91 % cure rate with two treatments. Three adverse events Grade 2 or above, deemed related or possibly related to FMT, were observed.

CONCLUSIONS

We confirm the effectiveness and safety of oral administration of frozen encapsulated fecal material, prepared from unrelated donors, in treating recurrent CDI. Randomized studies and FMT registries are still needed to ascertain long-term safety.

摘要

背景

粪便微生物群移植(FMT)已被证明在治疗难治性或复发性艰难梭菌感染(CDI)方面是安全有效的,但其应用受到实际障碍的限制。我们最近报告了一项使用口服冷冻粪便胶囊的小型初步可行性研究。基于这些早期结果,我们现在报告我们在一个进行结构化随访的大型队列中的临床经验。

方法

我们前瞻性地跟踪了一组在我们机构接受冷冻封装FMT治疗的复发性或难治性CDI患者。主要终点定义为在最后一次摄入胶囊后8周停用抗生素时CDI的临床缓解。安全性定义为任何2级或以上与FMT相关的不良事件。

结果

总体而言,分析纳入了180例年龄在7至95岁之间、最短随访8周的患者。单次治疗后82%的患者CDI得到缓解,两次治疗后治愈率升至91%。观察到3例2级或以上不良事件,被认为与FMT相关或可能相关。

结论

我们证实了口服由无关供体制备的冷冻封装粪便材料治疗复发性CDI的有效性和安全性。仍需要进行随机研究和FMT登记以确定长期安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de19/5016994/603e269a77c7/12916_2016_680_Fig1_HTML.jpg

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