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口服万古霉素序贯粪便移植与逐渐减少口服万古霉素治疗复发性艰难梭菌感染:一项开放标签、随机对照试验。

Oral Vancomycin Followed by Fecal Transplantation Versus Tapering Oral Vancomycin Treatment for Recurrent Clostridium difficile Infection: An Open-Label, Randomized Controlled Trial.

机构信息

Department of Infection Prevention and Control, University Health Network, Toronto,

Department of Medicine, University of Toronto.

出版信息

Clin Infect Dis. 2017 Feb 1;64(3):265-271. doi: 10.1093/cid/ciw731. Epub 2016 Nov 9.

Abstract

BACKGROUND

Fecal transplantation (FT) is a promising treatment for recurrent Clostridium difficile infection (CDI), but its true effectiveness remains unknown. We compared 14 days of oral vancomycin followed by a single FT by enema with oral vancomycin taper (standard of care) in adult patients experiencing acute recurrence of CDI.

METHODS

In a phase 2/3, single-center, open-label trial, participants from Ontario, Canada, experiencing recurrence of CDI were randomly assigned in a 1:1 ratio to 14 days of oral vancomycin treatment followed by a single 500-mL FT by enema, or a 6-week taper of oral vancomycin. Patients with significant immunocompromise, history of fulminant CDI, or irreversible bleeding disorders were excluded. The primary endpoint was CDI recurrence within 120 days. Microbiota analysis was performed on fecal filtrate from donors and stool samples from FT recipients, as available.

RESULTS

The study was terminated at the interim analysis after randomizing 30 patients. Nine of 16 (56.2%) patients who received FT and 5 of 12 (41.7%) in the vancomycin taper group experienced recurrence of CDI, corresponding with symptom resolution in 43.8% and 58.3%, respectively. Fecal microbiota analysis of 3 successful FT recipients demonstrated increased diversity. A futility analysis did not support continuing the study. Adverse events were similar in both groups and uncommon.

CONCLUSIONS

In patients experiencing an acute episode of recurrent CDI, a single FT by enema was not significantly different from oral vancomycin taper in reducing recurrent CDI. Further research is needed to explore optimal donor selection, FT preparation, route, timing, and number of administrations.

CLINICAL TRIALS REGISTRATION

NCT01226992.

摘要

背景

粪便移植(FT)是治疗复发性艰难梭菌感染(CDI)的一种很有前途的方法,但其实效仍不清楚。我们比较了 14 天口服万古霉素后再行单次灌肠 FT 与口服万古霉素逐渐减量(标准治疗)在成人急性复发性 CDI 患者中的疗效。

方法

在一项 2/3 期、单中心、开放性试验中,来自加拿大安大略省的复发性 CDI 患者以 1:1 的比例随机分为两组,一组接受 14 天的口服万古霉素治疗,然后进行单次 500 毫升灌肠 FT,另一组则接受 6 周的口服万古霉素逐渐减量。排除有严重免疫功能低下、暴发性 CDI 病史或不可逆转的出血性疾病的患者。主要终点是 120 天内 CDI 复发。如可行,对供体粪便滤液和 FT 受者粪便样本进行微生物组分析。

结果

在随机分配 30 例患者后,该研究在中期分析时终止。接受 FT 的 16 例患者中有 9 例(56.2%)和接受万古霉素逐渐减量的 12 例患者中有 5 例(41.7%)出现 CDI 复发,相应的症状缓解率分别为 43.8%和 58.3%。3 例成功 FT 受者的粪便微生物组分析显示多样性增加。无效性分析不支持继续该研究。两组的不良事件相似且不常见。

结论

在急性复发性 CDI 患者中,单次灌肠 FT 在降低复发性 CDI 方面与口服万古霉素逐渐减量无显著差异。需要进一步研究以探索最佳供体选择、FT 准备、途径、时间和给药次数。

临床试验注册

NCT01226992。

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