A 5-day course of oral antibiotics followed by faecal transplantation to eradicate carriage of multidrug-resistant Enterobacteriaceae: a randomized clinical trial
Details
Serval ID
serval:BIB_82180A9565B0
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A 5-day course of oral antibiotics followed by faecal transplantation to eradicate carriage of multidrug-resistant Enterobacteriaceae: a randomized clinical trial
Journal
Clin Microbiol Infect
Working group(s)
R. Gnosis WP3 study group
ISSN
1469-0691 (Electronic)
ISSN-L
1198-743X
Publication state
Published
Issued date
07/2019
Volume
25
Number
7
Pages
830-838
Language
english
Notes
Huttner, B D
de Lastours, V
Wassenberg, M
Maharshak, N
Mauris, A
Galperine, T
Zanichelli, V
Kapel, N
Bellanger, A
Olearo, F
Duval, X
Armand-Lefevre, L
Carmeli, Y
Bonten, M
Fantin, B
Harbarth, S
eng
Equivalence Trial
Multicenter Study
England
2019/01/08
Clin Microbiol Infect. 2019 Jul;25(7):830-838. doi: 10.1016/j.cmi.2018.12.009. Epub 2019 Jan 4.
de Lastours, V
Wassenberg, M
Maharshak, N
Mauris, A
Galperine, T
Zanichelli, V
Kapel, N
Bellanger, A
Olearo, F
Duval, X
Armand-Lefevre, L
Carmeli, Y
Bonten, M
Fantin, B
Harbarth, S
eng
Equivalence Trial
Multicenter Study
England
2019/01/08
Clin Microbiol Infect. 2019 Jul;25(7):830-838. doi: 10.1016/j.cmi.2018.12.009. Epub 2019 Jan 4.
Abstract
OBJECTIVES: Intestinal carriage with extended spectrum beta-lactamase Enterobacteriaceae (ESBL-E) and carbapenemase-producing Enterobacteriaceae (CPE) can persist for months. We aimed to evaluate whether oral antibiotics followed by faecal microbiota transplantation (FMT) can eradicate intestinal carriage with ESBL-E/CPE. METHODS: Randomized, open-label, superiority trial in four tertiary-care centres (Geneva (G), Paris (P), Utrecht (U), Tel Aviv (T)). Non-immunocompromised adult patients were randomized 1: 1 to either no intervention (control) or a 5-day course of oral antibiotics (colistin sulphate 2 x 10(6) IU 4x/day; neomycin sulphate 500 mg 4x/day) followed by frozen FMT obtained from unrelated healthy donors. The primary outcome was detectable intestinal carriage of ESBL-E/CPE by stool culture 35-48 days after randomization (V4). ClinicalTrials.govNCT02472600. The trial was funded by the European Commission (FP7). RESULTS: Thirty-nine patients (G = 14; P = 16; U = 7; T = 2) colonized by ESBL-E (n = 36) and/or CPE (n = 11) were enrolled between February 2016 and June 2017. In the intention-to-treat analysis 9/22 (41%) patients assigned to the intervention arm were negative for ESBL-E/CPE at V4 (1/22 not receiving the intervention imputed as positive) whereas in the control arm 5/17 (29%) patients were negative (one lost to follow up imputed as negative) resulting in an OR for decolonization success of 1.7 (95% CI 0.4-6.4). Study drugs were well tolerated overall but three patients in the intervention group prematurely stopped the study antibiotics because of diarrhoea (all received FMT). CONCLUSIONS: Non-absorbable antibiotics followed by FMT slightly decreased ESBL-E/CPE carriage compared with controls; this difference was not statistically significant, potentially due to early trial termination. Further clinical investigations seem warranted.
Keywords
Administration, Oral, Aged, Anti-Bacterial Agents/*therapeutic use, Carbapenem-Resistant Enterobacteriaceae/*drug effects, Carrier State/drug therapy/microbiology, Colistin/therapeutic use, Drug Administration Schedule, Drug Resistance, Multiple, Bacterial, Enterobacteriaceae Infections/*drug therapy, *Fecal Microbiota Transplantation, Feces/microbiology, Female, Humans, Male, Middle Aged, Tertiary Care Centers, beta-Lactamases, Carbapenemase, Colistin, Extended-spectrum beta-lactamase, Faecal microbiota transplantation, Neomycin
Pubmed
Create date
30/01/2023 11:16
Last modification date
31/01/2023 6:55