A 5-day course of oral antibiotics followed by faecal transplantation to eradicate carriage of multidrug-resistant Enterobacteriaceae: a randomized clinical trial

Détails

ID Serval
serval:BIB_82180A9565B0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
A 5-day course of oral antibiotics followed by faecal transplantation to eradicate carriage of multidrug-resistant Enterobacteriaceae: a randomized clinical trial
Périodique
Clin Microbiol Infect
Auteur⸱e⸱s
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.
Collaborateur⸱rice⸱s
R. Gnosis WP3 study group
ISSN
1469-0691 (Electronic)
ISSN-L
1198-743X
Statut éditorial
Publié
Date de publication
07/2019
Volume
25
Numéro
7
Pages
830-838
Langue
anglais
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.
Résumé
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.
Mots-clé
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
Création de la notice
30/01/2023 12:16
Dernière modification de la notice
31/01/2023 7:55
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