One-day prevalence of asymptomatic carriage of toxigenic and non-toxigenic Clostridioides difficile in 10 French hospitals.


Journal

The Journal of hospital infection
ISSN: 1532-2939
Titre abrégé: J Hosp Infect
Pays: England
ID NLM: 8007166

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 16 02 2022
revised: 02 05 2022
accepted: 02 05 2022
pubmed: 1 6 2022
medline: 27 10 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

Asymptomatic faecal carriage of Clostridioides difficile has been widely evaluated, but its prevalence across a wide range of clinical departments and related risk factors are not well described. The objectives of the PORTADIFF study were to evaluate the prevalence and identifying risk factors leading to asymptomatic carriage of both toxigenic and non-toxigenic C. difficile. The PORTADIFF study was a 1-day prevalence study carried out in 10 different French hospitals. Adult patients, who agreed to participate, were included in this study and provided a fresh stool sample. C. difficile strains isolated from carriage were characterized by polymerase chain reaction (PCR) detection of tcdA, tcdB, cdtA and cdtB, and PCR ribotyping. In total, 721 patients were included in this study. The median age was 73 years (range 18-101 years) and the male/female ratio was 1.06. C. difficile (either toxigenic or non-toxigenic strains) was isolated from 79 (11%) patients; 42 (5.8%) strains were toxigenic. The prevalence rates of asymptomatic carriage ranged from 5% on surgical wards to 19% on long-term care wards. The main risk factors associated with asymptomatic carriage were antibiotic treatment within the preceding 3 months (81.8% vs 53.7%; P<0.01), hospitalization within the preceding 2 months (55.8% vs 33%; P<0.01), cumulative duration of hospital stay before study inclusion (mean 50.1 vs 34.5 days; P<0.047), and hospitalization on a ward with high global incidence of C. difficile infection. Eleven percent of hospitalized patients were asymptomatic carriers of toxigenic or non-toxigenic C. difficile, and may constitute a potential reservoir of C. difficile strains.

Sections du résumé

BACKGROUND BACKGROUND
Asymptomatic faecal carriage of Clostridioides difficile has been widely evaluated, but its prevalence across a wide range of clinical departments and related risk factors are not well described. The objectives of the PORTADIFF study were to evaluate the prevalence and identifying risk factors leading to asymptomatic carriage of both toxigenic and non-toxigenic C. difficile.
METHODS METHODS
The PORTADIFF study was a 1-day prevalence study carried out in 10 different French hospitals. Adult patients, who agreed to participate, were included in this study and provided a fresh stool sample. C. difficile strains isolated from carriage were characterized by polymerase chain reaction (PCR) detection of tcdA, tcdB, cdtA and cdtB, and PCR ribotyping.
RESULTS RESULTS
In total, 721 patients were included in this study. The median age was 73 years (range 18-101 years) and the male/female ratio was 1.06. C. difficile (either toxigenic or non-toxigenic strains) was isolated from 79 (11%) patients; 42 (5.8%) strains were toxigenic. The prevalence rates of asymptomatic carriage ranged from 5% on surgical wards to 19% on long-term care wards. The main risk factors associated with asymptomatic carriage were antibiotic treatment within the preceding 3 months (81.8% vs 53.7%; P<0.01), hospitalization within the preceding 2 months (55.8% vs 33%; P<0.01), cumulative duration of hospital stay before study inclusion (mean 50.1 vs 34.5 days; P<0.047), and hospitalization on a ward with high global incidence of C. difficile infection.
CONCLUSION CONCLUSIONS
Eleven percent of hospitalized patients were asymptomatic carriers of toxigenic or non-toxigenic C. difficile, and may constitute a potential reservoir of C. difficile strains.

Identifiants

pubmed: 35640734
pii: S0195-6701(22)00162-1
doi: 10.1016/j.jhin.2022.05.011
pii:
doi:

Substances chimiques

Bacterial Toxins 0
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

65-74

Investigateurs

C Hartmann (C)
A Kazhalawi (A)
S Lambert-Bordes (S)
S Bleunven (S)
J-P Bedos (JP)
A Greder-Belan (A)
S Rigaudea (S)
H Lecuyer (H)
A Jousset (A)
D Lebeaux (D)
B Levy (B)
C Rabate (C)
A Collignon (A)
J Batah (J)
V Francois (V)
G Sebbane (G)
P-L Woerther (PL)
G Loggia (G)
J Michon (J)
R Verdon (R)
D Samba (D)
J-B Méar (JB)
T Guillard (T)
Y Nguyen (Y)
F Banisadr (F)
A Delmer (A)
C Himberlin (C)
S Diallo (S)
I Furet (I)
B Achouri (B)
A Reksa (A)
S Jouveshomme (S)
E Menage (E)
F Philippart (F)
M Hadj-Abdeslam (M)
B Durand-Gasselin (B)
M Eveillard (M)
A Kouatchet (A)
A Schmidt (A)
C Salanoubat (C)
M-N Heurtaux (MN)
P Cronier (P)
A Foufa (A)

Informations de copyright

Copyright © 2022 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.

Auteurs

A Le Monnier (A)

Service de Microbiologie Clinique, Groupe Hospitalier Paris Saint-Joseph, Paris, France; Institut Micalis, UMR1319, Université Paris-Saclay, INRAe, AgroParisTech, Chatenay-Malabry, France.

T Candela (T)

Institut Micalis, UMR1319, Université Paris-Saclay, INRAe, AgroParisTech, Chatenay-Malabry, France.

A Mizrahi (A)

Service de Microbiologie Clinique, Groupe Hospitalier Paris Saint-Joseph, Paris, France; Institut Micalis, UMR1319, Université Paris-Saclay, INRAe, AgroParisTech, Chatenay-Malabry, France.

E Bille (E)

Laboratoire de Microbiologie, Hôpital Necker Enfants-malades, Paris, France.

N Bourgeois-Nicolaos (N)

Service de Bactériologie et Hygiène, APHP Université Paris-Saclay, Hôpital Antoine Béclère, Clamart, France.

V Cattoir (V)

Laboratoire de Microbiologie, CHU de Caen, Caen, France.

E Farfour (E)

Service de Biologie Clinique, Hôpital Foch, Suresnes, France.

I Grall (I)

Clinique de Champigny, Ramsay Générale de Santé, Champigny Sur Marne, France.

D Lecointe (D)

Service d'Hygiène, Prévention et Contrôle des Infections, Hôpital Sud-Francilien, Corbeil-Essonnes, France.

A Limelette (A)

Laboratoire de Microbiologie, CHU de Reims, Hôpital Robert Debré, Reims, France.

G Marcade (G)

Laboratoire Microbiologie-Hygiène, Hôpital Louis Mourier, Colombes, France.

I Poilane (I)

Laboratoire de Microbiologie, Hôpital Jean Verdier, Bondy, France.

P Poupy (P)

Laboratoire de Microbiologie, Centre Hospitalier de Versailles, Le Chesnay, France.

I Kansau (I)

Institut Micalis, UMR1319, Université Paris-Saclay, INRAe, AgroParisTech, Chatenay-Malabry, France; Service de Médecine Interne et Immunologie Clinique, Hôpital Antoine Béclère, Clamart, France.

J-R Zahar (JR)

Unité de Prévention du Risque Infectieux, CHU Angers, Angers, France.

B Pilmis (B)

Institut Micalis, UMR1319, Université Paris-Saclay, INRAe, AgroParisTech, Chatenay-Malabry, France; Équipe Mobile de Microbiologie Clinique, Groupe Hospitalier Paris Saint-Joseph, Paris, France. Electronic address: bpilmis@ghpsj.fr.

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Classifications MeSH