Clostridioides difficile infection in immunocompromised hospitalized patients is associated with a high recurrence rate.
Aged
Aged, 80 and over
Antibodies, Monoclonal
/ therapeutic use
Broadly Neutralizing Antibodies
/ therapeutic use
Clostridioides difficile
/ classification
Clostridium Infections
/ drug therapy
Female
Fidaxomicin
/ therapeutic use
Hospitalization
Humans
Immunocompromised Host
Male
Middle Aged
Multivariate Analysis
Odds Ratio
Recurrence
Risk Factors
Vancomycin
/ therapeutic use
Chemotherapy
Clostridioides difficile
Immunocompromised
Recurrence
Transplantations
Journal
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933
Informations de publication
Date de publication:
Jan 2020
Jan 2020
Historique:
received:
29
08
2019
revised:
20
10
2019
accepted:
22
10
2019
pubmed:
2
11
2019
medline:
24
3
2020
entrez:
2
11
2019
Statut:
ppublish
Résumé
Clostridioides difficile infection (CDI) may pose a serious threat to immunocompromised patients (IMC). Herein, we evaluated the clinical outcomes of IMC patients with CDI. All consecutive hospitalized patients between January 1, 2013 and December 31, 2018 with laboratory confirmed CDI were included in the study. Subjects were divided into two groups: IMC patients and controls. Primary outcome was the recurrence rate of CDI (rCDI) at 30 and 90 days after the first CDI episode. Secondary outcomes included 30 and 90 day all-cause mortality, length of hospital stay (LOS) and readmission rates. A multivariate analysis adjusted other risk factors for recurrence. An analysis of IMC patient subgroups (based on type of IMC conditions) was also performed. Results are reported as odds ratios (OR) with a 95% confidence interval (95% CI). A total of 573 patients were included, amongst them 149 IMC patients (36 solid organ transplants, 38 undergoing chemotherapy, 62 haematological conditions, 13 receiving high dose prednisone) and 424 controls. IMC patients were younger, independent and exhibited less significant comorbidities. On multivariable analysis, the rate of rCDI was significantly higher in IMC patients (OR 2.7, 95% CI 1.6-5). rCDI was also associated with vancomycin therapy, haemodialysis and previous hospitalizations. Mortality, LOS, CDI complications and rehospitalization rates were similar in both. IMC patients with CDI have an increased risk of 90 days rCDI. Vancomycin treatment for CDI endangers recurrence in IMC patients. Further research should explore other therapies for IMC patients with CDI with alternative agents such as Fidaxomicin and Bezlotoxumab.
Identifiants
pubmed: 31672656
pii: S1201-9712(19)30421-7
doi: 10.1016/j.ijid.2019.10.028
pii:
doi:
Substances chimiques
Antibodies, Monoclonal
0
Broadly Neutralizing Antibodies
0
bezlotoxumab
4H5YMK1H2E
Vancomycin
6Q205EH1VU
Fidaxomicin
Z5N076G8YQ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
237-242Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.