TY - JOUR
T1 - Clostridioides difficile infection in paediatric patients with cancer and haematopoietic stem cell transplant recipients
AU - Haeusler, Gabrielle M.
AU - Lehrnbecher, Thomas
AU - Agyeman, Phillip K.A.
AU - Loves, Robyn
AU - Castagnola, Elio
AU - Groll, Andreas H.
AU - van de Wetering, Marianne
AU - Aftandilian, Catherine C.
AU - Phillips, Bob
AU - Chirra, Krishna M.
AU - Schneider, Christine
AU - Dupuis, Lee L.
AU - Sung, Lillian
N1 - Copyright © 2022 Elsevier Ltd. All rights reserved.
PY - 2022/8
Y1 - 2022/8
N2 - Background: Epidemiology of Clostridioides difficile infection (CDI) in paediatric cancer patients is uncertain. The primary objective was to describe the prevalence of CDI outcomes among paediatric patients receiving cancer treatments. Secondary objectives were to describe clinical features of CDI, propose a definition of severe CDI and to determine risk factors for CDI clinical outcomes. Methods: A multi-centre retrospective cohort study that included paediatric patients (1–18 years of age) receiving cancer treatments with CDI. Severe CDI definition was achieved by consensus. Univariable and multivariable regression was conducted to evaluate risk factors for CDI outcomes. Results: There were 627 eligible patients who experienced 721 CDI episodes. The prevalence of clinical cure was 82.9%, recurrence was 9.6%, global cure was 75.0% and repeated new CDI episode was 12.8%. The proposed definition of severe CDI was the presence of colitis, pneumatosis intestinalis, pseudomembranous colitis, ileus or surgery for CDI, occurring in 70 (9.7%) episodes. In univariable regression, initial oral metronidazole or initial oral vancomycin were not significantly associated with failure to achieve clinical cure or CDI recurrence. In multiple regression, oral metronidazole was significantly associated with higher odds (odds ratio (OR) 1.7, 95% confidence interval (CI) 1.0–2.7) and oral vancomycin was significantly associated with lower odds (OR 0.4, 95% CI 0.2–0.8) of repeated new episodes. Conclusion: The prevalence of clinical cure was 82.9% and recurrence was 9.6% in pediatric patients receiving cancer treatments. Severe CDI, as per our proposed definition, occurred in 9.7% episodes. Initial oral vancomycin was significantly associated with a reduction in repeated new CDI episodes.
AB - Background: Epidemiology of Clostridioides difficile infection (CDI) in paediatric cancer patients is uncertain. The primary objective was to describe the prevalence of CDI outcomes among paediatric patients receiving cancer treatments. Secondary objectives were to describe clinical features of CDI, propose a definition of severe CDI and to determine risk factors for CDI clinical outcomes. Methods: A multi-centre retrospective cohort study that included paediatric patients (1–18 years of age) receiving cancer treatments with CDI. Severe CDI definition was achieved by consensus. Univariable and multivariable regression was conducted to evaluate risk factors for CDI outcomes. Results: There were 627 eligible patients who experienced 721 CDI episodes. The prevalence of clinical cure was 82.9%, recurrence was 9.6%, global cure was 75.0% and repeated new CDI episode was 12.8%. The proposed definition of severe CDI was the presence of colitis, pneumatosis intestinalis, pseudomembranous colitis, ileus or surgery for CDI, occurring in 70 (9.7%) episodes. In univariable regression, initial oral metronidazole or initial oral vancomycin were not significantly associated with failure to achieve clinical cure or CDI recurrence. In multiple regression, oral metronidazole was significantly associated with higher odds (odds ratio (OR) 1.7, 95% confidence interval (CI) 1.0–2.7) and oral vancomycin was significantly associated with lower odds (OR 0.4, 95% CI 0.2–0.8) of repeated new episodes. Conclusion: The prevalence of clinical cure was 82.9% and recurrence was 9.6% in pediatric patients receiving cancer treatments. Severe CDI, as per our proposed definition, occurred in 9.7% episodes. Initial oral vancomycin was significantly associated with a reduction in repeated new CDI episodes.
KW - Clostridioides difficile infection
KW - Haematopoietic stem cell transplantation
KW - Oncology
KW - Pediatric
KW - Risk factors
KW - Recurrence
KW - Hematopoietic Stem Cell Transplantation/adverse effects
KW - Humans
KW - Clostridioides difficile
KW - Clostridium Infections/drug therapy
KW - Retrospective Studies
KW - Metronidazole
KW - Vancomycin/adverse effects
KW - Child
KW - Neoplasms/chemically induced
KW - Anti-Bacterial Agents/adverse effects
UR - http://www.scopus.com/inward/record.url?scp=85131718454&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2022.05.001
DO - 10.1016/j.ejca.2022.05.001
M3 - Article
C2 - 35696884
AN - SCOPUS:85131718454
SN - 0959-8049
VL - 171
SP - 1
EP - 9
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -