[Risk factors of Clostridium difficile-associated diarrhea in children]

Shu Guo1, Xi-wei Xu, Fang Dong

  • 1Department of Gastroenterology, Beijing Children's Hospital, Beijing, China.

Zhonghua Yi Xue Za Zhi
|September 5, 2012
PubMed

Insights

Nonsteroidal anti-inflammatory drugs (NSAIDs), elevated C-reactive protein (CRP), and abnormal white blood cell (WBC) counts are significant risk factors for Clostridium difficile-associated diarrhea (CDAD) in children. These findings aid in identifying children at higher risk for this infection.

Area of Science:

  • Pediatric Infectious Diseases
  • Gastroenterology
  • Microbiology

Background:

  • Clostridium difficile-associated diarrhea (CDAD) is a significant cause of healthcare-associated infections in children.
  • Identifying risk factors for CDAD is crucial for prevention and timely treatment.

Purpose of the Study:

  • To investigate the risk factors associated with Clostridium difficile-associated diarrhea (CDAD) in hospitalized children.
  • To identify independent predictors of CDAD in a pediatric population.

Main Methods:

  • A case-control study was conducted involving hospitalized diarrheal patients under 18 years old.
  • Patients were tested for Clostridium difficile, with cases confirmed by PCR for tcdA and/or tcdB genes.
  • Multivariate logistic regression analysis was used to identify independent predictors of CDAD, considering factors like prior hospitalization, medication use, C-reactive protein (CRP), and white blood cell (WBC) count.

Main Results:

  • Out of 93 PCR tests, 35 were positive for Clostridium difficile.
  • Multivariate analysis identified prior hospitalization (OR = 0.002), elevated CRP (OR = 3.465), nonsteroidal anti-inflammatory drug (NSAID) use (OR = 13.950), and elevated WBC count (OR = 8.063) as significant predictors of CDAD.
  • Healthcare facility-associated-CDAD (HCFA-CDAD) was observed in 30 patients.

Conclusions:

  • The use of NSAIDs, elevated CRP levels, and abnormal WBC counts are significantly associated with CDAD in children.
  • These factors can aid in the early identification and management of pediatric CDAD.
Abstract

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