Clostridium difficile infection in the pediatric transplant patient

Maribeth R Nicholson1, Christy L Osgood2, Sari A Acra1

  • 1Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Vanderbilt University School of Medicine, Nashville, TN, USA.

Pediatric Transplantation
|September 26, 2015
PubMed

Insights

Clostridium difficile infection (CDI) is increasing in children, especially those with cancer or a transplant history. Further research is needed to understand risk factors and treatment efficacy in this vulnerable group.

Area of Science:

  • Infectious Diseases
  • Pediatric Oncology
  • Transplant Medicine

Background:

  • Clostridium difficile infection (CDI) incidence is rising in pediatric and adult populations across healthcare settings.
  • Children with cancer or a history of hematopoietic stem cell transplant (HSCT) or solid organ transplant (SOT) face elevated risks for primary, recurrent, and severe CDI.
  • Current understanding of specific risk factors for CDI in pediatric transplant recipients remains limited.

Purpose of the Study:

  • To investigate the risk factors associated with CDI in pediatric transplant patients.
  • To clarify the diagnostic challenges in differentiating colonization from symptomatic CDI in immunocompromised children.
  • To evaluate the potential safety and efficacy of fecal microbiota transplantation (FMT) for severe or recurrent CDI in this population.

Main Methods:

  • This study reviews existing literature and clinical observations regarding CDI in pediatric cancer and transplant patients.
  • Analysis focuses on identifying predisposing factors, clinical presentations, and outcomes.
  • The current evidence on fecal transplantation as a therapeutic option is assessed.

Main Results:

  • Children with cancer and a transplant history exhibit higher colonization rates with Clostridium difficile.
  • Distinguishing between asymptomatic colonization and active CDI presents a significant clinical challenge.
  • Preliminary data suggest fecal transplantation may be safe and effective for severe/recurrent CDI in this cohort.

Conclusions:

  • Pediatric cancer and transplant patients are a high-risk group for Clostridium difficile infection.
  • Further dedicated research is essential to elucidate specific risk factors and optimize management strategies.
  • Fecal transplantation warrants more rigorous investigation as a therapeutic option for severe CDI in immunosuppressed pediatric transplant recipients.

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