Related Experiment Video
Updated: Jun 20, 2026

Studying Cryptosporidium Infection in 3D Tissue-derived Human Organoid Culture Systems by Microinjection
Published on: September 14, 2019
Cryptosporidiosis in paediatric renal transplantation
Flavio Bandin1, Theresa Kwon, Marie-Denise Linas
1Department of Paediatric Nephrology, Children's Hospital, Centre de Référence du Sud Ouest des Maladies Rénales Rares, Toulouse, France.
Insights
Infectious diarrhea is common in pediatric transplant patients, often linked to immunosuppressants like mycophenolic acid. Cryptosporidium is a significant cause, necessitating early screening and specific treatment with nitazoxanide.
Area of Science:
- Pediatric Nephrology
- Transplant Infectious Diseases
- Gastroenterology
Background:
- Diarrhea in transplant recipients can stem from infections or immunosuppressive drugs.
- Combined immunosuppressive therapy increases the risk of infectious diarrhea.
Observation:
- A retrospective study analyzed 64 diarrhea episodes in 199 pediatric renal transplant recipients over 3 years.
- Mycophenolic acid (MPA) was associated with diarrhea in 19% of patients, often attributable to the drug.
- Infectious agents caused 38 episodes, with Cryptosporidium being a notable pathogen.
Findings:
- Cryptosporidium accounted for 18% of infectious diarrhea and 11% of all diarrhea cases, affecting 3.5% of newly transplanted patients.
- Patients with Cryptosporidium experienced profuse, persistent diarrhea and acute renal failure.
- Modifying MPA dosage or switching immunosuppressants did not lead to graft rejection.
Implications:
- Screening for Cryptosporidium oocysts in stool is recommended for early diagnosis of infectious diarrhea.
- Early, specific treatment with nitazoxanide and supportive rehydration are crucial for managing Cryptosporidium infections.
- These findings support proactive management strategies for diarrhea in pediatric transplant populations.
Abstract:
Diarrhoea in transplantation may be secondary to infectious agents and immunosuppressive drugs. The use of combined immunosuppressive drugs increases the incidence of infectious diarrhoea. We retrospectively collected all diarrhoea episodes during a 3-year period in 199 pediatric renal transplant recipients, including 47 patients receiving a kidney transplant during this period. We diagnosed 64 diarrhoea episodes (32% of the patients, 10.7% per year). Fourteen diarrhoea episodes could be attributed to the immunosuppressive treatment, and 12 remained without diagnosis. Nineteen patients (<10%) receiving mycophenolic acid (MPA) developed diarrhoea, 14 of whom had episodes attributable to the immunosuppressive treatment. Reducing the MPA dose or switching to another immunosuppressant did not induce graft rejection, if at all, for at least 6 months. Thirty-eight diarrhoea episodes were caused by infectious agents: viruses in 16 patients, bacterial agents in ten patients, Candida albicans in four cases and parasitic agents in eight cases (Giardia lambdia in one patient and Cryptosporidium in seven patients). In our cohort, Cryptosporidium was responsible for 18% of the infectious diarrhoea and 11% of all causes of diarrhoea, and it affected 3.5% of the newly transplanted patients during the 3-year study period. The clinical presentation of the disease was profuse and persistent diarrhoea with acute renal failure in all patients. We propose that oocysts be screened for in the stool during the early stages of tests for determining the origin of infectious diarrhoea. Disease treatment requires early specific treatment (nitazoxanide) for extended periods of time in conjunction with supportive rehydration.
More Related Videos
Related Concept Videos
Kidney Transplant II: Surgical Procedure
Kidney Transplant I: Introduction
Pharmacokinetics in Pediatric Patients: Drug Excretion
Cryptococcal Meningitis
Kidney Transplant III: Nursing Management
Fungal Phylum Microsporidia
