carnitine defeciensy, constipatin\on
Conditions
Interventions
Supplementation with 10-50 mg/kg/day carnitine (P<
0.001). No other changes of medication were made during the supplementation period.
Sponsors
Department of Pediatrics, Hirakata City Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with severe motor and intellectual disabilities were defined as having an inability to move by themselves and IQ <35
Exclusion criteria
Exclusion criteria: The patients with infection or prescribed with antibiotics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First, we examined the correlation between level of free carnitine and severity of constipation. Second, we compared the constipation group with the non-constipation group in terms of age, sex, BMI, bed rest period (years), use of anti-epileptic drugs, use of valproate sodium, use of enteral nutrition, recurrent pulmonary infection (more than twice a year), presence of pressure ulcer, and results of blood tests for nutritional assessment (including serum levels of albumin, pre-albumin, total cholesterol, free carnitine, folic acid, and the trace elements Cu, Fe, Se, and Zn). Blood samples were collected in all cases during times when there were no observed inflammation reactions and no prescribed antibiotics. Carnitine levels also were obtained from patients without motor and intellectual disabilities who had severe chronic constipation requiring disimpaction with an enema on a daily basis. Third, we compared the frequency of defecation and the form of feces before and after therapeutic supplementation with carnitine. | — |
Countries
Japan
Contacts
Public ContactShinya Murata
Hirakata City Hospital, Department of Pediatrics,
Outcome results
None listed