In this cohort study, 62 children aged 1 to 18 years with functional constipation, referred to Ekbatan Hospital in Hamedan, Iran (during 2024), were studied. First, a blood sample from the basilic vein was obtained from all patients, and after centrifugation, the serum level of D(OH)25 was measured by the Enzyme-Linked Fluorescent Assay method (Biomerieux company kit made in France was used).
Based on vitamin D levels, patients were divided into two equal groups: Patients with vitamin D deficiency (study group) and patients without vitamin D deficiency (control group). Then, patients in both groups underwent constipation treatment, and the results of the treatment were evaluated and compared at the end of the second week, the first month, and the second month of treatment.
A vitamin D level equal to or higher than 30 ng/mL was considered normal. Treatment of functional constipation included dietary changes and consumption of Pidrolox powder without electrolytes (manufactured by Sepidage Company) with a dose of 0.7 g/kg twice a day (maximum dose 13.8 - 40 g per day). For patients with fecal impaction, a bisacodyl suppository of 5 mg per day was used for 3 to 5 days.
Diagnosis of fecal impaction was conducted through abdominal examination, digital rectal examination, and, if necessary, simple abdominal radiography. Inclusion criteria included age 1 to 18 years, functional constipation diagnosed by a pediatric gastroenterologist based on the Rome IV criteria (
14), and informed consent of the patient or parents to participate in the study. Patients with organic constipation and those taking medications that could alter bowel movements were excluded from the study.
In this study, the descriptive statistics section utilized mean and standard deviation to describe and report quantitative variables, while frequency and percentage were used for qualitative variables. In the analytical statistics section, demographic and basic characteristics were first compared between the two groups. An independent t-test was used to examine quantitative variables in the two groups. A chi-square test was used to compare qualitative variables in the two groups. To check the status of the response to the treatment at the investigated times, the frequency of recovery in the two groups was compared using the chi-square test.
Data analysis was conducted using SPSS version 20 software, and the significance level was considered less than 0.05 in all cases.
The Ethics Committee of the Hamadan University of Medical Sciences approved this study with the ethics code, the Deputy of Research and Technology
IR.UMSHA.REC.1402.060.