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1.
Paediatr Int Child Health ; 36(1): 39-44, 2016 Feb.
Article in English | MEDLINE | ID: mdl-25496416

ABSTRACT

BACKGROUND: There are no large epidemiological studies of Clostridium difficile-associated disease (CDAD) in hospitalised children. AIM: To describe the frequency, demography, clinical features and outcome of nosocomial CDAD in children admitted to Assiut University Children's Hospital, Egypt. PATIENTS AND METHODS: In this descriptive cross-sectional study, 72 children developed nosocomial diarrhoea between April 2010 and March 2011. A medical history, clinical assessment and culture for Clostridium difficile and direct toxin detection from stool samples by enzyme immuno-assay were undertaken in all patients. RESULTS: CDAD was diagnosed in 17 (23·6%) patients. Those aged ≤12 months were the most commonly affected (eight, 47%). The main cause of admission was respiratory disorders (eight, 47% of cases), followed by surgical problems (three, 17·7%). Ten patients (58·8%) had severe symptoms. There were no statistically significant differences between any of the demographic or laboratory data for children with CDAD and children with other causes of nosocomial diarrhoea. None of the patients developed complications. Seven children with CDAD (41·2%) had recurrence. CONCLUSION: CDAD is an important cause of nosocomial diarrhoea in children in Assiut University Children's Hospital. Established guidelines should be followed in all hospitals to minimise exposure to the pathogen. Physicians can do much to reduce the risk of a severe outcome in children by early identification and rapid management. Further research should be undertaken to identify the risk factors for recurrence.


Subject(s)
Clostridioides difficile/isolation & purification , Cross Infection/epidemiology , Diarrhea/epidemiology , Enterocolitis, Pseudomembranous/epidemiology , Child, Preschool , Cross Infection/microbiology , Cross-Sectional Studies , Diarrhea/microbiology , Egypt/epidemiology , Enterocolitis, Pseudomembranous/microbiology , Feces/microbiology , Female , Hospitals, Pediatric , Hospitals, University/statistics & numerical data , Humans , Infant , Infant, Newborn , Male
2.
Arab J Gastroenterol ; 12(4): 178-83, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22305497

ABSTRACT

BACKGROUND AND STUDY AIMS: Auto-immune hepatitis (AIH) in children is a rare chronic progressive liver disorder. It is characterised serologically by high aminotransferase levels, elevated immunoglobulin G (IgG) and the presence of autoantibodies. AIH is divided into two types according to the autoantibody profile. This study aims to assess frequency, clinical manifestations, biochemical features and outcome of AIH in children attending Assuit University Hospitals in Upper Egypt with acute icteric hepatitis and seronegative viral markers (anti-hepatitis A virus (HAV) IgM, HbsAg, anti-hepatitis C virus (anti-HCV) Ab). PATIENTS AND METHODS: The study includes 34 children with AIH, diagnosed on the basis of the International Scoring Criteria of Auto-immune Hepatitis, recruited from Assuit University Hospitals, during the period from January 2005 to December 2009. All patients received prednisolone 2mgkg(-1)day(-1). Follow-up was done for 1year. RESULTS: Among 34 children diagnosed as AIH, 24 were females (70.5%) and 10 were males (29.5%). Jaundice represented the most consistent finding in all patients. According to the autoantibody profile, 25 children were classified as type 1 and nine children were classified as type 2. Corticosteroid therapy was started. Complete remission was observed in 67.6% of patients and partial remission in 17.6%. There was no significant statistical difference in clinical and biochemical features of AIH in patients regarding the response to treatment. Mild side effects of steroid therapy were encountered in 48.2% of patients. After complete withdrawal of corticosteroids, six patients (20.7%) developed relapse. CONCLUSION: AIH type 1 was the main form of AIH in children referred to Assiut University Hospitals. Girls were more affected than boys. AIH type 1 exhibited a more active, ongoing immunologic process. Steroid alone can be used successfully in most cases. Children with AIH type 2 had a higher frequency of relapse after corticosteroid withdrawal. Further studies on a larger number of cases and long-term follow-up are recommended.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Hepatitis, Autoimmune/blood , Hepatitis, Autoimmune/drug therapy , Prednisolone/therapeutic use , Adolescent , Anti-Inflammatory Agents/adverse effects , Autoantibodies/blood , Child , Child, Preschool , Egypt , Female , Hepatitis, Autoimmune/diagnosis , Humans , Immunoglobulin G/blood , Jaundice/etiology , Male , Prednisolone/adverse effects , Recurrence , Treatment Outcome
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