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1.
Pediatr Infect Dis J ; 8(2): 75-8, 1989 Feb.
Article in English | MEDLINE | ID: mdl-2649867

ABSTRACT

A 6-year multicenter therapeutic study was performed on 1100 children with brucellosis in order to compare several antibiotic combinations and duration of treatment. The patients were randomized to receive oral therapy with oxytetracycline, doxycycline, rifampin and trimethoprim-sulfamethoxazole (TMP/SMX) either alone or in combination with each other or combined with streptomycin or gentamicin injections. The patients were also randomized into three groups based on the duration of oral therapy: 500 patients were treated for 3 weeks; 350 for 5 weeks; and 250 for 8 weeks. When intramuscular aminoglycosides were used, streptomycin was given for 2 weeks and gentamicin for 5 days. In oral monotherapy oxytetracycline, doxycycline and rifampin showed comparable results with low relapse rates (less than or equal to 9%) and no statistically significant differences were found among 3-, 5- or 8-week durations of therapy. TMP/SMX alone showed an unacceptably high relapse rate (30%) with all durations of therapy. In combined oral therapy rifampin plus oxytetracycline, rifampin plus TMP/SMX and oxytetracycline plus TMP/SMX showed comparable results with low relapse rates ranging from 4 to 8% in patients receiving therapy for 3 or 5 weeks, no relapses occurred in patients treated for 8 weeks. When oral monotherapy was combined with either streptomycin or gentamicin, very few relapses were seen, irrespective of the duration of treatment.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Brucellosis/drug therapy , Drug Therapy, Combination/therapeutic use , Administration, Oral , Adolescent , Child , Child, Preschool , Doxycycline/administration & dosage , Drug Administration Schedule , Female , Humans , Infant , Infant, Newborn , Male , Multicenter Studies as Topic , Oxytetracycline/administration & dosage , Random Allocation , Rifampin/administration & dosage , Sulfamethoxazole/administration & dosage , Time Factors , Trimethoprim/administration & dosage
2.
Eur J Pediatr ; 148(4): 333-6, 1989 Jan.
Article in English | MEDLINE | ID: mdl-2651131

ABSTRACT

Congenital chloride diarrhoea was diagnosed in 16 Kuwaiti children over a 7 year period (1980-1986) with an estimated incidence of 7.6 per 100,000 live births. The mean age at diagnosis was 3.2 months (range 1 week to 5 months). There were 9 boys and 7 girls with a mean age of 3 years 10 months (range 10 months to 7 years). All children had a shortened gestational period, abdominal distension and chronic diarrhoea. The serum electrolytes in all patients prior to treatment showed hyponatraemia, hypokalaemia, hypochloraemia and metabolic alkalosis. The diagnosis was confirmed by a stool chloride content that exceeded the sum of faecal sodium and potassium. Fifteen patients survived and showed catch-up growth with adequate replacement therapy and 1 died with renal failure.


Subject(s)
Chlorides/blood , Developing Countries , Diarrhea, Infantile/blood , Feces/analysis , Infant, Premature, Diseases/blood , Aldosterone/blood , Angiotensin II/blood , Child , Child, Preschool , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Male , Renin/blood
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