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1.
J Pediatr ; 128(2): 203-7, 1996 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-8636812

RESUMEN

OBJECTIVE: To evaluate the frequency of small-bowel bacterial overgrowth (SBBO) as a cause of chronic digestive symptoms in a large cohort of children, using the glucose breath hydrogen test (BHT). DESIGN: Patients were 53 children (aged 2 months to 12 years) with chronic diarrhea, abdominal pain, or both. Diagnosis of SBBO was defined with a BHT by a change in H2 concentration of 10 ppm H2 or more in expired air after an oral glucose load. Patients with a positive BHT result were included in group 1 and treated with a combination of colistin and metronidazole for 10 days; a second BHT was performed 1 month later. Group 2 comprised patients with a negative BHT result. Group 3 (n = 15) was a control group of healthy subjects, and group 4 (n = 6) a comparison group of subjects with bacteriologically documented SBBO. RESULTS: Eighteen patients (34%) had a positive BHT result and 35 a negative result. The BHT results were comparable in groups 1 and 4 and in groups 2 and 3, respectively. Fasting H2 levels were higher in group 1 than in groups 2 (p < 0.001) and 3 (p < 0.01). In group 1, children were younger than in group 2 (1 +/- 1 year vs 3.9 +/- 3 years; p < 0.001) and diarrhea was frequent (83%), but 17% of patients had abdominal pain alone. Fetid stools (p < 0.01), mucus in stools (p < 0.01), and flatulence (p < 0.05) were more frequent in group 1 than in group 2. Antibiotic treatment of children in group 1 led to a rapid disappearance of symptoms and normalization of BHT results. CONCLUSION: SBBO appears to be a frequent cause of chronic digestive symptoms in children, especially before the age of 2 years. The BHT provides a simple and noninvasive method of detecting it. The recognition of SBBO in children leads to effective treatment.


Asunto(s)
Dolor Abdominal/microbiología , Clostridioides difficile/aislamiento & purificación , Diarrea/microbiología , Giardia lamblia/aislamiento & purificación , Intestino Delgado/microbiología , Staphylococcus aureus/aislamiento & purificación , Dolor Abdominal/diagnóstico , Dolor Abdominal/epidemiología , Animales , Antibacterianos/uso terapéutico , Pruebas Respiratorias , Niño , Preescolar , Enfermedad Crónica , Comorbilidad , Diarrea/tratamiento farmacológico , Diarrea/epidemiología , Heces/microbiología , Femenino , Humanos , Lactante , Masculino
2.
J Pediatr ; 121(1): 12-6, 1992 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-1625069

RESUMEN

Twenty-nine children with typical Schönlein-Henoch purpura (SHP) were tested at the initial phase of the disease for respiratory function. Of the 29 patients, 28 had a decrease of lung transfer for carbon monoxide (TLCO) as measured by a steady-state method. Lung volumes and blood gas values were normal; slight radiologic signs of interstitial lung involvement were observed in 18 of 26 patients. There was a decrease in TLCO to 56.8% of normal values for height and gender and to 58.5% when normal values were volume-adjusted to functional residual capacity. In 19 of 25 patients, TLCO measurements were performed at 3-month intervals during follow-up. In all cases, normalization of TLCO values was observed only after complete clinical recovery from SHP. All children with persisting symptoms, even limited to microscopic hematuria or slight proteinuria, had low TLCO values. In one patient low TLCO during follow-up preceded a late relapse of SHP in the form of acute nephritic disease with characteristic IgA deposits on renal biopsy. We conclude that low TLCO in SHP is probably related to alteration of the alveolar-capillary membrane by circulating immune complexes. This noninvasive technique may be useful in diagnosis, and during the follow-up of the disease as an early indicator of reactivation.


Asunto(s)
Vasculitis por IgA/fisiopatología , Pulmón/metabolismo , Capacidad de Difusión Pulmonar/fisiología , Monóxido de Carbono/metabolismo , Niño , Preescolar , Femenino , Estudios de Seguimiento , Capacidad Residual Funcional , Hematuria/orina , Hemoglobinas/análisis , Humanos , Vasculitis por IgA/sangre , Vasculitis por IgA/metabolismo , Vasculitis por IgA/orina , Masculino , Oxígeno/sangre , Proteinuria/orina , Capacidad Vital
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