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1.
Braz. j. med. biol. res ; 37(11): 1623-1630, Nov. 2004. ilus, tab
Artículo en Inglés | LILACS | ID: lil-385881

RESUMEN

The objective of the present study was to assess esophageal motor function in 21 children (7.5 ± 2.9 years) with caustic strictures. Esophageal manometry was performed using a water-infusion system interfaced with a polygraph and displayed on a computer screen. The data were compared with those obtained from 9 healthy children. Radionuclide transit was determined by studying deglutition of a single bolus of 99mTc pertechnetate in 10 ml of water. Non-peristaltic low-amplitude and long-duration waves were the most common findings detected in patients with strictures longer than 20 percent of esophageal length (N = 11). Compared with the control group, these patients presented lower mean amplitude and longer mean duration of waves (24.4 ± 11.2 vs 97.9 ± 23.7 mmHg, P < 0.05, and 6.7 ± 2.4 vs 1.6 ± 0.1 s, P < 0.05, respectively). Six patients presented low-amplitude waves just below the constricted site. Ten children presented delayed esophageal transit. There was an association between dysphagia and abnormalities on manometry (P = 0.02) and between symptoms and scintigraphy data (P = 0.01). Dysphagia in caustic strictures is due to esophageal motility abnormalities, which are closely related to the scarred segment.


Asunto(s)
Humanos , Preescolar , Niño , Adolescente , Quemaduras Químicas/fisiopatología , Trastornos de la Motilidad Esofágica/inducido químicamente , Estenosis Esofágica/inducido químicamente , Hidróxido de Sodio/toxicidad , Quemaduras Químicas/etiología , Trastornos de la Motilidad Esofágica/fisiopatología , Trastornos de la Motilidad Esofágica , Estenosis Esofágica/fisiopatología , Estenosis Esofágica , Manometría/métodos , Índice de Severidad de la Enfermedad
2.
Braz. j. med. biol. res ; 36(10): 1391-1396, Oct. 2003. ilus, tab
Artículo en Inglés | LILACS | ID: lil-346500

RESUMEN

The efficacy of erythromycin was assessed in the treatment of 14 children aged 4 to 13 years with refractory chronic constipation, and presenting megarectum and fecal impaction. A double-blind, placebo- controlled, crossover study was conducted at the Pediatric Gastroenterology Outpatient Clinic of the University Hospital. The patients were randomized to receive placebo for 4 weeks followed by erythromycin estolate, 20 mg kg-1 day-1, divided into four oral doses for another 4 weeks, or vice versa. Patient outcome was assessed according to a clinical score from 12 (most severe clinical condition) to 0 (complete recovery). At enrollment in the study and on the occasion of follow-up medical visits at two-week intervals, patient score and laxative requirements were recorded. During the first 30 days, the mean ± SD clinical score for the erythromycin group (N = 6) decreased from 8.2 ± 2.3 to 2.2 ± 1.0 while the score for the placebo group (N = 8) decreased from 7.8 ± 2.1 to 2.9 ± 2.8. During the second crossover phase, the score for patients on erythromycin ranged from 2.9 ± 2.8 to 2.4 ± 2.1 and the score for the patients on placebo worsened from 2.2 ± 1.0 to 4.3 ± 2.3. There was a significant improvement in score when patients were on erythromycin (P < 0.01). Mean laxative requirement was lower when patients ingested erythromycin (P < 0.05). No erythromycin-related side effects occurred. Erythromycin was useful in this group of severely constipated children. A larger trial is needed to fully ascertain the prokinetic efficacy of this drug as an adjunct in the treatment of severe constipation in children


Asunto(s)
Preescolar , Adolescente , Humanos , Niño , Estreñimiento , Estolato de Eritromicina , Fármacos Gastrointestinales , Enfermedad Crónica , Estudios Cruzados , Estudios Transversales , Método Doble Ciego , Estudios de Seguimiento , Índice de Severidad de la Enfermedad
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