Affiliation:
1. Department of Pediatric Surgery, Uppsala University
Children's Hospital, S-751 85 Uppsala, Sweden
Abstract
Twenty-four adolescents, mean age 13.5 years, with primary nocturnal enuresis (PNE), were studied to evaluate the efficacy of long-term oral desmopressin use. Reduction in mean number of wet nights per week was the criterion for response. Results showed that during 12-week treatment Period I, 48% were full responders (≤1 wet night/wk); 22% were intermediate responders (2 to 3 wet nights/wk); and 30% were nonresponders (>3 wet nights/wk). During 12-week treatment Period II, 53% were full responders, 23.5% were intermediate responders, and 23.5% were nonresponders. Despite a high relapse rate (50% after Period I, 56% after Period II), 17 patients (71%) were completely dry 2 years posttreatment, suggesting a possible curative effect of oral desmopressin. It was concluded that oral desmopressin is comparable to the intranasal formulation, with a good, long-term therapeutic effect in adolescents with PNE.
Subject
Pediatrics, Perinatology and Child Health
Cited by
8 articles.
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1. NHG-Standaard Enuresis nocturna;NHG- Standaarden voor de huisarts 2011;2011
2. NHG-Standaard Enuresis nocturna;NHG-Standaarden voor de huisarts 2009;2009
3. The Canadian Enuresis Study and Evaluation Short- and Long-term Safety and Efficacy of an Oral Desmopressin Preparation;Scandinavian Journal of Urology and Nephrology;2003-01-01
4. Desmopressin for nocturnal enuresis in children;Cochrane Database of Systematic Reviews;2002-07-22
5. Disorders of Elimination;Handbook of Developmental Psychopathology;2000