TY - JOUR
T1 - The adverse effects of oral desmopressin lyophilisate (MELT): personal experience on enuretic children
AU - Ferrara, Pietro
AU - Franceschini, Giulia
AU - Mercurio, Serena
AU - Del Vescovo, Ester
AU - Ianniello, Francesca
AU - Petitti, Tommasangelo
PY - 2018
Y1 - 2018
N2 - Objective: The aim of this study was to evaluate adverse effects of oral desmopressin lyophilisate (MELT)
in enuretic children.
Material and methods: We enrolled 260 children with nocturnal enuresis (NE) referred to the Pediatric
Service, ‘Campus Bio-Medico’ University of Rome, from April 2014 to April 2017 in the study, of these 23
were excluded. The study was characterized by 2 phases. During Phase 1 a careful patient’s medical history
was obtained and physical examination was performed. After 3 months of treatment with MELT (Minirin/
DDAVP®) at the dose of 120 mcg a day, a micturition diary was kept, adherence to therapy and any possible
adverse effects were checked during the Phase 2. The study was carried out in compliance with the Helsinki
Declaration.
Results: Among 237 patients included in the study 11 male and 6 female (n=17; 7.2%) patients with a mean
age 10.06±2.49 years, reported 22 adverse effects, with an absolute risk of 7.17%. In particular, 5 neurological
symptoms, 3 gastrointestinal effects, 4 sleep disturbances, 8 psycho-behavioral disorders, 2 symptoms
of fatigue were reported.
Conclusion: In our study MELT with its higher bioavailability guaranteed lower frequency of adverse effects
which resolved spontaneously and rapidly. The MELT formulation actually represents the first line and
safe treatment for the NE.
AB - Objective: The aim of this study was to evaluate adverse effects of oral desmopressin lyophilisate (MELT)
in enuretic children.
Material and methods: We enrolled 260 children with nocturnal enuresis (NE) referred to the Pediatric
Service, ‘Campus Bio-Medico’ University of Rome, from April 2014 to April 2017 in the study, of these 23
were excluded. The study was characterized by 2 phases. During Phase 1 a careful patient’s medical history
was obtained and physical examination was performed. After 3 months of treatment with MELT (Minirin/
DDAVP®) at the dose of 120 mcg a day, a micturition diary was kept, adherence to therapy and any possible
adverse effects were checked during the Phase 2. The study was carried out in compliance with the Helsinki
Declaration.
Results: Among 237 patients included in the study 11 male and 6 female (n=17; 7.2%) patients with a mean
age 10.06±2.49 years, reported 22 adverse effects, with an absolute risk of 7.17%. In particular, 5 neurological
symptoms, 3 gastrointestinal effects, 4 sleep disturbances, 8 psycho-behavioral disorders, 2 symptoms
of fatigue were reported.
Conclusion: In our study MELT with its higher bioavailability guaranteed lower frequency of adverse effects
which resolved spontaneously and rapidly. The MELT formulation actually represents the first line and
safe treatment for the NE.
KW - Adverse effects
KW - desmopressin
KW - enuresis.
KW - Adverse effects
KW - desmopressin
KW - enuresis.
UR - http://hdl.handle.net/10807/111664
U2 - 10.5152/tud.2018.03285
DO - 10.5152/tud.2018.03285
M3 - Article
SN - 2149-3235
VL - 44
SP - 51
EP - 55
JO - Turkish Journal of Urology
JF - Turkish Journal of Urology
ER -