Our aim was to assess the hypothesis that a high-dose regimen of ibuprofen is more effective than the standarddose regimen in closing patent ductus arteriosus (PDA) without increasing adverse effects. Infants of gestational age <29 weeks, with respiratory distress syndrome (RDS) and echocardiographic evidence of significant PDA at 12–24 h of life, were randomized to receive a standard (10-5-5 mg/kg/day) or high-dose (20-10-10 mg/kg/day) course of ibuprofen. We studied 70 infants, 35 of whom received the standard dose of ibuprofen and the other 35 the high dose. Of the infants treated with the standard-dose regimen, 37% had persistent PDA as compared with 14% of those treated with the highdose regimen (P = 0.03). No differences in the occurrence of adverse effects were observed between the two groups. The high-dose ibuprofen regimen is more effective than the standard-dose regimen in closing PDA in preterm infants <29 weeks of gestation without increasing the adverse effect rate.

High-Dose Ibuprofen for Patent Ductus Arteriosus in Extremely Preterm Infants: A Randomized Controlled Study / C. Dani; V. Vangi; G. Bertini; S. Pratesi; I. Lori I; F. Favelli; R. CiutI; A. Bandinelli; C. Martano; P. Murru; H. Messner; F. Schena ; F. Mosca. - In: CLINICAL PHARMACOLOGY & THERAPEUTICS. - ISSN 0009-9236. - STAMPA. - 91:(2012), pp. 590-596.

High-Dose Ibuprofen for Patent Ductus Arteriosus in Extremely Preterm Infants: A Randomized Controlled Study.

DANI, CARLO;S. Pratesi;
2012

Abstract

Our aim was to assess the hypothesis that a high-dose regimen of ibuprofen is more effective than the standarddose regimen in closing patent ductus arteriosus (PDA) without increasing adverse effects. Infants of gestational age <29 weeks, with respiratory distress syndrome (RDS) and echocardiographic evidence of significant PDA at 12–24 h of life, were randomized to receive a standard (10-5-5 mg/kg/day) or high-dose (20-10-10 mg/kg/day) course of ibuprofen. We studied 70 infants, 35 of whom received the standard dose of ibuprofen and the other 35 the high dose. Of the infants treated with the standard-dose regimen, 37% had persistent PDA as compared with 14% of those treated with the highdose regimen (P = 0.03). No differences in the occurrence of adverse effects were observed between the two groups. The high-dose ibuprofen regimen is more effective than the standard-dose regimen in closing PDA in preterm infants <29 weeks of gestation without increasing the adverse effect rate.
2012
91
590
596
C. Dani; V. Vangi; G. Bertini; S. Pratesi; I. Lori I; F. Favelli; R. CiutI; A. Bandinelli; C. Martano; P. Murru; H. Messner; F. Schena ; F. Mosca
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/605517
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