Effect of bosentan therapy in persistent pulmonary hypertension of the newborn

被引:30
作者
Maneenil, Gunlawadee [1 ]
Thatrimontrichai, Anucha [1 ]
Janjindamai, Waricha [1 ]
Dissaneevate, Supaporn [1 ]
机构
[1] Prince Songkla Univ, Dept Pediat, Fac Med, Hat Yai 90110, Songkhla, Thailand
关键词
bosentan; newborn; persistent pulmonary hypertension; RESPIRATORY-FAILURE; INFANTS; MANAGEMENT; MILRINONE; SAFETY;
D O I
10.1016/j.pedneo.2017.02.003
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Persistent pulmonary hypertension of the newborn (PPHN) contributes to neonatal hypoxemia and is associated with a high mortality. Some PPHN patients are unresponsive to inhaled nitric oxide (iNO). Bosentan, an oral endothelin-1 receptor antagonist, reduces pulmonary vascular resistance and hence may play a role in the treatment of PPHN. Methods: A retrospective medical records review was performed in newborns who received oral bosentan as an adjunctive therapy for treatment of PPHN between January 2013 and February 2016 at the neonatal intensive care unit of Songklanagarind Hospital. The main outcomes were the effect of bosentan on oxygenation and hemodynamic status after commencement of treatment and the safety of bosentan. Results: Forty neonates at a median (IQR) gestation of 38 (36.8-40) weeks and an initial median (IQR) oxygen index (01) of 29.2 (13.4-40.1) received bosentan therapy. Oral bosentan was commenced at a median (IQR) age of 27 (14.5-40.2) hours and the mean (SD) duration of treatment was 6.2 (3.1) days. The OI, alveolar-arterial oxygen difference (AaDO(2)) and oxygen saturation (SpO(2)) improved significantly at 2 h after treatment (p = 0.002, p = 0.01 and p < 0.001, respectively). In 21 (52.5%) neonates who received iNO and bosentan, the median OI (IQR) was 34.2 (29.0-42.6) with a significant decrease of OI at 6 h (p = 0.005) after treatment. In 19 (47.5%) neonates who received bosentan alone, the median OI (IQR) was 13.0 (9.8-30.9) with a significant decrease of OI in 2 h (p = 0.01) after treatment. The blood pressures before and after bosentan treatment were not statistically significantly different. The mortality rate was 12.5% (5/40). Conclusion: Oral bosentan may be a safe and effective treatment to improve oxygenation in neonates with PPHN. Bosentan can be used as an adjuvant therapy with iNO and can be an alternative therapy option in mild-to-moderate PPHN. Copyright (C) 2017, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:58 / 64
页数:7
相关论文
共 26 条
[1]   Pediatric Pulmonary Hypertension Guidelines From the American Heart Association and American Thoracic Society [J].
Abman, Steven H. ;
Hansmann, Georg ;
Archer, Stephen L. ;
Ivy, D. Dunbar ;
Adatia, Ian ;
Chung, Wendy K. ;
Hanna, Brian D. ;
Rosenzweig, Erika B. ;
Raj, J. Usha ;
Cornfield, David ;
Stenmark, Kurt R. ;
Steinhorn, Robin ;
Theobaud, Bernard ;
Fineman, Jeffrey R. ;
Kuehne, Titus ;
Feinstein, Jeffrey A. ;
Friedberg, Mark K. ;
Earing, Michael ;
Barst, Robyn J. ;
Keller, Roberta L. ;
Kinsella, John P. ;
Mullen, Mary ;
Deterding, Robin ;
Kulik, Thomas ;
Mallory, George ;
Humpl, Tilman ;
Wessel, David L. .
CIRCULATION, 2015, 132 (21) :2037-2099
[2]   Oral sildenafil in infants with persistent pulmonary hypertension of the newborn: A pilot randomized blinded study [J].
Baquero, H ;
Soliz, A ;
Neira, F ;
Venegas, ME ;
Sola, A .
PEDIATRICS, 2006, 117 (04) :1077-1083
[3]   Pharmacokinetics, safety, and efficacy of bosentan in pediatric patients with pulmonary arterial hypertension [J].
Barst, RJ ;
Ivy, D ;
Dingemanse, J ;
Widlitz, A ;
Schmitt, K ;
Doran, A ;
Bingaman, D ;
Nguyen, N ;
Gaitonde, M ;
van Giersbergen, PLM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2003, 73 (04) :372-382
[4]   Neonatal persistent pulmonary hypertension treated with milrinone: Four case reports [J].
Bassler, D ;
Choong, K ;
McNamara, P ;
Kirpalani, H .
BIOLOGY OF THE NEONATE, 2006, 89 (01) :1-5
[5]   Pharmacokinetic and clinical profile of a novel formulation of bosentan in children with pulmonary arterial hypertension: the FUTURE-1 study [J].
Beghetti, Maurice ;
Haworth, Sheila G. ;
Bonnet, Damien ;
Barst, Robyn J. ;
Acar, Philippe ;
Fraisse, Alain ;
Ivy, Dunbar D. ;
Jais, Xavier ;
Schulze-Neick, Ingram ;
Galie, Nazzareno ;
Morganti, Adele ;
Dingemanse, Jasper ;
Kusic-Pajic, Andjela ;
Berger, Rolf M. F. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2009, 68 (06) :948-955
[6]   Diagnosis and management of persistent pulmonary hypertension of the newborn [J].
Bendapudi, Perraju ;
Rao, Gopinath Gangadhara ;
Greenough, Anne .
PAEDIATRIC RESPIRATORY REVIEWS, 2015, 16 (03) :157-161
[7]   Clinical pharmacology of bosentan, a dual endothelin receptor antagonist [J].
Dingemanse, J ;
van Giersbergen, PLM .
CLINICAL PHARMACOKINETICS, 2004, 43 (15) :1089-1115
[8]   Blood pressure disorders in the neonate: Hypotension and hypertension [J].
Fanaroff, Jonathan M. ;
Fanaroff, Avroy A. .
SEMINARS IN FETAL & NEONATAL MEDICINE, 2006, 11 (03) :174-181
[9]   Nitric oxide for respiratory failure in infants born at or near term [J].
Finer, N. N. ;
Barrington, K. J. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2006, (04)
[10]   Persistent pulmonary hypertension of the newborn with transposition of the great arteries: successful treatment with bosentan [J].
Goissen, C. ;
Ghyselen, L. ;
Tourneux, P. ;
Krim, G. ;
Storme, L. ;
Bou, P. ;
Maingourd, Y. .
EUROPEAN JOURNAL OF PEDIATRICS, 2008, 167 (04) :437-440