Raja Shahzad G, Danton Mark D, MacArthur Kenneth J, Pollock James C
Department of Cardiac Surgery, Royal Hospital for Sick Children, Glasgow, UK.
J Cardiothorac Vasc Anesth. 2007 Apr;21(2):203-7. doi: 10.1053/j.jvca.2006.02.010. Epub 2006 May 18.
Sildenafil (Viagra, Pfizer) is being increasingly used to treat pulmonary hypertension in children. However, there are limited data available to suggest dosage regimens. The purpose of this study was to determine the effects of escalating doses of sildenafil on hemodynamics and gas exchange in children with pulmonary hypertension because of congenital cardiac defects.
Prospective, observational study.
Pediatric intensive care unit in a tertiary care children's hospital.
Ten children with pulmonary hypertension because of congenital cardiac defects who were in the intensive care unit and on nitric oxide after cardiac surgery.
Patients received sildenafil every 4 hours via a gastric tube in incremental doses of 0.5 mg/kg, 1 mg/kg, 1.5 mg/kg, and 2.0 mg/kg along with nitric oxide during their stay in the intensive care unit until they were extubated. Hemodynamic and arterial blood gas measurements were taken before (baseline) and 60 minutes after the administration of sildenafil.
All doses of sildenafil caused significant reduction in pulmonary artery pressure with no significant effect on systemic arterial and central venous pressures. Arterial partial pressure of oxygen was decreased after a 2.0 mg/kg dose of sildenafil but not significantly. No significant differences were found among the 4 doses.
For the treatment of pulmonary hypertension in children with congenital cardiac defects, a 0.5 mg/kg dose of sildenafil every 4 hours is therapeutically as effective as a 2.0 mg/kg dose every 4 hours. However, a large dose-ranging and pharmacokinetic study of sildenafil in children with pulmonary hypertension because of congenital cardiac defects is needed to validate the safety and efficacy of the dose-range and dosing interval suggested by this study.
西地那非(万艾可,辉瑞公司)越来越多地用于治疗儿童肺动脉高压。然而,关于给药方案的数据有限。本研究的目的是确定递增剂量的西地那非对先天性心脏病所致肺动脉高压患儿血流动力学和气体交换的影响。
前瞻性观察性研究。
一家三级儿童医院的儿科重症监护病房。
10名因先天性心脏病导致肺动脉高压且在心脏手术后入住重症监护病房并接受一氧化氮治疗的儿童。
患者在重症监护病房期间,每4小时通过胃管接受递增剂量(0.5mg/kg、1mg/kg、1.5mg/kg和2.0mg/kg)的西地那非治疗,同时接受一氧化氮治疗,直至拔管。在给予西地那非前(基线)和给药后60分钟进行血流动力学和动脉血气测量。
所有剂量的西地那非均导致肺动脉压显著降低,而对体动脉压和中心静脉压无显著影响。给予2.0mg/kg剂量的西地那非后动脉血氧分压降低,但不显著。4种剂量之间未发现显著差异。
对于先天性心脏病所致肺动脉高压患儿的治疗,每4小时给予0.5mg/kg剂量的西地那非与每4小时给予2.0mg/kg剂量的西地那非疗效相同。然而,需要对先天性心脏病所致肺动脉高压患儿进行大规模的剂量范围和药代动力学研究,以验证本研究建议的剂量范围和给药间隔的安全性和有效性。