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Sildenafil Therapy for Pulmonary Hypertension Before and After Pediatric Congenital Heart Surgery

机译:西地那非治疗小儿先天性心脏病手术前后的肺动脉高压

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摘要

Pulmonary hypertension associated with pediatric congenital heart defects is a major cause of postoperative morbidity and death. Sildenafil has been combined with inhaled nitric oxide to treat pulmonary hypertension. We retrospectively studied the pre- and postoperative effects of oral sildenafil as monotherapy in children with pulmonary hypertension who underwent surgery to correct congenital cardiac defects.From September 2005 through November 2009, 38 children with moderate-to-severe pulmonary arterial hypertension (pulmonary arterial/aortic pressure ratio, >0.7) underwent cardiac surgery at our institution. Fifteen patients were given sildenafil (0.35 mg/kg, every 4 hr) orally or through nasogastric tubes 1 week before and 1 week after surgery. Twenty-three patients of comparable medical status were given sildenafil only upon the institution of cardiopulmonary bypass and for 1 week after surgery.Postoperatively, the 15 patients who were given preoperative sildenafil had significantly lower mean pulmonary arterial pressures (25.6 ± 3.1 vs 30.4 ± 5.7 mmHg; P = 0.005) and pulmonary arterial/aortic pressure ratios (0.35 ± 0.05 vs 0.42 ± 0.07; P = 0.002) than did the other 23 patients. The preoperative therapy also shortened cardiopulmonary bypass time, mechanical ventilation time, and lengths of intensive care unit and hospital stays. No sildenafil-related hypertensive crises or sequelae occurred.As monotherapy, oral sildenafil in low doses appears to control pulmonary hypertension safely and effectively in children undergoing operations to correct congenital heart defects, particularly when it is given both preoperatively and postoperatively. Further study is warranted.
机译:与小儿先天性心脏缺陷相关的肺动脉高压是术后发病和死亡的主要原因。西地那非已与吸入一氧化氮合用治疗肺动脉高压。我们回顾性研究口服西地那非单药疗法对接受手术纠正先天性心脏缺陷的肺动脉高压患儿的术前和术后效果.2005年9月至2009年11月,38例中重度肺动脉高压患儿(肺动脉/主动脉压力比,> 0.7)在我们机构接受了心脏手术。 15例患者在手术前1周和术后1周口服或通过鼻胃管给予西地那非(0.35 mg / kg,每4小时)。 23例具有可比医学状态的患者仅在进行体外循环后以及手术后1周才接受西地那非治疗。术后15例接受术前西地那非治疗的患者平均肺动脉压明显降低(25.6±3.1 vs 30.4±5.7) mmHg; P = 0.005)和肺动脉/主动脉压力比(0.35±0.05 vs 0.42±0.07; P = 0.002)比其他23例患者高。术前治疗还缩短了体外循环时间,机械通气时间,并缩短了重症监护室和住院时间。没有西地那非相关的高血压危机或后遗症发生。作为单一疗法,口服小剂量西地那非似乎可以安全有效地控制正在纠正先天性心脏缺陷的手术患儿的肺动脉高压,特别是在术前和术后给予的情况下。值得进一步研究。

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