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一项关于波生坦治疗新生儿持续性肺动脉高压的随机、双盲、安慰剂对照、前瞻性研究。

A randomized, double-blind, placebo-controlled, prospective study of bosentan for the treatment of persistent pulmonary hypertension of the newborn.

机构信息

Department of Pediatrics, El-Minia University, El-Minia, Egypt.

出版信息

J Perinatol. 2012 Aug;32(8):608-13. doi: 10.1038/jp.2011.157. Epub 2011 Nov 10.

Abstract

OBJECTIVE

To assess the efficacy and safety of bosentan as an adjuvant therapy of persistent pulmonary hypertension of the newborn (PPHN).

STUDY DESIGN

Forty-seven neonates with PPHN were randomly assigned to receive either bosentan (n=24) or placebo (n=23). Efficacy was evaluated with a favorable outcome defined as fulfilling all the following criteria (for example, oxygenation index <15, normal pulmonary artery pressure (<20 mm Hg) and no premature discontinuation of the drug because of drug-related toxicity or lack of efficacy). Evaluation of safety was done by monitoring drug-related adverse events.

RESULT

Bosentan treatment was superior to placebo with a favorable response in 87.5% of patients treated with bosentan as compared with 20% of those who received placebo (P<0.0001). None of patients in the bosentan group had drug-related clinical or laboratory adverse events.

CONCLUSION

Bosentan may be a useful adjuvant therapy of PPHN.

摘要

目的

评估波生坦作为新生儿持续性肺动脉高压(PPHN)辅助治疗的疗效和安全性。

研究设计

47 例 PPHN 新生儿被随机分为波生坦(n=24)或安慰剂(n=23)组。以满足以下所有标准(例如,氧合指数<15,肺动脉压正常(<20mmHg),并且没有因药物相关毒性或缺乏疗效而提前停止药物治疗)作为疗效评估的良好结局。通过监测与药物相关的不良事件来评估安全性。

结果

与接受安慰剂治疗的患者(20%)相比,接受波生坦治疗的患者有 87.5%的患者有良好的反应(P<0.0001),波生坦组无患者出现与药物相关的临床或实验室不良事件。

结论

波生坦可能是治疗 PPHN 的一种有效辅助治疗药物。

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