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Borneol-mediated vardenafil hydrochloride patch for pediatric pulmonary arterial hypertension: Preparation, characterization and in vivo study.冰片介导的盐酸伐地那非贴剂治疗小儿肺动脉高压:制备、表征及体内研究。
Int J Pharm. 2020 Dec 15;591:119864. doi: 10.1016/j.ijpharm.2020.119864. Epub 2020 Sep 28.
2
Efficacy of Milrinone Plus Sildenafil in the Treatment of Neonates with Persistent Pulmonary Hypertension in Resource-Limited Settings: Results of a Randomized, Double-Blind Trial.米力农联合西地那非治疗资源有限地区持续性肺动脉高压新生儿的疗效:一项随机、双盲试验的结果。
Paediatr Drugs. 2020 Dec;22(6):685-693. doi: 10.1007/s40272-020-00412-4.
3
Persistent Pulmonary Hypertension of the Newborn: Pathophysiological Mechanisms and Novel Therapeutic Approaches.新生儿持续性肺动脉高压:病理生理机制与新型治疗方法
Front Pediatr. 2020 Jul 24;8:342. doi: 10.3389/fped.2020.00342. eCollection 2020.
4
A Comparative Study of Inhaled Nitric Oxide and an Intravenously Administered Nitric Oxide Donor in Acute Pulmonary Hypertension.吸入一氧化氮与静脉给予一氧化氮供体治疗急性肺动脉高压的对比研究。
Drug Des Devel Ther. 2020 Feb 17;14:635-645. doi: 10.2147/DDDT.S237477. eCollection 2020.
5
Ophthalmic findings in neonates receiving sildenafil.接受西地那非治疗的新生儿的眼科检查结果
J Paediatr Child Health. 2020 Jun;56(6):884-888. doi: 10.1111/jpc.14766. Epub 2020 Jan 9.
6
In the child with pulmonary hypertension, does treatment with enteral sildenafil compared with a slow wean from nitric oxide alone prevent rebound pulmonary hypertension and allow for discontinuation of nitric oxide?在患有肺动脉高压的儿童中,与仅缓慢停用一氧化氮相比,肠内给予西地那非治疗能否预防肺动脉高压反弹并实现一氧化氮的停用?
Arch Dis Child. 2020 Apr;105(4):410-412. doi: 10.1136/archdischild-2019-318233. Epub 2019 Nov 28.
7
Pharmacokinetic modeling of intravenous sildenafil in newborns with congenital diaphragmatic hernia.静脉注射西地那非在先天性膈疝新生儿中的药代动力学模型。
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8
The CoDiNOS trial protocol: an international randomised controlled trial of intravenous sildenafil versus inhaled nitric oxide for the treatment of pulmonary hypertension in neonates with congenital diaphragmatic hernia.CoDiNOS 试验方案:一项国际性、随机对照试验,旨在比较静脉注射西地那非与吸入一氧化氮治疗先天性膈疝新生儿肺动脉高压的疗效。
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10
Prophylactic Sildenafil in Preterm Infants at Risk of Bronchopulmonary Dysplasia: A Pilot Randomized, Double-Blinded, Placebo-Controlled Trial.预防性应用西地那非治疗有支气管肺发育不良风险的早产儿:一项随机、双盲、安慰剂对照的初步试验。
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西地那非在新生儿肺动脉高压中的应用进展:关于其历史、当前给药方式及未来方向的叙述性综述

Update on the use of sildenafil in neonatal pulmonary hypertension: a narrative review of the history, current administration, and future directions.

作者信息

Li Zhenyu, Lv Xiaoming, Liu Qinmei, Dang Dan, Wu Hui

机构信息

Department of Neonatology, The First Hospital of Jilin University, Changchun, China.

出版信息

Transl Pediatr. 2021 Apr;10(4):998-1007. doi: 10.21037/tp-20-277.

DOI:10.21037/tp-20-277
PMID:34012848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8107873/
Abstract

Pulmonary hypertension (PH) is a life-threatening syndrome in neonates and has multiple and varied etiologies. However, few clinical studies have systematically evaluated the treatment regimens for this population. Phosphodiesterase (PDE) inhibitors, such as milrinone, tadalafil, dipyridamole, and sildenafil, are the most important regulators of vascular relaxation in the normal pulmonary vascular transition after birth, and these agents are widely used in the treatment of PH. Sildenafil, a representative PDE-5 inhibitor, has an important role as a single mode of therapy. However, the lack of evidence from pharmacokinetic and clinical trials has limited the emergence of standardized treatment regimens for sildenafil. There are also differing opinions among researchers regarding the best route of sildenafil administration. Due to the interindividual variability in the neonatal population, it is worth selecting the most suitable route of sildenafil administration according to the specific conditions of the neonatal population. These may be evaluated using the oxygenation index (OI), pulmonary artery pressure, mean blood pressure, and the serological index. This article reviews the clinical data on the use of sildenafil, focusing on the current and promising alternative routes of administration, which may affect subsequent clinical research in term and preterm neonates.

摘要

肺动脉高压(PH)是一种危及新生儿生命的综合征,病因多样。然而,很少有临床研究系统评估该人群的治疗方案。磷酸二酯酶(PDE)抑制剂,如米力农、他达拉非、双嘧达莫和西地那非,是出生后正常肺血管转变过程中血管舒张的最重要调节因子,这些药物广泛用于治疗PH。西地那非作为一种代表性的PDE-5抑制剂,在单一治疗模式中具有重要作用。然而,药代动力学和临床试验缺乏证据限制了西地那非标准化治疗方案的出现。研究人员对于西地那非的最佳给药途径也存在不同意见。由于新生儿群体存在个体差异,根据新生儿群体的具体情况选择最合适的西地那非给药途径是值得的。这些可以通过氧合指数(OI)、肺动脉压、平均血压和血清学指标来评估。本文综述了使用西地那非的临床数据,重点关注当前和有前景的替代给药途径,这可能会影响足月儿和早产儿随后的临床研究。