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Inhaled pulmonary vasodilators for persistent pulmonary hypertension of the newborn: safety issues relating to drug administration and delivery devices

机译:吸入型肺血管扩张剂用于新生儿持续性肺动脉高压:与药物给药和给药装置有关的安全性问题

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Treatment for persistent pulmonary hypertension of the newborn (PPHN) aims to reduce pulmonary vascular resistance while maintaining systemic vascular resistance. Selective pulmonary vasodilation may be achieved by targeting pulmonary-specific pathways or by delivering vasodilators directly to the lungs. Abrupt withdrawal of a pulmonary vasodilator can cause rebound pulmonary hypertension. Therefore, use of consistent delivery systems that allow for careful monitoring of drug delivery is important. This manuscript reviews published studies of inhaled vasodilators used for treatment of PPHN and provides an overview of safety issues associated with drug delivery and delivery devices as they relate to the risk of rebound pulmonary hypertension. Off-label use of aerosolized prostacyclins and an aerosolized prostaglandin in neonates with PPHN has been reported; however, evidence from large randomized clinical trials is lacking. The amount of a given dose of aerosolized drug that is actually delivered to the lungs is often unknown, and the actual amount of drug deposited in the lungs can be affected by several factors, including patient size, nebulizer used, and placement of the nebulizer within the breathing circuit. Inhaled nitric oxide (iNO) is the only pulmonary vasodilator approved by the US Food and Drug Administration for the treatment of PPHN. The iNO delivery device, INOmax DSIR?, is designed to constantly monitor NO, NO2, and O2 deliveries and is equipped with audible and visual alarms to alert providers of abrupt discontinuation and incorrect drug concentration. Other safety features of this device include two independent backup delivery systems, a backup drug cylinder, a battery that provides up to 6 hours of uninterrupted medication delivery, and 27 alarms that monitor delivery, dosage, and system functions. The ability of the drug delivery device to provide safe, consistent dosing is important to consider when selecting a pulmonary vasodilator.
机译:新生儿持续性肺动脉高压(PPHN)的治疗旨在降低肺血管阻力,同时保持全身血管阻力。选择性肺血管舒张可以通过靶向肺特异性途径或通过将血管舒张剂直接递送至肺来实现。突然停用肺血管扩张药会导致反弹性肺动脉高压。因此,使用能够仔细监控药物输送的一致的输送系统非常重要。该手稿回顾了用于PPHN治疗的吸入性血管舒张药的研究,并概述了与药物输送和输送装置相关的安全性问题,因为它们涉及反弹性肺动脉高压的风险。据报道,PPHN新生儿在标签上使用雾化的前列环素和雾化的前列腺素;但是,缺乏大型随机临床试验的证据。实际输送到肺部的给定剂量的雾化药物的量通常是未知的,并且沉积在肺部的药物的实际量会受到多种因素的影响,包括患者人数,使用的雾化器以及雾化器在体内的放置位置呼吸回路。吸入一氧化氮(iNO)是美国食品和药物管理局批准的用于PPHN治疗的唯一肺血管扩张剂。 iNO输送设备INOmax DS IR 设计用于不断监控NO,NO 2 和O 2 交货,并配备听觉和视觉警报,以警告提供者突然停药和药物浓度不正确。该设备的其他安全功能包括两个独立的备用输送系统,一个备用药瓶,一个电池,可提供长达6小时的不间断药物输送,以及27个警报,用于监视输送,剂量和系统功能。选择肺血管扩张药时,必须考虑药物输送装置提供安全,一致剂量的能力。

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