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用于新生儿持续性肺动脉高压的吸入性肺血管扩张剂:与药物给药及输送装置相关的安全性问题。

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

作者信息

Cosa Nathan, Costa Edward

机构信息

Department of Respiratory Care, Banner Desert Medical Center, Cardon Children's Medical Center, Mesa, AZ, USA.

Department of Medical Affairs, Mallinckrodt Pharmaceuticals, Hampton, NJ, USA.

出版信息

Med Devices (Auckl). 2016 Apr 12;9:45-51. doi: 10.2147/MDER.S99601. eCollection 2016.

Abstract

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®IR, 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.

摘要

新生儿持续性肺动脉高压(PPHN)的治疗旨在降低肺血管阻力,同时维持体循环血管阻力。选择性肺血管舒张可通过靶向肺特异性途径或直接将血管舒张剂输送至肺部来实现。突然停用肺血管舒张剂可导致肺动脉高压反弹。因此,使用能够仔细监测药物输送的一致输送系统很重要。本文综述了已发表的用于治疗PPHN的吸入性血管舒张剂的研究,并概述了与药物输送和输送装置相关的安全问题,这些问题与肺动脉高压反弹风险有关。已有报道在患有PPHN的新生儿中使用雾化前列环素和气雾化前列腺素的超说明书用药情况;然而,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雾化药物的量通常未知,并且沉积在肺部的实际药物量可能受到多种因素影响,包括患者体型、使用的雾化器以及雾化器在呼吸回路中的位置。吸入一氧化氮(iNO)是美国食品药品监督管理局批准用于治疗PPHN的唯一肺血管舒张剂。iNO输送装置INOmax DSIR®IR旨在持续监测一氧化氮、二氧化氮和氧气的输送情况,并配备了听觉和视觉警报,以提醒医护人员突然停药和药物浓度不正确的情况。该装置的其他安全特性包括两个独立的备用输送系统、一个备用药筒、一个可提供长达6小时不间断药物输送的电池以及27个监测输送情况、剂量和系统功能的警报装置。在选择肺血管舒张剂时,考虑药物输送装置提供安全、一致给药剂量的能力很重要。

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