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为重症患者定制的雾化伊洛前列素。

Aerosolized iloprost customized for the critically ill.

作者信息

Harris Keith W, O'Riordan Thomas G, Smaldone Gerald C

机构信息

Division of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, State University of New York at Stony Brook, Stony Brook, NY 11794-8172, USA.

出版信息

Respir Care. 2007 Nov;52(11):1507-9.

Abstract

BACKGROUND

Aerosolized iloprost, an inhaled synthetic analogue of prostacyclin, is an approved therapy for stage III and IV pulmonary hypertension. However, currently iloprost is delivered via a device that requires a clinically stable patient who can use a hand-held nebulizer. We designed separate aerosol delivery systems to nebulize iloprost to critically ill patients during (1) mechanical ventilation and (2) spontaneous breathing that requires a high fraction of inspired oxygen. The goal was to deliver doses similar to the currently approved high-efficiency I-neb nebulizer system.

METHODS

For the intubated patient we used the high-efficiency AeroTech II jet nebulizer and a breath-actuated ventilator circuit, without humidification. For spontaneous breathing, our delivery system consisted of a Pulmanex Hi-Ox disposable oxygen mask and an AeroTech II nebulizer. With a nebulizer charge of 20 microg, the drug presented to the patient (inhaled mass) was captured on a filter and analyzed using radioactivity (technetium-99m). The accuracy of the radiolabel was quantified by directly measuring iloprost with high-performance liquid chromatography and comparing the results. A cascade impactor measured particle distribution.

RESULTS

A line of identity confirmed that the radiolabel accurately represented the drug. The mean +/- SD inhaled mass was 6.02 +/- 0.87 microg (n = 5) on the ventilator and 3.77 +/- 0.46 microg (n = 5) during spontaneous ventilation. The mass median aerodynamic diameter and fine-particle fraction were 0.7 microm, 0.99, and 0.7 microm, 0.99, respectively.

CONCLUSIONS

Clinically effective doses of iloprost can be delivered to patients who require high-flow oxygen or mechanical ventilation.

摘要

背景

雾化吸入依洛前列素,一种吸入性前列环素合成类似物,是治疗III期和IV期肺动脉高压的一种已获批准的疗法。然而,目前依洛前列素是通过一种要求患者临床状况稳定且能够使用手持雾化器的装置来给药的。我们设计了单独的雾化给药系统,以便在以下两种情况下为重症患者雾化吸入依洛前列素:(1)机械通气期间;(2)需要高浓度吸氧的自主呼吸期间。目标是输送与目前已获批准的高效I-neb雾化器系统相似的剂量。

方法

对于插管患者,我们使用高效AeroTech II喷射雾化器和呼吸驱动通气回路,不进行湿化。对于自主呼吸患者,我们的给药系统由一个Pulmanex Hi-Ox一次性吸氧面罩和一个AeroTech II雾化器组成。雾化器装药20微克,将给予患者的药物(吸入质量)收集在滤器上,并用放射性(锝-99m)进行分析。通过用高效液相色谱法直接测量依洛前列素并比较结果来量化放射性标记物的准确性。用串联冲击器测量颗粒分布。

结果

一条恒等线证实放射性标记物准确代表了药物。在通气期间,平均±标准差吸入质量为6.02±0.87微克(n = 5),自主通气期间为3.77±0.46微克(n = 5)。质量中值空气动力学直径和细颗粒分数分别为0.7微米、0.99和0.7微米、0.99。

结论

可以向需要高流量吸氧或机械通气的患者输送临床有效剂量的依洛前列素。

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