Service de Médecine Intensive Réanimation, CHRU de Tours, Tours, France.
INSERM, Centre d'Étude des Pathologies Respiratoires (CEPR) UMR 1100, Université de Tours, Tours, France.
J Aerosol Med Pulm Drug Deliv. 2021 Sep;34(5):303-310. doi: 10.1089/jamp.2020.1643. Epub 2021 Mar 24.
Obstructive patients may benefit from nasal high-flow (NHF) therapy, but the use of pressurized metered-dose inhalers (pMDIs) has not been evaluated in this situation. Using an adult circuit and medium-sized cannula, we have tested different NHF rates, pMDI positions, breathing patterns, spacers, and spacer orientation. First, we evaluated albuterol delivery at the nasal cannula outlet. The second set of experiments made use of a nasopharyngeal cast to estimate the mass of albuterol potentially reaching the lungs. Albuterol was caught on filters placed at the cannula outlet and downstream of the nasal cast, and albuterol was quantified by spectrophotometry. The highest amounts of albuterol delivered at the cannula outlet were observed with a 30 L/min flow rate (vs. 45 and 60 L/min) and placing the device close to the nasal cannula (in comparison with a position on the dry side of the humidification chamber). The use of a spacer was associated with higher delivery. The highest albuterol delivery was observed placing the spacer close to the nasal cannula, oriented for aerosol delivery following the gas flow and a 30 L/min NHF rate. Using this optimal setting, activating the pMDI at the beginning of inspiration (compared to expiration) increased albuterol delivery downstream of the nasopharyngeal cast. Whether in a quiet- or distress-breathing pattern, our measurements showed an amount of albuterol potentially delivered to the lungs exceeding 10% of the actuated dose in optimal conditions. Albuterol delivery with pMDIs is feasible within NHF circuits. Drug delivery sufficient to induce bronchodilation can be achieved using a spacer placed just upstream of the nasal cannula, a low NHF rate, and activation of the pMDI at the beginning of inspiration. Further testing in a clinical setting is required, however.
阻塞性患者可能受益于经鼻高流量(NHF)治疗,但在此情况下尚未评估加压计量吸入器(pMDI)的使用。我们使用成人回路和中号套管,测试了不同的 NHF 流速、pMDI 位置、呼吸模式、喷雾器和喷雾器方向。首先,我们评估了在鼻套管出口处沙丁胺醇的输送。第二组实验利用鼻咽铸型来估计潜在到达肺部的沙丁胺醇质量。将沙丁胺醇放置在套管出口和鼻铸型下游的过滤器上进行收集,并通过分光光度法对其进行定量。在套管出口处观察到输送的沙丁胺醇量最高的是 30 L/min 的流速(与 45 和 60 L/min 相比),并且将设备靠近鼻套管放置(与在加湿室干燥侧的位置相比)。使用喷雾器与更高的输送量相关。在靠近鼻套管放置、朝向气流方向输送气溶胶且 NHF 流速为 30 L/min 的情况下,观察到最高的沙丁胺醇输送量。使用这种最佳设置,在吸气(与呼气相比)开始时激活 pMDI 会增加鼻咽铸型下游的沙丁胺醇输送量。无论在安静呼吸还是窘迫呼吸模式下,我们的测量结果显示,在最佳条件下,有超过 10%的触发剂量的沙丁胺醇潜在输送到肺部。在 NHF 回路中使用 pMDI 可以输送沙丁胺醇。通过在鼻套管上游放置喷雾器、使用低 NHF 流速以及在吸气开始时激活 pMDI,可以实现足以诱导支气管扩张的药物输送。然而,还需要在临床环境中进行进一步的测试。