新的神经压力支持(NPS)模式和头盔:我们是否找到了动态二重奏?

Alessandro Costa, Federico Merlo, Aline Pagni, Paolo Navalesi, Giacomo Grasselli, Gianmaria Cammarota, Davide Colombo
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引用次数: 0

摘要

背景:无创通气(NIV)通常用于临床实践,以缩短插管时间并提高患者舒适度。然而,由于死腔和顺应性等因素,无创通气过程中患者与呼吸机的交互(PVI),尤其是头盔接口,可能具有挑战性。神经调节通气辅助(NAVA)在改善头盔 NIV 期间的 PVI 方面已显示出前景,但仍存在局限性。神经压力支持(NPS)是一种新模式,旨在通过提供同步和陡峭的加压来解决这些局限性。本研究旨在评估与标准压力支持通气(PSV)相比,神经压力支持本身是否能改善头盔 NIV 期间的 PVI:研究对象包括需要使用头盔进行 NIV 的成年患者。患者被随机分为两组:一组从 NPS 开始,另一组从 PSV 开始;初始通气参数始终由值班临床医生设定。通气试验期间收集生理参数和动脉血气分析。记录专家对初始呼吸机设置的调整,以研究临床医生的专业知识作为混杂变量的影响。主要目标是同步时间(Timesync),即呼吸机和患者(基于神经信号)都处于吸气阶段的时间。作为次要目标,神经通气时间指数(NVTI)的计算方法也是 Timesync 除以神经吸气总时间,即 Timesync 所占神经吸气时间的比率:共有 24 名患者入选,没有人因安全问题中断研究。NPS 明显延长了 Timesync 时间(0.64±0.03 秒 vs. 0.37±0.03 秒,p I(78±2% vs. 45±2%,p 结论:NPS 改善了头盔呼吸过程中的 PVI:与 PSV 相比,NPS 可通过更长的 Timesync 和更好的耦合改善头盔 NIV 期间的 PVI。专家对呼吸机设置的调整对 PVI 的影响微乎其微。这些发现支持使用 NPS 提高患者与呼吸机的同步性,值得进一步研究其临床效果以及在不同患者群体和界面中的适用性:本研究于 2023 年 9 月 8 日在 www.Clinicaltrials: gov NCT06004206 注册,注册网址:https://clinicaltrials.gov/study/NCT06004206。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The new neural pressure support (NPS) mode and the helmet: did we find the dynamic duo?

Background: Noninvasive ventilation (NIV) is commonly used in clinical practice to reduce intubation times and enhance patient comfort. However, patient-ventilator interaction (PVI) during NIV, particularly with helmet interfaces, can be challenging due to factors such as dead space and compliance. Neurally adjusted ventilatory assist (NAVA) has shown promise in improving PVI during helmet NIV, but limitations remain. A new mode, neural pressure support (NPS), aims to address these limitations by providing synchronized and steep pressurization. This study aims to assess whether NPS per se improves PVI during helmet NIV compared to standard pressure support ventilation (PSV).

Methods: The study included adult patients requiring NIV with a helmet. Patients were randomized into two arms: one starting with NPS and the other with PSV; the initial ventilatory parameters were always set as established by the clinician on duty. Physiological parameters and arterial blood gas analysis were collected during ventilation trials. Expert adjustments to initial ventilator settings were recorded to investigate the impact of the expertise of the clinician as confounding variable. Primary aim was the synchrony time (Timesync), i.e., the time during which both the ventilator and the patient (based on the neural signal) are on the inspiratory phase. As secondary aim neural-ventilatory time index (NVTI) was also calculated as Timesync divided to the total neural inspiratory time, i.e., the ratio of the neural inspiratory time occupied by Timesync.

Results: Twenty-four patients were enrolled, with no study interruptions due to safety concerns. NPS demonstrated significantly longer Timesync (0.64 ± 0.03 s vs. 0.37 ± 0.03 s, p < 0.001) and shorter inspiratory delay (0.15 ± 0.01 s vs. 0.35 ± 0.01 s, p < 0.001) compared to PSV. NPS also showed better NVTI (78 ± 2% vs. 45 ± 2%, p < 0.001). Ventilator parameters were not significantly different between NPS and PSV, except for minor adjustments by the expert clinician.

Conclusions: NPS improves PVI during helmet NIV, as evidenced by longer Timesync and better coupling compared to PSV. Expert adjustments to ventilator settings had minimal impact on PVI. These findings support the use of NPS in enhancing patient-ventilator synchronization and warrant further investigation into its clinical outcomes and applicability across different patient populations and interfaces.

Trial registration: This study was registered on www.

Clinicaltrials: gov NCT06004206 Registry URL: https://clinicaltrials.gov/study/NCT06004206 on September 08, 2023.

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