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在实验室台架环境下对四种不同呼气末正压(EPAP)设备产生的呼气压力进行比较。

Comparison of expiratory pressures generated by four different EPAP devices in a laboratory bench setting.

作者信息

Sleeper Geoffrey, Rashidi Majid, Strohl Kingman P, Najimi Neda, Chen Pai-Lien, El Ghoul Rawad, Chiang Ambrose A

机构信息

BRYGGS Medical, Avon, OH, USA.

BRYGGS Medical, Avon, OH, USA; Department of Mechanical and Aerospace Engineering, Case Western Reserve University, Cleveland, OH, USA.

出版信息

Sleep Med. 2022 Aug;96:87-92. doi: 10.1016/j.sleep.2022.05.004. Epub 2022 May 13.

Abstract

OBJECTIVE/BACKGROUND: Expiratory positive airway pressure (EPAP) has been a treatment option for patients with obstructive sleep apnea (OSA). ULTepap is a new FDA-cleared EPAP device that seals the nares with a nasal pillow interface. Comparisons of expiratory pressures generated by ULTepap and other EPAP devices like Provent, Bongo Rx, and Theravent are not available. We aimed to compare the backpressures created by these devices in an in vitro laboratory bench setting.

METHODS

A test rig was designed and fabricated to test the expiratory pressures generated by ULTepap, Provent, Bongo Rx, and Theravent. Airflow was generated by a linear actuator-driven piston in a syringe, and a range of flow rates was provided by varying the voltage input to the actuator. The resulting expiratory and inspiratory pressures were measured and resistances were calculated.

RESULTS

The backpressures generated by ULTepap and Provent were comparable at all flow rates. For flow rates at 99/142/212 ml/s, the expiratory pressures were 3.5/7.5/13.8 cmH2O for ULTepap and 4.5/8.5/14.5 cmH2O for Provent. Bongo Rx and Theravent devices produced substantially lower backpressures compared to ULTepap devices (0.8/1.8/3.5 cmH2O for Bongo Rx and 0.9/2.2/5.3 cmH2O for Theravent at flow rates of 99/142/212 ml/s). All four devices presented very low inspiratory flow resistance, with all generating 0.5 cmH2O or less at all flow rates.

CONCLUSION

Not all FDA-cleared EPAP devices produce similar expiratory pressure profiles. ULTepap generated backpressures closest to that of Provent. Clinical trials comparing the efficacy, tolerance, and adherence of these EPAP devices in patients with OSA are warranted.

摘要

目的/背景:呼气末正压通气(EPAP)一直是阻塞性睡眠呼吸暂停(OSA)患者的一种治疗选择。ULTepap是一种新的获得美国食品药品监督管理局(FDA)批准的EPAP设备,它通过鼻枕接口密封鼻孔。目前尚无ULTepap与其他EPAP设备(如Provent、Bongo Rx和Theravent)产生的呼气压力的比较。我们旨在在体外实验室台架环境中比较这些设备产生的背压。

方法

设计并制造了一个试验台,以测试ULTepap、Provent、Bongo Rx和Theravent产生的呼气压力。气流由注射器中线性致动器驱动的活塞产生,通过改变输入致动器的电压来提供一系列流速。测量产生的呼气和吸气压力,并计算阻力。

结果

ULTepap和Provent在所有流速下产生的背压相当。对于99/142/212毫升/秒的流速,ULTepap的呼气压力分别为3.5/7.5/13.8厘米水柱,Provent为4.5/8.5/14.5厘米水柱。与ULTepap设备相比,Bongo Rx和Theravent设备产生的背压要低得多(在99/142/212毫升/秒的流速下,Bongo Rx为0.8/1.8/3.5厘米水柱,Theravent为0.9/2.2/5.3厘米水柱)。所有四种设备的吸气流动阻力都非常低,在所有流速下均产生0.5厘米水柱或更低的阻力。

结论

并非所有获得FDA批准的EPAP设备都产生相似的呼气压力曲线。ULTepap产生的背压最接近Provent。有必要进行临床试验,比较这些EPAP设备在OSA患者中的疗效、耐受性和依从性。

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