提高高循环增益睡眠呼吸暂停治疗的呼气再呼吸空间

Thomas Quinn, Robert Joseph Thomas, Eric James Heckman
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摘要

睡眠呼吸暂停的病理生理学不仅仅是解剖学上对气道塌陷的易感性,还包括唤醒阈值和循环增益等其他因素。高环路增益是中枢性和复杂性睡眠呼吸暂停(伴有阻塞性和中枢性混合特征)的一个显著特征,其中相对低碳酸血症可导致呼吸不稳定和周期性呼吸。现有的治疗方法,包括持续气道正压通气(CPAP)和自适应伺服呼吸机,往往不能充分治疗具有高环路增益特征的睡眠呼吸暂停。增强呼气再呼吸空间(EERS)的目标是通过增加少于典型潮气量的死亡空间来预防低碳酸血症,低碳酸血症会引发睡眠中的中枢事件。这是通过覆盖气道正压面罩上的传统呼气口,并添加带有远端呼气和安全阀的小附加管来实现的。该技术减少了唤醒期间的二氧化碳(co2)释放和相关的大恢复期呼吸,通常会使静息二氧化碳最大增加1-2毫米汞柱,从而增加二氧化碳储备,使其不太可能遇到低碳呼吸暂停阈值。通常,EERS的量是根据中心事件和周期性呼吸来滴定的,而不是以目标二氧化碳水平为目标。理想情况下,在EERS滴定期间使用二氧化碳监测,在基线高碳酸血症的情况下避免使用该技术。该方法已在我们睡眠中心的临床实践中使用超过15年,回顾性数据表明其具有良好的安全性和高成功率,包括先前CPAP治疗失败的患者。限制包括泄漏设置的有效性降低和体积较大的电路的容忍度降低。EERS代表了一种简单的,负担得起的修改现有的气道正压模式治疗中枢和复杂的睡眠呼吸暂停。未来的研究领域包括技术的随机对照试验和EERS与适应性通气联合使用的研究,以及针对高环路增益生理学的药物辅助。
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Enhanced expiratory rebreathing space for high loop gain sleep apnea treatment
The pathophysiology of sleep apnea goes beyond anatomic predisposition to airway collapse and includes additional factors such as arousal threshold and loop gain. High loop gain is a prominent feature in central and complex sleep apnea (with a mixture of obstructive and central features) where relative hypocapnia can lead to respiratory instability and periodic breathing. Existing therapies, including continuous positive airway pressure (CPAP) and adaptive servo-ventilators, often inadequately treat sleep apnea with high loop gain features. Enhanced expiratory rebreathing space (EERS) targets prevention of the hypocapnia that triggers central events in sleep by increasing dead space in amounts less than typical tidal volumes. This is accomplished by covering traditional exhalation ports on positive airway pressure masks and adding small additional tubing with distal exhalation and safety valves. This technique reduces carbon dioxide (CO 2 ) blow-off during arousals and the associated large recovery breaths, typically producing a maximal increase in resting CO 2 by 1–2 mmHg, thus increasing the CO 2 reserve and making it less likely to encounter the hypocapnic apneic threshold. Typically, the amount of EERS is titrated in response to central events and periodic breathing rather than aiming for a goal CO 2 level. Ideally CO 2 monitoring is used during titration of EERS and the technique is avoided in the setting of baseline hypercapnia. This method has been used in clinical practice at our sleep center for over 15 years, and retrospective data suggests an excellent safety profile and high rates of successful therapy including in patients who have previously failed CPAP therapy. Limitations include decreased effectiveness in the setting of leak and decreased tolerance of the bulkier circuit. EERS represents a simple, affordable modification of existing positive airway pressure modalities for treatment of central and complex sleep apnea. Areas of future study include randomized controlled trials of the technique and study of use of EERS in combination with adaptive ventilation, and pharmacologic adjuncts targeting high loop gain physiology.
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