Department of Respiratory and Critical Care Medicine, West China School of Medicine and West China Hospital, Sichuan University, 610041, China.
Division of Pulmonary, Critical Care and Sleep Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Sleep Med. 2023 Jul;107:137-148. doi: 10.1016/j.sleep.2023.04.010. Epub 2023 Apr 19.
The acute effect during positive pressure titration and long term efficacy of acetazolamide (AZT) in high loop gain sleep apnea (HLGSA) is inadequately assessed. We predicted that AZT may improve HLGSA in both conditions.
A retrospective analysis of polysomnograms from patients with presumed HLGSA and residual respiratory instability administered AZT (125 or 250 mg) about 3 h into an initially drug-free positive pressure titration. A responder was defined as ≥ 50% reduction of the apnea hypopnea index(AHI 3% or arousal) before and after AZT. A multivariable logistic regression model estimated responder predictors. Long term efficacy of AZT was assessed by comparing both auto-machine (aREI) and manually scored respiratory events (sREI) extracted from the ventilator, prior to and after 3 months of AZT, in a subset.
Of the 231 participants (median age of 61[51-68] years) and 184 (80%) males in the acute effect testing: 77 and 154 patients were given 125 mg and 250 mg AZT. Compared to PAP alone, PAP plus AZT was associated with a lower breathing related arousal index (8 [3-16] vs. 5 [2-10], p < 0.001), and AHI3% (19 [7-37] vs. 11 [5-21], p < 0.001); 98 patients were responders. The non-rapid eye movement sleep (NREM) AHI3% (OR 1.031, 95%CI [1.016-1.046], p < 0.001) was a strong predictor for responder status with AZT exposure. In the 109 participants with 3-month data, both aREI and sREIwere significantly reduced after AZT.
AZT acutely and chronically reduced residual sleep apnea in presumed HLGSA; NREM AHI3% is a response predictor. AZT was well tolerated and beneficial for at least 3 months.
正压滴定过程中的急性作用以及高环路增益睡眠呼吸暂停(HLGSA)的长期疗效中,乙酰唑胺(AZT)的作用评估并不充分。我们预测 AZT 可能会改善这两种情况下的 HLGSA。
对疑似 HLGSA 且残留呼吸不稳定的患者进行多导睡眠图分析,在最初无药物正压滴定约 3 小时后给予 AZT(125 或 250mg)。将 AHI 降低≥50%(或觉醒减少≥3%)定义为应答者。使用多变量逻辑回归模型估计应答者的预测因子。在 AZT 治疗 3 个月前后,从通气机中提取自动机器(aREI)和手动评分呼吸事件(sREI),评估 AZT 的长期疗效。
在 231 名参与者(中位年龄 61[51-68]岁)和 184 名男性(80%)中进行了急性作用测试:77 名和 154 名患者分别接受了 125mg 和 250mg AZT。与单独使用 PAP 相比,PAP 加 AZT 与较低的呼吸相关觉醒指数(8 [3-16]与 5 [2-10],p<0.001)和 AHI3%(19 [7-37]与 11 [5-21],p<0.001)相关;98 名患者为应答者。非快速眼动睡眠(NREM)AHI3%(OR 1.031,95%CI [1.016-1.046],p<0.001)是 AZT 暴露后应答状态的有力预测因子。在 109 名有 3 个月数据的参与者中,AZT 后 aREI 和 sREI 均显著降低。
AZT 急性和慢性降低了疑似 HLGSA 中的残余睡眠呼吸暂停;NREM AHI3%是反应预测因子。AZT 耐受性良好,至少 3 个月有益。