Neurologisches Rehabilitationszentrum Rosenhügel (NRZ), Vienna, Austria.
Department of Sleep Medicine, LKH Graz Südwest, Austria.
J Clin Sleep Med. 2018 Sep 15;14(9):1495-1501. doi: 10.5664/jcsm.7322.
To study the feasibility and accuracy of home sleep apnea testing (HSAT) in the diagnosis of obstructive sleep apnea (OSA) in a stroke rehabilitation unit.
Stroke patients referred to a neurorehabilitation center underwent OSA screening by means of HSAT within the Home Polygraphic Recording with Telemedicine Monitoring for Diagnosis and Treatment of Sleep Apnea in Stroke, or HOPES study (ClinicalTrials.gov identifier: NCT02748681). Feasibility was determined by evaluating the acceptability of recording quality. Patients in whom moderate OSA was diagnosed subsequently underwent unattended polysomnography (PSG) confirmation. Accuracy was studied by comparing the respiratory event index (REI)/monitoring time (MT) of screening HSAT with the apnea-hypopnea index (AHI)/total sleep time (TST) obtained during subsequent PSG with Bland-Altman plots. The influence of PSG-evaluated wake time and arousals on OSA classification was studied by comparing the AHI and REI of the same night.
A total of 265 patients (58 ± 9 years, 70% male) were screened. A total of 92% of HSAT studies were performed with acceptable recording quality. In total, 33 patients (63 ± 5 years, 58% male) with moderate OSA (REI ≥ 15 to < 30 events/h) were included in the HSAT/PSG comparison. The Bland-Altman plot shows acceptable limits of agreement from -19.5 to +16.4, with a mean difference of -1.33. The REI detected in the PSG night demonstrated no significant differences to the AHI and a high correlation ( = .97; < .001). The 95% confidence interval of the Bland-Altman plots varied from -7.61 to +4.80.
These findings confirm a good feasibility and sufficient accuracy of HSAT attached in a stroke rehabilitation unit. Therefore, the authors suggest that American Academy of Sleep Medicine recommendations for HSAT should include stroke patients.
研究家庭睡眠呼吸暂停测试(HSAT)在中风康复单元中诊断阻塞性睡眠呼吸暂停(OSA)的可行性和准确性。
参与神经康复中心的中风患者在 HOPES 研究(ClinicalTrials.gov 标识符:NCT02748681)中通过 HSAT 进行 OSA 筛查。通过评估记录质量的可接受性来确定可行性。在诊断为中度 OSA 的患者中,随后进行无人值守的多导睡眠图(PSG)确认。通过比较筛查 HSAT 的呼吸事件指数(REI)/监测时间(MT)与随后 PSG 中获得的呼吸暂停-低通气指数(AHI)/总睡眠时间(TST)的 Bland-Altman 图来研究准确性。通过比较同一晚上的 AHI 和 REI,研究 PSG 评估的清醒时间和唤醒对 OSA 分类的影响。
共筛选出 265 例患者(58±9 岁,70%为男性)。HSAT 研究中有 92%的研究可获得可接受的记录质量。共有 33 例(63±5 岁,58%为男性)患有中度 OSA(REI≥15 至<30 次/小时),纳入 HSAT/PSG 比较。Bland-Altman 图显示,从-19.5 到+16.4 的一致性界限可接受,平均差异为-1.33。PSG 夜间检测到的 REI 与 AHI 无显著差异,且相关性高(=0.97;<0.001)。Bland-Altman 图的 95%置信区间从-7.61 到+4.80 不等。
这些发现证实了在中风康复单元中附加 HSAT 的良好可行性和足够的准确性。因此,作者建议美国睡眠医学学会关于 HSAT 的建议应包括中风患者。