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本文引用的文献

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The utility of a portable recording device for screening of obstructive sleep apnea in obese adolescents.便携记录设备在肥胖青少年阻塞性睡眠呼吸暂停筛查中的应用。
J Clin Sleep Med. 2012 Jun 15;8(3):271-7. doi: 10.5664/jcsm.1912.
2
Sleep apnea treatment after stroke (SATS) trial: is it feasible?中风后睡眠呼吸暂停治疗(SATS)试验:是否可行?
J Stroke Cerebrovasc Dis. 2013 Nov;22(8):1216-24. doi: 10.1016/j.jstrokecerebrovasdis.2011.06.010. Epub 2011 Jul 23.
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pROC: an open-source package for R and S+ to analyze and compare ROC curves.pROC:一个用于 R 和 S+的开源软件包,用于分析和比较 ROC 曲线。
BMC Bioinformatics. 2011 Mar 17;12:77. doi: 10.1186/1471-2105-12-77.
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Evaluation of the accuracy of manual and automatic scoring of a single airflow channel in patients with a high probability of obstructive sleep apnea.评估手动和自动评分在高度疑似阻塞性睡眠呼吸暂停患者单个气流通道中的准确性。
Med Sci Monit. 2011 Feb;17(2):MT13-9. doi: 10.12659/msm.881379.
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Utility of ApneaLink for the diagnosis of sleep apnea-hypopnea syndrome.ApneaLink在睡眠呼吸暂停低通气综合征诊断中的应用价值。
Medicina (B Aires). 2010;70(1):53-9.
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Diagnostic performance of single airflow channel recording (ApneaLink) in home diagnosis of sleep apnea.单气流通道记录(ApneaLink)在睡眠呼吸暂停家庭诊断中的诊断性能。
Sleep Breath. 2010 Jun;14(2):109-14. doi: 10.1007/s11325-009-0290-2. Epub 2009 Aug 28.
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Validation of a portable recording device (ApneaLink) for identifying patients with suspected obstructive sleep apnoea syndrome.验证一种便携式记录设备(ApneaLink)识别疑似阻塞性睡眠呼吸暂停综合征患者的能力。
Intern Med J. 2009 Nov;39(11):757-62. doi: 10.1111/j.1445-5994.2008.01827.x. Epub 2008 Nov 3.
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Evaluation of a portable recording device (ApneaLink) for case selection of obstructive sleep apnea.用于阻塞性睡眠呼吸暂停病例筛选的便携式记录设备(ApneaLink)的评估
Sleep Breath. 2009 Aug;13(3):213-9. doi: 10.1007/s11325-008-0232-4. Epub 2008 Dec 4.
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Clinical guidelines for the use of unattended portable monitors in the diagnosis of obstructive sleep apnea in adult patients. Portable Monitoring Task Force of the American Academy of Sleep Medicine.成人患者阻塞性睡眠呼吸暂停诊断中使用无人值守便携式监测仪的临床指南。美国睡眠医学学会便携式监测特别工作组。
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Validation of the ApneaLink for the screening of sleep apnea: a novel and simple single-channel recording device.用于睡眠呼吸暂停筛查的ApneaLink验证:一种新颖且简单的单通道记录设备。
J Clin Sleep Med. 2007 Jun 15;3(4):387-92.

家庭睡眠呼吸暂停研究后是否需要技师对原始数据进行审核?

Is technologist review of raw data necessary after home studies for sleep apnea?

机构信息

Stroke Program, University of Michigan, Ann Arbor, MI.

Sleep Disorders Center, University of Michigan, Ann Arbor, MI.

出版信息

J Clin Sleep Med. 2014 Apr 15;10(4):371-5. doi: 10.5664/jcsm.3606.

DOI:10.5664/jcsm.3606
PMID:24733981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3960378/
Abstract

STUDY OBJECTIVES

As the importance of portable monitors for detection of sleep apnea increases, efficient and cost-minimizing methods for data interpretation are needed. We sought to compare in stroke patients, for whom portable studies often have particular advantages, results from a cardiopulmonary monitoring device with and without manual edits by a polysomnographic technologist.

METHODS

Participants in an ongoing stroke surveillance study in Corpus Christi, Texas, underwent sleep apnea assessments with the ApneaLink Plus device within 45 days of stroke onset. Recordings were analyzed by the device's software unedited, and again after edits were made to the raw data by a registered polysomnographic technologist. Sensitivity and specificity were calculated, with the edited data as the reference standard. Sleep apnea was defined by 3 different apnea-hypopnea index (AHI) thresholds: ≥ 5, ≥ 10, and ≥ 15.

RESULTS

Among 327 subjects, 54% were male, 59% were Hispanic, and the median age was 65 years (interquartile range: 57, 77). The median AHI for the unedited data was 9 (4, 22), and for the edited data was 13 (6, 27) (p < 0.01). Specificity was above 98% for each AHI cutoff, while sensitivity was 81% to 82%. For each cutoff threshold, the edited data yielded a higher proportion of positive sleep apnea screens (p < 0.01) by approximately 10% in each group.

CONCLUSIONS

For stroke patients assessed with a cardiopulmonary monitoring device, manual editing by a technologist appears likely to improve sensitivity, whereas specificity of unedited data is already excellent.

摘要

研究目的

随着便携式监测器在睡眠呼吸暂停检测中的重要性日益增加,需要寻找高效且能最小化成本的数据解读方法。我们旨在比较在中风患者中,便携式研究通常具有特殊优势的情况下,心肺监测设备的原始数据和经睡眠技师手动编辑后的数据结果。

方法

在德克萨斯州科珀斯克里斯蒂市进行的一项正在进行的中风监测研究中,参与者在中风发作后 45 天内使用 ApneaLink Plus 设备进行睡眠呼吸暂停评估。原始记录未经编辑,由设备软件进行分析;之后,由注册睡眠技师对原始数据进行编辑。以编辑后的数据作为参考标准,计算敏感性和特异性。通过 3 种不同的呼吸暂停低通气指数(apnea-hypopnea index,AHI)阈值定义睡眠呼吸暂停:≥5、≥10 和≥15。

结果

在 327 名受试者中,54%为男性,59%为西班牙裔,中位年龄为 65 岁(四分位间距:57,77)。未编辑数据的中位 AHI 为 9(4,22),编辑后数据的中位 AHI 为 13(6,27)(p<0.01)。每个 AHI 截止值的特异性均高于 98%,而敏感性为 81%至 82%。对于每个截止阈值,编辑后数据在每组中增加了约 10%的阳性睡眠呼吸暂停筛查比例(p<0.01)。

结论

对于使用心肺监测设备评估的中风患者,由技师手动编辑似乎可以提高敏感性,而未经编辑的数据特异性已经很高。