2017
DOI: 10.1016/j.hrthm.2016.11.033
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Variability in obstructive sleep apnea: Analysis of pacemaker-detected respiratory disturbances

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Cited by 20 publications
(14 citation statements)
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“…Specifically, in 36% of patients in whom multiple measurements were taken over a period of 7 days prior to the sleep study, we recorded RDI values both below and above the identified cutoff for severe SA. Similar observations of a wide intra-individual variability in AHI/RDI values were reported in a series of patients undergoing multiple polysomnographic recordings [23] at different time points (mean interval 3.3 weeks), as well as in a cohort of 58 patients [24] with PMKs equipped with a respiratory sensor from a different brand (mean intraindividual day-to-day RDI variability 19% ± 21%). In our opinion, this preliminary result seems to question the clinical validity of a single assessment by means of PSG, in that the variability of the value overtime could result in inaccurate diagnoses and therapeutic decisions.…”
Section: Discussionsupporting
confidence: 82%
“…Specifically, in 36% of patients in whom multiple measurements were taken over a period of 7 days prior to the sleep study, we recorded RDI values both below and above the identified cutoff for severe SA. Similar observations of a wide intra-individual variability in AHI/RDI values were reported in a series of patients undergoing multiple polysomnographic recordings [23] at different time points (mean interval 3.3 weeks), as well as in a cohort of 58 patients [24] with PMKs equipped with a respiratory sensor from a different brand (mean intraindividual day-to-day RDI variability 19% ± 21%). In our opinion, this preliminary result seems to question the clinical validity of a single assessment by means of PSG, in that the variability of the value overtime could result in inaccurate diagnoses and therapeutic decisions.…”
Section: Discussionsupporting
confidence: 82%
“…The large sample size may explain why the RESPIRE study showed a statistically significant association between increased severity of SA and AF, which was not found in the smaller 6-month pilot study by Moubarak et al 9 The findings of RESPIRE, however, confirm those of a recent study by Mazza et al, 15 which showed that pacemaker patients with device-diagnosed severe SA at baseline have twice the risk of AF compared with pacemaker patients with nonsevere SA (hazard ratio 2.38; 95% CI 1.21-4.66; P 5 .025). Severe SA at baseline and history of AF (paroxysmal) were also found to be independent predictors of AF.…”
Section: Discussionmentioning
confidence: 83%
“…7 Pacemakers capable of detecting respiratory disturbance may be used as a screening tool for detecting SAS and provide long-term information on changes in the severity of SA over time. [8][9][10] The feature has the added advantage vs polysomnography of monitoring sleep continuously every night.…”
Section: Introductionmentioning
confidence: 99%
“…Some recent publications have added significant information about the detection of SA in patients with cardiac implants 2,913 . D’Onofrio et al .…”
Section: Discussionmentioning
confidence: 99%