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0568 Phrenic Nerve Stimulation to Treat Idiopathic Central Sleep Apnea

Introduction Central sleep apnea (CSA) is common in patients with cardiovascular disease (CVD), but also occurs in patients without CVD. In a randomized double arm parallel design trial of 151 participants with moderate to severe CSA, 18/151 (twelve percent) had no known CVD defined as coronary dise...

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Published in:Sleep (New York, N.Y.) N.Y.), 2019-04, Vol.42 (Supplement_1), p.A226-A226
Main Authors: Javaheri, Shahrokh, Graff, Jason, Khayat, Rami, Schwartz, Alan, Germany, Robin, Costanzo, Maria Rosa
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Graff, Jason
Khayat, Rami
Schwartz, Alan
Germany, Robin
Costanzo, Maria Rosa
description Introduction Central sleep apnea (CSA) is common in patients with cardiovascular disease (CVD), but also occurs in patients without CVD. In a randomized double arm parallel design trial of 151 participants with moderate to severe CSA, 18/151 (twelve percent) had no known CVD defined as coronary disease, left ventricular dysfunction, heart failure, arrhythmias, or hypertension. Echocardiography showed normal LVEF and absence of significant diastolic dysfunction (posterior wall thickness ≤ 1.2 cm, E/a ratio between >0.8 and < 2.0). Methods All polysomnograms were scored centrally. Sleep metrics and quality of life (QOL) were assessed by patient global assessment (PGA) and Epworth Sleepiness Scale (ESS). Change between 6 months and baseline was calculated for continuous endpoints. Safety was assessed by related serious adverse events (SAE) through 12 months. Results There were six participants with idiopathic CSA in the treatment arm (TX) and 12 in the Control (Ctrl) arm. The mean age was 50 years, 83% were male and 50% had depression. The median apnea hypopnea index (AHI) was 37 events/hr, central apnea index (CAI) 25 events/hr, and Epworth Sleepiness Scale (ESS) score was 12. Following 6 months of PNS therapy, the mean AHI improved by 21±16 events/hr (TX) whereas Ctrl improved by 7±17 events/hr (p=0.049), with similar changes in the oxygen desaturation index. The median TX CAI improved from of 35 (Q1-Q3:20-53) to 9 (Q1-Q3:5-22) events/hr, whereas Ctrl changed from 24 (Q1-Q3:17-34) to 15 (Q1-Q3:4-31) events/hr (p=0.030). The arousal index decreased by a median 9 (Q1-Q3: -15 to 0) with TX and Ctrl decreased by 1 (Q1-Q3:-8 to 4) events/hour (p=0.241). Moderate or marked improvement in the patient global assessment was reported by 50% in TX versus 0% in Ctrl. The ESS improved by a median of 5.5 (Q1-Q3:-6.0 to -1.0) points in TX compared to 0.5 (Q1-Q3:-1 to 3.0) in Ctrl. Conclusion PNS appears to improve sleep and quality of life safely and effectively in patients with idiopathic CSA. Support (If Any) Respicardia funded this research.
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In a randomized double arm parallel design trial of 151 participants with moderate to severe CSA, 18/151 (twelve percent) had no known CVD defined as coronary disease, left ventricular dysfunction, heart failure, arrhythmias, or hypertension. Echocardiography showed normal LVEF and absence of significant diastolic dysfunction (posterior wall thickness ≤ 1.2 cm, E/a ratio between &gt;0.8 and &lt; 2.0). Methods All polysomnograms were scored centrally. Sleep metrics and quality of life (QOL) were assessed by patient global assessment (PGA) and Epworth Sleepiness Scale (ESS). Change between 6 months and baseline was calculated for continuous endpoints. Safety was assessed by related serious adverse events (SAE) through 12 months. Results There were six participants with idiopathic CSA in the treatment arm (TX) and 12 in the Control (Ctrl) arm. The mean age was 50 years, 83% were male and 50% had depression. The median apnea hypopnea index (AHI) was 37 events/hr, central apnea index (CAI) 25 events/hr, and Epworth Sleepiness Scale (ESS) score was 12. Following 6 months of PNS therapy, the mean AHI improved by 21±16 events/hr (TX) whereas Ctrl improved by 7±17 events/hr (p=0.049), with similar changes in the oxygen desaturation index. The median TX CAI improved from of 35 (Q1-Q3:20-53) to 9 (Q1-Q3:5-22) events/hr, whereas Ctrl changed from 24 (Q1-Q3:17-34) to 15 (Q1-Q3:4-31) events/hr (p=0.030). The arousal index decreased by a median 9 (Q1-Q3: -15 to 0) with TX and Ctrl decreased by 1 (Q1-Q3:-8 to 4) events/hour (p=0.241). Moderate or marked improvement in the patient global assessment was reported by 50% in TX versus 0% in Ctrl. The ESS improved by a median of 5.5 (Q1-Q3:-6.0 to -1.0) points in TX compared to 0.5 (Q1-Q3:-1 to 3.0) in Ctrl. Conclusion PNS appears to improve sleep and quality of life safely and effectively in patients with idiopathic CSA. Support (If Any) Respicardia funded this research.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsz067.566</identifier><language>eng</language><publisher>Westchester: Oxford University Press</publisher><subject>Patients ; Quality of life ; Sleep apnea</subject><ispartof>Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A226-A226</ispartof><rights>Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Javaheri, Shahrokh</creatorcontrib><creatorcontrib>Graff, Jason</creatorcontrib><creatorcontrib>Khayat, Rami</creatorcontrib><creatorcontrib>Schwartz, Alan</creatorcontrib><creatorcontrib>Germany, Robin</creatorcontrib><creatorcontrib>Costanzo, Maria Rosa</creatorcontrib><title>0568 Phrenic Nerve Stimulation to Treat Idiopathic Central Sleep Apnea</title><title>Sleep (New York, N.Y.)</title><description>Introduction Central sleep apnea (CSA) is common in patients with cardiovascular disease (CVD), but also occurs in patients without CVD. In a randomized double arm parallel design trial of 151 participants with moderate to severe CSA, 18/151 (twelve percent) had no known CVD defined as coronary disease, left ventricular dysfunction, heart failure, arrhythmias, or hypertension. Echocardiography showed normal LVEF and absence of significant diastolic dysfunction (posterior wall thickness ≤ 1.2 cm, E/a ratio between &gt;0.8 and &lt; 2.0). Methods All polysomnograms were scored centrally. Sleep metrics and quality of life (QOL) were assessed by patient global assessment (PGA) and Epworth Sleepiness Scale (ESS). Change between 6 months and baseline was calculated for continuous endpoints. Safety was assessed by related serious adverse events (SAE) through 12 months. Results There were six participants with idiopathic CSA in the treatment arm (TX) and 12 in the Control (Ctrl) arm. The mean age was 50 years, 83% were male and 50% had depression. The median apnea hypopnea index (AHI) was 37 events/hr, central apnea index (CAI) 25 events/hr, and Epworth Sleepiness Scale (ESS) score was 12. Following 6 months of PNS therapy, the mean AHI improved by 21±16 events/hr (TX) whereas Ctrl improved by 7±17 events/hr (p=0.049), with similar changes in the oxygen desaturation index. The median TX CAI improved from of 35 (Q1-Q3:20-53) to 9 (Q1-Q3:5-22) events/hr, whereas Ctrl changed from 24 (Q1-Q3:17-34) to 15 (Q1-Q3:4-31) events/hr (p=0.030). The arousal index decreased by a median 9 (Q1-Q3: -15 to 0) with TX and Ctrl decreased by 1 (Q1-Q3:-8 to 4) events/hour (p=0.241). Moderate or marked improvement in the patient global assessment was reported by 50% in TX versus 0% in Ctrl. The ESS improved by a median of 5.5 (Q1-Q3:-6.0 to -1.0) points in TX compared to 0.5 (Q1-Q3:-1 to 3.0) in Ctrl. Conclusion PNS appears to improve sleep and quality of life safely and effectively in patients with idiopathic CSA. 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In a randomized double arm parallel design trial of 151 participants with moderate to severe CSA, 18/151 (twelve percent) had no known CVD defined as coronary disease, left ventricular dysfunction, heart failure, arrhythmias, or hypertension. Echocardiography showed normal LVEF and absence of significant diastolic dysfunction (posterior wall thickness ≤ 1.2 cm, E/a ratio between &gt;0.8 and &lt; 2.0). Methods All polysomnograms were scored centrally. Sleep metrics and quality of life (QOL) were assessed by patient global assessment (PGA) and Epworth Sleepiness Scale (ESS). Change between 6 months and baseline was calculated for continuous endpoints. Safety was assessed by related serious adverse events (SAE) through 12 months. Results There were six participants with idiopathic CSA in the treatment arm (TX) and 12 in the Control (Ctrl) arm. The mean age was 50 years, 83% were male and 50% had depression. The median apnea hypopnea index (AHI) was 37 events/hr, central apnea index (CAI) 25 events/hr, and Epworth Sleepiness Scale (ESS) score was 12. Following 6 months of PNS therapy, the mean AHI improved by 21±16 events/hr (TX) whereas Ctrl improved by 7±17 events/hr (p=0.049), with similar changes in the oxygen desaturation index. The median TX CAI improved from of 35 (Q1-Q3:20-53) to 9 (Q1-Q3:5-22) events/hr, whereas Ctrl changed from 24 (Q1-Q3:17-34) to 15 (Q1-Q3:4-31) events/hr (p=0.030). The arousal index decreased by a median 9 (Q1-Q3: -15 to 0) with TX and Ctrl decreased by 1 (Q1-Q3:-8 to 4) events/hour (p=0.241). Moderate or marked improvement in the patient global assessment was reported by 50% in TX versus 0% in Ctrl. The ESS improved by a median of 5.5 (Q1-Q3:-6.0 to -1.0) points in TX compared to 0.5 (Q1-Q3:-1 to 3.0) in Ctrl. Conclusion PNS appears to improve sleep and quality of life safely and effectively in patients with idiopathic CSA. Support (If Any) Respicardia funded this research.</abstract><cop>Westchester</cop><pub>Oxford University Press</pub><doi>10.1093/sleep/zsz067.566</doi><oa>free_for_read</oa></addata></record>
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subjects Patients
Quality of life
Sleep apnea
title 0568 Phrenic Nerve Stimulation to Treat Idiopathic Central Sleep Apnea
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