Sleep-disordered breathing in heart failure
Sleep‐disordered breathing—comprising obstructive sleep apnoea (OSA), central sleep apnoea (CSA), or a combination of the two—is found in over half of heart failure (HF) patients and may have harmful effects on cardiac function, with swings in intrathoracic pressure (and therefore preload and afterl...
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Veröffentlicht in: | European journal of heart failure 2016-04, Vol.18 (4), p.353-361 |
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description | Sleep‐disordered breathing—comprising obstructive sleep apnoea (OSA), central sleep apnoea (CSA), or a combination of the two—is found in over half of heart failure (HF) patients and may have harmful effects on cardiac function, with swings in intrathoracic pressure (and therefore preload and afterload), blood pressure, sympathetic activity, and repetitive hypoxaemia. It is associated with reduced health‐related quality of life, higher healthcare utilization, and a poor prognosis. Whilst continuous positive airway pressure (CPAP) is the treatment of choice for patients with daytime sleepiness due to OSA, the optimal management of CSA remains uncertain. There is much circumstantial evidence that the treatment of OSA in HF patients with CPAP can improve symptoms, cardiac function, biomarkers of cardiovascular disease, and quality of life, but the quality of evidence for an improvement in mortality is weak. For systolic HF patients with CSA, the CANPAP trial did not demonstrate an overall survival or hospitalization advantage for CPAP. A minute ventilation‐targeted positive airway therapy, adaptive servoventilation (ASV), can control CSA and improves several surrogate markers of cardiovascular outcome, but in the recently published SERVE‐HF randomized trial, ASV was associated with significantly increased mortality and no improvement in HF hospitalization or quality of life. Further research is needed to clarify the therapeutic rationale for the treatment of CSA in HF. Cardiologists should have a high index of suspicion for sleep‐disordered breathing in those with HF, and work closely with sleep physicians to optimize patient management. |
doi_str_mv | 10.1002/ejhf.492 |
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It is associated with reduced health‐related quality of life, higher healthcare utilization, and a poor prognosis. Whilst continuous positive airway pressure (CPAP) is the treatment of choice for patients with daytime sleepiness due to OSA, the optimal management of CSA remains uncertain. There is much circumstantial evidence that the treatment of OSA in HF patients with CPAP can improve symptoms, cardiac function, biomarkers of cardiovascular disease, and quality of life, but the quality of evidence for an improvement in mortality is weak. For systolic HF patients with CSA, the CANPAP trial did not demonstrate an overall survival or hospitalization advantage for CPAP. A minute ventilation‐targeted positive airway therapy, adaptive servoventilation (ASV), can control CSA and improves several surrogate markers of cardiovascular outcome, but in the recently published SERVE‐HF randomized trial, ASV was associated with significantly increased mortality and no improvement in HF hospitalization or quality of life. Further research is needed to clarify the therapeutic rationale for the treatment of CSA in HF. Cardiologists should have a high index of suspicion for sleep‐disordered breathing in those with HF, and work closely with sleep physicians to optimize patient management.</description><identifier>ISSN: 1388-9842</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1002/ejhf.492</identifier><identifier>PMID: 26869027</identifier><language>eng</language><publisher>Oxford, UK: John Wiley & Sons, Ltd</publisher><subject>Atrial Fibrillation - etiology ; Atrial Fibrillation - physiopathology ; Continuous Positive Airway Pressure - methods ; Diagnosis ; Health Services - utilization ; Heart - physiopathology ; Heart failure ; Heart Failure - complications ; Heart Failure - physiopathology ; Heart Failure, Systolic ; Hospitalization ; Humans ; Inflammation ; Myocardial Ischemia - etiology ; Myocardial Ischemia - physiopathology ; Positive-Pressure Respiration - methods ; Pressure ; Prognosis ; Quality of Life ; Reactive Oxygen Species ; Sleep Apnea Syndromes ; Sleep Apnea, Central - complications ; Sleep Apnea, Central - physiopathology ; Sleep Apnea, Central - therapy ; Sleep Apnea, Obstructive - complications ; Sleep Apnea, Obstructive - physiopathology ; Sleep Apnea, Obstructive - therapy ; Sleep-disordered breathing ; Survival Rate ; Sympathetic Nervous System - physiopathology ; Thoracic Cavity ; Treatment</subject><ispartof>European journal of heart failure, 2016-04, Vol.18 (4), p.353-361</ispartof><rights>2016 The Authors © 2016 European Society of Cardiology</rights><rights>2016 The Authors European Journal of Heart Failure © 2016 European Society of Cardiology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4592-8103ff2342bb04e04f8b642a33c638e444e81b627fa84f05f3dac881cc7020f43</citedby><cites>FETCH-LOGICAL-c4592-8103ff2342bb04e04f8b642a33c638e444e81b627fa84f05f3dac881cc7020f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejhf.492$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejhf.492$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,1435,27933,27934,45583,45584,46418,46842</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26869027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pearse, Simon G.</creatorcontrib><creatorcontrib>Cowie, Martin R.</creatorcontrib><title>Sleep-disordered breathing in heart failure</title><title>European journal of heart failure</title><addtitle>Eur J Heart Fail</addtitle><description>Sleep‐disordered breathing—comprising obstructive sleep apnoea (OSA), central sleep apnoea (CSA), or a combination of the two—is found in over half of heart failure (HF) patients and may have harmful effects on cardiac function, with swings in intrathoracic pressure (and therefore preload and afterload), blood pressure, sympathetic activity, and repetitive hypoxaemia. It is associated with reduced health‐related quality of life, higher healthcare utilization, and a poor prognosis. Whilst continuous positive airway pressure (CPAP) is the treatment of choice for patients with daytime sleepiness due to OSA, the optimal management of CSA remains uncertain. There is much circumstantial evidence that the treatment of OSA in HF patients with CPAP can improve symptoms, cardiac function, biomarkers of cardiovascular disease, and quality of life, but the quality of evidence for an improvement in mortality is weak. For systolic HF patients with CSA, the CANPAP trial did not demonstrate an overall survival or hospitalization advantage for CPAP. A minute ventilation‐targeted positive airway therapy, adaptive servoventilation (ASV), can control CSA and improves several surrogate markers of cardiovascular outcome, but in the recently published SERVE‐HF randomized trial, ASV was associated with significantly increased mortality and no improvement in HF hospitalization or quality of life. Further research is needed to clarify the therapeutic rationale for the treatment of CSA in HF. Cardiologists should have a high index of suspicion for sleep‐disordered breathing in those with HF, and work closely with sleep physicians to optimize patient management.</description><subject>Atrial Fibrillation - etiology</subject><subject>Atrial Fibrillation - physiopathology</subject><subject>Continuous Positive Airway Pressure - methods</subject><subject>Diagnosis</subject><subject>Health Services - utilization</subject><subject>Heart - physiopathology</subject><subject>Heart failure</subject><subject>Heart Failure - complications</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Failure, Systolic</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Myocardial Ischemia - etiology</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>Positive-Pressure Respiration - methods</subject><subject>Pressure</subject><subject>Prognosis</subject><subject>Quality of Life</subject><subject>Reactive Oxygen Species</subject><subject>Sleep Apnea Syndromes</subject><subject>Sleep Apnea, Central - complications</subject><subject>Sleep Apnea, Central - physiopathology</subject><subject>Sleep Apnea, Central - therapy</subject><subject>Sleep Apnea, Obstructive - complications</subject><subject>Sleep Apnea, Obstructive - physiopathology</subject><subject>Sleep Apnea, Obstructive - therapy</subject><subject>Sleep-disordered breathing</subject><subject>Survival Rate</subject><subject>Sympathetic Nervous System - physiopathology</subject><subject>Thoracic Cavity</subject><subject>Treatment</subject><issn>1388-9842</issn><issn>1879-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M1PwjAYx_HGaATRxL_AcDQxw76t7Y6G8CISTUTjsem2p1IcDNstyn_vCIgnT89z-OR3-CJ0SXCPYExvYTG3PZ7QI9QmSiYRVpwfNz9TKkoUpy10FsICYyIbfYpaVCiRYCrb6GZWAKyj3IXS5-Ah76YeTDV3q_euW3XnYHzVtcYVtYdzdGJNEeBifzvodTh46Y-j6dPovn83jTIeJzRSBDNrKeM0TTEHzK1KBaeGsUwwBZxzUCQVVFqjuMWxZbnJlCJZJjHFlrMOut7trn35WUOo9NKFDIrCrKCsgyYywVxIJdgfzXwZgger194tjd9ogvU2jd6m0U2ahl7tV-t0CfkB_rZoQLQDX66Azb9DejAZD3eDe-9CBd8Hb_yHFpLJWL89jnT83J_hB670hP0AjvB6dw</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Pearse, Simon G.</creator><creator>Cowie, Martin R.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201604</creationdate><title>Sleep-disordered breathing in heart failure</title><author>Pearse, Simon G. ; Cowie, Martin R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4592-8103ff2342bb04e04f8b642a33c638e444e81b627fa84f05f3dac881cc7020f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Atrial Fibrillation - etiology</topic><topic>Atrial Fibrillation - physiopathology</topic><topic>Continuous Positive Airway Pressure - methods</topic><topic>Diagnosis</topic><topic>Health Services - utilization</topic><topic>Heart - physiopathology</topic><topic>Heart failure</topic><topic>Heart Failure - complications</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Failure, Systolic</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Myocardial Ischemia - etiology</topic><topic>Myocardial Ischemia - physiopathology</topic><topic>Positive-Pressure Respiration - methods</topic><topic>Pressure</topic><topic>Prognosis</topic><topic>Quality of Life</topic><topic>Reactive Oxygen Species</topic><topic>Sleep Apnea Syndromes</topic><topic>Sleep Apnea, Central - complications</topic><topic>Sleep Apnea, Central - physiopathology</topic><topic>Sleep Apnea, Central - therapy</topic><topic>Sleep Apnea, Obstructive - complications</topic><topic>Sleep Apnea, Obstructive - physiopathology</topic><topic>Sleep Apnea, Obstructive - therapy</topic><topic>Sleep-disordered breathing</topic><topic>Survival Rate</topic><topic>Sympathetic Nervous System - physiopathology</topic><topic>Thoracic Cavity</topic><topic>Treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pearse, Simon G.</creatorcontrib><creatorcontrib>Cowie, Martin R.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of heart failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pearse, Simon G.</au><au>Cowie, Martin R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sleep-disordered breathing in heart failure</atitle><jtitle>European journal of heart failure</jtitle><addtitle>Eur J Heart Fail</addtitle><date>2016-04</date><risdate>2016</risdate><volume>18</volume><issue>4</issue><spage>353</spage><epage>361</epage><pages>353-361</pages><issn>1388-9842</issn><eissn>1879-0844</eissn><abstract>Sleep‐disordered breathing—comprising obstructive sleep apnoea (OSA), central sleep apnoea (CSA), or a combination of the two—is found in over half of heart failure (HF) patients and may have harmful effects on cardiac function, with swings in intrathoracic pressure (and therefore preload and afterload), blood pressure, sympathetic activity, and repetitive hypoxaemia. It is associated with reduced health‐related quality of life, higher healthcare utilization, and a poor prognosis. Whilst continuous positive airway pressure (CPAP) is the treatment of choice for patients with daytime sleepiness due to OSA, the optimal management of CSA remains uncertain. There is much circumstantial evidence that the treatment of OSA in HF patients with CPAP can improve symptoms, cardiac function, biomarkers of cardiovascular disease, and quality of life, but the quality of evidence for an improvement in mortality is weak. For systolic HF patients with CSA, the CANPAP trial did not demonstrate an overall survival or hospitalization advantage for CPAP. A minute ventilation‐targeted positive airway therapy, adaptive servoventilation (ASV), can control CSA and improves several surrogate markers of cardiovascular outcome, but in the recently published SERVE‐HF randomized trial, ASV was associated with significantly increased mortality and no improvement in HF hospitalization or quality of life. Further research is needed to clarify the therapeutic rationale for the treatment of CSA in HF. Cardiologists should have a high index of suspicion for sleep‐disordered breathing in those with HF, and work closely with sleep physicians to optimize patient management.</abstract><cop>Oxford, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>26869027</pmid><doi>10.1002/ejhf.492</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Atrial Fibrillation - etiology Atrial Fibrillation - physiopathology Continuous Positive Airway Pressure - methods Diagnosis Health Services - utilization Heart - physiopathology Heart failure Heart Failure - complications Heart Failure - physiopathology Heart Failure, Systolic Hospitalization Humans Inflammation Myocardial Ischemia - etiology Myocardial Ischemia - physiopathology Positive-Pressure Respiration - methods Pressure Prognosis Quality of Life Reactive Oxygen Species Sleep Apnea Syndromes Sleep Apnea, Central - complications Sleep Apnea, Central - physiopathology Sleep Apnea, Central - therapy Sleep Apnea, Obstructive - complications Sleep Apnea, Obstructive - physiopathology Sleep Apnea, Obstructive - therapy Sleep-disordered breathing Survival Rate Sympathetic Nervous System - physiopathology Thoracic Cavity Treatment |
title | Sleep-disordered breathing in heart failure |
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