Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial
Quadriplegia is a severe, catastrophic injury that predominantly affects people early in life, resulting in lifelong physical disability. Obstructive sleep apnoea is a direct consequence of quadriplegia and is associated with neurocognitive deficits, sleepiness and reduced quality of life. The usual...
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creator | Berlowitz, David J Ayas, Najib Barnes, Maree Brown, Douglas J Cistulli, Peter A Geraghty, Tim Graham, Alison Lee, Bonsan Bonne Morris, Meg O'Donoghue, Fergal Rochford, Peter D Ross, Jack Singhal, Balraj Spong, Jo Wadsworth, Brooke Pierce, Robert J |
description | Quadriplegia is a severe, catastrophic injury that predominantly affects people early in life, resulting in lifelong physical disability. Obstructive sleep apnoea is a direct consequence of quadriplegia and is associated with neurocognitive deficits, sleepiness and reduced quality of life. The usual treatment for sleep apnoea is nasal continuous positive airway pressure (CPAP); however, this is poorly tolerated in quadriplegia. To encourage patients to use this therapy, we have to demonstrate that the benefits outweigh the inconvenience. We therefore propose a prospective, multinational randomized controlled trial of three months of CPAP for obstructive sleep apnoea after acute quadriplegia.
Specialist spinal cord injury centres across Australia, New Zealand, the UK and Canada will recruit medically stable individuals who have sustained a (new) traumatic quadriplegia (complete or incomplete second cervical to first thoracic level lesions). Participants will be screened for obstructive sleep apnoea using full, portable sleep studies. Those with an apnoea hypopnoea index greater than 10 per hour will proceed to an initial three-night trial of CPAP. Those who can tolerate CPAP for at least 4 hours on at least one night of the initial trial will be randomized to either usual care or a 3-month period of auto-titrating CPAP. The primary hypothesis is that nocturnal CPAP will improve neuropsychological functioning more than usual care alone. The secondary hypothesis is that the magnitude of improvement of neuropsychological function will be predicted by the severity of baseline sleepiness measures, sleep fragmentation and sleep apnoea. Neuropsychological tests and full polysomnography will be performed at baseline and 3 months with interim measures of sleepiness and symptoms of autonomic dysfunction measured weekly. Spirometry will be performed monthly. Neuropsychological tests will be administered by blinded assessors. Recruitment commenced in July 2009.
The results of this trial will demonstrate the effect of nocturnal CPAP treatment of obstructive sleep apnoea in acute quadriplegia. If CPAP can improve neurocognitive function after injury, it is likely that rehabilitation and subsequent community participation will be substantially improved for this group of predominantly young and severely physically disabled people.
Australian New Zealand Clinical Trial Registry ACTRN12605000799651. |
doi_str_mv | 10.1186/1745-6215-14-181 |
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Specialist spinal cord injury centres across Australia, New Zealand, the UK and Canada will recruit medically stable individuals who have sustained a (new) traumatic quadriplegia (complete or incomplete second cervical to first thoracic level lesions). Participants will be screened for obstructive sleep apnoea using full, portable sleep studies. Those with an apnoea hypopnoea index greater than 10 per hour will proceed to an initial three-night trial of CPAP. Those who can tolerate CPAP for at least 4 hours on at least one night of the initial trial will be randomized to either usual care or a 3-month period of auto-titrating CPAP. The primary hypothesis is that nocturnal CPAP will improve neuropsychological functioning more than usual care alone. The secondary hypothesis is that the magnitude of improvement of neuropsychological function will be predicted by the severity of baseline sleepiness measures, sleep fragmentation and sleep apnoea. Neuropsychological tests and full polysomnography will be performed at baseline and 3 months with interim measures of sleepiness and symptoms of autonomic dysfunction measured weekly. Spirometry will be performed monthly. Neuropsychological tests will be administered by blinded assessors. Recruitment commenced in July 2009.
The results of this trial will demonstrate the effect of nocturnal CPAP treatment of obstructive sleep apnoea in acute quadriplegia. If CPAP can improve neurocognitive function after injury, it is likely that rehabilitation and subsequent community participation will be substantially improved for this group of predominantly young and severely physically disabled people.
Australian New Zealand Clinical Trial Registry ACTRN12605000799651.</description><identifier>ISSN: 1745-6215</identifier><identifier>EISSN: 1745-6215</identifier><identifier>DOI: 10.1186/1745-6215-14-181</identifier><identifier>PMID: 23777510</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Activities of daily living ; Acute Disease ; Australia ; Autonomic Nervous System - physiopathology ; Canada ; Care and treatment ; Clinical Protocols ; Complications and side effects ; Continuous Positive Airway Pressure ; Humans ; Medical equipment and supplies industry ; Medical test kit industry ; Neuropsychological Tests ; New Zealand ; Patient outcomes ; Physically disabled persons ; Polysomnography ; Predictive Value of Tests ; Prospective Studies ; Quadriplegia ; Quadriplegia - complications ; Quadriplegia - physiopathology ; Quadriplegia - psychology ; Quality of Life ; Research Design ; Sleep ; Sleep apnea syndromes ; Sleep Apnea, Obstructive - diagnosis ; Sleep Apnea, Obstructive - etiology ; Sleep Apnea, Obstructive - physiopathology ; Sleep Apnea, Obstructive - psychology ; Sleep Apnea, Obstructive - therapy ; Spirometry ; Study Protocol ; Surveys and Questionnaires ; Time Factors ; Treatment Outcome ; United Kingdom</subject><ispartof>Trials, 2013-06, Vol.14 (1), p.181-181</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>Copyright © 2013 Berlowitz et al.; licensee BioMed Central Ltd. 2013 Berlowitz et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-be048df48f58e94fe57c61af998ff9c0b2c89f9a0edc277457ae5c04d1920df33</citedby><cites>FETCH-LOGICAL-c463t-be048df48f58e94fe57c61af998ff9c0b2c89f9a0edc277457ae5c04d1920df33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706386/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706386/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23777510$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Berlowitz, David J</creatorcontrib><creatorcontrib>Ayas, Najib</creatorcontrib><creatorcontrib>Barnes, Maree</creatorcontrib><creatorcontrib>Brown, Douglas J</creatorcontrib><creatorcontrib>Cistulli, Peter A</creatorcontrib><creatorcontrib>Geraghty, Tim</creatorcontrib><creatorcontrib>Graham, Alison</creatorcontrib><creatorcontrib>Lee, Bonsan Bonne</creatorcontrib><creatorcontrib>Morris, Meg</creatorcontrib><creatorcontrib>O'Donoghue, Fergal</creatorcontrib><creatorcontrib>Rochford, Peter D</creatorcontrib><creatorcontrib>Ross, Jack</creatorcontrib><creatorcontrib>Singhal, Balraj</creatorcontrib><creatorcontrib>Spong, Jo</creatorcontrib><creatorcontrib>Wadsworth, Brooke</creatorcontrib><creatorcontrib>Pierce, Robert J</creatorcontrib><title>Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial</title><title>Trials</title><addtitle>Trials</addtitle><description>Quadriplegia is a severe, catastrophic injury that predominantly affects people early in life, resulting in lifelong physical disability. Obstructive sleep apnoea is a direct consequence of quadriplegia and is associated with neurocognitive deficits, sleepiness and reduced quality of life. The usual treatment for sleep apnoea is nasal continuous positive airway pressure (CPAP); however, this is poorly tolerated in quadriplegia. To encourage patients to use this therapy, we have to demonstrate that the benefits outweigh the inconvenience. We therefore propose a prospective, multinational randomized controlled trial of three months of CPAP for obstructive sleep apnoea after acute quadriplegia.
Specialist spinal cord injury centres across Australia, New Zealand, the UK and Canada will recruit medically stable individuals who have sustained a (new) traumatic quadriplegia (complete or incomplete second cervical to first thoracic level lesions). Participants will be screened for obstructive sleep apnoea using full, portable sleep studies. Those with an apnoea hypopnoea index greater than 10 per hour will proceed to an initial three-night trial of CPAP. Those who can tolerate CPAP for at least 4 hours on at least one night of the initial trial will be randomized to either usual care or a 3-month period of auto-titrating CPAP. The primary hypothesis is that nocturnal CPAP will improve neuropsychological functioning more than usual care alone. The secondary hypothesis is that the magnitude of improvement of neuropsychological function will be predicted by the severity of baseline sleepiness measures, sleep fragmentation and sleep apnoea. Neuropsychological tests and full polysomnography will be performed at baseline and 3 months with interim measures of sleepiness and symptoms of autonomic dysfunction measured weekly. Spirometry will be performed monthly. Neuropsychological tests will be administered by blinded assessors. Recruitment commenced in July 2009.
The results of this trial will demonstrate the effect of nocturnal CPAP treatment of obstructive sleep apnoea in acute quadriplegia. If CPAP can improve neurocognitive function after injury, it is likely that rehabilitation and subsequent community participation will be substantially improved for this group of predominantly young and severely physically disabled people.
Australian New Zealand Clinical Trial Registry ACTRN12605000799651.</description><subject>Activities of daily living</subject><subject>Acute Disease</subject><subject>Australia</subject><subject>Autonomic Nervous System - physiopathology</subject><subject>Canada</subject><subject>Care and treatment</subject><subject>Clinical Protocols</subject><subject>Complications and side effects</subject><subject>Continuous Positive Airway Pressure</subject><subject>Humans</subject><subject>Medical equipment and supplies industry</subject><subject>Medical test kit industry</subject><subject>Neuropsychological Tests</subject><subject>New Zealand</subject><subject>Patient outcomes</subject><subject>Physically disabled persons</subject><subject>Polysomnography</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Quadriplegia</subject><subject>Quadriplegia - complications</subject><subject>Quadriplegia - physiopathology</subject><subject>Quadriplegia - psychology</subject><subject>Quality of Life</subject><subject>Research Design</subject><subject>Sleep</subject><subject>Sleep apnea syndromes</subject><subject>Sleep Apnea, Obstructive - diagnosis</subject><subject>Sleep Apnea, Obstructive - etiology</subject><subject>Sleep Apnea, Obstructive - physiopathology</subject><subject>Sleep Apnea, Obstructive - psychology</subject><subject>Sleep Apnea, Obstructive - therapy</subject><subject>Spirometry</subject><subject>Study Protocol</subject><subject>Surveys and Questionnaires</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>United Kingdom</subject><issn>1745-6215</issn><issn>1745-6215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUk1rFTEUHUSxtbp3JQE3dTE1eclMJi4Kj4dfUCiirsN9mZtnJDOZJplK_U3-SDPv1dKCZHEvN-cczr2cqnrJ6BljXfuWSdHU7Yo1NRM169ij6vhu9Phef1Q9S-knpYIrLp5WRysupWwYPa7-rOcc6uxyhOzGHTFhLHUOcyJTSC67ayTg4i-4IVPElOaIJEeEPOCYiQ2RhG3KcTZ7ZPKIE4FpDAgEbMZIwMwZydUMfXSTx50Dcrq5_Lr-8uYdSXnuF92Qgwl-rwYkwtiHwf3Gfm8mBu9Lm6MD_7x6YsEnfHFbT6rvH95_23yqLy4_ft6sL2ojWp7rLVLR9VZ0tulQCYuNNC0Dq1RnrTJ0uzKdsgoo9mYly40kYGOo6Jla0d5yflKdH3SneTsUUFk1gtdTdAPEGx3A6Yc_o_uhd-Fac0lb3rVF4PRWIIarGVPWg0sGvYcRy2k140o1VHZUFejrA3QHHrUbbSiKZoHrdcOFlErRxdHZf1Dl9Ti4cia0rswfEOiBYGJIKaK9c8-oXrKjl3DoJRyaCV2yUyiv7m99R_gXFv4X5sDEWQ</recordid><startdate>20130619</startdate><enddate>20130619</enddate><creator>Berlowitz, David J</creator><creator>Ayas, Najib</creator><creator>Barnes, Maree</creator><creator>Brown, Douglas J</creator><creator>Cistulli, Peter A</creator><creator>Geraghty, Tim</creator><creator>Graham, Alison</creator><creator>Lee, Bonsan Bonne</creator><creator>Morris, Meg</creator><creator>O'Donoghue, Fergal</creator><creator>Rochford, Peter D</creator><creator>Ross, Jack</creator><creator>Singhal, Balraj</creator><creator>Spong, Jo</creator><creator>Wadsworth, Brooke</creator><creator>Pierce, Robert J</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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><scope>5PM</scope></search><sort><creationdate>20130619</creationdate><title>Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial</title><author>Berlowitz, David J ; Ayas, Najib ; Barnes, Maree ; Brown, Douglas J ; Cistulli, Peter A ; Geraghty, Tim ; Graham, Alison ; Lee, Bonsan Bonne ; Morris, Meg ; O'Donoghue, Fergal ; Rochford, Peter D ; Ross, Jack ; Singhal, Balraj ; Spong, Jo ; Wadsworth, Brooke ; Pierce, Robert J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-be048df48f58e94fe57c61af998ff9c0b2c89f9a0edc277457ae5c04d1920df33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Activities of daily living</topic><topic>Acute Disease</topic><topic>Australia</topic><topic>Autonomic Nervous System - physiopathology</topic><topic>Canada</topic><topic>Care and treatment</topic><topic>Clinical Protocols</topic><topic>Complications and side effects</topic><topic>Continuous Positive Airway Pressure</topic><topic>Humans</topic><topic>Medical equipment and supplies industry</topic><topic>Medical test kit industry</topic><topic>Neuropsychological Tests</topic><topic>New Zealand</topic><topic>Patient outcomes</topic><topic>Physically disabled persons</topic><topic>Polysomnography</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Quadriplegia</topic><topic>Quadriplegia - complications</topic><topic>Quadriplegia - physiopathology</topic><topic>Quadriplegia - psychology</topic><topic>Quality of Life</topic><topic>Research Design</topic><topic>Sleep</topic><topic>Sleep apnea syndromes</topic><topic>Sleep Apnea, Obstructive - diagnosis</topic><topic>Sleep Apnea, Obstructive - etiology</topic><topic>Sleep Apnea, Obstructive - physiopathology</topic><topic>Sleep Apnea, Obstructive - psychology</topic><topic>Sleep Apnea, Obstructive - therapy</topic><topic>Spirometry</topic><topic>Study Protocol</topic><topic>Surveys and Questionnaires</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>United Kingdom</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Berlowitz, David J</creatorcontrib><creatorcontrib>Ayas, Najib</creatorcontrib><creatorcontrib>Barnes, Maree</creatorcontrib><creatorcontrib>Brown, Douglas J</creatorcontrib><creatorcontrib>Cistulli, Peter A</creatorcontrib><creatorcontrib>Geraghty, Tim</creatorcontrib><creatorcontrib>Graham, Alison</creatorcontrib><creatorcontrib>Lee, Bonsan Bonne</creatorcontrib><creatorcontrib>Morris, Meg</creatorcontrib><creatorcontrib>O'Donoghue, Fergal</creatorcontrib><creatorcontrib>Rochford, Peter D</creatorcontrib><creatorcontrib>Ross, Jack</creatorcontrib><creatorcontrib>Singhal, Balraj</creatorcontrib><creatorcontrib>Spong, Jo</creatorcontrib><creatorcontrib>Wadsworth, Brooke</creatorcontrib><creatorcontrib>Pierce, Robert J</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Trials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berlowitz, David J</au><au>Ayas, Najib</au><au>Barnes, Maree</au><au>Brown, Douglas J</au><au>Cistulli, Peter A</au><au>Geraghty, Tim</au><au>Graham, Alison</au><au>Lee, Bonsan Bonne</au><au>Morris, Meg</au><au>O'Donoghue, Fergal</au><au>Rochford, Peter D</au><au>Ross, Jack</au><au>Singhal, Balraj</au><au>Spong, Jo</au><au>Wadsworth, Brooke</au><au>Pierce, Robert J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial</atitle><jtitle>Trials</jtitle><addtitle>Trials</addtitle><date>2013-06-19</date><risdate>2013</risdate><volume>14</volume><issue>1</issue><spage>181</spage><epage>181</epage><pages>181-181</pages><issn>1745-6215</issn><eissn>1745-6215</eissn><abstract>Quadriplegia is a severe, catastrophic injury that predominantly affects people early in life, resulting in lifelong physical disability. Obstructive sleep apnoea is a direct consequence of quadriplegia and is associated with neurocognitive deficits, sleepiness and reduced quality of life. The usual treatment for sleep apnoea is nasal continuous positive airway pressure (CPAP); however, this is poorly tolerated in quadriplegia. To encourage patients to use this therapy, we have to demonstrate that the benefits outweigh the inconvenience. We therefore propose a prospective, multinational randomized controlled trial of three months of CPAP for obstructive sleep apnoea after acute quadriplegia.
Specialist spinal cord injury centres across Australia, New Zealand, the UK and Canada will recruit medically stable individuals who have sustained a (new) traumatic quadriplegia (complete or incomplete second cervical to first thoracic level lesions). Participants will be screened for obstructive sleep apnoea using full, portable sleep studies. Those with an apnoea hypopnoea index greater than 10 per hour will proceed to an initial three-night trial of CPAP. Those who can tolerate CPAP for at least 4 hours on at least one night of the initial trial will be randomized to either usual care or a 3-month period of auto-titrating CPAP. The primary hypothesis is that nocturnal CPAP will improve neuropsychological functioning more than usual care alone. The secondary hypothesis is that the magnitude of improvement of neuropsychological function will be predicted by the severity of baseline sleepiness measures, sleep fragmentation and sleep apnoea. Neuropsychological tests and full polysomnography will be performed at baseline and 3 months with interim measures of sleepiness and symptoms of autonomic dysfunction measured weekly. Spirometry will be performed monthly. Neuropsychological tests will be administered by blinded assessors. Recruitment commenced in July 2009.
The results of this trial will demonstrate the effect of nocturnal CPAP treatment of obstructive sleep apnoea in acute quadriplegia. If CPAP can improve neurocognitive function after injury, it is likely that rehabilitation and subsequent community participation will be substantially improved for this group of predominantly young and severely physically disabled people.
Australian New Zealand Clinical Trial Registry ACTRN12605000799651.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>23777510</pmid><doi>10.1186/1745-6215-14-181</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activities of daily living Acute Disease Australia Autonomic Nervous System - physiopathology Canada Care and treatment Clinical Protocols Complications and side effects Continuous Positive Airway Pressure Humans Medical equipment and supplies industry Medical test kit industry Neuropsychological Tests New Zealand Patient outcomes Physically disabled persons Polysomnography Predictive Value of Tests Prospective Studies Quadriplegia Quadriplegia - complications Quadriplegia - physiopathology Quadriplegia - psychology Quality of Life Research Design Sleep Sleep apnea syndromes Sleep Apnea, Obstructive - diagnosis Sleep Apnea, Obstructive - etiology Sleep Apnea, Obstructive - physiopathology Sleep Apnea, Obstructive - psychology Sleep Apnea, Obstructive - therapy Spirometry Study Protocol Surveys and Questionnaires Time Factors Treatment Outcome United Kingdom |
title | Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial |
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