Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16839
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dc.contributor.authorGainche, Laura-
dc.contributor.authorBerlowitz, David J-
dc.contributor.authorLeGuen, Mariannick-
dc.contributor.authorRuehland, Warren R-
dc.contributor.authorO'Donoghue, Fergal J-
dc.contributor.authorTrinder, John-
dc.contributor.authorGraco, Marnie-
dc.contributor.authorSchembri, Rachel-
dc.contributor.authorEckert, Danny J-
dc.contributor.authorRochford, Peter D-
dc.contributor.authorJordan, Amy S-
dc.date.accessioned2017-09-13T03:51:39Z-
dc.date.available2017-09-13T03:51:39Z-
dc.date.issued2016-11-15-
dc.identifier.citationJournal of Clinical Sleep Medicine 2016; 12(11): 1487-1492en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16839-
dc.description.abstractSTUDY OBJECTIVES: Obstructive sleep apnea (OSA) is common in individuals with tetraplegia and associated with adverse health outcomes. The causes of the high prevalence of OSA in this population are unknown, but it is important to understand as standard treatments are poorly tolerated in tetraplegia. Nasal congestion is common in tetraplegia, possibly because of unopposed parasympathetic activity. Further, nasal obstruction can induce OSA in healthy individuals. We therefore aimed to compare nasal resistance before and after topical administration of a sympathomimetic between 10 individuals with tetraplegia (T) and 9 able-bodied (AB) controls matched for OSA severity, gender, and age. METHODS: Nasal, pharyngeal, and total upper airway resistance were calculated before and every 2 minutes following delivery of ≈0.05 mL of 0.5% atomized phenylephrine to the nostrils and pharyngeal airway. The surface tension of the upper airway lining liquid was also assessed. RESULTS: At baseline, individuals with tetraplegia had elevated nasal resistance (T = 7.0 ± 1.9, AB = 3.0 ± 0.6 cm H2O/L/s), that rapidly fell after phenylephrine (T = 2.3 ± 0.4, p = 0.03 at 2 min) whereas the able-bodied did not change (AB = 2.5 ± 0.5 cm H2O/L/s, p = 0.06 at 2 min). Pharyngeal resistance was non-significantly higher in individuals with tetraplegia than controls at baseline (T = 2.6 ± 0.9, AB = 1.2 ± 0.4 cm H2O/L/s) and was not altered by phenylephrine in either group. The surface tension of the upper airway lining liquid did not differ between groups (T = 64.3 ± 1.0, AB = 62.7 ± 0.6 mN/m). CONCLUSIONS: These data suggest that the unopposed parasympathetic activity in tetraplegia increases nasal resistance, potentially contributing to the high occurrence of OSA in this population.en_US
dc.subjectNasal congestionen_US
dc.subjectQuadriplegiaen_US
dc.subjectSleep apneaen_US
dc.subjectUpper airway physiologyen_US
dc.titleNasal resistance is elevated in people with tetraplegia and is reduced by topical sympathomimetic administrationen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Clinical Sleep Medicineen_US
dc.identifier.affiliationThe Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationThe University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationNeuroscience Research Australia and the University of New South Wales, Randwick, NSW, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27568894en_US
dc.identifier.doi10.5664/jcsm.6272en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-2543-8722en_US
dc.identifier.orcid0000-0001-6048-0147en_US
dc.type.austinJournal Articleen_US
local.name.researcherBerlowitz, David J
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
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