Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12087
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dc.contributor.authorSheers, Nicoleen
dc.contributor.authorBerlowitz, David Jen
dc.contributor.authorRautela, Lindaen
dc.contributor.authorBatchelder, Ianen
dc.contributor.authorHopkinson, Kimen
dc.contributor.authorHoward, Mark Een
dc.date.accessioned2015-05-16T01:44:02Z
dc.date.available2015-05-16T01:44:02Z
dc.date.issued2014-02-20en
dc.identifier.citationAmyotrophic Lateral Sclerosis & Frontotemporal Degeneration 2014; 15(3-4): 180-4en
dc.identifier.govdoc24555916en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12087en
dc.description.abstractNon-invasive ventilation (NIV) increases survival and quality of life in motor neuron disease (MND). NIV implementation historically occurred during a multi-day inpatient admission at this institution; however, increased demand led to prolonged waiting times. The aim of this study was to evaluate the introduction of an ambulatory model of NIV implementation. A prospective cohort study was performed. Inclusion criteria were referral for NIV implementation six months pre- or post-commencement of the Day Admission model. This model involved a 4-h stay to commence ventilation with follow-up in-laboratory polysomnography titration and outpatient attendance. Outcome measures included waiting time, hospital length of stay, adverse events and polysomnography data. Results indicated that after changing to the Day Admission model the median waiting time fell from 30 to 13.5 days (p < 0.04) and adverse events declined (4/17 pre- (three deaths, one acute admission) vs. 0/12 post-). Survival was also prolonged (median (IQR) 278 (51-512) days pre- vs 580 (306-1355) days post-introduction of the Day Admission model; hazard ratio 0.41, p = 0.04). Daytime PaCO2 was no different. In conclusion, reduced waiting time to commence ventilation and improved survival were observed following introduction of an ambulatory model of NIV implementation in people with MND, with no change in the effectiveness of ventilation.en
dc.language.isoenen
dc.subject.otherNon-invasive ventilationen
dc.subject.otherambulatory model of careen
dc.subject.othermotor neuron diseaseen
dc.subject.othersurvivalen
dc.subject.otherAmbulatory Careen
dc.subject.otherCohort Studiesen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherKaplan-Meier Estimateen
dc.subject.otherMaleen
dc.subject.otherMotor Neuron Disease.complications.mortalityen
dc.subject.otherNoninvasive Ventilation.methodsen
dc.subject.otherOutcome Assessment (Health Care)en
dc.subject.otherOutpatientsen
dc.subject.otherPolysomnographyen
dc.subject.otherRespiratory Insufficiency.etiology.mortality.therapyen
dc.subject.otherStatistics, Nonparametricen
dc.subject.otherTime Factorsen
dc.subject.otherWaiting Lists.mortalityen
dc.titleImproved survival with an ambulatory model of non-invasive ventilation implementation in motor neuron disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleAmyotrophic lateral sclerosis & frontotemporal degenerationen
dc.identifier.affiliationVictorian Respiratory Support Service (VRSS), Austin Health , Heidelberg, Victoria , Australiaen
dc.identifier.doi10.3109/21678421.2014.881376en
dc.description.pages180-4en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24555916en
dc.type.austinJournal Articleen
local.name.researcherBerlowitz, David J
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
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