Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35567
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dc.contributor.authorSheers, Nicole L-
dc.contributor.authorHannan, Liam M-
dc.contributor.authorRautela, Linda-
dc.contributor.authorGraco, Marnie-
dc.contributor.authorJones, Jennifer R A-
dc.contributor.authorRetica, Sarah-
dc.contributor.authorSaravanan, Krisha-
dc.contributor.authorBurgess, Nicola-
dc.contributor.authorMcGaw, Rebekah-
dc.contributor.authorDonovan, Ashleigh-
dc.contributor.authorClohessy, Talia-
dc.contributor.authorChao, Caroline-
dc.contributor.authorCharles, Cameron-
dc.contributor.authorHoward, Mark E-
dc.contributor.authorBerlowitz, David J-
dc.date2024-
dc.date.accessioned2024-12-02T00:02:52Z-
dc.date.available2024-12-02T00:02:52Z-
dc.date.issued2024-10-21-
dc.identifier.citationAmyotrophic Lateral Sclerosis & Frontotemporal Degeneration 2024-10-21en_US
dc.identifier.issn2167-9223-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35567-
dc.description.abstractObjective: Noninvasive ventilation (NIV) is the primary treatment for respiratory insufficiency in neuromuscular disease. NIV implementation is usually conducted within hospitals; however, in-home implementation with intensive follow-up is an effective alternative. This pilot study aimed to assess model feasibility, acceptability, and NIV usage at 12-weeks after a single visit in-home implementation of NIV with remote monitoring follow-up (NIV@Home) compared to an in-hospital day admission NIV initiation plus planned polysomnography (Usual care). Methods: A single-blinded randomized controlled trial (www.anzctr.org.au ACTRN12620000682943) of adults with neuromuscular disease referred for NIV implementation. Participants were stratified by disease (MND or Other diagnoses) and bulbar symptoms before randomization to NIV@Home or Usual care, with follow-up at 12-weeks. The primary outcome was NIV usage. Secondary outcomes included feasibility, health-related quality of life, symptoms, carer burden, and NIV experience (semi-structured qualitative interviews). Results: Twenty-three participants (MND bulbar = 9, MND non-bulbar = 11, Other = 3) were randomized (NIV@Home = 9). No statistical differences were observed in the percentage of MND participants using NIV for >4 hours/day (NIV@Home = 33% vs. Usual care = 60%, p = 0.370), average use (NIV@Home = 2.4 [1.5-9.3] vs. 5.3 [1.8-7.0] hours/day, p = 0.568), or secondary outcomes. In-home NIV implementation was feasible and safe but took more therapist time (NIV@Home = 278 [270-305] vs. 172 [130-200] minutes, p < 0.001). Participants in the NIV@Home group reported substantial advantages to receiving care in home. Conclusion: In-home NIV implementation is feasible and acceptable to people with MND but requires more therapist time. Larger studies are required to determine whether there are clinically important differences between this model of NIV initiation and a traditional hospital-based model.en_US
dc.language.isoeng-
dc.subjectALSen_US
dc.subjectMNDen_US
dc.subjectNIVen_US
dc.subjectNoninvasive ventilationen_US
dc.subjectamyotrophic lateral sclerosisen_US
dc.subjectmotor neurone diseaseen_US
dc.subjectrespiratory insufficiencyen_US
dc.subjectventilationen_US
dc.titleNIV@Home: a pilot randomized controlled trial of in-home noninvasive ventilation initiation compared to a single-day admission model.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAmyotrophic Lateral Sclerosis & Frontotemporal Degenerationen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationThe University of Melbourne, Parkville, Australia.;Department of Respiratory Medicine, Northern Health, Epping, Australia.en_US
dc.identifier.affiliationPhysiotherapyen_US
dc.identifier.affiliationThe University of Melbourne, Parkville, Australia.;Department of Physiotherapy, Austin Health, Heidelberg, Australia, and.en_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Australia.;Institute for Breathing and Sleep, Heidelberg, Australia.;The University of Melbourne, Parkville, Australia.;Turner Institute for Brain and Mental Health, Monash University, Clayton, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Australia.;Institute for Breathing and Sleep, Heidelberg, Australia.;The University of Melbourne, Parkville, Australia.;Department of Physiotherapy, Austin Health, Heidelberg, Australia, and.en_US
dc.identifier.doi10.1080/21678421.2024.2416668en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-1847-4266en_US
dc.identifier.orcid0000-0001-6517-6507en_US
dc.identifier.orcid0000-0001-6048-0147en_US
dc.identifier.orcid0000-0002-9443-3426en_US
dc.identifier.orcid0000-0001-8791-761Xen_US
dc.identifier.orcid0009-0009-8638-8109en_US
dc.identifier.orcid0000-0001-6225-1495en_US
dc.identifier.orcid0000-0001-7772-1496en_US
dc.identifier.orcid0000-0003-2543-8722en_US
dc.identifier.pubmedid39431591-
dc.description.startpage1-
dc.description.endpage10-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptPhysiotherapy-
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-
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