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Title: | NIV@Home: a pilot randomized controlled trial of in-home noninvasive ventilation initiation compared to a single-day admission model. | Austin Authors: | Sheers, Nicole L;Hannan, Liam M ;Rautela, Linda ;Graco, Marnie ;Jones, Jennifer R A ;Retica, Sarah;Saravanan, Krisha ;Burgess, Nicola ;McGaw, Rebekah;Donovan, Ashleigh;Clohessy, Talia ;Chao, Caroline ;Charles, Cameron;Howard, Mark E ;Berlowitz, David J | Affiliation: | Institute for Breathing and Sleep The University of Melbourne, Parkville, Australia.;Department of Respiratory Medicine, Northern Health, Epping, Australia. Physiotherapy The University of Melbourne, Parkville, Australia.;Department of Physiotherapy, Austin Health, Heidelberg, Australia, and. Respiratory and Sleep Medicine Department 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. Department 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. |
Issue Date: | 21-Oct-2024 | Date: | 2024 | Publication information: | Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration 2024-10-21 | Abstract: | Objective: 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. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/35567 | DOI: | 10.1080/21678421.2024.2416668 | ORCID: | 0000-0003-1847-4266 0000-0001-6517-6507 0000-0001-6048-0147 0000-0002-9443-3426 0000-0001-8791-761X 0009-0009-8638-8109 0000-0001-6225-1495 0000-0001-7772-1496 0000-0003-2543-8722 |
Journal: | Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration | Start page: | 1 | End page: | 10 | PubMed URL: | 39431591 | ISSN: | 2167-9223 | Type: | Journal Article | Subjects: | ALS MND NIV Noninvasive ventilation amyotrophic lateral sclerosis motor neurone disease respiratory insufficiency ventilation |
Appears in Collections: | Journal articles |
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