Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28935
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dc.contributor.authorKatz, Sherri L-
dc.contributor.authorMah, Jean K-
dc.contributor.authorMcMillan, Hugh J-
dc.contributor.authorCampbell, Craig-
dc.contributor.authorBijelić, Vid-
dc.contributor.authorBarrowman, Nick-
dc.contributor.authorMomoli, Franco-
dc.contributor.authorBlinder, Henrietta-
dc.contributor.authorAaron, Shawn D-
dc.contributor.authorMcAdam, Laura C-
dc.contributor.authorNguyen, The Thanh Diem-
dc.contributor.authorTarnopolsky, Mark-
dc.contributor.authorWensley, David F-
dc.contributor.authorZielinski, David-
dc.contributor.authorRose, Louise-
dc.contributor.authorSheers, Nicole-
dc.contributor.authorBerlowitz, David J-
dc.contributor.authorWolfe, Lisa-
dc.contributor.authorMcKim, Doug-
dc.date2022-
dc.date.accessioned2022-03-23T05:10:56Z-
dc.date.available2022-03-23T05:10:56Z-
dc.date.issued2022-03-02-
dc.identifier.citationThorax 2022-08; 77(8): 805-811en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28935-
dc.description.abstractImpaired cough results in airway secretion retention, atelectasis and pneumonia in individuals with Duchenne muscular dystrophy (DMD). Lung volume recruitment (LVR) stacks breaths to inflate the lungs to greater volumes than spontaneous effort. LVR is recommended in DMD clinical care guidelines but is not well studied. We aimed to determine whether twice-daily LVR, compared with standard of care alone, attenuates the decline in FVC at 2 years in boys with DMD. In this multicentre, assessor-blinded, randomised controlled trial, boys with DMD, aged 6-16 years with FVC >30% predicted, were randomised to receive conventional treatment or conventional treatment plus manual LVR twice daily for 2 years. The primary outcome was FVC % predicted at 2 years, adjusted for baseline FVC % predicted, age and ambulatory status. Secondary outcomes included change in chest wall distensibility (maximal insufflation capacity minus FVC) and peak cough flow. Sixty-six boys (36 in LVR group, 30 in control) were evaluated (median age (IQR): 11.5 years (9.5-13.5), median baseline FVC (IQR): 85% predicted (73-96)). Adjusted mean difference in FVC between groups at 2 years was 1.9% predicted (95% CI -6.9% to 10.7%; p=0.68) in the direction of treatment benefit. We found no differences in secondary outcomes. There was no difference in decline in FVC % predicted with use of twice-daily LVR for boys with DMD and relatively normal lung function. The burden associated with routine LVR may outweigh the benefit. Benefits of LVR to maintain lung health in boys with worse baseline lung function still need to be clarified. NCT01999075.en
dc.language.isoeng-
dc.subjectDuchenne muscular dystrophyen
dc.subjectchilden
dc.subjectlung volume recruitmenten
dc.subjectrandomized controlled trialen
dc.subjectrespiratory therapyen
dc.titleRoutine lung volume recruitment in boys with Duchenne muscular dystrophy: a randomised clinical trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleThoraxen
dc.identifier.affiliationDepartment of Physiotherapy, The University of Melbourne, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Medicine and Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA..en
dc.identifier.affiliationDepartment of Respiratory Care, Shirley Ryan AbilityLab, Chicago, Illinois, USA..en
dc.identifier.affiliationFaculty of Medicine Dentistry and Health Sciences, The University of Melbourne, Melbourne, Victoria, Australia..en
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.affiliationDepartment of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada..en
dc.identifier.affiliationDepartment of Pediatric and Clinical Neurosciences, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada..en
dc.identifier.affiliationInstitute for Breathing and Sleepen
dc.identifier.affiliationDivision of Pediatric Neurology, Alberta Children's Hospital, Calgary, Alberta, Canada..en
dc.identifier.affiliationDepartment of Pediatrics, London Health Sciences Centre Children's Hospital, London, Ontario, Canada..en
dc.identifier.affiliationDepartment of Pediatrics, Epidemiology and Clinical Neurological Sciences, University of Western Ontario, London, Ontario, Canada..en
dc.identifier.affiliationCHEO Research Institute, Ottawa, Ontario, Canada..en
dc.identifier.affiliationFaculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada..en
dc.identifier.affiliationAlberta Children's Hospital Research Institute, Calgary, Alberta, Canada..en
dc.identifier.affiliationDivision of Respirology, Department of Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada..en
dc.identifier.affiliationOttawa Hospital Research Institute, Ottawa, Ontario, Canada..en
dc.identifier.affiliationHolland Bloorview Kids Rehabilitation Hospital, Toronto, Ontario, Canada..en
dc.identifier.affiliationDepartment of Respiratory Medicine, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada..en
dc.identifier.affiliationDivision of Neuromuscular and Neurometabolic Disease, McMaster University, Hamilton, Ontario, Canada..en
dc.identifier.affiliationDivision of Pediatric Respirology, Department of Pediatrics, BC Children's Hospital, Vancouver, British Columbia, Canada..en
dc.identifier.affiliationDivision of Pediatric Respirology, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada..en
dc.identifier.affiliationDepartment of Midwifery and Palliative Care, King's College London Florence Nightingale School of Nursing and Midwifery, London, London, UK..en
dc.identifier.affiliationOttawa Hospital Research Institute, Ottawa, Ontario, Canada..en
dc.identifier.affiliationCritical Care Directorate and Lane Fox Respiratory Unit, Guy's and St Thomas' NHS Foundation Trust, London, London, UK..en
dc.identifier.affiliationDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada..en
dc.identifier.affiliationDepartment of Pediatrics, The University of British Columbia, Vancouver, British Columbia, Canada..en
dc.identifier.affiliationResearch Institute of the McGill University Health Centre, Montreal, Quebec, Canada..en
dc.identifier.affiliationCANVent Respiratory Rehabilitation Services, Ottawa Hospital Rehabilitation Centre, Ottawa, Ontario, Canada..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35236763/en
dc.identifier.doi10.1136/thoraxjnl-2021-218196en
dc.type.contentTexten
dc.identifier.orcidhttp://orcid.org/0000-0001-6307-6094en
dc.identifier.orcidhttp://orcid.org/0000-0003-1847-4266en
dc.identifier.orcidhttp://orcid.org/0000-0003-2543-8722en
dc.identifier.pubmedid35236763-
local.name.researcherBerlowitz, David J
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
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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