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      Routine lung volume recruitment in boys with Duchenne muscular dystrophy: a randomised clinical trial

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          Abstract

          Background

          Impaired 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.

          Methods

          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.

          Results

          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.

          Conclusion

          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.

          Trial registration number

          NCT01999075.

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          Most cited references40

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          Standardisation of the measurement of lung volumes.

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            Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management

            Since the publication of the Duchenne muscular dystrophy (DMD) care considerations in 2010, multidisciplinary care of this severe, progressive neuromuscular disease has evolved. In conjunction with improved patient survival, a shift to more anticipatory diagnostic and therapeutic strategies has occurred, with a renewed focus on patient quality of life. In 2014, a steering committee of experts from a wide range of disciplines was established to update the 2010 DMD care considerations, with the goal of improving patient care. The new care considerations aim to address the needs of patients with prolonged survival, to provide guidance on advances in assessments and interventions, and to consider the implications of emerging genetic and molecular therapies for DMD. The committee identified 11 topics to be included in the update, eight of which were addressed in the original care considerations. The three new topics are primary care and emergency management, endocrine management, and transitions of care across the lifespan. In part 1 of this three-part update, we present care considerations for diagnosis of DMD and neuromuscular, rehabilitation, endocrine (growth, puberty, and adrenal insufficiency), and gastrointestinal (including nutrition and dysphagia) management.
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              Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management

              A coordinated, multidisciplinary approach to care is essential for optimum management of the primary manifestations and secondary complications of Duchenne muscular dystrophy (DMD). Contemporary care has been shaped by the availability of more sensitive diagnostic techniques and the earlier use of therapeutic interventions, which have the potential to improve patients' duration and quality of life. In part 2 of this update of the DMD care considerations, we present the latest recommendations for respiratory, cardiac, bone health and osteoporosis, and orthopaedic and surgical management for boys and men with DMD. Additionally, we provide guidance on cardiac management for female carriers of a disease-causing mutation. The new care considerations acknowledge the effects of long-term glucocorticoid use on the natural history of DMD, and the need for care guidance across the lifespan as patients live longer. The management of DMD looks set to change substantially as new genetic and molecular therapies become available.
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                Author and article information

                Journal
                Thorax
                Thorax
                thoraxjnl
                thorax
                Thorax
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0040-6376
                1468-3296
                August 2022
                2 March 2022
                : 77
                : 8
                : 805-811
                Affiliations
                [1 ] departmentDepartment of Pediatrics , Children's Hospital of Eastern Ontario , Ottawa, Ontario, Canada
                [2 ] CHEO Research Institute , Ottawa, Ontario, Canada
                [3 ] departmentFaculty of Medicine , University of Ottawa , Ottawa, Ontario, Canada
                [4 ] departmentDivision of Pediatric Neurology , Alberta Children's Hospital , Calgary, Alberta, Canada
                [5 ] departmentDepartment of Pediatric and Clinical Neurosciences , University of Calgary Cumming School of Medicine , Calgary, Alberta, Canada
                [6 ] Alberta Children's Hospital Research Institute , Calgary, Alberta, Canada
                [7 ] departmentDepartment of Pediatrics, Epidemiology and Clinical Neurological Sciences , University of Western Ontario , London, Ontario, Canada
                [8 ] departmentDepartment of Pediatrics , London Health Sciences Centre Children's Hospital , London, Ontario, Canada
                [9 ] Ottawa Hospital Research Institute , Ottawa, Ontario, Canada
                [10 ] departmentDivision of Respirology, Department of Medicine , The Ottawa Hospital , Ottawa, Ontario, Canada
                [11 ] Holland Bloorview Kids Rehabilitation Hospital , Toronto, Ontario, Canada
                [12 ] departmentDepartment of Pediatrics , University of Toronto , Toronto, Ontario, Canada
                [13 ] departmentDepartment of Respiratory Medicine , Centre Hospitalier Universitaire Sainte-Justine , Montreal, Quebec, Canada
                [14 ] departmentDivision of Neuromuscular and Neurometabolic Disease , McMaster University , Hamilton, Ontario, Canada
                [15 ] departmentDivision of Pediatric Respirology, Department of Pediatrics , BC Children's Hospital , Vancouver, British Columbia, Canada
                [16 ] departmentDepartment of Pediatrics , The University of British Columbia , Vancouver, British Columbia, Canada
                [17 ] departmentDivision of Pediatric Respirology, Department of Pediatrics , Montreal Children's Hospital , Montreal, Quebec, Canada
                [18 ] Research Institute of the McGill University Health Centre , Montreal, Quebec, Canada
                [19 ] departmentDepartment of Midwifery and Palliative Care , King's College London Florence Nightingale School of Nursing and Midwifery , London, London, UK
                [20 ] departmentCritical Care Directorate and Lane Fox Respiratory Unit , Guy's and St Thomas' NHS Foundation Trust , London, London, UK
                [21 ] departmentDepartment of Respiratory and Sleep Medicine , Austin Health , Heidelberg, Victoria, Australia
                [22 ] Institute for Breathing and Sleep , Heidelberg, Victoria, Australia
                [23 ] departmentFaculty of Medicine Dentistry and Health Sciences , The University of Melbourne , Melbourne, Victoria, Australia
                [24 ] departmentDepartment of Respiratory and Sleep Medicine , Institute for Breathing and Sleep , Heidelberg, Victoria, Australia
                [25 ] departmentDepartment of Physiotherapy , The University of Melbourne , Melbourne, Victoria, Australia
                [26 ] departmentDepartment of Medicine and Neurology , Northwestern University Feinberg School of Medicine , Chicago, Illinois, USA
                [27 ] departmentDepartment of Respiratory Care , Shirley Ryan AbilityLab , Chicago, Illinois, USA
                [28 ] departmentCANVent Respiratory Rehabilitation Services , Ottawa Hospital Rehabilitation Centre , Ottawa, Ontario, Canada
                Author notes
                [Correspondence to ] Dr Sherri L Katz, Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada; skatz@ 123456cheo.on.ca
                Author information
                http://orcid.org/0000-0001-6307-6094
                http://orcid.org/0000-0003-1847-4266
                http://orcid.org/0000-0003-2543-8722
                Article
                thoraxjnl-2021-218196
                10.1136/thoraxjnl-2021-218196
                9340020
                35236763
                8bf193ed-4507-48fd-b041-f75f29f1f002
                © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 08 September 2021
                : 25 January 2022
                Funding
                Funded by: Jesse's Journey;
                Award ID: N/A
                Categories
                Paediatric Lung Disease
                1506
                2313
                Original research
                Custom metadata
                unlocked

                Surgery
                child,duchenne muscular dystrophy,lung volume recruitment,randomized controlled trial,respiratory therapy

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