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Routine lung volume recruitment in boys with Duchenne muscular dystrophy: a randomised clinical trial.
Katz, Sherri L; Mah, Jean K; McMillan, Hugh J; Campbell, Craig; Bijelic, Vid; Barrowman, Nick; Momoli, Franco; Blinder, Henrietta; Aaron, Shawn D; McAdam, Laura C; Nguyen, The Thanh Diem; Tarnopolsky, Mark; Wensley, David F; Zielinski, David; Rose, Louise; Sheers, Nicole; Berlowitz, David J; Wolfe, Lisa; McKim, Doug.
Afiliação
  • Katz SL; Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada skatz@cheo.on.ca.
  • Mah JK; CHEO Research Institute, Ottawa, Ontario, Canada.
  • McMillan HJ; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Campbell C; Division of Pediatric Neurology, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Bijelic V; Department of Pediatric and Clinical Neurosciences, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
  • Barrowman N; Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Momoli F; Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Blinder H; CHEO Research Institute, Ottawa, Ontario, Canada.
  • Aaron SD; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • McAdam LC; Department of Pediatrics, Epidemiology and Clinical Neurological Sciences, University of Western Ontario, London, Ontario, Canada.
  • Nguyen TTD; Department of Pediatrics, London Health Sciences Centre Children's Hospital, London, Ontario, Canada.
  • Tarnopolsky M; CHEO Research Institute, Ottawa, Ontario, Canada.
  • Wensley DF; CHEO Research Institute, Ottawa, Ontario, Canada.
  • Zielinski D; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Rose L; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Sheers N; CHEO Research Institute, Ottawa, Ontario, Canada.
  • Berlowitz DJ; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Wolfe L; Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • McKim D; Division of Respirology, Department of Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.
Thorax ; 77(8): 805-811, 2022 08.
Article em En | MEDLINE | ID: mdl-35236763
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Thorax Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Thorax Ano de publicação: 2022 Tipo de documento: Article