Long-term effects of lung volume recruitment on maximal inspiratory capacity and vital capacity in duchenne muscular dystrophy

Annals of the American Thoracic Society

Volumn 13, Issue 2, 2016, Pages 217-222

  Katz, Sherri L ^a,b   Barrowman, Nicholas ^a,b   Monsour, Andrea ^a   Su, Santana ^a   Hoey, Lynda ^a   McKim, Douglas ^b,c,d  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^b UNIVERSITY OF OTTAWA   (Canada)

^c Rehabilitation Centre   (Canada)

^d OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

Cough; Neuromuscular diseases; Pulmonary function test; Respiratory therapy; VC

Indexed keywords

ADOLESCENT; ADULT; AIRWAY PRESSURE; ARTICLE; BREATHING EXERCISE; BREATHING MUSCLE; CHILD; CLINICAL ARTICLE; COHORT ANALYSIS; DUCHENNE MUSCULAR DYSTROPHY; FORCED VITAL CAPACITY; HUMAN; INSPIRATORY CAPACITY; LUNG CHARACTERISTICS AND FUNCTIONS; LUNG COMPLIANCE; LUNG VOLUME RECRUITMENT; MAXIMAL INSPIRATORY CAPACITY; MAXIMUM EXPIRATORY PRESSURE; MAXIMUM INSPIRATORY PRESSURE; MUSCLE WEAKNESS; PEAK COUGH FLOW; RETROSPECTIVE STUDY; TERTIARY CARE CENTER; THERAPY EFFECT; VITAL CAPACITY; LUNG; MALE; MUSCULAR DYSTROPHY, DUCHENNE; PATHOPHYSIOLOGY; PHYSIOLOGY; POSITIVE END EXPIRATORY PRESSURE; PROCEDURES; RESPIRATORY CARE; TIME; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; COHORT STUDIES; HUMANS; INSPIRATORY CAPACITY; LUNG; LUNG COMPLIANCE; MALE; MUSCULAR DYSTROPHY, DUCHENNE; POSITIVE-PRESSURE RESPIRATION; RESPIRATORY THERAPY; RETROSPECTIVE STUDIES; TIME; VITAL CAPACITY; YOUNG ADULT;

EID: 84988915506     PISSN: 23256621     EISSN: None     Source Type: Journal    
DOI: 10.1513/AnnalsATS.201507-475BC     Document Type: Article

References (27)

1. Panitch HB. The pathophysiology of respiratory impairment in pediatric neuromuscular diseases. Pediatrics 2009;123:S215-S218.
2. Kravitz RM. Airway clearance in Duchenne muscular dystrophy. Pediatrics 2009;123:S231-235.
3. Kang SW, Bach JR. Maximum insufflation capacity. Chest 2000;118: 61-65.
4. Chatwin M, Ross E, Hart N, Nickol AH, Polkey MI, Simonds AK. Cough augmentation with mechanical insufflation/exsufflation in patients with neuromuscular weakness. Eur Respir J 2003;21:502-508.
5. Bach JR. Mechanical insufflation/exsufflation: has it come of age? A commentary. Eur Respir J 2003;21:385-386.
6. Gomez-Merino E, Bach JR. Duchenne muscular dystrophy: prolongation of life by noninvasive ventilation and mechanically assisted coughing. Am J Phys Med Rehabil 2002;81:411-415.
7. Bach JR, Ishikawa Y, Kim H. Prevention of pulmonary morbidity for patients with Duchenne muscular dystrophy. Chest 1997;112: 1024-1028.
8. Marchant WA, Fox R. Postoperative use of a cough-assist device in avoiding prolonged intubation. Br J Anaesth 2002;89:644-647.
9. McKim D. Keeping ventilated and 'at-risk' patients out of intensive care unit. Can Respir J 2008;15:9C-10C.
10. McKim DA, Road J, Avendano M, Abdool S, Cote F, Duguid N, Fraser J, Maltais F, Morrison DL, O'Connell C, et al.; Canadian Thoracic Society Home Mechanical Ventilation Committee. Home mechanical ventilation: a Canadian Thoracic Society clinical practice guideline. Can Respir J 2011;18:197-215.
11. Finder JD, Birnkrant D, Carl J, Farber HJ, Gozal D, Iannaccone ST, Kovesi T, Kravitz RM, Panitch H, Schramm C, et al.; American Thoracic Society. Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement. Am J Respir Crit Care Med 2004;170:456-465.
12. Birnkrant DJ, Bushby KM, Amin RS, Bach JR, Benditt JO, Eagle M, Finder JD, Kalra MS, Kissel JT, Koumbourlis AC, et al. The respiratory management of patients with Duchenne muscular dystrophy: a DMD care considerations working group specialty article. Pediatr Pulmonol 2010;45:739-748.
13. Hull J. British Thoracic Society guideline for respiratory management of children with neuromuscular weakness: commentary. Thorax 2012; 67:654-655.
14. Kang SW, Kang YS, Moon JH, Yoo TW. Assisted cough and pulmonary compliance in patients with Duchenne muscular dystrophy. Yonsei Med J 2005;46:233-238.
15. Bach JR, Mahajan K, Lipa B, Saporito L, Goncalves M, Komaroff E. Lung insufflation capacity in neuromuscular disease. Am J Phys Med Rehabil 2008;87:720-725.
16. Marques TB, Neves JdeC, Portes LA, Salge JM, Zanoteli E, Reed UC. Air stacking: effects on pulmonary function in patients with spinal muscular atrophy and in patients with congenital muscular dystrophy. J Bras Pneumol 2014;40:528-534.
17. Panitch HB. Airway clearance in children with neuromuscular weakness. Curr Opin Pediatr 2006;18:277-281.
18. Bach JR. Mechanical insufflation-exsufflation: comparison of peak expiratory flows with manually assisted and unassisted coughing techniques. Chest 1993;104:1553-1562.
19. Bach JR, Smith WH, Michaels J, Saporito L, Alba AS, Dayal R, Pan J. Airway secretion clearance by mechanical exsufflation for post-poliomyelitis ventilator-assisted individuals. Arch Phys Med Rehabil 1993;74:170-177.
20. McKim DA, Katz SL, Barrowman N, Ni A, LeBlanc C. Lung volume recruitment slows pulmonary function decline in Duchenne muscular dystrophy. Arch Phys Med Rehabil 2012;93:1117-1122.
21. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)-a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform 2009;42:377-381.
22. McKim D, LeBlanc C, Walker K, Liteplo J. Respiratory care protocols for spinal cord injuries and neuromuscular diseases. Institute for Rehabilitation Research and Development. Ottowa, Ontario, Canada. 2002.
23. Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med 1999;159:179-187.
24. R Core Team. R: a language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. 2014.
25. Abresch T, McDonald CM, Han JJ, Leshner R, Escolar D, Cnaan A, Hoffman E, Arrieta A, Duong T, Hu F, et al. Pulmonary function characteristics of boys with Duchenne and Becker muscular dystrophy by age groups and steroid use: one year data from the Cooperative International Neuromuscular Research Group (CINRG) Longitudinal Study Project. Presented at the American Academy of Neurology Conference. Toronto, Ontario, 2010.
26. Katz S. Stacking Exercises Aid the Decline in FVC and Sick Time (STEADFAST). Children's Hospital of Eastern Ontario. ClinicalTrials. gov Identifier: NCT01999075 [2013 Nov 14; updated 2015 Oct 13].
27. Bach JR, Saporito LR. Criteria for extubation and tracheostomy tube removal for patients with ventilatory failure: a different approach to weaning. Chest 1996;110:1566-1571.