Inspiratory flow reserve in boys with Duchenne muscular dystrophy

Patients with advanced muscular dystrophy frequently develop ventilatory failure. Currently respiratory impairment usually is assessed by measuring vital capacity and the mouth pressure generated during a maximal inspiratory maneuver (PI,max), neither of which directly measures ventilatory capacity....

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Veröffentlicht in:	Pediatric pulmonology 2001-06, Vol.31 (6), p.451-457
Hauptverfasser:	De Bruin, Pedro F., Ueki, Jun, Bush, Andrew, Y. Manzur, Adnan, Watson, Ann, Pride, Neil B.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Biological and medical sciences boys Case-Control Studies Child Humans Inspiratory Reserve Volume Investigative techniques of respiratory function Investigative techniques, diagnostic techniques (general aspects) Male maximum inspiratory flow maximum inspiratory pressure Medical sciences muscle weakness muscular dystrophy Muscular Dystrophy, Duchenne - complications neuromuscular disease neuromuscular disease, boys pulmonary functions Respiratory Insufficiency - diagnosis Respiratory Insufficiency - etiology Respiratory Mechanics Sensitivity and Specificity tidal inspiratory flow ventilatory reserve Vital Capacity
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