Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Pediatr Rehabil Med ; 7(3): 255-65, 2014.
Article in English | MEDLINE | ID: mdl-25260508

ABSTRACT

PURPOSE: Respiratory muscle weakness is a primary therapeutic challenge for patients with infantile Pompe disease. We previously described the clinical implementation of a respiratory muscle training (RMT) regimen in two adults with late-onset Pompe disease; both demonstrated marked increases in inspiratory and expiratory muscle strength in response to RMT. However, the use of RMT in pediatric survivors of infantile Pompe disease has not been previously reported. METHOD: We report the effects of an intensive RMT program on maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP) using A-B-A (baseline-treatment-posttest) single subject experimental design in two pediatric survivors of infantile Pompe disease. Both subjects had persistent respiratory muscle weakness despite long-term treatment with alglucosidase alfa. RESULTS: Subject 1 demonstrated negligible to modest increases in MIP/MEP (6% increase in MIP, d=0.25; 19% increase in MEP, d=0.87), while Subject 2 demonstrated very large increases in MIP/MEP (45% increase in MIP, d=2.38; 81% increase in MEP, d=4.31). Following three-month RMT withdrawal, both subjects maintained these strength increases and demonstrated maximal MIP and MEP values at follow-up. CONCLUSION: Intensive RMT may be a beneficial treatment for respiratory muscle weakness in pediatric survivors of infantile Pompe disease.


Subject(s)
Breathing Exercises , Glycogen Storage Disease Type II/physiopathology , Glycogen Storage Disease Type II/rehabilitation , Respiratory Muscles/physiology , Airway Resistance/physiology , Child , Exhalation/physiology , Humans , Inhalation/physiology , Lung/physiopathology , Muscle Contraction/physiology
2.
Mol Genet Metab ; 104(3): 417-20, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21641843

ABSTRACT

Respiratory muscle strength training (RMST) is an exercise-based intervention which targets respiratory muscle weakness. We implemented RMST in two patients with late-onset Pompe disease (LOPD), both who had received long-term enzyme replacement therapy and had severe respiratory weakness. Over 16-32 weeks, inspiratory muscle strength increased by 73-74%. Expiratory muscle strength increased 31-48% over 12-22 weeks. These findings suggest that RMST may increase respiratory muscle strength, even in the setting of LOPD and severe baseline weakness.


Subject(s)
Glycogen Storage Disease Type II/rehabilitation , Muscle Strength/physiology , Resistance Training/methods , Respiratory Muscles/physiology , Exhalation/physiology , Female , Glycogen Storage Disease Type II/drug therapy , Humans , Inhalation/physiology , Male , Middle Aged , alpha-Glucosidases/therapeutic use
SELECTION OF CITATIONS
SEARCH DETAIL
...