Document Detail


Respiratory muscle function in cystic fibrosis.
MedLine Citation:
PMID:  2247866     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Maximal static expiratory and inspiratory mouth pressures (PEmax and PImax) and quadriceps femoris muscle strength were measured in 25 patients aged 16-28 years with cystic fibrosis (mean FEV1 46% predicted). Mean (SD) PEmax was 64% (18%) predicted (below 75% predicted in 16 of the 25 patients), and PImax was 64% (24%) predicted (below 75% predicted in 14 patients). Quadriceps muscle strength was 68% (20%) predicted (below 75% predicted in 17 patients). The relatively small reduction in respiratory muscle strength in these patients was unlikely to have contributed appreciably to their respiratory problems.
Authors:
A Mier; A Redington; C Brophy; M Hodson; M Green
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Thorax     Volume:  45     ISSN:  0040-6376     ISO Abbreviation:  Thorax     Publication Date:  1990 Oct 
Date Detail:
Created Date:  1991-01-09     Completed Date:  1991-01-09     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  0417353     Medline TA:  Thorax     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  750-2     Citation Subset:  IM    
Affiliation:
Brompton Hospital, London.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Air Pressure
Cystic Fibrosis / physiopathology*
Female
Humans
Male
Muscle Contraction / physiology
Respiration / physiology
Respiratory Muscles / physiopathology*
Thigh / physiopathology
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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