RESPIRATORY MUSCLE FUNCTION IN CYSTIC-FIBROSIS

被引：39
|
作者：
MIER, A [1 ]
REDINGTON, A [1 ]
BROPHY, C [1 ]
HODSON, M [1 ]
GREEN, M [1 ]
机构：
[1] BROMPTON HOSP,LONDON SW3 6HP,ENGLAND
来源：
THORAX | 1990年 / 45卷 / 10期
关键词：
D O I：
10.1136/thx.45.10.750
中图分类号：
R56 [呼吸系及胸部疾病];
学科分类号：
摘要：
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.
引用
收藏
页码：750 / 752
页数：3
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