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呼气末正压(PEP)作为囊性纤维化的肺部物理治疗:一项初步研究。

Positive expiratory pressure (PEP) as lung physiotherapy in cystic fibrosis: a pilot study.

作者信息

Tønnesen P, Støvring S

出版信息

Eur J Respir Dis. 1984 Aug;65(6):419-22.

PMID:6381080
Abstract

Positive expiratory pressure (PEP) on a face mask was compared with conventional lung physiotherapy in 12 patients with cystic fibrosis. Residual volume (p less than 0.02) and functional residual capacity (NS) was reduced and vital capacity increased (NS) during 6-9 months of PEP treatment. The subjective sputum production was significantly greater during the PEP period. PEP is easy to administer and is inexpensive.

摘要

在12例囊性纤维化患者中,对面罩式呼气末正压通气(PEP)与传统肺部物理治疗进行了比较。在PEP治疗6 - 9个月期间,残气量(p<0.02)减少,功能残气量(无显著差异)减少,肺活量增加(无显著差异)。在PEP治疗期间,主观痰液生成量显著增加。PEP易于实施且成本低廉。

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