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Impairment of respiratory muscle function in pulmonary hypertension.

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Impairment of respiratory muscle function in pulmonary hypertension. / Kabitz, Hans-Joachim; Schwoerer, Anja; Bremer, Hinrich-Cordt; Sonntag, Florian; Walterspacher, Stephan; Walker, David; Schaefer, Vanessa; Ehlken, Nicola; Staehler, Gerd; Halank, Michael; Klose, Hans; Ghofrani, Hossein A; Hoeper, Marius M; Gruenig, Ekkehard; Windisch, Wolfram.

in: CLIN SCI, Jahrgang 114, Nr. 2, 2, 2008, S. 165-171.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Kabitz, H-J, Schwoerer, A, Bremer, H-C, Sonntag, F, Walterspacher, S, Walker, D, Schaefer, V, Ehlken, N, Staehler, G, Halank, M, Klose, H, Ghofrani, HA, Hoeper, MM, Gruenig, E & Windisch, W 2008, 'Impairment of respiratory muscle function in pulmonary hypertension.', CLIN SCI, Jg. 114, Nr. 2, 2, S. 165-171. <http://www.ncbi.nlm.nih.gov/pubmed/17764445?dopt=Citation>

APA

Kabitz, H-J., Schwoerer, A., Bremer, H-C., Sonntag, F., Walterspacher, S., Walker, D., Schaefer, V., Ehlken, N., Staehler, G., Halank, M., Klose, H., Ghofrani, H. A., Hoeper, M. M., Gruenig, E., & Windisch, W. (2008). Impairment of respiratory muscle function in pulmonary hypertension. CLIN SCI, 114(2), 165-171. [2]. http://www.ncbi.nlm.nih.gov/pubmed/17764445?dopt=Citation

Vancouver

Kabitz H-J, Schwoerer A, Bremer H-C, Sonntag F, Walterspacher S, Walker D et al. Impairment of respiratory muscle function in pulmonary hypertension. CLIN SCI. 2008;114(2):165-171. 2.

Bibtex

@article{67df96cc2dfd43f6ac18a79430e78949,
title = "Impairment of respiratory muscle function in pulmonary hypertension.",
abstract = "It has been suggested that impaired respiratory muscle function occurs in patients with PH (pulmonary hypertension); however, comprehensive investigations of respiratory muscle function, including the application of non-volitional tests, needed to verify impairment of respiratory muscle strength in patients with PH have not yet been performed. In the present study, respiratory muscle function was assessed in 31 patients with PH (20 females and 11 males; mean pulmonary artery pressure, 51+/-20 mmHg; median World Health Organization class 3.0+/-0.5; 25 patients with pulmonary arterial hypertension and six patients with chronic thromboembolic PH) and in 31 control subjects (20 females and 11 males) well-matched for gender, age and BMI (body mass index). A 6-min walking test was performed to determine exercise capacity. Volitionally assessed maximal inspiratory (7.5+/-2.1 compared with 6.2+/-2.8 kPa; P=0.04) and expiratory (13.3+/-4.2 compared with 9.9+/-3.4 kPa; P",
author = "Hans-Joachim Kabitz and Anja Schwoerer and Hinrich-Cordt Bremer and Florian Sonntag and Stephan Walterspacher and David Walker and Vanessa Schaefer and Nicola Ehlken and Gerd Staehler and Michael Halank and Hans Klose and Ghofrani, {Hossein A} and Hoeper, {Marius M} and Ekkehard Gruenig and Wolfram Windisch",
year = "2008",
language = "Deutsch",
volume = "114",
pages = "165--171",
journal = "CLIN SCI",
issn = "0143-5221",
publisher = "PORTLAND PRESS LTD",
number = "2",

}

RIS

TY - JOUR

T1 - Impairment of respiratory muscle function in pulmonary hypertension.

AU - Kabitz, Hans-Joachim

AU - Schwoerer, Anja

AU - Bremer, Hinrich-Cordt

AU - Sonntag, Florian

AU - Walterspacher, Stephan

AU - Walker, David

AU - Schaefer, Vanessa

AU - Ehlken, Nicola

AU - Staehler, Gerd

AU - Halank, Michael

AU - Klose, Hans

AU - Ghofrani, Hossein A

AU - Hoeper, Marius M

AU - Gruenig, Ekkehard

AU - Windisch, Wolfram

PY - 2008

Y1 - 2008

N2 - It has been suggested that impaired respiratory muscle function occurs in patients with PH (pulmonary hypertension); however, comprehensive investigations of respiratory muscle function, including the application of non-volitional tests, needed to verify impairment of respiratory muscle strength in patients with PH have not yet been performed. In the present study, respiratory muscle function was assessed in 31 patients with PH (20 females and 11 males; mean pulmonary artery pressure, 51+/-20 mmHg; median World Health Organization class 3.0+/-0.5; 25 patients with pulmonary arterial hypertension and six patients with chronic thromboembolic PH) and in 31 control subjects (20 females and 11 males) well-matched for gender, age and BMI (body mass index). A 6-min walking test was performed to determine exercise capacity. Volitionally assessed maximal inspiratory (7.5+/-2.1 compared with 6.2+/-2.8 kPa; P=0.04) and expiratory (13.3+/-4.2 compared with 9.9+/-3.4 kPa; P

AB - It has been suggested that impaired respiratory muscle function occurs in patients with PH (pulmonary hypertension); however, comprehensive investigations of respiratory muscle function, including the application of non-volitional tests, needed to verify impairment of respiratory muscle strength in patients with PH have not yet been performed. In the present study, respiratory muscle function was assessed in 31 patients with PH (20 females and 11 males; mean pulmonary artery pressure, 51+/-20 mmHg; median World Health Organization class 3.0+/-0.5; 25 patients with pulmonary arterial hypertension and six patients with chronic thromboembolic PH) and in 31 control subjects (20 females and 11 males) well-matched for gender, age and BMI (body mass index). A 6-min walking test was performed to determine exercise capacity. Volitionally assessed maximal inspiratory (7.5+/-2.1 compared with 6.2+/-2.8 kPa; P=0.04) and expiratory (13.3+/-4.2 compared with 9.9+/-3.4 kPa; P

M3 - SCORING: Zeitschriftenaufsatz

VL - 114

SP - 165

EP - 171

JO - CLIN SCI

JF - CLIN SCI

SN - 0143-5221

IS - 2

M1 - 2

ER -