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Verfasst von:Filusch, Arthur [VerfasserIn]   i
 Ewert, Ralf [VerfasserIn]   i
 Altesellmeier, Maike [VerfasserIn]   i
 Zugck, Christian [VerfasserIn]   i
 Hetzer, Roland [VerfasserIn]   i
 Borst, Mathias M. [VerfasserIn]   i
 Katus, Hugo [VerfasserIn]   i
 Meyer, Franz Joachim [VerfasserIn]   i
Titel:Respiratory muscle dysfunction in congestive heart failure
Titelzusatz:the role of pulmonary hypertension
Verf.angabe:Arthur Filusch, Ralf Ewert, Maike Altesellmeier, Christian Zugck, Roland Hetzer, Mathias M. Borst, Hugo A. Katus, F. Joachim Meyer
Jahr:2011
Umfang:4 S.
Fussnoten:Online verfügbar: 4 Mai 2010 ; Gesehen am 03.11.2022
Titel Quelle:Enthalten in: International journal of cardiology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1981
Jahr Quelle:2011
Band/Heft Quelle:150(2011), 2 vom: Juli, Seite 182-185
ISSN Quelle:1874-1754
Abstract:Background - Inspiratory muscle weakness has been described in patients with congestive heart failure (CHF), and only recently in patients with idiopathic pulmonary arterial hypertension. However, the relationship between pulmonary hemodynamics and respiratory muscle function has not been investigated in patients with CHF. - Methods and results - In two tertial referral centers for CHF patients, 532 consecutive CHF patients (159 female, age 59±12years, NYHA I-IV) were studied by right heart catheterization, maximal inspiratory mouth occlusion pressure (Pimax) and pressure 0.1s after beginning of inspiration during tidal breathing at rest (P0.1). There was a significant correlation between Pimax and mean pulmonary artery pressure (PAPm) (r=−0.65, p=0.0023), mean pulmonary capillary wedge pressure (PCWPm) (r=−0.56; p=0.0018), PVR (r=−0.73; p=0.0031), and cardiac output (r=0.51; p=0.0022). Moreover, the ratio P0.1/Pimax showed a linear correlation with PAPm (r=0.54; p=0.0019), and with TPG (r=0.64; p=0.0014) respectively. Vital capacity was reduced in relation to increased PAPm (r=−0.54; p=0.0029). Pimax and P0.1/Pimax were independent from VC. - Conclusions - This study provides the first evidence of a close relation between inspiratory muscle dysfunction, increased ventilatory drive and pulmonary hypertension in a large patient cohort with CHF. Pimax and P0.1 can easily be measured in clinical routine and might become an additional parameter for the non-invasive monitoring of the hemodynamic severity of disease.
DOI:doi:10.1016/j.ijcard.2010.04.006
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.ijcard.2010.04.006
 Volltext: https://www.sciencedirect.com/science/article/pii/S0167527310002214
 DOI: https://doi.org/10.1016/j.ijcard.2010.04.006
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Congestive heart failure
 Pulmonary hypertension
 Respiratory muscles
 Ventilatory drive
K10plus-PPN:1820672689
Verknüpfungen:→ Zeitschrift

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