A CHALLENGING CASE OF PULMONARY HYPERTENSION IN THE SETTING OF PRIMARY MYELOFIBROSIS

A CHALLENGING CASE OF PULMONARY HYPERTENSION IN THE SETTING OF PRIMARY MYELOFIBROSIS

Right heart catheterization revealed a pulmonary artery systolic pressure (PASP) of 54 mmHg, which decreased to 41 mmHg after infusion of adenosine.

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Veröffentlicht in:Journal of the American College of Cardiology 2015-03, Vol.65 (10), p.A649-A649
Hauptverfasser: Abrich, Victor, Simper, David, Scott, Robert
Format: Artikel
Sprache:eng
Schlagworte:
Cardiology
Cardiovascular
Internal Medicine
Intubation
Lungs
Medical treatment
Pulmonary arteries
Pulmonary hypertension
Ultrasonic imaging
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Zusammenfassung:Right heart catheterization revealed a pulmonary artery systolic pressure (PASP) of 54 mmHg, which decreased to 41 mmHg after infusion of adenosine.
ISSN:0735-1097
1558-3597
DOI:10.1016/S0735-1097(15)60649-0