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Pulmonary artery catheters

Pediatric Critical Care Medicine, 2011
After its introduction in 1970, the use of the pulmonary artery catheter became a central part of the management of critically ill patients in adult and pediatric intensive care units. However, because it was introduced as a class II device, efficacy for its safety and clinical benefit did not exist during the early years of use.
Ronald M, Perkin, Nick, Anas
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Pulmonary artery leiomyosarcoma

Respiratory Medicine, 1991
A 47-year-old man presented to his general practitioner complaining of a persistent cough associated with wheezing. It was felt that he may have had asthma and was treated with a salbutamol inhaler. However, returned to his G.P. 1 month later with the same symptoms. Oral theophylline was commenced.
M, Sanderson, M, Britton
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Pulmonary Arterial Hypertension

Heart Failure Clinics, 2018
This article provides an overview of pulmonary arterial hypertension (PAH), beginning with the initial pathologic recognition of pulmonary hypertension more than 100 years ago and progressing to the current diagnostic categorization of PAH. It reviews the epidemiology, pathophysiology, genetics, and modern treatment of PAH.
Mark W, Dodson   +2 more
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Pulmonary Artery Sling

The Annals of Thoracic Surgery, 1976
A case of pulmonary artery sling in a 1-year-old boy, treated by resection of the left pulmonary artery (LPA) at its origin from the right pulmonary artery (RPA) and reanastomosis of the LPA to the main pulmonary artery (MPA), is reported. In this patient the LPA-MPA anastomosis was demonstrated to be patent in a follow-up pulmonary angiogram six ...
A, AytaƧ   +3 more
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Pulmonary Artery Calcification

Scottish Medical Journal, 1972
Pulmonary artery calcification detected radiologically is invariably associated with the Eisenmenger Syndrome. Its appearance is relatively uncommon and 4 further cases are described. It is suggested that the relative rarity of the cases of pulmonary artery calcification in this syndrome is due to the fact that the majority of patients die before the ...
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Pulmonary Arterial Hypertension

Critical Care Nursing Quarterly, 2007
Pulmonary arterial hypertension (PAH) is a rare and debilitating disease characterized by abnormal proliferation and contraction of pulmonary vascular smooth muscle cells. The resulting increase in pressure and pulmonary vascular resistance results in progressive right heart failure, low cardiac output, and ultimately death if left untreated.
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[Pulmonary arterial reconstruction with autologous pulmonary arterial tissue for pulmonary artery sling].

[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai, 1997
One-year and two-month-old boy with pulmonary artery sling underwent pulmonary artery reconstruction with autologous pulmonary arterial tissue. Surgical repair consisted of the transection of the left pulmonary artery at its origin with trimming a button hole and the creation of an oval hole with the same size to the left pulmonary button.
Y, Koh   +5 more
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Anomalous Pulmonary Arteries

Archives of Surgery, 1955
A diagnosis of anomalous pulmonary arteries is seldom made before surgery. Preoperative recognition of this condition is most important in cases of pulmonary disease requiring surgery of a lower lobe. The severance of such a vessel may result in exsanguination.
S F, LANDRY, J S, SALATICH
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Pulmonary artery banding

Multimedia Manual of Cardio-Thoracic Surgery, 2012
Pulmonary artery banding (PAB) is a simple surgical technique to reduce pulmonary overcirculation in some congenital heart disease. In the beginning, when the use of cardiopulmonary bypass was affected by many deleterious effects, this technique played a fundamental role in the treatment of patients with congenital heart defects and an intracardiac ...
ANGELI, EMANUELA   +4 more
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