Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2661371 | The Journal for Nurse Practitioners | 2008 | 8 Pages |
Abstract
Pulmonary hypertension (PH) is a condition that is becoming more recognized. It remains a devastating disease and is not just seen in the offices of pulmonologists. Patients with liver disease may be referred for liver transplant. Of the many patients referred for liver transplant, approximately 4% to 15% will have PH. PH in this population is called portopulmonary hypertension (POPH). As the number of liver transplants continues to grow, the importance of recognizing POPH increases. This article focuses on pathophysiology, recognition, and treatment of patients with this condition.
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Authors
Susan Steinbis,