Literature DB >> 19502663

The use of sildenafil to treat portopulmonary hypertension prior to liver transplantation.

Ian S H Cadden1, Erica D Greanya, Siegfried R Erb, Charles H Scudamore, Eric M Yoshida.   

Abstract

Portopulmonary hypertension (PPH) is an infrequent, but well-recognized complication of liver cirrhosis. PPH in those with end-stage liver disease has a significant impact on per-operative and intra-operative mortality, with liver transplantation being contraindicated in those individuals with mean pulmonary artery pressure exceeding 50 mmHg. Vasodilatory therapy is the mainstay of pharmacotherapy for PPH, although the evidence of benefit is largely extrapolated from the pulmonary hypertension literature. We report the use of the phosphodiesterase inhibitor, sildenafil, in a patient with end stage liver disease and PPH, with a pulmonary artery pressure before transplantation of 75 mmHg, to reduce pulmonary artery pressure prior to a successful liver transplant.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19502663

Source DB:  PubMed          Journal:  Ann Hepatol        ISSN: 1665-2681            Impact factor:   2.400


  3 in total

Review 1.  Trends on gastrointestinal bleeding and mortality: where are we standing?

Authors:  Ahmed Mahmoud El-Tawil
Journal:  World J Gastroenterol       Date:  2012-03-21       Impact factor: 5.742

Review 2.  Phosphodiesterase type 5 and cancers: progress and challenges.

Authors:  Ines Barone; Cinzia Giordano; Daniela Bonofiglio; Sebastiano Andò; Stefania Catalano
Journal:  Oncotarget       Date:  2017-10-12

3.  Perioperative management with phosphodiesterase type 5 inhibitor and prostaglandin E1 for moderate portopulmonary hypertension following adult-to-adult living-donor liver transplantation: a case report.

Authors:  Takashi Onoe; Asuka Tanaka; Kohei Ishiyama; Kentaro Ide; Hirotaka Tashiro; Hideki Ohdan
Journal:  Surg Case Rep       Date:  2018-02-07
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.