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The use of sildenafil to treat portopulmonary hypertension prior to liver transplantation
被引:0
|作者:
Cadden, Ian S. H.
Greanya, Erica D.
Erb, Siegfried R.
[3
]
Scudamore, Charles H.
[1
,2
]
Yoshida, Eric M.
[1
,3
]
机构:
[1] Univ British Columbia, Div Gastroenterol, Vancouver, BC V5Z 1M9, Canada
[2] Univ British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
[3] Vancouver Gen Hosp, Vancouver, BC, Canada
关键词:
Liver transplantation;
sildenafil;
cirrhosis;
pulmonary hypertension;
portopulmonary;
PRIMARY PULMONARY-HYPERTENSION;
COMPLICATING PORTAL-HYPERTENSION;
HEPATOPULMONARY SYNDROME;
BOSENTAN THERAPY;
CIRRHOSIS;
MANIFESTATIONS;
HEMODYNAMICS;
EPOPROSTENOL;
DATABASE;
PATIENT;
D O I:
暂无
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
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.
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页码:158 / 161
页数:4
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