Haemodynamic assessment and therapeutic studies in portal hypertension and ascites

Portal, systemic, cardiopulmonary and renal haemodynamics of 96 patients with alcohol related cirrhosis were measured. Their inter-relationship and predictive value for variceal haemorrhage and survival during a mean follow-up of 19 months was investigated. Severity of liver disease was related to t...

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Main Author: Stanley, Adrian John
Published: University of Edinburgh 1998
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.662359
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spelling ndltd-bl.uk-oai-ethos.bl.uk-6623592017-08-30T03:11:48ZHaemodynamic assessment and therapeutic studies in portal hypertension and ascitesStanley, Adrian John1998Portal, systemic, cardiopulmonary and renal haemodynamics of 96 patients with alcohol related cirrhosis were measured. Their inter-relationship and predictive value for variceal haemorrhage and survival during a mean follow-up of 19 months was investigated. Severity of liver disease was related to the hepatic venous pressure gradient (HVPG), azgos blood flow (AzBF) and systemic hypotension. During follow-up, HVPG predicted survival and variceal bleeding. Propranolol and isosorbide-5-mononitrate are widely used in the prophylaxis of variceal haemorrhage, but recent reports have suggested they may compromise renal function. Renal blood flow (RBF), HVPG, AzBF and systemic haemodynamics were measured in 26 cirrhotic patients before and after each drug or combination therapy. Despite significant changes in the other parameters, no fall in RBF was detected. The novel vasodilating beta-blocker carvedilol offers potential in the treatment of portal hypertension, but little data currently exist. Portal, cardiopulmonary and systemic haemodynamics and renal function were assessed in 17 cirrhotic patients after acute and chronic (1 month) therapy. Although carvedilol had a continued portal hypotensive effect after 1 month with no detrimental effect on liver blood flow or renal function, a significant minority of patients were unable to tolerate chronic therapy. Adenosine-antagonism offers a new therapeutic approach to cirrhotic ascites and renal dysfunction. The effects on renal and systemic haemodynamics and renal function were assessed following administration of FK352 (a novel adenosine-1 antagonist) to 12 cirrhotic patients with ascites. An improvement in natriuresis, diuresis and RBF was detected.615.1University of Edinburghhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.662359http://hdl.handle.net/1842/22648Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 615.1
spellingShingle 615.1
Stanley, Adrian John
Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
description Portal, systemic, cardiopulmonary and renal haemodynamics of 96 patients with alcohol related cirrhosis were measured. Their inter-relationship and predictive value for variceal haemorrhage and survival during a mean follow-up of 19 months was investigated. Severity of liver disease was related to the hepatic venous pressure gradient (HVPG), azgos blood flow (AzBF) and systemic hypotension. During follow-up, HVPG predicted survival and variceal bleeding. Propranolol and isosorbide-5-mononitrate are widely used in the prophylaxis of variceal haemorrhage, but recent reports have suggested they may compromise renal function. Renal blood flow (RBF), HVPG, AzBF and systemic haemodynamics were measured in 26 cirrhotic patients before and after each drug or combination therapy. Despite significant changes in the other parameters, no fall in RBF was detected. The novel vasodilating beta-blocker carvedilol offers potential in the treatment of portal hypertension, but little data currently exist. Portal, cardiopulmonary and systemic haemodynamics and renal function were assessed in 17 cirrhotic patients after acute and chronic (1 month) therapy. Although carvedilol had a continued portal hypotensive effect after 1 month with no detrimental effect on liver blood flow or renal function, a significant minority of patients were unable to tolerate chronic therapy. Adenosine-antagonism offers a new therapeutic approach to cirrhotic ascites and renal dysfunction. The effects on renal and systemic haemodynamics and renal function were assessed following administration of FK352 (a novel adenosine-1 antagonist) to 12 cirrhotic patients with ascites. An improvement in natriuresis, diuresis and RBF was detected.
author Stanley, Adrian John
author_facet Stanley, Adrian John
author_sort Stanley, Adrian John
title Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
title_short Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
title_full Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
title_fullStr Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
title_full_unstemmed Haemodynamic assessment and therapeutic studies in portal hypertension and ascites
title_sort haemodynamic assessment and therapeutic studies in portal hypertension and ascites
publisher University of Edinburgh
publishDate 1998
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.662359
work_keys_str_mv AT stanleyadrianjohn haemodynamicassessmentandtherapeuticstudiesinportalhypertensionandascites
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