[The noninvasive assessment of the effects of penbutolol on liver hemodynamics in cirrhotic patients using angioscintigraphy. A randomized controlled double-blind study].

Author: BestettiA, BrunoS, ChiesaA, GaglianoG, GrugniM C, OpocherE, RossiS, SantambrogioR, VignatiL, ZattaG

Paper Details 
Original Abstract of the Article :
This randomized double-blind controlled study analyzed the hemodynamic effects of penbutolol, a new levo-rotatory betablocker, using radionuclide angiography. Twenty cirrhotics with esophageal varices were randomized: 10 received 40 mg/day of penbutolol orally and the others a placebo. Angioscintigr...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/1962892

データ提供:米国国立医学図書館(NLM)

Assessing Liver Hemodynamics in Cirrhotic Patients

Liver cirrhosis, a serious condition affecting the liver, can lead to complications such as [portal hypertension] and [esophageal varices]. This study investigates the hemodynamic effects of penbutolol, a beta-blocker medication, in patients with cirrhosis, using a non-invasive technique called [angioscintigraphy].

Penbutolol's Impact on Liver Hemodynamics

The study reveals that penbutolol significantly reduced portal perfusion index and increased hepatic artery index in patients with cirrhosis, suggesting a potential therapeutic benefit in managing hemodynamic imbalances associated with the condition.

Angioscintigraphy: A Valuable Tool for Liver Assessment

The study underscores the importance of angioscintigraphy as a safe, accurate, and reproducible method for assessing liver hemodynamics in patients with cirrhosis. This technique offers a valuable tool for monitoring treatment response and guiding clinical decision-making.

Dr.Camel's Conclusion

This study delves deep into the intricate world of liver hemodynamics, revealing the potential of penbutolol in managing this challenging condition. It emphasizes the importance of non-invasive techniques like angioscintigraphy, providing a powerful tool for navigating the complexities of liver disease.

Date :
  1. Date Completed 1991-03-28
  2. Date Revised 2016-11-23
Further Info :

Pubmed ID

1962892

DOI: Digital Object Identifier

1962892

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