Beta-adrenergic blockade in cirrhosis–harmful or helpful?
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Beta-adrenergic blockade in cirrhosis–harmful or helpful? / Møller, Søren; Danielsen, Karen V.; Nabilou, Puria; Kimer, Nina; Bendtsen, Flemming.
I: Expert Review of Gastroenterology and Hepatology, Bind 17, Nr. 6, 2023, s. 519-529.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Beta-adrenergic blockade in cirrhosis–harmful or helpful?
AU - Møller, Søren
AU - Danielsen, Karen V.
AU - Nabilou, Puria
AU - Kimer, Nina
AU - Bendtsen, Flemming
N1 - Publisher Copyright: © 2023 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023
Y1 - 2023
N2 - Introduction: Portal hypertension exacerbates the disease course of cirrhosis and is responsible for major complications, including bleeding from esophageal varices, ascites, and encephalopathy. More than 40 years ago, Lebrec and colleagues introduced beta-blockers to prevent esophageal bleeding. However, evidence now suggests that beta-blockers may cause adverse reactions in patients with advanced cirrhosis. Areas covered: This review addresses current evidence for the pathophysiology of portal hypertension, focusing on the pharmacological effects of treatment with beta-blockers, indications for preventing variceal bleeding, their effects on decompensated cirrhosis, and the risk of treating patients suffering from decompensated ascites and renal dysfunction with beta-blockers. Expert opinion: The diagnosis of portal hypertension should be based on direct measurements of portal pressure. Carvedilol or nonselective beta-blockers are the first-line treatment for patients with medium-to-large varices as primary or secondary prophylaxis, in Child C patients with small varices, and sometimes for patients with clinically significant portal hypertension (HVPG ≥ 10 mm Hg, irrespective of the presence of varices) to prevent decompensation. Caution should be used when treating decompensated patients who are suspected of imminent cardiac and renal dysfunction. Future strategies for managing patients with portal hypertension should aim for more personalized treatment that takes into account the disease stage.
AB - Introduction: Portal hypertension exacerbates the disease course of cirrhosis and is responsible for major complications, including bleeding from esophageal varices, ascites, and encephalopathy. More than 40 years ago, Lebrec and colleagues introduced beta-blockers to prevent esophageal bleeding. However, evidence now suggests that beta-blockers may cause adverse reactions in patients with advanced cirrhosis. Areas covered: This review addresses current evidence for the pathophysiology of portal hypertension, focusing on the pharmacological effects of treatment with beta-blockers, indications for preventing variceal bleeding, their effects on decompensated cirrhosis, and the risk of treating patients suffering from decompensated ascites and renal dysfunction with beta-blockers. Expert opinion: The diagnosis of portal hypertension should be based on direct measurements of portal pressure. Carvedilol or nonselective beta-blockers are the first-line treatment for patients with medium-to-large varices as primary or secondary prophylaxis, in Child C patients with small varices, and sometimes for patients with clinically significant portal hypertension (HVPG ≥ 10 mm Hg, irrespective of the presence of varices) to prevent decompensation. Caution should be used when treating decompensated patients who are suspected of imminent cardiac and renal dysfunction. Future strategies for managing patients with portal hypertension should aim for more personalized treatment that takes into account the disease stage.
KW - bleeding
KW - cardiovascular dysfunction
KW - carvedilol
KW - esophageal varices
KW - hyperdynamic circulation
KW - Portal hypertension
KW - propranolol
KW - renal failure
UR - http://www.scopus.com/inward/record.url?scp=85160705478&partnerID=8YFLogxK
U2 - 10.1080/17474124.2023.2215428
DO - 10.1080/17474124.2023.2215428
M3 - Journal article
C2 - 37202907
AN - SCOPUS:85160705478
VL - 17
SP - 519
EP - 529
JO - Expert Review of Gastroenterology & Hepatology
JF - Expert Review of Gastroenterology & Hepatology
SN - 1747-4124
IS - 6
ER -
ID: 362978363