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药物预防静脉曲张出血和再出血。

Pharmacologic prevention of variceal bleeding and rebleeding.

机构信息

Hepatic Hemodynamic Laboratory, Liver Unit, Hospital Clínic-IDIBAPS, University of Barcelona, C.Villarroel 170, 08036, Barcelona, Spain.

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Barcelona, España.

出版信息

Hepatol Int. 2018 Feb;12(Suppl 1):68-80. doi: 10.1007/s12072-017-9833-y. Epub 2017 Dec 5.

Abstract

BACKGROUND

Variceal bleeding is a major complication of portal hypertension, which is associated with significant mortality. Moreover, patients surviving a variceal bleeding episode have very high risk of rebleeding, which is associated with mortality as high as that of the first bleed. Because of this, prevention of bleeding from gastroesophageal varices has been one of the main therapeutic goals since the advent of the first effective therapies for portal hypertension.

AIM

This review deals with the present day state-of-the-art pharmacological prevention of variceal bleeding in primary and secondary prophylaxis.

RESULTS

Pharmacological therapy aims to decrease portal pressure (PP) by acting on the pathophysiological mechanisms of portal hypertension such as increased hepatic vascular tone and splanchnic vasodilatation. Propranolol and nadolol block the beta-1 in the heart and the peripheral beta-2 adrenergic receptors. Beta-1 blockade of cardiac receptors reduces heart rate and cardiac output and subsequently decreases flow into splanchnic circulation. Beta-2 blockade leads to unopposed alpha-1 adrenergic activity that causes splanchnic vasoconstriction and reduction of portal inflow. Both effects contribute to reduction in PP. Carvedilol is more powerful in reducing hepatic venous pressure gradient (HVPG) than traditional nonselective beta-blockers (NSBBs) and achieves good hemodynamic response in nearly 75 % of cases. Simvastatin and atorvastatin improve endothelial dysfunction mainly by enhancing endothelial nitric oxide synthase (eNOS) expression and phosphorylation and NO production. In addition, statins deactivate hepatic stellate cells and ameliorate hepatic fibrogenesis. These effects cause a decrease in HVPG and improve liver microcirculation and hepatocyte perfusion in patients with cirrhosis. In addition, several promising drugs under development may change the management of portal hypertension in the coming years.

CONCLUSION

This review provides a background on the most important aspects of the treatment of portal hypertension in patients with compensated and decompensated liver cirrhosis. However, despite the great improvement in the prevention of variceal bleeding over the last years, further therapeutic options are needed.

摘要

背景

静脉曲张出血是门静脉高压的主要并发症,与显著的死亡率相关。此外,存活于静脉曲张出血事件的患者再出血风险极高,再出血死亡率与首次出血相当。正因为如此,自治疗门静脉高压的第一种有效疗法问世以来,预防胃食管静脉曲张出血一直是主要治疗目标之一。

目的

本综述涉及目前在一级和二级预防中预防静脉曲张出血的药理学方法。

结果

药物治疗旨在通过作用于门静脉高压的病理生理机制来降低门静脉压力(PP),如增加肝血管张力和内脏血管舒张。普萘洛尔和纳多洛尔阻断心脏的β-1 和外周的β-2 肾上腺素能受体。心脏β-1 受体阻断减少心率和心输出量,随后减少内脏循环的血流量。β-2 受体阻断导致无拮抗的α-1 肾上腺素能活性,引起内脏血管收缩和门静脉流入减少。这两种作用都有助于降低 PP。卡维地洛在降低肝静脉压力梯度(HVPG)方面比传统非选择性β受体阻滞剂(NSBB)更有效,并且在近 75%的情况下实现良好的血液动力学反应。辛伐他汀和阿托伐他汀通过增强内皮型一氧化氮合酶(eNOS)表达和磷酸化以及 NO 产生来改善内皮功能障碍。此外,他汀类药物还能使肝星状细胞失活,并改善肝纤维化。这些作用导致 HVPG 降低,并改善肝硬化患者的肝微循环和肝细胞灌注。此外,几种有前途的开发中的药物可能会在未来几年改变门静脉高压的治疗管理。

结论

本综述提供了关于代偿和失代偿性肝硬化患者门静脉高压治疗的最重要方面的背景信息。然而,尽管近年来在预防静脉曲张出血方面取得了巨大进展,但仍需要进一步的治疗选择。

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