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用于门静脉高压症早期临床开发的研究性药物。

Investigational drugs in early clinical development for portal hypertension.

机构信息

Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Department for BioMedical Research, Visceral Surgery and Medicine, University of Bern, Bern, Switzerland.

出版信息

Expert Opin Investig Drugs. 2022 Aug;31(8):825-842. doi: 10.1080/13543784.2022.2095259. Epub 2022 Jul 5.

Abstract

INTRODUCTION

Advanced chronic liver disease is considered a reversible condition after removal of the primary etiological factor. This has led to a paradigm shift in which portal hypertension (PH) is a reversible complication of cirrhosis. The pharmacologic management of PH is centered on finding targets to modify the natural history of cirrhosis and PH.

AREAS COVERED

This paper offers an overview of the use of pharmacological strategies in early clinical development that modify PH. Papers included were selected from searching clinical trial sites and PubMed from the last 10 years.

EXPERT OPINION

A paradigm shift has generated a new concept of PH in cirrhosis as a reversible complication of a potentially curable disease. Decreasing portal pressure to prevent decompensation and further complications of cirrhosis that may lead liver transplantation or death is a goal. Therapeutic strategies also aspire achieve total or partial regression of fibrosis, thus eliminating the need for treatment or screening of PH.

摘要

简介

在去除原发性病因后,晚期慢性肝脏疾病被认为是一种可逆转的状况。这导致了一种范式转变,即门静脉高压(PH)是肝硬化的一种可逆转的并发症。PH 的药物治疗集中在寻找目标以改变肝硬化和 PH 的自然病程。

涵盖领域

本文概述了在早期临床开发中使用药物策略来改变 PH 的情况。入选的论文是从过去 10 年的临床试验网站和 PubMed 中检索出来的。

专家意见

一种范式转变产生了肝硬化 PH 的新概念,即肝硬化潜在可治愈疾病的一种可逆转并发症。降低门静脉压力以预防肝硬化失代偿和进一步并发症,从而避免肝移植或死亡,这是一个目标。治疗策略还旨在实现纤维化的完全或部分消退,从而消除对 PH 的治疗或筛查的需要。

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