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首页> 外文期刊>Digestive diseases >Current Management of the Complications of Cirrhosis and Portal Hypertension: Variceal Hemorrhage, Ascites, and Spontaneous Bacterial Peritonitis
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Current Management of the Complications of Cirrhosis and Portal Hypertension: Variceal Hemorrhage, Ascites, and Spontaneous Bacterial Peritonitis

机译:肝硬化和门静脉高压并发症的当前处理:静脉曲张出血,腹水和自发性细菌性腹膜炎

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摘要

Cirrhosis is not a single entity but represents a disease progression across different prognostic stages, with the compensated and decompensated stages being the most important. Variceal hemorrhage (VH) and ascites are complications of cirrhosis that denote the presence of a decompensated stage. Spontaneous bacterial peritonitis (SBP) is a common bacterial infection unique to patients with cirrhosis that can precipitate the development of recurrent VH and hepatorenal syndrome (HRS), complications that denote the presence of a 'further decompensated' stage of cirrhosis. Main current issues in the management of VH include identification of different prognostic stages that allow for individualized patient care. Management of VH cannot be performed in an isolated manner, and the presence of other complications of cirrhosis (ascites, encephalopathy) should be taken into account both in the management and in the design of clinical trials. Because management of ascites per se has not resulted in significant changes in mortality, main management issues consist of preventing further decompensating events by preventing factors that will lead to worsening vasodilatation and hemodynamic status (infections, vasodilators), preventing volume depletion (overdiuresis, GI hemorrhage) and preventing structural kidney injury (nephrotoxins). Prophylaxis of bacterial infections such as SBP currently consists of the administration of antibiotics. By preventing infections, there is evidence that recurrent VH and HRS can also be prevented. However, response to recommended empirical antibiotics in patients with suspected infection, such as SBP, is currently significantly lower than in the past because of an increase in infections secondary to multidrug resistant (MDR) organisms. One of the main predictors of the development of MDR organisms is antibiotic prophylaxis and unnecessary and prolonged use of antibiotics in hospital. Therefore, appropriate antibiotics should be used in patients with a high suspicion of infection, and antibiotic prophylaxis should be restricted to patients with the highest risk of infection. (C) 2016 S. Karger AG, Basel
机译:肝硬化不是一个单一的实体,而是代表不同预后阶段的疾病进展,其中补偿和失代偿期是最重要的。静脉曲张出血(VH)和腹水是肝硬化的并发症,表明存在代偿期。自发性细菌性腹膜炎(SBP)是肝硬化患者特有的常见细菌感染,可导致复发性VH和肝肾综合征(HRS)的发展,并发症表示肝硬化处于“进一步失代偿”阶段。 VH管理中当前的主要问题包括确定允许个体化患者护理的不同预后阶段。 VH的管理不能孤立地进行,在管理和临床试验设计中都应考虑是否存在其他肝硬化并发症(腹水,脑病)。由于腹水管理本身并没有导致死亡率的显着变化,因此主要的管理问题包括通过预防会导致血管扩张和血液动力学状况恶化的因素(感染,血管扩张剂),防止容量减少(过度利尿,胃肠道出血)来防止进一步的代偿失调事件。 )并预防肾脏的结构性损伤(肾毒素)。预防细菌感染(例如SBP)目前包括施用抗生素。通过预防感染,有证据表明还可预防VH和HRS复发。但是,由于多重耐药性(MDR)生物继发感染的增加,目前对怀疑感染的患者(如SBP)对推荐的经验性抗生素的反应明显低于过去。耐多药生物发展的主要预测指标之一是抗生素的预防以及医院中不必要和长期使用抗生素。因此,对于高度怀疑感染的患者,应使用适当的抗生素,并且应仅对感染风险最高的患者进行抗生素的预防。 (C)2016 S.Karger AG,巴塞尔

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