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[肝肺综合征]

[Hepatopulmonary syndrome].

作者信息

Sayadi A, Duhaut L, Robert F, Savale L, Coilly A

机构信息

UMR-S 1193, hôpital Paul-Brousse, centre hépato-biliaire, université Paris-Saclay, AP-HP, 94800 Villejuif, France.

Inserm UMR_S 999, 94270 Le Kremlin-Bicêtre, France.

出版信息

Rev Med Interne. 2024 Mar;45(3):156-165. doi: 10.1016/j.revmed.2023.03.008. Epub 2023 Mar 31.

Abstract

The hepatopulmonary syndrome (HPS) is one of the lung diseases associated with cirrhosis and portal hypertension. It should be discussed for any dyspnea in cirrhotic patients. HPS is a pulmonary vascular disease characterized by intrapulmonary vascular dilatations (IPVD). The pathogenesis is complex and seems to rely on communications between the portal and pulmonary circulations. The diagnosis is based on a triad of liver disease and portal hypertension, evidence of IPVDs, and impaired gas exchange (alveolar-arterial oxygen difference [A-aO]≥15mmHg). HPS impairs prognosis (23% survival at 5years) and patients' quality of life. Liver transplantation (LT) allows regression of IPDVD in almost 100% of cases, normalization of gas exchange and improves survival with a 5-year post-LT survival between 76 and 87%. It is the only curative treatment, indicated in patients with severe HPS, defined by an arterial partial pressure of oxygen (PaO) below 60mmHg. When LT is not indicated or feasible, long-term oxygen therapy may be proposed as a palliative treatment. A better understanding of the pathophysiological mechanisms is needed to improve the therapeutic possibilities in a near future.

摘要

肝肺综合征(HPS)是与肝硬化和门静脉高压相关的肺部疾病之一。对于肝硬化患者出现的任何呼吸困难都应考虑到该病。HPS是一种以肺内血管扩张(IPVD)为特征的肺血管疾病。其发病机制复杂,似乎依赖于门静脉循环和肺循环之间的联系。诊断基于肝病和门静脉高压三联征、IPVD的证据以及气体交换受损(肺泡-动脉血氧分压差[A-aO]≥15mmHg)。HPS会影响预后(5年生存率为23%)和患者的生活质量。肝移植(LT)几乎可使100%的病例中IPDVD消退,气体交换恢复正常,并提高生存率,肝移植后5年生存率在76%至87%之间。这是唯一的治愈性治疗方法,适用于严重HPS患者,严重程度定义为动脉血氧分压(PaO)低于60mmHg。当不适合或无法进行肝移植时,可建议长期氧疗作为姑息治疗。需要更好地了解其病理生理机制,以便在不久的将来改善治疗方法。

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