Bera Chinmay, Wong Florence
Division of Gastroenterology and Hepatology, Department of Medicine, Toronto General Hospital, University Health Network, University of Toronto, Toronto, ON, Canada.
Division of Gastroenterology and Hepatology, Department of Medicine, Toronto General Hospital, University Health Network, University of Toronto, 9EN/222 Toronto General Hospital, 200 Elizabeth Street, 9EN222, Toronto, ON M5G2C4, Canada.
Therap Adv Gastroenterol. 2022 Jun 14;15:17562848221102679. doi: 10.1177/17562848221102679. eCollection 2022.
Hepatorenal syndrome (HRS) is a serious form of renal dysfunction in patients with cirrhosis and ascites. It is an important component of the acute-on-chronic liver failure (ACLF) syndrome. Significant recent changes in the understanding of the pathophysiology of renal dysfunction in cirrhosis include the role of inflammation in addition to hemodynamic changes. The term acute kidney injury (AKI) is now adopted to include all functional and structural forms of acute renal dysfunction in cirrhosis, with various stages describing the severity of the condition. Type 1 hepatorenal syndrome (HRS1) is renamed HRS-AKI, which is stage 2 AKI [doubling of baseline serum creatinine (sCr)] while fulfilling all other criteria of HRS1. Albumin is used for its volume expanding and anti-inflammatory properties to confirm the diagnosis of HRS-AKI. Vasoconstrictors are added to albumin as pharmacotherapy to improve the hemodynamics. Terlipressin, although not yet available in North America, is the most common vasoconstrictor used worldwide. Patients with high grade of ACLF treated with terlipressin are at risk for respiratory failure if there is pretreatment respiratory compromise. Norepinephrine is equally effective as terlipressin in reversing HRS1. Recent data show that norepinephrine may be administered outside the intensive care setting, but close monitoring is still required. There has been no improvement in overall or transplant-free survival shown with vasoconstrictor use, but response to vasoconstrictors with reduction in sCr is associated with improvement in survival. Non-responders to vasoconstrictor plus albumin will need liver transplantation as definite treatment with renal replacement therapy as a bridge therapy. Combined liver and kidney transplantation is recommended for patients with prolonged history of AKI, underlying chronic kidney disease or with hereditary renal conditions. Future developments, such as the use of biomarkers and metabolomics, may help to identify at risk patients with earlier diagnosis to allow for earlier treatment with improved outcomes.
肝肾综合征(HRS)是肝硬化腹水患者中一种严重的肾功能不全形式。它是慢加急性肝衰竭(ACLF)综合征的重要组成部分。近期对肝硬化肾功能不全病理生理学的认识有显著变化,包括除血流动力学改变外炎症的作用。现在采用急性肾损伤(AKI)这一术语来涵盖肝硬化中急性肾功能不全的所有功能和结构形式,并用不同阶段描述病情的严重程度。1型肝肾综合征(HRS1)现更名为HRS - AKI,即符合HRS1的所有其他标准,同时血清肌酐(sCr)较基线水平翻倍的2期AKI。白蛋白因其扩容和抗炎特性用于确诊HRS - AKI。血管收缩剂与白蛋白联合作为药物治疗以改善血流动力学。特利加压素虽在北美尚未上市,但却是全球最常用的血管收缩剂。接受特利加压素治疗的重度ACLF患者若治疗前存在呼吸功能不全则有呼吸衰竭风险。去甲肾上腺素在逆转HRS1方面与特利加压素同样有效。近期数据表明去甲肾上腺素可在重症监护室外给药,但仍需密切监测。使用血管收缩剂并未显示总体生存率或无移植生存率有所改善,但对血管收缩剂有反应且sCr降低与生存率提高相关。对血管收缩剂加白蛋白无反应者需要进行肝移植作为确定性治疗,肾替代治疗作为过渡治疗。对于有AKI病史较长、潜在慢性肾病或遗传性肾病的患者,推荐进行肝肾联合移植。未来的发展,如生物标志物和代谢组学的应用,可能有助于识别高危患者并早期诊断,从而实现早期治疗并改善预后。