Liver Unit, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEReHD), Barcelona, Spain.
Liver Unit, Hospital Vall d'Hebron, Barcelona, Spain.
J Hepatol. 2018 Dec;69(6):1250-1259. doi: 10.1016/j.jhep.2018.08.006. Epub 2018 Aug 21.
BACKGROUND & AIMS: Patients with decompensated cirrhosis on the waiting list for liver transplantation (LT) commonly develop complications that may preclude them from reaching LT. Circulatory dysfunction leading to effective arterial hypovolemia and activation of vasoconstrictor systems is a key factor in the pathophysiology of complications of cirrhosis. The aim of this study was to investigate whether treatment with midodrine, an alpha-adrenergic vasoconstrictor, together with intravenous albumin improves circulatory dysfunction and prevents complications of cirrhosis in patients awaiting LT.
A multicenter, randomized, double-blind, placebo-controlled trial (NCT00839358) was conducted, including 196 consecutive patients with cirrhosis and ascites awaiting LT. Patients were randomly assigned to receive midodrine (15-30 mg/day) and albumin (40 g/15 days) or matching placebos for one year, until LT or drop-off from inclusion on the waiting list. The primary endpoint was incidence of any complication (renal failure, hyponatremia, infections, hepatic encephalopathy or gastrointestinal bleeding). Secondary endpoints were mortality, activity of endogenous vasoconstrictor systems and plasma cytokine levels.
There were no significant differences between both groups in the probability of developing complications of cirrhosis during follow-up (p = 0.402) or one-year mortality (p = 0.527). Treatment with midodrine and albumin was associated with a slight but significant decrease in plasma renin activity and aldosterone compared to placebo (renin -4.3 vs. 0.1 ng/ml.h, p < 0.001; aldosterone -38 vs. 6 ng/dl, p = 0.02, at week 48 vs. baseline). Plasma norepinephrine only decreased slightly at week 4. Neither arterial pressure nor plasma cytokine levels changed significantly.
In patients with cirrhosis awaiting LT, treatment with midodrine and albumin, at the doses used in this study, slightly suppressed the activity of vasoconstrictor systems, but did not prevent complications of cirrhosis or improve survival.
Patients with cirrhosis who are on the liver transplant waiting list often develop complications which prevent them from receiving a transplant. Circulatory dysfunction is a key factor behind a number of complications. This study was aimed at investigating whether treating patients with midodrine (a vasoconstrictor) and albumin would improve circulatory dysfunction and prevent complications. This combined treatment, at least at the doses administered in this study, did not prevent the complications of cirrhosis or improve the survival of these patients.
等待肝移植(LT)的失代偿性肝硬化患者常出现并发症,这些并发症可能使他们无法接受 LT。导致有效动脉血容量不足和血管收缩系统激活的循环功能障碍是肝硬化并发症病理生理学的关键因素。本研究旨在探讨米多君(一种α-肾上腺素能血管收缩剂)联合静脉注射白蛋白治疗是否能改善等待 LT 的患者的循环功能障碍并预防肝硬化并发症。
进行了一项多中心、随机、双盲、安慰剂对照试验(NCT00839358),纳入 196 例连续的肝硬化伴腹水等待 LT 的患者。患者被随机分配接受米多君(15-30mg/天)和白蛋白(40g/15 天)或匹配的安慰剂治疗 1 年,直到 LT 或从等待名单中脱落。主要终点是任何并发症(肾衰竭、低钠血症、感染、肝性脑病或胃肠道出血)的发生率。次要终点是死亡率、内源性血管收缩系统的活性和血浆细胞因子水平。
在随访期间,两组发生肝硬化并发症的概率(p=0.402)或 1 年死亡率(p=0.527)无显著差异。与安慰剂相比,米多君和白蛋白治疗与血浆肾素活性和醛固酮的轻微但显著下降相关(肾素 -4.3 与 0.1ng/ml.h,p<0.001;醛固酮 -38 与 6ng/dl,p=0.02,第 48 周与基线相比)。血浆去甲肾上腺素仅在第 4 周略有下降。动脉压和血浆细胞因子水平均无明显变化。
在等待 LT 的肝硬化患者中,使用本研究中使用的剂量的米多君和白蛋白治疗,轻度抑制血管收缩系统的活性,但不能预防肝硬化并发症或改善生存率。
等待肝移植的肝硬化患者常出现并发症,这些并发症会阻止他们接受移植。循环功能障碍是许多并发症的关键因素。本研究旨在研究治疗患者使用米多君(一种血管收缩剂)和白蛋白是否会改善循环功能障碍并预防并发症。这种联合治疗,至少在本研究中使用的剂量下,并没有预防肝硬化的并发症或改善这些患者的生存率。