Gupta Tarana, Saini Anjali, Gaur Vaibhav, Goel Ashank
Medicine, Division of Hepatology, Pandit Bhagwat Dayal Sharma Post Graduate Institute of Medical Sciences, Rohtak, 124001, India.
J Clin Exp Hepatol. 2025 May-Jun;15(3):102494. doi: 10.1016/j.jceh.2024.102494. Epub 2025 Jan 10.
Sepsis is the most common acute insult in patients with acute-on-chronic liver failure (ACLF), and circulatory failure portends a poor prognosis in them.
This study aimed to compare terlipressin and noradrenaline as first-line vasopressors in patients with ACLF and septic shock.
This prospective, open-label, randomized controlled study was conducted from January 2021 to June 2022 at a tertiary care center. All patients presenting with ACLF as per the chronic liver failure consortium acute on chronic liver failure in cirrhosis study and septic shock were screened. Shock was defined as a mean arterial pressure (MAP) <65 mmHg/systolic blood pressure <90 mmHg. Patients with septic shock nonresponsive to crystalloids/colloids were randomized to receive terlipressin (group I) at 2.6 μg/kg/min and noradrenaline (group II) at 0.1 μg/kg/min. The primary outcome was an MAP >65 mmHg at 6 h. The secondary outcomes were 3-, 7-, 14-, and 28-day mortality, duration of hospital stay, cumulative dose of drug, and new events such as upper gastrointestinal bleed, acute kidney injury, jaundice, and hepatic encephalopathy within 28 days.
A total of 70 patients were randomized to group I (n = 35) and group II (n = 35). According to per-protocol analysis, a higher number of patients achieved an MAP > 65 mmHg at 6 h in group II (n = 23/31, 74%) than in group I (5/34, 14%) ( < 0.001). The 3-and 7-day mortality was significantly higher in group I than in group II, with no difference at 14 and 28 days. The 28-day mortality was highest in ACLF grade-3 in both group II (22/25, 88%) and group I (15/20, 75%).
Terlipressin did not prove to be noninferior to norepinephrine, and therefore, norepinephrine should be the first-line vasopressor in ACLF patients with septic shock. The mortality rate was highest in ACLF grade-3 patients in both the groups, irrespective of the initial response to vasopressors. This indicates that holistic management of these patients is most important.
脓毒症是慢性肝衰竭急性发作(ACLF)患者中最常见的急性损伤,循环衰竭预示着他们的预后不良。
本研究旨在比较特利加压素和去甲肾上腺素作为ACLF合并感染性休克患者的一线血管升压药的效果。
本前瞻性、开放标签、随机对照研究于2021年1月至2022年6月在一家三级医疗中心进行。对所有符合肝硬化慢性肝衰竭联盟慢性肝衰竭急性发作研究标准且合并感染性休克的患者进行筛查。休克定义为平均动脉压(MAP)<65 mmHg/收缩压<90 mmHg。对晶体液/胶体液无反应的感染性休克患者被随机分为两组,一组接受特利加压素(I组),剂量为2.6 μg/kg/min,另一组接受去甲肾上腺素(II组),剂量为0.1 μg/kg/min。主要结局是6小时时MAP>65 mmHg。次要结局包括3天、7天、14天和28天的死亡率、住院时间、药物累积剂量以及28天内出现的新事件,如消化道出血、急性肾损伤、黄疸和肝性脑病。
共有70例患者被随机分为I组(n = 35)和II组(n = 35)。根据符合方案分析,II组在6小时时达到MAP>65 mmHg的患者数量(n = 23/31,74%)高于I组(5/34,14%)(P<0.001)。I组的3天和7天死亡率显著高于II组,14天和28天死亡率无差异。II组(22/25,88%)和I组(15/20,75%)中ACLF 3级患者的28天死亡率最高。
特利加压素并不优于去甲肾上腺素,因此,去甲肾上腺素应作为ACLF合并感染性休克患者的一线血管升压药。两组中ACLF 3级患者的死亡率最高,无论对血管升压药的初始反应如何。这表明对这些患者进行全面管理最为重要。