Departments of Internal Medicine.
Hepatology.
J Clin Gastroenterol. 2022 Jan 1;56(1):e11-e19. doi: 10.1097/MCG.0000000000001450.
Acute-on-chronic liver failure (ACLF) is associated with high short-term mortality in those with hepatic encephalopathy (HE). Polyethylene glycol (PEG) 3350 electrolyte solution can ensure rapid gut catharsis, which may resolve HE more effectively than lactulose. In this open-label-randomized trial, we compared PEG+lactulose versus lactulose alone in ACLF with HE grade ≥2 for efficacy and outcome.
Patients were randomized to receive PEG (2 L q12 h) followed by lactulose (30 mL q8 h) or standard medical treatment [SMT, lactulose (titrated 30 mL q8 h)]. Endpoints were HE grade improvement at 24 hours, 48 hours, and 7 days using hepatic encephalopathy scoring algorithm (HESA), ammonia reduction, HE resolution, and survival benefit.
Of 60 patients, 29 were randomized to PEG+lactulose arm and 31 to SMT. In the PEG arm, early reduction in HESA score was noted in more persons [18 (62.1%) vs. 10 (32.2%); P=0.021] with a shorter median time to HE resolution [4.5 (3 to 9) d vs. 9 (8 to 11) d; P=0.023]. On multivariate analysis, age [hazard ratio (HR),1.06 (1.00 to 1.13); P=0.03], HESA score [HR, 6.01 (1.27 to 28.5); P=0.024], and model for end-stage liver disease [HR, 1.26 (1.01 to 1.53); P=0.022] were predictors of mortality at 28 days. Ammonia level or reduction did not correlate with HE grades. Adverse events included excessive diarrhea (20.6% vs. 9.6%) in the PEG and SMT arms, albeit without dyselectrolytemia or worsened renal function. In the PEG versus SMT arm, survival at 28 days were 93.1% versus 67.7% (P=0.010) and at 90 days was 68.9% versus 48.3% (P=0.940), respectively, with fewer persons relapsing with HE in the PEG arm.
PEG resulted in early and sustained HE resolution with improved short-term survival making, it a suitable and safe drug in patients with acute HE in ACLF.
伴有肝性脑病(HE)的慢加急性肝衰竭(ACLF)患者短期死亡率较高。聚乙二醇(PEG)3350 电解质溶液可确保快速肠道通便,这可能比乳果糖更有效地解决 HE。在这项开放标签的随机试验中,我们比较了 PEG+乳果糖与单独使用乳果糖治疗 ACLF 合并 HE 分级≥2 的疗效和结局。
患者被随机分为接受 PEG(2 L q12 h),然后是乳果糖(30 mL q8 h)或标准治疗[SMT,乳果糖(滴定 30 mL q8 h)]。终点是使用肝性脑病评分算法(HESA)在 24 小时、48 小时和 7 天时 HE 分级改善、氨降低、HE 缓解和生存获益。
在 60 名患者中,29 名被随机分配到 PEG+乳果糖组,31 名分到 SMT 组。在 PEG 组中,更多的人早期 HESA 评分降低[18(62.1%)vs. 10(32.2%);P=0.021],HE 缓解的中位时间更短[4.5(3 至 9)d vs. 9(8 至 11)d;P=0.023]。多变量分析显示,年龄[风险比(HR),1.06(1.00 至 1.13);P=0.03]、HESA 评分[HR,6.01(1.27 至 28.5);P=0.024]和终末期肝病模型[HR,1.26(1.01 至 1.53);P=0.022]是 28 天死亡率的预测因素。氨水平或降低与 HE 分级无关。不良事件包括 PEG 和 SMT 组中过度腹泻(20.6% vs. 9.6%),但没有电解质紊乱或肾功能恶化。在 PEG 与 SMT 组中,28 天生存率分别为 93.1%和 67.7%(P=0.010),90 天生存率分别为 68.9%和 48.3%(P=0.940),PEG 组中 HE 复发的人数更少。
PEG 可早期和持续缓解 HE,改善短期生存率,因此是 ACLF 急性 HE 患者的一种合适且安全的药物。