Choudhury Ashok, Kedarisetty Chandan K, Vashishtha Chitranshu, Saini Deepak, Kumar Sachin, Maiwall Rakhi, Sharma Manoj K, Bhadoria Ajeet S, Kumar Guresh, Joshi Yogendra K, Sarin Shiv K
Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, India.
Department of Critical care, Institute of Liver and Biliary Sciences, New Delhi, India.
Liver Int. 2017 Apr;37(4):552-561. doi: 10.1111/liv.13252. Epub 2016 Oct 20.
BACKGROUND & AIMS: The choice of vasopressor for treating cirrhosis with septic shock is unclear. While noradrenaline in general is the preferred vasopressor, terlipressin improves microcirculation in addition to vasopressor action in non-cirrhotics. We compared the efficacy and safety of noradrenaline and terlipressin in cirrhotics with septic shock.
Cirrhotics with septic shock underwent open label randomization to receive either terlipressin (n=42) or noradrenaline (n=42) infusion at a titrated dose. The primary outcome was mean arterial pressure (MAP) >65 mm Hg at 48 h.
Baseline characteristics were comparable between the terlipressin and noradrenaline groups.SBP and pneumonia were major sources of sepsis. A higher proportion of patients on terlipressin were able to achieve MAP >65 mm of Hg (92.9% vs 69.1% P=.005) at 48 h. Subsequent discontinuation of vasopressor after hemodynamic stability was better with terlipressin (33.3% vs 11.9%, P<.05). Terlipressin compared to noradrenaline prevented variceal bleed (0% vs 9.5%, P=.01) and improved survival at 48 h (95.2% vs 71.4%, P=.003). Percentage lactate clearance (LC) is an independent predictor of survival [P=.0001, HR=3.9 (95% CI: 1.85-8.22)] after achieving the target MAP.Therapy related adverse effect were comparable in both the arms (40.5% vs 21.4%, P=.06), mostly minor (GradeII-88%) and reversible.
Terlipressin is as effective as noradrenaline as a vasopressor in cirrhotics with septic shock and can serve as a useful drug. Terlipressin additionally provides early survival benefit and reduces the risk of variceal bleed. Lactate clearance is a better predictor of outcome even after achieving target MAP, suggesting the role of microcirculation in septic shock.
治疗肝硬化合并感染性休克时血管升压药的选择尚不明确。虽然一般而言去甲肾上腺素是首选的血管升压药,但特利加压素除了具有血管升压作用外,还能改善非肝硬化患者的微循环。我们比较了去甲肾上腺素和特利加压素治疗肝硬化合并感染性休克的疗效和安全性。
肝硬化合并感染性休克患者接受开放标签随机分组,分别接受特利加压素(n = 42)或去甲肾上腺素(n = 42)滴定剂量输注。主要结局是48小时时平均动脉压(MAP)> 65 mmHg。
特利加压素组和去甲肾上腺素组的基线特征具有可比性。收缩压和肺炎是脓毒症的主要来源。48小时时,接受特利加压素治疗的患者中有更高比例能够达到MAP> 65 mmHg(92.9% 对69.1%,P = 0.005)。血流动力学稳定后,特利加压素组血管升压药的停药情况更好(33.3% 对11.9%,P < 0.05)。与去甲肾上腺素相比,特利加压素可预防静脉曲张出血(0% 对9.5%,P = 0.01),并提高48小时生存率(95.2% 对71.4%,P = 0.003)。达到目标MAP后,乳酸清除率(LC)百分比是生存的独立预测因素[P = 0.0001,HR = 3.9(95% CI:1.85 - 8.22)]。两组治疗相关不良反应具有可比性(40.5% 对21.4%,P = 0.06),大多为轻度(II级 - 88%)且可逆。
在肝硬化合并感染性休克患者中,特利加压素作为血管升压药与去甲肾上腺素效果相当,可作为一种有用的药物。特利加压素还能提供早期生存获益并降低静脉曲张出血风险。即使在达到目标MAP后,乳酸清除率也是更好的结局预测指标,提示微循环在感染性休克中的作用。