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World J Gastroenterol. Mar 21, 2012; 18(11): 1166-1175
Published online Mar 21, 2012. doi: 10.3748/wjg.v18.i11.1166
Published online Mar 21, 2012. doi: 10.3748/wjg.v18.i11.1166
Drug | Standard dosing | Duration | Mechanism of action |
Somatostatin | Initial iv bolus 250 μg (can be repeated in the first hour if ongoing bleeding); continuous iv infusion of 250 to 500 μg/h | Up to 5 d | Inhibits vasodilator hormones like glucagon causing splanchnic vasoconstriction and reduced portal blood flow |
Octreotide (somatostatin analogue) | Initial iv bolus of 50 μg (can be repeated in first hour if ongoing bleeding); continuous iv infusion of 50 μg/h | Up to 5 d | Same as somatostatin, longer duration of action |
Vapreotide (somatostatin analogue) | Bolus: 50 μg; continuous iv infusion of 50 μg/h | Up to 5 d | Similar to somatostatin with higher metabolic stability |
Vasopressin + nitroglycerine | 0.2-0.4 units/min continuous iv infusion intravenously, may titrate to a maximum of 0.8 units/min; always use in combination with nitroglycerine | Maximum of 24 h at lowest effective dose | Causes direct vasoconstriction on splanchnic circulation resulting in decreased portal blood flow |
Terlipressin (vasopressin analogue) | Initial 48 h: 2 mg iv every 4 h until control of bleeding; maintenance: 1 mg iv every 4 h to prevent re-bleeding | Up to 5 d | Splanchnic vasoconstriction; the active metabolite lysine-vasopressin is gradually released over several hours thus decreasing typical vasopressin side effects |
- Citation: Bari K, Garcia-Tsao G. Treatment of portal hypertension. World J Gastroenterol 2012; 18(11): 1166-1175
- URL: https://www.wjgnet.com/1007-9327/full/v18/i11/1166.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i11.1166