Terlipressin with Limited Fluid Resuscitation in a Swine Model of Hemorrhage
Abstract Background Principles of damage control resuscitation include minimizing intravenous fluid (IVF) administration while correcting perfusion pressure as quickly as possible. Recent studies have identified a potential advantage of vasopressin over catecholamines in traumatic shock. Terlipressi...
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Veröffentlicht in: | The Journal of emergency medicine 2013-07, Vol.45 (1), p.78-85 |
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Sprache: | eng |
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Zusammenfassung: | Abstract Background Principles of damage control resuscitation include minimizing intravenous fluid (IVF) administration while correcting perfusion pressure as quickly as possible. Recent studies have identified a potential advantage of vasopressin over catecholamines in traumatic shock. Terlipressin (TP) is a vasopressin analogue used to reverse certain shock etiologies in some European countries. Study Objective We evaluated three dosages of TP when combined with a limited colloid resuscitation strategy on mean arterial pressure (MAP) and lactatemia in a swine model of isolated hemorrhage. Methods Sixty anesthetized swine underwent intubation and severe hemorrhage. Subjects were randomized to one of four resuscitation groups: 4 mL/kg Hextend® (Hospira Inc, Lake Forest, IL) only, 3.75 μg/kg TP + Hextend, 7.5 μg/kg TP + Hextend, or 15 μg/kg TP + Hextend. MAP and heart rate were recorded every 5 min. Baseline and serial lactate values at 30-min intervals were recorded and compared. Results Subjects receiving 7.5 μg/kg TP had significantly higher MAPs at times t15 ( p = 0.012), t20 ( p = 0.004), t25 ( p = 0.018), t30 ( p = 0.032), t35 ( p = 0.030), and t40 ( p = 0.021). No statistically significant differences in lactate values between TP groups and controls were observed. Conclusion Subjects receiving 7.5 μg/kg of TP demonstrated improved MAP within 10 min of administration. When combined with minimal IVF resuscitation, TP doses between 3.75 and 15 μg/kg do not elevate lactate levels in hemorrhaged swine. |
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ISSN: | 0736-4679 2352-5029 |
DOI: | 10.1016/j.jemermed.2012.12.023 |