Zusammenfassung
Die hochgradige Störung der Hämodynamik im Schock führt zu einer Verringerung des Sauerstoffangebots lebenswichtiger Organe. Wird dieser Zustand nicht rasch behoben, kann es zu einem Multiorganversagen kommen. Neben der Beseitigung der Schockursache, wie z. B. einer Blutung oder eines septischen Fokus, müssen Maßnahmen eingeleitet werden, die zu einer Stabilisierung der Hämodynamik führen. In vielen Fällen gelingt dies durch Flüssigkeitsersatz oder durch Einsatz von Inotropika und Vasopressoren. Beim hypovolämischen Schock konnten hyperton/hyperonkotische Lösungen bisher keine Vorteile gegenüber herkömmlichen Infusionen zeigen, außer in Situationen, in denen nicht sofort genügend Ressourcen für eine primäre Versorgung zur Verfügung stehen. Im Tierexperiment konnte die Hämodynamik mit Vasopressin deutlich besser als mit Volumen stabilisiert werden, wenn eine unstillbare intraabdominelle Blutung vorlag. Auch die Letalität war bei den mit Vasopressin behandelten Tieren signifikant niedriger. Es fehlen aber noch klinische Arbeiten, die diese Ergebnisse bestätigen. Vasopressin trägt im septischen Schock sowohl in niedriger als auch in hoher Dosierung zu einer Stabilisierung der Hämodynamik bei. Allerdings kommt es dabei zu einer Beeinträchtigung der Splanchnikusperfusion. Deshalb kann der Einsatz von Vasopressin im septischen Schock zurzeit nicht empfohlen werden.
Abstract
The extreme disturbance of hemodynamics in shock leads to a minimized oxygen delivery to several vital organs. If this state is not rapidly lifted, a multi-organ-failure can occur. In addition to the removal of the underlying causes, for example, bleeding or septic focus, measures must be started to stabilize hemodynamics. In most cases shock can be successfully treated with standard therapeutic interventions including the use of crystalloid or colloid solutions as well as the infusion of inotropes or vasopressors. Up to now, there is not enough evidence to show that hypertonic/hyperoncotic solutions are better for treating hypovolemic shock than standard infusions, other than in situations, where only an inadequate equipment is available. Experimental data support the use of vasopressin instead of fluid loading in case of uncontrolled intra-abdominal bleeding. According to these studies vasopressin seems to be associated with an improved hemodynamic stabilization and a significantly lower mortality rate. However, no clinical tests have been done so far to confirm these results. In septic shock the plasma-levels of vasopressin are low. It has been shown that the infusion of vasopressin contributes to stabilization of hemodynamics in septic shock, in lower, as well as in higher concentrations. On the other hand vasopressin worsens splanchnic perfusion. Therefore the routine use of vasopressin in the treatment of sepsis can not be recommended.
Literatur
Argenziano M, Choudhri AF, Oz MC, Rose EA, Smith CR, Landry DW (1997) A prospective randomized trial of arginine vasopressin in the treatment of vasodilatory shock after left ventricular assist device placement. Circulation 96 (Suppl): 286–290
Asfar P, Pierrot M, Veal V et al. (2003) Low-dose terlipressin improves systemic and splanchnic hemodynamics in fluid-challenged endotoxic rats. Crit Care Med 31: 215–220
Asfar P (2003) Reply to the comment on „Terlipressin in chronic hyperdynamic endotoxic shock: Is it safe? Intensive Care Med 29: 855
Baue AE, Tragus ET, Parkins WM (1967) A comparison of isotonic and hypertonic solutions an blood flow and oxygen consumption in the initial treatment of hemorrhagic shock. J Trauma 7: 743–756
Bernadich C, Bandi JC, Bosch J (1998) Effects of F-180, a new selective vasoconstrictor peptide compared with terlipressin and vasopressin on systemic and splanchnic hemodynamics in a rat model of portal hypertension. Hepatology 27: 351–356
Bickell WH, Wall MJ Jr, Pepe PE, Martin RR, Ginger VF, Allen MK, Mattox KL (1994) Immediate versus delayed fluid resuscitation for hypotensive patients with penetrating torso injuries. N Engl J Med 331: 1105–1109
Bittermann H, Triolo J, Lefer AM (1987) Use of hypertonic saline in the treatment of hemorrhage shock. Circ Shock 21: 271–283
Bohrmann SW, Fabian, TC, Kudsk KA, Proctor KG (1991) Microcirculatory flow changes after initial resuscitation of hemorrhagic shock with 7,5% hypertonic saline/6% dextran 70. J Trauma 31: 589–600
Bone RC (1996) Toward a theory regarding the pathogenesis of the systemic inflammatory response syndrome: What we do and do not know about cytokine regulation. Crit Care Med 24: 163
Bunn F, Roberts I, Tasker R, Akpa E (2001) Hypertonic versus isotonic crystalloid for fluid resuscitation in critically ill patients (Cochrane Review). Cochrane Library
Chernow B, Roth B (1986) Pharmacologic manipulations of the peripheral vasculature in shock: clinical and experimental approaches. Circ Shock 18: 141–155
Chiara O, Pelosi P, Brazzi L et al. (2003) Resuscitation from hemorrhagic shock: Experimental model comparing normal saline, dextran, and hypertonic saline solutions. Crit Care Med 31: 1915–1922
De Felippe J, Timoner J, Velasco IT, Lopes OU, Rocha e Silva M (1980) Treatment of refractory hypovolaemic shock by 7,5% sodium chloride injections. Lancet 2: 1002–1004
Dünser M, Wenzel V, Mayr AJ, Hasibeder WR (2002) Arginin-Vasopressin im vasodilatatorischen Schock. Anaesthesist 51: 650–659
Dünser MW, Mayr AJ, Ulmer H et al. (2001) The effects of vasopressin on systemic hemodynamics in catecholamine-resistant septic and postcardiotomy shock: a retrospective analysis. Anesth Analg 93: 7–13
Dünser MW, Mayr AJ, Ulmer H et al. (2003) Arginine Vasopressin in advanced vasodilatory shock. Circulation 107: 2313–2319
Eyraud D, Brabant S, Dieudonne N, Fléron MH, Gilles G, Bertrand M, Coriat P (1999) Treatment of intraoperative refractory hypotension with terlipressin in patients chronically treated with an antagonist of the renin-angiotensin system. Anesth Anal 88: 980–984
Fox AW, May RE, Mitch WE (1992) Comparison of peptide and nonpeptide receptor-mediated responses in rat tail artery. J Cardiovasc Pharmacol 20: 282–289
Holcroft JW, Vassar MJ, Turner JE, Derlet RW, Kramer GC (1987) 3% NaCl and 7,5% NaCl/Dextran 70 in the resuscitation of severely injured patients. Ann Surg 206: 279–287
Horton JW, Walker PB (1991) Small-volume hypertonic saline dextran resuscitation from canine endotoxin shock. Ann Surg 214: 64–73
Ioannou G, Doust J, Rockey DC (2001) Terlipressin for acute esophageal variceal hemorrhage (Cochrane Review). Cochrane Database Syst Rev 1: CD002147
Kien ND, Kramer GC, White DA (1980) Immediate increase in cardiac contractility following hypertonic saline infusion. Euro Surg Res 22: 293–295
Klinzing S, Simon M, Reinhart K, Bredle DL, Meier-Hellmann A (2003) High-dose vasopressin is not superior to norepinephrine in septic shock. Crit Care Med 31: 2646–2650
Kramer GC, Perron PR, Lindsay DC, Ho HS, Gunther RA, Boyle WA, Holcroft JW (1986) Small-volume resuscitation with hypertonic saline dextran solution. Surgery 100: 239–247
Krausz MM (1995) Controversies in shock research. Hypertonic resuscitation—Pros and cons. Shock 3: 69–72
Kreimeier U, Peter K, Meßmer K (2001) Small volume—large benefit? Anaesthesist 50: 442–449
Kreimeier U, Frey L, Dentz J, Herbel T, Messmer K (1991) Hypertonic saline dextran resuscitation during the initial phase of acute endotoxemia: Effect on regional blood flow. Crit Care Med 19: 801–809
Kreimeier U, Christ F, Kraft D, Lauterjung L, Niklas M, Peter K, Messmer K (1995) Anaphylaxis due to hydroxy-ethyl-starch-reactive antibodies. Lancet 346: 49–50
Landry DW, Oliver JA (2001) The pathogenesis of vasodilatory shock. N Engl J Med 345: 588–595
Landry DW, Levin HR, Gallant HM et al. (1997) Vasopressin deficiency contributes to the vasodilation of septic shock. Circulation 95: 1122–1125
Mattox KL, Maningas PA, Moore EE et al. (1991) Prehospital hypertonic saline/dextran infusion for post-traumatic hypotension—the US AUCH multicenter trial. Ann Surg 213: 482–491
Mazzoni MC, Borgstrom P, Intaglietta M, Arfors KE (1990) Capillary narrowing in hemorrhagic shock is rectified by hyperosmotic saline-dextrane reinfusion. Circ Shock 31: 407–418
Mellander S, Johansson B, Gray S, Jonsson O, Lundvall J, Ljung B (1967) The effects of hyperosmolarity on intact and isolated vascular smooth muscle. Possible role in exercise hyperemia. Angiologica 4: 310–322
Messmer K, Kreimeier U (1989) Microcirculatory therapy in shock. Resuscitation (Suppl) 18: S51–S61
Muders F, Elsner D, Jandeleit K et al. (1997) Chronic ACE inhibition by quinapril modulates central vasopressinergic system. Cardiovasc Res 34: 575–581
Nerlich M, Gunther R, Demling RH (1983) Resuscitation from hemorrhagic shock with hyptertonic saline or lactated ringer’s (Effect on the pulmonary and systemic microcirculations). Circ Shock 10: 179–188
Nilsson G, Lindblom P, Ohlin M, Berling R, Vernersson E (1990) Pharmacokinetics of terlipressin after single i.v. doses to healthy volunteers. Drugs Exp Clin Res 16: 307–314
Nolte D, Bayer M, Lehr HA, Becker M, Krombacher F, Kreimeier U, Messmer K (1992) Attenuation of postischemic microvascular disturbances in striated muscle by hyperosmolar saline dextran. Am J Physiol 263: H1411–H1416
O’Brien A, Clapp L, Simger M (2002) Terlipressin for norepinephrine-resistant septic shock. Lancet 359: 1209–1210
Pascual JMS, Watson JC, Runyon AE, Wade CE, Kramer GC (1992) Resuscitation of intraoperative hypovolemia: A comparison of normal saline and hyperosmotic/hyperoncotic solutions in swine. Crit Care Med 20: 200–210
Patel BM, Chittock DR, Russell JA, Walley KR (2002) Beneficial effects of short-term vasopressin infusion during severe septic shock. Anesthesiology 96: 576–582
Pope A, French G, Longnecker DE, Institute of Medicine (IOM) (1999) Fluid resuscitation. State of the science for treating combat casualties and civilian injuries.
Rabinovici R, Krausz MM, Feuerstein G (1991) Control of bleeding is essential for a successful treatment of hemorrhagic shock with 7.5 per cent sodium chloride solution. Surg Gynecol Obstet 173: 98–106
Reed LL, Manglano R, Martin M, Hochman M, Kocka F, Barret J (1991) The effect of hypertonic saline resuscitation on bacterial translocation after hemorrhagic shock in rats. Surgery 110: 685–690
Reinhart K, Rudolph T, Bredle DL, Cain SM (1989) O2-Uptake in bled dogs after resuscitation with hypertonic saline of hydroxyethylstarch. Am J Physiol 257: H238–H243
Schimetta W, Schöchl H, Kröll W, Pölz W, Pölz G, Mauritz W (2001) Safety of hypertonic hyperoncotic solutions—A survey from Austria. Wien Klin Wochenschr 114: 89–95
Soliman MH, Ragab H, Waxman K (1990) Survival after hypertonic saline resuscitation from hemorrhage. Am Surg 56: 749–751
Solomonov E, Hirsh M, Yahiya A, Krausz M (2000) The effect of vigorous fluid resuscitation in uncontrolled hemorrhagic shock after massive splenic injury. Crit Care Med 28: 749–754
Sprung CL, Bernard GR, Dellinger RP (2001) Guidelines for the management of severe sepsis and septic shock. Intensive Care Med 27 (Suppl): 1–134
Stadlbauer KH, Wagner-Berger HG, Raedler C et al. (2003) Vasopressin, but not fluid resuscitaton, enhances survival in a liver trauma model with uncontrolled and otherwise lethal hemorrhagic shock in pigs. Anesthesiology 98: 699–704
Sun Q, Dimopoulos G, Nguyen DN et al. (2003) Low-dose vasopressin in the treatment of septic shock in sheep. Am J Respir Crit Care Med 168: 481–486
Tisherman S (2000) Regardless of origin, uncontrolled hemorrhage is uncontrolled hemorrhage. Crit Care Med 28: 892–894
Traverso LW, Bellamy RF, Hollenbach SJ, Witcher LD (1987) Hypertonic sodium chloride solutions: effects on hemodynamics and survival after hemorrhage in swine. J Trauma 27: 32–35
Trunkey DD (1983) Trauma. Sci Am 249: 20–27
Tsuneyohsi I, Kanmura Y, Yoshimura N (1996) Nitric oxide as a mediator of reduced arterial responsiveness in septic patients. Crit Care Med 24: 1083–1086
Tsuneyoshi I, Yamada H, Kakihana Y, Nakamura M, Nakano Y, Boyle WA (2001) Hemodynamic and metabolic effects of low-dose vasopressin infusions in vasodilatory septic shock. Crit Care Med 29: 487–493
Vassar MJ, Perry CA, Gannaway WL, Holcroft JW (1991) 7.5% sodium chloride/dextran for resuscitation of patients undergoing helicopter transport. Arch Surg 126: 1065–1072
Vassar MJ, Perry CA Holcroft JW (1990) Analysis of potential risks associated with 7,5% sodium chloride resuscitation of traumatic shock. Arch Surg 135: 1309–1315
Velasco IT, Pontierie V, Rocha e Silva M, Lopes OU (1980) Hyperosmotic NaCl and severe hemorrhagic shock. Am J Phyiol 239: H664-H673
Voelckel WG, Raedler C, Wenzel V et al. (2003) Arginine vasopressin, but not epinephrine, improves survival in uncontrolled hemorrhagic shock after liver trauma in pigs. Crit Care Med 31: 1160–1165
Welte M, Messmer K (1996) Cardiac function in small volume resuscitation. In: Messmer K (ed) Compromised perfusion. Progr Appl Microcirc 21: 1–19
Wenzel V, Lindner KH (2001) Employing vasopressin during cardiopulmonary resuscitation and vasodilatory shock as a lifesaving vasopressor. Cardiovasc Res 51: 529–541
Wildenthal K, Mierzwiak DS, Mitchell JH (1969) Acute effects of increased serum osmolality on left ventricular performance. Am J Physiol 216: 890–904
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Meier-Hellman, A., Burgard, G. Neue Therapieansätze bei der prähospitalen und hospitalen Schockbehandlung. Internist 45, 305–314 (2004). https://doi.org/10.1007/s00108-003-1141-z
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DOI: https://doi.org/10.1007/s00108-003-1141-z
Schlüsselwörter
- Hyperton/hyperonkotische Lösungen
- Vasopressin
- Hypovolämischer Schock
- Intraabdominelle Blutung
- Septischer Schock