Early fluid resuscitation with hyperoncotic hydroxyethyl starch 200/0.5 (10%) in severe burn injury

Markus Béchir, Milo A Puhan, Simona B Neff, Merlin Guggenheim, Volker Wedler, John F Stover, Reto Stocker, Thomas A Neff, Markus Béchir, Milo A Puhan, Simona B Neff, Merlin Guggenheim, Volker Wedler, John F Stover, Reto Stocker, Thomas A Neff

Abstract

Introduction: Despite large experience in the management of severe burn injury, there are still controversies regarding the best type of fluid resuscitation, especially during the first 24 hours after the trauma. Therefore, our study addressed the question whether hyperoncotic hydroxyethyl starch (HES) 200/0.5 (10%) administered in combination with crystalloids within the first 24 hours after injury is as effective as 'crystalloids only' in severe burn injury patients.

Methods: 30 consecutive patients were enrolled to this prospective interventional open label study and assigned either to a traditional 'crystalloids only' or to a 'HES 200/0.5 (10%)' volume resuscitation protocol. Total amount of fluid administration, complications such as pulmonary failure, abdominal compartment syndrome, sepsis, renal failure and overall mortality were assessed. Cox proportional hazard regression analysis was performed for binary outcomes and adjustment for potential confounders was done in the multivariate regression models. For continuous outcome parameters multiple linear regression analysis was used.

Results: Group differences between patients receiving crystalloids only or HES 200/0.5 (10%) were not statistically significant. However, a large effect towards increased overall mortality (adjusted hazard ratio 7.12; P = 0.16) in the HES 200/0.5 (10%) group as compared to the crystalloids only group (43.8% versus 14.3%) was present. Similarly, the incidence of renal failure was 25.0% in the HES 200/0.5 (10%) group versus 7.1% in the crystalloid only group (adjusted hazard ratio 6.16; P = 0.42).

Conclusions: This small study indicates that the application of hyperoncotic HES 200/0.5 (10%) within the first 24 hours after severe burn injury may be associated with fatal outcome and should therefore be used with caution.

Trial registration: NCT01120730.

Figures

Figure 1
Figure 1
Kaplan-Meier survival curve and causes of death. Large effect towards a seven-fold higher mortality in the HES group (adjusted hazard ratio 7.12; P = 0.16). ARDS, acute respiratory distress syndrome; HES, hydroxyethyl starch.
Figure 2
Figure 2
Bloodmarkers at days one, two, three and seven. (a) Hematocrit, (b) white blood count, (c) C-reactive protein, (d) glutamat-pyruvat-transaminase (GPT) and (e) glutamat-oxalacetat-transaminase (GOT). Baxter group black bars, hydroxyethyl starch (HES) group grey bars. Plots show mean ± standard deviation, analysis of variance for repeated measurements. There were no differences between the groups.

References

    1. Brunkhorst FM, Engel C, Bloos F, Meier-Hellmann A, Ragaller M, Weiler N, Moerer O, Gruendling M, Oppert M, Grond S, Olthoff D, Jaschinski U, John S, Rossaint R, Welte T, Schaefer M, Kern P, Kuhnt E, Kiehntopf M, Hartog C, Natanson C, Loeffler M, Reinhart K. Intensive insulin therapy and pentastarch resuscitation in severe sepsis. N Engl J Med. 2008;358:125–139. doi: 10.1056/NEJMoa070716.
    1. Reinhart K, Brunkhorst FM, Engel C, Bloos F, Meier-Hellmann A, Ragaller M, Weiler N, Moerer O, Gruendling M, Oppert M, Grond S, Olthoff D, Jaschinski U, John S, Rossaint R, Welte T, Schaefer M, Kern P, Kuhnt E, Kiehntopf M, Deufel T, Hartog C, Gerlach H, Stuber F, Volk HD, Quintel M, Loeffler M. [Study protocol of the VISEP study: Response of the SepNet study group] Anaesthesist. 2008;57:723–728. doi: 10.1007/s00101-008-1391-1.
    1. Zander R, Boldt J, Engelmann L, Mertzlufft F, Sirtl C, Stuttmann R. [The design of the VISEP trial. Critical appraisal] Anaesthesist. 2007;56:71–77. doi: 10.1007/s00101-006-1122-4.
    1. Pitt RM, Parker JC, Jurkovich GJ, Taylor AE, Curreri PW. Analysis of altered capillary pressure and permeability after thermal injury. J Surg Res. 1987;42:693–702. doi: 10.1016/0022-4804(87)90013-8.
    1. Youn YK, LaLonde C, Demling R. The role of mediators in the response to thermal injury. World J Surg. 1992;16:30–36. doi: 10.1007/BF02067111.
    1. Warden GD. Burn shock resuscitation. World J Surg. 1992;16:16–23. doi: 10.1007/BF02067109.
    1. Yowler CJ, Fratianne RB. Current status of burn resuscitation. Clin Plast Surg. 2000;27:1–10.
    1. Cocks AJ, O'Connell A, Martin H. Crystalloids, colloids and kids: a review of paediatric burns in intensive care. Burns. 1998;24:717–724. doi: 10.1016/S0305-4179(98)00102-8.
    1. Barrow RE, Jeschke MG, Herndon DN. Early fluid resuscitation improves outcomes in severely burned children. Resuscitation. 2000;45:91–96. doi: 10.1016/S0300-9572(00)00175-1.
    1. Kreimeier U, Messmer K. Small-volume resuscitation: from experimental evidence to clinical routine. Advantages and disadvantages of hypertonic solutions. Acta Anaesthesiol Scand. 2002;46:625–638. doi: 10.1034/j.1399-6576.2002.460601.x.
    1. Oda J, Ueyama M, Yamashita K, Inoue T, Noborio M, Ode Y, Aoki Y, Sugimoto H. Hypertonic lactated saline resuscitation reduces the risk of abdominal compartment syndrome in severely burned patients. J Trauma. 2006;60:64–71. doi: 10.1097/01.ta.0000199431.66938.99.
    1. Oda J, Yamashita K, Inoue T, Hosotsubo H, Aoki Y, Ode Y, Kasai K, Noborio M, Ueyama M, Sugimoto H. Acute lung injury and multiple organ dysfunction syndrome secondary to intra-abdominal hypertension and abdominal decompression in extensively burned patients. J Trauma. 2007;62:1365–1369. doi: 10.1097/TA.0b013e3180487d3c.
    1. Hershberger RC, Hunt JL, Arnoldo BD, Purdue GF. Abdominal compartment syndrome in the severely burned patient. J Burn Care Res. 2007;28:708–714. doi: 10.1097/BCR.0b013E318148C988.
    1. Oda J, Ueyama M, Yamashita K, Inoue T, Harunari N, Ode Y, Mega K, Aoki Y, Noborio M. Effects of escharotomy as abdominal decompression on cardiopulmonary function and visceral perfusion in abdominal compartment syndrome with burn patients. J Trauma. 2005;59:369–374. doi: 10.1097/01.ta.0000174917.90514.4a.
    1. Boldt J, Papsdorf M. Fluid management in burn patients: results from a European survey-more questions than answers. Burns. 2008;34:328–338. doi: 10.1016/j.burns.2007.09.005.
    1. Human albumin administration in critically ill patients: systematic review of randomised controlled trials. Cochrane Injuries Group Albumin Reviewers. BMJ. 1998;317:235–240.
    1. Wharton SM, Khanna A. Current attitudes to burns resuscitation in the UK. Burns. 2001;27:183–184. doi: 10.1016/S0305-4179(00)00097-8.
    1. Ennis JL, Chung KK, Renz EM, Barillo DJ, Albrecht MC, Jones JA, Blackbourne LH, Cancio LC, Eastridge BJ, Flaherty SF, Dorlac WC, Kelleher KS, Wade CE, Wolf SE, Jenkins DH, Holcomb JB. Joint Theater Trauma System implementation of burn resuscitation guidelines improves outcomes in severely burned military casualties. J Trauma. 2008;64:S146–151. doi: 10.1097/TA.0b013e318160b44c. discussion S151-142.
    1. Holm C, Tegeler J, Mayr M, Pfeiffer U, Henckel von Donnersmarck G, Muhlbauer W. Effect of crystalloid resuscitation and inhalation injury on extravascular lung water: clinical implications. Chest. 2002;121:1956–1962. doi: 10.1378/chest.121.6.1956.
    1. Cittanova ML, Leblanc I, Legendre C, Mouquet C, Riou B, Coriat P. Effect of hydroxyethylstarch in brain-dead kidney donors on renal function in kidney-transplant recipients. Lancet. 1996;348:1620–1622. doi: 10.1016/S0140-6736(96)07588-5.
    1. Holm C. Resuscitation in shock associated with burns. Tradition or evidence-based medicine? Resuscitation. 2000;44:157–164. doi: 10.1016/S0300-9572(00)00159-3.
    1. Baxter CR. Fluid volume and electrolyte changes of the early postburn period. Clin Plast Surg. 1974;1:693–703.
    1. Baxter CR, Marvin JA, Curreri PW. Early management of thermal burns. Postgrad Med. 1974;55:131–139.
    1. Uchino S, Bellomo R, Kellum JA, Morimatsu H, Morgera S, Schetz MR, Tan I, Bouman C, Macedo E, Gibney N, Tolwani A, Oudemans-Van Straaten HM, Ronco C. Patient and kidney survival by dialysis modality in critically ill patients with acute kidney injury. Int J Artif Organs. 2007;30:281–292.
    1. Uchino S, Kellum JA, Bellomo R, Doig GS, Morimatsu H, Morgera S, Schetz M, Tan I, Bouman C, Macedo E, Gibney N, Tolwani A, Ronco C. Acute renal failure in critically ill patients: a multinational, multicenter study. JAMA. 2005;294:813–818. doi: 10.1001/jama.294.7.813.
    1. Jungheinrich C, Scharpf R, Wargenau M, Bepperling F, Baron JF. The pharmacokinetics and tolerability of an intravenous infusion of the new hydroxyethyl starch 130/0.4 (6%, 500 mL) in mild-to-severe renal impairment. Anesth Analg. 2002;95:544–551. doi: 10.1097/00000539-200209000-00007. table of contents.
    1. Thompson WL, Fukushima T, Rutherford RB, Walton RP. Intravascular persistence, tissue storage, and excretion of hydroxyethyl starch. Surg Gynecol Obstet. 1970;131:965–972.
    1. De Labarthe A, Jacobs F, Blot F, Glotz D. Acute renal failure secondary to hydroxyethylstarch administration in a surgical patient. Am J Med. 2001;111:417–418. doi: 10.1016/S0002-9343(01)00873-7.
    1. Waldhausen P, Kiesewetter H, Leipnitz G, Scielny J, Jung F, Bambauer R, von Blohn G. [Hydroxyethyl starch-induced transient renal failure in preexisting glomerular damage] Acta Med Austriaca. 1991;18(Suppl 1):52–55.
    1. Peron S, Mouthon L, Guettier C, Brechignac S, Cohen P, Guillevin L. Hydroxyethyl starch-induced renal insufficiency after plasma exchange in a patient with polymyositis and liver cirrhosis. Clin Nephrol. 2001;55:408–411.
    1. Schortgen F, Lacherade JC, Bruneel F, Cattaneo I, Hemery F, Lemaire F, Brochard L. Effects of hydroxyethylstarch and gelatin on renal function in severe sepsis: a multicentre randomised study. Lancet. 2001;357:911–916. doi: 10.1016/S0140-6736(00)04211-2.
    1. Boldt J, Brenner T, Lehmann A, Lang J, Kumle B, Werling C. Influence of two different volume replacement regimens on renal function in elderly patients undergoing cardiac surgery: comparison of a new starch preparation with gelatin. Intensive Care Med. 2003;29:763–769.
    1. Winkelmayer WC, Glynn RJ, Levin R, Avorn J. Hydroxyethyl starch and change in renal function in patients undergoing coronary artery bypass graft surgery. Kidney Int. 2003;64:1046–1049. doi: 10.1046/j.1523-1755.2003.00186.x.
    1. Kumle B, Boldt J, Piper S, Schmidt C, Suttner S, Salopek S. The influence of different intravascular volume replacement regimens on renal function in the elderly. Anesth Analg. 1999;89:1124–1130. doi: 10.1097/00000539-199911000-00009.
    1. Legendre C, Thervet E, Page B, Percheron A, Noel LH, Kreis H. Hydroxyethylstarch and osmotic-nephrosis-like lesions in kidney transplantation. Lancet. 1993;342:248–249. doi: 10.1016/0140-6736(93)92345-T.
    1. Goodwin CW, Dorethy J, Lam V, Pruitt BA. Randomized trial of efficacy of crystalloid and colloid resuscitation on hemodynamic response and lung water following thermal injury. Ann Surg. 1983;197:520–531. doi: 10.1097/00000658-198305000-00004.
    1. Verheij J, van Lingen A, Raijmakers PGHM, Rijnsburger ER, Veerman DP, Wisselink W, Girbes ARJ, Groeneveld ABJ. Effect of fluid loading with saline or colloids on pulmonary permeability, oedema and lung injury score after cardiac and major vascular surgery. Br J Anaesth. 2006;96:21–30. doi: 10.1093/bja/aei286.
    1. Vincent JL, Taccone F, Schmit X. Classification, incidence, and outcomes of sepsis and multiple organ failure. Contrib Nephrol. 2007;156:64–74. full_text.
    1. Mandai R, Eguchi Y, Tanaka M, Sai Y, Nosaka S. Effects of Profound Hemodilution on Small-Intestinal Wound Healing in Rabbits. J Surg Res. 2001;99:107–113. doi: 10.1006/jsre.2001.6164.
    1. Mittlmeier T, Vollmar B, Menger MD, Schewior L, Raschke M, Schaser KD. Small volume hypertonic hydroxyethyl starch reduces acute microvascular dysfunction after closed soft-tissue trauma. J Bone Joint Surg Br. 2003;85:126–132. doi: 10.1302/0301-620X.85B1.11870.
    1. Jespersen CM, Als-Nielsen B, Damgaard M, Hansen JF, Hansen S, Helo OH, Hildebrandt P, Hilden J, Jensen GB, Kastrup J, Kolmos HJ, Kjoller E, Lind I, Nielsen H, Petersen L, Gluud C. Randomised placebo controlled multicentre trial to assess short term clarithromycin for patients with stable coronary heart disease: CLARICOR trial. BMJ. 2006;332:22–27. doi: 10.1136/bmj.38666.653600.55.

Source: PubMed

3
Subskrybuj