HIGH-DOSE VITAMIN C INFUSION REDUCES FLUID REQUIREMENTS IN THE RESUSCITATION OF BURN-INJURED SHEEP

Fluid resuscitation to maintain adequate tissue perfusion while reducing edema in the severely burned patient remains a challenge. Recent studies suggest that reactive oxygen species generated by thermal injury are involved in edema formation associated with burn. The present study tested the hypothesis that adding a free radical scavenger to the resuscitation fluid would reduce total fluid requirements in the treatment of severe thermal injury. Anesthetized chronically instrumented sheep received a 40% total body surface area full-thickness flame burn. At 1 h after injury, animals were resuscitated with lactated Ringer's (LR, n = 14) as control, LR containing high doses of vitamin C (VC, n = 6), 1000 mOsM hypertonic saline (HS, n = 7), or 1000 HS containing VC (HS/VC, n = 7) in coded bags so that investigators were blinded to the treatment. Fluids were infused at an initial Parkland rate of 10 mL/kg/h, adjusted hourly to restore and maintain urine output at 1 to 2 mL/kg/h. Sheep in the VC or HS/VC group received 250 mg/kg VC in the first 500 mL of LR or HS, and then 15 mg/kg/h thereafter. Hemodynamic variables and indices of antioxidant status were measured. At 48 h postburn, sheep were euthanized, and heart, liver, lung, skeletal muscle, and ileum were evaluated for antioxidant status. All fluid resuscitation regimens were equally effective in restoring cardiac output to near baseline levels; no treatment effects were apparent on arterial pressure or heart rate. VC infusion significantly reduced fluid requirements and, therefore, net fluid balance (fluid in, urine out) by about 30% at 6 h and about 50% at 48 h in comparison with the LR group (P < 0.05). HS and HS/VC reduced fluid requirements by 30% and 65%, respectively, at 6 h, but the volume-sparing effect of HS was not observed after 36 h and that of HS/VC was lost after 12 h. Plasma total antioxidant potential increased about 25-fold (P < 0.05) at 2 and 3 h in response to VC infusion compared with the LR and HS groups, and remained about 5- to 10-fold higher throughout the rest of the study. VC infusion also prevented the 4-fold increase in plasma thiobarbituric acid reactive substances seen in the LR group early after burn (P < 0.05). Tissue antioxidant status was similar between groups. In this sheep burn model, continuous high-dose VC infusion reduced net fluid balance, reduced indices of plasma lipid peroxidation, and maintained overall antioxidant status in comparison with standard-of-care LR treatment.

[1]  G. Koval The safety of antioxidant vitamins. , 1996, Archives of internal medicine.

[2]  H. Matsuda,et al.  Antioxidant therapy using high dose vitamin C: Reduction of postburn resuscitation fluid volume requirements , 1995, World Journal of Surgery.

[3]  P. Ward,et al.  Thermal injury, intravascular hemolysis, and toxic oxygen products. , 1986, The Journal of clinical investigation.

[4]  A. Mason,et al.  Update on current therapeutic approaches in burns. , 1996, Shock.

[5]  G. Warden,et al.  Management of the burn wound. , 1994, Clinics in dermatology.

[6]  C. Scott-Conner,et al.  Hypertonic Saline Resuscitation: Efficacy in a Community‐Based Burn Unit , 1991, Southern medical journal.

[7]  L. Cancio,et al.  The technique of fluid resuscitation for patients with severe thermal injuries: Strategies for maintaining organ perfusion while avoiding fluid overload , 1997 .

[8]  T. Matsuda,et al.  Reduced fluid volume requirement for resuscitation of third-degree burns with high-dose vitamin C. , 1991, The Journal of burn care & rehabilitation.

[9]  Y. Youn,et al.  Oxidants and the pathophysiology of burn and smoke inhalation injury. , 1992, Free radical biology & medicine.

[10]  J. Richards,et al.  Acute haemolysis induced by high dose ascorbic acid in glucose-6-phosphate dehydrogenase deficiency. , 1993, BMJ.

[11]  G. Kramer,et al.  A comparison of several hypertonic solutions for resuscitation of bled sheep. , 1985, The Journal of surgical research.

[12]  H. Matsuda,et al.  Reduction of resuscitation fluid volumes in severely burned patients using ascorbic acid administration: a randomized, prospective study. , 2000, Archives of surgery.

[13]  W. Tourtellotte,et al.  Oxygen radical dependent lung damage following thermal injury of rat skin. , 1983, The Journal of trauma.

[14]  H. Matsuda,et al.  Reduced resuscitation fluid volume for second-degree experimental burns with delayed initiation of vitamin C therapy (beginning 6 h after injury). , 1997, The Journal of surgical research.

[15]  A. Mason,et al.  Chapter 3 – Epidemiological, demographic, and outcome characteristics of burn injury , 2007 .

[16]  L. Phillips,et al.  A comparison of two different 2400 mOsm solutions for resuscitation of major burns. , 1997, The Journal of burn care & rehabilitation.

[17]  D. Herndon,et al.  Free radical activity and loss of plasma antioxidants, vitamin E, and sulfhydryl groups in patients with burns: the 1993 Moyer Award. , 1993, The Journal of burn care & rehabilitation.

[18]  W. Tourtellotte,et al.  Lipid peroxidation and acute lung injury after thermal trauma to skin. Evidence of a role for hydroxyl radical. , 1985, The American journal of pathology.

[19]  A. Bendich,et al.  The health effects of vitamin C supplementation: a review. , 1995, Journal of the American College of Nutrition.

[20]  J. Repine,et al.  Increased serum catalase activity in rats subjected to thermal skin injury , 1993, Inflammation.

[21]  J. Strain,et al.  Ferric reducing/antioxidant power assay: direct measure of total antioxidant activity of biological fluids and modified version for simultaneous measurement of total antioxidant power and ascorbic acid concentration. , 1999, Methods in enzymology.

[22]  J. Antognini,et al.  Small-Volume Resuscitation Using Hypertonic Saline Improves Organ Perfusion in Burned Rats , 1996, Anesthesia and analgesia.

[23]  F. Rozario,et al.  High-dose intravenous vitamin C is not associated with an increase of pro-oxidative biomarkers , 2004, European Journal of Clinical Nutrition.

[24]  B. Jordan,et al.  Indices of antioxidant status in rats subjected to wood smoke inhalation and/or thermal injury. , 2002, Toxicology.

[25]  C. Rock,et al.  Carotenoids and antioxidant vitamins in patients after burn injury. , 1997, The Journal of burn care & rehabilitation.

[26]  A. Sheet,et al.  Uniformed Services University of the Health Sciences. , 1976, Journal of the National Medical Association.

[27]  H. Matsuda,et al.  High-dose vitamin C therapy for extensive deep dermal burns. , 1992, Burns : journal of the International Society for Burn Injuries.

[28]  H. Matsuda,et al.  Reduced resuscitation fluid volume for second-degree burns with delayed initiation of ascorbic acid therapy. , 1997, Archives of surgery.

[29]  J. Kuo,et al.  Effect of acute skin thermal injury on subcutaneous glutathione, ascorbic acid and hydroxyl radical concentrations in anesthetized rats. , 1996, Redox report : communications in free radical research.

[30]  Stephen M Hewitt,et al.  Vitamin C Pharmacokinetics: Implications for Oral and Intravenous Use , 2004, Annals of Internal Medicine.

[31]  J. Šmahel [Pathophysiology of the burn wound]. , 1985, Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V....

[32]  N. Aikawa,et al.  Individualized fluid resuscitation based on haemodynamic monitoring in the management of extensive burns. , 1982, Burns, including thermal injury.

[33]  A. Belce,et al.  Evaluation of lipid peroxidation and total antioxidant status in plasma of rats following thermal injury. , 1997, Burns : journal of the International Society for Burn Injuries.

[34]  George C. Kramer,et al.  RESUSCITATION WITH HYPERTONIC SALINE DEXTRAN IMPROVES CARDIAC FUNCTION IN VIVO AND EX VIVO AFTER BURN INJURY IN SHEEP , 1998, Shock.

[35]  C. Baxter,et al.  Fluid volume and electrolyte changes of the early postburn period. , 1974, Clinics in plastic surgery.

[36]  H. Matsuda,et al.  How long do we need to give antioxidant therapy during resuscitation when its administration is delayed for two hours? , 1992, Journal of Burn Care and Rehabilitation.

[37]  D. Harrington,et al.  Management of the burn wound. , 1977, The Nursing clinics of North America.

[38]  E. Eriksson,et al.  Management of the burn wound. , 1986, Clinics in plastic surgery.

[39]  D. Traber,et al.  Burn resuscitation with two doses of 4 mL/kg hypertonic saline dextran provides sustained fluid sparing: a 48-hour prospective study in conscious sheep. , 2000, The Journal of trauma.

[40]  R. Forrest,et al.  The effects of high-dose vitamin C therapy on postburn lipid peroxidation. , 1993, The Journal of burn care & rehabilitation.

[41]  W. Monafo Initial management of burns. , 1996, The New England journal of medicine.

[42]  C. Wade,et al.  Resuscitation of conscious pigs following hemorrhage: comparative efficacy of small-volume resuscitation. , 1988, Circulatory shock.

[43]  Yorihiro Yamamoto,et al.  Lipid Peroxides as the Initiating Factor of Atherosclerosis , 1993, Annals of the New York Academy of Sciences.

[44]  M. Anderson,et al.  Determination of glutathione and glutathione disulfide in biological samples. , 1985, Methods in enzymology.

[45]  J. Vuilleumier,et al.  Urinary oxalate excretion after large intakes of ascorbic acid in man. , 1981, The American journal of clinical nutrition.