Hemorrhagic Shock in the Pediatric Patient: New Therapies and Practices

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Hemorrhagic Shock in the Pediatric Patient: New Therapies and Practices Richard P. Dutton, M.D., M.B.A. In trauma, as in other subspecialties, randomized controlled trials focused on pediatric patients are few and far between. This is especially so in emergency research, where issues of consent make a difficult challenge even harder. Nonetheless, resuscitation from hemorrhagic shock in adult trauma patients has seen a remarkable evolution in care over the past decade, and many of the lessons learned will be equally applicable or more so in children. Introduction: Why we like fluids. The concept of giving fluids as a treatment for hemorrhage is obvious, especially when blood loss is readily visible. If the body loses fluid it makes sense to replace it. Classic war movies portray the wounded soldier as thirsty, with the compassionate medic giving water to ease the distress. Modern TV shows emphasize 1 liter of normal saline, STAT. And indeed, few therapies are so immediately gratifying. In a fluid depleted, vasoconstricted patient, administration of an intravenous fluid bolus predictably increases myocardial wall tension, resulting (through Starling s law) in increased contractility and thus increased blood pressure. The thing we measure (blood pressure) responds immediately to the thing we do (give fluids). This makes us feel better, and in control. This physiology is even more compelling in children, with fewer chronic diseases to obscure the normal relationship of fluid to volume to pressure. Further, there is a wealth of research demonstrating the value of fluid therapy when the body is hypovolemic. The modern era of resuscitation science began with development of the Wiggers model of controlled hypotension in the 1950s, 1 followed by the work of Shires a decade later. 2 Bleeding was found to produce consistent organ system hypoperfusion, which led to a variety of bad outcomes, including mortality. Ischemic animals benefitted from fluid therapy: tissue perfusion improved, and morbidity and mortality were reduced. Even within the past few years, this concept has been further hammered home. Blow et al demonstrated worse outcomes in the ICU if occult hypoperfusion in trauma patients was not recognized and addressed, 3 while Rivers and colleagues showed the benefit of Early Goal Directed Therapy a thinly veiled excuse for greater fluid administration in patients presenting to the Emergency Department in septic shock. 4 Within anesthesia the concept of treating hypoperfusion with fluids is a cornerstone of residency training. We know how much anesthesia the patient needs 1 MAC, right? so if they re hypotensive it must be because they re hypovolemic. Failure to give fluids will lead to postoperative visual loss (maybe), acute renal failure (maybe) and the twin boogeymen called stroke and MI. Yet the data does not support these fears. Deliberate hypotension during anesthesia has been studied many, many times and generally found to be safe. 5 And all of us have seen adult patients with mean arterial pressure as low as 40 mmhg who woke up just fine. In fact, absent patients who need CPR, ischemic injury caused by hypotension is vanishingly rare. In children, these boundaries can likely be pushed even further.

Risks of Fluid Administration But why not give the fluid? Where s the harm in it? Not surprisingly, there are risks as well as benefits to fluid administration. The first is increased bleeding. Any elevation of blood pressure will increase bleeding from open vessels and will tend to wash away clots that have already formed. In the vasoconstricted shock patient even small boluses of fluid can produce sharp increases in pressure and subsequent rebleeding. And in the case of new tissue injury (i.e. surgery), the higher the blood pressure, the more blood will be lost and the harder the bleeding will be to control. 6 Further is the issue of blood dilution. Crystalloid or colloid fluids will dilute native clotting factors and red cell mass. While red cell dilution will not decrease oxygen delivery, it will increase the rate of tissue bleeding through a decrease in viscosity and a loss of red cell facilitation of clotting. It is well established (although little known) that clotting occurs more rapidly at a higher hematocrit. 7 Plasma dilution also lowers the concentration of soluble clotting factors and platelets at the site of bleeding, leading to slower and less solid clot formation. While the body has some capacity to respond by releasing stored factors, this capacity is limited and rapidly overwhelmed by trauma or major surgery. Then there is the potential for volume overload. Previously healthy adults can generally compensate for excessive fluid administration by rapid renal excretion, but in children, especially infants, this is not always true. Excessive administration of fluid can result in myocardial distention and dysfunction, with resultant pulmonary edema. Depending on the fluid administered, there is also a risk of electrolyte abnormalities and hypo- or hyper-glycemia. Finally, it is clear that the fluids themselves are not as benign as we would like. Both crystalloid and colloid fluids have immune-mediating effects, usually suppressive. 8 Fluid therapy by itself can damage vascular endothelium and lead to increased permeability. 9 Unless carefully managed, fluid administration will also make the patient colder, further contributing to both coagulopathy and immune suppression, and this is even more true in the pediatric population. Animal Studies of Fluid Restriction Although identified repeatedly during wartime surgery (all the way back to World War I), the concept of deliberate hypotension during active bleeding has been slow to sink in. In 1964 Shaftan published a study of coagulation in dogs, demonstrating that it is formation of a soft extraluminal clot that limits bleeding following arterial trauma. 10 This study compared blood loss from a standard arterial injury under various conditions. The least blood loss occurred in hypotensive animals (whether hypotensive from hemorrhage or from vasodilator administration), followed by controls, followed by vasoconstricted animals. Greatest blood loss occurred in animals that received vigorous fluid reinfusion during hemorrhage.

A series of reports in swine, rats, sheep and dogs established that, while some resuscitation was needed to prevent early death from exsanguination, the optimal target systolic pressure for best survival was in the range of 70-80 mmhg. 11-15 Attempts to normalize systolic pressure prior to anatomic control of hemorrhage lead to rebleeding, increased requirement for resuscitation, increased blood loss, and increased mortality. In the most sophisticated models, direct assessment of cardiac output and regional perfusion show no difference between moderate or large volume resuscitation in cardiac output, blood pressure, or regional perfusion of the heart, kidneys, and intestines. Burris studied both conventional resuscitation fluids and various combinations of hypertonic saline and dextran, finding that rebleeding was correlated with higher mean arterial pressure (MAP), and survival was best in groups resuscitated to lower than normal MAP. 16 A 1994 consensus panel on resuscitation from hemorrhagic shock noted that mammalian species are capable of sustaining MAP as low as 40 mmhg for periods as long as 2 hours without deleterious effects. 17 The panel concluded that spontaneous hemostasis and long-term survival were maximized by reduced administration of resuscitation fluids during the period of active bleeding, seeking to keep perfusion only just above the threshold for ischemia. This same principle is likely true in children (although poorly studied), when adjusting for the age-normal blood pressure. Human Trials of Deliberate Hypotensive Resuscitation Two large trials of deliberate hypotensive resuscitation have been conducted in adult trauma patients. The first, in Houston in the early 1990s, randomized hypotensive victims of penetrating torso trauma to conventional management or to no intravenous fluid during prehospital and ED care. 18 This trial demonstrated a significant improvement in outcome (62% vs. 70% survival) with fluid restriction, but was controversial because of its focus on penetrating trauma only, its failure to continue fluid restriction into the early operative period, and its all or none methodology. Following this, a retrospective review of resuscitation strategy in a large population of hemorrhagic shock patients demonstrated increased mortality when a rapid infusion system was used. 19 A second prospective trial enrolled both blunt and penetrating trauma patients at the time of hospital arrival, and randomized fluid therapy to target a systolic pressure of either 80 mmhg or 100+ mmhg. 20 There was no difference in mortality between groups, although the overall mortality (8%) was much lower than in the earlier trial due to the exclusion of moribund patients. Although not of themselves perfect evidence, these trials were convincing enough regarding the safety and potential benefit of deliberate hypotension that this approach has become the recommended policy in most major trauma centers. 21 Even so, fluid restriction requires very close attention to detail in the ED and OR, and a willingness to tolerate systolic blood pressures that would demand action in most other settings. This kind of discipline is rare, and it is likely that most bleeding patients, in most settings, still receive too much crystalloid fluid.

New Thinking about Fluid Resuscitation In the new millennium thinking about resuscitation has evolved even further, in an effort to reduce the long-term harms from hypoperfusion while maintaining the hemostatic benefits of keeping the blood pressure low. With the recognition that the coagulopathy of trauma is caused not just by dilution, hypothermia and acidosis (the so-called lethal triad ) but also by an acute inflammatory response to tissue injury, 22 there has been increasing focus on early support of the coagulation system. Several large retrospective series in both military and civilian trauma have demonstrated improved outcomes when plasma and platelets are given earlier, and in greater quantities. 23-27 Although not yet demonstrated in a prospective trial, these observations have led to the recommendation of empiric 1:1:1 RBC:plasma:platelet administration (instead of crystalloids or colloids) as the indicated fluid therapy for hemodynamically unstable patients with ongoing bleeding. Uncrossmatched type-o RBC have been used by major trauma centers for many years, and have a superior safety record. 28,29 In the past few years large centers have also begun using prethawed or liquid universal donor (type AB) plasma early in resuscitation. Using a whole blood mix as the resuscitation fluid for hemorrhaging patients largely avoids the issue of dilution, but what about concern for hypoperfusion? Postulated as beneficial, but not yet studied even retrospectively, is the aggressive use of anesthetic agents early in resuscitation. In theory, this approach would reverse vasoconstriction and improve perfusion while maintaining low blood pressure during the period of active hemorrhage. Rather than maintaining hypotension by fluid restriction, this approach accomplishes it by vasodilatation. The downside to this approach the risk of complete circulatory failure caused by administering anesthetics to a patient in shock requires careful management. In the early going, titration of small doses of anesthesia (usually fentanyl) are balanced by small boluses of fluid (1:1:1 blood products) until an adequate anesthetic state is achieved. In the face of the dynamic changes produced by injury and surgery, this requires excellent intravenous access, an efficient rapid infusion system, close monitoring of blood pressure, and an experienced provider. When successful, the result is a stable, vasodilated physiology that keeps blood pressure low, blood composition close to normal, and the circulation largely intact. Validation of these theories is lacking, even in adults, but will hopefully be accomplished by the next generation of resuscitation researchers. Summary and Recommendations Based on the evidence presented, the following is this author s recommended approach to early resuscitation while the patient is still actively bleeding following traumatic injury or major surgical misadventure: Maintain systolic blood pressure 80 100 mmhg Maintain functional blood composition, using empriric 1:1:1 transfusion therapy Maintain normal serum ionized calcium Maintain core temperature > 35 degrees C Follow base deficit and serum lactate as markers for hypoperfusion

Transition the patient to deep anesthesia References 1. Runciman WB, Skowronski GA: Pathophysiology of haemorrhagic shock. Anaesth Intensive Care 12:193-205, 1984. 2. Shires GT, Cunningham JN, Backer CR, et al: Alterations in cellular membrane function during hemorrhagic shock in primates. Ann Surg 176:288-295, 1972. 3. Blow O, Magliore L, Claridge JA, et al: The golden hour and the silver day: detection and correction of occult hypoperfusion within 24 hours improves outcome from major trauma. J Trauma 47:964-969, 1999 4. Rivers E, Nguyen B, Havstad S, et al: Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med 345:1368-1377, 2001 5. Enderby GEH: Hypotensive Anaesthesia. Edinburgh, Churhill Livingstone, 1985 6. Dutton RP. Pathophysiology and Treatment of Traumatic Shock, in Smith C (ed.) Trauma Anesthesia: Basic and Clinical Aspects, Cambridge: Cambridge University Press, 2008 7. Dutton RP. Initial resuscitation of the hemorrhaging patient in Speiss B, Shander A (eds) Perioperative transfusion medicine. Philadelphia: Lippincott, Williams & Wilkins pp 289-300, 2006 8. Rhee P, Burris D, Kaufmann C, et al: Lactated Ringer's solution resuscitation causes neutrophil activation after hemorrhagic shock. J Trauma 44:313-319, 1998 9. Chappell D, Jacob M, Hofmann-Kiefer K, Conzen P, Rehm M. A rational approach to perioperative fluid management. Anesthesiology 109: 723-40, 2008 10. Shaftan GW, Chiu CJ, Dennis C, et al: Fundamentals of physiologic control of arterial hemorrhage. Surgery 58:851-856, 1965 11. Kowalenko T, Stern S, Dronen S, et al. Improved outcome with hypotensive resuscitation of uncontrolled hemorrhagic shock in a swine model. J Trauma 1992;33:349-353 12. Capone AC, Safar P, Stezoski W, et al. Improved outcome with fluid restriction in treatment of uncontrolled hemorrhagic shock. J Am Coll Surg 1995;180:49-56 13. Owens TM, Watson WC, Prough DS, et al. Limiting initial resuscitation of uncontrolled hemorrhage reduces internal bleeding and subsequent volume requirements. J Trauma 1995;39:200-207 14. Riddez L, Johnson L, Hahn RG. Central and regional hemodynamics during crystalloid fluid therapy after uncontrolled intra-abdominal bleeding. J Trauma 1998;44:433-439 15. Mapstone J, Roberts I, Evans P. Fluid resuscitation strategies: a systematic review of animal trials. J Trauma 2003;55:571-589 16. Burris D, Rhee P, Kaufmann C, et al: Controlled resuscitation for uncontrolled hemorrhagic shock. J Trauma 46:216-223, 1999 17. Shoemaker WC, Peitzman AB, Bellamy R, et al: Resuscitation from severe hemorrhage. Crit Care Med 24:S12-S23, 1996 18. Bickell WH, Wall MJ, Jr., Pepe PE, et al. Immediate versus delayed fluid resuscitation for hypotensive patients with penetrating torso injuries. N Engl J Med 1994;331:1105-1109 19. Hambly PR, Dutton RP: Excess mortality associated with the use of a rapid infusion system at a level 1 trauma center. Resuscitation 31:127-133, 1996 20. Dutton RP, Mackenzie CF, Scalea TM. Hypotensive resuscitation during active

hemorrhage: impact on in-hospital mortality. J Trauma 2002;52:1141-1146 21. ATLS for Doctors Student Manual, 9th Edition. Chicago, IL, American College of Surgeons, 2009 22. Brohi K, Cohen MJ, Ganter MT, et al. Acute coagulopathy of trauma: hypoperfusion induces systemic anticoagulation and hyperfibrinolysis. J Trauma 2008;64:1211-1217 23. Borgman, M.A., et al., The ratio of blood products transfused affects mortality in patients receiving massive transfusions at a combat support hospital. J Trauma, 2007. 63(4): p. 805-13 24. Gunter, O.L., Jr., et al., Optimizing outcomes in damage control resuscitation: identifying blood product ratios associated with improved survival. J Trauma, 2008. 65(3): p. 527-34 25. Stinger, H.K., et al., The ratio of fibrinogen to red cells transfused affects survival in casualties receiving massive transfusions at an army combat support hospital. J Trauma, 2008. 64(2 Suppl): p. S79-85 26. Sperry, J.L., et al., An FFP:PRBC transfusion ratio >/=1:1.5 is associated with a lower risk of mortality after massive transfusion. J Trauma, 2008. 65(5): p. 986-93 27. Holcomb, J.B., et al., Increased plasma and platelet to red blood cell ratios improves outcome in 466 massively transfused civilian trauma patients. Ann Surg, 2008. 248(3): p. 447-58 28. Dutton RP, Shih D, Edelman BB, et al: Safety of uncrossmatched type-o red cells for resuscitation from hemorrhagic shock. J Trauma 59:1445-1449, 2005 29. Camp FR, Conte NF, Brewer JR: Military blood banking, 1941-1973: Lessons learned applicable to civil disasters and other considerations; a monograph. Fort Knox, KY, U.S. Army Medical Research Laboratory, 1973