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Education  |   February 2015
Acute and Perioperative Care of the Burn-injured Patient
Author Notes
  • From the Department of Anesthesiology, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts (E.A.B., E.S., J.A.J.M.); Shriners Hospitals for Children®, Boston, Massachusetts (E.A.B., E.S., J.A.J.M.); Department of Anesthesiology, University of Texas Medical Branch, Galveston, Texas (L.W.); and Shriners Hospitals for Children®, Galveston, Texas (L.W.).
  • This article is featured in “This Month in Anesthesiology,” page 1A.
    This article is featured in “This Month in Anesthesiology,” page 1A.×
  • Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are available in both the HTML and PDF versions of this article. Links to the digital files are provided in the HTML text of this article on the Journal’s Web site (www.anesthesiology.org).
    Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are available in both the HTML and PDF versions of this article. Links to the digital files are provided in the HTML text of this article on the Journal’s Web site (www.anesthesiology.org).×
  • Figures 1-4, 6, and 7 were prepared by Annemarie B. Johnson, C.M.I., Medical Illustrator, Vivo Visuals, Winston-Salem, North Carolina.
    Figures 1-4, 6, and 7 were prepared by Annemarie B. Johnson, C.M.I., Medical Illustrator, Vivo Visuals, Winston-Salem, North Carolina.×
  • Submitted for publication March 5, 2014. Accepted for publication September 30, 2014.
    Submitted for publication March 5, 2014. Accepted for publication September 30, 2014.×
  • Address correspondence to Dr. Martyn: Department of Anesthesiology, 51 Blossom Street, Room 206, Boston, Massachusetts 02114. jmartyn@mgh.harvard.edu. Information on purchasing reprints may be found at www.anesthesiology.org or on the masthead page at the beginning of this issue. Anesthesiology’s articles are made freely accessible to all readers, for personal use only, 6 months from the cover date of the issue.
Article Information
Education / Review Article / Airway Management / Pain Medicine / Trauma / Burn Care
Education   |   February 2015
Acute and Perioperative Care of the Burn-injured Patient
Anesthesiology 2 2015, Vol.122, 448-464. doi:10.1097/ALN.0000000000000559
Anesthesiology 2 2015, Vol.122, 448-464. doi:10.1097/ALN.0000000000000559
Abstract

Care of burn-injured patients requires knowledge of the pathophysiologic changes affecting virtually all organs from the onset of injury until wounds are healed. Massive airway and/or lung edema can occur rapidly and unpredictably after burn and/or inhalation injury. Hemodynamics in the early phase of severe burn injury is characterized by a reduction in cardiac output and increased systemic and pulmonary vascular resistance. Approximately 2 to 5 days after major burn injury, a hyperdynamic and hypermetabolic state develops. Electrical burns result in morbidity much higher than expected based on burn size alone. Formulae for fluid resuscitation should serve only as guideline; fluids should be titrated to physiologic endpoints. Burn injury is associated basal and procedural pain requiring higher than normal opioid and sedative doses. Operating room concerns for the burn-injured patient include airway abnormalities, impaired lung function, vascular access, deceptively large and rapid blood loss, hypothermia, and altered pharmacology.

Abstract

Major burn injury affects almost every organ. Understanding the complex and often paradoxical pathophysiological responses in the early and late phases of injury is imperative to provide expert care in the acute and perioperative period.

Supplemental Digital Content is available in the text.

IN the United States, approximately 450,000 people seek treatment for burn injury each year, of whom 40,000 are hospitalized and 3,400 die.*  The majority of these patients present in emergency rooms of hospitals without a burn center. Initial care of patients with serious burn injury presents challenges in airway management, vascular access, and hemodynamic and pulmonary support. Anesthesiologists are specialists in each of these areas. As a result, anesthesiologists staffing these hospitals with emergency rooms must be familiar with the pathophysiology of major burn injuries and resuscitation. In burn care facilities, anesthesiologists should be familiar with the unique features of perioperative management of burn-injured patients. This review will focus on early evaluation and perioperative management of burned patients in the acute (nonreconstructive) phase only.
Burn Injury Pathophysiology
Major burns cause massive tissue destruction and result in activation of a cytokine-mediated inflammatory response that leads to dramatic pathophysiologic effects at sites local and distant from the burn. The systemic effects occur in two distinct phases, a burn shock (ebb) phase followed by a hypermetabolic (flow) phase, first described by Cuthbertson in 1942.1  Understanding the pathophysiologic alterations and time course is essential for the clinician providing early resuscitation and perioperative care for these patients.
Generalized edema even in noninjured tissues occurs when the injury exceeds 25 to 30% total body surface area (TBSA). After major burn injury, continued loss of plasma into burned tissue can occur up to the first 48 h or even longer. Loss of intravascular fluid into burned areas and edema formation (in nonburned sites) can quickly result in burn shock with impaired tissue and organ perfusion. In contrast to nonburn trauma, burn-induced fluid loss occurs in the absence of marked red cell volume loss resulting in hemoconcentration rather than anemia. Thus, the initial therapeutic goal is the repletion of intravascular volume with clear fluids to preserve tissue perfusion and minimize the ischemia and inflammatory responses. Burn shock occurs not only because of depletion of intravascular volume but also because of increased systemic vascular resistance (due to release of catecholamines, antidiuretic hormone, and hemoconcentration) and depressed cardiac output (fig. 1). Depression of cardiac output occurs even before any detectable reduction in plasma volume. The depressed cardiac output continues for 24 to 36 h.2  The hypermetabolic and hyperdynamic phase that develops over 48 to 72 h after injury is characterized by increased oxygen consumption, carbon dioxide production, and protein wasting.3,4 Pari Passu with the hypermetabolism is the hyperdynamic phase evidenced by supranormal cardiac output (often more than two to three times normal), tachycardia, and decreased systemic vascular resistance (fig. 2). The onset of sepsis further increases the cardiac output and decreases systemic vascular resistance.3,4  Elderly patients may not exhibit signs of the hyperdynamic state, but protein catabolism is ubiquitous.
Fig. 1.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
Fig. 1.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
×
Fig. 2.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
Fig. 2.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
×
Inhalation Injury
The presence of an inhalation injury significantly increases the morbidity and mortality associated with burn injuries. Resuscitation fluid requirements are increased by up to 50%.5–7  Chest radiographs are usually normal until secondary complications of inflammation, infection, or atelectasis develop. The mechanisms of inhalation injury (fig. 3) consist of a combination of (a) direct injury to face and upper airway from inhalation of steam and/or hot gases; (b) chemical injury to the trachea and bronchi, and alveolar and endothelial lining due to inhalation of the toxic products from the fire; and (c) impairment of oxygen transport processes or oxygen utilization by inhalation of carbon monoxide and cyanide, respectively.5–10 
Fig. 3.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
Fig. 3.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
×
Direct heat and steam injury to the upper airway can lead to marked swelling of the face, tongue, epiglottis, and glottic opening resulting in airway obstruction. Because airway swelling may not occur immediately but may develop over a period of hours (especially with concurrent fluid resuscitation), a high index of suspicion and frequent reevaluations of the respiratory status are essential. Upper airway edema will have more immediate consequences in smaller children. A scald injury of the epiglottis mimics symptoms of epiglottitis (see video, Supplemental Digital Content 1, http://links.lww.com/ALN/B124). Upper airway edema usually resolves in 3 to 6 days and is facilitated by elevation of the head of the bed and avoidance of excessive fluid administration. Positive pressure ventilation may increase resuscitation fluid requirements.6 
Tracheobronchial injury is caused by inhalation of chemicals in smoke. Smoke from a house fire contains combustion products that are toxic and damaging to the airways and alveoli (fig. 3, see video, Supplemental Digital Content 2, http://links.lww.com/ALN/B125). Decreased mucociliary transport impairs clearance of bacteria and mucosal debris.8  Alveolar collapse and atelectasis can occur because of loss of surfactant production or from plugging of small airways by mucosal debris. Over a period of time, these changes result in obstruction of airways, bronchospasm, atelectasis, and/or pneumonia, which cause ventilation perfusion mismatch, shunt, impaired gas exchange, and decreased pulmonary compliance. Injury to the airways and lung can also occur with severe cutaneous burns in the absence of inhalational injury. Mechanisms include inflammatory mediators from the burn-injured area, effects of fluid resuscitation, and infection. For example, acute lung injury can occur in patients with scald injury without smoke exposure. Two to 3 days after scald injury, the bronchoscopic features can mimic airway injury5,8,9  seen with smoke exposure (see video, Supplemental Digital Content 3, http://links.lww.com/ALN/B126).
Systemic toxicity can also occur from smoke inhalation. Exposure to carbon monoxide decreases oxygen-carrying capacity of hemoglobin leading to tissue hypoxia. Carbon monoxide has a 200-fold higher affinity than oxygen to the same binding sites on hemoglobin.10  Binding of carbon monoxide to hemoglobin also shifts the oxyhemoglobin dissociation curve to the left and alters its shape. Carboxyhemoglobin levels greater than 15% are toxic; those exceeding 50% are lethal. The half-life of carboxyhemoglobin is 4 h for a person breathing room air. This is reduced to 40 to 60 min when breathing 100% oxygen. Hyperbaric oxygen therapy has been suggested as a therapy to reduce the neurologic sequelae from carbon monoxide toxicity. Hyperbaric oxygen therapy may play a beneficial role in reducing the inflammation and harmful effects of ischemia reperfusion injury caused by carbon monoxide exposure. However, a recent Cochrane review failed to demonstrate convincing benefit from hyperbaric oxygen therapy.11  The limited availability of hyperbaric chambers even in academic institutions makes its usefulness limited.
Cyanide is a toxic gas produced in fires by the burning of nitrogenous materials. Cyanide poisoning should be suspected in any patient with a history of smoke inhalation injury with an anion gap metabolic acidosis in the presence of apparently adequate oxygen delivery. Cyanide binds to mitochondrial cytochrome oxidase blocking the last step in the oxidative phosphorylation, preventing the use of oxygen for conversion of pyruvate to adenosine triphosphate. Thus, cells can only generate adenosine triphosphate via anaerobic metabolism, which results in a metabolic acidosis from lactic acid production. Concentrations of cyanide greater than 20 ppm are considered dangerous. Concentrations of 100 ppm can lead to seizures, coma, respiratory failure, and death.12  The mixed venous oxygen saturation in cyanide poisoning is often increased, suggesting inability to use the delivered oxygen.13,14 
The treatment of inhalation injury, other than carbon monoxide and cyanide, is supportive respiratory care with airway management, lung-protective mechanical ventilation, and aggressive pulmonary toilet. Clinical manifestations of an inhalation injury may be delayed up to several days postexposure. Nebulization of anticoagulants, antioxidants, and antiinflammatory agents are under investigation but are not part of routine management at this time.15–17  Prophylactic administration of antibiotics and steroids is not routinely recommended.
Mortality persists at a rate of approximately 4% for patients admitted to burn centers.* A large analysis revealed three risk factors as predictive of death after burns: age older than 60 yr, burn size greater than 40% body surface area, and inhalation injury. Mortality is a function of the number of risk factors present.18  The mortality was 0.3, 3, 33, or 90%, depending on whether 0, 1, 2, or 3 risk factors were present, respectively. Morality related to burn injury has improved over the past several decades.19  Causes include increased awareness and improved methods of resuscitation, early excision and grafting of burn wounds, better methods of wound coverage, improved anesthesia and intensive care techniques, early diagnosis and aggressive treatment of infections, and enhanced nutritional support methods, particularly early and continuous enteral feeding. Data exist linking improved outcomes from major burns with early referral to a burn center. It is recognized that burn care requires specialized expertise, personnel, and equipment that are not cost-effectively maintained in low-volume centers.
Initial Evaluation and Management
Successful management of the patient with burn injury begins at the scene of injury and continues in the emergency department with a thorough trauma assessment based on the Advanced Trauma Life Support guidelines. This requires a combined strategy of airway assessment and protection, initiation of resuscitation, and evaluation for coexisting injuries. Between 5 and 7% of patients admitted to burn centers experience nonthermal traumatic injuries.20  Therefore, all burned patients should be approached initially as multiple trauma patients. Assessing the airway is the first priority during the initial evaluation. The presence of airway injury, signs of airway obstruction, and the presence of preexisting airway abnormality should be assessed as soon as the patient arrives at the hospital. Airway injuries may not be evident initially, but with massive fluid resuscitation airway edema can result (see video, Supplemental Digital Content 1, http://links.lww.com/ALN/B124). As a general rule, when indicated, it is safer to intubate the patient early than risk a difficult intubation after airway swelling has occurred.
Laryngeal injuries are common in burn-injured patients and can be associated with long-term morbidity. Early recognition of laryngeal injury and consultation with a laryngologist can influence treatment choices (e.g., tracheostomy) and limit morbidity.21  Because anesthesiologists are most likely to view the larynx of patients with acute burns, it is important to make laryngeal examination part of the initial intubation whether during resuscitation or induction of general anesthesia. Decreased pulmonary compliance because of a circumferential eschar on the chest or abdomen can interfere with respiration. Chest wall escharotomy may be needed when this occurs.
It is important to recognize inhalation injury as soon as possible. A diagnosis of inhalation injury is usually based on a history of exposure to fire and smoke (especially in combination with impaired avoidance behavior such as loss of consciousness or entrapment in an enclosed space) along with the physical examination (burns over face, singed nasal or facial hair, carbonaceous sputum, hypoxia, hoarse voice, and bronchorrhea, and/or bronchospasm). Fiberoptic bronchoscopy may be used to support the diagnosis and may reveal carbonaceous debris, erythema, or ulceration (see video, Supplemental Digital Content 2, http://links.lww.com/ALN/B125). It has been difficult to identify reliable indicators of progressive respiratory failure in patients with smoke inhalation.22  Diagnostic criteria for inhalation injury are complicated by heterogeneous presentation.
Intubation of burn-injured patients, especially combined with interhospital transport, is not a benign intervention. In response to the death of a burn-injured patient from complications of intubation subsequently judged to not to be indicated, the Parkland Hospital burn staff performed a retrospective review of the hospital course of burn patients intubated before transport to their emergency department.23  A large number of these patients were extubated the same or the next day, suggesting that intubation was not indicated in these patients. Thus, they were exposed to risk without commensurate benefit. Out of concern for exacerbation of a thermal laryngeal injury, otolaryngologists at the Baltimore Regional Trauma Center performed a prospective study of patients presenting to their emergency department with risk factors for inhalation injury.24  If patients at risk were not in respiratory distress and did not have other indications for immediate intubation such as large full-thickness burns, inability to protect their airway, or signs of obstruction, then they were evaluated by flexible fiberoptic laryngoscopy. All the patients with an adequate glottis by endoscopy were managed safely without intubation, despite the fact that many met the institution’s traditional criteria for intubation. Although adult patients with facial burns may appear to be at significant risk, the airway may not be compromised and intubation may expose them to unnecessary risk. In contrast, we have seen pediatric patients with oral scald who did not appear in distress and who, on superficial examination, did not seem to have significant injury but actually had serious thermal injury resembling epiglottitis (see video, Supplemental Digital Content 1, http://links.lww.com/ALN/B124). All patients with significant risk for inhalation injury should have a thorough airway examination, and intubation should be performed early when the airway is compromised. Preemptive intubation of patients with inhalation injury can be lifesaving but should be performed for clear indications. Facial burns or glottic edema may make it difficult to secure an endotracheal tube (ETT) after edema develops. Therefore, extra effort and vigilance is required in these patients.
Standard pulse oximeters cannot distinguish between oxyhemoglobin and carboxyhemoglobin. The PaO2 can be normal or high in patients receiving oxygen therapy even with high levels of carboxyhemoglobin. The diagnosis of carbon monoxide poisoning is made by measuring the carboxyhemoglobin level in arterial blood or measuring oxygen-carrying capacity of hemoglobin by cooximeter. Some pulse oximeters can differentiate between oxyhemoglobin and carboxyhemoglobin.
As with carbon monoxide poisoning, cyanide toxicity can be difficult to diagnose. Cyanide toxicity, just like carbon monoxide poisoning, does not cause cyanosis, and direct detection of cyanide poisoning in blood is difficult. The deleterious effects of cyanide are normally neutralized by the conversion of cyanide to thiocyanate, which is excreted in the urine. This can be enhanced by the administration of exogenous thiosulfate. Exogenous thiosulfate has a slow onset of action, and therefore, coadministration of hydroxycobalamin (vitamin B12) has been recommended, which forms cyanocobalamin.
The magnitude of burns is classified according to TBSA involved, depth of the burn, and the presence or absence of inhalational injury. TBSA burned in adults can be estimated using the “rule of nines.” The Lund–Browder chart is an age-specific diagram that more precisely accounts for the changing body surface area relationships with age (fig. 4). The depth of skin destruction is characterized as first, second, or third degree, based on whether there is superficial, partial-thickness, or full-thickness destruction of the skin (table 1). Fourth degree is used to describe burns that have injured deeper structures, such as muscle, fascia, and bone. Deep second- and third-degree burns require surgical debridement and grafting, whereas more superficial burns do not.
Table 1.
Classification of Burn Depth
Classification of Burn Depth×
Classification of Burn Depth
Table 1.
Classification of Burn Depth
Classification of Burn Depth×
×
Fig. 4.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
Fig. 4.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
×
Fluid Resuscitation
Rapid and effective intravascular volume replenishment is pivotal for mitigation of burn shock. Delayed or inadequate fluid replacement results in hypovolemia, tissue hypoperfusion, shock, and multiple organ failure.25  Inadequate fluid resuscitation can also exacerbate the effects of smoke inhalation injury.26,27  Multiple fluid resuscitation formulae exist for estimating fluid needs. As a general rule, burns of less than 15% TBSA can be managed with oral or intravenous fluid administered at 1.5 times maintenance rate and careful attention to hydration status. Fluid resuscitation formulae have recently been reviewed by Alvarado et al.27 
The Parkland formula is the most common guide used in the United States and recommends isotonic crystalloid initially and the use of colloids 24 h after injury (table 2).27  Controversy remains as to ideal time for initiation of colloid therapy in burn resuscitation. There is a general trend now to initiate colloid infusions earlier than the previously recommended time of 24 h. Lactated Ringer’s solution is often the crystalloid chosen in view of the metabolic acidosis associated with normal (0.9%) saline. In younger children and in patients where hypoglycemia is a potential concern, 5% dextrose solution can be added to the lactated Ringer’s solution. Side effects of large-volume crystalloid resuscitation include exacerbation of generalized edema, pleural and pericardial effusions, and intestinal ileus with abdominal or limb compartment syndrome.28 
Table 2.
Formulae for Fluid Resuscitation after Burn Injury
Formulae for Fluid Resuscitation after Burn Injury×
Formulae for Fluid Resuscitation after Burn Injury
Table 2.
Formulae for Fluid Resuscitation after Burn Injury
Formulae for Fluid Resuscitation after Burn Injury×
×
No matter which formula is used, it should serve only as a guideline, and fluid resuscitation is titrated to physiologic endpoints (table 3). Catheterization of the bladder is important in patients with moderate-to-severe burns who require intravenous fluid resuscitation. A urinary catheter provides a means of following urine output to titrate fluid administration and provide samples for urinalysis. Although the best endpoints of resuscitation after major burn injury have not been conclusively determined, the current recommendation is that urinary output be maintained between 0.5 and 1 ml · kg−1 · h−1.29  Actual fluid requirements can vary, depending on size and depth of the burn, interval from injury to start of resuscitation, presence of associated injuries, and presence of inhalational injury. The liberal use of opioids may also increase fluid needs.30  Indicators and criteria used for assessment of adequate fluid volume are specified in table 3.
Table 3.
Indicators of Adequate Circulating Volume and/or Resuscitation
Indicators of Adequate Circulating Volume and/or Resuscitation×
Indicators of Adequate Circulating Volume and/or Resuscitation
Table 3.
Indicators of Adequate Circulating Volume and/or Resuscitation
Indicators of Adequate Circulating Volume and/or Resuscitation×
×
A small percentage of patients fail to respond to conventional fluid resuscitation. Some burn centers administer colloid fluids to patients who, approximately 8 h after injury, are responding inadequately to crystalloid resuscitation.31  Many burn centers including ours administer colloids earlier than 8 h after injury, particularly in children. Consistently, in a recent survey, approximately 50% of the respondents indicated that they add colloids within the first 24 h.32  A very small percentage of patients may require inotropic support during the early resuscitation phase even in the absence of sepsis. No systemic study has evaluated the utility and morbidity associated with the use of inotropes in patients with acute burn injury. After 36 to 48 h, capillary integrity returns to normal in nonburned areas and reabsorption of edema fluid occurs over the next 1 to 2 weeks.
Electrical Injury
Burns due to electric shock exhibit unique pathology. Soft tissue damage due to electrical burns can dramatically increase fluid needs. Survivors of severe electrical shock frequently experience some form of subsequent arrhythmia (10 to 46%).33,34  Patients without electrocardiographic changes on presentation are unlikely to experience life-threatening arrhythmias.33,35  Damage to the myocardium may occur after exposure to either high- or low-voltage current. The myocardial injury behaves more like a cardiac contusion than a myocardial infarction, with minimal hemodynamic consequences.
Bone experiences the highest heat accumulation during high-voltage current flow because it has the highest resistance to flow of electricity. The high heat produced by bone injury damages muscles surrounding the bone to a greater extent, with more superficial areas of muscle being spared. Subcutaneous tissue and skin also have less damage because they are better conductors than bone. Electrothermal injury of the musculature may manifest as edema formation and tissue necrosis and may lead to compartment syndrome and rhabdomyolysis. For treatment of these complications, patients may come to the operating room within 24 h of injury. Myoglobinuria as a result of muscle damage poses a risk for acute renal failure and requires prompt treatment with crystalloid loading to a target urine output of 2 ml · kg−1 · h−1. Additional treatment with sodium bicarbonate, mannitol, and furosemide facilitate myoglobin excretion and protect against renal tubular injury.
Anesthetic Management
Preoperative Evaluation
Patients are often brought to the operating room in the early phase of burn injury, when they are undergoing significant fluid shifts with corresponding cardiovascular instability and/or respiratory insufficiency. Early excision of dead/necrotic tissue with temporary or permanent coverage of the open areas decreases the chance of wound colonization and systemic sepsis and has become the standard of care. Along with the standard preoperative evaluation, there are specific features of the history and physical examination, which deserve additional focus in the burned patient (table 4). These include the time and extent of burn injury, airway evaluation, presence of inhalation injury, current resuscitation regimen and patient’s response, potential vascular access sites, and tolerance to enteral feeding and/or gastric residues (table 4). Communication with the surgeons and critical care team is crucial to manage perioperative care in a manner that is compatible with treatment goals of the intensive care unit (ICU). Details of the surgical plan are also essential to estimate blood loss to plan appropriate vascular access, invasive monitors, and to order appropriate blood products.
Table 4.
Major Preoperative Concerns for Burn Patients
Major Preoperative Concerns for Burn Patients×
Major Preoperative Concerns for Burn Patients
Table 4.
Major Preoperative Concerns for Burn Patients
Major Preoperative Concerns for Burn Patients×
×
Intraoperative Management
Airway Management
Key features of airway assessment include preexisting airway abnormality, current airway injury (i.e., inhalation injury, facial edema), and signs of glottic obstruction. Assessment of mandibular mobility may reveal tightness that will make laryngoscopy challenging. Mouth opening can be limited because of edema or developing contractures (fig. 5). Dressings and nasogastric tubes may make face mask seal difficult. Facial wounds may be painful, and exudate and topical antibiotics may make for a slippery surface and difficulty holding the mask. If the preoperative examination reveals concern for upper airway patency, mobility, or mask ventilation, fiberoptic intubation while maintaining spontaneous ventilation should be considered. In children, awake intubation is not a viable option. Ketamine-induced sedation/anesthesia maintains the pharyngeal muscle tone with good conditions for fiberoptic intubation. Gastric emptying may or may not be delayed in burn patients.36 Laryngeal Mask Airways™, with the usual precautions, have been used successfully in burn patients.37  Infection/sepsis, intestinal edema, and opioids may slow gastric emptying, with increased risk of aspiration. The utility of methylnaltrexone to improve laxation in burned patients on high-dose opiate equivalents has been confirmed in a retrospective study.38  Methylnaltrexone antagonizes peripheral but not central opiate effects as it does not cross the blood–brain barrier. No prospective studies have examined the utility of methylnaltrexone in the burn-injured population.
Fig. 5.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
Fig. 5.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
×
Securing the ETT is difficult with facial burns. Tape or ties crossing burned areas can irritate the wound or cause injury to grafts. It is essential to secure the ETT with a carefully secured tie harness to avoid unintentional extubation. Placement of a circumferential tie around the patient’s head, using wire to secure the tube to a tooth, or use of arch bars can provide safe fixation.39,40  The use of cuffed ETTs in the pediatric population, both in the operating room and in the ICU, is safe and recommended regardless of the child’s age.41–43  Severely burned patients may require tracheostomies because of potential complications from long-term translaryngeal ETT placement for mechanical ventilation and placement of nasogastric feeding tubes (see video, Supplemental Digital Content 4, http://links.lww.com/ALN/B127). The proper timing and indications for tracheostomy in burns remain controversial. Tracheostomy-induced dysphagia, dyphonia, and other laryngeal pathologies have been described.44  Whether these pathologies were present before the tracheostomy could not be identified.
Vascular Access
Managing vascular access in burn patients is difficult because of technical challenges (edema) and because of the increased risks for bloodstream infection. It may be necessary to place vascular catheters through burn wounds. On occasion, an alternative is to have the surgeons debride the insertion site just before placement of the vascular catheter. In addition to subclavian and internal jugular veins, the femoral veins can be used. If no intravenous access is available, temporary intraosseous cannulation may safely be placed in patients of any age. Localization of vessels using ultrasonographic guidance can be useful in placing peripheral and central catheters in patients when access is difficult.45 
Ventilatory Management
In providing perioperative mechanical ventilation, the same considerations used in the ICU must be followed to avoid ventilation-induced morbidity. The findings of the Acute Respiratory Distress Syndrome Network trial have changed ventilatory strategies and have become the standard of care for burn patients with acute lung injury.46  The empiric use of tidal volumes of less than equal to 6 ml/kg ideal body weight and plateau airway pressures less than 30 cm H2O in adults are recommended. Although this concept has not been tested in burned patients, a recent report confirms the importance of maintaining low tidal volume ventilation even in the operating room.47  Because of the hypermetabolic state and increased carbon dioxide production, ventilation rates need to be higher than normal. Some patients will require postoperative mechanical ventilation. Assessment of not only pulmonary status but also the upper airway and glottis is imperative before a trial of extubation. The presence of a good air leak after deflation of the endotracheal cuff is an indirect estimate of an adequate glottic opening. In the operating room, visualization of the laryngeal structures is often performed by direct laryngoscopy or with flexible fiberoptic bronchoscopy before extubation (see video, Supplemental Digital Content 4, http://links.lww.com/ALN/B127).
Monitoring
Burn-injured areas may involve sites where monitoring equipments have to be placed. Surgical staples can be used to fix adhesive electrocardiogram electrodes. Alternatively, placing the electrodes on the back or dependent sites may hold them in place. Sites for placement of pulse oximetry, if the finger or toe is unavailable, include the ear, nose, or tongue. Reflectance oximetry has been suggested as an alternative if skin sites for monitoring are limited.48  There may be periods when it is not possible to maintain an effective pulse oximeter monitor. When a blood pressure cuff must be placed over grafted wounds, great care should be taken to protect the underlying area and the cuff should be sterile. With expected extensive bleeding, an arterial line should be considered for continuous measurement of blood pressure and blood sampling. Respiratory variation in arterial waveforms can be used as a guide to volume and vasoactive therapy. Blood urea nitrogen to creatinine ratio (≥20) or fractional sodium (Na+) excretion percent (<1%) would also indicate hypovolemia.
Temperature monitoring is imperative as burned patients are quite prone to and intolerant to hypothermia. Monitoring of body temperature is also useful for detection of blood transfusion reactions intraoperatively (>2°C rise in temperature). Neuromuscular function monitoring is useful in patients receiving neuromuscular blocking drugs as dose requirements can be significantly altered in burn patients. Multiport central venous catheters are useful for simultaneous monitoring of central pressures and administering of drugs and fluids.
Intrahospital Patient Transport
Intrahospital transport of critically ill patients is associated with an overall adverse event rate of up to 70%.49  Patients requiring mechanical ventilation during transport require at least two anesthesia personnel or an anesthesia personnel and respiratory therapist or nurse to manage ventilation, observe the monitors, and administer medications during transport. A number of professional societies have developed guidelines to improve the safety of transport of critically ill patients by setting rules for pretransport planning and coordination, escort, equipment, and monitoring procedures.50,51  Because patient agitation and extubation during transfer can be disastrous, providing adequate sedation and analgesia and possibly muscle relaxation are essential during intrahospital transport and moving patients to or from the bed to the stretcher or to the operating table.
Pharmacologic Considerations
Large burns result in altered pharmacokinetic and pharmacodynamic responses to many drugs. Plasma protein loss through injured skin and further dilution of plasma proteins by resuscitation fluids decrease the concentration of albumin, an important drug-binding protein (vide infra). There is an increase in volume of distribution of almost every drug studied (propofol, fentanyl, muscle relaxants).52  In addition, pharmacodynamic changes at target organs alter drug–receptor interactions causing variable and at times unpredictable changes in response to drugs. Consequently, changes in the usual dosages of drugs or complete exclusion of other drugs (e.g., succinylcholine) may be necessary to ensure efficacy or avoid toxicity.
During the acute injury phase (0 to 48 h) and despite adequate volume resuscitation, cardiac output along with renal and hepatic blood flow is decreased (fig. 1). These changes may decrease elimination of some drugs by the kidney and liver. After the resuscitation phase, the hyperdynamic phase begins, with increased cardiac output and blood flow to the kidneys and liver (fig. 2). Drugs dependent on organ blood flow for elimination will have increased clearances; doses for these drugs may have to be adjusted upward.
The two major drug-binding proteins, albumin and α1-acid glycoprotein (AAG), are altered in opposite ways after burn injury. The concentration of albumin that binds to mostly acidic and neutral drugs is decreased in burn injury.53  AAG binds cationic drugs, such as lidocaine, propranolol, muscle relaxants, and some opioids. AAG is also an acute-phase reactant, and its concentration increases twofold or greater in burn-injured patients, which decreases the free fraction of drugs bound by AAG.53 
Hepatic clearance of drugs highly extracted by the liver depends primarily on hepatic blood flow and is relatively insensitive to alterations in protein binding. Clearance of these drugs may decrease during the early postburn phase as a result of decreased liver and renal blood flow. Later on clearance of these drugs may increase during the hyperdynamic phase when hepatic blood flow increases (e.g., propofol, fentanyl).54  During the hypermetabolic state, renal blood flow and glomerular filtration rate also increase. Thus, renal clearance of some drugs increases.55,56  Hepatic enzyme activity appears to be altered in patients with burns.57  Phase I reactions, which include oxidation, reduction, hydroxylation, and demethylation, are impaired in burn patients (e.g., diazepam). Phase II reactions involve conjugation, glucuronidation, and sulfation and seem to be relatively unaffected (e.g., lorazepam).58 
Muscle Relaxants
Muscle relaxant pharmacology is significantly and consistently altered after burn injury.59  In burn patients, exposure to succinylcholine can result in an exaggerated hyperkalemic response, which can induce cardiac arrest. The current recommendation is to avoid succinylcholine administration in patients 48 h after burn injury.60,61  An increase in the number of extrajunctional acetylcholine receptors that release potassium during depolarization with succinylcholine is the cause for increased hyperkalemia. Martyn and Richtsfeld62  have reviewed the topic of succinylcholine-induced hyperkalemia. Almost paralleling the hyperkalemia to succinylcholine, there is concomitantly a decreased sensitivity to the neuromuscular effects of nondepolarizing muscle relaxants (NDMRs). Because succinylcholine is contraindicated, treatment of laryngospasm in burned patients can include high-dose NDMRs, positive pressure ventilation, or deepening the anesthetic by intravenous (and inhalational routes, if possible). Approximately 3 to 7 days after burn injury, the dose of NDMRs required to achieve effective paralysis can be substantially increased. The etiology of the altered response to NDMRs is multifactorial: (a) up-regulation of acetylcholine receptors, including up-regulation of fetal and α7 (neuronal type) acetylcholine receptors at the muscle membrane; (b) increased binding to AAG and enhanced renal and hepatic elimination of the NDMRs. The pivotal role of de novo expression of α7AChRs at the neuromuscular junction in resistance to NDMRs has recently been characterized.63 
An increased rocuronium dose of 1.2 to 1.5 mg/kg for rapid sequence induction has been recommended in patients with major burn injury.64  It must be noted, however, that even with a dose of 1.5 mg/kg of rocuronium, the onset of time to effective paralysis approximates 90 seconds in burned patients compared with less than 60 s in nonburned patients with a dose of 0.9 mg/kg (fig. 6).64  Atracurium, broken down by organ-independent pathways (e.g., Hofmann elimination), also exhibits reduced effectiveness after burns. This suggests that the major component to resistance to NDMRs is pharmacodynamic in nature.
Fig. 6.
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104 
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104
Fig. 6.
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104 
×
Anesthetic Drugs
Choice of drug should be based on the patient’s hemodynamic and pulmonary status and potential difficulty in securing the patient’s airway. The choice of volatile anesthetic does not appear to influence outcome in burned patients.
Propofol clearance and volume of distribution are increased in patients with major burns during the hyperdynamic phase of burn injury.65  The pharmacokinetic changes, in combination with pharmacodynamic alterations centrally, could contribute to a decreased hypnotic effect of propofol. Therefore, in comparison with nonburned patients, those with major burn injuries may require larger bolus doses and/or increased infusion rates of propofol to attain or maintain therapeutic plasma drug concentrations.65  The hemodynamic consequences of administering larger doses of propofol should be kept in mind.
Opioids
Opioid requirements are increased in burn-injured patients. Opioid tolerance makes pain management challenging throughout all phases of burn care. It is not uncommon for burn-injured patients to manifest opioid tolerance requiring dosing that far exceeds standard textbook recommendations (fig. 7). If patients come to the operating room with infusions of sedatives and narcotics, these infusions should be continued and not stopped; the infusions have been maintained to reach a steady state of effect. Intraoperative analgesia can be achieved by increasing these infusions or turning to other drugs. Table 5 indicates some of the first-, second-, and third-line sedative and analgesic regimens used in our institutions during the acute hypermetabolic phase of burn injury. In addition to pharmacokinetic changes documented for morphine, fentanyl, and propofol, animal studies of burn injury document changes in the spinal cord receptors. These include down-regulation of μ-opioid receptors, and up-regulation of protein kinase C-γ and N-methyl-d-aspartate receptors.66  In view of the N-methyl-d-aspartate up-regulation after burns, it is not surprising that ketamine requirements to anesthetize patients are increased after burn injury.67  Clonidine, dexmedetomidine, ketamine, and methadone have been found to be effective in the treatment of pain for burn-injured patients who develop extreme tolerance to morphine (table 5).68,69 
Table 5.
Sedation and Analgesia Guidelines for Acute Burns
Sedation and Analgesia Guidelines for Acute Burns×
Sedation and Analgesia Guidelines for Acute Burns
Table 5.
Sedation and Analgesia Guidelines for Acute Burns
Sedation and Analgesia Guidelines for Acute Burns×
×
Fig. 7.
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
Fig. 7.
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
×
Ketamine
Ketamine has many potential advantages for induction and maintenance of anesthesia in burn patients and is used by some centers as the primary anesthetic. Ketamine in normal patients is associated with hemodynamic stability, preserving airway patency as well as hypoxic and hypercapnic responses, and decreasing airway resistance. Ketamine may exert beneficial antiinflammatory effects in patients with burns and/or sepsis.70–72  Ketamine may be the agent of choice if one wishes to avoid manipulation of the airway (e.g., after placement of fresh facial grafts, for splint or dressing removal, for brief procedures such as dressing or line changes, insertion of Foley catheters in pediatric patients, or for patients with toxic epidermal necrolysis syndrome).73  The addition of benzodiazepines is often recommended to reduce the incidence of dysphoria. Because of the increased secretions associated with ketamine, glycopyrrolate is frequently coadministered. Ketamine is now part of the pharmacologic armamentarium to treat burn- and opioid-induced tolerance to narcotics. Bolus doses of ketamine can cause hypotension in patients with burn injury, despite ketamine-induced catecholamine release. The persistently high levels of catecholamines in patients with major burns result in desensitization and down-regulation of β-adrenoreceptors.74  As a result, direct myocardial depressant effects of ketamine can become manifested.
Regional Anesthesia
Some studies have shown potential benefit of regional anesthesia in patients with burn injury by providing intraoperative anesthesia, improving postoperative analgesia and facilitating rehabilitation. Patients often have more intense postoperative pain from the split-thickness skin donor site than from the grafted burn wound. Regional anesthesia in its simplest form may be tumescent local anesthesia injected into a donor site before harvesting75  or it can take the form of subcutaneous catheter infusions,76  peripheral nerve, or central neuraxial blocks.77 
Central neuraxial techniques (spinals, epidurals) have been used with good effect as both primary anesthetics and postoperative adjuncts in burn-injured patients. There are no reports suggesting that epidural abscesses are more common in burn patients, but reports have suggested that intravascular catheters are more likely to become infected if placed in or near burned tissue78 ; similarly, caution is likely reasonable in selecting appropriate burn patients for central neuraxial techniques.
Truncal blocks (paravertebral and transversus abdominis plane) have been very useful to provide analgesia for donor site harvesting, and both block techniques are also amenable to placement of catheters to extend duration of postoperative analgesia. The lateral femoral cutaneous nerve block is particularly well suited to block because it is exclusively a sensory nerve and innervates an area (the lateral thigh) that is frequently chosen for split-thickness skin grafts. Sometimes there is a need to cover the anterior and medial thigh due to the extent of skin harvest, and therefore, a fascia iliaca block can also be performed.76–78 
Metabolic and Nutritional Management
The hypermetabolic response after burn injury is more severe and sustained than any other form of trauma.3,4  Continuous enteral or parenteral nutrition partially abates the hypermetabolic response and attenuates muscle protein loss of burns.79  Despite aggressive nutrition, intensive insulin therapy, and use of adjuvants (oxandrolone, propranolol, others), loss of muscle mass continues even after wound coverage.79  Burn-injured patients undergo multiple surgical procedures. Periods of 8-hour fasting before surgery make it difficult to meet the high caloric requirements of patients with major burn injury and may be poorly tolerated. The feasibility and safety of continuing enteral feeding throughout operative procedures has been studied. Enteral feeding during surgery beyond the pylorus has been successful, provided the airway was secured via a cuffed ETT or tracheostomy (to prevent aspiration of gastric contents).79  Nonetheless it is prudent to hold enteral feedings when there is potential for increasing abdominal pressure (e.g., prone position during surgery) or when an airway procedure such as tracheostomy is to be performed.
Blood Loss during Burn Wound Excision
It is difficult to estimate blood loss during burn excision because shed blood cannot be efficiently collected in a suction canister, surgical sponges may also contain irrigation fluid, blood can be concealed beneath the patient, and substantial bleeding can continue unobserved beneath bulky dressings. Vigilant attention to several physiological variables is necessary to effectively maintain intravascular volume during burn excision. Published estimates of the amount of blood loss during burn excision operations are in the range of 2.6 to 3.4% of the blood volume for every 1% TBSA excised.80,81  Multiple techniques have been used to minimize intraoperative bleeding, such as application of topical thrombin, staged procedures, and brisk operative pace, and topical application or subcutaneous injection of vasoconstrictors (epinephrine, vasopressin analogs, or phenylephrine).82,83  No prospective study has compared the efficiency or superiority of one drug over the other to decrease bleeding.
Intraoperative Fluid Administration and Blood Transfusion
If the patient is receiving parenteral nutrition, it is important that its infusion not be stopped because of the danger of hypoglycemia. After the initial massive fluid resuscitation for major burns, much effort is made restricting fluids and administering diuretics to hasten elimination of this edema. In the perioperative period, it is important to avoid giving more fluid than is necessary. The use of colloids can help limit the amount of fluid needed to maintain preload. The surgeons may inject large amounts of subcutaneous fluid to facilitate wound debridement and donor harvest. This fluid should also be limited. As with the initial resuscitation, there is no single physiological endpoint to rely on for titrating fluid replacement. Constant vigilance and attention to all available information (hemodynamic, metabolic, and urine output) are necessary. The point at which red cell transfusion is beneficial varies greatly between patients. Rather than focusing on hemoglobin or hematocrit, it is best to strive to maintain adequate preload and follow metabolic status. Blood component therapy should be reserved for patients with a demonstrated physiologic need, but anticipation of continued blood loss may indicate transfusion to prevent significant anemia rather than waiting to treat it when it occurs.
In the past, administration of fresh-frozen plasma was guided by American Society of Anesthesiologists Task Force on Perioperative Blood Transfusion and Adjuvant Therapies recommendations that fresh-frozen plasma only be given when microvascular bleeding is present and coagulation factor deficiency is demonstrated. Recent experience with civilian and military trauma has demonstrated that mortality is decreased by previous and more aggressive administration of fresh-frozen plasma with massive bleeding.84,85  There are a number of definitions of massive transfusion such as loss of total blood volume in 24 h, requirement of 4 units of packed erythrocytes in an hour, or ongoing loss of more than 150 ml of blood per minute. It is not unusual for patients with large burns to meet these criteria during burn wound excision. The clinical experience with burn patients with massive hemorrhage is not the equivalent of hemorrhagic shock in nonburned trauma patients who present with hypovolemic shock, acidemia, hypothermia, and coagulopathy. During burn wound excision, bleeding is simultaneously treated with fluid replacement, and measures are taken to support the circulation and prevent hypothermia. Still, it is logical to assume that more aggressive use of fresh-frozen plasma to prevent development of coagulopathy can also benefit burn patients who experience massive hemorrhage.
Temperature Management
Maintaining body temperature in burned patients is especially important and challenging. The inflammatory response to large burns causes an increase in the hypothalamic core temperature set point. The metabolic rate is increased to maintain this increased temperature. Hypothermia in these patients is poorly tolerated as it causes an exaggerated increase in oxygen consumption and exacerbates the catabolic response to the injuries.86  Decreased body temperature during burn excisions may also increase blood loss and worsen morbidity and mortality.87  Multiple strategies are used to maintain body temperature in the operating room, including use of warming blankets, radiant warmers, blood/fluid warmers, minimizing skin surface exposure, and wrapping the head and extremities with plastic or thermal insulation. Temperature in the operating room is commonly maintained at 80 to 100°F (27 to 38°C), depending on the age and severity of the burn.
Postoperative Care
There are several critical postoperative concerns for burn patients: whether to extubate in the operating room, safe transport to the ICU, transfer of care to the ICU staff, and control of postoperative pain. The decision to extubate in the operating room depends on standard criteria with concerns specific to burn patients, including an assessment of airway patency, metabolic status, potential for ongoing bleeding, and when the patient will return again for surgery.
The same concerns regarding transfer from the ICU to the operating room apply for transfer back to the ICU, except that the patient is likely to be less stable physiologically in the postoperative period. Continued bleeding may be concealed by dressings, the patient may be more prone to hypothermia, emergence may be associated with delirium, and analgesic requirements will be greater. Monitors appropriate to the patient’s physiological status, transport oxygen with appropriate respiratory support, a plan to keep the patient warm, adequate transport staff, resuscitation drugs, and an easily available intravenous drug administration site are all necessary for safe transport. During this period of exaggerated physiological fragility, it is important to be especially vigilant during transfer of the monitors, respiratory, and hemodynamic support equipment to the ICU staff.
Inadequate control of pain and anxiety can adversely affect wound healing and psychological status. The presence of newly excised tissue and harvested donor sites are very painful. As indicated previously, it is common for burned patients to become quite tolerant of sedatives and analgesics over time, and thus, doses substantially larger than normal may be required especially in the postoperative period. Other drugs, which act on receptors other than opiates (α2-adrenoceptor agonists, N-methyl-d-aspartate antagonists, others), may have benefits when added to the regimen (vide infra). The optimal method providing sedation and analgesia in patients with major burns is still unresolved.
Pain Management
All aspects of burn injury (e.g., dressing changes, excision and grafting procedures, physical therapy, and line insertion) are associated with pain. There is ongoing background pain, and there is procedure-related pain. Pain is exacerbated by anxiety if the pain is poorly controlled with sedatives and analgesics. Pain of burns has hyperalgesic (increased response to painful stimuli, e.g., wound debridement) and allodynic components (painful responses to nonpainful stimuli, e.g., touch).88  Posttraumatic stress disorder has been reported to occur in up to 30% of patients with severe burn injury, often developing in the setting of inadequate treatment of anxiety and pain.89,90  Patient-controlled analgesia has been shown to be a safe and effective method of opioid delivery for acute or procedure-related pain in both children and adults with burn injury.91–93 
Sensitivity to analgesics varies with time after burn injury from increased sensitivity and tolerance.94  Continuous administration of analgesics by itself can result in opioid-induced hyperalgesia and accentuate the need for higher opioid doses.95  To provide appropriate, consistent patient comfort, standardized pain and anxiety guidelines are used in many burn centers. The ideal characteristics of such a guideline include (a) safety and efficacy over a broad range of ages and burn injury severities, (b) explicit recommendations for drug selection, dosing, and increases in dosing, (c) a limited formulary to promote staff familiarity with drugs used, and (d) regular assessment of pain and anxiety levels with guidance for intervention through adjusted drug dosing.96,97 Table 5 gives one example of a pain and sedation treatment guideline. Treatment of opioid tolerance includes switching of opioids (morphine → fentanyl → methadone) and coadministration of drugs acting on nonopioid receptors (ketamine–N-methyl-d-aspartate [nonsteroidal antiiflammatory drugs] antagonist, dexmedetomidine- or clonidine-α2-agonist and gabapentin-like drugs).
Acetaminophen and nonsteroidal antiinflammatory drugs (NSAIDs) are useful first-line analgesic for minor burns. However, oral NSAIDs and acetaminophen exhibit a ceiling effect in their dose–response relationship, rendering them unsuitable for the treatment of severe burn pain.98  NSAIDs can also have deleterious effects on gastric mucosa and renal function. NSAIDs and benzodiazepines are commonly combined with opioids to relieve procedural pain. Pain is exacerbated by anxiety, which may be reduced by benzodiazepines. Antidepressants appear to enhance opiate-induced analgesia, especially in patients with chronic (neuropathic) pain. The tolerance to opiates seems to be exaggerated by long-term administration of the benzodiazepine, midazolam.99  Anticonvulsants may be useful after burns but have not been adequately tested. Clonidine or dexmedetomidine (α2-adrenoceptor agonists) can be a useful adjunct in reducing pain without causing pruritus (itching) or respiratory depression. However, it can cause hypotension in higher doses and in the presence of hypovolemia, therefore should not be given to hemodynamically unstable patients.100,101  Dexmedetomidine has been used to provide sedation–analgesia for burned patients and to decrease opioid requirements.101–103 
Summary
Burn-injured patients frequently require surgical treatment, yet pose a myriad of pathophysiologic challenges to acute and perioperative care. Optimal care of the burn-injured patients requires a comprehensive preoperative assessment and attention to risk factors (e.g., burn shock and resuscitation, difficult airway anatomy, inhalation injury) that predispose these patients to increased morbidity and mortality. Anticipation of these issues, as well as awareness of the alterations in pharmacokinetics and pharmacodynamics in patients with burn injury, is essential. Significant losses of blood volume and body temperature are not uncommon sequelae in the intraoperative period. Appropriate precautions should be taken to prevent these. Safe care can be provided by understanding, appreciating, and anticipating the unique preoperative, intraoperative, and postoperative issues and problems of the burn patient.
Acknowledgments
Supported, in part, by grants from the Shriners Hospital Research Philanthropy, Tampa, Florida, and from the National Institutes of Health, Bethesda, Maryland, P50-GM 2500 Project I (to Dr. Martyn).
Competing Interests
The authors declare no competing interests.
*American Burn Association: Burn incidence and treatment in the US: 2007 fact sheet. Available at: http://www.ameriburn.org/resources_factsheet.php. Accessed May 16, 2014.
American Burn Association: Burn incidence and treatment in the US: 2007 fact sheet. Available at: http://www.ameriburn.org/resources_factsheet.php. Accessed May 16, 2014.×
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Fig. 1.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
Fig. 1.
Pathophysiologic changes in the early phase (24–48 h) of burn injury. The early (ebb) phase of burn injury is characterized by decreased cardiac output and decreased blood flow to all organs. The decreased cardiac output is due to loss of intravascular volume, direct myocardial depression, increased pulmonary and systemic vascular resistance (PVR and SVR, respectively), and hemoconcentration and can lead to metabolic acidosis and venous desaturation (↓SvO2). Decreased urine flow results from decreased glomerular filtration and increased aldosterone and antidiuretic hormone (ADH) levels. Oxygenation and ventilation problems can occur due to inhalation injury and/or distant effects of burn on airways and lung. Compartment syndrome ensues if there is circumferential burn with no escharotomy performed to release the constriction. Compartment syndrome can also occur in abdomen, extremities, or orbits without local or circumferential burns. Mental status can be altered because of hypoxia, inhaled toxins, and/or drugs. The reasons why heart rate, blood pressure, and central venous pressure (CVP) can be poor indicators of volume status are explained in table 3.
×
Fig. 2.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
Fig. 2.
Pathophysiological changes during hypermetabolic/hyperdynamic phase of burn. At 48–72 h after burn, the hypermetabolic-hyperdynamic (flow) phase starts, characterized by increased oxygen consumption, carbon dioxide production, and cardiac output, with enhanced blood flow to all organs including skin, kidney (glomerular filtration rate), and liver, and decreased systemic vascular resistance (SVR). Increased venous oxygen saturation (↑SvO2) is related to peripheral arteriovenous shunting. The markedly decreased SVR mimics sepsis. Lungs and airways may continue to be affected because of inhalation injury. During this phase, pulmonary edema, pneumonia, and/or acute respiratory distress syndrome can be seen even in the absence of inhalation injury. Pulmonary edema can occur due to distant effects of major burn and reabsorption of edema fluid (hypervolemia). The altered mental status may be related to burn itself and/or concomitant drug therapy. Release of catabolic hormones and insulin resistance leads to muscle protein catabolism and hyperglycemia.
×
Fig. 3.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
Fig. 3.
Respiratory inadequacy due to direct injury: putative agents and site of injury. The noxious agents released from the burning material can affect different parts of the airway. The cartoon indicates which part of the respiratory system is affected by each gas, toxin or chemical (“Cause”). The pathophysiological effects of each of these noxious agents are also indicated (“Effects”). Thermal or chemical injury can lead to edema of face, pharynx, glottis, and larynx. Injury to trachea and bronchi leads to bronchospasm and bronchorrhea. Chemical and toxin injury can lead to alveolar damage and pulmonary edema.
×
Fig. 4.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
Fig. 4.
Lund–Browder burn diagram and table. Lund–Browder burn diagram and table indicate the varying proportions in surface area in persons with different ages. A careful burn diagram should be completed at the time of initial evaluation, including wound size, location, and estimated burn depth. Lund–Browder chart should be used in pediatric patients because the body surface area relationships vary with age. The letters and numbers on the y and x axes can be used to demarcate site-specific changes. TBSA = total body surface area.
×
Fig. 5.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
Fig. 5.
Severe scar contracture developing before complete wound coverage. In contrast to edema affecting airways in the early phase, burn scar contraction of mouth and neck can complicate airway management during acute recovery phase. Reduced mandibular mobility and contraction around oral commissures can make it difficult or impossible to advance the jaw and open mouth. Furthermore, the airway can become obstructed by collapse of pharyngeal tissues during induction of general anesthesia. In these instances, direct laryngoscopy can be difficult or impossible because the larynx also can be tethered to surrounding structures. Awake fiber optic intubation is an option. Ketamine provides analgesia and maintains respiratory drive and pharyngeal tone for pediatric patients and adults who will not tolerate awake intubation.
×
Fig. 6.
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104 
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104
Fig. 6.
Dose–response curves and time to maximal effect of rocuronium in adult burned and nonburned patients. Dose versus time to percentage twitch suppression for rocuronium in control subjects and burned subjects of mean 40% total body surface area burn and studied at least 1 week after burn. In normal patients, dose of 0.9 mg/kg rocuronium caused 95% twitch suppression in ≤60 s. The same dose has an onset of >120 s after major burn. Increasing doses of rocuronium shifted dose–response curves to the left. However, even with 1.5 mg/kg dose, the onset was still >90 s. Train-of-four ratio refers to the ratio between fourth and first twitch tensions recorded in muscle during 2 Hz nerve stimulation.64,104 
×
Fig. 7.
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
Fig. 7.
Burn injury–induced tolerance to narcotics and sedatives. A 17-yr-old male sustained 90% flame burn injury requiring mechanical ventilation, multiple surgeries, and anesthetics. The graph indicates the mg · kg−1 · h−1 doses of morphine and midazolam administered over time after burn starting from week 1 to week 25. At one stage, the intravenous morphine and midazolam doses required exceeded 55 mg/hr of each. During procedures (e.g., dressing changes) additional doses of ketamine, dexmedetomidine, fentanyl, and/or propofol were administered pro re nata. More recently, when the doses of morphine and midazolam exceed 0.5 ml · kg−1 · h−1, we institute dexmedetomidine or ketamine infusions as sedative and change the opioid from morphine to fentanyl or vice versa (see also table 5).
×
Table 1.
Classification of Burn Depth
Classification of Burn Depth×
Classification of Burn Depth
Table 1.
Classification of Burn Depth
Classification of Burn Depth×
×
Table 2.
Formulae for Fluid Resuscitation after Burn Injury
Formulae for Fluid Resuscitation after Burn Injury×
Formulae for Fluid Resuscitation after Burn Injury
Table 2.
Formulae for Fluid Resuscitation after Burn Injury
Formulae for Fluid Resuscitation after Burn Injury×
×
Table 3.
Indicators of Adequate Circulating Volume and/or Resuscitation
Indicators of Adequate Circulating Volume and/or Resuscitation×
Indicators of Adequate Circulating Volume and/or Resuscitation
Table 3.
Indicators of Adequate Circulating Volume and/or Resuscitation
Indicators of Adequate Circulating Volume and/or Resuscitation×
×
Table 4.
Major Preoperative Concerns for Burn Patients
Major Preoperative Concerns for Burn Patients×
Major Preoperative Concerns for Burn Patients
Table 4.
Major Preoperative Concerns for Burn Patients
Major Preoperative Concerns for Burn Patients×
×
Table 5.
Sedation and Analgesia Guidelines for Acute Burns
Sedation and Analgesia Guidelines for Acute Burns×
Sedation and Analgesia Guidelines for Acute Burns
Table 5.
Sedation and Analgesia Guidelines for Acute Burns
Sedation and Analgesia Guidelines for Acute Burns×
×