Burn injury

Abstract

Burn injuries are under-appreciated injuries that are associated with substantial morbidity and mortality. Burn injuries, particularly severe burns, are accompanied by an immune and inflammatory response, metabolic changes and distributive shock that can be challenging to manage and can lead to multiple organ failure. Of great importance is that the injury affects not only the physical health, but also the mental health and quality of life of the patient. Accordingly, patients with burn injury cannot be considered recovered when the wounds have healed; instead, burn injury leads to long-term profound alterations that must be addressed to optimize quality of life. Burn care providers are, therefore, faced with a plethora of challenges including acute and critical care management, long-term care and rehabilitation. The aim of this Primer is not only to give an overview and update about burn care, but also to raise awareness of the ongoing challenges and stigmata associated with burn injuries.

Burn injuries, particularly severe burns, are accompanied by a metabolic, immune and inflammatory response that can be challenging to manage, often leading to multiple organ failure or even death. This Primer discusses aspects of burn injury, from prevention to care of patients from both an acute and a long-term perspective.

Introduction

Burn injuries are an under-appreciated trauma that can affect anyone, anytime and anywhere. The injuries can be caused by friction, cold, heat, radiation, chemical or electric sources, but the majority of burn injuries are caused by heat from hot liquids, solids or fire¹. Although all burn injuries involve tissue destruction due to energy transfer, different causes can be associated with different physiological and pathophysiological responses. For example, a flame or hot grease can cause an immediate deep burn, whereas scald injuries (that is, from hot liquids or steam) tend to appear more superficial initially, due to rapid dilution of the source and energy. Alkaline chemicals cause colliquative necrosis (whereby the tissue is transformed into a liquid, viscous mass), whereas acidic burn causes a coagulation necrosis (whereby the architecture of the dead tissue can be preserved). Electrical injuries are entirely different because they can cause deep tissue damage that is greater than the visible skin injury; tissue damage in electrical injuries is correlated with the electric field strength (amperes and resistance of the tissue), although for ease of comprehension the voltage is often used to describe the circumstances of injury². Thermal injury can also occur through cold. Frostbite is caused by a number of mechanisms including direct cellular injury from crystallization of water in tissue and indirect injury from ischaemia and reperfusion. These mechanisms lead not only to skin necrosis but also to deep tissue damage³. The particular cause of a burn injury determines the treatment approach. For example, although deep thermal burns are operated on immediately, the same approach would be an error in frostbite, in which the therapy of choice is moist rewarming, possible thrombolysis and watchful waiting.

In addition to determining the cause of a burn injury it is imperative to classify the injury according to its severity — its depth and size. Burns that affect the uppermost layer of the skin (epidermis only) are classed as superficial (first-degree) burns (Fig. 1); the skin becomes red and the pain experienced is limited in duration. Superficial partial-thickness (second-degree) burns (formerly known as 2A burns) are painful, weep, require dressing and wound care, and may scar, but do not require surgery. Deep partial-thickness (second-degree) burns (formerly known as 2B burns) are less painful owing to partial destruction of the pain receptors, drier, require surgery and will scar. A full-thickness (third-degree) burn extends through the full dermis and is not typically painful owing to damage to the nerve endings, and requires protection from becoming infected and, unless very small, surgical management. Finally, a fourth-degree burn involves injury to deeper tissues, such as muscle or bone, is often blackened and frequently leads to loss of the burned part. Although superficial and superficial partial-thickness burns usually heal without surgical intervention, more severe burns need careful management, which includes topical antimicrobial dressings and/or surgery. Importantly, burns are classified as either minor or major. A minor burn is usually a burn that encompasses <10% of the total body surface area (TBSA), with superficial burns predominating. By contrast, the burn size that constitutes a major burn is not commonly well-defined; some guidance to classify severe burn injuries are: >10%TBSA in elderly patients, >20%TBSA in adults and >30%TBSA in children. Alongside injuries to the skin, burns can be accompanied by smoke inhalation or other physical trauma to other organs.

Fig. 1. Burn depth.

Burn depth is an important factor in assessing patient care needs and, in particular, surgical needs; in general, the deeper the burn the more challenges there are to achieve good scar outcomes. First-degree (superficial thickness, affecting the epidermis only) burns are typically benign, very painful, heal without scarring and do not require surgery. Burns extending into the underlying skin layer (dermis) are classed as partial thickness or second-degree; these burns frequently form painful blisters. These burns range from superficial partial thickness, which are homogeneous, moist, hyperaemic and blanch, to deep partial thickness, which are less sensate, drier, may have a reticular pattern to the erythema and do not blanch. Third-degree (full thickness) and fourth-degree burns require surgery and, paradoxically, usually present with almost no pain.

The uniqueness of a severe or major burn injury is anchored in the body responses to it. After the injury, an immediate systemic and local stress response is triggered that, unlike sepsis or trauma, does not recover quickly. Severe burns cause a complex pattern of responses that can last up to several years after the initial insult⁴. In general, immediately after the insult, an inflammatory response is triggered to promote the healing process^5,6. However, in severe burns, this inflammatory process can be extensive and become uncontrolled, leading to an augmented inflammation that does not induce healing but rather causes a generalized catabolic state and delayed healing. This response is almost unique to burns and is referred to as the hypermetabolic response; it is associated with catabolism, increased incidence of organ failure, infections and even death⁷.

Once the burn injury severity has been established, the patient needs to be appropriately referred and triaged. Care of a patient with major burn injury is resource-intensive, often takes place in a specialized centre⁸, and has a substantial impact not only on the life of the patient but also on the lives of caregivers and families^9,10 — often for a long period of time. A recent study demonstrated that burn injuries affect morbidity and mortality for at least 5–10 years after the injury¹¹. Thus, those involved in burn care must adapt their goals to move away from immediate survival as the main goal towards goals that address scarring, long-term well-being, mental health and quality of life. Indeed, the trauma care community recently adopted the goals of no death, no scar, no pain¹².

In this Primer, we discuss key aspects of burn injury and provide an up to date description of the epidemiology and clinical care of patients with burn injuries. Mechanistically, we focus our discussion on severe burns, as these injuries exhibit profound inflammatory and metabolic effects that increase the risk of long-term sequelae and death, but principles of wound care and acute management can also be applied to minor burn injuries. The goals to reduce scarring and safeguard mental health are also described alongside other long-term outcomes of quality of life. We also discuss promising future therapies.

Epidemiology

Burn injuries result in lifelong physical and psychological scarring¹³, causing pain and influencing mental health, quality of life, ability to return to work and subsequent mortality^10,11,14. Although information on burn epidemiology is essential for resource allocation and prevention, the available data are variable and inconsistent. The majority of data are from high-income countries and are directly related to access to health-care resources, differences in environments and the resources of the various health-care systems^15–17. In lower income countries, fewer resources, geographical constraints and cost limit data collection and access to health care¹⁸. Additionally, cultural factors such as open-air cooking areas and loose clothing (for example, saris), domestic violence and dowry deaths contribute to regional variation^19–21. To address the significant gap in information, the WHO is piloting an online, checkbox-based Global Burn Registry that aims to standardize reporting²².

Although burn injuries are decreasing in high-income countries, the prevalence of burn injuries remains high elsewhere, with ~90% of burns occurring in low- and middle-income areas^23,24. The WHO estimates that 11 million burn injuries of all types occur annually worldwide, 180,000 of which are fatal¹³. There is a wide variability in the incidence of burn injury²³. For example, the number of burn-related deaths per 100,000 population ranges from 14.53 in Cote D’Ivoire to 0.02 in Malta²⁵. Burn-related deaths of children are 7 to 11 times higher in low-income than in high-income countries^13,19.

In the USA, a bimodal age distribution of all burn injuries is evident, with the majority of injuries occurring in young children (1–15.9 years of age) and in those of working age (20–59 years of age)¹. Regardless of country, burns in children are more equally distributed between boys and girls, especially in toddlers^1,24. However, this ratio changes as age increases; in most countries, nearly twice as many men are injured as women. An exception to this trend has been noted in Ghana and India, where up to three times more women are injured and die from burn injuries than men^26,27.

The American Burn Association (ABA) National Burn Repository 2019 reports that, overall, flame burns are still the majority of injuries in the USA (41%), with scalds second at 31%¹. Chemical (3.5%) and electrical burn injuries (3.6%) occur much less commonly¹. Burns in children <5 years of age tend to be scald injuries, with increasing flame-related burns as age increases²⁸. Around the world, burns in the elderly population are increasing, and are predominantly flame-related. However, scald injuries are increasing substantially as well²⁹. Finally, depending on the environment, burn injuries are more frequent in some vulnerable populations, such as those with epilepsy³⁰.

Mechanisms/pathophysiology

Experimental and clinical studies have demonstrated that severe burns (regardless of the cause) result in the development of an extremely dysregulated inflammatory host response within a few hours of injury^24,31–35. The inflammatory and stress responses are characterized by elevated levels of cytokines, chemokines and acute phase proteins as well as a hypermetabolic state that is driven by a sustained sympathetic tone that can persist beyond the acute phase of care^5,36. A number of factors contribute to the magnitude of the host response: burn severity (percentage TBSA and burn depth); burn cause; concomitant inhalation injury; exposure to toxins; other traumatic injuries; and patient-related factors such as age, pre-existing chronic medical conditions, drug or alcohol intoxication, and timing of presentation to medical aid. Depending on the magnitude of the injury, the initial host response immediately after severe burn injury is similar to that after many other inflammatory conditions triggered by tissue destruction such as trauma or major surgery³³, which is helpful in initiating tissue repair and overall wound healing. However, after severe burns, the inflammatory cascade may be triggered multiple times during the course of clinical care after initial resuscitation, for example, during burn surgery or subsequent infectious complications. When the inflammatory cascade occurs repeatedly or remains uncontrolled, it can destroy host tissue and contribute to organ dysfunction and death. Although various pieces of the complex response after burn injury have been identified, how and in what sequence these pieces interact have not been resolved.

Initial injury

Immediately after injury, the burn wound can be divided into three zones: the zone of coagulation (with the most damage in the central portion); the zone of stasis or zone of ischaemia (characterized by decreased perfusion that is potentially salvageable); and the zone of hyperaemia (the outermost region of the wound characterized by increased inflammatory vasodilation). The degree of cellular injury varies depending on the zone of injury and spans the spectrum from immediate cellular autophagy within the first 24 hours following injury, delayed-onset apoptosis ~24–48 hours after the burn injury and the presence of reversible oxidative stress. The natural healing of these wounds involves dynamic and overlapping phases (Fig. 2) that include an inflammatory phase, which is initiated by neutrophils and monocytes homing to the injury site via localized vasodilation.

Fig. 2. Four phases of natural wound healing.

Haemostasis occurs immediately after the injury and involves vasoconstriction, platelet activation and aggregation, and release of clotting and growth factors (such as platelet-derived growth factor (PDGF), epidermal growth factor (EGF) and transforming growth factor-β (TGFβ)) by platelets, keratinocytes, macrophages and fibroblasts, resulting in fibrin clot deposition at the injury site, which serves as a provisional matrix for subsequent stages of healing. Monocytes (and macrophages) and neutrophils are recruited to the injury site owing to localized vasodilation and initiate the inflammation phase. Inflammation begins within 24 hours of the injury and lasts for weeks to months depending on the severity of injury. Neutrophils and macrophages release cytokines and chemokines (including IL-1, IL-8 and tumour necrosis factor (TNF)) and growth factors (including TGFβ, insulin-like growth factor (IGF) and vascular endothelial growth factor (VEGF)), and remove debris and pathogens from the injury site. The next phase, proliferation, involves the recruitment and activation of fibroblasts and keratinocytes to the wound site. Proliferation is characterized by replacement of the provisional matrix with a connective tissue matrix, granulation (new connective tissue and microscopic blood vessels), angiogenesis and epithelialization. Keratinocytes assist in both epithelialization (wound surface closure) and angiogenesis (restoration of blood flow), which are vital to wound healing. Endothelial cells are activated by growth factors (VEGF, hepatocyte growth factor (HGF) and fibroblast growth factors (FGFs)) to initiate angiogenesis. Resident fibroblasts are transformed to myofibroblasts, which are involved in extracellular matrix (ECM) deposition. In the final phase, remodelling, granulation tissue matures and the ECM is remodelled under the influence of growth factors, matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs), which leads to increased tensile strength. The length of healing depends on multiple factors including the injury severity, inflammatory cascade activation and nutrition. IFN, interferon.

This inflammatory phase naturally serves to degrade necrotic tissue and initiate the cascade of signals required for wound repair. Following the inflammatory response, activation of keratinocytes and fibroblasts via various cytokines and growth factors helps usher in the proliferative phase that aims to restore vascular perfusion and further promote wound healing. The final phase of healing involves wound remodelling, in which collagen and elastin are deposited and continuously transform fibroblasts to myofibroblasts. Over time, a delicate balance between contraction of myofibroblast and re-epithelialization determines the quality and pliability of the repaired wound, and determines the extent of scar formation, which is characterized by fibrous malposition of collagen fibres³⁶. We and others have hypothesized that optimal healing depends on an adequate ‘pool’ of cells derived from the bone marrow and on the balance between pro-inflammatory and anti-inflammatory mediators³⁷. In general, the complex healing response is targeted towards dermal and epidermal regeneration with the goal of restoring closure of the skin barrier as well as pliability and functionality of the skin. However, wounds can heal with abnormal scars that are characteristically active, red, itchy, painful and disfiguring — termed hypertrophic or keloid scars (see below).

Shock

Alongside cytokines and other inflammatory mediators at the site of injury, stress hormones such as catecholamines and cortisones are released by the adrenal glands, all of which have systemic effects. Burn injury usually results in a distributive shock³⁸, an abnormal physiological state in which tissue perfusion and oxygen delivery is severely compromised owing to marked capillary leakage of fluid from the intravascular to interstitial space, that contributes to profound tissue oedema and fluid accumulation^39,40. The marked capillary leakage can be attributed to oxidative stress that is characterized by increases in the levels of nitric oxide and inflammatory mediators, which damages the vascular endothelium. Burn injury also depresses cardiac function within a few hours of injury, lasting ~24–48 hours, via oxidative stress, the release of inflammatory mediators (such as IL-6 and tumour necrosis factor (TNF)) and cellular alterations (such as apoptosis and necrosis)^32,34,39,41. The decrease in cardiac function and relative hypovolaemia, along with low blood flow caused by vasoconstriction, affects perfusion of tissues and organs (that is, distributive shock), including the lungs, liver and gastrointestinal tract — augmenting tissue and organ dysfunction and damage. The state of shock continues even if hypovolaemia is corrected³⁸. Furthermore, the cardiovascular dysfunction can further exacerbate the systemic inflammatory response into a vicious cycle of accelerating organ dysfunction (summarized in ref.⁴²).

Hypermetabolic state

After an initial (~72–96 hours) hypometabolism (ebb phase)⁴³ — which is potentially caused by intracellular processes, e.g. increased endoplasmic reticulum stress and mitochondrial dysfunction⁴⁴ and characterized by decreased metabolic rate and intravascular volume, poor tissue perfusion and low cardiac output — a hypermetabolic state is typically observed after injury in patients with severe burns (flow phase)^45,46. The hypermetabolic state after burn injury persists for up to 36 months after the initial insult⁴. Stress hormones such as catecholamines, glucocorticoids (produced by the adrenal glands) and glucagon (produced by the pancreas) increase blood pressure, peripheral insulin resistance and breakdown of glycogen, proteins and lipids. The results of these effects are increased resting energy expenditure, increased body temperature, total body protein loss, muscle wasting and increased stimulated synthesis of acute-phase proteins (such as insulin-like growth factor 1 (IGF-1), which has anabolic effects), ultimately resulting in organ catabolism associated with organ dysfunction and death^4,47–49.

Although these responses are reported in patients with other types of trauma or critical illness, their magnitude and duration in patients with severe burn injury is of consequence. Sustained release of catecholamines, glucocorticoids, glucagon and dopamine (released from the brain) seem to initiate a cascade of events leading to an acute hypermetabolic response and an ensuing catabolic state (Fig. 3). The mechanism(s) underlying this complex response remain to be established, but studies have suggested that the continuous and sustained release of pro-inflammatory mediators such as cytokines, chemokines and acute phase proteins (namely, IL-1, IL-6, TNF and IGF-1)⁴ may further contribute to the hypermetabolic state in patients with moderate to severe burn injury. Regardless of the underlying mechanistic detail, an effective treatment to abolish or reduce the hypermetabolic response is not available. However, the recent discovery of the browning of the white adipose tissue due to inflammation or upregulation of mitochondrial brown fat uncoupling protein 1 (which is responsible for thermogenic respiration) after burn injury^47,50 seems to induce metabolic and immune changes that further augment hypermetabolism and immune dysfunction — an avenue that may lead to new treatment options.

Fig. 3. Hypermetabolic state in burn injury.

Severe burn injury induces a unique and remarkably complex response that involves the release of stress hormones and pro-inflammatory mediators. The immediate response leads to a hypometabolic response that lasts for ~72–96 hours (ebb phase), but then rapidly turns into the flow phase that can persist for years after the initial injury. Stress mediators, such as catecholamines, glucocorticoids and cytokines, are released into the system and cause a plethora of systemic responses. The heart goes into a hyperdynamic overdrive, increasing circulation and blood flow to increase oxygen and nutrient delivery. However, increased stress signalling causes changes in organ function and metabolic demand. Protein is degraded to deliver energy for hepatic function, the gut develops mucosal atrophy to absorb more nutrients but also enabling bacterial translocation. The kidneys are hyperperfused but oxygen delivery is decreased, leading to acute kidney injury and stress signals from the kidney. The interplay between these organs accumulates, leading to metabolic and inflammatory overdrive that subsequently causes white adipose tissue to change to brown adipose tissue. Brown adipose tissue releases energy and induces substantial lipolysis with the accompanying expression of lipotoxic intermediates, such as triglycerides, free fatty acids and diacylglycerols (DAG), all of which are transferred to the liver. The liver is unable to metabolize all of the accumulating substances and develops hepatomegaly. In turn, hyperlipidaemia and hyperglycaemia with insulin resistance is present, which worsens the hypermetabolic and inflammatory state. If hypermetabolism cannot be diminished or decreased, holistic catabolism ensues and, subsequently, multiple organ failure and death. CNS, central nervous system.

Immune dysregulation and infection

In addition to hypovolaemic and hypermetabolic responses, burn injury has a profound effect on the immune system^34,35,51,52. Immune cells, including monocytes, macrophages and neutrophils, which are activated in response to burn injury within a few hours, recognize endogenous factors such as damage-associated molecular patterns (DAMPs) or alarmins that are generated as a result of burn-mediated tissue damage. DAMPs and their exogenous counterparts, pathogen-associated molecular pattern molecules (PAMPs), are recognized via pattern recognition receptors, namely Toll-like receptors (TLRs) and NOD-like receptors (NLRs). The ligation of TLRs and NLRs by their specific ligands results in the activation of downstream inflammatory pathways, leading to activation of NF-κB, a master transcription factor involved in the release of multiple inflammatory mediators (such as IL-1, IL-6, IL-8, IL-18 and TNF). The release of these cytokines and chemokines furthers the cycle of inflammation leading to systemic inflammatory response syndrome (in which uncontrolled cytokine release leads to excessive leukocyte recruitment, fever or hypothermia, tachycardia and tachypnoea)⁵³. Interestingly, other immune functions are severely compromised, including macrophage antigen presentation or neutrophil killing of invading pathogens^54–56. Moreover, T cell proliferation and IL-2 production are also suppressed^57–62. Together, these events lead to the development of a compromised adaptive immune response, resulting in enhanced susceptibility to infection (Fig. 4).

Fig. 4. Events leading to sepsis and multiple organ failure following burn injury.

Tissue injury following severe burns results in release of endogenous damage-associated molecular patterns (DAMPs) such as mitochondrial DNA²⁶³ and double-stranded RNA (dsRNA), which along with exogenous pathogen-associated molecular pattern molecules (PAMPs) such as lipopolysaccharides (LPS) and peptidoglycans, can induce vascular leak, an inflammatory response and metabolic changes. Vascular leak and transfer of intravascular fluid to third spaces leads to tissue oedema and further injury. The inflammatory response can result in immunosuppression and ineffective response to bacterial invasion. Metabolic changes include increased muscle protein degradation, insulin resistance and increased cardiac load. The culmination of these events is often systemic inflammatory response syndrome (SIRS), an inflammatory state affecting the whole body, which can lead to multiple organ failure, and ultimately, death. MHC, major histocompatibility complex; PGE₂, prostaglandin E₂; TNF, tumour necrosis factor. Adapted from ref.²⁶⁴, Springer Nature Limited.

Indeed, patients with severe burn injuries are at higher risk of developing infectious complications. Ventilator-associated pneumonia is also a common finding in patients with severe burn injuries⁶³. Additional sources for infection in these patients can be their own microbiota associated with skin, respiratory tract and intestines. Compromised host defence from the disrupted skin barrier in patients with burn injury leads to increased susceptibility to infection (predominantly bacterial, but also yeast, fungal and viral), increase virulence from specific pathogenic organisms and the subsequent development of organ failure^33,59,64. Indeed, in a recent autopsy study, >60% of deaths in patients with burn injury were attributable to infectious complications and nearly all had at least one associated organ failure, with many having multiple organ failure^65–67. Each episode of sepsis (Box 1) can lead to organ dysfunction, which eventually leads to organ failure that affects different organs, including the kidneys, lungs, liver, gastrointestinal tract, heart and bone marrow.

Various studies support the suggestion that the gut, being the major source of bacteria and bacterial products, also plays an important part in pathogenesis after burn injury^68,69. Previous studies have shown an increase in intestinal bacterial growth after burn injury, resulting from diminished gut immunity, hypoperfusion and gut dysmotility⁷⁰. Furthermore, an increase in intestinal permeability (due to hypoperfusion and subsequent tissue inflammation and damage) has also been documented in patients and in animals within a few hours of burn injury^70–72 and enables the gut bacteria to enter extra-intestinal sites such as mesenteric lymph nodes, liver and lungs. Indeed, increased bacterial translocation has been noted within the first few days after burn injury^70–72. However, this process becomes recurrent when the burn injury is followed by additional triggers that lead to gut hypoperfusion, such as peri-operative haemorrhagic shock and infectious complications. The microbial communities in faecal samples from patients with burn injury have been shown to be different from those observed in faecal samples from healthy controls^73,74. Specifically, the faecal microbial communities of controls were dominated by the Bacteroidaceae, Lachnospiraceae, and Ruminococcaceae families. The faecal samples from patients with burn injuries exhibited a marked decrease in the relative abundance of these three families, but also demonstrated sharp increases in the relative abundance of the Enterobacteriaceae, a finding that has been replicated in mice⁷⁴. Furthermore, results obtained using in situ hybridization suggest large populations of Enterobacteriaceae in close proximity to the villi in the small intestine of mice receiving burn injury⁷⁴. This observation provides further evidence that intestinal bacteria and their products (such as endotoxin) can cross the intestinal epithelial barrier into the systemic or lymphatic circulation and contribute to the pathology after burn injury. Changes in the microbial community or diversity have been implicated in the development of many diseases including allergies, obesity, inflammatory bowel disease and many infectious diseases^75–80. However, a more systematic approach is needed to better appreciate the role of gut-derived bacteria or the microbiome in pathogenesis after burn injury.

Box 1 Sepsis.

ABA Sepsis Criteria

To fulfil these criteria, at least three of the following should be present:

• Temperature >39 °C or <36.5 °C.

• Progressive tachycardia (>110 bpm).

• Progressive tachypnoea.

• Thrombocytopenia.

• Hyperglycaemia.

• Inability to continue enteral feedings 24 hours.

Alongside infection, demonstrated by at least one of the following:

• Culture-positive infection.

• Pathological tissue source identified.

• Clinical response to antimicrobial agents.

Mann–Salinas novel predictors of sepsis

Score comprises:

• Tachycardia >130 bpm.

• MAP <60 mmHg.

• Base deficit <–6 mEq/l.

• Hypothermia <36 °C.

• Use of vasoactive medications.

• Hyperglycaemia >150 mg/dl.

Sepsis-3 consensus definition for sepsis and septic shock

Score comprises:

• Altered mental status (Glasgow coma scale score <13).

• Systolic blood pressure ≤100 mmHg.

• Respiratory rate ≥22 breaths per minute.

• Suspected or documented infection and qSOFA ≥2 and/or SOFA ≥2; SOF variables are PaO₂/FiO₂ ratio, Glasgow coma scale, mean arterial pressure, vasopressor requirements, serum creatinine or urine output, bilirubin and platelet count.

The criteria for septic shock are:

• Vasopressors required to maintain MAP >65 mmHg.

• Lactate >2 mmol/l (after adequate fluid resuscitation).

ABA, American Burn Association; bpm, beats per minute; MAP, mean arterial pressure; PaO₂, partial pressure of arterial oxygen; FiO₂, fraction of inspired oxygen; SOFA, Sequential Organ Failure Assessment; qSOFA, quick SOFA. Data from ref.²³⁹.

Other injuries

Burn injuries can also lead to alterations and injuries in other organs. A common injury occurring with burns is inhalation injury (respiratory tract or lung tissue injury), caused by heat or inhalation of smoke or chemical products of combustion and leading to various degrees of damage (Box 2). Usually, inhalation injury is present in conjunction with the burn and can range from a minor injury to a very severe and necrotic injury pattern. Inhalation injury increases the risk of pulmonary complications, including ventilator-associated pneumonia, fluid requirements and mortality⁸¹. However, measurement of the severity of inhalation injury is currently not well defined, despite some efforts and an existing grading system based on bronchoscopy⁸², making assessment of the true effect of inhalation injury challenging.

A small percentage of burn injuries are associated with concomitant trauma, which commonly includes traumatic brain injury, injury to the abdominal or thoracic cavities, fractures or complex soft tissue injury (such as crush injury or degloving injury, with multiple layers of tissue involved). In general, patients with burns and traumatic injuries have worse outcomes than those without trauma⁸³. A comprehensive assessment of patients by trauma and burn teams needs to be conducted to optimize outcomes in these patients with complex and challenging injuries.

Additionally, burn injury affects all organs to some degree, owing to the systemic response to the burn. Possible effects include brain atrophy, pulmonary damage leading to pneumonia and/or acute respiratory distress syndrome (ARDS), acute renal failure, liver failure, hepatic fatty infiltration, gut atrophy, lipolysis and fat catabolism, cardiac dysfunction, and thymus and immune dysfunction and depletion. These effects lead to immunocompromise, loss of bone mineral density, hormone depletion and dysfunction, and thyroid dysfunction, all of which are common in the complex picture of burn-associated hypermetabolism. In an autopsy study, for example, multiple organ failure was a primary cause of >70% of all burn-related deaths⁸⁴.

Although very rare, a potential complication that has been documented in patients with burn injuries is irritation of the eye⁸⁵. Exposure to hot air, steam or flames can burn the face and eyes or eyelids, which can affect the normal function of the eye. Furthermore, injury to the eyelid can compromise the barrier and predispose the burn wound to foreign bodies and infection.

Box 2 Inhalation injury.

Inhalation injury can be divided into three types: systemic toxicity due to products of combustion (carbon monoxide (CO) and cyanide poisoning); upper airway thermal injury; and lower (bronchi and distal) airway chemical injury. Patients can sustain all of these in a closed-space fire. CO poisoning, more accurately categorized as a systemic intoxication, is easily diagnosed from the serum carboxyhaemoglobin level determined as part of the arterial blood gas measurement at hospital admission. Administration of 100% oxygen reduces the carboxyhaemoglobin half-life from 4 hours on room air (21% O₂) to ~45 minutes; patients with CO poisoning can have normal carboxyhaemoglobin levels on arrival at the hospital. Even when early intubation is not indicated, 100% O₂ administration should be continued until carboxyhaemoglobin levels are confirmed to be <5%. Although proponents of hyperbaric oxygen (HBO) therapy — in which pure oxygen is delivered in a pressurized room or tube — have argued that the treatment reduces long-term neurological sequelae of CO poisoning, prospective randomized trials have presented conflicting data regarding long-term cognitive function²⁴⁹. Cyanide toxicity is often clinically diagnosed by persistent acidosis without another systemic source; empirical treatment with cyanocobalamin has increased despite limited evidence for its safety and effectiveness. Upper airway burns can be diagnosed by assessing symptoms of hoarseness, stridor or oropharyngeal soot and examining the posterior pharynx for oedema or mucosal slough. Injuries to the lower airway tend to be due to chemical pneumonitis from products of combustion. Thermoregulation by the oropharynx is sufficient to cool most gases before they reach the distal lung parenchyma; however, steam is less efficiently cooled and may cause a thermal injury to the lower airways. Lower airway burns can be diagnosed with fibre optic bronchoscopy or by evidence of small airway inflammation and obstruction on CT. Prolonged mechanical ventilation complicates the care of patients with burn injuries, with or without inhalation injury. Patients with inhalation injury are at risk of developing acute respiratory distress syndrome (ARDS) from direct airway injury and their increased fluid resuscitation requirements from the inflammatory response to the burn injury. Many burn centres have adopted the use of lower tidal volumes and reduced airway plateau pressures to treat ARDS based on compelling data from the ARDSnet²⁵⁰. The applicability of extracorporeal membrane oxygenation in patients with inhalation injury must also be determined.

Diagnosis, screening and prevention

Prevention

Burn injuries result in permanent scarring and adverse long-term sequelae that affect burn survivors and their caregivers^9,10,14. Unfortunately, as vulnerable populations are disproportionately injured, the burden from these injuries further marginalizes already disadvantaged groups¹⁸. A central tenet of modern burn care is that the majority of burn injuries are preventable^13,86. As a result, the ABA encourages participation in prevention programmes as part of burn centre verification, and the WHO has proposed a plan for burn prevention and care at a global level^87,88. To encourage prevention implementation globally, the WHO published a collection of successful strategies from high-, middle- and low-income countries. These strategies range from grassroots changes of lifestyle (for example, safe wood burning stoves) to legislative regulation (for example, on children’s sleepwear flammability)⁸⁹.

Alongside legislative strategies, successful implementation of prevention programmes (for example, the introduction of fire-safe cigarettes and reduced flammability of children’s clothing) has reduced the incidence of burn injuries in high-income countries^90–93. However, these efforts may not be as effective in low- and middle-income countries. In these settings, local social factors must be taken into consideration, for example, most low-income countries do not have water heaters or the resources for smoke detectors in each home. The Haddon Matrix (assessing pre-event, event-related and post-event factors) should be considered when constructing prevention programmes^89,94 as the matrix helps to organize interventions for appropriate upstream, midstream and downstream targets. This approach can be applied at a regional level or even at a case level^95,96. Figure 5 provides an example of a Haddon Matrix under development by the authors (S.L.) to guide a programme for prevention of paediatric burn injuries.

Fig. 5. The Haddon Matrix for burn prevention.

The Haddon Matrix is a means of understanding traumatic injury that examines aetiological relationships instead of using descriptive terms¹⁸. This approach is essential to transition from the concept of burn injury as an ‘accident’ that is unpreventable, to the concept of injury being related to factors that can be modified. For example, we shift the concept from a child ‘accidentally’ turning on the hot water in a bathtub, to an unsupervised (change supervision) child turning on the hot water (control the water temperature at the boiler, or with a mixing valve). In using this approach, it is important not to assign blame, but to recognize the resources needed or factors that influence the cause of the traumatic event. For example, by examining the reasons why the child was unsupervised (parental mental health, other young siblings in the family, overstretched parents) and how to control the hot water (turn down the water heater, child-proof lockable tap, preset water temperature at the tap), programmes can be established to address them.

To be successful, regional burn prevention programmes should concentrate on factors that influence the incidence of burn injury in the local environment, knowledge dissemination strategies and data collection methods to identify the areas of focus and evaluate programme effectiveness⁸⁹. For example, in some countries, factors such as loose clothing and cooking on open fires are important areas of focus. In other regions, the occurrence of electrical burns has increased substantially as industrialization has taken place²¹. Prevention strategies can also be applied at a more personal level. For example, a review of injuries sustained by firefighters identified that burns occurred in common patterns associated with gaps in equipment, which can guide future equipment modifications and improvements⁹⁷. Development of prevention programmes must also take into consideration knowledge access and engagement with the selected media. For example, strategies to ‘gamify’ knowledge acquisition using mobile phone applications could reach a wider audience than a television commercial in some regions and for certain age groups⁹⁸. Literacy patterns, cultural appropriateness (which is particularly challenging to address in countries with more than one official language and no clear common language) and access to the recommended technologies can be barriers to this approach; for example, it is not possible to avoid open fire cooking until a cheap, safe, readily available alternative is identified^95,98,99. Furthermore, correction of one risk factor might introduce another; for example, use of liquefied petroleum gas burners as an alternative to open fire cooking without proper training can result in more injuries¹⁰⁰. Robust data collection and reporting and evidence-based decision making is needed to provide the information to drive this process. Although this information is more readily available in high-income countries, the countries with the highest rates of burn injury may not currently have the infrastructure to collect these data⁸⁹. To address this need, the WHO has started the Global Burn Registry to aid data collection in low-resource settings and address this knowledge gap²².

Diagnosis

Accurate assessment of the severity of a burn injury is paramount because it forms the basis for all subsequent treatment decisions, triage plans and assessment of medical futility. Whenever possible, decisions about how to proceed after diagnosis and screening should incorporate patient preferences and expectations about quality of life¹⁰¹. Optimal assessment of the severity of burn injury must involve a systematic methodical approach, such as that described in course materials for the Advanced Trauma Life Support¹⁰² (ATLS) by the American College of Surgeons Committee on Trauma, Emergency Management of the Severe Burn¹⁰³ (EMSB) by the Australian and New Zealand Burn Association, and Advanced Burn Life Support¹⁰⁴ (ABLS) by the ABA. Such diagnostic approaches must involve an orderly sequential evaluation (phase I of management), including the primary and secondary survey, that considers the need for further consultation and possible transport to optimize outcomes at specialized centres¹⁰⁵.

Primary survey

The primary survey at the scene of the injury or in the emergency department comprises immediate standardized assessment — in this order — of: the airway, breathing, ventilation, circulation and cardiac status, disability, neurological deficit, gross deformity and degree of exposure (requiring complete disrobing to enable identification of associated injuries). To avoid hypothermia, especially in children and the elderly, this assessment must be conducted while maintaining a warm environment¹⁰⁶. A preliminary estimate of the size of the burn using Lund and Browder diagrams¹⁰⁷ for children and, for adults, the Rule of Nines¹⁰⁸ (Fig. 6) is essential at this time because the amount of oral or intravenous fluid resuscitation is based on the burn size (percentage TBSA). Given the life-threatening nature of respiratory failure, assessing burn severity must also include early determination of whether the patient has a smoke inhalation injury (Box 2). Exposure to products of combustion in a closed space, facial burns and soot in the oral cavity do not in themselves indicate an inhalation injury but strongly necessitate further physical examination of the posterior pharynx for evidence of thermal injury, including mucosal erythema, sloughing and swelling or soot in the vocal cords. Clinical signs such as stridor, hoarseness, carbonaceous sputum and dyspnoea also suggest inhalation injury and warrant further work-up¹⁰⁹. However, even in resource-rich settings, in the majority of patients, diagnosis is made primarily on clinical appearance.

Fig. 6. Lund and Browder diagrams for estimating burn size in terms of TBSA.

In adults, the ‘Rule of Nines’ (that is, using multiples of 9) is used to assess the proportion of the total body surface area (TBSA) affected and to help guide immediate treatment decisions, such as amount of fluid resuscitation, that are based on the size of the burn injury. However, owing to different head to body size ratios, the proportion of the TBSA affected in children is estimated differently; the Rule of Nines is inaccurate. Another challenge is the body habitus. For example, the Rule of Nines and the estimate that each hand comprises 1% of the TBSA are inaccurate in patients who have obesity or cachexia²⁶⁵. The body areas are separated by colour and the numbers are percentages of the TBSA and include front and back coverage; for example, ‘32’ in the diagram of the trunk relates to the chest, abdomen and back that make up 32% of the TBSA. The hand, including the palm, fingers and back of the hand, represents 2% of the TBSA and can be a useful tool for quick calculation of the size of a burn — especially irregularly shaped scald burns²⁶⁶.

Secondary survey

The secondary survey, often in the emergency department or the burn centre, includes laboratory analyses and imaging, as indicated by evidence of other trauma or comorbidities. The secondary survey includes ensuring adequate tetanus prophylaxis, as burns are open wounds. The initial laboratory analyses in patients with burn a size of ≥15%TBSA include complete blood count, electrolyte assessment, coagulation profile and arterial blood gas measurement. In patients with suspected smoke inhalation injury, normal oxygenation and chest radiographs do not rule out the diagnosis as the pulmonary inflammatory response may take time to develop^110,111.

The secondary survey importantly includes a definitive evaluation of the burn severity including depth (Fig. 1) and size based on TBSA (Fig. 6). Understanding which burn wounds will heal and which will benefit from early excision and grafting can be challenging, owing to a lack of widely accepted validated noninvasive imaging techniques to estimate burn depth. Furthermore, estimates of burn size and depth made before admission to a burn centre — and even by experts — have consistently been shown to be inaccurate in spite of standardization attempts and the availability of tools such as the Lund and Browder diagrams¹⁰⁷ and the Rule of Nines¹⁰⁸. Given the unreliability of burn size and depth assessment by clinicians who are not burn experts and the expense and logistics of transferring patients to higher levels of care, development of creative technological solutions for consultations is essential. New approaches in development include the use of computer-assisted programs to improve burn size estimation and enable focused and accurate telemedical consultation^112,113. Telemedicine programs encompassing either real-time video conferencing or store-forward pictures of the wounds provide an option for burn experts to facilitate triage by assessing injury severity prior to transfer. Precise burn depth assessment can be challenging especially in patients at extremes of age and with thinner skin. To address this issue, several innovative devices incorporating laser Doppler imaging^114,115, harmonic ultrasound imaging¹¹⁶, optical coherence tomography¹¹⁷ and high-resolution infrared thermography¹¹⁸ have been developed and introduced into preclinical and limited clinical trials. Validation of these modalities requires both comparison of digital images with histological specimens of burned skin as well as objective correlation of the data with burn depth assessments by clinical experts. Unfortunately, the expense of integrating these into daily practice has presented a barrier to widespread use.

A critical aspect of the secondary survey is to calculate the initial fluid infusion rate needed. Historically, resuscitation following burn injury has centred on a variety of established formulae that estimate total 24-hour crystalloid-based fluid requirements. Using these formulae, the ABA guidelines recommend the estimation of 24-hour fluid volume using 2–4 ml/kg per %TBSA burned¹¹⁹. In practice, these formulae are primarily used to calculate the initial fluid infusion rate that should be initiated in the early phases of resuscitation after a severe burn injury, after which there is immediate divergence from the hourly fluid infusion rate estimates. This divergence stems from the fact that fluids are titrated to a target urine output (0.3–0.5 ml/kg per hour) rather than remaining fixed as the traditional formulae estimate. Hence, these formulae are used only to derive the initial fluid infusion rate. More recently, the Rule of Tens has been introduced to simplify the estimation of the initial fluid infusion rate and comprises three steps. First, the burn size (percentage TBSA) is estimated to the nearest 10. Second, the percentage TBSA is multiplied by 10 to compute the initial fluid infusion rate in millilitres per hour. Finally, for every 10 kg above 80 kg, an additional 100 ml/hour is required¹²⁰. This simple method of calculating the initial fluid infusion rate in adults (>40 kg) enables clinicians to focus on applying basic critical care principles to titrate the fluid infusion rate based on a combination of various end points (for example, lactate levels, extent of case deficit, mixed venous oxygen saturation, central venous pressure and mean arterial pressure) that are centred on a target urine output. A recent in silico validation study of 100,000 simulated patient weights and burn sizes determined that the Rule of Tens provides a reasonable initial fluid infusion rate across the entire spectrum of burn sizes and patient weights >40 kg¹²⁰. However, traditional methods of deriving the initial fluid infusion rate should probably be used in those patients at the extremes of weight. For those <40 kg in weight, especially paediatric patients, the initial rates will be higher than for those calculated based on 4 ml/kg per %TBSA burned. For those >130 kg in weight, the initial rates will be lower than those calculated based in 2 ml/kg per %TBSA burned.

Screening

The concept of screening in a patient with a burn injury is multifaceted given the complexity of the different physical and psychological elements involved and our growing understanding of functional recovery after injury. For example, screening for multidrug-resistant microorganisms early after admission can inform antimicrobial choice in the event of an infection. Standardized predictive formulae can provide estimates of the risk of developing complications such as acute kidney injury^121,122 and ARDS¹²³ after burn injury, but success with their use has been variable. The optimal smoke inhalation screening tool should be highly sensitive to avoid airway loss or respiratory failure due to missed diagnosis but must also be specific to avoid unnecessary intubation. Indeed, unnecessary intubation is associated with increased rates of ventilator-associated pneumonia and other upper airway complications including vocal cord and tracheal injury¹²⁴. Identifying which patients require early intubation to prevent loss of airway after smoke inhalation represents an ongoing area of equipoise¹⁰⁹. Unfortunately, biomarker identification for the development of predictive clinical decision support tools has so far eluded us.

Additionally, given what we know about the risks of emotional and psychological ramifications after burn injury¹²⁵ (see below, Quality of life), early screening for depression, acute stress and even substance use disorder may facilitate timely psychological and social interventions that will reduce the likelihood of prolonged mental health issues¹²⁶. Emerging data about increased use of health service resources by patients prior to a burn injury suggests an unmet opportunity for injury prevention¹²⁷; furthermore, knowing that a patient has frequently sought emergency care prior to a burn injury could indicate risk of mental health sequelae that warrants targeted intervention.

Management

Over 95% of fire-related burn deaths occur in low- and middle-income countries¹²⁸, where centres with burn expertise are sparse (Box 3). Even in the USA, access to specialized burn care has been repeatedly found to be limited, with up to 20% of the US population living >2 hours by ground or air from a verified burn centre¹⁰⁵. As such, training of health-care workers at basic-level facilities is essential to reduce death and disability from inadequately treated burns, especially under austere and low-resource conditions, including in low- and middle-income countries, war zones and mass-casualty incidents^129,130.

For all minor burn injuries, the steps of first aid (Box 4) are sufficient treatment; these steps are also recommended for the immediate treatment of more severe burn injuries. Indeed, in patients with more severe burns, phase I of the acute management includes the aforementioned primary and secondary surveys¹³¹. After the acute management phase, four major components of care follow upon admission to a burn centre: resuscitation, burn wound coverage, critical care and/or supportive care, and rehabilitation¹³² (Fig. 7). Another important aspect of planning burn care is predictors of outcome. One of the unique characteristics of burn injury is its reliable dose–response between the extent of the burn and outcome (that is, the larger the burn size, the worse the outcome). The Baux score combines the effect of the extent of the burn injury with patient age, and was described half a century ago. The Baux score is used to predict mortality following burn injury, with patient age and burn size (percentage TBSA) being equal contributors to predicted mortality. The Modified Baux score includes inhalation injury (present or absent), and is now the most widely accepted outcome predictor to date; it is applicable to patients of a wide range of age, including children¹³³.

Fig. 7. The phases of burn care.

Acute care for severe burns can be compartmentalized into five distinct phases that overlap during the first days to weeks after burn injury. Phase I is the initial assessment and triage, in which the injurious cause is removed and the primary and secondary surveys are conducted. Phase II is focused on fluid resuscitation to address hypovolaemia. In phase III, the wound is covered to promote healing and reduce infection risk. Phase IV focuses on supportive or critical care. If the patient survives, phase V of care focuses on rehabilitation, which includes physical and mental health support to enable the patient in returning to regular life. IV, intravenous; TBSA, total body surface area.

Burn outcomes should be validated against benchmarks and this concept was introduced by a multicentre trial (Glue Grant study)¹³⁴. More importantly, the ABA is actively working on a prospective database that will assess outcomes and compare the outcomes of a single centre against those of other burn centres within the ABA burn centre community, enabling objective evaluation of outcomes following burn injury.

Box 3 Burn care in low-resource areas.

Advances in our understanding of burn pathophysiology and management have resulted in improved burn care. Unfortunately, the majority of burn injuries occur in resource-challenged or austere environments (RAEs), where even basic burn care may not be available. Furthermore, preparation for potential mass casualty events must include plans for resource limitations, even in normally plentiful regions. The importance of this topic led the American Burn Association to sponsor a series of publications providing guidelines on burn care in RAEs^251,252.

Some key factors to consider in RAEs specific to burn care are: the knowledge level of the care providers; access to resuscitation fluid; and access to wound care. Ensuring that the ‘burn team’ is aware of the goals of treatment and the current standards in burn care is essential in any setting to ensure optimal outcomes. Indeed, participants in a burn disaster training course scored only 30% before training, a score that increased to 65% after training²⁵³. Work on education in RAEs has been undertaken by a number of organizations, including the Canadian Network for International Surgery (CNIS) and Interburns. The CNIS developed and published a standardized course for burn care (Essential Burn Management) that was developed and piloted in Ethiopia and Tanzania to meet local provider needs, and has increased knowledge in participants^254,255. Interburns has published Essential Burn Care, a resource for burn care education in RAEs²⁵⁶. More work needs to be undertaken to ensure that these materials are evaluated and appropriately disseminated.

Another unique aspect of burn care is the need for ongoing resuscitation in patients with major burn injuries. Often RAEs do not have access to intravenous fluids and, accordingly, interest in using oral rehydration solutions has increased^257–259, most notably the WHO solution, which comprises anhydrous glucose and salts in a prepared package to which water can be added. Current guidelines suggest that oral rehydration solutions can be used for burns up to 40%TBSA in size, and as an adjunct for larger burns; although a porcine study has shown improved renal function²⁵⁹ with such solutions, optimization in humans is still needed. A final factor specific to burn care is the need for antimicrobial dressings. The complex, silver-based, moisture control dressings used in high-resource environments may not be available; locally available alternatives such as Dakin’s solution or iodine-based solutions should be considered^260,261.

Box 4 First aid.

The immediate care for a patient with a burn injury depends on the cause of the injury (thermal, chemical or electric), the location of the injury and the availability of care resources. If the burn occurs at a remote place, first aid will likely be conducted by a bystander or person without medical training. The first step is to stop the exposure and move the patient into a safe area, which might include getting the person out from a trapped situation (for example, in a vehicle). If the individual’s clothing is on fire, suffocation to extinguish the fire is recommended²⁶² (by rolling and covering the burning clothing); otherwise, water or another fire extinguisher should be used. Next, the injury site should be flushed with cool water. This not only extinguishes the fire but also cools the wound and reduces the convection of heat and pain. However, use of cool water in this way increases the risk for hypothermia; accordingly, patients should be wrapped in clean dry blankets. Clothing and jewellery should be removed. For a chemical burn, copious flushing with water is recommended, but increases the risk of contamination of rescuers. Use of neutralizing agents is contraindicated as they induce heat. For electrical injures, stopping the current or using an insulator is important prior to touching the patient. Once these steps have been achieved, rescue teams or emergency services can be alerted and usual primary and secondary surveys can commence (see Diagnosis, screening and prevention). Wound care at the site of the accident involves removing burnt textiles, which can be replaced by clean sheets to reduce the risk of contamination of the wound and to maintain body temperature. Use of ‘home remedies’ such as butter, lemon, toothpaste, hydrogen peroxide ointments or onions is not recommended as many will further damage tissue. Transport principles to the local hospital vary according to the local geographic situation, but air transport may be recommended when the road transport time exceeds 2 hours or 100 km.

Special considerations

Paediatric patients

In general, the care path of a paediatric patient with a burn injury is similar to that of an adult. The initial approach is based on the principles of primary and secondary survey. However, the predominant differences in the care of a paediatric patient with a burn injury stem from the fact that, in children, the head represents a larger proportion of the TBSA and from the reduced overall physiological reserve of children. Newborn babies, for example, have a bigger head to body ratio with correspondingly smaller legs. Additionally, because children have limited glycogen stores, they should be given weight-based maintenance intravenous fluid in the form of 5% dextrose in 4.5% normal saline in addition to burn resuscitation fluid. The most important aspects of the care of a paediatric patient, as in adults, are to close the wound, treat hypermetabolism and plan for the long-term outcome.

Elderly patients

In patients >65 years of age, who have the worst outcomes after burn injury, pre-existing frailty is a major determinant of outcome¹³⁵. Elderly patients have a unique acute phase response after burn injury that is characterized by decreased organ perfusion and oxygenation¹³⁶. Furthermore, elderly patients are particularly prone to infection, mental health alteration and malnutrition, all of which are associated with increased morbidity and mortality¹³⁷.

Phase II: resuscitation

Burn shock, which combines hypovolaemic, distributive and cardiogenic features, occurs in the initial 48 hours secondary to the dysregulated inflammatory response after burn injury, and is characterized by a diffuse capillary leak wherein losses of proteins, electrolytes and plasma further reduce intravascular volume, impair end-organ perfusion and produce cellular dysoxia (aberrant cellular oxygen metabolism). As discussed previously, a number of factors contribute to the magnitude of the response, the combination of which contributes to considerable complexity and requires an individualized approach. In general, those with burn sizes >20%TBSA will require fluid resuscitation. However, patients with smaller burns may also require fluid resuscitation under circumstances in which other insults exists, such as electrical injury, smoke inhalation or concomitant trauma. The ultimate goal of fluid resuscitation is to maintain end-organ perfusion while avoiding resuscitation-related morbidity such as extremity, abdominal and orbital compartment syndromes (conditions characterized by acute increases in pressure in specific compartments, requiring emergent decompression to avoid cell death).

The initial fluid of choice is a balanced crystalloid, most commonly warmed Ringer’s lactate solution³⁸. However, in most patients with severe burns, exclusive use of a crystalloid solution can result in over-resuscitation (that is, a sustained high-volume crystalloid resuscitation that is associated with the development of resuscitation-related morbidity). To address this situation, ‘colloid rescue’¹³⁸ using other adjuncts such as albumin or plasma has been suggested.

Colloids: albumin or plasma

A recent meta-analysis of burn resuscitation outcomes¹³⁹ indicated that albumin-augmented resuscitation with 5% albumin as early as 8 hours after burn injury in those who are projected to receive a massive resuscitation (defined as those needing >1,500 ml per hour for 2 hours or >250 ml/kg in 24 hours) enables the infusion of a lower total volume of crystalloid in the first 24 hours. A previous randomized controlled trial has shown that the use of plasma, an alternative to albumin, reduces 24-hour fluid volumes, decreases intra-abdominal pressure and reduces subsequent development of abdominal compartment syndrome compared with administration of crystalloid¹⁴⁰. Additionally, plasma seems to have important advantages related to preserving the microvascular endothelium by maintaining the cell wall glycocalyx compared with other resuscitative fluids¹⁴¹. Unique to the use of plasma are the known risks of pooled blood product transfusions, which include transfusion-related lung injury. However, recent improvements in screening have mitigated this risk¹⁴².

Vitamin C

The antioxidant and reactive oxygen scavenging ability of vitamin C¹⁴³ prompted interest in its use during burn resuscitation. Initial animal studies were favourable, with decreased fluid requirement, oedema and capillary leak, and reduced lipid peroxidation, compared with crystalloid alone^143,144. In a small randomized trial in humans, high-dose vitamin C reduced 24-hour crystalloid fluid volumes and improved some ventilation and oxygenation parameters without a significant difference in mortality¹⁴⁵. Recent clinical data on vitamin C in patients with ARDS also seems positive¹⁴⁶, suggesting that vitamin C might have a beneficial effect in patients with burn injury. However, conflicting data on renal safety^147,148 and falsely elevated point-of-care glucose levels have prevented adoption of resuscitative vitamin C¹⁴⁹ and highlight the need for robust clinical trials of its use in patients with burn injury.

Blood purification strategies

Blood purification strategies are appealing because they aim to remove circulating inflammatory mediators¹⁵⁰. Indeed, retrospective studies of therapeutic plasma exchange (TPE) have demonstrated reduced resuscitative volume needs, improved mean arterial blood pressure, increased urine output and decreased lactate levels^150,151. Unfortunately, a single TPE treatment requires high volumes of either donor plasma or colloid, and consequently TPE is used by few centres due to cost and the resources required.

A more practical alternative to TPE may be haemofiltration. High-volume haemofiltration (HVHF) (doses >70 ml/kg per hour) may benefit patients in shock and can be used as an adjunct in those with burn shock^152,153. A recent multicentre trial in patients with burn injuries demonstrated that HVHF was effective in reversing shock and improving organ function¹⁵⁴. Another trial demonstrated that HVHF decreased the incidence of sepsis, duration of vasopressor treatment needed and mortality in patients with severe burn injuries¹⁵⁵. This study demonstrated a significant decrease in circulating inflammatory markers in the HVHF group compared with controls¹⁵⁵. These blood purification strategies may not be practical in a resource-constrained environment.

Phase III: burn wound coverage

In the first half of the 20th century, burn injuries were managed expectantly and, unfortunately, patients frequently succumbed to overwhelming sepsis while waiting for their burn eschar (scab) to slough, or for their open wounds to close by secondary intention (that is, allowing the burn injury to heal on its own). Topical antimicrobials slow the septic process¹⁵⁶ and have been instrumental in preventing those with larger, more-severe burns from succumbing to sepsis. However, improvements in survival and shortened length of hospital stay were only realized after the introduction in the 1970s of early excision and grafting^157–159.

Prophylactic systemic antibiotics are not used in the care of patients with an acute burn. However, topical antimicrobials have been the mainstay of nonsurgical burn treatment. Topical agents take a variety of forms: creams, ointments, liquids and impregnated dressings. The majority of dressing protocols use silver in some form owing to little clinical resistance by microorganisms. The literature to support one type of dressing over another is of variable quality and, accordingly, no clear consensus favouring one dressing is available; each regional burn unit tends to favour a particular dressing based on availability, personnel preference and historical experience¹⁶⁰. Regardless of the dressing chosen, some form of antimicrobial activity is desirable¹⁶¹.

Early excision, the gold-standard treatment, attenuates the hypermetabolic state and removes the biological nidus for infection, thereby reducing the risk of burn wound sepsis. Early autografting (that is, where skin is transplanted from a healthy (donor) site on the patient to the burned part) then builds on these improvements by rapidly closing excised wounds, further reducing infection risk, decreasing pain and enabling earlier mobilization. However, the optimal timing for ‘early’ excision is debated; for example, whether a patient undergoes surgery during the first day after burn, or 2–3 days later after completion of the 24-hour resuscitation, remains unclear. Regardless, the principle of excision and grafting is clear: close the wound. If a patient has good donor skin sites and is stable in resuscitation, autografting should be conducted while the wound bed is fresh and uncontaminated. If there are concerns about the viability or bacterial load on the wound bed and/or the patient’s stability, allografting (that is, using skin from another person (usually cadaveric)) should be used to temporarily cover the debrided wound. The surgical approach is to leave no full-thickness burned tissue behind and debride down to viable tissue.

Although many surgeons believe excising and covering the largest areas, such as back and trunk, should be performed first, in some centres the face and hands are covered first before transitioning to the body. We (M.G.J., S.L. and N.S.G.) believe that excision and coverage of the back and trunk have priority followed by the joints, legs and arms. Occasionally, valuable uninjured patches of potential donor sites can be ‘saved’ for use on important functional and cosmetic areas such as the hands and face. Our approach is based on the hypothesis that large burned areas contribute most to and augment hypermetabolism and inflammation and are, therefore, directly linked to poor outcomes. Once the larger areas have been covered, ‘healed’ skin can be harvested for delicate areas such the face, eyelids and hands; although cosmetic outcomes may not be optimal (owing to the reduced thickness of the skin), later reconstructions can be addressed once the patient is stabilized and out of hospital. Regardless of the order, skin grafts are usually meshed (that is, processed to ‘punch’ apertures onto the graft, allowing it to expand in size and permit ingress of topical agents and egress of serous fluid or blood) for the back trunk, legs and arms; sheet grafts (that is, donor sites that are excised and used as-is) are used for cosmetic areas such as the hands, face and neck.

Autologous split-thickness skin grafts

The gold-standard burn coverage is autologous split-thickness skin grafts (STSGs). Uninjured skin is harvested using a dermatome instrument, and the STSGs are transferred to an excised burn site. In burns covering >30–40%TBSA, available uninjured skin may be insufficient to allow definitive coverage in a single operation. In such cases, STSGs are frequently meshed and expanded to cover a larger excised area (Fig. 8); this approach trades aesthetic and functional outcomes for rapid closure and reduced donor site morbidity. For larger burns, usually >60%TBSA, mesh ratios >1:3 may be required, but are very technically challenging to use owing to fragility of the meshed skin, often resulting in substantial portions of the ‘grafted’ areas remaining open, necessitating overgrafting with allograft to functionally close the wound¹⁶². A solution to this issue is provided by Meek meshing technology, which expands the skin graft up to a ratio of 1:9 (Fig. 8). The expanded mesh can cover larger areas and the morbidity of poor scarring (see below) can be alleviated by combining the Meek technique with a dermal regenerative matrix and/or spray of a cell suspension¹⁶³, which can assist in closing the wound.

Fig. 8. Autologous split-thickness skin grafts.

For a patient with a severe burn injury to survive, the burn wounds need to be excised and covered. Temporary measures using allograft or various biological substitutes are available but, at this time only the patient’s skin (autologous) can permanently accomplish coverage. Several graft methods are available to cover burn wounds using autologous skin. a | Sheet grafts are the most aesthetically pleasing but require a lot of skin to cover wounds and, therefore, are usually reserved for small burns or for skin grafts to complex and important areas such as the face, hands and breasts. Full-thickness sheet grafts are reserved for smaller defects (usually lower eyelids and re-occurring upper eyelids) and play a more important part during the reconstructive phase. These are harvested using a dermatome. A split-thickness graft can be placed as a sheet graft or used for meshing. b | Use of meshed split thickness skin grafts is usually the method of choice to cover larger areas. The goal of meshing skin is to expand the donor skin to obtain greater coverage; skin can be meshed in ratios of 1:1.5, 1:2, 1:3, 1:4 or 1:6. Although increased meshing increases the coverage size, meshed skin becomes increasingly fragile. c | An alternative technique is the Meek technique, in which skin squares can be spread out to a large extent and added to the wound bed, covering large areas (up to a ratio of 1:9). This technology is reserved for extensive burns for which donor sites are sparse. d | A freshly meshed split-thickness skin graft (left) and its healing over time (right). Images in part c courtesy of R. Nijlant, Humeca B.V., Netherlands.

Failure of engraftment is typically the result of inadequate recipient site excision, shear stress or wound infection¹⁶⁴. Definitive coverage following large burns rapidly exhausts available donor skin and must, therefore, be performed in stages. When the excised burned area exceeds the available donor skin, ‘temporary coverage’ is needed to both permit donor site re-epithelialization in anticipation of re-harvest and to avoid the complications of open excisions. Common skin substitutes include cadaver skin (allograft) and porcine skin (xenograft), which provide temporary coverage for up to 14 days before inevitable rejection³⁶. STSG quality, quantity and the ability to re-harvest are functions of donor site skin thickness, harvested STSG thickness and the interval between re-harvests.

Artificial skin substitutes

In cases in which autologous skin is insufficient, thin and/or frail, artificial skin substitutes³⁶ can be used (Fig. 9). Composed of various biological, synthetic and biosynthetic materials, artificial skin substitutes can provide either temporary or permanent coverage of open wounds^165,166. In manufacturing skin substitutes, the scaffold is always taken into consideration. Scaffolds are 3D structures that act as a substitutes for extracellular matrix, providing the framework for neovascularization, cell adhesion, proliferation and differentiation. In addition, growth factors and cells can be added to the scaffold to enhance healing^167,168. Many variations are available, although all skin substitutes should demonstrate the following: resistance to shearing forces when handled; structure and function of normal skin that protect from fluid loss and infection; ability to act as a scaffold and enable cells to proliferate for wound healing; non-inflammatory, nontoxic and non-immunogenic composition; and affordability^169,170. For example, Skin TE (Polarity) is a technology where a skin biopsy is digested, sent to the manufacturer and then incorporated into a gel that contains epidermal and dermal elements, as well as skin appendages, that is directly applied to the burn wound¹⁷¹. Additionally, there are different classification systems for skin substitutes¹⁷². The Davison–Kotler classification¹⁷³ categorizes skin substitutes based their composition (cellular¹⁷⁴ or acellular¹⁷²), whether they are single layer or bilayer, their structure (epidermal (derived from human placenta)^175,176, dermal or composite (for example, a composite skin substitute composed of a bovine collagen, glycosaminoglycan bilayer and with a silicone layer that acts as the epidermis¹⁷²)), the type of biomaterial used (synthetic, biosynthetic or biological), and the duration of cover (permanent, semi-permanent or temporary)¹⁷⁷.

Fig. 9. Skin substitutes.

Skin substitutes have undergone development over the past decade from temporary materials used to induce wound healing towards permanent tissue-engineered materials that offer definitive healing. This figures reflects a summary of some promising skin substitutes or treatments to induce wound regeneration. a | The common principle of skin substitutes is to the deliver proteins, growth factors and/or cells via a delivery vehicle or matrix that will then be integrated into the wound and form new autologous skin. b | ReCell is not a composite skin substitute, but a device that sprays a cell suspension of skin cells including epithelial cells, fibroblasts melanocytes and other resident cells onto the wound or grafted area to improve healing and scarring. c | The skin gun (RenovaCare) delivers autologous cells and/or stem cells to wounds to improve wound healing. Although this is a promising approach, no clinical trials or substantial evidence have been reported that indicate that the skin gun will enter the clinical arena. d | Recently, a hand-held device has been designed that can print 3D autologous skin²⁴⁸. This device is based on microfluidic technology and can deliver cells specifically and accurately in an ‘ink’, which serves as a matrix. e | A skin substitute using autologous cells from a healthy donor and a matrix shows self-assembly of dermal and epidermal structures. Although the ideal tissue-engineered skin derivative has not been described, this technology will change the way burn care is delivered and will improve acute and long-term outcomes. Image in part b courtesy of Avita Medical. Image in part c courtesy of RenovaCare Inc. Part d provided by A. Guenther (University of Toronto, Canada), and adapted with permission from ref.²⁴⁸, Royal Society of Chemistry. Panel e is reprinted from ref.²⁶⁷, CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/).

Skin substitutes have also been used as biological or bioactive dressings that facilitate re-epithelialization of superficial partial-thickness burns underneath the skin substitute, ultimately functioning as definitive coverage¹⁷⁸. In selected patients with large burns, cultured epithelial autograft (CEA) can be used (Table 1). Although CEA can be used to cover large burns, it is limited by fragility, cost and the technical expertise required for optimal engraftment. When selected, use with an acellular dermal matrix may improve CEA outcomes¹⁷⁹. Additionally, Epicel is cultured skin derived from an autologous skin biopsy specimen; autologous keratinocytes are incubated for 2–3 weeks and grown into sheets of epidermal autograft.

Table 1.

Example commercially available skin substitutes

Name (manufacturer)	Composition	Advantages	Disadvantages	Refs
Epidermal: CEA
Epicel (Vericel Corporation, Cambridge, MA, USA)	CEA from human keratinocytes embedded in fibrin mesh	Autologous coverage of epidermis	High cost; limited reliability; fragile; increased susceptibility to infections; complex postoperative care; tendency for blistering; poor healing	268–270
Epidermal: autologous skin suspension or cell spray
ReCell (Avita Medical, Woburn, Massachusetts, USA)	Autologous skin suspension produced using minimal donor skin and applied as a cell spray.	Induces acceleration of re-epithelialization and wound healing; for wide meshes, most likely to improve appearance of scar	High cost; no dermal substitute; limited to more superficial burns	271,272
MySkin (Regenerys, Cambridge, UK)	Suspended CEA delivered as spray	Promotes re-epithelialization	No RCT data	273,274
SkinGun (RenovaCare, Inc., NY, USA)	Epidermal cells and stem cells	Expansion ratio of skin donor site to treatment surface area of ~1:20	No RCT data	275
Keraheal (MCTT, Seoul, Korea)	Suspension formed of cultured epithelial cells plus fibrin glue	Facilitates epithelial cell attachment	No RCT data	276
Dermal
OASIS Wound Matrix (Healthpoint Ltd, Ft Worth, TX, USA)	Derived from the submucosal layers of the porcine intestine; contains glycosaminoglycans and growth factors	Dermal element to improve scar appearance	Porcine composition; high cost	277,278
Matriderm (MedSkin Solutions Dr. Suwelack AG, Billerbeck, Germany)	Made of type I collagen fibre coated with 3% α-elastin hydrosylate matrix	Can be used as single-stage procedure with split-thickness skin grafts; very good outcomes in initial clinical trials	Possible increased susceptibility to infections	279
NovoSorb BTM (Biodegradable Temporizing Matrix) (PolyNovo, Melbourne, Australia)	Biodegradable polyurethane foam plus a temporary nonbiodegradable polyurethane seal; fully synthetic	Low cost; improves appearance; good results in initial clinical trials	No RCT data	280
MatriStem (ACell, Inc., Columbia, MD, USA)	Composed of extracellular matrix derived from porcine urothelium	Provides barrier protection	No RCT data	281
Integra (Integra LifeSciences, Plainsboro, NJ, USA)	Bovine collagen matrix with a silicone layer	Most-studied dermal replacement matrix; improves scarring and skin appearance; used in acute and reconstructive surgery; efficacy shown in RCT	High cost; possible increased susceptibility to infections	282,283
Alloderm (Allergan, Dublin, Ireland)	Human cadaveric acellular matrix	Improves scarring	High cost	284
SUPRATHEL (Polymedics Innovations GmbH, Denkendorf, Germany)	Synthetic copolymer >70% dl-lactide polymerized with ε-caprolactone and methylenecarbonate	Promising results in initial clinical studies	No RCT data	280
Composite
Self-Assembled Skin Substitute (SASS) (Loex, Quebec, Canada)	Reconstruction of a fully autologous bilayered skin substitute	No exogenous scaffold or biomaterial needed; good scar development; autologous	Requires a 31-day production period; very high cost; limited clinical data	279,285,286
Epifix (MiMedx, Marietta, GA, USA)	Composed of dehydrated amniotic and chorionic membrane containing collagen, connective tissue, cytokines and growth factors	Improves wound healing and regeneration	Not a skin substitute per se; no RCT data	287
Cultured skin substitute (prepared at Shriners Hospitals for Children, Cincinnati, OH, USA)	Autologous keratinocytes and fibroblasts from patient biopsy, combined into a bilayer with bovine collagen matrix	Good scaring; epithelial and dermal elements	High cost; long production time; does not include melanocytes	288

CEA, cultured epithelial autograft; RCT, Randomized controlled trial.

Scarring

A central part of the long-term outcome after burn injury is scarring; scars are optimally flat and minimally discoloured. After burn injury, normal scars are characterized by increased collagenase activity, lower TGFβ expression and macrophages with a predominantly M1 phenotype, which promotes T helper 1 cell subsets. However, burns can result in the development of a pathological scar. In particular, deep partial-thickness or full-thickness burns take longer to heal, which results in an increased risk of pathological scarring, especially when combined with a prolonged acute inflammatory phase. Pathological scars are characterized by excess collagen deposition, resulting in a thick, non-pliable defect that can cause itch, pain and contractures, limiting functionality¹⁸⁰.

Two primary subtypes of pathological scars occur after thermal injury — hypertrophic scars and keloids. Hypertrophic scars are more common in burn injuries and occur in 30–90% of patients with burn injuries¹⁸⁰. Delay (>3 weeks) in wound healing increases the risk of hypertrophic scarring¹⁸⁰, which is typically restricted to the confines of the initial injury and does not recur after excision. Decreased collagenase activity in hypertrophic scars leads to perturbed collagen production and degradation, resulting in bundles of crosslinked collagen oriented parallel to the epidermal surface¹⁸⁰. In particular, mature type I collagen expression is reduced and type III collagen is over-synthesized¹⁸¹. Additionally, hypertrophic scars have higher TGFβ and PDGF expression, macrophages with a predominantly M2 phenotype, which promotes T helper 2 cell subsets, and increased myofibroblasts compared with normal scars. Hypertrophic scar colour ranges from hypopigmented to hyperpigmented.

By contrast, keloid scars are occur mainly in those with darker skin pigmentation¹⁸⁰ and develop several months or years after the initial insult. Keloid scars are raised fibroproliferative lesions composed of disorganized bundles of type I and type III collagen. They exhibit tumour-like properties and are characterized by a dependence on anaerobic glycolysis to produce metabolites necessary for cell proliferation¹⁸². Furthermore, keloid scars demonstrate uncontrolled growth, invasion of normal tissues and recurrence despite treatment¹⁸³. Importantly, persistence of the inflammatory and proliferative phases of wound healing are likely to predispose patients to keloid scarring and results in a scar that grows beyond the initial burn wound¹⁸⁰. Keloid scar pigmentation can be increased or decreased compared with normal skin but is typically increased compared with the normal ‘baseline’ skin pigmentation of the patient.

Both keloid and hypertrophic scars detrimentally affect quality of life and are managed with a combination of intralesional pharmacological therapy, contracture release, scar excision, scar massage and laser therapy depending on the scar presentation.

Phase IV: supportive care

Given that wound closure is tied to improvements in both mortality and morbidity¹⁸⁴, supportive critical care that promotes optimal conditions for wound healing should be the clear focus of post-engraftment care. All aspects of care should be focused on optimizing the conditions for wound healing while preventing common hospital-acquired complications (for example, venous thromboembolic complications, stress ulcers, hospital-acquired and ventilator-associated pneumonia, catheter-related bloodstream infection and catheter-related urinary tract infection). Optimizing the conditions of wound healing includes haemodynamic support in the early phases (fluid resuscitation and occasional vasopressor support), optimization of nutritional support and use of pharmacological adjuncts to mitigate the impacts of hypermetabolism while promoting healing (such as propranolol and oxandralone)³⁶. At every phase of care, adequate pain control with the appropriate use of opioids and opioid-sparing adjuncts are paramount.

Phase V: rehabilitation

Despite an appropriate focus on medical and surgical interventions, planning for reconstruction and rehabilitation after major burn injury should begin at admission. To ensure a focus on ‘functional survival’, multidisciplinary burn teams are involved early upon hospitalization. Within these teams, physical and occupational therapists integrate rehabilitative principles throughout the continuum of burn care. Simple interventions such as proper limb positioning, splinting and incremental weight-bearing even in mechanically ventilated patients, can reduce burn contracture, minimize oedema and improve functional outcomes^185,186. A multicentre observational study in 307 patients with acute burn injuries demonstrated a significant link between increased duration of therapy and a decrease in the development of burn wound contractures¹⁸⁷ — the first study to demonstrate such a link between rehabilitative interventions and patient outcomes.

Occupational therapy, physical therapy and mobilization are crucial elements of care after burn injuries. These therapeutic approaches can improve joint stiffness, prevent heterotopic ossification (the formation of bone within the tissue where bone should not form) and improve muscle and tendon function. Additionally, the hypermetabolic response can be reduced with exercise⁷. Accordingly, exercise and therapy should be initiated as early as possible and mobilization should be started immediately after admission, keeping movement restrictions after surgery as brief as possible⁴⁹. Additionally, positioning of patients with burn injuries is imperative and anti-contracture positioning is central in the prevention of contraction and in improving graft take.

Not surprisingly, the psychosocial cost of severe injury is high on patients and their families¹⁸⁸. For this reason, it is advisable to fully integrate social workers, vocational counsellors and psychologists into the multidisciplinary burn team. Phase V has been neglected or even ignored for some time; it was only recently that we learned about the essential importance and value of good quality long-term outcomes after burn injury^125,126.

Quality of life

Health-related quality of life (HRQOL) is a multidimensional concept that reflects an individual’s perception of how a condition affects health-related domains for physical, psychological, emotional and social wellbeing that considers quality of life in relation to other health-related components (personal and environmental factors)¹⁸⁹. HRQOL is an increasingly studied outcome after burn injuries, in both the short and long term¹⁹⁰. Indeed, several tools can assess HRQOL in adult patients after burn injuries. For example, the Burn-Specific Health Scale–Brief (BSHS), Medical Outcomes Survey Short Form-36 (SF-36) and EuroQol (EQ-5D) questionnaires are often used^191–198. The use of both burn-specific and generic instruments provides insight into consequences of burn injuries in themselves and also in reference to other conditions^195,198. However, emerging data cast doubt on the psychometric quality of several burn-specific instruments¹⁹⁹. For example, the SF-36 domains were shown to be more sensitive to change than BSHS-B domains 1 month after burn injury in one study²⁰⁰. In addition, the specific psychometric properties of the BSHS-B are not yet available, including test–retest reliability (whereby repeated measurements over time show similar results in unchanged patients), validity of hypothesis testing and item-total correlations (whereby all items of a domain measure the same construct)¹⁹⁵. Thus, the optimal burn-specific instrument is not yet available. Several new instruments, including the Brisbane Burn Scar Impact Profile^196,201, the CARe burn scale²⁰² and the LIBRE survey²⁰³, warrant further validation. Of special note, instruments developed for surveying patients in high-income countries may not pertain to burn survivors in lower income countries²⁰⁴ or those living in rural or remote areas.

Models that can predict recovery of quality of life after burn injury can inform patients and health-care professionals on the expected outcomes, identify patients with expected suboptimal outcomes and enable the tailoring of treatment to optimize outcomes. Also, such models can be used for benchmark purposes²⁰⁵. Indeed, prognostication models for HRQOL after burn injury have been developed for use in children and adolescents^206,207. Spronk et al.²⁰⁸ have recently developed a prognostication model for use in adult patients (submitted for publication), which should be further validated in different burn populations.

Adults

Two studies have indicated that women report worse HRQOL 1 year²⁰⁹ and 10 years after a burn injury²¹⁰, but other reports suggest less consistent correlations between female sex²¹¹, pain and post-burn substance use disorder and poor HRQOL²¹². Furthermore, although HRQOL improves over time overall, some domains, including physical and emotional role participation, anxiety, depression and pain or discomfort, demonstrate delayed return to baseline after a burn injury²¹². Compared with the general population, patients who sustain severe burn injuries report lower quality of life, especially related to anxiety and depression, and pain and discomfort^213,214.

With increasing focus on post-intensive care syndrome, an increasingly understood condition in which critically ill patients are recognized to have longstanding physical and cognitive conditions²¹⁵, health systems must consider the long-term effects of hospital-acquired complications on functional recovery. Patients with burn injuries who experience a urinary tract infection, venothromboembolism, pulmonary complication or acute kidney injury during hospitalization reported lower physical component summary scores on the SF-12 for up to 24 months after the injury²¹⁶. Although in most quality of life studies, follow-up has been limited to 24 months after burn injury, emerging data suggest that patients struggle with functional recovery and HRQOL for as long as 10 years after the injury is sustained²¹⁰. As we become more familiar with the issues that drive long-term functional recovery, use of additional instruments such as Satisfaction with Life (SWL^125,217, which measures global cognitive judgments of satisfaction with life), Satisfaction with Appearance (SWAP^218,219, which measures body image dissatisfaction in persons with visible disfigurement), and the Community Integration Questionnaire (CIQ²²⁰, which measures levels of community integration) provide alternative options for assessing patient perceptions of their HRQOL.

Even patients with minor burn injuries report more anxiety and depression than the general population, despite having overall comparable HRQOL²¹³. A review of 19 studies²¹² showed that burn severity, post-burn depression, post-traumatic stress symptoms, avoidance coping, less emotional or social support, higher levels of neuroticism and unemployment predict poorer HRQOL, suggesting that the mental health aspects in survivors of burn injury are substantial.

Children

In children after burn injury, the Burns Outcome Questionnaire for children 0–5 years of age (BOQ_0–5)²⁰³ and the BOQ_6–18 (ref.²²¹) are valuable resources for quality of life assessment. The BOQ_0–5 consists of ten scales, ranging from play to appearance, whereas the BOQ_6–18 consists of 12 scales addressing physical functioning, emotional health and social functioning including school re-entry. However, the domains in these questionnaires correlate poorly with those of the WHO International Classification of Functioning, Disability and Health²²², suggesting that further development and validation of the BOQ surveys is required²²³. Indeed, few studies have addressed HRQOL in paediatric patients after burn injuries, especially in young children up to 4 years of age. Burn size and depth, length of hospital stay, presence of facial and hand burns, comorbidity and long recovery time predict suboptimal HRQOL following burn injury in children²²⁴. Studies in paediatric patients have shown improvements in HRQOL over the first 6 months after injury^223,224. However, some domains, including ‘concern/worry’ and ‘appearance’ in young children and ‘appearance’ and ‘parental concern’ in children 5–18 years of age, show persistent lack of improvement^224,225. Thus, children and adolescents seem to have continuing problems with changes in appearance, and parents have concerns related to their children after burn injury.

Assessing quality of life in children, especially those <12 years of age can be challenging. However, using parents as surrogates may in fact not reliably predict individual perception of quality of life. For example, using the validated questionnaire designed for adolescents (BOQ), adolescents and parents’ assessments of appearance, itch and school re-entry differed²²⁶. Thus, results on parent-reported quality of life should always be interpreted with caution and should ideally be checked with the child.

Employment and school after injury

Return to work and school are acknowledged to be important outcomes after burn care. Beneficial for individual health, social and societal aspects for individuals, work is not only a source of income but represents evidence of community integration and participation. Two systematic reviews showed that 66–74% of burn survivors returned to any form of work 1–24 months after the burn injury^227,228. Several factors predicted return to work, including burn severity, length of hospital stay, age, psychosocial and work-related factors^227,228. For example, one single-site study in Europe showed a high return to work rate of 92% in their population, in whom the mean burn size was 8%TBSA²²⁹; systematic reviews of studies in patients with burn sizes in the range 18–22%TBSA showed lower return to work rates. Regardless, the economic burden of burn injuries is substantial; in one European study the mean number of days absent from work was 59.3 per patient and the mean cost due to loss in productivity was €11,916 per patient (ref.²²⁹).

In children, there is minimal literature available on time to school re-entry. One review showed a short time to school re-entry (mean 10.5 days) in children 6–18 years of age after admission to a burn centre for burn injury with a median size of 14.3%TBSA; longer time to school re-entry was associated with male sex, older age and a longer hospital stay²³⁰. A recent literature review on school reintegration programmes after burn injury in children showed a wide range for time to school re-entry, and emphasized the critical role of a formal school reintegration programme to facilitate the transition and educating school personnel²³¹. Such a programme involves three stakeholders: the injured child, the child’s parent(s) or caregiver(s), and the teacher. Indeed, teachers play a central part in keeping up academic skills and facilitating social reintegration after burn injury²³¹. Clearly, gaps in knowledge related to our understanding of the barriers to returning to work and school must be addressed.

No data have been published on return to work or school after burn injuries in low- and middle-income countries, although data are emerging. One important issue related to employment is our definition of ‘work’: in many low-resource communities, individuals have a subsistence form of living in which work may not actually involve a paid job.

Secondary conditions

Recent publications have addressed long-term medical consequences of burn injury²³². In a cohort of patients with burn injury in Western Australia, linked hospital and death data indicated that both minor and severe burn injuries result in increased long-term morbidity and mortality in all age groups, as well as increased risk of hospital re-admission, long-term hospitalization and prolonged hospital stay for musculoskeletal diseases^233–235. Adult patients with burn injuries and patients with trauma showed elevated rates of post-injury admissions for cardiovascular events and an increased incidence of diabetes mellitus-related admissions during the first 5 years after injury²³⁶. Children with burn injury had a 1.6-times greater rate of long-term mortality than children with no injury²³⁷.

Outlook

What will the future of burn care bring? We believe that burn care must change to adjust to the challenges ahead.

Epidemiology and prevention

In the area of epidemiology, it would be important to know what the exact burden and effects of burn injuries are globally. To better identify needs, treatment, prevention and knowledge translation, capturing data more accurately is imperative, which should then lead to the development of strategies that translate this knowledge into actions. We believe that global agencies such as the WHO and the International Society for Burn Injuries should be integral to initiatives. Indeed, the WHO is piloting an important check-list initiative that does not require considerable resources for data structuring²². How these are translated into practice depends on the local circumstances, needs and resources.

Development of international burn registries should facilitate better understanding of burn injury aetiologies in many vulnerable populations. Cooperation between non-governmental organizations, national research networks, national health ministries and local communities to collect and analyse data about specific local aetiologies should increase awareness and knowledge, which could be subsequently applied to preventing burns. These data should include information on number of injuries, at-risk individuals and risk factors to identify vulnerable populations that could be targeted with burn prevention strategies that reflect local culture and availability of resources.

Diagnosis

Accurate measurement of burn size and depth are central for various treatment interventions. Absence of adequate methods to measure burn depth for superficial partial and deep partial burns makes it difficult to determine which wounds require surgery and which will heal with conservative treatments. New tools have been introduced, many of which are based on laser or thermal imaging technology, to examine skin perfusion to determine burn depth¹¹⁵; laser Doppler is a promising example, but others are emerging. Additionally, accurate burn size estimation is particularly challenging in patients with different body shapes, especially those with cachexia or obesity. Several burn measurement tools²³⁸ are being developed that are provider-independent, with the goal of increased accuracy.

Prognosis

We also need to develop instruments to evaluate variability among patients, how a patient will respond to burn stress and a patient’s likelihood of survival, towards the goal of personalized medicine. For example, sepsis and multiple organ failure are the main causes of mortality in patients after burn injury but burn care providers do not have an accurate means to diagnose, let alone predict, sepsis. Recently, a study compared the ABA sepsis definition with the Mann–Salinas definition and with the Critical Care Sepsis-3 definition²³⁹ (Box 1). The study showed that Sepsis-3 is the best and most accurate of the three formulae for identifying sepsis, but was only accurate in 85% of patients with burn injury²³⁹. Thus, better definitions need to be developed that more accurately predict and identify sepsis in patients with burn injury.

Sepsis was prospectively predicted with 100% accuracy during the first surgery using flow cytometry analysis of adipose tissue in a recent study²⁴⁰. Although these results are very promising, the study only included 37 patients and this technology cannot easily be translated to every burn centre. However, several other studies are also investigating prediction of sepsis and organ function after burn injury, and it seems only a matter of time until we are able to predict sepsis, multiple organ failure and death in patients. Once we can achieve accurate prediction, the challenge will be to change the trajectory. Some factors are being studied in a holistic approach to predict outcomes in the Glue Grant trial^51,52,241, a multicentre study examining genomic and proteomic changes after burn injury that is producing substantial data. Although the Gluegrant has completed its study, there are still studies and data resulting from this initiative that will enhance our knowledge on personalized medicine.

Acute care

Aspects of burn care also need further development, including resuscitation²⁴². Adequate resuscitation in patients with burn injury is challenging because questions abound regarding volume, composition, formulae and outcome measurement. An emerging technology is the ‘burn navigator’, which determines resuscitation parameters from urinary output data as a closed loop — adjusting fluid infusion volume automatically based on prior algorithms^243,244. This technology certainly has potential given that organ function such as cardiac function, and liver and kidney perfusion can be integrated, but it does require optimization. For example, urinary output is not ideal as it depends on several variables and can be misleading in determining resuscitation parameters (see above).

Another area of care that requires improvement is wound coverage. To overcome the need for uninjured donor skin in autologous STSG, artificial skin substitutes have been introduced to the market, and include TransCyte, CEA, cultured skin substitutes and various others^245,246 (Table 1). However, their application is limited in patients with burn injury due to cost, labour time and availability. Nonetheless, these products have changed the way we think about tissue-engineered skin¹⁷⁰. Currently, various approaches could change the treatment paradigm for burn wound care including stem cells²⁴⁷, stem cell ‘guns’ and 3D printing of autologous cells²⁴⁸ to recreate a patient’s skin that would reduce the risk of scarring and the need for donor sites, moving closer to our goal of no scar, no pain.

Long-term care

The historical belief that once burn wounds have healed, the patient is recovered is no longer valid. Indeed, the last phase of burn care — rehabilitation — is becoming one of the most important. Burn survivors have a substantially greater mortality than their matched non-injured counterparts, with the greatest risk of death during the first year after the injury (declining each year thereafter)^11,127. This increased mortality is related to trauma and mental illness, clearly indicating that survivors of burn injury have considerable care needs that are not being met. Indeed, burn survivors also have a decreased quality of life and struggle for a long time to adjust to their new life²¹⁰. At this time, it is not fully understood how we will diagnose, treat and prevent these long-term morbidities and, therefore, long-term studies to gain better insights are urgently needed.

The response to a burn injury is very complex, and so is the approach to its care. Although we have made some important strides in terms of survival following a burn injury, burn care needs to change over the next decades. New technologies need to be adopted in all phases of the recovery process to further improve burn outcomes, acutely and in the long term.

Author contributions

Introduction (M.G.J.); Epidemiology (S.L.); Mechanisms/pathophysiology (M.A.C., K.K.C. and M.G.J.); Diagnosis, screening and prevention (N.S.G. and S.L.); Management (K.K.C.); Quality of life (M.E.v.B. and N.S.G.); Outlook (M.G.J.); Overview of the Primer (M.G.J.). With the exception of M.G.J., all authors are listed alphabetically.

Competing interests

The authors declare no competing interests.