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History and Advancement of Burn Treatments

Liu, Hai-Fei MD, PhD; Zhang, Feng MD, PhD; Lineaweaver, William C. MD

doi: 10.1097/SAP.0000000000000896
Burn Surgery and Research

Advances in burn care have accelerated within the last 50 years. The principal modalities of and approaches to burn treatment include dressings, antimicrobials, fluid resuscitation, burn wound excision, skin grafting, and use of skin substitutes. This review presents a historical outline of these approaches, their current status, and prospects for the future of burn care.

From the *Joseph M. Still Burn and Reconstructive Center, Jackson, MS; and †Department of Orthopedic Surgery, the Affiliated Hospital of Qingdao University, Shandong, China.

Received July 18, 2016, and accepted for publication, after revision August 1, 2016.

Conflicts of interest and sources of funding: none declared.

Reprints: William C. Lineaweaver, MD, Joseph M. Still Burn and Reconstructive Center, Jackson, MS 39216. E-mail:

Burn treatments have been described since ancient times.1 Burns and their treatments are recognized in cave paintings which are more than 3500 years old. Documentation in the Egyptian Ebers papyrus of 1500 BC advocated a 5-day treatment regimen using a mixture of cattle dung, bees wax, ram's horn, and barley porridge soaked in resin for the topical treatment of burns. In 600 BC, the Chinese treated burn wounds with extracts from tea leaves. Nearly 100 years later, Hippocrates described the use of porcine skin mixed with a resin of bitumen impregnated in bulky dressings which were alternated with warm vinegar soaks augmented with tanning solutions made from oak bark. Celsus recommended a lotion with wine and myrrh for burns in the first century AD. In 300 AD, Hong Ge described a treatment of topical ointment made of old calcarea blended with plant oil or pig fat cooked with willow bark.2

In the middle of the 16th century, Ambroise Paré treated burns with onions and probably was the first to describe early burn wound excision. In the early 17th century, Guilhelmus Fabricius Hildanus discussed the pathophysiology of burns and made unique contributions to the treatment of subsequent cicatricial contractures. In 1797, Edward Kentish described pressure dressings as a means to relieve burn pain and blisters. In 1839, Guillaume Dupuytren reviewed the treatment of 50 burn patients with occlusive dressings and developed a classification of burn depth that remains recognizable today.3 He was also the first to recognize gastric and duodenal ulceration as a complication of severe burns, a concept described in more detail by Curling in 1842.4

The recognition of the importance of burn surface area and skin grafting by Reverdin in the 1800s clarified both the diagnostic and surgical understanding of burns.5 During and after World War I, consensus was reached that the best management of deep burn wounds included excision, skin grafting, and pain management. However, despite a centuries-long history of treatments for burns, many patients still died of shock and infection mainly because the fundamental understanding of the pathophysiological effects of burns was not clear.6 Research inspired by fire disasters such as the Rialto fire in 1921 and Coconut Grove nightclub fire in 1942 provided the first operational understandings of the pathophysiology of burns.6

Based on the index of mortality, it is evident that our ability to treat burn injuries has improved remarkably since World War II. The statistic that 50% lethal area, which is fatal for 50% population, was approximately 40% total body surface area (TBSA) for young adults in the United States in the immediate postwar era. By the 1990s, it increased to approximately 80% TBSA.7 According to Bull and Fisher,8 complications such as shock, sepsis, and multi-organ failure resulted in a 50% mortality rate in children with burns covering 50% TBSA between 1942 and 1952. The mortality of children with 80% TBSA or greater burns was only 33% on a large sample study during 1982 to 1996.9 According to a more recent study, a 98% TBSA injury now has a 50% survival rate in burned children.10

Burn treatment is a complex undertaking and involves many components. Elements presented in this brief review include burn dressings, infection control of the burn wound, fluid resuscitation, and burn surgeries. Advances in each of these elements have continued to contribute to survival and functional recovery of burn victims.

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The application of dressings began in ancient times and included increasingly explicit goals of preventing infection, promoting reepithelialization, avoiding water and heat loss, keeping the wound moist, and decreasing pain. A variety of biological, semibiological, and other dressings can and have been used to cover burn wounds, to aid epithelialization, and to protect the excised wounds from desiccation, infection and mechanical trauma.11 Biological dressings, such as allograft skin,12 xenograft (e.g., porcine skin),11 and human amnion,13 have been used to cover the wound while reepithelialization occurs. The use of these biological dressings has been associated with problems, including availability, tissue collection, storage, and, importantly, transmission of infection and high costs.14

Conventional dressings such as Vaseline gauze or silicone sheets (i.e., Mepitel) and synthetic dressings such as Mepilex, DuoDERM, Omniderm, Tegaderm, and hydrocolloids can be used to cover the wound while reepithelialization takes place.15

A number of silver containing dressings are currently used for burn care including ACTICOAT*, Mepilex Ag and Aquacel Ag products. ACTICOAT* is a bilayered polyethylene nanocrystalline silver dressing attached to a soaking coat of polyester that can provide sustained release of silver for up to 7 days.16 ACTICOAT* was substantiated to have better antimicrobial activity and reduce grafting requirements compared to silver sulfadiazine.17,18 ACTICOAT* was also demonstrated to have fewer adverse effects and reduce healing times.19 Mepilex Ag is a soft and highly conformable antimicrobial foam dressing that absorbs exudate and maintains a moist wound environment. The soft silicone layer minimizes the risk for maceration and reduces pain and damage to the area during dressing changes. Mepilex Ag is clinically proven to heal burns faster and with less pain and cost compared to silver sulfadiazine.20 Aquacel Ag products use a hydrofiber for absorption plus ionic silver. The easy application and low frequency of dressing change make these dressings practical dressings in burn care.

Recent development in dressing and bioengineering technology have introduced dressings and gels containing naturally occurring glycosaminoglycan and chitin,21–24 with incorporation of growth factors into the gel.25,26 These dressings have been reported to prevent early extension of burns27 express antimicrobial properties,28,29 and promote fibroblast proliferation, angiogenesis, and wound healing.30 Carbon fiber dressings have been more recently studied and demonstrated to increase the absorptive capacity of the dressing, reduce inflammation and bacterial growth, and promote wound healing.31,32

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Sepsis has been the most frequent cause of death after burn injury and contributes to almost 75% to 85% of all burn deaths.33,34 An important advancement in burn care that has dramatically reduced mortality is infection control.

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Systemic Antibiotics

The origin of modern scientific infection control in burn patients began with Leonard Colebrook, a physician, bacteriologist, and colleague of Alexander Fleming. Colebrook proposed that burn wounds became infected with bacteria and that strict infection control practices could prevent infection by reducing transfer of organisms between patients in a specially designed burn unit.35–37 Colebrook also studied the use of dressings impregnated with sulfanilamide and penicillin creams,35,38 and serum and plasma for burn shock resuscitation at the Glasgow Royal Infirmary.39

Lyons et al,40 managing burn patients at Massachusetts General Hospital, found that hemolytic streptococcal infection responded to sulfa drugs and an effective blood level of sulfonamide offered the most certain control of systemic infection due to the hemolytic streptococcus. However, in 1943, based on a study with 1500 patients, Meleney concluded that neither local nor systemic sulfonamides were effective at controlling local wound infection, and that inadequate surgical excision predisposed to infection.41

Emerging resistance by staphylococcus and clostridium to sulfa drugs stimulated research on penicillin. The discovery of penicillin by Alexander Fleming, the Scottish biologist, pharmacologist, and botanist, in 1928 was a major breakthrough but its clinical utility was not appreciated until 1940, when Chain, Florey, and others demonstrated the new drug’s life-saving potential against streptococcus, staphylococcus, and clostridium infections in murine and human studies.42,43

Organisms associated with infection in burn patients include gram-positive, gram-negative, and viral and fungal organisms. Systemic antimicrobials must be thoughtfully considered for burn patients to prevent the emergence of resistant organisms.

Burn infections caused by the most common gram-positive organisms, streptococci, staphylococci, and enterococci, can be treated with penicillinase-resistant penicillins if the organisms are methicillin-sensitive. Staphylococcal infections resistant to penicillinase-resistant penicillins are termed methicillin-resistant staphylococcus aureus (MRSA) or methicillin-resistant staphylococcus epidermidis (MRSE). Vancomycin has been considered the antibiotic of choice for infections caused by MRSA and MRSE.44 Linezolid was considered the choice for oral treatment of MRSA and MRSE infections.45 Most enterococci are susceptible to vancomycin. Vancomycin-resistant enterococci will require treatment with combined medications, such as ampicillin/aminoglycosides, or a quinupristin/dalfopristin combination.

The aminoglycosides were historically the antibiotics of choice for gram-negative infections. However, some gram-negative bacteria in burn patient infections are now resistant to almost all the antibiotic classes and must be treated with the polymixins. Branski et al46 concluded that colistin, or polymyxin E, was a safe and efficacious antimicrobial drug for adult and pediatric burn population without a marked incidence of toxic side effects, but should be used only with close monitoring of renal function.

The 5 classes of systemic antifungal drugs used in this setting include the polyenes (Amphotericin B), azoles, nucleosides (Flucytosine), echinocandin, and allylamine.45,47 Drug choices for treating fungal infections should be based on specific organisms isolated or suspected.

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Topical Antimicrobials

The high susceptibility of burn wounds to infection, coupled with increased antibiotic resistance among pathogenic bacteria and fungi and the difficulty of systemically administered antibiotics in reaching injured tissue, have contributed to the ongoing development and use of topical antimicrobials in the treatment of burns.

The aim of topical therapies has changed with the increased understanding of the pathophysiology of burns. In the early 20th century, the goal of topical therapies was to counteract the “toxins” released from burn wounds and to minimize fluid loss. In 1925, Davidson asserted that use of tannic acid in burn care not only lessened toxemia, but also provided analgesia, prevented body fluid loss, limited infection, decreased scar formation, and generated a scaffold for healing.48 Its use was stopped when it was found to lead to lethal liver necrosis.49

Sodium hypochlorite (NaClO), one of the first topical antimicrobials, was discovered in the 18th century by Berthollet and was widely used as a disinfectant throughout the 19th century. Its use was hampered by the frequently encountered irritation and topical reactions, but these side effects were later discovered to be due to variables in quality and chlorine in different preparations of the solution.50 In 1915, Dakin successfully synthesized hypochlorite solutions without irritating contaminants and proposed the concentration of 0.5% NaClO as most effective.51 During World War I, Dakin teamed up with the famous French surgeon and Nobel Prize winner Alexis Carrel to develop a protocol for wounds and burns. They specified mechanical cleansing, surgical debridement, and topical application of hypochlorite solution.52 In 1985, Lineaweaver et al53 found that the cellular toxicity of hydrogen peroxide and acetic acid exceeded their bactericidal potency, but concentrations of povidone-iodine and sodium hypochlorite were identified without fibroblast toxicity but with persistent bactericidal activity. Recently, Heggers et al54,55 investigated concentrations of sodium hypochlorite for antibacterial activity and tissue toxicity in vitro and in vivo, and found that a modified “Dakin's” solution at a concentration of 0.025% NaClO had sufficient bactericidal properties but eliminated detrimental effects on wound healing.

Pruitt et al56 achieved a remarkable improvement in postburn mortality in 1964, with the use of a topical antimicrobial, mafenide acetate (Sulfamylon) cream, which was effective against Gram-negative burn wound infections. Meanwhile, mafenide acetate was also adapted for treating burns at the Institute of Surgical Research in San Antonio, Texas, by microbiologist Robert Lindberg and surgeon John Moncrief.57 This antibiotic could penetrate third-degree eschar and was extremely effective against a wide spectrum of pathogens. Because of its capacity for deep penetration of burn eschars, mafenide acetate appeared particularly effective in the treatment of full-thickness burns with significant devitalized tissue.58 It is however a carbonic anhydrase inhibitor and can cause systemic acidosis, compensatory hyperventilation, and pulmonary edema. Therefore, the duration and area of mafenide acetate application must be limited to prevent systemic toxicity associated with prolonged or extensive use.57,58

A major milestone in topical burn therapy was the application of silver compounds, mentioned above, which remarkably reduced the incidence of burn wound sepsis and death. Silver based topical therapies were especially effective in controlling Pseudomonas aeruginosa infections.

In 1965, Moyer et al59 used 0.5% silver nitrate solution as an effective topical antibacterial agent for the treatment of burn wounds. Simultaneously, Fox et al60,61 developed silver sulfadiazine cream (Silvadene), which has become a mainstay of topical antimicrobial therapy due to its success in controlling infection and minimal side effect profile.

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The history of burn resuscitation can be traced back to the treatments and subsequent studies of severely burned patients in large urban fire disasters such as those at the Rialto Theatre (New Haven, Conn) in 1921 and the Coconut Grove nightclub (Boston, Mass) in 1942, when physicians noticed that some patients survived the large burns but died from the secondary shock. As burn size approaches 15% to 20% TBSA, hypovolemic shock sets in if no appropriate fluid resuscitation is conducted.62 In adults with burns approaching 25% to 30% TBSA, damage to cell membranes also occurs in hypovolemic shock, resulting in a decrease in transmembrane potential and the accumulation of intracellular sodium and water.63

It has been advocated that for maximum benefit, fluid resuscitation should begin as early as 2 hours after burn.9,64 The goal of fluid resuscitation is to prevent hypovolemic shock by maintaining adequate end-organ perfusion. Meticulous attention to details and frequent reassessment is necessary to avoid the dangers of excessive or deficient fluid administration.

Mechanisms that control protein and fluid loss from the vascular space are compromised after severe burns and the subsequent inflammatory reaction that follows the burn injury. The margination of neutrophils, macrophages, and lymphocytes into these areas is associated with the release of a variety of inflammatory mediators, including histamine, serotonin, prostaglandins, platelet products, complement components, and members of the kinin family, which affect and disrupt local and systemic vascular permeability.65 The end result is an immediate shift of intravascular fluid into the interstitial space.

The foundation of current fluid resuscitation approaches began with the studies of Underhill, who found the composition of burn blister fluid was similar to that of plasma and suggested that early burn mortality might be due to loss of fluid rather than toxins. Underhill identified the significance of loss of the liquid and protein components of the blood in the burn area and proposed the concept of thermal injury–induced intravascular fluid deficits in the 1930s and 1940s.66,67 Moore et al subsequently developed the concept of the burn edema and introduced an initial formula of infusion therapy in relation to the severity of the injury.68 At that time, as little as 10% to 20% TBSA burns were associated with high rates of mortality. In the 1970s, a 30% TBSA in burns could lead to nearly 100% mortality in older patients.69

In 1930, Underhill proposed blood hemoglobin percentage as an index of resuscitation, and asserted that resuscitation aimed at preventing hemoconcentration is required for 24 to 36 hours postburn. Intravenous sodium chloride solutions were used, supplemented by oral, rectal, and subdermal solutions.66 Based on hemoconcentration, Harkins proposed a formula of fluid resuscitation for burn patients: 100 mL of plasma for each point when the hematocrit exceeds 45. Furthermore, when hematocrit detecting was unavailable, he recommended the “First Aid Method”: 500 mL of plasma for each 10% TBSA burned.70

In 1943, Cope et al71 suggested that the initial dosage of plasma should be determined on the basis of the surface area of the burns. For each 10% TBSA involved, they proposed to give 500 mL plasma in the first 24 hours. The plasma dosage was adjusted subsequently on the basis of repeated hematocrit and serum protein determinations. Meanwhile, the National Research Council (NRC) advocated 1000 mL of plasma for each 10 percent burned area over the first 24 hours.72

In 1944, Lund and Browder73 developed diagrams by which physicians could easily and accurately quantify burn surface area. This quantification led to fluid resuscitation strategies based on TBSA burn calculations. Knaysi et al74 advocated a simple “rule of nines” for evaluating the percentage of body surface area burned. In the late 1940s, Cope and Moore75 were able to quantify the amount of fluid for adequate resuscitation based on the percent of the body surface area burned and described a revised NRC formula called the Surface Area Formula in 1947: 75 mL of plasma and 75 mL of isotonic crystalloid solution for one percentage of TBSA, with one half given in the first 8 hours, and one half in the next 16 hours. Urine output was used as the primary index of resuscitation. Moore went on to develop a formula for estimating the amount of fluid for adequate resuscitation based on the burned percentage of body surface area in 1970.68

Multiple subsequent formulas included body weight in the calculations and variations in both the volumes per weight per TBSA and the types of crystalloid or crystalloid-colloid combinations administered. Well-known resuscitation recipes included Evans Formula (colloid 1 mL/kg/TBSA, crystalloid 1 mL/kg/TBSA, and 5% glucose 2000 mL for the first day; one half these amounts colloid and salt second day), Brooke Formula (colloid 0.5 mL/kg per TBSA, and crystalloid 1.5 mL/kg per TBSA, plus 2000 mL glucose for the first day; colloid, 0.25 mL/kg per TBSA; and crystalloid, 0.5 mL/kg per TBSA, plus 2000 mL glucose for the next day), and Modified Brooke Formula (crystalloid 2 mL/kg per TBSA, one half for the first 8 hours and one half over the next 16 hours).76–78

The use of colloid solutions in the fluid resuscitation of burns could effectively reduce the edema formation and amount of fluid required. Patients with severe burns, preexisting heart disease, and inhalation injuries may benefit the most from lower-volume resuscitations aided by colloid. Colloids used in burn resuscitation have included dextran, albumin and plasma.79–81

Baxter and Shires82 postulated that protein administered in the first 24 hours postburn would leak out of the vessels and exacerbate edema. They therefore developed a crystalloid based formula without colloid, which is now referred to as the Parkland formula and is perhaps the most widely used formula today. The Parkland Formula recommends 4 mL of Lactated Ringer’s solution (RL)/kg/% TBSA burned during the first 24 hours of resuscitation after a burn injury. Half the volume is given in the first 8 hours postburn, with the remaining volume delivered over the subsequent 16 hours.82

To date, no single recommendation has been established to be the best fluid resuscitation formula for burns.83,84 Fluid resuscitation formulae are only guides to assist in estimation of fluid requirements, as each patient reacts differently to burn injury and resuscitation. Regardless of the formula or strategy used, the first 24–48 hours require frequent adjustments by clinical indicators of the adequacy of resuscitation.83 Over-resuscitation can be a major source of morbidity for burn patients. Fluid overload during the critical early management can result in unnecessary edema, pulmonary dysfunction, and extended ventilator support.85,86

Although the end points for fluid resuscitation are still controversial, the hourly urine output is a well-established parameter for guiding fluid management. The urine output should approach 0.5 mL/kg per hour or approximately 30 to 50 mL/h in most adults and older children (>50 kg), and approximately 1 mL/kg per hour in small children.87 Yowler and Fratianne69 suggested that the goal of fluid resuscitation is to maintain urine output in the range of 0.5 to 1 mL/kg per hour for adults and 1% to 1.5 mL/kg per hour in children.

Certain patient populations frequently require higher fluid resuscitation volume. Patients with delayed resuscitation, alcohol abuse, trauma, or inhalation injury may require greater fluid resuscitations than predicted. Patients with inhalation injury sometimes required as much as 30% to 40% higher fluid supplement than calculated by fluid resuscitation formulae for adequate resuscitation.88

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In 1510 to 1590 AD, Ambroise Pare described early excision of burn wounds. In 1607, Hildanus also recommended removal of burn eschars to facilitate drainage of serous fluid and allow better medication penetration. Limitations of technique, blood replacement, and perioperative support made excision of large burns impossible.89

In the 1940s, along with advancements in topical infection control and fluid resuscitation, it was recognized that one of the most effective therapies to reduce mortality in thermal burn injury was the early excision of burn eschar and subsequent skin grafting.90 Physicians applied pyruvic acid and starch to full thickness burns, followed by grafting as early as 6 days postdebridement.91 Young, McCorkle and Silvani, and Saltonstall and Lee92–94 subsequently reported extensive experience with surgical excision of full thickness burns in the 1940s.

In the late 1950s, Jackson et al95 advanced the concept of early excision technique in a series of pilot and controlled trials by immediate fascial excision and grafting of small burn areas, and eventually covering up to 65% TBSA with autograft and homograft skin. They concluded that excision and grafting of 20% to 30% TBSA could be carried out on the day of injury safely as long as shock was controlled by red cell volume monitoring. In 1964, Walker et al96 advocated early excision, starting postburn day 4, for patients with large burns, and immediate coverage with a combination of autograft and cadaver allograft. This technique was not accepted by the majority of surgeons because of controversy over expected outcomes, including mortality, infection, unnecessary blood loss, and total healing time.

It was not until the introduction of tangential excision by Janzekovic97–99 in the 1970s that early excision in burns achieved greater acceptance. She reported 2615 patients treated for deep second-degree burns by tangential excision of eschar and the damaged dermis down to bleeding tissues and immediate grafting with autograft 3 to 5 days after burn injury.97 Application of the technique was limited to small burns that could be covered by autografted skin.100 For the treatment of larger burns, Monafo101 (early 1970s) was one of the first to advocate the use of tangential excision and grafting. Burke et al102 treated children with burns over 80% TBSA with a combination of tangential excision for the smaller burns and excision to the level of fascia for the larger burns, and coverage with split-thickness allografts, achieving a remarkable decrease in both hospital time and mortality. In a randomized prospective study, Engrav et al103 reported that early tangential excision and grafting of deep second-degree burns improved mortality and also reduced hospitalization time when compared with conservative treatment.

In a retrospective study, Tompkins et al104 reported an improvement in mortality over the course of 1974 to 1984 through the application of prompt eschar excision. Herndon and Parks105 implemented an early total excision (within 48–72 hours) to fascia with application of 4:1 expanded autograft and cadaver skin for complete closure in the treatment of large burns in children. The results included a decrease in length of stay but not in mortality. In a randomized prospective trial of 85 patients with third-degree burns greater than 30% TBSA, early excision gained significantly decreased mortality in patients who were 17 to 30 years old without inhalation injury, no different mortality in adult patients older than 30 years of age or with a concomitant inhalation injury, and significantly increased mortality in children when compared with therapy of topical antimicrobial and skin grafting after spontaneous eschar separation.100 In 1988, Tompkins et al106 also credited the use of prompt eschar excision and grafting for the dramatically decreased mortality in severely burned children. A recent meta-analysis found that early excision of burns was beneficial in reducing mortality in patients without inhalational injury.107

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The earliest record of skin grafting can be traced back to the fifth century AD, when Sushrutha, an Indian surgeon, repaired the wounds of noses using reversed skin from forehead and transplanted skin from the buttocks.108,109 The first documentation of modern skin graft in humans was in 1823, when Carl Bunger treated a nose wound with full thickness skin from the inner thigh. The early success rate of skin grafts was low because of the inefficient harvesting and use of thick grafts.109 In 1869, Reverdin, a Swiss medical student, introduced “pinch grafts,” small circular skin discs, to deal with slowly healing or chronic wounds.110 The method was soon popularized in England by George Pollock.111,112 Thiersh et al113 advocated the use of “razor flaps” in 1874. Generally, these methods were restricted to the treatment of small ulcerated wounds.

In the 1920s, Blair and Brown114 discovered that deep islands of hair follicles and epithelial cells could be the basis of healing at skin graft donor sites. Split-thickness skin grafts subsequently became popular in the 1930s. After free hand blades with imprecise control over graft thickness, such as the Blair and Catlin knives, tools allowing precise thickness control of skin grafts quickly developed.115

Padgett116 introduced an adjustable dermatome which allowed the harvest of consistent split-thickness skin grafts. Padgett117 also advocated a categorization of split skin grafts based on thickness. The meshing of grafts was first achieved by Lanz118 in 1907, who designed a special dermatome consisting of a series of small knives mounted in parallel to make multiple holes in a skin graft, forming a mesh. Meek successfully conducted microdermagrafting using the Meek-Wall microdermatome and prefolded gauzes to expand the graft size as much as nine times the original size.119,120 Due to its operational complexity, the Meek microdermatome was substituted by the simpler “mesh dermatome” developed by Tanner et al in 1964. This device allowed a three-fold expansion of the harvested graft and other mesh machinery can expand grafts in ratios of 1:1 to 9:1.121 Recent studies using the modified Meek technique have demonstrated some advantage over mesh grafts when donor sites are limited, especially in extensive burn wounds.122–124 Furthermore, Lyons and Kagan125 also recently found that there was great variability in the expected and observed expansion ratios achieved by skin graft meshing devices. Kamolz et al120 also demonstrated that the micrografting technique provided more reliable and valid expansion rates, when compared with the skin meshing techniques. They recommended using the micrograft technique when large expansion ratios are required, especially in severe and extensive burns.

The first successful use of allogeneic skin graft in burn wound coverage was reported by Girdner126 in 1881. In 1938, Bettman127 reported success in the treatment of children with large full-thickness burn injuries covered by allograft skin. Cadaveric allogenic skin grafts were often used to prepare the granulating wound bed for autografting. In 1954, Jackson128 introduced a combined grafting technique, which used narrow strips of allograft and autograft in a granulating or excised wound. Walker et al96 advocated an early excision and immediate coverage with a combination of autograft and cadaver allograft for patients with large burns. In massively burned patients with limited donor sites, Alexander et al129 developed a simple method of applying a widely meshed skin autograft and then covering it with allogenic skin.

With the advance of tissue engineering techniques, skin substitution became a prominent topic in wound-healing research. In the 1970s, Yannas and Burke developed the first bilayer artificial skin, Integra, which consists of a silastic epidermis and a porous collagen-chondroitin dermis. Burke et al130 were also the first to use this artificial skin on patients with 50% to 95% TBSA burn after prompt excision of burn wounds. Heimbach et al131 led the first multicenter randomized clinical trial using Integra in 1988. In 1989, Hansbrough et al132 reported burn wound closure with cultured autologous keratinocytes and fibroblasts attached to a collagen-glycosaminoglycan substrate (composite skin graft, CSS). Further study by Boyce133 substantiated that the use of CSS in extensive burns reduces the requirement for harvesting skin autografts, and that the quality of grafted skin was similar between CSS and skin autograft after 1 year. Fang et al134 reviewed the research using cultured epithelial autografts and the acellular dermal matrices in the treatment of extended burn injuries and concluded that the use of acellular dermal matrix with cultured epithelial autografts is becoming increasingly routine, particularly as a life-saving tool after acute thermal trauma. Cultured skin autografts provide possible material for wound closure for patients with extensive burns, although the hospital cost, length of hospital stay, and number of readmissions for reconstruction of contractures is reported to be higher than conventional autografts.135–137

After approval by the Food and Drug Administration in 1996, Integra has been widely used in burns and reconstructive surgery. Other artificial skin substitutes include Apligraf (a bilayered bioengineered skin substitute constructed by culturing human foreskin-derived neonatal fibroblasts in a bovine type I collagen matrix) and Matriderm (a scaffold consisting of native bovine types I, III, and V collagen fiber template incorporating elastin hydrolysate).138,139

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Although amniotic membrane has been used for well over a century as a biologic wound cover, in Western medicine its use was first reported for skin transplantation in 1910 by Davis, and as a treatment for burns in 1913 by Sabella.140,141 In the late 20th century, use of fresh amniotic membrane was precluded due to issues relative to obtaining, preparing, and storing the tissue for use in clinical practice, as well as concern regarding the potential for infectious disease transmission. More recent advanced processing methods to make amniotic membrane available in forms that are convenient and safe allow more widespread use of the tissue in contemporary practice. In 2006, a dehydrated amnion chorion membrane (dHACM) allograft (EpiFix; MiMedx Group, Inc., Marietta, GA), was made available in the market as a HCT/P tissue allograft for the treatment of acute and chronic wounds.

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The advancement of burn treatments has been very significant over the last 75 years. The mortality of severely and extensively burned patients has significantly decreased due to the improvements in infection control, early resuscitation, improved surgical approaches, and other treatments basing on the better understanding of the burn pathophysiology.

Establishment of a standardized, generally accepted, and effective formula of fluid resuscitation of burns still merits further investigation. Limited donor skin and deficiency of eligible skin substitutions in severely burned patients hinders early and effective wound excision and closure, leading to complications and prolonged hospitalizations. Biologic dressings and skin substitutes have contributed to improved outcomes for patients suffering from acute and chronic wounds.142 Tissue engineered skin substitutes with all the functions of intact human skin and amniotic membrane allografts, such as dHACM, may offer the best opportunity for better outcomes.142 Better understanding and management of the pathophysiology of burn scar contractures and hypertrophic scarring are also important areas deserving research.143,144

Having reviewed the History and Advancement of Burn Treatments, the following articles in this Supplement will address other important topics in the current and future management of burn patients. These will include articles by Herndon and Branski on advances in the use of amniotic membranes as biologic burn dressings; by Tenenhaus on the use of human amnion/chorion membranes in the treatment of burns and complex wounds—current and future applications; by Glat and Davenport on current techniques for burn reconstruction, including the use of dehydrated amnion/chorion membrane; and by Glat on the evolution of burn injury management in clinical practice. Lastly, a series of cases in which dHACM allografts were used in acute and reconstructive burn care are presented by Reilly, Goverman, Glat, and Lineaweaver. Together, these articles provide a comprehensive overview of the current approaches and future considerations in the treatment of these severely injured patients using dehydrated amniotic membrane allografts.

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1. Artz CP. Historical aspects of burn management. Surg Clin North Am. 1970;50:1193–1200.
2. Majno G. The healing hand: Man and wound in the ancient world. Harvard University Press Cambridge: Mass; 1975.
3. Dupuytren G, Brierre de Boismont AJF, Paillard ALM. Leçons orales de clinique chirurgicale, faites à l’Hôtel-Dieu de Paris. Baillière Paris. 1839.
4. Curling TB. On acute ulceration of the duodenum, in cases of burn. Med Chir Trans. 1842;25:260–281.
5. Reverdin J. Greffe epidermique. Bull Soc Chir (Paris). 1869;10:511–515.
6. Ribeiro PS, Jacobsen KH, Mathers CD, et al. Priorities for women's health from the Global Burden of Disease study. Int J Gynaecol Obstet. 2008;102:82–90.
7. Pruitt BA, Goodwin CW, Mason AD Jr. Epidemiological, emographic, and outcome characteristics of burn injury. In: Herndon DN (ed). Total Burn Care. London: W. B. Saunders; 2002:16–30.
8. Bull JP, Fisher AJ. A study of mortality in a burns unit: a revised estimate. Ann Surg. 1954;139:269–274.
9. Wolf SE, Rose JK, Desai MH, et al. Mortality determinants in massive pediatric burns. An analysis of 103 children with > or = 80% TBSA burns (> or = 70% full-thickness). Ann Surg. 1997;225:554–565. discussion 65–9.
10. Barrow RE, Spies M, Barrow LN, et al. Influence of demographics and inhalation injury on burn mortality in children. Burns. 2004;30:72–77.
11. Chester DL, Papini R. Skin and skin substitutes in burn management. Trauma. 2004;6:87–99.
12. Horch RE, Jeschke MG, Spilker G, et al. Treatment of second degree facial burns with allografts—preliminary results. Burns. 2005;31:597–602.
13. Branski LK, Herndon DN, Celis MM, et al. Amnion in the treatment of pediatric partial-thickness facial burns. Burns. 2008;34:393–399.
14. Jones I, Currie L, Martin R. A guide to biological skin substitutes. Br J Plast Surg. 2002;55:185–193.
15. Wasiak J, Cleland H, Campbell F. Dressings for superficial and partial thickness burns. Cochrane Database Syst Rev. 2013:CD002106.
16. Khundkar R, Malic C, Burge T. Use of Acticoat dressings in burns: what is the evidence? Burns. 2010;36:751–758.
17. Tredget EE, Shankowsky HA, Groeneveld A, et al. A matched-pair, randomized study evaluating the efficacy and safety of Acticoat silver-coated dressing for the treatment of burn wounds. J Burn Care Rehabil. 1998;19:531–537.
18. Cuttle L, Naidu S, Mill J, et al. A retrospective cohort study of Acticoat versus Silvazine in a paediatric population. Burns. 2007;33:701–707.
19. Silver GM, Robertson SW, Halerz MM, et al. A silver-coated antimicrobial barrier dressing used postoperatively on meshed autografts: a dressing comparison study. J Burn Care Res. 2007;28:715–719.
20. Silverstein P, Heimbach D, Meites H, et al. An open, parallel, randomized, comparative, multicenter study to evaluate the cost-effectiveness, performance, tolerance, and safety of a silver-containing soft silicone foam dressing (intervention) vs silver sulfadiazine cream. J Burn Care Res. 2011;32:617–626.
21. Alsarra IA. Chitosan topical gel formulation in the management of burn wounds. Int J Biol Macromol. 2009;45:16–21.
22. Singh R, Chacharkar MP, Mathur AK. Chitin membrane for wound dressing application–preparation, characterisation and toxicological evaluation. Int Wound J. 2008;5:665–673.
23. Ribeiro MP, Espiga A, Silva D, et al. Development of a new chitosan hydrogel for wound dressing. Wound Repair Regen. 2009;17:817–824.
24. Boucard N, Viton C, Agay D, et al. The use of physical hydrogels of chitosan for skin regeneration following third-degree burns. Biomaterials. 2007;28:3478–3488.
25. Travis TE, Mauskar NA, Mino MJ, et al. Commercially available topical platelet-derived growth factor as a novel agent to accelerate burn-related wound healing. J Burn Care Res. 2014;35:e321–e329.
26. Alemdaroğlu C, Değim Z, Celebi N, et al. An investigation on burn wound healing in rats with chitosan gel formulation containing epidermal growth factor. Burns. 2006;32:319–327.
27. Jin Y, Ling PX, He YL, et al. Effects of chitosan and heparin on early extension of burns. Burns. 2007;33:1027–1031.
28. Dai T, Tegos GP, Burkatovskaya M, et al. Chitosan acetate bandage as a topical antimicrobial dressing for infected burns. Antimicrob Agents Chemother. 2009;53:393–400.
29. Dai T, Tanaka M, Huang YY, et al. Chitosan preparations for wounds and burns: antimicrobial and wound-healing effects. Expert Rev Anti Infect Ther. 2011;9:857–879.
30. Nascimento EG, Sampaio TB, Medeiros AC, et al. Evaluation of chitosan gel with 1% silver sulfadiazine as an alternative for burn wound treatment in rats. Acta Cir Bras. 2009;24:460–465.
31. Li LG, Chai JK, Guo ZR, et al. Application of carbon fiber dressing on burn wounds. Zhonghua Wai Ke Za Zhi. 2006;44:1047–1049.
32. Chen J, Han CM, Su GL, et al. Randomized controlled trial of the absorbency of four dressings and their effects on the evaporation of burn wounds. Chin Med J (Engl). 2007;120:1788–1791.
33. Church D, Elsayed S, Reid O, et al. Burn wound infections. Clin Microbiol Rev. 2006;19:403–434.
34. Bang RL, Sharma PN, Sanyal SC, et al. Septicaemia after burn injury: a comparative study. Burns. 2002;28:746–751.
35. Turk JL. Leonard Colebrook: the chemotherapy and control of streptococcal infections. J R Soc Med. 1994;87:727–728.
36. Lerner BH. Scientific evidence versus therapeutic demand: the introduction of the sulfonamides revisited. Ann Intern Med. 1991;115:315–320.
37. Colebrook L. Treatment of human puerperal infections, and of experimental infections in mice, with prontosil. Lancet. 1936:1279–1286.
38. Clark AM, Gibson T, Colebrook L, et al. Penicillin and propamide in burns: elimination of haemolytic streptococci and staphylococci. Lancet. 1943:605–609.
39. Colebrook L, Gibson T, Todd JP, et al. Studies of burns and scalds. (Reports of the burns unit, Royal Infirmary, Glasgow, 1942–43). In: Medical Research Council Special Report Series No. 249. London: His Majesty’s Stationery Office; 1944.
40. Lyons C. Problems of infection and chemotherapy. In: Aub JC, Beecher HK, Cannon B, et al. (eds). Management of the Cocoanut Grove Burns at the Massachusetts General Hospital. J. B. Philadelphia: Lippincott Company. 1943;94–102.
41. Meleney FL. The study of the prevention of infection in contaminated accidental wounds, compound fractures and burns. Ann Surg. 1943;118:171–183.
42. Chain E, Florey HW, Gardner AD, et al. Penicillin as a chemotherapeutic agent. Lancet. 1940;ii:226–228.
43. Ligon BL. Penicillin: its discovery and early development. Semin Pediatr Infect Dis. 2004;15:52–57.
44. Rybak MJ. The pharmacokinetic and pharmacodynamic properties of vancomycin. Clin Infect Dis. 2006;42(suppl 1):S35–S39.
45. McEvoy GK. American Hospital Formulary Service. Bethesda MD: American Society of Health-System Pharmacists: American Society of Health-System Pharmacists; 2003.
46. Branski LK, Al-Mousawi A, Rivero H, et al. Emerging infections in burns. Surg Infect (Larchmt). 2009;10:389–397.
47. Woods GLaG Y. Diagnostic pathology of infectious diseases. 1st ed. Malvern, Pennsylvania: Lea & Febiger; 1993.
48. Davidson EC. Tannic acid in the treatment of burns. Surg Gynecol Obstet. 1925;41:202–221.
49. McClure RD. Problems in the treatment of burns; liver necrosis as a lethal factor. Southern Surg. 1940;9:223–234.
50. Barillo DJ. Topical antimicrobials in burn wound care: a recent history. Wounds. 2008;20:192–198.
51. Dakin HD. On the use of certain antiseptic substances in the treatment of infected wounds. Br Med J. 1915;2:318–320.
52. Haller JS Jr. Treatment of infected wounds during the Great War, 1914 to 1918. South Med J. 1992;85:303–315.
53. Lineaweaver W, McMorris S, Soucy D, et al. Cellular and bacterial toxicities of topical antimicrobials. Plast Reconstr Surg. 1985;75:394–396.
54. Lineaweaver W, Howard R, Soucy D, et al. Topical antimicrobial toxicity. Arch Surg. 1985;120:267–270.
55. Heggers JP, Sazy JA, Stenberg BD, et al. Bactericidal and wound-healing properties of sodium hypochlorite solutions: the 1991 Lindberg Award. J Burn Care Rehabil. 1991;12:420–424.
56. Pruitt BA Jr, O'Neill JA Jr, Moncrief JA, et al. Successful control of burn-wound sepsis. JAMA. 1968;203:1054–1056.
57. Lindberg RB, Moncrief JA, Switzer WE, et al. The successful control of burn wound sepsis. J Trauma. 1965;5:601–616.
58. Monafo WW, West MA. Current treatment recommendations for topical burn therapy. Drugs. 1990;40:364–373.
59. Moyer CA, Brentano L, Gravens DL, et al. Treatment of large human burns with 0.5 per cent silver nitrate solution. Arch Surg. 1965;90:812–867.
60. Fox CL Jr, Rappole BW, Stanford W. Control of pseudomonas infection in burns by silver sulfadiazine. Surg Gynecol Obstet. 1969;128:1021–1026.
61. Fox CL Jr. Silver sulfadiazine—a new topical therapy for Pseudomonas in burns. Therapy of Pseudomonas infection in burns. Arch Surg. 1968;96:184–188.
62. Cartotto R. Fluid resuscitation of the thermally injured patient. Clin Plast Surg. 2009;36:569–581.
63. Parks DH, Carvajal HF, Larson DL. Management of burns. Surg Clin North Am. 1977;57:875–894.
64. Barrow RE, Jeschke MG, Herndon DN. Early fluid resuscitation improves outcomes in severely burned children. Resuscitation. 2000;45:91–96.
65. Arturson G. Microvascular permeability to macromolecules in thermal injury. Acta Physiol Scand Suppl. 1979;463:111–122.
66. Underhill FP. The significance of anhydremia in extensive surface burns. JAMA. 1930;95:852–857.
67. Underhill FP, Carrington GL, Kapsinov R, et al. Blood concentration blood in extensive superficial burns, and their significance for systemic treatment. Arch Intern Med. 1923;32:31–39.
68. Moore FD. The body-weight burn budget. Basic fluid therapy for the early burn. Surg Clin North Am. 1970;50:1249–1265.
69. Yowler CJ, Fratianne RB. Current status of burn resuscitation. Clin Plast Surg. 2000;27:1–10.
70. Harkins HN. The treatment of burns in wartime. JAMA. 1942;119:385–390.
71. Cope O, Rhinelander FW. The problem of burn shock complicated by pulmonary damage. In: Aub JC, Beecher HK, Cannon B, et al. (eds). Management of the Cocoanut Grove Burns at the Massachusetts General Hospital. Philadelphia: J.B. Lippincott; 1943:115–128.
72. National Research Council Division of Medical Sciences. Treatment of burns. War Med. 1942;2:334–339.
73. Lund CC, Browder NC. The estimation of areas of burns. Surg Gynecol Obstet. 1944;79:352–358.
74. Knaysi GA, Crikelair GF, Cosman B. The role of nines: its history and accuracy. Plast Reconstr Surg. 1968;41:560–563.
75. Cope O, Moore FD. The redistribution of body water and the fluid therapy of the burned patient. Ann Surg. 1947;126:1010–1045.
76. Evans EI, Purnell OJ, Robinett PW, et al. Fluid and electrolyte requirements in severe burns. Ann Surg. 1952;135:804–817.
77. Reiss E, Stirmann JA, Artz CP, et al. Fluid and electrolyte balance in burns. J Am Med Assoc. 1953;152:1309–1313.
78. Pruitt BA Jr, Mason AD Jr, Moncrief JA. Hemodynamic changes in the early postburn patient: the influence of fluid administration and of a vasodilator (hydralazine). J Trauma. 1971;11:36–46.
79. Rosenqvist H. The primary treatment of extensive burns: a clinical study. Acta Chir Scand. 1947;(suppl 124).
80. Demling RH, Kramer GC, Gunther R, et al. Effect of nonprotein colloid on postburn edema formation in soft tissues and lung. Surgery. 1984;95:593–602.
81. Cartotto R, Callum J. A review of the use of human albumin in burn patients. J Burn Care Res. 2012;33:702–717.
82. Baxter CR, Shires T. Physiological response to crystalloid resuscitation of severe burns. Ann N Y Acad Sci. 1968;150:874–894.
83. Hettiaratchy S, Papini R. Initial management of a major burn: II—assessment and resuscitation. BMJ. 2004;329:101–103.
84. James MF. Place of the colloids in fluid resuscitation of the traumatized patient. Curr Opin Anaesthesiol. 2012;25:248–252.
85. Tricklebank S. Modern trends in fluid therapy for burns. Burns. 2009;35:757–767.
86. Dries DJ. Management of burn injuries—recent developments in resuscitation, infection control and outcomes research. Scand J Trauma Resusc Emerg Med. 2009;17:14.
87. Ahrns KS. Trends in burn resuscitation: shifting the focus from fluids to adequate endpoint monitoring, edema control, and adjuvant therapies. Crit Care Nurs Clin North Am. 2004;16:75–98.
88. Navar PD, Saffle JR, Warden GD. Effect of inhalation injury on fluid resuscitation requirements after thermal injury. Am J Surg. 1985;150:716–720.
89. Lee KC, Joory K, Moiemen NS. History of burns: the past, present and the future. Burns Trauma. 2014;2:169–180.
90. Cope O, Langohr JL, et al. Expeditious care of full-thickness burn wounds by surgical excision and grafting. Ann Surg. 1947;125:1–22.
91. Connor GJ, Harvey SC. The pyruvic acid method in deep clinical burns. Ann Surg. 1946;124:799–810.
92. Young F. Immediate skin grafting in the treatment of burns: a preliminary report. Ann Surg. 1942;116:445–451.
93. McCorkle HJ, Silvani H. Selection of the time for grafting of skin to extensive defects resulting from deep thermal burns. Ann Surg. 1945;121:285–290.
94. Saltonstall H, Lee WE. Modified technic in skin grafting of extensive deep burns. Ann Surg. 1944;119:690–693.
95. Jackson D, Topley E, Cason JS, et al. Primary excision and grafting of large burns. Ann Surg. 1960;152:167–189.
96. Walker HL, Mason AD Jr, Raulston GL. Surface infection with pseudomonas aeruginosa. Ann Surg. 1964;160:297–305.
97. Janzekovic Z. A new concept in the early excision and immediate grafting of burns. J Trauma. 1970;10:1103–1108.
98. Janzekovic Z. Once upon a time … how west discovered east. J Plast Reconstr Aesthet Surg. 2008;61:240–244.
99. Janzekovic Z. Early surgical treatment of the burned surface. Panminerva Med. 1972;14:228–232.
100. Herndon DN, Barrow RE, Rutan RL, et al. A comparison of conservative versus early excision. Therapies in severely burned patients. Ann Surg. 1989;209:547–552. discussion 52–3.
101. Monafo WW. Tangential excision. Clin Plast Surg. 1974;1:591–601.
102. Burke JF, Bondoc CC, Quinby WC. Primary burn excision and immediate grafting: a method shortening illness. J Trauma. 1974;14:389–395.
103. Engrav LH, Heimbach DM, Reus JL, et al. Early excision and grafting vs. nonoperative treatment of burns of indeterminant depth: a randomized prospective study. J Trauma. 1983;23:1001–1004.
104. Tompkins RG, Burke JF, Schoenfeld DA, et al. Prompt eschar excision: a treatment system contributing to reduced burn mortality. A statistical evaluation of burn care at the Massachusetts General Hospital (1974–1984). Ann Surg. 1986;204:272–281.
105. Herndon DN, Parks DH. Comparison of serial debridement and autografting and early massive excision with cadaver skin overlay in the treatment of large burns in children. J Trauma. 1986;26:149–152.
106. Tompkins RG, Remensnyder JP, Burke JF, et al. Significant reductions in mortality for children with burn injuries through the use of prompt eschar excision. Ann Surg. 1988;208:577–585.
107. Ong YS, Samuel M, Song C. Meta-analysis of early excision of burns. Burns. 2006;32:145–150.
108. Puthumana PP. Through the mists of time: Sushrutha, an enigma revisited. Indian J Plast Surg. 2009;42:219–223.
109. Hauben DJ, Baruchin A, Mahler A. On the history of the free skin graft. Ann Plast Surg. 1982;9:242–245.
110. Reverdin J. Greffe epidermique. Bull Soc Chir (Paris). 1869; 101 December 8 and 15.
111. Freshwater MF, Krizek TJ. George David Pollock and the development of skin grafting. Ann Plast Surg. 1978;1:96–102.
112. Freshwater MF, Krizek TJ. Skin grafting of burns: a centennial. A tribute to George David Pollock. J Trauma. 1971;11:862–865.
113. Thiersh JC. On skin grafting. Verhandl 2nd Deutsch Ges Chir. 1886;15:17–20.
114. Ameer F, Singh AK, Kumar S. Evolution of instruments for harvest of the skin grafts. Indian J Plast Surg. 2013;46:28–35.
115. Goldwyn RM. Kazanjian and Converse's surgical treatment of facial injuries. Arch Surg. 1975;110:227.
116. Padgett EC. Skin grafting and the “three-quarter”-thickness skin graft for prevention and correction of cicatricial formation. Ann Surg. 1941;113:1034–1049.
117. Padgett EC. Indications for determination of the thickness of split skin grafts. Am J Surg. 1946;72:683–693.
118. Lanz O. Over transplantatie. Ned Tijdschr Geneerskd. 1907;43:1335.
119. Meek CP. Successful microdermagrafting using the Meek-Wall microdermatome. Am J Surg. 1958;96:557–558.
120. Kamolz LP, Schintler M, Parvizi D, et al. The real expansion rate of meshers and micrografts: things we should keep in mind. Ann Burns Fire Disasters. 2013;26:26–29.
121. Tanner JC Jr, Vandeput J, Olley JF. The mesh skin graft. Plast Reconstr Surg. 1964;34:287–292.
122. Kreis RW, Mackie DP, Hermans RR, et al. Expansion techniques for skin grafts: comparison between mesh and Meek island (sandwich-) grafts. Burns. 1994;20(suppl 1):S39–S42.
123. Raff T, Hartmann B, Wagner H, et al. Experience with the modified Meek technique. Acta Chir Plast. 1996;38:142–146.
124. Hsieh CS, Schuong JY, Huang WS, et al. Five years' experience of the modified Meek technique in the management of extensive burns. Burns. 2008;34:350–354.
125. Lyons JL, Kagan RJ. The true meshing ratio of skin graft meshers. J Burn Care Res. 2014;35:257–260.
126. Girdner J. Skin grafting with grafts taken from the dead subject. Med Rec. 1881;20:119–120.
127. Bettman A. Homogeneous thiersch grafting as a life saving measure. Am J Surg. 1938;39:156–162.
128. Jackson D. A clinical study of the use of skin homografts for burns. Br J Plast Surg. 1954;7:26–43.
129. Alexander JW, MacMillan BG, Law E, et al. Treatment of severe burns with widely meshed skin autograft and meshed skin allograft overlay. J Trauma. 1981;21:433–438.
130. Burke JF, Yannas IV, Quinby WC Jr, et al. Successful use of a physiologically acceptable artificial skin in the treatment of extensive burn injury. Ann Surg. 1981;194:413–428.
131. Heimbach D, Luterman A, Burke J, et al. Artificial dermis for major burns. A multi-center randomized clinical trial. Ann Surg. 1988;208:313–320.
132. Hansbrough JF, Boyce ST, Cooper ML, et al. Burn wound closure with cultured autologous keratinocytes and fibroblasts attached to a collagen-glycosaminoglycan substrate. JAMA. 1989;262:2125–2130.
133. Boyce ST. Cultured skin substitutes: a review. Tissue Eng. 1996;2:255–266.
134. Fang T, Lineaweaver WC, Sailes FC, et al. Clinical application of cultured epithelial autografts on acellular dermal matrices in the treatment of extended burn injuries. Ann Plast Surg. 2014;73:509–515.
135. Gallico GG 3rd, O'Connor NE, Compton CC, et al. Permanent coverage of large burn wounds with autologous cultured human epithelium. N Engl J Med. 1984;311:448–451.
136. Rue LW 3rd, Cioffi WG, McManus WF, et al. Wound closure and outcome in extensively burned patients treated with cultured autologous keratinocytes. J Trauma. 1993;34:662–667. discussion 67–8.
137. Barret JP, Wolf SE, Desai MH, et al. Cost-efficacy of cultured epidermal autografts in massive pediatric burns. Ann Surg. 2000;231:869–876.
138. van Zuijlen PP, van Trier AJ, Vloemans JF, et al. Graft survival and effectiveness of dermal substitution in burns and reconstructive surgery in a one-stage grafting model. Plast Reconstr Surg. 2000;106:615–623.
139. Haslik W, Kamolz LP, Nathschläger G, et al. First experiences with the collagen-elastin matrix Matriderm as a dermal substitute in severe burn injuries of the hand. Burns. 2007;33:364–368.
140. Davis JW. Skin transplantation with a review of 550 cases at the Johns Hopkins Hospital. Johns Hopkins Med J. 1910;15:307–396.
141. Sabella N. Use of fetal membranes in skin grafting. Med Rec NY. 1913;83:478.
142. Supp DM, Boyce ST. Engineered skin substitutes: practices and potentials. Clin Dermatol. 2005;23:403–412.
143. Gurtner GC, Werner S, Barrandon Y, et al. Wound repair and regeneration. Nature. 2008;453:314–321.
144. Kwan P, Hori K, Ding J, et al. Scar and contracture: biological principles. Hand Clin. 2009;25:511–528.

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