- Review Article
- Open Access
History of burns: The past, present and the future
© Author 2014
- Received: 23 June 2014
- Accepted: 27 September 2014
- Published: 25 October 2014
Burn injuries are one of the most common and devastating afflictions on the human body. In this article we look back at how the treatment of burns has evolved over the centuries from a primarily topical therapy consisting of weird and wonderful topical concoctions in ancient times to one that spans multiple scientific fields of topical therapy, antibiotics, fluid resuscitation, skin excision and grafting, respiratory and metabolic care and nutrition. Most major advances in burn care occurred in the last 50 years, spurred on by wars and great fires. The use of systemic antibiotics and topical silver therapy greatly reduced sepsis related mortality. This along with the advent of antiseptic surgical techniques, burn depth classification and skin grafting allowed the excision and coverage of full-thickness burns which resulted in greatly improved survival rates. Advancements in the methods of assessing the surface area of burns paved way for more accurate fluid resuscitation, minimising the effects of shock and avoiding fluid over-loading. The introduction of metabolic care, nutritional support and care of inhalational injuries further improved the outcome of burn patients. We also briefly discuss some future directions in burn care such as the use of cell and pharmalogical therapies.
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The treatment of burns is a major undertaking and involves many components from the initial first aid, assessment of the burn size and depth, fluid resuscitation, wound excision, grafting and coverage, infection control and nutritional support. Progress in each of these areas has contributed significantly to the overall enhanced survival of burn victims and this article aims to explore the history of burns to identify milestones and step-changes in each of these areas in the patient’s care. As in the case of the advancement in the treatment of trauma, these step-changes were mainly related to wars. Napoleon’s surgeon’s contributions to wound management that are still applicable today is an example. In burns, fire disasters as the Rialto fire in 1921 and Coconut Grove nightclubs fire in 1942 led to research that provided the first glimpse of the modern understanding of the patho-physiology of burns.
The majority of ancient burn care consisted of topical therapies and can be traced back to centuries. One of the earliest records of burn treatment was described in an Egyptian Smith Papyrus written in 1600 BC which advocated the use of resin and honey salve for treating burns, and the Ebers Papyrus in 1500 BC described the use of a wide variety of substances to treat burn wounds. In 600 BC, Chinese described the use of tea leave abstracts and tinctures for burns. Many famous philosophers and physicians have contributed to burn wound management such as Hippocrates, who in 400 BC, described the use of bulky dressings impregnated with rendered pig fat and resin with alternated warm vinegar soaks, augmented with tanning solutions made from oak bark and in the 1st century AD, Celsus described the use of wine and myrrh as a burn lotion, which had bacteriostatic properties. The first description of first aid for burns was around 854 CE-925 CE, by Muhammad ibn Zakariya al-Razi (or otherwise known as Rhases in the west), an Arabian physician who recommended cold water for the relief of pain from burns. A more recent example can be found in the 19th century, where a mixture of linseed oil and lime-water (termed Carron oil) was being used to treat burns in Ironworkers in Scotland.
With our current understanding of microbiology and infection, it would be difficult to comprehend why faeces and excrement, rich in disease causing pathogens, was used in the open wounds caused by burn. The use of a myriad of other different substances is interesting, however few of the ancient methods have any modern applications as they are unable to prevent bacterial infection which is one of the major causes of death of burn victims (the exception being vinegar, first described by Hippocrates but which is now being rediscovered for its antibacterial properties especially in the treatment of Pseudomonal infections).
Burn injury damages the skin which is the primary barrier to infection. Damaged skin that provides a fertile ground to bacterial growth, together with immunosuppression that accompanies major burns, are the main contributors to wound infection, invasive sepsis and if not managed, death. With the advancement of resuscitation methods in burn patients, deaths due to hypovolemia and hyperosmolar shock are now uncommon. Meanwhile, sepsis is now the commonest cause of death following burn injury and contributes to almost 75–85% of all burn victim deaths.[8,9] Over the last few decades, many advancements have positively impacted on the incidence of burn wound infections and these include, topical and systemic antimicrobial therapies, early burn wound excision and closure and the introduction of infection control measures in modern burn units such as isolation facilities.
The discovery of penicillin by the Scottish scientist, Sir Alexander Fleming in 1928 was a major breakthrough in the fight against microbial infections but it was not until World War II (WW2) that a way to manufacture the drug in large industrial scale was achieved. Penicillin played a crucial part in the treatment of the burn victims of the Coconut Grove fire in Boston in 1942, as it combated the Staphylococcus bacteria which typically led to toxic shock syndrome and also infected skin grafts. The emergence of methicillin-resistant staphylococcal strains however curbed the effectiveness of natural penicillins as the penicillinase produced by these bacteria hydrolyse the penicillin B-lactam ring and render them ineffective which in turn necessitated the development of penicillinase-resistant penicillins such as methicillin and cloxacillin. Streptococcal organisms are a major bane in the treatment of burn injuries as even the presence of a few B-hemolytic streptococci such as Group A (Streptococcus pyogenes) and Group B (Streptococcus agalactiae) can lead to a wound infection, loss of skin grafts and failure of a primary wound closure. Fortunately, natural penicillins remain effective and are bactericidal to these bacteria. Although staphyloccocal and streptococcal infections remain a major problem in burns, the landscape of microbes in burns continues to evolve with the emergence of antibiotic resistant strains e.g. the vancomycin-resistant enterococci (VRE) and Pseudomonas spp. which is now one of the most repeatedly encountered wound pathogen and a leading cause of noscomial infections in burn patients.
The aim of topical therapies has changed over the centuries as we understand increasingly more about the pathophysiology of burn wounds. In the early 20th century, the goal of topical therapies was to prevent the release of ‘toxins’ from the burn wound and to dry out the wound to allow formation of a hard coagulum to minimize fluid loss. A variety of therapies were developed to achieve this such as the tannic acid spray described by Davidson in 1925 which was believed to produce a cleaner wound. However its use was stopped when it was found to be a hepatotoxic.
One of the first topical antimicrobial treatments discovered was sodium hypochlorite (NaClO) in the 18th century by Berthollet. Its use was hampered by irritation it caused, but this was later discovered to be due to its variable quality and the free alkali or chlorine it contained. In 1915, Dr. Henry Dakin successfully developed a method of synthesizing hypochlorite without its irritating contaminants and found initially that a concentration of 0.5% was most effective as an antiseptic solution (revised later to 0.025%). This was further developed and used successfully in the treatment of burn wounds with a protocol of mechanical cleansing, surgical debridement and topical application of hypochlorite solution.
The major milestone in topical burn therapy was the application of solutions of silver compounds or salts, which played an important role in reducing the rate of burn wound sepsis and mortality. Silver sulfadiazine was developed by Charles Fox in the 1960’s and has become the mainstay of topical antimicrobial therapy due to its success in controlling infection and minimal side effect profile. Mafenide acetate (Sulfamylon) briefly was a viable alternative to the use of silver compound solutions in the treatment of infections but due to its carbonic anhydrase inhibitory effects which can lead to systemic acidosis, its use was all but discontinued except in cases of treatment of invasive wound infections. The other common silver-based therapy was silver nitrate, described by Moyer et al. in 1965. Silver based topical treatments were successful in controlling infections especially Pseudomonas aeroginosa infections.
Recent development in dressing technology have seen the use of a variety of interesting materials incorporated into the dressing. There is emerging evidence for the use of dressings and gels[18–21] containing the naturally occurring glycosaminoglycan, chitin, which prevents early extension of burn injury, has antimicrobial properties,[23,24] promotes fibroblast proliferation and angiogenesis and may promote burn wounds to heal, effects that are augmented by the incorporation of growth factors into the gel.[26,27] There has also been studies on the use of carbon fibre in dressings which has been shown to increase the absorptive capacity of the dressing, reduce inflammation, reduce bacterial growth and promote healing.[28,29]
Role of non-pharmalogical therapies
Although antibiotic treatment is a major front in the war against infection, non-pharmalogical interventions play equally important roles, such as strict handwashing and hygenic nursing standards and patient isolation. The need for strict burn patient isolation became an important issue after WW2. State of the art burn centres were established in the United States then across the world. The Brooks Army center is an example of facility that was designed with infection control and patient isolation in mind.
It was only at the end of the 19th century that it was realized that a relationship existed between the size of a burn and mortality. An early attempt at linking the size of burns to prognosis was carried out by Smart CB (1876) who studied 12 burn victims from an explosion aboard a ship and concluded that burn severity was determined by their size and depth, in addition to other bodily systems that were affected such as the airway. Schjerning advanced this idea of the relation of mortality with burn size in 1884; he found that death always followed if two thirds of the body was burned, to be expected if 50% of the body was burned, and generally occurred if a third of the body was burned.
However it was not until the late 18th to early 19th century was there any real attempt at accurately measuring burn size. Meeh in 1879 first described a method of using graph paper to measure burn body surface area (BSA). Weidenfeld found this technique of measuring BSA too unwieldy and uncomfortable for the patients. By using his own and Meeh’s calculations, he discovered that there was a constant relationship of the surface area of well-defined body regions such as the head or arm and the total BSA. Using this knowledge he was then able much more accurately to indicate the extent of a burn injury and subsequently was able to correlate the size of a burn and the time of early death. Additionally he also found that other factors such as age, depth of burn and the general health (constitution) of the patient also played a role.
Berkow calculated the surface area of various body parts in relation to the total body surface area, incorporating the use of calculations of body surface area as a function of overall height and weight by Du Bois D and Du Bois EF. Berkow recognised as well that his formula needed to be corrected if used in children. Lund and Browder later modified this in 1944 by accurately defining the anatomical regions and dividing the BSA into 12 regions, as well as introducing an age correction factor for children based on a BSA calculations done by Boyd (1935) who in turn modified it from Du Bois D and Du Bois EF. The Lund and Browder chart is still widely used today. Notably, a Chinese scientist, Chu, estimated the bodily proportions in Chinese using a wet paper moulding method in 1982, however the differences between his findings and those of Lund and Browder were only slight, further supporting the accuracy of these two parallel methods.
Berkow’s method not only gave rise to the Lund Browder chart but is also credited with a simplified method of assessing BSA which is the Rule of Nines. Wallace published details in 1951 of this simplified method to measure burn BSA. This method is also sometimes credited to Pulaski and Tennison (especially in the USA), who had presented a very similar idea first in a symposium in 1950 and later combined his ideas with Wallace. The rule of nines estimates the patient’s hand surface area (defined as the area enclosed by a line drawn around the patient’s hand with extended fingers) as 1% of the BSA, although this has been shown as less than accurate. However it has its place in the quick assessment of small burns.
The assessment of burn size is now a standard part of the diagnostic and treatment process in terms of fluid replacement therapy and plays a role as a prognostic indicator.
The first classification of burn depth actually goes back to the 16th century. Guilhelmus Fabricus Hildanus, often regarded as the founder of surgery in Germany, in 1634 recognized the link between the length of time heats acts on the body and the resulting damage. He categorised it into three stages; the first stage was characterised by erythema and blisters with colorless fluid, the second stage by erythema and blisters with yellow fluid, and the third, most serious stage, by the lack of blistering, and hard, dry skin that was blue or black and the lack of pain. Hildanus went on to publish De Combustionibus in 1670, which discussed the pathophysiology of burns and contributed to treatment of contractures. The three stage method of description was also utilized by Van Alberding in 1681, but he categorised it as light burns with blistering, contraction of the skin and thirdly, separation of the skin and underlying flesh with crust and ulcer formation.
First degree: Heat, pain and small blisters.
Second degree: Severe pain and large blisters.
Third degree: Damage to the skin and underlying flesh, with crust formation.
Fourth degree: Damage to all soft tissues down to the bone.
First degree: Erythema.
Second degree: Skin inflammation with epidermal detachment.
Third degree: Partial destruction of the papillary layer and subpapillary network of the corium.
Fourth degree: Destruction of the skin down to the subcuticular layer.
Fifth degree: Crust formation over skin and muscle.
First degree: Erythema.
Second degree: Blistering of the skin leading to superficial ulceration.
Third degree: Tissue disorganization leading to a dry yellow crust.
The current convention for describing burns is using depth rather than degrees; that is superficial, mixed depth and full thickness and new techniques are now in development to help physicians determine the depth of burns more accurately and objectively. These include thermal imaging, the use of laser techniques such as laser doppler imaging and laser speckle perfusion imaging and also enhanced photographic methods which are aided by computer systems such as the spectrophotometric intracutaneous analysis scope.
The need for fluid resuscitation in burn injured patients was first recognised by Underhill. When he studied the composition of blister fluid of patients injured in the Rialto Theatre fire in 1921, he found that it was similar to that of plasma and suggested that burn mortality may be due to loss of fluid rather than toxins. The introduction of methods of accurately quantifying burn surface area such as the Lund and Browder chart in 1944 and ‘rule of nines’ by Wallace and Tennison led to fluid replacement strategies based on total body surface area burned. By the 1940’s, the link between a proportional relationship between the percentage body surface area burned and the volume of fluid resuscitation required was established by Cope and Moore, who were able to quantify the amount of fluid per area needed for adequate resuscitation by studying young adult burn victims in the Coconut Grove Nightclub in Boston in 1942. Moore went on to develop a formula for calculating the amount of replacement fluid required based on the percentage of body surface area burned. Evans et al., in 1952 added to this formula by including body weight in the calculations and Reiss modified Evans formula by substituting normal saline with Ringer’s lactate and reducing the amount of colloid given. Colloid was altogether removed by Baxter and Shires, whose formula is now commonly known as the Parkland formula for fluid resuscitation which is still widely used in current practice.
The use of colloidal solutions in the resuscitation of burns has had varied proponents and opposition over the years. Rosenquvist was the first to publish the use of dextran, a solution of polysaccharides in physiological saline, in the treatment of burn patients in 1947 and obtained good results with its use. In 1962, Muir and Barclay proposed a formula of resuscitation which centered on the provision of colloid in the form of freeze dried plasma for resuscitation over a 36-hour period and this was used intensively in the United Kingdom (UK). However Cochrane reviews in 1998 and 2003 (lastest version published in 2013), showed that there was no evidence from randomized controlled trials that resuscitation with colloids reduces the risk of death compared with crystalloids in patients with burns and discouraged their use.
Early excision of burns
The idea of excising burns existed in ancient times, in 1510–1590 AD, 400 years ahead of his time, Ambroise Pare, was one of the first to describe early burn wound excision. In 1607, Hildanus also recommended removal of incisions made into burn eschars to allow drainage of serous fluid and allow better penetration of medications. However the benefit of surgical eschar removal was hampered by poor hygiene and lack of antiseptic surgical techniques, which would lead to a high rate of infection and blood loss. Additionally, wound management was not fully understood. Therefore the practice of early burn excision was rightly abandoned even though physicians recognized the importance of the early removal of dead tissues to reduce the inflammatory response. Patients with full-thickness burns could only languish in hospitals while their eschars, which were invariably infected, sloughed off, leaving open wounds that heal by secondary intention with remarkable contractures and disabilities.
Significant advances in infection control made burn eschar excision possible, when Lister in 1865 started successfully utilising carbolic acid (or phenol) as a method to sterilise surgical instruments and clean wounds. This, along with advancements in topical infection control, led to a significant decrease in post-operative infections and improved survival. On the other hand, the understanding and management of burn shock in the late 1950s was already underway. Improvements in the treatment of shock such as improved fluid resuscitation techniques, blood volume monitoring and realisation of the importance of urine output measurement allowed a greater efficiency of burn shock treatment and consequently more patients survived the initial shock stage. This in turn allowed the excision of full thickness burns to be more feasible and safe.
WW2 brought about a tremendous increase in burn victims, and physicians had to find a way to help patients recover faster. Physicians approached the problem of full thickness burns initially by chemical debridement with pyruvic acid and starch, which allowed grafting as early as 6 days post debridement. Several other authors reported in the 1940s their successful attempts at surgical excision of full thickness burns.[54–57] However most reports have been anecdotal.
In 1960, Jackson et al., published a series of pilot and controlled trials which showed that excision and grafting (20–30% of TBSA) could be safely achieved as long as shock was controlled via red cell volume monitoring and recommended the technique in cases of full-thickness burns (as natural slough separation would take 6 weeks), burns of 15–20% and deep circumferential burns of the trunk which affect respiration. However due to small numbers, they could not conclusively demonstrate an impact of the technique on mortality, infection nor healing time which probably prevented it from being accepted by the majority of surgeons at the time. What probably changed practice was the introduction of the tangential excision technique by Zora Janzekovic in the 1970s which was a significant improvement in the technique. An important modification introduced by this technique was that the excision not only included slough but also of the damaged dermis down to bleeding tissues. Her technique was advocated by many, several (including herself) who have reported improvement in mortality and also decrease in hospital stay when compared with conservative treatment.[60,61] The technique became the standard of care in most leading burn centres across the globe, but was only limited to small burns that could be covered by skin from patients’ own donor sites.
Wound cover after major burn excision was the challenge that delayed the practice till the 1970’s, when xenograft, pig skin, and cadaver skin became more widely available. Although Bettman reported success in the treatment of children with large full-thickness burn injuries with allograft skin in way back in 1938, modern day skin bank only began following the establishment of the United States Navy tissue bank in 1949.
In the first publication of early burn excision of major burns, Tompkins et al., credited the introduction of early excision and grafting of large burns for the dramatic decrease in mortality in children from 24% to 27%. Dr. David Herndon in a series of landmark papers has demonstrated the benefit of total early burn wound excisions for survival and improved outcomes.[61,64]
Skin grafting and the development of skin substitutes
The earliest record of skin grafting goes back to the 5th century AD, where an Indian surgeon, Sushrutha, repaired noses, that were amputated as punishment for crimes, using strips of skin from the forehead which were flapped downwards and grafted over the wound[65,66]. Sushrutha has also been documented to transplant skin from the buttock to the nose. The first documentation of a modern skin graft in humans was by Carl Bunger in 1823. This again involved a nose wound, and full thickness skin from the inner thigh was used for this purpose. During this time however, the success of skin grafts was low due to inefficient harvesting and use of large and thick grafts. Free skin grafting was successfully reproduced by Reverdin, who was still a student at the time, in 1869 to encourage healing and closure of slow healing or chronic wounds. Reverdin utilized “pinch grafts”, which were small circular skin discs obtained by pinching a small amount of skin and cutting it out. This was done repeatedly to produce islands of small grafts that were used to cover the wound, and it left donor sites that healed quickly due to their small sizes. This was soon popularized in England by George Pollock in 1870. Advances in the quality of surgical instruments meant that thinner grafts than previously possible could be harvested. Thiersch took advantage of this and developed and advocated the use of razor thin skin flaps or “razor flaps” in 1874. However these grafts did not produce satisfactory results in general and were limited to the treatment of small ulcerated wounds. Seven years later, Girdner reported the first successful use of allogeneic skin in burn wound coverage.
In the 1920’s, Blair and Brown discovered that deep islands of hair follicles and sebaceous gland epithelial cells were the factor responsible for initiating the healing at donor sites. This meant that grafts could be harvested to different depths as long as these islands were preserved. Tools that allowed the surgeon to control the depth of skin harvested then quickly developed. Surgeons initially had to harvest thin grafts with the use of blades that afforded no mechanism to control graft thickness such as the Blair and Catlin knives. Hofman and Finochietto developed knives that permitted precise regulation of the thickness harvested via screw-adjusted knives. Split thickness skin grafts (so called as the tools used to harvest these grafts resembled the tools used for splitting leather) however only started becoming more popular in the 1930s due in part to the development and availability of more reliable instruments. Humby then developed a knife allowed control over the depth harvested in 1936, followed by an adjustable dermatome by E.C Padgett in 1939.
The method of meshing grafts can be traced back to Lanz in 1907, who designed a cutting tool consisting of a series of small knives mounted in parallel to make multiple holes in a graft, forming a mesh. A method of expanding the graft size was described by Meek in 1958 which utilizes a special dermatome (Meek Wall dermatome) and prefolded gauzes which allowed a nine fold expansion of the harvested graft. The Meek dermatome was however viewed as cumbersome and required much skill and was thus superseded in 1964 by the introduction of simpler ‘mesh dermatome’ developed by J.C. Tanner et al. which allowed a graft to be expanded three times the original donor site size. The Meek technique has in recent years though been seeing a revival in its use including the development of modified, air driven dermatome by Kreis et al., in 1994 and has an advantage over mesh grafts when donor sites are limited e.g. in larger burn wounds.[76–78] Additionally, a study investigating the real expansion rate of meshers and Meek micrografts showed the Meek technique provided more reliable and valid expansion rates compared to the skin meshers.[74,79]
Despite the introduction of meshing and micrografting techniques, these were still insufficient to meet the increased demand for skin in cases of large burns especially with the introduction of the concept of early total burn excision, and thus cryopreservation and long term storage of human skin for both autologous and allogenic skin transplantation were developed in the 1940–50’s[80,81], of which a major milestone was the introduction of the use of glycerol to cryopreserve skin.
Skin allografts allowed the coverage of burns in cases where there was extensive skin loss or where limited sources of sites for autograft harvesting were available and could be used with or without concurrent skin autografts. Jackson described a combined grafting technique which utilized alternate placement of narrow stripes of allograft and autograft onto a granulating or excised wound hence it was also known as ‘Tiger-striping’. Following the adherence of the grafts, a process termed ‘creeping substitution’ occurs, whereby migration of autologous epithelial cells occurs across the wound surface between the sheets of autograft and underneath the allograft sheet causes the allograft sheet to slowly lift and separate, leaving an epithelized wound bed. This technique has been used and adapted by the Chinese surgeons, Zhang and co-workers,[84–86] who minced autologous skin into pieces less than 1 mm in diameter and then seed these ‘micrografts’, into the dermis of large sheets of allograft skin prior to applying it onto the wound. The autograft epidermal cells proliferate and migrate and eventually via the process of creeping substitution, lifts and separates the allograft. While this method results in effective skin expansion ratios up to 1:18, it has been associated with severe wound contraction compared to sheet autografts. Currently, micrografting techniques including the Meek technique has been more widely adopted in China than any other country.
Unfortunately, allogenic skin transplants trigger a potent reaction and rejection by the host immune skin and are invariably rejected acutely and immunosuppressive treatments that have proven effective in preventing rejection of organ transplants have sadly little or no effect on skin transplants. Thus in the UK, the use of allografts has been slowly phased out.
Another method of wound cover had to be developed and in the 1970’s, Yannas, a scientist at the Massachusetts Institute of Technology and Burke, a surgeon at the Massachusetts General Hospital and Shriners Burns center collaborated to develop and produce the first artificial skin, Integra®. It consisted of two layers, a collagen-chondrotin matrix and a silicon layer on top. The first multicentered clinical trial was conducted and published in 1988 and was granted an FDA licence in 1996. Integra is now widely used in acute burns and reconstructive surgery. Other artificial skin substitutes include Apligraf, developed by Bell et al., and Matriderm by Otto Suwelack.
The catabolic response to injury has been noted as early as in the 18th century by Sir John Hunter, but the ‘ebb’ and ‘flow’ phases of injury was first clearly documented by a Scottish nutritional scientist, David Cuthbertson in the early 1940s while he was studying the urinary excretion of minerals in facture patients. The ‘ebb’ phase in burns (also known as the acute or shock phase) occurs within 48 h of injury and is characterized by a decrease in the metabolic rate with depressed oxygen consumption, cardiac output and glucose tolerance. If patients survive this shock phase, they then go into the ‘flow’ or chronic response phase which is typically characterized by an elevated hyperdynamic state with increased metabolism and cardiac output. This increased hypermetabolism is responsible for the highly catabolism seen in severe burn injuries with accelerated glycolysis, proteolysis, and lipolysis leading to weight loss and the erosion of lean body mass (LBM), generalized fatigue and a weakened immune response.[92,93] The loss of LBM has a particularly devastating effect on the outcome of patients as Chang et al., has shown that impaired immunity is seen with 10% loss in LBM, decreased wound healing with 20% loss in LBM and death with 40% loss of LBM.
Several therapeutic strategies have been devised to ameliorate the hypermetabolic response including environmental control, excision of injured and dead tissue to reduce inflammatory stimulation, nutritional support and pharmacological therapies.
Only since the early 1900s has it been recognized that burn patients require an increased caloric intake. High caloric feeding was advocated by Shaffer et al. in 1909 and more recently by Wilmore in 1979. An in-depth understanding of the importance of the nutrition support was only established in 1970s. A high protein and high calorie diet supplemented with multivitamins and trace elements are required for burn patients. The evidence of other dietary supplements such as glutamine is not firmly established yet.[97–99] The route of feeding has been shown to be important as well. Herndon et al. showed that nutritional support, when given parentally, was shown to be harmful as it increased both immune deficiency and mortality and thus continuous enteral feeding is advocated instead. A recent review of the evidence surrounding nutritional support for burns patients guided the recommendations made by the European Society for Clinical Nutrition and Metabolism (ESPEN), including the need for early enteral feeding via the nasojejunal or nasoduodenal route.
In the last few decades, various pharmalogical interventions have been trialled in burn patients, chiefly to attempt to reduce the hypermetabolic response. Examples include Propranolol (a B-receptor antagonist),[102,103] anabolic agents such as human recombinant growth hormone and oxandrolone, and anti-hyperglycaemic agents such as insulin[106,107] and metformin.
The loss of LBM can also be accomplished by early rehabilitation from day one after the injury with active rather than passive exercises, even with intubated patients, will preserve the LBM and reduce complications.
The interest in pulmonary function in burns patients probably started in the 1970s when physicans started to note that pulmonary complications were common in burn patients. With improvements in the treatment of burn shock and sepsis, inhalational injury has now replaced these two causes as the main cause of mortality in burn patients. Inhalational injury by itself has been shown to be associated with pulmonary dysfunction for at least 6 months after the injury.
Pulmonary complications in burn patients can arise from direct injury to the respiratory tract via the inhalation of heated air and chemicals released by combustion, and also iatrogenic factors such as fluid-overloading during resuscitation and lung damage by mechanical ventilation.
Airway and pulmonary inflammation can also result from smoke inhalation alone. An autopsy study by Zikria et al., in 1972 showed that 70% of all burn victims who died within 12 hours of injury had inhalational injury which could be linked to the toxic products of combustion. A study by Herndon et al., in 1985 using an experimental sheep model of smoke inhalation injury showed that the pulmonary edema that occurred after smoke inhalation was the result of an increase in microvascular permeability and hypothesized that this may be secondary to neutrophil degradation. The global immunosuppression that accompanies burn injuries increases the risk of developing respiratory tract infections.
The treatment of burns itself can contribute to the development of lung injury. Moore et al., noted that although fluid resuscitation and blood transfusions prevented acute renal failure in trauma patients, these patients went on to develop pulmonary complications. Pruitt et al., hypothesized that pulmonary insufficiency in burns patients was due to a complex mechanism of interstitial edema leading to alveolar epithelial cell (type 2) damage and pulmonary circulation constriction secondary to vasoactive substances. Achauer et al., proposed a number of measures to prevent pulmonary edema including the use of pulmonary artery wedge and central venous pressure monitoring and also the supplementation of crystalloids with albumin to reduce the amount of fluid required. This was supported by animal studies by Holleman et al., which found that animals that were given only crystalloids post-scald injury had a higher water content in their lungs and recommended the addition of colloids to resuscitation fluid. The view on using colloids however, has changed in the last 40 years. Moncrief, from the U.S. Army of Surgical Research, hypothesized that the use of colloid was of no benefit in the first 24 hours due to the disturbed capillary permeability.
In addition to overhydration, Moore et al., also recognized that inhalational lung injury could be exacerbated by tracheostomy and mechanical ventilation at high oxygen tension. Traditionally, mechanical ventilation is acheived using tidal volumes of 10–15 ml per kilogram of body weight which is larger than in normal subjects at rest (7–8 ml per kilogram), which can lead to an excessive distension of the lung leading to disruption of the pulmonary epithelium and endothelium, and the release of inflammatory mediators.[119,120] The use of lower tidal volumes (TV) during ventilation of patients with acute lung injury and acute respiratory distress syndrome has been shown by a landmark study by the Acute Respiratory Distress Syndrome Network in 2000 to reduce mortality by 22% and increase the number of ventilator-free days. There is evidence as well that low TV ventilation protects against pulmonary complications in patients without acute respiratory distress syndrome. Most burn centers now adopt this low TV approach to reduce ventilator-induced injury.
The last 50 years has seen a tremendous improvement in the advancement of burn treatment with a significant reduction in mortality which can be attributed to the developments in early burn excision, early fluid resuscitation, infection control and nutrition. There is still many areas in burn care left to explore and improve and here we highlight some of the interesting developments in the field of burn care.
Wound cover with cell therapy
Human keratinocytes can be cultured and are currently being used as an adjunct to burn wound healing.[123,124] Stem cells have been shown to accelerate burn wound healing in animal models may prove to revolutionize burn care. Early studies with ‘bioprinted’ scaffold incorporating bone marrow-derived mesenchyme derived stem cells and amniotic fluid-derived stem cells showed promising results in a wound healing model but these were attributed to the growth factors secreted by the stem cells which did not become incorporated into the healing tissue. This concept however may perhaps help to allay fears regarding the use of pluripotent cells and the potential for malignant transformation. Another exciting development in the field of stem cells in wound healing is the concept of healing without scarring as has been demonstrated in early fetal life.
Research is currently underway to unlock the molecular mechanisms underlying this process with the hope that this can be translated into clinical practice.
Pharmalogical and nutritional interventions
Recent advancement in pharmacological interventions include the use of statins, which have demonstrated anti-inflammatory properties alongside their ability to lower serum lipid concentrations. They have been shown to improve survival in an animal model of burns sepsis and there is some evidence that this benefit translates to patients.[129–131]
Systemic administration of erythropoietin (EPO) has been shown to decrease secondary evolution of experimental burn injuries and may therefore have a role in minor burns. However it has to be noted that recombinant EPO has been shown to be ineffective in preventing the anemia that occurs after a major burn injury and does not reduce the need for ongoing blood transfusions. This resistance to EPO treatment may be due to dampened erythropoiesis and lymphopoiesis and enhanced myelopoiesis in the bone marrow as demonstrated following burn injury in animal models.
Shock wave therapy
There have been promising early clinical results on the use of shock-wave therapy (ESWT) for healing burn wounds.[135,136] Animal studies have demonstrated dampening of the inflammatory response with a single dose of ESWL post-burn and expedition of healing with multiple doses as well as improved angiogenesis and blood flow along with increased numbers of rolling and sticking leukocytes. A large phase III clinical trial to further evaluate the use of this treatment modality in burns patients is currently underway.
In this article we have highlighted the major advances in the evolution of the care of burns patients over the past 3500 years. The advancement of burn care has been closely associated with our deeper understanding of its pathophysiology; we have now come to understand the impact that burn injuries have in the multiple fields of current medical science i.e. in metabolism and circulation, electrolyte balance and nutrition, immunology and infection, inflammation, pulmonary function and wound healing. The major advancement in burn care in this century, especially in the last 50 years, is a typical example of the positive feed-back between in-depth research and the improvement of clinical care. It has transformed from the limited attempts to prevent complications in the first half of the century to the current state of effective shock therapy and surgical interventions which has led to a massive increase in the survival of burn victims. Despite this, many challenges still remain and the focus of burns care in the future will be to overcome the problem of burns in the elderly, extensive burns, to improve the quality of the lives saved by shortening healing times and therefore lengths of hospital stay and to improve scarring. It is hoped that new technologies and advances in wound care will achieve wound cover with minimal scarring.
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- Ribeiro PS, Jacobsen KH, Mathers CD, Garcia-Moreno C. Priorities for women’s health from the Global Burden of Disease study. Int J Gynecol Obstet 2008;102:82–90.Google Scholar
- Reverdin J. Greffe epidermique. Bull Soc Chir Paris 1869.Google Scholar
- Majno G. The healing hand: Man and wound in the ancient world. Cambridge: Harvard University Press; 1975.Google Scholar
- Bryan C. The papyrus ebers. London: Geoffrey Bles; 1930.Google Scholar
- E. G. Geschichte der Chirurgie und ihre Ausubung. BD I. Berlin: A. Hirschwald; 1898.Google Scholar
- Van Hee R. From fat of old pigs to fenestrated skin grafts: A fascinating history of burn’s treatment. Acta Chir Belg 2007;107:481–92.PubMedGoogle Scholar
- Nagoba BS, Selkar SP, Wadher BJ, Gandhi RC. Acetic acid treatment of pseudomonal wound infections — a review. J Infect Public Health 2013;6:410–5.PubMedGoogle Scholar
- Church D, Elsayed S, Reid O, Winston B, Lindsay R. Burn wound infections. Clin Microbiol Rev 2006;19:403–34.PubMedPubMed CentralGoogle Scholar
- Bang RL, Sharma PN, Sanyal SC, Al Najjadah I. Septicaemia after burn injury: A comparative study. Burns 2002;28:746–51.PubMedGoogle Scholar
- Davidson EC. Tannic acid in the treatment of burns. Surg Gynecol Obstet 1925;41:202–21.Google Scholar
- McClure RD. Problems in the treatment of burns; liver necrosis as a lethal factor. Southern Surg 1940;9:223–34.Google Scholar
- Barillo, David J. Topical antimicrobials in burn wound care. A recent history of wounds. Wounds 2008;20:192–8.PubMedGoogle Scholar
- Dakin HD. On the use of certain antiseptic substances in the treatment of infected wounds. Br Med J 1915;2:318–20.PubMedPubMed CentralGoogle Scholar
- Heggers JP, Sazy JA, Stenberg BD, Strock LL, McCauley RL, Herndon DN, et al. Bactericidal and wound-healing properties of sodium hypochlorite solutions: The 1991 Lindberg Award. J Burn Care Rehabil 1991;12:420–4.PubMedGoogle Scholar
- Fox CL Jr. Silver sulfadiazine — a new topical therapy for Pseudomonas in burns. Therapy of Pseudomonas infection in burns. Arch Surg 1968;96:184–8.PubMedGoogle Scholar
- Lindberg RB, Moncrief JA, Switzer WE, Order SE, Mills W Jr. The successful control of burn wound sepsis. J Trauma 1965;5:601–16.PubMedGoogle Scholar
- Moyer CA, Brentano L, Gravens DL, Margraf HW, Monafo WW Jr. Treatment of large human burns with 0.5 per cent silver nitrate solution. Arch Surg 1965;90:812–67.PubMedGoogle Scholar
- Alsarra IA. Chitosan topical gel formulation in the management of burn wounds. Int J Biol Macromol 2009;45:16–21.PubMedGoogle Scholar
- Singh R, Chacharkar MP, Mathur AK. Chitin membrane for wound dressing application — preparation, characterisation and toxicological evaluation. Int Wound J 2008;5:665–73.PubMedGoogle Scholar
- Ribeiro MP, Espiga A, Silva D, Baptista P, Henriques J, Ferreira C, et al. Development of a new chitosan hydrogel for wound dressing. Wound Repair Regen 2009;17:817–24.PubMedGoogle Scholar
- Boucard N, Viton C, Agay D, Mari E, Roger T, Chancerelle Y, et al. The use of physical hydrogels of chitosan for skin regeneration following third-degree burns. Biomaterials 2007;28:3478–88.PubMedGoogle Scholar
- Jin Y, Ling PX, He YL, Zhang TM. Effects of chitosan and heparin on early extension of burns. Burns 2007;33:1027–31.PubMedGoogle Scholar
- Dai T, Tegos GP, Burkatovskaya M, Castano AP, Hamblin MR. Chitosan acetate bandage as a topical antimicrobial dressing for infected burns. Antimicrob Agents Chemother 2009;53:393–400.PubMedGoogle Scholar
- Dai T, Tanaka M, Huang YY, Hamblin MR. Chitosan preparations for wounds and burns: Antimicrobial and wound-healing effects. Expert Rev Anti Infect Ther 2011;9:857–79.PubMedPubMed CentralGoogle Scholar
- Nascimento EG, Sampaio TB, Medeiros AC, Azevedo EP. Evaluation of chitosan gel with 1% silver sulfadiazine as an alternative for burn wound treatment in rats. Acta Cir Bras 2009;24:460–5.PubMedGoogle Scholar
- Travis TE, Mauskar NA, Mino MJ, Prindeze N, Moffatt LT, Fidler PE, 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:e321–9.PubMedGoogle Scholar
- Alemdaroglu C, Degim Z, Celebi N, Zor F, Ozturk S, Erdogan D. An investigation on burn wound healing in rats with chitosan gel formulation containing epidermal growth factor. Burns 2006;32:319–27.PubMedGoogle Scholar
- Li LG, Chai JK, Guo ZR, Yang HM, Jia XM, Xu MH, et al. Application of carbon fiber dressing on burn wounds. Zhonghua Wai Ke Za Zhi 2006;44:1047–9.PubMedGoogle Scholar
- Chen J, Han CM, Su GL, Tang ZJ, Su SJ, Lin XW. Randomized controlled trial of the absorbency of four dressings and their effects on the evaporation of burn wounds. Chin Med J (Engl) 2007;120:1788–91.PubMedGoogle Scholar
- Smart C. ON burns by gunpowder and scalds by steam. Lancet 1876;2:421–2.Google Scholar
- Schjerning. About the death as a result of burning and scalding from the court physician standpoint. 1884;41:24–66, 273–300.Google Scholar
- Meeh K. Surface measurements of the human body. Z Biol 1879;15:425–58.Google Scholar
- Weidenfeld S, Zumbusch LV. More contributions to pathology and therapy of severe burns. Arch Dermatol Syph 1905:163–87.Google Scholar
- Du Bois D, Du Bois EF A formula to estimate the approximate surface area if height and weight be known. 1916. Nutrition 1989;5:303–11.PubMedGoogle Scholar
- Chu CS. Burns updated in China: I. Cutaneous thermal burns. J Trauma 1982;22:566–73.PubMedGoogle Scholar
- Wallace AB. The exposure treatment of burns. Lancet 1951:501–4.Google Scholar
- Rossiter ND, Chapman P, Haywood IA. How big is a hand? Burns 1996;22:230–1.PubMedGoogle Scholar
- Hildanus GF. Van de verbrandtheydt daarin bij na alle accidenten ofte toevallen derslver klaarlijck vertoont worden. Amstelredam: Hendrick Laurentsz; 1634.Google Scholar
- Dupuytren G, Brierre de Boismont AJ, ALM P. Oral lessons of clinical surgery, faites à l’Hôtel-Dieu de Paris: Baillière Paris; 1839.Google Scholar
- Boyer A. Traits of surgical diseases and operations of their choosing. Paris, Migneret: T.I; 1814.Google Scholar
- Hardwicke J, Thomson R, Bamford A, Moiemen N. A pilot evaluation study of high resolution digital thermal imaging in the assessment of burn depth. Burns 2013;39:76–81.PubMedGoogle Scholar
- Stewart CJ, Frank R, Forrester KR, Tulip J, Lindsay R, Bray RC. A comparison of two laser-based methods for determination of burn scar perfusion: Laser Doppler versus laser speckle imaging. Burns 2005;31:744–52.PubMedGoogle Scholar
- Tehrani H, Moncrieff M, Philp B, Dziewulski P. Spectrophotometric intracutaneous analysis: A novel imaging technique in the assessment of acute burn depth. Ann Plast Surg 2008;61:437–40.PubMedGoogle Scholar
- Underhill FP. Changes in blood concentration with special reference to the treatment of extensive superficial burns. Ann Surg 1927;86:840–9.PubMedPubMed CentralGoogle Scholar
- Cope O, Moore FD. The redistribution of body water and the fluid therapy of the burned patient. Ann Surg 1947;126:1010–45.PubMedPubMed CentralGoogle Scholar
- Moore FD. The body-weight burn budget. Basic fluid therapy for the early burn. Surg Clin North Am 1970;50:1249–65.PubMedGoogle Scholar
- Evans EI, Purnell OJ, Robinett PW, Batchelor A, Martin M. Fluid and electrolyte requirements in severe burns. Ann Surg 1952;135:804–17.PubMedPubMed CentralGoogle Scholar
- Reiss E, Stirmann JA, Artz CP, Davis JH, Amspacher WH. Fluid and electrolyte balance in burns. J Am Med Assoc 1953;152:1309–13.PubMedGoogle Scholar
- Baxter CR, Shires T. Physiological response to crystalloid resuscitation of severe burns. Ann N Y Acad Sci 1968;150:874–94.PubMedGoogle Scholar
- Rosenqvist H. The primary treatment of extensive burns: A clinical study. Acta Chir Scand 1947:suppl 124.Google Scholar
- Muir I, Barclay T. Burns and their treatment. 2nd ed., 1–14, Lloyd-Luke Ltd., London, 1974.Google Scholar
- Perel P, Roberts I, Ker K. Colloids versus crystalloids for fluid resuscitation in critically ill patients. Cochrane Database Syst Rev 2013;2:CD000567.PubMedGoogle Scholar
- Connor, Gervase J, Harvey, Samuel C. The pyruvic acid method in deep chemical burns. Ann Surg 1946:124, 799.PubMed CentralGoogle Scholar
- Young F. Immediate skin grafting in the treatment of burns: A preliminary report. Ann Surg 1942;116:445–51.PubMedPubMed CentralGoogle Scholar
- Ackman D, Gerrie JW, Pritchard JE, Mills ES. A report of the management of burns using the occlusive compression dressing, with sulfathiazole emulsion. Ann Surg 1944;119:161–77.PubMedPubMed CentralGoogle Scholar
- McCorkle HJ, Silvani H. Selection of the time for grafting of skin to extensive defects resulting from deep thermal burns. Ann Surg 1945;121:285–90.PubMedPubMed CentralGoogle Scholar
- Saltonstall H, Lee WE. Modified technic in skin grafting of extensive deep burns. Ann Surg 1944;119:690–3.PubMedPubMed CentralGoogle Scholar
- Jackson D, Topley E, Cason JS, Lowbury EJ. Primary excision and grafting of large burns. Ann Surg 1960;152:167–89.PubMedPubMed CentralGoogle Scholar
- Janzekovic Z. A new concept in the early excision and immediate grafting of burns. J Trauma 1971;10:1103–8.Google Scholar
- Engrav LH, Heimbach DM, Reus JL, Harnar TJ, Marvin JA. Early excision and grafting vs. nonoperative treatment of burns of indeterminant depth: A randomized prospective study. J Trauma 1983;23:1001–4.PubMedGoogle Scholar
- Herndon DN, Barrow RE, Rutan RL, Rutan TC, Desai MH, Abston S. A comparison of conservative versus early excision. Therapies in severely burned patients. Ann Surg 1989;209:547–52.PubMedPubMed CentralGoogle Scholar
- Bettman A. Homogeneous thiersch grafting as a life saving measure. Am J Surg 1938;39:156–62.Google Scholar
- Herndon DN. Total Burn Care. 4th edition. Saunders; June 2012.Google Scholar
- Tompkins RG, Remensnyder JP, Burke JF, Tompkins DM, Hilton JF, Schoenfeld DA, et al. Significant reductions in mortality for children with burn injuries through the use of prompt eschar excision. Ann Surg 1988;208:577–85.PubMedPubMed CentralGoogle Scholar
- Puthumana PP. Through the mists of time: Sushrutha, an enigma revisited. Indian J Plast Surg 2009;42:219–23.PubMedPubMed CentralGoogle Scholar
- Hauben DJ, Baruchin A, Mahler A. On the histroy of the free skin graft. Ann Plast Surg 1982;9:242–5.PubMedGoogle Scholar
- Freshwater MF, Krizek TJ. George David Pollock and the development of skin grafting. Ann Plast Surg 1978;1:96–102.PubMedGoogle Scholar
- Thiersh JC. On skin grafting. Verhandl 2nd Deutsch Ges Chir 1886;15:17–20.Google Scholar
- Girdner J. Skin grafting with grafts taken from the dead subject. Medical Record. 1881;20:119–20.Google Scholar
- Ameer F, Singh AK, Kumar S. Evolution of instruments for harvest of the skin grafts. Indian J Plast Surg 2013;46:28–35.PubMedPubMed CentralGoogle Scholar
- Goldwyn RM. Kazanjian and Converse’s Surgical treatment of facial injuries. Arch Surg 1975;110:227.Google Scholar
- Lanz O. Over transplantatie. About transplant. Vol 43. 1907. p. 1335.Google Scholar
- Meek CP. Successful microdermagrafting using the Meek-Wall microdermatome. Am J Surg 1958;96:557–8.PubMedGoogle Scholar
- Kamolz LP, Schintler M, Parvizi D, Selig H, Lumenta DB. The real expansion rate of meshers and micrografts: Things we should keep in mind. Ann Burns Fire Disasters 2013;26:26–9.PubMedPubMed CentralGoogle Scholar
- Tanner JC Jr, Vandeput J, Olley JF. The mesh skin graft. Plast Reconstr Surg 1964;34:287–92.PubMedGoogle Scholar
- Kreis RW, Mackie DP, Hermans RR, Vloemans AR. Expansion techniques for skin grafts: Comparison between mesh and Meek island (sandwich-) grafts. Burns 1994;20 Suppl 1:S39–42.PubMedGoogle Scholar
- Raff T, Hartmann B, Wagner H, Germann G. Experience with the modified Meek technique. Acta Chir Plast 1996;38:142–6.PubMedGoogle Scholar
- Hsieh CS, Schuong JY, Huang WS, Huang TT. Five years’ experience of the modified Meek technique in the management of extensive burns. Burns 2008;34:350–4.PubMedGoogle Scholar
- Lyons JL, Kagan RJ. The true meshing ratio of skin graft meshers. J Burn Care Res 2014;35:257–60.PubMedGoogle Scholar
- Webster JP. Refrigerated skin grafts. Ann Surg 1944;120: 431–48.PubMedPubMed CentralGoogle Scholar
- Matthews DN. Storage of skin for autogenous grafts. Lancet 1945;245:775–8.Google Scholar
- Billingham R, Medawar P. The freezing, drying, and storage of mammalian skin. J Exp Biol 1952;19:454–68.Google Scholar
- Jackson D. A clinical study of the use of skin homografts for burns. Br J Plast Surg 1954;7:26–43.PubMedGoogle Scholar
- Zhang ML, Chang ZD, Han X, Zhu M. Microskin grafting. I. Animal experiments. Burns Incl Therm Inj 1986;12:540–3.PubMedGoogle Scholar
- Zhang ML, Chang ZD, Wang CY, Fang CH. Microskin grafting in the treatment of extensive burns: A preliminary report. J Trauma 1988;28:804–7.PubMedGoogle Scholar
- Zhang ML, Wang CY, Chang ZD, Cao DX, Han X. Microskin grafting. II. Clinical report. Burns Incl Therm Inj 1986;12:544–8.PubMedGoogle Scholar
- Fang CH, Alexander JW. Wound contraction following transplantation of microskin autografts with overlaid skin allograft in experimental animals. Burns 1990;16:190–2.PubMedGoogle Scholar
- Heimbach D, Luterman A, Burke J, Cram A, Herndon D, Hunt J, et al. Artificial dermis for major burns. A multi-center randomized clinical trial. Ann Surg 1988;208:313–20.PubMedPubMed CentralGoogle Scholar
- van Zuijlen PP, van Trier AJ, Vloemans JF, Groenevelt F, Kreis RW, Middelkoop E. Graft survival and effectiveness of dermal substitution in burns and reconstructive surgery in a one-stage grafting model. Plast Reconstr Surg 2000;106:615–23.PubMedGoogle Scholar
- Cuthbertson DP. Second annual Jonathan E. Rhoads Lecture. The metabolic response to injury and its nutritional implications: Retrospect and prospect. JPEN J Parenter Enteral Nutr 1979;3:108–29.PubMedGoogle Scholar
- Wolfe RR. Review: Acute versus chronic response to burn injury. Circ Shock 1981;8:105–15.PubMedGoogle Scholar
- Newsome TW, Mason AD Jr, Pruitt BA Jr. Weight loss following thermal injury. Ann Surg 1973;178:215–7.PubMedPubMed CentralGoogle Scholar
- Reiss E, Pearson E, Artz CP. The metabolic response to burns. J Clin Invest 1956;35:62–77.PubMedPubMed CentralGoogle Scholar
- Chang DW, DeSanti L, Demling RH. Anticatabolic and anabolic strategies in critical illness: A review of current treatment modalities. Shock 1998;10:155–60.PubMedGoogle Scholar
- Shaffer PA, Coleman W, Somogyi M, Reinoso EA, Cutler E. Protein metabolism in typhoid fever. Arch Intern Med 1909;IV:538–600.Google Scholar
- Wilmore DW, Curreri PW, Spitzer KW, Spitzer ME, Pruitt BA Jr. Supranormal dietary intake in thermally injured hypermetabolic patients. Surg Gynecol Obstet 1971;132:881–6.PubMedGoogle Scholar
- Juang P, Fish DN, Jung R, MacLaren R. Enteral glutamine supplementation in critically ill patients with burn injuries: A retrospective case-control evaluation. Pharmacotherapy 2007;27:11–9.PubMedGoogle Scholar
- Garrel D, Patenaude J, Nedelec B, Samson L, Dorais J, Champoux J, et al. Decreased mortality and infectious morbidity in adult burn patients given enteral glutamine supplements: A prospective, controlled, randomized clinical trial. Crit Care Med 2003;31:2444–9.PubMedGoogle Scholar
- Hall KL, Shahrokhi S, Jeschke MG. Enteral nutrition support in burn care: A review of current recommendations as instituted in the Ross Tilley Burn Centre. Nutrients 2012;4:1554–65.PubMedPubMed CentralGoogle Scholar
- Herndon DN, Barrow RE, Stein M, Linares H, Rutan TC, Rutan R, et al. Increased mortality with intravenous supplemental feeding in severely burned patients. J Burn Care Rehabil 1989;10:309–13.PubMedGoogle Scholar
- Rousseau AF, Losser MR, Ichai C, Berger MM. ESPEN endorsed recommendations: Nutritional therapy in major burns. Clin Nutr 2013;32:497–502.PubMedGoogle Scholar
- Herndon DN, Rodriguez NA, Diaz EC, Hegde S, Jennings K, Mlcak RP, et al. Long-term propranolol use in severely burned pediatric patients: A randomized controlled study. Ann Surg 2012;256:402–11.PubMedPubMed CentralGoogle Scholar
- Norbury W. Propranolol attenuates factors affecting hypermetabolism in pediatric burn patients. Crit Care. 2007; 11(Suppl 2):152.Google Scholar
- Breederveld RS, Tuinebreijer WE. Recombinant human growth hormone for treating burns and donor sites. Cochrane Database Syst Rev 2012;12:CD008990.PubMedGoogle Scholar
- Hart DW, Wolf SE, Ramzy PI, Chinkes DL, Beauford RB, Ferrando AA, et al. Anabolic effects of oxandrolone after severe burn. Ann Surg 2001;233:556–64.PubMedPubMed CentralGoogle Scholar
- Hrynyk M, Neufeld RJ. Insulin and wound healing. Burns 2014.Google Scholar
- Pidcoke HF, Baer LA, Wu X, Wolf SE, Aden JK, Wade CE. Insulin effects on glucose tolerance, hypermetabolic response and circadian-metabolic protein expression in a rat burn and disuse model. Am J Physiol Regulat Integrat Comp Physiol 2014;307:R1–R10.Google Scholar
- Gore DC, Wolf SE, Sanford A, Herndon DN, Wolfe RR. Influence of metformin on glucose intolerance and muscle catabolism following severe burn injury. Ann Surg 2005;241:334–42.PubMedPubMed CentralGoogle Scholar
- Park GY, Park JW, Jeong DH, Jeong SH. Prolonged airway and systemic inflammatory reactions after smoke inhalation. Chest 2003;123:475–80.PubMedGoogle Scholar
- Zikria BA, Weston GC, Chodoff M, Ferrer JM. Smoke and carbon monoxide poisoning in fire victims. J Trauma 1972;12:641–5.PubMedGoogle Scholar
- Herndon DN, Thompson PB, Traber DL. Pulmonary injury in burned patients. Crit Care Clin 1985;1:79–96.PubMedGoogle Scholar
- Pruitt BA Jr, Flemma RJ, DiVincenti FC, Foley FD, Mason AD Jr, Young WG Jr. Pulmonary complications in burn patients. A comparative study of 697 patients. J Thorac Cardiovasc Surg 1970;59:7–20.PubMedGoogle Scholar
- Moore FD, Lyons JH, Pierce EC, Morgan AP, Drinker PA, MacArthur JD, et al. Post-traumatic pulmonary insufficiency. Philadelphia: W.B. Saunders; April 1969.Google Scholar
- Pruitt BA Jr, Erickson DR, Morris A. Progressive pulmonary insufficiency and other pulmonary complications of thermal injury. J Trauma 1975;15:369–79.PubMedGoogle Scholar
- Achauer BM, Allyn PA, Furnas DW, Bartlett RH. Pulmonary complications of burns: The major threat to the burn patient. Ann Surg 1973;177:311–9.PubMedPubMed CentralGoogle Scholar
- Holleman JH, Gabel JC, Hardy JD. Pulmonary effects of intravenous fluid therapy in burn resuscitation. Surg Gynecol Obstet 1978;147:161–6.PubMedGoogle Scholar
- Moncrief JA. Burns. N Engl J Med 1973;288:444–54.PubMedGoogle Scholar
- Bernard GR, Artigas A, Brigham KL, Carlet J, Falke K, Hudson L, et al. The American-European Consensus Conference on ARDS. Definitions, mechanisms, relevant outcomes, and clinical trial coordination. Am J Respirat Crit Care Med 1994;149 (3 Pt 1):818–24.Google Scholar
- Tsuno K, Miura K, Takeya M, Kolobow T, Morioka T. Histopathologic pulmonary changes from mechanical ventilation at high peak airway pressures. Am Rev Respir Dis 1991;143 (5 Pt 1):1115–20.PubMedGoogle Scholar
- Tremblay L, Valenza F, Ribeiro SP, Li J, Slutsky AS. Injurious ventilatory strategies increase cytokines and c-fos m-RNA expression in an isolated rat lung model. J Clin Invest 1997;99:944–52.PubMedPubMed CentralGoogle Scholar
- Serpa Neto A, Nagtzaam L, Schultz MJ. Ventilation with lower tidal volumes for critically ill patients without the acute respiratory distress syndrome: A systematic translational review and meta-analysis. Curr Opin Crit Care 2014;20:25–32.PubMedGoogle Scholar
- Peck MD, Koppelman T. Low-tidal-volume ventilation as a strategy to reduce ventilator-associated injury in ALI and ARDS. J Burn Care Res 2009;30:172–5.PubMedGoogle Scholar
- Gardien KL, Middelkoop E, Ulrich MM. Progress towards cell-based burn wound treatments. Regen Med 2014;9:201–18.PubMedGoogle Scholar
- Lootens L, Brusselaers N, Beele H, Monstrey S. Keratinocytes in the treatment of severe burn injury: An update. Int Wound J 2013;10:6–12.PubMedGoogle Scholar
- Liu L, Yu Y, Hou Y, Chai J, Duan H, Chu W, et al. Human umbilical cord mesenchymal stem cells transplantation promotes cutaneous wound healing of severe burned rats. PloS One 2014;9:e88348.PubMedPubMed CentralGoogle Scholar
- Skardal A, Mack D, Kapetanovic E, Atala A, Jackson JD, Yoo J, et al. Bioprinted amniotic fluid-derived stem cells accelerate healing of large skin wounds. Stem Cells Transl Med 2012;1:792–802.PubMedPubMed CentralGoogle Scholar
- Hu MS, Rennert RC, McArdle A, Chung MT, Walmsley GG, Longaker MT, et al. The role of stem cells during scarless skin wound healing. Adv Wound Care (New Rochelle) 2014;3:304–14.Google Scholar
- Beffa DC, Fischman AJ, Fagan SP, Hamrahi VF, Paul KW, Kaneki M, et al. Simvastatin treatment improves survival in a murine model of burn sepsis: Role of interleukin 6. Burns 2011;37:222–6.PubMedGoogle Scholar
- Jansen JO, Lord JM, Thickett DR, Midwinter MJ, McAuley DF Gao F. Clinical review: Statins and trauma — a systematic review. Crit Care 2013;17:227.PubMedPubMed CentralGoogle Scholar
- Fogerty MD, Efron D, Morandi A, Guy JS, Abumrad NN, Barbul A. Effect of preinjury statin use on mortality and septic shock in elderly burn patients. J Trauma 2010;69:99–103.PubMedGoogle Scholar
- Akcay MN, Akcay G, Kiziltunc A, Ozturk G, Aydinli B. The effect of short-term treatment with atorvastatin on E-selectin levels in severely burned patients. Int J Clin Pharmacol Res 2005;25:65–9.PubMedGoogle Scholar
- Tobalem M, Harder Y, Rezaeian F, Wettstein R. Secondary burn progression decreased by erythropoietin. Crit Care Med 2013;41:963–71.PubMedGoogle Scholar
- Still JM Jr., Belcher K, Law EJ, Thompson W, Jordan M, Lewis M, et al. A double-blinded prospective evaluation of recombinant human erythropoietin in acutely burned patients. J Trauma 1995;38:233–6.PubMedGoogle Scholar
- Posluszny JA Jr, Muthumalaiappan K, Kini AR, Szilagyi A, He LK, Li Y, et al. Burn injury dampens erythroid cell production through reprioritizing bone marrow hematopoietic response. J Trauma 2011;71:1288–96.PubMedPubMed CentralGoogle Scholar
- Arno A, Garcia O, Hernan I, Sancho J, Acosta A, Barret JP. Extracorporeal shock waves, a new non-surgical method to treat severe burns. Burns 2010;36:844–9.PubMedGoogle Scholar
- Meirer R, Kamelger FS, Piza-Katzer H. Shock wave therapy: An innovative treatment method for partial thickness burns. Burns 2005;31:921–2.PubMedGoogle Scholar
- Davis TA, Stojadinovic A, Anam K, Amare M, Naik S, Peoples GE, et al. Extracorporeal shock wave therapy suppresses the early proinflammatory immune response to a severe cutaneous burn injury. Int Wound J 2009;6:11–21.PubMedGoogle Scholar
- Goertz O, von der Lohe L, Lauer H, Khosrawipour T, Ring A, Daigeler A, et al. Repetitive extracorporeal shock wave applications are superior in inducing angiogenesis after full thickness burn compared to single application. Burns 2014.Google Scholar
- Goertz O, Lauer H, Hirsch T, Ring A, Lehnhardt M, Langer S, et al. Extracorporeal shock waves improve angiogenesis after full thickness burn. Burns 2012;38:1010–8.PubMedGoogle Scholar