- •Preface
- •List of contributers
- •History, epidemiology, prevention and education
- •A history of burn care
- •“Black sheep in surgical wards”
- •Toxaemia, plasmarrhea, or infection?
- •The Guinea Pig Club
- •Burns and sulfa drugs at Pearl Harbor
- •Burn center concept
- •Shock and resuscitation
- •Wound care and infection
- •Burn surgery
- •Inhalation injury and pulmonary care
- •Nutrition and the “Universal Trauma Model”
- •Rehabilitation
- •Conclusions
- •References
- •Epidemiology and prevention of burns throughout the world
- •Introduction
- •Epidemiology
- •The inequitable distribution of burns
- •Cost by age
- •Cost by mechanism
- •Limitations of data
- •Risk factors
- •Socioeconomic factors
- •Race and ethnicity
- •Age-related factors: children
- •Age-related factors: the elderly
- •Regional factors
- •Gender-related factors
- •Intent
- •Comorbidity
- •Agents
- •Non-electric domestic appliances
- •War, mass casualties, and terrorism
- •Interventions
- •Smoke detectors
- •Residential sprinklers
- •Hot water temperature regulation
- •Lamps and stoves
- •Fireworks legislation
- •Fire-safe cigarettes
- •Children’s sleepwear
- •Acid assaults
- •Burn care systems
- •Role of the World Health Organization
- •Conclusions and recommendations
- •Surveillance
- •Smoke alarms
- •Gender inequality
- •Community surveys
- •Acknowledgements
- •References
- •Prevention of burn injuries
- •Introduction
- •Burns prevalence and relevance
- •Burn injury risk factors
- •WHERE?
- •Burn prevention types
- •Burn prevention: The basics to design a plan
- •Flame burns
- •Prevention of scald burns
- •Conclusions
- •References
- •Burns associated with wars and disasters
- •Introduction
- •Wartime burns
- •Epidemiology of burns sustained during combat operations
- •Fluid resuscitation and initial burn care in theater
- •Evacuation of thermally-injured combat casualties
- •Care of host-nation burn patients
- •Disaster-related burns
- •Epidemiology
- •Treatment of disaster-related burns
- •The American Burn Association (ABA) disaster management plan
- •Summary
- •References
- •Education in burns
- •Introduction
- •Surgical education
- •Background
- •Simulation
- •Education in the internet era
- •Rotations as courses
- •Mentorship
- •Peer mentorship
- •Hierarchical mentorship
- •What is a mentor
- •Implementation
- •Interprofessional education
- •What is interprofessional education
- •Approaches to interprofessional education
- •References
- •European practice guidelines for burn care: Minimum level of burn care provision in Europe
- •Foreword
- •Background
- •Introduction
- •Burn injury and burn care in general
- •Conclusion
- •References
- •Pre-hospital and initial management of burns
- •Introduction
- •Modern care
- •Early management
- •At the accident
- •At a local hospital – stabilization prior to transport to the Burn Center
- •Transportation
- •References
- •Medical documentation of burn injuries
- •Introduction
- •Medical documentation of burn injuries
- •Contents of an up-to-date burns registry
- •Shortcomings in existing documentation systems designs
- •Burn depth
- •Burn depth as a dynamic process
- •Non-clinical methods to classify burn depth
- •Burn extent
- •Basic principles of determining the burn extent
- •Methods to determine burn extent
- •Computer aided three-dimensional documentation systems
- •Methods used by BurnCase 3D
- •Creating a comparable international database
- •Results
- •Conclusion
- •Financing and accomplishment
- •References
- •Pathophysiology of burn injury
- •Introduction
- •Local changes
- •Burn depth
- •Burn size
- •Systemic changes
- •Hypovolemia and rapid edema formation
- •Altered cellular membranes and cellular edema
- •Mediators of burn injury
- •Hemodynamic consequences of acute burns
- •Hypermetabolic response to burn injury
- •Glucose metabolism
- •Myocardial dysfunction
- •Effects on the renal system
- •Effects on the gastrointestinal system
- •Effects on the immune system
- •Summary and conclusion
- •References
- •Anesthesia for patients with acute burn injuries
- •Introduction
- •Preoperative evaluation
- •Monitors
- •Pharmacology
- •Postoperative care
- •References
- •Diagnosis and management of inhalation injury
- •Introduction
- •Effects of inhaled gases
- •Carbon monoxide
- •Cyanide toxicity
- •Upper airway injury
- •Lower airway injury
- •Diagnosis
- •Resuscitation after inhalation injury
- •Other treatment issues
- •Prognosis
- •Conclusions
- •References
- •Respiratory management
- •Airway management
- •(a) Endotracheal intubation
- •(b) Elective tracheostomy
- •Chest escharotomy
- •Conventional mechanical ventilation
- •Introduction
- •Pathophysiological principles
- •Low tidal volume and limited plateau pressure approaches
- •Permissive hypercapnia
- •The open-lung approach
- •PEEP
- •Lung recruitment maneuvers
- •Unconventional mechanical ventilation strategies
- •High-frequency percussive ventilation (HFPV)
- •High-frequency oscillatory ventilation
- •Airway pressure release ventilation (APRV)
- •Ventilator associated pneumonia (VAP)
- •(a) Prevention
- •(b) Treatment
- •References
- •Organ responses and organ support
- •Introduction
- •Burn shock and resuscitation
- •Post-burn hypermetabolism
- •Individual organ systems
- •Central nervous system
- •Peripheral nervous system
- •Pulmonary
- •Cardiovascular
- •Renal
- •Gastrointestinal tract
- •Conclusion
- •References
- •Critical care of thermally injured patient
- •Introduction
- •Oxidative stress control strategies
- •Fluid and cardiovascular management beyond 24 hours
- •Other organ function/dysfunction and support
- •The nervous system
- •Respiratory system and inhalation injury
- •Renal failure and renal replacement therapy
- •Gastro-intestinal system
- •Glucose control
- •Endocrine changes
- •Stress response (Fig. 2)
- •Low T3 syndrome
- •Gonadal depression
- •Thermal regulation
- •Metabolic modulation
- •Propranolol
- •Oxandrolone
- •Recombinant human growth hormone
- •Insulin
- •Electrolyte disorders
- •Sodium
- •Chloride
- •Calcium, phosphate and magnesium
- •Calcium
- •Bone demineralization and osteoporosis
- •Micronutrients and antioxidants
- •Thrombosis prophylaxis
- •Conclusion
- •References
- •Treatment of infection in burns
- •Introduction
- •Clinical management strategies
- •Pathophysiology of the burn wound
- •Burn wound infection
- •Cellulitis
- •Impetigo
- •Catheter related infections
- •Urinary tract infection
- •Tracheobronchitis
- •Pneumonia
- •Sepsis in the burn patient
- •The microbiology of burn wound infection
- •Sources of organisms
- •Gram-positive organisms
- •Gram-negative organisms
- •Infection control
- •Pharmacological considerations in the treatment of burn infections
- •Topical antimicrobial treatment
- •Systemic antimicrobial treatment (Table 3)
- •Gram-positive bacterial infections
- •Enterococcal bacterial infections
- •Gram-negative bacterial infections
- •Treatment of yeast and fungal infections
- •The Polyenes (Amphotericin B)
- •Azole antifungals
- •Echinocandin antifungals
- •Nucleoside analog antifungal (Flucytosine)
- •Conclusion
- •References
- •Acute treatment of severely burned pediatric patients
- •Introduction
- •Initial management of the burned child
- •Fluid resuscitation
- •Sepsis
- •Inhalation injury
- •Burn wound excision
- •Burn wound coverage
- •Metabolic response and nutritional support
- •Modulation of the hormonal and endocrine response
- •Recombinant human growth hormone
- •Insulin-like growth factor
- •Oxandrolone
- •Propranolol
- •Glucose control
- •Insulin
- •Metformin
- •Novel therapeutic options
- •Long-term responses
- •Conclusion
- •References
- •Adult burn management
- •Introduction
- •Epidemiology and aetiology
- •Pathophysiology
- •Assessment of the burn wound
- •Depth of burn
- •Size of the burn
- •Initial management of the burn wound
- •First aid
- •Burn blisters
- •Escharotomy
- •General care of the adult burn patient
- •Biological/Semi biological dressings
- •Topical antimicrobials
- •Biological dressings
- •Other dressings
- •Exposure
- •Deep partial thickness wound
- •Total wound excision
- •Serial wound excision and conservative management
- •Full thickness burns
- •Excision and autografting
- •Topical antimicrobials
- •Large full thickness burns
- •Serial excision
- •Mixed depth burn
- •Donor sites
- •Techniques of wound excision
- •Blood loss
- •Antibiotics
- •Anatomical considerations
- •Skin replacement
- •Autograft
- •Allograft
- •Other skin replacements
- •Cultured skin substitutes
- •Skin graft take
- •Rehabilitation and outcome
- •Future care
- •References
- •Burns in older adults
- •Introduction
- •Burn injury epidemiology
- •Pathophysiologic changes and implications for burn therapy
- •Aging
- •Comorbidities
- •Acute management challenges
- •Fluid resuscitation
- •Burn excision
- •Pain and sedation
- •End of life decisions
- •Summary of key points and recommendations
- •References
- •Acute management of facial burns
- •Introduction
- •Anatomy and pathophysiology
- •Management
- •General approach
- •Airway management
- •Facial burn wound management
- •Initial wound care
- •Topical agents
- •Biological dressings
- •Surgical burn wound excision of the face
- •Wound closure
- •Special areas and adjacent of the face
- •Eyelids
- •Nose and ears
- •Lips
- •Scalp
- •The neck
- •Catastrophic injury
- •Post healing rehabilitation and scar management
- •Outcome and reconstruction
- •Summary
- •References
- •Hand burns
- •Introduction
- •Initial evaluation and history
- •Initial wound management
- •Escharotomy and fasciotomy
- •Surgical management: Early excision and grafting
- •Skin substitutes
- •Amputation
- •Hand therapy
- •Secondary reconstruction
- •References
- •Treatment of burns – established and novel technology
- •Introduction
- •Partial thickness burns
- •Biological membranes – amnion and others
- •Xenograft
- •Full thickness burns
- •Dermal analogs
- •Keratinocyte coverage
- •Facial transplantation
- •Tissue engineering and stem cells
- •Gene therapy and growth factors
- •Conclusion
- •References
- •Wound healing
- •History of wound care
- •Types of wounds
- •Mechanisms of wound healing
- •Hemostasis
- •Proliferation
- •Epithelialization
- •Remodeling
- •Fetal wound healing
- •Stem cells
- •Abnormal wound healing
- •Impaired wound healing
- •Hypertrophic scars and keloids
- •Chronic non-healing wounds
- •Conclusions
- •References
- •Pain management after burn trauma
- •Introduction
- •Pathophysiology of pain after burn injuries
- •Nociceptive pain
- •Neuropathic pain
- •Sympathetically Maintained Pain (SMP)
- •Pain rating and documentation
- •Pain management and analgesics
- •Pharmacokinetics in severe burns
- •Form of administration [21]
- •Non-opioids (Table 1)
- •Paracetamol
- •Metamizole
- •Non-steroidal antirheumatics (NSAID)
- •Selective cyclooxygenasis-2-inhibitors
- •Opioids (Table 2)
- •Weak opioids
- •Strong opioids
- •Other analgesics
- •Ketamine (see also intensive care unit and analgosedation)
- •Anticonvulsants (Gabapentin and Pregabalin)
- •Antidepressants with analgesic effects
- •Regional anesthesia
- •Pain management without analgesics
- •Adequate communication
- •Psychological techniques [65]
- •Transcutaneous electrical nerve stimulation (TENS)
- •Particularities of burn pain
- •Wound pain
- •Breakthrough pain
- •Intervention-induced pain
- •Necrosectomy and skin grafting
- •Dressing change of large burn wounds and removal of clamps in skin grafts
- •Dressing change in smaller burn wounds, baths and physical therapy
- •Postoperative pain
- •Mental aspects
- •Intensive care unit
- •Opioid-induced hyperalgesia and opioid tolerance
- •Hypermetabolism
- •Psychic stress factors
- •Risk of infection
- •Monitoring [92]
- •Sedation monitoring
- •Analgesia monitoring (see Fig. 2)
- •Analgosedation (Table 3)
- •Sedation
- •Analgesia
- •References
- •Nutrition support for the burn patient
- •Background
- •Case presentation
- •Patient selection: Timing and route of nutritional support
- •Determining nutritional demands
- •What is an appropriate initial nutrition plan for this patient?
- •Formulations for nutritional support
- •Monitoring nutrition support
- •Optimal monitoring of nutritional status
- •Problems and complications of nutritional support
- •Conclusion
- •References
- •HBO and burns
- •Historical development
- •Contraindications for the use of HBO
- •Conclusion
- •References
- •Nursing management of the burn-injured person
- •Introduction
- •Incidence
- •Prevention
- •Pathophysiology
- •Severity factors
- •Local damage
- •Fluid and electrolyte shifts
- •Cardiovascular, gastrointestinal and renal system manifestations
- •Types of burn injuries
- •Thermal
- •Chemical
- •Electrical
- •Smoke and inhalation injury
- •Clinical manifestations
- •Subjective symptoms
- •Possible complications
- •Clinical management
- •Non-surgical care
- •Surgical care
- •Coordination of care: Burn nursing’s unique role
- •Nursing interventions: Emergent phase
- •Nursing interventions: Acute phase
- •Nursing interventions: Rehabilitative phase
- •Ongoing care
- •Infection prevention and control
- •Rehabilitation medicine
- •Nutrition
- •Pharmacology
- •Conclusion
- •References
- •Outpatient burn care
- •Introduction
- •Epidemiology
- •Accident causes
- •Care structures
- •Indications for inpatient treatment
- •Patient age
- •Total burned body surface area (TBSA)
- •Depth of the burn
- •Pre-existing conditions
- •Accompanying injuries
- •Special injuries
- •Treatment
- •Initial treatment
- •Pain therapy
- •Local treatment
- •Course of treatment
- •Complications
- •Infections
- •Follow-up care
- •References
- •Non-thermal burns
- •Electrical injury
- •Introduction
- •Pathophysiology
- •Initial assessment and acute care
- •Wound care
- •Diagnosis
- •Low voltage injuries
- •Lightning injuries
- •Complications
- •References
- •Symptoms, diagnosis and treatment of chemical burns
- •Chemical burns
- •Decontamination
- •Affection of different organ systems
- •Respiratory tract
- •Gastrointestinal tract
- •Hematological signs
- •Nephrologic symptoms
- •Skin
- •Nitric acid
- •Sulfuric acid
- •Caustic soda
- •Phenol
- •Summary
- •References
- •Necrotizing and exfoliative diseases of the skin
- •Introduction
- •Necrotizing diseases of the skin
- •Cellulitis
- •Staphylococcal scalded skin syndrome
- •Autoimmune blistering diseases
- •Epidermolysis bullosa acquisita
- •Necrotizing fasciitis
- •Purpura fulminans
- •Exfoliative diseases of the skin
- •Stevens-Johnson syndrome
- •Toxic epidermal necrolysis
- •Conclusion
- •References
- •Frostbite
- •Mechanism
- •Risk factors
- •Causes
- •Diagnosis
- •Treatment
- •Rewarming
- •Surgery
- •Sympathectomy
- •Vasodilators
- •Escharotomy and fasciotomy
- •Prognosis
- •Research
- •References
- •Subject index
P. Dziewulski, J.-L. Villapalos
It is our practice to use endo or naso tracheal tubes in patients with partial thickness burn injury that require short to medium term ventilation (> 14 days). Patients who have a pan facial full thickness burn, who require long term ventilation and have an associated major burn (> 60%) TBSA are usually managed with a tracheostomy [11]. This allows easy access to the face for wound and graft care, prevents shearing and allows the benefits of sedation reduction associated with tracheostomy. However this may increase the incidence of subsequent neck contracture when associated with a deep neck burn.
If an endo or naso tracheal intubation is preferred, the tube can be secured by standard tube tapes, however, these make wound care difficult and can rub against the cheek wound deepening it. Our preferred method in this circumstance is dental wiring or a trans-septal silk suture that secures the tube without the need for tapes. Other tubes can be secured in this way or alternatively to the endotracheal tube once it is secured.
Facial burn wound management
Initial wound care
Following admission patients with facial burns undergo cleaning with an antiseptic and debridement of debris and blisters. Superficial partial thickness wounds are cleaned twice daily and a topical antimicrobial is applied until epithelialization and healing occur. Deep burns are cleaned and dressed twice daily with Flammazine or Acticoat on alternate days until surgical excision is undertaken, usually within the first 5–7 days following admission. In indeterminate injury a topical antimicrobial such as twice daily Flammazine or alternate day Acticoat is applied until an assessment is made at or before day 10 to determine whether healing will occur by day 21. This cleaning and debridement may require a general anaesthetic in the operating theatre to adequately clean the wound, remove pseudo eschar and assess the underlying wound.
Conservative management is continued if the wound is believed to heal within 21 days, if not the patient is prepared for surgical debridement and wound closure. In male patients regular shaving of
the beard area prevents excessive accumulation of hair and wound debris that if left can lead to folliculitis, infection and deepening of the wound.
Topical agents
There are many topical agents that have been used in the management of facial burns. These include antiseptics, antimicrobial agents and dressings [12].
Antiseptics are topical agents designed to limit (bacteriostatic) or eliminate (bactericidal) the presence of microorganisms in the surgical wound. They are the mainstay of wound cleansing both following admission and afterwards during repeated wound bathing and cleaning. They include chlorhexidene and povidone iodine products that have similar anti gram-positive, gram-negative bactericidal and viricidal effects. The iodine-based antiseptics are also active against fungi, spores, protozoa, and yeasts. Iodine based preparations can be painful and irritating and in the past have been associated with toxicity [13].
Antimicrobial agents are topical agents that control and limit burn infection. The characteristics of the ideal prophylactic topical antimicrobial agent include a broad spectrum with long standing action, lack of toxicity and adequate local eschar penetration without systemic absorption. They should be inexpensive, and easy to apply and store. They need to provide a favorable wound healing environment and deliver a high concentration of active principle to a devitalized, devascularized and potentially necrotic wound [14]. The use of topical antimicrobials in facial burns is intended to limit bacterial colonization and invasive infection, which has a detrimental effect on the zone of stasis injury leading to deepening of the burn wound.
Silver preparations and silver sulfadiazine in particular are key products in burn surgery as they act on the potentially infected burn eschar limiting the extent of the non-viable tissue but can be irritant, stain the skin and can be absorbed systemically [15].
Silver sulfadiazine cream 1% (Flammazine1, Smith and Nephew; Silvadene1, King Pharmaceuticals) is a water-based cream containing the insoluble active principle silver sulfadiazine in micronized form. Fox introduced it in 1968 and at the time
294
Acute management of facial burns
revolutionized burn wound management. It must be applied repeatedly at least every 12h with a layer thickness of about 3–5 mm and provides effective local antibacterial effect against gram-positive bacteria, gram-negative bacteria, viruses and fungal species such as candida albicans.
It can produce a transient consumptive leucopenia, methahemoglobinemia and is contraindicated in cases of sulfa allergy. Its use can produce a thick yellow pseudo-eschar that can make the differential diagnosis with full thickness burns difficult. It can delay wound healing due to keratinocyte and fibroblast inhibition rendering its use in facial burns questionable although the evidence in this group of patients is limited [16].
Comparison of the use of silver sulfadiazine against bio-engineered skin substitutes showed a significant decrease in wound care time, pain and re-epithelialization time in the skin substitute group [17]. A similar report comparing silver sulfadiazine and allografts found decreased re-epithelialization time and hypertrophic scar incidence in the allograft group [18].
Cerium nitrate can be combined with silver sulfadiazine (Flammacerium) and has excellent penetration, forms a hard eschar and reduces bacterial colonization with gram positive, gram negative and fungal species [19]. Its use has been popularized in Europe with varying results [20] and the results of a randomized controlled study comparing it to Flammazine in the management of facial burns are awaited (ClinicalTrials.gov IdentifierNCT00 297 752).
Acticoat (Smith and Nephew, Hull, UK) is a bilayered polyethylene nanocrystalline silver-based dressing attached to a soaking coat of polyester. It delivers silver at a regular rate to the wound once it becomes saturated with water, avoids the rapid neutralization of silver occurring in other silverbased preparations and limits the need for dressing changes. It needs to be kept hydrated with water. Acticoat is useful in the management of facial burns and is a successful alternative to traditional silver sulfadiazine [21]. It has been compared to silver sulfadiazine and was noted to reduce grafting requirements [22].
Neosporin, Polysporin and Bacitracin are commonly used antibiotic ointments in North America for the treatment of superficial burned areas. Their
eschar penetration is limited. The Neosporin contains bacitracin (gram-positive activity) and neomycin and polymyxin B (gram-negative activity) [23].
Moist exposed burn ointment (MEBO) has been popularized in the Far East and Middle East recently. It contains herbs in a wax ointment but it is not clear what the active ingredient and comparative studies have shown varying results [24, 25].
Beta-Glucan preparations have been reported as reducing pain and promoting healing with Glucancollagen being reported as being useful in partial thickness burns in children [26].
Biological dressings
There are a number of biological and semi-biological dressings that can be used to physiologically close the burn wound to aid epithelialisation in partial thickness injury and to protect the deeper, excised wound from desiccation, infection and mechanical trauma [27].
Prior to application of any of these dressings the wounds need thorough cleaning, decontaminating and debridement of blisters, debris and devitalized tissue. This can only be adequately achieved in most cases under a general anaesthetic in a dedicated facility.
A popular semi-biological dressing Biobrane has been popularized in the management of superficial partial thickness wounds. It is a bilaminar dressing with an external silicone layer bonded to a nylon mesh impregnated with porcine collagen. It has been shown to have advantages over conventional open technique topical management in terms of ease of care, reduction in costs, decrease of pain and decrease in time to healing [28, 29] (Fig. 3).
Cadaver allograft can be used to physiologically close partial thickness wounds. to enhance epithelialsation and healing. A prospective study demonstrated cadaver allograft to be superior when compared to open treatment with silver sulphadiazine. in shallow and deep partial thickness burns [18].
Porcine skin xenografts can also be used for temporary physiological wound closure to promote epithelialisation and healing or as interim prior to autografting [27].
Human amnion can also be used a biological dressing to physiologically close the wound and pro-
295