- •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
Nursing management of the burn-injured person
improvements the burn patient wishes to see first. For many, the wish is for functional improvements first before the esthetic procedures.
Surgical care
Full-thickness burn wounds do not have sufficient numbers of skin-reproducing cells in the dermal appendages to satisfactorily heal on their own. The area may slowly fill in with granulation and fibrous scar tissues, migrating in from the wound margins and underlying connective tissue. However, the process is very slow and the results unacceptable from a functional wound closure and esthetic outcome perspective. Common practice in surgical burn management is to begin surgically removing (excising) full-thickness burn wounds within a week of admission. This technique of early excision has had a significant positive impact on survival, especially for those patients with moderate to large-sized burn wounds. In the past, patients with extensive burns frequently died of overwhelming sepsis and/or malnutrition while awaiting surgery to remove the devitalized burn tissue (eschar). Most patients undergo excision and grafting in the same operative procedure. In some instances, if there is concern the wound bed may not be ready for a graft, the wounds are excised and covered with topical antimicrobials, followed by a temporary biologic or synthetic dressing. The donor skin (skin graft), which is harvested in this first O. R., is then wrapped up in sterile fashion and placed in a skin fridge for later application. Two days later, if the the recipient bed is clean, the patient returns to the OR to have the donor skin laid as a skin graft on the clean recipient bed. With large burn areas, it is necessary to serially excise and graft over a period of days to several weeks. Concern over blood loss and lack of sufficient donor sites are the two limiting factors when attempting to excise and graft patients with extensive wounds.
Burn surgery involves excision of the non-viable eschar down to the point of punctate bleeding at the level of subcutaneous tissue or fascia (Fig. 16). Harvesting of donor sites for skin grafts is performed using a dermatome (Fig. 17). Hemostasis of both surgical sites must then be achieved and the donor skin placed onto the freshly excised recipient bed. Attempts are made to match skin thickness and colour
Fig. 16. Surgical excision of full-thickness burn wound
as closely as possible between donor sites and recipient sites. Grafts can be split-thickness or full-thick- ness in depth, meshed or unmeshed in appearance, temporary or permanent in nature (Table 11). The skin grafts are very thin (about.017 of an inch thick), but may be thicker, depending on the location of the recipient bed. For example, skin for an upper eyelid site would be much thinner than that intended for the back or a leg. Grafts should be left as unmeshed sheets for application to highly visible areas, such as the face, neck or back of the hand (Fig. 18). Sheet grafts are generally left open and frequently observed for evidence of serosanguinous exudate under the skin. In order to encourage a good blood supply from the recipient site to the donor site, the exudate needs to be removed. Two strategies fre-
Fig. 17. Harvesting a split-thickness skin graft
413
J. Knighton, M. Jako
Table 11. Sources of skin grafts
Type |
Source |
Coverage |
Autograft |
Patient’s own skin |
Permanent |
Isograft |
Identical twin’s skin |
Permanent |
Allograft/Homograft |
Cadaver skin |
Temporary |
Xenograft/Heterograft |
Pigskin, amnion |
Temporary |
quently recommended include aspirating the exudate using a small gauge needle and syringe, or creating a small slit in the blister and gently using normal-saline soaked, cotton-tipped applicators to roll the fluid from the centre of the “bleb” to the opening. On other parts of the body, grafts can be meshed using a dermatome mesher (Fig. 19). The mesher is set to an expansion ratio chosen by the surgeon. If there are sufficient donor sites to cover the excised areas, a 1½: 1 ratio is selected. This expansion ratio allows for exudate to come through and be wicked into a protective dressing, while at the same time be cosmetically acceptable (Fig. 20). Wider expansion ratios (3:1, 6:1) allow for increased coverage when there are limited donor sites. However, the long-term appearance is less acceptable as the mesh pattern is more visible after healing and scar maturation are complete. Meshed skin grafts are generally covered with one of a number of possible options, including silver-impregnated, vacuum-as- sisted closure, greasy gauze, or cotton gauze dressings. Most are left intact for 5 days to allow for good vascularization between the recipient bed and the skin graft. Following the initial “takedown” at postop day 5, the dressings are changed every day until the graft has become adherent and stable, usually
Fig. 19. Putting a skin graft through a dermatome mesher
around day 8. It is possible to gradually determine the percentage of “graft take” during these dressing changes. If necessary, “touch-up” surgeries can be arranged over the next few weeks. For the next year or so post-burn, the skin grafts mature and their appearance improves (Fig. 21). In the Operating Room, once hemostasis has been assured through the application of pressure and thrombin/adrenalin soaks, the donor site can be dressed with either a transparent occlusive, hydrophilic foam or greasy gauze dressing (Fig. 22). To encourage moist wound healing, the dressing should be left intact for several days, inspected and reapplied if indicated. Donor sites generally heal in 10–14 days and can be reharvested, if necessary, at subsequent operative procedures (Fig. 23).
Blood loss during burn excisions poses significant concerns from an operative point of view. The burn surgeon must carefully gauge how much excision and grafting can be performed in a single opera-
Fig. 18. Unmeshed split-thickness sheet graft |
Fig. 20. Meshed split-thickness skin graft |
414
Nursing management of the burn-injured person
Fig. 21. Mature split-thickness skin graft |
Fig. 23. Healed donor site |
tion and be prepared to conclude earlier if the blood loss is too great. From the anaesthetist’s perspective, it is a challenge to estimate blood loss during a burn excision and then to know what blood replacement to give intraoperatively. From the patient’s point of view, he/she may not wish to receive donated blood unless it is absolutely necessary. Today, with modern operative techniques, blood loss is less of a problem. The application of pressure, thrombin/adrenalin soaks, use of surgical tourniquets and the newer tumescent technique have decreased blood loss significantly for burn excision procedures.
Over the past 10 years, there have been major advancements in the development, manufacture and clinical application of a number of temporary and permanent, biologic skin substitutes. Most of these products were initially developed in response to the
Fig. 22. Harvested donor site
problemsfacedwhengraftingthemassive(i. e. > 70%) burn wound where donor sites are limited (Table 12). As experience increases with these products, alternate applications are also being explored in both the burn patient and wound care populations. The search for a permanent skin substitute continues.
Table 12. Biologic skin replacements
Source |
Product |
Description |
|
Cultured |
Epicel |
– |
cultured, autologous keratino- |
epithelial |
(Genzyme |
|
cytes grown from patient’s |
autograft |
Corpor- |
|
donated skin cells |
(CEA) |
ation, |
– |
6–8 cells thick, 2–3 weeks |
|
Massach- |
|
culture time |
|
usetts) |
– lacks dermal component; |
|
|
|
|
susceptible to infection |
|
|
– |
lacks epidermal cell-to-connect- |
|
|
|
ive tissue attachment and is, |
|
|
|
therefore, very fragile |
Dermal |
Integra |
– |
synthetic, dermal substitute |
replace- |
(Johnson & |
– neodermis formed by fibrovas- |
|
ment |
Johnson, |
|
cular ingrowth of wound bed |
|
Texas) |
|
into 2 mm thick glycosamino- |
|
|
|
glycan matrix dermal analog |
–epidermal component, Silastic, removed in 2–3 weeks and replaced with ultrathin
–autograft
–functional burn wound cover
–requires 2 O.R.’s: 1 for dermal placement, 1 for epidermal graft
Dermal |
AlloDerm |
– |
cadaver allograft dermis |
replace- |
(LifeCell |
|
rendered acellular and nonim- |
ment |
Corpor- |
|
munogenic |
|
ation, Texas) |
– |
covered with autograft in same |
|
|
|
O.R. procedure |
415