Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4581_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
02.09.2026
Размер:
19 Мб
Скачать
11.2 Minor Burns: Ambulatory Treatment
129
advantage of these agents over petrolatum­impregnated gauze (Heinrich et al. 1988; Genuino et al. 2014). However, if the treating physician wishes to use a topical antimicrobial agent, there are several choices. The most popu­lar is 1% silver sulfadiazine. In comparative studies, it delayed spontaneous reepithelializa­tion of partial- thickness burn wounds (due to its silver component; Barret etal. 2000). However, if the wound is covered with an eschar, 1% sil­ver sulfadiazine has the fewest side effects and is probably the best recommendation. It is not used on patients allergic to sulfa products, preg­nant women, nursing mothers, and infants less than 2months of age (increases the possibility of kernicterus). Bacitracin is an alternative topi­cal prophylactic antibiotic. Several authors favor its use because it is cheaper than silver sulfadiazine. Alternatively, there has been increasing interest in the use of combinations of antibiotics in ointment (neomycin, bacitracin, polymyxin B). They are effective against the Gram-positive cocci and some of the aerobic Gram-negative bacilli that most frequently colo­nize small burn wounds.
Infection can involve the depth and extent of a burn converting a supercial dermal burn into a deep dermal burn or even a full-thickness burn. An infected burn is also more susceptible to sep­sis. The appearance of gray or black spots, espe­cially if there are other manifestations of infection, should raise concern for invasive infec­tion. Fortunately, it rarely occurs among those treated as outpatients. However, when it occurs, the patient should be admitted to a hospital. All patients with a suspected burn infection should therefore be managed aggressively as inpatients with parenteral antibiotics. The view of a full­thickness skin biopsy of all infected burns to con­rm the presence of infection and identify the responsible microorganism has also been sup­ported (Morgan etal. 2000; Hartford and Kealy
2007). Burns, even minor ones, are regarded as
tetanus-prone wounds (Larkin and Moylan 1975; Solanki etal. 2014). Tetanus prophylaxis should be provided, unless the patient has received teta­nus immunization within 10 years (Rhee etal.
2005).
Covering burns serves a number of purposes. Dressings provide anesthetic relief; they act as a barrier against infection and keep the wound dry by absorbing drainage. A wide variety of dress­ings exist, and the choice depends on the depth of the burn. Non-medicinal white petrolatum­impregnated ne mesh or porous mesh gauze, biologic dressings (allogenic amnion), and syn­thetic tissue-engineered dressings (Biobrane®, hydrocolloid dressings, TransCyte®, other wound dressings containing cultured autogenous kerati­nocytes with or without broblasts like Apligraf, Integra, and AlloDerm) are readily available and can be used for burn cover. Varkey etal. (2015) in a recent review of covering materials suggested that those containing supercial dermal bro­blasts (tissue-engineered skin with supercial broblasts and keratinocytes) may prove bene­cial for postburn wound healing due to the anti­brotic properties of the latter.
Supercial partial-thickness burns, the equiv­alent of sunburn, with intact epidermis, require neither topical medication, nor a dressing. Hartford and Kealy (2007) reported that most burns of the face are treated without a dressing for practical reasons. Many physicians prefer to use a thin layer of bland ointment combined with a topical antibiotic (e.g., Baciguent, bacitracin in anhydrous lanolin, mineral oil, and white petrola­tum), because it is more comfortable for the patient and moist wounds heal more quickly than dry wounds. Mabrouk etal. (2012) observed an improvement in management and healing rate and a better long-term outcome of partial­thickness facial burns when treating those with a moist occlusive dressing (Aquacel® Ag) com­pared to moist open dressing (MEBO®). Wasiak etal. (2013) reviewed the literature regarding the effects of burn wound dressings on supercial and partial-thickness burns. Despite the poor quality of trial reporting and trial conduct, the authors concluded that burns treated with hydro­gel dressings appear to heal more quickly than those treated with usual care. Hoogewerf et al. (2013a, b) conducted a literature search on the effects of topical interventions on wound healing in people with facial burns of any depth. Five ran­domized controlled trials were included. All stud-
130
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
11 Burns oftheScalp, Face, andNeck
ies had small sample sizes and were at high risk of bias. Heterogeneity of interventions and out­comes prevented pooling of data. In these stud­ies, time to complete wound healing was signicantly shorter for those using a skin substi­tute than for those using an antibacterial agent, but the quality of evidence was low. Pain was sig­nicantly reduced with the use of skin substitutes in both studies that reported this outcome in all groups (range mean difference– 2.00 to 4.80 on a 10-point scale). They concluded that there is insufcient high-quality research and evidence to enable conclusions to be drawn on wound heal­ing in patients with facial burns.
More recently, Slaviero etal. (2018) reviewed the effect of various antiseptics and antiseptic dressings on the healing of burn wounds and reached similar conclusions to Hoogewerf etal. (2013a, b), namely that at the present moment, it is still uncertain whether the different products used on burn wounds are associated with differ­ent healing rates. They, too, suggest that further efforts are needed in order to provide stronger evidence. Hoogewerf et al. (2020) reached the same conclusion after a thorough literature search on randomized controlled trials that evaluated the effects of topical treatment for facial burns. Due to low/very low certainty evidence, no differ­ences could be established regarding wound infections, pain, time to partial and complete wound healing, adverse effects, length of hospital stay, scar quality, and patient satisfaction between the various used topical agents (Hoogewerf etal.
2020).
Recommendations regarding blister manage­ment are varied and range from leaving them intact to removing the blistered skin immediately or delaying removal. The author recommends leaving blisters intact or, when indicated, decom­pressing the blisters, leaving the blistered skin to protectively cover the wound. An intact blister usually indicates a supercial dermal wound, which will probably heal spontaneously within 3 weeks. If the blistered skin is removed, the wound is converted from a painless one to a pain­ful, open wound exposed to colonization by bac­teria and potential infection (Hartford and Kealy
2007). A burn wound with an intact blister, how-
ever, rarely, if ever, gets infected. The uid will be resorbed within the next 10–15days, and the wound will heal spontaneously. If spontaneous healing looks unlikely at follow-up, surgical intervention to facilitate healing should be undertaken.
Instructions regarding wound care, position­ing, physical therapy, clinical signs of infection, access to medical care, and pain medication are given to the patient before release from the emer­gency room. Follow-up in 2–3days is mandatory to check on the wound and the patient’s compli­ance with instructions. Further follow-up visits are arranged accordingly. The objective in burn care is to have all wounds healed within 1month. In cases of a problematic spontaneous healing, surgical removal of residual necrotic and granu­lation tissue by tangential excision and skin graft­ing is undertaken.
Most burn patients develop pruritus (itching), an annoying and often unrelenting manifestation of healing and healed burn wounds. A few studies on this subject are methodologically robust. In recent years, there has been an attempt to design and implement treatment strategies and algo­rithms; however, there is currently no agreed and consistent management plan for the treatment of pruritus due to a burn injury. A variety of treat­ments are available for the relief of this annoying symptom ranging from antihistamines (histamine has been implicated in the genesis of itching) and topical emollients to psychological therapies, massage, and dermatological treatments. Oral antihistamines are used most commonly, yet research indicates that they are not always effec­tive. The rst-line treatment should be simple; however, if single therapies are unsuccessful, combination therapy should be introduced early, in order to reduce the onset of chronic itch (Richardson etal. 2014).
Occasionally, patients with moderate or even severe burns can be treated in the ambulatory set­ting. Lower cost, less chance of exposure to antibiotic- resistant microorganisms, and a more comfortable environment are the main advan­tages. However, the conditions that need to be met in order to consider ambulatory care for any patient include completion of intravenous resus-
11.3 Moderate andSevere Burns
131
citation; no ongoing complications; no wound or systemic manifestation of sepsis; adequate nutri­tion established; and satisfactory pain control (oral analgesics). Furthermore, wound care and physical and/or occupational therapy need to be arranged (Hartford and Kealy 2007).
11.3 Moderate andSevere Burns
Primary assessment of patients with moderate and severe burns aims at quick identication and treatment of life-threatening conditions. Exposure to heated gases and smoke may result in damage to the respiratory tract, formation of edema, and airway obstruction. Progressive hoarseness is a sign of impending obstruction. The latter may develop rapidly following injury, and the respira­tory status should be continually monitored, in order to assess the need for airway control and ventilator support. Initially, 100% humied oxy­gen should be given to all patients, when no obvi­ous signs of respiratory distress are present. If deemed necessary, an airway is established by means of nasal endotracheal intubation. Early intubation of patients with signicant burns, inhalation injury, and facial/neck burns before transfer has been emphasized (Table 11.2). However, this has led to many potentially unnec­essary intubations that expose patients to unnec­essary complications. Although early intubation is lifesaving for many burn patients, criteria should be developed to determine when intuba­tion is not needed (Romanowski et al. 2016). After an airway is established, breathing must be assessed in order to ensure an adequate chest expansion. Assisted ventilation with 100% humi­ed oxygen is required for all intubated patients. Appropriate cervical spine stabilization must be accomplished by, preferably, a cervical collar to keep the head immobilized until the patient’s condition can be evaluated.
The American Burn Association recommends that if a patient is less than 60min from a hospi­tal, an iv line is not essential and can be deferred until a patient is at a hospital. If an iv line is established, Ringer’s lactate solution should be infused at 500mL/h in an adult and 250mL/h in
a child 5years of age or older. Children younger than 5years need no iv lines (Mlcak and Buffalo
2007).
Prehospital care of wounds is basic and simple
because it requires only protection from the envi­ronment with application of a clean dressing to cover the involved part. This is also the rst step in diminishing pain. If there are further burn wounds, the patient should be wrapped in a clean sheet to minimize heat loss and to control tem­perature during transport.
The assessment of a burn patient in an A&E
department is essentially the same as outlined for a prehospital phase of care. The primary care begins with the ABCs, and the establishment of an adequate airway is vital. Following the pri­mary survey, a thorough head-to-toe evaluation of the patient should be done.
Establishment of iv lines, preferably two
large-caliber iv catheters through unburned areas, for uid resuscitation, is necessary for all patients with major burns including those with inhalation injury or other associated injuries (Table 11.3). The lines are best placed in the upper extremities peripherally. Ringer’s lactate solution should be infused at 2–4 mL/kg/% total body surface area (TBSA), which is burned (ABA 2005). Children must have addi­tional uid for maintenance (Herndon et al.
1993). The initial resuscitation should begin
with 5000 ml/m2/% TBSA burned/day +2000 ml/m2/TBSA/day 5% dextrose in Ringer’s lactate. This formula calls for one-half of the total amount to be given in the rst 8h post-injury with the remainder given over the
Table 11.3 Specic protocol for preparing burned patients for medical evaluation
Cannulation of several venous routes of which one should be central if possible (followed by chest radiograph)
Monitoring of diuresis—Lactate, base decit, and central venous saturation
Insertion of nasogastric tube Sedation and/or analgesia Cleansing of wounds Tracheal intubation (if necessary) Application of sanitary devices to prevent excessive
heat loss
132
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
11 Burns oftheScalp, Face, andNeck
following 16h (Herndon etal. 1993). The uid requirements in patients with an inhalation injury have been studied, but largely in retro­spective cohorts (Holley etal. 2020). The con­sensus opinion currently indicates an increased uid demand in the presence of inhalation injury compared to patients with the same per­centage cutaneous burn but without inhalation injury (Yeung etal. 2013). However, other stud­ies have failed to demonstrate this increased resuscitation uid requirement in patients with an inhalation injury (Holley etal. 2020).
All resuscitation formulas are designed to serve as a guide only. Adjustments according to the individual patient’s response and needs ought to be made. The best monitor of uid replace­ment is urine output. Acceptable hydration is indicated by a urine output of more than 30mL/h in an adult (0.5 mL/kg/h) and 1 mL/kg/h in a child (Table11.3). Fagan etal. (2014) support the notion that global parameters of perfusion (lac­tate, base decit, and central venous saturation) are more appropriate than urine output alone in reecting the degree and recovery from a hypo­perfused state, or a state of shock. Inadequate resuscitation can cause diminished perfusion of renal and mesenteric vascular beds, whereas uid overload can cause undesired pulmonary or cere­bral edema. Decompression of the stomach with a nasogastric tube is usually necessary (air, diminished peristalsis due to pain medication/ narcotics).
Patients with facial burns occasionally have an associated inhalation injury. In a recent retro­spective study of 808 facial burns, the incidence of inhalation injury was reported to be 3.06% (Kalantar Motamedi et al. 2015). The classic paper describing the effects of inhalation injury on mortality in burn patients from the U.S.Army Institute of Surgical Research in San Antonio, Texas, reported a diagnosed inhalation injury in 373/1000 patients (ca 37%) (Shirani etal. 1987). A decrease in the incidence of inhalation injury (34% vs. 27% from 1996 to 2007) has been observed in the Netherlands (Mackie etal. 2011), whereas it is uncommon in other studies of burn patients (1.9%, 5000 burns during a 7-year period, Israel) (Haik etal. 2007).
Thermal airway injury is generally limited to supraglottic structures, whereas injury to the lower airway is chemical in nature. Toxic gases (CO2, CO, HCN) exert their effects through asphyxiation, systemic toxicity, or direct effects on respiratory tissue (halogen acids, formalde­hyde, etc.). The chemical injury stimulates vaso­motor and sensory nerve endings to produce neuropeptides, which can induce inammatory response, increased vascular permeability and vasodilation, bronchoconstriction, and nitric oxide synthase (NOS) to generate reactive oxy­gen species (ROS) (Walker et al. 2015). These factors potentiate local cellular damage and loss of hypoxic pulmonary vasoconstriction, which in turn causes increased bronchial blood ow. The loss of an intact bronchial epithelium and the effects of ROS result in a loss of plasma proteins into the alveoli and bronchioles and cast forma­tion within the airways, leading to alveolar col­lapse or complete occlusion of the airways (Murakami and Traber 2003). The abovemen­tioned processes contribute to ventilation­perfusion mismatch as a primary mechanism of hypoxemia following the smoke inhalation injury (Walker et al. 2015). Respiratory failure may occur 12–48h after smoke exposure. Because of necrosis of respiratory epithelium, patients are predisposed to secondary bacterial invasion and superimposed bacterial pneumonia (Shirani etal.
1987). Tissue factor expressed by damaged respi-
ratory epithelial cells and alveolar macrophages initiates the extrinsic coagulation cascade, dis­rupting pro- and anticoagulant alveolar homeo­stasis. Furthermore, smoke inhalation injury contributes to a hypercoagulable state in the lung by inducing plasminogen activator inhibitor 1 and stabilizing its mRNA (Middle etal. 2011).
Inhalation injury signicantly increases mor­bidity and mortality. It has been found to be an independent factor of mortality in burn patients and worsens survival even among patients with similar age and burn size (Walker et al. 2015). Physical ndings including facial injury, singed nasal hairs, soot in the proximal airways, carbo­naceous sputum production, and changes in voice may help support the diagnosis (Dries and Endorf
2013). A recent study from Florida, however,
11.3 Moderate andSevere Burns
133
showed that singed nasal hair, carbonaceous spu­tum, and facial burns are unreliable evidence for inhalation injury even in the context of an enclosed space mechanism of injury (Ching etal.
2015). These ndings may be conrmed by diag-
nostic studies including ber-optic bronchoscopy (FOB), typically performed within 24h of admis­sion (Endorf and Gamelli 2007). Despite its limi­tations, FOB continues to be the standard technique to assess the presence and severity of inhalation injury. Its relative ease and availability allow the initial diagnosis to be made and allow the inhalation injury to be followed serially (Walker et al. 2015). The use of scheduled sequential bronchoscopy as a therapeutic tool after inhalation injury showed several strong trends towards less morbidity, fewer days of mechanical ventilation, a shorter length of stay, less antibiotic use, and shorter duration of treat­ment. These promising data should promote a larger, multi-institutional trial in the future (Carr and Crowley 2013). Other means of evaluating the severity of inhalation injury include chest CT. Problems with CT include determining the optimal timing of the test and how to interpret abnormal radiographic ndings in the setting of a negative bronchoscopy (Walker et al. 2015). Yamamura et al. (2013) reported that bronchial wall thickness measured by using the chest CT scans obtained within a few hours of admission was predictive of the total number of ventilator days, ICU-stay days, and development of pneu­monia in patients with smoke inhalation injury. Thermal injury to the upper airway may cause, as mentioned previously, massive swelling of the tongue, epiglottis, and aryepiglottic folds with obstruction. Some physicians support early intu­bation (Palmieri 2007). However, airway edema develops over a matter of hours as uid resuscita­tion is ongoing. Initial evaluation is not a good indicator of the severity of obstruction that may occur later (McCall and Cahill 2005). Respiratory status should be continuously monitored in order to assess the need for airway control and the indi­cation for intubation to protect the airway (Dries and Endorf 2013). Targeted therapies for inhala­tion injury are limited. Supportive respiratory care (pulmonary toilet, mechanical ventilation
when indicated) is one of the fundamental tenets (Walker et al. 2015). Bronchial hygiene (early ambulation, chest physiotherapy, airway suction­ing, and therapeutic bronchoscopy) is paramount in patients with inhalation injury. There is no ideal respiratory support strategy. Many studies support benet with noninvasive ventilation due to the avoidance of endotracheal intubation and its associated complications. Reduction in inci­dence, cost impact, and subsequent mortality of pneumonia is particularly discussed as an advan­tage of noninvasive ventilation. The most serious complication of the latter is failure to recognize when this therapy is not providing adequate ven­tilation oxygenation or airway support resulting in deterioration of the patient (Endorf and Dries
2010). Consensus recommendations for mechan-
ical ventilation continue to serve as general guidelines (Mlcak etal. 2007). Ventilator strate­gies must support oxygenation and ventilation and reect the experience of the clinicians man­aging the patient. Limitation of pressure, accep­tance of permissive hypercapnia, and strategies to manage secretions are important (Dries and Endorf 2013).
A number of ventilation modes have been rec­ommended for the patient with inhalation injury. High-frequency percussive ventilation (HFPV) has been shown to increase the Pa O2/Fi O2 (arte­rial partial pressure of oxygen/fraction of inspired oxygen) ratio (Walker etal. 2015). A recent sys­tematic review concluded that high-frequency percussive ventilation may decrease in-hospital mortality and pneumonia incidence when com­pared to standard controlled mechanical ventila­tion. However, the authors conceded that the absence of “good-quality” evidence precluded performing a meta-analysis (Miller etal. 2018). Airway pressure release ventilation (Dries and Marini 2009) and high tidal volume ventilation (Sousse etal. 2015) have been shown to be ben­ecial for patients with inhalation injury.
Treatment of carbon monoxide (CO) poison­ing involves providing 100% oxygen, which shortens the half-life of carboxyhemoglobin (COHb) to about 45 min. Hyperbaric oxygen therapy (HBO) has been used and can further reduce the COHb half-life to about 20 min. A
134
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
11 Burns oftheScalp, Face, andNeck
systematic review found that there is not enough evidence to determine denitively whether HBO reduces adverse neurologic outcomes after CO poisoning (Buckley et al. 2011). Hydroxycobalamin is the antidote of rst resort in cyanide exposure. It binds to hydrogen cyanide (HCN) to form cyanocobalamin, which is non­toxic and excreted in the urine (Walker et al.
2015).
Supportive clinical treatment involves the use
of medical adjuncts like bronchodilators (B2­adrenergic agonists such as albuterol and salbuta­mol or nebulized epinephrine), mucolytic agents (N-acetylcysteine), anticoagulants (heparin, hep­arinoids, antithrombin, and brinolytics), and anti-inammatory agents, which have been used primarily in animal models (Dries and Endorf
2013; Holley etal. 2020).
The most common complication following
inhalation injury is respiratory tract infection and more specically pneumonia. Whereas mortality with burns and concomitant inhalation injury was reported to increase by 20%, it increased to 60% with the development of pneumonia. Delayed complications of intubation or complications associated with tracheostomy, long-term tracheal stenosis, vocal cord problems, and bronchiectasis are also encountered after inhalation injury. Long-term follow-up is necessary in order to identify and monitor the development of these complications (Walker etal. 2015; Holley etal.
2020; Charles etal. 2021).
11.4 Surgical Wound Care
Most burns go on to heal spontaneously and do not require operation. Their treatment is directed towards promoting healing, and a wide variety of dressings are currently available. Dressing selec­tion should be based on their healing effects; however, ease of application and removal, dress­ing change requirements, cost, and patient com­fort should also be considered. According to a recent study, which reviewed all randomized con­trolled trials evaluating the effects of burn wound dressings on the healing of supercial and partial­thickness burns, there is a paucity of high-quality
evidence regarding their effect (Wasiak et al.
2013). Silver sulfadiazine was consistently asso-
ciated with poorer healing outcomes than biosyn­thetic, silicon-coated, and silver dressings, while hydrogel-treated burns had better healing out­comes than those treated with usual care (Wasiak etal. 2013).
Some burns are indeterminate or of mixed depth. Some of these may require debridement and/or escharotomy and ultimately skin grafting of a portion of the wound, but that is not obvious on presentation. Demarcation of the areas which need tangential excision of the formed eschar (3–4 days post-incident) and skin grafting will aid surgical treatment of the burned face.
Full-thickness facial burns which need graft­ing are less problematic. The operative procedure can be scheduled as soon as facial edema has subsided. Face masks are used in some centers in order to exert pressure so that the grafts can be applied to a more normal surface. Tangential excision of the eschars can be a very bloody oper­ation. The use of epinephrine is indicated; fur­thermore, excision with needle-point electrocautery works well. If there is any doubt regarding depth, tangential excision with a Goulian knife is more appropriate as preservation of any viable dermal elements is essential for optimum results (Muller etal. 2007). Temporary wound closure with allografts is a good option if one decides to delay the reconstructive phase in order to decrease graft loss due to hematoma formation.
Selection of site and depth of donor skin har­vest needs careful consideration. Color match is important; therefore, skin grafts from the “blush” area above the line of the nipples should be used whenever possible.
Respecting the aesthetic units of the face gives better results, and grafts should be placed accord­ingly. Fibrin glue is often used in some centers in order to increase graft adherence limiting hema­toma formation. In cases where not the whole aesthetic unit is involved, the question arises as to what to do with unburned areas. It is not custom­ary to excise and graft the whole unit in order to achieve a better aesthetic outcome (Muller etal.
2007).
11.4 Surgical Wound Care
135
Fraulin etal. (1996) conducted a comparative study in order to assess the cosmetic and func­tional results of conservative versus surgical man­agement of facial burns. Forty patients were categorized in four groups according to the depth and management of their burns: (A) healed with­out surgery in less than 21days, (B) healed with­out surgery in 21 days or more, (C) early debridement and thick split-thickness skin graft (STSG) in 18days or less after the burn, and (D) delayed debridement and thick STSG in more than 18days after the burn. Group A patients had a sig­nicantly better overall rating on the scar assess­ment scale than the patients in the other groups that required more than 21days to heal, B, C, and D.Also, skin-grafted areas in the surgically treated groups C and D had a signicantly better scar rat­ing than wounds that healed spontaneously in group B. There was no signicant difference among groups B, C, and D when the total number of persistent functional problems after treatment was compared. The most common functional problems for these patients were microstomia and eyelid ectropion (Fraulin etal. 1996).
Philp etal. (2012) assessed the late outcomes after grafting 35 patients with full-thickness facial burns. Fourteen patients were available for late (40±33months, range 5–91months) follow­ up. The most problematic late outcomes that the authors identied included relatively poor sen­sory return, elevation of graft edges, eyelid ectro­pion, gaps between grafts and hairline, and marked hypertrophic scarring around the mouth and chin. The results of different methods of
facial grafting in 160 children with facial burns were assessed by Greenhalgh et al. (2013). In addition, the authors determined the efcacy of using allograft skin or Integra as temporary cov­ers. Allograft and Integra were used for massive burns. Of these, 39% died, 17% developed an Integra infection, and 43% required regrafting before autografting. The authors concluded that when there is a shortage of autograft, allograft or Integra is a good option, but Integra does not reduce the need for reconstructive surgery.
Occasionally, deep facial burns result in bro­proliferative scarring, skin contractures, or chronic wounds that take weeks or months to heal (Hall etal. 2017). This in turn leads to disg­urement and functional impairment constituting a major therapeutic challenge. Postburn treatment of these deformities is possible with Z-plasties, new skin grafts, pre-expanded local aps, pre­expanded prefabricated locoregional aps, and free and perforator aps (Spence 2008; Li etal.
2009; Zan et al. 2013; Lazzeri et al. 2013)
(Fig. 11.12). Partial unit to subtotal/total face deformities can be satisfactorily resurfaced, occasionally in combination with full-thickness skin grafts (especially for the central portion of the face, Spence 2008). Complications associated with the tissue expander have been reported in 18% of patients and signicant ap loss in 5% (Spence 2008). Free and perforator aps (e.g., the anterolateral thigh ap, the thoracodorsal artery perforator ap) provide good functional and aesthetic results especially for reconstruction of severe postburn neck contractures with a low
Fig. 11.12 (a–c) Forty ve-year old patient with full thickness (deep) burn of the posterior scalp. The burned tissue has been excised and replaced with a free latissimus dorsi muscular ap covered with split thickness skin grafts
abc
136
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
11 Burns oftheScalp, Face, andNeck
necessity for secondary procedures and low donor-site morbidity (Yang et al. 2002; Mun etal. 2007). Some regional perforator aps (ante­rior supraclavicular artery perforator ap) can be used either as pedicled or as free aps (Pallua and Wolter 2013). In highly selected cases of severe panfacial burns, facial vascularized composite tissue allotransplantation is a realistic option which can be considered, especially in cases of devastating electrical facial injuries. However, determining whether the patient is a candidate for face transplantation is crucial, in order to avoid a series of unwanted sequelae (Janis et al. 2015; Bharadia etal. 2017).
Specic problems encountered in cases of burns of the various facial units will be high­lighted in the following sections.
11.5 Perioral Burns
Acute reconstructive surgery is carried out during the rst months after burn injury and aims at facilitating patient care or at preventing acute contractures from causing permanent secondary damage. Acute reconstructive intervention is most frequently indicated in cases of perioral, eyelid, or cervical burns.
Partial- and/or full-thickness perioral facial burns may lead to a contracture of the tissues sur­rounding the oral commissures resulting in microstomia (Fig. 11.13). The latter negatively affects speech, eating, dental hygiene, expres­sion, social interaction, psychosocial well-being, and, when necessary, administration of general anesthesia. Orofacial contracture management
combining exercise and stretching which was ini­tiated within 48 h of admission and continued until functional goals were consistently achieved was shown to have positive outcomes for patients with partial-thickness orofacial burns. Some functional loss, however, remained with patients demonstrating persistent reduced vertical mouth opening at conclusion of treatment compared to their healthy counterparts (Clayton etal. 2015a). Nonsurgical exercise after full-thickness burns can result in positive gains; however, the duration of rehabilitation is considerable (eventually lon­ger than 2years) and some degree of long-term loss in functional mouth opening remains (Clayton etal. 2015b).
Mouth splints are widely utilized at burn cen­ters and by medical professionals for the preven­tion of oral microstomia. These devices may be obtained commercially or are custom made by hospitals’ therapists. Mouth splints may be fabri­cated static or dynamic for the horizontal or verti­cal opening of the mouth (Taylor and Walker
1997; Dougherty and Warden 2003). The use of
stacked tongue depressors is a simple acceptable technique to aid in reversing oral microstomia. In cases of microstomia, the vermilion becomes scaled, cracked, and inelastic, increasing the retraction of the commissures. The main objec­tive of surgical treatment is to obtain sufcient mouth opening, while maintaining the function of the orbicularis oris muscle, and to secure nor­mal function (eating, talking, oral hygiene). The Z-plasty and the V-Y plasty are powerful tools in the surgeon’s armamentarium for facial burn reconstruction. They lengthen linear scars by recruiting lax-adjacent lateral tissue (Ivy 1971).
abc
Fig. 11.13 (a–c) Twenty eight-year old male patient with perioral burns. The microstomia is clearly noticeable (Courtesy: Prof. DAM McGrouther, Consultant P/R Surgeon, Phoenix Professor of Plastic Surgery)
11. 6 E yelids
137
Z-plasty can also cause a profound benecial inuence on the physiology of scar tissue through the immediate and continuing breakdown of col­lagen, which occurs in hypertrophic burn scars, which occurs following the relief of tension (Longacre et al. 1976). Z-plasty also narrows a scar at the same time that it lengthens it. The improvement in the appearance and functionality of the mouth area following a Z-plasty can be dramatic (Grishkevich 2011), particularly when combined with pulsed-dye laser treatment. Free skin grafts used after opening the commissures will retract, unless the graft is kept distended for a long period of time. This can be achieved with appropriately shaped wires, which are buried under the borders of the wound after excision of the scar tissue. Full-thickness skin grafts can then be sutured in place. The wires are removed in 3–4 months (Planas et al. 1999). Mucosal V-Y advancement aps and rhomboid trapezoid mucosal aps have been used with success after scar excision for the reconstruction of the oral commissures. Acceptable aesthetic results and a good functional outcome were achieved with only minor wound-healing disturbances and no complications (Zweifel etal. 2010; Grishkevich
2011). Reconstruction of the philtrum, when
indicated, is best performed by the technique of Schmid (1964) using a composite graft from the triangular fossa of the ear. Local skin aps (the nasolabial ap) have been used by other authors. Favorable results were achieved with no postop­erative use of a splint (Makiguchi etal. 2014). Expanded skin aps have also been used for the reconstruction of perioral burn deformities. Sakurai et al. (2007) reported the use of an expanded frontal scalp ap with which postburn lip deformities were reconstructed. The result was aesthetically and functionally successful.
In cases of severe cicatricial microstomia and associated facial/neck scarring, a free perforator ap has been utilized. Jin etal. (2009) reported favorable experience with the deep inferior epi­gastric perforator (DIEP) ap, which is suitable for the repair of massive defects of the face and neck due to its size (especially when used as a bipedicled ap), has reliable blood perfusion, provides soft and pliable tissue, and causes mini-
mal donor-site morbidity. Smaller lower lip and chin burn deformities can be satisfactorily recon­structed with a free radial forearm ap. Lee etal. (2006) reported favorable results with the latter ap in seven patients with hypertrophic burn scar contractures of the lower face. In order to achieve a better outcome, the authors limited the ap to at least one nger breadth above the hyoid bone because its low setting may deteriorate the cervi­comental angle. Furthermore, they attached the ap dermis to the wound bed for reconstruction of the labiomental sulcus.
Macrostomia is caused by rapid contraction of open wounds or grafts in the perioral region and cheek. This contraction results in eversion of the upper and lower lips and lateral movements of the oral commissures widening the mouth open­ing. Drooling and desiccation of the oral mucosa, which can lead to irreversible damage to the den­tition, are the result of macrostomia. Early inter­vention with release and grafting of the lower and/or upper lip is indicated, whereas denitive reconstruction is best carried out at a later period (Donelan 2007).
11.6 Eyelids
Facial burns might well be associated with sig­nicant ocular trauma, dened as globe or eyelid pathology. In a series of 865 patients admitted to Temple University Health Sciences Burn Center, 127 (15%) presented with burn injuries to the globe and/or eyelids (Stern etal. 1996). In another series of 189 patients with facial burns referred for consultation by an ophthalmologist, 143/189 had burn injuries of the eyes or lids that required care. Lid involvement was encountered in 122/189 (78 bilateral, 44 unilateral). In 61 cases, thermal or chemical burns to the conjunctiva or lens were present (Still Jr etal. 1995).
The most important clinical recommendation is to rinse a thermally or chemically burnt eye as soon and as extensively as possible. Any delay worsens prognosis (Schrage etal. 2011). This is often only achievable when ordinary tap water is being used (Claassen etal. 2021). For chemical eye burns, the most efcacious decontamination
138
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
11 Burns oftheScalp, Face, andNeck
solution is currently uncertain. For some other proposed alternatives to water, such as the Diphoterine® solution, there is growing evidence of possible superiority in the duration and out­come of the healing process and in the treatment of pain (Wiesner etal. 2019). Early ophthalmo­logical review and prophylactic ocular lubrica­tion are mandatory in burns involving the eyelids (Mustardé 1991; Malhotra etal. 2009). The use of prophylactic ocular surface lubrication may provide early corneal protection, thereby mini­mizing ulceration in patients who may otherwise have required surgery, especially in those with mild-to-moderate exposure. In a series of 66 patients with facial burns involving the lids or eyes, 18.4% of those treated with lubrication required ocular surgery as opposed to 30% when prophylaxis was not used (Spencer etal. 2002). It is difcult to accurately assess initially the sever­ity of burns of the eyelids, unless they are coagu­lated or charred. Initial debridement is therefore not indicated. All burns of the lids should be treated, primarily, with antibiotic drops or oint­ment into the conjunctival sac every 4h, plus a mydriatic when the cornea has been damaged (Mustardé 1991). When necessary, further cor­neal damage due to exposure may be prevented by creating a “moist chamber” over the affected eye (plastic watch glass on a ring of twisted fatty gauze built up on the periorbital area). As soon as the sloughs separate, split skin grafts should be applied to the granulating areas to provide skin cover. Further grafting will be required once the phase of contraction has passed.
Burns to the periorbital region can cause upper and lower lid ectropion (intrinsic contracture), which can also arise secondarily due to contrac­ture of open wounds and/or skin grafts at distant sites (extrinsic contracture). If eyelid retraction (ectropion) causing corneal exposure occurs, early surgical intervention often requiring repeat procedures is indicated (Malhotra et al. 2009). Permanent visual impairment is rare with such prompt management. No standard rules exist regarding the tissue used for eyelid reconstruc­tion. Each case requires an individual approach based on the available skin (Malhotra etal. 2009). Release of the contracture and resurfacing of the
area with split-thickness skin grafts are consid­ered effective methods to restore protective eye­lid function (Mustardé 1991; Donelan 2007). A medium-thickness split skin graft should be used for the upper eyelid, which will give the supple­ness which is required to permit rapid blinking. Because the thinner skin will contract more, about twice as large a graft (in a vertical direc­tion) is used as will eventually be required. In the lower eyelid, a full-thickness skin graft from behind the ear should be used. This will contract less than split skin grafts and overlying the tarsus it offers no obstruction to movement, despite the fact that it is a rather thick graft (Mustardé 1991). A tarsorrhaphy is totally unnecessary and may cause damage to the lid margin (Mustardé 1991, Donelan 2007). In severe burns, the underlying brosis may cause more contraction than was rst anticipated. Therefore, a second and some­times a third graft may be required, each on the marginal side of the last (Mustardé 1991). During overlying scar release, care ought to be taken to prevent damage to the underlying orbicularis oculi which is often rolled up and contracted. It must be unfolded to its normal at broad shape before skin grafting. However, in cases of deep burns with destruction of the underlying orbicu­laris oculi muscle, the freeing of deeper tissue is more cumbersome and much scarred muscle may require to be excised. Repeated excisions and grafting may lead to a rather stiff lid, which in the case of the lower lid is of no great importance. In the case of the upper lid, however, the lid must be long enough to allow the cornea to roll under it during sleep and be completely covered. The dis­ability of such a lid xation is overcome by retracting the head, rolling the eyes down, and looking out from below the xed lid, provided that there is a gap of some sort between the lids (Mustardé 1991).
It has been reported that 50% of eyelid burns are partial-thickness burns which heal spontane­ously in 1week, whereas 12% are full-thickness burns that require release and grafting (Frank etal. 1983). Early release within 7days of burn and grafting was reported to prevent the develop­ment of exposure keratitis, progressive conjuncti­vitis, and corneal ulceration and should be