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Innovation and clinical specialities: burns<br />

under diagnosis 20 or a true difference given that the vast majority<br />

of burns occur outdoors. Researchers have found prevalence<br />

rates of inhalational injury in South Africa of 2.2 % of pediatric burn<br />

patients 19 and 14.5% of adult burn patients. 21<br />

Successful management of inhalation injuries relies on early<br />

suspicion and resuscitation, as well as minimizing post-injury<br />

complications such as bronchopneumonia and acute respiratory<br />

distress syndrome (ARDS).<br />

In the early resuscitation phase (< 36hrs), it is key to suspect<br />

inhalation injury, consider early intubation and empirically<br />

oxygenate these patients. Patients who have had prolonged<br />

exposure to smoke (ie. trapped indoors), loss of consciousness,<br />

flash burns with singed facial hair, carbonaceous sputum,<br />

hoarseness should all be closely observed for impending airway<br />

obstruction. Suspicion should also be high in patient with facial<br />

scald injuries, where airway compromise is often misdiagnosed.<br />

Scald burns can be associated with direct thermal injury to the<br />

upper airway from ingestion of hot liquids or steam inhalation. 19<br />

Intubation with a large endotracheal tube (to enable suctioning)<br />

should be done in patients with stridor, increased work to<br />

breathing, respiratory distress, hypoxia, hypercapnea, deep burns<br />

to the face or edema/erythema of the oropharynx on<br />

laryngoscopic exam. Respiratory distress may not develop for<br />

several hours, and intubation should be performed in the case of<br />

transfer in high risk patients even in absence of stridor as<br />

obstruction may progress quickly as a result of airway<br />

inflammation from injury or edema from resuscitation. 22<br />

Smoke inhalation injury is often associated with significant<br />

carbon monoxide exposure, resulting in carboxyhemoglobinemia.<br />

Carbon monoxide poisonings account for the majority of deaths,<br />

which occur at the scene or early in the pre-hospital phase.<br />

Asphyxia or anoxic brain injury develop quickly; as the oxygencarrying<br />

capacity of the blood is decreased. The clinical<br />

manifestations of carbon monoxide poisoning are non-specific<br />

and can include headache, malaise, confusion, dyspnea, seizures<br />

and loss of consciousness. The diagnosis of carbon monoxide<br />

poisoning may be hard to confirm, given its imprecise<br />

presentation, unavailable carboxyhemoglobin levels, and<br />

misleading O 2 saturation measurement. Conventional pulse<br />

oxymetry monitors are unable to distinguish O 2 saturation from CO<br />

saturation, and therefore the patient may have a falsely normal O 2<br />

saturation reading. Patients may also appear pink/red and wellperfused,<br />

classically described as “cherry red”. PaO 2 should be<br />

confirmed by blood gas if possible. Clinical suspicion is the<br />

mainstay for diagnosis and treatment. Given poor outcomes<br />

associated with neurologic findings or loss of consciousness in the<br />

setting of carbon monoxide poisoning 23 , administration of high flow<br />

oxygen should be used liberally to reverse tissue hypoxia and to<br />

accelerate the displacement of carbon monoxide (as well as<br />

cyanide) from their binding sites. The half-life of<br />

carboxyhemoglobin can be decreased from 240 minutes to 75-80<br />

minutes by using 100% FiO 2 instead of room air (21% FiO 2). 24<br />

In the post-resuscitation phase (2-5 days) many competing<br />

factors can contribute to exacerbate pulmonary insufficiency.<br />

Direct thermal injury or exposure to bronchopulmonary toxins from<br />

smoke exposure can lead to airway edema, inflammatory changes<br />

and activation of systemic inflammatory response, as well as<br />

disruption of the muco-ciliary transport, increased capillary<br />

Table 1: Burn Wound Dressings [Modified from Sabiston 33 ]<br />

Antimicrobial Salves<br />

Silver sulfadiazine (Flamazine, Silvadene)<br />

Mafenide acetate (Sulfamylon)<br />

Bacitracin<br />

Neomycin<br />

Polymyxin B<br />

Nystatin (Mycostatin)<br />

Mupirocin (Bactroban)<br />

Broad-spectrum antimicrobial; painless and easy to use; does not penetrate eschar; deeply may leave black tattoos<br />

from silver ion; mild inhibition of epithelialization<br />

Broad-spectrum antimicrobial; penetrates eschar well; may cause pain in sensate skin; wide application causes metabolic<br />

acidosis, therefore only suitable for small areas; mild inhibition of epithelialization.<br />

Ease of application; painless; antimicrobial spectrum not as wide as above agents<br />

Ease of application; painless; antimicrobial spectrum not as wide<br />

Ease of application; painless; antimicrobial spectrum not as wide<br />

Effective in inhibiting most fungal growth; cannot be used in combination with mafenide acetate<br />

More effective staphylococcal coverage; does not inhibit epithelialization; expensive<br />

Antimicrobial Soaks<br />

0.5% Silver nitrate Effective against all microorganisms; stains contacted areas; leaches sodium from wounds; may cause methemoglobinemia<br />

5% Mafenide acetate Wide antibacterial coverage; no fungal coverage; painful on application to sensate wound; wide application associated with<br />

metabolic acidosis, and therefore generally used for small high-risk areas such as cartilage coverage in nose and ears.<br />

0.025% Sodium hypochlorite (Dakin solution) Effective against almost all microbes, particularly gram-positive organisms; mildly inhibits epithelialization<br />

0.25% Acetic acid Effective against most organisms, particularly gram-negative ones; mildly inhibits epithelialization<br />

Synthetic Coverings<br />

OpSite<br />

Biobrane<br />

Transcyte<br />

Integra<br />

Biologic Coverings<br />

Xenograft (pig skin)<br />

Allograft (homograft, cadaver skin)<br />

Provides a moisture barrier; inexpensive; decreased wound pain; use complicated by accumulation of transudate and exudate<br />

requiring removal; no antimicrobial properties<br />

Provides a wound barrier; associated with decreased pain; use complicated by accumulation of exudate risking invasive<br />

wound infection; no antimicrobial properties<br />

Provides a wound barrier; decreased pain; accelerated wound healing; use complicated by accumulation of exudate;<br />

no antimicrobial properties<br />

Provides complete wound closure and leaves a dermal equivalent; sporadic take rates; no antimicrobial properties.<br />

Allows for coverage with a very thin skin graft with no dermis. Very expensive product<br />

Completely closes the wound; provides some immunologic benefits; must be removed or allowed to slough<br />

Provides all the normal functions of skin; can leave a dermal equivalent; epithelium must be removed or allowed to slough<br />

58 <strong>Hospital</strong> and Healthcare Innovation Book 2009/2010

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