Full document - International Hospital Federation
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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