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SunBurn |
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Background:
A sunburn is an intense, delayed,
transient inflammatory response caused by acute
overexposure to ultraviolet radiation (UVR) in
sunlight, primarily ultraviolet B (UV-B). UVR
accounts for 5% of the total energy reaching the
earth's surface. UVR is composed of ultraviolet A
([UV-A], 320-400 nm), UV-B (290-320 nm), and
ultraviolet C ([UV-C], 200-290 nm). UV-A is
further divided into UV-A II (320-340 nm) and UV-A
I (340-400 nm). While sunlight contains the entire
UVR spectrum, only UV-A and UV-B reach the earth's
surface. Approximately 95-98% of the solar UVR at
the earth's surface is UV-A. UV-A can penetrate
glass; UV-B cannot.
Unlike UV-A, all UV-C and
approximately 90% of UV-B is filtered by the ozone
layer, so no UV-C and only 10% of UV-B reaches the
earth. Exposure to UV-C may result from welding
arcs, bactericidal lamps, and mercury arc lamps.
UVR's depth of skin penetration depends upon the
wavelength, with longer wavelengths having deeper
penetration. Approximately 90% of UV-B is absorbed
by the epidermis, while 50% of UV-A reaches the
basal layer or deeper.
Since the 1920s, a tanned
appearance has been a symbol of health and wealth,
often indicating the ability to travel to sunny
areas. Outdoor recreational activities have
increased sun exposure and thus the risk of
sunburn. In 1996, 79% of Canadians reported an
average of at least 30 minutes daily exposure to
the summer sun; 32% reported 1-2 hours, and 28%
reported 2 or more hours. A 1996 US survey of
adults older than 18 years showed that 83% had at
least 1 hour of weekday exposure during the
summer, and 93% had more than 1 hour of weekend
exposure; most of this exposure occurred between
10 am and 4 pm.
A tan is the skin's response to
injury produced by UVR; there is no such thing as
a "safe" tan.
Children receive approximately 3
times more sun exposure than adults. Approximately
50-80% of an individual's estimated lifetime sun
exposure occurs during childhood and adolescence.
In quest of a tan, use of
artificial tanning beds and sun lamps has become
common, particularly by women, but artificial
tanning devices are associated with the same risks
as exposure to UVR from sunlight. Over the past 10
years, the idea that a tan is healthy has
gradually lost favor because sun exposure has
become strongly associated with skin cancer,
immunosuppression, cataract formation, and
photoaging. Blistering sunburns, particularly
during childhood, significantly increase an
individual's subsequent risk of developing
cutaneous melanoma.
Ozone layer thickness varies
with the seasons. The layer above North America is
thickest in late winter, thinnest in late summer
and early fall. The ozone layer has been
decreasing. Reactive nitrogen compounds (eg,
nitrous oxide, nitrogen dioxide), halogens (eg,
chlorine, bromine), and hydrogen compounds can
destroy the ozone layer. Nitrogen gases (from
supersonic aircraft, air pollution, fertilizers,
and microorganisms), chlorofluorocarbons (CFCs)
(used as refrigerants and in aerosols, extruded
foam, and solvents), and bromine-containing halons
(in fire extinguishers) contribute to ozone layer
depletion.
Buildup of greenhouse gas (eg,
carbon dioxide) traps heat near the earth's
surface, cools the stratosphere, and increases
ozone loss. A 1% decrease in ozone results in a
1-2% increase in UV-B and a consequent 2% increase
in skin cancers. Clouds and air pollution have
little effect on UVR, since as much as 80% of UVR
penetrates. UVR also penetrates 1-meter depths of
water.
UVR exposure increases 4% for
each 300-meter rise in altitude. Reflection from
sand, pavement, snow, and water also increases UVR
exposure. Humidity increases susceptibility to
sunburn. The equator receives the greatest amount
of UVR throughout the year.
UV index
The UV index was introduced in
1994 to forecast UVR intensity. UV index ratings
and associated risks, based upon the estimated
extent of exposure required to cause sunburn in a
fair-skinned person, are as follows:
- Zero to 2 - Minimal risk
(1-hr exposure required to sunburn)
- Three to 4 - Low risk (20-min
exposure required to sunburn)
- Five to 6 - Moderate risk
(<15-min exposure required to sunburn)
- Seven to 9 - High risk
(<10-min exposure required to sunburn)
- Ten or more - Extreme risk
(<5-min exposure required to sunburn)
Measurements of sunburn and
skin protection
The unit of measurement for
sunburn is the minimal erythema dose (MED),
defined as the minimum UV-B exposure required to
produce a clearly marginated erythema in an
irradiated site following a single exposure.
Sunscreens are rated with a sun protection factor
(SPF) number, a number that primarily reflects the
sunscreen's protection from UV-B. (No standard
measurement exists for UV-A photoprotection.) SPF
numbers are calculated by dividing the MED with
sunscreen applied by the MED without sunscreen.
Note that this degree of protection is determined
under ideal laboratory conditions and may be
considerably less with thin application and
outdoor use.
Pathophysiology:
UV-B radiation causes most
sunburn reactions and is 1000 times as
erythemogenic as UV-A. UV-B also is most likely to
induce and promote deoxyribonucleic acid (DNA)
damage.
UV-A causes approximately 15% of
sunburn reactions but causes most phototoxic drug
reactions.
UV-A and UV-B are absorbed by
chromophores, which resonate at the same
wavelength as UVR and become excited, then
subsequently degraded. The chromophores for
wavelengths less than 300 nm are the nucleic,
amino, and urocanic acids. Melanin is the
chromophore for longer wavelengths.
The DNA in epidermal
keratinocytes absorbs UVR, resulting in pyrimidine
dimer formation.
Cells with damaged DNA either
can repair the damaged DNA, or they can be
eliminated through p53 gene-dependent
sunburn cell (apoptotic keratinocyte) formation.
Sunburn cell formation depends on Fas ligand, a
proapoptotic protein induced by DNA damage. UVR
may cause p53 gene mutations, resulting
in diminished surveillance against UVR-induced
cancer. Many cytokines and inflammatory mediators
are synthesized and released, probably due to DNA
damage.
UVR causes increased synthesis
and release of arachidonic acid metabolites (eg,
prostaglandin E2 [PGE2], prostaglandin
D2 [PGD2], prostaglandin F2a
[PGF2a], and
12 hydroxyeicosatetraenoic acid [12-HETE]),
cytokines (eg, interleukin [IL]-1, IL-6, IL-8,
IL-10, IL-12, tumor necrosis factor [TNF]-a),
adhesion molecules, histamines, kinins, substance
P, calcitonin gene-related peptide, and nitric
oxide.
Reactive oxygen species can
induce membrane lipid peroxidation and
destruction.
Frequency:
- In the US:
A 1996 national survey
of US adults reported 39% had experienced a
sunburn that year; the mean number of sunburns
per adult was 1.75. A telephone survey of 503
continental US households during the summer of
1997 found that 13% of children had sunburned
during the week or weekend prior to the survey
contact, as had 9% of their parents during the
prior weekend.
- Internationally:
A 1996 Canadian
national survey showed that half of the
population had experienced at least 1 sunburn
during the summer months. A third reported 2 or
more sunburns, and 13% reported 4 or more
sunburns. A mild sunburn (ie, erythema with
sensitivity) was reported by 40% of Canadians,
moderate sunburn (ie, erythema with sensitivity
and peeling) was reported by 28%, and blistering
sunburn every summer was reported by 4%.
Mortality/Morbidity:
Sunburns, for the
most part, are a symptomatic nuisance that results
in pruritic and tender erythematous skin. In the
long term, sunburns are associated with
nonmelanoma skin cancer (NMSC) and malignant
melanoma, which can add to morbidity and shorten
lifespan. Severe sunburns infrequently require the
attention of a burn unit, and more rarely, result
in death.
Breed:
N/A
Race:
Whites are more susceptible to
sunburn, although all races may experience sunburn
with prolonged exposure.
Sunburns occur most frequently
in persons with skin phototype (SPT) 1 or 2 (ie,
individuals with light skin who have difficulty
tanning). Type 1 phototypes are fair skinned,
often with freckles, burn easily, and never tan.
Individuals with Type 5 (ie, brown skin) and 6 (ie,
black skin) are less likely to sunburn, but can
burn with prolonged UVR exposure.
SPTs are genetically determined
but also are based in part on individuals'
histories of sun exposure and reactions. SPT is
based on a person's own estimate of sunburning and
tanning, so patients should be asked, "Do you tan
easily?" A negative response to this question from
a white person implies an SPT 1 or SPT 2
designation (25% of the US population), while
affirmative responses imply designations of SPT 3
or SPT 4.
Sex:
Males typically experience more
sunburns, employ fewer sun protective measures,
and tend to be less informed about skin
malignancies and UV indices than women.
In the 1996 Canadian national
survey, 57% of the men reported at least 1 sunburn
in the summer, compared to 49% of the women. Men
reported longer sun exposure; 35% had an average
of at least 2 hours exposure daily in the summer,
compared to 21% of the women. Most outdoor workers
responding to this survey were men.
No difference exists in the
anatomical distribution of painful sunburns in men
and women.
Age:
Although sunburn occurs in people
of all ages, incidence of sunburns increases from
childhood to adolescence. The highest prevalence
of multiple sunburns in the summer occurs in
individuals aged 15-24 years.
History:
Patients with sunburn have a history of
excessive sun exposure from outdoor recreation or
work, and, less frequently, a history of
concomitant ingestion of PO medications or
application of topical agents.
- All individuals develop
sunburns from large doses of UVR, although
persons with darker skin burn less frequently.
- Persons with blue or green
eye color, lighter skin, and those who tan
poorly and freckle easily are more prone to
sunburn.
- If the patient has received
the threshold dose of UVR, delayed skin erythema
in exposed areas occurs in 2-6 hours, peaks at
15-36 hours, and resolves within 72-120 hours.
- Individuals with fair skin (eg,
SPT 1 and 2) may have a history of immediate
transient flush.
- The trunk, neck, and head
burn at lower UVR doses than upper limbs; upper
limbs burn more readily than lower limbs.
- According to the 1996
Canadian National Survey, the area most commonly
sunburned was the back and shoulders, followed
by the arms and legs, then face, scalp and neck,
and chest.
- Erythema following UV-A
exposure from sun beds begins immediately, peaks
at approximately 8 hours, and persists 24-48
hours.
Physical:
- Confluent erythema and warmth
are present in exposed areas.
- Edema, pain and tenderness,
and pruritus may occur as a result of
moderate-to-severe sun exposure.
- Vesiculation occurs in severe
cases of sunburn and may require a week or
longer to resolve.
- Complications due to
secondary infection are infrequent.
- Scaling or peeling occurs a
few days following exposure.
- Nausea, abdominal cramping,
weakness and malaise, fever, chills, and
headache also may occur, most often with severe
sunburn.
- Patients with severe sunburn
may have a rapid pulse rate.
Causes:
Although exposure to UV-B light
causes most sunburns, use of tanning salons and
home tanning devices have made UV-A–induced
sunburn increasingly common.
- Severe sunburns often result
after falling asleep at the beach or under a UV
lamp or from prolonged exposure at swimming
areas.
- Both outdoor work and outdoor
recreational activities are risk factors for
sunburn.
- Sunburn is common when
residents of northern latitudes have prolonged
sun exposure while vacationing in southern
latitudes or near the equator.
- Outdoor exposure on cloudy
days may give people a false sense of
protection. As much as 80% of UVR penetrates
clouds.
- Reflective surfaces such as
sand, snow, water, and cement may contribute to
sunburn development.
- Increased humidity reduces
the threshold for erythema caused by UVR.
- Medical treatments that
expose patients to UV-B and UV-A may cause a
sunburn reaction.
- UV-C exposure from welding
arcs, bactericidal lamps, and mercury arc lamps
may cause sunburn.
- The degree of sunburn depends
upon duration and intensity of exposure,
patient’s skin type or complexion, and previous
conditioning of the skin.
- The unit of measurement of a
sunburn is the MED, defined as the minimum UV-B
exposure required to produce a clearly
marginated erythema in an irradiated site
following a single exposure. MED is expressed as
mJ/cm2.
- Phototoxic reactions
resulting in a sunburn reaction usually occur in
the UV-A range and can be caused by topical and
systemic agents. In contrast to photoallergic
reactions, phototoxic reactions may occur after
the initial exposure and do not affect areas of
the body that were protected from light.
- Topical agents causing
phototoxic reactions
- Bergamot oil
(5-methoxypsoralen)
- Coal tar derivatives
- Acridine
- Anthracene
- Fluoranthene
- Naphthalene
- Phenanthrene
- Pyridine
- Thiopene
- Dyes/pigments
- Acriflavine
- Anthraquinone
- Cadmium sulfate
- Eosin
- Methylene blue
- Rose bengal
- Toluidine blue
- Plants (furocoumarins)
- Leguminoseae family
- Moraceae family - Figs
- Rutaceae family -
Bergamot orange, gas plant, lemon, lime
- Umbellifereae family -
Angelica, anise, bishop weed, celery, cow
parsley, dill, fennel, giant hogweed, wild
parsnip, wild carrot
- Retinoids (after continued
use)
- Adapalene
- Tazarotene
- Vitamin A acid
- Systemic agents causing
phototoxic reactions
- Antimicrobials
- Ceftazidime
- Griseofulvin
- Quinolones -
Ciprofloxacin, nalidixic acid, norfloxacin,
ofloxacin
- Sulfonamides
- Tetracyclines -
Doxycycline, tetracycline
- Trimethoprim
- Antineoplastic agents
- Dacarbazine
- 5-fluorouracil
- Vinblastine
- Diuretics
- Furosemide
- Hydrochlorothiazide
- Hypolipidemics - Clofibrate
- Nonsteroidal
anti-inflammatory agents (NSAIDs)
- Diclofenac
- Ibuprofen
- Indomethacin
- Ketoprofen
- Naproxen
- Piroxicam
- Sulindac
- Tiaprofenic acid
- Antipsychotics
- Alprazolam
- Chlordiazepoxide
- Chlorpromazine
- Desipramine
- Imipramine
- Perphenazine
- Prochlorperazine
- Thioridazine
- Trifluoperazine
- Sulfonylureas - Tolbutamide
Burns, Chemical
Burns, Electrical
Burns, Thermal
Toxic Shock Syndrome
Other Problems to be
Considered:
Drug-induced photosensitivity
or photosensitivity from topical agents including
sunscreens
Collagen vascular disease (eg,
dermatomyositis, systemic lupus erythematosus)
Polymorphous light eruption (PMLE)
Erythropoietic protoporphyria
Chronic actinic dermatitis
(actinic reticuloid, persistent light reactivity,
photosensitive eczema)
Skin cancers: Because of the
risk of NMSC and malignant melanoma, physicians
should be vigilant during skin examinations and
should educate patients about this risk,
especially when treating patients with SPTs 1 or 2
who have a history of extensive sun exposure,
sunburns, and family history of skin cancer.
Vitamin D deficiency:
Aggressive photoprotection in individuals with a
normal diet does not cause vitamin D deficiency.
Vitamin D-3 is ingested in foods or is formed in
the presence of UV-B from epidermal and dermal
7-dehydrocholesterol, which is converted to
previtamin D-3 and then vitamin D-3.
Lab Studies:
- Except for patients with
severe sunburn, laboratory studies rarely are
indicated and usually are ordered only if the
diagnosis is unclear.
- Manage cases of severe
sunburn as burn cases; order appropriate
laboratory studies and monitor for fluid and
electrolyte imbalance and for risk of secondary
infection.
Imaging Studies:
- No imaging studies are
required for patients with sunburn.
Other Tests:
- If porphyria is suspected,
order blood, urine, and stool porphyrins.
- If systemic lupus
erythematosus (SLE) is suspected, order
antinuclear antibody (ANA) serology, anti-Ro,
and anti-La antibody titers.
- Phototesting may show an
abnormally low erythemal threshold in chronic
actinic dermatitis and may induce the disorder.
- Patch testing and photopatch
testing may identify a contact or photocontact
allergen.
- If secondary infection is
suspected, order microbiology tests.
Procedures:
- Skin biopsy usually is
unnecessary because diagnosis usually is easy to
confirm from the history and clinical findings.
Histologic Findings:
Histology rarely is
required because diagnosis usually is confirmed
clinically, although it may help distinguish
sunburn from photosensitivity disorders.
Histologic changes may occur before clinical signs
or symptoms appear, sometimes as early as 30
minutes after exposure.
In patients with sunburn,
examination of the epidermis reveals sunburn cells
(ie, dyskeratotic and vacuolated keratinocytes
with pyknotic nuclei), mild spongiosis,
vacuolization of melanocytes, and decreased
numbers of Langerhans cells (see
Picture 1).
Examination of the dermis
reveals mast cell degranulation, endothelial cell
swelling of superficial and deep venular plexuses,
and a mixed perivascular infiltrate, primarily
around superficial vessels. Endothelial cell
swelling is apparent within 30 minutes after
irradiation and peaks at 24 hours.
Medical Care:
A sunburn is considered a
self-limited injury. Even a mild sunburn requiring
no treatment, however, provides an excellent
opportunity to teach patients about the risks of
sun exposure and use of photoprotection.
Patients with moderate sunburn
should be encouraged to replenish their fluids
with nonalcoholic beverages. Those with
mild-to-moderate sunburn may require relief of
pain or pruritus.
Severe sunburn requires
admission to a burn unit for parenteral fluid
replacement, pain control, and prophylaxis against
infection.
Patients presenting with a
vesicular reaction should not have the vesicles
unroofed, since the epidermal surface of the
blister provides protection against secondary
infection.
After a sunburn, the skin should
not be exposed to the sun for at least a week
because the skin is more susceptible to burning.
Nonpharmacologic treatment for sunburn includes
the following:
- Direct the patient to stay in
a shaded cool environment for a few days, with
bed rest as necessary.
- Cool baths or cool tap water
(depending on the affected surface area) or
saline solution compresses for 20 minutes,
repeated 3-4 times daily may offer some relief
from pain and pruritus.
- Applying calamine or
pramoxine lotion 3 times daily to affected areas
may help.
- Moisturizers, applied
liberally and frequently, help reduce dryness
and peeling in mild sunburns.
- Bath preparations (eg,
colloidal oatmeal) are helpful, but direct
patients to use soaps sparingly.
- Ointments or butter do not
help a mild-to-moderate sunburn and may be
painful to wash off.
Surgical Care:
Blistering sunburns may
require treatment within a hospital burn unit.
Consultations:
Refer patients who have
experienced a bad sunburn or who have burned while
on a photosensitizing medication to a
dermatologist. Other possible consultations
include the following:
- Ophthalmology (if corneal
injury suspected)
Diet:
N/A
Activity:
N/A
Topical vitamin E, if applied
within 2 minutes of excessive UV exposure, may
reduce erythema and edema. However, because
clinical effects of sunburn do not appear for some
time after exposure, the risk of sunburn may not
be appreciated at the time of exposure.
Oral indomethacin or ibuprofen,
or topical indomethacin 1%, administered
immediately after sun exposure may reduce erythema
and degree of epidermal insult.
Decrease erythema by applying
glycolic acid 12% topically qid starting 4 h after
UV-B exposure and glycolic acid 8% daily starting
24 h after UV-B exposure. Three weeks of
pretreatment with 8% glycolic acid cream 8%
results in an SPF of approximately 2.4.
Some emergency departments and
burn units continue to administer systemic
corticosteroids, although the effectiveness of
these drugs has not been established. Systemic
corticosteroid administration has little
beneficial effect in sunburn treatment and may
increase the risk of secondary infection.
Potent topical corticosteroids
transiently reduce erythema, but do not influence
epidermal damage. Topical corticosteroids may
provide some relief of stinging or itching when
applied bid/tid and provide an additive effect to
indomethacin or ibuprofen. Avoid prolonged
administration of potent steroids.
Acetaminophen or aspirin may
offer some relief of associated pain, although
opioid analgesics may be necessary in severe
situations.
Diphenhydramine (Benadryl) or
hydroxyzine HCL (Atarax) 25-75 mg hs may help
patients sleep and relieve itching, but provide no
other sunburn management benefits.
Discourage use of topical
diphenhydramine and topical anesthetic sprays
because of allergic contact dermatitis risk.
Drug Category:
Anti-inflammatory agents -- Help reduce
erythema and degree of epidermal insult.
Drug Name
|
Indomethacin (Indocin) --
Rapidly absorbed orally. Metabolism occurs in
liver by demethylation, deacetylation, and
glucuronide conjugation. Inhibits
prostaglandin synthesis. Topical indomethacin
1% applied immediately after sun exposure, may
reduce erythema and the degree of epidermal
insult. |
| Adult Dose |
25-50 mg PO bid/tid
75 mg SR PO bid; not to exceed 200 mg/d
|
| Pediatric
Dose |
1-2 mg/kg/d PO divided bid/qid;
not to exceed 4 mg/kg/d or 150-200 mg/d
|
|
Contraindications |
Documented hypersensitivity; GI
bleeding; renal insufficiency |
|
Interactions |
Coadministration with aspirin
increases risk of inducing serious NSAID-related
adverse effects; probenecid may increase
concentrations and, possibly, toxicity of
NSAIDs; may decrease effect of hydralazine,
captopril, and beta-blockers; may decrease
diuretic effects of furosemide and thiazides;
monitor PT closely (instruct patients to watch
for signs of bleeding); may increase risk of
methotrexate toxicity; phenytoin levels may be
increased when administered concurrently
|
| Pregnancy |
B - Usually safe but benefits
must outweigh the risks. |
|
Precautions |
Category D in third trimester
of pregnancy; acute renal insufficiency,
hyperkalemia, hyponatremia, interstitial
nephritis, and renal papillary necrosis may
occur; increases risk of acute renal failure
in patients with preexisting renal disease or
compromised renal perfusion; reversible
leukopenia may occur, (discontinue if there is
persistent leukopenia, granulocytopenia, or
thrombocytopenia) |
Drug Name
|
Ibuprofen (Advil, Motrin) --
DOC for patients with mild to moderate pain;
also used to reduce fever. Inhibits
inflammatory reactions and pain by decreasing
prostaglandin synthesis. Ibuprofen 400 mg q6h
initiated immediately after sun exposure may
reduce erythema and degree of epidermal
insult. |
| Adult Dose |
200-400 mg PO q4-6h while
symptoms persist; not to exceed 3.2 g/d
|
| Pediatric
Dose |
6 months to 12 years: 4-10
mg/kg PO tid/qid
>12 years: Administer as in adults
|
|
Contraindications |
Documented hypersensitivity;
peptic ulcer disease, recent GI bleeding or
perforation; renal insufficiency; high risk of
bleeding |
|
Interactions |
Coadministration with aspirin
increases risk of inducing serious NSAID-related
adverse effects; probenecid may increase
concentrations and, possibly, toxicity of
NSAIDs; may decrease effect of hydralazine,
captopril, and beta-blockers; may decrease
diuretic effects of furosemide and thiazides;
monitor PT closely (instruct patients to watch
for signs of bleeding); may increase risk of
methotrexate toxicity; phenytoin levels may be
increased when administered concurrently
|
| Pregnancy |
B - Usually safe but benefits
must outweigh the risks. |
|
Precautions |
Category D in third trimester
of pregnancy; caution in congestive heart
failure, hypertension, and decreased renal and
hepatic function; caution in anticoagulation
abnormalities or during anticoagulant therapy |
Drug Category: Analgesics
-- May offer some pain relief, although opioid
analgesics may be necessary in severe situations.
Drug Name
|
Acetaminophen (Tylenol) -- DOC
for pain in patients with documented
hypersensitivity to aspirin or NSAIDs, with
upper GI disease, or who are taking PO
anticoagulants. |
| Adult Dose |
325-650 mg PO q4-6h or 1000 mg
PO tid/qid; not to exceed 4 g/d |
| Pediatric
Dose |
<12 years: 10-15 mg/kg PO q4-6h
prn; not to exceed 2.6 g/d
>12 years: 325-650 mg PO q4h; not to exceed 5
doses in 24 h
|
|
Contraindications |
Documented hypersensitivity;
G-6-PD deficiency |
|
Interactions |
Rifampin can reduce analgesic
effects; coadministration with barbiturates,
carbamazepine, hydantoins, or isoniazid may
increase hepatotoxicity |
| Pregnancy |
B - Usually safe but benefits
must outweigh the risks. |
|
Precautions |
Hepatotoxicity possible with
overdose or chronic use; severe or recurrent
pain or high or continued fever may indicate a
serious illness; contained in many OTC
products, and combined use with these products
may result in cumulative doses exceeding
recommended maximum dose |
Drug Name
|
Aspirin (Anacin, Ascriptin,
Bayer Aspirin, Bayer Buffered Aspirin) --
Treatment for mild to moderate pain. Inhibits
prostaglandin synthesis, which prevents
formation of platelet-aggregating thromboxane
A2. |
| Adult Dose |
325-650 mg PO q4-6h; not to
exceed 4 g/d |
| Pediatric
Dose |
10-15 mg/kg PO q4-6h; not to
exceed 60-80 mg/kg/d |
|
Contraindications |
Documented hypersensitivity;
liver damage; hypoprothrombinemia; vitamin K
deficiency; bleeding disorders; asthma;
because of association of aspirin with Reye
syndrome, do not use in children (<16 y) with
flu |
|
Interactions |
Effects may decrease with
antacids and urinary alkalinizers;
corticosteroids decrease salicylate serum
levels; additive hypoprothrombinemic effects
and increased bleeding time may occur with
coadministration of anticoagulants; may
antagonize uricosuric effects of probenecid
and increase toxicity of phenytoin and
valproic acid; doses >2 g/d may potentiate
glucose lowering effect of sulfonylurea drugs
|
| Pregnancy |
D - Unsafe in pregnancy
|
|
Precautions |
May cause transient decrease in
renal function and aggravate chronic kidney
disease; avoid use in patients with severe
anemia, with history of blood coagulation
defects, or taking anticoagulants |
Drug Category: Dermatologic
agents -- Used to decrease erythema.
Drug Name
|
Glycolic acid -- It is an
organic acid contained in various topical
preparations and used to treat
hyperpigmentation and photodamaged skin.
Reduces erythema following sunburn.
Pretreatment for 3 wk with glycolic acid cream
8% provides an SPF of approximately 2.4.
|
| Adult Dose |
Apply 12% cream topically qid,
starting 4 h after UV-B exposure and 8% cream
qd starting 1 d after UV-B exposure
|
| Pediatric
Dose |
Administer as in adults
|
|
Contraindications |
Documented hypersensitivity
|
|
Interactions |
None reported |
| Pregnancy |
C - Safety for use during
pregnancy has not been established.
|
|
Precautions |
None known |
Drug Category:
Antihistamines -- May help patient sleep and
provide relief from itching, but provide no
additional benefit in management of sunburn.
Drug Name
|
Diphenhydramine (Benadryl) --
For symptomatic relief of symptoms caused by
release of histamine. |
| Adult Dose |
25-50 mg PO q6-8h prn; not to
exceed 400 mg/d |
| Pediatric
Dose |
12.5-25 mg PO tid/qid, or 5
mg/kg/d, or 150 mg/m2/d divided tid/qid;
not to exceed 300 mg/d
5 mg/kg/d IV/IM or 150 mg/m2/d,
divided qid; not to exceed 300 mg/d
|
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Contraindications |
Documented hypersensitivity;
MAOIs |
|
Interactions |
Potentiates effect of CNS
depressants; due to alcohol content, do not
give syrup dosage form to patient taking
medications that can cause disulfiramlike
reactions |
| Pregnancy |
C - Safety for use during
pregnancy has not been established.
|
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Precautions |
May exacerbate angle-closure
glaucoma, hyperthyroidism, peptic ulcer, or
urinary tract obstruction; xerostomia may
occur |
Drug Name
|
Hydroxyzine hydrochloride (Atarax)
-- Antagonizes H1-receptors in periphery; may
suppress histamine activity in subcortical
region of CNS. |
|
Adult Dose |
25-100 mg PO qd/qid
|
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Pediatric Dose |
0.6 mg/kg/dose PO q6h
|
|
Contraindications |
Documented hypersensitivity
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Interactions |
CNS depression may increase
with alcohol or other CNS depressants
|
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Pregnancy |
C - Safety for use during
pregnancy has not been established.
|
|
Precautions |
Associated with clinical
exacerbations of porphyria (may not be safe
for porphyric patients); ECG abnormalities
(alterations in T waves) may occur; may cause
drowsiness |
Further Inpatient Care:
Further Outpatient Care:
- Patients with
mild-to-moderate sunburn do not require close
monitoring.
- Closely follow patients with
extensive burns and dehydration to assess their
needs for fluid replacement and treatment of
infection.
- Caution patients and parents
to watch for signs of secondary infection in
cases of severe sunburn. Instruct patients and
parents to seek medical care for drainage, foul
smell, or increasing redness or fevers
associated with disruption of the natural skin
barrier.
In/Out Patient Meds:
Transfer:
Deterrence/Prevention:
- The association between
repeated sun exposure and sunburns with the
development of skin cancer and premature aging
highlights the importance of preventive
practices.
- Early intervention and
education during childhood maximize the effects
of preventive practices. Encourage adults to
teach sun protection to their children. Infants
and small children may be unable to avoid sun
exposure on their own.
- Encourage patients who desire
a tanned appearance to try self-tanning gels or
lotions (eg, dihydroxyacetone), which do not
increase the risk of skin cancer or wrinkling.
(These gels and lotions offer no sun
protection.)
- Sunburn prevention may
involve behavioral and pharmacological
components. The following behaviors minimize the
risk of sunburn:
- Avoid prolonged exposure
during the middle of the day (ie, 10 am-4 pm),
particularly during summer months.
- Avoid prolonged sun
exposure when the UV index is high.
- Sit or play in the shade
whenever possible. Umbrellas may decrease UVR
by approximately 70% but offer little
protection against reflected radiation. Shade
from trees (unless in a dense forest),
awnings, and buildings, while helpful, provide
insufficient UVR protection (ie, SPF typically
<4).
- Wear appropriate protective
clothing and accessories (eg, long pants,
long-sleeved shirts, hats, and sunglasses).
- Patients who have
excessive exposure to sunlight or who have
histories of skin cancer should consider
buying clothing specifically designed to
protect from UVR.
- Dark, dry, tightly woven
clothing offers the most protection. When
fabric is wet, water occupies the spaces
between the fibers and allows greater UVR
penetration. Women’s stockings provide
minimal protection. Synthetic fabrics (eg,
rayon) offer greater protection than cotton
clothing.
- Recently developed
commercial products (eg, Rit Sun Guard with
Tinosorb) add UV protection to clothing. The
product is added to the clothes washing
cycle, and a single treatment reportedly
remains effective through 20 washings.
- Wear hats with wide brims
(eg, >7.5 cm) of tightly woven material (not
straw) to protect the face, ears, and neck.
Baseball caps, depending upon how they are
worn, often inadequately protect the ears,
nose, and back of the neck.
- Avoid cosmetic tanning and
tanning salons.
- Avoid or minimize sun
exposure while taking phototoxic medications
or topical agents that may interact with
UV/visible light to cause a dose-related
sunburn.
- Pharmacologic aspects of
sunburn prevention include chemical and physical
sunscreens. No sunscreen offers 100%
photoprotection, so consider sunscreen only as
an adjunctive photoprotective measure.
- No truly effective PO
sunscreens exist. Antimalarial drugs, vitamin A
or E, betacarotene, and PO p-aminobenzoic
acid (PABA) do not provide adequate sun
protection. Combined systemic vitamin C at 2 g/d
and vitamin E at 1000 IU/d provide minimal
protection (SPF 1.4); topical application in a
sunscreen may enhance sun protection.
- Sunscreens are meant to
protect the skin and not to prolong sun
exposure. Although sunscreens can prevent
sunburn, UVR-induced immunosuppression and
carcinogenicity may occur before the UV erythema
threshold is reached. Daily sunscreen use for
4.5 years has been associated with a decline in
the incidence of squamous cell carcinoma.
- Sunscreen selection
- Seek out a sunscreen with
an SPF number of 30 or more (ie, "high
protection"), preferably a product that offers
protection against both UV-B and UV-A. (SPFs
ranging from 1-11 are rated "minimal
protection" and SPFs ranging from 12-29 are
rated "moderate protection.")
- If sunscreens with high SPF
ratings are unavailable, use sunscreens with
an SPF of at least 15. Sunscreens rated at SPF
15 block approximately 93% of UV-B radiation,
compared to the 97% block provided by SPF 30.
- Apply sunscreen 15-60
minutes prior to UV exposure to allow proper
skin binding.
- Generously apply topical
sunscreens to all exposed surfaces, including
often forgotten areas such as the lips, ears,
neck, and dorsum of feet; approximately 30 mL
is required to cover the body completely.
- Reapply sunscreens after
swimming, toweling, or sweating because these
activities remove some of the sunscreen.
Waterproof sunscreens are more substantive (ie,
maintain efficacy after 80-min water
immersion) than water-resistant sunscreens (ie,
maintain efficacy after 40-min water
immersion); either is more effective than
sweat-resistant sunscreens (ie, maintain
efficacy after 30-min continuous heavy
sweating).
- Reapplication does not
extend the period of protection.
- Physical sunscreens reflect
and scatter UV and are useful for all ages.
Examples include titanium dioxide, zinc oxide,
talc, kaolin, ferric chloride, and melanin.
Titanium dioxide and zinc oxide also absorb UVR
and, therefore, are considered both chemical and
physical sunscreens.
- Physical sunscreens tend to
be thicker, less cosmetically appealing, and
more easily rubbed off, although micronized
titanium dioxide and zinc oxide are relatively
transparent and more cosmetically pleasing.
- Although physical
sunscreens offer reduced risk of
sensitization, their occlusive effect may
cause miliaria and folliculitis.
- UV-B absorbers
- Benzylidene camphor
derivative (4-methylbenzylidene camphor) -
Photostabilizer for dibenzoylmethanes
- Cinnamates - Easily removed
with swimming and sweating; may cross react
with balsam of Peru, benzyl and methyl
cinnamate, cinnamic alcohol, cinnamic aldehyde,
cinnamon, cinnamon oil, cocoa leaves
- 2-ethoxyethyl p-methoxycinnamate
(Cinoxate)
- Octocrylene
- Octyl methoxycinnamate (Parsol
MCX)
- PABA esters (eg, octyl
dimethyl PABA [Padimate O]) - May induce
contact/photocontact dermatitis; may
cross-react with ester anesthetics,
sulfonamides, sulfonylurea hypoglycemics,
thiazides
- Salicylates - Easily
removed with swimming or sweating; rare cause
of contact dermatitis
- Octyl salicylate
- Homomenthyl salicylate (homosalate)
- Triethanolamine
salicylate
- UV-A absorbers
- Anthranilates (methyl
anthranilate) - Incomplete UV-A protection
(max absorption: 332-345 nm); rare cause of
contact dermatitis
- Benzophenones -
Broad-spectrum with UV-A II/UV-B protection
- Dioxybenzone
(benzophenone-8) - may induce contact
dermatitis and contact urticaria
- Oxybenzone
(benzophenone-3) - may induce contact and
photocontact dermatitis
- Dibenzoylmethanes (eg, t-butylmethoxy-dibenzoylmethane,
avobenzone, Parsol 1789) - Broad UV-A II and I
protection; photodegradable; may induce
contact and photocontact sensitization
Complications:
- Closely monitor patients with
extensive burns and dehydration to assess their
need for fluid replacement and their risk of
secondary infection.
- Sunburned skin rarely leads
to scarring after healing unless secondary
infection occurs.
Prognosis:
- Prognosis for most sunburns
is excellent.
- The long-term effects of
sunburn increase the patient's risk for skin
cancer, lentigines, and photoaging.
Patient Education:
- Teach patients about the
harmful effects of the sun and how to provide
appropriate sun protection for the entire
family. Patients should be taught that there is
no such thing as a “healthy” tan, and that
sunburns are more easily prevented than treated.
- Direct patients to avoid or
minimize sun exposure during the peak times of
sunburning (ie, 10 am-4 pm) when the UV index is
high. (A memorable reminder for patients is to
tell them the peak times are "whenever your
shadow is shorter than you.")
- Instruct patients to avoid
sunbathing.
- Encourage parents to use sun
protection themselves as well as to provide it
for their children. Research has found that
parents who used sun protection themselves were
more likely to provide sun protection for their
child, compared to parents who do not use sun
protection for themselves.
- Encourage susceptible persons
(eg, those with SPTs 1 or 2 and/or those with
outdoor occupations) to apply sunscreen every
day along with their daily cosmetic regimen.
- Remind young patients who
enjoy tanning about the unattractive
dyspigmentation and wrinkling associated with
chronic sun exposure, not to mention the
increased future risk of developing cutaneous
malignancy.
- Make patients aware of the UV
index, which indicates the sunlight intensity
based on weather conditions. Many weather
forecasts now feature this information.
- Encourage patients to perform
regular skin self-examinations and to seek
periodic professional examinations from their
physicians.
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