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Warning Endpoints How To Avoid Side Effects

1) Lasers are commonly used in dermatology to treat conditions like vascular lesions, hair removal, and pigmented lesions. 2) Immediate skin responses, called endpoints, provide indicators of desired treatment effects or unwanted tissue injury. 3) Different laser treatments produce specific endpoints depending on the laser type, settings, and target tissue. Observing endpoints guides safe adjustment of laser parameters to increase efficacy while avoiding side effects.

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0% found this document useful (0 votes)
74 views13 pages

Warning Endpoints How To Avoid Side Effects

1) Lasers are commonly used in dermatology to treat conditions like vascular lesions, hair removal, and pigmented lesions. 2) Immediate skin responses, called endpoints, provide indicators of desired treatment effects or unwanted tissue injury. 3) Different laser treatments produce specific endpoints depending on the laser type, settings, and target tissue. Observing endpoints guides safe adjustment of laser parameters to increase efficacy while avoiding side effects.

Uploaded by

cristianne
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Immediate skin responses to laser and light treatments

Warning endpoints: How to avoid side effects


Molly Wanner, MD, MBA,a Fernanda H. Sakamoto, MD, PhD,a,b
Mathew M. Avram, MD, JD,a,b and R. Rox Anderson, MDa,b
Boston, Massachusetts

Learning objectives
After completing this learning activity, participants should be able to recognize warning endpoints for different laser applications; detail the laser tissue interaction underlying these
responses; and select the appropriate endpoints to optimize safety.

Disclosures
Editors
The editors involved with this CME activity and all content validation/peer reviewers of the journal-based CME activity have reported no relevant financial relationships with
commercial interest(s).

Authors
The authors involved with this journal-based CME activity have reported no relevant financial relationships with commercial interest(s).

Planners
The planners involved with this journal-based CME activity have reported no relevant financial relationships with commercial interest(s). The editorial and education staff involved
with this journal-based CME activity have reported no relevant financial relationships with commercial interest(s).

Lasers are versatile, commonly used treatment tools in dermatology. While it is tempting to follow
manufacturer’s guidelines or other ‘‘recipes’’ for laser treatment, this approach alone can be a recipe for
disaster. Specific and immediate skin responses or endpoints exist and are clinically useful because they
correlate with underlying mechanisms that are either desirable (ie, therapeutic), undesirable (ie, warning
signs of injury or side effects), or incidental. The observation of clinical endpoints is a safe and reliable
guide for appropriate treatment. This article presents the warning endpoints during specific dermatologic
laser treatments, and the accompanying article presents the therapeutic endpoints, their underlying
mechanisms, and the utility of these endpoints. ( J Am Acad Dermatol 2016;74:807-19.)

Key words: adverse effects; endpoint; laser; light; skin; warning.

INTRODUCTION
Key points Abbreviations used:
d Immediate or short-term tissue reactions, IPL: intense pulsed light
called endpoints, can provide a reliable in- MTZ: microthermal zone
Nd:YAG: neodymium-doped yttrium aluminum
dicator of desired treatment response or of garnet
unwanted tissue injury RF: radiofrequency
SP: selective photothermolysis

From the Department of Dermatologya and Wellman Center for Accepted for publication June 3, 2015.
Photomedicine,b Massachusetts General Hospital, Harvard Reprint requests: Molly Wanner, MD, MBA, Department of Derma-
Medical School, Boston, Massachusetts. tology, Massachusetts General Hospital, 50 Staniford St, Ste 200,
Drs Wanner and Sakamoto contributed to this article equally. Boston, MA 02114. E-mail: mwanner@partners.org.
Funding sources: None. 0190-9622/$36.00
Massachusetts General Hospital receives royalties from laser Ó 2015 by the American Academy of Dermatology, Inc.
companies, but none are related to this manuscript. Dr Avram http://dx.doi.org/10.1016/j.jaad.2015.06.025
is on the advisory board of and a consultant for Zeltiq, is a Date of release: May 2016
consultant for Kythera, and is an investigator for Cutera. The Expiration date: May 2019
other authors declare no conflicts of interest.

807
808 Wanner et al J AM ACAD DERMATOL
MAY 2016

d The specific endpoints vary with the type of inside the tissue. The absorbed energy is converted
laser, with proper use of the laser, and with to heat, mechanical motion, or chemical reactions.
the histologic target(s) involved Most laser- and other energyebased treatments in
d Observation of clinical endpoints is crucial dermatology work by creating heat within tissue at
for the adjustment of laser parameters dur- specific target locations or in specific patterns.
ing treatment, both to increase efficacy and When using light sources, basic parameters that
to avoid side effects describe the dosimetry of treatment must be under-
Lasers and other energy sources are frequently stood. These include wavelength of light (nm), pulse
used in dermatology to treat vascular lesions, hyper- duration (in seconds), frequency of pulse delivery
trichosis, tattoos, various pigmented lesions, scars, (Hertz [Hz]), energy (Joule [J]), fluence (the incident
photoaging, and skin laxity (Table I). Of all surgical energy per unit area, J/cm2), power (watts [W], the
tools, lasers are both the most precise and the most rate of energy delivery), power density or irradiance
selective. For many applications, there are specific (the rate of incident energy delivery per unit area,
‘‘target’’ structures or distinct patterns of intended W/cm2) and exposure spot size (cm). For fractional
skin injury that achieve the therapeutic response lasers, the area density (ie, the fraction of skin
without causing significant collateral injury or scar- treated, expressed as %) and pulse energy (ie, J per
ring. Different anatomic, physical, and physiologic pulse, corresponding to depth of treatment) are also
mechanisms are involved in these various applica- important.84
tions. As a result, specific immediate and early skin Many of the lasers used in dermatology affect
responses or ‘‘endpoints’’ are seen during various specific light-absorbing ‘‘targets’’ (eg, blood vessels,
laser treatments that correlate with therapeutic out- pigmented cells, hair follicles, or tattoo ink) based on
comes. Other early responses are harbingers of the process of selective photothermolysis (SP).1,85 SP
unwanted injury or phenomena that lead to side depends on the preferential absorption of light by
effects. the targets, provided by light-absorbing molecules
We present the clinically useful early response called chromophores. For example, blood vessels
endpoints and their mechanisms that arise during are treated using hemoglobin as the target chromo-
treatment with laser and other energy-based devices phores; melanin is the target chromophore for the
in dermatology. Knowledge of specific desired (ie, treatment of hair and for various pigmented lesions;
therapeutic) and undesired (ie, warning) endpoints and tattoo inks or exogenous pigments are the
is key for the proper clinical use of lasers in chromophores for tattoo and traumatic tattoo
dermatology. The mechanisms underlying these removal. Flashlamp sources (intense pulsed light
early response endpoints are also fundamental to [IPL]) mimic lasers to some extent, using broad
understanding laseretissue interactions. There are 2 spectrum light through cutoff filters to target chro-
articles in this series; the current article presents the mophores. By choosing different wavelengths of
warning endpoints, following an overview of lasers, light, different chromophores are affected. IPL sour-
other energy sources, and their tissue interactions ces are generally less selective than lasers and may
and laser safety. The accompanying article presents be associated with a greater number of side effects.86
the specific therapeutic endpoints that are correlated For SP, a brief pulse of light is used to limit damage
with providing effective treatment. to the tissue surrounding the targets. By delivering
the energy in a pulse, the light-absorbing targets
become hot before much heat can diffuse into the
LASEReTISSUE INTERACTIONS
surrounding tissue. This produces a specific reaction
Key points
in the target chromophore and in the skin called an
d Selective photothermolysis depends on the
endpoint. The pulse duration is chosen to be about
preferential absorption of light by the histo-
equal or somewhat less than the time needed for a
logic target or chromophore
target to cool, called the thermal relaxation time.
d The laseretissue reaction in the histologic
Smaller targets cool faster and need shorter pulse
target produces a specific endpoint in the
durations for SP. Dermatologic lasers for SP span a
skin
wide range of pulse durations. For example, a tattoo
d Nonselective devices produce nonspecific
ink particle (;0.05-1 m) cools in \1 microsecond;
endpoints
nanosecond and picoseconds laser pulses are there-
Light, radiofrequency, microwave, ultrasonogra- fore used for tattoo removal. In contrast, a terminal
phy, plasma, and other sources that transfer energy hair follicle (;75-200 m) takes several milliseconds
into the skin produce their various effects based on to cool, such that 1- to 100-millisecond laser or IPL
the location, amount, and rate of energy absorption pulses are typically used for permanent hair
J AM ACAD DERMATOL Wanner et al 809
VOLUME 74, NUMBER 5

Table I. Devices and potential applications (including off-label)


Devices Applications
Pulsed dye laser1-5 Vascular lesionsdtelangiectasia, port wine stain,
hemangioma, angioma, and venous lake; lentigines;
keratosis pilaris; photoaging; poikiloderma; pyogenic
granuloma; sebaceous hyperplasia; scars (red); stria
(red); and verruca
KTP laser6-9 Similar to pulsed dye laser, for KTP lasers with similar
pulse durations
Alexandrite, long pulsed10-16 Hair removal; vascular lesionsdhypertrophic port wine
stains and lentigines; and benign melanocytic nevi, if
appropriate
Q-switched (alexandrite, ruby, Nd:YAG, and frequency Pigmented lesionsdlentigines, nevus of Ota, caf e au lait
doubled Nd:YAG) and picosecond lasers (alexandrite, macules, some nevi; tattoos; drug-induced
Nd:YAG, frequency doubled Nd:YAG)17-24 pigmentation (eg, minocycline and amiodarone);
melasma (low fluence)
810-nm diode15,16,25-27 Hair removal; venous lakes; veins; and venous
malformations
1064-nm Nd:YAG, long pulsed28-31 Hair removal; veins; photoaging; and laxity
Nonablative, nonfractional mid-infrared (1320- Acne; scars; rhinophyma; hidradenitis suppurativa; and
1550 nm)32-45 photoaging
Intense pulsed light46-51 Acne; lentigines; hair removal; photoaging; poikiloderma;
vascular lesionsdtelangiectasia, leg veins, and port
wine stains
Ablative resurfacing (eg, erbium and CO2 lasers)52 Photoaging; scars; actinic keratoses and cheilitis;
seborrheic keratoses; adnexal tumors; rhinophyma;
and verruca
Nonablative fractional (wavelengths: 1320, 1440, 1540, Scars; photoaging; lentigines; rhytides; poikiloderma;
1550, 1410, and 1927 nm)53-63 melasma; minocyline-induced hyperpigmentation;
residual hemangioma; telangiectatic matting;
granuloma annulare; milia; striae; and
postinflammatory hyperpigmentation
Ablative fractional (wavelengths: 2790, 2940, and Scars; striae; photoaging; laxity; lentigines; rhytides;
10600 nm)64-71 morphea; drug delivery; anetoderma; and residual
hemangioma
Radiofrequency72-76 Laxity; rhytides; and cellulite/body contouring
Ultrasonography77-83 Laxity; noninvasive fat reduction

KTP, Potassium titanyl phosphate; Nd:YAG, neodymium-doped yttrium aluminum garnet.

reduction. A millisecond is 1 million times longer ultrasonography. Nonselective treatment devices


than a nanosecond. The wide range of pulse heat tissue with a depth or pattern that depends on
duration correlates with different damage mecha- where the energy is delivered.
nisms and with different corresponding clinical Ablative treatments remove tissue by vaporizing
endpoints. Because IPLs emit broad spectrum light it. For example, laser skin resurfacing is a classic
in a range of wavelengths, endpoints can be less technique that ablates a thin layer of epidermis and
specific. superficial dermis, using CO2 or erbium lasers.52,87
Nonselective treatment devices emit energy that is These lasers emit at wavelengths that are strongly
absorbed by water. Because water is present absorbed by water.88 For laser skin resurfacing, the
throughout the skin, these wavelengths are not laser energy is delivered uniformly at the skin
selectively absorbed by specific targets in the skin. surface, and immediate response endpoints are
There are endpoints associated with these devices, used to verify treatment depth.
but they are, in general, nonspecific. These include Nonablative treatments are those that heat but do
infrared, ablative, and nonablative lasers emitting at not vaporize tissue. The immediate response end-
wavelengths absorbed by water, various electrosur- points for these devices typically relate to thermal
gical devices, radiofrequency, and focused coagulation of tissue. Lasers for nonablative
810 Wanner et al J AM ACAD DERMATOL
MAY 2016

treatments, including fractional nonablative lasers, America releases an annual Laser Safety Guide.91
emit at infrared wavelengths that are weakly or All operators should have eye protection, fire pre-
moderately absorbed by water. The nonablative cautions, and fume extraction. It is the responsibility
treatment devices in dermatology also include radio- of the operator to protect the patient and everyone
frequency and ultrasonography, which can produce present in the treatment room.
thermal coagulation of tissue deep in the dermis or The eye is particularly susceptible to irreversible
subcutaneous fat.72,73 Focused ultrasonographic en- damage.92 Eye damage and blindness can result with
ergy is able to create a pattern of small zones of even a nanosecond of laser exposure. Retinas,
thermal injury deep inside soft tissue, near a focal corneas, and lenses are all susceptible.
point.77,78 The endpoints described in these papers are often
Fractional laser treatments53 use ablative or non- best seen in visible light without laser goggles. It is
ablative lasers that are delivered in differing patterns paramount that the laser should be placed in the
to produce different clinical results. The laser energy ‘‘standby’’ mode when the endpoint is evaluated
is delivered as an array of small beams, creating a without goggles and that laser goggles are replaced
pattern of up to 1000 small wounds per square before firing the laser.
centimeter of skin called microthermal zones
(MTZs). A fraction (#50%) of the skin can be injured, The warning endpoints
but healing is rapid because each MTZ is surrounded Heat produces a wide range of tissue responses
by unexposed, intact tissue. Nonablative fractional depending on the location, temperature, duration,
lasers produce columns of thermal injury that extend and rate of heating. Well below the boiling point of
up to about 2 mm deep.53 Ablative fractional lasers water, heat can destroy the structure of macromole-
vaporize an array of small (0.1-0.3 mm in diameter) cules including enzymes, structural proteins, mem-
vertical channels into the skin that can extend up to branes, DNA, and RNA. At nonlethal temperatures
3 mm deep.89 Energy delivered per MTZ controls the above about 428C, cells go into ‘‘heat shock,’’ a survival
depth of treatment while the number of MTZ per unit response that potently inhibits normal metabolism
area of skin controls the treatment fraction or the and partially blocks apoptosis. Heat shock is a
fraction of the area treated. clinically invisible cellular response. From about
The laseretissue interaction between a target 508C to 1008C, most proteins denature and then
chromophore (or histologic target) and a light source coagulate (stick to one another), killing cells and
elicits a reproducible clinical response. Some clinical causing some visible changes. Protein denaturation is
responses are suggestive of a therapeutic treatment a rate-dependent process that depends on both tem-
that will result in removal or partial removal of the perature and time. As such, skin cells can withstand
intended target. Other clinical responses are warning high temperatures for short periods of time (eg, 1008C
signs of excess damage to the skin that may result in a for a few thousandths of a second) but are killed at the
scar or other adverse event. modest temperature of 558C in a few seconds.93,94
There is little difference among cutaneous cell types in
LASER SAFETY their tolerance for thermal injury.95,96
Key points
d Lasers and light sources pose serious Look for the Nikolsky sign
hazards Key points
d Lasers and intense pulsed lights can result in d Warning endpoints are skin responses seen

blindness and irreversible eye damaged immediately or soon after laser irradiation,
never fire a laser without eye protection suggestive of tissue injury
and fire precautions in place d The Nikolsky sign is an indication of
d Always place laser and light devices in epidermal necrosis, corresponding to loss
standby mode before removing goggles of dermoepidermal adhesion.
d Always replace goggles before firing a laser d The Nikolsky sign can be desirable in spe-

cific situations
Laser and IPL devices pose serious and potent
hazards, especially for eye injury. There are physical Keratinocyte necrosis is manifested by a positive
hazards, such as fire and electrocution, eye and skin Nikolsky sign appearing within 5 minutes. When
hazards, and biologic hazards, such as plume inha- lateral pressure is gently applied with the clinician’s
lation of infectious pathogens.90 Any individual finger, the epidermis separates from its underlying
working with these devices should receive compre- dermis.97 In this setting, the Nikolsky sign (Figs 1
hensive safety training. The Laser Institute of and 2 ; Table II) is caused by loss of the actively
J AM ACAD DERMATOL Wanner et al 811
VOLUME 74, NUMBER 5

Fig 2. Superficial erosion of the lip after unintended bulk


heating during treatment with a nonablative fractional
laser (1540 nm). This photograph was taken 20 minutes
posttreatment. The patient washed her face and removed
the epidermis in the process, eliciting a positive Nikolsky
sign.

cool the skin during treatment. Signs of a skin burn


can be difficult to assess because after laser/IPL
treatment, the entire field is usually erythematous
and edematous. The Nikolsky sign can be present
without any other detectable sign of a first- or
second-degree burn. Checking for the Nikolsky
sign about 5 minutes after a test spot exposure is
strongly recommended in these settings.
The Nikolsky sign can be a desired therapeutic
endpoint. After the first pass of laser resurfacing or
during treatment of congenital melanocytic nevi
using the Kono technique,103-105 the Nikolsky sign
Fig 1. Angioma before (A), immediately after (B), and is often present.106 Gently removing the epidermis
8 weeks after (C) treatment with an 810-nm diode laser. with a sterile gauze pad is performed in these
There was inadequate compression of the sapphire tip. procedures to allow for deeper penetration of a
Note the deep blue color of the angioma that was cooled second laser pass (Fig 3). The risk of side effects and
appropriately. In the areas that were not cooled, there is scarring in these procedures is strongly related to
the Nikolsky sign (arrow); dermal whitening and a subtle
clinical experience. Otherwise, there is no clinical
elevation of the skin (double arrow); and charring of the
skin (asterisk). C, Hypopigmentation is evident at 8 weeks
setting for which the Nikolsky sign is a desired
posttreatment. This hypopigmentation has persisted therapeutic endpoint during laser treatment.
1.5 years after treatment.
Skin cooling: Too little, or too much?
maintained adhesion between keratinocytes and
Key points
dermis. This endpoint is a warning that the epidermis d Second- and third-degree and ‘‘stamping’’
is necrotic and that an open wound is likely to follow
burns correspond to injury because of the
with blistering, erosion, or ulceration, along with an
failure or misuse of skinecontact window
increased risk of infection, pigmentary changes, or cooling or the use of an incorrect device
scarring. d Spotty or crescent-shaped burns or ery-
One should look for the Nikolsky sign especially
thema can indicate inadequate or misaligned
when the risk of unwanted epidermal necrosis is
skin cooling or poor application technique
high or if the patient reports strong pain during
treatment. Typical situations include treatments of Actively cooling the skin during laser, IPL, or other
tanned or pigmented skin with any visible or near- energyebased treatments is useful to protect the
infrared laser or flash lamps (IPLs); the use of high pigmented epidermis, to reduce pain, and to
fluences or energy settings with any nonablative decrease the risk of skin burns. Skin cooling is
device; inadvertent pulse stacking (rapidly repeating accomplished by applying a cold external medium,
exposure of a skin site); and a failure to adequately which can be solid (as with cold windows in some
812 Wanner et al J AM ACAD DERMATOL
MAY 2016

Table II. Warning endpoints*


Warning endpoint Description
Nikolsky sign (Figs 1 and 2) Epidermal separation upon lateral pressure, indicating
loss of adhesion between epidermis and dermis
because of epidermal necrosis
Second- and third-degree burns (Figs 4 and 5) Pain, erythema, edema, blistering, and erosion
Stamping epidermal burn (Fig 6) Epidermal injury caused by the presence of tissue or hair
residue on a skin contact window
Crescent mooneshaped injuries (Fig 7) Epidermal injury caused by cryogen/laser misalignment
Pucker sign (Fig 8) Immediate skin shrinkage caused by thermal injury of the
dermis
Charring (Figs 1 and 9) Black or brown carbon on the skin caused by tissue
carbonization
Chrysiasis98,99 (Fig 10) Immediate, blue-grey discoloration caused by a Q-
switched laser effect on gold particles in the skin
Immediate tattoo darkening100,101 Immediate dark discoloration caused by laser treatment
of ferric oxide or titanium dioxide
Metallic-gray blanching102 (Fig 11) Dermal blood and protein denaturation

*Level IV evidence.

Fig 3. A, Congenital nevus treated with a long pulse plus short pulse approach93 before
treatment on the left knee. B, The Nikolsky sign was induced after 3 milliseconds of exposure to
a 755-nm alexandrite laser. Gentle removal of the epidermis was performed with sterile wet
gauze in preparation for the second laser irradiation with a Q-switched 1064-nm laser.

IPL and laser delivery handpieces), liquid (as with This can occur with diode lasers, IPLs, and radio-
cryogen spray cooling) or gas (as with forced cold frequency (RF) or ultrasonographic treatments.
air). When operating properly, skin cooling reduces Deeply penetrating monopolar RF or ultrasono-
the risk of side effects and allows the use of higher graphic treatments can result in fat damage with
treatment fluence. However, injury can also occur by dimpling of the overlying skin. The warning end-
misuse or malfunction of skin cooling points of second- and third-degree burns are as
methods.98,107,108 The skin can be injured by either follows: severe pain, intense erythema, local edema,
too little cooling or by freezing from too much blistering, epidermal splatter (ie, pieces of epidermis
cooling. Freezing the skin is easily observed as a detach from skin and attach to the laser handpiece
frosty-white color change. window), erosion, or ulceration (Figs 4-6). These
With cold window devices, poor contact with iatrogenic burns may heal with erosion/ulceration,
the skin is an operator-dependent problem that can crusting, pigmentary changes, secondary infection,
cause skin burns immediately after exposure (Fig 1). and scarring.
J AM ACAD DERMATOL Wanner et al 813
VOLUME 74, NUMBER 5

Fig 5. A second-degree burn showing the value of cool-


ing to protect pigmented epidermis. The arrow points to a
second-degree burn of porcine skin after failure of skin
cooling. The double arrow points to an area treated with
the same laser and proper epidermal cooling. There are no
signs of a burn.

Fig 4. A second-degree burn with blistering after the use


of a 755-nm alexandrite laser for the treatment of a deep, Skin shrinkage is a sign of dermal injury
unresponsive port wine stain. Key points
d Skin contraction and the ‘‘pucker sign’’ are

indications of a dermal burn, corresponding


Inappropriate use of cold window devices can
to thermal denaturation of collagen
pose additional risks. During laser/IPL hair removal, d Immediate shrinkage of the dermis can
when a piece of charred hair adheres to a contact
cause the skin to become slightly elevated
window device, energy is strongly absorbed by the
and firm
charred tissue with each laser pulse. This can cause a d Unintended ablation is an indication of ther-
‘‘stamping’’ burn pattern with each subsequent pulse
mal burn
(Fig 6). This potential adverse effect can be simply d ‘‘Charring’’ indicates a severe burn, corre-
avoided by cleaning the window both before and
sponding to carbonization of tissue
during treatment.
Some laser devices incorporate ‘‘dynamic’’ cryogen Type I collagen is the most abundant protein in
spray cooling, which coats the skin surface with a the dermis. When heated above about 708C, type I
spurt of very cold (approximately 508C) fluoro- collagen undergoes a helix-to-coil conformational
carbon liquid just before or just after the laser pulse change, leading to immediate skin shrinkage.94 This
is delivered. Cryogen spray cooling is available on endpoint is always an indication of significant ther-
some pulsed dye lasers, alexandrite, and neodymium- mal injury to the dermis. For some applications, a
doped yttrium aluminum garnet (Nd:YAG) lasers. moderate amount of immediate shrinkage is a useful
When used properly, cryogen spray cooling is therapeutic endpoint (eg, during the final pass of
extremely helpful in protecting the pigmented ablative laser resurfacing or during high-density
epidermis from laser-induced injury and reducing ablative fractional laser treatments). However, in
the risk of blisters, pain, and swelling. However, any application where dermal injury is unwanted,
excessive cryogen spray duration (eg, [100 ms) can immediate shrinkage is an ominous warning
freeze the skin, particularly if used in combination endpoint that should lead the clinician to stop
with other cooling devices, such as cold air. treatment and reassess the situation. For example,
The warning endpoint consists of a bright white immediate skin shrinkage should not be seen during
frosting that persists for several seconds (Fig 7). nonablative laser treatments or during any applica-
Misalignment between the cryogen spray and laser tion of selective photothermolysis (eg, vascular
beam can also cause arcuate or crescent ‘‘moon- lesions, pigmented lesions, tattoo removal, or hair
shaped’’ patterns of skin injury. Even if the device is removal). This warning sign is not limited to laser
properly aligned, moon-shaped injury can occur if treatments and can also occur during IPL, RF, ultra-
the laser handpiece is not held perpendicular to the sonographic, or plasma exposure.
skin surface. Sometimes it is unclear whether such Shrinkage can be observed in several ways. First,
arcuate injuries were caused by a cryogen injury or a the skin will visibly contract during laser exposure.
laser burn injury, but both mechanisms can be However, it can be difficult to see this endpoint
prevented by proper alignment and positioning of through protective laser goggles and impossible to
the laser/cryogen handpiece and close observation see when using an occlusive handpiece. The
of treatment endpoints. ‘‘pucker sign’’ is another, more reliable indicator of
814 Wanner et al J AM ACAD DERMATOL
MAY 2016

Fig 6. A, Stamping burn pattern after the use of an 800-nm diode laser with a dirty cold contact
window. B, Hair char is present on the cold window.

Fig 7. Freezing of the skin from excessive cryogen spray


cooling. In this case, 100-ms of cryogen spray was applied
both before and after delivery of an 8-mm diameter
alexandrite laser pulse. A halo of skin surrounding the Fig 8. ‘‘Pucker sign,’’ a radial pattern of superficial skin
laser exposure is frozen. When the frost persists for more lines caused by immediate skin shrinkage. The pucker sign
than a few seconds, freeze injury is likely to occur. The is illustrated by this test exposure using a defocused CO2
cryogen spray duration should be reduced. laser. Immediate shrinkage is a warning endpoint of
significant thermal injury to the dermis. Some immediate
skin shrinkagedthe skin surface lines assume a shrinkage is normally seen during ablative laser resurfac-
ing, but in most other settings this is an ominous endpoint.
radial pattern pointing to the center of the exposure
from a laser or other device (Fig 8 ). A more subtle
sign of immediate shrinkage of the dermis is slight laser treatment of tattoos, pieces of live tissue can be
elevation of the skin and firmness to palpation explosively expelled from the skin, flying rapidly
(Fig 1). toward the treating physician. Depending on
One unfortunately common and preventable country of origin, people with tattoos are more
cause of scarring is the use of any IPL device for likely to have viral hepatitis or HIV.100,101,109 If the
treatment of tattoos. The pulse duration of all IPL patient harbors viral hepatitis or HIV, health care
devices is too long for selective photothermolysis of personnel can be directly exposed to ablated, infec-
tattoos.99 The puckered lip sign is sometimes seen tious tissue fragments. In addition, laser plumes from
during this inappropriate use of an IPL. tissue ablation or from partial combustion of hair
Controlled tissue ablation is the goal during during laser or IPL hair removal can be irritating or
vaporization of verrucae and other lesions, during toxic.88
laser resurfacing, and during ablative fractional Charring is another warning endpoint. When
resurfacing; however, ablation during other types energy continues to be applied to tissue after most
of procedures is a sign of excessive tissue injury. of its water is removed, partial combustion occurs,
During any nonablative procedure, ablation of the and the tissue surface becomes charred. Charring
skin should not be seen. In addition to signaling a consists of a thin layer of black or dark brown carbon
thermal burn, tissue ablation poses a biohazard, and adhered to the tissue surface (Figs 1 and 9). Skin
protective measures should be taken whenever tis- charring is generally associated with excessive ther-
sue ablation is seen. For example, during Q-switched mal damage (eg, caused by the improper use or
J AM ACAD DERMATOL Wanner et al 815
VOLUME 74, NUMBER 5

Fig 9. Charring of the skin appears as black or dark brown


material adherent to the tissue surface (arrow). The
material is carbon released by partial combustion. During
ablative laser procedures, charring of the skin is a sign of
excessive thermal injury.
Fig 11. Metallic gray blanching of the skin after the use of
a high-fluence 755-nm alexandrite laser for the treatment
of port wine stain.

immediate, permanent blue-grey discoloration of


skin. This is laser-induced chrysiasis,110 a specific
warning endpoint created by the interaction of the
Q-switched laser with gold deposits that remain in
the skin for a lifetime. The situation can be avoided
by obtaining a history of gold therapy before any
Q-switched laser treatment. However, some patients
may not recall taking gold decades ago or may not
recognize gold exposure unless made aware that
‘‘aurothiomalate’’ is a gold-based medication used
Fig 10. Laser-induced chrysiasis is a blue-grey discolor- for arthritis, for example. Particularly in a patient
ation of the skin caused by Q-switched laser exposure. It with a history of rheumatoid arthritis, a good habit is
occurs in patients with a history of gold intake. Chrysiasis to deliver 1 test pulse in a hidden, nonesun exposed
is permanent and difficult to treat.
skin site, such as the inner upper arm, then look for a
blue-grey skin discoloration without laser goggles
malfunction of a resurfacing laser [conventional or (Fig 10). In some cases, laser-induced chrysiasis
fractional] or plasma device). can be improved by subsequent treatment with
long-pulse lasers or IPLs.102
Tattoo ink darkening is another warning endpoint
Other specific warning endpoints
that is specific to Q-switched laser treatment.111,112
Key points
d Immediate blue-grey darkening during Q-
Tattoo inks that contain red iron oxide or white
titanium dioxide generally turn black or dark gray
switched laser treatment indicates chrysia-
immediately upon exposure to a Q-switched laser.
sis, a potentially permanent side effect in
patients with a history of gold intake This darkening is thought to be caused by the
d Immediate
chemical reduction of ferric oxide to ferrous oxide.
tattoo darkening during Q-
Tattoo ink darkening is irreversible, but the dark-
switched laser treatment indicates a chemi-
ened tattoo ink can sometimes be removed by
cal alteration of tattoo inks that may not be
subsequent laser treatments.113 The most common
removed with subsequent treatments
d Immediate metallic-gray blanching of skin is
setting for laser-induced tattoo ink darkening is
during treatment of cosmetic tattoos used as perma-
a sign of dermal overheating
nent lip liner or for eyebrows. Common colors
Some warning endpoints are highly specific. include flesh, pink, rose, or reddish colors.114
Q-switched laser treatment of a patient who has Finally, when using vascular-targeting lasers, the
been treated at any time with gold often causes an immediate metallic-gray blanching of the vascular lesion
816 Wanner et al J AM ACAD DERMATOL
MAY 2016

can indicate nonspecific dermal injury and the need to with the 585 nm pulsed dye laser. J Am Acad Dermatol.
immediately reduce the treatment fluence or provide 1996;35:428-431.
5. Bernstein EF, Kligman A. Rosacea treatment using the
better skin cooling (Fig 11). This is especially important new-generation, high-energy, 595 nm, long pulse-duration
when using near-infrared lasers, such as alexandrite, pulsed-dye laser. Lasers Surg Med. 2008;40:233-239.
Nd:YAG, or diode lasers for vascular destruction.10 6. Clark C, Cameron H, Moseley H, Ferguson J, Ibbotson SH.
Overheating the vessels will cause heat propagation Treatment of superficial cutaneous vascular lesions: experi-
beyond the target vessels, damaging the surrounding ence with the KTP 532 nm laser. Lasers Med Sci. 2004;19:1-5.
7. Pancar GS, Aydin F, Senturk N, Bek Y, Canturk MT, Turanli AY.
dermis. Clinically, the injury progresses with necrosis, Comparison of the 532-nm KTP and 1064-nm Nd:YAG lasers
ulceration, crusting, and possibly scarring. for the treatment of cherry angiomas. J Cosmet Laser Ther.
In conclusion, specific and observable responses 2011;13:138-141.
during laser or IPL treatments can be indicators of 8. Ho SG, Chan NP, Yeung CK, Shek SY, Kono T, Chan HH. A
therapeutic benefit or a warning of unwanted skin retrospective analysis of the management of freckles and
lentigines using four different pigment lasers on Asian skin. J
injury or other unwanted events. These endpoints are Cosmet Laser Ther. 2012;14:74-80.
more useful than a list of ‘‘dosimetry’’ settings for 9. Uebelhoer NS, Bogle MA, Stewart B, Arndt KA, Dover JS. A
various devices and indications. It is the physician’s split-face comparison study of pulsed 532-nm KTP laser and
responsibility to recommend and use appropriate 595-nm pulsed dye laser in the treatment of facial telangi-
devices for treatment of a given problem and individ- ectasias and diffuse telangiectatic facial erythema. Dermatol
Surg. 2007;33:441-448.
ual patient; to take a relevant history; to prepare the 10. Izikson L, Anderson RR. Treatment endpoints for resistant
patient and the skin before treatment; to use skillful port wine stains with a 755 nm laser. J Cosmet Laser Ther.
application techniques; and to adjust the treatment 2009;11:52-55.
device for proper parameters. Appropriate wave- 11. Badawi A, Kashmar M. Treatment of trichostasis spinulosa
length choice for each chromophore, dosimetry, pulse with 0.5-millisecond pulsed 755-nm alexandrite laser. Lasers
Med Sci. 2011;26:825-829.
duration, and skin cooling are crucial for success. 12. Lee SJ, Chung WS, Kim J, Cho SB. Combination of 595-nm
The Nikolsky sign, second- and third-degree burn pulsed dye laser, long-pulsed 755-nm alexandrite laser and
signs, stamping epidermal burns, immediate skin microdermabrasion treatment for keratosis pilaris. J Derma-
shrinkage, and charring of the skin are warning tol. 2011;39:479-480.
endpoints related to the use of an inappropriate 13. Choi JE, Kim JW, Seo SH, Son SW, Ahn HH, Kye YC. Treatment
of Becker’s nevi with a long-pulse alexandrite laser. Dermatol
fluence, an incorrect device, the wrong pulse dura- Surg. 2009;35:1105-1108.
tion, or the failure of cooling devices. Q-switched 14. Trafeli JP, Kwan JM, Meehan KJ, et al. Use of a long-pulse
lasers have specific warning signs, such as chrysiasis alexandrite laser in the treatment of superficial pigmented
and immediate tattoo ink darkening. Overheating of lesions. Dermatol Surg. 2007;33:1477-1482.
vessels can be observed as an immediate metallic- 15. Handrick C, Alster TS. Comparison of long-pulsed diode and
long-pulsed alexandrite lasers for hair removal: a long-term
gray blanching of the skin. Skin response endpoints clinical and histologic study. Dermatol Surg. 2001;27:622-626.
should be used in lieu of a ‘‘cookbook’’ approach 16. Eremia S, Li C, Newman N. Laser hair removal with
because variations in skin pigmentation and sensi- alexandrite versus diode laser using four treatment sessions:
tivity are common, and because the output or 1-year results. Dermatol Surg. 2001;27:925-929. discussion
calibration accuracy of devices vary between manu- 9-30.
17. Taylor CR, Gange RW, Dover JS, et al. Treatment of tattoos by
facturers and usually change over time and after Q-switched ruby laser. A dose-response study. Arch Dermatol.
routine maintenance. Careful observation of warn- 1990;126:893-899.
ing endpoints after a test spot treatment and during 18. Taylor CR, Anderson RR. Treatment of benign pigmented
treatment can decrease the risk of severe side effects. epidermal lesions by Q-switched ruby laser. Int J Dermatol.
1993;32:908-912.
We thank Steve Conley at the Massachusetts General 19. Taylor CR, Flotte TJ, Gange RW, Anderson RR. Treatment of
Hospital Media Lab for his work on this paper. nevus of Ota by Q-switched ruby laser. J Am Acad Dermatol.
1994;30:743-751.
20. Bernstein EF. Q-switched laser treatment of amiodarone
REFERENCES pigmentation. J Drugs Dermatol. 2011;10:1316-1319.
1. Anderson RR, Parrish JA. Microvasculature can be selectively 21. Kim YJ, Whang KU, Choi WB, et al. Efficacy and safety of 1,064
damaged using dye lasers: a basic theory and experimental nm Q-switched Nd:YAG laser treatment for removing mela-
evidence in human skin. Lasers Surg Med. 1981;1:263-276. nocytic nevi. Ann Dermatol. 2012;24:162-167.
2. Bernstein EF. The new-generation, high-energy, 595-nm, long 22. Goyal S, Arndt KA, Stern RS, O’Hare D, Dover JS. Laser
pulse-duration pulsed-dye laser improves the appearance of treatment of tattoos: a prospective, paired, comparison study
photodamaged skin. Lasers Surg Med. 2007;39:157-163. of the Q-switched Nd:YAG (1064 nm), frequency-doubled
3. Park HS, Choi WS. Pulsed dye laser treatment for viral warts: a Q-switched Nd:YAG (532 nm), and Q-switched ruby lasers. J
study of 120 patients. J Dermatol. 2008;35:491-498. Am Acad Dermatol. 1997;36:122-125.
4. Gonzalez S, Vibhagool C, Falo LD Jr, Momtaz KT, 23. Green D, Friedman KJ. Treatment of minocycline-induced
Grevelink J, Gonzalez E. Treatment of pyogenic granulomas cutaneous pigmentation with the Q-switched Alexandrite
J AM ACAD DERMATOL Wanner et al 817
VOLUME 74, NUMBER 5

laser and a review of the literature. J Am Acad Dermatol. 43. Wada T, Kawada A, Hirao A, Sasaya H, Oiso N. Efficacy and
2001;44:342-347. safety of a low-energy double-pass 1450-nm diode laser for
24. Kauvar AN. Successful treatment of melasma using a com- the treatment of acne scars. Photomed Laser Surg. 2011;30:
bination of microdermabrasion and Q-switched Nd:YAG 107-111.
lasers. Lasers Surg Med. 2012;44:117-124. 44. Bernstein EF. Double-pass, low-fluence laser treatment using
25. Wall TL, Grassi AM, Avram MM. Clearance of multiple venous a large spot-size 1,450 nm laser improves acne. Lasers Surg
lakes with an 800-nm diode laser: a novel approach. Dermatol Med. 2009;41:116-121.
Surg. 2007;33:100-103. 45. Doshi SN, Alster TS. 1,450 nm long-pulsed diode laser for
26. Williams RM, Gladstone HB, Moy RL. Hair removal using an nonablative skin rejuvenation. Dermatol Surg. 2005;31:
810 nm gallium aluminum arsenide semiconductor diode 1223-1226. discussion 6.
laser: a preliminary study. Dermatol Surg. 1999;25:935-937. 46. Fitzpatrick RE, Lowe NJ, Goldman MP, Borden H, Behr KL,
27. Eremia S, Li C, Umar SH. A side-by-side comparative study of Ruiz-Esparza J. Flashlamp-pumped pulsed dye laser treat-
1064 nm Nd:YAG, 810 nm diode and 755 nm alexandrite ment of port-wine stains. J Dermatol Surg Oncol. 1994;20:
lasers for treatment of 0.3-3 mm leg veins. Dermatol Surg. 743-748.
2002;28:224-230. 47. Faurschou A, Togsverd-Bo K, Zachariae C, Haedersdal M.
28. Taylor MB, Prokopenko I. Split-face comparison of radio- Pulsed dye laser vs. intense pulsed light for port-wine stains:
frequency versus long-pulse Nd-YAG treatment of facial a randomized side-by-side trial with blinded response
laxity. J Cosmet Laser Ther. 2006;8:17-22. evaluation. Br J Dermatol. 2009;160:359-364.
29. Alster TS, Bryan H, Williams CM. Long-pulsed Nd:YAG 48. Tanghetti EA. Split-face randomized treatment of facial
laser-assisted hair removal in pigmented skin: a clinical and telangiectasia comparing pulsed dye laser and an intense
histological evaluation. Arch Dermatol. 2001;137:885-889. pulsed light handpiece. Lasers Surg Med. 2011;44:97-102.
30. Lorenz S, Brunnberg S, Landthaler M, Hohenleutner U. Hair 49. Sadick NS, Shea CR, Burchette JL Jr, Prieto VG. High-intensity
removal with the long pulsed Nd:YAG laser: a prospective flashlamp photoepilation: a clinical, histological, and mech-
study with one year follow-up. Lasers Surg Med. 2002;30: anistic study in human skin. Arch Dermatol. 1999;135:
127-134. 668-676.
31. Tan MH, Dover JS, Hsu TS, Arndt KA, Stewart B. Clinical 50. Babilas P, Schreml S, Eames T, Hohenleutner U, Szeimies RM,
evaluation of enhanced nonablative skin rejuvenation using Landthaler M. Split-face comparison of intense pulsed light
a combination of a 532 and a 1,064 nm laser. Lasers Surg Med. with short- and long-pulsed dye lasers for the treatment of
2004;34:439-445. port-wine stains. Lasers Surg Med. 2010;42:720-727.
32. Sadick N, Schecter AK. Utilization of the 1320-nm Nd:YAG 51. Lee EJ, Lim HK, Shin MK, Suh DH, Lee SJ, Kim NI. An
laser for the reduction of photoaging of the hands. Dermatol open-label, split-face trial evaluating efficacy and safty of
Surg. 2004;30:1140-1144. photopneumatic therapy for the treatment of acne. Ann
33. Goldberg DJ. Non-ablative subsurface remodeling: clinical Dermatol. 2012;24:280-286.
and histologic evaluation of a 1320-nm Nd:YAG laser. J Cutan 52. Fitzpatrick RE, Goldman MP, Ruiz-Esparza J. Clinical advan-
Laser Ther. 1999;1:153-157. tage of the CO2 laser superpulsed mode. Treatment of
34. Orringer JS, Kang S, Maier L, et al. A randomized, controlled, verruca vulgaris, seborrheic keratoses, lentigines, and actinic
split-face clinical trial of 1320-nm Nd:YAG laser therapy in the cheilitis. J Dermatol Surg Oncol. 1994;20:449-456.
treatment of acne vulgaris. J Am Acad Dermatol. 2007;56: 53. Manstein D, Herron GS, Sink RK, Tanner H, Anderson RR.
432-438. Fractional photothermolysis: a new concept for cutaneous
35. Paithankar DY, Ross EV, Saleh BA, Blair MA, Graham BS. Acne remodeling using microscopic patterns of thermal injury.
treatment with a 1,450 nm wavelength laser and cryogen Lasers Surg Med. 2004;34:426-438.
spray cooling. Lasers Surg Med. 2002;31:106-114. 54. Tierney E, Mahmoud BH, Srivastava D, Ozog D, Kouba DJ.
36. Jih MH, Friedman PM, Goldberg LH, Robles M, Glaich AS, Treatment of surgical scars with nonablative fractional laser
Kimyai-Asadi A. The 1450-nm diode laser for facial inflam- versus pulsed dye laser: a randomized controlled trial.
matory acne vulgaris: dose-response and 12-month Dermatol Surg. 2009;35:1172-1180.
follow-up study. J Am Acad Dermatol. 2006;55:80-87. 55. Wanner M, Tanzi EL, Alster TS. Fractional photothermolysis:
37. Angel S, Boineau D, Dahan S, Mordon S. Treatment of active treatment of facial and nonfacial cutaneous photodamage
acne with an Er:Glass (1.54 microm) laser: a 2-year follow-up with a 1,550-nm erbium-doped fiber laser. Dermatol Surg.
study. J Cosmet Laser Ther. 2006;8:171-176. 2007;33:23-28.
38. Kassir M, Newton D, Maris M, Euwer R, Servell P. Er:glass 56. Rokhsar CK, Fitzpatrick RE. The treatment of melasma with
(1.54m) laser for the treatment of facial acne vulgaris fractional photothermolysis: a pilot study. Dermatol Surg.
[abstract]. Lasers Surg Med. 2004;34:S65. 2005;31:1645-1650.
39. Bhatia AC, Dover JS, Arndt KA, Stewart B, Alam M. Patient 57. Tannous ZS, Astner S. Utilizing fractional resurfacing in the
satisfaction and reported long-term therapeutic efficacy treatment of therapy-resistant melasma. J Cosmet Laser Ther.
associated with 1,320 nm Nd:YAG laser treatment of acne 2005;7:39-43.
scarring and photoaging. Dermatol Surg. 2006;32:346-352. 58. Rokhsar CK, Ciocon DH. Fractional photothermolysis for the
40. Chou CL, Chiang YY. Moderate rhinophyma successfully treatment of postinflammatory hyperpigmentation after
treated with a Smoothbeam laser. J Dermatolog Treat. carbon dioxide laser resurfacing. Dermatol Surg. 2009;35:
2010;23:153-155. 535-537.
41. Downs A. Smoothbeam laser treatment may help improve 59. Goldberg DJ, Berlin AL, Phelps R. Histologic and ultrastruc-
hidradenitis suppurativa but not HaileyeHailey disease. J tural analysis of melasma after fractional resurfacing. Lasers
Cosmet Laser Ther. 2004;6:163-164. Surg Med. 2008;40:134-138.
42. Tanzi EL, Williams CM, Alster TS. Treatment of facial rhytides 60. Behroozan DS, Goldberg LH, Glaich AS, Dai T, Friedman PM.
with a nonablative 1,450-nm diode laser: a controlled clinical Fractional photothermolysis for treatment of poikiloderma of
and histologic study. Dermatol Surg. 2003;29:124-128. civatte. Dermatol Surg. 2006;32:298-301.
818 Wanner et al J AM ACAD DERMATOL
MAY 2016

61. Jih MH, Goldberg LH, Kimyai-Asadi A. Fractional photo- 79. Alam M, White LE, Martin N, Witherspoon J, Yoo S, West DP.
thermolysis for photoaging of hands. Dermatol Surg. 2008; Ultrasound tightening of facial and neck skin: a rater-blinded
34:73-78. prospective cohort study. J Am Acad Dermatol. 2010;62:
62. Katz TM, Goldberg LH, Marquez D, et al. Nonablative 262-269.
fractional photothermolysis for facial actinic keratoses: 80. Moreno-Moraga J, Valero-Altes T, Riquelme AM,
6-month follow-up with histologic evaluation. J Am Acad Isarria-Marcosy MI, de la Torre JR. Body contouring by
Dermatol. 2011;65:349-356. non-invasive transdermal focused ultrasound. Lasers Surg
63. Weiss ET, Brauer JA, Anolik R, et al. 1927-nm fractional Med. 2007;39:315-323.
resurfacing of facial actinic keratoses: a promising new 81. Jewell ML, Baxter RA, Cox SE, et al. Randomized
therapeutic option. J Am Acad Dermatol. 2012;68:98-102. sham-controlled trial to evaluate the safety and effectiveness
64. Tierney EP, Hanke CW, Watkins L. Treatment of lower eyelid of a high-intensity focused ultrasound device for noninvasive
rhytids and laxity with ablative fractionated carbon-dioxide body sculpting. Plast Reconstr Surg. 2011;128:253-262.
laser resurfacing: Case series and review of the literature. J 82. Capla JM, Rubin JP. Discussion: Randomized sham-controlled
Am Acad Dermatol. 2011;64:730-740. trial to evaluate the safety and effectiveness of a
65. Chapas AM, Brightman L, Sukal S, et al. Successful treatment high-intensity focused ultrasound device for noninvasive
of acneiform scarring with CO2 ablative fractional resurfacing. body sculpting. Plast Reconstr Surg. 2011;128:263-264.
Lasers Surg Med. 2008;40:381-386. 83. Shek S, Yu C, Yeung CK, Kono T, Chan HH. The use of focused
66. Cervelli V, Gentile P, Spallone D, et al. Ultrapulsed fractional ultrasound for non-invasive body contouring in Asians. Lasers
CO2 laser for the treatment of post-traumatic and patholog- Surg Med. 2009;41:751-759.
ical scars. J Drugs Dermatol. 2010;9:1328-1331. 84. Sakamoto FH, Avram M, Anderson RR. Laser and other
67. Kineston D, Kwan JM, Uebelhoer NS, Shumaker PR. Use of a energy technologies principles and skin interactions. In:
fractional ablative 10.6-mum carbon dioxide laser in the Bolognia JL, Jorizzo JL, Schaffer JV, eds. Dermatology. 3rd
treatment of a morphea-related contracture. Arch Dermatol. ed. New York: Elsevier Saunders; 2012:2251-2259.
2011;147:1148-1150. 85. Anderson RR, Parrish JA. Selective photothermolysis: precise
68. Haedersdal M, Katsnelson J, Sakamoto FH, et al. Enhanced microsurgery by selective absorption of pulsed radiation.
uptake and photoactivation of topical methyl aminolevuli- Science. 1983;220:524-527.
nate after fractional CO2 laser pretreatment. Lasers Surg Med. 86. Jalian HR, Jalian CA, Avram MM. Common causes of injury
2011;43:804-813. and legal action in laser surgery. JAMA Dermatol. 2013;149:
69. Haedersdal M, Togsverd-Bo K, Paasch U. Case reports on the 188-193.
potential of fractional laser-assisted photodynamic therapy 87. Kamat BR, Tang SV, Arndt KA, Stern RS, Noe JM, Rosen S.
for basal cell carcinomas. Lasers Med Sci. 2012;27:1091-1093. Low-fluence CO2 laser irradiation: selective epidermal dam-
70. Cho S, Jung JY, Lee JH. Treatment of anetoderma occurring age to human skin. J Invest Dermatol. 1985;85:274-278.
after resolution of StevenseJohnson syndrome using an 88. Sakamoto FH, Wall T, Avram MM, Anderson RR. Lasers and
ablative 10,600-nm carbon dioxide fractional laser. Dermatol flashlamps in dermatology. In: Freedberg IM, ed. Fitzpatrick’s
Surg. 2012;38:677-679. dermatology in general medicine. New York: The McGraw-Hill
71. Zachary CB, Rofagha R. Laser therapy. In: Bolognia JL, Companies Inc; 2007:2263-2279.
Jorizzo JL, Schaffer JV, eds. Dermatology. 3rd ed. New York: 89. Hantash BM, Bedi VP, Chan KF, Zachary CB. Ex vivo histolog-
Elsevier Inc; 2012:2261-2281. ical characterization of a novel ablative fractional resurfacing
72. Nahm WK, Su TT, Rotunda AM, Moy RL. Objective changes in device. Lasers Surg Med. 2007;39:87-95.
brow position, superior palpebral crease, peak angle of the 90. Landthaler M, B€aumler W, Hohenleutner U. Lasers and
eyebrow, and jowl surface area after volumetric radiofre- flashlamps in dermatology. In: Wolff K, Goldsmith LA,
quency treatments to half of the face. Dermatol Surg. 2004; Katz SI, Gilchrest BA, Paller AS, Leffell DJ, eds. Fitzpatrick’s
30:922-928. dermatology in general medicine. New York: McGraw-Hill;
73. Sadick NS, Mulholland RS. A prospective clinical study to 2012:2869-2890.
evaluate the efficacy and safety of cellulite treatment using 91. Laser Institute of America Laser Safety Committee. A laser
the combination of optical and RF energies for subcutaneous safety guide. Orlando (FL): Laser Safety Institute; 2015.
tissue heating. J Cosmet Laser Ther. 2004;6:187-190. 92. Hammes S, Augustin A, Raulin C, Ockenfels HM, Fischer E.
74. Atiyeh BS, Dibo SA. Nonsurgical nonablative treatment of Pupil damage after periorbital laser treatment of a port-wine
aging skin: radiofrequency technologies between aggressive stain. Arch Dermatol. 2007;143:392-394.
marketing and evidence-based efficacy. Aesthetic Plast Surg. 93. Polla BS, Anderson RR. Thermal injury by laser pulses:
2009;33:283-294. protection by heat shock despite failure to induce
75. Wanner M, Avram M. An evidence-based assessment of heat-shock response. Lasers Surg Med. 1987;7:398-404.
treatments for cellulite. J Drugs Dermatol. 2008;7:341-345. 94. Gevorkian SG, Allahverdyan AE, Gevorgyan DS, Simonian AL.
76. Kaplan H, Gat A. Clinical and histopathological results Thermal (in)stability of type I collagen fibrils. Phys Rev Lett.
following TriPollar radiofrequency skin treatments. J Cosmet 2009;102:048101.
Laser Ther. 2009;11:78-84. 95. Purschke M, Anderson RR, Zurakowski D, Manstein D. Cell--
77. White WM, Makin IR, Barthe PG, Slayton MH, Gliklich RE. cycle-dependent active thermal bystander effect (ATBE).
Selective creation of thermal injury zones in the superficial Lasers Surg Med. 2011;43:230-235.
musculoaponeurotic system using intense ultrasound ther- 96. Bhuyan BK, Day KJ, Edgerton CE, Ogunbase O. Sensitivity of
apy: a new target for noninvasive facial rejuvenation. Arch different cell lines and of different phases in the cell cycle to
Facial Plast Surg. 2007;9:22-29. hyperthermia. Cancer Res. 1977;37:3780-3784.
78. Gliklich RE, White WM, Slayton MH, Barthe PG, Makin IR. 97. Arndt KA, Feingold DS. The sign of Pyotr Vasilyewich
Clinical pilot study of intense ultrasound therapy to deep Nikolsky. N Engl J Med. 1970;282:1154-1155.
dermal facial skin and subcutaneous tissues. Arch Facial Plast 98. Cho SB, Lee SJ, Kang JM, Kim YK, Lee JH. Formation of
Surg. 2007;9:88-95. arcuate crusted lesions after non-ablative 1450-nm diode
J AM ACAD DERMATOL Wanner et al 819
VOLUME 74, NUMBER 5

laser treatment equipped with a dynamic cooling device. J 106. Chan HH, Ying SY, Ho WS, Kono T, King WW. An in vivo trial
Cosmet Laser Ther. 2010;12:124-125. comparing the clinical efficacy and complications of
99. Wenzel S, Landthaler M, B€aumler W. Recurring mistakes in Q-switched 755 nm alexandrite and Q-switched 1064 nm
tattoo removal. A case series. Dermatology. 2009;218: Nd:YAG lasers in the treatment of nevus of Ota. Dermatol
164-167. Surg. 2000;26:919-922.
100. Urbanus AT, van den Hoek A, Boonstra A, et al. People with 107. Datrice N, Ramirez-San-Juan J, Zhang R, et al. Cutaneous
multiple tattoos and/or piercings are not at increased risk for effects of cryogen spray cooling on in vivo human skin.
HBV or HCV in The Netherlands. PLoS One. 2011;6:e24736. Dermatol Surg. 2006;32:1007-1012.
101. Entz AT, Ruffolo VP, Chinveschakitvanich V, Soskolne V, van 108. Lee SJ, Park SG, Kang JM, Kim YK, Kim DH. Cryogen-induced
Griensven GJ. HIV-1 prevalence, HIV-1 subtypes and risk arcuate shaped hyperpigmentation by dynamic cooling
factors among fishermen in the Gulf of Thailand and the device. J Eur Acad Dermatol Venereol. 2008;22:883-884.
Andaman Sea. AIDS. 2000;14:1027-1034. 109. Briggs ME, Baker C, Hall R, et al. Prevalence and risk factors
102. Yun PL, Arndt KA, Anderson RR. Q-switched laser-induced for hepatitis C virus infection at an urban Veterans Admin-
chrysiasis treated with long-pulsed laser. Arch Dermatol. istration medical center. Hepatology. 2001;34:1200-1205.
2002;138:1012-1014. 110. Trotter MJ, Tron VA, Hollingdale J, Rivers JK. Localized
103. Kono T, Ercocen AR, Chan HH, Kikuchi Y, Nozaki M. Effec- chrysiasis induced by laser therapy. Arch Dermatol. 1995;
tiveness of the normal-mode ruby laser and the combined 131:1411-1414.
(normal-mode plus Q-switched) ruby laser in the treatment 111. Anderson RR, Geronemus R, Kilmer SL, Farinelli W,
of congenital melanocytic nevi: a comparative study. Ann Fitzpatrick RE. Cosmetic tattoo ink darkening. A complication
Plast Surg. 2002;49:476-485. of Q-switched and pulsed-laser treatment. Arch Dermatol.
104. Kono T, Ercocen AR, Kikuchi Y, Isago T, Honda T, Nozaki M. A 1993;129:1010-1014.
giant melanocytic nevus treated with combined use of 112. Ross EV, Yashar S, Michaud N, et al. Tattoo darkening and
normal mode ruby laser and Q-switched alexandrite laser. J nonresponse after laser treatment: a possible role for tita-
Dermatol. 2003;30:538-542. nium dioxide. Arch Dermatol. 2001;137:33-37.
105. Kono T, Sakurai H, Groff WF, et al. Comparison study of a 113. Kirby W, Kaur RR, Desai A. Paradoxical darkening and removal
traditional pulsed dye laser versus a long-pulsed dye laser in of pink tattoo ink. J Cosmet Dermatol. 2010;9:149-151.
the treatment of early childhood hemangiomas. Lasers Surg 114. Ortiz AE, Alster TS. Rising concern over cosmetic tattoos.
Med. 2006;38:112-115. Dermatol Surg. 2011;38:424-429.

Answers to CME examination


Identification No. JC0516
May 2016 issue of the Journal of the American Academy of Dermatology.

Wanner M, Sakamoto FH, Avram MM, Anderson RR. J Am Acad Dermatol 2016;74:807-19.

1. c 3. a
2. b

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