Treatment of Photodamaged Skin Focus
on Combination Therapy
Gary D. Monheit, M.D.
Associate Professor
Department of Dermatology
University of Alabama at Birmingham
Birmingham, Alabama
Needs
Assessment
Chronic exposure to ultraviolet radiation results in histological damage
to the skin that can produce undesirable visible alterations, such as
rhytides, telangiectasias and dyschromia, as well as precancerous lesions.
A wide variety of non-invasive treatments, including cosmoceutical topicals
such as retinoids, hydroxy acids and bleaching agents, nonablative light
therapies, and ablative procedures such as chemical peels, laser resurfacing,
and dermabrasion, are available. Topicals
are often a starting point for the treatment of milder cases of photodamage,
and can also be used before, during, and after office-based procedures
to augment outcomes for patients with more extensive damage. A review
of current treatment options, including the application of combination
therapy regimens, can assist clinicians in the development of individualized
treatment plans for patients with photodamaged skin.
Learning
Objectives
Upon completion of this continuing education activity, participants
should be better able to:
• Describe the categories of change that occur in photodamaged
skin.
• Discuss the available treatments for the signs of photoaging.
• Discuss the role of topical agents in the treatment of photodamaged
skin.
• Discuss the advantages of using both topical and procedure-based
treatments as part of a combination therapy regimen.
Introduction
Chronic exposure
to solar ultraviolet (UV) radiation results in premature skin aging.
The clinical manifestations of photoaged skin include wrinkling, mottled
pigmentation, roughness, sallow color, and loss of elasticity. Underlying
these visible signs of photoaging are various histological and cytological
changes induced by chronic UV exposure. The loss of collagen fibers,
which normally provide structural stability, and the degradation of
elastin fibers, which gives skin its natural elasticity, result in a
general breakdown of the skin’s fibrous matrix. This creates an
inelastic, thin, dull-appearing skin. In addition to the structural
damage to the dermal extracellular matrix, chronic exposure to the sun’s
UV rays causes a generalized dysplasia of a variety of epidermal cell
types, including keratinocytes and melanocytes. This type of cellular
damage contributes to the mottled and/or hyperpigmented appearance of
photoaged skin.
Photoaging (extrinsic
aging) differs histologically from intrinsic aging, the changes that
occur normally over time. The histological signs of intrinsic aging
include epidermal atrophy, resulting in thin, translucent skin with
hypocellular changes of the dermis, and increased crosslinking of the
collagen matrix. Extrinsic aging, on the other hand, produces changes
such as thickening rigidity and scaling of the epidermis with a concomitant
destruction of collagen and elastin and the deposition of colloid material
with hypercellularity of the dermis. Susceptibility to photodamage is
largely determined by an individual’s Fitzpatrick skin type. Lighter
skin tones—Fitzpatrick types I through III—are more susceptible
to extrinsic photoaging than darker skin tones—Fitzpatrick types
IV through VI. The intrinsic photoprotection present in darker skin
makes it less prone to damage from actinic exposure.
[FACULTY—PLEASE
PROVIDE chart/pictures outlining extrinsic vs intrinsic aging
to be inserted here]
|
Skin
Type |
Skin
Color |
Tanning
Response |
|
Type
I |
White
|
Always
burn, never tan |
|
Type
II |
White
|
Usually
burn, tans with difficulty |
|
Type
III |
White
|
Sometimes
mild burn, tan average |
|
Type
IV |
Brown |
Rarely
burn, tan with ease |
|
Type
V |
Dark
Brown |
Very
rarely burn, tan very easily |
|
Type
VI |
Black |
No
burn, tan very easily |
Photodamage can
be classified into three categories of change. Color changes include
the redness of inflammation, irritation, and telangeictases, and areas
of brown coloration in the form of lentigines and postinflammatory hyperpigmentation.
Dermal changes, in the form of the irregular destruction of collagen
and elastin, are the cause of wrinkling, surface irregularities, and
skin sagginess/loss of elasticity. Finally, epidermal dysplasia, hyperkeratosis
with actinic keratoses fall into the category of pre-pre or precancerous
changes; these are atypical proliferations on the skin that stem from
deeper cellular damage and that may evolve into cancerous lesions.
[FACULTY—PLEASE
PROVIDE histology images representing these categories of change
to be inserted here]
Recognizing
the specific types of changes that have occurred in a patient’s
skin and quantifying the extent of the damage are crucial first steps
in designing an effective treatment plan. In 1996, Glogau published
a system for classifying patient photoaging types (the “Glogau
wrinkle scale”; Table 1), with the aim of facilitating discussion
and rational comparison of therapies and their outcomes. The Glogau
wrinkle scale may be a valuable tool for determining which treatment
modalities may be of the most benefit for patients.
|
GLOGAU
PHOTOAGING CLASSIFICATION |
RECOMMENDED
TREATMENT |
|
Type
1: “no wrinkles”
• Patient age: 20s or 30s
• Early photoaging
o Mild pigmentary changes
o No keratoses
o Minimal wrinkles |
•
Sunscreens and education
• Education
• Tropical tretinoin
• Creams: 15-30%
• Glycolic acid peels: 40-70%
• Botulinum toxin |
|
Type
2: “wrinkles in motion”
•
Patient age: late 30s or 40s
• Early to moderate photoaging
o Early senile lentigines visible
o Keratoses palpable but not visible
o Parallel smile lines appearing |
•
Sunscreens and education
• Education
• Tropical tretinoin
• Creams: 15-30%
• Glycolic acid peels: 40-70%
• Botulinum toxin |
|
Type
3: “wrinkles at rest”
•
Patient age: 50s and up
• Advanced photoaging
o Obvious dyschromia, telangiectasia
o Visible keratoses
o Wrinkles, even at rest |
•
Sunscreens and education
• TCA chemical peel: 30-50%
• Combination TCA peels
• Laser resurfacing (periorbital, perioral)
• Combination laser resurfacing
• Soft tissue augmentation
• Botulinum toxin
• Combination procedures |
|
Type
4: “only wrinkles”
•
Patient age: 60s or 70s
• Severe photoaging
o Yellow-gray skin color
o Prior skin malignancies
o Wrinkled skin throughout |
•
Full facial CO2 laser resurfacing
• Combination CO2 laser and TCA peel
• Deep peel
• Facelift
• Brow lift
• Blepharoplasty
• Botulinum toxin |
Table 2.
Glogau Wrinkle Scale
Many treatment options,
including both topical agents and office-based procedures, are available
for treating photodamage, and different treatment modalities can target
different features of photoaged skin. For this reason, combination therapy
plans that incorporate more than one treatment modality may help patients
achieve the greatest benefit.
In a recent roundtable discussion, experts in the treatment of photoaging
skin discussed the available treatments, and the benefits of a combination
therapy approach to the treatment of sun damage and related conditions.
Available Options
for the Treatment of Photodamage
Dr. Alster: In addition to all the options that will be discussed, it
is very important to emphasize to our patients that every single aspect
of photoaging starts and ends with photoprotection. We have to make
it very clear to our patients when we’re attempting to treat them
that we want to prevent further photoaging as much as possible, and
photoprotection is a big part of that.
Dr Nestor: Peels
have been used for the longest time for photodamage. Peels help treat
some of color changes that occur with photodamage—specifically
the brown type of coloration. In my experience, peels are only minimally
effective for the telangiectatic changes. They are certainly beneficial
for the sun damage aspect of hyperkeratotic, precancerous changes, and,
depending on the depth of the peel, they can help improve rhytides and
related dermal changes.
Recently, a lot
of peels have been supplanted by ablative laser treatments. The CO2
and erbium laser are still being used, and they have the same general
type of effect as peels. In some hands they can be specifically targeted
to be deeper or more superficial, depending upon the laser and how it’s
used.
For nonablative
treatments, the classic treatment for me is photorejuvenation, with
intense pulsed light (IPL). IPL can treat two aspects of photoaging:
coloration, both red (telangiectases) and brown (lentigines), and dermal
remodeling, though perhaps not as dramatically as with the ablative
lasers.
The newest treatment
on the block is photodynamic therapy, the topical application of aminolevulinic
acid, followed by exposure to blue light. Photodynamic therapy, when
combined with IPL or other devices, can improve all three aspects of
photoaging: color changes, dermal remodeling, and precancerous changes.
There are a variety
of laser devices that can affect change in one or more of the processes
of photoaging. From the standpoint of the telangiectatic red changes,
certainly lasers such as the pulsed dye 532 nm laser, as well as other
lasers in that general category, can affect change in the blood vessels,
in addition to having an impact on dermal remodeling. The Q-switched
ruby, Q-switched YAG, and Alexandrite lasers can affect changes in pigmentary
states. Lasers in the 1320 nm to 1450 nm range can be used to target
changes related to dermal remodeling.
I look at the topical
treatments as either a step-up process or an augmentation process to
the procedural treatments. Certainly retinoids, such as Renova and Retin-A,
to me are a very, very good adjunctive treatment, and a starting point
for people who are not ready for more significant laser or other physical
treatments. A variety of different topical agents, such as cosmeceutical
agents containing glycolic acid, other over-the-counter topical agents,
and a variety of other categories, from amino acid filagrin-based antioxidants
(AFAs) to azelaic acid, can be used adjunctively as part of a combination
treatment plan to target several different histological aspects of photodamage.
DR. NESTOR—PLEASE ELABORATE ON HOW YOU CHOOSE A TOPICAL AGENT
Dr. Alster: We next
turn to Gary Monheit for background on fillers, dermabrasions, Botox,
and peels.
Dr. Monheit: My
first approach is always to ask “where is the problem, what are
we looking at, and what is the best way that we can solve the problem?”
I developed an index of photoaging skin that I use with my patients.
It categorizes the problems of photoaging skin into textural changes
and lesional changes, quantifies the level of damage, and gives it a
score. It is a good tool for identifying where the problem is, and it
allows the clinician to individualize the treatment plann.
[DR. MONHEIT—PLEASE
PROVIDE YOUR INDEX to be inserted here]
The aging face must
be considered in addition to aging skin, when we target our treatments.
In order to target problems of volume loss, both in the skin and below
the skin, fillers can be used. Muscle spasms are responsible for the
development of dynamic wrinkles and furrows, and for this we use botulinum
toxin, a relaxing agent to ease muscle spasms that have caused crow’s
feet, forehead wrinkles, and glabellar lines.
Before resurfacing
techniques are used, we have to determine where the damage lies in the
skin: is it superficial, medium depth, or is it deep? Superficial damage,
involving just the epidermis, can be targeted by a superficial agent
that exfoliates the stratum corneum in the uppermost epidermis. Light
chemical peels, including glycolic acid, Jessner’s solution, salicylic
acid, or some of the other combination peels, can be used. The very
superficial peels are designed to to remove the stratum corneum,stimulate
epidermal proliferation and encourage the growth of a plumper, fresher
epidermis. Microdermabrasion, a mechanical abrasive method, can also
be used to remove the stratus corneum and stimulate epidermal growth.
Lasers aren’t used for superficial exfoliation at all.
Medium depth techniques
destroy the epidermis, and either inflame or destroy a portion of the
papillary dermis. For medium depth chemical peeling, my favorite is
the combination Jessner’s solution and 35% trichloracetic acid,
a very safe, effective, peeling formula. It completely destroys the
epidermis, and also inflames the papillary dermis, causing enough destruction
to get regeneration of a new epidermis that does not have the pigmentation,
hyperkeratosis, or atrophy that the patient had before. The creation
of a newly rejuvenated epidermis also addresses the fine line changes
we find in the papillary dermis. A medium depth peel will not have an
effect on blood vessels, so there will not be a change in telangiectases
or reddening. For medium depth dermabrasion, I mainly use manual dermasanding.
This technique uses silicon carbide sandpaper on water to sand off epidermis
until we get to petechial bleeding. I like to use this in combination
with superficial or medium depth peeling as a background, and we can
sand into lesions all the way into the mid-papillary dermis. Erbium
lasers can also be used for medium depth resurfacing. [DR. MONHEIT:
PLEASE DISCUSS HOW YOU CHOOSE A MODALITY FOR AN INDIVIDUAL PATIENT-
See below]
For deep levels
of resurfacing, we can use a deep chemical peel. Deep chemical peels
destroy the epidermis, the papillary dermis, and portions of the reticular
dermis or the mid-reticular dermal area. The Baker’s (phenol)
peel is the major peel used. It has major side effects and is a major
surgical procedure that is not used as much as it used to be, but it
still has a place. [FACULTY PLEASE PROVIDE ADDITIONAL INPUT] A mechanical
dermabrasion procedure can bring the destruction and removal down to
the mid-reticular dermis. Finally, CO2 laser resurfacing can be used,
which can reach the reticular dermis in order to achieve regeneration
of new collagen and a completely new epidermis.
For example, this patient has significant rhytids in the periorbital
and perioral areas. They require deep resurfacing. The remaining face
has medium depth damage of epidermal growths, dyschromias and fine rhytids.
I have chosen a combination procedure utilizing C02 laser resurfacing
– perioral and periorbital medium depth chemical peel (Jessner’s
+ 35% TCA) – remaining face with light chemical peeling on the
neck. This will blend the cosmetic units giving a natural appearing
skin rejuvenation.
See Figures 1, 2,
3, 4 and 5
Dr. Alster: Dr.
Lask, how are lasers used in your practice, versus other types of surgeries
you perform? I think it’s important to note that some people still
do some mainstay surgical procedures in addition to some of these other
cosmetic enhancement procedures.
Dr. Lask: Like phenol
peels, I think deeper laser resurfacing has gone out of fashion. I think
that now, more nonablative techniques are used for photoaging, primarily
vascular and pigmented lasers for removing erythema, telangiectases,
and dyschromia. The ones we like best are intense pulsed light, pulsed
dye lasers, and Q-switched lasers, which all seem to work very well.
Because downtime with most of these devices is quite minimal, and the
improvement is fairly significant, these are very popular in our practice.
Topical Agents and
Combination Therapy
Dr?-can someone
identify the speaker?Dr. Monheit: Combination therapy has two major
benefits: number one, enhancing the ultimate effect of the treatment,
and number two, prolonging the effect for the longest period of time
and preventing problems from occurring. With any type of treatment,
we want to get the best effect with the least amount of problems or
side effects and the least amount of treatment for the patient. The
ultimate treatment would give superior results without any side effects
or downtime. Combination therapy using retinoids and other topicals,
along with the other treatments we’ve been talking about, gets
us much closer towards this best-case scenario.
Dr-identify speaker
Dr. Monheit: Topicals add a pharmacologic aspect to the destructive
procedures we are using. Everything mentioned—whether it is nonablative,
selective thermolysis, peeling, or dermabrasion—is destructive
in the sense that we are destroying one cell or one structure or generally
destroying a layer of epidermis or dermis. We are stimulating a regeneration
of skin. Topicals can allow us to tailor the regeneration process to
fit the result we’re seeking.
Hydroquinone blocks
the enzyme tyrosine, thus preventing the production of new melanin and
stopping pigment production. This pharmacologic effect is combined with
light chemical peels to lighten dyschromic skin.
Dr. Alster: Another
reason we use topicals is really as a primer for some of the other procedures
we do. There Is a certain amount of improvement we can get by using
a combination of topicals alone, and they “prepare the canvas”
for the other destructive methods that we use in our office, and enable
us to use either fewer, or less intense, treatments.
Dr. ?identify speaker:Dr.
Monheit: I think an important point is that we are all talking about
long-term care of people with an ongoing problem: photoaging skin. What
we suggest at the beginning of treatment may be different from what
the patient will have a year from now, or two years, or five years,
but what we are doing is incorporating these patients into a program
where we are going to be the primary physicians for their skin. Many
times the topical treatment is the glue that holds the treatment plan
together temporally—we start with some of the less aggressive
treatments, such as IPL, and then as the patient gets older and the
photodamage increases, we can move on to other things like fillers,
or some of the more aggressive ablative treatments. But, that’s
down the road, and they will continue to look to us for continued improvement,
and to protect the skin from further photodamage.
Dr. Alster: That’s
a very good point, not only in terms of moving patients up to other,
more aggressive forms of treatment, but also in terms of using some
of these topicals as maintenance. The topicals are like steps to the
bridge. We use them as primers, throughout the treatments, and then
as maintenance down the line.
There’s been
a trend towards using a combination of lighter therapies, as opposed
to the more invasive treatments like ablative lasers or even dermabrasion,
because when you can do this with topicals, and with some of these other
nonablative treatments that we have been talking about, you can get
very much the same results without as much downtime or as many side
effects.
[FACULTY—PLEASE
PROVIDE A SIMPLE LIST/TABLE BRIEFLY COMPARING THE TOPICAL AGENTS FOR
PHOTODAMAGE YOU USE MOST FREQUENTLY IN YOUR PRACTICES (EG SUNSCREEN,
TAZAROTENE, AHAs, HYDROQUINONE, AZELAIC ACID, ETC ). FOR EACH, PLEASE
PROVIDE GENERIC NAME, PURPOSE, AND TYPICAL PROTOCOL FOR USE - Below]
Topical Agents Most Commonly Used to Correct Photoaging Skin
1. Sunscreens
2. Retinoids: Retinoic acid
3. Tazarotene
4. Glycolic Acid
5. Hydroquinone
6. Ascorbic Acid
[separate box]
Tretinoin in the Treatment of Photodamage
Tretinoin (all-trans-retinoic
acid), a compound derived from retinol (Vitamin A), is the only topical
pharmaceutical agent proven to repair photodamaged skin. While the exact
mechanisms of action are not fully understood, treatment of photodamaged
skin with topical tretinoin is known to result in the regeneration of
the dermal collagen matrix, epidermal thickening, compaction of the
stratum corneum, and promotion of epidermal hyperplasia and angiogenesis.
Studies have demonstrated that retinoids are able to induce collagen
synthesis in cultured human dermal fibroblasts, and that retinoic acid
applied topically to the skin prevents UV induction of the matrix metalloproteinases
(MMPs) that play a role in the destruction of the extracellular matrix.
The histological alterations induced by tretinoin treatment have been
correlated with clinical improvements, including smoothening of the
skin, lightening of hyperpigmented lesions, disappearance or significant
improvement of fine wrinkles, and, to a lesser extent, of coarse wrinkles.
Tretinoin has also been shown to protect skin against photodamage induced
by repeated UV exposure, making it an ideal agent for maintenance therapy.
Tretinoin is available
in several formulations and concentrations, the choice of which is usually
determined by the patient’s tolerance. Tolerance of topical retinoids
by patients may vary with age, race, skin type, extent of photodamage,
and local climate. Treatment should be combined with photoprotection
in order to prevent further photodamage. Clinical effects may be noted
as early as the first month of treatment.
Summary of the cytological, histological and vascular effects of topical
tretinoin on photodamaged human skin:
? Epidermal thickness
Compaction of the stratum corneum
? Stratum granulosum thickness
? Melanin content and ? melanocytotic hypertrophy/hyperplasia
Reduced epidermal atrophy and promotion of epidermal hyperplasia
? Epidermal atypia and dysplasia
? Synthesis of collagen
? Number of collagen-containing anchoring fibrils in the cutaneous basement
membrane zone
? Skin elasticity at high test loads
Exfoliation of retained keratinous horn in follicles
New blood vessel formation and ? blood flow
Symbols: ? indicates significantly increased; ? indicates significantly
decreased.
Table adapted from Noble & Wagstaff, 1995.
The first step in treating a patient with photodamaged skin is the assessment
of the type and extent of damage. Our faculty experts discussed possible
combination therapies for several hypothetical patients.
Case Study #1: A
patient with dyschromia (redness or brown mottling of the skin, with
very little loss of elasticity).
Dr. Lask: If a person
comes in with dyschromia, I almost always start them on some bleaching
agents first. The biggest problem with bleaching agents we have is local
irritation. In people that irritate, obviously we have to stop, but
we still find improvement without irritation, even using it once every
second or third day. For dyschromia, we almost always also put patients
on retinoids. They diminish pigmentation, which has been proven in many
different clinical studies, and improve skin texture and quality. [DR.
LASK, PLEASE EXPAND ON PROTOCOL FOR USE (DOSE, TIMING, ETC)]
For the next step
with dyschromia, we primarily use the Q-switched lasers. We also use
intense pulsed light (IPL) for dyschromia, but I think the Q-switched
lasers like the YAG or the Alexandrite give you a quicker response.
There is a little bit of downtime, five or seven days, but the response
is much quicker.
And for the erythema
or vascular component of photoaging, we primarily use the V Beam or
pulsed dye laser, as well as IPL. I do think the V Beam is a little
better for erythema, and it is certainly safer to use and a little more
user friendly than IPL, but both work fine. They both require multiple
treatments.
Dr. Monheit: I think
you have to separate the younger patient with dyschromia, who really
doesn’t have a lot of atrophy, poikiloderma of the skin, or telangiectasia,
but who mainly has more of a melasmic discoloration and sun dyschromia
as the major problem. Like Dr. Lask, I would begin with topical therapy.
I would include a bleaching agent such as a hydroquinone: depending
on the severity of the dyschromia, I would either go from 2% or even
up to 8%. As you increase the concentration of hydroquinone you get
more irritation, so you must be careful with it.
I like to combine
that with a topical retinoid, because I think that with our bleaching
agent, we essentially stop or inhibit the transformation of dopa to
tyrosine through tyrosinase by blocking it, so we’re mechanically
stopping the production of new pigment. At the same time we want to
speed up epidermal proliferation to push out old pigment, and that’s
what we’re doing with the topical retinoid. In addition, the use
of sunscreen is essential to protect the skin from further sun damage.
So, those three
topicals (a bleaching agent, a retinoid, and sunscreen) are the real
baseline we want to have the patient using readily before we add on
office procedures. For this particular kind of patient I would start
with a light chemical peel. I like salicylic acid peels better than
the others because they are less inflammatory with less of a chance
of postinflammatory hyperpigmentation occurring. They remove the stratum
corneum, stimulate more epidermal proliferation, and pull out more pigmentation.
I would do this as a repetitive peel every three to four weeks, along
with topical treatment, and follow them along on this regimen first.
If the response
is not significant, I would then go on to a medium depth chemical peel,
which would obliterate the entire epidermis but then have to be followed
carefully with both bleaching agents and anti-inflammatories, such as
topical steroids, to prevent postinflammatory hyperpigmentation. After
that, I would use some selective lasers such as the Q-switched YAG,
or if more extensive damage is present, even intense pulsed light (we
use the Quantum laser). That is my basic regimen for treating pigmentation
as a major sign of photoaging.
Dr. Nestor: I like to look at it more from the aspect of what patients
can and will tolerate. In my patient population, more and more of them
really want as much benefit as possible without the downtime. I rarely
see a lot of dyschromia in and of itself without other changes. Certainly,
it occurs, but I would really categorize this as spot dyschromia versus
generalized photoaging. I look at photoaging much less as spot dyschromia,
which would be lentigines here or there, or something that would occur
separately from the photodamage type of dyschromia, which is more generalized.
Certainly lentigines are a part of it, but it is much more of an overwhelming
presentation than individual lentigines or brown areas. I would agree
with Dr. Monheit that the melasma picture is something different, and
I think that’s really not necessarily associated as much with
photoaging as it is with a genetic predisposition and hormonal changes.
I look at photoaging in a different category.
For the majority
of my patients I tend to use and start with photorejuventation or IPL
because of the benefit of having no downtime for many of them, and because
this is not just pure hyperpigmentation. We generally see some degree
of redness and telangiectases, as well as some degree of dermal change.
I believe IPL does a nice job of helping all of these at the same time.
I generally use
a Q-switched laser as a secondary treatment for this category, but for
the category I mentioned earlier—the individual lentigines or
areas—I tend to use it much sooner, because those patients tend
to have a lesser degree of photoaging, and the individual lesions are
very easy to remove with the Q-switched laser.
For patients that
can tolerate downtime, in the past I’ve started with an erbium
laser or in some cases a CO2 laser, but recently I have been using more
photodynamic therapy, because it really augments the photorejuvenation
process significantly. It does have at least two or three days of downtime,
possibly more depending upon how you use it.
When it comes to
topicals along with these treatments, I look at them as adjuncts in
this case. For the hyperpigmentation aspects I use a combination agent
containing fluocinolone acetonide 0.01%, hydroquinone 4%, and tretinoin
0.05%, which can, I believe, significantly augment the problem of repigmentation,
and can also help with the overall improvement. I also use retinoids
in this category. [DR. NESTOR, PLEASE EXPAND ON THIS—HOW AND WHY
ARE THEY USED]
Again, I want to
stress the issue of photoprotection. For a lot of these patients, I
use a broad spectrum physical block with titanium dioxide or zinc oxcide.
I think that we tend to make many of our patients significantly better,
and they tend to go down the tubes pretty quickly by just creating more
sun damage so I think that’s a big factor.
[FACULTY—PLEASE
PROVIDE before & after pictures of patient(s) treated for dyschromia]
Dr. Alster: To summarize
the various treatment regimens for dyschromia, everyone uses some sort
of adjunctive topical. Most people use it preliminarily to prime the
skin, and keep their patients on this therapy while they pursue other
treatments, most notably in the case of Dr. Lask—pulsed dye laser
and intense pulsed light for the erythema, and then Q-switched pigment-specific
lasers with IPL for the pigment. In the case of Dr. Monheit, he starts
with topicals, goes through light peels and medium peels, depending
on the amount of dyschromia, and then finishes up with laser or light
sources for any residual erythema. Dr. Nestor uses the adjunctive topicals
and quite a bit of photodynamic therapy for the more generalized dyschromia,
versus Q-switched pigment-specific lasers for spot dyschromia. Photoprotection
is also very important.
Case Study #2: A
patient with periorbital and perioral rhytides.
Dr. Alster: How
do you mix and match treatments for a patient with rhytides around the
eyes and mouth?
Dr. Lask: Well,
now if anybody comes in with periorbital rhytides, usually the first
thing I will suggest is botulinum toxin, because most people do get
significant improvement. Again, I put almost everybody on a topical
retinoid as well in order to enhance the outcome and improve skin texture.
I do not use peeling
much anymore. I used to use some laser peeling for the eye area, but
I’ve found it not to be dramatically rewarding for eyelid wrinkles.
The skin is very thin, so if you peeled to a certain depth you either
got pigment loss or some texture change on the lower eyelids. I do think
it helps texture, but not really wrinkling. The only thing I believe
helps with significant wrinkling of the lower eyelids is phenol peeling,
but I do think it often results in some long-term or permanent pigment
loss.
As far as the upper
lip rhytides, I think they’re the hardest, I find, to treat in
my office. The simplest approach may be a topical retinoid; I’ve
seen some studies showing that retinoids actually enhance even upper
lip wrinkling to some degree, though in very small amounts, so I think
using retinoids on the upper lip is a worthwhile endeavor. Some people
will try botulinum toxin injections for the upper lip, and I do think
it helps. The problem is that botulinum toxin does alter the upper lip
a little bit, making it a little bit flatter, and it can also cause
the patient to have a strange sensation in their mouth. A lot of people
don’t like that, so I don’t do it a lot. It does help wrinkling
for some patients.
The fillers such
as Hylaform, Restylane, and the human and bovine collagens can be useful
as well. Patients who are relatively young and whose lip lines are small
may benefit from CosmoDerm, CosmoPlast, Zyderm or Zyplast, but these
only provide short-term improvement, so the patient has to be willing
to come back quite often. Hylaform, which I’ve only been using
for a short time now, seems to last at least a few months, so it seems
to have a longer duration than Zyderm, Zyplast, CosmoDerm, and CosmoPlast.
These products may have a bigger role in upper lip treatments than the
collagen products.
The ablative processes
(laser abrasion, chemical peeling, dermabrasion) all can improve upper
lip rhytides, but in a fair amount of patients they do result in some
long-term pigment loss. Some patients, especially younger patients,
do not want to deal with that. So I think that unless you’re willing
to face that potential complication, it is a hard road to go down.
Dr. Monheit: The
first thing I do is quantify the problem: how much damage is there,
and how much do we have to correct? Most of the “lunchtime procedures”
work very well for people who have either Glogau I or II levels of rhytides
and damage. The other factor we have to consider, as Dr. Nestor mentioned
earlier, is how much downtime a patient is willing to put up with. My
initial approach is to be conservative and to explain and make suggestions
about what we can offer to the patient as far as the lunchtime procedures.
All of my patients get a topical program to begin with, and that includes
a retinoid, some form of exfoliating agent, such as glycolic acid or
mechanical exfoliation, and sunscreen protection. [DR. MONHEIT, PLEASE
EXPAND ON HOW THESE AGENTS ARE USED—DURATION? DOSE?]
The patients are treated for two to six weeks prior to other resurfacing
procedures. Topical home therapy is the cornerstone of all other procedural
therapy to be performed in the dermatologist’s office.
First I address
wrinkles around the eyes and the periorbital area. Using botulinum toxin,
we can relax frown lines and glabellar lines, and a unit or two of botulinum
toxin directly below the tarsal plate may relax a hypertrophic orbicularis
muscle and actually smooth some of the larger wrinkles under the eye.
The next step is resurfacing, and for nonablative procedures we use
the Cool Touch laser for periorbital areas; we also use IPL around parts
of the forehead. Again, these are conservative—minimal to moderate—changes
we will see. As I get into the ablative procedures, I still use CO2
laser resurfacing around the eyes but I do not use phenol peeling. When
I use CO2 laser resurfacing, I like to do at least a medium depth chemical
peel on the rest of the face to blend it so that if there is a pigmentary
change, it won’t be apparent.
As we move down
to the lower aspects of the face, volume changes are very important,
especially in the perioral area. I find that rhytides need a combination
of both volume filling and some nonablative or ablative resurfacing
to get results. I like to combine filling agents together for these
patients, for example using a hyaluronic acid like Hylaform or Restylane
and then combining it with CosmoDerm, first to take care of the deeper
filling in the dermis, and then the very superficial fine lines with
a lighter filling agent. I also believe when combining hyaluronic acid
along with a collagen, we are in essence adding back the substances
that are being lost in the skin: the collagen fibers, the elastic fibers,
and the hyaluronic acid. When we put them back together again, we’re
adding back the bricks and mortar of the dermis, filling it back up.
After we accomplish the filling, then we look at what we can do with
nonablative resurfacing.
For the population
of people with more severe photodamage, I use blepharoplasty. I will
do transconjunctival blepharoplasty for removal of fat and relocation
of fat to resurface the area. We will do fat filling for sad pockets
underneath the eye and to augment the tear trough, and we’ll take
skin out from the upper lid. For around the mouth, I’m now using
the Feather Lift to bring up some of the skin on the perioral area to
raise the nasolabial fold, as well as filling. For more permanent filling,
we’re using fat injections and fat autograft muscle injections
(FAMI) as filling material, and we combine that with resurfacing techniques
for patients with more severe forms of aging (Glogau III and IV).
So we really have
a step-wise program we go through, based on the patient’s needs
and desires. While many patients prefer lunchtime procedures with no
downtime, I often say “go for the gold”: give up some downtime,
have more permanent procedures and address more severe problems with
the more aggressive procedures we use.
Dr. Nestor: Around
the eyes, I also use a step-wise process and approach it from the patient’s
needs. One thing we have not covered is the issue of either dyschromia
or dark circles under the eyes, which can accompany superficial or deep
rhytides. I tend to use a fair amount of erbium laser resurfacing for
these patients to combine the improvement in both the pigmentation and
the fine lines. [DR. NESTOR—HOW MANY TREATMENTS?]
In patients who
are not significantly affected around the eyes, I do see some benefit
with nonablative laser, either the Cool Touch, Smooth Beam, or even
pulsed dye laser. The nonablative laser seems to be less effective around
the mouth. Certainly I have found that, for more superficial damage,
combining the deeper tightening agents such as Thermage or ThermaCool
with photodynamic therapy can result in some degree of significant improvement.
Certainly this can be augmented with the use of fillers.
Since the advent
of Restylane, we’ve seen wonderful improvement in treating perioral
rhytides in those patients that really don’t want to have the
downtime of the deeper laser procedures. For the lips, I often use a
combination of CosmoPlast and Restylane, and I’ve found that this
works well for improving the perioral area, as well as the areas of
the mesiolabial fold. We can inject Botox into some areas, including
the musculature that pulls down the angle of the mouth, to improve any
sagging.
I do use topicals
as adjunctive treatments, including Renova and Retin-A. With my population
of patients here in this warm climate, I tend to use a lot more .025%
Retin-A; studies have compared the lower to the higher concentrations
of Retin-A, and found little difference except for the degree of side
effects and irritation. I do think that the combination therapy gives
us a dramatic degree of improvement.
[FACULTY—PLEASE
PROVIDE before & after pictures of patient(s) treated for perioral/periorbital
rhytides See figures 6 and 7]
Dr. Alster: So,
for dyschromia, and perioral and periorbital rhytides, we all incorporate
some sort of topical, typically a retinoid product, to get the process
started. Very rarely will we see enough change in our patients to not
go at least an extra step, particularly around the mouth. Sometimes
people can improve enough with the topical retinoid around the eyes,
but if there is any movement association there, which I think the majority
of our patients have, Botox comes into play. Fillers are useful around
the mouth, and of course, as was pointed out, ablative or nonablative
lasers and peels also play a role in treating some of the deeper rhytides.
If downtime is not an issue, they can go through some of these more
intensive procedures. In terms of the dark circles under the eyes, in
addition to the erbium laser, you can still use a CO2 laser at a lower
energy in order to get the same peeling effect; peels also work very
nicely in that area.
Case Study #3: Patients
with photoaging and acne and/or rosacea.
Dr. Alster: In our
aging population, we see a lot of people who have acne and rosacea;
many of the procedures we’ve been talking about also apply to
these conditions. [FACULTY—IS IT ACCURATE TO SAY YOU SEE A LOT
OF PATIENTS WITH PHOTODAMAGE AND ACNE OR ROSACEA?]
Dr. Nestor: Acne
and rosacea are physiologically different conditions, although there
certainly is some crossover. In the photoaging population, we’re
probably dealing more with rosacea than with acne in general. My regimen
for acne has changed dramatically over the past year or so because of
the advent of both the blue light therapy (420 nm) and photodynamic
therapy. For rosacea, I tend to use a lot of intense pulsed light; I
think this works great. Certainly pulsed dye laser also works in this
case, and I’ve combined that more and more with photodynamic therapy,
mainly because of the effects it has on sebaceous glands and the augmentation
that occurs in the other aspects of rosacea. For acne, this has also
proven to be a tremendous advancement because of the effect on the sebaceous
unit, and we tend to get very, very significant effects, especially
in the older populations. In my hands, we get more of a long-term clearing
in the older patients than the younger patients, for whatever reasons.
The blue light has also helped us as an augmentation. Again, I tend
to see even better results in the older population of patients than
I do with the younger patients, and for all of these patients, I almost
always augment with a retinoid. I tend to use a lot of adapalene, just
because for many of my patients there’s less of an issue of irritation,
but I certainly use a lot of Retin-A Micro in these patients. I tend
not to use Renova because the emollient formulation tends to aggravate
the acne. For my patients with rosacea, I will add a metronidazole cream
or another topical to help augment the treatment.
[FACULTY: HOW DO
YOU COMBINE TREATMENTS FOR PHOTODAMAGE WITH TREATMENTS FOR ACNE/ROSACEA?
IS ONE TREATED FIRST, THEN THE OTHER, OR IS TREATMENT CONCURRENT? PLEASE
REVISE THIS SECTION ACCORDINGLY]
It is best to control the active rosacea first with topical and systemic
antibiotic therapy before the vessels and dyschromia are treated with
specific lasers. Rosacea exhibits vasomotor flushing which can be triggered
by facial trauma; i.e. chemical peels, Microdermabrasion or lasers.
Thus, the inflammatory condition must be controlled first.
Dr. Monheit: I think
it’s important to separate the adult acne population and the photodamaged
patient who has true acne from the rosacea population, mainly because
of the vasomotor phenomena that occurs in rosacea, which some of our
acne therapies can actually make worse. I usually start with a topical
regimen, then I suggest to them physical modalities that will augment
it. I want them on a topical treatment program that they can adapt to
for long periods of time, and to know that the lasers, or the peels
I’m going to use, are not going to cure the situation, and they’re
not going to maintain it. They will augment what the patient’s
basic home care is going to do for this condition, which is a long-term
condition.
Starting with patients
with adult acne, if I need to I put them on antibiotics, and on topical
therapy a retinoid is very important. I like Retin-A Microgel. If the
patient has sensitive skin we use the 0.04%; we use the stronger one
(0.1%) if the patient has an oily complexion and can tolerate it. This
is a daily regimen. Along with that, I add an azelaic acid and/or a
benzoyl peroxide to be used at night, depending on their skin tolerance.
We use a blue light
laser, and I think that a series of four to six treatments can really
put a lot of lesions to rest and cut down on the frequency of topical
therapy. One other treatment that I think is invaluable is salicyclic
acid peels for acne. They are lipid soluble; the crystals will penetrate
into the comedones and break up the blockage, and this can really be
a nice adjunct to help make the retinoid work much better, and more
quickly.
In contrast, when
we treat rosacea, I really do not use a lot of inflammatory peels, or
even microdermabrasion, because of the flushing response these patients
get. Metronidazole and sulfacetamide are important for basic maintenance
therapy. In addition, I use IPL and pulsed dye lasers. I tend to use
IPL more for the flushing and the telangeictases. I tell my patients
that we need to control the acne component of the rosacea first, and
once we see that this has resolved with either antibiotics or topicals,
I’ll then put them on an IPL program to deal with the flushing
and the telangiectases.
Dr. Lask: Two different
lasers have been used a lot more recently for acne, the Smooth Beam
and the Cool Touch, both of which have FDA clearance for acne treatments.
As mentioned earlier, a lot of these devices are used for three to six
treatments. I don’t think there’s any set numbers of how
many times you treat these patients, but I do see quite a variety of
responses. Some do very well, and some don’t respond at all, but
there are nice new innovations for acne besides the topical medications.
For the rosacea,
besides the effect on the erythema, flushing, and heat response that
the B Beam and the intense pulsed light can give, I think there’s
some correlation diminishing the breakouts in these patients as well,
so these make very nice adjunctive therapies.
[FACULTY—PLEASE
PROVIDE before & after pictures of patient(s) treated for photodamage
and acne and/or rosacea See figures 8 and 9]
Case Study #4: Treatment
of darker-skinned patients.
Dr. Alster: In general, do you modify your treatments for different
ethnicities? I know in my practice I will tend to use less aggressive
forms of treatment in my patients with darker skin types, and incorporate
more of the topical and lighter peels, compared to somebody with lighter
skin tones.
Dr. Lask: People
with darker skin types tend to come to me because of dyschromias, not
generally the classic photoaging problems, and in this population I
use primarily the bleaching agents, and the retinoids. I do sometimes
use less aggressive treatments, i.e. lower concentration of hydroquinone
or fewer applications, or how often they apply it, because if they irritate,
as we all know, they will discolor more than a fair-skinned patient,
so I have to be more careful.
Dr. Alster: Dr.
Nestor, how do you treat these individuals, especially in terms of the
intense pulsed light and PDT combination? Do you scale back what you
use, in terms of energies, or do you tend to use other forms of treatment?
Dr. Nestor: I think
these patients of different Fitzpatrick skin types come in with different
aspects of photoaging. I think that the classical triad of hyperpigmentation,
redness, and actinic-type changes, with actinic keratoses, are much
more geared toward type I, II, and maybe some type III. We see more
rhytides, though certainly not to the same extent as in types I, II,
or III, and dyschromia with types IV or V, and the type VI patients
tend to have more acneform eruption, much less rosacea, and certainly
much less of the other classical signs of sun damage, though there could
be some dyschromia.
I tend to individualize
my treatment plan based on the presentations of the patients. In darker-skinned
individuals, we tend to use more nonablative procedures if we’re
targeting rhytides and those types of changes, as we’ll certainly
use botulinum toxin and fillers, because those are not necessarily sensitive
to Fitzpatrick skin types. In this population there is much less of
a need for the more aggressive, more ablative, procedures.
I find that the
other nonablative procedures that we’ve talked about (Cool Touch,
Smooth Beam, and others), are equally tolerated by darker-skinned and
lighter-skinned individuals, although with the pulsed dye laser and
IPL, you have to be much more careful with the darker skin types—using
less energy, and possibly using different filters for the IPL. With
regard to topicals, the only thing I would stress is that with the darker
skin types, when there is a lot of irritation associated with topical
treatments, you may see some hyperpigmentation, so you have to be a
lot more careful with a postinflammatory change. This is just something
to keep in the back of the mind. [DR. NESTOR—CAN YOU PROVIDE AN
GENERAL TREATMENT PROTOCOL?]
[FACULTY—PLEASE
PROVIDE before & after pictures demonstrating treatments for darker-skinned
patients]
Conclusion
Chronic sun exposure results in deleterious effects on the skin, a process
known as photoaging. Characteristics of photoaged skin include fine
and coarse wrinkles, roughness, laxity, mottled pigmentation, actinic
lentigines and keratoses, coarseness, sallowness, and telangiectasia.
Depending on the extent of photodamage and the desires of the individual
patient, there are many available options for treatment, including both
topical agents and office procedures such as lasers, dermabrasion, peels,
and fillers. The use of multiple treatment modalities as part of a combination
therapy plan may provide the most benefit to patients, as this approach
allows for concurrent treatment of multiple symptoms. Topical retinoids
are recommended for priming the skin prior to office procedures, and
as maintenance therapy to maintain treatment results and to prevent
further sun damage. Photoprotection should be an essential part of any
photoaging treatment regimen.