Cosmetic Fillers:
Restylane, Perlane, Radiesse, Sculptra, and Artefill
While bovine Collagen (Zyderm
® and Zyplast ®) has been the
main product used for correction of facial wrinkles and folds since the
late 1970's the field of facial fillers has mushroomed over the last
several years to an amazing array of exciting new products. In Dr. Zemplenyi's practice Collagen and Cosmoderm have been
replaced with new fillers including Restylane, Perlane, Juvederm, Radiesse, Sculptra and Artefill.
Each of these substances has its own
advantages for wrinkle treatment discussed below. Injection of any of these fillers may be
combined with an addition rejuvenation of forehead and crows feet with Botox.
All of the available fillers are very useful for treatment of
wrinkles, folds
and depressed scars (acne and traumatic) as well as sagging of tissues
due to age-related volume loss. For reduction of bruising and swelling
Dr. Zemplenyi suggests use of Arnica Montana and
avoidance of aspirin and ANSAIDs such as Motrin and Alleve for
about one week prior to the
wrinkle treatment injection. Cooling with ice or a special cooling machine is sometimes
used for increased comfort. Dr. Zemplenyi also sometimes
prescribes oral Prednisone on the day of the wrinkle treatment for further
decrease of swelling especially with injection of the lips. Following resolution of mild redness, swelling and bruising (if any), all
fillers look about the same a few days following their injection if used
in equivalent volumes.
However, persistence of the fillers
depends on many variables such as the site of injection, the natural rate
of degradation and absorption and patient's metabolism and
the injection technique utilized. All of these substances with
the exception of Artefill are fully absorbable by the body, and
thus they require periodic re-injections.
Restylane
® (hyalorunic acid) became available in the United
States in
2004 while it has been used extensively and very successfully in Canada and Europe since
late 1990's. Restylane™ is available as a clear, smoothly-injecting gel packaged in 1cc syringes. Hyalorunic acid, a large sugar molecule (polysaccharide),
occurs naturally in
the base membrane of the human skin. Commercially it is manufactured using bacterial
amplification technology. Hyalorunic acid molecules do not produce allergic
reactions, and thus skin testing for allergies is not necessary prior to the treatment.
Correction of folds and lines may be achieved during the first
consultation with Dr. Zemplenyi. Mild burning, redness, tenderness,
swelling and bruising may sometimes be seen at the site of the injected
folds and may last for a few days. The procedure is tolerated very well,
cover-up make-up may be applied immediately following the injections and
downtime is eliminated or minimized. The vast majority of patients do
not experience any need for interruption of work or social
obligations. Correction of the lines and folds lasts about six months
but some additional filling of lines may be needed sooner and is
recommended on a follow-up visit within two weeks of the original
injection. Upper and lower lips may be enhanced with Restylane or
Perlane, and Dr.
Zemplenyi often performs this wrinkle treatment procedure using a topical and a local
anesthetic block for maximum patient comfort.
Juvederm
® is another hyalorunic acid
released in the United States in 2007 by Allergan (the manufacturer of
Botox A) designed to compete with the very successful Restylane. While each syringe contains
more cross-linked material in a higher concentration than Restylane
uniformly dispersed in a gel, Dr. Zemplenyi finds Juvederm Ultra
™ to be
very comparable but not superior to Restylane with respect to duration,
filling or ease of use.
Perlane ® is a sister substance of Restylane
containing larger particles of hyalorunic acid in a higher
concentration. It stays longer than Restylane in the augmented, treated folds, wrinkles, lips and
scars. It was released by the FDA in the United States in
2007, and is quickly becoming a very popular hyalorunic acid product. Perlane may be used in the same sites as Restylane and Juvederm
but it is injected into a deeper plane under the skin surface. Because of its longer duration Perlane
may also be used for volumetric augmentation (correction) of cheeks,
orbital rim hollowing, wasting of the temples, etc. Patient's own
(native) collagen synthesis may be induced by the longer presence of Perlane in the
tissues.
Radiesse
® (synthetic hydroxyl apatite), formerly called Radience, is a naturally occurring component of the matrix found in
bones. While large experience exists with this product in an "off-label
" application since about 2002 the FDA approved Radiesse for cosmetic
application in 2006. For increased comfort Radiesse is injected
along with small amounts of a local anesthetic at the injection sites,
and the treatments are very well tolerated. Application
of ice diminishes the discomfort. In some patients persistence of
augmentation exceeding one to two years, especially if a touch-up
correction is performed in two to four weeks following the initial treament. Radiesse is somewhat more expensive than
the hyalorunic acids but each 1.3 cc syringe contains more of the filler
substance material making the higher charge a cost-effective choice.
Radiesse is now FDA-approved for cosmetic improvement of facial folds
and wrinkles as well as for augmentation treatment of volumetric loss
and lipo-atrophy such as seen with aging or in patients with HIV.
Sculptra
®, known in Europe as Nufill, that has been available outside of the United States for about
ten
years for treatment of volumetric defects of cheeks related to loss of
fat and muscle. In 2004 it was officially
approved by the FDA for treatment of lipo-atrophy such as seen in men
infected with HIV. It is now used very successfully for volumetric
augmentation and reversal of soft tissue atrophy as seen with the aging
process of the face.
Sculptra (L-polylactic acid) has been demonstrated to induce synthesis
of patient's own (native) collagen at the injection site, and this effect may persist
for more than two years. While it is clear that new collagen
formation occurs, there exists individual variation in the actual amount
of collagen produced by each treatment. In general three
or more serial treatment sessions spaced about four weeks apart are needed to
promote enough collagen synthesis. Due to the actual particulate size,
Sculptra is injected through a larger gauge needle than Restylane and
Collagen, and some bruising is possible. Sculptra plays an important
role not only for patients needing augmentation of larger volumes of
soft tissue, but it may be used as the main cosmetic filler for
three-dimensional improvement of all facial regions. While Sculptra is
injected into the deeper tissues and takes several weeks for a maximal
effect to appear, it may be combined with Restylane injected into the
superficial layers of skin for an immediate improvement.
Artefill
® has stirred much excitement over its
approval - after much investigation by the FDA in 2007 for
augmentation of naso-labial (melolabial) folds. Artefill is an
improved reformulation of Artecoll that has been used since mid 1990's
in Europe and Canada. It consists of a permanent, non-absorbable
substance (polymethyl methacrylate microspheres) that has been used for
hard contact lenses for many years. The non-absorbable microspheres are
suspended in a bovine, absorbable collagen gel. As the bovine
collagen is broken down by the body, new native collagen is synthesized
as a reaction to the non-absorbable polymethyl methacrylate microspheres.
This native collagen has been shown to persist for at least five years.
Thus, patients may achieve very longstanding or permanent
correction of folds. However, a patient being treated with
Artefill must accept a very small risk of a significant, local foreign
body reaction that may rarely occur as the skin over-reacts to the
injected, permanent foreign substance. While such a rare foreign
body granuloma is treatable a permanent scarring at the site of the
reaction could result. A collagen skin test is required
prior to treatment with Artefill. While Dr. Zemplenyi has been
selective and cautious with the use of Artefill, the treated
patients have been so far extremely pleased with the achieved results.
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