Laser, non
laser methods compared in treatment of red nose syndrome.
Telangiectasia:
Plastic surgeon investigates different modalities - finds speed,
low cost, convenience beneficial nonlaser technique.
Reprinted from
Cosmetic Surgery Times June 2001, Vol. 5, No. 5 By Lisette Hilton
(Contributing Editor)
New York -- Board-certified
plastic surgeon Gregory E. Rauscher, M.D., wanted to know how
current laser treatments compared with the nonlaser modality Telangitron
(Clareblend, Reno, Nev.) for the treatment of red nose.
Dr. Rauscher,
professor of plastic surgery, New Jersey Medical School and director
of cosmetic surgery, Hackensack University Medical Center, presented
the results of his study recently at the Rhinoplasty Society meeting
in New York City.
Where does
it originate?
Red nose syndrome, a term used to describe patients who complain
of objectionable redness of their nose, is commonly associated
with chronic UV exposure, rosacea, chronic use of topical corticosteroids,
and rhinoplasty.
There was no
successful treatment for red nose until 1981 when Joel Noe. M.D.,
described the use of an Argon laser. The argon laser was a non-pulsed
continuous light with a wavelength of 433 nm and 514 nm. Charles
Dicken, M.D., of the Mayo Clinic, concurred that the argon worked
to diminish red nose in studies he reported in 1986.
The theory of
Selective Photothermolysis was described in 1983, hypothesizing
that choosing the appropriate wavelength, pulse duration, and
pulse energy could achieve thermal destruction of a target. Wavelengths
of 418 nm, 524 nm, and 577 nm destroyed vascular structures.
Dr. Rauscher
said the argon laser never caught on as the treatment of choice
for red nose due to the time for treatment and the cost. It posed
a high risk for scarring.
The next modality
that came along was the pulsed dye laser, from 577 nm to 600 nm
wavelength. The wavelengths were only partially effective, required
multiple treatments, and caused significant purpura, Dr. Rauscher
said.
Other treatments
used throughout the years to treat red nose syndrome include:
- The Hyfrecator,
a high-frequency generator that's connected to high voltage. Unfortunately,
the needle would adhere to the skin and burn the skin, often leaving
pitted scars.
- The Ellman Unit, a radiofrequency generator, another form of
treatment. The partially
rectified current in the unit was capable of sealing telangiectasias,
but the operation was
imprecise.
According to
Dr. Rauscher, comparative therapies with more current lasers include
the 532 nm laser and the Coherent (now Lumenis) VersaPulse V with
HELP-G. "The problem with laser treatment is when the vessel
is destroyed the patient can develop telangiectatic matting, which
are multiple small blood vessels," Dr. Rauscher said.
Another treatment
option for red nose syndrome is the Telangitron. Telangitron works
by a direct current, coagulating unwanted blood vessels with a
32-guage needle-a small acupuncture needle, according to Dr. Rauscher.
The needle diameter is 0.003inch and the length is 6 nm.
Lasers have a
fluence as a measure of energy, which is J/cm2, that measures
the energy through a surface area. For lasers, Dr. Rauscher advised
using topical anesthetic - either ELA-Max, a topical (analgesic)
that will numb the skin if it is covered with an occlusive plastic
dressing; or Beta cain that does not require an occlusive dressing.
Treatment begins
after application of an anesthetic. The settings for each modality
are:
532 nm Diode
¨ Spot size: 400 mmn
¨ Pulse duration: 40 msec
¨ Repetition rate: 5 Hz
¨ Fluence: 140 J/cm2
¨ Chill tip: 5 degrees C
Coherent (now Lumenis) VersaPulse VPW
¨ Fluence: 9.5 to 10 J/cm2
¨ Chill tip: 4.0 degrees C
¨ Spot size: 4.0 mm
¨ Pulse width: 10 msec
VersaPulse V with HELP-G
¨ Fluence: 10 J/cm2
¨ Wavelength: 532 nm
¨ Spot size: 5 mm
¨ Pulse width: 50 msec
"If you
are using an updated VersaPulse V with HELP-G, you can extend
the pulse so you're probably going to be able to treat the telangiectasia
in one treatment," Dr. Rauscher said.
Laser versus
nonlaser treatment
The patients in Dr. Rauscher's study were caucasian, and all except
one were Fitzgerald class I or II skin type. Dr. Rauscher treated
23 patients with the 532 nm diode Laser and 18 with Telangitron.
These patients have had about a two-and-a-half year follow up.
According to Dr. Rauscher, treatment with the Telangitron is fast
and there is a low cost to purchase and maintain.
The Telangitron
generator uses 55 V per pulse of energy.
The direct current
permits entrance and exit of blood vessels without sticking, so
Dr. Rauscher noted minimal collateral damage or pitting.
"If you
use the Ellman or old Hyfrecator, you don't have a direct current
upon entering the vessel so when you cauterize the vessel and
pull the needle out of the skin, the needle pulls out the clot
and bleeding starts," he said.
During the Telangitron
procedure, the operator inserts a needle with DC current and initiates
radio frequency current for up to two seconds. The operator then
removes the needle.
"If you're
using 40 V with Telangitron, you're delivering 2.8 W. If you're
using 60 watts, you're delivering 4.2 W," Dr. Rauscher said.
Dr. Rauscher
noted the convenience of Telangitron. "If you have the laser--you'll
use it. At the same time, if you have more than one office you
can easily bring the Telangitron unit with you," he said.
The cost differences
between the lasers versus nonlaser treatment was considerable.
"The laser treatment and physician time are considerable,"
he said.
Dr. Rauscher
reported that the efficiency of the treatment of Telangitron and
532-nm pulse diode and VersaPulse VPW are about the same, "except
for the telangiectatic matting with the lasers. The patient downtime
is almost zero with the laser or Telangitron," he said.
He noted that
patients presenting vessels around the nose and face objected
to the swelling after laser treatment.
"Everyone's
skin improved with the new lasers and with Telangitron,"
he said. "At this point, I always use Telangitron. As I can
have my nurse or aesthetician perform the treatment."
(Dr. Rauscher
has no financial interest in the Telangitron unit nor its manufacture.)