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At Agewell we customize each
prescription formulation
specifically to each
patients' individual
requirements. We
strive to provide the utmost
in customer care on every
order. Please call us
with any questions
pertaining to your
compounding request, we are
here to discuss any
questions or concerns you
may have pertaining to your
prescription.
Compounding medications for dermatological diseases allows for:
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Unique delivery
vehicles to be
utilized (i.e.
topical cream, scalp
lotion, nail
lacquer); which
makes administering
the medication
easier, more
pleasant, and
potentially more
effective
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Multiple
medications, that
have been shown to
have modest effects
individually, to be
combined to form a
more potent
customized
medication. This may
speed the healing
process and save
patients valuable
time and money,
eliminating needlessly
switching from one
therapy to the next
ACNE:
We can compound customized
formulations which contain
numerous medications to
provide a synergistic effect
for treatment of resistant
acne.
Int J Dermatol
1995
Jun;34(6):434-7
Topical nicotinamide
compared with clindamycin
gel in the treatment of
inflammatory acne vulgaris.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Dermatol
1996
Apr;23(4):243-6
Topical spironolactone
reduces sebum secretion
rates in young adults.
In order to access the
PubMed abstract of this
article, visit this
website link.
ATHLETES FOOT:
There are various
synergistic combinations
which are used for
antifungal therapy. Research
points to the practicality
"of using ibuprofen, alone
or in combination with
azoles, in the treatment of
candidosis, particularly
when applied topically,
taking advantage of the
drug's antifungal and
anti-inflammatory
properties."
J Med Microbiol 2000
Sep;49(9):831-40
Antifungal activity
of ibuprofen alone and in
combination with fluconazole
against Candida species.
In order to access the
PubMed abstract of this
article, visit this
website link.
CHEMICAL
PEELS:
Chemical peelings with
kojic acid, glycolic acid,
and trichloroacetic acid,
either alone or in
combination, are effective
therapy for diffuse melasma
and localized
hyperpigmentations (lentigo).
Dermatol Surg 1999
Jun;25(6):450-4
The use of chemical
peelings in the treatment of
different cutaneous
hyperpigmentations.
In order to access the
PubMed abstract of this
article, visit this
website link.
DIAPER RASH / INCONTINENCE:
Ann Pharmacother
1996 Sep;30(9):954-6
Cholestyramine
ointment to treat buttocks
rash and anal excoriation in
an infant.
In order to access the
PubMed abstract of this
article, visit this
website link.
Dis Colon Rectum 1987
Feb;30(2):106-7
Cholestyramine
ointment in the treatment of
perianal skin irritation
following ileoanal
anastomosis.
In order to access the
PubMed abstract of this
article, visit this
website link.
HEAD LICE AND SCABIES:
There are concerns about
emerging resistance and the
potential harm of using
permethrins have prompted a
search for effective
pediculicidal therapies that
are not harmful to children
with repeated use. An herbal
formulation has been shown
to be effective for head
lice. Ivermectin can also be
compounded for topical
application or as an oral
dose titrated for each
patient for the treatment of
head lice and scabies.
Clin Exp Dermatol 2002
Jun;27(4):264-7
The below mentioned
article describes the
treatment of 18 children
with scabies or cutaneous
larva migrans using
ivermectin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Twenty six male and female
patients aged 5 to 17 years
had head lice infestation
confirmed by eggs presence
and received treatments with
a single 200 microgram/kg
oral dose of. At day 14
after treatment, 20 had
responded to the treatment
(77%), and 6 patients (23%)
presented with a complete
disappearance of eggs and
all clinical symptoms. At
day 28, 7 patients appeared
clear of infestation (27%),
but 4 of the 6 patients with
no eggs at day 14 presented
with signs of reinfestation.
This study suggests that
ivermectin is a promising
treatment of head lice, and
a second dose at day 10 may
be appropriate.
Trop Med Parasitol
1994 Sep;45(3):253-4
The below mentioned
article depicts the efficacy
of ivermectin for the
treatment of head lice (Pediculosis
capitis).
In order to access the
PubMed abstract of this
article, visit this
website link.
Two hundred scabies
patients were randomly
allocated to receive either
oral ivermectin in a single
dose of 200 micrograms/kg
body weight, or 1% lindane
lotion for topical
application overnight.
Patients were assessed after
48 hours, two weeks and four
weeks. After a period of
four weeks, 82.6% of the
patients in the ivermectin
group showed marked
improvement; only 44.44% of
the patients in the lindane
group showed a similar
response. Oral ivermectin is
easy to administer as a
single oral dose, induces an
early and effective
improvement in signs and
symptoms, and compliance is
accordingly increased.
J Dermatol 2001
Sep;28(9):481-4
Oral ivermectin in
scabies patients: a
comparison with 1% topical
lindane lotion.
In order to access the
PubMed abstract of this
article, visit this
website link.
Isr Med Assoc J. 2002
Oct;4(10):790-3
The in vivo
pediculicidal efficacy of a
natural remedy.
In order to access the
PubMed abstract of this
article, visit this
website link.
MOLLUSCUM CONTAGIOSUM:
The following study found
that 5% KOH aqueous solution
proved to be as effective
and less irritating when
compared to the 10% KOH
solution. This trial also
emphasizes the effectiveness
of topical KOH in the
treatment of molluscum
contagiosum, sparing
affected children from more
aggressive physical
modalities of treatment.
Pediatr Dermatol 2000
Nov-Dec;17(6):495
Evaluation of the
effectiveness of 5%
potassium hydroxide for the
treatment of molluscum
contagiosum.
In order to access the
PubMed abstract of this
article, visit this
website link.
NAIL INFECTION / REMOVAL:
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Treatment of Fingernail Lichen Planus
Nail lichen planus most commonly occurs during the fifth and sixth decade of life and can be notoriously recalcitrant to many forms of treatment. Prevost and English of the University of Pittsburgh Department of Dermatology reported a case of successful treatment of destructive inflammatory lichen planus of the nails with combined topical therapy of tazarotene gel and clobetasol gel, without the occurrence of potential adverse affects of systemic treatments.
J Drugs Dermatol. 2007 Feb;6(2):202-4.
Palliative treatment of fingernail lichen planus.
In order to access the
PubMed abstract of this
article, visit this
website link.
Although surgical excision
is the most popular method
for removing nails, the use
of concentrated urea
plasters applied under
occlusion may be superior.
The use of urea plasters has
inherent advantages - they
are inexpensive, several
nails can be treated in one
session, and the procedure
is essentially painless.
Various synergistic
combinations and topical
medications with penetrant
enhancers can be compounded
for antifungal therapy.
Topical medications usually
have a lower adverse
drug-reaction profile than
systemic medications.
Cutis. 1980 Jun;25(6):609-12
Urea ointment in the nonsurgical avulsion of nail dystrophies--a reappraisal.
In order to access the
PubMed abstract of this
article, visit this
website link.
Cutis. 1980 Apr;25(4):397, 405
Combination urea and salicyclic acid ointment nail avulsion in nondystrophic nails: a follow-up observation.
In order to access the
PubMed abstract of this
article, visit this
website link.
JAMA 1979 Apr
13;241(15):1559, 1563
Urea plasters alternative to
surgery for nail removal.
PMID:
430701 (No abstract
available)
Clin Exp Dermatol 1982 May;7(3):273-6
The treatment of fungus and yeast infections of nails by the method of "chemical removal".
PMID: 7105479 (No abstract available)
Management of onychomycosis, a fungal infection of the fingernails and toenails, usually consists of systemic antifungal medications, topical therapy (e.g., urea ointment, desiccating solutions, keratolytics, vital dyes), or surgical intervention (e.g., nail plate avulsion, laser therapy). Topical prescription antifungal preparations, containing the active ingredient of your choice, may be less likely to cause the serious systemic side effects that can occur with oral antifungal therapy and can provide a more economical alternative, as lower doses are needed when the medication is applied topically at the site. Penetrant enhancers can be included in the preparation to improve the effectiveness of topical antifungals.
Trop Med Int Health 1999 Apr;4(4):284-7
Treatment of toenail onychomycosis with 2% butenafine and 5% Melaleuca alternifolia (tea tree) oil in cream.
In order to access the
PubMed abstract of this
article, visit this
website link.
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PIGMENTATION ABNORMALITIES:
Patients with vitiligo
have low catalase levels in
their epidermis in
association with high levels
of hydrogen peroxide.
Topical application of a UVB-activated
pseudocatalase cream can
successfully remove
epidermal H2O2
resulting in a remarkable
repigmentation.
J Investig Dermatol Symp
Proc 1999 Sep;4(1):91-6
In vivo and in vitro
evidence for hydrogen
peroxide (H2O2)
accumulation in the
epidermis of patients with
vitiligo and its successful
removal by a UVB-activated
pseudocatalase.
In order to access the
PubMed abstract of this
article, visit this
website link.
PLANTAR WARTS / WARTS:
Topical 5-fluorouracil
(5-FU) 5% with tape
occlusion produced complete
eradication of all plantar
warts within 12 weeks of
treatment in 19 of 20
patients. It was concluded
that use of topical 5%
5-fluorouracil cream for
plantar warts is safe,
efficacious, and accepted by
the patient.
J Drugs Dermatol. 2006
May;5(5):418-24.
Topical 5%
5-fluorouracil cream in the
treatment of plantar warts:
a prospective, randomized,
and controlled clinical
study.
In order to access the
PubMed abstract of this
article, visit this
website link.
A medical record review was
conducted by the Podiatry
Division, Department of
Orthopedics, Cabrini Medical
Center, New York, NY to
determine the clinical
outcome and average time to
resolution of verruca
plantaris (plantar warts) in
20 patients treated with
twice-daily applications of
topical fluorouracil (5-FU)
combined with topical 17%
and 40% salicylic acid.
Twice-daily application of
topical fluorouracil and
salicylic acid is a safe and
effective treatment for
verruca plantaris.
J Am Podiatr Med Assoc. 2005
Jul-Aug;95(4):366-9.
Treatment of verruca
plantaris with a combination
of topical fluorouracil and
salicylic acid.
In order to access the
PubMed abstract of this
article, visit this
website link.
Phys Ther. 2002
Dec;82(12):1184-91
Treatment of plantar
verrucae using 2% sodium
salicylate iontophoresis.
In order to access the
PubMed abstract of this
article, visit this
website link.
Cantharidin
in a collodion vehicle has
been used by dermatologists
as a treatment for molluscum
contagiosum and warts since
the 1950s. Cantharidin lost
FDA approval in 1962 because
its manufacturers failed to
submit data attesting to
cantharidin's efficacy.
However, in 1999, the FDA
included cantharidin on its
"Bulk Substances List" of
drugs which although not
available as commercial
products, were approved for
compounding on a customized
basis for individual
patients.
Because of cantharidin's
potential for toxicity, the
FDA has proposed that
cantharidin should be
limited to "topical use in
the professional office
setting only." Severe
blistering can result from
improper use, and ingestion,
especially by children, can
be fatal. Treatment of
mucous membranes is
contraindicated and
placement of cantharidin
near the eyes and eyelids
should be avoided to prevent
scleral erosion.
Caution:
The treatment of
plantar warts with
cantharidin is NOT
recommended and may
have a higher rate of
significant complications
including lymphangitis and
refractory lymphedema.
Arch Dermatol. 2001;137:1357-1360
Cantharidin
revisited: a blistering
defense of an ancient
medicine.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Am Acad Dermatol.
2000;43:503-507
Childhood molluscum
contagiosum: experience with
cantharidin therapy in 300
patients.
In order to access the
PubMed abstract of this
article, visit this
website link.
Squaric Acid
Dibutylester (SADBE) for
Cutaneous Warts in Children
Warts are a common
pediatric skin infection and
clearance may be enhanced by
contact sensitizers, such as
squaric acid dibutylester (SADBE).
Contact immunotherapy with
SADBE is relatively safe and
an effective alternative in
the management of multiple
and resistant cutaneous
warts in children.
J Am Acad Dermatol. 2000
May;42(5 Pt 1):803-8
Squaric acid
immunotherapy for warts in
children.
In order to access the
PubMed abstract of this
article, visit this
website link.
Pediatr Dermatol. 2000
Jul-Aug;17(4):315-8
Use of squaric acid
dibutylester (SADBE) for
cutaneous warts in children.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Am Acad Dermatol. 1999
Oct;41(4):595-9
Contact
immunotherapy with squaric
acid dibutylester for the
treatment of recalcitrant
warts.
In order to access the
PubMed abstract of this
article, visit this
website link.
ROSACEA:
Clin Exp Dermatol 2003
Jan;28(1):61-3
Topical application
of NADH for the treatment of
rosacea and contact
dermatitis.
In order to access the
PubMed abstract of this
article, visit this
website link.
SCARRING AND KELOIDS:
Br J Plast Surg
1998 Sep;51(6):462-9
Topical tamoxifen--a
potential therapeutic regime
in treating excessive dermal
scarring?
In order to access the
PubMed abstract of this
article, visit this
website link.
TOPICAL ANESTHETICS:
Topical anesthesia is needed
for common procedures such
as suturing, wound cleaning,
and injection
administration. The ideal
topical anesthetic would
provide complete anesthesia
following a simple pain-free
application, not contain
narcotics or controlled
substances, and have an
excellent safety profile.
The combination of topical
anesthetics lidocaine and
tetracaine and the
vasoconstrictor epinephrine
has been used successfully
for anesthesia prior to
suturing linear scalp and
facial lacerations in
children. A
triple-anesthetic gel
containing benzocaine,
lidocaine, and tetracaine
("BLT") has also been
reported to be effective
when applied prior to laser
and cosmetic procedures.
Convenience of application
without need for occlusion
is an advantage of these
topical anesthetics.
The following article
concludes: "LAT gel (4%
lidocaine, 1:2000
adrenaline, 0.5% tetracaine)
worked as well as TAC gel
(0.5% tetracaine, 1:2000
adrenaline, 11.8% cocaine)
for topical anesthesia in
facial and scalp
lacerations. Considering the
advantages of a
noncontrolled substance and
less expense, LAT gel
appears to be better suited
than TAC gel for topical
anesthesia in laceration
repair in children."
Pediatrics 1995
Feb;95(2):255-8
Lidocaine adrenaline
tetracaine gel versus
tetracaine adrenaline
cocaine gel for topical
anesthesia in linear scalp
and facial lacerations in
children aged 5 to 17 years.
In order to access the
PubMed abstract of this
article, visit this
website link.
The following article
reported that a
triple-anesthetic gel
containing benzocaine,
lidocaine, and tetracaine
("BLT") applied prior to
treatment with a 532-nm KTP
laser resulted in
significantly lower pain
scores than with 3 other
topical anesthetics at 15,
30, 45, and 60 minutes after
application.
Cosmetic Dermatology
2003 Apr;16(4):35-7
Topical
Triple-Anesthetic Gel
Compared With 3 Topical
Anesthetics
TOPICAL THERAPY WITH
5-Flourourcil:
G. Thomas Jansen, M.D.
University of Arkansas
Medical Center, Little Rock
Veterans Administration
Hospital, Little Rock,
Arkansas
Actinic keratoses are
unsightly and may be
precancerous. Solitary or
localized lesions respond
adequately to many forms of
treatment. However,
widespread multiple actinic
keratoses can best be
treated with topical
5-fluorouracil. The exact
mode of action is not known,
but we can presume it is
related to the clearly
established effect of this
drug upon RNA and DNA
synthesis. This treatment is
almost ideal, since it
usually destroys the
keratoses selectively,
without significant
alteration in normal skin. A
1 or 2 percent solution is
made by diluting the 10 ml
ampule with propylene
glycol. This liquid is
applied two times daily to
the involved areas for a 2-4
week period. Lesions on the
face and neck respond more
quickly than those of the
hands and arms. A brisk,
painful, inflammatory
reaction at the site of the
keratoses is anticipated and
used as an indicator of the
end point of treatment. Once
treatment is discontinued,
the erythema usually
subsides in 2 weeks and the
skin becomes smooth and free
of keratoses. Not all
keratoses respond, and
untoward reactions such as
phototoxicity, irritation of
the mucous membranes,
contact sensitivity, and
alteration of pigmentation
can occur. Although
resolution of the keratoses
persists for years, should
they return reapplication is
usually effective again.
At
agewell, we can compound the
following 5fu combination:
Fluorouracil 5% / Salicylic
Acid 30% / Retinoic Acid
0.1% Gel
SUN PROTECTION / PHOTOAGED
SKIN / WRINKLES:
Topically applied
antioxidants
exert their benefits by
offering protection from
damaging free radicals
produced when skin is
exposed to ultraviolet light
or allowed to age naturally.
Appropriate formulation and
use which is supervised by a
knowledgeable healthcare
professional will maximize
the benefits while
minimizing any potential
side effects of these
therapies.
Biofactors
1999;9(2-4):371-8
Coenzyme Q10, a cutaneous
antioxidant and energizer.
In order to access the
PubMed abstract of this
article, visit this
website link.
Coenzyme Q10
(ubiquinone, CoQ10) is an
important antioxidant that
is taken to strengthen
immune and cardiac function.
The processes of aging and
photoaging of the skin (due
to sunlight) are associated
with an increase in cellular
oxidation, which may occur
as the body’s own levels of
CoQ10 decline. A reduction
in wrinkle depth was shown
following topical
application of CoQ10 0.3%,
and results indicated that
CoQ10 has the efficacy to
prevent many of the
detrimental effects of
photoaging. Wrinkles around
the region of the eyes
(“crow’s feet”) may be
reduced by long-term
application of CoQ10.
Z Gerontol Geriatr 1999
Apr;32(2):83-8
Modulation of oxidative
stresses in human aging skin
In order to access the
PubMed abstract of this
article, visit this
website link.
Vitamin C
has been incorporated into a
variety of cosmeceuticals
designed to protect and
rejuvenate photoaged skin.
Ascorbyl Palmitate (Vitamin
C Ester) is
a lipid soluble, neutral pH,
non-acidic (thus,
non-irritating and
non-stinging) form of
Vitamin C which can reach
cells within the skin
rapidly in amounts greater
than can be achieved by
water soluble Vitamin C
(L-Ascorbic Acid).
Dermatol Surg. 2005 Jul;31(7
Pt 2):814-7
Topical vitamin C: a useful
agent for treating
photoaging and other
dermatologic conditions.
In order to access the
PubMed abstract of this
article, visit this
website link.
Alpha Lipoic Acid
(ALA) is a powerful
antioxidant and scavenger
with anti-inflammatory
properties that promotes
optimum efficiency for
production of energy and
removal of intracellular
waste products, essential
for cellular healing and
elimination of wrinkles and
facial scars. Twelve weeks
of treatment with a cream
containing 5% ALA improves
clinical characteristics
related to photoaging of
facial skin.
Br J Dermatol. 2003 Oct;
149(4): 841-9
Randomized,
placebo-controlled, double
blind study on the clinical
efficacy of a cream
containing 5% alpha-lipoic
acid related to photoageing
of facial skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical niacinamide 5%
(vitamin B3) reduces
yellowing, wrinkling, red
blotchiness, and
hyperpigmented spots in
aging facial skin.
Int J Cosmet Sci. 2004
Oct;26(5):231-8.
Topical niacinamide reduces
yellowing, wrinkling, red
blotchiness, and
hyperpigmented spots in
aging facial skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical
application of 0.01%
estradiol and 0.3% estriol
markedly improved elasticity
and firmness of the skin,
substantially decreased
pore sizes, increased skin
moisture, and decreased
wrinkle depth.
Eur J Obstet Gynecol
Reprod Biol. 2007
Feb;130(2):202-5.
Effects of topical estradiol
on the facial skin collagen
of postmenopausal women
under oral hormone therapy:
a pilot study.
In order to access the
PubMed abstract of this
article, visit this
website link.
Int J Dermatol. 1996
Sep;35(9):669-74.
Treatment of skin aging with
topical estrogens.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical 2% progesterone
increases elasticity and
firmness in the skin of peri-
and postmenopausal women.
Br J Dermatol. 2005
Sep;153(3):626-34.
Effects and side-effects of
2% progesterone cream on the
skin of peri- and
postmenopausal women:
results from a double-blind,
vehicle-controlled,
randomized study.
In order to access the
PubMed abstract of this
article, visit this
website link.
DMAE
(2-dimethylaminoethanol,
deanol), when applied
topically to the skin, may
improve the appearance of
sagging skin, boost the
effects of other
antioxidants, increase
smoothness, reduce fine
lines and give facial
muscles a leaner look. In a
randomized clinical study,
3% DMAE facial gel applied
daily for 16 weeks has been
shown to be safe and
efficacious in the
mitigation of forehead lines
and periorbital fine
wrinkles, and in improving
lip shape and fullness and
the overall appearance of
aging skin.
Br J Dermatol. 2007
Mar;156(3):433-9.
The antiwrinkle effect of
topical concentrated
2-dimethylaminoethanol
involves a vacuolar
cytopathology.
In order to access the
PubMed abstract of this
article, visit this
website link.
Am J Clin Dermatol.
2005;6(1):39-47.
The role of
dimethylaminoethanol in
cosmetic dermatology.
In order to access the
PubMed abstract of this
article, visit this
website link.
Antioxidants
such as vitamins E and C,
coenzyme Q10, alpha-lipoic
acid, glutathione, and
others can reduce signs of
aging.
Acta Dermatovenerol Alp
Panonica Adriat. 2008
Jun;17(2):47-54.
Skin aging.
In order to access the
PubMed abstract of this
article, visit this
website link.
Alpha-lipoic
acid
(ALA) 0.5% and
proanthocyanidin (PA) 0.3%
administered transdermally
in a cosmetic formulation
supplemented with 2% benzyl
alcohol as a penetration
enhancer,
significantly enhanced
collagen synthesis and
deposition.
Connect Tissue Res.
2005;46(4-5):251-7.
Transdermal delivery of
amino acids and antioxidants
enhance collagen synthesis:
in vivo and in vitro
studies.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical Application of
Phytonadione, Retinol and
Vitamins C and E to Reduce
Infraorbital Dark Circles
and Wrinkles of the Lower
Eyelids
Infraorbital dark circles
and wrinkles of the lower
eyelids are cosmetic
problems that worsen with
age. Fifty-seven healthy
adult volunteers with dark
under-eye circles and
wrinkles were enrolled in an
open label study to
determine whether a gel
containing 2% phytonadione,
0.1% retinol and 0.1%
vitamins C and E is
effective in reducing dark
under-eye circles and
wrinkles of the lower
eyelids. The gel formulation
was applied twice daily to
the lower eyelid site for 8
weeks. Hemostasis,
pigmentation and wrinkles
were evaluated by a
physician and by the
patients after 4 and 8 weeks
of treatment. Topical
application of the gel
decreased not only
hemostasis but also wrinkles
after 8 weeks of treatment.
Of 57 patients, 27 (47%) had
reductions in hemostasis.
However, pigmentation was
not clearly removed by this
gel.
J Cosmet Dermatol. 2004
Apr;3(2):73-5
The effects of topical
application of phytonadione,
retinol and vitamins C and E
on infraorbital dark circles
and wrinkles of the lower
eyelids.
In order to access the
PubMed abstract of this
article, visit this
website link.
Protection and Reversal of
Photodamage with Topical
Antioxidants
Topical vitamins C and E, as
well as topical selenium,
protect skin against
sunburn, suntan and skin
cancer and also reverse the
mottled pigmentation and
wrinkles of photoaging.
However, only certain forms
of these antioxidants are
stable and active after
percutaneous absorption.
Benefits of topical
application are that the
skin attains far higher
levels of each antioxidant
than can be achieved by
taking these vitamins orally
and topical application arms
the skin with a reservoir of
antioxidants that cannot be
washed or rubbed off,
protecting the skin for
several days after
application.
J Cosmet Dermatol. 2004
Jul;3(3):149-55
Photodamage of the skin:
protection and reversal with
topical antioxidants.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical application of
niacinamide (such as in a 2%
cream) has a stabilizing
effect on epidermal barrier
function, seen as a
reduction in transepidermal
water loss and an
improvement in the moisture
content of the horny layer,
and it may be used as a
treatment adjunct in atopic
dermatitis. In aging skin,
topical application of
niacinamide improves the
surface structure and
pigmentary disorders,
smoothes out wrinkles and
inhibits photocarcinogenesis.
Cutis 2006 Jan;77(1
Suppl):11-6.
Pharmacologic doses of
nicotinamide in the
treatment of inflammatory
skin conditions: a review.
In order to access the
PubMed abstract of this
article, visit this
website link.
Int J Dermatol 2005
Mar;44(3):197-202.
Moisturizing effects of
topical nicotinamide on
atopic dry skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Cosmet Dermatol 2004
Apr;3(2):88-93
Nicotinic acid/niacinamide
and the skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Niacinamide can be combined
with other active
ingredients such as DMAE,
sodium hyaluronate, benzoyl
peroxide, or metronidazole
in a customized medication
that can be used as
anti-wrinkle or anti-aging
therapy or to treat acne or
rosacea
Br J Dermatol. 2003 Oct;
149(4): 841-9
Randomized,
placebo-controlled, double
blind study on the clinical
efficacy of a cream
containing 5% alpha-lipoic
acid related to photoageing
of facial skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Estrogen Therapy to Prevent
or Reverse Skin Aging
Declining estrogen levels
are associated with a
variety of cutaneous
changes, many of which can
be reversed or improved by
topical or systemic estrogen
supplementation. Studies of
postmenopausal women
indicate that estrogen
deprivation is associated
with declining dermal
collagen content, diminished
elasticity and skin
strength, loss of moisture
in the skin, epidermal
thinning, atrophy, fine
wrinkling, and impaired
wound healing. Keratinocytes,
Langerhans' cells,
melanocytes, sebaceous
glands, collagen content and
the synthesis of hyaluronic
acid are under hormonal
influence. Estrogen may
attenuate inflammation in
psoriatic lesions. Alone or
together with progesterone,
estrogen prevents or
reverses skin atrophy,
dryness and wrinkles
associated with
chronological or
photo-aging. Estrogen and
progesterone stimulate
proliferation of
keratinocytes while estrogen
suppresses apoptosis and
thus prevents epidermal
atrophy. Estrogen maintains
skin moisture by increasing
acid mucopolysaccharide or
hyaluronic acid levels in
the dermis, and accelerates
cutaneous wound healing.
Low estrogen levels
that accompany menopause
exacerbate the deleterious
effects of both intrinsic
and environmental aging.
Estrogens clearly have a key
role in skin aging
homeostasis as evidenced by
the accelerated decline in
skin appearance seen in the
perimenopausal years.
At Yale University
School of Medicine, the
effects of long-term hormone
replacement therapy (HRT) on
skin rigidity and wrinkling
at 11 facial locations was
assessed using the Lemperle
scale by a plastic surgeon
who was blinded to HRT use.
Skin rigidity at the cheek
and forehead was measured
with a durometer.
Demographics including age,
race, sun exposure,
sunscreen use, tobacco use,
and skin type were similar.
Rigidity was significantly
decreased in HRT users
compared to nonusers at both
the cheek and forehead.
Average wrinkle scores were
lower in hormone users than
in nonhormone users. The
study concluded that
long-term postmenopausal HRT
users have more elastic skin
and less severe wrinkling
than women who never used
HRT, suggesting that hormone
therapy may have cosmetic
benefits.
In another study, the dermal
collagen of 15
postmenopausal women who had
received systemic estrogen
replacement was analyzed
before and after using a
topical 0.01% estrogen
treatment. Epithelial and
dermal thickness improved
after topical estrogen
therapy. Facial skin
collagen significantly
increased after 16 weeks of
treatment. Systemic estrogen
levels did not significantly
increase after topical
therapy.
Exp Dermatol. 2004;13 Suppl
4:36-40
Skin aging and sex hormones
in women -- clinical
perspectives for
intervention by hormone
replacement therapy.
In order to access the
PubMed abstract of this
article, visit this
website link.
Exp Dermatol. 2006
Feb;15(2):83-94
Biology of estrogens in
skin: implications for skin
aging.
In order to access the
PubMed abstract of this
article, visit this
website link.
Eur J Obstet Gynecol Reprod
Biol. 2006 Jun 22
J Am Acad Dermatol. 2005
Oct;53(4):555-68; quiz
569-72
Estrogen and skin: the
effects of estrogen,
menopause, and hormone
replacement therapy on the
skin.
In order to access the
PubMed abstract of this
article, visit this
website link.
Fertil Steril. 2005
Aug;84(2):285-8
Long-term effects of hormone
therapy on skin rigidity and
wrinkles.
In order to access the
PubMed abstract of this
article, visit this
website link.
Am J Clin Dermatol.
2003;4(6):371-8
Skin aging and menopause :
implications for treatment.
In order to access the
PubMed abstract of this
article, visit this
website link.
Am J Clin Dermatol.
2001;2(3):143-50
Estrogen and skin. An
overview.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Dermatol Sci. 2005
Apr;38(1):1-7
Regulatory roles of sex
hormones in cutaneous
biology and immunology.
In order to access the
PubMed abstract of this
article, visit this
website link.
In the following study, the
effects of topical 0.01%
estradiol and 0.3% estriol
compounds were measured in
preclimacteric women with
skin aging symptoms. After
treatment for 6 months,
elasticity and firmness of
the skin had markedly
improved; wrinkle depth and
pore sizes had decreased by
61 to 100%; skin moisture
had increased; and wrinkle
depth decreased
significantly.
Int J Dermatol 1996
Sep;35(9):669-74
Treatment of skin aging with
topical estrogens.
In order to access the
PubMed abstract of this
article, visit this
website link.
A low-dose, topical gel form
of diclofenac sodium has
been developed in Europe for
pain relief and reduction of
redness after sunburn.
Eur J Dermatol. 2004
Jul-Aug;14(4):238-46
The efficacy and safety of
low-dose diclofenac sodium
0.1% gel for the symptomatic
relief of pain and erythema
associated with superficial
natural sunburn.
In order to access the
PubMed abstract of this
article, visit this
website link.
PRURITUS:
Pramoxine Reduces Uremic
Pruritus
Wake Forest University
School of Medicine conducted
a randomized, double-blind,
controlled comparative trial
in a community hemodialysis
center to evaluate the
efficacy of 1% pramoxine
hydrochloride lotion versus
control lotion in the
treatment of uremic pruritus
in adult hemodialysis
patients. Pramoxine 1%
lotion was applied twice
daily to all affected areas
of pruritus for 4 weeks,
resulting in a 61% decrease
in itch intensity. “This
safe, convenient and
effective topical lotion may
potentially benefit the
large number of patients
affected by pruritus
associated with end-stage
renal disease.”
J Dermatolog Treat. 2008 Sep
24:1-5.
A pramoxine-based anti-itch
lotion is more effective
than a control lotion for
the treatment of uremic
pruritus in adult
hemodialysis patients.
In order to access the
PubMed abstract of this
article, visit this
website link.
Hydroxyethyl Starch-Induced
Pruritus Relieved by
Menthol/Camphor Lotion
Hydroxyethyl starch (HES) is
a key component of many
colloid volume expanders
used in hypovolemic shock
and otologic disease.
Pruritus is a common side
effect. Although classically
refractory to treatment with
corticosteroids and
antihistamines, some benefit
has been achieved with
topical capsaicin,
ultraviolet light therapy,
and oral naltrexone.
A man
with severe symptoms and
refractory course was
treated with a topical
lotion containing 0.5%
camphor and 0.5% menthol,
which was dramatically
successful.
A randomized,
double-blind,
placebo-controlled trial
showed a combination of
menthol and phenol to be
beneficial in mustard-gas
induced pruritis.
J Am Acad Dermatol. 2008
Jul;59(1):151-3.
Hydroxyethyl starch-induced
pruritus relieved by a
combination of menthol and
camphor.
In order to access the
PubMed abstract of this
article, visit this
website link.
Singapore
Med J 2007;48:392-5.
Phenol and menthol in the
treatment of chronic skin
lesions following mustard
gas exposure.
In order to access the
PubMed abstract of this
article, visit this
website link.
Naltrexone for Post-Burn
Pruritus and Severe
Generalized Pruritus in
Biliary Atresia
“Severe pruritus is one of
the many complications that
burn survivors endure as a
consequence of healing or
healed burn or donor site
wounds, [and] continues to
be a clinical challenge that
is inadequately addressed by
traditional therapies. The
success of naltrexone, an
opioid antagonist, in
treating pruritus in other
patient populations,
supported the concept that
it may also be effective in
burn survivors.” Opioid
antagonists have been shown
to suppress pruritus in
patients with chronic
cholestasis, uremia, atopic
dermatitis, and chloroquine-induced
itching.
“Naltrexone is a
well-tolerated medication
with little adverse effects
[and] may be an effective
adjuvant treatment in the
management of cholestatic
pruritus in the pediatric
population.”
Two studies used a topical
formulation of 1% naltrexone
(or placebo) for 2 weeks to
treat patients with
localized and generalized
atopic dermatitis with
severe itching. More than
70% of the patients using
the 1% naltrexone cream
experienced a significant
reduction of pruritus. The
cream containing naltrexone
had an overall 29.4% better
effect than placebo.
Burns. 2008
Sep;34(6):797-802.
Add article title
Click here to access the
PubMed abstract of this
article.
Pediatr Dermatol. 2008
May-Jun;25(3):403-4.
The use of naltrexone in the
management of severe
generalized pruritus in
biliary atresia: report of a
case.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Am Acad Dermatol. 2007
Jun;56(6):979-88
Treatment of pruritus with
topically applied opiate
receptor antagonist.
In order to access the
PubMed abstract of this
article, visit this
website link.
The following studies
evaluated a topical
formulation of 1% naltrexone
to treat patients with
localized and generalized
atopic dermatitis with
severe itching, and more
than 70% of patients using
the 1% naltrexone cream
experienced a significant
reduction of pruritus.
J Am Acad Dermatol. 2007
Jun;56(6):979-88
Treatment of pruritus with
topically applied opiate
receptor antagonist.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Cutan Med Surg. 2005
Oct;9(5):215-6
Successful treatment of
refractory aquagenic
pruritus with naltrexone.
In order to access the
PubMed abstract of this
article, visit this
website link.
Itching Relieved with
Topical Naltrexone
Pruritus is a very common
and distressing skin
problem. More than 70% of
patients with localized and
generalized atopic
dermatitis with severe
itching who used topical
naltrexone 1% cream
experienced a significant
reduction of pruritus.
J Am Acad Dermatol. 2007
Jun;56(6):979-88
Treatment of pruritus with
topically applied opiate
receptor antagonist.
In order to access the
PubMed abstract of this
article, visit this
website link.
Aquagenic pruritus is an
intense prickling sensation
that develops in affected
individuals immediately
after contact with water at
any temperature. Endogenous
opiates, like naltrexone,
can modify pruritus by
influencing the peripheral
and central sensation of
itch, and have been found to
be successful in suppressing
the perception of pruritus
from many diverse origins
including aquagenic pruritus.
J Cutan Med Surg. 2005
Oct;9(5):215-6
Successful treatment of
refractory aquagenic
pruritus with naltrexone
In order to access the
PubMed abstract of this
article, visit this
website link.
PSORIASIS:
Topical vitamin B12 offers a
new therapeutic approach for
eczema (atopic dermatitis)
and psoriasis, and may be
suitable for long-term
therapy as no long term
adverse effects have been
reported.
British Journal of
Dermatology 2004; 150:
977-983.
Topical vitamin B12--anew
therapeutic approach in
atopic dermatitis-evaluation
of efficacy andtolerability
in a randomized
placebo-controlled
multicentre clinicaltrial.
In order to access the
PubMed abstract of this
article, visit this
website link.
Dermatology 2001;203:141-147
Vitamin B(12) cream
containing avocado oil in
thetherapy of plaque
psoriasis.
In order to access the
PubMed abstract of this
article, visit this
website link.
Salicylic acid has been used
alone as a treatment for
psoriasis, but is most
commonly used to increase
the penetration of other
topical preparations,
primarily corticosteroids.
In this small study, the use
of 6% salicylic acid gel in
conjunction with tacrolimus
ointment showed
statistically significant
improvement for the
treatment of plaque
psoriasis compared with the
use of salicylic acid alone.
"For patients with localized
psoriasis, and for many of
those with moderate
psoriasis as well, the
mainstay of treatment is
still topical therapy. The
quality of life is greatly
affected in such patients,
and they often express high
levels of dissatisfaction
with current treatment
options. Safe, convenient,
and effective topical
regimens, such as
combination therapy with
topical tacrolimus and
salicylic acid, can be of
great benefit in this large
population."
Arch Dermatol.
2005;141:43-46
Topical tacrolimus ointment
combined with 6% salicylic
acid gel for plaque
psoriasis treatment.
In order to access the
PubMed abstract of this
article, visit this
website link.
"Methotrexate has been used
as an effective systemic
chemotherapeutic drug for
psoriasis by dermatologists
for over 30 years.
Nevertheless,
pharmacokinetic data
indicate that oral
methotrexate can cause a
decrease in red and white
blood cell and platelet
counts and can also cause
severe liver damage,
diarrhea, and stomach
irritation, as dose-related
drug-induced side effects.
Such indications have
limited its prescription by
physicians. However, [Syed
and Nordstrom of the
Department of Dermatology,
University of California-San
Francisco, and researchers
from three other locations
note that] if its
incorporation in a gel as a
topical agent, in a proper
dosage. imparts better
results without the cited
side effects, then such a
formulation appears to
justify a clinical
evaluation. Furthermore,
published data have
indicated that 70% of
patients prefer topical
therapy for treating
psoriasis."
This article concludes: "methotrexate
0.25% in a hydrophilic gel
is well tolerated and
significantly more effective
than placebo as a
patient-applied topical
medication to treat
psoriasis vulgaris."
J Cutan Med Surg 2001;
299-302
Management of psoriasis
vulgaris with methotrexate
0.25% in a hydrophilic gel:
a placebo-controlled,
double-blind study.
In order to access the
PubMed abstract of this
article, visit this
website link.
This article concludes: "Methotrexate
0.25% in a hydrophilic gel
is well tolerated but is not
very effective in
controlling the lesions of
psoriasis on the palms and
soles; however, a higher
concentration in a different
base with better penetration
could possibly provide
better results."
J Dermatol 2004
Oct;31(10):798-801
Topical 0.25% methotrexate
gel in a hydrogel base for
palmoplantar psoriasis.
In order to access the
PubMed abstract of this
article, visit this
website link.
Tiwari, Kumar, et al.
published a case report of
topical methotrexate
delivered by iontophoresis
for the treatment of
recalcitrant palmoplantar
psoriasis. In a 46 y.o. male
with well-defined bilateral
palmar plaques of 6 years
duration which were
resistant to several
therapies, the right palm
was treated, as it had more
severe lesions.
Iontophoresis was performed
using cotton gauze soaked in
4 to 6 ml of methotrexate
disodium solution 10 mg/ml,
once a week for four weeks.
The researchers reported 75%
improvement after four weeks
of therapy. Iontophoresis
allows high concentrations
of drug to be delivered to a
limited area, and may offer
a method of reducing total
drug accumulation and
reduced side effects.
Int J Dermatol. 2003
Feb;42(2):157-9
Topical methotrexate
delivered by iontophoresis
in the treatment of
recalcitrant psoriais--a
case report.
In order to access the
PubMed abstract of this
article, visit this
website link.
VITILIGO:
Treatment Options for Vitiligo
Pseudocatalase Cream
Vitiligo is a spontaneous
irregular depigmentation of
skin. Patients with vitiligo
have low catalase levels in
their epidermis with high
levels of hydrogen peroxide.
Pseudocatalase cream is an
externally applied UVB-activated
product that can lead to
recovery of the oxidative
damage in the epidermis and
remarkable repigmentation.
Skin Pharmacol Appl Skin
Physiol 1999
May-Jun;12(3):132-8
Successful treatment of
oxidative stress in vitiligo.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Pathol 2000
Aug;191(4):407-16
Melanocytes are not absent
in lesional skin of long
duration vitiligo.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Investig Dermatol Symp
Proc 1999 Sep;4(1):91-6
In vivo and in vitro
evidence for hydrogen
peroxide (H2O2) accumulation
in the epidermis of patients
with vitiligo and its
successful removal by a UVB-activated
pseudocatalase.
In order to access the
PubMed abstract of this
article, visit this
website link.
Dermatology
1995;190(3):223-9
Treatment of vitiligo with a
topical application of
pseudocatalase and calcium
in combination with
short-term UVB exposure: a
case study on 33 patients.
In order to access the
PubMed abstract of this
article, visit this
website link.
Topical Phenylalanine
Melanocytes may still be
present in long-standing
(>25 years) depigmented skin
of patients with vitiligo.
L-phenylalanine uptake and
turnover in the pigment
forming melanocytes is vital
for initiation of
melanogenesis. Phenylalanine
hydroxylase activities
increase linearly with
inherited skin color
yielding eightfold more
activities in black skin
compared to white skin.
Camacho and Mazuecos
performed an uncontrolled
retrospective survey of a
group of 193 patients (171
participants after
screening) with evolving
vitiligo who were treated
with oral (50 or 100 mg/kg
daily) and topical (10% gel)
phenylalanine plus sun
exposure . When the study
closed, 100% repigmentation
was achieved in 122 patients
on the face, 35 on the
trunk, and 33 on the limbs.
Patients who were treated
during the months of high
solar radiation (and
therefore also used the
topical phenylalanine)
achieved greater
repigmentation. No side
effects were reported.
Arch Dermatol. 1999;135:216-217
Treatment of vitiligo with
oral and topical
phenylalanine: 6 years of
experience.
In order to access the
PubMed abstract of this
article, visit this
website link.
J Drugs Dermatol 2002
Sep;1(2):127-31
Oral and topical
L-phenylalanine, clobetasol
propionate, and UVA/sunlight--a
new study for the treatment
of vitiligo.
In order to access the
PubMed abstract of this
article, visit this
website link.
Mol Genet Metab 2005
Dec;86(4):27-33
Decreased phenylalanine
uptake and turnover in
patients with vitiligo.
In order to access the
PubMed abstract of this
article, visit this
website link.
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