Topical Tretinoin benefit risk danger side effects, cream use for acne,
Topical tretinoin helps reduce wrinkles on the skin and it is very effective. However, perhaps this skin product should be used less frequently in order to avoid side effects or potential dangers. Tretinoin is a syntheic form of vitamin a.
Topical tretinoin therapy and all-cause mortality.
Arch Dermatol. 2009 Jan;145(1):18-24.Weinstock MA, Bingham SF, Lew RA, Hall R, Eilers D, Kirsner R, Naylor M, Kalivas
J, Cole G, Marcolivio K, Collins J, Digiovanna JJ, Vertrees JE; Veterans Affairs
Topical Tretinoin Chemoprevention (VATTC) Trial Group.Dermatoepidemiology Unit,
VA Medical Center, 111D, 830 Chalkstone Ave, Providence, RI 02908, USA.
To evaluate the relation of topical tretinoin, a commonly used
retinoid cream, with all-cause mortality in the Veterans Affairs Topical
Tretinoin Chemoprevention Trial (VATTC). The planned outcome of this trial was
risk of keratinocyte carcinoma, and systemic administration of certain retinoid
compounds has been shown to reduce risk of this cancer but has also been
associated with increased mortality risk among smokers. The VATTC Trial
was a blinded randomized chemoprevention trial, with 2- to 6-year follow-up.
Oversight was provided by multiple independent committees. A total of 1131
veterans were randomized. Their mean age was 71 years. Patients with a very high
estimated short-term risk of death were excluded. Interventions Application of tretinoin, 0.1%, or vehicle control cream twice daily to the face and ears. The intervention was terminated 6 months early
because of an excessive number of deaths in the tretinoin-treated group. Post
hoc analysis of this difference revealed minor imbalances in age, comorbidity,
and smoking status, all of which were important predictors of death. After
adjusting for these imbalances, the difference in mortality between the
randomized groups remained statistically significant. We observed
an association of topical tretinoin therapy with death, but we do not infer a
causal association that current evidence suggests is unlikely.
Efficacy of 5% minoxidil versus combined 5% minoxidil
and 0.01% topical tretinoin for male pattern hair loss: a randomized,
double-blind, comparative clinical trial.
Am J Clin Dermatol. 2007. Department of Dermatology, Seoul National University
College of Medicine, and Seoul National University Boramae Hospital, Seoul,
Korea.
5% topical minoxidil solution has been widely used to stimulate new hair growth
and help stop hair loss in men with androgenetic alopecia. However, it is not
convenient for patients to continue applying the solution twice daily on a
regular basis. Topical tretinoin is known to increase the percutaneous
absorption of minoxidil and, therefore, to enhance the response of AGA to
minoxidil. For this reason, it was assumed that topical tretinoin would be
helpful in alleviating the inconvenience associated with the recommended
twice-daily application of minoxidil. We compared the efficacy and safety of
therapy using a combined solution of 5% minoxidil and 0.01% topical tretinoin
once daily with those of the conventional 5% topical minoxidil therapy applied
twice daily in the treatment of androgenetic alopecia. The efficacy and safety
of combined 5% minoxidil and 0.01% topical tretinoin once-daily therapy appear
to be equivalent to those of conventional 5% minoxidil twice-daily therapy for
the treatment of androgenetic alopecia.
Tolerability of high-dose topical tretinoin: the
Veterans Affairs Topical Tretinoin Chemoprevention Trial.
Br J Dermatol. 2009 Oct; Geng A, Weinstock MA, Hall R, Eilers D, Naylor M,
Kalivas J; VATTC Trial Group. Weinstock M, Marcolivio K, Weinstock M, Bingham S,
DiGiovanna JJ, Hall R, Naylor M, Taylor JR, Vertrees J, White C, Hall R, Sidhu-Malik
N, Hannah D, Eilers D, Liang T, Sakla N, Kreuger A, Cole G, Jeffes E, Labrador
T, Taylor JR, Kirsner R, Kerri JE, Falabella AG, Givens M, Naylor M, Benson MB,
Perry L, Kalivas J, Yanni C, Targovnik S, Austin J, Collier S, Collins JF,
Bingham S, Calvert B, Connor P, Crigler C, Davis D, Grubb P, Kelly J, Kirk G,
Lawson K, Linzy L, Palmer L, Rhoads M, Sather M, Copeland E, Fye C, Gagne W, de
Naranjo PG, Messick C, Vertrees J, Piepkorn M, White C, Lew R, Braverman I, Cole
B, Kalish R, McLean D, Thiers BH. Boston Dermatology and Laser Center, Boston,
MA, USA.
Topical tretinoin is a medication commonly used for acne that has potential
application in the long-term treatment of photodamaged skin. However, there are
few published data regarding the tolerability of high-dose tretinoin with
long-term use. To assess the long-term tolerability of tretinoin 0.1% cream. A
randomized, multicentre, double-blind, controlled trial for chemoprevention of
keratinocyte carcinomas (i.e. basal cell or squamous cell carcinomas) using
topical tretinoin cream to the face and ears was conducted. All participants
were veterans and had a history of two or more keratinocyte carcinomas over the
previous 5 years. Participants were examined (by a study dermatologist) and
interviewed every 6 months (for up to 5.5 years to May 2004). Treatment
comprised tretinoin 0.1% cream or vehicle control cream once daily, then twice
daily as tolerated. Participants were instructed to step down application
frequency to once daily or less if twice daily was not tolerated. The main
outcome measures were reported side-effects, frequency of cream application and
attendance at study visits. Appropriate data were available for four of the six
clinical sites of this trial. Data from 736 randomized participants (mean age 71
years; 97% men) from four clinical sites were analysed. The tretinoin group more
commonly reported one or more side-effects at the 6-month follow-up than the
control group (61% vs. 42%, P < 0.0001). Side-effects decreased over time in
both groups, but to a greater extent in the tretinoin group, and the difference
became nonsignificant at 30 months. Burning was the most common side-effect. No
unexpected adverse events were reported. Overall, the tolerability level of
topical tretinoin was high in this study population, with almost 40% of the
tretinoin group reporting no side-effects, and the majority (67%) tolerating at
least once-daily dosing at 6-month follow-up. High-dose topical tretinoin is
feasible for long-term use in this population.