Koenraad De Boulle, Alastair Carruthers, Nowell Solish, Jean Carruthers, Wolfgang G.Philipp-Dormston, Steven Fagien, Sara Sangha, Michael Silberberg, Cheri Mao
Background:
With onabotulinumtoxinA approved for the
treatment of glabellar and crow’s feet lines
and, most recently, for forehead lines (FHL), it
is possible to simultaneously treat multiple
areas of the upper face that are of high
concern and treatment priority for aesthetically
oriented individuals. This review aims to
present key insights on the use of
onabotulinumtoxinA for the treatment of
moderate to severe FHL.
Methods:
Double-blind, placebo-controlled registration
trials of onabotulinumtoxinA for the treatment
of FHL were included. Using findings from 3
such published studies, we discuss key
concepts and clinical experience for the
treatment of moderate to severe FHL with
onabotulinumtoxinA (20 U in the frontalis and
20 U in the glabellar complex, with/without 24
U in crow’s feet lines), including injection
pattern, dose selection, efficacy and safety
data, and considerations for patient selection.
Results:
Across the 2 pivotal phase 3 studies,
responder rates on investigator- and subject-
assessed measures of appearance of FHL
severity were significantly higher with
onabotulinumtoxinA versus placebo for the
treatment of FHL at day 30 (P < 0.0001), and
results were maintained through 3 cycles of
onabotulinumtoxinA.
Conclusions:
OnabotulinumtoxinA treatment also resulted in
high patient satisfaction rates. The incidence
of eyebrow and of eyelid ptosis was low, and
no new safety signals were detected.
OnabotulinumtoxinA is safe and effective and
an appropriate option for patients with
moderate to severe FHL encountered in clinical
practice.
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