Hypertrophic scars and keloids are one of the most challenging scars to treat, as
their high rate of relapse, functional disability, and their psychosocial effects on
patients make their management a formidable task. Various treatment options are
available for treating hypertrophic scars, including corticosteroid injection, silicone
treatment, pressure garments, and laser therapy. However, the results obtained
with these techniques have been inconsistent. None of these treatment modalities
has been proven as a gold standard. Growing evidence suggests that botulinum
toxin type A (BTX-A) may play an important role in both preventing and treating
pathological scarring. We decided to assess the clinical and experimental data of
utmost importance regarding the role of BTX-A in the management of hypertrophic
and keloid scarring. According to experimental research, BTX-A reduces neurogenic
inflammation, alters fibroblast function, and lessens mechanical tension in wounds
by inhibiting the P-neurokinin-1 receptor system. Clinical trials spanning a range of
surgical and traumatic patient populations, such as thyroidectomy, facial wounds,
blepharoplasty, mastectomy, and burn scars, have all consistently demonstrated
enhanced scar height, pliability, erythema/skin redness, and pain, as well as an
improvement in patients’ subjective assessment. Meta-analyses also show that BTXA
is statistically more effective than placebo and other treatments. Differences in
dose schedules and administration timing, as well as insufficient information on
long-term effects, make these results impossible to be generalizable. In general,
BTX-A appears to be a safe and effective complement to the multimodal,
personalized treatment of hypertrophic and keloid scars.
Keywords: Botulinum Toxin Type A; Hypertrophic Scar; Keloid; Non-Surgical
Treatment; Scar Management
