METHOD
Since 2003, we followed 162 facial paralysis patients performing BTXA applications in the NPS every 6 months for symmetry. From this group, 33 patients with synkinesis were selected, average age 39.7 years.
The oculo-oral synkinesis was observed in all patients. In 12 (36.4%) there were also other types: oro-ocular, oro-oral etc. BTXA points in the NPS followed published protocol1. Not all identified synkinesis were necessarily treated, predefined criteria were observed: deepening of the PS naso-labial fold, intensity of contraction and patient's complaint. The dosage needed for synkinesis management, adverse effects and satisfaction were evaluated and compared to traditional treatment.
RESULTS
BTXA dosage used in the PS ranged from 2 to 18 units (U), average 4,4U/session, compared to average 38U/session on the NPS. Muscle groups more often treated were the zygomaticus and risorius. Treatment points used 1 (21.2%) or 2U (76.5%). There was no increase in side effects frequency (64% temporary difficulty to speak, eat or drink).
There was partial improvement of synkinesis in 92% and complete improvement in 8%. The goal is to weaken the muscles, without complete paralysis. There was progressive improvement of symptoms during subsequent sessions.
CONCLUSIONS
We didn’t find reports treating synkinesis in the way presented, with low doses BTXA injection in the middle and lower thirds of the PS. The technique presented favorable results, with satisfactory control of involuntary movements, without increasing the frequency of adverse effects and greater patient satisfaction when compared to traditional treatment.
1. Salles AG et al. Botulinum toxin injection in long-standing facial paralysis patients: improvement of facial symmetry observed up to 6 months. Aesth Plast Surg 2009;33:582-90
2. Armstrong MW et al. Treatment of facial synkinesis and facial asymmetry with botulinum toxin type A following facial nerve palsy. Clin Otolaryngol Allied Sci 1996;21:15–20
3. Borodic G et al. Botulinum toxin for aberrant facial nerve regeneration: double-blind, placebo-controlled trial. Plast Reconstr Surg 2005;116:36-43