When used to treat focal dystonias, botulinum toxin may cause a transi
ent impairment of neuromuscular transmission in muscles distant from t
hose injected. These systemic effects are not clinically evident, but
should not be ignored when patients are exposed to other drugs or cond
itions that also impair neuromuscular transmission. A patient is descr
ibed who underwent general anesthesia twice during treatment with botu
linum toxin for a long history of blepharospasm. On both occasions, th
e neuromuscular block produced by vecuronium (0.05 mg kg(-1)) was moni
tored in the abductor digiti minimi muscle. Compared with that observe
d in 24 individuals who were free from neuromuscular problems, the pat
ient's sensitivity to vecuronium was low 90 days after the seventh tre
atment with toxin and normal 8 days after the ninth. The possibility i
s considered that repeated treatments with the toxin may cause continu
ous remodeling of neuromuscular junctions and may cause the patient to
develop some tolerance to the action of neuromuscular blockers.