Neuropathic pain is often resistant to opioids, so other medication classes
, such as tricyclic antidepressants, anticonvulsants, and local anesthetics
, are often used. Central sensitization, or pain 'wind-up', may perpetuate
chronic neuropathic pain even when ongoing peripheral sensory input is abse
nt. Wind-up is thought to cause allodynia, hyperalgesia, and hyperpathia. R
eceptors such as NMDA, AMPA, and M-glu hale recently been identified for th
eir role in central sensitization or pain 'windup'. Ketamine has been propo
sed recently for neuropathic pain secondary to its NMDA receptor activity.
The current application as a topical gel sterns from the theory that ketami
ne has peripheral action at both opioid and Na+-K+ channels. This case stud
y involved 5 patients from 25 to 70 years old (3 RSD, 1 lumbar radiculopath
y, 1 post-herpetic neuralgia). Dose used was determined by site and surface
area of involvement and ranged from 0.093 mg/kg to 9.33 mg/kg. All five pa
tients reported significant pain relief at initial application and wished t
o continue treatment. The average numerical analogue scale (NAS) score prea
pplication was 8.8. The average IS minutes post application NAS was 1.6. Pa
tients reported alterations in temperature sensation, feelings of relaxatio
n and decreased tension in the area of application, and pain relief. Reduct
ion in numerical pain scores postapplication of ketamine gel ranged from 53
-100% using a 1-10 numerical pain intensity scale. No significant side effe
cts were reported. Ketamine Gel may provide clinicians with a new option in
the battle against chronic neuropathic pain. Until further information is
available and larger trials can be conducted, we can only recommend this ty
pe of therapy for refractory cases in which all primary and secondary optio
ns have been exhausted.