Anesth Analg 2004;98:1581-1584
© 2004 International Anesthesia Research Society
doi: 10.1213/01.ANE.0000113258.31039.C8
PAIN MEDICINE
The Long-Term Effect of Repeated Intravenous Lidocaine on Central Pain and Possible Correlation in Positron Emission Tomography Measurements
Alex Cahana, MD, DAAPM*,
Antonio Carota, MD ,
Marie-Louise Montadon, MSc , and
Jean Marie Annoni, MD
*Interventional Pain Program, Department of Anesthesiology;
Clinic of Neurological Rehabilitation;
Department of Radiology, Division of Nuclear Medicine; and
Clinic of Neurology, Department of Clinical Neuroscience, Geneva University Hospitals, Geneva, Switzerland
Address correspondence and reprint requests to Alex Cahana, MD, DAAPM, Interventional Pain Program, Department of Anesthesiology, Pharmacology and Surgical Intensive Care, Geneva University Hospital, 1211 Geneva 14, Switzerland. Address e-mail to alex.cahana{at}hcuge.ch
Functional neuroimaging suggests that similar brain regions are involved in the processing of pain in healthy subjects and in patients with chronic neuropathic central pain. We present a patient with chronic neuropathic central pain due to a unique lesion to the trigeminal and spinothalamic pathway who had persistent pain relief after repeated IV lidocaine infusions. Positron emission tomography scan results showed a relative hypoactivity of the left posterolateral thalamus before treatment which disappeared after therapy. This case may suggest a stereo-selective analgesic effect of lidocaine accompanied by regional cerebral blood flow changes in the thalamus, indicating that sodium channels could, in fact, be highly expressed or modified in the thalamus after thalamic deafferentation.
IMPLICATIONS: We present a case of persistent central pain after encephalitis in a patient who had long-term pain relief after a series of IV lidocaine infusions. A positron emission tomography scan study, done before and after treatment, suggested that lidocaine for the diagnosis of chronic neuropathic pain may have a specific site of action in the brain.
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109(6):
1972 - 1980.
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