EFFECT OF INTRAVENOUS-SODIUM AMYTAL ON CUTANEOUS SENSORY ABNORMALITIES, SPONTANEOUS PAIN AND ALGOMETRIC PAIN PRESSURE THRESHOLDS IN NEUROPATHIC PAIN PATIENTS - A PLACEBO-CONTROLLED STUDY .2.

Citation
A. Mailis et al., EFFECT OF INTRAVENOUS-SODIUM AMYTAL ON CUTANEOUS SENSORY ABNORMALITIES, SPONTANEOUS PAIN AND ALGOMETRIC PAIN PRESSURE THRESHOLDS IN NEUROPATHIC PAIN PATIENTS - A PLACEBO-CONTROLLED STUDY .2., Pain, 70(1), 1997, pp. 69-81
Citations number
45
Categorie Soggetti
Neurosciences,"Clinical Neurology
Journal title
PainACNP
ISSN journal
03043959
Volume
70
Issue
1
Year of publication
1997
Pages
69 - 81
Database
ISI
SICI code
0304-3959(1997)70:1<69:EOIAOC>2.0.ZU;2-D
Abstract
This study investigated the behaviour exhibited by 17 neuropathic pain patients (almost half of whom had documented neurological injury) wit h diffuse pain and extratenitorial sensory, sudomotor and vasomotor ab normalities, under the influence of intravenous administration of sali ne-controlled sodium amytal (SA), a medium action barbiturate. After S A (but not after normal saline) infusion, there was a dramatic and sel ective reduction of allodynia (touch-evoked pain) in all patients disp laying this phenomenon, while pin prick and cold hypo- or hyperalgesia , as well as algometric pressure thresholds of the symptomatic Limb (a s a measurement of deep pain) were minimally changed in most patients. Spontaneous subjective pain was reduced substantially but not totally . The patients were able (once allodynia was eliminated) to recognize a deep-seated pain of which they were unaware before, evoked by firm b ut gentle palpation of the Limb. Sympathetic blocks and A-fibre ischem ic blocks in several patients and spinal stimulation in one patient pr oduced effects identical to those observed during SA administration. T he deep pain component was maintained despite elimination of allodynia even under stages of sleep induced by SA, at which time the patients would withdraw only the symptomatic limb upon firm but gentle that neu ropathic pain patients have two separate pain components, a cutaneous one (touch-evoked pain or allodynia) mediated by large fibres as a pro duct of central sensitization, and a deep pain component mediated via nociceptors, which can be easily discriminated during systemic adminis tration of SA. (C) 1997 International Association for the Study of Pai n.