LACK OF EFFECT OF SPHENOPALATINE GANGLION BLOCK WITH INTRANASAL LIDOCAINE ON SUBMAXIMAL EFFORT TOURNIQUET TEST PAIN

Citation
Dg. Silverman et al., LACK OF EFFECT OF SPHENOPALATINE GANGLION BLOCK WITH INTRANASAL LIDOCAINE ON SUBMAXIMAL EFFORT TOURNIQUET TEST PAIN, Regional anesthesia, 18(6), 1993, pp. 356-360
Citations number
NO
Categorie Soggetti
Anesthesiology
Journal title
ISSN journal
0146521X
Volume
18
Issue
6
Year of publication
1993
Pages
356 - 360
Database
ISI
SICI code
0146-521X(1993)18:6<356:LOEOSG>2.0.ZU;2-F
Abstract
Background and Objectives. The present study examined whether sphenopa latine ganglion block (SPGB) causes a reduction in the response to acu te nociceptive input that may account for the SPGB-induced relief repo rted by many patients with chronic pain. Methods. In a double-blind, c ross-over design, 16 healthy volunteers underwent separate 15-minute s ubmaximal effort tourniquet tests before and after SPGB with 20% lidoc aine plus 1:100,000 epinephrine (SPGB(lidocaine)) or placebo (SPGB(sal ine)). Responses during each minute of tourniquet inflation were conve rted to a 1 to 16 scale and classified as nothing (1), mild sensation (2-4), strong sensation (5-7), slightly painful (8-10), definitely pai nful (11-13), and severely painful (14-16). Results. Maximum pain scor es reached 12.6 +/- 2.5 (mean +/- SD) pm-SPGB, 10.9 +/- 3.5 after SPGB (saline) and 11.1 +/- 2.5 after SPGB(lidocaine). No significant differ ences were noted between SPGB(lidocaine) and SPGB(saline) at any of th e 15 time points (p = NS by repeated measures ANOVA and paired t-test) . However, retrospective grouping of time points noted that scores aft er SPGB(lidocaine) were lower in the ''strong sensation'' range. Concl usion. SPGB does not lessen scute extremity pain to a significant degr ee and is not in and of itself an effective means of analgesia for acu te pain. Its potential impact on nociceptive stimuli that elicit a ''s trong sensation'' (i.e., a score of 5-7 in the present study) should b e evaluated in hyperpathic pain states and in states with exaggerated aversive responses.