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Intra-articular morphine as analgesic in temporomandibular joint arthralgia/osteoarthritis

List, T. (författare)
Tegelberg, A. (författare)
Department of Stomatognathic Physiology, Central Hospital, SE-721, 89 Västerås, Sweden
Haraldson, T. (författare)
Department of Stomatognathic Physiology, Borås Hospital, SE-501, 82 Borås, Sweden
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Isacsson, G. (författare)
AstraZeneca Clinical RandD, SE-151, 85 Södertälje, Sweden
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 (creator_code:org_t)
2001
2001
Engelska.
Ingår i: Pain. - 0304-3959 .- 1872-6623. ; 94:3, s. 275-282
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The aim of this study was to determine the analgesic efficacy of a single dose intra-articular injection (i.a.) of morphine in 53 patients with unilateral arthralgia/osteoarthritis of the temporomandibular joint (TMJ). This randomized, double-blind, parallel group, multicenter study included a screening visit, a treatment visit, and a follow-up visit 1 week after treatment. Recordings of visual analog scales (VAS) pain intensity scores at maximum mouth opening (main efficacy variable) and at jaw rest were made directly before a 1-ml i.a. injection into one TMJ of either 1.0 mg morphine-HCl, 0.1 mg morphine-HCl, or saline (placebo). The pain intensity was also recorded at the follow-up and in a diary 3 days before and 5 days after the injection. The VAS pain score at maximum mouth opening was considerably reduced 1-10 h after injection but without significant differences between groups. At the follow-up, the median VAS pain score at maximal mouth opening was significantly lower in the 0.1-mg morphine group than in the 1.0-mg morphine group (P < 0.043) or the saline group (P < 0.021). A significant increase in pain pressure threshold over the affected joint was seen in the 0.1-mg morphine group compared with the saline group at the follow-up but not 1 and 2 h post-injection. The incidence of adverse events was small and did not differ between the treatment groups. In conclusion, one i.a. injection of 0.1 mg morphine significantly increased the pain pressure threshold and mouth opening ability, but evidence for the analgesic property of the locally applied opioid was inconclusive. No dose-effect relation and no significant short-term analgesic property were seen. Although statistically significant, the magnitude of the reduced VAS pain intensity score was not clinically relevant at the 1-week follow-up. © 2001 International Association for the Study of Pain. Published by Elsevier Science B.V. All rights reserved.

Nyckelord

Analgesia
Human
Intra-articular
Morphine
Osteoarthritis
Randomized Clinical Trial
Temporomandibular joint
NATURAL SCIENCES
NATURVETENSKAP

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List, T.
Tegelberg, A.
Haraldson, T.
Isacsson, G.
Artiklar i publikationen
Pain
Av lärosätet
Linköpings universitet

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