Phenytoin as a coanalgesic in cancer pain
The efficacy of phenytoin (PHT), buprenorphine (Bu), and Bu + PHT for the relief of cancer pain of various etiologies was evaluated in a randomized, double-blind study of 3 groups, each comprised of 25 patients. Treatment duration was 1 month. PHT (100 mg by mouth twice daily) provided >50% pain...
Saved in:
Published in | Journal of pain and symptom management Vol. 7; no. 4; pp. 209 - 213 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.05.1992
Elsevier Science |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | The efficacy of phenytoin (PHT), buprenorphine (Bu), and Bu + PHT for the relief of cancer pain of various etiologies was evaluated in a randomized, double-blind study of 3 groups, each comprised of 25 patients. Treatment duration was 1 month. PHT (100 mg by mouth twice daily) provided >50% pain relief to 18 patients (72%) and >75% relief to 4 (16%). Bu (0.2 mg sublingually twice daily) gave 21 patients (84%) >50% relief and 15 patients (60%) >75% relief. Of the Bu-treated patients, 8 had major side effects, while none of the PHT-treated patients experienced significant untoward reactions. Combined therapy (PHT, 50 mg PO + Bu 0.1 mg SL twice daily) provided >50% pain relief to 22 patients (88%) and >75% to 18 (72%); only 3 patients experienced a significant side effect. This study suggests that phenytoin has mild-to-moderate pain-relieving properties of its own and can significantly enhance buprenorphine analgesia. By permitting a lower opioid dose, it may reduce the occurrence of opioid-related side effects. PHT's lack of serious side effects, as well as its documented anxiolytic and antidepressant actions, may add to its comparative usefulness. Further clinical trials of PHT as a coanalgesic and/or adjuvant agent in cancer pain are warranted. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 ObjectType-News-3 content type line 23 |
ISSN: | 0885-3924 1873-6513 |
DOI: | 10.1016/0885-3924(92)90077-U |