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Evaluation of two opioid-acetaminophen combinations and placebo in postoperative oral surgery pain.
Pharmacotherapy. 1994 Mar-Apr; 14(2):139-46.P

Abstract

STUDY OBJECTIVE

To determine the relative analgesic potency and adverse effect liability of hydrocodone bitartrate 7.5 mg with acetaminophen 500 mg, codeine phosphate 30 mg with acetaminophen 300 mg, and placebo in the treatment of pain following oral surgery.

DESIGN

Randomized, double-blind, single-dose, placebo-controlled, parallel-group study with self-ratings at 30 minutes and then at hourly intervals from hour 1 to hour 6.

SETTING

Private, oral surgery practice sites.

PATIENTS

Three hundred twenty-four outpatients with moderate or severe pain after the surgical removal of impacted third molars were selected. One was lost to follow-up and 32 did not need an analgesic; 232 patients had valid efficacy data.

INTERVENTIONS

Patients were treated with a single oral dose of hydrocodone bitartrate 7.5 mg with acetaminophen 500 mg, codeine phosphate 30 mg with acetaminophen 300 mg, or placebo when they experienced steady, moderate or severe pain that, in their opinion, required an analgesic. Using a self-rating record, subjects rated their pain and its relief for 6 hours after medicating; estimates of peak and total analgesia were derived from these subjective reports.

MEASUREMENTS AND MAIN RESULTS

This study was a valid analgesic assay. Both active treatments were significantly superior to placebo for all measures of analgesic efficacy. The hydrocodone-acetaminophen combination was significantly superior to the codeine-acetaminophen combination for total pain relief and the number of evaluations with 50% relief. Both active treatments manifested an analgesic effect within 30 minutes; the effect persisted for 5 hours for the codeine combination and 6 hours for the hydrocodone combination. Adverse effects were transient, consistent with the pharmacologic profiles of opioids, and none required treatment.

CONCLUSIONS

A slight advantage in analgesic efficacy was demonstrated in this single-dose study for the hydrocodone-acetaminophen combination. Repeat-dose studies, however, should be conducted to determine the clinical significance of the difference in analgesic effect of these opioid combinations.

Authors+Show Affiliations

Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, Maryland.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Clinical Trial
Comparative Study
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

8197031

Citation

Forbes, J A., et al. "Evaluation of Two Opioid-acetaminophen Combinations and Placebo in Postoperative Oral Surgery Pain." Pharmacotherapy, vol. 14, no. 2, 1994, pp. 139-46.
Forbes JA, Bates JA, Edquist IA, et al. Evaluation of two opioid-acetaminophen combinations and placebo in postoperative oral surgery pain. Pharmacotherapy. 1994;14(2):139-46.
Forbes, J. A., Bates, J. A., Edquist, I. A., Burchfield, W. H., Smith, F. G., Schwartz, M. K., Kit, V., Hyatt, J., Bell, W. E., & Beaver, W. T. (1994). Evaluation of two opioid-acetaminophen combinations and placebo in postoperative oral surgery pain. Pharmacotherapy, 14(2), 139-46.
Forbes JA, et al. Evaluation of Two Opioid-acetaminophen Combinations and Placebo in Postoperative Oral Surgery Pain. Pharmacotherapy. 1994 Mar-Apr;14(2):139-46. PubMed PMID: 8197031.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Evaluation of two opioid-acetaminophen combinations and placebo in postoperative oral surgery pain. AU - Forbes,J A, AU - Bates,J A, AU - Edquist,I A, AU - Burchfield,W H, AU - Smith,F G, AU - Schwartz,M K, AU - Kit,V, AU - Hyatt,J, AU - Bell,W E, AU - Beaver,W T, PY - 1994/3/1/pubmed PY - 1994/3/1/medline PY - 1994/3/1/entrez SP - 139 EP - 46 JF - Pharmacotherapy JO - Pharmacotherapy VL - 14 IS - 2 N2 - STUDY OBJECTIVE: To determine the relative analgesic potency and adverse effect liability of hydrocodone bitartrate 7.5 mg with acetaminophen 500 mg, codeine phosphate 30 mg with acetaminophen 300 mg, and placebo in the treatment of pain following oral surgery. DESIGN: Randomized, double-blind, single-dose, placebo-controlled, parallel-group study with self-ratings at 30 minutes and then at hourly intervals from hour 1 to hour 6. SETTING: Private, oral surgery practice sites. PATIENTS: Three hundred twenty-four outpatients with moderate or severe pain after the surgical removal of impacted third molars were selected. One was lost to follow-up and 32 did not need an analgesic; 232 patients had valid efficacy data. INTERVENTIONS: Patients were treated with a single oral dose of hydrocodone bitartrate 7.5 mg with acetaminophen 500 mg, codeine phosphate 30 mg with acetaminophen 300 mg, or placebo when they experienced steady, moderate or severe pain that, in their opinion, required an analgesic. Using a self-rating record, subjects rated their pain and its relief for 6 hours after medicating; estimates of peak and total analgesia were derived from these subjective reports. MEASUREMENTS AND MAIN RESULTS: This study was a valid analgesic assay. Both active treatments were significantly superior to placebo for all measures of analgesic efficacy. The hydrocodone-acetaminophen combination was significantly superior to the codeine-acetaminophen combination for total pain relief and the number of evaluations with 50% relief. Both active treatments manifested an analgesic effect within 30 minutes; the effect persisted for 5 hours for the codeine combination and 6 hours for the hydrocodone combination. Adverse effects were transient, consistent with the pharmacologic profiles of opioids, and none required treatment. CONCLUSIONS: A slight advantage in analgesic efficacy was demonstrated in this single-dose study for the hydrocodone-acetaminophen combination. Repeat-dose studies, however, should be conducted to determine the clinical significance of the difference in analgesic effect of these opioid combinations. SN - 0277-0008 UR - https://www.unboundmedicine.com/medline/citation/8197031/Evaluation_of_two_opioid_acetaminophen_combinations_and_placebo_in_postoperative_oral_surgery_pain_ DB - PRIME DP - Unbound Medicine ER -