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Parecoxib Provides Analgesic and Opioid-Sparing Effects Following Major Orthopedic Surgery: A Subset Analysis of a Randomized, Placebo-Controlled Clinical Trial.
Diaz-Borjon, Efrain; Torres-Gomez, Armando; Essex, Margaret Noyes; Salomon, Patricia; Li, Chunming; Cheung, Raymond; Parsons, Bruce.
Affiliation
  • Diaz-Borjon E; Orthopedics and Traumatology, Hospital Angeles Lomas, Huixquilucan, Mexico.
  • Torres-Gomez A; Orthopaedics, ABC Medical Center, Mexico City, Mexico.
  • Essex MN; Global Medical Affairs, Pfizer Inc, New York, NY, USA. Margaret.essex@pfizer.com.
  • Salomon P; Pain Division for Latin America, Pfizer Inc, Mexico City, Mexico.
  • Li C; Statistics, Pfizer Inc, Madison, NJ, USA.
  • Cheung R; Global Medical Affairs, Pfizer Inc, New York, NY, USA.
  • Parsons B; Global Medical Affairs, Pfizer Inc, New York, NY, USA.
Pain Ther ; 6(1): 61-72, 2017 Jun.
Article in En | MEDLINE | ID: mdl-28255955
ABSTRACT

INTRODUCTION:

Orthopedic surgeries are among the most common and most painful surgeries performed. A multimodal analgesic approach is recommended to reduce opioid consumption, provide effective pain relief, and improve outcomes following surgery. This study examined the efficacy and opioid-sparing effects of parecoxib following major orthopedic surgery.

METHODS:

This subset analysis of a large, multicenter, randomized, double-blind, placebo-controlled study of parecoxib examined treatment effects on postoperative pain severity, pain interference with function, opioid consumption, occurrence of opioid-related symptoms, safety, and patient satisfaction following major orthopedic surgery.

RESULTS:

Pain scores were significantly lower in the parecoxib group (n = 142) compared with placebo (n = 139) on day 2 (-22%; p < 0.001) and day 3 (-17%; p = 0.004). Pain interference with function scores were also significantly lower in the parecoxib group on day 2 (-32%; p < 0.001) and day 3 (-27%; p = 0.003) relative to placebo. Additionally, significantly less supplemental morphine was required in the parecoxib group relative to placebo through 24 h (-28%; p = 0.008) and 48 h (-33%; p < 0.001). Patients in the parecoxib group had a reduced risk of experiencing opioid-related symptoms including fatigue, drowsiness, inability to concentrate, confusion, nausea, constipation, and confusion on day 2 and/or day 3. Finally, more patients receiving parecoxib (42%) rated treatment as "excellent" compared to those receiving placebo (21%).

CONCLUSIONS:

These findings support the use of parecoxib for the management of pain following major orthopedic surgery.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Pain Ther Year: 2017 Document type: Article Affiliation country: Mexico

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Pain Ther Year: 2017 Document type: Article Affiliation country: Mexico