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Meta-Analysis
. 2011 Feb 16;2011(2):CD007556.
doi: 10.1002/14651858.CD007556.pub2.

Single dose oral fenoprofen for acute postoperative pain in adults

Affiliations
Meta-Analysis

Single dose oral fenoprofen for acute postoperative pain in adults

Maria X Traa et al. Cochrane Database Syst Rev. .

Abstract

Background: Fenoprofen is a non-steroidal anti-inflammatory drug (NSAID), available in several different countries, but not widely used.

Objectives: To assess the efficacy of single dose oral fenoprofen in acute postoperative pain, and associated adverse events.

Search strategy: We searched Cochrane CENTRAL, MEDLINE, EMBASE and the Oxford Pain Relief Database for studies to December 2010.

Selection criteria: Single oral dose, randomised, double-blind, placebo-controlled trials of fenoprofen for relief of established moderate to severe postoperative pain in adults.

Data collection and analysis: Studies were assessed for methodological quality and data extracted by two review authors independently. Summed total pain relief (TOTPAR) or pain intensity difference (SPID) over 4 to 6 hours was used to calculate the number of participants achieving at least 50% pain relief. These derived results were used to calculate, with 95% confidence intervals, the relative benefit compared to placebo, and the number needed to treat (NNT) for one participant to experience at least 50% pain relief over 4 to 6 hours. Numbers of participants using rescue medication over specified time periods, and time to use of rescue medication, were sought as additional measures of efficacy. Information on adverse events and withdrawals was collected.

Main results: Five studies (696 participants) met the inclusion criteria; 24 participants were treated with fenoprofen 12.5 mg, 23 with fenoprofen 25 mg, 79 with fenoprofen 50 mg, 78 with fenoprofen 100 mg, 146 with fenoprofen 200 mg, 55 with fenoprofen 300 mg, 43 with zomepirac 100 mg, 30 with morphine 8 mg, 77 with codeine 60 mg, and 141 with placebo. Participants had pain following third molar extraction, laparoscopy, minor day surgery and episiotomy. The NNT for at least 50% pain relief over 4 to 6 hours with a single dose of fenoprofen 200 mg compared to placebo was 2.3 (1.9 to 3.0). There were insufficient data to analyse other doses or active comparators, time to use of rescue medication, or numbers of participants needing rescue medication. There was no difference in numbers of participants experiencing any adverse events between fenoprofen 200 mg and placebo. No serious adverse events or adverse event withdrawals were reported in these studies.

Authors' conclusions: Oral fenoprofen 200 mg is effective at treating moderate to severe acute postoperative pain, based on limited data for at least 50% pain relief over 4 to 6 hours. Efficacy of other doses, other efficacy outcomes, and safety and tolerability could not be assessed.

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Conflict of interest statement

SD and RAM have received research support from charities, government and industry sources at various times, but no such support was received for this work. RAM has consulted for various pharmaceutical companies and received lecture fees from pharmaceutical companies related to analgesics and other healthcare interventions. MXT has no interests to declare.

Figures

1
1
Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
2
2
Forest plot comparing fenoprofen 200 mg versus placebo for the outcome of ≥50% total pain relief over 4 to 6 hours.
3
3
Forest plot comparing fenoprofen 200 mg versus placebo for the outcome of adverse effects over 4 to 6 hours.
1.1
1.1. Analysis
Comparison 1 Fenoprofen 200 mg versus placebo, Outcome 1 Participants with ≥ 50% pain relief over 4 to 6 hours.
1.2
1.2. Analysis
Comparison 1 Fenoprofen 200 mg versus placebo, Outcome 2 Participants with ≥1 adverse effect over 4 to 6 hours.

Update of

  • doi: 10.1002/14651858.CD007556

References

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