Low-Dose Methoxyflurane versus Standard of Care Analgesics for Emergency Trauma Pain: A Systematic Review and Meta-Analysis of Pooled Data
- PMID: 33505170
- PMCID: PMC7829133
- DOI: 10.2147/JPR.S292521
Low-Dose Methoxyflurane versus Standard of Care Analgesics for Emergency Trauma Pain: A Systematic Review and Meta-Analysis of Pooled Data
Abstract
Purpose: Undertreatment of trauma-related pain is common in the pre-hospital and hospital settings owing to barriers to the use of traditional standard of care analgesics. Low-dose methoxyflurane is an inhaled non-opioid analgesic with a rapid onset of pain relief that is approved for emergency relief of moderate-to-severe trauma-related pain in adults. This analysis was performed to compare the efficacy and safety of low-dose methoxyflurane with standard of care analgesics in adults with trauma-related pain.
Methods: A meta-analysis was performed on pooled data from randomized controlled trials identified via a systematic review. The primary endpoint was the pain intensity difference between baseline and various time intervals (5, 10, 15, 20, and 30 minutes) after initiation of treatment.
Results: The pain intensity difference was statistically superior with low-dose methoxyflurane compared with standard of care analgesics (overall estimated treatment effect=11.88, 95% CI=9.75-14.00; P<0.0001). The superiority of low-dose methoxyflurane was demonstrated at 5 minutes after treatment initiation and was maintained across all timepoints. Significantly more patients treated with methoxyflurane achieved response criteria of pain intensity ≤30 mm on a visual analog scale, and relative reductions in pain intensity of ≥30% and ≥50%, compared with patients who received standard of care analgesics. The median time to pain relief was shorter with methoxyflurane than with standard of care analgesics. The findings were consistent in a subgroup of elderly patients (aged ≥65 years).
Conclusion: Methoxyflurane can be considered as an alternative to standard of care analgesics in pre-hospital and hospital settings for treatment of adult patients with acute trauma-related pain.
Keywords: acute pain; analgesia; emergency service; inhaled analgesic; pain management; wounds and injury.
© 2021 Fabbri et al.
Conflict of interest statement
Dr Fabbri has received fees from Mundipharma as a member of the scientific committee for the MEDITA study, and was corresponding author for that study. Dr Borobia has received fees from Mundipharma as a member of the scientific committee for InMEDIATE, as well as speaker fees from Mundipharma and Menarini. Dr Borobia is Principal Investigator on clinical trials sponsored by GSK, Daiichi Sankyo, Janssen and Farmalider. Dr Ricard-Hibon has served as an advisory board member for Mundipharma. Professor Coffey was chief investigator for the STOP! Study and has received honoraria to present at symposia sponsored by Mundipharma. Aurore Caumont-Prim and François Montestruc are employees of eXYSTAT, a contract research organization which received fees from Mundibiopharma Limited to perform the meta-analysis. Amedeo Soldi is an employee of Mundipharma Srl. Susana Traseira Lugilde is an employee of Mundipharma S.L. Sara Dickerson is an employee of Mundibiopharma Limited. The authors report no other conflicts of interest in this work.
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