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      Evaluation of pain relief treatment and timelines in emergency care in six European countries and Australia

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          Abstract

          Purpose

          Inadequate relief of pain is common in prehospital and hospital emergency department (ED) settings. We investigated pain treatments and timelines in patients receiving pre-hospital and hospital ED care to provide insight into potential approaches to reduce the burden of trauma-related pain.

          Patients and methods

          In this observational, retrospective chart review, patients had received emergency care for musculoskeletal trauma injuries and analgesic treatment for moderate-to-severe pain in Belgium, France, Germany, Italy, Spain or Sweden. As inhaled low-dose methoxyflurane (LDM) is used extensively in Australia but was not widely available in Europe at the time of this analysis, data from Australia were collated to provide insight into the potential utility of this analgesic in Europe. The primary endpoint was time to administration of first pain relief treatment following arrival of paramedic/ED care.

          Results

          Randomly selected physicians (n=189) collated data from 856 patients (Europe: n=585; Australia: n=271) via an online survey. Time to first pain relief treatment varied between countries and was significantly longer across Europe versus Australia (mean [SD] 38.1 [34.7] vs 29.9 [35.5] mins; P=0.0017). Patients from Australia who received LDM experience a shorter mean (SD) time to first pain treatment following arrival of emergency care versus patients who received other analgesics (propensity score matched [n=85] per group: 21.7 [24.2] vs 39.1 [43.0] mins; P=0.0013). Across all countries, mean (SD) time to first analgesic was shorter when treatment was administered by paramedics versus hospital ED staff (15.7 [14.7] vs 49.1 [38.4] mins).

          Conclusions

          While there was a large variation in analgesia timelines across countries, mean times are shorter in Australia compared with Europe overall. In Australia, use of LDM was associated with a significantly shorter time from emergency assistance to first pain treatment compared with non-LDM treatments. Further studies are needed to investigate the utility of LDM in Europe.

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          Most cited references15

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          Causes and consequences of inadequate management of acute pain.

          Intense acute pain afflicts millions of patients each year. Despite the recently increased focus on the importance of pain control, management of acute pain has remained suboptimal.
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            Undertreatment of acute pain (oligoanalgesia) and medical practice variation in prehospital analgesia of adult trauma patients: a 10 yr retrospective study.

            Prehospital oligoanalgesia is prevalent among trauma victims, even when the emergency medical services team includes a physician. We investigated if not only patients' characteristics but physicians' practice variations contributed to prehospital oligoanalgesia.
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              STOP!: a randomised, double-blind, placebo-controlled study of the efficacy and safety of methoxyflurane for the treatment of acute pain

              Objective To evaluate the short-term efficacy and safety of methoxyflurane for the treatment of acute pain in patients presenting to an emergency department (ED) with minor trauma. Methods STOP! was a randomised, double-blind, multicentre, placebo-controlled study conducted at six sites in the UK. A total of 300 patients, 90 of whom were adolescent patients (age 12–17 years), were randomised 150:150 to receive either methoxyflurane via a Penthrox inhaler or placebo. The primary end point of the study was the change in pain intensity as measured using the visual analogue scale (VAS) from baseline to 5, 10, 15 and 20 min after the start of study drug inhalation. Patients were supplied with one inhaler containing 3 mL methoxyflurane or 5 mL placebo after enrolment and initial assessments. Age group (adolescent/adult) and baseline VAS score were controlled for in the statistical analyses. Results A total of 149 patients received methoxyflurane, and 149 patients received placebo. Demographic and baseline characteristics were comparable between the groups. Methoxyflurane reduced pain severity significantly more than placebo (p<0.0001) at all time points tested, with the greatest estimated treatment effect of −18.5 mm (adjusted change from baseline) seen at 15 min after the start of treatment. Methoxyflurane was well tolerated, with the majority of adverse reactions being mild, transient and in line with anticipated pharmacological action. Conclusion The results of this study suggest that methoxyflurane administered via the Penthrox inhaler is an efficacious, safe, and rapidly acting analgesic. Trial registration number: NCT01420159.
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                Author and article information

                Journal
                Open Access Emerg Med
                Open Access Emerg Med
                OAEM
                oaem
                Open Access Emergency Medicine : OAEM
                Dove
                1179-1500
                17 September 2019
                2019
                : 11
                : 229-240
                Affiliations
                [1 ]Mundipharma International Limited , Cambridge, UK
                [2 ]Mundibiopharma Limited , Cambridge, UK
                [3 ]Canterbury and Concord Hospitals , Sydney, NSW, Australia
                [4 ]Covance Market Access Inc ., Solna, Sweden
                [5 ]Covance Market Access Inc , Sydney, NSW, Australia
                [6 ]Covance Market Access Inc ., Leeds, UK
                Author notes
                Correspondence: Sara L DickersonMundibiopharma Limited , Cambridge Science Park, Milton Road, CambridgeCB4 0AB, UKTel +44 0 122 339 7684Email sara.dickerson@mundipharma.com
                Author information
                http://orcid.org/0000-0002-0002-7217
                http://orcid.org/0000-0002-9321-1602
                http://orcid.org/0000-0001-6955-6339
                http://orcid.org/0000-0002-7749-6345
                http://orcid.org/0000-0002-5880-3354
                Article
                214396
                10.2147/OAEM.S214396
                6756271
                3243cfc0-ccdb-4d7b-bc3f-e4543af71c32
                © 2019 Xia et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 14 May 2019
                : 21 August 2019
                Page count
                Figures: 3, Tables: 3, References: 20, Pages: 12
                Categories
                Original Research

                methoxyflurane,pain management,ambulance,retrospective study,emergency medical service,analgesia

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