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dc.contributor.authorFriesgaard, Kristian D.
dc.contributor.authorVist, Gunn Elisabeth
dc.contributor.authorHyldmo, Per Kristian
dc.contributor.authorRaatiniemi, Lasse
dc.contributor.authorKurola, Jouni
dc.contributor.authorLarsen, Robert
dc.contributor.authorKongstad, Poul
dc.contributor.authorMagnusson, Vidar
dc.contributor.authorSandberg, Mårten
dc.contributor.authorRehn, Marius
dc.contributor.authorRognås, Leif
dc.date.accessioned2022-04-12T08:09:28Z
dc.date.available2022-04-12T08:09:28Z
dc.date.created2022-04-11T14:10:54Z
dc.date.issued2022-01
dc.identifier.citationFriesgaard, K.D., Vist, G.E., Hyldmo, P.K., Raatiniemi, L., Kurola, J., Larsen, R., Kongstad, P., Magnusson, V., Sandberg, M., Rehn, M. & Rognås, L. (2022) Opioids for Treatment of Pre-hospital Acute Pain: A Systematic Review. Pain and Therapy, 11, 17-36.en_US
dc.identifier.issn2193-8237
dc.identifier.urihttps://hdl.handle.net/11250/2991009
dc.description.abstractIntroduction Acute pain is a frequent symptom among patients in the pre-hospital setting, and opioids are the most widely used class of drugs for the relief of pain in these patients. However, the evidence base for opioid use in this setting appears to be weak. The aim of this systematic review was to explore the efficacy and safety of opioid analgesics in the pre-hospital setting and to assess potential alternative therapies. Methods The PubMed, EMBASE, Cochrane Library, Centre for Reviews and Dissemination, Scopus, and Epistemonikos databases were searched for studies investigating adult patients with acute pain prior to their arrival at hospital. Outcomes on efficacy and safety were assessed. Risk of bias for each included study was assessed according to the Cochrane approach, and confidence in the evidence was assessed using the GRADE method. Results A total of 3453 papers were screened, of which the full text of 125 was assessed. Twelve studies were ultimately included in this systematic review. Meta-analysis was not undertaken due to substantial clinical heterogeneity among the included studies. Several studies had high risk of bias resulting in low or very low quality of evidence for most of the outcomes. No pre-hospital studies compared opioids with placebo, and no studies assessed the risk of opioid administration for subgroups of frail patients. The competency level of the attending healthcare provider did not seem to affect the efficacy or safety of opioids in two observational studies of very low quality. Intranasal opioids had a similar effect and safety profile as intravenous opioids. Moderate quality evidence supported a similar efficacy and safety of synthetic opioid compared to morphine. Conclusions Available evidence for pre-hospital opioid administration to relieve acute pain is scarce and the overall quality of evidence is low. Intravenous administration of synthetic, fast-acting opioids may be as effective and safe as intravenous administration of morphine. More controlled studies are needed on alternative routes for opioid administration and pre-hospital pain management for potentially more frail patient subgroups.en_US
dc.language.isoengen_US
dc.publisherSpringer Nature Switzerland AGen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.subjectsmertelindringen_US
dc.subjectsmertestillendeen_US
dc.subjectopioideren_US
dc.subjectsystematic reviewen_US
dc.titleOpioids for Treatment of Pre-hospital Acute Pain: A Systematic Reviewen_US
dc.title.alternativeOpioids for Treatment of Pre-hospital Acute Pain: A Systematic Reviewen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s) 2022en_US
dc.subject.nsiVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750en_US
dc.source.pagenumber17-36en_US
dc.source.volume11en_US
dc.source.journalPain and Therapyen_US
dc.identifier.doi10.1007/s40122-021-00346-w
dc.identifier.cristin2016756
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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