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dc.contributor.authorBugge, Helge Fagerheim
dc.contributor.authorGuterud, Mona
dc.contributor.authorBache, Kristi Cecilie Grønvold
dc.contributor.authorBraarud, Anne-Cathrine
dc.contributor.authorEriksen, Erik
dc.contributor.authorFremstad, Kjell Otto
dc.contributor.authorIhle-Hansen, Hege
dc.contributor.authorIngebretsen, Svein Håkon
dc.contributor.authorKramer-Johansen, Jo
dc.contributor.authorLarsen, Karianne
dc.contributor.authorRøislien, Jo
dc.contributor.authorThorsen, Kjetil
dc.contributor.authorToft, Mathias
dc.contributor.authorSandset, Else Charlotte
dc.contributor.authorHov, Maren Ranhoff
dc.coverage.spatialNorwayen_US
dc.date.accessioned2022-09-27T11:55:45Z
dc.date.available2022-09-27T11:55:45Z
dc.date.created2022-05-20T08:18:33Z
dc.date.issued2022-02-04
dc.identifier.citationTrials. 2022, 23 (1), .en_US
dc.identifier.issn1745-6215
dc.identifier.urihttps://hdl.handle.net/11250/3021778
dc.description.abstractBackground: Less than 50% of stroke patients in Norway reach hospital within 4 h of symptom onset. Early prehospital identification of stroke and triage to the right level of care may result in more patients receiving acute treatment. Quality of communication between paramedics and the stroke centre directly affects prehospital on-scene time, emphasising this as a key factor to reduce prehospital delay. Prehospital stroke scales are developed for quick and easy identification of stroke, but have poor sensitivity and specificity compared to an in-hospital assessment with the National Institutes of Health Stroke Scale (NIHSS). The aim of the Paramedic Norwegian Acute Stroke Prehospital Project (ParaNASPP) is to assess whether a structured learning program, prehospital NIHSS and a mobile application facilitating communication with the stroke physician may improve triage of acute stroke patients. Methods: A stepped wedge cluster randomised controlled intervention design will be used in this trial in Oslo, Norway. Paramedics at five ambulance stations will enrol adult patients with suspected stroke within 24 h of symptom onset. All paramedics will begin in a control phase with standard procedures. Through an e-learning program and practical training, a random and sequential switch to the intervention phase takes place. A mobile application for NIHSS scoring, including vital patient information for treatment decisions, transferring data from paramedics to the on-call stroke physician at the Stroke Unit at Oslo University Hospital, will be provided for the intervention. The primary outcome measure is positive predictive value (PPV) for prehospital identification of patients with acute stroke defined as the proportion of patients accepted for stroke evaluation and discharged with a final stroke diagnosis. One thousand three hundred patients provide a 50% surplus to the 808 patients needed for 80% power to detect a 10% increase in PPV. Discussion: Structured and digital communication using a common scale like NIHSS may result in increased probability for better identification of stroke patients and less stroke mimics delivered to a stroke team for acute diagnostics and treatment in our population.en_US
dc.description.sponsorshipThe study is funded by the Norwegian Air Ambulance Foundation and Oslo University Hospital, Norway.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.ispartofseriesTrials;23, Article number: 113 (2022)
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectParamedicsen_US
dc.subjectAmbulancesen_US
dc.subjectStrokesen_US
dc.subjectNational Institutes of Health Stroke Scaleen_US
dc.subjectTriagesen_US
dc.subjectPositive predictive valuesen_US
dc.subjectMobile applicationsen_US
dc.titleParamedic Norwegian Acute Stroke Prehospital Project (ParaNASPP) study protocol: a stepped wedge randomised trial of stroke screening using the National Institutes of Health Stroke Scale in the ambulanceen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s). 2022en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1186/s13063-022-06006-4
dc.identifier.cristin2025813
dc.source.journalTrialsen_US
dc.source.volume23en_US
dc.source.issue1en_US
dc.source.pagenumber1-11en_US


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