Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11828
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dc.contributor.authorTaylor, Simone Een
dc.contributor.authorTaylor, David McDen
dc.contributor.authorJao, Kathyen
dc.contributor.authorGoh, Shyanen
dc.contributor.authorWard, Meaganen
dc.date.accessioned2015-05-16T01:27:25Z
dc.date.available2015-05-16T01:27:25Z
dc.date.issued2013-07-21en
dc.identifier.citationEmergency Medicine Australasia : EMA 2013; 25(4): 316-23en
dc.identifier.govdoc23911022en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11828en
dc.description.abstractThe study aims to evaluate the impact of a nurse-initiated analgesia pathway (NIAP) intervention for paediatric patients in the ED.We undertook a pre- and post-intervention trial in a large, tertiary referral, mixed ED. The intervention comprised development and implementation of a comprehensive NIA Standing Order. In addition to paracetamol, which nurses could initiate pre-intervention, they were authorised to administer ibuprofen, paracetamol/codeine combinations and topical local anaesthetics prior to a doctor assessing the patient. All nurses were trained and credentialed prior to administering the NIAP. Patients aged 5-17 years with a triage pain score of ≥4 (Wong-Baker or numerical rating scale) were eligible for enrolment. The primary outcome was time to analgesia. Secondary outcomes were the proportion of patients who received 'adequate analgesia' and parental satisfaction with ED pain management (measured 48 h post-discharge).Fifty-one children were enrolled in both the pre- and post-intervention periods. Patient sex and mean age, weight and triage pain score did not differ between the groups (P > 0.05). At post-intervention, significantly more patients received nurse-initiated analgesia (3.0% vs 43.9%; P < 0.001) and the median time to analgesia was significantly reduced (58 min vs 23 min; P < 0.01). Also, significantly more patients received 'adequate analgesia' post-intervention (41.2% vs 72.5%; P < 0.001). At follow up, the proportion of parents who were very satisfied with their child's overall pain management trended upwards in the post-intervention period (47.1% vs 66.7%; P = 0.07). No adverse events were observed during either period.The NIAP significantly reduced time to analgesia. It was associated with high levels of parental satisfaction.en
dc.language.isoenen
dc.subject.otheremergency departmenten
dc.subject.otherpaediatricsen
dc.subject.otherpainen
dc.subject.otherAdolescenten
dc.subject.otherAnalgesia.nursingen
dc.subject.otherChilden
dc.subject.otherChild, Preschoolen
dc.subject.otherCritical Pathways.organization & administrationen
dc.subject.otherEmergency Service, Hospitalen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherPain Management.nursingen
dc.subject.otherParents.psychologyen
dc.subject.otherPatient Satisfactionen
dc.titleNurse-initiated analgesia pathway for paediatric patients in the emergency department: a clinical intervention trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleEmergency Medicine Australasia : EMAen
dc.identifier.affiliationDepartment of Pharmacy, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1111/1742-6723.12103en
dc.description.pages316-23en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23911022en
dc.type.austinJournal Articleen
local.name.researcherTaylor, David McD
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptPharmacy-
crisitem.author.deptEmergency-
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