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Title: | Sub-dissociative-dose intranasal ketamine for moderate to severe pain in adult emergency department patients. | Authors: | Yeaman F.;Graudins A. ;Rosengarten P.;Egerton-Warburton D. ;Meek R. | Institution: | (Yeaman, Meek, Egerton-Warburton, Graudins) Southern Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia (Meek) Emergency Medicine Research, Dandenong Hospital, Monash Health, Melbourne, VIC, Australia (Egerton-Warburton) Emergency Medicine Research, Monash Medical Centre, Monash Health, Melbourne, VIC, Australia (Rosengarten) Department of Emergency Medicine, Frankston Hospital, Peninsula Health, Melbourne, VIC, Australia (Graudins) Monash Emergency Research, Monash Medical Centre, Melbourne, VIC, Australia | Issue Date: | 17-Jun-2014 | Copyright year: | 2014 | Publisher: | Blackwell Publishing (E-mail: info@asia.blackpublishing.com.au) | Place of publication: | Australia | Publication information: | EMA - Emergency Medicine Australasia. 26 (3) (pp 237-242), 2014. Date of Publication: June 2014. | Journal: | EMA - Emergency Medicine Australasia | Abstract: | Background: There are currently no studies assessing effectiveness of sub-dissociative intranasal (IN) ketamine as the initial analgesic for adult patients in the ED. Objective(s): The study aims to examine the effectiveness of sub-dissociative IN ketamine as a primary analgesic agent for adult patients in the ED. Method(s): This is a prospective, observational study of adult ED patients presenting with severe pain (>=6 on 11-point scale at triage). IN ketamine dose was 0.7mg/kg, with secondary dose of 0.5mg/kg at 15min if pain did not improve. After 6 months, initial dose was increased to 1.0mg/kg with the same optional secondary dose. Primary outcomes: The primary outcomes are change in VAS rating at 30min; percentage of patients reporting clinically significant reduction in VAS (>=20mm) at 30min; dose resulting in clinically significant pain reduction. Result(s): Of the 72 patients available for analysis, median age was 34.5 years and 64% were men. Median initial VAS rating was 76mm (interquartile range [IQR]: 65-82). Median total dose of IN ketamine for all patients was 0.98mg/kg (IQR: 0.75-1.15, range: 0.59-1.57). Median reduction in VAS rating at 30min was 24mm (IQR: 2-45). Forty (56%, 95% CI: 44.0-66.7) reported VAS reduction >=20mm, these patients having had a total median ketamine dose of 0.94mg/kg (IQR: 0.72-1.04). Conclusion(s): IN ketamine, at a dose of about 1mg/kg, was an effective analgesic agent in 56% of study patients. The place of IN ketamine in analgesic guidelines for adults requires further investigation. © 2014 Australasian College for Emergency Medicine and Australasian Society for Emergency Medicine. | DOI: | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/1742-6723.12173 | PubMed URL: | 24712757 [http://www.ncbi.nlm.nih.gov/pubmed/?term=24712757] | ISSN: | 1742-6731 | URI: | https://repository.monashhealth.org/monashhealthjspui/handle/1/41689 | Type: | Article | Type of Clinical Study or Trial: | Observational study (cohort, case-control, cross sectional or survey) |
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