Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26092
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dc.contributor.authorGrayson, Kim E-
dc.contributor.authorBailey, Michael-
dc.contributor.authorBalachandran, Mayurathan-
dc.contributor.authorBanneheke, Piyusha P-
dc.contributor.authorBelletti, Alessandro-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorNaorungroj, Thummaporn-
dc.contributor.authorSerpa Neto, Ary-
dc.contributor.authorWright, Jason D-
dc.contributor.authorYanase, Fumitaka-
dc.contributor.authorYoung, Paul J-
dc.contributor.authorShehabi, Yahya-
dc.date2021-02-23-
dc.date.accessioned2021-03-24T21:38:57Z-
dc.date.available2021-03-24T21:38:57Z-
dc.date.issued2021-07-01-
dc.identifier.citationCritical Care Medicine 2021; 49(7): 1118-1128en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26092-
dc.description.abstractPrevious case series reported an association between dexmedetomidine use and hyperthermia. Temperature data have not been systematically reported in previous randomized controlled trials evaluating dexmedetomidine. A causal link between dexmedetomidine administration and elevated temperature has not been demonstrated. Post hoc analysis. Four ICUs in Australia and New Zealand. About 703 mechanically ventilated ICU patients. Early sedation with dexmedetomidine versus usual care. The primary outcome was mean daily body temperature. Secondary outcomes included the proportions of patients with body temperatures greater than or equal to 38.3°C and greater than or equal to 39°C, respectively. Outcomes were recorded for 5 days postrandomization in the ICU. The mean daily temperature was not different between the dexmedetomidine (n = 351) and usual care (n = 352) groups (36.84°C ± SD vs 36.78°C ± SD; p = 0.16). Over the first 5 ICU days, more dexmedetomidine group (vs usual care) patients had a temperature greater than or equal to 38.3°C (43.3% vs 32.7%, p = 0.004; absolute difference 10.6 percentage points) and greater than or equal to 39.0°C (19.4% vs 12.5%, p = 0.013; absolute difference 6.9 percentage points). Results were similar after adjusting for diagnosis, admitting temperature, age, weight, study site, sepsis occurrence, and the time from dexmedetomidine initiation to first hyperthermia recorded. There was a significant dose response relationship with temperature increasing by 0.30°C ±0.08 for every additional 1 μg/kg/hr of dexmedetomidine received p < 0.0002. Our study suggests potentially important elevations in body temperature are associated with early dexmedetomidine sedation, in adults who are mechanically ventilated in the ICU.en
dc.language.isoeng-
dc.titleThe Effect of Early Sedation With Dexmedetomidine on Body Temperature in Critically Ill Patients.en
dc.typeJournal Articleen
dc.identifier.journaltitleCritical Care Medicineen
dc.identifier.affiliationIntensive Care Unit, Wellington Hospital, Wellington, New Zealanden
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australiaen
dc.identifier.affiliationUniversity of Melbourne, Parkville, VIC, Australiaen
dc.identifier.affiliationMonash University, School of Clinical Sciences, Clayton, VIC, Australiaen
dc.identifier.affiliationData Analytics Research and Evaluation Centre, Austin Hospital and University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.affiliationDepartment of Anaesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italyen
dc.identifier.affiliationIntensive Care Unit, Austin Hospital, Heidelberg, VIC, Australiaen
dc.identifier.affiliationIntensive Care, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailanden
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, São Paulo, Brazilen
dc.identifier.affiliationIntensive Care Unit, Royal Melbourne Hospital, Parkville, VIC, Australiaen
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellington, New Zealanden
dc.identifier.affiliationIntensive Care Unit, Monash Medical Centre, Clayton, VIC, Australiaen
dc.identifier.affiliationUniversity of New South Wales, Prince of Wales Clinical School of Medicine, Randwick, NSW, Australiaen
dc.identifier.doi10.1097/CCM.0000000000004935en
dc.type.contentTexten
dc.identifier.pubmedid33729724-
local.name.researcherBellomo, Rinaldo
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
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