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dc.contributor.authorBruera E.en
dc.contributor.authorHui D.en
dc.contributor.authorBush S.H.en
dc.contributor.authorGallo L.E.en
dc.contributor.authorPalmer J.L.en
dc.contributor.authorYennurajalingam S.en
dc.date.accessioned2021-05-14T10:30:02Zen
dc.date.available2021-05-14T10:30:02Zen
dc.date.copyright2010en
dc.date.created20100305en
dc.date.issued2012-10-11en
dc.identifier.citationJournal of Pain and Symptom Management. 39 (2) (pp 186-196), 2010. Date of Publication: February 2010.en
dc.identifier.issn0885-3924en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/31044en
dc.description.abstractNeuroleptics are commonly used in the management of delirium. Limited information is available regarding the dosage requirements and efficacy of neuroleptics in the palliative care setting. We determined the type and dose of neuroleptic use by delirium subtype. The medical records of 99 inpatients with advanced cancer were reviewed retrospectively. The doses of different neuroleptics, expressed as haloperidol equivalent daily doses (HEDDs), were correlated with delirium recall, recalled delirium symptom frequency, and associated distress from the patients', family caregivers', nurses' and palliative care specialists' perspectives. Subtypes of delirium included hypoactive in 20 (20%), mixed in 66 (67%), and hyperactive in 13 (13%). The median HEDD was 2.5 mg, interquartile range (Q1-Q3) 1-4.7 mg (mean 4.0 +/- 5.9 mg), and it was significantly higher in agitated and mixed delirium as compared with hypoactive delirium (P = 0.008). The neuroleptic dose was low and appeared to be ineffective in preventing patient delirium recall, with 73 (74%) patients remembering their episode of delirium as distressing. HEDD did not correlate with delirium recall, recalled symptom frequency, or distress for patients and family caregivers. However, HEDD increased with nurses' distress related to patients' symptoms (disorientation to place P = 0.002, disorientation to time P = 0.008, delusions P = 0.041, and agitation P < 0.001), and palliative care specialists' distress related to patients' hallucinatory symptoms (P = 0.006) and agitation (P = 0.006). In this study, the administered neuroleptic dose was influenced more by health care professional distress than by delirium symptom frequency. Future studies should examine the efficacy of neuroleptic dose according to individual delirium symptoms. © 2010 U.S. Cancer Pain Relief Committee.en
dc.languageEnglishen
dc.languageenen
dc.publisherElsevier Inc. (360 Park Avenue South, New York NY 10010, United States)en
dc.titleNeuroleptic Dose in the Management of Delirium in Patients with Advanced Cancer.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.jpainsymman.2009.07.009en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid20152585 [http://www.ncbi.nlm.nih.gov/pubmed/?term=20152585]en
dc.identifier.source358227056en
dc.identifier.institution(Hui, Bush, Gallo, Palmer, Yennurajalingam, Bruera) Department of Palliative Care and Rehabilitation Medicine, University of Texas M. D. Anderson Cancer Center, Houston, TX, United States (Bush) McCulloch House, Southern Health Care Network, Melbourne, Vic., Australia (Bush) Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton, Vic., Australiaen
dc.description.addressE. Bruera, Department of Palliative Care and Rehabilitation Medicine, University of Texas M. D. Anderson Cancer Center, Houston, TX, United States. E-mail: ebruera@mdanderson.orgen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2012 Elsevier B.V., All rights reserved.en
dc.subect.keywordsDelirium haloperidol neoplasms neuroleptic agents palliative careen
dc.identifier.authoremailBruera E.; ebruera@mdanderson.orgen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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