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Cited 9 time in webofscience Cited 8 time in scopus
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Association between continuous deep sedation and survival time in terminally ill cancer patients

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dc.contributor.authorPark, So-Jung-
dc.contributor.authorAhn, Hee Kyung-
dc.contributor.authorAhn, Hong Yup-
dc.contributor.authorHan, Kyu-Tae-
dc.contributor.authorHwang, In Cheol-
dc.date.available2021-02-22T01:40:05Z-
dc.date.created2020-05-28-
dc.date.issued2021-05-
dc.identifier.issn0941-4355-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/80004-
dc.description.abstractPurpose Our study aimed to evaluate the association between CDS and survival time using the likelihood of receiving CDS to select a matched non-CDS group through an accurate measurement of survival time based on initiation of CDS. Methods A retrospective cohort study was performed using an electronic database to collect data regarding terminally ill cancer patients admitted to a specialized palliative care unit from January 2012 to December 2016. We first used a Cox proportional hazard model with receiving CDS as the outcome to identify individuals with the highest plausibility of receiving CDS among the non-CDS group (n = 663). We then performed a multiple regression analysis comparing the CDS group (n = 311) and weighted non-CDS group (n = 311), using initiation of CDS (actual for the CDS group; estimated for the non-CDS group) as the starting time-point for measuring survival time. Results Approximately 32% of participants received CDS. The most common indications were delirium or agitation (58.2%), intractable pain (28.9%), and dyspnea (10.6%). Final multiple regression analysis revealed that survival time was longer in the CDS group than in the non-CDS group (Exp(beta), 1.41; P < 0.001). Longer survival with CDS was more prominent in females, patients with renal dysfunction, and individuals with low C-reactive protein (CRP) or ferritin, compared with their counterpart subgroup. Conclusions CDS was not associated with shortened survival; instead, it was associated with longer survival in our terminally ill cancer patients. Further studies in other populations are required to confirm or refute these findings.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER-
dc.relation.isPartOfSUPPORTIVE CARE IN CANCER-
dc.titleAssociation between continuous deep sedation and survival time in terminally ill cancer patients-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000533038800001-
dc.identifier.doi10.1007/s00520-020-05516-8-
dc.identifier.bibliographicCitationSUPPORTIVE CARE IN CANCER, v.29, no.1, pp.525 - 531-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85084810143-
dc.citation.endPage531-
dc.citation.startPage525-
dc.citation.titleSUPPORTIVE CARE IN CANCER-
dc.citation.volume29-
dc.citation.number1-
dc.contributor.affiliatedAuthorAhn, Hee Kyung-
dc.contributor.affiliatedAuthorHwang, In Cheol-
dc.type.docTypeArticle; Early Access-
dc.subject.keywordAuthorContinuous deep sedation-
dc.subject.keywordAuthorPalliative sedation-
dc.subject.keywordAuthorSurvival-
dc.subject.keywordAuthorSedative-
dc.subject.keywordAuthorPalliative care-
dc.subject.keywordAuthorHospice-
dc.subject.keywordPlusPALLIATIVE SEDATION-
dc.subject.keywordPlusREFRACTORY SYMPTOMS-
dc.subject.keywordPlusCARE-
dc.subject.keywordPlusEND-
dc.subject.keywordPlusLIFE-
dc.subject.keywordPlusNETHERLANDS-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusPAIN-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaHealth Care Sciences & Services-
dc.relation.journalResearchAreaRehabilitation-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryHealth Care Sciences & Services-
dc.relation.journalWebOfScienceCategoryRehabilitation-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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