Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/50249
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dc.contributor.authorBall K.-
dc.contributor.authorCamilleri S.-
dc.contributor.authorKiefel S.-
dc.contributor.authorSchulz I.-
dc.contributor.authorWeston L.-
dc.contributor.authorSacks B.-
dc.date.accessioned2023-09-21T00:29:58Z-
dc.date.available2023-09-21T00:29:58Z-
dc.date.copyright2023-
dc.date.issued2023-09-11en
dc.identifier.citationJournal of Palliative Medicine. 26(8) (pp 1159-1164), 2023. Date of Publication: 01 Aug 2023.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/50249-
dc.description.abstractBackground: Epidermolysis bullosa (EB) comprises a group of rare genetic conditions that are characterized by fragility of the skin and mucous membranes and formation of blisters with minor trauma. Severe forms can be life limiting. The palliative care needs of children with severe EB are poorly described. Aim(s): The aim of this case series was to examine the contribution of a pediatric palliative care service to the complex health care needs of children with severe EB. Method(s): We present a case series of five children with severe forms of EB who were known to the state-wide Victorian Paediatric Palliative Care Service, with a discussion of our learnings in caring for these children and their families. Result(s): Medical treatment decision making in EB provokes complex ethical, psychological, personal, and professional dilemmas. This case series highlights the diversity of management approaches that may be considered, each tailored to the unique context of the child and family.Copyright © Mary Ann Liebert, Inc.-
dc.publisherMary Ann Liebert Inc.-
dc.relation.ispartofJournal of Palliative Medicine-
dc.subject.meshanalgesia-
dc.subject.meshblister-
dc.subject.meshdistress syndrome-
dc.subject.meshepidermolysis bullosa-
dc.subject.meshgastrointestinal hemorrhage-
dc.subject.meshglomerulonephritis-
dc.subject.meshimmunoglobulin A nephropathy-
dc.subject.meshmusic therapy-
dc.subject.meshnurse consultant-
dc.subject.meshnutritional intolerance-
dc.subject.meshpain-
dc.subject.meshpalliative therapy-
dc.subject.meshpediatric patient-
dc.subject.meshpruritus-
dc.subject.meshsepsis-
dc.subject.meshsleep disorder-
dc.subject.meshteleconsultation-
dc.subject.meshwound-
dc.subject.meshanalgesic agent-
dc.subject.meshbath-
dc.titleEpidermolysis Bullosa in Pediatric Palliative Care: A Case Series.-
dc.typeArticle-
dc.identifier.affiliationSupportive and Palliative Care-
dc.type.studyortrialCase series or case report-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1089/jpm.2022.0559-
dc.publisher.placeUnited States-
dc.identifier.pubmedid36888536 [https://www.ncbi.nlm.nih.gov/pubmed/?term=36888536]-
dc.identifier.institution(Ball) Department of Pediatrics, Women's and Children's Hospital, SA, Australia-
dc.identifier.institution(Camilleri, Kiefel, Schulz, Sacks) Department of Paediatric Palliative Care, Royal Children's Hospital, Melbourne, VIC, Australia-
dc.identifier.institution(Weston) Department of Dermatology, Royal Children's Hospital, Melbourne, VIC, Australia-
dc.identifier.institution(Sacks) Murdoch Children's Research Institute, Monash Health, Parkville, VIC, Australia-
dc.identifier.affiliationmh(Sacks) Murdoch Children's Research Institute, Monash Health, Parkville, VIC, Australia-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
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