Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12904-017-0267-z
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dc.titlePaediatric palliative care improves patient outcomes and reduces healthcare costs: Evaluation of a home-based program
dc.contributor.authorChong, P.H
dc.contributor.authorDe Castro Molina, J.A
dc.contributor.authorTeo, K
dc.contributor.authorTan, W.S
dc.date.accessioned2020-10-27T10:16:54Z
dc.date.available2020-10-27T10:16:54Z
dc.date.issued2018
dc.identifier.citationChong, P.H, De Castro Molina, J.A, Teo, K, Tan, W.S (2018). Paediatric palliative care improves patient outcomes and reduces healthcare costs: Evaluation of a home-based program. BMC Palliative Care 17 (1) : 11. ScholarBank@NUS Repository. https://doi.org/10.1186/s12904-017-0267-z
dc.identifier.issn1472684X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181228
dc.description.abstractBackground Around the world, different models of paediatric palliative care have responded to the unique needs of children with life shortening conditions. However, research confirming their utility and impact is still lacking. This study compared patient-related outcomes and healthcare expenditures between those who received home-based paediatric palliative care and standard care. The quality of life and caregiver burden for patients receiving home-based paediatric palliative care were also tracked over the first year of enrolment to evaluate the service's longitudinal impact. Method A structured impact and cost evaluation of Singapore-based HCA Hospice Care's Star PALS (Paediatric Advance Life Support) programme was conducted over a three-year period, employing both retrospective and prospective designs with two patient groups. Results Compared to the control group (n = 67), patients receiving home-based paediatric palliative care (n = 71) spent more time at home than in hospital in the last year of life by 52 days (OR = 52.30, 95% CI: 25.44-79.17) with at least two fewer hospital admissions (OR = 2.46, 95% CI: 0.43-4.48); and were five times more likely to have an advance care plan formulated (OR = 5.51, 95% CI: 1.55-19.67). Medical costs incurred by this group were also considerably lower (by up to 87%). Moreover, both patients' quality of life (in terms of pain and emotion), and caregiver burden showed improvement within the first year of enrolment into the programme. Discussion Our findings suggest that home-based paediatric palliative care brings improved resource utilization and cost-savings for both patients and healthcare providers. More importantly, the lives of patients and their caregivers have improved, with terminally ill children and their caregivers being able to spend more quality time at home at the final stretch of the disease. Conclusions The benefits of a community paediatric palliative care programme have been validated. Study findings can become key drivers when engaging service commissioners or even policy makers in appropriate settings. © 2018, The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadult
dc.subjectadvance care planning
dc.subjectArticle
dc.subjectcaregiver burden
dc.subjectcohort analysis
dc.subjectcontrolled study
dc.subjectcystic fibrosis
dc.subjectDuchenne muscular dystrophy
dc.subjecteconomic aspect
dc.subjectethnicity
dc.subjectfemale
dc.subjecthealth care cost
dc.subjecthealth care policy
dc.subjecthealth care utilization
dc.subjecthospice care
dc.subjecthospitalization
dc.subjecthuman
dc.subjectlength of stay
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectpalliative therapy
dc.subjectpediatric advanced life support
dc.subjectpediatric palliative care
dc.subjectprematurity
dc.subjectprospective study
dc.subjectquality of life
dc.subjectretrospective study
dc.subjectterminal care
dc.subjectadolescent
dc.subjectchild
dc.subjecthealth care cost
dc.subjecthome care
dc.subjectinfant
dc.subjectorganization and management
dc.subjectoutcome assessment
dc.subjectpalliative therapy
dc.subjectpediatrics
dc.subjectpreschool child
dc.subjectpsychology
dc.subjectSingapore
dc.subjectstandards
dc.subjectstatistics and numerical data
dc.subjectAdolescent
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectCohort Studies
dc.subjectFemale
dc.subjectHealth Care Costs
dc.subjectHome Care Services
dc.subjectHumans
dc.subjectInfant
dc.subjectMale
dc.subjectPalliative Care
dc.subjectPatient Outcome Assessment
dc.subjectPediatrics
dc.subjectProspective Studies
dc.subjectQuality of Life
dc.subjectRetrospective Studies
dc.subjectSingapore
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s12904-017-0267-z
dc.description.sourcetitleBMC Palliative Care
dc.description.volume17
dc.description.issue1
dc.description.page11
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