Healthcare utilization at the end of life in people dying from amyotrophic lateral sclerosis: A retrospective cohort study using linked administrative data
Background: ALS is an incurable neurodegenerative disorder, with the recommendation that symptom management and palliative care start immediately or soon after diagnosis. However, little is known about healthcare utilization at the end of life in this patient group. Aim: To describe healthcare utilization at the end of life in patients who died from ALS. Design: We performed a retrospective cohort study using population-level administrative databases. The description of healthcare utilization was based on (1) validated quality indicators for end-of-life care, and (2) the European Federation of... Mehr ...
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Dokumenttyp: | Artikel |
Erscheinungsdatum: | 2019 |
Verlag/Hrsg.: |
Elsevier
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Schlagwörter: | Neurodegenerative disease / Palliative care / Registries / Retrospective studie / Aged / 80 and over / Amyotrophic Lateral Sclerosi / Belgium / Cohort Studie / Databases / Factual / Female / Human / Male / Middle Aged / Terminal Care / Patient Acceptance of Health Care / Settore MED/06 - Oncologia Medica / Settore MED/09 - Medicina Interna |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-26573384 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://hdl.handle.net/2434/909145 |