The Economic Impact on Australian Patients with Neuroendocrine Tumours.


Journal

The patient
ISSN: 1178-1661
Titre abrégé: Patient
Pays: New Zealand
ID NLM: 101309314

Informations de publication

Date de publication:
06 2020
Historique:
pubmed: 20 2 2020
medline: 28 5 2021
entrez: 20 2 2020
Statut: ppublish

Résumé

Little is known about the economic burden to patients and families with neuroendocrine tumours (NETs) for medical out-of-pocket expenses and employment decisions. This study was performed to determine the extent and factors influencing the financial consequences of living with NETs and their effect on quality of life. We undertook an online cross-sectional survey using a targeted approach and collected Australian Medicare claims data. Validated surveys measured health-related quality of life (EuroQol 5-dimension 5-level [EuroQol-5D-5L]) and financial toxicity (COmprehenSive Financial Toxicity [COST]), supplemented with questions on employment and retirement, insurance and out-of-pocket medical expenses. Generalised linear models were performed to assess determinants of quality of life and out-of-pocket expenses recorded by Medicare. The survey was answered by 204 patients with a mean age of 59 years who were diagnosed on average 5.2 years ago. Self-reported mean costs were 1698 Australian dollars ($A) (standard deviation [SD] $A2132) over 3 months (median $A877) and were highest for medical tests (mean $A376 [17% of total costs], SD $A722), travel-related expenses (mean $A289 [13%], SD $A559), and specialist visits (mean $A225 [10%], SD $A342) ($A1 = $US0.69). Imaging scans, surgery and travel expenses were the most common cost burdens reported by patients. Having private health insurance was the key determinant of higher out-of-pocket costs. Poorer quality of life was significantly associated with higher financial toxicity, not working due to cancer, nausea/diarrhoea, two or more co-morbidities and younger age. Medical expenses are substantial for some patients with NETs. Quality of life is adversely affected for patients experiencing financial toxicity and avoiding early retirement is an important issue for supportive care services.

Sections du résumé

BACKGROUND AND OBJECTIVE
Little is known about the economic burden to patients and families with neuroendocrine tumours (NETs) for medical out-of-pocket expenses and employment decisions. This study was performed to determine the extent and factors influencing the financial consequences of living with NETs and their effect on quality of life.
METHODS
We undertook an online cross-sectional survey using a targeted approach and collected Australian Medicare claims data. Validated surveys measured health-related quality of life (EuroQol 5-dimension 5-level [EuroQol-5D-5L]) and financial toxicity (COmprehenSive Financial Toxicity [COST]), supplemented with questions on employment and retirement, insurance and out-of-pocket medical expenses. Generalised linear models were performed to assess determinants of quality of life and out-of-pocket expenses recorded by Medicare.
RESULTS
The survey was answered by 204 patients with a mean age of 59 years who were diagnosed on average 5.2 years ago. Self-reported mean costs were 1698 Australian dollars ($A) (standard deviation [SD] $A2132) over 3 months (median $A877) and were highest for medical tests (mean $A376 [17% of total costs], SD $A722), travel-related expenses (mean $A289 [13%], SD $A559), and specialist visits (mean $A225 [10%], SD $A342) ($A1 = $US0.69). Imaging scans, surgery and travel expenses were the most common cost burdens reported by patients. Having private health insurance was the key determinant of higher out-of-pocket costs. Poorer quality of life was significantly associated with higher financial toxicity, not working due to cancer, nausea/diarrhoea, two or more co-morbidities and younger age.
CONCLUSIONS
Medical expenses are substantial for some patients with NETs. Quality of life is adversely affected for patients experiencing financial toxicity and avoiding early retirement is an important issue for supportive care services.

Identifiants

pubmed: 32072460
doi: 10.1007/s40271-020-00412-z
pii: 10.1007/s40271-020-00412-z
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

363-373

Auteurs

Louisa G Gordon (LG)

Population Health Department, QIMR Berghofer Medical Research Institute, Royal Brisbane Hospital, Herston, Locked Bag 2000, Brisbane, QLD, 4029, Australia. louisa.gordon@qimrberghofer.edu.au.
School of Nursing and Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Brisbane, QLD, 4059, Australia. louisa.gordon@qimrberghofer.edu.au.
The University of Queensland, Herston, Brisbane, QLD, 4006, Australia. louisa.gordon@qimrberghofer.edu.au.

Thomas M Elliott (TM)

Population Health Department, QIMR Berghofer Medical Research Institute, Royal Brisbane Hospital, Herston, Locked Bag 2000, Brisbane, QLD, 4029, Australia.

Kate Wakelin (K)

Unicorn Foundation, PO Box 384, Blairgowrie, VIC, 3942, Australia.

Simone Leyden (S)

Unicorn Foundation, PO Box 384, Blairgowrie, VIC, 3942, Australia.

John Leyden (J)

Unicorn Foundation, PO Box 384, Blairgowrie, VIC, 3942, Australia.

Michael Michael (M)

Neuroendocrine Unit (ENETs Centre of Excellence), Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.

Nick Pavlakis (N)

Royal North Shore Hospital, Sydney, NSW, 2065, Australia.
The University of Sydney, Sydney, NSW, 2006, Australia.

Jan Mumford (J)

Australian Gastro Intestinal Trials Group, CommNETS, Sydney, NSW, 2000, Australia.

Eva Segelov (E)

Monash University and Monash Health, Melbourne, VIC, 3800, Australia.

David K Wyld (DK)

School of Nursing and Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Brisbane, QLD, 4059, Australia.
The University of Queensland, Herston, Brisbane, QLD, 4006, Australia.
Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, 4006, Australia.

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