The trajectory of patients who die from metastatic prostate cancer: a population-based study.


Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 30 10 2018
medline: 13 3 2020
entrez: 30 10 2018
Statut: ppublish

Résumé

To describe health service use, symptom and survival characteristics in metastatic prostate cancer (mPCa) in order to outline usual care practices and identify future opportunities to improve the quality of care in this patient group. This population cohort study, conducted in Victoria, Australia, used 10 years (2000-2010) of linked hospital discharge, emergency visit, and death registration data, to track patients from their first inpatient admission with mPCa until death. Descriptive statistics on inpatient health service use, symptoms, procedures, survival, and place of death are presented. In all, 4436 patients survived a median (interquartile range [IQR]) of 4 (1, 12) months from their first multiday admission with mPCa. They had a median (IQR) of 3 (1, 9) admissions, 1 (0, 2) emergency department presentation, and 35 (18, 63) days admitted to hospital. Lower urinary tract symptoms were common (50%), and 21% underwent lower urinary tract procedures, whilst 48% had blood product transfusions. In the last month of life, 3685 (83%) had at least one indicator of aggressive end-of-life care, including 48% with more than one acute hospital admission, and 55% staying ≥14 days. Hospital-based palliative care was accessed by 2657 (60%), occurring a median (IQR) of 30 (11, 74) days before death. In all, 23% died in the community, whilst 77% died in hospital, of whom 55% died in an acute hospital bed. Half of all decedents first admitted for a multiday stay with mPCa survived <4 months thereafter. They had a marked symptom burden, underwent multiple procedures and had multiple admissions. In all, 40% of patients did not receive any hospital-based palliative care. Several opportunities exist to improve the timely transition to palliative care services with mPCa. These data form a benchmark against which future improvements to palliative care integration may be measured.

Identifiants

pubmed: 30371986
doi: 10.1111/bju.14593
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

19-26

Informations de copyright

© 2018 The Authors BJU International © 2018 BJU International Published by John Wiley & Sons Ltd.

Auteurs

Anna Collins (A)

Department of Medicine, St Vincent's Hospital, University of Melbourne, Melbourne, Vic., Australia.

Vijaya Sundararajan (V)

Department of Medicine, St Vincent's Hospital, University of Melbourne, Melbourne, Vic., Australia.
Department of Public Health, La Trobe University, Melbourne, Vic., Australia.

Jeremy Millar (J)

Radiation Oncology, Alfred Health, Melbourne, Vic., Australia.

Jodie Burchell (J)

Department of Medicine, St Vincent's Hospital, University of Melbourne, Melbourne, Vic., Australia.

Brian Le (B)

Parkville Integrated Palliative Care Service, Victorian Comprehensive Cancer Centre, Melbourne, Vic., Australia.

Mei Krishnasamy (M)

Department of Nursing, University of Melbourne, Melbourne, Vic., Australia.

Sue-Anne McLachlan (SA)

Medical Oncology, St Vincent's Hospital, Melbourne, Vic., Australia.

Peter Hudson (P)

Centre for Palliative Care, St Vincent's Hospital Melbourne, University of Melbourne, Melbourne, Vic., Australia.
Vrije University, Brussels, Belgium.

Linda Mileshkin (L)

Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Vic., Australia.

Jennifer Philip (J)

Department of Medicine, St Vincent's Hospital, University of Melbourne, Melbourne, Vic., Australia.
Parkville Integrated Palliative Care Service, Victorian Comprehensive Cancer Centre, Melbourne, Vic., Australia.

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