Literature DB >> 18722748

Using national health policies to improve access to palliative care medications in the community.

Debra Rowett1, Peter J Ravenscroft, Janet Hardy, David C Currow.   

Abstract

Access to affordable priority palliative care medicines needs to be informed by good clinical data from well-conducted clinical trials designed to address efficacy, cost-effectiveness, and safety. Availability of priority palliative care symptom control medicines improves the provision of palliation in the place of patient's choice including the community. Within Australia, a National Medicines Policy and a Palliative Care Strategy endorsed by Federal and State and Territory health ministers have facilitated a process to improve the evidence for palliative clinical practice and, through this, improve community availability of key medications for people at the end of life. The initiative, coordinated by a working party under government auspices, has brought together medicine regulators, the pharmaceutical industry, government, policy makers, and clinicians. The brief was to improve availability of key palliative care medications within the current national drug regulatory and funding frameworks. The results to date include: a palliative care section within the Pharmaceutical Benefits Scheme generating the first ever patient-defined section; medicines not previously listed now available; commitment of AU$9.46 M for a national multisite collaborative clinical study network to improve the evidence for clinical interventions in the palliative care setting through systematic investigation with rigorous Phase III and IV studies to inform registration and subsidy applications; and establishing a national Communication Network of the Palliative Care Medications Working Group for the health workforce and community to improve the quality use where improved access has been achieved.

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Year:  2008        PMID: 18722748     DOI: 10.1016/j.jpainsymman.2008.03.013

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  5 in total

1.  Cancer pain--progress and ongoing issues in Australia.

Authors:  David C Currow; Debra S Rowett
Journal:  Pain Res Manag       Date:  2009 Sep-Oct       Impact factor: 3.037

2.  Planning phase III multi-site clinical trials in palliative care: the role of consecutive cohort audits to identify potential participant populations.

Authors:  David Christopher Currow; Tania M Shelby-James; Meera Agar; John Plummer; Deborah Rowett; Paul Glare; Odette Spruyt; Janet Hardy
Journal:  Support Care Cancer       Date:  2009-11-29       Impact factor: 3.603

3.  Palliative care in Uganda: quantitative descriptive study of key palliative care indicators 2018-2020.

Authors:  Ainur Kagarmanova; Mark Donald Mwesiga; Matthew L Sisk; Cynthia Kabagambe; Sheba Nyakaisiki; Tom Marentette; Lacey N Ahern
Journal:  BMC Palliat Care       Date:  2022-04-22       Impact factor: 3.113

4.  Patients attended by palliative care teams: are they always comparable populations?

Authors:  Maria Nabal; Miquel Barcons; Roberto Moreno; Xavier Busquets; Javier J Trujillano; Antonio Requena
Journal:  Springerplus       Date:  2013-04-22

5.  Preliminary development and validation of a new end-of-life patient-reported outcome measure assessing the ability of patients to finalise their affairs at the end of life.

Authors:  Nikki McCaffrey; Pawel Skuza; Katrina Breaden; Simon Eckermann; Janet Hardy; Sheila Oaten; Michael Briffa; David Currow
Journal:  PLoS One       Date:  2014-04-15       Impact factor: 3.240

  5 in total

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