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Ministry of Health — Review of Adult Palliative Care Services in New Zealand, March 2017

Ministry of Health — Manatū Hauora

Publisher: Ministry of Health — Manatū Hauora; historical report hosted by Health NZ

End-of-Life & Palliative
PDF
Ministry of Health — Manatū Hauora
Published 30 March 2017
Authority5/5Freshness2/5Relevance5/5KB value5/5
Evidence class

Official guidance

Official primary

Reviewed

2026-10-10

Next review: 2027-04-10

Scope

New Zealand

High confidence

Status

verified

Primary-source future-planning audit, 10 October 2026

Evidence boundary: Historical Ministry of Health report published March 2017, based on adult review work October 2015–September 2016; it is not a new Health NZ 2026 review. The 22-page summary is distinct from the larger reference document and companion action plan. DHB self-assessments, four-region visits and targeted consultation are not a representative patient survey or independent proof of outcomes. 2016 forecasts, 2013/2015 setting data, historical funding, workforce predictions and DHB arrangements are not verified current observations, contracts, service access or treatment instructions. Recommendations and later proposed models do not prove implementation. All 22 pages were read and the current linked official PDF is byte-identical; this identity/full-source review does not verify every clinical/legal proposition against current guidance. Original filename/hash/category and June 2026 capture label are preserved separately from the July 2026 webpage update and October 2026 review.

Short Answer

Historical 2017 Ministry of Health summary of a 2015–2016 adult palliative-care review, now hosted by Health NZ; not a 2026 service review.

Why it matters

Use this historical baseline to trace palliative-care integration, equity, information and carer-support priorities into later policy and research. Compare forecasts only with their stated 2016 basis, consult Health NZ’s later work-programme sources for subsequent direction, and verify local care/referral/funding arrangements separately.

Key Points

  • •The cover says Released 2017 and the publication page identifies Ministry of Health, March 2017, HP 6516 and online ISBN 978-0-947515-82-9. Health NZ’s current hosting page gives publication as 30 March 2017; its separate last-update date is 22 July 2026 (physical pp.1–2).
  • •The original has 22 physical pages: four front-matter pages, including a blank page, followed by printed pp.1–18. It is a high-level summary of a larger reference document, not the separate Palliative Care Action Plan (physical pp.3–6).
  • •Review work ran October 2015–September 2016 and covered adult services. Sources include Ministry-commissioned projections, DHB self-assessments, stakeholder input, site visits in four regions and targeted consultation in July 2016; the appendix lists respondents, not a nationally representative patient sample (physical pp.5, 9–10, 16, 22).
  • •The report distinguishes primary and specialist palliative care, including direct specialist care and indirect advice/training. Figure 2 illustrates continuous or episodic specialist involvement alongside primary providers (physical pp.7–8 / printed pp.3–4). These are historical explanatory models, not individual referral or treatment instructions.
  • •It warns that place of death may not reflect the main place or provider of care, because people move between settings. Its setting statistics come from 2013 and Hospice NZ’s 2015 review, rather than current patient flows (physical p.9 / printed p.5).
  • •Reported barriers include uneven rural specialist coverage, variable referral criteria, information-sharing difficulties, funding/reporting differences and cultural appropriateness concerns. These are 2015–2016 review findings, not verified present-day regional service conditions (physical p.10 / printed p.6).

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Full Summary & Notes

Published by the Ministry of Health in March 2017, this report summarises a review conducted from October 2015 to September 2016. It draws on commissioned projections, DHB self-assessments, stakeholder engagement and targeted consultation to examine adult palliative care across homes, hospitals, hospices and aged residential care. It describes uneven integration and access, workforce and information gaps, and proposes five priorities: stronger primary palliative care, quality across settings, support for informal carers, patient/whānau voice and strategic coordination. Its 2016 projections, historical funding and DHB arrangements are not current service measurements or 2026 forecasts. Health NZ now hosts the byte-identical 22-page report; its July 2026 webpage update and the preserved 2026 filename do not make this a new review, clinical protocol or guarantee of current care availability.

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Document Details & Metadata

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