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Disability data gaps leave health inequities hidden, new report finds
New report exposes major gaps in NZ health data, leaving disabled people’s needs invisible. Linked data reveals systemic barriers, poorer outcomes, and urgent need for better data to drive equitable care improvements.
- About our patient experience surveys
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Pānui/information for whānau/families about post-mortem examination
This pānui is for whānau, families, parents, kaitiaki and caregivers who are trying to decide whether or not to consent to a post-mortem to be undertaken on their baby who has died during the perinatal period.
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Window on the quality of health care
A window on the quality of health care provides a snapshot of the quality of health care in New Zealand
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Eleventh Annual Report of the Perinatal and Maternal Mortality Review Committee
This report considers perinatal and maternal mortality and morbidity from 1 January to 31 December 2015; perinatal mortality from 2007 to 2015; maternal mortality from 2006 to 2015; and babies with neonatal encephalopathy from 2010 to 2015.
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Harm (adverse) event submission portal
Use this portal to report and manage harm (adverse) events, as part of the Healing, Learning and Improving from Harm policy. You can complete Part A and Part B sections, edit and review, and download your data.
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Sepsis information for patients and whānau
Information to help patients and whānau understand sepsis, treatment, intensive care and recovery.
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Publications
This page contains links to reports, journal articles and other publications related to the patient experience surveys.
- Guidance for engagement with consumers and whānau
- Health quality & safety news: Issue #45