Serious adverse patient safety event review report
128T Serious adverse patient safety event review report
A SAPSE review panel must prepare and produce a report for the health service entities which appointed it as soon as practicable after completing an investigation into a serious adverse patient safety event.
A report under subsection (1) must contain one or more of the following elements as considered appropriate by the SAPSE review panel—
a description of the serious adverse patient safety event;
analysis identifying why the event happened and any factors that contributed to the event;
any recommendations about changes or improvements in a policy, procedure or practice relating to the provision of a health service that are intended to reduce the likelihood of, or prevent, the same type of event happening again;
any prescribed matter or requirement.
A report under subsection (1) must not contain—
the name or address of the following—
a person involved in providing the relevant health service;
a person who received the relevant health service;
a member of the SAPSE review panel;
any other prescribed information.
S. 128U inserted by No. 4/2022 s. 5.
This provision refers to the regulations (prescribed matter
, prescribed information
). Made under this Act:
- Health Services (Health Service Establishments) Regulations 2024 · under section 158
- Health Services (Quality and Safety) Regulations 2020 · under section 158
This Act’s bill:Second reading speech
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