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Privacy of PMMRC Information

As with all people who deal with health information, the PMMRC and its agents must adhere to the Privacy Act 1993 and the associated
Health Information Privacy Code.

The purpose of the data collection*

Broadly, the purpose of data collection for the PMMRC is outlined in the New Zealand Public Health and Disability Act 2000 (Part 2 s18(1)(a) and (b)), which describes the PMMRC’s function to review and report to the Minster with a view to reducing the numbers of death and to continuous quality improvement.


Sources of the PMMRC data

The death of a baby or a mother is likely to be a difficult time for family members and so information is usually obtained from reliable ‘indirect’ sources such as health professionals and national databases, not directly from the family. Family are welcome to provide information if they wish to do so.

The legislation gives agents of PMMRC the authority to collect data however families should not feel coerced into to supplying information and it is essential that family members or others do not find the data collection process for the PMMRC intrusive.

Transfer, storage, security, and accuracy

Data is treated with utmost care. It is not emailed but is transferred using a password, protected website, sending discs via registered courier post or by using a secure fax machine. Paper records are kept to a minimum and are stored in locked filing cabinets. Any documents which need destruction are destroyed by an approved Document Security Service.

Everyone involved with mortality review is encouraged to have their unique, complex password.

The database uses secure socket layer (SSL) connections for the transmission of data. This involves the encryption of the information transmitted between the web server and the web client, such that it will be unreadable by anyone intercepting it at any point between. It also allows the user to be certain that they are connected to the correct web server. SSL is widely used for online financial transactions by banks and companies around the world.

All agents of the PMMRC have to sign a confidentiality statement before they are appointed as agents and every three years thereafter. Agents who do not adhere to the confidentially requirements are liable to a fine up to $10,000.

The formal agreement (contract) that the Ministry of Health undertakes with the Mortality Database Group to run the PMMRC database outlines the requirements for the Database Group to manage the data safely.

Accuracy of information is important for the work of the PMMRC and families who are involved in a death may also want assurance that every effort is made to ensure the PMMRC data are accurate. The agreement (mentioned above) outlines the requirements for the Database Group to make every effort to ensure data is accurate.

The system used by the Mortatliy Database Group means that there is triangulation of data coming in from various sources (including family if they choose).

The Maori committee members of both PMMRC and CYMRC along with those of the Quality Improvement Committee (QIC) meet as a group at least annually and are available to consider issues about access to and security of the data in relation to Maori.

Disclosure of data

PMMRC data does not have to be released under the Official Information Act 1982.

PMMRC data cannot be obtained by the Police and the Coroner (unless they are investigating a crime punishable by 2 years, or more imprisonment) or the Health and Disability Commissioner.

Reports to the Minister (which are released publicly) do not identify any individual.

All requests for PMMRC data (including those for research) are required to be in writing and are reviewed by a Scientific Group of the Committee.

PMMRC and Protected Quality Assurance Activities (PQAA)

People involved in the PMMRC process may also be involved in protected quality assurance activities (PQAA) which are described in the Health Practitioners Competence Assurance Act 2003 and approved by the Minster. The purpose of PQAA is to improve the competence and practice of individual health practitioners.

The purpose of the PMMRC is to review and report to the Minster on baby or mother deaths with a review to reducing the number of those death. Thus the two processes are quite different, one focuses on improving the competence of individual health practitioners and the other on providing high level policy advice to the Minister.

However relevant information generated in a PQAA can be disclosed to the PMMRC or an agent unless one of the exemptions listed in Schedule 5 of the New Zealand Public Health and Disability Act 2000 appy.


* Headings adapted from Elisabeth Harding’s Privacy Framework.