​​​NSW Perinatal Data Collection

The New South Wales Perinatal Data Collection (PDC) is a population-based surveillance system covering all births in NSW public and private hospitals, as well as home births. It encompasses all live births, and stillbirths of at least 20 weeks gestation or at least 400 grams birthweight.

The PDC relies on the attending midwife or doctor to complete an electronic notification when a birth occurs. The electronic notification captures items described in PD2015_025 NSW Perinatal Data Collection (PDC) Reporting and Submission Requirements from 1 January 2016.1 These items include demographic, maternal health, pregnancy, labour, birth, and perinatal outcomes. Completed notifications are transferred electronically to the state database, which is managed by System Information and Analytics Branch within the Patient Experience and System Performance Division of the NSW Ministry of Health. The PDC data dictionary can be found at CHeReL - Datasets.

There are several maternity information systems used in NSW hospitals that contribute information to the PDC. In 2022, the largest source of PDC records was eMaternity, which supplied 57.9% of all PDC records. Cerner systems supplied 17.1% of PDC records (public hospitals in Sydney and South Western Sydney Local Health Districts). Meditech, which includes 5 Ramsay Private Hospitals (North Shore Private Hospital, Westmead Private Hospital, St George Private Hospital, Kareena Private Hospital and Wollongong Private Hospital), supplied 8.2% of all PDC records. Healthscope Hospitals (Prince of Wales Private Hospital, Norwest Private Hospital, Sydney South West Private Hospital, Nepean Private Hospital, and Newcastle Private Hospital) supplied 7.6% of PDC records. The Mater Hospital, North Sydney, database supplied 2.4% of PDC records, 2.6% of PDC records were supplied from the Sydney Adventist Hospital database and 1.9% of PDC records were supplied from the Northern Beaches Hospital database.

The PDC receives notifications of women whose usual place of residence is outside NSW but who give birth in NSW. However, the PDC does not receive notifications of births outside NSW to women usually resident in NSW.

Maternal and Child Health Register

The Maternal and Child Health Register is a dataset of linked de-identified records that has been established under the Public Health and Disease Registers provisions of the NSW Public Health Act 2010. It includes records from the following data collections for children and young people aged less than 16 years and women aged 12 to 55 years:

  • NSW PDC for the period 1994 onwards (all records)
  • NSW Admitted Patient Data Collection (public hospitals) and the NSW Private Hospital Inpatient Statistics Collection for the period 1 July 2001 onwards (children and young people aged less than 16 years and women aged 12 to 55 years)
  • NSW Emergency Department Data Collection for the period 1 July 2005 onwards (children and young people aged less than 16 years and women aged 12 to 55 years)
  • NSW Register of Congenital Conditions for the most recently available 5-year period (all records)
  • Australian Bureau of Statistics Cause of Perinatal Death Unit Record File for the period 2017 onwards
  • Notifiable Conditions Information Management System for the period 1994 onwards (children and young people aged less than 16 years and women aged 12 to 55 years)
  • NSW Registry of Births, Deaths and Marriages death registrations for the period 1994 onwards (children and young people aged less than 16 years and women aged 12 to 55 years)
  • Australian Coordinating Registry Cause of Death Unit Record File for the period 1994 onwards (children and young people aged less than 16 years and women aged 12 to 55 years)
  • NSW Perinatal Death Review database for the period 1 January 2000 onwards (all records).

An Enhanced Reporting of Aboriginality (ERA) variable is available on the Maternal and Child Heath Register. This variable uses linkage with routinely collected population-based health and health-related data collections in NSW to obtain more accurate information about Aboriginal people than is currently available in individual collections, and thus is able to more accurately identify and monitor risk factors for diseases and conditions that are different for Aboriginal people compared to non-Aboriginal people.

Enhanced reporting relies on having independent sources of information on whether a person is Aboriginal or Torres Strait Islander.2 Each independent report is counted as a “unit of information” that contributes to the weight of evidence as to whether a person is reported as Aboriginal or Torres Strait Islander. ERA uses the following algorithm to determine whether a person is reported as Aboriginal:

  1. if a person is consistently reported as Aboriginal or Torres Strait Islander on all contributing sources of data, then the person is reported as Aboriginal or Torres Strait Islander
  2. if the person is not consistently reported as Aboriginal or Torres Strait Islander, then:
    1. if the person has 3 or more units of information across all contributing data sets, at least 2 indicating that the person is Aboriginal or Torres Strait Islander are required to report the person as Aboriginal or Torres Strait Islander
    2. otherwise, if the person has 1 or 2 units of information in all contributing data sets, 1 is sufficient to report the person as Aboriginal or Torres Strait Islander.
  3. if a person is consistently reported as unknown, not stated or the information is missing on all contributing data sets, then the person’s Aboriginality is reported as "missing".

For mothers and babies, ERA is based on the weight of evidence from linked records of the PDC, Admitted Patient Data Collection (APDC), Emergency Department Data Collection, Australian Coordinating Registry Cause of Death Unit Record File, and Register of Births, Deaths and Marriages (RBDM) birth registration data. In this web report, APDC records do not contribute to the mother’s or baby’s ERA where there is a corresponding linked PDC birth record. This is because, from 2012, information on a person’s Aboriginality as reported on the PDC is usually obtained from the hospital’s patient administration system and is not an independent source of information.

The Maternal and Child Health Register linkage is updated regularly for all years of data. Reported numbers of Aboriginal mothers and babies according to ERA for a particular birth year are subject to change as additional information on health service use is made available.

NSW Maternal and Perinatal Mortality Review Committee

The NSW Maternal and Perinatal Mortality Review Committee (MPMRC) was established under the Health Administration Act 1982​ (NSW), and is privileged under the Act to carry out confidential reviews of both maternal and perinatal deaths. Members are appointed by the Minister for Health.

The MPMRC reviews each maternal death to classify the death, identify the cause of death, ascertain any possible avoidable factors and identify lessons to be learnt. A sub-committee of MPMRC members, known as the Perinatal Mortality Review Subcommittee, reviews perinatal deaths among liveborn babies, and stillbirths of at least 20 weeks gestation or at least 400 grams birthweight. The information obtained from these reviews assists in the development of policies aimed at improving the health of mothers and newborns in NSW. Information considered by the Committee is confidential.

Perinatal Death Review Data Collection

Information on causes of death were obtained from the NSW Perinatal Death Review (PDR) for 2021. The PDR includes information on all perinatal deaths, including deaths that occurred after discharge or transfer from the hospital of birth; however, the PDR does not include death information for babies who were born in NSW and died interstate. Stillbirths and neonatal cause of death were classified to the Perinatal Society of Australia and New Zealand (PSANZ) Perinatal Death Classification.3 Information on causes of death is reported on the basis of the year of birth.

Map of NSW local health districts

Refer to Map of local health districts.

References

  1. NSW Ministry of Health. NSW Perinatal Data Collection (PDC) Reporting and Submission Requirements from 1 January 2016. Accessed 22 November 2023.
  2. Population and Public Health Division. Improved reporting of Aboriginal and Torres Strait Islander peoples on population datasets in New South Wales using record linkage – a feasibility study. Sydney: NSW Ministry of Health, 2012. Accessed 22 November 2023.
  3. Perinatal Society of Australia and New Zealand. Clinical Practice Guideline for Care Around Stillbirth and Neonatal Death, version 4.3, August 2020. Accessed 22 November 2023.

Current as at: Wednesday 31 July 2024