- Status Complete
- Type Re-application
- Pre-PASC consultation -
- Pre-MSAC consultation -
- Outcome Not supported
Application details
Reason for application
New MBS item.
Service or technology in this application
Non-invasive prenatal testing through the analysis of cell free fetal DNA is a major technological advancement in testing for fetal aneuploidy.
Type: Investigative
Medical condition this application addresses
The medical conditions relevant to the proposed service are conditions such as Down syndrome, Edward syndrome, Patau syndrome and Turner syndrome that arise where the number of chromosomes present in the patient is abnormal (aneuploidy). Prenatal screening is a routine medical service for a pregnant woman to evaluate her personal risk of fetal aneuploidy. These aneuploidies include but are not limited to; trisomy 21 (Down syndrome), trisomy 18 (Edward syndrome), trisomy 13 (Patau syndrome) and monosomy X (Turner syndrome).
Previous applications
Application documents
Consultation survey
PICO confirmation
Public summary document
Final stakeholder meeting minutes
Public summary document
Final stakeholder meeting minutes
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Meetings to consider this application
- PASC meeting:
- 8 December 2016
- ESC meeting:
- 8 June 2018
- 10-11 October 2019
- MSAC meeting:
- 26-27 July 2018
- 28-29 November 2019
Stakeholder meeting
Tuesday 6 November 2018, members of MSAC, clinicians with experience and expertise in obstetrics and gynaecology, pathology, clinical genetics and genetic counselling; representatives of the applicant; representatives from consumer organisations; and representatives from the Department of Health met to discuss Non-Invasive Prenatal Testing (NIPT) for Common Trisomies (21, 18 and 13). This was not an MSAC decision forum, but a meeting that would inform the issues considered by MSAC, following its July 2018 consideration of application 1492. The final minutes of this meeting are above.