Health Insurance (Pathology Services Table) Amendment Regulations 2010 (No. 1) (Cth)

Health Insurance (Pathology Services Table) Amendment Regulations 2010 (No. 1)¹

Select Legislative Instrument 2010 No. 68

I, QUENTIN BRYCE, Governor-General of the Commonwealth of Australia, acting with the advice of the Federal Executive Council, make the following Regulations under the Health Insurance Act 1973.

Dated 14 April 2010

QUENTIN BRYCE

Governor-General

By Her Excellency’s Command

NICOLA ROXON

Minister for Health and Ageing

Name of Regulations

These Regulations are the Health Insurance (Pathology Services Table) Amendment Regulations 2010 (No. 1).

Commencement

These Regulations commence on 1 May 2010.

Amendment of Health Insurance (Pathology Services Table) Regulations 2009

Schedule 1 amends the Health Insurance (Pathology Services Table) Regulations 2009.

Schedule 1 Amendment

(regulation 3)

[1] Schedule 1, Part 3, items 73287 and 73289

substitute

73287	Study of the whole of every chromosome by cytogenetics or other techniques, performed on 1 or more of any tissue or fluid except blood (including a service mentioned in item 73293, if performed) — 1 or more tests	397.20
73289	Study of the whole of every chromosome by cytogenetics or other techniques, performed on blood (including a service mentioned in item 73294, if performed) — 1 or more tests	361.35
73290	Study of the whole of every chromosome by cytogenetics or other techniques, performed on blood or bone marrow, to diagnose or monitor haematological malignancy (including a service mentioned in item 73287 or 73289, if performed) — 1 or more tests	397.20
73291	Analysis of 1 or more chromosome regions, performed on blood or fresh tissue, for specific constitutional genetic abnormalities in: (a) diagnostic studies of a person with developmental delay, intellectual disability, autism, or at least 2 congenital abnormalities, in whom a study by cytogenetics or other techniques mentioned in item 73287 or 73289 is normal or has not been performed — 1 or more tests; or (b) studies of a relative of the person for an abnormality previously identified in the person — 1 or more tests	232.50
73292	Analysis of chromosomes by genome-wide microarray, including targeted assessment of specific regions for constitutional genetic abnormalities in diagnostic studies of a person with developmental delay, intellectual disability, autism, or at least 2 congenital abnormalities (including a service mentioned in item 73287, 73289 or 73291, if performed) — 1 or more tests	593.85
73293	Analysis of 1 or more regions on all chromosomes, performed on fresh tissue, for specific constitutional genetic abnormalities in diagnostic studies of the products of conception, including exclusion of maternal cell contamination — 1 or more tests	232.50
73294	Analysis of the PMP22 gene for constitutional genetic abnormalities causing peripheral neuropathy, as: (a) diagnostic studies of a person with peripheral neuropathy — 1 or more tests; or (b) studies of a relative of the person for an abnormality previously identified in the person — 1 or more tests	232.50

Note

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