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Results 1 to 10 of 158 matches

Category 6 - PATHOLOGY SERVICES

73287

73287 - Additional Information

Item Start Date:
01-Jul-1993
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

The study of the whole of every chromosome by cytogenetic 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



Fee: $394.55 Benefit: 75% = $295.95 85% = $335.40

(See para PR.7.3 of explanatory notes to this Category)

Category 6 - PATHOLOGY SERVICES

73289

73289 - Additional Information

Item Start Date:
01-Jul-1993
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

The study of the whole of every chromosome by cytogenetic or other techniques, performed on blood (including a service mentioned in item 73293, if performed) - 1 or more tests



Fee: $358.95 Benefit: 75% = $269.25 85% = $305.15

Category 6 - PATHOLOGY SERVICES

73290

73290 - Additional Information

Item Start Date:
01-May-2010
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

The study of the whole of each chromosome by cytogenetic or other techniques, performed on blood or bone marrow, in the diagnosis and monitoringof haematological malignancy (including a service in items 73287 or 73289, if performed). - 1 or more tests.



Fee: $394.55 Benefit: 75% = $295.95 85% = $335.40

(See para PR.7.2 of explanatory notes to this Category)

Category 6 - PATHOLOGY SERVICES

73291

73291 - Additional Information

Item Start Date:
01-May-2010
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

Analysis of one or more chromosome regions for specific constitutional genetic abnormalities of blood or fresh tissue in

a)    diagnostic studies of a person with developmental delay, intellectual disability, autism, or at least two congenital abnormalities, in whom cytogenetic studies (item 73287 or 73289) are either normal or have not been performed; or

b)    studies of a relative for an abnormality previously identified in such an affected person.

- 1 or more tests.



Fee: $230.95 Benefit: 75% = $173.25 85% = $196.35

Category 6 - PATHOLOGY SERVICES

73292

73292 - Additional Information

Item Start Date:
01-May-2010
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

Analysis of chromosomes by genome-wide micro-array 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 two congenital abnormalities (including a service in items 73287, 73289 or 73291, if performed)

- 1 or more tests.



Fee: $589.90 Benefit: 75% = $442.45 85% = $501.45

Category 6 - PATHOLOGY SERVICES

73293

73293 - Additional Information

Item Start Date:
01-May-2010
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

Analysis of one or more regions on all chromosomes for specific constitutional genetic abnormalities of fresh tissue in diagnostic studies of the products of conception, including exclusion of maternal cell contamination.

- 1 or more tests.



Fee: $230.95 Benefit: 75% = $173.25 85% = $196.35

Category 6 - PATHOLOGY SERVICES

73294

73294 - Additional Information

Item Start Date:
01-May-2010
Description Updated:
01-May-2010
Schedule Fee Updated:
01-Jan-2013

Group
P7 - Genetics

Analysis of the PMP22 gene for constitutional genetic abnormalities causing peripheral neuropathy, either as:

a)    diagnostic studies of an affected person; or

b)    studies of a relative for an abnormality previously identified in an affected person

- 1 or more tests.



Fee: $230.95 Benefit: 75% = $173.25 85% = $196.35

Category 6 - PATHOLOGY SERVICES

73295

73295 - Additional Information

Item Start Date:
01-Sep-2022
Description Updated:
01-Sep-2022
Schedule Fee Updated:
01-Feb-2017

Group
P7 - Genetics

Detection of germline BRCA1 or BRCA2 pathogenic or likely pathogenic gene variants, in a patient with advanced (FIGO III-IV) high-grade serous or high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer for whom testing of tumour tissue is not feasible, requested by a specialist or consultant physician, to determine eligibility for treatment with a poly (adenosine diphosphate [ADP]-ribose) polymerase (PARP) inhibitor under the Pharmaceutical Benefits Scheme (PBS) 

Maximum of one test per patient’s lifetime



Fee: $1,200.00 Benefit: 75% = $900.00 85% = $1,101.30

(See para PN.0.23 of explanatory notes to this Category)

Category 6 - PATHOLOGY SERVICES

73296

73296 - Additional Information

Item Start Date:
01-Nov-2017
Description Updated:
01-Nov-2023
Schedule Fee Updated:
01-Nov-2017

Group
P7 - Genetics

Characterisation of germline gene variants, including copy number variation where appropriate, requested by a specialist or consultant physician:

(a) in genes associated with breast, ovarian, fallopian tube or primary peritoneal cancer, which must include at least:

(i) BRCA1 and BRCA 2 genes; and

(ii) one or more STK11, PTEN, CDH1, PALB2 and TP53 genes; and

(b) in a patient:

(i) with breast, ovarian, fallopian tube or primary peritoneal cancer; and

(ii) for whom clinical and family history criteria place the patient at greater than 10% risk of having a pathogenic or likely pathogenic gene associated with breast, ovarian, fallopian tube or primary peritoneal cancer

Once per cancer diagnosis



Fee: $1,200.00 Benefit: 75% = $900.00 85% = $1,101.30

(See para PN.0.23 of explanatory notes to this Category)

Category 6 - PATHOLOGY SERVICES

73297

73297 - Additional Information

Item Start Date:
01-Nov-2017
Description Updated:
01-Nov-2023
Schedule Fee Updated:
01-Nov-2017

Group
P7 - Genetics

Characterisation of germline gene variants, including copy number variation where appropriate, requested by a specialist or consultant physician:

(a) in genes associated with breast, ovarian, fallopian tube or primary peritoneal cancer, which may include the following genes:

(i) BRCA1 or BRCA2;

(ii) STK11, PTEN, CDH1, PALB2 and TP53; and

(b) in a patient:

(i) who has a biological relative who has had a pathogenic or likely pathogenic gene variant identified in one or more of the genes mentioned in paragraph (a); or

(ii) who has not previously received a service to which item 73295, 73296 or 73302 applies

Once per variant



Fee: $400.00 Benefit: 75% = $300.00 85% = $340.00

(See para PN.0.23 of explanatory notes to this Category)

Results 1 to 10 of 158 matches


Legend

  • Assist - Addition/Deletion of (Assist.)
  • Amend - Amended Description
  • Anaes - Anaesthetic Values Amended
  • Emsn - EMSN Change
  • Fee - Fee Amended
  • Renum - Item Number Change (renumbered)
  • New - New Item
  • NewMin - New Item (previous Ministerial Determination)
  • Qfe - QFE Change