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Results 121 to 126 of 126 matches

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)

Category 6 - PATHOLOGY SERVICES

73357

73357 - Additional Information

Item Start Date:
01-May-2020
Description Updated:
01-Mar-2021
Schedule Fee Updated:
01-May-2020

Group
P7 - Genetics

Characterisation of germline gene variants, including copy number variation, in the genes mentioned in item 73354, 73355 or 73356, requested by a specialist or consultant physician, for a patient:

(a) who has a biological relative with a pathogenic mutation identified in one or more of those genes; and

(b) who has not previously received a service to which any of items 73354, 73355 and 73356 apply



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

Category 6 - PATHOLOGY SERVICES

73375

73375 - Additional Information

Item Start Date:
01-May-2020
Description Updated:
01-May-2020
Schedule Fee Updated:
01-May-2020

Group
P7 - Genetics

Analysis of tumour tissue, requested by a specialist or consultant physician, that:

(a) is for the characterisation of copy number changes, gene rearrangements, or other molecular changes, in 2 or 3 of the genes mentioned in item 73374; and

(b) is for a patient with clinical or laboratory evidence, including morphological features, of sarcoma

Applicable only once per lifetime



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

Category 6 - PATHOLOGY SERVICES

73376

73376 - Additional Information

Item Start Date:
01-May-2020
Description Updated:
01-May-2020
Schedule Fee Updated:
01-May-2020

Group
P7 - Genetics

Analysis of tumour tissue, requested by a specialist or consultant physician, that:

(a) is for the characterisation of copy number changes, gene rearrangements, or other molecular changes, in 4 or more of the genes mentioned in item 73374; and

(b) is for a patient with clinical or laboratory evidence, including morphological features, of sarcoma

Applicable only once per lifetime



Fee: $800.00 Benefit: 75% = $600.00 85% = $701.30

Category 6 - PATHOLOGY SERVICES

73440

73440 - Additional Information

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

Group
P7 - Genetics

Genomic testing and copy number variant analysis of genes known to be causative or likely causative of childhood hearing loss in a patient, if:
(a) the testing and analysis is requested by a specialist or consultant physician; and
(b) the patient has congenital or childhood onset hearing loss that presented before the patient was 18 years of age and is permanent moderate, severe, or profound (>40 dB in the worst ear over 3 frequencies) and classified as sensorineural, auditory neuropathy or mixed; and
(c) the patient is not eligible for a service to which item 73358 or 73359 applies; and
(d) the testing and analysis is not associated with a service to which item 73441 applies

Applicable once per lifetime



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

(See para PN.0.23, PN.7.13 of explanatory notes to this Category)

Category 6 - PATHOLOGY SERVICES

73441

73441 - Additional Information

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

Group
P7 - Genetics

Genomic testing and copy number variant analysis of relevant genes known to be causative or likely causative of childhood hearing loss in a patient, if:
(a) the testing and analysis is requested by a specialist or consultant physician; and
(b) the patient has congenital or childhood onset hearing loss that presented before the patient was 18 years of age and is permanent bilateral moderate, severe, or profound (>40 dB in the worst ear over 3 frequencies) and classified as sensorineural, auditory neuropathy or mixed; and
(c) the testing and analysis is performed using a sample from the patient and a sample from each of the patient’s biological parents; and
(d) the patient is not eligible for a service to which item 73358 or 73359 applies; and
(e) the testing and analysis is not associated with a service to which item 73440 applies

Applicable once per lifetime



Fee: $2,100.00 Benefit: 75% = $1,575.00 85% = $2,001.30

(See para PN.0.23, PN.7.13 of explanatory notes to this Category)

Results 121 to 126 of 126 matches


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  • 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