1 November 2023 pathology MBS changes

This page provides information on the 1 November 2023 changes to MBS pathology items.

Page last updated: 08 December 2023

Effective from 1 November 2023, new and amended pathology items were listed on the Medicare Benefits Schedule, which includes:

  • New pathology items 73437, 73438 and 73439, which allow testing for genetic variants in patients with non-squamous non-small cell lung carcinoma to be performed as a pathologist-determinable service;
  • A fee increase for item 73418 for genetic testing for cardiac arrhythmias;
  • New items 73440, 73441, 73442, 73443 and 73444 will be introduced for genetic testing for childhood hearing loss;
  • New items 73445, 73446, 73447 and 73448 will be introduced for gene panel testing for haematological malignancies;
  • New items 73451 and 73452 will be introduced for genetic testing to determine carrier status of cystic fibrosis, spinal muscular atrophy, and fragile X syndrome in patients who are planning pregnancy or already pregnant, and their reproductive partner;
  • New items 73453, 73454 and 73455 will be introduced for reproductive carrier testing for specific genetic variants that cause nine severe conditions commonly found in the Ashkenazi Jewish population, with testing available to individuals of reproductive age who identify as being of Ashkenazi Jewish decent;
  • New items 73456, 73457, 73458, 73459, 73460, 73461 and 73462 will introduced for the diagnosis of mitochondrial disease in patients who are suspected of having either acute or chronic diseases, and the cascade testing of their biological relatives;
  • Amendment to the schedule fee for item 73418 from $400.00 to $1,200.00;
  • New item 66585 will be introduced for the quantification of N-terminal pro B-type natriuretic peptide (NT-proBNP) or B-type natriuretic peptide (BNP) in patients with systemic sclerosis, to assess the risk of pulmonary arterial hypertensions;
  • Amendments to prostate specific antigen testing items 66655, 66656, 66659 and 66660 and introduction of new item 66654 for testing patients with a first degree relative diagnosed with prostate cancer as a ‘high risk’ patient;
  • New items 71202 and 73310 will be introduced for the detection of measurable residual disease (MRD) in patients with acute lymphoblastic leukaemia using flow cytometry and next-generation sequencing methods;
  • New item 73306 will be introduced for the EndoPredict brand gene expression profiling test, which is a genetic test that looks at expression levels of several genes that can be involved in breast cancer;
  • Pathology item 73343 will be incorporated into the PST; and
  • Amendments to item 73296 and 73297 to expand the eligible patient population which can access testing of genes associated with breast, ovarian, fallopian tube or primary peritoneal cancer.
Further information and guidance can be found in the below factsheets:
Fact SheetPDF and Word versions
Amendment to genetic testing of reproductive partners for cardiac arrhythmia to align with genetic testing of reproductive partners for cardiomyopathy
(Last updated: 22 November 2023)
PDF Version - Amendment to genetic testing of reproductive partners for cardiac arrhythmia to align with genetic testing of reproductive partners for cardiomyopathy (PDF 122 KB)
Word Version - Amendment to genetic testing of reproductive partners for cardiac arrhythmia to align with genetic testing of reproductive partners for cardiomyopathy (Word 122 KB)
New and amended items for prostate specific antigen testing
(Last updated: 22 November 2023)
PDF Version - New and amended items for prostate specific antigen testing (PDF 134 KB)
Word Version - New and amended items for prostate specific antigen testing (Word 125 KB)
New MBS items for genetic testing for childhood hearing loss
(Last updated: 22 November 2023)
PDF Version - New MBS items for genetic testing for childhood hearing loss (PDF 191 KB)
Word Version - New MBS items for genetic testing for childhood hearing loss (Word 127 KB)
Genetic testing for variants associated with haematological malignancies
(Last updated: 22 November 2023)
PDF Version - Genetic testing for variants associated with haematological malignancies (PDF 128 KB)
Word Version - Genetic testing for variants associated with haematological malignancies (Word 126 KB)
Detection of measurable residual disease (MRD) in patients with acute lymphoblastic leukaemia (ALL)
(Last updated: 22 November 2023)
PDF Version - Detection of measurable residual disease in patients with acute lymphoblastic leukaemia (PDF 175 KB)
Word Version - Detection of measurable residual disease in patients with acute lymphoblastic leukaemia (Word 124 KB)
Reproductive carrier testing for cystic fibrosis, spinal muscular atrophy and fragile X syndrome
(Last updated: 22 November 2023)
PDF Version - Reproductive carrier testing for cystic fibrosis, spinal muscular atrophy and fragile X syndrome (PDF 188 KB)
Word Version - Reproductive carrier testing for cystic fibrosis, spinal muscular atrophy and fragile X syndrome (Word 128 KB)
New MBS item for prognostic gene expression profile test to determine the risk of early and late metastasis in node negative and positive cancer under endocrine treatment
(Last updated: 22 November 2023)
PDF Version - New MBS item for prognostic gene expression profile test to determine the risk of early and late metastasis in node negative and positive cancer under endocrine treatment (PDF 155 KB)
Word Version - New MBS item for prognostic gene expression profile test to determine the risk of early and late metastasis in node negative and positive cancer under endocrine treatment (Word 123 KB)
New MBS item for N-terminal pro B-type natriuretic peptide (NT proBNP) testing in patients with systemic sclerosis
(Last updated: 22 November 2023)
PDF Version - New MBS item for N-terminal pro B-type natriuretic peptide testing in patients with systemic sclerosis (PDF 156 KB)
Word Version - New MBS item for N-terminal pro B-type natriuretic peptide testing in patients with systemic sclerosis (Word 123 KB)
Small Gene Panel Testing for Non-Small Cell Lung Carcinoma (NSCLC)
(Last updated: 22 November 2023)
PDF Version - Small Gene Panel Testing for Non-Small Cell Lung Carcinoma (PDF 155 KB)
Word Version - Small Gene Panel Testing for Non-Small Cell Lung Carcinoma (Word 132 KB)
New pathology items for targeted carrier testing for severe monogenic conditions
(Last updated: 22 November 2023)
PDF Version - New pathology items for targeted carrier testing for severe monogenic conditions (PDF 196 KB)
Word Version - New pathology items for targeted carrier testing for severe monogenic conditions (Word 126 KB)
Amendments to items for pathology testing for breast fallopian tube or primary peritoneal cancer
(Last updated: 22 November 2023)
PDF Version - Amendments to items for pathology testing for breast, fallopian tube or primary peritoneal cancer (PDF 172 KB)
Word Version - Amendments to items for pathology testing for breast, fallopian tube or primary peritoneal cancer (Word 122 KB)
Whole genome sequencing for the diagnosis of mitochondrial disease
(Last updated: 22 November 2023)
PDF Version - Whole genome sequencing for the diagnosis of mitochondrial disease (PDF 202 KB)
Word Version - Whole genome sequencing for the diagnosis of mitochondrial disease (Word 132 KB)

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