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Service Update - New amniocentesis collection tubes 01 November 2024 Please be advised that amniocentesis collection tubes ordered from PathWest Diagnostic Genomics have changed. The 10mL black top collection tubes are no longer in production and have been replaced with 10mL blue top collection tubes. Any remaining black top tubes can still be used until your stocks are depleted.New blue-top tubes can be ordered via the contact details below. Contact us PathWest Diagnostic Genomics E: diagnosticgenomicsqe.pathwest@health.wa.gov.au T: 13 PATH (7284) -
Laboratory Assistant from our Media Manufacturing Unit featured in TAFE’s success stories 29 August 2024 After completing his Certificate IV in Laboratory Techniques at TAFE, Trevor Bentley began working at PathWest as a Technical Assistant in Microbiology, and currently as a Laboratory Assistant at the Media Manufacturing Unit. While working at PathWest, Trevor was contacted by one of his lecturers at TAFE to be featured in their online success stories as an inspiration for their current and future students. In Trevor’s feature story, he shared ‘I have been continuously learning new skills at PathWest and building upon the training I received at TAFE.’ As a Technical Assistant in Microbiology, Trevor was responsible for receiving specimens, interpreting request forms, and processing a variety of samples using aseptic techniques. He has performed thousands of streak plates and spread plates for antibiotic sensitivity testing,operation of urinalysis, PCR and rapid flu/C... -
Medical Scientist shares key takeaways from the TSANZ Annual Scientific Meeting 2024 29 August 2024 Held annually, the Transplantation Society of Australia and New Zealand (TSANZ) Annual Scientific Meeting (ASM) focuses on advancing research, clinical practices, and advocacy to improve outcomes and increase access to organ transplantation in Australia and New Zealand. At the 42nd TSANZ ASM that took place in Melbourne from 16 to 18 June 2024, Babette Vogels, Medical Scientist – Transplant Immunology from Immunology FSH, was one of the attendees and shares her key takeaways. ‘I found the event very educational and overall, a highly valuable experience,’ Babette said. She was particularly impressed by the diverse perspectives on transplantation, including clinical aspects, research, and emerging technologies. Babette appreciated the opportunity to learn from experts across various fields and to gain a broader understanding beyond her role as a Medical Scientist in Trans... -
External Awards: PathWest staff achievements in 2023-24 30 June 2024 Anatomical Pathology Dr Priyanthi Kumarasinghewas appointed President Elect of the International Academy of Pathology (IAP) in 2023 and assumed the role of IAP President in 2024. Dr Ming Chaiwas appointed President of the Australasian Gastrointestinal Pathology Society and won the IAP 2024 Poster Prize for the Sunday Masterclass titled ‘Oh, the Places You’ll Go with Cytology!’ Dr Disna Abeysuriyawon the IAP 2024 Oral Presentation Prize for her presentation on ‘Birth Asphyxia and Early Neonatal Death.’ Dr Kimberley Chungreceived the award for Best Oral Presentation by a Registrar Award at the Australian Society of Cytology (ASC) Annual Scientific Meeting held at the Gold Coast in November 2023. Mr Neville Hattersleywas honoured with the Best Scientific Presentation Award at the WA Branch ASC Annual Meeting. Dr Ronan Knittelwas awarded... -
Non-syndromic Hearing Loss Gene Panel Service Update 25 June 2024 In line with the recent additions to the Medicare Benefits Schedule (MBS)1, the Department of Diagnostic Genomics at PathWest is pleased to announce that we will be offering a non-syndromic hearing loss gene panel which will replace the current GJB2/GJB6 testing from 1 July 2024. The genes included in the non-syndromic hearing loss panel (including some overlap with syndromic conditions) performed at PathWest are: AIFM1, BDP1, CDH23, COL11A2, DIAPH1, EPS8L2, GJB2, GJB6, LOXHD1, MYO15A, MYO7A, OTOA, PCDH15, POU3F4, PRPS1, SLC26A4, STRC, TECTA, TMC1, TMPRSS3, USH1C, WFS1, WHRN. Genes in this panel reflect local data as well as local and international literature2-4 with an expected diagnostic pick-up rate of up to 60%. Please note, the diagnostic yield of this panel is maximized in the following instances: Congenital hearing impairment with no identifiable infectious or traumatic caus...
Last Updated:
20/05/2025