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Response to: ‘Sentinel lymph node biopsy for in situ melanoma is unlikely in Australia’ by Morton and Thompson
  1. Tim Badgery-Parker1,2,
  2. Sallie-Anne Pearson3,
  3. Ian A Scott4,
  4. Adam G Elshaug1
  1. 1 Faculty of Medicine and Health, School of Public Health, Menzies Centre for Health Policy, Charles Perkins Centre, The University of Sydney, Sydney, New South Wales, Australia
  2. 2 Capital Markets CRC, Sydney, New South Wales, Australia
  3. 3 Medicines Policy Research Unit, Centre for Big Data Research in Health, University of New South Wales, Sydney, New South Wales, Australia
  4. 4 School of Clinical Medicine, Princess Alexandra Hospital, Brisbane, Queensland, Australia
  1. Correspondence to Tim Badgery-Parker, Faculty of Medicine and Health, School of Public Health, Menzies Centre for Health Policy, The University of Sydney, Sydney, NSW 2006, Australia; tim.badgeryparker{at}sydney.edu.au

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We thank Drs Morton and Thompson1 for their comments on our indicator for low-value sentinel lymph node biopsy (SLNB). They provide a plausible explanation for our finding that SLNB appears to be used for melanoma in situ in public hospitals in New South Wales (NSW). Their explanation is based on an understanding of care processes that cannot be inferred from our data. We hoped to gain such understanding through our clinician workshop, for which invitations were sent out widely through various channels. We agree it is unfortunate that no dermatologists, pathologists or oncologists chose to participate.

Morton and Thompson suggest that melanoma in situ is recorded when a wide-excision specimen is taken from a site that was previously biopsied and found to have invasive melanoma. If the wide-area specimen has residual melanoma in situ, this diagnosis is recorded, while the SLNB is done because of …

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