Reasonable Hypothesis SOP [1] | 63 of 2017 as amended |
Balance of Probabilities SOP [1] | 64 of 2017 as amended |
SOP Bulletin 199 [2]
SOP Bulletin 230 [3]
ICD Coding
Immune thrombocytopaenia is an autoimmune disorder resulting in destruction of platelets and a low platelet count. It can be a stand alone condition or occur in conjunction with another disorder.
This diagnosis is complex. Clinical manifestations (bleeding) or a need for treatment are required. Non-immunological causes and haematological disorders also involving other blood components need to be excluded. The condition can be temporary and may no longer be present.
The relevant medical specialist is a haematologist.
* another SOP applies
# non-SOP condition
Clinical onset may be when bleeding manifestations were first noticed or may be when a low platelet count was first noted on testing.
This may be evidenced by a fall in the platelet count or more severe bleeding manifestations.
Links
[1] http://www.rma.gov.au/sops/condition/immune-thrombocytopaenia
[2] https://clik.dva.gov.au/system/files/media/SOP%20Bulletin%20199_0.pdf
[3] https://clik.dva.gov.au/system/files/media/SOP%20Bulletin%20230.pdf