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Heparin induced thrombocytopaenia
Type I
Type II
Heparin induced thrombocytopaenia and thrombosis syndrome (HITTS)
Incidence
2.5% of patients exposed to heparin for ³
5 days
Aetiology
Pathogenesis
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Antibody (usually IgG) against heparin-platelet factor
4 complex. Platelet factor 4 is secreted by during platelet activation.
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When IgG binds to heparin/PF4 complexes on platelet
surface it causes platelet aggregation resulting in thrombus formation and
further PF4 release.
Clinical features
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Usually presents after exposure of ³5
days to heparin (2-3 days in patients previously exposed to heparin). Rare
after >14 days exposure
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Heparin dose may be very low
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Thrombocytopaenia. Nadir often around 50x109/L.
Severe thrombocytopaenia (<20x109/L) uncommon
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Haemorrhage very rare
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Approximately 50% of patients develop thrombosis (new
or extension of pre-existing thrombus). Usually presents after onset of
thrombocytopaenia. Arterial in 20%
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Loss commonly:
Diagnosis
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Requires clinical vigilance
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No completely sensitive and specific test
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Heparin/PF4 antibody can be detected by bioassay (more
specific) or immunoassay.
Treatment
Further reading
Greaves M. Heparin-induce thrombocytopaenia
and thrombosis. Prescribers’ Journal, 2000; 40:59-64
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