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Performance Evaluation of the Biological Diagnosis of HIT

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

Heparin-induced Thrombocytopenia (HIT)

Study type

Observational

Funder types

Other

Identifiers

NCT06180785
8665 (Other Identifier)

Details and patient eligibility

About

Heparin-induced thrombocytopenia (HIT) is a severe complication of heparin therapy with a non-negligible incidence (estimated at 2.6% of unfractionated heparin treatments and 0.2% of low molecular weight heparin treatments). It is generally secondary to the appearance of IgG antibodies directed against the platelet factor 4 (PF4) - heparin complex. These antibodies, once bound to this complex, are likely to activate platelets: the thrombotic risk generated can be potentially fatal.

Enrollment

894 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  • Adult patient (≥ 18 years of age)
  • Hospitalized at HUS between 01/01/2009 and 31/12/2019
  • Specimen sent to the HUS Hematology Laboratory for biological diagnosis of HIT between 01/01/2009 and 31/12/2019
  • Data collected by the CRPV and analyzed by the HIT multidisciplinary group in order to reach a consensus decision on the presence or absence of HIT
  • Patient does not object to the reuse of his medical data for scientific research purposes.

Exclusion criteria:

  • Patient for whom no test has been performed at the HUS Hematology Laboratory
  • Patient for whom no data has been collected by the CRPV
  • Patient for whom the HIT group could not confirm or deny the presence of HIT

Trial contacts and locations

1

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Central trial contact

Agathe HERB, PharmD

Data sourced from clinicaltrials.gov

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