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  3. Outcomes of Patients with Suspected Heparin-Induced Thrombocytopenia in a Contemporary Multicenter Cohort.
 

Outcomes of Patients with Suspected Heparin-Induced Thrombocytopenia in a Contemporary Multicenter Cohort.

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BORIS DOI
10.48620/90757
Publisher DOI
10.1182/bloodadvances.2025016639
PubMed ID
40758946
Description
Managing patients with suspected heparin-induced thrombocytopenia (HIT) poses significant clinical challenges. Limited evidence exists on how management decisions impact clinical outcomes, leading to treatment recommendations based on low-certainty evidence. This study aimed to evaluate the treatment strategies and clinical outcomes of patients with suspected heparin-induced thrombocytopenia (HIT) in a contemporary multicenter cohort. We conducted a prospective, multicenter cohort study including consecutive patients with suspected HIT from 11 centers. Patients were stratified into three groups: (a) HIT confirmed, (b) HIT-negative but heparin/PF4 antibody-positive, and (c) HIT-negative without antibodies. Clinical and laboratory data were systematically collected. HIT was diagnosed using the washed-platelet heparin-induced platelet activation (HIPA) test as the reference standard. Among 1,393 patients (46% female, median age 67), HIT was confirmed in 119 (8.5%). Most patients were in intensive care (37%) or had undergone cardiac surgery (32%). Argatroban was the predominant treatment (70%), and platelet recovery occurred in 77% of HIT patients. Among patients with HIT, subsequent venous thromboembolism occurred in 23%, arterial thromboembolism in 9%, major bleeding in 12.6%, and mortality in 18%, with no significant differences between anticoagulants. Treatment with argatroban, bivalirudin, or direct oral anticoagulants (DOACs) significantly reduced arterial thromboembolism risk. Outcomes did not differ between HIT-negative patients with or without heparin/PF4 antibodies. HIT, as well as the mere suspicion of HIT, remains a serious condition with a high risk of adverse outcomes, including death. Our findings provide further evidence supporting the effectiveness of DOACs, argatroban, and bivalirudin in reducing arterial thromboembolism risk.
Date of Publication
2025-11-11
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
500 Science > 540 Chemistry
Language(s)
en
Contributor(s)
Nilius, Henning
Sinitsa, Ekaterina
Studt, Jan-Dirk
Tsakiris, Dimitrios A
Greinacher, Andreas
Mendez, Adriana
Schmidt, Adrian Emanuel
Wuillemin, Walter A
Gerber, Bernhard
Vishnu, Prakash
Graf, Lukas
Kremer Hovinga, Johanna A.orcid-logo
Clinic of Haematology and Central Haematological Laboratory
Bakchoul, Tamam
Nagler, Michael
Institute of Clinical Chemistry
Additional Credits
Clinic of Haematology and Central Haematological Laboratory
Institute of Clinical Chemistry
Series
Blood Advances
Publisher
American Society of Hematology (ASH Publications)
ISSN
2473-9537
2473-9537
Access(Rights)
open.access
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