Outcomes of patients with suspected heparin-induced thrombocytopenia in a contemporary multicenter cohort

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 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 3 groups: (1) HIT confirmed, (2) HIT-negative but heparin/platelet factor 4 (PF4) antibody-positive, and (3) HIT-negative without antibodies. Clinical and laboratory data were systematically collected. HIT was diagnosed using the washed-platelet heparin-induced platelet activation test as the reference standard. Among 1393 patients (46% female, median age 67 years), 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 patients with HIT. 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 patients who were HIT-negative 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.

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Journal
Blood Advances
Published
2025-08-04
DOI
https://doi.org/10.1182/bloodadvances.2025016639
Citations
1
Primary Topic
Heparin-Induced Thrombocytopenia and Thrombosis
Type
article
Field-Weighted Citation Impact
2.01

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article

Outcomes of patients with suspected heparin-induced thrombocytopenia in a contemporary multicenter cohort

Dimitrios A. Tsakiris, Michael Nagler, Prakash Vishnu, Lukas Graf et al.
1 citations
Blood Advances
Heparin-Induced Thrombocytopenia and Thrombosis
2.01
article

Outcomes of patients with suspected heparin-induced thrombocytopenia in a contemporary multicenter cohort

Dimitrios A. Tsakiris, Michael Nagler, Prakash Vishnu, Lukas Graf, Bernhard Gerber, Walter A. Wuillemin, Tamam Bakchoul, Johanna A. Kremer Hovinga, Henning Nilius, Andreas Greinacher, Ekaterina Sinitsa, Adrián Schmidt, Adriana Méndez, Jan–Dirk Studt
article en
1 citations

Abstract

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 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 3 groups: (1) HIT confirmed, (2) HIT-negative but heparin/platelet factor 4 (PF4) antibody-positive, and (3) HIT-negative without antibodies. Clinical and laboratory data were systematically collected. HIT was diagnosed using the washed-platelet heparin-induced platelet activation test as the reference standard. Among 1393 patients (46% female, median age 67 years), 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 patients with HIT. 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 patients who were HIT-negative 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.

Blood AdvancesVol. 9(21)
University of Bern (CH), Bern University of Applied Sciences (CH), Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA), University of Lucerne (CH), University of St.Gallen (CH), Universitätsmedizin Greifswald (DE), Triemli Hospital (CH), University Hospital of Bern (CH), University Hospital of Basel (CH), Institute for Transfusion Medicine (US), Fred Hutch Cancer Center (US), Cancer Consortium (US), Ente Ospedaliero Cantonale (CH), University Hospital of Zurich (CH), Institute of Oncology Research (CH), University Children's Hospital Tübingen (DE), Kantonsspital Aarau (CH), University of Tübingen (DE)
Falk Foundation, Pfizer, AstraZeneca, Sanofi, CSL Behring, Mylan, Deutsche Forschungsgemeinschaft, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Bundesamt für Gesundheit, Deutsche Herzstiftung, Swedish Orphan Biovitrum, Robert Koch Institut, Bayer Vital
Good health and well-being
Openalex Percentile: Top 13%
Heparin-Induced Thrombocytopenia and Thrombosis
2.01
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