Management of heparin-induced thrombocytopenia: systematic reviews and meta-analyses
- PMID: 33095876
- PMCID: PMC7594379
- DOI: 10.1182/bloodadvances.2020002963
Management of heparin-induced thrombocytopenia: systematic reviews and meta-analyses
Abstract
Heparin-induced thrombocytopenia (HIT) is a prothrombotic adverse drug reaction occurring in <0.1% to 7% of patients receiving heparin products depending on the patient population and type of heparin. Management of HIT is highly dependent on a sequence of tests for which clinicians may or may not have the results when care decisions need to be made. We conducted systematic reviews of the effects of management strategies in persons with acute HIT, subacute HIT A or B, and remote HIT. We searched Medline, EMBASE, and the Cochrane Database through July 2019 for previously published systematic reviews and primary studies. Two investigators independently screened and extracted data and assessed the certainty of the evidence using the Grading of Recommendations Assessment, Development and Evaluation approach. We found primarily noncomparative studies and case series assessing effects of treatments, which led to low to very low certainty evidence. There may be little to no difference in the effects between nonheparin parenteral anticoagulants and direct oral anticoagulants in acute HIT. The benefits of therapeutic-intensity may be greater than prophylactic-intensity anticoagulation. Using inferior vena cava filters or platelet transfusion may result in greater harm than not using these approaches. Evidence for management in special situations, such as for patients undergoing cardiovascular interventions or renal replacement therapy, was also low to very low certainty. Additional research to evaluate nonheparin anticoagulants is urgently needed, and the development of novel treatments that reduce thrombosis without increasing hemorrhage should be a priority.
© 2020 by The American Society of Hematology.
Conflict of interest statement
Conflict-of-interest disclosure: A.C. has served as a consultant for Synergy and CRO and received institutional research support on his behalf from Alexion, Bayer, Novo Nordisk, Pfizer, Sanofi, Spark, and Takeda. B.H.C. has received institutional research support on his behalf from Bayer and Alexion. T.E.W. has served as a consultant for Aspen Global, Ergomed, and Octapharma; receives honoraria from Alexion; and serves on advisory boards for Bayer, CSL Behring, and Instrumentation Laboratory. The remaining authors declare no competing financial interests.
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