ArticleFrontiers in medicine2026
Possible atypical heparin-induced thrombocytopenia presenting with splenic infarction despite preserved platelet counts after cardiac surgery - a case report.
Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Heparin-induced thrombocytopenia (HIT) type 2 is a major complication of heparin therapy and associated with considerable morbidity and mortality. Correct diagnosis, especially in the intensive care setting where thrombocytopenia occurs frequently, is of paramount importance. We report a 44-year-old female patient undergoing surgical replacement of the tricuspid valve due to Ebstein anomaly. Peri-operatively, the patient was treated with unfractionated heparin (UFH). Sixteen days after treatment initiation, computed tomography incidentally revealed multiple splenic infarctions consistent with embolic infarction. The 4T score was 3 points, suggesting a low pre-test probability for HIT; however, its applicability was limited by post-cardiac surgery platelet kinetics and the absence of a typical platelet fall. A PF4/heparin antibody immunoassay was therefore performed and showed strong positivity (optical density 2.07, lower limit of normal <0.51). Anticoagulation was changed to argatroban, followed by apixaban. Importantly, although an initial perioperative platelet decline of 59% was observed consistent with cardiopulmonary bypass-related consumption, platelet counts had recovered to within the normal range at the time of diagnosis, and no classical secondary platelet fall was observed. In summary, we report a case of possible HIT in which platelet count-based risk stratification may not have fully captured an atypical presentation in this selected clinical setting.
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