Heparin-induced thrombocytopenia: treatment options and special considerations.
Review published in Pharmacotherapy (2007)
Abstract
Heparin-induced thrombocytopenia (HIT) is an immune-mediated adverse effect that typically manifests several days after the start of heparin therapy, although both rapid- and delayed-onset HIT have been described. Its most serious complication is thrombosis. Although not all patients develop thrombosis, it can be life threatening. The risk of developing HIT is related to many factors, including the type of heparin product administered, route of administration, duration of therapy, patient population, and previous exposure to heparin. The diagnosis of HIT is typically based on clinical presentation, exposure to heparin, and presence of thrombocytopenia with or without thrombosis. Antigen and activation laboratory assays are available to support the diagnosis of HIT. However, because of the limited sensitivity and specificity of these assays, bedside probability scales for HIT were developed. When HIT is suspected, prompt cessation of all heparin therapy is necessary, along with initiation of alternative anticoagulant therapy. Two direct thrombin inhibitors--argatroban and lepirudin--are approved for the management of HIT in the United States, and bivalirudin is approved for use in patients with HIT who are undergoing percutaneous coronary intervention. Other agents, although not approved to manage HIT, have also been used; however, their role in therapy requires further evaluation. A comprehensive HIT management strategy involves the evaluation of numerous factors. Many patients, including those undergoing coronary artery bypass surgery, those with acute coronary syndromes, those with hepatic or renal insufficiency, and children, require special attention. Clinicians must become familiar with the available information on this serious adverse effect and its treatment so that optimum patient management strategies may be formulated.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
Heparin-induced thrombocytopenia (HIT) is an immune-mediated adverse effect that typically manifests several days after the start of heparin therapy, although both rapid- and delayed-onset HIT have been described. Its most serious complication is thrombosis.
Why This Matters for Hirudotherapy
This review describes heparin-induced thrombocytopenia (HIT), an immune-mediated reaction to heparin whose most serious complication is thrombosis, and surveys treatment, noting that all heparin must be stopped and an alternative anticoagulant started, with the direct thrombin inhibitors argatroban and lepirudin approved in the United States for managing HIT and bivalirudin approved for HIT patients undergoing percutaneous coronary intervention. Its direct tie to the leech secretome is lepirudin, a recombinant hirudin analog, demonstrating that a molecule originating in the medicinal leech became an approved clinical anticoagulant for a setting where heparin is contraindicated. Caveat: this is a narrative review of pharmacologic HIT management, not a study of hirudotherapy, and the approval status it reports is for recombinant hirudin-derived drugs, not for leech therapy itself.
Citation
Heparin-induced thrombocytopenia: treatment options and special considerations.
Dager et al. · Pharmacotherapy, 2007
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