Survey of Practice Pattern in Patients With Heparin-Induced Thrombocytopenia Requiring Cardiopulmonary Bypass
Research article published in Anesthesia and analgesia (2021)
Abstract
BACKGROUND: Heparin-induced thrombocytopenia (HIT) is an immune-mediated adverse reaction to heparin. Patients undergoing cardiac surgery with cardiopulmonary bypass (CPB) are routinely anticoagulated with heparin before the initiation of bypass. Heparin is contraindicated, however, in patients with acute HIT, and alternatives to routine practice are often used. While guidelines have recently been published addressing this topic 10, there remains variance between institutions in how these cases are treated. Our goal was to better delineate practice trends in the diagnosis and management of HIT patients requiring CPB. METHODS: We surveyed members of the Society of Cardiovascular Anesthesiologists (SCA) and the American Society for Extracorporeal Technology (AmSECT) using an online survey tool. RESULTS: We received 304 completed surveys (5.8% response rate), 75% completed by an anesthesiologist, and 24% by a perfusionist. The majority of respondents used clinical history and/or antibody testing (71% and 63%, respectively) to diagnose HIT. Seventy-five percent of respondents reported using an institutional protocol for HIT-CPB cases. Most respondents (89%) reported having at least 1 case in the last 3 years, with a total case experience of at least 785 cases (785 = the minimum number of cases in each case volume category × the number of respondents choosing that category). The strategy recommended in published guidelines, bivalirudin, was the most commonly reported alternative anticoagulation strategy (75%) used by respondents in HIT cases, with most (83%) using the activated clotting time (ACT) to monitor anticoagulation. CONCLUSIONS: Most responding SCA and AmSECT members reported that their institution used a protocol or guideline for HIT/CPB cases, and most guidelines directed the use of bivalirudin as an alternative anticoagulant. Various other methods such as plasmapheresis are also being used with success in this patient population. Further research, including comparison studies of alternative anticoagulant strategies, is required to elucidate the best approach to these difficult cases.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
A survey of 304 SCA and AmSECT members on anticoagulation for heparin-induced thrombocytopenia during cardiopulmonary bypass found that 75% used institutional protocols and that bivalirudin, used by 75% of respondents, was the most common alternative anticoagulant, typically monitored with activated clotting time.
Why This Matters for Hirudotherapy
This survey examined practice patterns for anticoagulating heparin-induced thrombocytopenia (HIT) patients requiring cardiopulmonary bypass, analyzing 304 completed surveys from Society of Cardiovascular Anesthesiologists and American Society for Extracorporeal Technology members. Bivalirudin—a direct thrombin inhibitor originally developed as 'hirulog' and structurally derived from the medicinal-leech anticoagulant hirudin—was the most commonly reported alternative anticoagulant (75% of respondents), making these data illustrate how a pharmacological descendant of the leech secretome has become established in a complex clinical setting. The findings document real-world clinical uptake rather than efficacy, however: this is a self-reported survey with a 5.8% response rate, and the authors explicitly note that comparison studies are still needed to determine the best approach. It therefore demonstrates adoption of a hirudin-based agent in HIT/CPB management, not proof that hirudotherapy-derived anticoagulation is superior to other strategies.
Citation
Reference (Vancouver style)
Wanat-Hawthorne A, Tanaka K, Angona R, Feng C, Eaton M. Survey of Practice Pattern in Patients With Heparin-Induced Thrombocytopenia Requiring Cardiopulmonary Bypass. Anesth Analg. 2021;133(5):1180-1186. doi:10.1213/ANE.0000000000005721. PMID: 34415867
Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.
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