Evaluation of bivalirudin-based anticoagulation for extracorporeal membrane oxygenation, including patients with COVID-19
Clinical research published in J Extra Corpor Technol (2026)
Abstract
BACKGROUND: Although unfractionated heparin (UFH) has traditionally been used for anticoagulation during extracorporeal membrane oxygenation (ECMO), bivalirudin may be preferred due to fewer complications. A prior medication use evaluation of ECMO patients who received bivalirudin resulted in dosing updates for our pharmacist-directed bivalirudin protocol. This study intended to evaluate the efficacy and safety of bivalirudin for anticoagulation during ECMO support post-protocol initiation. METHODS: This was a retrospective, single-center, pre-post study. Adult patients requiring ECMO support for at least 24 h and who received bivalirudin between January 1, 2015 to July 31, 2018 (pre-group) and May 1, 2019 to June 30, 2021 (post-group) were included. RESULTS: There were 38 patients in the pre- and 35 patients in the post-group. The primary outcome, median time to two consecutive activated partial thromboplastin times (aPTTs) within therapeutic range for the initial goal range, was 8.9 h in the pre- and 14.2 h in the post-group (p = 0.517). In a subgroup analysis of the post-group, the primary outcome was higher in patients with COVID-19 (26.5 vs. 8.6 h, p = 0.018). The median number of dose adjustments to achieve goal aPTT was higher in COVID-19 patients (4 vs. 2, p = 0.017). CONCLUSION: These results suggest that a standardized pharmacist-directed protocol for bivalirudin in ECMO achieves timely therapeutic anticoagulation levels. Patients with COVID-19 trended toward longer times to two consecutive therapeutic aPTTs. Further studies are needed to evaluate dosing strategies in patients with and without COVID-19.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Evaluation of bivalirudin-based anticoagulation during ECMO support across patient cohorts including those with COVID-19, comparing bleeding/thrombosis outcomes against heparin-based protocols.
Warum dies für die Hirudotherapie relevant ist
Diese retrospektive, monozentrische Pre-Post-Studie evaluierte ein apothekergelenktes Bivalirudin-Dosierungsprotokoll zur ECMO-Antikoagulation bei 73 Patienten (38 vor dem Protokoll, 35 nach dem Protokoll) und berichtete, dass das standardisierte Protokoll zeitgerechte therapeutische aPTT-Werte erreichte, während eine COVID-19-Subgruppe längere Zeiten bis zu zwei aufeinanderfolgenden therapeutischen aPTT-Werten (26,5 vs. 8,6 h, P=0,018) sowie mehr Dosisanpassungen aufwies. Der Abstract erwähnt weder Hirudin noch Blutegel oder Blutegeltherapie, und Bivalirudin wird ausschließlich als Alternative zu Heparin ohne jeglichen Bezug auf aus Blutegeln stammende Substanzen diskutiert. Es lässt sich keine vertretbare Verbindung zur Hirudotherapie oder zum Blutegelsekretom aus diesem Artikel herleiten. Die Studie ist daher für das Fachgebiet der ASH nicht relevant.
Zitation
Evaluation of bivalirudin-based anticoagulation for extracorporeal membrane oxygenation, including patients with COVID-19.
Raguindin M et al. · The journal of extra-corporeal technology, 2026
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