Bivalirudin Anticoagulation Dosing Protocol for Extracorporeal Membrane Oxygenation: A Retrospective Review.
Research article published in The journal of extra-corporeal technology (2018)
Abstract
Anticoagulation with unfractionated heparin during extracorporeal membrane oxygenation (ECMO) is common, but alternative agents are being evaluated for safety and efficacy. The objective of this analysis was to assess if a comprehensive bivalirudin dosing and monitoring protocol effectively guides dose adjustments and monitoring of bivalirudin in patients during ECMO. Our analysis included 11 patients who received bivalirudin during ECMO therapy and had dosing managed using our hospital derived protocol. Patients treated over a 1-year period were included in this retrospective analysis. Clinical characteristics and changes in activated partial thromboplastin time (aPTT) were evaluated from medical records to determine the efficacy of the dosing protocol. ECMO was initiated for acute respiratory distress syndrome in eight (72.7%) patients and for cardiac arrest in three (27.3%) patients. A total of 178 protocol guided dose adjustments were made during the study. Among the dose adjustments, 56 (31.5%) attained the protocol predicted aPTT level change, 96 (53.9%) of the measured aPTT changes were less than predicted, and 26 (14.6%) of the measured aPTT changes were more than predicted. On average, patients were within their defined therapeutic aPTT target range 66.3% of the time. All patients reached their designated aPTT target range within the first 24 hours of therapy. Significant bleeding was documented in eight (72.7%) patients. No clinically evident thromboembolic events were identified in vivo while cannulated. This analysis suggests that bivalirudin can be managed using a dosing protocol to provide anticoagulation therapy to patients during ECMO and can provide foundational guidance for dose adjustment and monitoring for other institutions.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Anticoagulation with unfractionated heparin during extracorporeal membrane oxygenation (ECMO) is common, but alternative agents are being evaluated for safety and efficacy. The objective of this analysis was to assess if a comprehensive bivalirudin dosing and monitoring protocol effectively guides...
Warum dies für die Hirudotherapie relevant ist
Diese retrospektive Auswertung untersuchte 11 ECMO-Patienten, deren Bivalirudin-Antikoagulation über ein hauseigenes Dosierungsprotokoll gesteuert wurde, und ergab, dass alle Patienten ihren Ziel-aPTT-Bereich innerhalb von 24 Stunden erreichten, wobei jedoch bei 72,7 % signifikante Blutungen auftraten und nur 31,5 % von 178 Dosisanpassungen die vorhergesagte aPTT-Veränderung erzielten. Für die ASH besitzt diese Studie echte Relevanz, da Bivalirudin ein synthetischer direkter Thrombininhibitor ist, der aus Hirudin abgeleitet ist – dem potenten Antikoagulans, das ursprünglich aus dem Speichel des medizinischen Blutegels isoliert wurde – und zeigt, wie ein Derivat des Blutegelsekretoms für die intensivmedizinische Antikoagulation weiterentwickelt wird. Diese Praxisdaten zur Dosierung tragen zum Verständnis des Managements Hirudin-basierter Antikoagulanzien außerhalb der klassischen Blutegeltherapie bei. Allerdings sind mit nur 11 Patienten an einem einzigen Zentrum, retrospektivem Studiendesign und einer hohen Blutungsrate die Sicherheit und Generalisierbarkeit des Protokolls nicht belegt, und aus dieser kleinen Fallserie lassen sich keine Wirksamkeitsaussagen ableiten.
Zitation
Bivalirudin Anticoagulation Dosing Protocol for Extracorporeal Membrane Oxygenation: A Retrospective Review.
Netley et al. · The journal of extra-corporeal technology, 2018
Verwandter klinischer Kontext
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