Abstract 4143330: Pediatric Paracorporeal VAD Antiplatelet Protocol

Background: Ischemic stroke remains a dreaded complication of paracorporeal (continuous-PC; pulsatile-PP) ventricular assist devices (VADs) in pediatric patients. Advancements in anticoagulation management have improved the stroke rate to 12-17%, however, the management of antiplatelet therapy varies across centers. This study examines the outcomes of an antiplatelet protocol for patients with paracorporeal VADs at our center. Methods: We developed an antiplatelet protocol (Fig. 1) with dose adjustments guided by platelet function assays, VAD fibrin burden, and bleeding risk. We retrospectively reviewed patients with a paracorporeal VAD between December 2018 to December 2023. Demographic variables, incidence of thrombotic and bleeding events, and outcomes were assessed using descriptive statistics. Results: The cohort comprised 44 patients (52% male), median age 19 months (1 month - 8 years), with 22 (50%), 9 (20.5%), and 13 (29.5%) patients supported on PP, PC, and multiple VAD types respectively. Median support duration was 131 (PP; IQR 87, 183), 31 (PC; IQR 16, 46), and 88 (multiple VADs; IQR 66, 196) days. Diagnoses included cardiomyopathy 38% (n=17), congenital heart disease 57% (n=25) and others 5% (n=2). Thrombotic complications included: ischemic stroke in 6.8% (n=3) (1.9 events/100 patient months compared to 6-11 events/100 months reported in recent multicenter registry data); 11% (n=5) patients underwent 6 pump exchanges for fibrin burden. Major bleeding rate was 29.5% (n=13), most commonly gastrointestinal bleed; there were no hemorrhagic strokes. Five (11.3%) patients had an asymptomatic subdural hematoma (n=4 tiny/small, n=1 moderate). A positive clinical outcome was achieved in 86%, with 77% (n=34) bridged to transplant, 5% (n=2) explanted for recovery, and 5% (n=2) alive on device. Overall mortality was 14% (2 died on device, 4 transitioned to ECMO and died). Conclusions: Our experience underscores the efficacy of a structured antiplatelet protocol in managing pediatric patients with paracorporeal VADs associated with a low stroke rate. Future studies are needed to assess the generalizability of these findings.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4143330
Primary Topic
Cardiac Arrhythmias and Treatments
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article
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article

Abstract 4143330: Pediatric Paracorporeal VAD Antiplatelet Protocol

Michael C. Mongé, Rachel S. Bercovitz, Ashish Garg, Philip T. Thrush et al.
Circulation
Cardiac Arrhythmias and Treatments
article

Abstract 4143330: Pediatric Paracorporeal VAD Antiplatelet Protocol

Michael C. Mongé, Rachel S. Bercovitz, Ashish Garg, Philip T. Thrush, Naomi E. Hammond, Anna Joong
article en

Abstract

Background: Ischemic stroke remains a dreaded complication of paracorporeal (continuous-PC; pulsatile-PP) ventricular assist devices (VADs) in pediatric patients. Advancements in anticoagulation management have improved the stroke rate to 12-17%, however, the management of antiplatelet therapy varies across centers. This study examines the outcomes of an antiplatelet protocol for patients with paracorporeal VADs at our center. Methods: We developed an antiplatelet protocol (Fig. 1) with dose adjustments guided by platelet function assays, VAD fibrin burden, and bleeding risk. We retrospectively reviewed patients with a paracorporeal VAD between December 2018 to December 2023. Demographic variables, incidence of thrombotic and bleeding events, and outcomes were assessed using descriptive statistics. Results: The cohort comprised 44 patients (52% male), median age 19 months (1 month - 8 years), with 22 (50%), 9 (20.5%), and 13 (29.5%) patients supported on PP, PC, and multiple VAD types respectively. Median support duration was 131 (PP; IQR 87, 183), 31 (PC; IQR 16, 46), and 88 (multiple VADs; IQR 66, 196) days. Diagnoses included cardiomyopathy 38% (n=17), congenital heart disease 57% (n=25) and others 5% (n=2). Thrombotic complications included: ischemic stroke in 6.8% (n=3) (1.9 events/100 patient months compared to 6-11 events/100 months reported in recent multicenter registry data); 11% (n=5) patients underwent 6 pump exchanges for fibrin burden. Major bleeding rate was 29.5% (n=13), most commonly gastrointestinal bleed; there were no hemorrhagic strokes. Five (11.3%) patients had an asymptomatic subdural hematoma (n=4 tiny/small, n=1 moderate). A positive clinical outcome was achieved in 86%, with 77% (n=34) bridged to transplant, 5% (n=2) explanted for recovery, and 5% (n=2) alive on device. Overall mortality was 14% (2 died on device, 4 transitioned to ECMO and died). Conclusions: Our experience underscores the efficacy of a structured antiplatelet protocol in managing pediatric patients with paracorporeal VADs associated with a low stroke rate. Future studies are needed to assess the generalizability of these findings.

CirculationVol. 150(Suppl_1)
Northwestern University (US), Lurie Children's Hospital (US)
Good health and well-being
Openalex Percentile: Top 62%
Cardiac Arrhythmias and Treatments
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