Platelet-mapping assay for monitoring antiplatelet therapy during mechanical circulatory support in children: A retrospective observational study
Autor: | Christilla Bachelot-Loza, Tiffany Pascreau, Tiphaine Belleville-Rolland, Philippe Pouard, Olivier Raisky, Myrto Costopoulos, Dominique Lasne, Chiara Giorni, Delphine Borgel |
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Rok vydání: | 2017 |
Předmět: |
pediatrics
medicine.medical_treatment 030204 cardiovascular system & hematology Fibrin 03 medical and health sciences 0302 clinical medicine platelet function tests medicine Platelet activation platelet aggregation inhibitors Aspirin biology medicine.diagnostic_test business.industry ventricular‐assist device Retrospective cohort study thromboelastography Hematology Original Articles Thromboelastography Dipyridamole 030228 respiratory system Online‐only Articles Ventricular assist device Anesthesia platelets biology.protein Platelet aggregation inhibitor Original Article business medicine.drug |
Zdroj: | Research and Practice in Thrombosis and Haemostasis |
ISSN: | 2475-0379 |
Popis: | Essentials Thromboelastography (TEG)-platelet mapping (PM) assay is used for antiplatelet-drug monitoring. The TEG-PM was evaluated for dypiridamole and aspirin monitoring in 4 BH-implanted children. Some TEG-PM tracings were atypical leading to wrong results. The TEG-PM has to be improved for antiplatelet-drug monitoring during ventricular assistance. Introduction The complex hemostatic changes associated with Berlin Heart (BH) implantation in children require a challenging antithrombotic treatment. The aim of this retrospective analysis was to evaluate the thromboelastography (TEG)-platelet mapping (PM) assay to monitor antiplatelet therapy in children implanted with a BH. Methods TEG-PM was performed in 4 BH-implanted patients receiving dipyridamole and aspirin, and 9 healthy volunteers. Patients’ antiplatelet therapy was adjusted to TEG-PM results. Light transmission aggregometry (LTA) was also available for 2 of these patients. Results Between 2009 and 2014, 4 BH-implanted patients received a dual antiplatelet therapy monitored by TEG-PM. In 2 patients, 18 of 34 tracings were atypical, because the maximum amplitude due to fibrin never stabilized, which made difficult antiplatelet therapy adjustment as recommended by BH's guidelines. To overcome this difficulty, TEG-PM and LTA were next performed in parallel. However, both methods led to different decisions to adjust antiplatelet therapy in 57% of the cases. In order to better understand this atypical tracing, TEG-PM was also performed in 9 volunteers and surprisingly 3 of them had the same atypical tracing. This atypical tracing was corrected by adding apyrase, suggesting that adenosine diphosphate (ADP) participates to spontaneous platelet activation in heparinized samples. In addition, we evidenced a high variability in the responses of TEG-PM with ADP in volunteers. Conclusions Antiplatelet therapy monitoring in BH-implanted children remains challenging, as TEG-PM is sensitive to several preanalytical and analytical conditions. |
Databáze: | OpenAIRE |
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