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The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery

BACKGROUND: An antiplatelet therapy with acetylsalicylic acid (ASA) is prescribed in the prevention of cardiovascular events, but around 24% of ASA takers are resistant to the treatment. AIM: In this prospective, observational cohort study, we aimed to identify the prevalence and risk factors of ASA...

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Autores principales: Kazimi, Alia Uzra, Weber, Christian Friedrich, Keese, Michael, Miesbach, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642110/
https://www.ncbi.nlm.nih.gov/pubmed/34609920
http://dx.doi.org/10.1177/10760296211044723
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author Kazimi, Alia Uzra
Weber, Christian Friedrich
Keese, Michael
Miesbach, Wolfgang
author_facet Kazimi, Alia Uzra
Weber, Christian Friedrich
Keese, Michael
Miesbach, Wolfgang
author_sort Kazimi, Alia Uzra
collection PubMed
description BACKGROUND: An antiplatelet therapy with acetylsalicylic acid (ASA) is prescribed in the prevention of cardiovascular events, but around 24% of ASA takers are resistant to the treatment. AIM: In this prospective, observational cohort study, we aimed to identify the prevalence and risk factors of ASA nonresponse in patients who underwent vascular surgery. METHODS: The study was conducted in the University hospital in Frankfurt am Main. In total, 70 patients were pre-treated with 100 mg of ASA per day and underwent either elective carotid thromboendarterectomy, femoral thromboendarterectomy or endovascular aneurysm repair of the abdominal aorta. The platelet function was measured on the first preoperative and the second or fourth postoperative day with the multiple electrode aggregometry by in-vitro stimulation with arachidonic acid (ASPItest) and thrombin receptor activating peptide 6 (TRAPtest). The primary end point was the in-vitro induced platelet aggregation in the ASPItest. If the ASPItest amounted ≥400 AU × min, the patients were categorized as ASA nonresponders. RESULTS: The total prevalence of ASA nonresponse in our study was 20% preoperatively and 35.7% postoperatively (p = 0.005). As significant predictors for ASA nonresponse, we demonstrated the area under the aggregation curve in the TRAPtest preoperatively (p = 0.04) and postoperatively (p = 0.02), and the two comorbidities arterial hypertension (P < .001; rho 0.44) and diabetes mellitus (p = 0.04; rho 0.39), which are already well known to be associated with ASA nonresponse. CONCLUSION: In conclusion, data of the study indicate a high incidence of perioperative, laboratory ASA nonresponse in patients undergoing vascular surgery.
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spelling pubmed-86421102021-12-04 The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery Kazimi, Alia Uzra Weber, Christian Friedrich Keese, Michael Miesbach, Wolfgang Clin Appl Thromb Hemost Original Manuscript BACKGROUND: An antiplatelet therapy with acetylsalicylic acid (ASA) is prescribed in the prevention of cardiovascular events, but around 24% of ASA takers are resistant to the treatment. AIM: In this prospective, observational cohort study, we aimed to identify the prevalence and risk factors of ASA nonresponse in patients who underwent vascular surgery. METHODS: The study was conducted in the University hospital in Frankfurt am Main. In total, 70 patients were pre-treated with 100 mg of ASA per day and underwent either elective carotid thromboendarterectomy, femoral thromboendarterectomy or endovascular aneurysm repair of the abdominal aorta. The platelet function was measured on the first preoperative and the second or fourth postoperative day with the multiple electrode aggregometry by in-vitro stimulation with arachidonic acid (ASPItest) and thrombin receptor activating peptide 6 (TRAPtest). The primary end point was the in-vitro induced platelet aggregation in the ASPItest. If the ASPItest amounted ≥400 AU × min, the patients were categorized as ASA nonresponders. RESULTS: The total prevalence of ASA nonresponse in our study was 20% preoperatively and 35.7% postoperatively (p = 0.005). As significant predictors for ASA nonresponse, we demonstrated the area under the aggregation curve in the TRAPtest preoperatively (p = 0.04) and postoperatively (p = 0.02), and the two comorbidities arterial hypertension (P < .001; rho 0.44) and diabetes mellitus (p = 0.04; rho 0.39), which are already well known to be associated with ASA nonresponse. CONCLUSION: In conclusion, data of the study indicate a high incidence of perioperative, laboratory ASA nonresponse in patients undergoing vascular surgery. SAGE Publications 2021-10-05 /pmc/articles/PMC8642110/ /pubmed/34609920 http://dx.doi.org/10.1177/10760296211044723 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Manuscript
Kazimi, Alia Uzra
Weber, Christian Friedrich
Keese, Michael
Miesbach, Wolfgang
The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title_full The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title_fullStr The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title_full_unstemmed The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title_short The Pre- and Postoperative Prevalence and Risk Factors of ASA Nonresponse in Vascular Surgery
title_sort pre- and postoperative prevalence and risk factors of asa nonresponse in vascular surgery
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642110/
https://www.ncbi.nlm.nih.gov/pubmed/34609920
http://dx.doi.org/10.1177/10760296211044723
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