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Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study

BACKGROUND AND AIMS: The therapeutic strategy for the treatment of known sequelae of COVID‐19 has shifted from reactive to preventative. In this study, we aim to evaluate the effects of acetylsalicylic acid (ASA), and anticoagulants on COVID‐19 related morbidity and mortality. METHODS: This record‐b...

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Autores principales: Malik, Muhammad B., Amer, Samar A., Merrell, Eric, Russo, Ronald, Riley, Jeffrey B., Scro, Austin, James, Elizabeth, Anuforo, Anderson, Adhikari, Soumya, Siciliano, Rosalie, Chebaya, Philip, Darling, Edward, Kuhn, Michael, Nieman, Gary, Shawkat, Ahmed, Aiash, Hani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273938/
https://www.ncbi.nlm.nih.gov/pubmed/35844823
http://dx.doi.org/10.1002/hsr2.699
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author Malik, Muhammad B.
Amer, Samar A.
Merrell, Eric
Russo, Ronald
Riley, Jeffrey B.
Scro, Austin
James, Elizabeth
Anuforo, Anderson
Adhikari, Soumya
Siciliano, Rosalie
Chebaya, Philip
Darling, Edward
Kuhn, Michael
Nieman, Gary
Shawkat, Ahmed
Aiash, Hani
author_facet Malik, Muhammad B.
Amer, Samar A.
Merrell, Eric
Russo, Ronald
Riley, Jeffrey B.
Scro, Austin
James, Elizabeth
Anuforo, Anderson
Adhikari, Soumya
Siciliano, Rosalie
Chebaya, Philip
Darling, Edward
Kuhn, Michael
Nieman, Gary
Shawkat, Ahmed
Aiash, Hani
author_sort Malik, Muhammad B.
collection PubMed
description BACKGROUND AND AIMS: The therapeutic strategy for the treatment of known sequelae of COVID‐19 has shifted from reactive to preventative. In this study, we aim to evaluate the effects of acetylsalicylic acid (ASA), and anticoagulants on COVID‐19 related morbidity and mortality. METHODS: This record‐based analytical cross‐sectional study targeted 539 COVID‐19 patients in a single United States medical center between March and December 2020. Through a random stratified sample, we recruited outpatient (n = 206) and inpatient (n = 333) cases from three management protocols, including standard care (SC) (n = 399), low‐dose ASA only (ASA) (n = 112), and anticoagulation only (AC) (n = 28). Collected data included demographics, comorbidities, and clinical outcomes. The primary outcome measure was inpatient admission. Exploratory secondary outcome measures included length of stay, 30‐day readmission rates, medical intensive care unit (MICU) admission, need for mechanical ventilation, the occurrence of acute respiratory distress syndrome (ARDS), bleeding events, clotting events, and mortality. The collected data were coded and analyzed using standard tests. RESULTS: Age, mean number of comorbidities, and all individual comorbidities except for asthma, and malignancy were significantly lower in the SC compared to ASA and AC. After adjusting for age and comorbidity via binary logistic regression models, no statistical differences were found between groups for the studied outcomes. When compared to the SC group, ASA had lower 30‐day readmission rates (odds ration [OR] 0.81 95% confidence interval [CI] 0.35–1.88, p = 0.63), MICU admission (OR 0.63 95% CI 0.34–1.17, p = 0.32), ARDS (OR 0.71 95% CI 0.33–1.52, p = 0.38), and death (OR 0.85 95% CI 0.36–1.99, p = 0.71). CONCLUSION: Low‐dose ASA has a nonsignificant but potentially protective role in reducing the risk of COVID‐19 related morbidity and mortality. Our data suggests a trend toward reduced 30‐day readmission rates, ARDS, MICU admissions, need for mechanical ventilation, and mortality compared to the standard management protocol. Further randomized control trials are needed to establish causal effects.
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spelling pubmed-92739382022-07-15 Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study Malik, Muhammad B. Amer, Samar A. Merrell, Eric Russo, Ronald Riley, Jeffrey B. Scro, Austin James, Elizabeth Anuforo, Anderson Adhikari, Soumya Siciliano, Rosalie Chebaya, Philip Darling, Edward Kuhn, Michael Nieman, Gary Shawkat, Ahmed Aiash, Hani Health Sci Rep Original Research BACKGROUND AND AIMS: The therapeutic strategy for the treatment of known sequelae of COVID‐19 has shifted from reactive to preventative. In this study, we aim to evaluate the effects of acetylsalicylic acid (ASA), and anticoagulants on COVID‐19 related morbidity and mortality. METHODS: This record‐based analytical cross‐sectional study targeted 539 COVID‐19 patients in a single United States medical center between March and December 2020. Through a random stratified sample, we recruited outpatient (n = 206) and inpatient (n = 333) cases from three management protocols, including standard care (SC) (n = 399), low‐dose ASA only (ASA) (n = 112), and anticoagulation only (AC) (n = 28). Collected data included demographics, comorbidities, and clinical outcomes. The primary outcome measure was inpatient admission. Exploratory secondary outcome measures included length of stay, 30‐day readmission rates, medical intensive care unit (MICU) admission, need for mechanical ventilation, the occurrence of acute respiratory distress syndrome (ARDS), bleeding events, clotting events, and mortality. The collected data were coded and analyzed using standard tests. RESULTS: Age, mean number of comorbidities, and all individual comorbidities except for asthma, and malignancy were significantly lower in the SC compared to ASA and AC. After adjusting for age and comorbidity via binary logistic regression models, no statistical differences were found between groups for the studied outcomes. When compared to the SC group, ASA had lower 30‐day readmission rates (odds ration [OR] 0.81 95% confidence interval [CI] 0.35–1.88, p = 0.63), MICU admission (OR 0.63 95% CI 0.34–1.17, p = 0.32), ARDS (OR 0.71 95% CI 0.33–1.52, p = 0.38), and death (OR 0.85 95% CI 0.36–1.99, p = 0.71). CONCLUSION: Low‐dose ASA has a nonsignificant but potentially protective role in reducing the risk of COVID‐19 related morbidity and mortality. Our data suggests a trend toward reduced 30‐day readmission rates, ARDS, MICU admissions, need for mechanical ventilation, and mortality compared to the standard management protocol. Further randomized control trials are needed to establish causal effects. John Wiley and Sons Inc. 2022-07-11 /pmc/articles/PMC9273938/ /pubmed/35844823 http://dx.doi.org/10.1002/hsr2.699 Text en © 2022 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Malik, Muhammad B.
Amer, Samar A.
Merrell, Eric
Russo, Ronald
Riley, Jeffrey B.
Scro, Austin
James, Elizabeth
Anuforo, Anderson
Adhikari, Soumya
Siciliano, Rosalie
Chebaya, Philip
Darling, Edward
Kuhn, Michael
Nieman, Gary
Shawkat, Ahmed
Aiash, Hani
Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title_full Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title_fullStr Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title_full_unstemmed Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title_short Effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in COVID‐19, analytical cross‐sectional study
title_sort effect of low dose acetylsalicylic acid and anticoagulant on clinical outcomes in covid‐19, analytical cross‐sectional study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273938/
https://www.ncbi.nlm.nih.gov/pubmed/35844823
http://dx.doi.org/10.1002/hsr2.699
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