TY - JOUR
T1 - Thrombotic Events in COVID-19 Are Associated With a Lower Use of Prophylactic Anticoagulation Before Hospitalization and Followed by Decreases in Platelet Reactivity
AU - Dutch COVID & Thrombosis Coalition
AU - Clark, Chantal C.
AU - Jukema, Bernard N.
AU - Barendrecht, Arjan D.
AU - Spanjaard, Judith S.
AU - Jorritsma, Nikita K.N.
AU - Smits, Simone
AU - de Maat, Steven
AU - Seinen, Cor W.
AU - Verhoef, Sandra
AU - Parr, Naomi M.J.
AU - Sebastian, Silvie A.E.
AU - Koekman, Arnold C.
AU - van Wesel, Annet C.W.
AU - van Goor, Harriet M.R.
AU - Spijkerman, Roy
AU - Bongers, Suzanne H.
AU - van der Vries, Erhard
AU - Nierkens, Stefan
AU - Boes, Marianne
AU - Koenderman, Leo
AU - Kaasjager, Karin A.H.
AU - Maas, Coen
N1 - Publisher Copyright:
© Copyright © 2021 Clark, Jukema, Barendrecht, Spanjaard, Jorritsma, Smits, de Maat, Seinen, Verhoef, Parr, Sebastian, Koekman, van Wesel, van Goor, Spijkerman, Bongers, van der Vries, Nierkens, Boes, Koenderman, Kaasjager and Maas.
PY - 2021/4/22
Y1 - 2021/4/22
N2 - Background: Coronavirus disease of 2019 (COVID-19) is associated with a prothrombotic state and a high incidence of thrombotic event(s) (TE). Objectives: To study platelet reactivity in hospitalized COVID-19 patients and determine a possible association with the clinical outcomes thrombosis and all-cause mortality. Methods: Seventy nine hospitalized COVID-19 patients were enrolled in this retrospective cohort study and provided blood samples in which platelet reactivity in response to stimulation with ADP and TRAP-6 was determined using flow cytometry. Clinical outcomes included thrombotic events, and all-cause mortality. Results: The incidence of TE in this study was 28% and all-cause mortality 16%. Patients that developed a TE were younger than patients that did not develop a TE [median age of 55 vs. 70 years; adjusted odds ratio (AOR) = 0.96 per 1 year of age, 95% confidence interval (CI) 0.92–1.00; p = 0.041]. Furthermore, patients using preexisting thromboprophylaxis were less likely to develop a thrombotic complication than patients that were not (18 vs. 54%; AOR = 0.19, 95% CI 0.04–0.84; p = 0.029). Conversely, having asthma strongly increased the risk on TE development (AOR = 6.2, 95% CI 1.15–33.7; p = 0.034). No significant differences in baseline P-selectin expression or platelet reactivity were observed between the COVID-19 positive patients (n = 79) and COVID-19 negative hospitalized control patients (n = 21), nor between COVID-19 positive survivors or non-survivors. However, patients showed decreased platelet reactivity in response to TRAP-6 following TE development. Conclusion: We observed an association between the use of preexisting thromboprophylaxis and a decreased risk of TE during COVID-19. This suggests that these therapies are beneficial for coping with COVID-19 associated hypercoagulability. This highlights the importance of patient therapy adherence. We observed lowered platelet reactivity after the development of TE, which might be attributed to platelet desensitization during thromboinflammation.
AB - Background: Coronavirus disease of 2019 (COVID-19) is associated with a prothrombotic state and a high incidence of thrombotic event(s) (TE). Objectives: To study platelet reactivity in hospitalized COVID-19 patients and determine a possible association with the clinical outcomes thrombosis and all-cause mortality. Methods: Seventy nine hospitalized COVID-19 patients were enrolled in this retrospective cohort study and provided blood samples in which platelet reactivity in response to stimulation with ADP and TRAP-6 was determined using flow cytometry. Clinical outcomes included thrombotic events, and all-cause mortality. Results: The incidence of TE in this study was 28% and all-cause mortality 16%. Patients that developed a TE were younger than patients that did not develop a TE [median age of 55 vs. 70 years; adjusted odds ratio (AOR) = 0.96 per 1 year of age, 95% confidence interval (CI) 0.92–1.00; p = 0.041]. Furthermore, patients using preexisting thromboprophylaxis were less likely to develop a thrombotic complication than patients that were not (18 vs. 54%; AOR = 0.19, 95% CI 0.04–0.84; p = 0.029). Conversely, having asthma strongly increased the risk on TE development (AOR = 6.2, 95% CI 1.15–33.7; p = 0.034). No significant differences in baseline P-selectin expression or platelet reactivity were observed between the COVID-19 positive patients (n = 79) and COVID-19 negative hospitalized control patients (n = 21), nor between COVID-19 positive survivors or non-survivors. However, patients showed decreased platelet reactivity in response to TRAP-6 following TE development. Conclusion: We observed an association between the use of preexisting thromboprophylaxis and a decreased risk of TE during COVID-19. This suggests that these therapies are beneficial for coping with COVID-19 associated hypercoagulability. This highlights the importance of patient therapy adherence. We observed lowered platelet reactivity after the development of TE, which might be attributed to platelet desensitization during thromboinflammation.
KW - COVID-19
KW - platelets
KW - pulmonary thrombosis
KW - SARS-CoV-2
KW - thromboinflammation
KW - thrombosis
KW - thrombotic event
UR - http://www.scopus.com/inward/record.url?scp=85105384673&partnerID=8YFLogxK
U2 - 10.3389/fmed.2021.650129
DO - 10.3389/fmed.2021.650129
M3 - Article
AN - SCOPUS:85105384673
SN - 2296-858X
VL - 8
JO - Frontiers in Medicine
JF - Frontiers in Medicine
M1 - 650129
ER -