tetano
Editor, Senior Moderator
J Am Coll Cardiol
. 2022 Jul 26;80(4):316-328.
doi: 10.1016/j.jacc.2022.04.060.
Association of Blood Viscosity With Mortality Among Patients Hospitalized With COVID-19
Daein Choi[SUP] 1 [/SUP], Ori Waksman[SUP] 2 [/SUP], Aleesha Shaik[SUP] 2 [/SUP], Phyu Mar[SUP] 2 [/SUP], Qinzhong Chen[SUP] 2 [/SUP], Daniel J Cho[SUP] 3 [/SUP], HyoungSup Kim[SUP] 3 [/SUP], Robin L Smith[SUP] 4 [/SUP], Sascha N Goonewardena[SUP] 5 [/SUP], Robert S Rosenson[SUP] 6 [/SUP]
Affiliations
Abstract
Background: Coronavirus disease-2019 (COVID-19) is characterized by a dysfunctional immune response and abnormal blood rheology that contribute to endothelial dysfunction and thrombotic complications. Whole blood viscosity (WBV) is a clinically validated measure of blood rheology and an established predictor of cardiovascular risk. We hypothesize that increased WBV is associated with mortality among patients hospitalized with COVID-19.
Objectives: This study sought to determine the association between estimated BV (eBV) and mortality among hospitalized COVID-19 patients.
Methods: The study population included 5,621 hospitalized COVID-19 patients at the Mount Sinai Health System from February 27, 2020, to November 27, 2021. eBV was calculated using the Walburn-Schneck model. Multivariate Cox proportional hazards models were used to evaluate the association between eBV and mortality. Considered covariates included age, sex, race, cardiovascular and metabolic comorbidities, in-house pharmacotherapy, and baseline inflammatory biomarkers.
Results: Estimated high-shear BV (eHSBV) and estimated low-shear BV were associated with increased in-hospital mortality. One-centipoise increases in eHSBV and estimated low-shear BV were associated with a 36.0% and 7.0% increase in death, respectively (P < 0.001). Compared with participants in the lowest quartile of eHSBV, those in the highest quartile of eHSBV had higher mortality (adjusted HR: 1.53; 95% CI: 1.27-1.84). The association was consistent among multiple subgroups, notably among patients without any comorbidities (adjusted HR: 1.69; 95% CI: 1.28-2.22).
Conclusions: Among hospitalized COVID-19 patients, increased eBV is significantly associated with higher mortality. This suggests that eBV can prognosticate patient outcomes in earlier stages of COVID-19, and that future therapeutics aimed at reducing WBV should be evaluated.
Keywords: COVID-19; blood viscosity; cardiovascular disease; mortality; rheology epidemiology.
. 2022 Jul 26;80(4):316-328.
doi: 10.1016/j.jacc.2022.04.060.
Association of Blood Viscosity With Mortality Among Patients Hospitalized With COVID-19
Daein Choi[SUP] 1 [/SUP], Ori Waksman[SUP] 2 [/SUP], Aleesha Shaik[SUP] 2 [/SUP], Phyu Mar[SUP] 2 [/SUP], Qinzhong Chen[SUP] 2 [/SUP], Daniel J Cho[SUP] 3 [/SUP], HyoungSup Kim[SUP] 3 [/SUP], Robin L Smith[SUP] 4 [/SUP], Sascha N Goonewardena[SUP] 5 [/SUP], Robert S Rosenson[SUP] 6 [/SUP]
Affiliations
- PMID: 35863848
- DOI: 10.1016/j.jacc.2022.04.060
Abstract
Background: Coronavirus disease-2019 (COVID-19) is characterized by a dysfunctional immune response and abnormal blood rheology that contribute to endothelial dysfunction and thrombotic complications. Whole blood viscosity (WBV) is a clinically validated measure of blood rheology and an established predictor of cardiovascular risk. We hypothesize that increased WBV is associated with mortality among patients hospitalized with COVID-19.
Objectives: This study sought to determine the association between estimated BV (eBV) and mortality among hospitalized COVID-19 patients.
Methods: The study population included 5,621 hospitalized COVID-19 patients at the Mount Sinai Health System from February 27, 2020, to November 27, 2021. eBV was calculated using the Walburn-Schneck model. Multivariate Cox proportional hazards models were used to evaluate the association between eBV and mortality. Considered covariates included age, sex, race, cardiovascular and metabolic comorbidities, in-house pharmacotherapy, and baseline inflammatory biomarkers.
Results: Estimated high-shear BV (eHSBV) and estimated low-shear BV were associated with increased in-hospital mortality. One-centipoise increases in eHSBV and estimated low-shear BV were associated with a 36.0% and 7.0% increase in death, respectively (P < 0.001). Compared with participants in the lowest quartile of eHSBV, those in the highest quartile of eHSBV had higher mortality (adjusted HR: 1.53; 95% CI: 1.27-1.84). The association was consistent among multiple subgroups, notably among patients without any comorbidities (adjusted HR: 1.69; 95% CI: 1.28-2.22).
Conclusions: Among hospitalized COVID-19 patients, increased eBV is significantly associated with higher mortality. This suggests that eBV can prognosticate patient outcomes in earlier stages of COVID-19, and that future therapeutics aimed at reducing WBV should be evaluated.
Keywords: COVID-19; blood viscosity; cardiovascular disease; mortality; rheology epidemiology.