SSRN Electronic Journal | 2021

Lupus Anticoagulant is Associated With Critical Cases and High Mortality in COVID-19

 
 
 
 
 
 
 
 

Abstract


Background: In severe COVID-19 cases, hypercoagulable state may occur. Antiphospholipid syndrome related auto-antibodies (APSRAs) contribute to coagulopathy, but their role in COVID-19 remains unclear. We aimed to investigate the prevalence of positive APSRAs and their effect on clinical outcomes in confirmed COVID-19 patients. \n \nMethod In this cross-sectional study, severe hospitalized COVID-19 cases were enrolled. Demographic and clinical data were obtained from the day of admission. APSRAs including IgG and/or IgM anticardiolipin (aCL) and anti-β2-glycoprotein1 (anti-β2GP1) as well as lupus anticoagulant (LAC) were measured.\xa0 \n \nFinding: In this study, 54 severe COVID-19 cases with positive RT-PCR and/or chest CT scan were recruited. Positive APSRAs was found in 7 (12.9%) patients. Positive LAC was more prevalent marker as compared to other tests (11.1%). The prevalence of positive aCL (IgM or IgG) and anti-s2 GPI (IgM or IgG) was 1.8% (in an elderly woman). Lower oxygen saturation was found in positive APSRAs group as opposed to negative APSRAs group (70.3±9 vs 84.8±9.7%). Mortality rate in positive APSRAs group was significantly higher relative to negative APSRAs group (83.3% vs 27.1%; P-value: 0.01). Likewise, the mechanical ventilation requirement in the positive group was also higher (50% vs 27.1%, P-value: 0.28).\xa0 \n \nConclusion: This study indicated that LAC directly is associated with critical cases and high mortality of COVID-19. Nonetheless the mortality was not related to macrothrombotic incidence. \n \nFunding Information: There is no funding. \n \nDeclaration of Interests: We declare no competing interests. \n \nEthics Approval Statement: The study was confirmed by the Ethics in Medical Research Committee IR.SBMU.RETECH.REC.1399.1362. Signed informed consents were obtained from all the participants or their legally authorized representatives.

Volume None
Pages None
DOI 10.2139/ssrn.3880443
Language English
Journal SSRN Electronic Journal

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