Abstract

IntroductionCoagulation parameters are important determinants for COVID-19 infection. We conducted meta-analysis to assess the association between early hemostatic parameters and infection severity.MethodsElectronic search was made for papers that addressed clinical characteristics of COVID-19 patients and disease severity. Results were filtered using exclusion and inclusion criteria and then pooled into a meta-analysis to estimate the standardized mean difference (SMD) with 95% confidence interval (CI) for D-dimers, fibrinogen, prothrombin time, platelet count (PLT), activated partial thromboplastin time. To explore the heterogeneity and robustness of our fundings, sensitivity and subgroup analyses were conducted. Publication bias was assessed with contour-enhanced funnel plots and Egger's test by linear regression. Coagulation parameters data from retrospective cohort study of 451 patients with COVID-19 at National Research Center for Cardiac Surgery were included in meta-analysis of published studies.ResultsOverall, 41 original studies (17,601 patients) on SARS-CoV-2 were included. For the two groups of patients, stratified by severity, we identified that D-dimers, fibrinogen, activated partial thromboplastin time, and prothrombin time were significantly higher in the severe group [SMD 0.6985 with 95%CI (0.5155; 0.8815); SMD 0.661 with 95%CI (0.3387; 0.9833); SMD 0.2683 with 95%CI (0.1357; 0.4009); SMD 0.284 with 95%CI (0.1472; 0.4208)]. In contrast, PLT was significantly lower in patients with more severe cases of COVID-19 [SMD −0.1684 with 95%CI (−0.2826; −0.0542)]. Neither the analysis by the leave-one-out method nor the influence diagnostic have identified studies that solely cause significant change in the effect size estimates. Subgroup analysis showed no significant difference between articles originated from different countries but revealed that severity assessment criteria might have influence over estimated effect sizes for platelets and D-dimers. Contour-enhanced funnel plots and the Egger's test for D-dimers and fibrinogen revealed significant asymmetry that might be a sign of publication bias.ConclusionsThe hemostatic laboratory parameters, with exception of platelets, are significantly elevated in patients with severe COVID-19. The two variables with strongest association to disease severity were D-dimers and fibrinogen levels. Future research should aim outside conventional coagulation tests and include analysis of clotting formation and platelet/platelet progenitors characteristics.

Highlights

  • Coagulation parameters are important determinants for COVID-19 infection

  • We aimed to identify the relationship between coagulation biomarkers taken at admission and severity of COVID-19 in adult patients by estimating the effect size of five laboratory coagulation tests: D-dimers (DD), platelet count (PLT), fibrinogen (FIB), activated partial thromboplastin time (APTT), and prothrombin time (PT)

  • APTT, and PT were significantly higher in more severe cases [standardized mean difference (SMD) 0.6985 with 95% confidence interval (CI) (0.5155; 0.8815); SMD 0.661 with 95% CI (0.3387; 0.9833); SMD 0.2683 with 95% CI (0.1357; 0.4009); SMD 0.284 with 95% CI (0.1472; 0.4208)]

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Summary

Introduction

Coagulation parameters are important determinants for COVID-19 infection. We conducted meta-analysis to assess the association between early hemostatic parameters and infection severity. Evidence of abnormal COVID-19associated coagulation parameters has already appeared in early publications from Wuhan [9–12] and was supported by further publications worldwide [rev. The reported hemostatic abnormalities with COVID-19 infection include increased D-dimers (DD) levels [14, 15], fibrinogen levels [16, 17], changes in the quantities and levels of activation of platelets [14, 18–20], elevated von Willebrand factor (VWF) [(21, 22), rev. Elevated risk of thromboembolic events, even with the initiation of prophylactic anti-coagulation, suggest the presence of hypofibrinolysis, in addition to detected hypercoagulability in COVID-19 [24, 25]. It is consistent with the results of thromboelastography (TEG) reported by Wright et al [26]

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