Research article

A meta-analysis to estimate the incidence of thromboembolism in hospitalized COVID-19 patients

  • Received: 06 September 2020 Accepted: 12 November 2020 Published: 19 November 2020
  • Coronavirus disease 2019 (COVID-19) is associated with an increased risk of venous and arterial thrombosis in patients. Numerous studies have been conducted on COVID-19 and its association with thromboembolism is well known. We conducted a meta-analysis to find out the incidence of thromboembolism in hospitalised patients with COVID-19 to provide more generalized results. A systematic literature search was conducted in PubMed and SCOPUS to find observational studies reporting outcomes of interest. Amongst the studied thromboembolic events, the meta-analysis showed the prevalence of pulmonary embolism (PP: 12.4% [7.2%, 18.6%]; I2 = 97.23%) to be the highest. It was followed by deep vein thrombosis (PP: 8.6% [4.2%, 14.3%]; I2 = 97.52%), myocardial infarction (PP: 2.3% [0.2%, 11.2%]; I2 = 99.3%), and stroke (PP: 1.2% [0.8%, 1.6%]; I2 = 65.09%). The results of this analysis further warrant the timely and appropriate use of pharmacological thromboprophylaxis and identification of risk factors in hospitalized COVID-19 patients.

    Citation: Ayema Haque, Areeba Minhaj, Areeba Ahmed, Owais Khan, Palvisha Qasim, Hasan Fareed, Fatima Nazir, Ayesha Asghar, Kashif Ali, Sobia Mansoor. A meta-analysis to estimate the incidence of thromboembolism in hospitalized COVID-19 patients[J]. AIMS Medical Science, 2020, 7(4): 301-310. doi: 10.3934/medsci.2020020

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  • Coronavirus disease 2019 (COVID-19) is associated with an increased risk of venous and arterial thrombosis in patients. Numerous studies have been conducted on COVID-19 and its association with thromboembolism is well known. We conducted a meta-analysis to find out the incidence of thromboembolism in hospitalised patients with COVID-19 to provide more generalized results. A systematic literature search was conducted in PubMed and SCOPUS to find observational studies reporting outcomes of interest. Amongst the studied thromboembolic events, the meta-analysis showed the prevalence of pulmonary embolism (PP: 12.4% [7.2%, 18.6%]; I2 = 97.23%) to be the highest. It was followed by deep vein thrombosis (PP: 8.6% [4.2%, 14.3%]; I2 = 97.52%), myocardial infarction (PP: 2.3% [0.2%, 11.2%]; I2 = 99.3%), and stroke (PP: 1.2% [0.8%, 1.6%]; I2 = 65.09%). The results of this analysis further warrant the timely and appropriate use of pharmacological thromboprophylaxis and identification of risk factors in hospitalized COVID-19 patients.


    Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) might put patients at a risk of venous and arterial thrombosis [1]. A thrombus is a solid mass composed of platelets and fibrin with a few trapped red and white blood cells that forms within a blood vessel. Its formation is potentiated by either a hypercoagulable state or obstruction. SARS-CoV-2 uses angiotensin converting enzyme 2 (ACE2) receptor for entry into endothelial cells and replicates, which causes infiltration of inflammatory cells, endothelial cell death, and prothrombotic effects in the microvasculature. This may lead to systemic hypercoagulability and increased risk for thromboembolic events [2]. There are a number of studies highlighting the occurrence of thromboembolism in COVID-19 positive patients. However, these studies have reported varied findings. Therefore, this meta-analysis would help us analyze the prevalence of thromboembolic events in the hospitalized COVID-19 patients.

    PubMed and SCOPUS were searched up till July 21, 2020 using the following keywords and their MeSH terms: “COVID-19”, “Thromboembolism”, “Pulmonary Embolism”, “Deep Venous Thrombosis”, “Stroke”, “Myocardial Infarction”. Two reviewers (SSA and AA) independently conducted the literature search. A third reviewer was consulted to resolve any conflict faced by the two authors. We included retrospective, cross-sectional, case-control, and cohort studies on COVID-19 hospitalized patients that reported the incidence of thromboembolic events. Both genders were included and there was no age limit. We included studies that were published in English only. The studies that did not report the incidence of thromboembolic events and which were conducted in out of hospital patients were excluded. Initially, 571 potential studies were identified from the search strategy. PRISMA flow chart (Figure 1) summarizes our literature search [3]. After exclusions based on sequential screening of titles, abstracts, and full-texts, 20 studies (Table 1) were included. The outcomes of interest were presence of pulmonary embolism (PE), deep vein thrombosis (DVT), stroke, and myocardial infarction (MI). Outcomes were presented as proportions. Arcsine of square root proportions and corresponding 95% confidence intervals (CI) were pooled using a random effects model. P value <0.05 was considered significant.

    The analysis includes 20 studies (Table 1) with a total of 15,452 patients [4][23]. The incidence of venous thromboembolism was found to be greater than arterial thromboembolism. Amongst the studied thromboembolic events, the prevalence of pulmonary embolism (PP: 12.4% [7.2%, 18.6%]; I2 = 97.23%) was the highest. It was followed by deep vein thrombosis (PP: 8.6% [4.2%, 14.3%]; I2 = 97.52%), myocardial infarction (PP: 2.3% [0.2%, 11.2%]; I2 = 99.3%), and stroke (PP: 1.2% [0.8%, 1.6%]; I2 = 65.09%), (Table 2 and Figue 2, 3, 4, and 5). The Forest plots (Figure 6) show the combined incidence of arterial thromboembolism including MI and stroke (PP: 2.5% [0.2%, 0.7%]; I2 = 98.91%). Figure 7 shows Forest plots of venous thromboembolism, including pulmonary embolism and deep venous thrombosis (PP: 15.8% [10.0%, 22.6%]; I2 = 98.21%).

    Figure 1.  PRISMA flow chart.
    Table 1.  Study Characteristics of Included Studies.
    Author Country Study type Outcomes reported Sample size Age Sex (%)
    Male Female
    Klok et al. [11] Netherlands Cross-sectional Stroke, DVT, PE 184 64 76 24
    Lodigiani et al. [13] Italy Retrospective Stroke, MI, DVT, PE 388 66 (55–85) 68 32
    Angeli et al. [4] Italy Cross-sectional PE 50 64 72 28
    Demelo-Rodríguez et al. [8] Spain Prospective DVT 156 68.1 ± 14.5 65.4 34.6
    Helms et al. [9] France Prospective Stroke, DVT, PE 150 63 (53–71) 81.3 18.7
    Llitjos et al. [12] France Retrospective DVT, PE 26 68 (51.5–74.5) 77 23
    Middledorp et al. [14] Netherlands Retrospective DVT, PE 198 61 65.7 34.3
    Jain et al. [10] United States Retrospective Stroke 3218 64 60.7 39.3
    Pyoiadji et al. [15] United States Retrospective PE 328 61.3 45.9 54.1
    Bompard et al. [6] France Retrospective PE 135 64 69.6 30.4
    Cantador et al. [7] Spain Retrospective Stroke, MI, DVT 1419 69 78.6 21.4
    Zhang et al. [17] China Cross Sectional DVT 143 63 51.7 48.3
    Yaghi et al. [16] United States Retrospective Stroke 3556 62.5 71.9 28.1
    Bilaloglu et al. [5] United States Cross-sectional Stroke, MI, DVT 3334 64 (51–75) 60.4 39.6
    Bi et al. [18] China Prospective DVT 420 45 47.6 52.4
    Cui et al. [19] China Retrospective DVT 81 59.9 46 54
    Grillet et al. [20] France Retrospective PE 100 66 ± 13 70 30
    Li et al. [22] USA Retrospective PE 1453 N/R N/R N/R
    Léonard-Lorant et al. [21] France Retrospective PE 106 N/R 56.6 34.4
    Poissy et al. [23] France Cross-sectional DVT, PE 107 N/R N/R N/R

     | Show Table
    DownLoad: CSV
    Table 2.  Pooled prevalence in COVID-19 patients.
    Variable Number of patients affected Total number of patients Pooled percentage % (95% CI, %) Heterogeneity
    Stroke 143 12249 1.2 (0.8–1.6) 65.09
    MI 305 5141 2.3 (0.2–11.2) 99.3
    DVT 278 6606 8.6 (4.2–14.3) 97.52
    PE 379 6559 12.4 (7.2–18.6) 97.23

     | Show Table
    DownLoad: CSV
    Figure 2.  Forest plots showing the incidence of pulmonary embolism in COVID-19 patients.
    Figure 3.  Forest plots showing the incidence of deep vein thrombosis in COVID-19 patients.
    Figure 4.  Forest plots showing the incidence of myocardial infarction in COVID-19 patients.
    Figure 5.  Forest plots showing the incidence of stroke in COVID-19 patients.
    Figure 6.  Forest plots showing the incidence of arterial thromboembolism in COVID-19 patients.
    Figure 7.  Forest plots showing the incidence of venous thromboembolism in COVID-19 patients.

    The results of this meta-analysis demonstrate that pulmonary embolism is the most prevalent thromboembolic event in COVID-19 hospitalized patients. This finding concurs with that of prior studies, such as that by Al-Ani et al. where they reported a high frequency of PE, along with an overall venous thromboembolism (VTE) frequency of 20% of patients, and of stroke 3% [24]. Klok et al., which was an analysis of incidence of thromboembolic events in critically ill COVID19 patients in three Dutch hospitals, reported a cumulative incidence of 31%, with the highest being that of PE [25]. This high prevalence of PE can be attributed to the hypoxia induced coagulation leading to an in-situ thrombosis [24]. In contrast, studies on hospitalized patients without COVID-19 have generally shown a lower incidence of VTE. A study on VTE (reporting DVT and PE) risk stratification in patients without COVID-19 reported a low incidence of 0.3% of VTE development during hospital admissions [26]. Another study reported the trends in the incidence of PE and DVT in hospitalized patients over the course of 20 years. The incidence in DVT amplified from 0.8% to 1.3% of admissions while the incidence of PE was 0.4% and remained constant [27]. This suggests that the virus may increase the risk of thrombosis. However, further investigation is needed to confirm this. Post-mortem findings in COVID-19 patients have shown evidence of subclinical thromboembolism, mainly in the pulmonary vasculature [28]. DVT thromboprophylaxis is recommended in all hospitalized patients but the guidelines for prophylaxis in COVOD-19 are heterogenous [24]. In COVID-19 patients with severe disease and elevated D-dimer levels, heparin use was found to decrease mortality. This benefit was not seen in non-COVID pneumonia patients admitted to intensive care unit [29]. Apart from PE, COVID-19 can also be complicated by DVT, MI and stroke as the continued inflammatory response to COVID-19 with cytokine overproduction, raised D-dimer levels and fibrin degradation products leads to a prothrombotic state [30]. Increased risk of myocardial infarction is also seen in influenza and other virus illness [31]. Myocardial infarction can also be the first presenting feature of COVID-19 [32]. A rise in catecholamines due to the systemic inflammation in COVID-19 can cause plaque disruption and acute myocardial infarction [33]. Myocardial infarction due to COVID-19 can also occur in the absence of a culprit lesion in the coronary artery [32]. Compared with other anticoagulation medicines, low molecular weight heparin (LMWH) is associated with better prognosis in COVID-19 patients [33]. Tissue plasminogen activator (tPA) can be considered in patients with COVID-19 associated acute respiratory distress syndrome who are on mechanical ventilation [33]. Rapid rising data on varied neurological symptoms associated with Covid-19 individuals emphasizes more on the risk of thrombotic vascular events associated with this disease course. A rapid review on Covid-19 related stroke in young individuals reported that SARS-CoV-2 is more likely to cause stroke than the other coronavirus and seasonal infectious diseases [34]. In fact, a 7.5-fold increased rate of cerebrovascular events is documented in nearly 1.5% covid-19 hospitalizations than in patients with influenza [35].

    Due to the lack of sufficient data, we were unable to analyze the impact of baseline factors such as age and sex on our results. This meta-analysis included COVID-19 hospitalized patients and does not represent all the patients with COVID-19, including asymptomatic carriers and patients who are treated at home. The studies are heterogenous and include studies with self-reported outcomes which increases the risk of bias. Due to difference in pathophysiology, prophylaxis and treatment of arterial and venous thrombotic complications, more studies are required to fill the gap in this area. The impact of treatment and drugs administered on these outcomes was not taken into account in this analysis.

    Based on the results of our meta-analysis, thromboembolism may prove to be a significant factor in the pathogenesis of COVID-19. These complications should be anticipated in patients with COVID-19 and effective treatment should be given. Use of thromboprophylaxis should be considered to reduce the risk of thromboembolism [25]. Future studies should focus on establishing a link between the severity of COVID-19 infection and its thromboembolic complications. Serum markers should be identified which relate to increased risk of thromboembolic complications and worse prognosis. The dose and mode of thromboprophylaxis should also be studied to improve outcomes in COVID-19 patients.



    Conflict of interest



    The authors declare no conflict of interest.

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