Introduction

COVID-19 is a multisystem disease which increases risk of coagulopathy and thus, venous thromboembolism (VTE) and pulmonary embolism (PE) in critically ill patients. The incidence rate for VTE and arterial thrombosis and related thrombo-embolic complications remain very high in COVID-19 patients [1]. There are three possible mechanisms associated with this observation: (1) through cytokine storm by interleukin-1, interleukin-6, tumor necrosis factor-alpha and others leading to endothelial activation and widespread thrombosis as seen in pulmonary vessels in acute respiratory distress syndrome; (2) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has shown an affinity for angiotensin-converting enzyme 2 located at alveolar epithelial cells, endothelial cells of extrapulmonary tissues leading to thrombosis by microvascular injury and multiorgan failure; and (3) lupus anticoagulant antibodies can lead to thrombosis by the “two hit” thrombosis model [1].

Methods

After a thorough review of the literature from PubMed, Scopus, and Google Scholar, data were collected from four studies. Random effects models were obtained to perform a meta-analysis, and I2 statistics were used to measure inter-study heterogeneity. I2 > 75% was interpreted as substantial heterogeneity and prevalence was further explored using subgroup analysis.

Results

Among 3066 COVID-19 patients, the pooled prevalence of PE was 15.8% (95% CI (6.0–28.8%)) with I2 = 98%. The pooled rate in younger cohort (age < 65 years) showed a higher prevalence of 20.5% (95% CI (17.6–24.8%)) compared to the older cohort (age > 65 years) showing 14.3% (95% CI (2.9–30.1%)) (p < 0.00001) (Fig. 1). Single-center studies showed a prevalence of 12.9% (95% CI 1.0–30.2%), while that of multicenter studies was 19.5% (95% CI 14.9–25.2%).

Fig. 1
figure 1

Pooled prevalence of pulmonary embolism. a The pooled rate in younger cohort (age < 65 years) showed a higher prevalence of 20.5% (95% CI (17.6–24.8%)) compared to the older cohort (age > 65 years) showing 14.3% (95% CI (2.9–30.1%)) (p < 0.00001). b The pooled rate of pulmonary embolism in single-center studies was 12.9% (95% CI 1.0–30.2%) as compared to 19.4% (95% CI 14.9–25.2%) in multicenter studies (p < 0.00001)

Discussion

Due to underlying thrombotic milieu that is characteristic of COVID-19, patients suffering from this infection are highly predisposed to pulmonary embolism which is a major cause of mortality associated with this disease. Patients diagnosed with COVID-19 run the risk of incident pulmonary embolism even in the absence of regular risk factors [2]. Stringent movement restrictions applied as a consequence of this pandemic can lead to a delay in seeking medical attention, subsequently leading to progression of low-risk PE cases to high-risk life-endangering cases of fatal PE [3].

To the best of our knowledge, this is the first pooled estimate of the prevalence of PE in COVID-19 patients with a variation by age (mean age 65 years) and study centers (single vs. multi). Several single-center/multi-center studies along with case reports have shown increased incidence of PE in COVID-19 patients despite being on prophylactic anticoagulant therapy. In our analysis, we thus proved that multicenter studies with a larger and diverse study sample showed an increased prevalence of PE, thus the need for a low threshold of PE suspicion. The results of our pooled analysis also showed a higher prevalence of PE in the younger cohort (age < 65 years) compared to elderly patients. A study of 137 critically ill patients in Hubei province with median age of sample 57 (20–83) years showed that nearly 1/5th patients had an underlying co-morbidity of hypertension, diabetes mellitus, cardiovascular disease, COPD, malignancy, and others which could further increase the risk of thrombotic events [4]. Thus, in addition to older patients who are known to be at high risk of thrombotic events due to comorbidities, young, or middle-aged groups diagnosed with COVID-19 with underlying diseases must also be screened for PE with a high index of suspicion.

A presentation of PE could range from asymptomatic to chest pain, shortness of breath, hemoptysis, syncope, and overlapping with COVID-19 disease. Thus, initial suspicion towards DVT/PE can be gauged from elevated D-dimer levels. With a higher threshold for D-dimer levels of 1.5 μg/ml, the negative predictive value is reported to be 94.7% [5]. Thus, with elevated D-dimer levels or clinical symptoms, compression ultrasound could be preceded before CT pulmonary angiography since 90% of pulmonary emboli are known to originate from lower extremity DVT [5, 6]. Cardiac investigations such as ECG or TTE should not be heavily relied upon; clinical suspicion should be the most important factor driving the clinician towards suspecting and investigation for PE in COVID-19 patients [7].

Risk stratification methods such as Caprini, IMPROVE, Padua models, and VELTAS (Venous and Lymphatic Triage and Acuity Scale) are proven to be useful for clinical assessment of VTE and PE in COVID-19 [8, 9]. Prophylactic anticoagulant therapy is recommended with LMWH or unfractionated heparin with or without mechanical compression [10]. However, recently a case report described fatal thromboembolism in a patient who was already on the usual anticoagulation dose and had a normal D-dimer level until the event [11]. This warrants further research on the effective anticoagulation and therapeutic dose to prevent mortality from this life-threatening complication of COVID-19.

With this pooled analysis, we report that nearly 1 in every 7 COVID-19 patients could present with PE, higher odds of being detected in those with a mean age of less than 65 years (20.5% vs. 14.3%) compared to relatively younger cohorts (mean age < 65 years). As expected, the pooled prevalence in single-center studies remain underreported (12.9% vs. 19.4%) compared to the pooled rate observed in multicenter studies.

Conclusions

The level of surveillance for PE and threshold for conducting diagnostic tests such as D-dimer levels need to be increased considering fatal outcomes of a PE with COVID-19. Our study gives preliminary data for further large-scale analysis to understand the prevalence of PE in young to middle-aged COVID-19 patients and development of algorithms to speculate and timely diagnose PE and venous thromboembolism and curtail mortality rate and pertinent complications.