Pulmonary Embolism or Pulmonary Thrombosis in COVID-19? Is the Recommendation to Use High-Dose Heparin for Thromboprophylaxis Justified?

Acutely ill medical patients are at heightened risk for venous thromboembolism, a term that combines deep vein thrombosis (DVT) and its more severe complication, pulmonary embolism.[1] [2] Although the incidence of venous thromboembolism in medical patients might have been overestimated in some instances, according to a recent study,[3] treatment by low, prophylactic doses of low molecular weight heparin (LMWH) is recommended for these patients when additional risk factors coexist.[1] [2] COVID-19 is an acute, complex disorder that is associated with SARS-CoV-2 infection, which, in its most severe presentation, is characterized by the development of interstitial pneumonia and acute respiratory distress syndrome.[4] According to many reports, COVID-19 exposes patients to a particularly high risk for venous thromboembolism.[5] [6] [7] [8] Hence, hospitalized COVID-19 patients are generally treated with higher LMWH doses than recommended for thromboprophylaxis. A recent document by the Italian Drug Agency (AIFA) suggested the use of 80 to 100 mg enoxaparin daily, instead of the usual 40 mg, while in some hospitals, even higher, up to full anticoagulant doses of LMWH or unfractionated heparin[9] are used. In our hospital we use 40 mg enoxaparin daily, as recommended for high-risk, acutely ill medical patients.[1] [2]

From the COVID-19 outbreak in Northern Italy until April 14, 388 patients have been admitted to our non-intensive care unit (ICU) wards, none of whom developed symptomatic DVT during their hospital stay. As DVT may be asymptomatic in a proportion of patients at risk, we performed leg compression ultrasonography, which failed to detect DVT in any of the 64 tested patients, independently of the severity of their condition and length of in-hospital bed rest ([Table 1]). The absence of reports in the literature of DVT in COVID-19 patients under LMWH thromboprophylaxis confirms our experience. This is apparently in contrast with the relatively frequent reports of pulmonary embolism in hospitalized COVID-19 patients,[5] [6] [7] [8] which is diagnosed based on the clinical observation of rapid worsening of respiratory insufficiency and blood oxygenation that is out of proportion to the extent of pulmonary infiltration and on the evidence of pulmonary vessel occlusions, generally interpreted as caused by pulmonary emboli, when computed tomography angiography (CTA) is performed. These patients, however, usually do not have symptoms or signs of DVT. As an example, a study of 184 severe COVID-19 patients, all hospitalized in ICU and treated mostly with standard doses of LMWH for thromboprophylaxis, reported a high incidence of venous thromboembolism (n = 28).[5] However, only one patient had DVT (diagnosed by compression ultrasonography), while pulmonary embolism (diagnosed by CTA) was by far the most frequent thrombotic event (n = 25) (highlighting the importance of performing CTA in symptomatic patients whenever possible), followed by two cases of catheter-related upper extremity venous thrombosis.[5] The discrepancy between the frequencies of pulmonary embolism and DVT is surprising, because, although pulmonary embolism may occur in the absence of detectable DVT, this happens in only approximately 20% of studied patients.[10] Therefore, we question whether the observed pulmonary vessels occlusions that have been described in reports on COVID-19 patients are exclusively caused by pulmonary embolism. In our experience and in some reports,[11] [12] filling defects of pulmonary vessels that are detected by CTA scans are in many instances more reminiscent of pulmonary thrombi rather than emboli, because they are not fully occlusive. This observation is compatible with postmortem descriptions of “…presence of manifestations of thrombotic, or thrombo-hemorrhagic microangiopathy…; …enlarged pulmonary blood vessels containing microthrombi….” Diffuse thrombotic material is observed also in other organs, compatibly with the development of clinical signs of multiorgan failure.[13] Therefore, local thrombi both in the lungs and other organs, rather than emboli from peripheral veins, appear to be the hallmark of severe COVID-19, which are responsible for the severe ischemic clinical manifestations of the disease.

Table 1 Characteristics of 64 hospitalized COVID-19 patients who underwent bilateral leg compression ultrasonography to unravel asymptomatic deep vein thrombosis

Age (y)	70 [min = 35; max = 97; IQR = 58–77.5]
Days of in-hospital bed rest	9 [min = 1; max = 45; IQR = 4–15]
Days in NIV	0 [min = 0; max = 20; IQR = 0–5]
Respiratory rate (breaths/min)	20 [min = 8; max = 32; IQR = 16–24]
PaO2/FiO2	300 [min = 60; max = 600; IQR = 249–392.5]
D-dimer (µg/mL)	0.458 [min = 0.1; max = 11.970; IQR = 0.252–0.903]
Fibrinogen (g/L)	4.76 [min = 1.30; max = 9.50; IQR = 3.878–5.38]
Ferritin (µg/L)	320 [min = 30; max = 9,000; IQR = 185–776]
Prothrombin time (P/N ratio)	1.13 [min = 0.97; max = 1.51; IQR = 1.07–1.2]
Platelet count (×109/L)	286 [min = 126; max = 754; IQR = 222–384]
Sex	Male = 35; Female = 29
Obesity	Yes = 4; No = 60
Previous VTE	Yes = 0; No = 64
Malignancy	Yes = 7; No = 57

Abbreviations: IQR, interquartile range; NIV, noninvasive ventilation; VTE, venous thromboembolism.

Note: Median [min = lowest value; max = highest value; IQR = interquartile range].

Distinction between pulmonary thrombi and pulmonary emboli is not trivial, because their pathogenesis and, hence, treatment are arguably different. If the rarity of DVT in our COVID-19 patients and also in other more severe patients described in the literature strongly suggests that prophylactic LMWH is effective in preventing VTE, it is quite evident that the same treatment is not effective to prevent pulmonary thrombosis in COVID-19 patients. Higher LMWH doses may not be necessarily more effective, considering that anticoagulant doses of heparin are not indicated for treatment of other types of thrombotic microangiopathies, which possibly share some pathogenic mechanisms with the COVID microangiopathy,[14] with the exception of catastrophic antiphospholipid syndrome.[15] Pulmonary thrombi in COVID-19 probably develop as a consequence of vascular damage associated with viral infection and severe inflammation, with the pathogenic contribution of platelets interacting with the vascular wall and leukocytes (contributing to boost inflammation), factor XIIa with other components of the contact phase of coagulation, von Willebrand factor, complement, and other players in thromboinflammation,[16] [17] [18] [19] [20] [21] [22] [23] [24] some of which have been shown to be implicated in the pathogenesis of acute respiratory distress syndrome already many years ago.[25] High-dose heparin in this setting may not only be ineffective, but it may also be dangerous, possibly contributing to the described hemorrhagic component of microangiopathy. While only randomized clinical trials can answer this question, it is well established that high-dose LMWH administration is associated with increased incidence of major and fatal bleeding (which actually occurred in some COVID-19 Italian patients, most likely in association with the high degree of anticoagulation).

Pending the results of randomized clinical trials, which will hopefully test not only high-dose heparin, but also drugs targeting platelets, von Willebrand factor, complement, contact phase of coagulation, and/or other players in thromboinflammation, we believe that we should continue to use 40 mg enoxaparin for thromboprophylaxis of COVID-19 patients, at least in non-ICU wards.

Publication History

Received: 19 April 2020

Accepted: 23 April 2020

Article published online:
29 April 2020

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