key: cord-0820032-56h2jmn9
authors: Zamboni, Paolo
title: COVID-19 as a Vascular Disease: Lesson Learned from Imaging and Blood Biomarkers
date: 2020-06-29
journal: Diagnostics (Basel)
DOI: 10.3390/diagnostics10070440
sha: f2e8ed2fa1f4fb34d9b7a911002e0532565d7eaa
doc_id: 820032
cord_uid: 56h2jmn9

COVID-19, a disease initially thought to be prominently an interstitial pneumonia with varying degrees of severity, can be considered a vascular disease with regards to serious complications and causes of mortality. Quite recently, blood clots have emerged as the common factor unifying many of the symptoms initially attributed without an explanation to COVID-19. Cardiovascular biomarkers and particularly, D-dimer and troponin appear to be very powerful prognostic markers, signaling the need for earlier and more aggressive interventions and treatments in order to avoid and/or minimize arterial/venous thromboembolism and myocardial infarct. The ultrasound imaging patterns at both the lung and peripheral vascular level can also be very useful weapons that have the advantage of being able to monitor longitudinally the clinical picture, something that real-time PCR/nasopharyngeal swab is not able to do and that CT can only pursue with significant radiation exposure. A lesson learned in the early phase of the COVID-19 pandemic suggests quitting and starting again with targeted imaging and blood vascular biomarkers.

Italy was the first western country to be stricken by the coronavirus pandemic. From the outset, it became mandatory to identify and isolate COVID-19 patients, many of whom were then admitted to hospital. The most common symptoms of the disease at onset were fever, fatigue, dry cough, dyspnea, runny nose or other upper respiratory tract symptoms. Ageusia and anosmia were also found to be characteristic symptoms, albeit with more rare presentation, while gastrointestinal symptoms account for a minority of cases. Laboratory tests also found COVID-19 to be associated with changes in blood chemistry, with D-dimer, lactate dehydrogenase (LDH) and the aspartate transaminase to alanine transaminase ratio (AST-ALT) all showing interesting changes in the negative predictive value to positive predicted value (NPV-PPV) relationship [1, 2] .

As the COVID-19 outbreak progressed, chest X-rays were found to display relatively low sensitivity, whereas chest CT exhibited higher sensitivity scores, with the latter achieving: sensitivity of 97%, specificity of 25%, PPV of 65%, and NPV of 83%, with real-time PCR/nasopharyngeal swab (swab-PCR) as the reference method [2] . Given such a low specificity score, the use of dedicated software up to the introduction of artificial intelligence can allow chest CT to significantly improve the reporting speed and the diagnostic accuracy, as well [3, 4] . An alternative approach that has great potential is lung ultrasound (LUS), which has been shown to be capable of diagnosing interstitial pneumonia with great accuracy compared with chest CT [5] . Indeed, the receiver operating characteristic curves for LUS have shown a strong relationship between sensitivity and specificity, with area under the curve scores of 0.95 and 0.93, respectively, achieved in two distinct meta-analyses [6, 7] .

Unfortunately, the use of swab-PCR as the primary diagnostic tool for COVID-19 leaves much to be desired. Indeed, of the 72,314 COVID-19 patients at the Wuhan University Hospital, only 62% had a positive swab-PCR [1] , with diagnosis in the remaining 38% of cases achieved through contact history, symptoms, blood chemistry tests and pulmonary CT. Furthermore, in another large study, in 75% of patients with negative swab-PCR, chest CT demonstrated interstitial pneumonia often consistent with COVID-19 etiology. Moreover, by means of analysis of serial swab-PCR assays and CT scans, the mean interval time between the initial negative to positive swab-PCR result was 5.1 ± 1.5 days [2] . As such, there is general agreement that a negative swab-PCR test should be interpreted with caution and a repeat test may be needed [2, 8, 9] .

Finally, we must not to forget serology testing for viral antibodies, which is an important indicator of previous exposure to the virus. In a longitudinal study, sensitivity and specificity for detecting seropositivity at ≥ 15 days following a positive SARS-CoV-2 swab-PCR result, was 100.0% and 98.7% when assaying for the panels of IgM and IgG. The median time to seropositivity observed for a reactive IgM and IgG result from the date of a positive PCR was 5 days (IQR: 2.75-9 days) and 4 days (IQR: 2.75-6.75 days), respectively [10] .

The SARS-CoV-2 spike protein is known to bind to the angiotensin-converting enzyme 2 (ACE2) receptor on the surface of human cells. The spike protein is processed by membrane proteases, including TMPRSS2, and is internalized into the cell, leading to infection [11] . ACE2 receptors are abundantly expressed by endothelial cells. In a paper published in April 2020, it has been demonstrated that the SARS-CoV-2 virus can infect the endothelial cells in the lungs, heart, kidneys, liver, and intestines of patients with COVID-19 infection [11] . The demonstration of endothelial cell injury across vascular beds of different organs gives light to unexplained symptoms and clinical courses described in early reports of the COVID-19 pandemic. In particular, histological analysis revealed the presence of the virus within endothelial cells was associated with clusters of inflammatory cells. This finding suggests that SARS-CoV-2 infection initiates endothelial inflammation throughout the entire human organism, as well as apoptosis, something that explains the systemic macro and microcirculatory involvement in different vascular beds and their clinical sequelae in patients with COVID-19 [12] . Moreover, evidence of viral endothelial injury helps to explain why patients with pre-existing cardiovascular disease are particularly associated with adverse outcomes in COVID-19. Notwithstanding this, awareness that COVID-19 targets the endothelial cells provides a rationale for exploring several established cardiovascular therapies known to protect the endothelium in the hope of reducing viral replication [13] [14] [15] [16] [17] .

In the past few months, blood clots have emerged as the common factor unifying many of the mysterious symptoms attributed to COVID-19, a disease that had initially been thought to largely affect the lungs in the form of pneumonia. Early findings in COVID-19 autopsies showed deep vein thrombosis (DVT) in 58% of cases, complicated by fatal venous thromboembolism (VTE) in 30% of patients. In addition, sudden cardiac death and kidney infarct complications were found in the other 30% of patients of this initial cohort [18] . Recently, the hypothesis that COVID-19 pneumonia might be complicated by VTE has been supported by an increased number of reports in the COVID-19 literature [19] [20] [21] [22] [23] [24] (Figure 1 ).

Since the initial reports, an increase in circulating D-dimer levels has been reported, without being clarified if the cause was the cytokine storm of COVID-19 interstitial pneumonia or if there were overlapping thrombotic phenomena. Furthermore, increased levels of such a biomarker are associated with poor prognosis and/or death [19] . Indeed, it has been determined that a cutoff value 2.0 µg/mL of D-dimer can predict in-hospital mortality, with a sensitivity of 92.3% and a specificity of 83.3%. COVID-19 patients with D-dimer levels ≥2.0 µg/mL have been shown to have a significantly higher Diagnostics 2020, 10, 440 3 of 10 incidence of mortality when comparing to those who with D-dimer levels < 2.0 µg/mL (p < 0.001). Fatal VTE in course of COVID-19 is preceded by changes in blood coagulation biomarkers such as increased values of D-dimer, decreased antithrombin values, prothrombin time, and thrombin time [24] . The addition of systemic proinflammatory cytokines release as a consequence of endothelial inflammation, as well as the expression of the ACE2 receptors for SARS-CoV-2 on the membrane of the vascular muscle and endothelial cells, may help to explain why COVID-19 patients are also susceptible to arterial thrombosis, even in young non-arteriosclerotic individuals [25] . Furthermore, cerebral circulation may also be involved, as retrospective analysis in Wuhan revealed, where 6% of the deaths among COVID-19 patients were stroke-related [26] . Since the initial reports, an increase in circulating D-dimer levels has been reported, without being clarified if the cause was the cytokine storm of COVID-19 interstitial pneumonia or if there were overlapping thrombotic phenomena. Furthermore, increased levels of such a biomarker are associated with poor prognosis and/or death [19] . Indeed, it has been determined that a cutoff value 2.0 µg/ml of D-dimer can predict in-hospital mortality, with a sensitivity of 92.3% and a specificity of 83.3%. COVID-19 patients with D-dimer levels ≥2.0 µg/ml have been shown to have a significantly higher incidence of mortality when comparing to those who with D-dimer levels < 2.0 µg/ml (P<0.001). Fatal VTE in course of COVID-19 is preceded by changes in blood coagulation biomarkers such as increased values of D-dimer, decreased antithrombin values, prothrombin time, and thrombin time [24] . The addition of systemic proinflammatory cytokines release as a consequence of endothelial inflammation, as well as the expression of the ACE2 receptors for SARS-CoV-2 on the membrane of the vascular muscle and endothelial cells, may help to explain why COVID-19 patients are also susceptible to arterial thrombosis, even in young non-arteriosclerotic individuals [25] . Furthermore, cerebral circulation may also be involved, as retrospective analysis in Wuhan revealed, where 6% of the deaths among COVID-19 patients were stroke-related [26] .

Finally, elevated cardiac troponin levels are associated with myocardial injury, and in turn, with a fatal outcome in the clinical course of COVID-19 [27] [28] [29] . This is evident by the paradox that patients with underlying cardiovascular disease but without increased troponin achieve better outcomes than younger patients without comorbidities but higher troponin levels. In a single center study, the stratification of the mortality rate in the subgroups of patients during hospitalization for COVID-19 was respectively: 7.62% for patients without underlying chronic cardiovascular disease and normal troponin T levels; 13.33% for those with comorbidities and normal troponin levels; 37.50% for those without associated cardiovascular diseases but elevated troponin levels; 69.44% for those with both underlying cardiovascular diseases and elevated troponin. However, patients with underlying comorbidities were more likely to exhibit elevation of troponin T as compared with the patients without previous cardiovascular diseases, respectively 54.5% versus 13.2% [29] . Given this, it is important to triage patients with suspected COVID-19 according to their history of cardiovascular disease, assessing, at least, their D-dimer and troponin levels. Finally, elevated cardiac troponin levels are associated with myocardial injury, and in turn, with a fatal outcome in the clinical course of COVID-19 [27] [28] [29] . This is evident by the paradox that patients with underlying cardiovascular disease but without increased troponin achieve better outcomes than younger patients without comorbidities but higher troponin levels. In a single center study, the stratification of the mortality rate in the subgroups of patients during hospitalization for COVID-19 was respectively: 7.62% for patients without underlying chronic cardiovascular disease and normal troponin T levels; 13.33% for those with comorbidities and normal troponin levels; 37.50% for those without associated cardiovascular diseases but elevated troponin levels; 69.44% for those with both underlying cardiovascular diseases and elevated troponin. However, patients with underlying comorbidities were more likely to exhibit elevation of troponin T as compared with the patients without previous cardiovascular diseases, respectively 54.5% versus 13.2% [29] . Given this, it is important to triage patients with suspected COVID-19 according to their history of cardiovascular disease, assessing, at least, their D-dimer and troponin levels.

There is a growing body of evidence suggesting that SARS-CoV-2 can bind the glycosaminoglycans (GAGs), including heparin. The latter acts as a decoy, preferentially binding to the SARS-CoV-2 S1 spike protein and inhibiting SARS-CoV-2 entry into cells. Initial binding with heparin appears also to change the conformation of the spike protein inhibiting downstream binding and processing of the ACE2 receptor and TMPRSS2, respectively. It has been recently demonstrated that intact recombinant S1S2 spike protein from SARS-CoV-2 can bind to a human cell line that expresses ACE2 and TMPRSS2, and shown that unfractionated heparin and some low molecular weight heparins (LMWH), particularly enoxaparin in routine clinical use, determines a robust inhibition of S1S2 binding [30] [31] [32] [33] .

In light of what has been previously reported on the pathophysiological, diagnostic, and prognostic value of D-dimer, the dual role of heparin as a therapeutic weapon becomes clear-on the one hand, as a powerful inhibitor of the entry of the virus into cells, and on the other, as a preventer of the thromboembolic process. This is something which appears to be confirmed in clinical practice, since early analysis of in-hospital patients has revealed that anticoagulant treatment is associated with decreased mortality in COVID-19 patients. The 28-day mortality in COVID-19 patients with alteration of coagulation parameters including D-dimer in the LMWH group was significantly lower than in the non-user group. Again, the rate of mortality was significantly higher in patients with D-dimer >6-fold with respect to the upper limit of normality than in those below, respectively 52.4% versus 32.8% p = 0.017 [34] .

I do not want to comment here on the consequences of the high percentage of false negatives of swab-PCR in a pandemic, nor discuss the reasons for swab-PCR vulnerability. Rather, we simply point out that there is an urgent need for a faster and more sensitive test to regulate access to hospitals, including the surgical unit, especially in emergency circumstances. As such, this issue continues to be an open diagnostic problem that affects both patients and health care professionals. Looking at the current diagnosis of COVID-19, it would appear that both chest CT and LUS have a valuable role to play in the triaging of patients into hospitals, especially in cases of emergency surgery or in situations where surgery cannot be procrastinated. However, the use of CT scans to identify COVID-19 carriers has the disadvantage that it increases their exposure to radiation, as well as being a relatively costly health care procedure [35] . Recently, a group of LUS experts developed a standardized protocol for investigation of COVID-19 pneumonia [36] . To this end, they suggested to use a tablet E-connected to a wireless probe, with both wrapped in single use plastic film covers [36] [37] [38] [39] [40] . As such, this strategy minimizes the risk of contamination and facilitates easy disinfection and sterilization of equipment ( Figure 2 ). Diagnostics 2020, 10, 440 4 of 10 that intact recombinant S1S2 spike protein from SARS-CoV-2 can bind to a human cell line that expresses ACE2 and TMPRSS2, and shown that unfractionated heparin and some low molecular weight heparins (LMWH), particularly enoxaparin in routine clinical use, determines a robust inhibition of S1S2 binding [30] [31] [32] [33] .

In light of what has been previously reported on the pathophysiological, diagnostic, and prognostic value of D-dimer, the dual role of heparin as a therapeutic weapon becomes clear-on the one hand, as a powerful inhibitor of the entry of the virus into cells, and on the other, as a preventer of the thromboembolic process. This is something which appears to be confirmed in clinical practice, since early analysis of in-hospital patients has revealed that anticoagulant treatment is associated with decreased mortality in COVID-19 patients. The 28-day mortality in COVID-19 patients with alteration of coagulation parameters including D-dimer in the LMWH group was significantly lower than in the non-user group. Again, the rate of mortality was significantly higher in patients with Ddimer >6-fold with respect to the upper limit of normality than in those below, respectively 52.4% versus 32.8% p = 0.017 [34] .

I do not want to comment here on the consequences of the high percentage of false negatives of swab-PCR in a pandemic, nor discuss the reasons for swab-PCR vulnerability. Rather, we simply point out that there is an urgent need for a faster and more sensitive test to regulate access to hospitals, including the surgical unit, especially in emergency circumstances. As such, this issue continues to be an open diagnostic problem that affects both patients and health care professionals. Looking at the current diagnosis of COVID-19, it would appear that both chest CT and LUS have a valuable role to play in the triaging of patients into hospitals, especially in cases of emergency surgery or in situations where surgery cannot be procrastinated. However, the use of CT scans to identify COVID-19 carriers has the disadvantage that it increases their exposure to radiation, as well as being a relatively costly health care procedure [35] . Recently, a group of LUS experts developed a standardized protocol for investigation of COVID-19 pneumonia [36] . To this end, they suggested to use a tablet E-connected to a wireless probe, with both wrapped in single use plastic film covers [36] [37] [38] [39] [40] . As such, this strategy minimizes the risk of contamination and facilitates easy disinfection and sterilization of equipment ( Figure 2 ).

A wireless ultrasound probe with respectively a 4.5 mHz convex probe on the right side, and a 7.5 mHz linear probe on the left one. The transducer, wrapped with a single use plastic cover to avoid contamination, is wi-fi connected with the tablet which in turn, is encircled by a plastic film. Wireless ultrasound equipment to avoid contamination. A wireless ultrasound probe with respectively a 4.5 mHz convex probe on the right side, and a 7.5 mHz linear probe on the left one. The transducer, wrapped with a single use plastic cover to avoid contamination, is wi-fi connected with the tablet which in turn, is encircled by a plastic film.

It has been also suggested that LUS should involve two operators in the acquisition protocol in order to reduce their exposure time to COVID-19 patients, with the first scanning and the second one storing the images. Both convex and linear probes can be used. Moreover, the standard LUS Diagnostics 2020, 10, 440 5 of 10 investigation is composed by 14 intercostal windows, seven for each side: three posteriorly along the paravertebral line; two laterally along the mid-axillary line; two anteriorly along the mid-clavicular line, these latter ones below and above the inter-nipple line, respectively. The LUS in patients not able to maintain a sitting position can be performed in lateral decubitus. COVID-19 pneumonia can be also scored for severity by LUS (Figure 3 ).

It has been also suggested that LUS should involve two operators in the acquisition protocol in order to reduce their exposure time to COVID-19 patients, with the first scanning and the second one storing the images. Both convex and linear probes can be used. Moreover, the standard LUS investigation is composed by 14 intercostal windows, seven for each side: three posteriorly along the paravertebral line; two laterally along the mid-axillary line; two anteriorly along the mid-clavicular line, these latter ones below and above the inter-nipple line, respectively. The LUS in patients not able to maintain a sitting position can be performed in lateral decubitus. COVID-19 pneumonia can be also scored for severity by LUS (Figure 3) . The introduction of the severity score leads us to prefer LUS to both swab-PCR and CT scan for the following clinical needs:  When following-up the evolution of COVID-19 pneumonia, in situations where the use of a CT scan would expose the patient to an excess of radiation.  When monitoring longitudinally health care professionals. Since it is expected that the pandemic will continue for some time, it will also be necessary to monitor medical staff. For this purpose, LUS would be ideal. Based on the incubation time, it would seem reasonable to repeat the survey every two weeks. Ideally, preliminary LUS screening would be undertaken before admission, in general, to hospital, and particularly to surgical departments. In the case of a positive LUS test, ideally corroborated by hepatic and coagulation blood markers (as discussed above), the patient would be isolated and surgically treated according to COVID-19 hospital protocol. By contrast, in the case of negative LUS outcome and blood laboratory test, the patient would follow the standard route. In a department of surgery, this approach could represent a fast, sensitive, cost effective assessment, which would protect other patients and health care staff during the pandemic. Finally, LUS would permit the avoidance of X-rays and can be rapidly performed by the surgeons, reducing the overwhelming of the radiology services. From this point of view, the development of an e-learning LUS educational program represents a matter of urgency. The introduction of the severity score leads us to prefer LUS to both swab-PCR and CT scan for the following clinical needs:

• When following-up the evolution of COVID-19 pneumonia, in situations where the use of a CT scan would expose the patient to an excess of radiation. • When monitoring longitudinally health care professionals. Since it is expected that the pandemic will continue for some time, it will also be necessary to monitor medical staff. For this purpose, LUS would be ideal. Based on the incubation time, it would seem reasonable to repeat the survey every two weeks.

Ideally, preliminary LUS screening would be undertaken before admission, in general, to hospital, and particularly to surgical departments. In the case of a positive LUS test, ideally corroborated by hepatic and coagulation blood markers (as discussed above), the patient would be isolated and surgically treated according to COVID-19 hospital protocol. By contrast, in the case of negative LUS outcome and blood laboratory test, the patient would follow the standard route. In a department of surgery, this approach could represent a fast, sensitive, cost effective assessment, which would protect other patients and health care staff during the pandemic. Finally, LUS would permit the avoidance of X-rays and can be rapidly performed by the surgeons, reducing the overwhelming of the radiology services. From this point of view, the development of an e-learning LUS educational program represents a matter of urgency.

As described above, an elevation in D-dimer levels is a common finding in patients with COVID-19. Throughout the pandemic, several reported cases have associated this biomarker with acute DVT and/or VTE. Clinical suspicion of VTE is thought to be higher in cases with DVT symptoms, with rapid and disproportionate hypoxemia, or acute unexplained right ventricular dysfunction [12] . At the beginning of the pandemic, the presence of elevated D-dimer did not warrant routine ultrasound investigation. Ultrasound investigation, currently used to diagnose DVT, was therefore not adopted, given the risk of transmitting infection to other patients or health care workers. However, with the subsequent introduction of wireless ultrasound probes, which can be rapidly covered in single use transparent films, has completely changed this scenario ( Figure 2 ). As such, LUS is rapidly becoming a useful, cost effective, and safe diagnostic tool for identifying and clinically assessing COVID-19 pneumonia.

The first-line imaging test in the diagnostic management of patients presenting with clinically suspected DVT is compression ultrasonography (CUS), a powerful ultrasound biomarker [41] [42] [43] (Figure 4 ).

Diagnostics 2020, 10, 440 6 of 10

As described above, an elevation in D-dimer levels is a common finding in patients with COVID-19. Throughout the pandemic, several reported cases have associated this biomarker with acute DVT and/or VTE. Clinical suspicion of VTE is thought to be higher in cases with DVT symptoms, with rapid and disproportionate hypoxemia, or acute unexplained right ventricular dysfunction [12] . At the beginning of the pandemic, the presence of elevated D-dimer did not warrant routine ultrasound investigation. Ultrasound investigation, currently used to diagnose DVT, was therefore not adopted, given the risk of transmitting infection to other patients or health care workers. However, with the subsequent introduction of wireless ultrasound probes, which can be rapidly covered in single use transparent films, has completely changed this scenario ( Figure 2 ). As such, LUS is rapidly becoming a useful, cost effective, and safe diagnostic tool for identifying and clinically assessing COVID-19 pneumonia.

The first-line imaging test in the diagnostic management of patients presenting with clinically suspected DVT is compression ultrasonography (CUS), a powerful ultrasound biomarker [41] [42] [43] ( Figure 4 ). The ultrasound scan might include a second CUS examination after 5 to 10 days following an initial negative CUS to evaluate if a possible distal DVT has propagated to the proximal veins. Single limited, serial limited, and whole-leg CUS are the current imaging strategies for the diagnosis of DVT. Preference for one strategy over the other differs between centers and sonographers [41] [42] [43] [44] .

Due to frequent association with VTE, it could be reasonable to complete the LUS screening protocol with CUS investigation at the level of the jugular, subclavian, femoral, popliteal, and calf muscular venous segment, according to the above protocols. The addition of ultrasound venous images to the LUS protocol takes just a few minutes and is able to provide fundamental prognostic and therapeutic information (Figure 4) . Finally, taking into account all the above data for the diagnosis of COVID-19 and the frequent VTE complications, the usual DVT diagnostic algorithm could be usefully modified by means of blood and ultrasound vascular biomarkers, according to a novel flowchart illustrated in Figure 5 . The ultrasound scan might include a second CUS examination after 5 to 10 days following an initial negative CUS to evaluate if a possible distal DVT has propagated to the proximal veins. Single limited, serial limited, and whole-leg CUS are the current imaging strategies for the diagnosis of DVT. Preference for one strategy over the other differs between centers and sonographers [41] [42] [43] [44] .

Due to frequent association with VTE, it could be reasonable to complete the LUS screening protocol with CUS investigation at the level of the jugular, subclavian, femoral, popliteal, and calf muscular venous segment, according to the above protocols. The addition of ultrasound venous images to the LUS protocol takes just a few minutes and is able to provide fundamental prognostic and therapeutic information (Figure 4) . Finally, taking into account all the above data for the diagnosis of COVID-19 and the frequent VTE complications, the usual DVT diagnostic algorithm could be usefully modified by means of blood and ultrasound vascular biomarkers, according to a novel flowchart illustrated in Figure 5 . 

As mentioned above, both CT and LUS detect subpleural consolidation areas in the course of COVID-19 pneumonia. Some authors, in the light of frequent VTE complications, have raised the question as to whether these areas of consolidation might actually be indicative of segmental pulmonary embolus [45] . To answer their question, it has recently been proposed that contrastenhanced ultrasound (CEUS) be used when performing LUS scans [46] . Tee et al., were able to demonstrate by means of CEUS that irregular areas of subpleural consolidation at LUS are avascular and therefore, most likely represent microinfarcts. Conversely, consolidation of non-thrombotic origin would be seen to have some enhancement at CEUS investigation. The same cannot be seen by using CT due to the superior spatial resolution of ultrasound.

Vascular biomarkers confirm that COVID-19, a disease initially thought to be exclusively an interstitial pneumonia with varying degrees of severity, can also be considered a vascular disease, especially with regards to more serious complications and causes of mortality. Particularly, both Ddimer and troponin appear to be very powerful prognostic markers, signaling the need for earlier and more aggressive interventions and treatments. The ultrasound imaging pattern at both lung and peripheral vascular level can also be very useful weapons that have the advantage of being able to monitor longitudinally the clinical picture, something that swab-PCR is not able to do and that CT can only pursue with significant radiation exposure. 

As mentioned above, both CT and LUS detect subpleural consolidation areas in the course of COVID-19 pneumonia. Some authors, in the light of frequent VTE complications, have raised the question as to whether these areas of consolidation might actually be indicative of segmental pulmonary embolus [45] . To answer their question, it has recently been proposed that contrast-enhanced ultrasound (CEUS) be used when performing LUS scans [46] . Tee et al., were able to demonstrate by means of CEUS that irregular areas of subpleural consolidation at LUS are avascular and therefore, most likely represent microinfarcts. Conversely, consolidation of non-thrombotic origin would be seen to have some enhancement at CEUS investigation. The same cannot be seen by using CT due to the superior spatial resolution of ultrasound.

Vascular biomarkers confirm that COVID-19, a disease initially thought to be exclusively an interstitial pneumonia with varying degrees of severity, can also be considered a vascular disease, especially with regards to more serious complications and causes of mortality. Particularly, both D-dimer and troponin appear to be very powerful prognostic markers, signaling the need for earlier and more aggressive interventions and treatments. The ultrasound imaging pattern at both lung and peripheral vascular level can also be very useful weapons that have the advantage of being able to monitor longitudinally the clinical picture, something that swab-PCR is not able to do and that CT can only pursue with significant radiation exposure.

Funding: This research received no external funding.

Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

Correlation of Chest CT and RT-PCR Testing in Coronavirus Disease 2019 (COVID-19) in China: A Report of 1014 Cases

Artificial intelligence-enabled rapid diagnosis of patients with COVID-19

Clinically Applicable AI System for Accurate Diagnosis, Quantitative Measurements, and Prognosis of COVID-19 Pneumonia Using Computed Tomography

Lung ultrasound for the diagnosis of pneumonia in adults: A systematic review and meta-analysis

Lung ultrasound for the diagnosis of pneumonia in adults: A meta-analysis

Accuracy of Lung Ultrasonography in the Diagnosis of Pneumonia in Adults: Systematic Review and Meta-Analysis

Performance du frottis nasopharyngé-PCR pour le diagnostic du Covid-19-Recommandations pratiques sur la base des premières données scientifiques (Covid-19 diagnosis: Clinical recommendations and performance of nasopharyngeal swab-PCR)

Negative Nasopharyngeal and Oropharyngeal Swabs Do Not Rule Out COVID-19

Longitudinal Monitoring of SARS-CoV-2 IgM and IgG Seropositivity to Detect COVID-19

Endothelial cell infection and endotheliitis in COVID-19

COVID-19 and Thrombotic or Thromboembolic Disease: Implications for Prevention, Antithrombotic Therapy, and Follow-up

The effect of cholesterol-lowering and antioxidant therapy on endothelium-dependent coronary vasomotion

Effects of angiotensin converting enzyme inhibition on endothelium-dependent vasodilatation in essential hypertensive patients

Angiotensin-converting enzyme inhibition improves vascular function in rheumatoid arthritis

Anti-tumor necrosis factor-alpha treatment improves endothelial function in patients with rheumatoid arthritis

Trials of anti-tumour necrosis factor therapy for COVID-19 are urgently needed

Autopsy Findings and Venous Thromboembolism in Patients With COVID-19

Diagnostics 2020

D-dimer levels on admission to predict in-hospital mortality in patients with Covid-19

Venous thromboembolism in COVID-19 patients

High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study

Incidence of thrombotic complications in critically ill ICU patients with COVID-19

Deep Vein Thrombosis and Pulmonary Embolism: Two Complications of COVID-19 Pneumonia?

Prominent changes in blood coagulation of patients with SARS-CoV-2 infection

Acute limb ischaemia in two young, non-atherosclerotic patients with COVID-19

Neurologic Manifestations of Hospitalized Patients With Coronavirus Disease

Sanchis-Gomar, F. Cardiac troponin I in patients with coronavirus disease 2019 (COVID-19): Evidence from a meta-analysis

High-Sensitivity Cardiac Troponin Can Be an Ally in the Fight Against COVID-19

Cardiovascular Implications of Fatal Outcomes of Patients With Coronavirus Disease 2019 (COVID-19)

SARS-CoV-2 spike protein binds heparan sulfate in a length-and sequence-dependent manner

Glycosaminoglycans induce conformational change in the SARSCoV-Spike S1 Receptor Binding Domain. BioRxiv

Effective Inhibition of SARS-CoV-2 Entry by Heparin and Enoxaparin Derivatives

Anticoagulant treatment is associated with decreased mortality in severe corona-virus disease 2019 patients with coagulopathy

COVID-19 pneumonia: A review of typical CT findings and differential diagnosis

Proposal for International Standardization of the Use of Lung Ultrasound for Patients With COVID-19: A Simple, Quantitative, Reproducible Method

Our Italian experience using lung ultrasound for identification, grading and serial follow-up of severity of lung involvement for management of patients with COVID-19

Point of care and intensive care lung ultrasound: A reference guide for practitioners during COVID-19

Point-of-Care Lung Ultrasound findings in novel coronavirus disease-19 pnemoniae: A case report and potential applications during COVID-19 outbreak

Chinese Critical Care Ultrasound Study Group (CCUSG). Findings of lung ultrasonography of novel corona virus pneumonia during the 2019-2020 epidemic

Prévalence de la thrombose veineuse diagnostiquée par échographie-doppler des membres inférieurs dans la suspicion d'embolie pulmonaire et dans l'embolie pulmonaire confirmée

Risk of deep vein thrombosis following a single negative whole-leg compression ultrasound: A systematic review and meta-analysis

Diagnostic accuracy of three ultrasonography strategies for deep vein thrombosis of the lower extremity: A systematic review and meta-analysis

Advances in the Diagnosis of Venous Thromboembolism: A Literature Review

Are subpleural consolidations indicators for segmental pulmonary embolism in COVID-19?

Contrast-enhanced ultrasound (CEUS) of the lung reveals multiple areas of microthrombi in a COVID-19 patient

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license

The author thanks Basel Plus SRL Milan, Italy, for the free loan of wireless ultrasound equipment during the COVID-19 pandemic.

The author declares no conflicts of interest.

The author thanks Basel Plus SRL Milan, Italy, for the free loan of wireless ultrasound equipment during the COVID-19 pandemic.

The author declares no conflict of interest.Diagnostics 2020, 10, 440