Role of advanced imaging in COVID-19 cardiovascular complications

Catapano, Federica; Marchitelli, Livia; Cundari, Giulia; Cilia, Francesco; Mancuso, Giuseppe; Pambianchi, Giacomo; Galea, Nicola; Ricci, Paolo; Catalano, Carlo; Francone, Marco

doi:10.1186/s13244-021-00973-z

Role of advanced imaging in COVID-19 cardiovascular complications

Critical Review
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Published: 24 February 2021

Volume 12, article number 28, (2021)
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Role of advanced imaging in COVID-19 cardiovascular complications

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Federica Catapano¹,
Livia Marchitelli¹,
Giulia Cundari¹,
Francesco Cilia¹,
Giuseppe Mancuso¹,
Giacomo Pambianchi¹,
Nicola Galea^1,2,
Paolo Ricci^1,3,
Carlo Catalano¹ &
…
Marco Francone ORCID: orcid.org/0000-0002-7906-3420¹

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Abstract

Clinical manifestations of COVID-19 patients are dominated by respiratory symptoms, but cardiac complications are commonly observed and associated with increased morbidity and mortality. Underlying pathological mechanisms of cardiac injury are still not entirely elucidated, likely depending on a combination of direct viral damage with an uncontrolled immune activation. Cardiac involvement in these patients ranges from a subtle myocardial injury to cardiogenic shock. Advanced cardiac imaging plays a key role in discriminating the broad spectrum of differential diagnoses. Present article aims to review the value of advanced multimodality imaging in patients with suspected SARS-CoV-2-related cardiovascular involvement and its essential role in risk stratification and tailored treatment strategies. Based on our experience, we also sought to suggest possible diagnostic algorithms for the rationale utilization of advanced imaging tools, such as cardiac CT and CMR, avoiding unnecessary examinations and diagnostic delays.

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Key points

1.
Cardiac involvement is common in COVID-19 patients, leading to a morbidity/mortality increase.
2.
Cardiac complication includes, among others, myocarditis, acute coronary syndrome and thromboembolic events.
3.
Advanced imaging plays a key role in differential diagnosis of cardiac manifestations.

Introduction

Coronavirus disease 2019 (COVID-19) is a pandemic disease caused by a novel single-stranded enveloped RNA virus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the 7th known human coronavirus.

The virus enters cells through the angiotensin-converting enzyme 2 (ACE2) receptor, mostly expressed in lung alveolar cells, cardiac myocytes and vascular endothelial cells.

Clinical manifestations of COVID-19 are dominated by respiratory symptoms, due to the tropism of the SARS-CoV-2 for the lungs, where it causes interstitial pneumonia [1]. The most common severe complications are acute respiratory disease syndrome (ARDS) and systemic inflammatory response syndrome (SIRS), which can lead to multiorgan failure (MOF) and shock.

Both direct and indirect involvement of other organs is common, and, although the underlying pathological mechanism is still under investigation, the cardiovascular system seems to be particularly affected.

Cardiac injury was early recognized among COVID-19 cases in China; in the report from the National Health Commission almost 11.8% of patients without underlying cardiovascular disease had cardiac injury during hospitalization, showed by elevated T-troponin (TnT) levels and/or new onset of ECG/echocardiographic abnormalities [2].

In addition to its prevalence, cardiac injury seems to be significantly associated with fatal outcome.

Retrospective studies among hospitalized COVID-19 patients have reported a more severe respiratory disease in patients with cardiac injury, requiring in greater proportion both noninvasive and invasive mechanical ventilation [3], and markedly higher mortality rate [3, 4].

Several case reports and case series released so far describe cardiovascular manifestations among COVID-19 patients, such as myocarditis [5, 6], acute coronary syndrome (ACS) [7], arrhythmias, pericarditis [8] and venous thromboembolic events.

Along with the understanding of the underlying pathological mechanisms of myocardial injury, a prompt diagnosis becomes essential for risk stratification and to define tailored treatment strategies.

Present article aimed to review the role of advanced multimodality imaging in patients with suspected SARS-CoV-2-related cardiovascular involvement.

Current emerging scientific evidence has been combined with our 8-month clinical work as one of the national referrals for COVID-19 infection. Based on our experience, we also sought to suggest possible diagnostic algorithms for the rationale utilization of advanced imaging tools in this specific clinical setting.

Pathophysiology of myocardial injury

Although underlying mechanism leading to cardiac injury in COVID-19 patients is not entirely understood, several potential pathophysiological pathways have been proposed [9, 10].

Most likely scenario comprehends a multifactorial etiology based on a synergic effect of several mechanism, both direct or indirect, including:

the so-called “cytokine storm,” whereby an uncontrolled immune cells activation leads to overproduction of pro-inflammatory cytokines, with disruptive consequences ranging from high fever to vascular malfunction, which can lead to inadequate organ blood supply, resulting in MOF. The increase levels of reactive oxygen species (ROS), caused by the pro-inflammatory state, result in endothelial dysfunction, which plays a pivotal role in the genesis of hypertension, atherosclerosis and other cardiovascular diseases (CVD);
direct cytotoxic effects on interstitial cells or macrophages within cardiac tissue, hypothesis supported by viral genome detection within the myocardium in recent autoptic studies [11];
potential downregulation of ACE2 expression in the heart, as demonstrated in a murine model of SARS-CoV-2 infection by Oudit et al. [12]. ACE2 seems to provide a protective effect on cardiovascular system, through several mechanism, including anti-inflammation, anti-fibrosis, anti-oxidation, and vasodilation [13]. Therefore, ACE2 under expression in COVID-19 patients is supposed to lead to cardiac dysfunction and progression of atherosclerosis;
low oxygen blood levels, detected in this cohort of patients as a consequence of pulmonary disfunction, can cause an insufficient energy intake to cardiomyocyte, increasing anaerobic fermentation. Accordingly, intracellular acidosis and ROS production destroy the cell membrane. Moreover, hypoxia can lead to intracellular influx of calcium ions, contributing apoptosis of cardiomyocytes [14];
collateral effects of several drugs widely used in COVID-19 patients, such as antiretroviral therapy, azithromycin and tocilizumab. Indeed, these drugs could lead to electrophysiological alteration as well as be involved in drug–drug interaction with some cardiovascular treatments.

Possible pathogenesis of myocardial involvement is illustrated in Fig. 1.

From this background emerges clearly that SARS-CoV-2 infection is associated with a wide spectrum of cardiovascular (CV) manifestation, ranging from a subtle myocardial injury to cardiogenic shock.

Overall, pneumonia, older age, pre-existing cardiovascular diseases and greater severity of the disease at presentation lead to an increased risk of CV events [15].

Underlying cardiovascular comorbidities

Similarly to influenza virus infections [16, 17], people affected by SARS-CoV-2 with pre-existing CVD have an increased risk of develo** acute myocardial injury [18], resulting in a poor prognosis. It has been described a more severe and acute systemic response to the infection in these patients, with increased leukocyte count, higher levels of cardiac necrosis biomarkers and greater incidence of ARDS [18]. In particular, patients with underlying CVD and higher levels of TnT showed the worst outcome (mortality 69.44%), as compared to both individuals with increased TnT but without CVD comorbidities (mortality 37.5%) and subjects with previous CVD and normal TnT (mortality 13.3%) [4]. As reported in previous studies, the overall percentage of pre-existing CVD in patients with COVID-19 was 24–48%, and the most frequent comorbidities were hypertension (15–31%), diabetes (7–20%), coronary artery disease (CAD) (3–8%) and other CVD (15%) [19,20,21,22]. The prevalence of these diseases was greater among patients admitted to the intensive care unit (ICU) [10].

As explained before, the genesis of CV involvement in COVID-19 remains debated. For what concerns cardiac injury in patients with CVD, several studies speculated about different etiologies of secondary cardiac involvement. The increase in myocardial oxygen demand during the infection could bring to a cardiac decompensation in patients with pre-existing heart failure [18], while the systemic inflammatory release of cytokines could lead to a major risk for atherosclerotic plaque rupture [21]. Then, the increased coagulation activity, expressed by increased D-dimer levels, could induce thrombosis and ischemia [21]. Furthermore, other studies hypothesized that hypoxia could reduce the oxygen supply to the heart, unmasking a CAD or a microvascular pathology causing myocardial infarction with non-obstructive coronary artery (MINOCA) [23].

Finally, in predisposed patients, hypoxia, together with drugs and systemic inflammation, could lead to arrhythmias.

Myocarditis

Myocarditis is a well-recognized complication of acute viral infections [24], as a wide spectrum of viral genomes has been identified in the endomyocardial specimens of patients with clinical suspicion of myocarditis and parvovirus B-19, adenovirus or influenza infection [25].

Myocarditis has also been reported as a complication of middle east respiratory syndrome (MERS), caused by another severe coronavirus [26].

Several case reports of COVID-19 patients with acute myocardial injury, defined as troponin release, provide evidence of cardiac inflammation [27] with cardiac magnetic resonance (CMR) findings compatible with acute myocarditis [28, 29].

Notably, Esposito et al. [30] reported a series of 8 patients with elevated concentrations of TnT and electrocardiography alterations whom CMR findings fulfilled the 2018 Lake Louise Criteria for the diagnosis of myocarditis. In all cases, CMR showed diffuse intense myocardial edema, increased T1 and T2 map** and also a mild pericardial effusion in 75% of patients.

Worth noticing, all patients had no remarkable previous history of cardiovascular disease.

Even Inciardi et al. [31] reported a case of a 53-year-old woman with no CV history presented to the emergency department with severe fatigue and abnormal ECG findings with elevated levels of markers of myocyte necrosis. After urgent invasive coronary angiography (ICA) was performed with no evidence of obstructive coronary disease, CMR showed marked biventricular myocardial interstitial edema and diffuse transmural late gadolinium enhancement (LGE) with circumferential pericardial effusion, with the final diagnosis of myopericarditis.

Although the gold standard in the diagnosis of myocarditis is endomyocardial biopsy (EMB), through histological, immunological and molecular evidences [32], it is rarely performed in COVID-19 patients for obvious implications related to the complexity of organizing a procedure which is invasive and poses all involved operators at risk of infection. In this setting, CMR represents the ideal noninvasive imaging tool for clinical diagnosis of myocarditis.

CMR patterns have been reported to be heterogeneous, as aforementioned, but in general not different from any other typical form of active inflammation characterized by diffuse myocardial edema. LGE seems to be less-frequently observed in these patients [30], reflecting a limited myocyte necrosis at least in acute phase, and highlighting the key role of the new Lake Louise Criteria in myocarditis diagnosis [33].

We noted similar findings in our experience with a crucial role of map** techniques for the assessment of myocardial inflammation.

When present LGE has a non-ischemic pattern, as in case showed in Fig. 2, with a predominant location at inferior and inferior-lateral segments [34].

In their echocardiographic study, Moody et al. have found an independent association between reduced RV systolic dysfunction and all-cause mortality in severe COVID-19 patients with elevated TnT. Besides the effects of thromboembolic disease, authors hypothesized a possible primary RV involvement as a concurrent factor to RV injury [35]. In this clinical setting, a significant contribution could be provided by CMR, which has shown to be the gold standard for the evaluation of RV function together with tissue characterization [36].

Up to date, histopathological confirmation of myocarditis was found in only one patient with CMR findings of reverse Takotsubo syndrome and final diagnosis of lymphocytic myocarditis, with no evidence of SARS-CoV-2 genome within the myocardium [37].

In a cohort study of 39 autopsy cases of patients with COVID-19, Lindner et al. found viral genome in the myocardial tissue in 61.5% of autopsies (n = 24/39), with virus load above 1000 copies in most cases (n = 16/24) [11].

Other autopsy studies [Full size image

Additionally, in COVID-19 era, conventional echocardiography (i.e. not bedside) is potentially underused due to an increased infection risk for healthcare providers during the examination [50].

Myocardial Infarction: obstructive versus MINOCA syndromes

As mentioned above, SARS-CoV-2 infection can increase the risk of ACS [51]. This finding was confirmed by previous studies conducted on influenza virus [17] and community acquired pneumonia [52], demonstrating an improved risk of acute myocardial infarction (AMI), which was maximum within 7 days from the diagnosis in the affected patients [53].

Uncontrolled inflammatory response has been observed to be the most important determinant of ACS in COVID-19: stimulation of macrophages, endothelial and smooth muscle cells, activation of platelets and the expression of tissue factor in the atheromatous plaque concur to plaque rupture and ACS [24]. The effective incidence of ACS among patients with COVID-19 is still unknown and probably underestimated, due to the relative inaccessibility to healthcare services during the pandemic [10, 32]. For the same reasons, we do not have a realistic ACS risk evaluation in COVID-19 patients without CVD.

According to the American College of Cardiology, patients with diagnosis of ST-Elevation Myocardial Infarction (STEMI) should undergo ICA, for a combined diagnostic and therapeutic approach.

As interesting remark, a delay in revascularization of STEMI patients has been reported in Italy during the first wave of COVID-19 outbreak [50], highlighting the logistical difficulties in the management of even the most critical medical conditions during the pandemic.

For an imaging perspective, this could lead to the observation of subacute patterns, with mild, if not reabsorbed, myocardial edema and initial healing of myocyte necrosis.

For patients with active SARS-CoV-2 infection and Non-ST Elevation Myocardial Infarction (NSTEMI), diagnostic testing prior to catheterization is recommended [51]. In hemodynamically stable cases and equivocal presentation, cardiac CT could be considered as a valid alternative to ICA [54]. CT allows the comprehensive assessment of pulmonary parenchyma, pulmonary vessels and coronary arteries and allows to rule-out CAD with a nearly100% negative predictive value [23].

Pontone et al. reported their experience performing cardiac CT in a patient with dyspnea and chest pain tested positive for SARS-CoV-2, proposing a CT protocol to “quadruple rule-out” out pneumonia, pulmonary embolism, myocarditis and ACS in selected COVID-19 patients [54].

CMR findings of AMI include myocardial edema, detected by T2-weighted short tau inversion recovery (STIR) and confirmed by elevated T2 map** values, along with matched subendocardial distribution of LGE, as shown in Fig. 5.

After excluding CAD, other possible differential diagnoses of AMI should be investigated. [23].

Several articles reported the evidence of MINOCA or AMI type 2 among patients with COVID-19. The former explained with the presence of high levels of ACE-2 receptors in pericytes and in endothelial cells, which hampers a severe microvascular dysfunction also associated with cytokines storm [24]. The latter caused by a mismatch between oxygen supply and demand [55]. In both of these clinical entities, ICA would be of limited use [24] and other imaging technique should be considered in order to exclude other CVD with similar clinical presentations [23], such as myocarditis with infarct-like onset and Takotsubo cardiomyopathy.

Accordingly, few cases of Takotsubo syndrome have been reported, likely triggered by both intense emotional stress and systemic inflammation COVID-19 related [37, 56, 57].

CMR findings of Takotsubo syndrome in COVID-19 patients showed no significant differences from the classic pattern: a diffuse hyperintensity in T2 STIR images in mid-apical segments matched the area of regional dysfunction [58] (Fig. 6).

CMR has been poorly used to investigate myocardial injury in COVID-19 patients so far, especially during the acute phases of the disease [28, 30, 40, 59], and MINOCA phenotypes could reasonably be underdiagnosed in this group.

In selected COVID-19 patients, CMR allows to noninvasively characterize underlying pathological substrate, offering a comprehensive evaluation of biventricular morphology, function and myocardial tissue characterization.

Further studies are needed to better define the role of CMR in this subset of patients.

Arrhythmias and sudden cardiac arrest: role of advanced imaging?

Cardiac arrhythmias, of both atrial and ventricular origin, are a common complication in SARS-CoV-2 infection [60, 61].

In the report by Colon et al., 19 out of 119 (16.5%) patients, all admitted in ICU, developed new-onset atrial arrhythmias, including atrial fibrillation (63%), atrial flutter (32%) and atrial tachycardia (5%) [62]. Atrioventricular/ventricular block and QT prolongation have been reported in association with SARS-CoV-2 infection, with incidence of 11.8% and 13% respectively [60]. Malignant arrhythmias, as ventricular tachycardia and fibrillation, have been described as well since early reports from China, especially in patients with elevated TnT levels [4].

Furthermore, sudden cardiac arrest was reported as fatal outcome in COVID-19 patients, in both in—[63] and out-of-hospital settings [64].

A special mention is finally needed for arrhythmogenic effects of COVID-19-related drugs. Specifically, antiviral therapies, such as Lopinavir and Ritonavir, are associated with atrioventricular block while azithromycin, chloroquine and hydroxychloroquine with QT prolongation [10]. Although there are no indications in the acute setting, advanced cardiac imaging is an essential tool in the assessment of dysrhythmias, improving sudden cardiac death risk stratification. CMR provides reliable and reproducible evaluation of structural changes and can be applied to identify underlying arrhythmogenic substrate (e.g. myocardial edema, ischemia and/or fibrosis). Thus, it could play a role to identify pathological substrates in patients with new onset arrhythmias and to improve arrhythmic event prediction in selected patients recovered from COVID-19 with infection-related cardiac injury.

Coagulation abnormalities and pulmonary embolism

Thromboembolic disease represents another piece in the mosaic of SARS-CoV-2 infection, which is commonly observed in COVID-19 and associated with poor prognosis. Increased D-dimer levels in COVID-19 patients have been early reported in China [65], with higher levels in patients in ICU [median IQR 414 (191–1324) vs. 166 (101–285), p value < 0.001] [20].

Fei Zhou et al., in one of the largest retrospective cohort studies, not only reported increased coagulation activity in about 90% of COVID-19 in patients affected by pneumonia, but also pointed out elevated D-dimer levels at admission to be one of the main risk factors of in-hospital death [21].

It has not been fully elucidated yet whether this hypercoagulable state depends on a direct endothelial damage inflicted by the virus or represents a consequence of cytokine storm precipitating the onset of SIRS [66]. The blood coagulation activation in COVID-19, also substantiated by elevated levels of fibrinogen, Von Willebrand factor activity and factor VIII, seems not meet the criteria for disseminate intravascular coagulation, as platelet count and prothrombin time have been mostly reported within normal ranges, or just slightly increased, in these patients [67, 68].

Moreover, Helms et al. reported in ICU population with ARDS a much higher incidence of pulmonary embolism (PE) in COVID-19 patients than in non-COVID-19 (11.7 vs. 2.1%) [67].

Reasonably, SARS-CoV-2-associated thromboembolic disease has a multifactorial etiology, clinically revealed mainly by the onset of PE.

In a retrospective study conducted in France among 100 COVID-19 inpatients undergone CT pulmonary angiography (CTPA), 23% had acute PE. This group was more frequently in ICU (17 [74%] vs. 22 [29%]; P, 0.001) than non-PE-group and required mechanical ventilation more often (15 of 23 patients [65%] vs. 19 of 77 patients [25%], P, 0.001) [69]. Several other studies with CTPA confirmed these findings [67, 70, 71], raising the needing of a more defined role of contrast chest CT in COVID-19 diagnostic work-up. CTPA is the imaging modality of choice in clinical suspicion of PE [72], and although is still not recommended in COVID-19 patients by current guidelines [73,74,75] it could significantly impact clinical outcome in selected groups, such as patients with elevated D-dimer levels, sudden clinical worsening and/or new onset of dyspnea (Fig. 7).

Recommended patient’s workflow in suspected COVID-19

In clinical suspicion of CV involvement in COVID-19 patients, supported by typical or atypical chest pain, worsening of dyspnea and/or new onset of arrhythmias, bedside echocardiography represents the first essential imaging tool in diagnostic work-up. Considering the high exposure risk for operators, it is not routinely performed in COVID-19 patients. Anyway, a fast and focused bedside echocardiography evaluation can be pivotal in referring selected patients to second level imaging, such as cardiac CT, CMR and ICA, to avoid unnecessary examinations and diagnostic delay, as shown in Fig. 8.

According to our proposed algorithm, cardiac CT can be used to rule-out ACS when coronary obstruction is suspected, while CMR plays a key role in the differential diagnosis of myocardial injury with normal coronary arteries [76].

Safety precautions should be implemented to prevent risk of infection for both healthcare professionals and patients. If available, utilization of COVID-19 dedicated scanners with appropriate cleaning and decontamination of the area at the end of the shift would be highly recommended.

A full personal protective equipment is needed for healthcare staff, which need to be reduced to the minimum necessary, while all patients should wear surgical masks [77, 78].

In our experience, we implemented the use of rapid and tailored CT and CMR protocols to reduce exposure time related infection risk and patient discomfort [79].

Conclusions and future perspectives

Rationale utilization of advanced cardiac imaging services in COVID-19 should serve to avoid or, at least, minimize the unnecessary use of invasive, potentially contagious and time-consuming procedures like cardiac catheterization or transesophageal echocardiography and to speed-up diagnostic pathways.

While bedside echocardiography remains a first-line and ease-of-use diagnostic tool, appropriate use of second-line techniques, such as cardiac CT and CMR, allows the reliable exclusion of CAD together with the characterization of underlying pathological substrate (see Fig. 8).

Our clinical experience, also supported by scientific literature [40], has shown that a progressive shift from acute to chronic cardiovascular damage is not uncommon, even in apparently healed patients and includes conditions like chronic thrombo-embolic pulmonary hypertension, recurrent arrhythmias and progression to dilated cardiomyopathy. Accordingly, careful follow-up of these patients should be offered in the convalescent stage.

In conclusion, besides pulmonary manifestation, radiologists should be aware of the wide and heterogeneous spectrum of cardiovascular complications in COVID-19 and rationalized utilization of advanced imaging tools which may be used to drive therapeutic approach and stratify patients’ prognosis.

Availability of data and materials

Not applicable.

Abbreviations

ACE2:: Angiotensin-converting enzyme 2
ACS:: Acute coronary syndrome
AMI:: Acute myocardial infarction
ARDS:: Acute respiratory distress syndrome
CAD:: Coronary artery disease
CMR:: Cardiovascular magnetic resonance
COVID-19:: Coronavirus disease 2019
CT:: Computed tomography
CTPA:: Computed tomography pulmonary angiography
CV:: Cardiovascular
CVD:: Cardiovascular disease
DWI:: Diffusion-weighted imaging
ECV:: Extra-cellular volume
ICA:: Invasive coronary angiography
ICU:: Intensive care unit
LGE:: Late gadolinium enhancement
MERS:: Middle east respiratory syndrome
MINOCA:: Myocardial infarction with non-obstructive coronary artery
MOF:: Multiorgan failure
NSTEMI:: Non-ST elevation myocardial infarction
PE:: Pulmonary embolism
ROS:: Reactive oxygen species
SARS-CoV-2:: Severe acute respiratory syndrome coronavirus 2
SIRS:: Systemic inflammatory response syndrome
STEMI:: ST-elevation myocardial infarction
STIR:: Short Tau inversion recovery
TnT:: T-troponin

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Department of Radiological, Oncological and Pathological Sciences, “Sapienza” University of Rome, Viale del Policlinico 155, 00161, Rome, Italy
Federica Catapano, Livia Marchitelli, Giulia Cundari, Francesco Cilia, Giuseppe Mancuso, Giacomo Pambianchi, Nicola Galea, Paolo Ricci, Carlo Catalano & Marco Francone
Department of Experimental Medicine, “Sapienza” University of Rome, Viale del Policlinico 155, 00161, Rome, Italy
Nicola Galea
Unit of Emergency Radiology, Policlinico Umberto I, Policlinico Umberto I, Sapienza University of Rome, Viale del Policlinico 155, 00161, Rome, Italy
Paolo Ricci

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Federica Catapano
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Livia Marchitelli
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Giulia Cundari
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Francesco Cilia
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Giuseppe Mancuso
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Giacomo Pambianchi
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Nicola Galea
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Paolo Ricci
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Carlo Catalano
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Marco Francone
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Catapano, F., Marchitelli, L., Cundari, G. et al. Role of advanced imaging in COVID-19 cardiovascular complications. Insights Imaging 12, 28 (2021). https://doi.org/10.1186/s13244-021-00973-z

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Received: 20 November 2020
Accepted: 28 January 2021
Published: 24 February 2021
DOI: https://doi.org/10.1186/s13244-021-00973-z

Role of advanced imaging in COVID-19 cardiovascular complications

Abstract

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