Abstract

The pathophysiology of some non-communicable diseases (NCDs) such as hypertension, cardiovascular disease (CVD), diabetes, and cancer includes an alteration of the endothelial function. COVID-19 is a pulmonary and vascular disease with a negative impact on patients whose damaged endothelium is particularly vulnerable. The peculiar SARS-CoV-2-induced “endothelitis” triggers an intriguing immune-thrombosis that affects both the venous and arterial vascular beds. An increased liability for infection and an increased likelihood of a worse outcome have been observed during the pandemic in patients with active cancer and in cancer survivors. “Overlapping commonalities” between COVID-19 and Cardio-Oncology have been described that include shared phenotypes of cardiovascular toxicities such as left ventricular dysfunction, ischemic syndromes, conduction disturbances, myocarditis, pericarditis and right ventricular failure; shared pathophysiologic mechanisms such as inflammation, release of cytokines, the renin-angiotensin-aldosterone-pathway, coagulation abnormalities, microthrombosis and endothelial dysfunction. For these features and for the catalyst role of NCDs (mainly CVD and cancer), we should refer to COVID-19 as a “syndemic.” Another challenging issue is the persistence of the symptoms, the so-called “long COVID” whose pathogenesis is still uncertain: it may be due to persistent multi-organ viral attacks or to an abnormal immune response. An intensive vaccination campaign is the most successful pharmacological weapon against SARS-CoV-2, but the increasing number of variants has reduced the efficacy of the vaccines in controlling SARS-CoV-2 infections. After a year of vaccinations we have also learned more about efficacy and side-effects of COVID-19 vaccines. An important byproduct of the COVID-19 pandemic has been the rapid expansion of telemedicine platforms across different care settings; this new modality of monitoring cancer patients may be useful even in a post pandemic era. In this paper we analyze the problems that the cardio-oncologists are facing in a pandemic scenario modified by the extensive vaccination campaign and add actionable recommendations derived from the ongoing studies and from the syndemic nature of the infection.

Highlights

  • SARS-CoV-2 causes primarily pulmonary disease due to a high expression of Angiotensin Converting Enzyme 2 (ACE2), the entry receptor of the virus, in many epithelial cell types of the respiratory tract such as alveolar epithelial type II cells in the lungs [2, 3]

  • A recent review of 22 publications with a total of 277 autopsied hearts found myocarditis in 7.2% of hearts, but a closer examination of the cases revealed that most cases were not functionally significant and the authors conclude that the true prevalence is

  • ACE2 is a receptor for SARS-CoV-2, concern was initially raised in the medical and scientific community that the use of angiotensinconverting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) could result in increased mortality and severity of COVID19

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Summary

INTRODUCTION

SARS-CoV-2 causes primarily pulmonary disease due to a high expression of ACE2, the entry receptor of the virus, in many epithelial cell types of the respiratory tract such as alveolar epithelial type II cells in the lungs [2, 3]. Since the early studies published in China, patients hospitalized for COVID showed a high prevalence of CVD risk factors and CVD and this accounted for a more severe course of the disease and higher case fatality rates [24]. ACE2 is a receptor for SARS-CoV-2, concern was initially raised in the medical and scientific community that the use of ACEIs and ARBs could result in increased mortality and severity of COVID19. A recent meta-analysis of 26 studies confirmed that treatment with ACEIs and ARBs compared with other antihypertensive drugs or no treatment was associated with reduced mortality as well as a lower risk of ventilatory support among COVID-19-infected hypertensive patients [52]. Major scientific Societies have provided recommendations in favor of continued treatment with ACEIs and ARBs in patients with hypertension, HF, and ischemic heart disease [53,54,55] (Table 1)

Myocarditis and Pericarditis After
ADAPTED CARDIAC MONITORING IN THE VACCINATION ERA
Recommendation during vaccination
General Considerations
Baseline Evaluation of Cancer Patient
Findings
Surveillance During Treatment
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