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      The cardiovascular burden of congenital heart disease - not only in times of COVID-19

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          Abstract

          Thank you for the article of Tan and Aboulhosn who address cardiovascular burden of patients with congenital heart defects (CHD) in the context of COVID-19 [1]. However, we argue to expand our outlook on cardiovascular burden beyond the connection with COVID-19 to better understand the general peculiarities of the vessels in CHD – which is what we currently do not do well enough [2]. In terms of cardiovascular abnormalities, there is still a great need for clarification of how genetic factors regulate blood pressure and endothelial function. Furthermore, the extent to which surgical factors like surgical scars, conduits, patches and early inflammatory processes due to cardiopulmonary bypass and oxidative stress - which come along with surgery - play a role in cardiovascular outcomes needs to be determined [3]. More than that, lifelong medication which fosters the hardening of the arterial vessels, or environmental factors, such as reduced physical activity patterns, might also play a role in not only a limited immune defense of COVID-19 specifically but the prevention of secondary diseases in general. Interdisciplinary work is needed to solve the puzzle of why the arteries of individual patients or patient groups are harder, the vessel walls thicker, the function of endothelium impaired [4]. While in contrast the risk for a cardiovascular event within the next ten years, estimated with a general risk scores, is low [5], we need to start understanding how these patients age in more detail and how they can benefit from lifelong primary prevention of cardiovascular diseases.

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          Most cited references5

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          The cardiovascular burden of coronavirus disease 2019 (COVID-19) with a focus on congenital heart disease

          Coronavirus disease 2019 (COVID-19), caused by a novel betacoronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first described in a cluster of patients presenting with pneumonia symptoms in Wuhan, China, in December of 2019. Over the past few months, COVID-19 has developed into a worldwide pandemic, with over 400,000 documented cases globally as of March 24, 2020. The SARS-CoV-2 virus is most likely of zoonotic origin, but has been shown to have effective human-to-human transmission. COVID-19 results in mild symptoms in the majority of infected patients, but can cause severe lung injury, cardiac injury, and death. Given the novel nature of COVID-19, no established treatment beyond supportive care exists currently, but extensive public-health measures to reduce person-to-person transmission of COVID-19 have been implemented globally to curb the spread of disease, reduce the burden on healthcare systems, and protect vulnerable populations, including the elderly and those with underlying medical comorbidities. Since this is an emerging infectious disease, there is, as of yet, limited data on the effects of this infection on patients with cardiovascular disease, particularly so for those with congenital heart disease. We summarize herewith the early experience with COVID-19 and consider the potential applicability to and implications for patients with cardiovascular disease in general and congenital heart disease in particular.
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            Cardiovascular risk factors in adults with congenital heart defects — Recognised but not treated? An analysis of the German National Register for Congenital Heart Defects

            As adult congenital heart disease (ACHD) patients are aging, a high prevalence of cardiovascular risk factors is encountered similar to the general population. Currently, data regarding the primary and secondary prevention of acquired cardiovascular disease in ACHD is lacking.
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              Increased arterial stiffness in children with congenital heart disease.

              Objective Central systolic blood pressure (SBP) is a measure of arterial stiffness and strongly associated with atherosclerosis and end-organ damage. It is a stronger predictor of cardiovascular events and all-cause mortality than peripheral SBP. In particular, for children with congenital heart disease, a higher central SBP might impose a greater threat of cardiac damage. The aim of the study was to analyse and compare central SBP in children with congenital heart disease and in healthy counterparts. Patients and methods Central SBP was measured using an oscillometric method in 417 children (38.9% girls, 13.0 ± 3.2 years) with various congenital heart diseases between July 2014 and February 2017. The test results were compared with a recent healthy reference cohort of 1466 children (49.5% girls, 12.9 ± 2.5 years). Results After correction for several covariates in a general linear model, central SBP of children with congenital heart disease was significantly increased (congenital heart disease: 102.1 ± 10.2 vs. healthy reference cohort: 100.4 ± 8.6, p < .001). The analysis of congenital heart disease subgroups revealed higher central SBP in children with left heart obstructions (mean difference: 3.6 mmHg, p < .001), transpositions of the great arteries after arterial switch (mean difference: 2.2 mmHg, p = .017) and univentricular hearts after total cavopulmonary connection (mean difference: 2.1 mmHg, p = .015) compared with the reference. Conclusion Children with congenital heart disease have significantly higher central SBP compared with healthy peers, predisposing them to premature heart failure. Screening and long-term observations of central SBP in children with congenital heart disease seems warranted in order to evaluate the need for treatment.
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                Author and article information

                Contributors
                Journal
                Int J Cardiol
                Int. J. Cardiol
                International Journal of Cardiology
                Elsevier B.V.
                0167-5273
                1874-1754
                13 July 2020
                13 July 2020
                Affiliations
                [a ]Department of Pediatric Cardiology and Congenital Heart Disease, Deutsches Herzzentrum München, Technische Universität München, Germany
                [b ]Institute of Preventive Pediatrics, Technische Universität München, Germany
                Author notes
                [* ]Corresponding author at: Institute of Preventive Pediatrics, Technische Universität München, Georg-Brauchle-Ring 60/62, 80992 München, Germany. j.mueller@ 123456tum.de
                Article
                S0167-5273(20)32857-6
                10.1016/j.ijcard.2020.05.071
                7357463
                252aedc0-28bc-4768-8009-7ea5743607db
                © 2020 Elsevier B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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                Cardiovascular Medicine
                Cardiovascular Medicine

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