Cardiovascular Heart Disease from the Myocyte to the Pathology: The Cutting Edge

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Cardiology".

Deadline for manuscript submissions: 25 August 2024 | Viewed by 6816

Special Issue Editors


E-Mail
Guest Editor
Cardiology Department, Mauriziano Umberto I Hospital, 10128 Torino, Italy
Interests: atrial fibrillation; heart failure; cardiac resynchronization therapy; catheter ablationmitral valve; aortic valve; coronary artery bypass; echocardiography; doppler echocardiography; defibrillators

E-Mail Website
Guest Editor
Cardiology Department, Mauriziano Umberto I Hospital, 10128 Torino, Italy
Interests: atrial fibrillation; anticoagulant agent; cardio-oncology; arrhythmia; acute coronary syndrome

Special Issue Information

Dear Colleagues,

Cardiovascular disease (CVD), which includes coronary heart disease, heart failure (HF), valvular heart disease, congenital heart disease, rhythm disorders, cardiomyopathies, peripheral artery disease and arrhythmias,  remains a major challenge influencing the quality of care of patients and the economic global burden.

For patients suffering from CVD, several evidence-based treatments have remarkably improved the outcome; however, despite the best care, the percentage of undiagnosed or undertreated cases remains high.

It has been well-assessed that coronary artery disease (CAD) is one of the most significant causes of morbidity and mortality worldwide. CAD is characterized by atherosclerotic plaque accumulation in the epicardial arteries, which causes obstructive or non-obstructive disease. Various clinical presentations have been reported. However, acute coronary syndrome (ACS) or chronic coronary syndromes (CCS) are the leading forms of CAD. Long, stable periods followed by unstable phases are likely to occur typically due to acute atherothrombotic events caused by plaque rupture or erosion in ischemic patients.

Although patients with ACS have recently been provided with more advanced strategies due to the innovations in revascularization and pharmacological approaches, a high long-term risk of cardiovascular events remains in ACS. Accurate risk stratification of patients plays a crucial role in preventing long-term ischemic events.

HF is a syndrome consisting of acute or chronic symptoms (with reduced ejection fraction (HFrEF), with mildly reduced ejection fraction (HFmrEF), and with preserved ejection fraction (HFpEF)). Heart failure often complicates the treatment of cancer. Moreover, cardiovascular (CV) toxicities of most of cancer therapies have been reported. The cardio-oncology field has rapidly grown in the last few years.

Cardiomyopathies are myocardial disorders in which the muscles are structurally and/or functionally abnormal with a wide range of myocardial phenotypes or genotypes.

The aim of this Special Issue is to address the more debated aspect of lifestyle adjustments, the most innovative pharmacological therapies, and invasive interventions in contributing to obtaining CVD stabilization or regression.

Dr. Carmelo Massimiliano Rao
Dr. Iris Parrini
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Journal of Clinical Medicine is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • coronary heart disease
  • heart failure
  • valvular heart disease
  • congenital heart disease
  • rhythm disorders
  • cardiomyopathies
  • peripheral artery disease
  • arrhythmias

Published Papers (3 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Review

Jump to: Other

28 pages, 22618 KiB  
Review
Clinical Utility of Three-Dimensional Echocardiography in the Evaluation of Mitral Valve Disease: Tips and Tricks
by Paolo G. Pino, Andrea Madeo, Fabiana Lucà, Roberto Ceravolo, Stefania Angela di Fusco, Francesco Antonio Benedetto, Giovanni Bisignani, Fabrizio Oliva, Furio Colivicchi, Michele Massimo Gulizia and Sandro Gelsomino
J. Clin. Med. 2023, 12(7), 2522; https://doi.org/10.3390/jcm12072522 - 27 Mar 2023
Cited by 2 | Viewed by 2756
Abstract
Although real-time 3D echocardiography (RT3DE) has only been introduced in the last decades, its use still needs to be improved since it is a time-consuming and operator-dependent technique and acquiring a good quality data can be difficult. Moreover, the additive value of this [...] Read more.
Although real-time 3D echocardiography (RT3DE) has only been introduced in the last decades, its use still needs to be improved since it is a time-consuming and operator-dependent technique and acquiring a good quality data can be difficult. Moreover, the additive value of this important diagnostic tool still needs to be wholly appreciated in clinical practice. This review aims at explaining how, why, and when performing RT3DE is useful in clinical practice. Full article
Show Figures

Figure 1

15 pages, 1580 KiB  
Review
Patent Foramen Ovale and Cryptogenic Stroke: Integrated Management
by Fabiana Lucà, Paolo G. Pino, Iris Parrini, Stefania Angela Di Fusco, Roberto Ceravolo, Andrea Madeo, Angelo Leone, Mark La Mair, Francesco Antonio Benedetto, Carmine Riccio, Fabrizio Oliva, Furio Colivicchi, Michele Massimo Gulizia and Sandro Gelsomino
J. Clin. Med. 2023, 12(5), 1952; https://doi.org/10.3390/jcm12051952 - 01 Mar 2023
Cited by 5 | Viewed by 2382
Abstract
Patent foramen ovale (PFO) is a common cardiac abnormality with a prevalence of 25% in the general population. PFO has been associated with the paradoxical embolism causing cryptogenic stroke and systemic embolization. Results from clinical trials, meta-analyses, and position papers support percutaneous PFO [...] Read more.
Patent foramen ovale (PFO) is a common cardiac abnormality with a prevalence of 25% in the general population. PFO has been associated with the paradoxical embolism causing cryptogenic stroke and systemic embolization. Results from clinical trials, meta-analyses, and position papers support percutaneous PFO device closure (PPFOC), especially if interatrial septal aneurysms coexist and in the presence of large shunts in young patients. Remarkably, accurately evaluating patients to refer to the closure strategy is extremely important. However, the selection of patients for PFO closure is still not so clear. The aim of this review is to update and clarify which patients should be considered for closure treatment. Full article
Show Figures

Figure 1

Other

Jump to: Review

6 pages, 1802 KiB  
Case Report
Congenital Ventricular Diverticulum
by Carmelo Massimiliano Rao, Fabiana Lucà, Claudio Franzutti, Giuseppe Scappatura, Nicola Arcadi, Pasquale Fratto, Francesco Antonio Benedetto and Sandro Gelsomino
J. Clin. Med. 2023, 12(9), 3153; https://doi.org/10.3390/jcm12093153 - 27 Apr 2023
Viewed by 1306
Abstract
Herein, we describe a 54-year-old patient with a congenital ventricular diverticulum (CVD), referred to our emergency department for presyncope episodes and multiple re-entrant ventricular tachycardias (VT). Significantly, echocardiographic findings were not clear, and the diagnosis was made by cardiac magnetic resonance imaging (CMRI), [...] Read more.
Herein, we describe a 54-year-old patient with a congenital ventricular diverticulum (CVD), referred to our emergency department for presyncope episodes and multiple re-entrant ventricular tachycardias (VT). Significantly, echocardiographic findings were not clear, and the diagnosis was made by cardiac magnetic resonance imaging (CMRI), which showed the presence of an apical accessory cavity connected to the ventricle and contracting synchronously. CMRI allowed the differential diagnosis with other outpouching cardiac defects. The patient underwent a subcutaneous implantable cardioverter defibrillator (S-ICD) implant and was referred for heart transplantation (HT). The diagnosis, treatment, and main findings of the CVD are discussed in this case report. Full article
Show Figures

Figure 1

Back to TopTop