Antonio Francesco Amico

Dr. Antonio Francesco Amico


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 September 2023 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
FLFabiana Lucà
Fabiana Lucà
OFOliva Fabrizio
Oliva Fabrizio
MAMaurizio Giuseppe ABRIGNANI
Maurizio Giuseppe ABRIGNANI
SFStefania Angela Di Fusco
Stefania Angela Di Fusco
IPIris Parrini
Iris Parrini
MGMichele Massimo Gulizia
Michele Massimo Gulizia
It is well established that direct oral anticoagulants (DOACs) are the cornerstone of anticoagulant strategy in atrial fibrillation (AF) and venous thromboembolism (VTE) and should be preferred over vitamin K antagonists (VKAs) since they are superior or non-inferior to VKAs in reducing thromboembolic risk and are associated with a lower risk of intracranial hemorrhage (IH). In addition, many factors, such as fewer pharmacokinetic interactions and less need for monitoring, contribute to the favor of this therapeutic strategy. Although DOACs represent a more suitable option, several issues should be considered in clinical practice, including drug–drug interactions (DDIs), switching to other antithrombotic therapies, preprocedural and postprocedural periods, and the use in patients with chronic renal and liver failure and in those with cancer. Furthermore, adherence to DOACs appears to remain suboptimal. This narrative review aims to provide a practical guide for DOAC prescription and address challenging scenarios.

15 September 2023 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
SGSimona Giubilato
Simona Giubilato
FLFabiana Lucà
Fabiana Lucà
MAMaurizio Giuseppe ABRIGNANI
Maurizio Giuseppe ABRIGNANI
LGLaura Gatto
Laura Gatto
CRCarmelo Massimiliano Rao
Carmelo Massimiliano Rao
MGMichele Massimo Gulizia
Michele Massimo Gulizia
Chronic coronary syndrome (CCS), which encompasses a broad spectrum of clinical presentations of coronary artery disease (CAD), is the leading cause of morbidity and mortality worldwide. Recent guidelines for the management of CCS emphasize the dynamic nature of the CAD process, replacing the term “stable” with “chronic”, as this disease is never truly “stable”. Despite significant advances in the treatment of CAD, patients with CCS remain at an elevated risk of major cardiovascular events (MACE) due to the so-called residual cardiovascular risk. Several pathogenetic pathways (thrombotic, inflammatory, metabolic, and procedural) may distinctly contribute to the residual risk in individual patients and represent a potential target for newer preventive treatments. Identifying the level and type of residual cardiovascular risk is essential for selecting the most appropriate diagnostic tests and follow-up procedures. In addition, new management strategies and healthcare models could further support available treatments and lead to important prognostic benefits. This review aims to provide an overview of the diagnostic and therapeutic challenges in the management of patients with CCS and to promote more effective multidisciplinary care.

4 August 2023 in Metabolites
Verified
Journal Article
Open access
PDF file
FLFabiana Lucà
Fabiana Lucà
FOFabrizio Oliva
Fabrizio Oliva
CRCarmelo Massimiliano Rao
Carmelo Massimiliano Rao
MAMaurizio Giuseppe ABRIGNANI
Maurizio Giuseppe ABRIGNANI
AAAntonio Francesco Amico
Antonio Francesco Amico
MGMichele Massimo Gulizia
Michele Massimo Gulizia
It has been consistently demonstrated that circulating lipids and particularly low-density lipoprotein cholesterol (LDL-C) play a significant role in the development of coronary artery disease (CAD). Several trials have been focused on the reduction of LDL-C values in order to interfere with atherothrombotic progression. Importantly, for patients who experience acute coronary syndrome (ACS), there is a 20% likelihood of cardiovascular (CV) event recurrence within the two years following the index event. Moreover, the mortality within five years remains considerable, ranging between 19 and 22%. According to the latest guidelines, one of the main goals to achieve in ACS is an early improvement of the lipid profile. The evidence-based lipid pharmacological strategy after ACS has recently been enhanced. Although novel lipid-lowering drugs have different targets, the result is always the overexpression of LDL receptors (LDL-R), increased uptake of LDL-C, and lower LDL-C plasmatic levels. Statins, ezetimibe, and PCSK9 inhibitors have been shown to be safe and effective in the post-ACS setting, providing a consistent decrease in ischemic event recurrence. However, these drugs remain largely underprescribed, and the consistent discrepancy between real-world data and guideline recommendations in terms of achieved LDL-C levels represents a leading issue in secondary prevention. Although the cost-effectiveness of these new therapeutic advancements has been clearly demonstrated, many concerns about the cost of some newer agents continue to limit their use, affecting the outcome of patients who experienced ACS. In spite of the fact that according to the current recommendations, a stepwise lipid-lowering approach should be adopted, several more recent data suggest a "strike early and strike strong" strategy, based on the immediate use of statins and, eventually, a dual lipid-lowering therapy, reducing as much as possible the changes in lipid-lowering drugs after ACS. This review aims to discuss the possible lipid-lowering strategies in post-ACS and to identify those patients who might benefit most from more powerful treatments and up-to-date management.

1 September 2017 in Minerva Cardiology and Angiology
Verified
Journal Article
Closed access
AAAntonio Francesco Amico
Antonio Francesco Amico
FNFederico Nardi
Federico Nardi
Article: Clinical cardiac imaging in cardiac arrest and periarrest - Minerva Cardioangiologica 2017 December;65(6):621-8 - Minerva Medica - Journals

1 January 2011 in Journal of Cardiovascular Medicine
Verified
Journal Article
Closed access
AAAntonio Francesco Amico
Antonio Francesco Amico