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Patients with the Wolff-Parkinson-White syndrome may experience benign and malignant arrhythmias, the most common being atrioventricular reentrant tachycardias. This arrhythmia may degenerate into atrial fibrillation, which can be conducted over an accessory pathway capable of exceptionally fast conduction to the ventricles and degenerate into ventricular fibrillation, leading to sudden cardiac death. These life-threatening events generally affect symptomatic patients in their third or fourth decade. Although rare, ventricular fibrillation may be the first clinical manifestation in subjects who are asymptomatic or unaware of their conditions. Electrophysiologic study may be useful to identify subjects at high risk of sudden cardiac death.In some cases, atrioventricular reentrant arrhythmias are sustained by accessory pathways with peculiar electrophysiologic properties related to their specific anatomy. Most of these fibers, which may be responsible for variants of ventricular preexcitation, show decremental conduction properties due to a nodelike aspect or a peculiar tortuous anatomic route across the atrioventricular groove. Moreover, some fibers do not actively sustain any reentrant circuit and can be only involved as bystander in other arrhythmias. Although rare, these accessory pathway variants should be properly diagnosed using noninvasive and invasive methods to guide catheter ablation procedures when needed.An accessory pathway (AP) could manifest its presence exclusively during an orthodromic supraventricular tachycardia or with preexcitation during sinus rhythm (SR). The manifestations of the presence of an AP depend on its ability to conduct antegradely from atrium (A) to ventricle (V), retrogradely (V to A), or both. AP retrograde conduction is necessary to establish an atrioventricular reentrant tachycardia circuit. If an AP can only conduct antegradely, it will function as a bystander AV connection during independent arrhythmias. The correct diagnosis of this condition is very important, as it will determine the immediate and long-term management.An accessory pathway (AP) can be apparent during sinus rhythm if it depolarizes part of the ventricles ahead of the normal wave front from the conduction system. An AP can generate an anatomic circuit able to sustain a macroreentrant atrioventricular reentrant tachycardia. This arrhythmia can engage the normal conducting system in an antegrade direction or retrogradely, generating, respectively, a narrow or a wide complex tachycardia. The combined use of a standard electrocardiogram and an esophageal recording-pacing can be particularly useful in the first approach to patients with Wolff-Parkinson-White syndrome, further stratifying patients requiring electrophysiology study and transcatheter ablation.The ability to estimate accessory pathway (AP) position enables pre-procedural planning, reduces mapping times, and improves risk estimates as part of the patient consent process. In this article, the nomenclature and important concepts of AP localization algorithms are outlined. An overview of three prominent algorithms is then provided. Each represents an era of invasive treatment of APs surgical therapy, endocardial ablation, and contemporary electroanatomic mapping. In this manner, the premises, pitfalls, and evolution of AP localization algorithms are illustrated. In addition, the pertinent features of their work are distilled in a simplified topographic algorithm with the interventional electrophysiologist in mind.Ventricular preexcitation is a depolarization of the ventricles that occurs before the conventional sequence, and the electrocardiogram is the specific test for diagnosis. A Kent bundle is the paradigm of ventricular preexcitation, and it is associated with short PR, wide QRS and delta wave. This finding is not always very evident, as it can have different degrees of pre-eccitazione; therefore great diagnostic care must be taken in this field. If not properly identified, the pattern of ventricular preexcitation may lead to an incorrect diagnosis. The methodology of precision electrocardiology is able to confront all these aspects.Accessory pathways that bypass all or part of the normal atrioventricular conduction system traverse the atrioventricular junction. The atrioventricular junction comprises of a limited septal component and much more extensive right and left parietal components. Its composition forms a plane of insulation between atrial and ventricular myocardium, preventing direct continuity between them. Typical accessory atrioventricular pathways located anywhere along the atrioventricular junction are muscle bundles or may involve muscle around the walls of coronary sinus aneurysms or coronary veins. Navarixin mw Increasingly, variants or unusual accessory pathways, some involving an accessory node, are reported in clinical studies.Over the last decades, the approach to the Wolff-Parkinson-White syndrome, as well as its treatment, has substantially changed, leading to improvement in the prognosis and quality of life of these patients. From the first diagnostic electrophysiologic studies to the most recent evaluations, important data on pathophysiologic and clinical aspects have been gathered, and this learning journey is still not concluded. This body of knowledge is a fundamental part of any cardiologists’ armamentarium despite the fact that this syndrome is rarely observed in adult patients.The fluorescence-based assay of iodide ion (I-) has been extensively studied by the use of different sensing probes and techniques, but it remains a tricky task to eliminate the interference of chloride ion (Cl-) for the analysis of low-level I- in complex genuine samples. Herein, we develop a redox pretreatment strategy for specific separating I- from human urine. Simultaneously, a novel ratiometric fluorescent probe is constructed by a simple mixing of dimer DNA silver nanoclusters (dDNA-AgNCs) and carbon dots (CDs) with the ratio of 51 in fluorescent intensity, and used for visual assay of I-. After addition of I-, the fluorescence of orange dDNA-AgNCs can be quenched by I- as the result of I–induced oxidative etching and aggregation of dDNA-AgNCs, while blue CDs as the stable internal standard are unresponsive to I-. With the increase of I-, the fluorescence intensity ratio (I577/I446) of binary-color probe gradually decreased, which leads to color variation from salmon pink to lighter salmon pink to lilac to light steel blue to final deep sky blue (under a UV lamp) with a sensitive detection limit of 19.