Feasibility of Intercity and Trans-Atlantic Telerobotic Remote Ultrasound Assessment Facilitated by a Nondedicated Bandwidth Connection

AbstractWe discuss the concept of ultrasound imaging at a distance by presenting the evaluation of a customized, lightweight, human-safe robotic arm for low-force, long-distance, telerobotic ultrasonography. We undertook intercity and trans-Atlantic telerobotic ultrasound simulation from master stations located in New York, New York and Munich, Germany, and imaged a phantom and a human volunteer located at a slave station in Burlington, Massachusetts, using standard Internet bandwidth <100 Mbps and <50 Mbps, respectively. The data from the robotic arm were tracked for understanding the time efficiency of the human interactions at the master stations. Comparison of a beginner in ultrasound operation with a professional sonographer revealed that although proficiency in using ultrasound was not a prerequisite for operating the robotic arm, previous experience in using clinical ultrasound was associated with progressively lower probe maneuvering time and speed due to an enhanced ability of the veteran operator in adjusting the finer angular motions of the probe. These results suggest that long-distance telerobotic echocardiography over a local nondedicated Internet bandwidth is feasible and can be rapidly learned by sonographers for cost-effective resource utilization

Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A

We report the case of a boy who was first addressed to medical attention when he was 2-years-old because of an episode of Salmonellosis. His cardiologic evaluation was normal. There were no clinical signs of myocarditis. Three years later he was admitted to the hospital due to a prolonged episode of flu with persistent fever. At that time, his electrocardiogram (ECG) showed junctional rhythm (JR) at 35 bpm. Further ECGs revealed sinus rhythm (SR) with first degree atrio-ventricular block, episodes of sinoatrial (SA) exit blocks, sinus arrests and phases of JR, supporting the diagnosis of sick sinus syndrome (SSS) [1]. Although the boy did not complain of symptoms, Holter monitoring showed frequent pauses of sinus arrest (max interval = 5.4 s) and chronotropic incompetence. At the age of 8 years, he underwent permanent pacemaker (PM) implantation. Although ventricular pacing is less indicated in SSS [2], the patient was treated with VVIR modality because an attempt at right atrial catheter positioning failed, due to inexcitability of the atrium. Since then, the boy has been asymptomatic. Further Holter monitoring showed episodes of paroxysmal atrial fibrillation (Fig. 1) and showed rate responsive pacing with an acceptable mean heart rate of 66 bp

Impact of acute TTE-evidenced cardiac dysfunction on in-hospital and outpatient mortality: A multicenter NYC COVID-19 registry study.

BackgroundCOVID-19 is associated with cardiac dysfunction. This study tested the relative prognostic role of left (LV), right and bi- (BiV) ventricular dysfunction on mortality in a large multicenter cohort of patients during and after acute COVID-19 hospitalization.Methods/resultsAll hospitalized COVID-19 patients who underwent clinically indicated transthoracic echocardiography within 30 days of admission at four NYC hospitals between March 2020 and January 2021 were studied. Images were re-analyzed by a central core lab blinded to clinical data. Nine hundred patients were studied (28% Hispanic, 16% African-American), and LV, RV and BiV dysfunction were observed in 50%, 38% and 17%, respectively. Within the overall cohort, 194 patients had TTEs prior to COVID-19 diagnosis, among whom LV, RV, BiV dysfunction prevalence increased following acute infection (pConclusionsLV, RV and BiV function declines during acute COVID-19 infection with each contributing to increased in- and out-patient mortality risk. RV dysfunction independently increases mortality risk

Prevalence and complications of aberrant subclavian artery in patients with heritable and nonheritable arteriopathies

Background: An aberrant subclavian artery (ASA) (or lusoria) is the most common congenital anomaly of the aortic arch (0.5%-2.2%; female-to-male ratio 2:1 to 3:1). ASA can become aneurysmal and result in dissection, involving Kommerell\u27s diverticulum when present and the aorta. Data of its significance in genetic arteriopathies are not available. Objectives: The purpose of this study was to assess the prevalence and complications of ASA in gene-positive and -negative nonatherosclerotic arteriopathies. Materials: The series includes 1,418 consecutive patients with gene-positive (n = 854) and gene-negative arteriopathies (n = 564) diagnosed as part of institutional work-up for nonatherosclerotic syndromic and nonsyndromic arteriopathies. Comprehensive evaluation includes genetic counseling, next-generation sequencing multigene testing, cardiovascular and multidisciplinary assessment, and whole-body computed tomography angiography. Results: ASA was found in 34 of 1,418 cases (2.4%), with a similar prevalence in gene-positive (n = 21 of 854, 2.5%) and gene-negative (n = 13 of 564, 2.3%) arteriopathies. Of the former 21 patients, 14 had Marfan syndrome, 5 had Loeys-Dietz syndrome, 1 had type-IV Ehlers-Danlos syndrome, and 1 had periventricular heterotopia type 1. ASA did not segregate with genetic defects. Dissection occurred in 5 of 21 patients with genetic arteriopathies (23.8%; 2 Marfan syndrome and 3 Loeys-Dietz syndrome), all with associated Kommerell\u27s diverticulum. No dissections occurred in gene-negative patients. At baseline, none of the 5 patients with ASA dissection fulfilled criteria for elective repair according to guidelines. Conclusions: The risk of complications of ASA is higher in patients with genetic arteriopathies and is difficult to predict. In these diseases, imaging of the supra-aortic trunks should enter baseline investigations. Determination of precise indications for repair can prevent unexpected acute events such as those described