Search results for "TACHYCARDIA"

showing 10 items of 119 documents

Angiotensin converting enzyme gene polimorfism and central obesity: relationship with blood pressure and left ventricular structure and function

2001

medicine.medical_specialtyEjection fractionMegalencephalic leukoencephalopathy with subcortical cystsbiologybusiness.industryDiastoleAngiotensin-converting enzymemedicine.diseaseInappropriate sinus tachycardiaBlood pressureWaist–hip ratioEndocrinologyInternal medicineInternal Medicinemedicinebiology.proteinCardiologySystolebusinessAmerican Journal of Hypertension
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Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype.

2020

Background: Pathogenic variants in the filamin C (FLNC) gene are associated with inherited cardiomyopathies including dilated cardiomyopathy with an arrhythmogenic phenotype. We evaluated FLNC variants in arrhythmogenic cardiomyopathy (ACM) and investigated the disease mechanism at a molecular level. Methods: 120 gene-elusive ACM patients who fulfilled diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy (ARVC) were screened by whole exome sequencing. Fixed cardiac tissue from FLNC variant carriers who had died suddenly was investigated by histology and immunohistochemistry. Results: Novel or rare FLNC variants, four null and five variants of unknown significance, were id…

medicine.medical_specialtyFilaminsCardiomyopathyContrast MediaGadolinium030204 cardiovascular system & hematologyVentricular tachycardiaSudden deathRight ventricular cardiomyopathy03 medical and health sciences0302 clinical medicineCardiac magnetic resonance imagingInternal medicinemedicineHumansCor030212 general & internal medicineFLNCcardiovascular diseasesArrhythmogenic Right Ventricular DysplasiaExome sequencingmedicine.diagnostic_testbusiness.industryDilated cardiomyopathymedicine.diseasePatologiaPhenotypeMutationCardiologyCardiomyopathiesCardiology and Cardiovascular Medicinebusiness
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Prevalence, management, and outcome of adverse rhythm disorders in takotsubo syndrome: insights from the international multicenter GEIST registry

2019

One important complication related to takotsubo syndrome (TTS) is adverse rhythm disorders. Our study was conducted to determine the incidence and management of adverse rhythm disorders in TTS and its long-term prognostic impact. We analyzed 906 TTS patients from 9 European centers. Patients were divided into the adverse rhythm disorders group (encompassing ventricular tachycardia, ventricular fibrillation, torsade de pointes, and asystole or complete atrioventricular block) and non-adverse rhythm disorders group. In our study cohort, we identified 67 (7.4%) patients with presence of adverse rhythm disorders. TTS patients were followed up over a period of 2.8 years. In the adverse rhythm di…

medicine.medical_specialtyMalignant arrhythmia030204 cardiovascular system & hematologyGlobal HealthVentricular tachycardia03 medical and health sciences0302 clinical medicineHeart RateRisk FactorsTakotsubo CardiomyopathyInternal medicinePrevalencemedicineHumansMulticenter Studies as TopicRegistries030212 general & internal medicineAsystoleOutcomebusiness.industryIncidenceICDCardiogenic shockMortality rateDisease ManagementArrhythmias CardiacVentricular tachycardiaTorsade de pointePrognosismedicine.diseaseManagementHeart failureVentricular fibrillationCohortTakotsubo syndromeCardiology and Cardiovascular MedicineComplicationbusinessHeart Failure Reviews
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Phrenic nerve displacement by intrapericardial balloon inflation during epicardial ablation of ventricular tachycardia: Four case reports

2020

BACKGROUND Phrenic nerve (PN) injury is one of the recognized possible complications following epicardial ablation of ventricular tachycardia (VT). High-output pacing is a widely used maneuver to establish a relationship between the PN and the ablation catheter tip. An absence of PN capture is usually considered an indication that it is safe to ablate, and that successful ablation may be performed at adjacent sites. However, PN capture may impact the procedural outcome. Only a few cases have been reported in the literature that avoid PN injury by using different techniques. CASE SUMMARY Three patients with a previous history of myocarditis and one patient with ischemic cardiomyopathy underw…

medicine.medical_specialtyMyocarditismedicine.medical_treatmentEpicardial ablationCatheter ablationCase ReportEpicardial access030204 cardiovascular system & hematologyVentricular tachycardiaBalloon inflationPhrenic nerve03 medical and health sciences0302 clinical medicineInternal medicinemedicineDisplacement (orthopedic surgery)cardiovascular diseases030212 general & internal medicineCase seriesPhrenic nervebusiness.industryNonischemic cardiomyopathyVentricular tachycardiamusculoskeletal systemmedicine.diseaseMyocarditisNonischemic cardiomyopathynervous systemcardiovascular systemCardiologyCatheter ablationCardiology and Cardiovascular Medicinebusinesscirculatory and respiratory physiologyWorld Journal of Cardiology
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Causality-based diagnosis of histamine-related cardiorespiratory disturbances in surgical patients

1998

medicine.medical_specialtyNeurologyImmunologyPharmacology toxicologyHistamine ReleaseSkin Diseaseschemistry.chemical_compoundDouble-Blind MethodTachycardiaInternal medicineBradycardiamedicineHumansIntensive care medicineAnaphylaxisPharmacologybusiness.industryCardiorespiratory fitnessCausalityRheumatologyHistamine H2 AntagonistschemistryHypertensionHistamine H1 AntagonistsHypotensionbusinessHistamineHistamineSurgical patientsInflammation Research
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Tetralogy of Fallot as a Model to Study Cardiac Progenitor Cell Migration and Differentiation During Heart Development

2009

Tetralogy of Fallot (ToF) has long been considered a congenital disorder that occurs due to environmental alterations during gestation. Recently, several mutated genes have been discovered that are thought to be responsible for the malformations observed in ToF. These genetic mutations, which are microdeletions, are sporadic and are frequently also present in trisomy 21 patients. The ToF malformations can be lethal, but for the last 50 years, surgical repairs that place an artificial patch to repair the four features of ToF have improved the survival of patients with ToF. However, 0.5% to 6% of patients who survive after surgical repair of ToF die of sudden cardiac death caused by ventricul…

medicine.medical_specialtyOrganogenesisBiologyVentricular tachycardiaSudden cardiac deathHomeobox protein Nkx-2.5Cell MovementInternal medicinemedicineAnimalsHumansCell LineageCell ProliferationTetralogy of FallotHomeodomain ProteinsSurgical repairHeart developmentMyocardiumStem CellsGene Expression Regulation DevelopmentalCell DifferentiationToF Cardiac Stem Cellsmedicine.diseaseGATA4 Transcription Factormedicine.anatomical_structureVentricleMutationHomeobox Protein Nkx-2.5Tetralogy of FallotCardiologyCardiology and Cardiovascular MedicineTranscription FactorsCongenital disorderTrends in Cardiovascular Medicine
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Is there a role for verapamil beyond rate control in paroxysmal atrial fibrillation?

2021

medicine.medical_specialtyParoxysmal atrial fibrillationbusiness.industryRate controlVerapamilPhysiology (medical)Internal medicineAtrial FibrillationmedicineCardiologyVerapamilHumansCardiology and Cardiovascular MedicinebusinessTachycardia ParoxysmalAnti-Arrhythmia Agentsmedicine.drugEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
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A 35-year effective treatment of catecholaminergic polymorphic ventricular tachycardia with propafenone

2018

Key Teaching Points • Despite proven catecholaminergic polymorphic ventricular tachycardia (CPVT) with pathogen RyR2 mutation and recurrent syncope, patients could have a favorable long-term outcome over 35 years under treatment. • Propafenone could be effective for treatment of patients with CPVT. • The beneficial effect of the monotherapy with propafenone in our patient may result from the combined antiarrhythmic effect of this drug with Na+ channel blockade and beta blocker capabilities.

medicine.medical_specialtyPolymorphic premature ventricular beatsmedicine.drug_classCase ReportPropafenone030204 cardiovascular system & hematologyCatecholaminergic polymorphic ventricular tachycardiaRyanodine receptor 203 medical and health sciences0302 clinical medicinePropafenoneInternal medicineMedicineEffective treatment030212 general & internal medicineExercise-induced syncopeBeta blockerbusiness.industrymedicine.diseaseBlockadeExercise-induced syncopeCatecholaminergic polymorphic ventricular tachycardiacardiovascular systemCardiologyAntiarrhythmic effectCardiology and Cardiovascular MedicinebusinessRyanodine receptor mutationmedicine.drugHeartRhythm Case Reports
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Simplified Electrophysiology Modeling Framework to Assess Ventricular Arrhythmia Risk in Infarcted Patients

2021

Patients that have suffered a myocardial infarction are at lifetime high risk for sudden cardiac death (SCD). Personalized 3D computational modeling and simulation can help to find non-invasively arrhythmogenic features of patients’ infarcts, and to provide additional information for stratification and planning of radiofrequency ablation (RFA). Currently, multiscale biophysical models require high computational resources and long simulations times, which make them impractical for clinical environments. In this paper, we develop a phenomenological solver based on cellular automata to simulate cardiac electrophysiology, with results comparable to those of biophysical models. The solver can ru…

medicine.medical_specialtyRadiofrequency ablationCardiac electrophysiologyComputer scienceSolvermedicine.diseaseVentricular tachycardiaCellular automatonlaw.inventionSudden cardiac deathModeling and simulationlawInternal medicinecardiovascular systemmedicineCardiologyMyocardial infarction
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Personalized Cardiac Computational Models: From Clinical Data to Simulation of Infarct-Related Ventricular Tachycardia.

2019

In the chronic stage of myocardial infarction, a significant number of patients develop life-threatening ventricular tachycardias (VT) due to the arrhythmogenic nature of the remodeled myocardium. Radiofrequency ablation (RFA) is a common procedure to isolate reentry pathways across the infarct scar that are responsible for VT. Unfortunately, this strategy show relatively low success rates; up to 50% of patients experience recurrent VT after the procedure. In the last decade, intensive research in the field of computational cardiac electrophysiology (EP) has demonstrated the ability of three-dimensional (3D) cardiac computational models to perform in-silico EP studies. However, the personal…

medicine.medical_specialtyRadiofrequency ablationPhysiologyborder zone (BZ)030204 cardiovascular system & hematologyVentricular tachycardialcsh:Physiologylaw.invention03 medical and health sciences0302 clinical medicineelectrical remodeling (ER)lawventricular tachycardia (VT)Physiology (medical)Internal medicinemedicineSinus rhythmMyocardial infarctionslow conducting channel (SCC)myocardial infarction (MI)030304 developmental biologyOriginal Research0303 health sciencesComputational modellcsh:QP1-981Cardiac electrophysiologybusiness.industryfibrosiscomputational simulationReentryTorsomedicine.diseasemedicine.anatomical_structureCardiologycardiovascular systemradiofrequency ablation (RFA)businessFrontiers in physiology
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