Subject(s)
Brugada Syndrome/complications , Wolff-Parkinson-White Syndrome/complications , Brugada Syndrome/diagnosis , Brugada Syndrome/physiopathology , Defibrillators, Implantable , Diabetes Complications/diagnosis , Diabetes Complications/physiopathology , Dyslipidemias/complications , Electric Countershock/methods , Electrocardiography , Female , Humans , Middle Aged , Obesity/complications , Risk Factors , Treatment Outcome , Wolff-Parkinson-White Syndrome/diagnosis , Wolff-Parkinson-White Syndrome/physiopathologySubject(s)
Friedreich Ataxia/physiopathology , Hypertrophy, Left Ventricular/diagnosis , Adolescent , Adult , Antihypertensive Agents/therapeutic use , Antioxidants/therapeutic use , Female , Follow-Up Studies , Friedreich Ataxia/complications , Friedreich Ataxia/drug therapy , Friedreich Ataxia/epidemiology , Friedreich Ataxia/genetics , Humans , Hypertrophy, Left Ventricular/drug therapy , Hypertrophy, Left Ventricular/epidemiology , Hypertrophy, Left Ventricular/genetics , Incidence , Male , Middle Aged , Prevalence , Retrospective Studies , Sampling Studies , Sicily/epidemiologyABSTRACT
AIM: Long QT syndrome is a rare arrhythmic disease with a low incidence in the general population. There are no sure clinical or electrocardiographic parameters that could lead to a correct prognostic stratification in patients affected by this syndrome. The correlation between the incidence of a sudden death or dangerous ventricular arrhythmias and the duration of QTc interval is still a controversial topic. METHODS: Twenty nine children affected by QT long syndrome were admitted to the Division of Pediatric Cardiology of the Casa del Sole Hospital of Palermo (Italy). Their diagnosis was made by electrocardiogram (ECG). The average age of the patients was 7.6 years. The average follow-up was 4 years and three months. A therapy with beta-blocker was administered to all the children. During the follow-up of 4 year and three months, patients were genotyped. Twenty-three out of 29 children had at least one relative affected by the syndrome. Three of them had a familiar dead because of this syndrome and everyone had a duration of maximum QTc higher than the cut off (P=0.0002). All the people who died had not followed the therapy with beta-blocker. Patients with a maximum QTc recorded <500 had not familiar death by this syndrome. RESULTS: Holter and echocardiogram recorded periodically during the observation did not show dangerous arrhythmic events. All children maintained a good health during the follow-up. CONCLUSION: Although conducted on a small study population, the data analysis recorded during this study suggests that in patients affected by QT long syndrome younger than 16 years old undergoing a beta-blocker therapy the prognosis is excellent. The duration of QTc interval appears as a negative prognostic factor, although the beta-blocker therapy has been reduced considerably the incidence of sudden death.
Subject(s)
Long QT Syndrome , Adolescent , Child , Child, Preschool , Follow-Up Studies , Humans , Infant , Long QT Syndrome/genetics , Mutation , Prognosis , Risk FactorsSubject(s)
Arrhythmias, Cardiac/virology , Heart Conduction System/physiopathology , Myocarditis/complications , Paramyxoviridae Infections/complications , Paramyxoviridae , Arrhythmias, Cardiac/diagnosis , Arrhythmias, Cardiac/physiopathology , Arrhythmias, Cardiac/therapy , Child , Diagnosis, Differential , Electric Countershock/methods , Electrocardiography , Humans , Male , Myocarditis/diagnosis , Myocarditis/physiopathology , Myocarditis/therapy , Myocarditis/virology , Paramyxoviridae/isolation & purification , Paramyxoviridae Infections/diagnosis , Paramyxoviridae Infections/physiopathology , Paramyxoviridae Infections/therapy , Treatment OutcomeABSTRACT
AIM: Recent scientific evidence has emphasized the possible role of inhibitors of the renin-angiotensin system in preventing arrhythmic relapses in patients with paroxysmal or persistent atrial fibrillation and co-existing left ventricular hypertrophy or left ventricular dysfunction. METHODS: In order to verify the effects of these drugs on patients with a normal heart, we collected a series of 187 patients admitted to our division of cardiology for paroxysmal or persistent atrial fibrillation. All patients underwent cardioversion (with antiarrhythmic drugs and/or by electrical cardioversion) and were discharged in sinus rhythm. Episodes of recurrent arrhythmia were recorded during a mean follow-up period was 2 years. Patients were subdivided into 2 groups according to therapy: group 1 comprised patients receiving renin-angiotensin system inhibitors, group 2 comprised those not receiving therapy with these agents. All 91 patients in group 1 and 76 of those in group 2 had hypertension. Among the 91 patients in the group 1, 55 were treated with angiotensin-converting enzyme (ACE) inhibitors and 36 with angiotensin receptor blockers. There were no statistically significant differences in cardiovascular risk factors or antiarrhythmic drug use between the 2 groups. RESULTS: In group 1, 83% of patients experienced <2 recurrences of atrial fibrillation during the follow-up period, while 17% had >2 episodes. In group 2, 86% of patients experienced <2 relapses during the follow-up period, while the remaining 14% had >2 relapses. There was no statistically significant difference between the 2 groups (P=0.85). A subgroup analysis showed that treatment with angiotensin receptor blockers, beta-blockers, diuretics, and calcium-channel blockers brought no advantage in sinus rhythm maintenance. CONCLUSION: In our sample of hypertensive patients with a healthy heart, treatment with ACE inhibitors showed no statistically significant advantage in the prevention of atrial fibrillation relapses.
