6 results on '"Autore C"'
Search Results
2. Syncope and risk of sudden death in hypertrophic cardiomyopathy.
- Author
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Spirito P, Autore C, Rapezzi C, Bernabò P, Badagliacca R, Maron MS, Bongioanni S, Coccolo F, Estes NA, Barillà CS, Biagini E, Quarta G, Conte MR, Bruzzi P, and Maron BJ
- Published
- 2009
- Full Text
- View/download PDF
3. Syncope and risk of sudden death in hypertrophic cardiomyopathy
- Author
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Barry J. Maron, Roberto Badagliacca, Giovanni Quarta, Caterina S. Barillà, Paola Bernabò, N.A. Mark Estes, Fabio Coccolo, Martin S. Maron, Elena Biagini, Sergio Bongioanni, Claudio Rapezzi, Paolo Spirito, Paolo Bruzzi, Camillo Autore, Maria Rosa Conte, Spirito P, Autore C, Rapezzi C, Bernabò P, Badagliacca R, Maron MS, Bongioanni S, Coccolo F, Estes NA, Barillà CS, Biagini E, Quarta G, Conte MR, Bruzzi P, and Maron BJ
- Subjects
Adult ,Male ,medicine.medical_specialty ,Heart disease ,Adolescent ,Cardiomyopathy ,Neurological disorder ,Kaplan-Meier Estimate ,Sudden death ,Syncope ,Young Adult ,Age Distribution ,Risk Factors ,Physiology (medical) ,Internal medicine ,medicine ,Humans ,Aged ,Proportional Hazards Models ,Proportional hazards model ,business.industry ,Hypertrophic cardiomyopathy ,Cardiomyopathy, Hypertrophic ,Middle Aged ,medicine.disease ,Prognosis ,Confidence interval ,Defibrillators, Implantable ,Death, Sudden, Cardiac ,Anesthesia ,Relative risk ,Multivariate Analysis ,Cardiology ,Female ,cardiomyopathy ,hypertrophic ,death ,sudden ,syncope ,Cardiology and Cardiovascular Medicine ,business ,Follow-Up Studies - Abstract
Background— The prognostic significance of syncope has not been investigated systematically in hypertrophic cardiomyopathy, and treatment strategies have been based largely on intuition and experience. Methods and Results— We assessed the relationship between syncope and sudden death in 1511 consecutive patients with hypertrophic cardiomyopathy. Unexplained (n=153) or neurally mediated (n=52) syncope occurred in 205 patients (14%). Over a 5.6±5.2-year follow-up, 74 patients died suddenly. Relative risk of sudden death was 1.78 (95% confidence interval 0.88 to 3.51, P =0.08) in patients with unexplained syncope and 0.91 (95% confidence interval 0.00 to 3.83, P =1.0) in those with neurally mediated syncope compared with patients without syncope. In multivariable analysis, the temporal proximity of unexplained syncope to initial patient evaluation was independently associated with risk of sudden death ( P =0.006). Patients with unexplained syncope within 6 months before the initial evaluation showed a 5-fold increase in risk compared with patients without syncope (adjusted hazard ratio 4.89, 95% confidence interval 2.19 to 10.94), a relationship that was maintained throughout all age groups (5 years before initial evaluation) did not show an increased risk of sudden death (adjusted hazard ratio 0.38, 95% confidence interval 0.05 to 2.74). Conclusions— In the present large cohort of patients with hypertrophic cardiomyopathy, unexplained syncope was a risk factor for sudden death. Patients with syncopal events that occurred in close temporal proximity to the initial evaluation showed a substantially higher risk of sudden death than patients without syncope. Older patients with remote syncopal events did not show an increased risk.
- Published
- 2009
4. Prevalence and Clinical Outcome of Athletes With Mitral Valve Prolapse.
- Author
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Caselli S, Mango F, Clark J, Pandian NG, Corrado D, Autore C, and Pelliccia A
- Subjects
- Adolescent, Adult, Echocardiography, Electrocardiography, Female, Humans, Italy epidemiology, Male, Mitral Valve diagnostic imaging, Mitral Valve Prolapse diagnosis, Mitral Valve Prolapse physiopathology, Prevalence, Prognosis, Risk Assessment, Risk Factors, Severity of Illness Index, Time Factors, Young Adult, Athletes, Mitral Valve physiopathology, Mitral Valve Prolapse epidemiology
- Published
- 2018
- Full Text
- View/download PDF
5. Prognostic value of quantitative contrast-enhanced cardiovascular magnetic resonance for the evaluation of sudden death risk in patients with hypertrophic cardiomyopathy.
- Author
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Chan RH, Maron BJ, Olivotto I, Pencina MJ, Assenza GE, Haas T, Lesser JR, Gruner C, Crean AM, Rakowski H, Udelson JE, Rowin E, Lombardi M, Cecchi F, Tomberli B, Spirito P, Formisano F, Biagini E, Rapezzi C, De Cecco CN, Autore C, Cook EF, Hong SN, Gibson CM, Manning WJ, Appelbaum E, and Maron MS
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Child, Cohort Studies, Female, Humans, Male, Middle Aged, Prognosis, Risk Factors, Single-Blind Method, Young Adult, Cardiomyopathy, Hypertrophic diagnosis, Cardiomyopathy, Hypertrophic mortality, Contrast Media, Death, Sudden, Cardiac epidemiology, Gadolinium, Magnetic Resonance Imaging, Cine standards
- Abstract
Background: Hypertrophic cardiomyopathy (HCM) is the most common cause of sudden death in the young, although not all patients eligible for sudden death prevention with an implantable cardioverter-defibrillator are identified. Contrast-enhanced cardiovascular magnetic resonance with late gadolinium enhancement (LGE) has emerged as an in vivo marker of myocardial fibrosis, although its role in stratifying sudden death risk in subgroups of HCM patients remains incompletely understood., Methods and Results: We assessed the relation between LGE and cardiovascular outcomes in 1293 HCM patients referred for cardiovascular magnetic resonance and followed up for a median of 3.3 years. Sudden cardiac death (SCD) events (including appropriate defibrillator interventions) occurred in 37 patients (3%). A continuous relationship was evident between LGE by percent left ventricular mass and SCD event risk in HCM patients (P=0.001). Extent of LGE was associated with an increased risk of SCD events (adjusted hazard ratio, 1.46/10% increase in LGE; P=0.002), even after adjustment for other relevant disease variables. LGE of ≥15% of LV mass demonstrated a 2-fold increase in SCD event risk in those patients otherwise considered to be at lower risk, with an estimated likelihood for SCD events of 6% at 5 years. Performance of the SCD event risk model was enhanced by LGE (net reclassification index, 12.9%; 95% confidence interval, 0.3-38.3). Absence of LGE was associated with lower risk for SCD events (adjusted hazard ratio, 0.39; P=0.02). Extent of LGE also predicted the development of end-stage HCM with systolic dysfunction (adjusted hazard ratio, 1.80/10% increase in LGE; P<0.03)., Conclusions: Extensive LGE measured by quantitative contrast enhanced CMR provides additional information for assessing SCD event risk among HCM patients, particularly patients otherwise judged to be at low risk., (© 2014 American Heart Association, Inc.)
- Published
- 2014
- Full Text
- View/download PDF
6. Infective endocarditis in hypertrophic cardiomyopathy: prevalence, incidence, and indications for antibiotic prophylaxis.
- Author
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Spirito P, Rapezzi C, Bellone P, Betocchi S, Autore C, Conte MR, Bezante GP, and Bruzzi P
- Subjects
- Acute Disease, Adult, Age Factors, Aged, Cardiomyopathy, Hypertrophic diagnostic imaging, Cardiomyopathy, Hypertrophic epidemiology, Echocardiography, Endocarditis, Bacterial complications, Endocarditis, Bacterial drug therapy, Female, Humans, Incidence, Italy epidemiology, Male, Middle Aged, Prevalence, Retrospective Studies, Risk Factors, Antibiotic Prophylaxis, Cardiomyopathy, Hypertrophic complications, Endocarditis, Bacterial epidemiology
- Abstract
Background: The literature on infective endocarditis in hypertrophic cardiomyopathy (HCM) is virtually confined to case reports. Consequently, the risk of endocarditis in HCM remains undefined., Methods and Results: We assessed the occurrence of endocarditis in 810 HCM patients evaluated between 1970 and 1997. Endocarditis was diagnosed in 10 patients, 2 of whom were excluded from analysis of prevalence and incidence because they were referred for acute endocarditis. At first evaluation, echocardiographic features consistent with prior endocarditis were identified in 3 of 808 patients, a prevalence of 3.7 per 1000 patients (95% CI, 0.8 to 11). Of 681 patients who were followed, 5 developed endocarditis, an incidence of 1.4 per 1000 person-years (95% CI, 0.5 to 3.2); outflow obstruction was present in each of these 5 patients and was associated with the risk of endocarditis (P=0.006). In the 224 obstructive patients, incidence of endocarditis was 3.8 per 1000 person-years (95% CI, 1.6 to 8.9) and probability of endocarditis 4. 3% at 10 years. Left atrial size was also associated with the risk of endocarditis (P=0.007). In patients with both obstruction and atrial dilatation (>/=50 mm), incidence of endocarditis increased to 9.2 per 1000 person-years (95% CI, 2.5 to 23.5). Analysis of all 10 patients with endocarditis identified outflow obstruction in each and atrial dilatation in 7., Conclusions: Endocarditis in HCM is virtually confined to patients with outflow obstruction and is more common in those with both obstruction and atrial dilatation. These results indicate that antibiotic prophylaxis is required only in patients with obstructive HCM.
- Published
- 1999
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- View/download PDF
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