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1 n 64 families (230 relatives, 80 unexplained sudden cardiac death).
2 (HCM) is an uncommon but important cause of sudden cardiac death.
3 ies have focused on identifying high-risk of sudden cardiac death.
4 olongation, which poses an increased risk of sudden cardiac death.
5 n HFpEF, which in turn predisposes to VA and sudden cardiac death.
6 turely from ventricular tachycardia (VT) and sudden cardiac death.
7 rdiac hypertrophy are major risk factors for sudden cardiac death.
8 n associated with delayed repolarization and sudden cardiac death.
9 rs are indicated for prevention of secondary sudden cardiac death.
10 of lesions lead to heart attack, stroke, or sudden cardiac death.
11 main goal of treatment is the prevention of sudden cardiac death.
12 She had no family history of sudden cardiac death.
13 S2), a heart rhythm disorder associated with sudden cardiac death.
14 ias, leading to ventricular fibrillation and sudden cardiac death.
15 riggered syncope, aborted cardiac arrest, or sudden cardiac death.
16 ricular tachycardia (VT) is a major cause of sudden cardiac death.
17 table cardioverter-defibrillator shocks, and sudden cardiac death.
18 act obstruction, and risk stratification for sudden cardiac death.
19 All-cause mortality and sudden cardiac death.
20 ricular arrhythmias and an increased risk of sudden cardiac death.
21 e been linked to ventricular arrhythmias and sudden cardiac death.
22 achycardia, aborted sudden cardiac death, or sudden cardiac death.
23 ical interventions with potential to prevent sudden cardiac death.
24 osis (CS) may manifest as arrhythmia or even sudden cardiac death.
25 -myocyte junction and are a leading cause of sudden cardiac death.
26 ading to impaired mechanical contraction and sudden cardiac death.
27 tor (ICD) in the treatment and prevention of sudden cardiac death.
28 ardial repolarization and are susceptible to sudden cardiac death.
29 roke, invasive cardiovascular procedures, or sudden cardiac death.
30 ication and treatment of patients at risk of sudden cardiac death.
31 h risk indicator for cardiac arrhythmias and sudden cardiac death.
32 den cardiac death as compared with explained sudden cardiac death.
33 lications of heart disease and can result in sudden cardiac death.
34 tricular tachycardia or long QT syndrome and sudden cardiac death.
35 eading cause of mortality on hemodialysis is sudden cardiac death.
36 h risk indicator for cardiac arrhythmias and sudden cardiac death.
37 is a risk factor for cardiac arrhythmias and sudden cardiac death.
38 lock, atrial or ventricular arrhythmias, and sudden cardiac death.
39 evation myocardial infarction and 6 (17%) as sudden cardiac death.
40 for a group known to have elevated rates of sudden cardiac death.
41 e to ischemia-associated QT prolongation and sudden cardiac death.
42 scar and hibernation can inform the risk of sudden cardiac death.
43 d by cardiac hypertrophy, heart failure, and sudden cardiac death.
44 and the mechanisms of arrhythmias leading to sudden cardiac death.
45 r ICD implantation for primary prevention of sudden cardiac death.
46 inherited cardiac disorders associated with sudden cardiac death.
47 ventricular arrhythmias, cardiac arrest, and sudden cardiac death.
48 to advance the science and clinical care of sudden cardiac death.
49 for studying arrhythmic disorders leading to sudden cardiac death.
50 interval (Tp-e) is an independent marker of sudden cardiac death.
51 nsive research, as it increases the risk for sudden cardiac death.
52 to model and study disorders associated with sudden cardiac death.
53 s associated with poor cardiac prognosis and sudden cardiac death.
54 such as epilepsy, schizophrenia, cancer, and sudden cardiac death.
55 ncreasing the risk of Torsade de pointes and sudden cardiac death.
56 ts with myocardial ischemia, arrhythmia, and sudden cardiac death.
57 adian pattern of ventricular tachyarrhythmia/sudden cardiac death.
58 contributing to ventricular arrhythmias and sudden cardiac death.
59 syndrome type 1, which can cause syncope and sudden cardiac death.
60 es the risk for ventricular fibrillation and sudden cardiac death.
61 ide range of symptoms and may even result in sudden cardiac death.
62 ay result in serious consequences, including sudden cardiac death.
63 pathogenesis of ventricular arrhythmias and sudden cardiac death.
64 tent >15% it is associated with high risk of sudden cardiac death.
65 opathy and a low-intermediate 5-year risk of sudden cardiac death.
66 eating heart failure and reduce the risk for sudden cardiac death.
67 function, life-threatening arrhythmias, and sudden cardiac death.
68 man (QTc, >480 ms) with a family history of sudden cardiac death.
69 entricular Arrhythmias and the Prevention of Sudden Cardiac Death.
70 ted fat increase the risk of arrhythmias and sudden cardiac death.
71 ventricular walls and is a leading cause of sudden cardiac death.
72 seases and is associated with a high risk of sudden cardiac death.
73 ral regurgitation, and it is associated with sudden cardiac death.
74 luding myocardial fibrofatty replacement and sudden cardiac death.
75 d with malignant ventricular arrhythmias and sudden cardiac death.
76 es de pointes, and aborted cardiac arrest or sudden cardiac death.
77 eart disease, cardiomyopathy, arrhythmia, or sudden cardiac death.
78 e myocardium, resulting in heart failure and sudden cardiac death.
79 int of significant ventricular arrhythmia or sudden cardiac death.
80 nisms leading to acute coronary syndrome and sudden cardiac death.
81 from cardiovascular causes, of which 15 were sudden cardiac deaths.
82 age had the highest incidence of unexplained sudden cardiac death (0.8 cases per 100,000 persons per
84 al]) of cardiac death (1.45 [1.24 to 1.69]), sudden cardiac death [1.70 (1.34 to 2.15)], first cardio
85 strongest predictor for all-cause death and sudden cardiac death (10.09%, 95% CI 4.72-20.42% and 16.
86 ost common cause of cardiovascular death was sudden cardiac death (20.1%); while myocardial infarctio
87 35 years of age had the highest incidence of sudden cardiac death (3.2 cases per 100,000 persons per
88 ventricular arrhythmias (82%); and frequent sudden cardiac death (40 cases in 21 of 28 families).
90 revealed highly prevalent family history of sudden cardiac death (51%) and cardiomyopathy (72%) amon
91 hronic heart failure (42%), pneumonia (10%), sudden-cardiac death (7%), cancer (6%), and hemorrhage (
92 cturally normal heart carries a low risk for sudden cardiac death; accordingly, there is typically no
93 potential was associated with higher risk of sudden cardiac death (adjusted hazard ratio, 1.18; 95% c
94 ad disease progression and one patient died (sudden cardiac death after 17 months of ibrutinib mainte
95 ilure (aHR: 1.95; 95% CI: 1.11 to 3.41), and sudden cardiac death (aHR: 3.75; 95% CI: 1.26 to 11.2) o
96 romycin increases risk of cardiovascular and sudden cardiac death, although the underlying mechanisms
97 However, the recognition of the risk for sudden cardiac death among basketball players is challen
98 hic, and autopsy information on all cases of sudden cardiac death among children and young adults 1 t
100 ed the identification of a possible cause of sudden cardiac death among children and young adults.
101 ulation-based, clinical and genetic study of sudden cardiac death among children and young adults.
102 ew-user design to compare the 1-year risk of sudden cardiac death among hemodialysis patients initiat
103 in reducing risk of all-cause mortality and sudden cardiac death among patients with an EF </=35% at
104 muM) had a 4-fold higher risk of cardiac or sudden cardiac death and a 2-fold higher risk of any-cau
105 d cardiomyopathy (DCM) is a leading cause of sudden cardiac death and a major indicator for heart tra
106 ndividuals, can acutely increase the risk of sudden cardiac death and acute myocardial infarction in
108 of myocardial fibrosis predicts both risk of sudden cardiac death and likelihood of LV functional rec
109 myectomy with long-term follow-up, (aborted) sudden cardiac death and mortality rates were found to b
111 ons for prediction and prevention of SCA and sudden cardiac death and provides justification for a re
112 f creating parametric risk models to predict sudden cardiac death and pump failure in the DCM populat
114 ations: For this review, we analyzed data on sudden cardiac death and SCA available from population s
116 ciated with a transient elevation in risk of sudden cardiac death and that appropriate training subst
118 nt of our analyses, whereas the composite of sudden cardiac death and ventricular tachycardia requiri
120 sease severity expression, high-incidence of sudden cardiac death, and absence of skeletal myopathy o
121 all-cause mortality, heart transplantation, sudden cardiac death, and appropriate implantable cardio
123 pically required due to an elevated risk for sudden cardiac death, and catheter ablation can be used
124 ar tachycardia, syncope, a family history of sudden cardiac death, and severe cardiac hypertrophy are
125 ications known as the stroke-heart syndrome, sudden cardiac death, and Takotsubo syndrome, among othe
126 years, 22 patients had hard cardiac events (sudden cardiac death, appropriate implantable cardiovert
127 ars (2 to 8 years), the combined endpoint of sudden cardiac death, appropriate implantable cardiovert
128 ter defibrillators for primary prevention of sudden cardiac death are less likely to experience susta
129 nce of sustained ventricular arrhythmias and sudden cardiac death are lower in women than in men.
131 ations, including pulmonary hypertension and sudden cardiac death, are significantly higher for peopl
132 s worse compared with other etiologies, with sudden cardiac death as an important mode of death.
133 re independently associated with unexplained sudden cardiac death as compared with explained sudden c
135 peripheral artery disease, heart failure and sudden cardiac death, as well as how to select available
136 based on an estimate of a patient's risk of sudden cardiac death, as well as their preferences and v
139 icologic and histologic studies (unexplained sudden cardiac death), at least 59 cardiac genes were an
140 ecutive families who experienced unexplained sudden cardiac death before 45 years of age were include
141 cardiac syncope, aborted cardiac arrest, and sudden cardiac death, but a 38.8-fold (95% CI, 5.6-269.1
142 as emerged as a novel tool for prevention of sudden cardiac death, but clinical performance data for
143 Ds) improve survival in patients at risk for sudden cardiac death, but complications remain an import
144 recommended at autopsy in suspected cases of sudden cardiac death, but data on the role of nonselecti
145 onventionally been used as a risk marker for sudden cardiac death, but has performed poorly in trials
146 cardiomyopathy (ARVC) is a leading cause of sudden cardiac death, but its progression over time and
147 ic heart failure are at an increased risk of sudden cardiac death, but more discriminating tools are
148 hERG) ion channel, have been associated with sudden cardiac death, but only a subset of these variant
150 nes can pre-dispose to 4 important causes of sudden cardiac death: cardiomyopathy, coronary artery di
151 in a case-control cohort of 600 adult-onset sudden cardiac death cases and 600 matched controls from
153 ine receptor-2 (RyR2) gene in both SUDEP and sudden cardiac death cases linked to catecholaminergic p
154 he prevalence of rare pathogenic variants in sudden cardiac death cases versus controls, and the prev
157 15 individuals, all of whom had experienced sudden cardiac death-corresponding to a pathogenic varia
158 is review article, part of the Compendium on Sudden Cardiac Death, discusses the major issues related
164 ound that the mice developed CCD, leading to sudden cardiac death from complete heart block, but no l
167 ; 95% confidence interval, 1.31 to 6.82) and sudden cardiac death (hazard ratio, 4.52; 95% confidence
169 tes conferred a higher risk of non-CV death, sudden cardiac death, hospitalization, CV hospitalizatio
170 id not receive defibrillators was related to sudden cardiac death in 8.0% among those with ICM but in
171 ong QT syndrome (LQTS) is a leading cause of sudden cardiac death in early life and has been implicat
172 32% versus 17%, P=0.020), and higher rate of sudden cardiac death in first degree relatives<age 30 (4
173 relatives without children and families with sudden cardiac death in first-degree relatives <40 years
176 tive analysis examined data collected in the Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT),
179 ormance was assessed in the SCD-HeFT cohort (Sudden Cardiac Death in Heart Failure Trial; n=2521).
180 rillator (ICD) use for primary prevention of sudden cardiac death in heart failure with reduced eject
181 s generally and patients at risk for SCA and sudden cardiac death in particular is limited by the div
182 dioverter-defibrillators are used to prevent sudden cardiac death in patients with cardiac sarcoidosi
183 tor (ICD) is the standard therapy to prevent sudden cardiac death in patients with coronary artery di
185 bility is a well-established risk factor for sudden cardiac death in survivors of acute myocardial in
186 sociation between these 'maladaptations' and sudden cardiac death in the general population raises th
187 Current risk stratification strategies for sudden cardiac death in the heart failure patient are no
188 hly increased and so far unexplained risk of sudden cardiac death in the hemodialysis patient populat
190 review will outline the underlying causes of sudden cardiac death in the young and outline our univer
192 fied in 31 of 113 cases (27%) of unexplained sudden cardiac death in which genetic testing was perfor
195 e diseases are often the underlying cause of sudden cardiac death in young individuals and result fro
198 associates with cardiovascular mortality and sudden cardiac death independent of traditional risk fac
206 In individuals aged <35 years, unexplained sudden cardiac death is the most common presentation.
207 Long QT syndrome has been associated with sudden cardiac death likely caused by early afterdepolar
209 omnolence and gastrointestinal symptoms; one sudden cardiac death occurred in the SEP-363856 group.
212 l, 0.92-0.98; P=0.004) and family history of sudden cardiac death (odds ratio, 3.5; 95% confidence in
214 lant and a secondary arrhythmic end point of sudden cardiac death or appropriate implantable cardiove
215 admission for heart failure, 8% experienced sudden cardiac death or equivalent, 4% required heart tr
219 Patients with Brugada syndrome and aborted sudden cardiac death or syncope have higher risks for ve
220 t failure (HR, 1.48; 95% CI, 1.43-1.53), and sudden cardiac death or ventricular arrhythmia (HR, 1.65
223 for major arrhythmic events (sustained VAs, sudden cardiac death, or appropriate ICD therapy) in asy
224 d with a history of ventricular arrhythmias, sudden cardiac death, or implantable cardioverter-defibr
226 inheritance of the condition and the risk of sudden cardiac death, other family members are tested fo
227 However, HCM is also an important cause of sudden cardiac death, particularly in adolescents and yo
228 rited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and
230 vices in heart failure with primary focus on sudden cardiac death prevention and cardiac resynchroniz
233 ibrillators (ICDs) for primary prevention of sudden cardiac death (primary prevention ICDs) in patien
234 ars, whereas for patients >70 years old, the sudden cardiac death rate was 1.6 (95% CI, 0.8-3.2) and
236 , 0.66; 95% confidence interval, 0.50-0.87), sudden cardiac death (relative hazard, 0.57; 95% confide
237 ommon cyanotic congenital heart disease, and sudden cardiac death represents an important mode of dea
238 as a base case, the complex epidemiology of sudden cardiac death risk and the substantial new fundin
240 l decision is whether a particular patient's sudden cardiac death risk is sufficient to justify place
243 In the current therapeutic era, the risk for sudden cardiac death (SCD) after non-ST-segment elevatio
244 ic heart failure (HF) have increased risk of sudden cardiac death (SCD) and death from progressive pu
245 ite recent progress in profiling of risk for sudden cardiac death (SCD) and prevention and interventi
254 ophic cardiomyopathy is the leading cause of sudden cardiac death (SCD) in children and young adults.
255 s have a higher incidence of out-of-hospital sudden cardiac death (SCD) in comparison with whites.
256 ime physical activity (LTPA) and the risk of sudden cardiac death (SCD) in coronary artery disease pa
259 cardiomyopathy for the primary prevention of sudden cardiac death (SCD) in those with a left ventricu
268 tachyarrhythmias with device-based therapy, sudden cardiac death (SCD) remains an enormous public he
269 assessed the echocardiographic predictors of sudden cardiac death (SCD) within 2 population-based coh
271 l heart disease carries an elevated risk for sudden cardiac death (SCD), and implantable cardioverter
272 dialysis are reported to be at high risk of sudden cardiac death (SCD), and to date, no therapy has
288 st device implantation (DHF/HTx/VAD); and 3) sudden cardiac death/sustained ventricular tachycardia/v
289 ally important subset of adults experiencing sudden cardiac death; these variants are present in ~1%
290 leads to the pandemics of heart failure and sudden cardiac death, thus calling for a reappraisal of
292 hy and a low- or intermediate 5-year risk of sudden cardiac death underwent cardiac magnetic resonanc
293 hanical circulatory support/transplantation, sudden cardiac death, vascular outcomes in coarctation o
295 rillators (ICDs) for secondary prevention of sudden cardiac death were conducted nearly 2 decades ago
298 defined as stroke, myocardial infarction, or sudden cardiac death, were assessed prospectively over a
299 s to very low values before they suffer from sudden cardiac death with an unexplained high incidence.