Research Topics
| E S KaufmanSummaryAffiliation: Case Western Reserve University Country: USA Publications
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Detail Information
Publications
Microvolt-level T-wave alternans determination using the spectral method in patients with QT prolongation: value of adjusting the T-wave windowElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, OH 44109 1998, USA
J Electrocardiol 45:758-63. 2012..MTWA analysis software selects a segment of the ECG that encompasses the T-wave in most individuals, but may miss the T-wave end in patients with QT prolongation...
Positive predictive value of device-detected atrial high-rate episodes at different rates and durations: an analysis from ASSERTElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, Ohio 44109, USA
Heart Rhythm 9:1241-6. 2012..As AHREs may lead to the initiation of oral anticoagulation, it is crucial to understand the relationship between AHREs and true AT/AF...
Arrhythmic risk in congenital long QT syndromeElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, OH 44109 1998, USA
J Electrocardiol 44:645-9. 2011....
Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndromeElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, Ohio 44109 1998, USA
Heart Rhythm 6:S51-5. 2009..ICD implantation is the primary therapy; quinidine may be a useful adjunctive therapy...
Risk of death in the long QT syndrome when a sibling has diedElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus, Case Western Reserve University, Cleveland, Ohio, USA
Heart Rhythm 5:831-6. 2008..Sudden death of a sibling is thought to be associated with greater risk of death in long QT syndrome (LQTS). However, there is no evidence of such an association...
"Indeterminate" microvolt T-wave alternans tests predict high risk of death or sustained ventricular arrhythmias in patients with left ventricular dysfunctionElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, Ohio 44109 1998, USA
J Am Coll Cardiol 48:1399-404. 2006..This study tested the hypothesis that an "indeterminate" microvolt T-wave alternans (MTWA) test, when due to ectopy, unsustained MTWA, or low exercise heart rate (HR), has prognostic significance similar to a positive MTWA test...
Use of autonomic maneuvers to probe phenotype/genotype discordance in congenital long QT syndromeElizabeth S Kaufman
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, Ohio, USA
Am J Cardiol 96:1425-30. 2005..01, at 1 minute into recovery) but not in subjects with LQT2. In conclusion, sympathetic stimulation can reveal the LQT1 phenotype even in subjects with normal baseline electrocardiographic findings...
Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family membersE S Kaufman
The Heart and Vascular Research Center, Case Western Reserve University, Cleveland, Ohio 44109 1998, USA
J Cardiovasc Electrophysiol 12:455-61. 2001..We hypothesized that a combination of clinical and ECG techniques could identify gene carriers within a single family with congenital LQTS...
Risk of proarrhythmic events in the Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) study: a multivariate analysisElizabeth S Kaufman
Heart and Vascular Research Center, Hamann 3rd Floor, MetroHealth Campus, Case Western Reserve University, 2500 MetroHealth Drive, Cleveland, Ohio 44109 1998, USA
J Am Coll Cardiol 44:1276-82. 2004..This study examined the risk of proarrhythmic events in patients receiving antiarrhythmic drugs for treatment of atrial fibrillation (AF) according to present-day safety guidelines...
Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutationsElizabeth S Kaufman
The Heart and Vascular Research Center and Rammelkamp Center for Education and Research, MetroHealth Campus, Case Western Reserve University, Cleveland, Ohio 44109 1998, USA
J Cardiovasc Electrophysiol 14:320-2. 2003
Heart rate variability in cocaine-exposed newborn infantsS K Mehta
Fairview Hospital and MetroHealth Medical Center, Department of Pediatrics and Heart and Vascular Center, MetroHealth Campus, Case Western Reserve University, Cleveland, Ohio 44111 5656, USA
Am Heart J 142:828-32. 2001..Its underlying cause, in part, may be attributed to abnormal autonomic function. We proposed to study heart rate variability, reflecting autonomic control of the heart, in cocaine-exposed infants...
Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndromeJenny B Hobbs
Cardiology Unit of the Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA
JAMA 296:1249-54. 2006..Among patients with recent syncope, beta-blocker treatment was associated with reduced risk...
Microvolt T-wave alternans and the risk of death or sustained ventricular arrhythmias in patients with left ventricular dysfunctionDaniel M Bloomfield
Columbia University Medical Center, New York, New York 10032, USA
J Am Coll Cardiol 47:456-63. 2006..This study hypothesized that microvolt T-wave alternans (MTWA) improves selection of patients for implantable cardioverter-defibrillator (ICD) prophylaxis, especially by identifying patients who are not likely to benefit...
Long-QT syndrome after age 40Ilan Goldenberg
Cardiology Division of the Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA
Circulation 117:2192-201. 2008....
I(Kr) channel blockade to unmask occult congenital long QT syndromeDarwin Jeyaraj
Heart and Vascular Research Center, MetroHealth Campus of Case Western Reserve University, Cleveland, Ohio 44109 1998, USA
Heart Rhythm 5:2-7. 2008..Beta-adrenergic stimulation may unmask occult LQT1, but no maneuver has consistently unmasked the LQT2 phenotype...
Quinidine in short QT syndrome: an old drug for a new diseaseElizabeth S Kaufman
J Cardiovasc Electrophysiol 18:665-6. 2007
Repolarization dynamics in patients with long QT syndromeJuha S Perkiomaki
Department of Medicine, University of Rochester School of Medicine and Dentistry, New York, USA
J Cardiovasc Electrophysiol 13:651-6. 2002..The aim of the present study was to assess the dynamics of repolarization duration and the dynamics of repolarization complexity in LQTS patients and their unaffected family members...
Long QT syndrome in adultsAndrew J Sauer
Cardiology Unit of the Department of Medicine, University of Rochester Medical Center, Rochester, New York 14642 8653, USA
J Am Coll Cardiol 49:329-37. 2007....
Long QT syndrome and pregnancyRahul Seth
Cardiology Division of the Department of Medicine, University of Rochester Medical Center, Rochester, New York 14642, USA
J Am Coll Cardiol 49:1092-8. 2007..This study was designed to investigate the clinical course of women with long QT syndrome (LQTS) throughout their potential childbearing years...
Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndromeIlan Goldenberg
Cardiology Division of the Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA
Circulation 117:2184-91. 2008..However, specific risk factors for life-threatening cardiac events in children with this genetic disorder have not been identified...
Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channelArthur J Moss
Cardiology Unit of the Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA
Circulation 105:794-9. 2002..We investigated the clinical features and prognostic implications of mutations involving pore and nonpore regions of the HERG channel in the LQT2 form of this disorder...
Variable expression of long QT syndrome among gene carriers from families with five different HERG mutationsJesaia Benhorin
Department of Cardiology, Bikur Cholim Hospital, Jerusalem, Israel
Ann Noninvasive Electrocardiol 7:40-6. 2002..These findings highlight the complexity of the clinical phenotype in this Mendelian dominant disorder and suggest that one or more modifier genes contribute to the variable expression of this syndrome...
AHA scientific statement: practice standards for electrocardiographic monitoring in hospital settings: an American Heart Association Scientific Statement from the Councils on Cardiovascular Nursing, Clinical Cardiology, and Cardiovascular Disease in the YBarbara J Drew
J Cardiovasc Nurs 20:76-106. 2005..Currently available ECG lead systems are described, and recommendations related to staffing, training, and methods to improve quality are provided...
Practice standards for electrocardiographic monitoring in hospital settings: an American Heart Association scientific statement from the Councils on Cardiovascular Nursing, Clinical Cardiology, and Cardiovascular Disease in the Young: endorsed by the InteBarbara J Drew
Circulation 110:2721-46. 2004..Currently available ECG lead systems are described, and recommendations related to staffing, training, and methods to improve quality are provided...
Microvolt T-wave alternans distinguishes between patients likely and patients not likely to benefit from implanted cardiac defibrillator therapy: a solution to the Multicenter Automatic Defibrillator Implantation Trial (MADIT) II conundrumDaniel M Bloomfield
Data Coordinating Center, The MTWA in CHF Study, PH 9 103D, Department of Medicine, Columbia University, 630 W 168th St, New York, NY 10032, USA
Circulation 110:1885-9. 2004..We compared the ability of microvolt T-wave alternans and QRS duration to identify groups at high and low risk of dying among heart failure patients who met MADIT II criteria for ICD prophylaxis...
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndromeWojciech Zareba
Cardiology Unit of the Department of Medicine, Heart Research Follow Up Program, Box 653, University of Rochester Medical Center, Rochester, NY 14642, USA
J Cardiovasc Electrophysiol 14:1149-53. 2003..The aim of this study was to determine whether there is an association between the location of mutations in the KCNQ1 gene and cardiac events in LQT1 patients...
Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 geneArthur J Moss
Cardiology Division, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
Circulation 115:2481-9. 2007..We evaluated the effect of location, coding type, and biophysical function of KCNQ1 mutations on the clinical phenotype of this disorder...
A surprise wireless remote transmissionElizabeth S Kaufman
Heart Rhythm 5:1092. 2008
Heart rate variability in healthy newborn infantsSudhir Ken Mehta
Fairview Hospital and MetroHealth Medical Center, Cleveland, Ohio 44111 5656, USA
Am J Cardiol 89:50-3. 2002..Because the data are reported as means +/- SD, medians, and 5th and 95th percentiles, their use facilitates the study of parasympathetic and sympathetic activity in comparable populations...
Saving lives in congenital long QT syndrome: who benefits from implantable cardioverter defibrillator therapy?Elizabeth S Kaufman
J Cardiovasc Electrophysiol 14:342-3. 2003
The impact of asymptomatic atrial fibrillationElizabeth S Kaufman
J Am Coll Cardiol 43:53-4. 2004
How to find the high-risk patient among individuals with a Brugada syndrome-type electrocardiogramElizabeth S Kaufman
J Cardiovasc Electrophysiol 16:52-3. 2005
Occurrence and characteristics of stroke events in the Atrial Fibrillation Follow-up Investigation of Sinus Rhythm Management (AFFIRM) studyDavid G Sherman
University of Texas Health Science Center, San Antonio, USA
Arch Intern Med 165:1185-91. 2005..The Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) Study was a multicenter comparison of high-risk patients with AF who were randomized to either a sinus rhythm control or a rate control strategy...
Can common genetic variations combine to produce the long QT syndrome phenotype?Elizabeth S Kaufman
Heart Rhythm 2:748-9. 2005
Autonomic alterations in cocaine-exposed infantsSudhir Ken Mehta
Fairview Hospital and MetroHealth Medical Center, Cleveland, Ohio 44111 5656, USA
Am Heart J 144:1109-15. 2002..It is unknown whether these alterations are transient (acute effect) or persist in older infants and possibly reflect a teratogenic effect of cocaine...
Heart rate variability by triangular index in infants exposed prenatally to cocaineSudhir Ken Mehta
Department of Pediatrics, MetroHealth Campus, Case Western Reserve University, Fairview Hospital, 18101 Lorain Avenue, Cleveland, Ohio 44111 5656, USA
Ann Noninvasive Electrocardiol 7:374-8. 2002..Although normative data have been published for newborns, studies in infants with pathological conditions are lacking...
Efficient genotyping for congenital long QT syndromeElizabeth S Kaufman
JAMA 294:3027-8. 2005
Arrhythmogenic right ventricular cardiomyopathy: how should genetic information be integrated with clinical diagnostic criteria?Elizabeth S Kaufman
Heart Rhythm 3:945-7. 2006
Evaluation of suspected arrhythmic syncope: leaning away from tiltingElizabeth S Kaufman
J Cardiovasc Electrophysiol 16:943-4. 2005
