12 results on '"Qrs morphology"'
Search Results
2. Patient With Presyncope and Variable PR Interval and QRS Morphology
- Author
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Ismael A. Vergara, Alex Bittner, Alejandro Paredes, and Lars Eckardt
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Qrs morphology ,medicine.medical_specialty ,RBBB - Right bundle branch block ,Conduction disturbance ,RBBB, right bundle branch block ,Internal medicine ,Female patient ,bundle branch block ,Medicine ,cardiovascular diseases ,PR interval ,conduction disturbance ,LBBB - Left bundle branch block ,Presyncope ,Ecg Teaching Competition ,Bundle branch block ,business.industry ,LAFB, left anterior fascicular block ,AV, atrioventricular ,Imaging Vignette: ECG Challenge ,LBBB, left bundle branch block ,medicine.disease ,Cardiology ,cardiovascular system ,ECG, electrocardiogram ,sense organs ,Cardiology and Cardiovascular Medicine ,business ,infra-his block ,circulatory and respiratory physiology - Abstract
We describe the case of a 72-year-old female patient, presenting with presyncope and variable PR Interval and changing QRS morphology on the electrocardiogram. Differential diagnosis is discussed. (Level of Difficulty: Beginner.), Central Illustration
- Published
- 2021
3. Verapamil-sensitive ventricular tachycardia demonstrating multiform QRS morphology in a patient with ischemic cardiomyopathy
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Akihiko Matsumura, Shunsuke Kuroda, Akira Mizukami, Tatsuya Hayashi, Makoto Suzuki, and Kenji Yoshioka
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Qrs morphology ,medicine.medical_specialty ,Cardiomyopathy ,medicine.medical_treatment ,Infarction ,Catheter ablation ,Case Report ,His-Purkinje system ,030204 cardiovascular system & hematology ,Ventricular tachycardia ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,cardiovascular diseases ,030212 general & internal medicine ,Ischemic cardiomyopathy ,business.industry ,Reentry ,medicine.disease ,QRS morphology ,Verapamil ,cardiovascular system ,Cardiology ,Cardiology and Cardiovascular Medicine ,business ,medicine.drug - Abstract
The His-Purkinje system (HPS) is known to be involved in the reentrant circuit of ventricular tachycardia (VT), even in patients with structural heart disease.1, 2, 3 Catheter ablation may be an effective strategy for this entity; however, there is a potential risk of conduction delay or even high-degree atrioventricular (AV) block. Therefore, detailed understanding of the reentry circuit is crucial. However, the mechanism and role of HPS in this entity are debatable. We experienced a case of post–myocardial infarction VT with involvement of the HPS demonstrating a change in QRS morphology without termination, which provided us clues for understanding the mechanisms underlying this type of VT.
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- 2019
4. Depolarization spatial variance as a cardiac dyssynchrony descriptor
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Luis D. Barja, Maria Paula Bonomini, Nicolas Mangani, Daniel Felipe Ortega, and Pedro David Arini
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Qrs morphology ,medicine.medical_specialty ,INTRAVENTRICULAR DYSSYNCHRONY ,Otras Ingenierías y Tecnologías ,medicine.medical_treatment ,0206 medical engineering ,Cardiac resynchronization therapy ,Health Informatics ,02 engineering and technology ,INGENIERÍAS Y TECNOLOGÍAS ,Spatial variance ,03 medical and health sciences ,QRS complex ,0302 clinical medicine ,Internal medicine ,ECG SIGNAL PROCESSING ,medicine ,Sinus rhythm ,Ventricular depolarization ,Mathematics ,Depolarization ,Control subjects ,020601 biomedical engineering ,Signal Processing ,Cardiology ,CARDIAC RESYNCHRONIZATION THERAPY ,030217 neurology & neurosurgery - Abstract
Ventricular depolarization dispersion refers mainly to heterogeneity in interlead QRS durations. Here, we propose the spatial variance (SVd) to describe depolarization dispersion about a mean QRS morphology. We hypothesize that waveform changes can be more accurate than interval changes at measuring QRS heterogeneity, and less sensitive to delineation errors. To prove this, SVd was computed on 36 dyssyn-chrony patients either in sinus rhythm (SVdB) or under nHB (SVdHB), and on 32 control subjects with native conduction (SVdN). In the normal ECG, there are interlead sets that produce maximal (SVdNmax) and minimal (SVdNmin) spatial variance. In Baseline patients, SVdB significantly increased from controls in the minimal variance situation (p < 0.005), deviating one or more leads from the normal morphology (similar in all the ensemble) and consequently increasing the interlead distance. The opposite held for the maximal variance situation, where it was expected a wide span of morphologies in health, there was a tendency to stacking in morphologies at baseline (p
- Published
- 2019
5. Tachycardiomyopathy a Rare Manifestation of Left Ventricular Outflow Tract Tachycardia. Treatment with Radiofrequency Catheter Ablation
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Guillermo Mora, Nohra Romero, and van Rendon
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Tachycardia ,Qrs morphology ,medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Idiopathic ventricular tachycardia ,business.industry ,Case Report ,Ventricular tachycardia ,medicine.disease ,Radiofrequency catheter ablation ,lcsh:RC666-701 ,Physiology (medical) ,Anesthesia ,Internal medicine ,cardiovascular system ,medicine ,Cardiology ,Ventricular outflow tract ,cardiovascular diseases ,medicine.symptom ,tachycardiomyopathy ,Cardiology and Cardiovascular Medicine ,business ,left ventricular outflow tract - Abstract
It is recognized that a type of idiopathic ventricular tachycardia (VT) arises from the left ventricular outflow tract (LVOT). This VT exhibits sustained or nonsustained forms, but also appears as frequent premature ventricular contractions (PVCs) of monomorphic QRS morphology. The prognosis is almost uniformly benign. We describe a patient with tachycardiomyopathy resulting from LVOT VT.
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- 2013
6. An S wave in ECG lead V 6 predicts poor response to cardiac resynchronization therapy and long-term outcome.
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Jiang Z, Qiu Y, Qian Z, Wang Y, Zhao Y, Hou X, Liang Y, Zheng L, Xu G, Su Y, Gu X, and Zou J
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- Bundle-Branch Block physiopathology, Female, Follow-Up Studies, Humans, Male, Middle Aged, Patient Selection, Retrospective Studies, Time Factors, Treatment Outcome, Bundle-Branch Block therapy, Cardiac Resynchronization Therapy methods, Electrocardiography, Ventricular Function, Left physiology
- Abstract
Background: Cardiac resynchronization therapy (CRT) is a standard treatment for selected patients with chronic heart failure (HF). However, up to 30%-50% of patients still do not respond to CRT., Objective: Our aim was to identify the predictive value of an S wave in lead V
6 in CRT response in patients with complete left bundle branch block (CLBBB)., Methods: The CLBBB definition included the Strauss left bundle branch block criteria and the absence of q waves in leads I, V5 , and V6 . According to the electrocardiogram at baseline, CLBBB patients were divided into 3 groups: T-CLBBB group (CLBBB without an S wave in lead V5 or V6 ), V5 S group (CLBBB with an S wave in lead V5 and no S wave in lead V6 ), and V5 &V6 S group (CLBBB with S waves in leads V5 and V6 ). CRT response was defined as left ventricular end-systolic volume reduction ≥ 15% at 6-month follow-up. The combined end point included HF rehospitalization or all-cause death., Results: Of 181 patients with left bundle branch block-like pattern, 112 patients with CLBBB were included into 3 groups: 54 in the T-CLBBB group, 32 in the V5 S group, and 26 in the V5 &V6 S group. The CRT response rate was 85.2% (46), 65.6% (21), and 38.5% (10), respectively (P < .001). Kaplan-Meier curves demonstrated that patients in the V5 &V6 S group had a higher incidence of HF rehospitalization or all-cause death than those in the other 2 groups (P < .001). In a multivariate logistic regression model analysis, an S wave in lead V6 was significantly associated with CRT nonresponse (hazard ratio 0.33; 95% confidence interval 0.11-0.96; P = .042)., Conclusion: An S wave in lead V6 can predict poor response to CRT and long-term outcome., (Copyright © 2019 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.)- Published
- 2020
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7. Comentário a «Definir bloqueio completo do ramo esquerdo na era da terapêutica de ressincronização cardíaca»
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Mário Oliveira
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Qrs morphology ,medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Left bundle branch block ,business.industry ,medicine.medical_treatment ,Cardiac resynchronization therapy ,Right bundle branch block ,medicine.disease ,Left ventricular hypertrophy ,QRS complex ,Notching ,lcsh:RC666-701 ,Internal medicine ,medicine ,Cardiology ,cardiovascular system ,cardiovascular diseases ,Left anterior fascicular block ,Cardiology and Cardiovascular Medicine ,business - Abstract
Cardiac resynchronization therapy (CRT) has emerged as an attractive intervention to improve left ventricular mechanical function by changing the sequence of electrical activation.Unfortunately, many patients receiving CRT do not benefit but are subjected to device complications and costs. Thus, there is a need for better selection criteria. Current criteria for CRT eligibility include a QRS duration >120 ms. However, QRS morphology is not considered, although it can indicate the cause of delayed conduction. Recent studies have suggested that only patients with left bundle branch block (LBBB) benefit from CRT, and not patients with right bundle branch block or nonspecific intraventricular conduction delay. The authors review the pathophysiologic and clinical evidence supporting why only patients with complete LBBB benefit from CRT. Furthermore, they review how the threshold of 120 ms to define LBBB was derived subjectively at a time when criteria for LBBB and right bundle branch block were mistakenly reversed. Three key studies over the past 65 years have suggested that 1/3 of patients diagnosed with LBBB by conventional electrocardiographic criteria may not have true complete LBBB, but likely have a combination of left ventricular hypertrophy and left anterior fascicular block. On the basis of additional insights from computer simulations, the investigators propose stricter criteria for complete LBBB that include a QRS duration >140 ms for men and >130 ms for women, along with mid-QRS notching or slurring in >2 contiguous leads. Further studies are needed to reinvestigate the electrocardiographic criteria for complete LBBB and the implications of these criteria for selecting patients for CRT. Keywords: Left bundle branch block, Cardiac resynchronization therapy
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- 2011
8. Large variability in clinical judgement and definitions of left bundle branch block to identify candidates for cardiac resynchronisation therapy.
- Author
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van Stipdonk AMW, Vanbelle S, Ter Horst IAH, Luermans JG, Meine M, Maass AH, Auricchio A, Prinzen FW, and Vernooy K
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- Bundle-Branch Block physiopathology, Humans, ROC Curve, Bundle-Branch Block therapy, Cardiac Resynchronization Therapy methods, Clinical Decision-Making methods, Electrocardiography, Patient Selection
- Abstract
Background: Left bundle branch block (LBBB) morphology is associated with improved outcome of cardiac resynchronisation therapy (CRT) and is an important criterion for patient selection. There are, however, multiple definitions for LBBB. Moreover, applying these definitions seems subjective. We investigated the inter- and intraobserver agreement in the determination of LBBB using available definitions, and clinicians' judgement of LBBB., Methods: Observers were provided with 12‑lead ECGs of 100 randomly selected CRT patients. Four observers judged the ECGs based on different LBBB-definitions (ESC, AHA/ACC/HRS, MADIT, and Strauss). Additionally, four implanting cardiologists scored the same 100 ECGs based on their clinical judgement. Observer agreement was summarized through the proportion of agreement (P) and kappa coefficient (k)., Results: Relative intra-observer agreement using different LBBB definitions, and within clinical judgement was moderate (range k 0.47-0.74 and k = 0.76 (0.14), respectively). The inter-observer agreement between observers using LBBB definitions as well as between clinical observers was minimal to weak (range k 0.19-0.44 and k = 0.35 (0.20), respectively). The probability of classifying an ECG as LBBB by available definitions varied considerably (range 0.20-0.76). The agreement between different definitions of LBBB ranged from good (P = 0.95 (0.07)) to weak (P = 0.40 (0.22)). Furthermore, correlation between the different LBBB definitions and clinical judgement was poor (range phi 0.30-0.55)., Conclusion: Significant variation in the probability of classifying LBBB is present in using different definitions and clinical judgement. Considerable intra- and inter-observer variability adds to this variation. Interdefinition agreement varies significantly and correlation of clinical judgement with LBBB classification by definitions is modest at best., (Copyright © 2019 Elsevier B.V. All rights reserved.)
- Published
- 2019
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9. Prominent R wave in ECG lead V1 predicts improvement of left ventricular ejection fraction after cardiac resynchronization therapy in patients with or without left bundle branch block.
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Bode WD, Bode MF, Gettes L, Jensen BC, Mounsey JP, and Chung EH
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- Aged, Bundle-Branch Block diagnosis, Bundle-Branch Block physiopathology, Echocardiography, Female, Humans, Male, Middle Aged, Predictive Value of Tests, Retrospective Studies, Time Factors, Treatment Outcome, Bundle-Branch Block therapy, Cardiac Resynchronization Therapy methods, Electrocardiography, Stroke Volume physiology, Ventricular Function, Left physiology
- Abstract
Background: QRS morphology on postprocedural ECG indicating posterolateral left ventricular pacing may be predictive of response to cardiac resynchronization therapy (CRT)., Objective: The purpose of this study was to assess whether a positive vector in V1 and/or negative vector in lead I on the first postprocedural ECG, suggesting posterolateral capture from CRT, correlates with improvement in left ventricular ejection fraction (LVEF)., Methods: A retrospective chart review was conducted on all patients who underwent CRT implantation at our institution between April 2008 and December 2011. Biventricular (BiV) paced QRS morphology was defined as R/S ≥1 in V1 and/or R/S ≤ 1 in lead I. The primary outcome was improvement of LVEF ≥7.5%. The χ(2) and t tests were used for analysis., Results: Of 68 patients, 49 (72%) met our BiV paced QRS morphology criteria. Thirty-four of these 49 patients (69%) had improvement in LVEF. Of the 19 patients who did not meet our criteria, 17 (89%) did not have an improvement in LVEF (sensitivity 94%, specificity 53%, χ(2) = 19.04, P < .0001). The average LVEF improvement in patients who met our BiV paced QRS morphology criteria was significantly greater than in those who did not (14.27% vs 2.63%, P = .0001). Preprocedural left bundle branch block was not a predictor of echocardiographic response., Conclusion: Our results highlight the importance of periprocedural ECG analysis to optimize response to CRT. Moreover, patients without left bundle branch block still benefited from CRT if they met our BiV paced morphology criteria. This suggests that postprocedural left ventricular activation as reflected on the ECG may supersede the baseline conduction delay., (Copyright © 2015 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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10. Nonspecific intraventricular conduction delay: Definitions, prognosis, and implications for cardiac resynchronization therapy.
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Eschalier R, Ploux S, Ritter P, Haïssaguerre M, Ellenbogen KA, and Bordachar P
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- Arrhythmias, Cardiac diagnosis, Arrhythmias, Cardiac etiology, Arrhythmias, Cardiac physiopathology, Cardiac Resynchronization Therapy methods, Electrocardiography methods, Humans, Practice Guidelines as Topic, Prognosis, Arrhythmias, Cardiac therapy, Heart Conduction System physiopathology, Heart Ventricles physiopathology
- Abstract
Cardiac resynchronization therapy (CRT) is an electrical treatment of heart failure with reduced ejection fraction and wide QRS. It aims to correct the electrical dyssynchrony present in 30% to 50% of patients in this population. Dyssynchrony results in widening of the QRS complex on the electrocardiogram (ECG). CRT was initially developed to treat patients who had left bundle branch block (LBBB) and delayed activation of the lateral left ventricular wall. However, a large proportion of heart failure patients present with a widened QRS that is neither an LBBB nor a right bundle branch block (RBBB): nonspecific intraventricular conduction delay (NICD). Less studied than RBBB or LBBB, its pathophysiology is both complex and varied yet still reflects intramyocardial conduction delay. NICD is most often associated with cardiomyopathy (eg, ischemic or hypertensive). Conduction pathways can be either healthy or affected. Results from CRT are contradictory in this patient group, despite a seemingly neutral trend. Unfortunately, prospective studies are lacking. Guidelines recommending implantation of CRT devices in this group are based solely on analyses of subgroups with small sample sizes. A dedicated prospective study is therefore warranted for this question to be answered properly. A detailed study of the ECG and noninvasive study of ventricular electrical activation may enable clinicians to better identify patients with NICD who will respond to CRT., (Copyright © 2015 Heart Rhythm Society. All rights reserved.)
- Published
- 2015
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11. Opportunity to increase life span in narrow QRS cardiac resynchronization therapy recipients by deactivating ventricular pacing: evidence from randomized controlled trials.
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Sohaib SM, Finegold JA, Nijjer SS, Hossain R, Linde C, Levy WC, Sutton R, Kanagaratnam P, Francis DP, and Whinnett ZI
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- Cardiac Resynchronization Therapy mortality, Defibrillators, Implantable, Disease-Free Survival, Electrocardiography, Heart Failure mortality, Humans, Kaplan-Meier Estimate, Life Expectancy, Multicenter Studies as Topic, Randomized Controlled Trials as Topic, Treatment Outcome, Cardiac Resynchronization Therapy methods, Heart Failure therapy
- Abstract
Objectives: This study examined the time course of clinical events in cardiac resynchronization therapy (CRT) trials., Background: Recent randomized controlled trial results suggest that in heart failure with narrow QRS, biventricular pacing (CRT) may increase mortality. The authors proposed implant complications as the cause, rather than a progressive adverse physiological effect., Methods: The study identified all trials comparing CRT with no CRT, which reported Kaplan-Meier curves in groups defined by QRS: narrow, non-left bundle branch block (LBBB) broad, and LBBB broad. For each trial, the change in life span every 3 months up to 3.5 years (the longest time for which data are available) was calculated and a power law was fitted, that is, ∝ time(n)., Results: Four trials (MADIT-CRT [Multicenter Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy], RAFT [Resynchronization-Defibrillation for Ambulatory Heart Failure Trial], REVERSE [REsynchronization reVErses Remodeling in Systolic left vEntricular dysfunction], and EchoCRT [Echocardiography Guided Cardiac Resynchronization Therapy]), totaling 4,717 patients, reported curves for mortality or heart failure-related hospitalization, or for mortality. In patients with LBBB broad QRS (within MADIT-CRT), life span gain increased in proportion to time(1.94). In contrast, in patients with non-LBBB broad QRS (within MADIT-CRT) and patients with narrow QRS (EchoCRT), life span was lost in proportion to time(1.92) and time,(1.96) respectively. Hospitalization-free survival showed similar patterns., Conclusions: The nonlinear growth of life span gained when a CRT device is implanted in patients with LBBB broad QRS is unfortunately mirrored by a similarly progressive loss in life span in narrow QRS heart failure. This suggests the culprit is a progressive physiological effect of pacing rather than implant complications. If these data are not sufficient, a randomized controlled trial of deactivating CRT in patients with narrow QRS may now be needed, with a primary endpoint of increasing survival., (Copyright © 2015 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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12. Computerized analysis of the 12-lead electrocardiogram to identify epicardial ventricular tachycardia exit sites.
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Yokokawa M, Jung DY, Joseph KK, Hero AO 3rd, Morady F, and Bogun F
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- Algorithms, Female, Humans, Male, Middle Aged, Electrocardiography, Signal Processing, Computer-Assisted, Tachycardia, Ventricular physiopathology
- Abstract
Background: Twelve-lead electrocardiogram (ECG) criteria for epicardial ventricular tachycardia (VT) origins have been described. In patients with structural heart disease, the ability to predict an epicardial origin based on QRS morphology is limited and has been investigated only for limited regions in the heart., Objective: The purpose of this study was to determine whether a computerized algorithm is able to accurately differentiate epicardial vs endocardial origins of ventricular arrhythmias., Methods: Endocardial and epicardial pace-mapping were performed in 43 patients at 3277 sites. The 12-lead ECGs were digitized and analyzed using a mixture of gaussian model (MoG) to assess whether the algorithm was able to identify an epicardial vs endocardial origin of the paced rhythm. The MoG computerized algorithm was compared to algorithms published in prior reports., Results: The computerized algorithm correctly differentiated epicardial vs endocardial pacing sites for 80% of the sites compared to an accuracy of 42% to 66% of other described criteria. The accuracy was higher in patients without structural heart disease than in those with structural heart disease (94% vs 80%, P = .0004) and for right bundle branch block (82%) compared to left bundle branch block morphologies (79%, P = .001). Validation studies showed the accuracy for VT exit sites to be 84%., Conclusion: A computerized algorithm was able to accurately differentiate the majority of epicardial vs endocardial pace-mapping sites. The algorithm is not region specific and performed best in patients without structural heart disease and with VTs having a right bundle branch block morphology., (Copyright © 2014 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2014
- Full Text
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