197 results on '"Mitchell LB"'
Search Results
2. The relative importance of barriers to the prescription of warfarin for nonvalvular atrial fibrillation
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Bungard, TJ, Ghali, WA, McAlister, FA, Buchan, AM, Cave, AJ, Hamilton, PG, Mitchell, LB, Shuaib, A, Teo, KK, and Tsuyuki, RT
- Abstract
BACKGROUND AND PURPOSE: Despite the publication of a number of randomized, controlled trials demonstrating a substantial reduction in stroke with anticoagulation in patients with nonvalvular atrial fibrillation, the 'real world' use of warfarin is sub-optimal. Previous surveys have attempted to explain this problem but have significant limitations. The purpose of this study was to assess the relative importance of various barriers that may influence the prescription of warfarin in patients with nonvalvular atrial fibrillation. METHODS: This cross-sectional survey was mailed to all practising cardiologists, neurologists and internists, as well as a random sample of family physicians within Alberta. Physicians caring for patients with NVAF rated the relative importance of potential barriers using a Likert scale. RESULTS: Sixty-seven per cent of all physicians returned the survey. Overall, barriers pertaining to the patient's clinical characteristics were rated to be more important than those pertaining to the physician or to the organization required when prescribing these therapies. Specifically, an ongoing history of falls, a history of bleeding within the previous year and an inability to comply with therapy were rated as important barriers by 64%, 55% and 53% of physicians, respectively. Most physicians strongly believed that patients should receive information on the benefits and risks of warfarin (96%) and that patients should have a say in whether warfarin is prescribed (86%). IMPLICATIONS: This study suggests that most of the barriers to warfarin use pertain to patient clinical characteristics and the need for patients to be involved in the decision to initiate therapy. The use of decision support technologies would facilitate involvement of the patient and serve to educate both the patient and physician on the risks and benefits of warfarin therapy.
- Published
- 2016
3. Long-term Reproducibility of Ventricular Tachycardia Induction in Patients With Implantable Cardioverter/Defibrillators
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George J. Klein, Raymond Yee, Robert S. Sheldon, A M Gillis, Mitchell Lb, Wyse Dg, James W. Leitch, and Duff Hj
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Male ,Tachycardia ,medicine.medical_specialty ,Time Factors ,Heart disease ,Defibrillation ,medicine.medical_treatment ,Ventricular tachycardia ,Physiology (medical) ,Internal medicine ,medicine ,Hospital discharge ,Humans ,In patient ,Aged ,Reproducibility ,business.industry ,Reproducibility of Results ,Middle Aged ,medicine.disease ,Defibrillators, Implantable ,Electrophysiology ,Heart Function Tests ,Ventricular fibrillation ,Tachycardia, Ventricular ,Cardiology ,Female ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - Abstract
Background Noninvasive electrophysiological studies (EPSs) can be performed in current implantable antitachycardia pacemaker/cardioverter/defibrillators (ICDs). Thus, these devices may be used as tools to study changes in the electrophysiological substrate and ventricular tachycardia characteristics over time. Methods and Results Fifty-five patients receiving an ICD for treatment of sustained ventricular tachyarrhythmias underwent serial EPSs after implantation of the ICD. Studies were performed before hospital discharge and 1, 3, 5, 9, 12, 18, 24, and 36 months after ICD implantation. Sustained monomorphic ventricular tachycardia (VT) was induced in 37 patients (group 1) at the predischarge EPS, whereas no sustained arrhythmia could be induced in 18 patients (group 2) at baseline. Group 1 patients underwent 165 noninvasive EPSs after discharge. Sustained monomorphic VT was induced during 72% of the follow-up EPSs, ventricular fibrillation (VF) was induced during 11% of follow-up EPSs, and no sustained VT or VF was induced during 17% of follow-up visits. Sustained VT was induced at every follow-up EPS in 23 patients (62%), whereas no sustained VT/VF could be induced at least once during follow-up in 14 patients (38%). Clinical or electrophysiological variables did not predict noninducibility during follow-up. However, the probability that a patient would experience spontaneous VT decreased significantly over time in patients in whom VT was not inducible during at least 1 follow-up EPS ( P =.05). Group 2 patients underwent 86 noninvasive EPSs after discharge. Sustained monomorphic VT was induced during 22% of follow-up EPSs, VF was induced during 19% of follow-up EPSs, and no sustained VT/VF could be induced during 68% of follow-up EPSs. No sustained VT/VF could be induced during every follow-up EPS in 9 patients (50%), whereas sustained monomorphic VT was induced at least once during follow-up in 7 patients (34%). Persistent noninducibility of VT during follow-up was associated with low probability of occurrence of spontaneous VT (11%), whereas inducibility of VT at least once during follow-up was associated with the occurrence of spontaneous VT (89%, P =.003). Conclusions Considerable variability of VT induction is observed over a lengthy period in patients presenting with sustained VT/VF. Persistent noninducibility of VT is associated with a reduced probability of spontaneous VT. These observations suggest that the substrates for inducible and spontaneous VT change in parallel over time.
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- 1995
4. TREATMENT OF VENTRICULAR ARRHYTHMIAS AFTER RECOVERY FROM MYOCARDIAL INFARCTION
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Mitchell Lb
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Cardiac Complexes, Premature ,medicine.medical_specialty ,medicine.medical_treatment ,Myocardial Infarction ,Infarction ,Ventricular tachycardia ,Amiodarone ,General Biochemistry, Genetics and Molecular Biology ,Internal medicine ,medicine ,Humans ,cardiovascular diseases ,Myocardial infarction ,Randomized Controlled Trials as Topic ,business.industry ,General Medicine ,Implantable cardioverter-defibrillator ,medicine.disease ,Defibrillators, Implantable ,Clinical trial ,Ventricular Fibrillation ,Ventricular fibrillation ,Catheter Ablation ,Tachycardia, Ventricular ,cardiovascular system ,Cardiology ,Complication ,business ,Anti-Arrhythmia Agents ,medicine.drug - Abstract
▪ Abstract Demonstrated associations between postmyocardial infarction ventricular arrhythmias and a higher subsequent risk of both sudden and all-cause mortality have prompted a search for effective and safe treatment modalities. Recently completed clinical trials have provided a rationale for treatment recommendations in some specific settings. Beta-blocking therapy is recommended for postinfarction patients with frequent or complex ventricular premature beats. In contrast, calcium antagonist therapy is not helpful in these cases, and Class I antiarrhythmic therapy is actually harmful. Early indications of benefit from Class III antiarrhythmic therapies, particularly amiodarone, are under evaluation in large trials. Patients with sustained ventricular tachycardia (VT) or ventricular fibrillation (VF) occuring late after myocardial infarction require therapy. Viable therapeutic methods include individualized antiarrhythmic therapy selected by the noninvasive approach, individualized antiarrhythmic therapy selected by the invasive approach, empiric amiodarone therapy, transcatheter or surgical ablative therapy (for VT), and use of an implantable cardioverter defibrillator. Clinical trial data have yet to determine which of these approaches is most effective under which circumstances. Postinfarction patients with nonsustained VT are the focus of several ongoing treatment trials. Early data suggest that risks requiring specific therapy are reached only by those patients who also have significant left ventricular dysfunction. The presence of inducible sustained ventricular tachycardia at an electrophysiologic study may further risk stratify such patients. High-risk patients with nonsustained ventricular tacycardia, left ventricular dysfunction, and inducible sustained ventricular tachycardia should participate in ongoing clinical trials. In the absence of this opportunity, intensive treatment should be considered.
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- 1994
5. Clinical trials of antiarrhythmic drugs in patients with sustained ventricular tachyarrhythmias
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Mitchell Lb
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medicine.medical_specialty ,Clinical Trials as Topic ,business.industry ,Ventricular Tachyarrhythmias ,medicine.medical_treatment ,Adrenergic beta-Antagonists ,Amiodarone ,Implantable cardioverter-defibrillator ,Primary therapy ,Defibrillators, Implantable ,Clinical trial ,Pharmacotherapy ,Internal medicine ,Concomitant ,Ventricular Fibrillation ,medicine ,Cardiology ,Catheter Ablation ,Tachycardia, Ventricular ,Humans ,In patient ,Cardiology and Cardiovascular Medicine ,business ,medicine.drug - Abstract
Patients with sustained ventricular tachyarrhythmias in the absence of a reversible cause require long-term therapy. Six approaches may have value in this setting, including individualized drug therapy selected by the invasive approach, individualized drug therapy selected by the noninvasive approach, beta-blocking therapy, amiodarone, transcatheter or electrosurgical ablation, and the implantable cardioverter defibrillator. Data supporting the four pharmacologic approaches and data comparing these approaches to one another and to the implantable cardioverter defibrillator are reviewed. Support for primary therapy with a beta-blocker is the weakest. Nevertheless, a role for concomitant beta-blockade is established. Comparisons of the invasive and noninvasive approaches suggest that, in drug-naive patients, the invasive approach is effective but the noninvasive approach is not, whereas in drug-resistant patients, neither approach is adequate. Data suggesting that amiodarone is more effective than individualized drug therapy is not compelling but is widely accepted. Given these uncertainties, many authorities have embraced the implantable cardioverter defibrillator as the therapy of choice.
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- 1997
6. Implantable Cardioverter–Defibrillators in Hypertrophic Cardiomyopathy
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Robert S. Sheldon, Raj, and Mitchell Lb
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medicine.medical_specialty ,Text mining ,business.industry ,Internal medicine ,Hypertrophic cardiomyopathy ,Cardiology ,Medicine ,General Medicine ,business ,medicine.disease - Published
- 2000
7. Impact of implantable cardioverter-defibrillator, amiodarone, and placebo on the mode of death in stable patients with heart failure: analysis from the sudden cardiac death in heart failure trial.
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Packer DL, Prutkin JM, Hellkamp AS, Mitchell LB, Bernstein RC, Wood F, Boehmer JP, Carlson MD, Frantz RP, McNulty SE, Rogers JG, Anderson J, Johnson GW, Walsh MN, Poole JE, Mark DB, Lee KL, Bardy GH, Packer, Douglas L, and Prutkin, Jordan M
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- 2009
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8. Entrainment mapping of a concealed nodoventricular accessory pathway in a man with complete heart block and tachycardia-induced cardiomyopathy.
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Quinn FR, Mitchell LB, Mardell AP, Dal Disler RN, and Veenhuyzen GD
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True nodoventricular (NV) accessory connections, as originally described by Mahaim, are rare entities, with the majority of previously reported cases now recognized as being due to decremental atriofascicular pathways. Here, we present a patient with incessant narrow and wide QRS complex tachycardia occurring in the setting of prior complete heart block. Entrainment mapping proved useful in diagnosing orthodromic reentry utilizing a concealed right septal NV pathway. The patient was successfully treated with radiofrequency ablation, resulting in a marked improvement in left ventricular function. [ABSTRACT FROM AUTHOR]
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- 2008
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9. Addendum to 'Personal and public safety issues related to arrhythmias that may affect consciousness: implications for regulation and physician recommendations: a medical/scientific statement from the American Heart Association and the North American Society of Pacing and Electrophysiology': public safety issues in patients with implantable defibrillators: a scientific statement from the American Heart Association and the Heart Rhythm Society.
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Epstein AE, Baessler CA, Curtis AB, Estes NA 3rd, Gersh BJ, Grubb B, Mitchell LB, and American Heart Association
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- 2007
10. Prophylactic therapy to prevent atrial arrhythmia after cardiac surgery.
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Mitchell LB
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- 2007
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11. Child welfare reform in the United States: findings from a local agency survey.
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Mitchell LB, Barth RP, Green R, Wall A, Biemer P, Berrick JD, Webb MB, and National Survey of Child and Adolescent Well-Being Research Group
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Efforts to improve the public welfare and child welfare system sparked an unprecedented amount of federal legislation in the 1990s, including the Adoption and Safe Families Act of 1997 (ASFA), the Multiethnic Placement Act of 1994 and Interethnic Adoption Provisions of 1996 (MEPA-IEP), and welfare reform. Such reforms allow an unprecedented degree of flexibility, but little is known about their implementation. Researchers administered the Local Agency Survey to the first national probability sample of public child welfare agencies from 1999 to 2000. Findings indicate that ASFA has had the most effect on child welfare service delivery. Welfare reform has had less effect, and MEPA-IEP seems to have had little effect at all. [ABSTRACT FROM AUTHOR]
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- 2005
12. Survival after coronary revascularization among patients with kidney disease.
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Hemmelgarn BR, Southern D, Culleton BF, Mitchell LB, Knudtson ML, Ghali WA, and Alberta Provincial Project for Outcomes Assessment in Coronary Heart Disease Investigators
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- 2004
13. Effect of ramipril in reducing sudden deaths and nonfatal cardiac arrests in high-risk individuals without heart failure or left ventricular dysfunction.
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Teo KK, Mitchell LB, Pogue J, Bosch J, Dagenais G, Yusuf S, and HOPE Investigators
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- 2004
14. Are lipid-lowering drugs also antiarrhythmic drugs? An analysis of the Antiarrhythmics versus Implantable Defibrillators (AVID) trial.
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Mitchell LB, Powell JL, Gillis AM, Kehl V, Hallstrom AP, AVID (Antiarrhythmics Versus Implantable Defibrillators) Investigators, Mitchell, L Brent, Powell, Judy L, Gillis, Anne M, Kehl, Victoria, Hallstrom, Alfred P, and AVID Investigators
- Abstract
Objectives: This study sought to evaluate the antiarrhythmic effects of lipid-lowering drug therapy as assessed by ventricular tachyarrhythmia (ventricular tachycardia [VT]/ventricular fibrillation [VF]) recurrences recorded by an implantable cardioverter defibrillator (ICD) in patients with atherosclerotic heart disease (ASHD).Background: Randomized trials of lipid-lowering drugs suggest reduction of sudden death (SD) in patients with ASHD. Because SD is usually secondary to VT/VF, this observation suggests that lipid-lowering therapy has antiarrhythmic effects.Methods: The probability of VT/VF recurrence in patients with ASHD treated with an ICD in the Antiarrhythmics Versus Implantable Defibrillators (AVID) trial who did not receive lipid-lowering drug therapy (n = 279) was compared with that in patients who received early and consistent lipid-lowering therapy (n = 83). In addition, all-cause mortality and cardiac mortality of all patients in the AVID trial with ASHD who did not receive lipid-lowering therapy (n = 564) were compared with that of those who received early and consistent lipid-lowering therapy (n = 149).Results: Using multivariate analyses, lipid-lowering therapy was associated with a reduction in the relative hazard for VT/VF recurrence of 0.40 (95% confidence interval [CI] 0.15 to 0.58) (adjusted p = 0.003) in the ICD subgroup. Lipid-lowering therapy was also associated with a reduction in the relative hazard for all-cause mortality of 0.36 (95% CI 0.15 to 0.68) (adjusted p = 0.03) and a reduction in the relative hazard for cardiac mortality of 0.39 (95% CI 0.16 to 0.78) (adjusted p = 0.04) in the larger study population.Conclusions: In patients with ASHD who have received an ICD, lipid-lowering therapy is associated with reduction in the probability of VT/VF recurrence, suggesting that part of the benefit of lipid-lowering therapy may be due to an antiarrhythmic effect. [ABSTRACT FROM AUTHOR]- Published
- 2003
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15. A Randomized Clinical Trial of the Noninvasive and Invasive Approaches to Drug Therapy of Ventricular Tachycardia
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Henry J. Duff, Wyse Dg, Dante E. Manyari, and Mitchell Lb
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Male ,Programmed stimulation ,medicine.medical_specialty ,medicine.medical_treatment ,Ventricular tachycardia ,law.invention ,Electrocardiography ,Random Allocation ,Pharmacotherapy ,Randomized controlled trial ,Recurrence ,law ,Tachycardia ,Internal medicine ,Humans ,Medicine ,cardiovascular diseases ,Monitoring, Physiologic ,Clinical Trials as Topic ,Chemotherapy ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Signal-averaged electrocardiogram ,Anesthesia ,Ventricular Fibrillation ,Ventricular fibrillation ,Ambulatory ,Exercise Test ,cardiovascular system ,Cardiology ,Female ,business ,Anti-Arrhythmia Agents ,Follow-Up Studies - Abstract
There is controversy over whether therapy to prevent ventricular tachyarrhythmias should be selected noninvasively (by trying drugs and monitoring the patient electrocardiographically) or invasively (by selecting a drug that prevents induction of the arrhythmia by programmed stimulation). We randomly assigned 57 patients with symptomatic and demonstrable ventricular tachyarrhythmias to therapy selected either noninvasively or invasively. The tachyarrhythmias involved were sustained ventricular tachycardia (35 patients), nonsustained ventricular tachycardia with hypotension (15 patients), and ventricular fibrillation (7 patients). The noninvasive approach sought reduction of ventricular premature beats by more than 80 percent and of couplets by more than 90 percent, with elimination of three or more successive ventricular beats on ambulatory monitoring and exercise testing. The invasive approach sought to prevent the induction of five or more repetitive beats by programmed stimulation. The noninvasive approach required fewer drug trials (3.2 +/- 1.8 [mean +/- SD] vs. 5.5 +/- 2.8, P less than 0.001) and fewer hospital days (20 +/- 15 vs. 33 +/- 24, P = 0.01) and identified a therapy predicted to be effective for more patients than did the invasive approach (29 of 29 vs. 15 of 28, P less than 0.001). When a predicted effective therapy was not found, amiodarone was prescribed despite persisting inducibility of ventricular tachycardia. Patients randomly assigned to the noninvasive approach had more symptomatic recurrences of tachyarrhythmia than those treated by the invasive approach (two-year actuarial probabilities of 0.50 +/- 0.10 vs. 0.20 +/- 0.08, P = 0.02). Similar differences were observed when amiodarone recipients were excluded. There were only three deaths from recurrent ventricular tachyarrhythmias--two in the group whose treatment was selected noninvasively and one in the group whose treatment was selected invasively (not significant). We conclude that therapy selected by the invasive approach prevents recurrences of ventricular tachyarrhythmias better than that selected by the noninvasive approach.
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- 1987
16. Use of the implantable cardioverter-defibrillator in patients with coronary artery spasm as the apparent cause of spontaneous life-threatening ventricular tachycardia or ventricular fibrillation: crossing the spasm sudden death chasm.
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Mitchell LB
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- 2012
- Full Text
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17. The power spectrum analyser as an indicator of cerebral ischaemia during carotid endarterectomy
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Mitchell Lb, Michael A. Ashburn, Callahan A, String St, and Dean Df
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Male ,medicine.medical_specialty ,medicine.medical_treatment ,Analyser ,Carotid endarterectomy ,Electroencephalography ,Eeg machines ,Critical Care and Intensive Care Medicine ,Brain Ischemia ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,Humans ,cardiovascular diseases ,030212 general & internal medicine ,Major complication ,Stroke ,Aged ,medicine.diagnostic_test ,business.industry ,030208 emergency & critical care medicine ,Middle Aged ,medicine.disease ,Cerebrovascular Disorders ,Anesthesiology and Pain Medicine ,Carotid Arteries ,Cardiology ,Cerebral ischaemia ,Female ,business ,Eeg monitoring - Abstract
Stroke is a potential major compliction of carotid endarterectomy and may be caused by cerebral ischaemia or embolisation from the operative site. Conventional EEC monitoring has been used intraoperatively to identify periods of cerebral ischaemia, but this monitoring technique can be difficult to operate and interpret in the operating room. This study reports the use of a new signal analyser, the power spectrum analyser (PSA-1, Neurologics, Inc., Nashville, Tennessee), and its impact on active patient management. Thirty-six patients undergoing carotid endarterectomies were monitored with the PSA-1 in conjunction with routine EEG. Eight patients (22%) showed evidence of ischaemia 22 times on both PSA-1 and routine EEG. At no time did the routine EEG show evidence of ischaemia when the PSA-1 did not. The PSA-1 has proven to be a reliable neurophysiologic monitor for the identification of periods of cerebral ischaemia. Use of this small, easily operated and interpreted machine could enhance safety in operating rooms lacking sufficient resources to use conventional EEG machines.
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- 1985
18. The HOPE (Heart Outcomes Prevention Evaluation) Study: The design of a large, simple randomized trial of an angiotensin converting enzyme inhibitor (ramipril) and vitamin E in patients at high risk of cardiovascular events
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Mindlen, F., Nordaby, R., Ruiz, M., Zavala, A., Guzman, L., Martinez, F., Diaz, Rr, Mackey, C., Marino, M., Romero, G., Zapata, G., Cuneo, C., Kawamura, T., Coelho, O., Massayochi, O., Braga, J., Labrunie, A., Bodanese, L., Manenti, E., Vitola, D., Nicolau, J., Amodeo, C., Armaganijan, D., Bertolami, M., Caramelli, B., Carvalho, A., Cirenza, C., Fichino, M., Franken, R., Ghorayeb, N., Kadri, T., Leao, P., Malheiros, F., Pavanello, R., Ramires, F., Ramires, J., Savioli, F., Sousa, A., Tanajura, L., Topps, D., Korner, L., Martinez, V., Baptie, B., Basinger, M., Baylis, B., Beresford, P., Edwards, A., Giannaccaro, P., Groenewoud, Y., Grose, M., Kellen, J., Lam, S., Lesoway, R., Ma, P., Meldrum, D., Mitchell, D., Mitchell, Lb, Roth, D., Shumak, S., Simon, M., Stone, J., Warnica, W., Wyse, D., Neffgen, C., Neffgen, J., Armstrong, F., Armstrong, W., Bell, N., Black, W., Brass, N., Brenneis, F., Brownoff, R., Chaytors, G., Debanne, D., Derksen, C., Donoff, M., Dzavik, V., Goeres, M., Greenwood, P., Gulamhusein, S., Hui, W., Hutchison, K., Kasian, L., Kasza, L., Krikke, E., Kvill, L., Lakhani, Z., Linklater, D., Mackel, J., Martin, S., Montague, T., Moores, D., Musseau, A., Muzyka, T., Paradis, J., Prosser, A., Ryan, E., Senaratne, M., Stenerson, P., Talibi, T., Teo, K., Young, C., Zuk, V., White, R., Browne, K., Browne, M., Happel, K., Irving, A., Plesko, A., Donnelly, R., Radomsky, N., Felker, P., Larsen, D., Morse, J., Rowntree, C., Thompson, J., Wedel, R., Bloomberg, G., Chomin, G., Dahl, M., Leong, W., Moy, V., Heath, J., Marshall, J., Terwiel, M., Kenefick, G., Kuritzky, R., Stevens, K., Weddings, K., Barban, K., Imrie, J., Woo, K., Ashton, T., Calvert, K., Bishop, W., Sweeney, R., Breakwell, L., Kornder, J., Pearce, S., Polasek, P., Richardson, P., Ghosh, S., Rielly, M., Wagner, K., Bemstein, V., Dawson, K., Lee, P., Lewis, J., Macdonald, K., Mcgee, L., Thompson, C., Hilton, D., Illott, K., Klinke, P., Mcconnell, J., Rabkin, S., Ong, A., Ong, G., Bedard, D., Hoeschen, R., Mehta, P., Mohammad, I., Morris, A., Bessoudo, R., Dobbins, N., Mclellan, L., Milton, J., Davis, R., Okeefe, D., Smith, R., Joyce, C., Parsons, M., Skanes, J., Sussex, B., Tobini, M., Ravalia, M., Sherman, G., Worrall, G., Atkinson, A., Hatheway, R., Johnson, B., Barnhill, S., Bata, I., Cosseet, J., Johnstone, D., Macfarlane, M., Sheridan, W., Crossman, L., Folkins, D., Shirley, M., Machel, T., Morash, J., Gupta, M., Mayich, M., Vakani, T., Baitz, T., Macphee, E., Turton, E., Turton, M., Chan, N., Misterski, J., Raco, D., Curnew, G., Fallen, E., Finkelstein, L., Gerstein, H., Hardman, P., Lawand, S., Lonn, E., Magi, W., Mcqueen, M., Panju, A., Patterson, R., Sullivan, B., Sullivan, H., Sullivan, M., Taylor, K., Worron, I., Yusuf, S., Cameron, W., Noseworthy, C., Houlden, R., Lavalle, T., Fowlis, R., Janzen, I., Arnold, M., Cann, M., Carroll, S., Dumaresq, S., Edmonds, M., Furlong, P., Geddes, C., Graham, E., Harris, K., Hramiak, I., Kennedy, R., Kostuk, W., Krupa, M., Lent, B., Lovell, M., Maclean, C., Massel, D., Mcmanus, R., Mcsherry, J., Munoz, C., Occhipinti, J., Oosterveld, L., Pflugfelder, P., Powers, S., Southern, R., Spence, D., Squires, P., Wetmore, S., Willing, J., Wisenberg, G., Wolfe, B., Kannampuzha, P., Rebane, T., Sluzar, V., Hess, A., Chan, Y., Thomson, D., Baigrie, R., Dubbin, J., Liuni, C., Tan, Kw, Brankston, E., Hewson, P., Hrycyshyn, B., Kapusta, W., Knox, L., Lockner, C., Whitsitt, P., Baird, M., Conroy, D., Davies, Ra, Davies, Rf, Fraser, M., Hagar, S., Hierlihy, P., Keely, E., Khan, S., Lau, Dgw, Marois, L., Nemeth, K., Reeves, E., Turek, M., Vexler, R., Young, D., Kumar, G., Kuruvilla, G., Kuruvilla, P., Lowe, D., Kwok, K., Blakely, J., Styling, S., Bozek, B., Charles, J., Fell, D., Fell, Da, Goode, E., Grossman, Ld, Matthews, E., Nitkin, R., Ricci, J., Selby, A., Singh, N., Swan, J., Emmett, J., Weingert, M., Ganjavi, F., Hill, D., Nawaz, S., Hessian, R., Kwiatkowski, K., Lai, C., Mulaisho, C., Okeefe, H., Smith, H., Weeks, A., Andrews, J., Barnie, A., Drobac, M., Hacker, P., Hanna, A., Iwanochko, M., Kenshole, A., Langer, A., Liu, P., Maclean, S., Moe, G., Sasson, Z., Sternberg, L., Trachuk, C., Walters, J., Zinman, B., Cheung, M., Cina, C., Yao, L., Man, K., Fulop, J., Glanz, A., Sibbick, M., Carter, P., Hickey, J., Mcmillian, E., Dion, D., Sthilaire, R., Coutu, D., Damours, G., Starra, R., Brooks, J., Dechamps, P., Kiwan, G., Kouz, S., Laforest, M., Remillard, C., Bellamy, D., Brossoit, R., Carrier, S., Houde, A., Labonte, I., Belanger, A., Kandalaft, N., Quenneville, L., Sandi, M., Auger, P., Bilodeau, N., Delage, F., Dumont, F., Giroux, R., Loisel, R., Poirier, C., Saulnier, D., Carmichael, P., Lemay, C., Lenis, J., Arisjilwan, N., Bedard, H., Casavant, C., Chiasson, J., Dagenais, D., Fitchett, D., Gossard, D., Halle, H., Hamel, N., Joyal, M., Magnan, O., Methe, M., Pedneault, L., Pilon, C., Poisson, D., Primeau, L., Rondeau, C., Roy, C., Ruel, M., Serpa, A., Sestier, F., Smilovitch, M., Theroux, P., Beaudoin, J., Boudreault, Jr, D Amours, D., Douville, T., Giguere, G., Houde, G., Labbe, R., Lachance, S., Lessard, L., Mercier, G., Noel, Hp, Talbot, P., Tremblay, J., Karabatsos, A., Maclellan, K., Wilson, P., Bogaty, P., Laforge, D., Langlais, M., Leblanc, M., Samson, M., Turcotte, J., Campeau, J., Dupuis, R., Lauzon, C., Ouimet, F., Pruneau, G., Desmaris, C., Frechetto, I., Gervais, P., James Brophy, Leroux, S., Bester, S., Meunier, L., Sayeed, M., Hart, M., Moumne, I., Thomasse, G., Walker, J., Walker, M., Ahmed, S., Habib, Nm, Kuny, P., Lopez, J., Klein, W., Grisold, M., Heyndrickx, L., Fiasse, A., Degaute, Jp, Mockel, J., Duprez, D., Chaudron, Jm, Bodson, A., Krzentowski, G., Boland, J., Kolendorf, K., Winther, B., Juhl, H., Hamalainen, T., Siitonen, O., Gin, H., Rigalleau, V., Hensen, J., Riel, R., Oehmenbritsch, R., Schulzeschleppinghoff, B., Hopf, R., Moller, A., Rosak, C., Wetzel, H., Hasslacher, C., Martin, T., Stein, J., Erdmann, E., Bohm, M., Hartmann, D., Breidert, M., Fritzen, R., Scherbaum, W., Mann, J., Maus, J., Schroeder, C., Henrichs, H., Unger, H., Ickenstein, G., Kromer, E., Riegger, G., Schunkert, H., Basan, B., Hampel, R., Crean, P., Garadah, T., White, U., Marini, N., Paciaroni, E., Saccomano, G., Diluzio, S., Magnani, B., Mantovani, B., Pareschi, P., Stucchi, N., Nanni, D., Rusticali, F., Simoni, C., Brunelli, C., Caponnetto, S., Gatto, E., Mazzantini, A., Molinari, O., Morello, R., Degiorgio, L., Imparato, C., Barbaresi, F., Cotogni, A., Pasqualini, M., Frigeni, G., Landoni, M., Polese, A., Cernigoi, A., Merni, M., Tortul, C., Velussi, M., Aina, F., Cernigliaro, C., Dellavesa, P., Dejoannon, U., Pierfranceschi, G., Zavaroni, D., Emilia, R., Manicardi, E., Minelli, E., Penazzoli, F., Portioli, I., Rossi, E., Giani, P., Roccaforte, R., Casaccia, M., Larovere, R., Miglierina, E., Repetto, S., Centofante, P., Vincenzi, M., Nieuwenhuijzen, Ac, Sels, J., Wolffenbuttel, Bhr, Kip, J., Mantingh, L., Mulder, H., Vandoorn, Lg, Hjerkinn, E., Reikvam, A., Cardona, M., Sanz, G., Karoni, A., Bescos, Ll, Albert, X., Masia, R., Alvarez, A., Saenz, L., Astrom, L., Press, R., Sjostedt, P., Tabrizi, F., Bergbom, I., Hansson, P., Held, C., Kahan, T., Ryden, B., Andersson, O., Wysocki, M., Karlsson, E., Sartor, G., Smith, L., Katzman, P., Ljungdahl, L., Noren, P., Hallberg, A., Olsson, Po, Asbrink, S., Molgaard, J., Nilsson, V., Nystrom, F., Ohman, P., Andersson, C., Ekholm, L., Svensson, Ka, Torebo, E., Fagher, B., Svenstam, I., Thulin, T., Ericsson, Ub, Ahnberg, K., Henning, R., Jacobsson, L., Taghavi, A., Ahlstrom, P., Rosenqvist, U., Ericson, C., Gertow, O., Kristensson, Be, Stahl, L., Bergsten, L., Harden, R., Jagren, C., Leijd, B., Lennerhagen, P., Ostergrens, J., Sandstrom, V., Sundelin, R., Hagg, A., Morlin, C., Pettersson, F., Wanders, A., Bjorkman, H., Karlsson, G., Larsson, H., Lonndahl, Y., Weber, P., Cozzi, R., Gerber, P., Moccetti, T., Safwan, E., Sessa, F., Binder, T., Boman, P., Kiowski, W., Lehman, R., Lull, B., Spinas, G., Jamieson, A., Kennedy, Ja, Kesson, C., Gryczka, R., Parker, P., Sidiki, S., Small, M., Struthers, S., Manns, J., Smithurst, H., Begg, A., Fisher, Bm, Bedford, C., Heller, S., Marlow, S., Munoz, Ec, Garcia, Hh, Ruiz, Ro, Meaney, E., Flores, Mi, Brown, E., Perry, G., Patel, G., Sarma, R., Szlachcic, Y., Dorman, J., Singh, B., Bailey, G., Clegg, L., Horwitz, L., Leahy, J., Rashkow, A., Hudson, M., Miller, A., Umberger, J., Zoble, R., Orander, P., Sridharan, M., Defrancisco, G., Davidson, M., Islam, N., Mathew, J., Rajanahally, R., French, D., Wickemeyer, W., Effron, M., Goldstein, M., Utley, K., Pierpont, G., Weigenant, J., Farkouh, M., Kubly, V., Rich, M., Wisneski, L., Abrams, J., Garcia, D., Bonora, M., Kohn, R., Muffoletto, E., Brink, D., Lader, E., Singler, A., Pande, P., Powers, J., Hoogwerf, B., Moore, J., Yanak, F., Gupta, S., Williams, D., Danisa, K., Kirk, C., Wescott, B., Grover, J., Mackenzie, M., Amidi, M., Bell, M., Farmer, J., Kingry, C., Young, J., Harms, V., Kennedy, Jw, Letterer, R., Heller, C., and Mack, R.
19. EFFECT OF THE ANTIARRHYTHMIC AGENT MORICIZINE ON SURVIVAL AFTER MYOCARDIAL-INFARCTION
- Author
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ROGERS, WJ, EPSTEIN, AE, ARCINIEGAS, JG, CROSSLEY, GH, DAILEY, SM, KAY, GN, LITTLE, RE, MACLEAN, WAH, PAPAPIETRO, SE, PLUMB, VJ, SILBER, S, BAKER, AR, CARLISLE, K, COHEN, N, COX, M, THOMAS, C, LEVSON, L, VONHAGEL, D, WALTON, AE, PRATT, CM, MAHMARIAN, J, MORRIS, G, CAPONE, RJ, BERGER, EE, CHMIELEWSKI, C, GORKIN, L, KHAN, AH, KORR, K, HANDSHAW, K, CONNOLLY, E, FITZPATRICK, D, CAMERON, T, WYSE, DG, DUFF, HJ, MITCHELL, LB, GILLIS, AM, WARNICA, JW, SHELDON, RS, LESOWAY, NR, KELLEN, J, HALE, C, INKSTER, M, BRODSKY, M, WOLFF, L, ALLEN, B, ZELMAN, R, THOMAS, G, CAUDILLO, G, TAKEDA, D, SHERWOOD, C, RANAZZI, R, RAPAPORT, E, DOHRMANN, ML, RASKIN, S, DREW, DW, SOMELOFSKI, CA, DANFORTH, JW, HUI, PY, JOHNSON, MR, LABARCA, JR, WALDO, AL, CARLSON, MD, ADLER, DS, HOLLAND, JB, BUCHTER, CM, BAHLER, RC, PAMELIA, FX, JOSEPHSON, RA, HENTHORN, RW, ZUELGARAY, JG, WOOD, K, REDMON, P, VARGAS, MA, VARGO, L, SCHALLER, SE, KOBUS, CE, CHOBAN, NL, BIGGER, JT, GREENBERG, HM, GREGORY, JJ, HOCHMAN, JS, RADOSLOVICH, G, STEINBERG, JS, ROTHBART, ST, CASE, R, DWYER, EM, SQUATRITO, A, KELLY, M, CAMPION, JM, TORMEY, D, ANTHONY, R, CALLAGHAN, E, CHAPNICK, M, RIPLEY, B, FONTANA, C, SCHLANT, RC, ARENSBERG, D, CORSO, JA, HURST, JW, MORRIS, DC, SHERMAN, SW, SILVERMAN, BD, SILVERMAN, ME, ROBERTS, JS, BALLOU, SK, JEFFRIES, VD, BRACKNEY, BA, SEALS, AA, HARTLEY, J, BAKER, RM, GILMOUR, KE, BAKER, SB, HOWARD, J, KATZ, RJ, BESCH, GA, BRILL, D, DIBIANCO, R, DONOHUE, D, FISHER, G, FRANCIS, C, FRIEDMAN, D, GOLDBERG, D, GOLDBERG, S, KOSS, G, LARCA, L, LEONARD, R, LINDGREN, K, RONAN, J, ROSENBLATT, A, ROSING, D, ROSS, A, ROTSZTAIN, A, SHAWL, F, SINDERSON, T, STEVENSON, R, TINKER, B, VARGHESE, J, YACKEE, J, BIGHAM, H, FRANKLIN, W, GOLD, R, GRAHAM, G, GROSSBERG, D, HOARE, R, LEVY, W, MAHMOOD, T, TANNENBAUM, E, TULLNER, W, EISENHOWER, E, GERACI, T, WILHELMSEN, L, BERGSTRAND, R, FREDLUND, BO, SIGURDSSON, A, SIVERTSSON, R, SWEDBERG, K, HOULTZ, B, WIKLUND, I, SCHLYTER, G, HEDELIN, G, LEIJON, M, MORGANROTH, J, CARVER, J, HOROWITZ, L, KUTALEK, S, PAPA, L, SANDBERG, J, VICTOR, M, CESARE, S, VRABEL, C, TALARICO, K, LUHMANN, S, PALAZZO, D, GOLDSTEIN, S, GOLDBERG, AD, FRUMIN, H, WESTVEER, D, DEBUTLIER, M, SCHAIRER, J, STOMEL, R, FRANK, DM, JARANDILLA, R, DAVEY, D, HASSE, C, SHINNEY, S, MORLEDGE, JH, FARNHAM, DJ, HINDERACKER, PH, MUSSER, WE, DEVRIES, K, KUSHNER, JA, RAO, R, PETERSON, DT, MCCAULEY, CS, BERGEN, TS, BOWMAN, KO, GILLMAN, A, FULLER, L, OBRIEN, J, MORLEDGE, J, DEMARIA, AN, KUO, CS, KAMMERLING, JM, CORUM, J, THIEMANN, M, SCHRODT, R, PETERS, R, SUTTON, F, GOTTLIEB, S, PAPUCHIS, G, MATTIONI, T, TODD, L, CUSACK, C, SCHECK, J, HUANG, SKS, ALPERT, JS, GORE, JM, RYAN, M, COLLETTWILLEY, P, CHAHINE, RA, SEQUEIRA, RF, LOWERY, MH, DELGADO, LM, CORREA, JL, LASO, LJ, HODGES, M, SALERNO, D, ANDERSON, B, COLLINS, R, DENES, P, DUNBAR, D, GRANRUD, G, HAUGLAND, J, HESSION, W, MCBRIDE, J, GORNICK, C, SIMONSON, J, TOLINS, M, ETTINGER, A, PETERSON, S, SLIVKEN, R, GRIMALDI, L, ROY, D, THEROUX, P, LEMERY, R, MORISSETTE, D, BEAUDOIN, D, GIRARD, L, LAVALLEE, E, MCANULTY, JH, REINHART, SE, MAURICE, G, MURPHY, ES, KRON, J, MARCHANT, C, BOXER, J, PRINCEHOUSE, L, SINNER, K, BEANLANDS, D, DAVIES, R, GREEN, M, WILLIAMS, W, BAIRD, MJ, GARRARD, L, HEAL, S, HASPECT, A, BORTHWICK, J, MAROIS, L, WOODEND, K, AKIYAMA, T, HOOD, WB, EASLEY, R, RYAN, G, KENIEN, G, PATT, M, KAZIERAD, D, GOLDFARB, A, BUTLER, LL, KELLER, ML, STANLEY, P, PEEBLES, J, SYROCKI, D, LAVIN, D, SCHOENBERGER, JA, LIEBSON, PR, STAMATO, NJ, PETROPULOS, AT, BUCKINGHAM, TA, REMIJAS, T, KOCOUREK, J, JANKO, K, BARKER, AH, ANDERSON, JL, FOWLES, RE, KEITH, TB, WILLIAMS, CB, MORENO, FL, DORAN, EN, FOWLER, B, SUMMERS, K, WHITE, C, OHARA, G, ROULEAU, JL, PLANTE, S, VINCENT, C, BOUCHARD, D, ZOBLE, RG, OTERO, JE, BUGNI, WJ, SCHWARTZ, KM, SHETTIGAR, UR, BREWINGTON, JA, UMBERGER, J, COHEN, JD, BJERREGAARD, P, HAMILTON, WP, GARNER, M, ANDERSON, S, ELSHERIF, N, URSELL, SN, GABOR, GE, IBRAHIM, B, ASSADI, M, BREZSNYAK, ML, PORTER, AV, STANIORSKI, A, WOOSLEY, RL, RODEN, DM, CAMPBELL, WB, ECHT, DS, LEE, JT, MURRAY, KT, SPELL, JD, BONHOTAL, ST, JARED, LL, THOMAS, TI, GOLDNER, F, RICHARDSON, DW, ROMHILT, DW, ELLENBOGEN, KA, BANE, BB, FIELDS, J, SHRADER, S, POWELL, E, CHAFFIN, CF, WELLS, A, CONWAY, KT, PLATIA, EV, ODONOGHUE, S, TRACY, CM, ALI, N, BOWEN, P, BROOKS, KM, OETGEN, W, WESTON, LT, CARSON, P, OBIASMANNO, D, HARRISON, J, SAYLOR, A, POWELL, S, HAAKENSON, CM, SATHER, MR, MALONE, LA, HALLSTROM, AP, MCBRIDE, R, GREENE, HL, BROOKS, MM, LEDINGHAM, R, REYNOLDSHAERTLE, RA, HUTHER, M, SCHOLZ, M, MORRIS, M, FRIEDMAN, LM, SCHRON, E, VERTER, J, JENNINGS, C, PROSCHAN, M, BRISTOW, JD, DEMETS, DL, FISCH, C, NIES, AS, RUSKIN, J, STRAUSS, H, WALTERS, L, ROGERS, WJ, EPSTEIN, AE, ARCINIEGAS, JG, CROSSLEY, GH, DAILEY, SM, KAY, GN, LITTLE, RE, MACLEAN, WAH, PAPAPIETRO, SE, PLUMB, VJ, SILBER, S, BAKER, AR, CARLISLE, K, COHEN, N, COX, M, THOMAS, C, LEVSON, L, VONHAGEL, D, WALTON, AE, PRATT, CM, MAHMARIAN, J, MORRIS, G, CAPONE, RJ, BERGER, EE, CHMIELEWSKI, C, GORKIN, L, KHAN, AH, KORR, K, HANDSHAW, K, CONNOLLY, E, FITZPATRICK, D, CAMERON, T, WYSE, DG, DUFF, HJ, MITCHELL, LB, GILLIS, AM, WARNICA, JW, SHELDON, RS, LESOWAY, NR, KELLEN, J, HALE, C, INKSTER, M, BRODSKY, M, WOLFF, L, ALLEN, B, ZELMAN, R, THOMAS, G, CAUDILLO, G, TAKEDA, D, SHERWOOD, C, RANAZZI, R, RAPAPORT, E, DOHRMANN, ML, RASKIN, S, DREW, DW, SOMELOFSKI, CA, DANFORTH, JW, HUI, PY, JOHNSON, MR, LABARCA, JR, WALDO, AL, CARLSON, MD, ADLER, DS, HOLLAND, JB, BUCHTER, CM, BAHLER, RC, PAMELIA, FX, JOSEPHSON, RA, HENTHORN, RW, ZUELGARAY, JG, WOOD, K, REDMON, P, VARGAS, MA, VARGO, L, SCHALLER, SE, KOBUS, CE, CHOBAN, NL, BIGGER, JT, GREENBERG, HM, GREGORY, JJ, HOCHMAN, JS, RADOSLOVICH, G, STEINBERG, JS, ROTHBART, ST, CASE, R, DWYER, EM, SQUATRITO, A, KELLY, M, CAMPION, JM, TORMEY, D, ANTHONY, R, CALLAGHAN, E, CHAPNICK, M, RIPLEY, B, FONTANA, C, SCHLANT, RC, ARENSBERG, D, CORSO, JA, HURST, JW, MORRIS, DC, SHERMAN, SW, SILVERMAN, BD, SILVERMAN, ME, ROBERTS, JS, BALLOU, SK, JEFFRIES, VD, BRACKNEY, BA, SEALS, AA, HARTLEY, J, BAKER, RM, GILMOUR, KE, BAKER, SB, HOWARD, J, KATZ, RJ, BESCH, GA, BRILL, D, DIBIANCO, R, DONOHUE, D, FISHER, G, FRANCIS, C, FRIEDMAN, D, GOLDBERG, D, GOLDBERG, S, KOSS, G, LARCA, L, LEONARD, R, LINDGREN, K, RONAN, J, ROSENBLATT, A, ROSING, D, ROSS, A, ROTSZTAIN, A, SHAWL, F, SINDERSON, T, STEVENSON, R, TINKER, B, VARGHESE, J, YACKEE, J, BIGHAM, H, FRANKLIN, W, GOLD, R, GRAHAM, G, GROSSBERG, D, HOARE, R, LEVY, W, MAHMOOD, T, TANNENBAUM, E, TULLNER, W, EISENHOWER, E, GERACI, T, WILHELMSEN, L, BERGSTRAND, R, FREDLUND, BO, SIGURDSSON, A, SIVERTSSON, R, SWEDBERG, K, HOULTZ, B, WIKLUND, I, SCHLYTER, G, HEDELIN, G, LEIJON, M, MORGANROTH, J, CARVER, J, HOROWITZ, L, KUTALEK, S, PAPA, L, SANDBERG, J, VICTOR, M, CESARE, S, VRABEL, C, TALARICO, K, LUHMANN, S, PALAZZO, D, GOLDSTEIN, S, GOLDBERG, AD, FRUMIN, H, WESTVEER, D, DEBUTLIER, M, SCHAIRER, J, STOMEL, R, FRANK, DM, JARANDILLA, R, DAVEY, D, HASSE, C, SHINNEY, S, MORLEDGE, JH, FARNHAM, DJ, HINDERACKER, PH, MUSSER, WE, DEVRIES, K, KUSHNER, JA, RAO, R, PETERSON, DT, MCCAULEY, CS, BERGEN, TS, BOWMAN, KO, GILLMAN, A, FULLER, L, OBRIEN, J, MORLEDGE, J, DEMARIA, AN, KUO, CS, KAMMERLING, JM, CORUM, J, THIEMANN, M, SCHRODT, R, PETERS, R, SUTTON, F, GOTTLIEB, S, PAPUCHIS, G, MATTIONI, T, TODD, L, CUSACK, C, SCHECK, J, HUANG, SKS, ALPERT, JS, GORE, JM, RYAN, M, COLLETTWILLEY, P, CHAHINE, RA, SEQUEIRA, RF, LOWERY, MH, DELGADO, LM, CORREA, JL, LASO, LJ, HODGES, M, SALERNO, D, ANDERSON, B, COLLINS, R, DENES, P, DUNBAR, D, GRANRUD, G, HAUGLAND, J, HESSION, W, MCBRIDE, J, GORNICK, C, SIMONSON, J, TOLINS, M, ETTINGER, A, PETERSON, S, SLIVKEN, R, GRIMALDI, L, ROY, D, THEROUX, P, LEMERY, R, MORISSETTE, D, BEAUDOIN, D, GIRARD, L, LAVALLEE, E, MCANULTY, JH, REINHART, SE, MAURICE, G, MURPHY, ES, KRON, J, MARCHANT, C, BOXER, J, PRINCEHOUSE, L, SINNER, K, BEANLANDS, D, DAVIES, R, GREEN, M, WILLIAMS, W, BAIRD, MJ, GARRARD, L, HEAL, S, HASPECT, A, BORTHWICK, J, MAROIS, L, WOODEND, K, AKIYAMA, T, HOOD, WB, EASLEY, R, RYAN, G, KENIEN, G, PATT, M, KAZIERAD, D, GOLDFARB, A, BUTLER, LL, KELLER, ML, STANLEY, P, PEEBLES, J, SYROCKI, D, LAVIN, D, SCHOENBERGER, JA, LIEBSON, PR, STAMATO, NJ, PETROPULOS, AT, BUCKINGHAM, TA, REMIJAS, T, KOCOUREK, J, JANKO, K, BARKER, AH, ANDERSON, JL, FOWLES, RE, KEITH, TB, WILLIAMS, CB, MORENO, FL, DORAN, EN, FOWLER, B, SUMMERS, K, WHITE, C, OHARA, G, ROULEAU, JL, PLANTE, S, VINCENT, C, BOUCHARD, D, ZOBLE, RG, OTERO, JE, BUGNI, WJ, SCHWARTZ, KM, SHETTIGAR, UR, BREWINGTON, JA, UMBERGER, J, COHEN, JD, BJERREGAARD, P, HAMILTON, WP, GARNER, M, ANDERSON, S, ELSHERIF, N, URSELL, SN, GABOR, GE, IBRAHIM, B, ASSADI, M, BREZSNYAK, ML, PORTER, AV, STANIORSKI, A, WOOSLEY, RL, RODEN, DM, CAMPBELL, WB, ECHT, DS, LEE, JT, MURRAY, KT, SPELL, JD, BONHOTAL, ST, JARED, LL, THOMAS, TI, GOLDNER, F, RICHARDSON, DW, ROMHILT, DW, ELLENBOGEN, KA, BANE, BB, FIELDS, J, SHRADER, S, POWELL, E, CHAFFIN, CF, WELLS, A, CONWAY, KT, PLATIA, EV, ODONOGHUE, S, TRACY, CM, ALI, N, BOWEN, P, BROOKS, KM, OETGEN, W, WESTON, LT, CARSON, P, OBIASMANNO, D, HARRISON, J, SAYLOR, A, POWELL, S, HAAKENSON, CM, SATHER, MR, MALONE, LA, HALLSTROM, AP, MCBRIDE, R, GREENE, HL, BROOKS, MM, LEDINGHAM, R, REYNOLDSHAERTLE, RA, HUTHER, M, SCHOLZ, M, MORRIS, M, FRIEDMAN, LM, SCHRON, E, VERTER, J, JENNINGS, C, PROSCHAN, M, BRISTOW, JD, DEMETS, DL, FISCH, C, NIES, AS, RUSKIN, J, STRAUSS, H, and WALTERS, L
20. Empiric antiarrhythmic drug therapy in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia: pragmatism or anachronism?
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Mitchell LB
- Published
- 2009
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21. Prevention of atrial fibrillation following cardiac surgery.
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Arias MA, Potter BJ, LeLorier J, Kwatra MM, Mitchell LB, and Exner DV
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- 2006
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22. Are transthoracic echocardiographic parameters associated with atrial fibrillation recurrence or stroke? Results from the Atrial Fibrillation Follow-Up Investigation of Rhythm Management (AFFIRM) study.
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Olshansky B, Heller EN, Mitchell LB, Chandler M, Slater W, Green M, Brodsky M, Barrell P, Greene HL, AFFIRM (Atrial Fibrillation Follow-Up Investigation of Rhythm Management) Investigators, Olshansky, Brian, Heller, Eliot N, Mitchell, L Brent, Chandler, Mary, Slater, William, Green, Martin, Brodsky, Michael, Barrell, Patrick, and Greene, H Leon
- Abstract
Objectives: The purpose of this study was to evaluate the associations of transthoracic echocardiographic parameters with recurrent atrial fibrillation (AF) and/or stroke.Background: The Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) study, an evaluation of elderly patients with AF at risk for stroke, provided an opportunity to evaluate the implications of echocardiographic parameters in patients with AF.Methods: Transthoracic echocardiographic measures of mitral regurgitation (MR), left atrial (LA) diameter, and left ventricular (LV) function were evaluated in the AFFIRM rate- and rhythm-control patients who had sinus rhythm resume and had these data available. Risk for recurrent AF or stroke was evaluated with respect to transthoracic echocardiographic measures.Results: Of 2,474 patients studied, 457 had > or =2(+)/4(+) MR, and 726 had a LA diameter >4.5 cm. The LV ejection fraction was abnormal in 543 patients. The cumulative probabilities of at least one AF recurrence/stroke were 46%/1% after 1 year and 84%/5% by the end of the trial (> 5 years), respectively. Multivariate analysis showed that randomization to the rhythm-control arm (hazard ratio [HR] = 0.64; p < 0.0001) and a qualifying episode of AF being the first known episode (HR = 0.70; p < 0.0001) were associated with decreased risk. Duration of qualifying AF episode >48 h (HR = 1.55; p < 0.0001) and LA diameter (p = 0.008) were associated with an increased risk of recurrent AF. Recurrent AF was more likely with larger LA diameters (HR = 1.21, 1.16, and 1.32 for mild, moderate, and severe enlargement, respectively). No transthoracic echocardiographic measures were associated with risk of stroke.Conclusions: In the AFFIRM study, large transthoracic echocardiographic LA diameters were associated with recurrent AF, but no measured echocardiographic parameter was associated with stroke. [ABSTRACT FROM AUTHOR]- Published
- 2005
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23. Resumption of driving after life-threatening ventricular tachyarrhythmia.
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Akiyama T, Powell JL, Mitchell LB, Ehlert FA, Baessler C, and Antiarrhythmics Versus Implantable Defibrillators Investigators
- Published
- 2001
24. Noninvasive risk assessment early after a myocardial infarction the REFINE study.
- Author
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Exner DV, Kavanagh KM, Slawnych MP, Mitchell LB, Ramadan D, Aggarwal SG, Noullett C, Van Schaik A, Mitchell RT, Shibata MA, Gulamhussein S, McMeekin J, Tymchak W, Schnell G, Gillis AM, Sheldon RS, Fick GH, Duff HJ, and REFINE Investigators
- Published
- 2007
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25. Antiarrhythmic drug effects on QT interval dispersion in patients undergoing electropharmacologic testing for ventricular tachycardia and fibrillation.
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Gillis AM, Traboulsi M, Hii JTY, Wyse DG, Duff HJ, McDonald M, Mitchell LB, Gillis, A M, Traboulsi, M, Hii, J T, Wyse, D G, Duff, H J, McDonald, M, and Mitchell, L B
- Abstract
The effects of antiarrhythmic drugs on QT interval dispersion as a predictor of antiarrhythmic drug therapy has not been rigorously assessed. This study was performed to determine whether the effects of antiarrhythmic drugs on QT interval dispersion predict antiarrhythmic drug response in patients undergoing electropharmacologic testing for ventricular tachycardiarrythmias. Precordial QT intervals and QT interval dispersions were measured at baseline and during steady-state antiarrhythmic drug therapy in 72 consecutive patients with documented coronary artery disease and remote myocardial infarction presenting with spontaneous sustained ventricular tachyarrhythmias who underwent electropharmacologic studies to assess arrhythmia suppression. QT interval dispersion was similar at baseline in drug responders (42 +/- 21 ms) and drug nonresponders (46 +/- 21 ms), whereas during antiarrhythmic therapy QT interval dispersion was shorter in drug responders (33 +/- 15 ms) than in drug nonresponders (55 +/- 29 ms, p <0.001). QT interval dispersion was shorter in 7 drug responders during their effective drug trials (27 +/- 14 ms) than during their ineffective drug trials (47 +/- 24 ms, n = 9, p <0.05). QT dispersion < or = 50 ms (p <0.002) and a patent infarct-related artery (p <0.003) were independent predictors of antiarrhythmic therapy. The positive and negative predictive value of QT interval dispersion during drug therapy to predict a successful drug response was 32% and 96%, respectively. QT interval dispersion predicted the outcome of electropharmacologic studies independent of infarct-related artery patency. QT interval dispersion >50 ms during drug therapy was associated with ineffective drug therapy. [ABSTRACT FROM AUTHOR]
- Published
- 1998
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26. Driving after life-threatening ventricular tachyarrhythmia.
- Author
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Lowenfels AB, Kriatselis H, Göhl K, Gottwik M, Akiyama T, Powell JL, and Mitchell LB
- Published
- 2002
27. Selecting Persistent Atrial Fibrillation Patients for Adjunctive Right Atrial Ablation: When You're Right, You're Right.
- Author
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Veenhuyzen G and Mitchell LB
- Subjects
- Humans, Heart Atria surgery, Atrial Fibrillation surgery, Atrial Appendage, Catheter Ablation
- Published
- 2024
- Full Text
- View/download PDF
28. ICDs for Patients With Stable VT, Cardiomyopathy, and Relatively Preserved LVEF: Core Therapy, Precision Medicine, or Indication Creep?
- Author
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Mitchell LB and Exner DV
- Subjects
- Humans, Precision Medicine, Ventricular Fibrillation, Cardiomyopathies therapy, Defibrillators, Implantable, Tachycardia, Ventricular therapy
- Published
- 2022
- Full Text
- View/download PDF
29. Anticoagulation Therapy for Patients With New-Onset Postoperative Atrial Fibrillation After Noncardiac Surgery: Must Do, May Do, or Don't Do?
- Author
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Pollak PT and Mitchell LB
- Subjects
- Anticoagulants therapeutic use, Hemorrhage, Humans, Risk Factors, Atrial Fibrillation drug therapy, Atrial Fibrillation epidemiology, Thromboembolism
- Published
- 2021
- Full Text
- View/download PDF
30. The 2020 Canadian Cardiovascular Society/Canadian Heart Rhythm Society Comprehensive Guidelines for the Management of Atrial Fibrillation.
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Andrade JG, Aguilar M, Atzema C, Bell A, Cairns JA, Cheung CC, Cox JL, Dorian P, Gladstone DJ, Healey JS, Khairy P, Leblanc K, McMurtry MS, Mitchell LB, Nair GM, Nattel S, Parkash R, Pilote L, Sandhu RK, Sarrazin JF, Sharma M, Skanes AC, Talajic M, Tsang TSM, Verma A, Verma S, Whitlock R, Wyse DG, and Macle L
- Subjects
- Aged, 80 and over, Canada epidemiology, Cardiovascular Diseases epidemiology, Cardiovascular Diseases therapy, Female, Heart Disease Risk Factors, Humans, Male, Middle Aged, Prevalence, Risk Adjustment methods, Risk Adjustment standards, Societies, Medical, Anticoagulants administration & dosage, Anticoagulants adverse effects, Atrial Fibrillation classification, Atrial Fibrillation complications, Atrial Fibrillation epidemiology, Atrial Fibrillation therapy, Catheter Ablation adverse effects, Catheter Ablation methods, Hemorrhage chemically induced, Hemorrhage prevention & control, Patient Care Management methods, Patient Care Management standards, Stroke etiology, Stroke prevention & control
- Abstract
The Canadian Cardiovascular Society (CCS) atrial fibrillation (AF) guidelines program was developed to aid clinicians in the management of these complex patients, as well as to provide direction to policy makers and health care systems regarding related issues. The most recent comprehensive CCS AF guidelines update was published in 2010. Since then, periodic updates were published dealing with rapidly changing areas. However, since 2010 a large number of developments had accumulated in a wide range of areas, motivating the committee to complete a thorough guideline review. The 2020 iteration of the CCS AF guidelines represents a comprehensive renewal that integrates, updates, and replaces the past decade of guidelines, recommendations, and practical tips. It is intended to be used by practicing clinicians across all disciplines who care for patients with AF. The Grading of Recommendations, Assessment, Development and Evaluations (GRADE) system was used to evaluate recommendation strength and the quality of evidence. Areas of focus include: AF classification and definitions, epidemiology, pathophysiology, clinical evaluation, screening and opportunistic AF detection, detection and management of modifiable risk factors, integrated approach to AF management, stroke prevention, arrhythmia management, sex differences, and AF in special populations. Extensive use is made of tables and figures to synthesize important material and present key concepts. This document should be an important aid for knowledge translation and a tool to help improve clinical management of this important and challenging arrhythmia., (Copyright © 2020 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
31. Emotional Reactivity as a Vulnerability for Psychogenic Nonepileptic Seizures? Responses While Reliving Specific Emotions.
- Author
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Roberts NA, Burleson MH, Torres DL, Parkhurst DK, Garrett R, Mitchell LB, Duncan CJ, Mintert M, and Wang NC
- Subjects
- Adult, Female, Humans, Male, Middle Aged, Pilot Projects, Wounds and Injuries psychology, Young Adult, Affective Symptoms physiopathology, Conversion Disorder physiopathology, Emotional Regulation physiology, Psychophysiologic Disorders physiopathology, Respiratory Sinus Arrhythmia physiology, Seizures physiopathology
- Abstract
Objective: Dysfunction in emotional processes is a hypothesized contributor to functional neurological disorders (FNDs), yet few studies have evoked real-time emotion during multimethod assessment incorporating subjective, behavioral, and psychophysiological indicators. This approach may reveal clinical and neurobiological vulnerability to FND and clarify how dysfunctional emotional processes serve as perpetuating factors., Methods: Eleven participants with video-EEG-confirmed diagnoses of psychogenic nonepileptic seizures (PNES) were compared with 49 seizure-free trauma control subjects (TCs) with or without clinically elevated posttraumatic stress symptoms (25 clinically elevated [TC-clin], 24 not clinically elevated [TC-nonclin]). Participants recalled and described memories evoking anger, shame, happiness, and neutral feelings., Results: Even though PNES patients and TCs reported similar amounts of emotional experience, PNES patients reported more difficulty reliving emotions and were less likely to complete the relived shame task. During and after reliving happiness, PNES and TC-clin groups showed respiratory sinus arrhythmia (RSA) decreases, indicating parasympathetic withdrawal, whereas the TC-nonclin group showed RSA increases., Conclusions: Findings from this pilot study are consistent with previous research and clinical observations that emotional engagement may be more effortful for PNES patients. Patterns of RSA change, which may also point to greater effortful engagement, were similar in PNES and TC-clin groups, suggesting that traumatic stress reactions may play a part. At the same time, experience of greater difficulty or avoidance may be even greater among PNES patients. Especially when regulatory resources are already limited, accumulated effort, coupled with self-threatening contexts such as shame, may be particularly problematic for those with PNES and perhaps other FNDs.
- Published
- 2020
- Full Text
- View/download PDF
32. Review of Stereotactic Arrhythmia Radioablation Therapy for Cardiac Tachydysrhythmias.
- Author
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Chiu MH, Mitchell LB, Ploquin N, Faruqi S, and Kuriachan VP
- Abstract
Cardiac tachyarrhythmias are a major cause of morbidity and mortality. Treatments for these tachyarrhythmias include antiarrhythmic drugs, catheter ablation, surgical ablation, cardiac implantable electronic devices, and cardiac transplantation. Each of these treatment approaches is effective in some patients but there is considerable room for improvement, particularly with respect to the most common of the tachydysrhythmias, atrial fibrillation, and the most dangerous of the tachydysrhythmias, ventricular tachycardia (VT) or ventricular fibrillation. Noninvasive stereotactic ablative radiation therapy is emerging as an effective treatment for refractory tachyarrhythmias. Animal models have shown successful ablation of arrhythmogenic myocardial substrates with minimal short-term complications. Studies of stereotactic radioablation involving patients with refractory VT have shown a reduction in VT recurrence and promising early safety data. In this review, we provide the background for the application of stereotactic arrhythmia radioablation therapy along with promising results from early applications of the technology., (© 2020 Canadian Cardiovascular Society. Published by Elsevier Inc.)
- Published
- 2020
- Full Text
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33. Comment on "The Canadian Cardiovascular Society 2018 guideline update for atrial fibrillation - A different perspective".
- Author
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Andrade JG, Macle L, Verma A, and Mitchell LB
- Subjects
- Anticoagulants, Canada, Electric Countershock, Humans, Atrial Fibrillation
- Published
- 2020
- Full Text
- View/download PDF
34. Periprocedural Anticoagulation for Cardioversion of Acute Onset Atrial Fibrillation and Flutter: Evidence Base for Current Guidelines.
- Author
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Andrade JG and Mitchell LB
- Subjects
- Acute Disease, Atrial Fibrillation complications, Atrial Flutter complications, Humans, Practice Guidelines as Topic, Stroke etiology, Stroke prevention & control, Thromboembolism etiology, Anticoagulants therapeutic use, Atrial Fibrillation therapy, Atrial Flutter therapy, Electric Countershock adverse effects, Thromboembolism prevention & control
- Abstract
The practice of electrical or pharmacological cardioversion (CV) to restore sinus rhythm in patents with symptomatic atrial fibrillation (AF) or atrial flutter has been a part of clinical practice for more than 100 years. For almost as long as CV has been performed, it has been recognized that the act of restoring sinus rhythm is associated with an increased risk of stroke and systemic embolism, and that oral anticoagulant (OAC) therapy can be used to prevent peri-CV thromboembolism. Although it has been widely accepted that OAC therapy is necessary to prevent thromboembolism in patients with chronic AF/atrial flutter who undergo CV, previous clinical practice recommendations have suggested that OAC therapy may be omitted in patients at low risk of stroke. However, in recent years, evidence has emerged from several sources challenging these historical conventions. In 2018 the Canadian Cardiovascular Society AF guidelines updated the previous recommendations regarding CV of acute onset AF, and the use of peri-CV anticoagulation. In this article we present an extensive review of the evidence informing the previous recommendations, as well as the novel evidence that informed the change in recommendations. In addition, the current Canadian Cardiovascular Society AF guideline recommendations are examined within the context of contemporary international major society guidelines., (Copyright © 2019 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2019
- Full Text
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35. Monitoring Direct Oral Anticoagulants: Longing for the Days When We Were in Control?
- Author
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Pollak PT and Mitchell LB
- Subjects
- Administration, Oral, Anticoagulants, Humans, Atrial Fibrillation
- Published
- 2019
- Full Text
- View/download PDF
36. Effect of Catheter Ablation vs Antiarrhythmic Drug Therapy on Mortality, Stroke, Bleeding, and Cardiac Arrest Among Patients With Atrial Fibrillation: The CABANA Randomized Clinical Trial.
- Author
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Packer DL, Mark DB, Robb RA, Monahan KH, Bahnson TD, Poole JE, Noseworthy PA, Rosenberg YD, Jeffries N, Mitchell LB, Flaker GC, Pokushalov E, Romanov A, Bunch TJ, Noelker G, Ardashev A, Revishvili A, Wilber DJ, Cappato R, Kuck KH, Hindricks G, Davies DW, Kowey PR, Naccarelli GV, Reiffel JA, Piccini JP, Silverstein AP, Al-Khalidi HR, and Lee KL
- Subjects
- Aged, Anti-Arrhythmia Agents adverse effects, Atrial Fibrillation complications, Atrial Fibrillation mortality, Female, Heart Arrest etiology, Hemorrhage etiology, Hospitalization statistics & numerical data, Humans, Intention to Treat Analysis, Kaplan-Meier Estimate, Male, Middle Aged, Recurrence, Registries, Risk Factors, Stroke etiology, Anti-Arrhythmia Agents therapeutic use, Atrial Fibrillation drug therapy, Atrial Fibrillation surgery, Catheter Ablation adverse effects, Heart Arrest prevention & control, Hemorrhage prevention & control, Stroke prevention & control
- Abstract
Importance: Catheter ablation is effective in restoring sinus rhythm in atrial fibrillation (AF), but its effects on long-term mortality and stroke risk are uncertain., Objective: To determine whether catheter ablation is more effective than conventional medical therapy for improving outcomes in AF., Design, Setting, and Participants: The Catheter Ablation vs Antiarrhythmic Drug Therapy for Atrial Fibrillation trial is an investigator-initiated, open-label, multicenter, randomized trial involving 126 centers in 10 countries. A total of 2204 symptomatic patients with AF aged 65 years and older or younger than 65 years with 1 or more risk factors for stroke were enrolled from November 2009 to April 2016, with follow-up through December 31, 2017., Interventions: The catheter ablation group (n = 1108) underwent pulmonary vein isolation, with additional ablative procedures at the discretion of site investigators. The drug therapy group (n = 1096) received standard rhythm and/or rate control drugs guided by contemporaneous guidelines., Main Outcomes and Measures: The primary end point was a composite of death, disabling stroke, serious bleeding, or cardiac arrest. Among 13 prespecified secondary end points, 3 are included in this report: all-cause mortality; total mortality or cardiovascular hospitalization; and AF recurrence., Results: Of the 2204 patients randomized (median age, 68 years; 37.2% female; 42.9% had paroxysmal AF and 57.1% had persistent AF), 89.3% completed the trial. Of the patients assigned to catheter ablation, 1006 (90.8%) underwent the procedure. Of the patients assigned to drug therapy, 301 (27.5%) ultimately received catheter ablation. In the intention-to-treat analysis, over a median follow-up of 48.5 months, the primary end point occurred in 8.0% (n = 89) of patients in the ablation group vs 9.2% (n = 101) of patients in the drug therapy group (hazard ratio [HR], 0.86 [95% CI, 0.65-1.15]; P = .30). Among the secondary end points, outcomes in the ablation group vs the drug therapy group, respectively, were 5.2% vs 6.1% for all-cause mortality (HR, 0.85 [95% CI, 0.60-1.21]; P = .38), 51.7% vs 58.1% for death or cardiovascular hospitalization (HR, 0.83 [95% CI, 0.74-0.93]; P = .001), and 49.9% vs 69.5% for AF recurrence (HR, 0.52 [95% CI, 0.45-0.60]; P < .001)., Conclusions and Relevance: Among patients with AF, the strategy of catheter ablation, compared with medical therapy, did not significantly reduce the primary composite end point of death, disabling stroke, serious bleeding, or cardiac arrest. However, the estimated treatment effect of catheter ablation was affected by lower-than-expected event rates and treatment crossovers, which should be considered in interpreting the results of the trial., Trial Registration: ClinicalTrials.gov Identifier: NCT00911508.
- Published
- 2019
- Full Text
- View/download PDF
37. Association Between Patient and Physician Sex and Physician-Estimated Stroke and Bleeding Risks in Atrial Fibrillation.
- Author
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Lee H, Tan MK, Yan AT, Angaran P, Dorian P, Bucci C, Gregoire JC, Bell AD, Green MS, Gross PL, Skanes A, Kerr CR, Mitchell LB, Cox JL, Essebag V, Heilbron B, Ramanathan K, Fournier C, Wheeler BH, Lin PJ, Berall M, Langer A, Goldin L, and Goodman SG
- Subjects
- Aged, Atrial Fibrillation drug therapy, Canada epidemiology, Female, Hemorrhage epidemiology, Humans, Incidence, Male, Risk Factors, Sex Factors, Stroke epidemiology, Stroke prevention & control, Anticoagulants therapeutic use, Atrial Fibrillation complications, Hemorrhage etiology, Risk Assessment methods, Stroke etiology
- Abstract
Background: Physicians treating nonvalvular atrial fibrillation (AF) assess stroke and bleeding risks when deciding on anticoagulation. The agreement between empirical and physician-estimated risks is unclear. Furthermore, the association between patient and physician sex and anticoagulation decision-making is uncertain., Methods: We pooled data from 2 national primary care physician chart audit databases of patients with AF (Facilitating Review and Education to Optimize Stroke Prevention in Atrial Fibrillation and Coordinated National Network to Engage Physicians in the Care and Treatment of Patients with Atrial Fibrillation Chart Audit) with a combined 1035 physicians (133 female, 902 male) and 10,927 patients (4567 female and 6360 male)., Results: Male physicians underestimated stroke risk in female patients and overestimated risk in male patients. Female physicians estimated stroke risk well in female patients but underestimated the risk in male patients. Risk of bleeding was underestimated in all. Despite differences in risk assessment by physician and patient sex, > 90% of patients received anticoagulation across all subgroups. There was modest agreement between physician estimated and calculated (ie, CHADS
2 score) stroke risk: Kappa scores were 0.41 (0.35-0.47) for female physicians and 0.34 (0.32-0.36) for male physicians., Conclusions: Our study is the first to examine the association between patient and physician sex influences and stroke and bleeding risk estimation in AF. Although there were differences in agreement between physician estimated stroke risk and calculated CHADS2 scores, these differences were small and unlikely to affect clinical practice; further, despite any perceived differences in the accuracy of risk assessment by sex, most patients received anticoagulation., (Copyright © 2018 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)- Published
- 2019
- Full Text
- View/download PDF
38. 2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
- Author
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Andrade JG, Verma A, Mitchell LB, Parkash R, Leblanc K, Atzema C, Healey JS, Bell A, Cairns J, Connolly S, Cox J, Dorian P, Gladstone D, McMurtry MS, Nair GM, Pilote L, Sarrazin JF, Sharma M, Skanes A, Talajic M, Tsang T, Verma S, Wyse DG, Nattel S, and Macle L
- Subjects
- Algorithms, Anti-Arrhythmia Agents therapeutic use, Anticoagulants therapeutic use, Antidotes therapeutic use, Atrial Fibrillation complications, Catheter Ablation, Coagulants therapeutic use, Comorbidity, Coronary Artery Disease complications, Coronary Artery Disease drug therapy, Drug Therapy, Combination, Echocardiography, Transesophageal, Electric Countershock, Fibrinolytic Agents therapeutic use, Heart Failure complications, Heart Failure therapy, Hemorrhage chemically induced, Hemorrhage drug therapy, Humans, Risk Factors, Societies, Medical, Stroke etiology, Stroke prevention & control, Atrial Fibrillation therapy
- Abstract
The Canadian Cardiovascular Society (CCS) Atrial Fibrillation Guidelines Committee provides periodic reviews of new data to produce focused updates that address clinically important advances in atrial fibrillation (AF) management. This 2018 Focused Update addresses: (1) anticoagulation in the context of cardioversion of AF; (2) the management of antithrombotic therapy for patients with AF in the context of coronary artery disease; (3) investigation and management of subclinical AF; (4) the use of antidotes for the reversal of non-vitamin K antagonist oral anticoagulants; (5) acute pharmacological cardioversion of AF; (6) catheter ablation for AF, including patients with concomitant AF and heart failure; and (7) an integrated approach to the patient with AF and modifiable cardiovascular risk factors. The recommendations were developed using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) standards. Individual studies and literature were reviewed for quality and bias; the literature review process and evidence tables are included as Supplementary Material and are available on the CCS Web site. Details of the updated recommendations are presented, along with their background and rationale. This document is linked to an updated summary of all CCS AF guidelines recommendations, from 2010 to the present 2018 Focused Update, which is provided in the Supplementary Material., (Copyright © 2018 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
39. Ranolazine in High-Risk Patients With Implanted Cardioverter-Defibrillators: The RAID Trial.
- Author
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Zareba W, Daubert JP, Beck CA, Huang DT, Alexis JD, Brown MW, Pyykkonen K, McNitt S, Oakes D, Feng C, Aktas MK, Ayala-Parades F, Baranchuk A, Dubuc M, Haigney M, Mazur A, McPherson CA, Mitchell LB, Natale A, Piccini JP, Raitt M, Rashtian MY, Schuger C, Winters S, Worley SJ, Ziv O, and Moss AJ
- Subjects
- Aged, Defibrillators, Implantable adverse effects, Double-Blind Method, Female, Follow-Up Studies, Humans, Male, Middle Aged, Prospective Studies, Risk Factors, Tachycardia, Ventricular epidemiology, Tachycardia, Ventricular physiopathology, Ventricular Fibrillation epidemiology, Ventricular Fibrillation physiopathology, Cardiovascular Agents therapeutic use, Defibrillators, Implantable trends, Ranolazine therapeutic use, Tachycardia, Ventricular prevention & control, Ventricular Fibrillation prevention & control
- Abstract
Background: Ventricular tachycardia (VT) and ventricular fibrillation (VF) remain a challenging problem in patients with implantable cardioverter-defibrillators (ICDs)., Objectives: This study aimed to determine whether ranolazine administration decreases the likelihood of VT, VF, or death in patients with an ICD., Methods: This was double-blind, placebo-controlled clinical trial in which high-risk ICD patients with ischemic or nonischemic cardiomyopathy were randomized to 1,000 mg ranolazine twice a day or placebo. The primary endpoint was VT or VF requiring appropriate ICD therapy or death, whichever occurred first. Pre-specified secondary endpoints included ICD shock for VT, VF, or death and recurrent VT or VF requiring ICD therapy., Results: Among 1,012 ICD patients (510 randomized to ranolazine and 502 to placebo) the mean age was 64 ± 10 years and 18% were women. During 28 ± 16 months of follow-up there were 372 (37%) patients with primary endpoint, 270 (27%) patients with VT or VF, and 148 (15%) deaths. The blinded study drug was discontinued in 199 (39.6%) patients receiving placebo and in 253 (49.6%) patients receiving ranolazine (p = 0.001). The hazard ratio for ranolazine versus placebo was 0.84 (95% confidence interval: 0.67 to 1.05; p = 0.117) for VT, VF, or death. In a pre-specified secondary analysis, patients randomized to ranolazine had a marginally significant lower risk of ICD therapies for recurrent VT or VF (hazard ratio: 0.70; 95% confidence interval: 0.51 to 0.96; p = 0.028). There were no other significant treatment effects in other pre-specified secondary analyses, which included individual components of the primary endpoint, inappropriate shocks, cardiac hospitalizations, and quality of life., Conclusions: In high-risk ICD patients, treatment with ranolazine did not significantly reduce the incidence of the first VT or VF, or death. However, the study was underpowered to detect a difference in the primary endpoint. In prespecified secondary endpoint analyses, ranolazine administration was associated with a significant reduction in recurrent VT or VF requiring ICD therapy without evidence for increased mortality. (Ranolazine Implantable Cardioverter-Defibrillator Trial [RAID]; NCT01215253)., (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
40. Use of Evidence-Based Therapy for Cardiovascular Risk Factors in Canadian Outpatients With Atrial Fibrillation: From the Facilitating Review and Education to Optimize Stroke Prevention in Atrial Fibrillation (FREEDOM AF) and Co-ordinated National Network to Engage Physicians in the Care and Treatment of Patients With Atrial Fibrillation (CONNECT AF).
- Author
-
Silberberg A, Tan MK, Yan AT, Angaran P, Dorian P, Bucci C, Gregoire JC, Bell AD, Gladstone DJ, Green MS, Gross PL, Skanes A, Demchuk AM, Kerr CR, Mitchell LB, Cox JL, Talajic M, Essebag V, Heilbron B, Ramanathan K, Fournier C, Wheeler BH, Lin PJ, Berall M, Langer A, Goldin L, and Goodman SG
- Subjects
- Aged, Atrial Fibrillation complications, Canada epidemiology, Clinical Competence, Female, Humans, Incidence, Male, Physicians, Primary Care standards, Program Evaluation, Registries, Risk Factors, Stroke epidemiology, Stroke etiology, Atrial Fibrillation therapy, Evidence-Based Medicine standards, Outpatients, Physicians, Primary Care education, Practice Guidelines as Topic, Risk Assessment, Stroke prevention & control
- Abstract
Using data collected from 2 national atrial fibrillation (AF) primary care physician chart audits (Facilitating Review and Education to Optimize Stroke Prevention in Atrial Fibrillation [FREEDOM AF] and Co-ordinated National Network to Engage Physicians in the Care and Treatment of Patients With Atrial Fibrillation [CONNECT AF]), we evaluated the frequency of, and factors associated with, the use of cardiovascular (CV) evidence-based therapies in Canadian AF outpatients with at least 1 CV risk factor or co-morbidity. Of the 11,264 patients enrolled, 9,495 (84.3%) were eligible for one or more CV evidence-based therapies. The proportions of patients with AF receiving all eligible guideline-recommended therapies were 40.8% of patients with coronary artery disease, 48.9% of patients with diabetes mellitus, 40.2% of patients with heart failure, 96.7% of patients with hypertension, and 55.1% of patients with peripheral arterial disease. Factors that were independently associated with nonreceipt of all indicated evidence-based therapies included sinus rhythm rather than AF at baseline and liver disease. In conclusion, although most Canadian outpatients with AF have CV risk factors or co-morbidities, a substantial portion of these patients did not receive all guideline-recommended therapies. These findings suggest that there is an opportunity to improve the quality of care for patients with AF in Canada., (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
41. A unique form of a brady-tachy syndrome.
- Author
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Ilhan E, Quinn FR, Exner DV, Mitchell LB, and Veenhuyzen GD
- Subjects
- Aged, Humans, Male, Syndrome, Bradycardia diagnosis, Tachycardia diagnosis
- Published
- 2017
- Full Text
- View/download PDF
42. 2016 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
- Author
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Macle L, Cairns J, Leblanc K, Tsang T, Skanes A, Cox JL, Healey JS, Bell A, Pilote L, Andrade JG, Mitchell LB, Atzema C, Gladstone D, Sharma M, Verma S, Connolly S, Dorian P, Parkash R, Talajic M, Nattel S, and Verma A
- Subjects
- Acute Coronary Syndrome therapy, Algorithms, Anticoagulants therapeutic use, Atrial Appendage surgery, Atrial Fibrillation complications, Cardiac Pacing, Artificial, Cardiotonic Agents administration & dosage, Cardiotonic Agents adverse effects, Catheter Ablation, Coronary Artery Disease complications, Digoxin administration & dosage, Digoxin adverse effects, Drug Therapy, Combination, Factor Xa Inhibitors therapeutic use, Fibrinolytic Agents therapeutic use, Hemorrhage chemically induced, Hemorrhage prevention & control, Humans, Magnesium therapeutic use, Percutaneous Coronary Intervention, Platelet Aggregation Inhibitors therapeutic use, Postoperative Complications prevention & control, ST Elevation Myocardial Infarction therapy, Stroke prevention & control, Atrial Fibrillation therapy
- Abstract
The Canadian Cardiovascular Society (CCS) Atrial Fibrillation (AF) Guidelines Committee provides periodic reviews of new data to produce focused updates that address clinically important advances in AF management. This 2016 Focused Update deals with: (1) the management of antithrombotic therapy for AF patients in the context of the various clinical presentations of coronary artery disease; (2) real-life data with non-vitamin K antagonist oral anticoagulants; (3) the use of antidotes for the reversal of non-vitamin K antagonist oral anticoagulants; (4) digoxin as a rate control agent; (5) perioperative anticoagulation management; and (6) AF surgical therapy including the prevention and treatment of AF after cardiac surgery. The recommendations were developed with the same methodology used for the initial 2010 guidelines and the 2012 and 2014 Focused Updates. Using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) standards, individual studies and literature were reviewed for quality and bias; the literature review process and evidence tables are included in the Supplementary Material, and on the CCS Web site. The section on concomitant AF and coronary artery disease was developed in collaboration with the CCS Antiplatelet Guidelines Committee. Details of the updated recommendations are presented, along with their background and rationale. This document is linked to an updated summary of all CCS AF Guidelines recommendations, from 2010 to the present 2016 Focused Update., (Copyright © 2016. Published by Elsevier Inc.)
- Published
- 2016
- Full Text
- View/download PDF
43. The Risk Stratification and Stroke Prevention Therapy Care Gap in Canadian Atrial Fibrillation Patients.
- Author
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Angaran P, Dorian P, Tan MK, Kerr CR, Green MS, Gladstone DJ, Mitchell LB, Fournier C, Cox JL, Talajic M, Lin PJ, Langer A, Goldin L, and Goodman SG
- Subjects
- Aged, Aged, 80 and over, Canada epidemiology, Female, Humans, Incidence, Male, Prognosis, Risk Factors, Stroke epidemiology, Stroke etiology, Survival Rate trends, Anticoagulants therapeutic use, Atrial Fibrillation complications, Patient Education as Topic, Risk Assessment, Stroke prevention & control
- Abstract
Background: Canadian atrial fibrillation (AF) guidelines recommend that all AF patients be risk stratified with respect to stroke and bleeding, and that most should receive antithrombotic therapy., Methods: As part of the Canadian Facilitating Review and Education to Optimize Stroke Prevention in Atrial Fibrillation (FREEDOM AF) chart audit, data were collected on 4670 patients ≥ 18 years old without significant valvular heart disease from the primary care practices of 474 physicians (February to September, 2011)., Results: Physicians did not provide an estimate of stroke and bleeding risk in 15% and 25% of patients, respectively. When risks were provided, they were on the basis of a predictive stroke and bleeding risk index in only 50% and 26% of patients, respectively. There were over- and underestimation of stroke and bleeding risk in a large proportion of patients. Antithrombotic therapy included warfarin (90%); 24% of patients had a time in the therapeutic range (TTR) < 50%, 9% between 50% and 60%, 11% between 60% and 70%, and 56% had a TTR ≥ 70%., Conclusions: In a large Canadian AF population, primary care physicians did not provide a stroke or bleeding risk in a substantial proportion of their AF patients. When estimates were provided, they were on the basis of a predictive stroke and bleeding risk index in less than half of the patients. Furthermore, there was under- and overestimation of stroke and bleeding risk in a substantial proportion of patients. As many as 1 in 3 patients receiving warfarin have their TTR < 60%. These findings suggest an opportunity to enhance knowledge translation to primary care physicians., (Copyright © 2016 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
44. Molecular Differentiation of the African Yellow Fever Vector Aedes bromeliae (Diptera: Culicidae) from Its Sympatric Non-vector Sister Species, Aedes lilii.
- Author
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Bennett KL, Linton YM, Shija F, Kaddumukasa M, Djouaka R, Misinzo G, Lutwama J, Huang YM, Mitchell LB, Richards M, Tossou E, and Walton C
- Subjects
- Animals, Benin, Cluster Analysis, DNA, Ribosomal Spacer chemistry, DNA, Ribosomal Spacer genetics, Ecosystem, Humans, Insect Proteins genetics, Molecular Sequence Data, Phylogeography, Sequence Analysis, DNA, Tanzania, Uganda, Yellow Fever transmission, Aedes classification, Aedes genetics, Entomology methods, Insect Vectors, Polymerase Chain Reaction methods
- Abstract
Introduction: Yellow fever continues to be a problem in sub-Saharan Africa with repeated epidemics occurring. The mosquito Aedes bromeliae is a major vector of yellow fever, but it cannot be readily differentiated from its non-vector zoophilic sister species Ae. lilii using morphological characters. Genetic differences have been reported between anthropophilic Ae. bromeliae and zoophilic Ae. lilii and between forest and domestic populations. However, due to the application of different molecular markers and non-overlapping populations employed in previous studies, interpretation of species delimitation is unclear., Methodology/principle Findings: DNA sequences were generated from specimens of Ae. simpsoni s.l. from the Republic of Benin, Tanzania and Uganda for two nuclear genes apolipophorin 2 (apoLp2) and cytochrome p450 (CYPJ92), the ribosomal internal transcribed spacer region (ITS) and the mitochondrial cytochrome c oxidase (COI) barcoding region. Nuclear genes apoLp2 and CYPJ92 were unable to differentiate between species Ae. bromeliae and Ae. lilii due to ancestral lineage sorting, while ITS sequence data provided clear topological separation on a phylogeny. The standard COI barcoding region was shown to be subject to species introgression and unable to clearly distinguish the two taxa. Here we present a reliable direct PCR-based method for differentiation of the vector species Ae. bromeliae from its isomorphic, sympatric and non-biomedically important sister taxon, Ae. lilii, based on the ITS region. Using molecular species verification, we describe novel immature habitats for Ae. lilii and report both sympatric and allopatric populations. Whereas only Ae. lilii is found in the Republic of Benin and only Ae. bromeliae in Tanzania, both species are sympatric in Uganda., Conclusions/significance: Our accurate identification method will allow informed distribution and detailed ecological studies that will facilitate assessment of arboviral disease risk and development of future targeted vector control.
- Published
- 2015
- Full Text
- View/download PDF
45. The 2014 Atrial Fibrillation Guidelines Companion: A Practical Approach to the Use of the Canadian Cardiovascular Society Guidelines.
- Author
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Macle L, Cairns JA, Andrade JG, Mitchell LB, Nattel S, and Verma A
- Subjects
- Algorithms, Canada, Humans, Risk Assessment, Risk Factors, Anticoagulants classification, Anticoagulants therapeutic use, Atrial Fibrillation complications, Atrial Fibrillation diagnosis, Atrial Fibrillation therapy, Cardiology, Societies, Medical, Stroke etiology, Stroke prevention & control
- Abstract
The Canadian Cardiovascular Society (CCS) Atrial Fibrillation Guidelines Program has generated a comprehensive series of documents regarding the management of atrial fibrillation (AF) between 2010 and 2014. The guidelines provide evidence-based consensus management recommendations in a broad range of areas. These guidelines have proven useful in informing clinical practice, but often lack detail in specifications related to practical application, particularly for areas in which the evidence base is limited or conflicting. Based on feedback from the community, the CCS Atrial Fibrillation Guidelines Committee has identified a number of areas that require clarification to address commonly asked practical questions related to guidelines application. In the present article a number of such questions are presented and suggestions about how they can be answered are suggested. Among the issues considered are: (1) What duration of AF is clinically significant? (2) How are the risk factors in the CCS Algorithm for selecting anticoagulation therapy derived and defined? (3) How is valvular heart disease defined and how do different forms of valve disease affect the choice of anticoagulant therapy for AF patients? (4) How should we quantify renal dysfunction and how does it affect therapeutic choices? The response to these questions and the underlying logic are provided, along with an indication of future research needed where no specific approach can presently be recommended based on the literature., (Copyright © 2015 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
46. Sudden cardiac death.
- Author
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Kuriachan VP, Sumner GL, and Mitchell LB
- Subjects
- Arrhythmias, Cardiac complications, Death, Sudden, Cardiac epidemiology, Death, Sudden, Cardiac prevention & control, Defibrillators, Implantable, Female, Heart Defects, Congenital complications, Humans, Myocardial Ischemia complications, Nervous System Diseases complications, Pregnancy, Pregnancy Complications, Cardiovascular, Risk Factors, Sports Medicine, Death, Sudden, Cardiac etiology
- Abstract
Sudden death accounts for 300,000-400,000 deaths annually in the United States. Most sudden deaths are cardiac, and most sudden cardiac deaths are related to arrhythmias secondary to structural heart disease or primary electrical abnormalities of the heart. The most common structural disease leading to sudden death is ischemic heart disease. Nonischemic cardiomyopathy and other structural abnormalities such as arrhythmogenic ventricular dysplasia and hypertrophic cardiomyopathy may also be causative. Patients without structural disease have a primary electrical abnormality, such as long-QT syndrome or Brugada syndrome. Severe left ventricular systolic dysfunction is the main marker for sudden death in patients with ischemic or nonischemic cardiomyopathy. In other conditions, other markers for structural heart disease and electrical abnormalities need to be considered. It is seen that β-blocker therapy is associated with a reduction in sudden cardiac death across a broad range of disorders. Nevertheless, the implantable cardioverter defibrillator remains the most effective treatment strategy in selected patients., (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
47. The new Canadian Cardiovascular Society algorithm for antithrombotic therapy of atrial fibrillation is appropriately based on current epidemiologic data.
- Author
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Cairns JA, Healey JS, Macle L, Mitchell LB, and Verma A
- Subjects
- Female, Humans, Male, Algorithms, Anticoagulants pharmacology, Atrial Fibrillation therapy, Brain Ischemia prevention & control, Practice Guidelines as Topic, Risk Assessment methods, Societies, Medical
- Published
- 2015
- Full Text
- View/download PDF
48. Prediction of stroke or TIA in patients without atrial fibrillation using CHADS2 and CHA2DS2-VASc scores.
- Author
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Mitchell LB, Southern DA, Galbraith D, Ghali WA, Knudtson M, and Wilton SB
- Subjects
- Acute Coronary Syndrome epidemiology, Acute Coronary Syndrome therapy, Age Factors, Aged, Canada epidemiology, Comorbidity, Decision Support Techniques, Female, Follow-Up Studies, Humans, Male, Middle Aged, Mortality, Outcome Assessment, Health Care, Platelet Aggregation Inhibitors therapeutic use, Propensity Score, Research Design standards, Risk Assessment methods, Risk Assessment standards, Sex Factors, Acute Coronary Syndrome complications, Diabetes Mellitus epidemiology, Ischemic Attack, Transient epidemiology, Ischemic Attack, Transient etiology, Ischemic Attack, Transient prevention & control, Stroke epidemiology, Stroke etiology, Stroke prevention & control
- Abstract
Objectives: To determine the accuracy of CHADS2 and CHA2DS2-VASc tools for predicting ischaemic stroke or transient ischaemic attack (TIA) and death in patients without a history of atrial fibrillation or flutter (AF)., Methods: The study included 20 970 patients without known AF enrolled in the Alberta Provincial Project for Outcomes Assessment in Coronary Heart disease (APPROACH) prospective registry who were discharged after an acute coronary syndrome (ACS) between 2005 and 2011. The outcome measures were incident ischaemic stroke, TIA or death from any cause., Results: Over a median follow-up of 4.1 years, 453 patients (2.2%) had a stroke (n=297) or TIA (n=156) and 1903 (9.0%) died. The incidence of stroke or TIA increased with increases in each risk score (p<0.001), with an absolute annual incidence ≥1% with CHADS2 ≥3 or CHA2DS2-VASc ≥4. Both CHADS2 and CHA2DS2-VASc scores had acceptable discrimination performance (C-statistic=0.68 and 0.71, respectively). The mortality rate was also greater in patients with higher CHADS2 and CHA2DS2-VASc scores (p<0.0001)., Conclusions: In patients with ACS but no AF, the CHADS2 and CHA2DS2-VASc scores predict ischaemic stroke/TIA events with similar accuracy to that observed in historical populations with non-valvular AF, but with lower absolute event rates. Further study of the utility of the CHADS2 and CHA2DS2-VASc scores for the assessment of thromboembolic risk and selection of antithrombotic therapy in patients without AF is warranted., (Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.)
- Published
- 2014
- Full Text
- View/download PDF
49. 2014 focused update of the Canadian Cardiovascular Society Guidelines for the management of atrial fibrillation.
- Author
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Verma A, Cairns JA, Mitchell LB, Macle L, Stiell IG, Gladstone D, McMurtry MS, Connolly S, Cox JL, Dorian P, Ivers N, Leblanc K, Nattel S, and Healey JS
- Subjects
- Algorithms, Anticoagulants therapeutic use, Antithrombins administration & dosage, Aspirin administration & dosage, Atrial Fibrillation epidemiology, Benzimidazoles administration & dosage, Canada, Clopidogrel, Comorbidity, Dabigatran, Electric Countershock, Humans, Renal Insufficiency, Chronic epidemiology, Risk Assessment, Stroke epidemiology, Stroke prevention & control, Ticlopidine administration & dosage, Ticlopidine analogs & derivatives, beta-Alanine administration & dosage, beta-Alanine analogs & derivatives, Atrial Fibrillation therapy
- Abstract
Atrial fibrillation (AF) is an extremely common clinical problem with an important population morbidity and mortality burden. The management of AF is complex and fraught with many uncertain and contentious issues, which are being addressed by extensive ongoing basic and clinical research. The Canadian Cardiovascular Society AF Guidelines Committee produced an extensive set of evidence-based AF management guidelines in 2010 and updated them in the areas of anticoagulation and rate/rhythm control in 2012. In late 2013, the committee judged that sufficient new information regarding AF management had become available since 2012 to warrant an update to the Canadian Cardiovascular Society AF Guidelines. After extensive evaluation of the new evidence, the committee has updated the guidelines for: (1) stroke prevention principles; (2) anticoagulation of AF patients with chronic kidney disease; (3) detection of AF in patients with stroke; (4) investigation and management of subclinical AF; (5) left atrial appendage closure in stroke prevention; (6) emergency department management of AF; (7) periprocedural anticoagulation management; and (8) rate and rhythm control including catheter ablation. This report presents the details of the updated recommendations, along with their background and rationale. In addition, a complete set of presently applicable recommendations, those that have been updated and those that remain in force from previous guideline versions, is provided in the Supplementary Material., (Copyright © 2014 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2014
- Full Text
- View/download PDF
50. Mosquitoes of eastern Amazonian Ecuador: biodiversity, bionomics and barcodes.
- Author
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Linton YM, Pecor JE, Porter CH, Mitchell LB, Garzón-Moreno A, Foley DH, Pecor DB, and Wilkerson RC
- Subjects
- Animals, Ecuador, Oviposition, Polymerase Chain Reaction, Rainforest, Biodiversity, Culicidae classification, Culicidae genetics, DNA Barcoding, Taxonomic methods, Ecology classification, Electron Transport Complex IV genetics
- Abstract
Two snapshot surveys to establish the diversity and ecological preferences of mosquitoes (Diptera: Culicidae) in the terra firme primary rain forest surrounding the Tiputini Biodiversity Station in the UNESCO Yasuní Biosphere Reserve of eastern Amazonian Ecuador were carried out in November 1998 and May 1999. The mosquito fauna of this region is poorly known; the focus of this study was to obtain high quality link-reared specimens that could be used to unequivocally confirm species level diversity through integrated systematic study of all life stages and DNA sequences. A total of 2,284 specimens were preserved; 1,671 specimens were link-reared with associated immature exuviae, all but 108 of which are slide mounted. This study identified 68 unique taxa belonging to 17 genera and 27 subgenera. Of these, 12 are new to science and 37 comprise new country records. DNA barcodes [658-bp of the mtDNA cytochrome c oxidase (COI) I gene] are presented for 58 individuals representing 20 species and nine genera. DNA barcoding proved useful in uncovering and confirming new species and we advocate an integrated systematics approach to biodiversity studies in future. Associated bionomics of all species collected are discussed. An updated systematic checklist of the mosquitoes of Ecuador (n=179) is presented for the first time in 60 years.
- Published
- 2013
- Full Text
- View/download PDF
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