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      Natural history of "high-risk" bundle-branch block: final report of a prospective study.

      The New England journal of medicine

      Aged, Arrhythmias, Cardiac, complications, mortality, Bradycardia, Bundle-Branch Block, physiopathology, Coronary Disease, Death, Sudden, epidemiology, Electrocardiography, Electrophysiology, Female, Follow-Up Studies, Heart Block, etiology, therapy, Heart Failure, Humans, Male, Middle Aged, Pacemaker, Artificial, Prospective Studies, Risk, Syncope

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          Abstract

          We conducted a prospective study in which 554 patients with chronic bifascicular and trifascicular conduction abnormalities were followed for an average of 42.4 +/- 8.5 months. Heart block occurred in 19 patients, and 17 were successfully treated. The actuarial five-year mortality from an event that could conceivably have been a bradyarrhythmia was 6 per cent (35 per cent from all causes). Of the 160 deaths 67 (42 per cent) were sudden; most of these were not ascribable to bradyarrhythmia but to tachyarrhythmia and myocardial infarction. Mortality was higher in patients with coronary-artery disease (P less than 0.01) and congestive heart failure (P less than 0.05). Patients in whom syncope developed before or after entry into the study had a 17 per cent incidence of heart block (2 per cent in those without syncope)(P less than 0.05); however, no single variable was predictive of which patients were at high risk of death from a bradyarrhythmia. The predictors of death were increasing age, congestive heart failure, and coronary-artery disease; the predictors of sudden death were coronary-artery disease and increasing age. The risks of heart block and of death from a bradyarrhythmia are low; in most patients, heart block can be recognized and successfully treated with a pacemaker.

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          Journal
          7088050
          10.1056/NEJM198207153070301

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