Literature DB >> 1552108

The Cardiac Arrhythmia Suppression Trial: first CAST ... then CAST-II.

H L Greene1, D M Roden, R J Katz, R L Woosley, D M Salerno, R W Henthorn.   

Abstract

The Cardiac Arrhythmia Suppression Trial (CAST) was a study designed to test the hypothesis that suppression of ventricular premature complexes after a myocardial infarction would improve survival. Preliminary results showed that suppression of ventricular premature complexes with encainide and flecainide worsened survival, and the CAST continued as the CAST-II with moricizine compared with its placebo. The protocol for the CAST-II was changed to attempt to enroll patients more likely to experience serious arrhythmias. The enrollment time was narrowed to 4 to 90 days after myocardial infarction; the qualifying ejection fraction was lowered to less than or equal to 0.40; a higher dose of moricizine could be used; early titration itself was double-blind with a placebo, and the definition of disqualifying ventricular tachycardia was changed to allow patients with more serious arrhythmias to be entered into the trial. The Cardiac Arrhythmia Suppression Trial-II was subsequently terminated prematurely because 1) patients treated with moricizine had an excessive cardiac mortality rate during the 1st 2 weeks of exposure to the drug, and 2) there appeared to be little chance of showing a long-term survival benefit from treatment with moricizine. This report outlines the rationale behind the Cardiac Arrhythmia Suppression Trial and the reasons for selection of the drugs used in the CAST and CAST-II.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1552108     DOI: 10.1016/0735-1097(92)90267-q

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  23 in total

1.  Decision support and safety of clinical environments.

Authors:  A H Morris
Journal:  Qual Saf Health Care       Date:  2002-03

Review 2.  Subclassification of class I antiarrhythmic drugs: enhanced relevance after CAST.

Authors:  T J Campbell
Journal:  Cardiovasc Drugs Ther       Date:  1992-10       Impact factor: 3.727

Review 3.  Depression and myocardial infarction. Implications for medical prognosis and options for treatment.

Authors:  T J Cleophas
Journal:  Drugs Aging       Date:  1997-08       Impact factor: 3.923

4.  A computational model to predict the effects of class I anti-arrhythmic drugs on ventricular rhythms.

Authors:  Jonathan D Moreno; Z Iris Zhu; Pei-Chi Yang; John R Bankston; Mao-Tsuen Jeng; Chaoyi Kang; Lianguo Wang; Jason D Bayer; David J Christini; Natalia A Trayanova; Crystal M Ripplinger; Robert S Kass; Colleen E Clancy
Journal:  Sci Transl Med       Date:  2011-08-31       Impact factor: 17.956

5.  Ranolazine for Atrial Fibrillation: Too Good to be True?

Authors:  Joseph J Gard; Samuel J Asirvatham
Journal:  J Atr Fibrillation       Date:  2010-08-23

6.  Note on a possible proarrhythmic property of antiarrhythmic drugs aimed at improving gap-junction coupling.

Authors:  Aslak Tveito; Glenn Terje Lines; Mary M Maleckar
Journal:  Biophys J       Date:  2012-01-18       Impact factor: 4.033

7.  In vitro cardiovascular effects of dihydroartemisin-piperaquine combination compared with other antimalarials.

Authors:  Franco Borsini; William Crumb; Silvia Pace; David Ubben; Barb Wible; Gan-Xin Yan; Christian Funck-Brentano
Journal:  Antimicrob Agents Chemother       Date:  2012-03-05       Impact factor: 5.191

Review 8.  Recent advances in cardiology.

Authors:  C S Lawson; D J Coltart
Journal:  Postgrad Med J       Date:  1994-04       Impact factor: 2.401

9.  Limitations of medical research and evidence at the patient-clinician encounter scale.

Authors:  Alan H Morris; John P A Ioannidis
Journal:  Chest       Date:  2013-04       Impact factor: 9.410

Review 10.  Pathophysiology of the cardiac late Na current and its potential as a drug target.

Authors:  Jonathan D Moreno; Colleen E Clancy
Journal:  J Mol Cell Cardiol       Date:  2011-12-16       Impact factor: 5.000

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.