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efecto cardiovascular en target (estudio de 12 meses) la variable cardiovascular (cv) principal estudiada fue la variable aptc de « antiplatelet trialists'collaboration »: infarto de miocardio confirmado o probable (sintomático o silente) , accidente cerebrovascular (isquémico o hemorrágico) y muerte cv.no hubo diferencias significativas entre
cardiovascular effect in target (12-month study) the primary cardiovascular (cv) endpoint studied was the antiplatelet trialists'collaboration (aptc) endpoint: confirmed or probable myocardial infarction (clinical or silent) , stroke (ischemic or haemorrhagic) and cv death.
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