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  • 57) a riziko ischemické mrtvice bylo mezi skupinami obdobné (3/45 u atorvastatinu vs. 2/48 u placeba, poměr rizika 1,64, IS 95 %, 0,27–9,82). • Riziko hemoragické mrtvice bylo zvýšené u pacientů, kteří vstupovali do studie s lakunárním infarktem v anamnéze (20/708 u atorvastatinu vs. 4/701 u placeba, poměr rizika 4,99, IS 95 %, 1,71-14,61), avšak riziko ischemické mrtvice bylo u těchto pacientů sníženo (79/708 u atorvastatinu vs.102/701 u placeba, poměr rizika 0,76,� IS 95 %, 0,57–1,02). (cs)
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