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It focused on immediate changes following FDA approval and hypothesized that, although use increased, overall uptake remained substantially below the level expected if all eligible patients were treated representing a missed opportunity, particularly among those at the higher end of cardiovascular risk

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10.1186/s13018-019-1242-6 86 PetekM.SikiricP.AnicT.BuljatG.SeparovicJ.Stancic-RokotovD.et al (1999)

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