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Clinical evidence in the context of muscle wasting The 2016 ESC guidelines [26] for the management of HF provided a general recommendation that “an n-3 PUFA preparation may be considered in symptomatic HF patients to reduce the risk of cardiovascular hospitalization and cardiovascular death” irrespective of the presence of sarcopenia (class of recommendation IIb, level of evidence B)
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En cas de pathologie ou en dose de « choc » : 450 à 600 mg par jour, mais ne pas dépasser 3 mois de cure
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