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The principal aim of this observational study was to investigate S-Se in a selenium deficient region at time of intensive attention entry, and likewise to monitor S-Se during high-dose selenium supplementation for protection. TECHNIQUES We sized S-Se in 100 successive customers admitted to a tertiary general intensive care unit. After preliminary sampling, high-dose intravenous selenium supplementation ended up being administered as much as twenty days. OUTCOMES At entry, in 95% of this

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