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- W2780373756 abstract "Objective – to evaluate the efficacy and safety of dexmedetomidine, propofol, and their combination for sedation of patients with alcohol drawalsyn drome in the intensive care unit.Materials and Methods. The study included 210 patients, which were assigned in four groups – group of dexmedetomidine , propofol, dexmedetomidine and propofol and control group. Duration of stay in the intensive care unit was 51h [46– 75], 68 h [48 –98], 68h [48–78] and 92h [70–102 ].Results. Diazepam consumption and the number of patients, who required haloperidol, were less and sedation quality and patients communication were better in study groups compared with the control group.Conclusion. Dexmedetomidine, propofol, and their combination are effective and safe for patients with alcohol drawal syndrome in the intensive care unit." @default.
- W2780373756 created "2018-01-05" @default.
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- W2780373756 date "2015-12-11" @default.
- W2780373756 modified "2023-09-25" @default.
- W2780373756 title "Dexmedetomidine, propofol and their combination for sedation o f patients with alcohol drawal syndrome in the intensive care unit: prospective controlled study" @default.
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- W2780373756 doi "https://doi.org/10.25284/2519-2078.4(73).2015.84129" @default.
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