Dexmedetomidine versus propofol/midazolam for long-term sedation during mechanical ventilation

Purpose To compare dexmedetomidine (DEX) with standard care (SC, either propofol or midazolam) for long-term sedation in terms of maintaining target sedation and length of intensive care unit (ICU) stay. Methods A pilot, phase III, double-blind multicenter study in randomized medical and surgical pa...

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Veröffentlicht in:Intensive care medicine 2009-02, Vol.35 (2), p.282-290
Hauptverfasser: Ruokonen, Esko, Parviainen, Ilkka, Jakob, Stephan M., Nunes, Silvia, Kaukonen, Maija, Shepherd, Stephen T., Sarapohja, Toni, Bratty, J. Raymond, Takala, Jukka
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Sprache:eng
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Zusammenfassung:Purpose To compare dexmedetomidine (DEX) with standard care (SC, either propofol or midazolam) for long-term sedation in terms of maintaining target sedation and length of intensive care unit (ICU) stay. Methods A pilot, phase III, double-blind multicenter study in randomized medical and surgical patients ( n  = 85) within the first 72 h of ICU stay with an expected ICU stay of ≥48 h and sedation need for ≥24 h after randomization. Patients were assigned to either DEX (≤1.4 μg kg −1  h −1 ; n  = 41) or SC ( n  = 44), with daily sedation stops. Results Non-inferiority of DEX versus SC was not confirmed. Target Richmond agitation–sedation score (RASS) was reached a median of 64% (DEX) and 63% (SC) of the sedation time (ns). The length of ICU stay was similar in DEX and SC. Patients with RASS target 0–3 (DEX 78%, SC 80%) were at target sedation 74% (DEX) and 64% (SC) of the time (ns), whereas those with RASS target −4 or less reached the target 42% (DEX) and 62% (SC) of the time ( P  = .006). Post hoc analyses suggested shorter duration of mechanical ventilation for DEX ( P  = 0.025). Conclusions This pilot study suggests that in long-term sedation, DEX is comparable to SC in maintaining sedation targets of RASS 0 to −3 but not suitable for deep sedation (RASS −4 or less). DEX had no effect on length of ICU stay. Its effects on other relevant clinical outcomes, such as duration of mechanical ventilation, should be tested further.
ISSN:0342-4642
1432-1238
DOI:10.1007/s00134-008-1296-0