2009
DOI: 10.1001/jama.2009.56
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Dexmedetomidine vs Midazolam for Sedation of Critically Ill Patients<subtitle>A Randomized Trial</subtitle>

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Cited by 1,419 publications
(985 citation statements)
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References 44 publications
(38 reference statements)
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“…The current PRE-DELIRIC model may require on-going validation as new therapies and interventions emerge. For example, the use of new sedatives or analgesics may affect the development of delirium [33][34][35] and consequently could affect the performance of the model. Different risk factors may emerge in the future that may need to be investigated and included in the current PRE-DELIRIC model.…”
Section: Discussionmentioning
confidence: 99%
“…The current PRE-DELIRIC model may require on-going validation as new therapies and interventions emerge. For example, the use of new sedatives or analgesics may affect the development of delirium [33][34][35] and consequently could affect the performance of the model. Different risk factors may emerge in the future that may need to be investigated and included in the current PRE-DELIRIC model.…”
Section: Discussionmentioning
confidence: 99%
“…Whereas there was no diff erence in the primary outcome, patients in the dexmedetomidine group had a lower prevalence of delirium and a larger number of delirium-free days. In addition, patients sedated with dexmede tomi dine had a shorter time to extubation [36].…”
Section: Comparative Trialsmentioning
confidence: 94%
“…Had lighter or 'cooperative' sedation goals been achieved (closer to 0 to -1), the incidence of drug-induced coma would likely have been less (particularly with lorazepam), and results may have diff ered. Another recent randomized, double-blind trial, the Safety and Effi cacy of Dexmedetomidine Compared with Midazolam (SEDCOM) trial, compared midazolam to dexmedetomidine [36], requiring daily awakening trials and a targeted RASS score of -2 to +1. Th e primary outcome was percent time within RASS goal and secondary outcomes included assessment of delirium, duration of mechanical ventilation and ICU LOS.…”
Section: Comparative Trialsmentioning
confidence: 99%
“…The ideal sedative agent should be fast acting, have a rapid onset, not be organ dependent in terms of degradation, not have metabolically active or toxic by-products, have little cardiovascular effects, and be cheap. Over the last 30 years, midazolam, propofol [9], and dexmedetomidine [10,11] have been rolled out with the promise of being better than the previous generation of drugs.Sedation management in the ICU is a complex process involving sedation level assessment, medication administration, and an overall strategy. These three components are essential for correct ICU sedation.…”
mentioning
confidence: 99%