Abstract
The US Food and Drug Administration (FDA) first approved dexmedetomidine in December 1999 for use as a continuous infusion in post-operative ventilated patients for up to 24 hours in the intensive care unit (ICU). It is not yet approved in the European Union. Its use is currently being evaluated in a number of different situations: Longer-term use, perioperative care, anesthesia, and postoperative analgesia. This chapter will focus on its potential for intensive care patients.
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Rahman West, R., Rhodes, A., Grounds, R.M. (2009). The Role of Dexmedetomidine in Intensive Care. In: Vincent, JL. (eds) Intensive Care Medicine. Springer, New York, NY. https://doi.org/10.1007/978-0-387-92278-2_81
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DOI: https://doi.org/10.1007/978-0-387-92278-2_81
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