Dexmedetomidine: pediatric pharmacology, clinical uses and safety

被引:79
作者
Su, Felice [1 ]
Hammer, Gregory B. [2 ,3 ]
机构
[1] Stanford Univ, Div Crit Care Med, Dept Pediat, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
关键词
alpha(2)-agonist; adverse effects; dexmedetomidine; indications; pediatrics; sedation; INTENSIVE-CARE-UNIT; DOSE DEXMEDETOMIDINE; CARDIAC-SURGERY; ALPHA(2A)-ADRENERGIC RECEPTOR; HYPNOTIC RESPONSE; INTRAVENOUS DEXMEDETOMIDINE; AGONIST DEXMEDETOMIDINE; INFLAMMATORY RESPONSES; SEVOFLURANE ANESTHESIA; PROCEDURAL SEDATION;
D O I
10.1517/14740338.2010.512609
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Importance of the field: Dexmedetomidine is an alpha(2)-adrenoceptor agonist with sedative, anxiolytic and analgesic properties. It is used off-label in pediatric patients due to its efficacy and lack of adverse respiratory effects. Dexmedetomidine may cause severe circulatory complications in adults. Despite its popularity, the safety of dexmedetomidine in the pediatric population has not been extensively studied. Areas covered in this review: This article reviews the current literature (up to 2010) focusing on applications and safety of dexmedetomidine administered to pediatric patients. What the reader will gain: Dexmedetomidine is a useful sedative and anxiolytic drug in the pediatric intensive care unit as well as during diagnostic and therapeutic procedures. Deleterious effects of dexmedetomidine include hypotension and bradycardia. Additionally, hypertension may occur during the "loading dose" or with high infusion rates. Few studies have been performed to evaluate the safety of dexmedetomidine in pediatrics. The development of tolerance and withdrawal has not been studied in children. Take home message: Despite its favorable respiratory profile, dexmedetomidine may cause deleterious cardiovascular effects. Close monitoring of circulatory dynamics and judicious titration is recommended. Further studies are needed to better define adverse effects following long-term infusions as well as in special populations such as pre-term infants.
引用
收藏
页码:55 / 66
页数:12
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