Closed-loop Continuous Infusions of Etomidate and Etomidate Analogs in Rats A Comparative Study of Dosing and the Impact on Adrenocortical Function

被引:43
作者
Cotten, Joseph F. [1 ,2 ]
Le Ge, Ri [2 ]
Banacos, Natalie [2 ]
Pejo, Ervin [2 ]
Husain, S. Shaukat [1 ,2 ]
Williams, James H. [1 ,2 ]
Raines, Douglas E. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Boston, MA USA
[2] Massachusetts Gen Hosp, Dept Anesthesia Crit Care & Pain Med, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
CRITICALLY-ILL PATIENTS; LOW-DOSE ETOMIDATE; CUSHINGS-SYNDROME; REMIFENTANIL GI87084B; ANESTHESIA; INDUCTION; PHARMACOKINETICS; RESPONSES; HYPERCORTISOLEMIA; SUPPRESSION;
D O I
10.1097/ALN.0b013e31821950de
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Background: Etomidate is a sedative-hypnotic that is often given as a single intravenous bolus but rarely as an infusion because it suppresses adrenocortical function. Methoxycarbonyl etomidate and (R)-ethyl 1-(1-phenylethyl)-1H-pyrrole-2-carboxylate (carboetomidate) are etomidate analogs that do not produce significant adrenocortical suppression when given as a single bolus. However, the effects of continuous infusions on adrenocortical function are unknown. In this study, we compared the effects of continuous infusions of etomidate, methoxycarbonyl etomidate, and carboetomidate on adrenocortical function in a rat model. Methods: A closed-loop system using the electroencephalo-graphic burst suppression ratio as the feedback was used to administer continuous infusions of etomidate, methoxycarbonyl etomidate, or carboetomidate to Sprague-Dawley rats. Adrenocortical function was assessed during and after infusion by repetitively administering adrenocorticotropic hormone 1-24 and measuring serum corticosterone concentrations every 30 min. Results: The sedative-hypnotic doses required to maintain a 40% burst suppression ratio in the presence of isoflurane, 1%, and the rate of burst suppression ratio recovery on infusion termination varied (methoxycarbonyl etomidate > carboetomidate > etomidate). Serum corticosterone concentrations were reduced by 85% and 56% during 30-min infusions of etomidate and methoxycarbonyl etomidate, respectively. On infusion termination, serum corticosterone concentrations recovered within 30 min with methoxycarbonyl etomidate but persisted beyond an hour with etomidate. Carboetomidate had no effect on serum corticosterone concentrations during or after continuous infusion. Conclusions: Our results suggest that methoxycarbonyl etomidate and carboetomidate may have clinical utility as sedative-hypnotic maintenance agents when hemodynamic stability is desirable.
引用
收藏
页码:764 / 773
页数:10
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