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Response surface modeling of the interaction between propofol and sevoflurane.

机译:异丙酚与七氟醚之间相互作用的响应面建模。

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BACKGROUND: Propofol and sevoflurane display additivity for gamma-aminobutyric acid receptor activation, loss of consciousness, and tolerance of skin incision. Information about their interaction regarding electroencephalographic suppression is unavailable. This study examined this interaction as well as the interaction on the probability of tolerance of shake and shout and three noxious stimulations by using a response surface methodology. METHODS: Sixty patients preoperatively received different combined concentrations of propofol (0-12 microg/ml) and sevoflurane (0-3.5 vol.%) according to a crisscross design (274 concentration pairs, 3 to 6 per patient). After having reached pseudo-steady state, the authors recorded bispectral index, state and response entropy and the response to shake and shout, tetanic stimulation, laryngeal mask airway insertion, and laryngoscopy. For the analysis of the probability of tolerance by logistic regression, a Greco interaction model was used. For the separate analysis of bispectral index, state and response entropy suppression, a fractional Emax Greco model was used. All calculations were performed with NONMEM V (GloboMax LLC, Hanover, MD). RESULTS: Additivity was found for all endpoints, the Ce(50, PROP)/Ce(50, SEVO) for bispectral index suppression was 3.68 microg. ml(-1)/ 1.53 vol.%, for tolerance of shake and shout 2.34 microg . ml(-1)/ 1.03 vol.%, tetanic stimulation 5.34 microg . ml(-1)/ 2.11 vol.%, laryngeal mask airway insertion 5.92 microg. ml(-1) / 2.55 vol.%, and laryngoscopy 6.55 microg. ml(-1)/2.83 vol.%. CONCLUSION: For both electroencephalographic suppression and tolerance to stimulation, the interaction of propofol and sevoflurane was identified as additive. The response surface data can be used for more rational dose finding in case of sequential and coadministration of propofol and sevoflurane.
机译:背景:丙泊酚和七氟醚显示对γ-氨基丁酸受体激活,意识丧失和皮肤切口耐受性具有可加性。无法获得有关其与脑电图抑制有关的相互作用的信息。这项研究通过使用响应面方法研究了这种相互作用以及对震动和呼喊以及三种有害刺激的耐受性的相互作用。方法:六十名患者根据交叉设计(274个浓度对,每位患者3至6个)接受了不同浓度的丙泊酚(0-12微克/毫升)和七氟醚(0-3.5体积%)的合并治疗。在达到伪稳态后,作者记录了双谱指数,状态和反应熵以及对震动和呼喊,强直刺激,喉罩气道插入和喉镜检查的反应。为了通过逻辑回归分析耐受性的可能性,使用了Greco相互作用模型。为了分别分析双谱指数,状态和响应熵抑制,使用了分数Emax Greco模型。所有计算均使用NONMEM V(GloboMax LLC,汉诺威,马里兰州)进行。结果:发现所有端点的可加性,用于抑制双光谱指数的Ce(50,PROP)/ Ce(50,SEVO)为3.68微克。 ml(-1)/ 1.53%(体积),可承受2.34微克的震动和吼叫声。 ml(-1)/1.03体积%,强直性刺激5.34微克。 ml(-1)/ 2.11 vol。%,喉罩气道插入5.92 microg。 ml(-1)/2.55 vol。%,喉镜检查6.55 microg。 ml(-1)/2.83体积%。结论:对于脑电图抑制和刺激耐受,丙泊酚和七氟醚的相互作用被确定为可加性作用。如果先后并用丙泊酚和七氟醚,则可以将响应表面数据用于更合理的剂量查找。

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