Male patients require higher optimal effect-site concentrations of propofol during i-gel insertion with dexmedetomidine 0.5 μg/kg

Jung Ju Choi, Ji Young Kim, Dongchul Lee, Young Jin Chang, Noo Ree Cho, Hyun Jeong Kwak, Jung Ju Choi, Ji Young Kim, Dongchul Lee, Young Jin Chang, Noo Ree Cho, Hyun Jeong Kwak

Abstract

Background: The pharmacokinetics and pharmacodynamics of an anesthetic drug may be influenced by gender. The purpose of this study was to compare effect-site half maximal effective concentrations (EC50) of propofol in male and female patients during i-gel insertion with dexmedetomidine 0.5 μg/kg without muscle relaxants.

Methods: Forty patients, aged 20-46 years of ASA physical status I or II, were allocated to one of two groups by gender (20 patients per group). After the infusion of dexmedetomidine 0.5 μg/kg over 2 min, anesthesia was induced with a pre-determined effect-site concentration of propofol by target controlled infusion. Effect-site EC50 values of propofol for successful i-gel insertion were determined using the modified Dixon's up-and-down method.

Results: Mean effect-site EC50 ± SD of propofol for successful i-gel insertion was significantly higher for men than women (5.46 ± 0.26 μg/ml vs. 3.82 ± 0.34 μg/ml, p < 0.01). The EC50 of propofol in men was approximately 40% higher than in women. Using isotonic regression with a bootstrapping approach, the estimated EC50 (95% confidence interval) of propofol was also higher in men [5.32 (4.45-6.20) μg/ml vs. 3.75 (3.05-4.43) μg/ml]. The estimated EC95 (95% confidence interval) of propofol in men and women were 5.93 (4.72-6.88) μg/ml and 4.52 (3.02-5.70) μg/ml, respectively.

Conclusions: During i-gel insertion with dexmedetomidine 0.5 μg/kg without muscle relaxant, male patients had higher effect-site EC50 for propofol using Schnider's model. Based on the results of this study, patient gender should be considered when determining the optimal dose of propofol during supraglottic airway insertion.

Trial registration: ClinicalTrials.gov identifier: NCT02268656. Registered August 26, 2014.

Keywords: Dexmedetomidine; I-gel; Propofol.

Figures

Fig. 1
Fig. 1
Consecutive effect-site concentration of propofol (Cepropofol) for i-gel insertion in male (upper) and female (lower) patients after preoperative dexmedetomidine (0.5 μg/ml) administration. Horizontal lines represent the half maximal effective effect-site concentrations (EC50). Mean EC50 (± SD) values in the male and female groups were 5.46 ± 0.26 and 3.82 ± 0.34 μg/ml, respectively (p < 0.01)
Fig. 2
Fig. 2
Pooled-adjacent-violators algorithm (PAVA) response rate in male (unfilled square) and female (filled square) patients. EC50 (95 % CI) values in male and female groups were 5.32 (4.45–6.20) and 3.75 (3.05–4.43) μg/ml, respectively, and corresponding EC95 (95 % CI) values were 5.93 (4.72–6.88) and 4.52 (3.02–5.70) μg/ml, respectively. Isotonic regression showed the EC50 value was significantly higher in the male group than in the female group

References

    1. Levitan RM, Kinkle WC. Initial anatomic investigations of the I-gel airway: a novel supraglottic airway without inflatable cuff. Anaesthesia. 2005;60:1022–6. doi: 10.1111/j.1365-2044.2005.04258.x.
    1. Janakiraman C, Chethan DB, Wilkes AR, Stacey MR, Goodwin N. A randomised crossover trial comparing the i-gel supraglottic airway and classic laryngeal mask airway. Anaesthesia. 2009;64:674–8. doi: 10.1111/j.1365-2044.2009.05898.x.
    1. Richebé P, Rivalan B, Baudouin L, Sesay M, Sztark F, Cros AM, Maurette P. Comparison of the anaesthetic requirement with target-controlled infusion of propofol to insert the laryngeal tube vs. the laryngeal mask. Eur J Anaesthesiol. 2005;22:858–63. doi: 10.1017/S0265021505001456.
    1. Baik HJ, Kim JH, Lee CH. Laryngeal mask insertion during target-controlled infusion of propofol. J Clin Anesth. 2001;13:175–81. doi: 10.1016/S0952-8180(01)00237-9.
    1. Jang YE, Kim YC, Yoon HK, Jeon YT, Hwang JW, Kim E, Park HP. A randomized controlled trial of the effect of preoperative dexmedetomidine on the half maximal effective concentration of propofol for successful i-gel insertion without muscle relaxants. J Anesth. 2015;29:338–45. doi: 10.1007/s00540-014-1949-9.
    1. Kim MK, Lee JW, Jang DJ, Shin OY, Nam SB. Effect-site concentration of remifentanil for laryngeal mask airway insertion during target-controlled infusion of propofol. Anaesthesia. 2009;64:136–40. doi: 10.1111/j.1365-2044.2008.05707.x.
    1. Kodaka M, Okamoto Y, Handa F, Kawasaki J, Miyao H. Relation between fentanyl dose and predicted EC50 of propofol for laryngeal mask insertion. Br J Anaesth. 2004;92:238–41. doi: 10.1093/bja/aeh033.
    1. Higuchi H, Adachi Y, Arimura S, Nitahara K, Satoh T. Oral clonidine premedication reduces the EC50 of propofol concentration for laryngeal mask airway insertion in male patients. Acta Anaesthesiol Scand. 2002;46:372–7. doi: 10.1034/j.1399-6576.2002.460407.x.
    1. Pleym H, Spigset O, Kharasch ED, Dale O. Gender differences in drug effects: implications for anesthesiologists. Acta Anaesthesiol Scand. 2003;47:241–59. doi: 10.1034/j.1399-6576.2003.00036.x.
    1. Kodaka M, Johansen JW, Sebel PS. The influence of gender on loss of consciousness with sevoflurane or propofol. Anesth Analg. 2005;101:377–81. doi: 10.1213/01.ANE.0000154534.71371.4F.
    1. Arya S, Asthana V, Sharma JP. Clinicalvs. Bispectral index-guided propofol induction of anesthesia: A comparative study. Saudi J Anaesth. 2013;7:75–9. doi: 10.4103/1658-354X.109819.
    1. Kwak HJ, Min SK, Yoo JY, Park KH, Kim JY. The median effective dose of dexmedetomidine for laryngeal mask airway insertion with propofol 2.0 mg/kg. Acta Anaesthesiol Scand. 2014;58:815–9. doi: 10.1111/aas.12338.
    1. Schnider TW, Minto CF, Gambus PL, Andresen C, Goodale DB, Shafer SL, Youngs EJ. The influence of method of administration and covariates on the pharmacokinetics of propofol in adult volunteers. Anesthesiology. 1998;88:1170–82. doi: 10.1097/00000542-199805000-00006.
    1. Dixon WJ. Staircase bioassay: the up-and-down method. Neurosci Biobehav Rev. 1991;15:47–50. doi: 10.1016/S0149-7634(05)80090-9.
    1. Pace NL, Stylianou MP. Advances in and limitations of up-and-down methodology: a précis of clinical use, study design, and dose estimation in anesthesia research. Anesthesiology. 2007;107:144–52. doi: 10.1097/01.anes.0000267514.42592.2a.
    1. Dilleen M, Heimann G, Hirsch I. Non-parametric estimators of a monotonic dose–response curve and bootstrap confidence intervals. Stat Med. 2003;22:869–82. doi: 10.1002/sim.1460.
    1. Payton ME, Greenstone MH, Schenker N. Overlapping confidence intervals or standard error intervals: what do they mean in terms of statistical significance? J Insect Sci. 2003;3:34. doi: 10.1673/031.003.3401.
    1. Gan TJ, Glass PS, Sigl J, Sebel P, Payne F, Rosow C, Embree P. Women emerge from general anesthesia with propofol/alfentanil/nitrous oxide faster than men. Anesthesiology. 1999;90:1283–7. doi: 10.1097/00000542-199905000-00010.
    1. Apfelbaum JL, Grasela TH, Hug CC, Jr, McLeskey CH, Nahrwold ML, Roizen MF, Stanley TH, Thisted RA, Walawander CA, White PF. The initial clinical experience of 1819 physicians in maintaining anesthesia with propofol: characteristics associated with prolonged time to awakening. Anesth Analg. 1993;77:S10–4.
    1. Fu F, Chen X, Feng Y, Shen Y, Feng Z, Bein B. Propofol EC50 for inducing loss of consciousness is lower in the luteal phase of the menstrual cycle. Br J Anaesth. 2014;112:506–13. doi: 10.1093/bja/aet383.
    1. Soh S, Park WK, Kang SW, Lee BR, Lee JR. Sex differences in remifentanil requirements for preventing cough during anesthetic emergence. Yonsei Med J. 2014;55:807–14. doi: 10.3349/ymj.2014.55.3.807.
    1. Card JW, Voltz JW, Ferguson CD, Carey MA, DeGraff LM, Peddada SD, Morgan DL, Zeldin DC. Male sex hormones promote vagally mediated reflex airway responsiveness to cholinergic stimulation. Am J Physiol Lung Cell Mol Physiol. 2007;292:908–14. doi: 10.1152/ajplung.00407.2006.
    1. Dyck JB, Maze M, Haack C, Azarnoff DL, Vuorilehto L, Shafer SL. Computer-controlled infusion of intravenous dexmedetomidine hydrochloride in adult human volunteers. Anesthesiology. 1993;78:821–8. doi: 10.1097/00000542-199305000-00003.
    1. Hendrickx JF, Eger EI, 2nd, Sonner JM, Shafer SL. Is synergy the rule? A review of anesthetic interactions producing hypnosis and immobility. Anesth Analg. 2008;107:494–506. doi: 10.1213/ane.0b013e31817b859e.
    1. Kumari K, Gombar S, Kapoor D, Sandhu HS. Clinical study to evaluate the role of preoperative dexmedetomidine in attenuation of hemodynamic response to direct laryngoscopy and tracheal intubation. Acta Anaesthesiol Taiwan. 2015
    1. Chang RN, Baik HJ, Kim DY, Lee GY, Chung RK, Lee HS. Effect-site target-controlled infusion of propofol: comparison of Schnider and modified Marsh model. Anesth Pain Med. 2012;7:293–300.
    1. Absalom AR, Mani V, De Smet T, Struys MM. Pharmacokinetic models for propofol-defining and illuminating the devil in the detail. Br J Anaesth. 2009;103:26–37. doi: 10.1093/bja/aep143.
    1. Hoymork SC, Raeder J. Why do women wake up faster than men from propofol anaesthesia? Br J Anaesth. 2005;95:627–33. doi: 10.1093/bja/aei245.
    1. Schnider TW, Minto CF, Shafer SL, Gambus PL, Andresen C, Goodale DB, Youngs EJ. The influence of age on propofol pharmacodynamics. Anesthesiology. 1999;90:1502–16. doi: 10.1097/00000542-199906000-00003.
    1. Milne SE, Troy A, Irwin MG, Kenny GN. Relationship between bispectral index, auditory evoked potential index and effect-site EC50 for propofol at two clinical end-points. Br J Anaesth. 2003;90:127–31. doi: 10.1093/bja/aeg035.
    1. Laosuwan S, Pongruekdee S, Thaharavanich R. Comparison of effective-site target controlled infusion and manually controlled infusion of propofol for sedation during spinal anesthesia. J Med Assoc Thai. 2011;94:965–71.
    1. Casati A, Fanelli G, Casaletti E, Cedrati V, Veglia F, Torri G. The target plasma concentration of propofol required to place laryngeal mask versus cuffed oropharyngeal airway. Anesth Analg. 1999;88:917–20.
    1. Tanabe K, Matsumoto S, Nakanishi M, Iida H. The concentration for loss of consciousness by propofol does not differ between morning and afternoon. Int J Anesthetic Anesthesiol. 2015;2:2–3.

Source: PubMed

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