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Target-controlled infusion of remifentanil or fentanyl during extra-corporeal shock-wave lithotripsy

Published online by Cambridge University Press:  13 April 2005

L. I. Cortínez
Affiliation:
Pontificia Universidad Católica de Chile, Department of Anesthesiology, Santiago, Chile
H. R. Muñoz
Affiliation:
Pontificia Universidad Católica de Chile, Department of Anesthesiology, Santiago, Chile
R. De la Fuente
Affiliation:
Pontificia Universidad Católica de Chile, Department of Anesthesiology, Santiago, Chile
D. Acuña
Affiliation:
Pontificia Universidad Católica de Chile, Department of Anesthesiology, Santiago, Chile
J. A. Dagnino
Affiliation:
Pontificia Universidad Católica de Chile, Department of Anesthesiology, Santiago, Chile
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Extract

Summary

Background and objective: Target-controlled infusions (TCIs) of remifentanil and fentanyl in conscious sedation regimes for extra-corporeal shock-wave lithotripsy have not been reported. We estimated the effect site concentrations of remifentanil and fentanyl needed to obtain adequate analgesia in 50% of patients (EC50) and compared both drugs in terms of intra- and post-procedure complications.

Methods: Forty-four adult patients were randomly distributed into two groups: Group R received remifentanil and Group F received fentanyl TCI with initial effect site concentrations of 1.5 and 2 ng mL−1, respectively. Pain was assessed using a 10-point verbal analogue scale and <3 was considered adequate analgesia. Increments or decrements of 0.5 ng mL−1 were then introduced for subsequent patients according to Dixon's up and down method. During the rest of the procedure, TCI was adjusted to maintain verbal analogue scale <3.

Results: Remifentanil and fentanyl EC50 were 2.8 ng mL−1 (95% confidence interval (CI): 1.8–3.7 ng mL−1) and 2.9 ng mL−1 (95% CI: 1.7–4.1 ng mL−1), respectively (n.s.). At EC50, the probability of having a respiratory rate <10 was 4% (95% CI: 0–57%) for remifentanil and 56% (95% CI: 13–92%) for fentanyl. Hypoxaemia, vomiting and sedation were more frequent in Group F during and after the procedure (P < 0.05).

Conclusions: A similar EC50 but more respiratory depression, sedation and PONV were found with fentanyl TCI than with remifentanil TCI.

Type
Original Article
Copyright
© 2005 European Society of Anaesthesiology

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References

Gravenstein D. Extracorporeal shock wave lithotripsy and percutaneous nephrolithotomy. Anesthesiol Clin North Am 2000; 18: 953971.Google Scholar
Coloma M, Chiu JW, White PF, et al. Fast-tracking after immersion lithotripsy: general anesthesia versus monitored anesthesia care. Anesth Analg 2000; 91: 9296.Google Scholar
Bromage PR, Bonsu AK, el-Faqih SR, Husain I. Influence of Dornier HM3 system on respiration during extracorporeal shock-wave lithotripsy. Anesth Analg 1989; 68: 363367.Google Scholar
Sa Rego MM, Inagaki Y, White PF. Remifentanil administration during monitored anesthesia care: are intermittent boluses an effective alternative to a continuous infusion? Anesth Analg 1999; 88: 518522.Google Scholar
Gesztesi Z, Rego MM, White PF. The comparative effectiveness of fentanyl and its newer analogs during extracorporeal shock wave lithotripsy under monitored anesthesia care. Anesth Analg 2000; 90: 567570.Google Scholar
Beloeil H, Corsia G, Coriat P, Riou B. Remifentanil compared with sufentanil during extra-corporeal shock wave lithotripsy with spontaneous ventilation: a double-blind, randomized study. Br J Anaesth 2002; 89: 567570.Google Scholar
Shafer SL, Gregg KM. Algorithms to rapidly achieve and maintain stable drug concentrations at the site of drug effect with a computer-controlled infusion pump. J Pharmacokinet Biopharm 1992; 20: 147169.Google Scholar
Goldman JM. A simple, easy, and inexpensive method for monitoring ETCO2 through nasal cannulae. Anesthesiology 1987; 67: 606.Google Scholar
Minto CF, Schnider TW, Shafer SL. Pharmacokinetics and pharmacodynamics of remifentanil. II. Model application. Anesthesiology 1997; 86: 2433.Google Scholar
McClain DA, Hug Jr CC. Intravenous fentanyl kinetics. Clin Pharmacol Ther 1980; 28: 106114.Google Scholar
Dixon W, Massey FJ. Introduction to Statistical Analysis New York, USA: McGraw-Hill, 1969.
Maitre PO, Vozeh S, Heykants J, et al. Population pharmacokinetics of alfentanil: the average dose–plasma concentration relationship and interindividual variability in patients. Anesthesiology 1987; 66: 312.Google Scholar
Ausems ME, Vuyk J, Hug Jr CC, Stanski DR. Comparison of a computer-assisted infusion versus intermittent bolus administration of alfentanil as a supplement to nitrous oxide for lower abdominal surgery. Anesthesiology 1988; 68: 851861.Google Scholar
Paul M, Fisher DM. Are estimates of MAC reliable? Anesthesiology 2001; 95: 13621370.Google Scholar
Shafer SL, Varvel JR, Aziz N, Scott JC. Pharmacokinetics of fentanyl administered by computer-controlled infusion pump. Anesthesiology 1990; 73: 10911102.Google Scholar
Mertens MJ, Engbers FH, Burm AG, Vuyk J. Predictive performance of computer-controlled infusion of remifentanil during propofol/remifentanil anaesthesia. Br J Anaesth 2003; 90: 132141.Google Scholar
McEwan AI, Smith C, Dyar O, et al. Isoflurane minimum alveolar concentration reduction by fentanyl. Anesthesiology 1993; 78: 864869.Google Scholar
Lang E, Kapila A, Shlugman D, et al. Reduction of isoflurane minimal alveolar concentration by remifentanil. Anesthesiology 1996; 85: 721728.Google Scholar
Puchner W, Egger P, Puhringer F, et al. Evaluation of remifentanil as single drug for awake fiberoptic intubation. Acta Anaesthesiol Scand 2002; 46: 350354.Google Scholar
Chen SW, Maguire PA, Davies MF, et al. Evidence for mu1-opioid receptor involvement in fentanyl-mediated respiratory depression. Eur J Pharmacol 1996; 312: 241244.Google Scholar
Joshi GP, Warner DS, Twersky RS, Fleisher LA. A comparison of the remifentanil and fentanyl adverse effect profile in a multicenter phase IV study. J Clin Anesth 2002; 14: 494499.Google Scholar
Joo HS, Perks WJ, Kataoka MT, et al. A comparison of patient-controlled sedation using either remifentanil or remifentanil–propofol for shock wave lithotripsy. Anesth Analg 2001; 93: 12271232.Google Scholar