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瑞芬太尼患者自控镇痛分娩在效应部位的浓度

作者:高翠歌 编译 来源: 日期:2015-11-17
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瑞芬太尼患者自控镇痛分娩在效应部位的浓度

Effect-site concentration of remifentanil during patient-controlled analgesia in labour

A. Jost, R. Blagus, B. Ban, M. Kamenik

Background

Intravenous remifentanil has been described for patient-controlled analgesia in labour. Recently, the application of target-controlled infusion pumps with Minto’s pharmacokinetic/pharmacodynamic model has been reported. Hypothetical effect-site remifentanil concentration during patient-controlled analgesia for labour has yet to be examined. The aim of this concept study was to explore characteristics of this parameter.

Methods

We performed a historical cohort study based on our previous randomised cross-over clinical trial and analysed hypothetical effect-site remifentanil concentration. Values at spontaneous vaginal delivery and Apgar scores were tested for correlation. The association between pain score and the corresponding effect-site remifentanil concentration before and after bolus administration, and their relative difference, was examined with a linear mixed-effects model, adjusted for other variables.

Results

A series of 23 parturients with uncomplicated singleton pregnancies were included. On average, effect-site remifentanil concentration was highest during the third quarter throughout our recordings (5.5 ng/mL; maximum 15.8 ng/mL). The mean (median) {IQR} [range] at spontaneous vaginal delivery (n=14) was 2.52 (1.32) {0.95–4.28} [0.65–6.88] ng/mL, all Apgar scores were >7, and no correlation was confirmed. A negative association between effect-site remifentanil concentration before bolus administration and pain score (scale 0–100) was observed (−3.9, 95% CI −5.16 to −2.61, P <0.01).

Conclusions

The residual value of hypothetical effect-site remifentanil concentration before uterine contraction, at the beginning of bolus administration, predicted lower pain scores. Monitoring effect-site remifentanil concentration may be potentially useful when remifentanil is administered for labour analgesia. However, our results need to be confirmed with a pharmacokinetic model optimized for pregnant patients.

International journal of obstetric anesthesia

August 2015Volume 24, Issue 3, Pages 230–236

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