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Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia

Background: Labor pain perception has been demonstrated to exhibit a circadian rhythm with lower pain scores during the day compared with the night. This study aimed to determine and compare the median effective dose (ED(50)) of ropivacaine in parturients having epidural labor analgesia during the d...

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Autores principales: Deng, Jiali, Wei, Changna, Liu, Lin, Qian, Jing, Xiao, Fei, Chen, Xinzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636744/
https://www.ncbi.nlm.nih.gov/pubmed/34869403
http://dx.doi.org/10.3389/fmed.2021.669264
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author Deng, Jiali
Wei, Changna
Liu, Lin
Qian, Jing
Xiao, Fei
Chen, Xinzhong
author_facet Deng, Jiali
Wei, Changna
Liu, Lin
Qian, Jing
Xiao, Fei
Chen, Xinzhong
author_sort Deng, Jiali
collection PubMed
description Background: Labor pain perception has been demonstrated to exhibit a circadian rhythm with lower pain scores during the day compared with the night. This study aimed to determine and compare the median effective dose (ED(50)) of ropivacaine in parturients having epidural labor analgesia during the day vs. during the night. Methods: The study group consisted of 60 nulliparous healthy parturients who were assigned to one of two groups according to the time they requested labor analgesia: Day Group (7:01 am to 7:00 pm) and Night Group (7:01 pm to 7:00 am). A bolus of.15% ropivacaine was administered epidurally and effective analgesia was defined as the attainment of a visual analog scale (VAS) pain score ≤ 10 mm within 30 min. The dose of ropivacaine for the first parturient in each group was 18 mg. The dose for each subsequent parturient was varied with increments or decrements of 3 mg based on the response of the previous subject. The ED(50) was calculated using up-down sequential analysis. Probit regression was used to estimate the relative mean potency of ropivacaine between groups. Results: The ED(50) (mean [95% CI]) of ropivacaine was lower in the Day Group (17.9 [16.5–19.4] mg) than in the Night Group (20.9 [19.2–22.7] mg) (P = 0.003). The estimate of relative potency for ropivacaine for the Night Group vs. the Day Group was 0.85 (95% CI:0.56–0.98). Conclusions: Under the conditions of this study, the dose requirement for epidural ropivacaine for labor analgesia was ~ 15% greater during the night than during the day. Clinical Trials Registration: Chinese Clinical Trial Registry (No.: ChiCTR1900025269. http://www.chictr.org.cn/showprojen.aspx?proj=36993).
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spelling pubmed-86367442021-12-03 Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia Deng, Jiali Wei, Changna Liu, Lin Qian, Jing Xiao, Fei Chen, Xinzhong Front Med (Lausanne) Medicine Background: Labor pain perception has been demonstrated to exhibit a circadian rhythm with lower pain scores during the day compared with the night. This study aimed to determine and compare the median effective dose (ED(50)) of ropivacaine in parturients having epidural labor analgesia during the day vs. during the night. Methods: The study group consisted of 60 nulliparous healthy parturients who were assigned to one of two groups according to the time they requested labor analgesia: Day Group (7:01 am to 7:00 pm) and Night Group (7:01 pm to 7:00 am). A bolus of.15% ropivacaine was administered epidurally and effective analgesia was defined as the attainment of a visual analog scale (VAS) pain score ≤ 10 mm within 30 min. The dose of ropivacaine for the first parturient in each group was 18 mg. The dose for each subsequent parturient was varied with increments or decrements of 3 mg based on the response of the previous subject. The ED(50) was calculated using up-down sequential analysis. Probit regression was used to estimate the relative mean potency of ropivacaine between groups. Results: The ED(50) (mean [95% CI]) of ropivacaine was lower in the Day Group (17.9 [16.5–19.4] mg) than in the Night Group (20.9 [19.2–22.7] mg) (P = 0.003). The estimate of relative potency for ropivacaine for the Night Group vs. the Day Group was 0.85 (95% CI:0.56–0.98). Conclusions: Under the conditions of this study, the dose requirement for epidural ropivacaine for labor analgesia was ~ 15% greater during the night than during the day. Clinical Trials Registration: Chinese Clinical Trial Registry (No.: ChiCTR1900025269. http://www.chictr.org.cn/showprojen.aspx?proj=36993). Frontiers Media S.A. 2021-11-18 /pmc/articles/PMC8636744/ /pubmed/34869403 http://dx.doi.org/10.3389/fmed.2021.669264 Text en Copyright © 2021 Deng, Wei, Liu, Qian, Xiao and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Deng, Jiali
Wei, Changna
Liu, Lin
Qian, Jing
Xiao, Fei
Chen, Xinzhong
Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title_full Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title_fullStr Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title_full_unstemmed Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title_short Circadian Variation in the Median Effective Dose of Epidural Ropivacaine for Labor Analgesia
title_sort circadian variation in the median effective dose of epidural ropivacaine for labor analgesia
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636744/
https://www.ncbi.nlm.nih.gov/pubmed/34869403
http://dx.doi.org/10.3389/fmed.2021.669264
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