Tianjin Medical Journal ›› 2023, Vol. 51 ›› Issue (10): 1146-1152.doi: 10.11958/20230652

• Drug Clinical Evaluations • Previous Articles    

Effect of epidural injection with different doses of 1.5% chloroprocaine in relieving breakthrough pain during labor analgesia

JI Tianzhen1(), XU Cheng2, LIU Hongxia1, LI Guofang1, LI Rui3, ZHU Haijuan1,()   

  1. 1. Department of Anesthesiology, Anhui Provincial Maternal and Child Health Hospital, Hefei 230011, China
    2. Department of Anesthesiology, Shanghai Jiaotong University Affiliated Sixth People's Hospital
    3. Department of Anesthesiology and Perioperative Medicine, the Second Hospital of Anhui Medical University
  • Received:2023-05-04 Revised:2023-05-19 Published:2023-10-15 Online:2023-10-18
  • Contact: E-mail:35880762@qq.com

Abstract:

Objective To investigate the effect of epidural injection of 1.5% chloroprocaine on breakthrough pain during labor analgesia. Methods A total of 128 primiparas with breakthrough pain after epidural labor analgesia were randomly divided into four groups (R, C1, C2 and C3 groups). When breakthrough pain occurred, 0.15% ropivacaine 6 mL was injected epidural in the group R, and 1.5% chloroprocaine 6, 8 and 10 mL were injected epidural in the group C1, the group C2 and the group C3, respectively. The visual analogue score (VAS) for pain was assessed every 3 minutes after the administration of local anesthetics. The primary outcome was recorded including the onset time of breakthrough pain after the administration and the success rate of breakthrough pain treatment. Secondary outcome included rescue analgesia rate, maternal satisfaction (5 minutes after administration of breakthrough pain, 24 hours after the delivery), VAS, modified Bromage score, fetal heart rate (FHR) at first breakthrough pain (T0), 3 min (T1), 6 min (T2), 9min (T3), 12 min (T4), 15 min (T5) and 18 min (T6) after administration, the interval and duration of uterine contraction at the onset time of breakthrough pain, the second, fourth, sixth, eighth, tenth and twelfth contractions after administration, Apgar score in 1 and 5 min and adverse reactions. Results Kaplan-Meier survival analysis showed that the median onset time (95%CI) of breakthrough pain in the group R, the group C1, the group C2 and the group C3 were 14.3 (13.4-15.2) min, 6.6 (5.6-7.6) min, 5.9 (5.0-6.8) min and 4.7 (3.9-5.4) min, respectively. The onset time of administration was significantly faster in the group C3 than that in the group C1 and the group C2 (Log-rank χ2 was 9.852 and 5.325, P<0.05). Compared with the group R, the success rate of breakthrough pain treatment and maternal satisfaction (5 minutes after administration, 24 hours after the delivery) were significantly increased in the group C2 and the group C3, and remedial analgesia rate was significantly decreased in the group C3 (P < 0.01). Compared with the group C1, the success rate of breakthrough pain treatment was increased and the remedial analgesia rate was decreased in the group C3 Maternal satisfaction (5 minutes after administration, 24 hours after the delivery ) was significantly increased in the group C2 and the group C3 (P < 0.01). At T1, the VAS score was significantly lower in the group C2 and the group C3 than that in the group R, and which was significantly lower in the group C3 than that in the group C1 (P < 0.05). At T2~5, the VAS score was significantly lower in the group C1, the group C2 and the group C3 than that in the group R, and which was significantly lower in the group C2 and the group C3 than that in the group C1 (P < 0.05). At T6, VAS scores were significantly lower in the group C2 and the group C3 than those of the group R and the group C1 (P<0.05). There were no significant differences in the interval of uterine contractions and duration of uterine contractions between the four groups. Compared with the group R and the group C1, the probability of lower limb numbness within 30 minutes after administration of breakthrough pain was significantly higher in the group C3 (P<0.05). There were no significant differences in modified Bromage score, FHR at different time points before and after administration, and Apgar score at 1 and 5 min between the four groups. Conclusion The optimal effective dose of epidural injection of 1.5% chloroprocaine for the treatment of breakthrough pain during labor analgesia is 8 mL.

Key words: labor pain, breakthrough pain, analgesia, obstetrical, analgesia, epidural, chloroprocaine, onset time

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