纳布啡剂量差异对剖宫产术后病人镇痛及恢复影响

    Effect of different dose of nalbuphine on analgesia and recovery after cesarean section

    • 摘要:
      目的: 探讨纳布啡差异对剖宫产术后病人镇痛及恢复影响。
      方法: 选取2021年4月至2023年4月期间在医院行剖宫产术的108例产妇,采用随机数字表法将产妇分为低剂量组(36例)、中剂量组(36例)、高剂量组(36例)。3组病人均采用统一静脉自控镇痛方案,低、中、高剂量组分别给予0.10 mg/kg、0.15 mg/kg、0.20 mg/kg纳布啡。评估3组病人Ramsay评分、舒适度评分(BCS)、术后疼痛视觉模拟量表(VAS)评分,比较3组血清疼痛指标前列腺素E2(PGE2)、心肌细胞P物质(SP)、术后恢复指标及不良反应。
      结果: 随着时间的增加,3组Ramsay评分降低、BCS评分升高(P < 0.05);与低剂量组比较,中、高剂量组术后2 h、6 h Ramsay评分更高,中、高剂量组术后2 h、6 h、12 h、24 h BCS评分更高(P < 0.05);与低剂量组比较,中、高剂量组术后6 h、12 h、24 h 静息、运动、压迫宫底VAS评分均降低(P < 0.05),与术后2 h比较,3组术后6 h、12 h、24 h静息、运动、压迫宫底 VAS评分均升高(P < 0.05),与术后6 h比较,3组术后12 h 静息、运动、压迫宫底VAS评分升高,术后24 h VAS评分则均降低(P < 0.05),与术后12 h比较,3组术后24 h 静息、运动、压迫宫底评分均降低(P < 0.05);与低剂量组比较,中、高剂量组术后12 h、24 h、48 h 血清PGE2、SP水平均降低(P < 0.05),与术前比较,3组术后12 h、24 h、48 h血清PGE2、SP水平均升高(P < 0.05),与术后12 h比较,三组术后24 h血清PGE2、SP水平均升高,术后48 h血清PGE2、SP水平均降低(P < 0.05),与术后24 h比较,3组术后48 h血清PGE2、SP水平均降低(P < 0.05);与低剂量组比较,中、高剂量组初次下床活动时间、胃肠排气时间、初次排尿时间均缩短(P < 0.05);高剂量组术后48 h内的不良反应总发生率(22.22%)高于低、中剂量组(P < 0.05)。
      结论: 纳布啡在剖宫产术后的镇痛效果良好,可减少疼痛介质的释放,有利于产后恢复,综合考虑0.15 mg/kg纳布啡即可达到良好的镇痛效果,且安全性好。

       

      Abstract:
      Objective To explore the effects of different dose of nalbuphine on analgesia and recovery in patients after cesarean section.
      Methods A total of 108 parturients who underwent cesarean section in the hospital from April 2021 to April 2023 were selected. The parturients were divided into the low-dose group (36 cases), medium-dose group (36 cases) and high-dose group (36 cases) by the random number table method. Three groups were treated with a unified patient-controlled intravenous analgesia regimen. The low-dose, medium-dose and high-dose groups were given 0.10 mg/kg, 0.15 mg/kg and 0.20 mg/kg nalbuphine, respectively. The Ramsay score, comfort score (BCS) and postoperative pain Visual Analogue Scale (VAS) score in three groups were evaluated. The serum pain indicatorsprostaglandin E2 (PGE2), substance P (SP) in myocardial cells, postoperative recovery indicators and adverse reactions among three groups were compared.
      Results With the increase of time, the Ramsay scores decreased, and the BCS scores increased in three groups (P < 0.05). Compared with the low-dose group, the Ramsay scores of the medium-dose and high-dose groups were higher after 2 h and 6 h of surgery, and the BCS scores of the medium-dose and high-dose groups were higher after 2 h, 6 h, 12 h and 24 h of surgery (P < 0.05). Compared with the low-dose group, the VAS scores of the fundus at rest, during exercise and under compression in the medium and high-dose groups after 6 h, 12 h, and 24 h of surgery were all decreased (P < 0.05). Compared with 2 hours after the operation, the VAS scores of resting, exercising and compressing the fundus of the uterus in the three groups increased at 6 hours, 12 hours and 24 hours after the operation (P < 0.05). Compared with 6 hours after the operation, the VAS scores of resting, exercising and compressing the fundus of the uterus in the three groups increased at 12 hours after operation, while the VAS scores decreased at 24 hours after the operation (P < 0.05). Compared with 12 hours after operation, the scores of rest, exercise and compression of the fundus at 24 hours after the operation in three groups decreased (P < 0.05). Compared with the low-dose group, the serum levels of PGE2 and SP in the medium and high-dose groups decreased at 12 h, 24 h and 48h after the operation (P < 0.05). Compared with that before the operation, the serum levels of PGE2 and SP in three groups increased at 12 h, 24 h nd 48h after the operation (P < 0.05). Compared with 12 h after the operation, the serum levels of PGE2 and SP in three groups increased after 24 hours of operation, and decreased after 48 hours of operation (P < 0.05). Compared with 24 hours after the operation, the serum levels of PGE2 and SP in three groups decreased after 48 hours of operation (P < 0.05). Compared with the low-dose group, the time of first getting out of bed for activity, time of gastrointestinal exhaust and time of first urination in the medium and high-dose groups were all shortened (P < 0.05). The total incidence of adverse reactions within 48 hours after surgery in the high-dose group (22.22%) was higher than that in the low-dose and medium-dose groups (P < 0.05).
      Conclusions Nalbuphine has a good analgesic effect after cesarean section, can reduce the release of pain mediators, and is conducive to postpartum recovery. Considering comprehensively, the 0.15 mg/kg of nalbuphine can achieve a good analgesic effect, and has good safety.

       

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