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剖宫产术后患者自控布比卡因伤口滴注:辅助使用氯胺酮无效

Patient-controlled bupivacaine wound instillation following cesarean section: the lack of efficacy of adjuvant ketamine.

作者信息

Zohar Edna, Luban Ilya, Zunser Igor, Shapiro Arie, Jedeikin Robert, Fredman Brian

机构信息

Department of Anesthesiology and Intensive Care, Meir Hospital, Kfar Saba, Israel.

出版信息

J Clin Anesth. 2002 Nov;14(7):505-11. doi: 10.1016/s0952-8180(02)00422-1.

Abstract

STUDY OBJECTIVE

To assess the analgesic efficacy of ketamine when administered as an adjuvant to bupivacaine for patient-controlled wound instillation following cesarean section.

DESIGN

Prospective, randomized, double-blind study.

SETTING

Large referral hospital.

PATIENTS

50 term parturients undergoing cesarean section.

INTERVENTION

In all cases, a standard spinal anesthetic was administered. On completion of the surgery, a multihole 20 G epidural catheter (B. Braun, Melsungen, Germany) was placed above the fascia such that the tip was sited at the point which demarcated 50% of the length of the surgical wound. Thereafter, the catheter was connected to a patient-controlled drug delivery device. The device was filled with either 0.125% bupivacaine (bupivacaine group) or 0.125% bupivacaine and ketamine (1 mg/mL) (bupivacaine-ketamine group). Postoperatively, wound instillation was performed via the patient-controlled analgesia device. During the first 6 postoperative hours, a co-investigator administered "rescue" morphine (2 mg IV). Thereafter, "rescue" dipyrone (1 g) was administered on patient request.

MEASUREMENTS AND MAIN RESULTS

At all time intervals, visual analog scale (VAS) for pain at rest, on coughing, and during leg raise were similar between the groups. All patients (100%) in both treatment groups received "rescue" morphine. Similarly, the number of doses of 2 mg "rescue" morphine administered was unaffected by patient randomization. The total "rescue" morphine administered during the first 6 postoperative hours was 11.2 +/- 4.6 mg versus 11.3 +/- 5.6 mg for the bupivacaine group and bupivacaine-ketamine group, respectively. The number of pump infusions during the 24-hour study period was 9 +/- 2 and 9 +/- 3 for the bupivacaine group and bupivacaine-ketamine group, respectively. The volume infused via the delivery device was similar between the groups (81 +/- 18 mL vs. 85 +/- 24 mL for the bupivacaine group and bupivacaine-ketamine group, respectively). Psychomental and cognitive function as measured by the Digit Symbol Substitution and Mini Mental Tests were unaffected by adjuvant ketamine administration. Patient satisfaction was similar between the groups.

CONCLUSION

Adjuvant local ketamine does not enhance bupivacaine-induced wound instillation following cesarean section.

摘要

研究目的

评估剖宫产术后患者自控伤口滴注时,氯胺酮作为布比卡因辅助用药的镇痛效果。

设计

前瞻性、随机、双盲研究。

地点

大型转诊医院。

患者

50名足月行剖宫产的产妇。

干预措施

所有病例均采用标准的脊髓麻醉。手术结束后,将一根20G多孔硬膜外导管(德国梅尔松根市贝朗公司生产)置于筋膜上方,使导管尖端位于手术伤口长度50%的分界点处。此后,将导管连接至患者自控给药装置。该装置中填充的要么是0.125%布比卡因(布比卡因组),要么是0.125%布比卡因和氯胺酮(1毫克/毫升)(布比卡因 - 氯胺酮组)。术后,通过患者自控镇痛装置进行伤口滴注。术后前6小时,由一名共同研究者给予“解救”吗啡(静脉注射2毫克)。此后,根据患者要求给予“解救”安乃近(1克)。

测量指标及主要结果

在所有时间间隔,两组患者静息、咳嗽及抬腿时疼痛的视觉模拟量表(VAS)评分相似。两个治疗组的所有患者(100%)均接受了“解救”吗啡。同样,给予2毫克“解救”吗啡的剂量不受患者随机分组的影响。布比卡因组和布比卡因 - 氯胺酮组术后前6小时给予的“解救”吗啡总量分别为11.2±4.6毫克和11.3±5.6毫克。在24小时研究期间,布比卡因组和布比卡因 - 氯胺酮组的泵注次数分别为9±2次和9±3次。两组通过给药装置输注的液体量相似(布比卡因组为81±18毫升,布比卡因 - 氯胺酮组为85±24毫升)。通过数字符号替换和简易精神状态测试评估的心理精神和认知功能不受氯胺酮辅助用药的影响。两组患者的满意度相似。

结论

剖宫产术后辅助使用局部氯胺酮并不能增强布比卡因诱导的伤口滴注镇痛效果。

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