超声引导下不同佐剂对全髋关节置换术后镇痛效果的临床研究
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(佛山市第一人民医院,广东 佛山 528000)

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戴鹏,男,主治医师,主要研究方向是外科学麻醉。

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R 614

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佛山市卫生和健康局医学科研项目资助课题(20200209)


Ultrasound-guided Different Adjuvants for Postoperative Analgesia after Total Hip Arthroplasty
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(Foshan First People's Hospital, Guangdong Foshan 528000)

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    摘要:

    〔摘 要〕 目的:研究超声引导下腰方肌阻滞中不同佐剂对全髋关节置换术(THA)术后镇痛效果的研究。方法:选取 佛山市第一人民医院 2019 年 12 月至 2020 年 12 月期间行 THA 的 90 例患者,采用随机分组的方法分成 Y 组、D 组和 R 组, 各 30 例。Y 组手术侧注入混合药:罗哌卡因 100 mg +右美托咪定 1 μg·kg-1(共 30 mL),D 组手术侧注入混合药:罗哌 卡因 100 mg +地塞米松 0.1 mg·kg-1(共 30 mL),R 组手术侧注入罗哌卡因 100 mg(共 30 mL)。各组患者术后均复合 静脉自控镇痛(PCIA)。术后根据镇痛效果静脉注射曲马多 50 mg 进行补救镇痛同时记录患者对术后镇痛的满意度评分。 记录三组患者术后 4、6、12、24、48 h 静息以及被动运动的视觉模拟评分法(VAS)评分。统计术后 48 h 内曲马多补救 镇痛情况和镇痛泵的按压次数。同时记录术后 48 h 内呼吸抑制、恶心呕吐以及术后谵妄的发生率。结果:术后 4、6、48 h 各组 VAS 评分比较,差异无统计学意义(P > 0.05)。术后 12、24 h, Y 组、D 组的 VAS 评分均低于 R 组,差异具有统 计学意义(P < 0.05),且术后 12、24 h Y 组的 VAS 评分与 D 组比较,差异无统计学意义(P > 0.05);术后 48 h 内, Y 组、D 组的镇痛泵的按压次数为(1.5 ± 1.1)次、(1.1 ± 0.9)次,曲马多的补救例数为 2 例(6.7 %)、2 例(6.7 %), 均低于 R 组的(3.5 ± 1.2)次及 8 例(26.7 %),差异具有统计学意义(P < 0.05)。且 Y 组的的曲马多的补救例数及镇痛 泵的按压次数与 D 组比较,差异无统计学意义(P > 0.05);呼吸抑制以及术后谵妄三组均未出现。Y 组恶心呕吐发生 1 例 (3.3 %)与 D 组的 2 例(6.7 %),均低于 R 组的 7 例(23.3 %),差异具有统计学意义(P < 0.05)。且 D 组与 Y 组的 恶心呕吐率比较,差异无统计学意义(P > 0.05)。术后 Y 组术后满意度评分为(5.8 ± 0.3)分、D 组为(5.3 ± 0.3)分, 均高于 R 组的(3.9 ± 0.5)分,差异具有统计学意义(P < 0.05)。且 D 组与 Y 组的术后满意度评分比较,差异无统计学 意义(P > 0.05)。结论:超声引导下腰方肌阻滞中加入佐剂(右美托咪定或地塞米松)对 THA 术后镇痛的效果更佳,同 时可以减少不良反应,提高患者对术后镇痛的满意度。但两者镇痛效果并无明显差别。

    Abstract:

    〔Abstract〕 Objective To study the effects of different adjuvants in ultrasound-guided quadratus lumborum block on postoperative analgesia after total hip arthroplasty (THA). Methods A total of 90 patients who underwent THA from December 2019 to December 2020 in Foshan First People's Hospital were selected and randomly divided into groups Y, D and R, 30 cases in each group. The operation side of group Y was injected with mixed medicine: ropivacaine 100 mg + dexmedetomidine 1 μg·kg-1 (total 30 mL), and the operation side of group D was injected with mixed medicine: ropivacaine 100 mg + dexamethasone 0.1 mg·kg-1 (30 mL in total), 100 mg of ropivacaine (30 mL in total) was injected on the surgical side of group R. All patients in each group used intravenous analgesia pump (PCIA) after operation. After surgery, 50 mg tramadol was injected intravenously according to the analgesic effect for salvage analgesia. At the same time, the patient's satisfaction score for postoperative analgesia was recorded. The visual analogue scale (VAS) scores of the three groups were recorded at 4, 6, 12, 24, and 48 hours after operation. Statistics of tramadol salvage analgesia and the number of compressions of the analgesic pump within 48 h after surgery. At the same time, the incidence of respiratory depression, nausea and vomiting, and postoperative delirium within 48 hours were recorded. Results There was no significant difference in the VAS scores of each group at 4, 6, and 48 hours after operation (P > 0.05). TheVAS scores of the Y group and D group were lower than that of the R group at 12 and 24 h after the operation, the difference was statistically significant (P < 0.05), and the VAS scores of the Y group and the D group were not different at 12 and 24 h after the operation. Statistical significance (P > 0.05); within 48 hours after surgery, the number of remedies for tramadol in group Y and group D was (1.5 ± 1.1) times and (1.1 ± 0.9) times, and the number of times the analgesic pump was pressed was 2 cases (6.7 %) and 2 cases (6.7 %) were lower than those in the R group (3.5 ± 1.2) and 8 cases (26.7%). The difference was statistically significant (P < 0.05). Moreover, the number of remedy cases of tramadol in group Y and the number of compressions of the analgesic pump were not statistically significant compared with group D (P > 0.05); respiratory depression and postoperative delirium did not appear in the three groups. Nausea and vomiting occurred in 1 case (3.3%) in group Y and 2 cases (6.7%) in group D, both lower than 7 cases in group R (23.3%), the difference was statistically significant (P < 0.05). Moreover, there was no statistically significant difference in the nausea and vomiting rates between group D and group Y (P > 0.05). The postoperative satisfaction score of group Y was (5.8 ± 0.3) points and group D was (5.3 ± 0.3) points, which were higher than those of group R, and the difference was statistically significant (P < 0.05). Moreover, there was no statistically significant difference between the postoperative satisfaction scores of group D and group Y (P > 0.05).ConclusionAdding an adjuvant (dexmedetomidine or dexamethasone) to the ultrasound-guided quadratus lumborum block has a better effect on postoperative analgesia after THA, while reducing adverse reactions and improving patients’ satisfaction with postoperative analgesia Degrees. However, there is no significant difference in efficacy between the two.

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  • 收稿日期:2021-06-09
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  • 在线发布日期: 2021-10-20
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