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不同浓度右美托咪定联合罗哌卡因腰丛神经阻滞对老年股骨粗隆间骨折手术的麻醉效果观察▲
Lumbar plexus block with different concentrations of dexmedetomidine combined with ropivacaine in elderly patients undergoing intertrochanteric femoral fracture: an observation of anesthetic effect

微创医学 页码:651-656

作者机构:南昌市第一医院麻醉科,江西省南昌市 300080

基金信息:江西省卫生计生委科技计划(编号:20197006)

DOI:10.11864/j.issn.1673.2025.06.05

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目的 探讨不同浓度右美托咪定联合罗哌卡因行腰丛神经阻滞(LPB)对老年股骨粗隆间骨折手术的麻醉效果。方法 选取180例老年股骨粗隆间骨折患者作为研究对象,按随机数字表法将其分为D0、D1、D2、D3组,各45例,4组患者均接受LPB,其中D0组药物为0.375%罗哌卡因;D1组药物为含0.5 μg/mL 右美托咪定的0.375%罗哌卡因;D2组药物为含1.0 μg/mL右美托咪定的0.375%罗哌卡因;D3组药物为含1.5 μg/mL 右美托咪定的0.375%罗哌卡因。比较4组患者神经阻滞起效时间、神经阻滞持续时间、麻醉苏醒时间、自主呼吸恢复时间;分别于术前(H0)、术后6 h(H1)、术后12 h(H2)、术后24 h(H3),采用视觉模拟评分法(VAS)评估患者疼痛程度;术后24 h(H3)采用15项恢复质量评分量表(QoR-15)评估4组麻醉恢复质量;比较4组患者寒战、恶心呕吐、心动过缓发生率。结果 D0组、D1组、D2组、D3组患者神经阻滞起效时间依次缩短(P<0.05);D0组患者神经阻滞持续时间短于其他3组,且D1组短于D2组和D3组(P<0.05);D0组患者自主呼吸恢复时间、麻醉苏醒时间短于其他3组,且D1组、D2组短于D3组(P<0.05)。在H1、H2、H3的相应时点,D0组、D1组、D2组、D3组患者疼痛VAS评分依次降低(P<0.05);H0、H1、H2、H3时点,4组患者疼痛VAS评分依次降低(P<0.05)。D0组、D1组、D2组、D3组患者QoR-15评分依次升高(P<0.05);D3组患者总不良反应发生率高于D0组和D1组(P<0.05)。结论 老年股骨粗隆间骨折行手术治疗,采用不同浓度右美托咪定联合罗哌卡因行LPB可缩短神经阻滞起效时间、延长神经阻滞持续时间、增强术后镇痛效果、提高麻醉恢复质量。中等浓度(1.0 μg/mL)右美托咪定使患者获益更大,高浓度(1.5 μg/mL )右美托咪定会延长麻醉苏醒和自主呼吸恢复时间、增加心动过缓不良反应发生率。

Objective To investigate the anesthetic effect of lumbar plexus block (LPB) with different concentrations of dexmedetomidine combined undergoing ropivacaine in elderly patients wndergoing intertrochanteric femoral fracture. Methods A total of 180 elderly patients with intertrochanteric fracture of femur were enrolled as research subjects and divided into groups D0, D1, D2, and D3 by using a random number table method, with 45 cases in each group. All four groups underwent LPB. Specifically, the D0 group received 0.375% ropivacaine; the D1 group was treated with 0.375% ropivacaine containing 0.5 μg/mL dexmedetomidine; the D2 group received 0.375% ropivacaine containing 1.0 μg/mL dexmedetomidine; the D3 group received 0.375% ropivacaine containing 1.5 μg/mL dexmedetomidine. The onset time and duration of nerve block anesthesia, anesthetic recovery time, and spontaneous breathing recovery time were compared between the four groups. Pain intensity was evaluated by using the visual analogue scale (VAS) at preoperative (H0), 6 hours postoperatively (H1), 12 hours postoperatively (H2), and 24 hours postoperatively (H3), respectively; the quality of anesthetic recovery was assessed with the quality of recovery scale-15 (QoR-15) at 24 hours postoperatively (H3), as well as the incidences of shivering, nausea and vomiting, and bradycardia were compared between the four groups. Results The onset time of nerve block anesthesia in group D0, D1, D2 and D3 was sequentially shortened (P<0.05). The duration of nerve block anesthesia in group D0 was shorter than that in the other three groups, and the duration in group D1 was shorter than that in groups D2 and D3 (P<0.05). The spontaneous breathing recovery time and the anesthetic recovery time in group D0 were shorter than those in the other three groups, while group D1 and D2 had shorter times than group D3 (P<0.05). At H1, H2 and H3, the pain VAS scores in group D0, D1, D2 and D3 decreased sequentially (P<0.05). Within each of the four groups, the pain VAS scores decreased sequentially at H0, H1, H2, and H3 (P<0.05). The QoR-15 scores in group D0, D1, D2 and D3 increased sequentially (P<0.05). The total incidence of adverse reactions in group D3 was higher than that in group D0 and D1 (P<0.05). Conclusion For elderly patients with intertrochanteric femoral fracture undergoing surgical treatment, LPB with different concentrations of dexmedetomidine combined with ropivacaine can shorten the onset time of nerve block anesthesia, prolong its duration, enhance the postoperative analgesic effect and improve the quality of anesthetic recovery. However, moderate concentration (1.0 μg/mL) of dexmedetomidine yields greater benefits for patients, and high concentration (1.5 μg/mL) of dexmedetomidine may prolong the anesthetic recovery time and spontaneous breathing recovery time, and increase the incidence of bradycardia as an adverse reaction.


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