不含吗啡和肾上腺素的关节周围多模态药物注射在前交叉韧带重建中的效果和安全性

IF 0.4 Q4 ORTHOPEDICS
Changhun Han, Yusuke Hashimoto, Sunao Nakagawa, S. Takahashi, Yohei Nishida, S. Yamasaki, J. Takigami, Hiroaki Nakamura
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The following clinical outcomes were compared between the groups: visual analog scale (VAS) score, C-reactive protein (CRP) concentration, number of times the patients used additional analgesics, complication rate, and postoperative time to achieve straight leg raise (SLR). Results Twenty-nine patients with PMDI and 29 controls were enrolled. The VAS score at 1 day postoperatively was lower in the PMDI than the control group (1.93  ±  1.44 vs. 3.41  ±  1.75, respectively; P < 0.001). The CRP concentration at 1 and 3 days was lower in the PMDI than the control group (0.46  ±  0.47 vs. 1.00  ±  0.69 mg/dL, P < 0.001; and 1.93  ±  1.71 vs. 4.01  ±  2.55 mg/dL, P < 0.001, respectively). The average number of additional analgesics used was significantly lower in the PMDI than the control group. There were no significant differences in the frequency of occurrence of postoperative complications between the two groups. 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引用次数: 0

摘要

背景:关节周围多模态药物注射(PMDI)是前交叉韧带重建(ACLR)后安全有效的疼痛管理技术;然而,添加吗啡和肾上腺素有时会引起不良反应。因此,我们评价ACLR术后不加吗啡和肾上腺素的PMDI的疗效。方法本回顾性匹配病例对照研究纳入了行原发性双束ACLR合并PMDI的患者,然后根据性别、年龄和体重指数采用倾向匹配分析与未行PMDI的对照组进行一对一匹配。比较两组间的临床结果:视觉模拟评分(VAS)评分、c反应蛋白(CRP)浓度、患者额外使用镇痛药次数、并发症发生率、术后达到直腿抬高(SLR)时间。结果入选PMDI患者29例,对照组29例。PMDI组术后1 d VAS评分低于对照组(分别为1.93±1.44∶3.41±1.75);p < 0.001)。PMDI组第1天和第3天CRP浓度低于对照组(0.46±0.47 vs 1.00±0.69 mg/dL, P < 0.001;和1.93±1.71和4.01±2.55 mg / dL, P < 0.001,分别)。PMDI组额外使用镇痛药的平均数量明显低于对照组。两组患者术后并发症发生频率差异无统计学意义。PMDI组患者在1 d内达到SLR的人数为27/29(93%),显著高于对照组(12/29,41%)(P < 0.001)。结论ACLR术后不使用吗啡和肾上腺素的PMDI降低了患者的主观疼痛水平和客观炎症反应,无并发症,使患者早日实现功能恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect and safety of periarticular multimodal drug injection without morphine and epinephrine in anterior cruciate ligament reconstruction
Background Periarticular multimodal drug injection (PMDI) is a safe and effective pain management technique after anterior cruciate ligament reconstruction (ACLR); however, adding morphine and epinephrine sometimes causes adverse effects. Therefore, we evaluated the efficacy of PMDI without morphine and epinephrine after ACLR. Methods This retrospective matched case-control study included patients who had undergone primary double-bundle ACLR with PMDI and were then matched one-to-one with a control group without PMDI based on sex, age, and body mass index using propensity-matched analysis. The following clinical outcomes were compared between the groups: visual analog scale (VAS) score, C-reactive protein (CRP) concentration, number of times the patients used additional analgesics, complication rate, and postoperative time to achieve straight leg raise (SLR). Results Twenty-nine patients with PMDI and 29 controls were enrolled. The VAS score at 1 day postoperatively was lower in the PMDI than the control group (1.93  ±  1.44 vs. 3.41  ±  1.75, respectively; P < 0.001). The CRP concentration at 1 and 3 days was lower in the PMDI than the control group (0.46  ±  0.47 vs. 1.00  ±  0.69 mg/dL, P < 0.001; and 1.93  ±  1.71 vs. 4.01  ±  2.55 mg/dL, P < 0.001, respectively). The average number of additional analgesics used was significantly lower in the PMDI than the control group. There were no significant differences in the frequency of occurrence of postoperative complications between the two groups. The number of patients who could achieve SLR within 1 day was 27/29 (93%) in PMDI group, which was significantly higher than the control group (12/29, 41%) (P < 0.001). Conclusion PMDI without morphine and epinephrine after ACLR reduced patients’ subjective pain level, objective inflammatory response without complications and enabled patients to achieve early functional recovery.
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
36
审稿时长
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