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掌侧钢板固定桡骨远端骨折术后术区多模式药物注射是否能改善疼痛评分?

Does Surgical-site Multimodal Drug Injection After Palmar Plating of Distal Radius Fractures Improve Pain Scores?

机构信息

H.-S. Jung, K.-J. Chun, J. Y. Kim, J. Lee, J. S. Lee, Department of Orthopaedic Surgery, Medical Center of Chung-Ang University School of Medicine, Seoul, Korea.

出版信息

Clin Orthop Relat Res. 2020 Nov;478(11):2663-2669. doi: 10.1097/CORR.0000000000001212.

Abstract

BACKGROUND

Although palmar locked plating is a stable fixation method frequently used to treat unstable distal radius fractures (DRFs), surgical treatment may be painful, and so interventions to decrease that pain might improve our patients' experiences with surgery. Some surgeons use local multimodal drug injections to decrease postoperative pain after lower-extremity arthroplasty, but little is known about the effectiveness of a local multimodal drug injection in patients who undergo palmar plating for DRFs.

QUESTIONS/PURPOSES: (1) Do patients who receive a local multimodal drug injection after palmar plating for unstable DRFs have better pain scores at 4, 8, 24, and 48 hours after surgery than patients who have not received such an injection? (2) Do patients who receive a local multimodal drug injection have lower fentanyl consumption and administration of anti-emetic drugs within the first 48 hours after surgery than patients who have not received such an injection?

METHODS

A randomized controlled study was performed between August 2018 and August 2019 at a single tertiary care referral center. Patients who underwent palmar plating for DRFs under general anesthesia were eligible for inclusion. Patients were allocated into two groups: Those who received a local multimodal drug injection, and those who did not receive an injection. During the study period, 101 patients treated with palmar plating for DRFs met the inclusion criteria and were enrolled and randomized. Fifty-two patients were allocated to the multimodal injection group and 49 were allocated to the control group. Three patients (two in the multimodal injection group and one in the control group) were excluded after randomization because their pain level was not registered at any timepoint and so they could not be analyzed; our analysis was by intention to treat, and there was no crossover. After palmar plating, patients in the multimodal injection group received an injection of ropivacaine (10 mL), morphine (5 mL), ceftezole (5 mL) as well as normal saline (5 mL) to the periosteal area, pronator quadratus muscle, subcutaneous area, and skin. There were no differences between the groups in terms of age (62 years ± 13 years in the multimodal injection group versus 62 years ± 11 years in the control group; p = 0.93), gender (84% [42 of 50] women in the multimodal injection group versus 77% [37 of 48] women in the control group; p = 0.39), hand dominance (70% [35 of 50] dominant wrist in the multimodal injection group versus 60% [29 of 48] dominant wrist in the control group; p = 0.32) and AO/Orthopaedic Trauma Association (AO/OTA) classification (p = 0.57). All patients underwent treatment with the same perioperative protocol, and 25 μg of fentanyl was injected intravenously when a patient complained of pain and asked for additional pain control after surgery. In addition, when a patient complained of nausea or vomiting associated with fentanyl use, an anti-emetic drug was also injected. All nursing staff who administered the analgesics and anti-emetic drugs were blinded to treatment allocation. These two groups were compared regarding their pain level using a 100-mm VAS at 4, 8, 24, and 48 hours postoperatively. The minimum clinically important difference (MCID) for the VAS score was set to 20 mm. VAS scores were also collected by nursing staff who remained blinded to the treatment allocation. The total amount of fentanyl use and the number of patients who received anti-emetic drugs associated with administration of fentanyl within the first 48 hours were also recorded.

RESULTS

With an MCID of 20 points, we found no clinically important reduction in VAS scores among patients who received a local multimodal injection compared with those who did not receive an injection at 4 hours (34 ± 15 versus 41 ± 20, mean difference -7.079 [95% CI -13.986 to -0.173]; p = 0.045), 8 hours (27 ± 16 versus 40 ± 19, mean difference -12.263 [95% CI -19.174 to -5.353]; p = 0.001), 24 hours (18 ± 12 versus 29 ± 20, mean difference -11.042 [95% CI -17.664 to -4.419]; p = 0.001), and 48 hours (9 ± 8 versus 10 ± 6, mean difference -1.318 [95% CI -4.000 to 1.365]; p = 0.33). Within the first 48 hours after surgery, fentanyl consumption was lower in patients receiving a local multimodal injection than in control patients (25 μg [range 0-100 μg] versus 37.5 μg [range 0-125 μg], difference of medians -12.5; p = 0.01). There was also a difference between the study groups in terms of the proportion of patients who received anti-emetic medications (16% [8 of 50] in the multimodal injection group versus 35% [17 of 48] in the control group, odds ratio = 2.879 [95% CI 1.102 to 7.519]; p = 0.03).

CONCLUSIONS

Our data suggest that patients who received a surgical-site multimodal analgesic injection after palmar plating for a distal radius fracture had no clinically important reduction in pain scores, but they did consume lower doses of opioid analgesics and fewer of these patients received anti-emetic drugs within 2 days of surgery. The high-potency opioids or other analgesia usually used for postoperative pain management have many side effects. Thus, reducing additional analgesia is as important as postoperative pain management and a surgical-site multimodal analgesic injection is one of the methods to achieve this a goal.

LEVEL OF EVIDENCE

Level I, therapeutic study.

摘要

背景

尽管掌侧锁定钢板固定是一种常用于治疗不稳定型桡骨远端骨折(DRF)的稳定固定方法,但手术治疗可能会引起疼痛,因此干预以减轻这种疼痛可能会改善我们患者的手术体验。一些外科医生在下肢关节置换术后使用局部多模式药物注射来减轻术后疼痛,但对于接受掌侧钢板固定治疗 DRF 的患者,局部多模式药物注射的有效性知之甚少。

问题/目的:(1)与未接受此类注射的患者相比,接受不稳定型 DRF 掌侧钢板固定术后局部多模式药物注射的患者在术后 4、8、24 和 48 小时的疼痛评分是否更好?(2)与未接受此类注射的患者相比,接受局部多模式药物注射的患者在术后 48 小时内芬太尼消耗和使用止吐药的情况是否更低?

方法

在 2018 年 8 月至 2019 年 8 月期间,在一家三级转诊中心进行了一项随机对照研究。接受掌侧钢板固定治疗 DRF 的全麻患者符合纳入标准。患者被分配到两组:接受局部多模式药物注射的患者和未接受注射的患者。在研究期间,101 名接受掌侧钢板固定治疗 DRF 的患者符合纳入标准并被纳入并随机分组。52 名患者被分配到多模式注射组,49 名患者被分配到对照组。3 名患者(2 名在多模式注射组,1 名在对照组)在随机分组后因任何时间点的疼痛水平均未登记而被排除,因此无法进行分析;我们的分析是基于意向治疗,没有交叉。掌侧钢板固定后,多模式注射组患者在骨膜、旋前方肌、皮下区域和皮肤的周围区域接受罗哌卡因(10 mL)、吗啡(5 mL)、头孢唑林(5 mL)和生理盐水(5 mL)注射。两组在年龄(多模式注射组 62 岁±13 岁,对照组 62 岁±11 岁;p = 0.93)、性别(多模式注射组 84%[50 名女性中的 42 名],对照组 77%[48 名女性中的 37 名];p = 0.39)、手优势(多模式注射组 70%[50 名中的 35 名]优势手腕,对照组 60%[48 名中的 29 名];p = 0.32)和 AO/矫形创伤协会(AO/OTA)分类(p = 0.57)方面无差异。所有患者均接受相同的围手术期方案治疗,术后当患者出现疼痛并要求额外的疼痛控制时,静脉注射 25 μg 芬太尼。此外,当患者出现与芬太尼使用相关的恶心或呕吐时,还会注射止吐药。所有给予镇痛和止吐药物的护理人员均对治疗分配保持盲法。通过术后 4、8、24 和 48 小时的 100-mm VAS 比较两组患者的疼痛程度。VAS 评分的最小临床重要差异(MCID)设定为 20mm。护理人员也记录了 VAS 评分,并对治疗分配保持盲法。还记录了芬太尼的总用量和在术后 48 小时内因给予芬太尼而接受止吐药的患者人数。

结果

以 MCID 为 20 分,与未接受注射的患者相比,接受局部多模式药物注射的患者在 4 小时(34 ± 15 比 41 ± 20,平均差值-7.079[95%CI-13.986 至-0.173];p = 0.045)、8 小时(27 ± 16 比 40 ± 19,平均差值-12.263[95%CI-19.174 至-5.353];p = 0.001)、24 小时(18 ± 12 比 29 ± 20,平均差值-11.042[95%CI-17.664 至-4.419];p = 0.001)和 48 小时(9 ± 8 比 10 ± 6,平均差值-1.318[95%CI-4.000 至 1.365];p = 0.33)时的 VAS 评分无明显差异。术后 48 小时内,接受局部多模式药物注射的患者芬太尼消耗量低于对照组(25 μg[0-100 μg]比 37.5 μg[0-125 μg],中位数差值-12.5;p = 0.01)。研究组之间在接受止吐药的患者比例方面也存在差异(多模式注射组 16%[50 名中的 8 名]比对照组 35%[48 名中的 17 名],优势比=2.879[95%CI1.102 至 7.519];p = 0.03)。

结论

我们的数据表明,接受掌侧钢板固定治疗桡骨远端骨折后接受手术部位多模式镇痛注射的患者疼痛评分无明显降低,但他们使用的阿片类药物剂量较低,且术后 2 天内接受止吐药治疗的患者比例也较低。高阿片类药物或其他通常用于术后疼痛管理的镇痛药物有许多副作用。因此,减少额外的镇痛治疗与术后疼痛管理一样重要,手术部位多模式镇痛注射是实现这一目标的方法之一。

证据水平

I 级,治疗性研究。

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