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罗哌卡因超声引导髂筋膜间隙阻滞的 95%有效容量。

95% effective volume of ropivacaine for ultrasound‑guided supra‑inguinal fascia iliaca compartment block.

机构信息

anesthesiology department, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

出版信息

BMC Anesthesiol. 2023 Mar 29;23(1):98. doi: 10.1186/s12871-023-02049-5.

DOI:10.1186/s12871-023-02049-5
PMID:36991333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10053470/
Abstract

BACKGROUND

Hip arthroplasty is effective in treating hip diseases, such as osteoarthritis and hip fracture, but it often brings severe trauma and pain. In recent years, ultrasound-guided supra-inguinal fascia iliaca compartment block(S-FICB) has become a widely used nerve block method for analgesia in hip arthroplasty.

METHODS

Fifty-three patients preparing for hip arthroplasty were prospectively enrolled. S-FICB was performed under ultrasound guidance, and inject 0.33% ropivacaine into the space. Using the biased-coin design (BCD) sequential allocation method. The initial volume of 0.33% ropivacaine was 30ml. In case of failure, the next patient received a higher volume (defined as the previous volume with an increment of 1.2 mL). If the previous patient had a successful block, the next patient was randomized to a lower volume (defined as the previous volume with a decrement of 1.2 mL), with a probability of b = 0.05, or the same volume, with a probability of 1 - b = 0.95. The study was stopped when 45 successful blocks were achieved.

RESULTS

Forty-five patients (84.9%) were blocked successfully. The 95% effective volume (EV95) was 34.06ml (95%CI 33.35 ~ 36.28ml). There were 31 patients with non-fracture in this study. The quadriceps muscle strength decreased in only two patients. Moreover, they both received 34.8ml of ropivacaine for S-FICB. Twenty-two patients had hip fractures. There were 3 patients (14%) with failed blocks and 19 patients (86%) with successful blocks. However, all fracture patients experienced less pain after S-FICB.

CONCLUSION

EV95 of 0.33% ropivacaine for ultrasound-guided S-FICB was 34.06ml.

TRIAL REGISTRATION

The trial was registered at the Chinese Clinical Trial Registry (registration number: ChiCTR2100052214, registration date: 2021 October 22).

摘要

背景

髋关节置换术在治疗髋关节疾病,如骨关节炎和髋部骨折等方面非常有效,但它通常会带来严重的创伤和疼痛。近年来,超声引导下骼筋膜间隙阻滞(S-FICB)已成为髋关节置换术镇痛的一种广泛应用的神经阻滞方法。

方法

前瞻性纳入 53 例准备行髋关节置换术的患者。在超声引导下进行 S-FICB,向间隙内注射 0.33%罗哌卡因。采用偏倚硬币设计(BCD)序贯分配方法。0.33%罗哌卡因的初始容量为 30ml。如果阻滞失败,下一位患者接受更高的容量(定义为前一容量增加 1.2ml)。如果前一位患者阻滞成功,下一位患者随机接受较低的容量(定义为前一容量减少 1.2ml),b 值为 0.05,或相同的容量,1-b 值为 0.95。当 45 例成功阻滞时,研究停止。

结果

45 例(84.9%)患者阻滞成功。95%有效容量(EV95)为 34.06ml(95%CI 33.35~36.28ml)。本研究中有 31 例患者无骨折。只有 2 例患者股四头肌力量减弱。而且,他们都接受了 34.8ml 的罗哌卡因进行 S-FICB。22 例患者髋部骨折。有 3 例(14%)患者阻滞失败,19 例(86%)患者阻滞成功。然而,所有骨折患者在 S-FICB 后疼痛均减轻。

结论

超声引导下 S-FICB 中 0.33%罗哌卡因的 EV95 为 34.06ml。

试验注册

该试验在中国临床试验注册中心注册(注册号:ChiCTR2100052214,注册日期:2021 年 10 月 22 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/caccd3375089/12871_2023_2049_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/63d364d2a6f5/12871_2023_2049_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/66eb0f2b30da/12871_2023_2049_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/caccd3375089/12871_2023_2049_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/63d364d2a6f5/12871_2023_2049_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/66eb0f2b30da/12871_2023_2049_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe6/10053470/caccd3375089/12871_2023_2049_Fig3_HTML.jpg

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