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血清TLR4水平升高作为不同镇痛方法的小儿患者术后慢性疼痛的潜在标志物。

Elevated serum TLR4 level as a potential marker for postsurgical chronic pain in pediatric patients with different approaches to analgesia.

作者信息

Semkovych Yaroslav, Dmytriiev Dmytro

机构信息

Department of Children Diseases of Postgraduate Medical Education Faculty, Ivano-Frankivsk National Medical University, Ivano-Frankivsk, Ukraine.

Department of Anesthesiology and Intensive Care, Vinnytsia National Pirogov Memorial Medical University, Vinnytsya, Ukraine.

出版信息

Front Med (Lausanne). 2022 Aug 17;9:897533. doi: 10.3389/fmed.2022.897533. eCollection 2022.

DOI:10.3389/fmed.2022.897533
PMID:36059845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9428710/
Abstract

INTRODUCTION

The perioperative period of any surgery is accompanied by immune suppression. The level of Toll-like receptor 4 (TLR4) is known to increase in inflammation and after nerve injury and contributes to the development of neuropathic pain. The interaction of TLRs in response to the effect of opioids results in paradoxical hyperalgesia. Regional anesthesia techniques are the standard of care for perioperative pain management in children.

AIM

The aim of the study was to determine and evaluate the indicators of TLR4 for different methods of pain relief in anesthetic management of hernia repair in children and their effect on pain chronification.

MATERIALS AND METHODS

There were examined 60 children with inguinal hernia during 2020-2022. Children were divided into 3 groups: Group I included 20 children who underwent surgery under general anesthesia using the block of the anterior abdominal wall-transversalis fascia plane block (TFPB), combined with the quadratus lumborum block (QLB-4) a single intramuscular injection; Group II included 20 children who underwent surgery under general anesthesia using the TFPB; Group III comprised 20 children who underwent surgery under general anesthesia using opioid analgesics. The levels of TLR4 were evaluated at a discharge from the hospital, 3 and 6 months after surgery.

RESULTS

There was no difference in age and body weight among all groups. In Group II, boys prevailed. In Group III, the length of hospital stay was the longest (3.28 ± 0.24 days, < 0.05, = 4.09) as compared to children of Group II and Group I (3.0 ± 0.30 ( < 0.05, = 2.647) and 2.1 ± 0.16 days, respectively). While staying in the surgical department, children of Group III demonstrated significantly higher FLACC and VAS scores. The prevalence of chronic pain was the highest among children of Group III (35%) as compared to those in Group II and Group I (20 and 15%, respectively). The highest increase in the level of TLR4 was found in the group of opioid analgesia on the third and sixth months after surgery (68.86 + 10.31 pg/ml and 143.15 + 18.77 pg/ml ( < 0.05, = 6.33), respectively) as compared to patients who received regional anesthesia.

CONCLUSIONS

There were confirmed the following advantages of the transversalis fascia plane block combined with the quadratus lumborum block (QLB + TFPB) a single intramuscular injection: ease of use; adequate perioperative pain control as evidenced by the FLACC and VAS pain assessment scales; reduced perioperative use of opioid analgesics; shortening the length of hospital stay.

摘要

引言

任何手术的围手术期都伴随着免疫抑制。已知Toll样受体4(TLR4)水平在炎症和神经损伤后会升高,并导致神经性疼痛的发展。TLR对阿片类药物作用的反应相互作用会导致矛盾性痛觉过敏。区域麻醉技术是儿童围手术期疼痛管理的标准治疗方法。

目的

本研究的目的是确定和评估儿童疝气修补麻醉管理中不同疼痛缓解方法的TLR4指标及其对疼痛慢性化的影响。

材料与方法

2020年至2022年期间对60例腹股沟疝患儿进行了检查。患儿分为3组:第一组包括20例在全身麻醉下接受手术的患儿,采用前腹壁-腹横筋膜平面阻滞(TFPB)联合腰方肌阻滞(QLB-4)单次肌肉注射;第二组包括20例在全身麻醉下接受手术的患儿,采用TFPB;第三组包括20例在全身麻醉下接受手术的患儿,使用阿片类镇痛药。在出院时、术后3个月和6个月评估TLR4水平。

结果

所有组之间在年龄和体重方面没有差异。第二组中男孩占多数。与第二组和第一组的患儿相比(分别为3.0±0.30(<0.05,F=2.647)和2.1±0.16天),第三组的住院时间最长(3.28±0.24天,<0.05,F=4.09)。在外科病房住院期间,第三组患儿的面部、腿部、活动、哭泣、安慰(FLACC)和视觉模拟评分(VAS)显著更高。与第二组和第一组(分别为20%和15%)相比,第三组患儿慢性疼痛的患病率最高(35%)。与接受区域麻醉的患者相比,在术后第三个月和第六个月,阿片类镇痛组的TLR4水平升高最高(分别为68.86+10.31 pg/ml和143.15+18.77 pg/ml(<0.05,F=6.33))。

结论

证实了腹横筋膜平面阻滞联合腰方肌阻滞(QLB+TFPB)单次肌肉注射具有以下优点:使用方便;通过FLACC和VAS疼痛评估量表证明围手术期疼痛控制充分;减少围手术期阿片类镇痛药的使用;缩短住院时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/9428710/7ada6b7b95cc/fmed-09-897533-g0006.jpg
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