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神经周围注射地塞米松:神经毒性还是神经保护作用?临床前证据的系统评价

Perineural dexamethasone: neurotoxicity or neuroprotection? A systematic review of preclinical evidence.

作者信息

De Cassai Alessandro, Santonastaso Domenico Pietro, Coppolino Francesco, D'Errico Cristiano, Melegari Gabriele, Dost Burhan, Aviani Fulvio Giulia, Boscolo Annalisa, Boscolo-Berto Rafael, Navalesi Paolo

机构信息

Department of Medicine (DIMED), University of Padua, Padua, Italy.

Institute of Anesthesia and Intensive Care Unit, University Hospital of Padua, Padua, Italy.

出版信息

J Anesth Analg Crit Care. 2025 Aug 6;5(1):50. doi: 10.1186/s44158-025-00271-w.

Abstract

BACKGROUND

Perineural dexamethasone is widely used as an adjuvant to local anesthetics in regional anesthesia to prolong analgesia. However, concerns persist regarding its potential neurotoxic effects, particularly when administered perineurally. This systematic review aims to synthesize preclinical evidence evaluating the neurotoxicity or neuroprotective properties of perineural dexamethasone.

METHODS

A systematic search of PubMed, CENTRAL, Scopus, and Embase was conducted through May 22, 2025. Eligible studies included in vivo or in vitro preclinical models assessing the neurotoxic or neuroprotective effects of perineural dexamethasone compared to control conditions. Risk of bias was assessed using the SYRCLE tool for in vivo studies and a narrative evaluation for in vitro studies. A total of 14 studies (11 in vivo, 3 in vitro) met inclusion criteria.

RESULTS

In vitro studies showed that dexamethasone alone was not neurotoxic at clinically relevant doses but could enhance cytotoxicity when combined with local anesthetics at higher concentrations. In vivo models generally demonstrated no significant long-term nerve inflammation, degeneration or demyelination, with some early protective effects observed in perineural dexamethasone groups. However, all in vivo studies were rated at high risk of bias. In nerve injury models, dexamethasone reduced apoptotic and inflammatory markers when administered immediately post-injury, with limited effect when delayed.

CONCLUSIONS

Preclinical evidence supports the general safety of low-dose, preservative-free perineural dexamethasone. Nonetheless, high-dose use, additives, and application in patients with neuropathies may pose risks. Given the high risk of bias in existing studies and minimal added benefit over systemic administration, clinical caution is advised.

摘要

背景

在区域麻醉中,神经周围注射地塞米松作为局部麻醉剂的辅助药物被广泛用于延长镇痛时间。然而,人们对其潜在的神经毒性作用仍存在担忧,尤其是在神经周围给药时。本系统评价旨在综合评估神经周围注射地塞米松神经毒性或神经保护特性的临床前证据。

方法

截至2025年5月22日,对PubMed、CENTRAL、Scopus和Embase进行了系统检索。符合条件的研究包括体内或体外临床前模型,评估与对照条件相比神经周围注射地塞米松的神经毒性或神经保护作用。使用SYRCLE工具评估体内研究的偏倚风险,对体外研究进行叙述性评价。共有14项研究(11项体内研究,3项体外研究)符合纳入标准。

结果

体外研究表明,单独使用地塞米松在临床相关剂量下无神经毒性,但与高浓度局部麻醉剂联合使用时可增强细胞毒性。体内模型一般未显示出明显的长期神经炎症、变性或脱髓鞘,在神经周围注射地塞米松的组中观察到一些早期保护作用。然而,所有体内研究的偏倚风险均被评为高风险。在神经损伤模型中,地塞米松在损伤后立即给药时可降低凋亡和炎症标志物水平,延迟给药时效果有限。

结论

临床前证据支持低剂量、无防腐剂的神经周围注射地塞米松的总体安全性。尽管如此,高剂量使用、添加剂以及在患有神经病变的患者中应用可能存在风险。鉴于现有研究存在高偏倚风险且与全身给药相比额外获益极小,建议临床谨慎使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c9/12329900/d6d23cf02f00/44158_2025_271_Fig1_HTML.jpg

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