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利多卡因滴眼液可减轻与眼部带状疱疹后神经痛相关的疼痛。

Lidocaine eye drops attenuate pain associated with ophthalmic postherpetic neuralgia.

机构信息

Department of Anesthesiology, Kitasato University School of Medicine, Sagamihara, Japan.

出版信息

Anesth Analg. 2010 May 1;110(5):1457-60. doi: 10.1213/ANE.0b013e3181d5adaf. Epub 2010 Mar 17.

Abstract

BACKGROUND

Topical lidocaine (LDC) treatment using a gel or patch preparation is effective in the treatment of postherpetic neuralgia (PHN), but neither is suited for the eye in patients with ophthalmic PHN. Herein, we examined the effect of LDC 4% eye drops on ophthalmic PHN pain.

METHODS

Twenty-four patients with ophthalmic PHN were randomized to receive 0.4 mL eye drops of either LDC 4% or saline placebo (PBO) in the painful eye. After a 7-day period, the patients were crossed over to receive the alternative eye drops. The pain in the eye and the forehead was assessed with a visual analog scale (VAS) before and 15 minutes after treatment. Patients used a descriptive scale to grade pain outcome and were asked to note whether the pain returned and how long after therapy it recurred.

RESULTS

LDC significantly decreased the VAS score of persistent pain in the eye (baseline: 5.9 +/- 2.2 cm; 15 minutes after eye drops: 0.9 +/- 1.8 cm, mean +/- SD [P < 0.01]) and in the forehead (baseline: 6.3 +/- 2.0 cm; 15 minutes after eye drops: 2.6 +/- 2.7 cm [P < 0.01]). The delta change in these VAS scores between LDC and PBO was significant (P < 0.01). Moreover, pain was described as moderate or better by 23 patients after they received LDC and 4 patients of the PBO group. The effect of LDC persisted for a median of 36 hours (range, 8-96 hours) after application.

CONCLUSIONS

This study suggests that LDC provides a significant improvement of ophthalmic PHN because of its prompt analgesia, lack of systemic side effects, and convenience of use.

摘要

背景

局部利多卡因(LDC)凝胶或贴剂治疗对治疗疱疹后神经痛(PHN)有效,但对于眼部 PHN 患者,这两种方法都不适合眼部使用。在此,我们研究了 4%LDC 滴眼液治疗眼部 PHN 疼痛的效果。

方法

24 例眼部 PHN 患者随机分为 LDC 4%滴眼液组和生理盐水安慰剂(PBO)组,分别于疼痛眼滴 0.4ml 药物。7 天后,患者交叉滴用另一种眼药。治疗前和治疗后 15 分钟,用视觉模拟评分(VAS)评估眼部和额部疼痛。患者用描述性量表评价疼痛缓解程度,并记录疼痛是否复发及治疗后多久复发。

结果

LDC 显著降低了眼部持续性疼痛的 VAS 评分(基线:5.9+/-2.2cm;滴眼后 15 分钟:0.9+/-1.8cm,平均值+/-标准差[P<0.01])和额部疼痛评分(基线:6.3+/-2.0cm;滴眼后 15 分钟:2.6+/-2.7cm[P<0.01])。LDC 与 PBO 组间 VAS 评分差值有显著差异(P<0.01)。23 例患者滴用 LDC 后疼痛描述为中度或更重度,而 PBO 组中只有 4 例患者如此描述。LDC 的作用可持续中位数 36 小时(范围 8-96 小时)。

结论

本研究表明,LDC 能够显著改善眼部 PHN 疼痛,且具有起效迅速、无全身不良反应、使用方便等优点。

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