肉毒杆菌毒素注射对带状疱疹后神经痛患者疼痛程度和生活质量的影响

R. Prasuna, Ajay Aeerabolli
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引用次数: 0

摘要

背景:带状疱疹和带状疱疹后神经痛(PHN)是水痘-带状疱疹病毒再激活的结果。疼痛随着年龄的增长而急剧增加,老年人更容易遭受痛苦。如果带状疱疹不及早治疗,患者可能会发展为PHN。对一些人来说,它可以持续1-2年。肉毒杆菌毒素注射(BTX-A)对患有PHN疼痛的患者是有用的。目的:研究肉毒杆菌毒素对PHN患者疼痛程度和生活质量的影响。方法:对30例接受皮下注射BTX-A治疗的PHN患者进行了基于医院记录的随访研究。注射前,我们使用SF-36评分测量了疼痛严重程度的视觉模拟评分(VAS)和生活质量(QOL)量表。给予BTX-A注射,患者每月随访6个月。在随访期间,测量VAS、生活质量、疼痛频率和镇痛药的使用情况。结果:大多数患者年龄在60-69岁之间(40%)。男性和女性的比例差别不大。6个月时,平均疼痛严重程度从8.9显著降低到5.8。生活质量在6个月内显著改善。疼痛频率在6个月时从22.33显著下降到18.56。平均镇痛药使用量为87.43,在BTX-A后2周显著降至7,然后在4周缓慢增至7.66,在12周增至8.23,在24周增至10.4。结论:BTX-A治疗PNH疗效确切,疗效确切。它可以被认为是治疗PNH的有效方法,尤其是在无反应的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of botulinum toxin injection on pain severity and quality of life among patients with postherpetic neuralgia
Background: Herpes zoster and postherpetic neuralgia (PHN) results from reactivation of varicella-zoster virus. Pain increases sharply with advancing age and the elderly are more inclined to suffer. If herpes zoster is not treated early, patients may develop PHN. For some, it can persist for 1–2 years. Botulinum toxin injection (BTX-A) has been useful for patients suffering from PHN pain. Objective: The objective of this study was to study the effect of botulinum toxin on pain severity and quality of life in patients with PHN. Methods: A hospital record-based follow-up study was carried out among 30 PHN patients treated with hypodermic injection of BTX-A. Before injection, we measured Visual Analog Score (VAS) for pain severity and the Quality of Life (QOL) Scale using short form survey-36 (SF-36) score. BTX-A injections were given, and patients were followed every month for 6 months. During follow-up, VAS, QOL, pain frequency, and analgesic use were measured. Results: Majority were 60–69 years (40%). The proportion of males and females was not much different. Mean pain severity reduced significantly from 8.9 to 5.8 at 6 months. QOL improved significantly in 6 months. Pain frequency decreased significantly from 22.33 to 18.56 at 6 months. Mean analgesics use was 87.43 which reduced significantly to 7 at 2 weeks after BTX-A and then slowly increased to 7.66 at 4 weeks, to 8.23 at 12 weeks, and 10.4 at 24 weeks. Conclusion: Using BTX-A for treating PNH is promising and gives long-lasting results. It can be considered a valid approach in the treatment of PNH, especially in nonresponsive patients.
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