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本文引用的文献

1
Injectable multiple sclerosis medications: a patient survey of factors associated with injection-site reactions.注射用多发性硬化症药物:一项关于与注射部位反应相关因素的患者调查。
Int J MS Care. 2012 Spring;14(1):46-53. doi: 10.7224/1537-2073-14.1.46.
2
Understanding and meeting injection device needs in multiple sclerosis: a survey of patient attitudes and practices.了解并满足多发性硬化症患者的注射装置需求:患者态度与行为调查
Patient Prefer Adherence. 2011 Mar 28;5:173-80. doi: 10.2147/PPA.S14903.
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Effect of oral antihistamine on local injection site reactions with self-administered glatiramer acetate.口服抗组胺药对自行注射醋酸格拉替雷所致局部注射部位反应的影响。
J Neurosci Nurs. 2010 Feb;42(1):40-6. doi: 10.1097/jnn.0b013e3181c71ab7.
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Factors that influence adherence with disease-modifying therapy in MS.影响多发性硬化症疾病修正治疗依从性的因素。
J Neurol. 2009 Apr;256(4):568-76. doi: 10.1007/s00415-009-0096-y. Epub 2009 Apr 27.
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Impact of warm compresses on local injection-site reactions with self-administered glatiramer acetate.热敷对自我注射醋酸格拉替雷局部注射部位反应的影响。
J Neurosci Nurs. 2008 Aug;40(4):232-9. doi: 10.1097/01376517-200808000-00007.
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Efficacy of EMLA cream to reduce fear and pain associated with interferon beta-1a injection in patients with multiple sclerosis.复方利多卡因乳膏减轻多发性硬化症患者干扰素β-1a注射相关恐惧和疼痛的疗效
J Neurosci Nurs. 2006 Aug;38(4):222-6. doi: 10.1097/01376517-200608000-00004.
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Clinically important changes in acute pain outcome measures: a validation study.急性疼痛结局指标的临床重要变化:一项验证性研究
J Pain Symptom Manage. 2003 May;25(5):406-11. doi: 10.1016/s0885-3924(03)00162-3.
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Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale.采用11点数字疼痛评分量表测量的慢性疼痛强度变化的临床重要性。
Pain. 2001 Nov;94(2):149-158. doi: 10.1016/S0304-3959(01)00349-9.
9
Comparison of vascular effects of ropivacaine and lidocaine on isolated rings of human arteries.罗哌卡因和利多卡因对人离体动脉环血管作用的比较。
Acta Anaesthesiol Scand. 1995 Aug;39(6):765-8. doi: 10.1111/j.1399-6576.1995.tb04167.x.

一种含有麻醉和加热成分的局部用粘合剂,用于减轻皮下注射多发性硬化症药物时的疼痛:一项试点研究。

A Topical Adhesive Containing Anesthetic and Heating Components to Reduce Injection Pain with Subcutaneous Multiple Sclerosis Medications: A Pilot Study.

作者信息

Brown Theodore R, Simnad Virginia I

出版信息

Int J MS Care. 2017 Mar-Apr;19(2):85-90. doi: 10.7224/1537-2073.2015-099.

DOI:10.7224/1537-2073.2015-099
PMID:32607066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7313407/
Abstract

BACKGROUND

Injection pain and fear of pain are common with subcutaneous medications for treating multiple sclerosis (MS). Synera is a peel-and-stick topical adhesive (S-TA) with a novel heating component to enhance the delivery of an anesthetic mixture of lidocaine and tetracaine. We studied the effect of S-TA on pain and other aspects of comfort after subcutaneous MS drug injection.

METHODS

Thirty participants with MS having injection reactions to subcutaneous interferon beta (IFNβ) or glatiramer acetate (GA) were enrolled in an open-label prospective study. We captured six to seven injections at baseline and with 60- and 30-minute S-TA application times. The primary outcome was immediate pain on injection. Secondary outcomes included 12- and 24-hour pain ratings, 24-hour local injection-site reaction scale scores, 24-hour tenderness, and fear of injection (FOI).

RESULTS

Twenty-nine participants completed the study (interferon beta = 4, GA = 25, mean age = 51 years, females = 86%). There were significant reductions in injection pain, pain at 12 and 24 hours, tenderness at 24 hours, local injection-site reaction scale scores, and FOI for the 30- and 60-minute applications of S-TA (all P < .01). Results were similar in the GA subgroup. Adverse events included muscle spasm and lightheadedness (n = 1) and mild dermatitis (n = 1).

CONCLUSIONS

These results suggest that S-TA applied 30 or 60 minutes before MS drug injection may reduce pain, tenderness, and FOI. Randomized controlled studies are needed to confirm the efficacy of ST-A.

摘要

背景

注射疼痛和对疼痛的恐惧在用于治疗多发性硬化症(MS)的皮下药物治疗中很常见。Synera是一种即揭即贴的局部贴剂(S-TA),具有一种新型加热组件,可增强利多卡因和丁卡因麻醉混合物的递送效果。我们研究了S-TA对皮下注射MS药物后疼痛及其他舒适度方面的影响。

方法

30名对皮下注射干扰素β(IFNβ)或醋酸格拉替雷(GA)有注射反应的MS患者参与了一项开放标签的前瞻性研究。我们在基线以及S-TA应用60分钟和30分钟时记录了六到七次注射情况。主要结局是注射时的即时疼痛。次要结局包括12小时和24小时的疼痛评分、24小时局部注射部位反应量表评分、24小时压痛以及注射恐惧(FOI)。

结果

29名参与者完成了研究(干扰素β组 = 4人,GA组 = 25人,平均年龄 = 51岁,女性 = 86%)。对于S-TA应用30分钟和60分钟的情况,注射疼痛、12小时和24小时的疼痛、24小时压痛、局部注射部位反应量表评分以及FOI均有显著降低(所有P < .01)。GA亚组的结果相似。不良事件包括肌肉痉挛和头晕(n = 1)以及轻度皮炎(n = 1)。

结论

这些结果表明,在MS药物注射前30或60分钟应用S-TA可能会减轻疼痛、压痛和FOI。需要进行随机对照研究来证实S-TA的疗效。