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A Topical Adhesive Containing Anesthetic and Heating Components to Reduce Injection Pain with Subcutaneous Multiple
A novel topical adhesive (S-TA) significantly reduced injection pain, tenderness, and fear of injection for multiple sclerosis (MS) patients receiving subcutaneous medications. This topical anesthetic patch offers improved comfort for MS treatment injections.
Area of Science:
- Neurology
- Dermatology
- Pharmacology
Background:
- Subcutaneous injections for multiple sclerosis (MS) commonly cause pain and fear.
- Synera, a novel topical adhesive with a heating component, delivers lidocaine and tetracaine to reduce injection discomfort.
- This study investigated the efficacy of Synera (S-TA) in mitigating pain and improving comfort during MS drug administration.
Purpose of the Study:
- To evaluate the impact of S-TA on immediate and delayed pain following subcutaneous MS drug injections.
- To assess the effect of S-TA on injection site reactions, tenderness, and fear of injection (FOI).
- To determine optimal application times for S-TA to maximize patient comfort.
Main Methods:
- An open-label prospective study involving 30 participants with MS experiencing injection site reactions.
- Participants received subcutaneous interferon beta (IFNβ) or glatiramer acetate (GA) with S-TA applied 30 and 60 minutes prior to injection.
- Pain, tenderness, local reactions, and FOI were measured at various time points post-injection.
Main Results:
- Significant reductions in immediate injection pain, 12- and 24-hour pain, 24-hour tenderness, and injection site reaction scores were observed with S-TA application (P < .01).
- Fear of injection (FOI) was also significantly reduced.
- Results were consistent across glatiramer acetate (GA) treated patients; adverse events were mild and infrequent.
Conclusions:
- S-TA applied 30 or 60 minutes before subcutaneous MS drug injection effectively reduces pain, tenderness, and fear of injection.
- The findings suggest S-TA as a promising intervention for improving patient comfort during MS therapy.
- Further randomized controlled trials are warranted to confirm the efficacy of S-TA.
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