Poonyathalang Anuchit, Tiraset Nanida, Rattanathamsakul Natthapon
From the Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Plast Reconstr Surg Glob Open. 2024 Aug 13;12(8):e6050. doi: 10.1097/GOX.0000000000006050. eCollection 2024 Aug.
This study evaluates the effectiveness of 0.3% hyaluronic acid (HA) eye drops in patients receiving concurrent botulinum toxin (BoNT) injections for benign essential blepharospasm (BEB) or hemifacial spasm (HFS).
This randomized controlled cross-over trial study involved 14 patients with BEB and 33 patients with HFS randomized into two groups (early treatment and deferred treatment) for 3 months of treatment with 0.3% HA eye drops. Data collected at baseline, 3 months, and 6 months included Blepharospasm Severity Scale (BSS) score in patients with BEB; Samsung Medical Class Grading Scale score in patients with HFS; and dry eye symptoms, lower eyelid tear meniscus height (TMH), tear breakup time (TBUT), and corneal fluorescein staining in both groups.
After 3 months of 0.3% HA instillation, patients with BEB in both groups showed significant improvement in BSS, TMH, TBUT, and the amelioration of subjective dry eye symptoms and corneal staining ( < 0.05). However, discontinuation of 0.3% HA eye drops worsened BSS, TMH, and TBUT. Patients with HFS also experienced significant improvement in Samsung Medical Class score, subjective dry eye symptoms, and objective corneal findings ( < 0.05).
Treatment with 0.3% HA eye drops led to significant improvement in spasm severity, and dry eye parameters, after 3 months of instillation in patients with BEB or HFS during concurrent treatment with BoNT injections. The 0.3% HA eye drops were safe and might serve as an add-on treatment for symptom improvement.
本研究评估了0.3%透明质酸(HA)滴眼液对同时接受肉毒杆菌毒素(BoNT)注射治疗良性特发性睑痉挛(BEB)或半面痉挛(HFS)患者的有效性。
这项随机对照交叉试验研究纳入了14例BEB患者和33例HFS患者,随机分为两组(早期治疗组和延迟治疗组),使用0.3% HA滴眼液治疗3个月。在基线、3个月和6个月收集的数据包括BEB患者的睑痉挛严重程度量表(BSS)评分;HFS患者的三星医学分级量表评分;以及两组的干眼症状、下睑泪液半月皱襞高度(TMH)、泪膜破裂时间(TBUT)和角膜荧光素染色。
滴注0.3% HA 3个月后,两组BEB患者的BSS、TMH、TBUT均有显著改善,主观干眼症状和角膜染色也有所改善(P<0.05)。然而,停用0.3% HA滴眼液会使BSS、TMH和TBUT恶化。HFS患者的三星医学分级评分、主观干眼症状和客观角膜检查结果也有显著改善(P<0.05)。
在BoNT注射同时治疗期间,对BEB或HFS患者滴注0.3% HA滴眼液3个月后,痉挛严重程度和干眼参数有显著改善。0.3% HA滴眼液安全,可作为改善症状的附加治疗。