The efficacy of a netilmicin/dexamethasone gel combination in the treatment of posterior blepharitis in moderate-severe dry eye patients.

IF 1.4 4区 医学 Q3 OPHTHALMOLOGY European Journal of Ophthalmology Pub Date : 2024-10-21 DOI:10.1177/11206721241293175
Giovanni William Oliverio, Leandro Inferrera, Elisa I Postorino, Paola Palino, Pasquale Aragona
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Abstract

Purpose: To evaluate the safety and efficacy of netilmicin/dexamethasone combination in the treatment of meibomian gland dysfunction (MGD)-associated posterior blepharitis.

Methods: In this prospective and controlled study were enrolled 40 patients with MGD and symptoms of dry eye disease. Two groups were established: 20 patients (group 1) received netilmicin 3 mg/ml and dexamethasone 1 mg/ml eye gel, whereas in group 2 (20 patients) received vehicle for 15 days. Patients were evaluated at baseline, 15 and 45 days, including SANDE and VARS questionnaire, non-invasive tear film breakup time (NIBUT), tear meniscus height (TMH), ocular redness and meibography score. Moreover, fluorescein tear-film breakup time (TBUT), fluorescein ocular surface staining, lid margin evaluation including hyperemia, edema and meibum expressibility and quality examinations were carried out. Furthermore, intraocular pressure (IOP) and best-corrected visual acuity (BCVA) were considered as safety parameters.

Results: In group 1, at 15 and 45 days there were statistically significant changes in VARS and SANDE score (p < 0.0001) as well as lid margin parameters, TBUT and fluorescein ocular surface staining (p < 0.0001). Comparing the two groups, a significant improvement of SANDE score was observed at 15 days in group 1 as well as lid margin parameters, TBUT and fluorescein ocular surface staining at 15 and 45 days (all p < 0.0001).

Conclusion: Netilmicin/dexamethasone combination is effective and safe to treat MGD-associated posterior blepharitis improving both symptoms and ocular surface signs.

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奈替米星/地塞米松凝胶组合治疗中重度干眼症患者后睑缘炎的疗效。
目的:评估奈替米星/地塞米松联合疗法治疗睑板腺功能障碍(MGD)相关后睑缘炎的安全性和有效性:在这项前瞻性对照研究中,共招募了40名患有睑板腺功能障碍并伴有干眼症状的患者。研究分为两组:20 名患者(第 1 组)使用 3 毫克/毫升的奈替米星和 1 毫克/毫升的地塞米松眼用凝胶,而第 2 组(20 名患者)使用 15 天的药物。分别在基线、15 天和 45 天对患者进行评估,包括 SANDE 和 VARS 问卷、无创泪膜破裂时间(NIBUT)、泪液半月板高度(TMH)、眼红和 meibography 评分。此外,还进行了荧光素泪膜破裂时间(TBUT)、荧光素眼表面染色、睑缘评估(包括充血、水肿和睑板腺分泌功能)和质量检查。此外,眼压(IOP)和最佳矫正视力(BCVA)也被视为安全参数:结果:在第 1 组中,15 天和 45 天后,VARS 和 SANDE 评分有显著的统计学变化(P奈替米星/地塞米松联合用药治疗 MGD 相关性后睑缘炎既有效又安全,可改善症状和眼表体征。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
372
审稿时长
3-8 weeks
期刊介绍: The European Journal of Ophthalmology was founded in 1991 and is issued in print bi-monthly. It publishes only peer-reviewed original research reporting clinical observations and laboratory investigations with clinical relevance focusing on new diagnostic and surgical techniques, instrument and therapy updates, results of clinical trials and research findings.
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