Andover Eye Associates, Andover, MA 01810, USA.
Curr Med Res Opin. 2011 Jan;27(1):171-8. doi: 10.1185/03007995.2010.539603. Epub 2010 Dec 7.
To evaluate the clinical efficacy and safety of tobramycin/dexamethasone (TobraDex ST ; 'ST') ophthalmic suspension 0.3%/0.05% compared to azithromycin (Azasite) ophthalmic solution (1%) in the treatment of moderate to severe blepharitis/blepharoconjunctivitis.
The study was a multicenter, randomized, investigator-masked, and active-controlled, 15-day study. Enrolled in the study were 122 adult subjects (at least 18 years of age) diagnosed with moderate to severe blepharitis/blepharoconjunctivitis, defined by a minimum score of at least '1' for one of the lid signs, one of the conjunctival signs, and one of the symptoms in at least one eye and a minimum global score (total signs and symptoms score) of '5' in the same eye. One group of 61 subjects received ST with instructions to dose 1 drop four times daily (QID) for 14 days. The other group of 61 subjects received azithromycin and dosed with 1 drop twice daily (BID) for 2 days followed by once daily (QD) dosing for 12 days. Visits were conducted at Day 1 (baseline), Day 8 and Day 15. The a priori primary outcome parameter of the study was the seven-item global score defined as the total score of lid margin redness, bulbar conjunctival redness, palpebral conjunctival redness, ocular discharge (0-3 scale), and lid swelling, itchy eyelids, and gritty eyes (0-4 scale). The study utilized standardized, validated photograph control scales developed by Ora, Inc. (Andover, MA).
The study was registered at ClinicalTrials.gov under the registry number NCT01102244.
A statistically significant lower mean global score (p = 0.0002) was observed in subjects treated with ST compared to subjects treated with azithromycin at Day 8. No serious adverse events were reported during the course of the study in either group.
ST provides a fast and effective treatment of acute blepharitis compared to azithromycin. Initial therapy with the combination of tobramycin/dexamethasone provides faster inflammation relief than azithromycin for moderate to severe blepharitis/blepharoconjunctivitis.
评估妥布霉素/地塞米松(TobraDex ST;'ST')滴眼液 0.3%/0.05%与阿奇霉素(Azasite)滴眼液(1%)治疗中重度睑缘炎/睑结膜炎的临床疗效和安全性。
这是一项多中心、随机、研究者盲法、阳性对照、为期 15 天的研究。共纳入 122 名年龄至少 18 岁的中重度睑缘炎/睑结膜炎成年患者(至少一眼的一项睑缘体征、一项结膜体征和一项症状评分至少为“1”,且同一眼的总体征和症状评分至少为“5”)。一组 61 名患者接受 ST 治疗,指导用药方案为每日 4 次(QID),共 14 天;另一组 61 名患者接受阿奇霉素治疗,前 2 天每日 2 次(BID)滴眼,之后 12 天每日 1 次(QD)滴眼。在第 1 天(基线)、第 8 天和第 15 天进行访视。研究的主要预先设定的终点参数是七项总评分,定义为睑缘红斑、球结膜充血、睑结膜充血、眼部分泌物(0-3 级)、眼睑肿胀、眼睑瘙痒和异物感(0-4 级)的总分。该研究使用 Ora,Inc.(马萨诸塞州安多弗)开发的标准化、经过验证的照片控制量表。
该研究在 ClinicalTrials.gov 注册,注册号为 NCT01102244。
在第 8 天,与阿奇霉素治疗组相比,接受 ST 治疗的患者的平均总评分显著降低(p=0.0002)。在研究过程中,两组均未报告严重不良事件。
与阿奇霉素相比,ST 可快速有效治疗急性睑缘炎。与阿奇霉素相比,对于中重度睑缘炎/睑结膜炎,妥布霉素/地塞米松的初始联合治疗能更快缓解炎症。