Francis Brian A, Vera Vanessa, Kim Joshua, Basha Mahdi M, Lum Bryant, Grayson Douglas, Vold Steven, Balaram Mini, Simonyi Susan, Ansari Husam, Nayak Kolomeyer Natasha
Doheny and Stein Eye Institutes, UCLA, Los Angeles.
Allergan, an AbbVie company, Irvine.
J Glaucoma. 2025 Apr 1;34(4):330-341. doi: 10.1097/IJG.0000000000002543. Epub 2025 Jan 29.
In the real-world, retrospective, EXPAND study of consecutive adults with glaucoma, ab-externo gel stent implantation effectively lowered intraocular pressure (34%) and the medication burden (61%), with transient/self-resolving hypotony as the most frequent adverse event (28%).
To assess effectiveness and safety of ab-externo gel stent (GS) implantation in glaucoma.
Multicenter, real-world, retrospective study. Consecutive adults with glaucoma and ab-externo GS implantation (with/without phacoemulsification or open/closed conjunctiva) ≥12 months before study entry. Data were extracted between the baseline/preoperative and last follow-up visit or date of secondary surgical intervention (SSI). Primary effectiveness endpoint: proportion of primary eyes (first eye in bilaterally implanted patients) at month 12 (M12) achieving ≥20% intraocular pressure (IOP) reduction from baseline without medication increase, clinical hypotony, vision loss to counting fingers, or SSI. Secondary effectiveness endpoints included complete success (IOP ≤18 mm Hg and ≥20% IOP reduction from medicated baseline without medication, clinical hypotony, or SSI); qualified success (same but without medication increase); and needling rate. Key safety endpoints (all eyes): intraoperative complications, postoperative adverse events (AEs), and SSIs.
The safety population included 466 eyes; 80.7% received the GS alone and 85.0% were implanted with closed conjunctiva. At M12, 39.1% of all primary eyes (N=413) and 54.9% of primary eyes with IOP and medication data at baseline and M12 (N=213) achieved the primary endpoint. At M12 among all primary eyes, the complete success, qualified success, and needling rates were 33.5%, 56.5%, and 28.6%. Most eyes (97.9%) had no intraoperative complications. The most frequent postoperative AE was transient/self-resolving hypotony (IOP <6 mm Hg; 28.1%). Sixty-nine (14.8%) eyes required an SSI.
Ab-externo GS placement effectively lowered IOP and the medication count without unexpected complications/AEs, expanding implantation options based on patients' needs and surgeons' preferences.
在一项针对连续性青光眼成年患者的真实世界回顾性EXPAND研究中,外路凝胶支架植入术有效降低了眼压(34%)和药物负担(61%),最常见的不良事件是短暂性/自行缓解的低眼压(28%)。
评估外路凝胶支架(GS)植入术治疗青光眼的有效性和安全性。
多中心、真实世界、回顾性研究。纳入研究前≥12个月接受外路GS植入术(有/无超声乳化或开放/闭合结膜)的连续性青光眼成年患者。在基线/术前和最后一次随访或二次手术干预(SSI)日期之间提取数据。主要有效性终点:在第12个月(M12)时,未增加药物、未出现临床低眼压、视力未下降至仅能数指或未进行SSI的情况下,主要眼(双侧植入患者的第一眼)眼压从基线降低≥20%的比例。次要有效性终点包括完全成功(眼压≤18 mmHg且眼压从用药基线降低≥20%,无需用药、无临床低眼压或SSI);合格成功(情况相同但未增加药物);以及针刺率。关键安全性终点(所有眼):术中并发症、术后不良事件(AE)和SSI。
安全人群包括466只眼;80.7%仅接受了GS植入,85.0%采用闭合结膜植入。在M12时,所有主要眼(N = 413)中的39.1%以及基线和M12时有眼压和药物数据的主要眼(N = 213)中的54.9%达到了主要终点。在所有主要眼中,M12时的完全成功率、合格成功率和针刺率分别为33.5%、56.5%和28.6%。大多数眼(97.9%)没有术中并发症。最常见的术后AE是短暂性/自行缓解的低眼压(眼压<6 mmHg;28.1%)。69只眼(14.8%)需要进行SSI。
外路GS植入有效降低了眼压和用药次数,且无意外并发症/AE,根据患者需求和外科医生偏好扩展了植入选择。