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Abstract #46649 Published in IGR 13-3

The Ahmed Versus Baerveldt Study One-Year Treatment Outcomes

Christakis PG; Kalenak JW; Zurakowski D; Tsai JC; Kammer JA; Harasymowycz PJ; Ahmed IIK
Ophthalmology 2011;

See also comment(s) by William Feuer & Keith Barton


Objective: To report the 1-year treatment outcomes of the Ahmed Versus Baerveldt (AVB) Study. Design: Multicenter randomized clinical trial. Participants: A total of 238 patients were enrolled in the study, including 124 in the Ahmed group and 114 in the Baerveldt group. Methods: Patients aged 18 years or older with uncontrolled glaucoma refractory to medicinal, laser, and surgical therapy were randomized to undergo implantation of an Ahmed-FP7 valve (New World Medical, Inc., Rancho Cucamonga, CA) or a Baerveldt-350 implant (Abbott Medical Optics, Inc., Santa Ana, CA), to be followed for 5 years. Main Outcome Measures: The primary outcome measure was failure, defined as intraocular pressure (IOP) out of target range (5-18 mmHg with (greater-than or equal to)20% reduction from baseline) for 2 consecutive visits after 3 months, vision-threatening complications, additional glaucoma procedures, or loss of light perception. Secondary outcome measures included IOP, medication use, visual acuity, complications, and interventions. Results: There were no significant differences in baseline ocular or demographic characteristics between the study groups with the exception of sex. Preoperatively, the study group had a mean IOP of 31.4(plus or minus)10.8 mmHg on a mean of 3.1(plus or minus)1.0 glaucoma medications with a median Snellen acuity of 20/100. The cumulative probability of failure a 1-year was 43% in the Ahmed group and 28% in the Baerveldt group (P=0.02). The mean IOP at 1 year was 16.5(plus or minus)5.3 mmHg in the Ahmed group and 13.6(plus or minus)4.8 mmHg in the Baerveldt group (P < 0.001). The mean number of glaucoma medications required was 1.6(plus or minus)1.3 in the Ahmed group and 1.2(plus or minus)1.3 in the Baerveldt group (P=0.03). Visual acuity was similar in both groups at all visits in the first year (P=0.66). In the first year after surgery, there were a similar number of patients who experienced postoperative complications in the 2 groups (45% Ahmed, 54% Baerveldt, P=0.19), but a greater number of patients in the Baerveldt group required interventions (26% Ahmed vs. 42% Baerveldt, P=0.009). Conclusions: The Baerveldt-350 group had a higher success rate than the Ahmed-FP7 group after 1 year of follow-up, but required a greater number of interventions. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.

I.I.K. Ahmed. Department of Ophthalmology and Vision Sciences, University of Toronto: Faculty of Medicine, Toronto, .


Classification:

12.8.2 With tube implant or other drainage devices (Part of: 12 Surgical treatment > 12.8 Filtering surgery)



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