TY - JOUR
T1 - Intermediate-term Results of a Randomized Clinical Trial of the 350- versus- the 500-mm2 Baerveldt Implant
AU - Lloyd, Mary Ann
AU - Baerveldt, George
AU - Fellenbaum, Paul S.
AU - Sidoti, Paul A.
AU - Minckler, Don S.
AU - Martone, James F.
AU - LaBree, Laurie
AU - Heuer, Dale K.
N1 - Funding Information:
Presented in part at the Association for Research in Vision and Ophthalmology Annual Meeting, Sarasota, May 1992 and May 1993, and at the American Academy ofOphthalmology Annual Meeting, Chicago, November 1993. Supported in part by the Foundation for Glaucoma Research, San Francisco, California; National Glaucoma Research, a program of the American Health Assistance Foundation, Beltsville, Maryland; and Research to Prevent Blindness, Inc, New York, New York. Dr. Baerveldt has a financial interest in the Baerveldt glaucoma implant; the other authors have no proprietary interest in glaucoma shunting devices. Reprint requests to Mary Ann Lloyd, MD, Department ofOphthalmology, Palo Alto Medical Foundation, 300 Homer Ave, Palo Alto, CA 94301.
PY - 1994
Y1 - 1994
N2 - Background: The Baerveldt glaucoma implant is a large equatorial aqueous shunting device that is installed through a single-quadrant conjunctival incision. The intermediateterm results of a randomized study comparing the 350- and 500-mm2 Baerveldt implants are reported. Methods: Seventy-three patients with medically uncontrollable, nonneovascular glaucomas associated with aphakia, pseudophakia, or failed filters were enrolled in a randomized, prospective study comparing 350- and 500-mm2 Baerveldt implants. Surgical success was defined as 6 mmHg ≤ final intraocular pressure ≤ 21 mmHg without glaucoma reoperation or devastating complication. Results: Of patients with 350- and 500-mm2 implants, 93% and 88%, respectively, achieved surgical success (18-month life-table analysis, P = 0.93). The 500-mm2 implants afforded intraocular pressure control with significantly fewer medications (0.7 versus 1.3; P = 0.006). The postoperative visual acuities remained within one line of the preoperative visual acuities or improved in 62% and 66% of patients in the 350- and 500mm2 groups, respectively (P = 0.93). Complication rates were statistically similar. The most frequent ones in the 350- and 500-mm2 groups, respectively, were serous choroidal effusion (16% and 32%), strabismus (16% and 19%), anterior uveitis (14% and 11 %), and corneal or corneal graft edema (11 % each). Conclusion: The intermediate-term results of the 350- and 500-mm2 Baerveldt implants were statistically comparable with respect to surgical and visual outcomes, as well as complications, although the larger implant was associated with a higher rate of some complications. However, the 500-mm2 Baerveldt implant afforded intraocular pressure control with fewer medications than the 350-mm2 implant.
AB - Background: The Baerveldt glaucoma implant is a large equatorial aqueous shunting device that is installed through a single-quadrant conjunctival incision. The intermediateterm results of a randomized study comparing the 350- and 500-mm2 Baerveldt implants are reported. Methods: Seventy-three patients with medically uncontrollable, nonneovascular glaucomas associated with aphakia, pseudophakia, or failed filters were enrolled in a randomized, prospective study comparing 350- and 500-mm2 Baerveldt implants. Surgical success was defined as 6 mmHg ≤ final intraocular pressure ≤ 21 mmHg without glaucoma reoperation or devastating complication. Results: Of patients with 350- and 500-mm2 implants, 93% and 88%, respectively, achieved surgical success (18-month life-table analysis, P = 0.93). The 500-mm2 implants afforded intraocular pressure control with significantly fewer medications (0.7 versus 1.3; P = 0.006). The postoperative visual acuities remained within one line of the preoperative visual acuities or improved in 62% and 66% of patients in the 350- and 500mm2 groups, respectively (P = 0.93). Complication rates were statistically similar. The most frequent ones in the 350- and 500-mm2 groups, respectively, were serous choroidal effusion (16% and 32%), strabismus (16% and 19%), anterior uveitis (14% and 11 %), and corneal or corneal graft edema (11 % each). Conclusion: The intermediate-term results of the 350- and 500-mm2 Baerveldt implants were statistically comparable with respect to surgical and visual outcomes, as well as complications, although the larger implant was associated with a higher rate of some complications. However, the 500-mm2 Baerveldt implant afforded intraocular pressure control with fewer medications than the 350-mm2 implant.
UR - http://www.scopus.com/inward/record.url?scp=0028000025&partnerID=8YFLogxK
U2 - 10.1016/S0161-6420(94)31152-3
DO - 10.1016/S0161-6420(94)31152-3
M3 - Article
C2 - 8058290
AN - SCOPUS:0028000025
SN - 0161-6420
VL - 101
SP - 1456
EP - 1464
JO - Ophthalmology
JF - Ophthalmology
IS - 8
ER -