SYMPOSIUM - GLAUCOMA
Year : 2009 | Volume
: 16 | Issue : 3 | Page : 107--111
Results from the tube versus trabeculectomy study
Steven J Gedde, the Tube Versus Trabeculectomy Study Group
Bascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida, USA
Steven J Gedde
Bascom Palmer Eye Institute, 900 N.W. 17th Street, Miami, Florida 33136
The Tube Versus Trabeculectomy (TVT) Study is a multicenter randomized clinical trial comparing the safety and efficacy of tube shunt surgery to trabeculectomy with mitomycin (MMC) in eyes with previous cataract and/or failed glaucoma surgery. Tube shunt surgery was more likely to maintain intraocular pressure (IOP) control and avoid persistent hypotony, reoperation for glaucoma, or loss of light perception vision than trabeculectomy with MMC during the first year of follow-up. Both surgical procedures had similar IOP reduction at 1 year, but less supplemental medical therapy was used following trabeculectomy. The incidence of postoperative complications was higher after trabeculectomy with MMC relative to tube shunt surgery, but serious complications associated with vision loss and/or reoperation developed with similar frequency after both of the procedures. There was no significant difference in the rate of vision loss following trabeculectomy with MMC and tube shunt surgery after 1 year of follow-up. Cataract progression was common, but occurred with similar frequency with both of the surgical procedures.
|How to cite this article:|
Gedde SJ, the Tube Versus Trabeculectomy Study Group. Results from the tube versus trabeculectomy study.Middle East Afr J Ophthalmol 2009;16:107-111
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Gedde SJ, the Tube Versus Trabeculectomy Study Group. Results from the tube versus trabeculectomy study. Middle East Afr J Ophthalmol [serial online] 2009 [cited 2021 Dec 7 ];16:107-111
Available from: http://www.meajo.org/text.asp?2009/16/3/107/56219
Recently, practice patterns in glaucoma surgery have undergone significant changes. The number of trabeculectomies performed among Medicare beneficiaries between 1995 and 2004 has steadily declined, and there has been a concurrent rise in tube shunt surgery.  Surveys of the American Glaucoma Society membership has also demonstrated an increase in the popularity of tube shunts as an alternative to trabeculectomy, especially in eyes that have undergone previous ocular surgery. , Despite these trends, there is no clear consensus among glaucoma specialists regarding the preferred surgical approach for managing glaucoma in eyes that have previously undergone cataract or glaucoma surgery, with some surgeons favoring a trabeculectomy with an adjunctive antifibrotic agent and others preferring a tube shunt. ,
The Tube Versus Trabeculectomy (TVT) Study is a multicenter randomized clinical trial comparing the safety and efficacy of tube shunt surgery to trabeculectomy with mitomycin C (MMC) in eyes that have undergone prior ocular surgery. Patients with uncontrolled glaucoma who had previously undergone cataract extraction with intraocular lens implantation and/or failed trabeculectomy were randomized to receive a 350-mm 2 Baerveldt glaucoma implant or trabeculectomy with MMC. The goal of this investigator initiated study is to provide information that will assist in surgical decision making in similar patient groups.
Material and Methods
The design and methods of the TVT Study were previously described in detail.  The study is registered with http://www.clinicaltrials.gov (NCT00306852). The inclusion and exclusion criteria for the study are listed in [Table 1]. Enrolled patients were randomly assigned to treatment with a tube shunt or trabeculectomy with MMC. Patients in the tube group underwent placement of a 350-mm 2 Baerveldt glaucoma implant superotemporally with a complete restriction of flow at the time of implantation [Figure 1]. Patients in the trabeculectomy group had a superior trabeculectomy with a standard dosage of MMC of 0.4 mg/ml for 4 min [Figure 2]. Follow-up visits were scheduled 1 day, 1 week, 1 month, 3 months, 6 months, 1 year, 18 months, 2 years, 3 years, 4 years, and 5 years postoperatively. Each examination included measurement of Snellen visual acuity (VA), intraocular pressure (IOP), slit lamp biomicroscopy, Seidel testing, and ophthalmoscopy. Humphrey perimetry, Early Treatment Diabetic Retinopathy Study (ETDRS) VA, and quality of life using the National Eye Institute Questionnaire (NEI VFQ-25) were assessed at baseline and at the annual follow-up visits. A formal motility evaluation was performed in all patients at baseline and at the 1-year and 5-year follow-up visits and at any visit after 3 months in which the patient reported diplopia. The examining clinician provided a reason for loss of 2 or more lines of Snellen VA at follow-up visits after 3 months.
Failure was prospectively defined as IOP > 21 mm Hg or not reduced by 20% below baseline on two consecutive follow-up visits after 3 months, IOP 5 mm Hg on two consecutive follow-up visits after 3 months, reoperation for glaucoma, or loss of light perception vision. Reoperation for glaucoma or a complication was defined as additional surgery requiring a return to the operating room. Cyclodestruction was also counted as a reoperation for glaucoma, and a vitreous tap with the injection of intravitreal antibiotics was a reoperation for a complication. Interventions performed at the slit lamp, such as needling procedures or reformation of the anterior chamber, were not considered reoperations. Serious complications were defined as surgical complications that were associated with loss of two or more lines of Snellen VA and/or reoperation to manage the complication.
A total of 212 eyes of 212 patients were enrolled at 17 Clinical Centers, including 107 in the tube group and 105 in the trabeculectomy group.  The mean age of the study population was 71.0 years, and 53% were women. The baseline IOP was 25.3 ± 5.3 mm Hg (mean ± SD) on 3.1 ± 1.2 glaucoma medications (mean ± SD), and 81% of patients had primary open-angle glaucoma. There were no significant differences in any of the demographic and ocular characteristics between the tube group and the trabeculectomy group, suggesting that randomization was very effective in creating two balanced treatment groups.
Postoperative interventions in the tube group included rip cord removal in 19 (18%) patients, laser suture lysis in 5 (5%) patients, anterior chamber reformation in 4 (4%) patients, needling procedures in 2 (2%) patients, and injection of 5-fluorouracil in 1 (1%) patient.  In the trabeculectomy group, laser suture lysis was performed in 51 (49%) patients, 5-fluorouracil injection in 23 (22%) patients, needling procedures in 8 (8%) patients, injection of intracameral tissue plasminogen activator in 2 (2%) patients, and suturing of a wound leak in 1 (1%) patient. 
[Table 2] presents the IOPs and number of glaucoma medications at baseline and 1 year. The trabeculectomy group had significantly lower mean IOPs than the tube group at all follow-up visits during the first 3 months, but there was no significant difference in the degree of IOP reduction between the treatment groups after 3 months.  There was a significantly increased use of adjunctive medical therapy in the tube group in comparison to the trabeculectomy group at all follow-up visits during the first postoperative year.  Kaplan-Meier plots of the probability of failure are shown in [Figure 3]. The cumulative probability of failure was 3.9% in the tube group and 13.5% in the trabeculectomy group at 1 year, a difference that was statistically significant (p = 0.017, log rank test).  A greater proportion of patients in the trabeculectomy group (5%) required reoperations for glaucoma in comparison to those of the tube group (1%) during the first year of follow-up. However, this difference did not quite reach the level of statistical significance (p = 0.086, log rank test). 
There was reduction in VA in both the tube group and the trabeculectomy group during the first year of follow-up, but Snellen and ETDRS VA were similar between treatment groups at 1 year.  There was no difference in the rate of loss of two or more lines of Snellen VA between the tube group (32%) and the trabeculectomy group (33%) after 1 year (p = 1.00, chi-square test).  Many causes of vision loss were not directly attributable to the surgical procedures under study, such as macular degeneration and posterior capsular opacification.
There were a large number of surgical complications in the TVT Study, but most were transient and self-limited. A similar rate of intraoperative complications was observed in the tube group (7%) and the trabeculectomy group (10%) (p = 0.59, chi-square test).  Significantly more patients in the trabeculectomy group (57%) experienced postoperative complications than those in the tube group (34%) during the first year of follow-up (p = 0.001, chi-square test).  However, all complications are not equal in severity, and serious complications associated with reoperation to manage the complication and/or loss of two Snellen lines of vision occurred with similar frequency in the trabeculectomy group (27%) and tube group (17%) at 1 year (p = 0.12, chi-square test).  Wound leaks (p = 0.004, chi-square test) and dysesthesia (p = 0.034, Fischer's exact test) were significantly more common in the trabeculectomy group than the tube group.  New postoperative motility disturbances developed more frequently in the tube group (9.9%) than the trabeculectomy group (0%) during the first year of follow-up (p = 0.005, Fisher's exact test), and there was a tendency for diplopia to occur more commonly in the tube group (5%) than the trabeculectomy group (0%) (p = 0.06, Fisher's exact test). 
Cataract progression was common among phakic patients in the TVT Study, but occurred with similar frequency in the tube group (33%) and the trabeculectomy group (48%) during the first year of follow-up (p = 0.50, chi-square test).  There was no statistical difference in the rate of cataract surgery between the tube group (17%) and the trabeculectomy group (5%) after 1 year (p = 0.35, Chi-square test). 
The TVT Study enrolled patients with medically uncontrolled glaucoma who had previous cataract extraction with intraocular lens implantation and/or failed filtering surgery and randomized them to surgical treatment with a trabeculectomy with MMC or tube shunt placement. During the first year of follow-up, patients who were treated with tube shunt surgery were more likely to maintain IOP control and avoid persistent hypotony, loss of light perception vision, or reoperation for glaucoma in comparison to those who underwent trabeculectomy with MMC. Both surgical procedures were associated with similar IOP reduction at 1 year, but there was less need for supplemental medical therapy after trabeculectomy. The incidence of postoperative complications was higher after trabeculectomy with MMC as compared with tube shunt surgery. However, serious complications associated with reoperation and/or vision loss occurred with similar frequency after both of the surgical procedures. After 1 year of follow-up, there was no significant difference in the rate of vision loss following trabeculectomy with MMC or tube shunt surgery. Cataract progression was common, but occurred with similar frequency with both surgical procedures.
The results of the TVT Study provide further evidence that the role of tube shunts in the surgical management of glaucoma should be expanded. Although these devices have historically been reserved for refractory glaucomas at high risk of failure with standard filtering surgery, this study enrolled eyes at lower risk for failure. The TVT Study does not demonstrate clear superiority of one glaucoma operation over the other. There are other factors that must be considered when selecting a surgical procedure, including the surgeon's skill and experience with both operations, the patient's willingness to undergo repeat glaucoma surgery, and the planned surgical approach if failure occurs. Because postoperative interventions and surgical complications were more common after trabeculectomy, tube shunt surgery may be the preferred surgical approach when follow-up is limited. Additional data will be forthcoming from the TVT Study, and it is needed to fully assess the risks and benefits of tube shunt surgery and trabeculectomy with MMC in managing medically uncontrolled glaucoma in similar patient groups.
This study is supported by research grants from Pfizer, Inc., New York, New York USA; Advanced Medical Optics, Irvine, California USA; the National Eye Institute (grant EY014801), National Institutes of Health, Bethesda, Maryland USA; and Research to Prevent Blindness, Inc., New York, New York USA.
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