Abstract
This study aims to evaluate the efficacy and safety of post-trabeculectomy topical bevacizumab, in preventing bleb failure. A total of 11 females and 12 males were enrolled for the study. After a complete ophthalmic evaluation, the patients underwent trabeculectomy. Full ophthalmic examination was done the next day, which included visual acuity, intraocular pressure (IOP), and bleb morphology. Next, two drops of bevacizumab [0.25 mg (0.01 ml)] were instilled over the wound area with a tuberculin (1 ml) syringe. Pressure was applied at the medial canthus to prevent it from going into the lacrimal passage. Similar postoperative procedures were repeated at 1, 2, 3, and 4 weeks. So in all, five instillations of bevacizumab were completed. Later, the patients were followed at 1-month interval for 6 months. Target IOP was achieved in all eyes and was maintained during the study period of 6 months without any anti-glaucoma medication. Average IOP before trabeculectomy was 27.27 ± 8.92 mmHg, which decreased postoperatively to 8.77 ± 0.97 mmHg at 3 months and 9.27 ± 1.16 mmHg at 6 months. This drop in IOP was statistically significant on both occasions (p = 0.00). A nice low filtering bleb was formed after the surgery, and it remained the same during the study period. The other parameters like cup-to-disc ratio and visual field did not change during the 6 months of study as expected because glaucoma is a slow progressive disease. Modulating the wound at multiple sites by bevacizumab (inflammation, proliferative, and remodeling stages) can lead to success of trabeculectomy.
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References
Addicks EM, Quigley HA, Green WR, Robin AL. Histologic characteristics of filtering blebs in glaucomatous eyes. Arch Ophthalmol. 1983;101:795–8.
Mills KB. Trabeculectomy: a retrospective long-term follow-up of 444 cases. Br J Ophthalmol. 1981;65:790–5.
Ridgway AE, Rubinstein K, Smith VH. Trabeculectomy. A study of 86 cases. Br J Ophthalmol. 1972;56:511–6.
Ridgway AE. Trabeculectomy. A follow-up study. Br J Ophthalmol. 1974;58:680–6.
Schwartz AL, Anderson DR. Trabecular surgery. Arch Ophthalmol. 1974;92:134–8.
Schwartz PL, Ackerman J, Beards J, Wesseley Z, Goodstein S, Ballen PH. Further experience with trabeculectomy. Ann Ophthalmol. 1976;8:207–17.
Kahook MY, Camejo L, Noecker RJ. Trabeculectomy with intraoperative retrobulbar triamcinolone acetonide. Clin Ophthalmol. 2009;3:29–31.
Lu D, Tai MC, Chiang C. Subconjunctival retention of perfluoropropane gas increases the success of rate of trabeculectomy. Asian J Ophthalmol. 1999;1:8–9.
Lu DW, Tai MC, Chiang CH. Subconjunctival retention of perfluoropropane (C3F8) gas increased the success rates of trabeculectomy. J Ocul Pharmacol Ther. 1997;13:235–42.
Skuta GL. Antifibrotic agents in glaucoma filtering surgery. Int Ophthalmol Clin. 1993;33:165–82.
Rockwood EJ, Parrish 2nd RK, Heuer DK, et al. Glaucoma filtering surgery with 5-fluorouracil. Ophthalmology. 1987;94:1071–8.
Akarsu C, Onol M, Hasanreisoglu B. Postoperative 5-fluorouracil versus intraoperative mitomycin C in high-risk glaucoma filtering surgery: extended follow up. Clin Exp Ophthalmol. 2003;31:199–205.
Membrey WL, Poinoosawmy DP, Bunce C, Hitchings RA. Glaucoma surgery with or without adjunctive antiproliferatives in normal tension glaucoma: 1 intraocular pressure control and complications. Br J Ophthalmol. 2000;84:586–90.
Yoon PS, Singh K. Update on antifibrotic use in glaucoma surgery, including use in trabeculectomy and glaucoma drainage implants and combined cataract and glaucoma surgery. Curr Opin Ophthalmol. 2004;15:141–6.
McGuigan LJ, Cook DJ, Yablonski ME. Dexamethasone, d-penicillamine, and glaucoma filtering surgery in rabbits. Invest Ophthalmol Vis Sci. 1986;27:1755–7.
Mc Guigan LJB, Mason RP, Sanchez R, Quigley HA. d-Penicillamine and beta-aminopropionitrile effects on experimental filtering surgery. Invest Ophthalmol Vis Sci. 1987;28:1625–9.
Moorhead LC. Inhibition of collagen cross-linking: a new approach to ocular scarring. Curr Eye Res. 1981;1:77–83.
Moorhead LC, Smith J, Stewart R, Kimbrough R. Effects of beta-aminopropionitrile after glaucoma filtration surgery; pilot human study. Ann Ophthalmol. 1987;19:223–5.
Cameron ME. Beta irradiation as an adjunct to surgery in refractory glaucoma. Trans Aust Coll Ophthalmol. 1970;2:53–60.
Skuta GL, Parrish RK. Wound healing in glaucoma filtering surgery. Surv Ophthalmol. 1987;32:149–70.
Jordan JF, Diestelhorst M, Grisanti S, Krieglstein GK. Photodynamic modulation of wound healing in glaucoma filtration surgery. Br J Ophthalmol. 2003;87:870–5.
Lu DW, Chang CJ, Chiang CH, Yeh MK, Chou PI. Wound modulation after trabeculectomy by different formulations of antimetabolites in rabbits. J Ocul Pharmacol Ther. 2000;16:529–38.
Demir T, Turgut B, Celiker U, et al. Effects of octreotide acetate and amniotic membrane on wound healing in experimental glaucoma surgery. Doc Ophthalmol. 2003;107:87–92.
Vandewalle E, Spielberg L, Zeyen T, Stalmans I. Can preoperative bevacizumab improve trabeculectomy outcome? “Avastin Trab Study”. Bull Soc Belge Ophthalmol. 2010;314:51–2.
Choi JY, Choi J, Y-De K. Subconjunctival bevacizumab as an adjunct to trabeculectomy in eyes with refractory glaucoma: a case series. Korean J Ophthalmol. 2010;24:47–52.
Li Z, Van Bergen T, Van de Veire S, et al. Inhibition of vascular endothelial growth factor reduces scar formation after glaucoma filtration surgery. Invest Ophthalmol Vis Sci. 2009;50:5217–25.
Cantor LB, Mantravadi A, WuDunn D, Swamynathan K, Cortes A. Morphologic classification of filtering blebs after glaucoma filtration surgery: the Indiana bleb appearance grading scale. Journal of Glaucoma. 2003;12:266–71.
World Health Organization and International Agency for the Prevention of Blindness. The state of the world’s sight. VISION 2020: the Right to Sight: 1999–2005. Geneva: WHO; 2005.
McEvan WK. Application of Poiseuille’s law to aqueous outflow. Arch Ophthalmol. 1958;60:290–4.
Hitchings RA, Grierson I. Clinico pathological correlation in eyes with failed fistulizing surgery. Trans Ophthalmol Soc UK. 1983;103:84–8.
Lama PJ, Fechtner RD. Antifibrotics and wound healing in glaucoma surgery. Surv Ophthalmol. 2003;48:314–46.
Esson DW, Popp MP, Liu L, Schultz GS, Sherwood MB. Microarray analysis of the failure of filtering “blebs” in a rat model of glaucoma filtering surgery. Invest Ophthalmol Vis Sci. 2004;45:4450–62.
Chang MR, Cheng Q, Lee DA. Basic science and clinical aspects of wound healing in glaucoma filtering surgery. J Ocul Pharmacol Ther. 1998;14:75–95.
Grierson I, Joseph J, Miller M, Day JE. Wound repair: the fibroblast and the inhibition of scar formation. Eye. 1988;2(Pt 2):135–48.
Tahery MM, Lee DA. Review: pharmacologic control of wound healing in glaucoma filtration surgery. J Ocul Pharmacol. 1989;5:155–79.
Cordeiro MF, Schultz GS, Ali RR, Bhattacharya SS, Khaw PT. Molecular therapy in ocular wound healing. Br J Ophthalmol. 1999;83:1219–24.
Siriwardena D, Kotecha A, Minassian D, Dart JKG, Khaw PT. Anterior chamber flare after trabeculectomy and after phacoemulsification. Br J Ophthalmol. 2000;84:1056–7.
Gordon CR, Rojavin Y, Patel M, et al. A review on bevacizumab and surgical wound healing: an important warning to all surgeons. Ann Plast Surg. 2009;62(6):707–9.
Wilgus TA, Ferreira AM, Oberyszyn TM, Bergdall VK, Dipietro LA. Regulation of scar formation by vascular endothelial growth factor. Lab Invest. 2008;88:579–90.
Methew R, Barton K. Anti vascular endothelial growth factor therapy in glaucoma filtration surgery. Am J Ophthalmol. 2011;152:10–5.
O’Neill EC, Qin Q, Van Bergen NJ, et al. Antifibrotic activity of bevacizumab on human Tenon’s fibroblast in vitro. Invest Ophthalmol Vis Sci. 2010;51:6524–32.
Nomoto H, Shiraga F, Kuno N, et al. Pharmacokinetics of bevacizumab after topical, subconjunctival, and intravitreal administration in rabbits. Invest Ophthalmol Vis Sci. 2009;50:4807–13.
Dastjerdi MH, Al-Arfaz KM, Nallasamy N, et al. Topical bevacizumab in the treatment of corneal neovascularization: results of a prospective, open-label, non-comparative study. Arch Ophthalmol. 2009;127:381–9.
Bock F, Onderka J, Rummelt C, et al. Safety profile of topical VEGF neutralization at the cornea. Invest Ophthalmol Vis Sci. 2009;50:2095–102.
Kim SW, Ha BJ, Kim EK, Tchah H, Kim TI. The effect of topical bevacizumab on corneal neovascularization. Ophthalmology. 2008;115:33–8.
Koenig Y, Bock F, Horn F, Kruse F, Straub K, Cursiefen C. Short- and long-term safety profile and efficacy of topical bevacizumab (Avastin) eye drops against corneal neovascularization. Graefes Arch Clin Exp Ophthalmol. 2009;247:1375–82.
Hosseini H, Khalili MR. Therapeutic potential of bevacizumab (Avastin) in herpetic stromal keratitis (HSK). Med Hypotheses. 2007;69:568–70.
Heindl LM, Cursiefen C. Pterygium. Etiology, clinical aspects and novel adjuvant therapies. Ophthalmologe. 2010;107(517–20):522–4.
Wu PC, Kuo HK, Tai MH, Shin SJ. Topical bevacizumab eyedrops for limbal-conjunctival neovascularization in impending recurrent pterygium. Cornea. 2009;28:103–4.
Uy HS, Chan PS, Ang RE. Topical bevacizumab and ocular surface neovascularization in patients with Stevens-Johnson syndrome. Cornea. 2008;27:70–3.
Broadway DC, Grierson I, O’Brien C, Hitchings RA. Adverse effects of topical antiglaucoma medication. I. The conjunctival cell profile. Arch Ophthalmol. 1994;112:1437–45.
Liesegang TJ. Conjunctival changes associated with glaucoma therapy: implications for the external disease consultant and the treatment of glaucoma. Cornea. 1998;17:574–83.
Cevenkel B, Kopitar AN, Ihan A. Mediat Inflamm: Inflammatory molecule in aqueous humour and on ocular surface and glaucoma surgery outcome; 2010. doi:10.1155/2010/939602.
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Bhasker, S.K., Saxena, S. & Singh, K. Post-trabeculectomy topical bevacizumab preventing bleb failure: a preliminary study. j ocul biol dis inform 5, 89–95 (2012). https://doi.org/10.1007/s12177-013-9108-3
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DOI: https://doi.org/10.1007/s12177-013-9108-3