Corneal Patch Graft for the Repair of Late-onset Hypotony or Filtering Bleb Leak After Trabeculectomy

2014 ◽  
Vol 23 (1) ◽  
pp. e76-e80 ◽  
Author(s):  
Frank Bochmann ◽  
Claude Kaufmann ◽  
Anna Kipfer ◽  
Michael A. Thiel
2001 ◽  
Vol 132 (1) ◽  
pp. 36-40 ◽  
Author(s):  
Alan Burnstein ◽  
Darrell WuDunn ◽  
Yoko Ishii ◽  
Christian Jonescu-Cuypers ◽  
Louis B Cantor

2002 ◽  
Vol 133 (6) ◽  
pp. 859
Author(s):  
Anita Panda ◽  
Sanjeev Nainiwal ◽  
Mayank S. Pangtey ◽  
Rajeev Sudan

Eye ◽  
2000 ◽  
Vol 14 (5) ◽  
pp. 802-804 ◽  
Author(s):  
Hidetaka Maeda ◽  
Ayako Eno ◽  
Makoto Nakamura ◽  
Akira Negi
Keyword(s):  

2020 ◽  
pp. 112067212092434
Author(s):  
Michael O’Rourke ◽  
Sarah Moran ◽  
Niamh Collins ◽  
Aoife Doyle

Purpose Bleb dysfunction may occur as a late complication following glaucoma filtration surgery. Over-filtering, thinning and cystic blebs can lead to hypotony, leak and corneal dellen. We report our surgical management and outcomes of this specific entity using donor scleral patch grafts. Methods This is a 10-year non-comparative, retrospective interventional case series. Bleb reconstruction involved excision of encysted conjunctiva and sclera to identify the original fistula. A functioning donor scleral patch graft was sited over this with fixed and releasable sutures and the conjunctiva advanced. Intraocular pressure, visual acuity and post-operative issues were assessed. Results A total of 18 eyes of 17 patients with mean age 65 years (standard deviation 13.5) were included. Trabeculectomy was the primary procedure in 72% ( n = 13) and deep sclerectomy in 28% ( n = 5). Bleb leak accounted for 61% ( n = 11), hypotony 33% ( n = 6) and corneal dellen 6% ( n = 1). Mean pre-operative intraocular pressure was 7 mm Hg (standard deviation 4.6) which increased to 18.5 mm Hg (standard deviation 12) at day 1 ( p < 0.001), 11.8 mm Hg (standard deviation 4.6) at 3 months ( p < 0.05), 12.1 mm Hg (standard deviation 4.2) at 1 year ( p < 0.01) which was maintained at 12.1 mm Hg (standard deviation 5.3) at last follow-up ( p < 0.001). Post-operative interventions included bleb needling, re-suturing, suture removal, further glaucoma management, bleb leak and cataract surgery. Visual acuity also improved post-operatively and was maintained. Conclusion Reconstruction of the filtering bleb architecture with donor sclera results in improved intraocular pressure while maintaining visual acuity. Post-operative care is required to support the restored bleb function. Our findings support the use of scleral patch graft as an effective and safe method for the long-term management of hypotony and bleb leak as a late complication of glaucoma filtration surgery.


Ophthalmology ◽  
2002 ◽  
Vol 109 (1) ◽  
pp. 71-75 ◽  
Author(s):  
Alan L Burnstein ◽  
Darrell WuDunn ◽  
Stephenie L Knotts ◽  
Yara Catoira ◽  
Louis B Cantor
Keyword(s):  

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Taher Eleiwa ◽  
Mariam Raheem ◽  
Nimesh A. Patel ◽  
Audina M. Berrocal ◽  
Alana Grajewski ◽  
...  

Purpose. This case series demonstrate diagnostic features, treatment options, and challenges for Brittle Cornea Syndrome. Observations. Three cases presented with bluish sclera and extremely thin cornea. Genetic workup was performed and confirmed the diagnosis of Brittle Cornea Syndrome, a rare autosomal recessive disorder characterized by corneal thinning and blue sclera. Case 1 was a 4-year-old boy who developed cataract and glaucoma after undergoing right tectonic penetrating keratoplasty (PK) secondary to a spontaneous corneal rupture. Glaucoma was controlled medically. Later, the kid underwent right transcorneal lensectomy and vitrectomy with synechiolysis. After 6 weeks, he sustained graft dehiscence that was repaired using onlay patch graft. Case 2 was a 7-year-old boy who underwent PK in the right eye, then a pericardial patch graft in the left eye following spontaneous corneal rupture. Glaucoma in both eyes was controlled medically. Case 3 was the 2-year-old sister of the 2nd case. She had a pachymetry of 238 μm OD and 254 μm OS. In the 3 cases, parents were instructed to take protective measures for both eyes and to continue with follow-up visits. Also, they were instructed to have regular screenings for late-onset hearing loss, dental abnormalities, and bone deformities. Conclusions. Long-term follow-up of children diagnosed with Brittle Cornea Syndrome is paramount to minimize the morbidity of corneal rupture and late-onset extraocular conditions.


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