COMBINED TRANSSCLERAL DIODE LASER CYCLOPHOTOCOAGULATION AND TRANSSCLERAL RETINAL PHOTOCOAGULATION FOR REFRACTORY NEOVASCULAR GLAUCOMA

Retina ◽  
1996 ◽  
Vol 16 (2) ◽  
pp. 164-165 ◽  
Author(s):  
JAMES C. TSAI ◽  
PHILIP A. BLOOM ◽  
WENDY A. FRANKS ◽  
PENG T. KHAW
2008 ◽  
Vol 39 (1) ◽  
pp. 22-29 ◽  
Author(s):  
Russell Pokroy ◽  
Yoel Greenwald ◽  
Ayala Pollack ◽  
Amir Bukelman ◽  
Miriam Zalish

2010 ◽  
Vol 38 (4) ◽  
pp. 353-357 ◽  
Author(s):  
Sudipta Ghosh ◽  
Dalveer Singh ◽  
Jonathan B Ruddle ◽  
Michael Shiu ◽  
Michael A Coote ◽  
...  

2009 ◽  
Vol 18 (3) ◽  
pp. 192-196 ◽  
Author(s):  
Nilgun Yildirim ◽  
Ilgaz Sagdic Yalvac ◽  
Afsun Sahin ◽  
Ahmet Ozer ◽  
Tark Bozca

2015 ◽  
Vol 62 (2) ◽  
pp. 19-23
Author(s):  
Nevena Bjelovic ◽  
Ivan Sencanic

Introduction: Transscleral diode laser cyclophotoco-agulation is new cyclodestructive procedure for the treatment of refractory, advanced glaucoma. Comparing to other cyclophotocoagulation it is more safe and selective. Aim of the study: To evaluate the efficacy and safety of transscleral diode laser cyclophotocoagulation in treatment of refractory glaucoma. Material: A retrospective cohort study included 35 patients (36 eyes) with refractory glaucoma treated in Centre for Sight "Oftalmika", form March 2008 to February 2012. All patients were treated by transscleral diode laser cyclophotocoagulation. The mean age was 68.8 ? 16.8 years. Most prevalent type was the neovascular glaucoma (23 ili 65.7%). The treatment consisted of 16-20 applications of 1.5-2.0 W energy applied for 1.5-2.0 seconds. Results: The average IOP reduction was 33.4mmHg or 63,1%. The best treatment result was achieved in the neovascular glaucoma, where IOP reduction 6 months after the procedure was 71,2 %. The poorest results were obtained in congenital glaucoma (28,5%). Prior ciclodestructive procedures and/or filtration glaucoma procedures did not influence laser treatment results. In only 5,7% patients repeated procedures were indicated. Overall complication rates was 22,8%, and the most prevalent complications were hyphema and reversible keratopathy (8,6% eyes). Postoperative hypothonia had one patient. Number of antiglaucoma medications, 6 months after the treatment, was reduced by 1,1 (45,7%). Medication reduction was most prevalent in the case of seconday glaucoma 1,4 (52,6%), and the least prevalent in congenital glaucoma 0,5 (14,3%). Only one patient had occasional pain after the procedure. Conclusion: Transscleral diode laser cyclophotoco-agulation is safe and effective procedure in the treatment of refractory glaucoma. The best treatment result was achieved in the neovascular glaucoma, and the poorest in congenital glaucoma. Effect of the procedure on pain relif is unequivocal.


2009 ◽  
Vol 19 (3) ◽  
pp. 20-23
Author(s):  
Ahmed M. Emarah ◽  
Mostafa A El-Helw ◽  
Mohammed A Hassaballa ◽  
Heba A ElGuindy ◽  
Mohammed A Fakery

2019 ◽  
Vol 2 (6) ◽  
pp. 402-412 ◽  
Author(s):  
Giancarlo A. Garcia ◽  
Christine V. Nguyen ◽  
Aleksandr Yelenskiy ◽  
Goichi Akiyama ◽  
Brett McKnight ◽  
...  

1990 ◽  
Vol 21 (7) ◽  
pp. 492-496
Author(s):  
Tom Jennings ◽  
Terry Fuller ◽  
John A Vukich ◽  
Tim T Lam ◽  
Brian C Joondeph ◽  
...  

Author(s):  
Ihsan Cakir ◽  
Cigdem Altan ◽  
Gulay Yalcinkaya ◽  
Nese Alagoz ◽  
Banu Solmaz ◽  
...  

2022 ◽  
Vol 8 ◽  
Author(s):  
Ling Bai ◽  
Yanfen Wang ◽  
Xindi Liu ◽  
Yuping Zheng ◽  
Wenjing Wang ◽  
...  

This study investigates the safety and efficacy of conbercept injection through different routes for neovascular glaucoma (NVG) treatment, in which seventy-four patients (81 eyes) with NVG caused by ischemia retinopathy had participated. Patients were divided into three stages according to the progression of NVG and were randomly assigned to receive intracameral or intravitreal conbercept injection. After conbercept injection, patients experienced improved best-corrected visual acuity (BCVA), good intraocular pressure (IOP) control, and neovascularization of Iris (NVI) regression. In stage III, patients required trabeculectomy with mitomycin C plus pan-retinal photocoagulation (PRP) to achieve complete NVI regression. Compared to the intravitreal group, the intracameral group had significantly lower IOP in 2 days in stage III and 1 day in stages I and II after injection, complete NVI regression before PRP in stages I and II, and better NVI regression in stage III. The rates of hyphema after trabeculectomy and malfunction filtering bleb suffering needle bleb revision were lower in the intracameral group, but only the hyphema rate was significantly different. Injections through different routes are all safe. We recommend intravitreal injections for patients in stages I and II, but for stage III, intracameral injection is better, and trabeculectomy with mitomycin C should be conducted within 2 days after injection to maximally reduce the risk of perioperative hyphema.Trial Registration:ClinicalTrials.gov, identifier NCT03154892.


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