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Table of Contents - WOC 2012

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FP-RET-FR 98 (5)<br />

Intravitreal (IVT) as Compared to Posterior Sub-Tenon (PST) Injection<br />

<strong>of</strong> Triamcinolone Acetonide (Kenacort) for Diffuse Diabetic Macular<br />

Edema<br />

Qamar Muhammad Rashad (1)<br />

1. Quaid e Azam Medical College<br />

Purpose: To assess the safety and efficacy <strong>of</strong> the intravitreal (IVT) injection as<br />

compared to posterior subtenon (PST) injection <strong>of</strong> Triamcinolone<br />

Acetonide(Kenacort) for the treatment <strong>of</strong> diffuse diabetic macular edema.<br />

Methods: We selected sixty cases with diffuse diabetic macular edema with the<br />

mean age fifty two years. All focal leaks were treated by laser photocoagulation.<br />

In the same patients, after taking written consent, one eye was assigned to 4<br />

mg IVT injection and the fellow eye was then treated with 40 mg PST injection<br />

<strong>of</strong> Kenacort.<br />

Results: BCVA improved in 80 % patients <strong>of</strong> IVT group as compared to 100%<br />

in PST group along with decrease in retinal thickness but it was more rapid<br />

and then recurred in IVT group at the end <strong>of</strong> 6-months.IOP was increased<br />

significantly in 30% <strong>of</strong> cases where intravitreal injection <strong>of</strong> Kenacort was used<br />

and none <strong>of</strong> the patients with posterior sub-tenon injection. Raised IOP was<br />

treated with topical anti- glaucoma medication without any permanent damage<br />

to the visual function. No other intraocular or extra ocular complications were<br />

noted.<br />

Conclusion: Posterior Sub-Tenon injection is an easy, safe and valid alternative<br />

to intravitreal one for the treatment <strong>of</strong> diffuse Diabetic Macular Edema.<br />

FP-RET-FR 98 (6)<br />

Analgesic Effect <strong>of</strong> Topical Sodium Dicl<strong>of</strong>enac during Retinal<br />

Photocoagulation for Diabetic Retinopathy; A Randomized Double-<br />

Masked Placebo-Controlled Crossover Clinical Trial<br />

Ramezani Alireza (1) , Entezari Morteza (1) , Shahbazi Mahdi (1) ,<br />

Semnani Yosef (1, 2) , Rajavi Zhaleh (1)<br />

1. Ophthalmic Research Center, Imam Hossein Medical Center, Shahid Beheshti<br />

University<br />

2. Imam Hossein Medical center, Shahid Beheshti University <strong>of</strong> Medical Sciences<br />

Purpose: To evaluate the analgesic effect <strong>of</strong> topical sodium dicl<strong>of</strong>enac during<br />

retinal laser photocoagulation for diabetic retinopathy.<br />

Methods: In a randomized placebo-controlled intra-individual two-period crossover<br />

clinical trial, patients with diabetic retinopathy candidate for retinal<br />

laser photocoagulation were included. At the first session, one eye received<br />

topical sodium dicl<strong>of</strong>enac 0.1% and the other placebo drop 3 times, about 60<br />

minutes before laser treatment. At the second session, the eyes were given<br />

the alternate drug. Patients scored their pain using a visual analogue scale<br />

(max=10cm) at both stages. The patients, nurse, and the surgeons were all<br />

masked to the drops given. The difference <strong>of</strong> the pain level was compared.<br />

Results: A total <strong>of</strong> 200 eyes <strong>of</strong> 100 patients (63 female) with mean age <strong>of</strong> 54±10<br />

years were enrolled. Both treatments were matched regarding the applied<br />

laser. The mean <strong>of</strong> pain scoring reported by the patients at first stage was<br />

5.8±3.1 and 5.3±2.7 for the eyes receiving topical dicl<strong>of</strong>enac and placebo,<br />

respectively. Corresponding features were 5.2±3.0 and 5.0±2.4 for the second<br />

stage. There was no significant difference between the treatments.<br />

Conclusion: Pretreatment with topical sodium dicl<strong>of</strong>enac 0.1% does not have<br />

any analgesic effect during peripheral retinal laser photocoagulation in diabetic<br />

cases.<br />

<strong>WOC</strong><strong>2012</strong> Abstract Book<br />

FP-RET-FR 98 (7)<br />

Long-Term Safety and Efficacy <strong>of</strong> 0.5 mg Ranibizumab in Patients<br />

with Visual Impairment Due to Diabetic Macular Edema: The<br />

RESTORE Extension Study<br />

Lang on behalf <strong>of</strong> the RESTORE Gabriele E. (1)<br />

1. Department <strong>of</strong> Ophthalmology, University Eye Hospital<br />

Objective/Purpose: To evaluate the long-term safety and efficacy <strong>of</strong> 0.5 mg<br />

ranibizumab (RBZ) in patients with visual impairment due to diabetic macular<br />

edema (DME) who completed the 12-month RESTORE core study.<br />

Methods: In the 2-year RESTORE extension study, RBZ was given open-label<br />

pro-re-nata (PRN) according to pre-specified criteria based on monthly<br />

best-corrected visual acuity (BCVA) assessments; monthly injections were<br />

suspended when BCVA was stable or better than 83 letters and reinitiated<br />

when BCVA decreased. Primary endpoint: incidences <strong>of</strong> ocular and non-ocular<br />

adverse events (AEs) during the 2-year extension period.<br />

Results: 240 (79%) <strong>of</strong> 303 patients, who completed the core study, were<br />

followed up. Key patients characteristics (mean±SD) at extension baseline:<br />

62.6±8.8 years <strong>of</strong> age, 7.5±1.2% HbA1c, BCVA <strong>of</strong> 70.4±11.1 letters, central<br />

retinal thickness <strong>of</strong> 309.5±111.3 µm. Demographic and disease characteristics<br />

at extension baseline were comparable to the entire core study patient<br />

population. Treatment numbers, AE incidences, and mean BCVA change were<br />

assessed during the 2-year extension and over the total 3-year treatment<br />

exposure period (including the core study).<br />

Conclusion: With the clinical trial outcomes <strong>of</strong> up to 3 years <strong>of</strong> RBZ treatment,<br />

the RESTORE extension study provides further evidence for long-term safety<br />

and efficacy <strong>of</strong> RBZ PRN treatment in DME.<br />

FP-RET-FR 98 (8)<br />

Association between HLA-DQB1 and Diabetic Retinopathy in Iranian<br />

Pateints with Type I Diabetes Mellitus<br />

Daneshvar Ramin (1) , Khazaei Mohammad Hassan (1) , Tavakol Afshari Jalil (1) ,<br />

Khazaei Bahram (1) , Ganjali Rashin (1)<br />

1. Mashhad University <strong>of</strong> Medical Sciences<br />

Purpose: Investigation <strong>of</strong> human leukocyte antigen (HLA) in diabetic patients<br />

with long disease duration and without retinopathy.<br />

Methods: In a retrospective, non-randomized study, two subsets <strong>of</strong> type 1<br />

diabetic patients were included in the study: Group 1: those who developed<br />

diabetic retinopathy with disease duration less than 20 years (23 patients);<br />

Group 2: those without diabetic retinopathy despite passing more than 20 years<br />

<strong>of</strong> diabetes (19 patients). HLA-DQB1 typing was done using a polymerase<br />

chain reaction with sequence-specific primer (PCR-SSP) method.<br />

Results: Diabetic groups were matched with regard to level <strong>of</strong> glycemic control,<br />

blood pressure, and lipid pr<strong>of</strong>ile. HLA-DQB1*0201/ HLA-DQB1*0501and HLA-<br />

DQB1*0201/ HLA-DQB1*0504 haplotypes were more common in Group 1 than<br />

Group 2 [26.1% vs. 0.0%; p= 0.019]. HLA-DQB1*0301 and HLA-DQB1*0304<br />

were less common among Group 1 than Group 2 [63.2% vs. 34.8%, p=0.067].<br />

Conclusion: HLA-DQB1 is associated with diabetic retinopathy in Iranian type<br />

1 diabetic patients. HLA typing may be beneficial for predicting the prognosis<br />

<strong>of</strong> diabetic retinopathy in younger diabetic patients. Study was previously<br />

presented in ‹European Journal <strong>of</strong> Ophthalmology›; however, the study results<br />

would be nice to present to the ophthalmologist in the MEACO region.<br />

127

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