Macular Degeneration: Zambarakji HJ

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A digest of articles written 1999 and later, on the topic "Macular Degeneration," originating from Planet Earth —» Zambarakji HJ.  Display:  All Citations ·  All Abstracts
1 Clinical Conference Assessment of the Heidelberg Retina Tomograph in the detection of sight-threatening diabetic maculopathy. 1999

Zambarakji HJ, Butler TK, Vernon SA. · Department of Ophthalmology, Queen's Medical Centre, University Hospital, Nottingham, UK. · Eye. · Pubmed #10450371 No free full text.

Abstract: PURPOSE: To assess the potential role of the Heidelberg Retina Tomograph (HRT) in screening for sight-threatening macular oedema in diabetes. METHODS: One hundred and thirty-one eyes of 81 consecutive diabetic patients who fitted the inclusion criteria were included in the study. On HRT, the volume above the reference plane bound within a 2 mm diameter circle centred at the fovea was measured. The volumetric indices were compared with the mean measurement index in a group of 20 age-matched controls (mean score = 1, mean +2 SD score = 1.8). We also assessed the sensitivity of the subjective analysis of the intensity image and the addition of the three-dimensional map to the intensity image for detecting macular oedema and clinically significant macular oedema (CSMO). RESULTS: One hundred and twelve eyes of 71 patients had a corrected Snellen visual acuity of 6/9 or better. When considering eyes with 6/9 or better vision only, the system's sensitivity for detecting CSMO was 58.33% 'per eye' examined, and 81.82% 'per patient' examined using a cut-off volumetric index of 1.8. In our study eyes with 6/9 or better vision, we found a 21% prevalence of CSMO. The predictive values of a positive test were 38.89% and 45% (cut-off score 1.8, 'per eye' and 'per patient' respectively) for CSMO. The predictive values of a negative test were 86.84% and 90.48% (cut-off score 1.8, 'per eye' and 'per patient' respectively) for CSMO. CONCLUSIONS: The volumetric assessment of diabetic maculopathy by HRT is a potentially useful method for screening eyes at risk. A larger group of patients with a greater number of eyes with minimal or no maculopathy is required to establish the specificity of this technique.

2 Article Pseudophakic macular edema and oral acetazolamide: an optical coherence tomography measurable, dose-related response. 2008

Ismail RA, Sallam A, Zambarakji HJ. · Whipps Cross University Hospital, London - UK. · Eur J Ophthalmol. · Pubmed #18988178 No free full text.

Abstract: PURPOSE. Although uncommon after phacoemulsification surgery, cystoid macular edema (CME) is an important cause of postoperative reduction of vision after cataract surgery. To demonstrate an optical coherence tomography (OCT) measurable, dose-related response to orally administered acetazolamide in a patient presenting with pseudophakic CME. METHODS. A 76-year-old woman with reduced vision in right eye due to cataract had uneventful phacoemulsification. Surgery was complicated by early onset endophthalmitis that was treated with intravitreal antibiotics with good visual recovery. At 6 months follow-up, she presented with further reduction of vision (0.5 LogMAR) due to CME and a central foveal thickness (CFT) of 587 microm. RESULTS. Acetazolamide treatment was started in combination with topical ketorolac. At a daily dose of 500 mg, CFT and visual acuity were 262 microm and 0.34 LogMAR, respectively. Dose reduction of acetazolamide to 250 mg/day was associated with worsening of the CFT to 335 microm. CFT was subsequently measured at 230 microm on increasing the acetazolamide dose to 500 mg/day and measured 353 microm when acetazolamide dose was halved. CFT was 478 microm when acetazolamide was ceased.CONCLUSIONS. In this report, the authors have shown a dose-related response of pseudophakic CME to oral acetazolamide. This would suggest that the clinical response to oral acetazolamide may be titrated to the extent of CME and monitored by OCT.

3 Article Proton beam irradiation for neovascular age-related macular degeneration. 2006

Zambarakji HJ, Lane AM, Ezra E, Gauthier D, Goitein M, Adams JA, Munzenrider JE, Miller JW, Gragoudas ES. · Retina Service, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts 02114, USA. · Ophthalmology. · Pubmed #16935343 No free full text.

Abstract: OBJECTIVE: To evaluate safety and visual outcomes after proton therapy for subfoveal neovascular age-related macular degeneration (AMD). DESIGN: Randomized dose-ranging clinical trial. PARTICIPANTS: One hundred sixty-six patients with angiographic evidence of classic choroidal neovascularization resulting from AMD and best-corrected visual acuity of 20/320 or better. METHODS: Patients were assigned randomly (1:1) to receive 16-cobalt gray equivalent (CGE) or 24-CGE proton radiation in 2 equal fractions. Visual acuity was measured using standardized protocol refraction. Complete ophthalmological examinations, color fundus photography, and fluorescein angiography were performed before and 3, 6, 12, 18, and 24 months after treatment. MAIN OUTCOME MEASURE: Proportion of eyes losing 3 or more lines of vision from baseline. Kaplan-Meier statistics were used to compare cumulative rates of vision loss between the 2 treatment groups. RESULTS: At 12 months after treatment, 36 eyes (42%) and 27 eyes (35%) lost 3 or more lines of vision in the 16-CGE and 24-CGE groups, respectively. Rates increased to 62% in the 16-CGE group and 53% in the 24-CGE group by 24 months after treatment (P = 0.40). Radiation complications developed in 15.7% of patients receiving 16 CGE and 14.8% of patients receiving 24 CGE. CONCLUSIONS: No significant differences in rates of visual loss were found between the 2 dose groups. Proton radiation may be useful as an adjuvant therapy or as an alternative for patients who decline or are not appropriate for approved therapies.

4 Article Reproducibility of volumetric macular measurements in diabetic patients with the Heidelberg Retina Tomograph. 1999

Zambarakji HJ, Vernon SA, Spencer AF, Amoaku WM. · Department of Ophthalmology, Queen's Medical Centre, University Hospital, Nottingham, UK. · Doc Ophthalmol. · Pubmed #10896350 No free full text.

Abstract: AIMS: To quantify diabetic macular edema by confocal scanning laser ophthalmoscopy and assess its usefulness by determining the reproducibility of topographic measurements at the macula. METHODS: The volumes above reference plane bound by a 2 mm diameter circle centred on the fovea were measured by two observers. The reference plane was adjusted to the lowest point of the height variation of the contour line. The reproducibility of this technique was assessed in 20 eyes of 20 diabetic patients of which 8 eyes had macular edema. Three HRT scans of each eye were obtained. The measurements of volume above reference plane of each scan were repeated three times. RESULTS: For all diabetic eyes, the intra scan coefficients of variability measured 14.71% to 21.21%, the inter scan coefficient of variability was 30.46%. The average standard deviations were 0.053 mm3 for one examination per scan, 0.047 mm3 for two examinations per scan and 0.044 mm3 for three examinations per scan. Linear regression demonstrated an increase in standard deviation with greater volumetric measurements (p < 0.001). We found good correlation (r = 0.959, p < 0.001) and strong agreement between the two observer's findings for all 20 eyes. For the 8 eyes with macular edema, the coefficients of variability were similar to those calculated for all 20 eyes. The average SD for one examination per scan were 0.078 mm3, 0.069 mm3 for two examinations per scan and 0.062 mm3 for three examinations per scan. We found good correlation (r = 0.945, p < 0.001) and strong agreement between the two observer's findings in eyes with edema. CONCLUSION: The reproducibility of this technique has been demonstrated in diabetic eyes. This may have useful clinical applications for the quantification of diabetic macular edema and monitoring of laser therapy.