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1.
Plast Reconstr Surg ; 2024 May 06.
Article in English | MEDLINE | ID: mdl-38722563

ABSTRACT

BACKGROUND: To compare the outcomes of two types of tarsoconjunctival pedicle flaps for reconstruction of large lower eyelid defects. METHODS: Retrospective medical record review of consecutive patients who underwent centrally-based or laterally-based tarsoconjunctival pedicle transconjunctival flap for lower eyelid reconstruction for defects greater than 50% of the lid margin. Full thickness skin grafts were used for anterior lamellar reconstruction in all cases. The primary outcome measure was eyelid position, function and satisfactory cosmesis. RESULTS: Forty-three patients were identified. Twenty-six patients underwent reconstruction with a centrally-based tarsoconjunctival pedicle flap; 17 patients underwent reconstruction with a laterally-based tarsoconjunctival pedicle flap. The average size of the lid defect was 77.7% (range 50-100%) in the central group and 75% (range 50-100%) in the lateral group (p=0.604). Mean follow up time was 61.5 weeks in the central group and 46.6 weeks in the lateral group (p=0.765). After division of the flap and during follow up, 27% of the centrally based group required revisional surgery with none in the laterally based group (p=0.03). 100% of the patients with centrally based flaps required second staged division of flap, whereas only 52% of patients with a laterally based flaps underwent second staged flap division. (p<0.001). CONCLUSION: Outcome suggests that for reconstruction of large lower lid defects requiring lid sharing procedures, both centrally and lateral-based procedures have equivalent functional outcome. However, the laterally based group has less need for revisional procedures and may not need a second stage division of the flap.

2.
J Craniofac Surg ; 35(4): e325-e329, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38385685

ABSTRACT

PURPOSE: To describe a modified approach for full-thickness lower eyelid defect reconstruction. METHODS: This is a retrospective review of 5 patients with large full-thickness lower eyelid defects after tumor resection requiring reconstruction. For these lower eyelid defects, a lateral-based or superior-based tarsoconjunctival pedicle flap from the upper eyelid was used to rebuild the posterior lamella. In all cases, the anterior lamella was supplied from an adjacent myocutaneous flap in a bucket handle configuration. Data collection included tumor type and location, size of eyelid defect, presence of canalicular involvement, postoperative eyelid position, patient satisfaction, and complication rates. RESULTS: Five eyelids of 5 patients underwent Mohs micrographic excision of basal cell carcinoma followed by reconstruction with a bucket handle flap. Age range was 68 to 96 years old (mean of 81 y). Five patients presented with lower eyelid involvement. The defect size ranged from 80% to 100% of the eyelid. Three patients had canalicular involvement and required bicanalicular nasolacrimal stent placement. After reconstruction, all patients showed good eyelid apposition to the globe with excellent esthetic outcome. No revision procedures were done. Average follow-up time was 13 months (range of 8 to 21 mo). CONCLUSION: The bucket handle flap for full-thickness eyelid reconstruction is a simple technique that allows for preservation of all anatomical layers of the anterior lamella. This technique shows promising functional and esthetic outcomes.


Subject(s)
Carcinoma, Basal Cell , Eyelid Neoplasms , Mohs Surgery , Surgical Flaps , Humans , Aged , Eyelid Neoplasms/surgery , Aged, 80 and over , Retrospective Studies , Male , Female , Carcinoma, Basal Cell/surgery , Treatment Outcome , Plastic Surgery Procedures/methods , Blepharoplasty/methods , Eyelids/surgery , Patient Satisfaction
3.
Eur J Pediatr ; 183(1): 235-242, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37870609

ABSTRACT

The purpose of this study is to examine the association between blepharoptosis and cognitive performance in late adolescence. This population-based, retrospective, cross-sectional study included 1,411,570 Israeli-born adolescents (620,107 women, 43.9%) aged 16-19 years who were medically examined before compulsory military service between 1993 and 2017. The diagnosis of blepharoptosis was verified by an ophthalmologist. Cognitive performance was assessed by a validated intelligence-quotient-equivalent test, comprising four domains (problem-solving, verbal abstraction and categorization, verbal comprehension, and mathematical abilities). Cognitive Z-scores were calculated and categorized as high (≥ 1 standard deviation (SD)), medium (- 1 to < 1 SD), and low (less than - 1 SD). Relationships were analyzed using regression models adjusted for sociodemographic variables including sex, year of birth, residential socioeconomic status, education level, body mass index, and familial country of origin. A total of 577 (41 per 100,000, 32.2% women) adolescents were diagnosed with blepharoptosis. The proportions of unilateral and bilateral visual impairment among adolescents with blepharoptosis were 13.0% and 3.5%, respectively. In a multivariable analysis, blepharoptosis was associated with a 0.18 SD reduction in cognitive Z-score (p < 0.001). The adjusted odds ratios for low and high cognitive Z-scores in adolescents with blepharoptosis were 1.54 (1.25-1.89) and 0.80 (0.62-1.04), respectively. This relationship persisted when adolescents with normal best-corrected visual acuity or unimpaired health status were analyzed separately.  Conclusions: Blepharoptosis is associated with reduced cognitive performance determined in late adolescence. Future prospective studies should investigate the causes of this link and their underlying mechanisms. What is Known: • While earlier investigations have examined the effects of blepharoptosis on vision and quality of life, the association between blepharoptosis and cognitive outcomes in youth has remained unexplored. What is New: • This nationwide study involving 1.4 million Israeli adolescents found a correlation between blepharoptosis and reduced cognitive performance. • Our findings suggest a potential interplay between blepharoptosis and cognitive development in the pediatric population, calling for increased focus on the educational needs of affected individuals.


Subject(s)
Blepharoptosis , Humans , Adolescent , Child , Female , Male , Blepharoptosis/epidemiology , Blepharoptosis/etiology , Prospective Studies , Quality of Life , Retrospective Studies , Cross-Sectional Studies , Cognition
4.
Orbit ; 42(1): 81-86, 2023 Feb.
Article in English | MEDLINE | ID: mdl-34284693

ABSTRACT

A 10-month-old female presented with a rapidly growing, painless mass in the right upper eyelid. Due to suspected malignancy, she underwent an urgent biopsy. Histopathological and immunohistochemical analyses revealed nodular fasciitis. Here, we describe the case and perform a literature review of orbital nodular fasciitis in the pediatric population.


Subject(s)
Eyelids , Fasciitis , Humans , Child , Female , Infant , Diagnosis, Differential , Biopsy , Eyelids/pathology , Fasciitis/diagnostic imaging , Fasciitis/surgery
5.
Harefuah ; 161(4): 223-227, 2022 Apr.
Article in Hebrew | MEDLINE | ID: mdl-35466606

ABSTRACT

OBJECTIVES: Thyroid Eye Disease (TED), also known as Graves' ophthalmopathy, is the most frequent extrathyroidal manifestation of autoimmune dysthyroidism. The most common ocular signs are eyelid retraction, proptosis, and strabismus, alongside specific dermatopathies. This article aims to review the options to improve TED manifestation by lifestyle adjustment. RESULTS: Tobacco smoking is the strongest risk factor for the development of TED and is associated with increased incidence and severity of TED and reduction in response to treatment. Smoking cessation decreases the incidence of TED and compares the risk level of ex-smokers to the risk level of the general population. Selenium is a chemical element with anti-oxidative properties. Selenium levels were significantly lower in Graves' disease patients with TED compared with those without TED. A double-blinded, randomized-control trial demonstrated that supplementation of selenium was associated with improved quality of life, decreased ocular involvement, and slowed TED progression while taken for a limited period. Statins administration to thyroid patients is associated with a reduced risk of TED. Recently, a few studies have shown an increased risk of developing TED and increased severity depending on the level of lipids in the blood, which suggests that balancing blood lipid levels by statins or by low-fat diet can help prevent TED. CONCLUSIONS: Lifestyle adjustment might be critical for a significant portion of patients. By supporting smoking cessation, the recommendation of selenium supplementation for a limited period and reducing serum cholesterol levels can prevent the development of TED, reduce its severity, and improve the patient's quality of life.


Subject(s)
Graves Disease , Graves Ophthalmopathy , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Selenium , Graves Disease/complications , Graves Disease/epidemiology , Graves Ophthalmopathy/epidemiology , Graves Ophthalmopathy/etiology , Graves Ophthalmopathy/therapy , Humans , Life Style , Quality of Life , Randomized Controlled Trials as Topic
6.
Ophthalmic Plast Reconstr Surg ; 38(1): 50-52, 2022.
Article in English | MEDLINE | ID: mdl-34085991

ABSTRACT

PURPOSE: To compare outcomes of Mueller's Muscle Conjunctival Resection (MMCR) between 2 groups of patients with different anatomy due to ethnic heritage. METHODS: The medical records of patients who underwent MMCR between 2013 and 2018 were retrospectively reviewed. Patients who underwent additional procedures, such as upper blepharoplasty and browplasty, were excluded from the study. Patients were divided in 2 groups based on self-identified ethnic groups (Asian and Caucasian). Image J software was used to calculate MRD1 from digital images. The improvement of MRD1 (net MRD1) after surgery was evaluated and compared between 2 groups. RESULTS: Eighty-three eyes of 68 patients were included in this study. The Asian group consisted of 41 eyelids from 28 patients. The Caucasian group consisted of 42 eyelids from 40 patients. The average age was 52.18 (SD 20.176) in the Asian group compared with the 66.45 years (SD 9.22, p < 0.005) in the Caucasian group. The mean improvement of MRD1 was 1.96 ± 0.75 mm in Asian group and 2.05 ± 0.72 mm in Caucasian group, which was not statistically significant (p = 0.62). The incidence of ptosis overcorrection and undercorrection between the groups was also not statistically significant. CONCLUSIONS: There was no statistically significant difference in the surgical outcomes among the 2 study groups. Despite differences in the anatomy of Caucasian and Asian eyelids, MMCR is a successful procedure in patients self-identified from both ethnic groups.


Subject(s)
Blepharoplasty , Blepharoptosis , Blepharoptosis/surgery , Ethnicity , Eyelids/surgery , Humans , Middle Aged , Oculomotor Muscles/surgery , Retrospective Studies , Sutures
7.
Ophthalmic Plast Reconstr Surg ; 38(2): 146-150, 2022.
Article in English | MEDLINE | ID: mdl-34293782

ABSTRACT

PURPOSE: To describe the use of a lateral wall implant as an adjunct in lateral orbital wall decompression in severe thyroid eye disease. METHODS: This study is a retrospective review of 6 patients who underwent prior orbital decompression but had persistent proptosis. These patients underwent lateral wall decompression with adjunct lateral wall implant placement with a manually vaulted 0.6-mm polyethylene-coated titanium mesh implant. Data collection included: visual acuity, intraocular pressure, exophthalmometry, ocular motility, eyelid position, and complication rates. RESULTS: Eight orbits in 6 patients underwent maximal lateral wall decompression and reconstruction using the polyethylene-coated titanium implant. Four males and 2 females were included with ages ranging from 25 to 73 years. Visual acuity improved an average of 2.4 lines (range 0-5 lines). Intraocular pressure improved an average of 7.5 mm Hg (2-13 mm Hg). There was reduction of proptosis by 3.4 mm on average (1-7 mm). Upper eyelid retraction improved on average by 1.8 mm (0-5 mm). Horizontal eye movements improved by 11% on average (-3.1% to +25%). Excellent cosmesis was achieved with no visible temple deformity, trismus, conjunctival scarring, orbital hemorrhage, or vision loss. CONCLUSIONS: The amount of volume created in lateral wall decompression is limited by the amount of native bone present and the temporalis muscle. In severe or recalcitrant cases, the authors propose the placement of a lateral wall implant as an adjunct to laterally displace the temporalis muscle and create additional volume. This technique accomplishes further reduction of proptosis in patients who have undergone prior orbital decompression.


Subject(s)
Exophthalmos , Graves Ophthalmopathy , Adult , Aged , Decompression, Surgical/methods , Exophthalmos/etiology , Female , Graves Ophthalmopathy/complications , Graves Ophthalmopathy/surgery , Humans , Male , Middle Aged , Orbit/surgery , Polyethylene , Retrospective Studies , Titanium , Treatment Outcome
9.
Ophthalmic Plast Reconstr Surg ; 36(4): 355-358, 2020.
Article in English | MEDLINE | ID: mdl-31809483

ABSTRACT

PURPOSE: To report adverse hemorrhagic outcomes in patients who received intravenous (IV) ketorolac during oculofacial plastic surgical procedures. METHODS: The medical records of 111 consecutive patients who underwent lacrimal or orbital surgery, between the years 2016 and 2018, performed by a single surgeon under general anesthesia were retrospectively reviewed. Patients were excluded if they had history of a bleeding coagulopathy, anticoagulant use prior to surgery, or insufficient follow up. Patients were divided into 2 groups based on whether they received intravenous ketorolac. The primary outcome measure was the occurrence of a major postoperative bleeding event, and the secondary outcome measures were the evaluation of postoperative ecchymosis graded at 1 week after surgery and the incidence of persistent ecchymosis beyond 4 weeks. RESULTS: A total of 111 patients were analyzed further, including 31 patients who received intraoperative IV ketorolac and 80 control patients who did not. The demographic characteristics between the 2 groups were similar. No major bleeding events occurred in either group. And there was no statistically significant difference between the 2 groups in terms of ecchymosis grade and the incidence of development of persistent ecchymosis. Comparing the subgroups of lacrimal and orbital cases, there was also no significance difference between these groups. CONCLUSIONS: This study suggests that intraoperative ketorolac use does not increase the risk of postoperative bleeding complications in oculofacial procedures. This alternative to opioids may assist with pain control and lessen the narcotic burden.


Subject(s)
Ketorolac , Pain, Postoperative , Analgesics, Opioid , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Humans , Ketorolac/adverse effects , Pain, Postoperative/drug therapy , Postoperative Hemorrhage/chemically induced , Postoperative Hemorrhage/epidemiology , Retrospective Studies
11.
Ophthalmic Plast Reconstr Surg ; 35(1): e16-e18, 2019.
Article in English | MEDLINE | ID: mdl-30562335

ABSTRACT

A 69-year-old woman presented to the oculofacial plastic service with a painless superotemporal subconjunctival mass in the OS. Over the past year, the lesion had been progressively enlarging, resulting in horizontal diplopia with lateral gaze. Visual acuity was within normal limits with no evidence of optic neuropathy. On examination, the lesion was tense, transilluminated, and was clinically consistent with a simple dacryops. Complete excision of the lesion was planned under local anesthesia with monitored care. To facilitate complete removal of the lesion, fibrinogen and a mixture of thrombin and trypan blue were injected to fill the cyst cavity. This blue-stained fibrin clot allowed for easy visualization of the border and ensured complete excision without collateral damage to surrounding normal tissue. Simple dacryops is often difficult to remove completely with its capsule intact and this technique allows for clear delineation of the cyst and preservation of epithelial integrity for complete and efficient removal.


Subject(s)
Cysts/surgery , Fibrin Tissue Adhesive/pharmacology , Lacrimal Apparatus Diseases/surgery , Lacrimal Apparatus/surgery , Ophthalmologic Surgical Procedures/methods , Trypan Blue/pharmacology , Aged , Coloring Agents/pharmacology , Cysts/diagnosis , Female , Humans , Lacrimal Apparatus Diseases/diagnosis , Slit Lamp Microscopy , Tissue Adhesives/pharmacology
12.
Arch Gynecol Obstet ; 298(6): 1095-1099, 2018 12.
Article in English | MEDLINE | ID: mdl-30276469

ABSTRACT

OBJECTIVE: To investigate whether delivery of small for gestational age (SGA) neonate poses a risk for subsequent long-term ophthalmic morbidity. METHODS: In this population-based study, all deliveries between 1991 and 2014 were included. Congenital malformations and multiple gestations were excluded from the analysis. Offspring were defined as either SGA (weight below the 5th percentile for gestational age) or non-SGA. Comparison was performed regarding the incidence of long-term ophthalmic morbidity in a cohort of neonates who were born SGA and those who were not. Ophthalmic morbidity was documented during any encounter with the hospital for a period of up to 18 years after delivery. Ophthalmic morbidity included infections of the eye or the adnexa, inflammation of any cause requiring admission, visual disturbances, and other hospital admissions carrying an ICD-9 code of ophthalmic designation. A Cox proportional hazards model was used to estimate the adjusted hazards ratio (HR) for ophthalmic morbidity During the study period, 243,682 deliveries met the inclusion criteria, of which 11,290 (4.63%) were defined as SGA. RESULTS: During the follow-up period, SGA neonates had higher rates of ophthalmic-related hospitalizations (1.2% versus 1.0%; OR = 1.22, 95% CI 1.02-1.46; p = 0.026). In a Cox proportional hazards model, adjusted for confounders such as maternal age, gestational age at delivery, child birth year, low 5 min Apgar scores (< 7), gestational diabetes, maternal hypertensive disorders, placental abruption and placenta previa, SGA neonate was independently associated with subsequent long-term ophthalmic morbidity (adjusted HR = 1.22; 95% CI 1.02-1.47; p = 0.024). CONCLUSION: Delivery of an SGA neonate is an independent risk factor for long-term ophthalmic morbidity.


Subject(s)
Eye Diseases/etiology , Infant, Small for Gestational Age/physiology , Morbidity/trends , Adult , Cohort Studies , Female , Humans , Incidence , Infant, Newborn , Male , Pregnancy , Pregnancy Complications , Retrospective Studies , Risk Factors
13.
J Refract Surg ; 33(9): 592-597, 2017 Sep 01.
Article in English | MEDLINE | ID: mdl-28880333

ABSTRACT

PURPOSE: To develop a decision forest for prediction of laser refractive surgery outcome. METHODS: Data from consecutive cases of patients who underwent LASIK or photorefractive surgeries during a 12-year period in a single center were assembled into a single dataset. Training of machine-learning classifiers and testing were performed with a statistical classifier algorithm. The decision forest was created by feature vectors extracted from 17,592 cases and 38 clinical parameters for each patient. A 10-fold cross-validation procedure was applied to estimate the predictive value of the decision forest when applied to new patients. RESULTS: Analysis included patients younger than 40 years who were not treated for monovision. Efficacy of 0.7 or greater and 0.8 or greater was achieved in 16,198 (92.0%) and 14,945 (84.9%) eyes, respectively. Efficacy of less than 0.4 and less than 0.5 was achieved in 322 (1.8%) and 506 (2.9%) eyes, respectively. Patients in the low efficacy group (< 0.4) had statistically significant differences compared with the high efficacy group (≥ 0.8), yet were clinically similar (mean differences between groups of 0.7 years, of 0.43 mm in pupil size, of 0.11 D in cylinder, of 0.22 logMAR in preoperative CDVA, of 0.11 mm in optical zone size, of 1.03 D in actual sphere treatment, and of 0.64 D in actual cylinder treatment). The preoperative subjective CDVA had the highest gain (most important to the model). Correlations analysis revealed significantly decreased efficacy with increased age (r = -0.67, P < .001), central corneal thickness (r = -0.40, P < .001), mean keratometry (r = -0.33, P < .001), and preoperative CDVA (r = -0.47, P < .001). Efficacy increased with pupil size (r = 0.20, P < .001). CONCLUSIONS: This model could support clinical decision making and may lead to better individual risk assessment. Expanding the role of machine learning in analyzing big data from refractive surgeries may be of interest. [J Refract Surg. 2017;33(9):592-597.].


Subject(s)
Clinical Decision-Making/methods , Corneal Stroma/surgery , Corneal Topography/methods , Machine Learning/statistics & numerical data , Myopia/surgery , Photorefractive Keratectomy/methods , Refraction, Ocular/physiology , Adult , Corneal Stroma/pathology , Databases, Factual , Female , Follow-Up Studies , Humans , Lasers, Excimer/therapeutic use , Male , Myopia/diagnosis , Myopia/physiopathology , Treatment Outcome
14.
Isr Med Assoc J ; 19(1): 49-54, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28457115

ABSTRACT

BACKGROUND: Pseudoexfoliation syndrome (PES) is a common age-related disorder affecting 60-70 million people worldwide. Patients with PES have abnormal production and deposition of fibrillar material in the anterior chamber of the eye. These exfoliated fibrils, easily detected by ocular slit-lamp examination, have also been found to exist systematically in the skin, heart, lungs, liver and kidneys. Recently, myriad studies have associated PES with systemic conditions such as increased vascular risk, risk of dementia and inflammatory state. We review here the most current literature on the systemic implications of PES. Our aim is to encourage further studies on this important clinical entity.


Subject(s)
Exfoliation Syndrome/complications , C-Reactive Protein/analysis , Cardiovascular Diseases/complications , Cognitive Dysfunction/complications , Coronary Vessel Anomalies/complications , Dementia/complications , Hearing Loss, Sensorineural/complications , Humans , Insulin Resistance , Life Expectancy , Obesity/complications , Tumor Necrosis Factor-alpha/blood , alpha 1-Antitrypsin/blood
15.
J Ocul Pharmacol Ther ; 32(9): 601-605, 2016 11.
Article in English | MEDLINE | ID: mdl-27513223

ABSTRACT

PURPOSE: Topical nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used for the prevention and treatment of inflammation and pain following cataract surgery. Preservative-free diclofenac and nepafenac drops are commonly used ophthalmic NSAIDs. The purpose of this study was to compare the tolerability of diclofenac to that of nepafenac. METHODS: In this prospective patient-blinded study, consecutive patients undergoing cataract surgery were included. One drop of nepafenac 0.1% and diclofenac sodium 0.1% were instilled in the right and left eyes, respectively, one immediately after the other, 1 day before surgery. Visual analog scale (scale 0-10) was used to measure patient discomfort, itching, burning, and pain at 1 second (s), 15 s, 1 minute (min), and 5 min postadministration. RESULTS: Overall, 44 eyes of 22 patients were included in this study. Diclofenac and nepafenac had high and similar tolerability at all time points with no significant difference regarding all aspects of tolerability. A vast majority of patients (72%) did not prefer 1 drop over the other in terms of overall comfort. CONCLUSIONS: Both diclofenac and nepafenac seem to have similar high tolerability. Diclofenac may be an affordable alternative to nepafenac and therefore should be considered by prescribing physicians, specifically in preoperative cataract patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Benzeneacetamides/adverse effects , Diclofenac/adverse effects , Inflammation/drug therapy , Ophthalmic Solutions/adverse effects , Pain, Postoperative/drug therapy , Phenylacetates/adverse effects , Administration, Topical , Aged , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Benzeneacetamides/administration & dosage , Benzeneacetamides/therapeutic use , Diclofenac/administration & dosage , Diclofenac/therapeutic use , Double-Blind Method , Female , Humans , Inflammation/surgery , Male , Molecular Structure , Ophthalmic Solutions/administration & dosage , Ophthalmic Solutions/therapeutic use , Pain Measurement , Pain, Postoperative/surgery , Phenylacetates/administration & dosage , Phenylacetates/therapeutic use , Prospective Studies , Visual Analog Scale
18.
Acta Ophthalmol ; 93(8): e649-53, 2015 Dec.
Article in English | MEDLINE | ID: mdl-25899144

ABSTRACT

PURPOSE: To quantify subjective visual metamorphopsia in newly diagnosed patients suffering from diabetic macular oedema (DME) and other macular abnormalities and to evaluate anti-VEGF treatment effect. METHODS: Patients with DME, subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) or retinal venous occlusion (RVO) were recruited. Metamorphopsia score (Mscore) was calculated using M-Charts at baseline and at the end of a series of anti-VEGF injections. RESULTS: Fifteen eyes of 10 patients with DME, 14 eyes of 13 patients with AMD-CNV and five patients with RVO were included in this study. At baseline, positive Mscore was observed in 46.6% of eyes with DME, 50% of eyes with AMD-CNV and four of five eyes with RVO. Treatment led to a complete metamorphopsia reduction (Mscore = 0) in 71.4% of DME patients, 35.7% of AMD and 0% of RVO patients. CONCLUSION: We suggest that the M-charts may serve as an additional test for diagnosis and follow-up, complementary to morphological evaluation by imaging, in diabetic patients facing their first anti-VEGF treatment.


Subject(s)
Diabetic Retinopathy/diagnosis , Macular Edema/diagnosis , Retinal Vein Occlusion/diagnosis , Vision Disorders/diagnosis , Wet Macular Degeneration/diagnosis , Aged , Aged, 80 and over , Angiogenesis Inhibitors/therapeutic use , Diabetic Retinopathy/drug therapy , Diabetic Retinopathy/physiopathology , Female , Humans , Intravitreal Injections , Macular Edema/drug therapy , Macular Edema/physiopathology , Male , Middle Aged , Retinal Vein Occlusion/drug therapy , Retinal Vein Occlusion/physiopathology , Tomography, Optical Coherence , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vision Disorders/drug therapy , Vision Disorders/physiopathology , Visual Acuity/physiology , Visual Field Tests , Visual Fields , Wet Macular Degeneration/drug therapy , Wet Macular Degeneration/physiopathology
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