Potential Risk Factors for Ocular Pain in Patients Undergoing Multiple Intravitreal Injections of Anti-Vascular Endothelial Growth Factor.

Purpose: To assess ocular pain in patients undergoing multiple intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF) who have previous factors that may influence pain sensitivity. Methodology: This is a prospective, observational, case series study involving patients who underwent multiple (≥3) pro re nata intravitreal injections of ranibizumab or aflibercept to treat any cause of chorioretinal vascular disease. Ocular pain was assessed by the numerical analog scale during intravitreal injection. For this study, the main variable was ocular pain and the secondary variables included age, sex, previous history of glaucoma, primary retinal vascular disease, severe dry eye history, trigeminal pain, scleral buckle surgery, collagen diseases, fibromyalgia, severe migraine history, pars plana vitrectomy, scleral thickness measurements, and type of anti-VEGF. Results: In a total of 894 patients, 948 eyes (4822 intravitreal injections), 793 patients (88.6%) had ocular pain sensitivity between no pain to mild pain, 80 patients (8.9%) had moderate ocular pain, 15 patients (1.6%) had severe ocular pain, and 6 patients (0.7%) had extremely severe ocular pain. Patients with severe dry eye (p = 0.01) and previous history of scleral buckle surgery (p = 0.01) showed a significant correlation with ocular pain during intravitreal injection. Pars plana scleral thickness (>550 um) and diabetic neuropathy were associated with ocular pain but did not meet the criteria for statistical significance (p = 0.09 and p = 0.06, respectively). Conclusion: Dry eye and prior scleral buckle surgery may contribute to pain associated with intravitreal injection. These issues should be taken into consideration in patients undergoing multiple intravitreal injections.

Perifoveal exudative vascular anomalous complex and resembling lesions treated with intravitreal triamcinolone.

PURPOSE: To report the use of intravitreal triamcinolone to treat macular edema associated with isolated perifoveal exudative vascular anomalous complex (PVAC) and resembling lesion (PVAC-RL). METHODS: In this case series, three diabetic patients (3 eyes) with PVAC-RLs and one healthy patient (1 eye) with PVAC lesion associated with cystic spaces underwent three intravitreal injections of aflibercept before switching to one intravitreal triamcinolone injection in each patient. RESULTS: Macular edema improved from 297.5 ± 8.10 µm, at baseline, to 269.2 ± 8.89 µm, after triamcinolone; whereas visual acuity improved from 20/38 to 20/26 (ETDRS). CONCLUSION: PVAC and PVAC-RL are rare and often misdiagnosed lesions that may be associated with decreased vision. Our outcomes suggest that intravitreal injection of triamcinolone may be an effective and affordable treatment for PVAC and PVAC-RL with intraretinal fluid.

Branch retinal artery occlusion with paracentral acute middle maculopathy related to a COVID-19 infection in a patient with Anosmia.

PURPOSE: To report a case of paracentral acute middle maculopathy (PAMM) due to branch retinal artery occlusion (BRAO) as a complication of COVID-19. METHODS: A case report evaluated through spectral-domain optical coherence tomography (SD-OCT), fluorescein angiography, and OCT angiography. RESULTS: A 55-year-old man complained of blurred vision in the right eye. He presented with anosmia and tested positive for COVID-19 one week before. Fundus examination revealed a superior temporal whitening of the retina, SD-OCT showed a hyperreflective band-like lesion on the nuclear layer consistent with PAMM. CONCLUSION: COVID-19 infection involves inflammatory and thrombotic events. Even patients with just anosmia may have complications such as BRAO associated with PAMM.

Retinal microvascular abnormalities, cotton wool-like lesions, and macular edema following COVID-19 in a patient previously vaccinated with AstraZeneca and idiopathic myopathy.

In this case study, the authors describe peculiar bilateral cotton wool-like retinal lesions associated with macular edema in a patient with COVID-19 who was vaccinated with a single dose of AstraZeneca one month earlier. This patient had no pulmonary or systemic cardiovascular complications from COVID-19, as reported in other papers that found retinal lesions. However, the patient was diagnosed with idiopathic myopathy when discovering the SARS-CoV-2 infection. The patient was a 22-year-old white female with no previous history of morbidity, complaining of blurred vision in both eyes seven days after testing positive for SARS-CoV-2 by PCR (using nasal and oral swab) and confirmed through ELISA blood test (IgM positive). There was no ancillary test revealing diabetes mellitus. The patient presented with scattered whitish cotton wool-like lesions and a few hemorrhages on the posterior pole in fundus examination. On spectral domain optical coherence tomography (SD-OCT), there were hyperreflective lesions in the nerve fiber layer, ganglion cell layer, inner nuclear layer, and inner and outer plexiform layers at the site corresponding to the whitish cotton wool-like lesions in the posterior fundus photos. Moreover, the macula of both eyes had intraretinal and subretinal fluid, reversible with corticosteroid therapy. In conclusion, COVID-19 has been associated with capillary disorders at different target sites such as retina, lungs, and central nervous system. Similarly, vaccination against SARS-CoV-2 has been linked to retinal complications in the literature; however, cotton wool-like lesions have not yet been reported. There are many questions yet to be answered about the implications of COVID-19 infection and its vaccines.

Perfil epidemiológico de pacientes com degeneração macular relacionada à idade / Epidemiological profile of patients with age-related macular degeneration

RESUMO Objetivo Demonstrar o perfil epidemiológico e fatores de riscos de pacientes com degeneração macular relacionada à idade. Métodos Estudo observacional e seccional. Foi incluído um olho de cada paciente com maior comprometimento visual por degeneração macular relacionada à idade atendido no Hospital Universitário Antônio Pedro. A variável principal a ser comparada foi a presença de degeneração macular relacionada à idade dividida nos estágios inexpressivo, inicial, intermediário e avançado, segundo classificação do estudo AREDS. As variáveis secundárias foram os dados demográficos (sexo, idade, raça, faixa etária), índice de massa corporal, cor da íris, história familiar de degeneração macular relacionada à idade, status do cristalino, longo tempo exposição à luz ultravioleta e tabagismo. Foram realizados testes estatísticos com análise de Kruskal-Wallis, do teste do qui-quadrado e teste t de Student. O nível de significância foi definido em 5%. Resultados Após os critérios de inclusão e exclusão, 126 pacientes foram incluídos neste estudo, sendo 20 pacientes com degeneração macular relacionada à idade inexpressiva, 30 pacientes com degeneração macular relacionada à idade inicial, 30 pacientes com degeneração macular relacionada à idade intermediária e 46 pacientes com degeneração macular relacionada à idade avançada. Dentre todos os fatores de risco pesquisados, apenas o tabagismo se mostrou estatisticamente significativo (p=0,03). Conclusão O tabagismo como fator de risco para degeneração macular relacionada à idade apresentou ter importância expressiva prevalente nesta pesquisa e até mesmo como fator preventivo dessa morbidade ocular.

ABSTRACT Purpose To demonstrate the epidemiological profile and risk factors of patients with age-related macular degeneration (ARMD). Methods Observational and sectional study. One eye of each patient with greater visual impairment due to AMD treated at the University Hospital Antônio Pedro was included. The main variable to be compared was the presence of AMD divided into inexpressive, initial, intermediate, and advanced stages, according to the classification of the AREDS study. The secondary variables were demographics (gender, age, race, age group), body mass index, iris color, family history of ARMD, lens status, long-term exposure to ultraviolet light and smoking. Statistical tests were performed with Kruskal-Wallis and Chi-square analyses and Student's t test. The significance level was set at 5%. Results After the inclusion and exclusion criteria, 126 patients were included in this study, 20 patients with non-expressive AMD, 30 patients with early AMD, 30 patients with intermediate AMD, and 46 patients with advanced AMD. Among all the risk factors surveyed, only smoking was statistically significant (p = 0.03). Conclusion Smoking as a risk factor for AMD had significant relevance prevalent in this research and even as a preventive factor for this ocular morbidity.

Transient central retina artery occlusion in patients undergoing intravitreal anti vegf injections.

PURPOSE: To evaluate the occurrence of transient central retinal artery occlusion following intravitreal anti-vascular endothelial growth factor injection. METHODS: Prospective, observational study of 807 patients (807 eyes) who were given intravitreal injections of ranibizumab or aflibercept to treat any cause of retinal vascular diseases between 1 January 2017 and 30 November 2018 at the Federal Fluminense University Hospital in Niteroi, and a private facility in Rio de Janeiro, Brazil. Patients who did not present transient central retinal artery occlusion were excluded. RESULTS: Among 4069 injections, only 18 patients (0.44%) presented transient central retinal artery occlusion, 14 mild cases (77.7%), and 4 severe cases (22.3%). The clinical factors associated with more severe cases of transient central retinal artery occlusion were the duration of the transient central retinal artery occlusion (p = 0.001), number of prior injections (p = 0.01), and a positive carotid Doppler test (p = 0.01). Twelve cases (66.6%) had positive carotid artery obstruction (atheroma plaque size ≥70%) while 6 cases (33.3%) had negative carotid artery obstruction (atheroma plaque size <70%). The age group >60 years old (p = 0.06), cup/disc ratio >0.6 (p = 0.06), and pseudophakic lens status were also factors with association with transient central retinal artery occlusion, although did not meet criteria for statistical significance. The only patient who experienced a recurrent episode of transient central retinal artery occlusion had diabetic macular edema, positive carotid Doppler test, and cup/optic disc ratio >0.6. CONCLUSION: Transient central retinal artery occlusion is a rare adverse event that can appear in patients with retinal vascular disease receiving anti-vascular endothelial growth factor therapy. The atheroma plaque size and the number of prior injections can be associated with the severity of the event.

Diferenças de mensuração de acuidade visual e velocidade de leitura para perto entre pacientes com retinopatia diabética. Repercussão entre conceitos de deficiência visual parcial e cegueira legal / Differences in measurement of visual acuity and reading speed for near vision among patients with diabetic retinopathy. Repercussion in concepts of partial vision loss and legal blindness

RESUMO Objetivo: Comparar a acurácia entre a acuidade visual com melhor correção óptica em pacientes com retinopatia diabética e acuidade visual com correção óptica menor ou igual a 20/200 em ambos os olhos mensurada pela tabela de Snellen e pela tabela ETDRS, além da avaliação do tempo de leitura com tabela de leitura de Jaeger. Métodos: Estudo observacional e transversal. ormação de Grupos de Pesquisa: o Grupo I foi formado por pacientes com acuidade visual de 20/200 e o Grupo II, por pacientes com acuidade visual maior de 20/200. Os pacientes de ambos os grupos foram subdivididos em aqueles com retinopatia diabética não proliferativa e os com retinopatia diabética proliferativa. As variáveis pesquisadas foram sexo, idade, tabela ETDRS nos subgrupos (igual a 20/200, igual a 20/400 e maior de 20/200 e 20/400) e tempo de leitura da tabela de Jaeger para perto. O índice de significância estatística deste estudo foi de 5%. Resultados: Participaram do estudo 62 pacientes diabéticos, sendo 33 com retinopatia diabética não proliferativa e 29 com retinopatia diabética proliferativa. Dentre os pacientes com retinopatia diabética não proliferativa, 19 tinham acuidade visual com melhor correção óptica de 20/200 (30,6% da amostra), e 13 pacientes eram portadores de retinopatia diabética proliferativa com acuidade visual com melhor correção óptica de 20/200 (20,9% da amostra). A correlação entre a tabela Snellen e a tabela ETDRS revelou que 16 pacientes (25,8% da amostra) com cegueira legal apresentaram acuidade visual entre 20/180 e 20/120 segundo a tabela ETDRS. Para os pacientes portadores de retinopatia diabética não proliferativa com acuidade visual de 20/200 pela tabela ETDRS, houve tempo médio de leitura para perto da tabela de Jaeger de 23,6±1,4 segundos. Na análise estatística da acuidade visual mensurada com a Tabela de Snellen em comparação com a Tabela de Leitura para perto (Jaeger), mensurando tempo de leitura, ahouve significância estatística (p=0,04). Conclusão: Pacientes diabéticos com cegueira legal segundo a tabela de Snellen apresentam sua real capacidade visual residual subavaliada. É importante levar em consideração o tempo de leitura e o uso da tabela ETDRS para melhor acurácia.

ABSTRACT Purpose: To compare the accuracy of best-corrected visual acuity in patients with diabetic retinopathy to corrected visual acuity ≤ 20/200 in both eyes, measured by Snellen and ETDRS charts, in addition to evaluation of reading time by Jaeger chart. Methods: An observational and cross-sectional study. Study Groups: Group I, patients with visual acuity 20/200, and Group II, patients with visual acuity >20/200. Patients were subdivided into those with non-proliferative diabetic retinopathy and with proliferative diabetic retinopathy. The study variables were sex, age, ETDRS chart in the subgroups (equal to 20/200; equal to 20/400 and greater than 20/200 and 20/400), and reading time by Jaeger chart on the near vision. The statistical significance was set at 5%. Results: A total of 62 diabetic patients participated in the study; in that, 33 with non-proliferative diabetic retinopathy and 29 with proliferative diabetic retinopathy. Among patients with non-proliferative diabetic retinopathy, 19 had best-corrected visual acuity 20/200 (30.6% of sample), and 13 patients had proliferative diabetic retinopathy with best-corrected visual acuity 20/200 (20.9% of sample). The correlation between the Snellen and ETDRS charts revealed 16 patients (25.8% of sample) with legal blindness presented visual acuity between 20/180 and 20/120, as per the ETDRS chart. For patients with non-proliferative diabetic retinopathy with visual acuity 20/200 measured by the ETDRS chart, the mean reading time to near vision was 23.6±1.4 seconds, as measured by Jaeger chart. In the statistical analysis, the comparison of visual acuity measured by Snellen chart, with the reading chart to near vision (Jaeger) measuring reading time, was statistically significant (p=0.04). Conclusion: Diabetic patients with legal blindness as per Snellen chart showed their real underestimated residual visual capacity. It is important to consider reading time and use of the ETDRS chart for better accuracy.

The Central Subfoveal Bouquet in Idiopathic Epiretinal Membranes.

PURPOSE: To report both the unoperated clinical course and the surgical outcomes of eyes with a central foveal bouquet (CB) secondary to idiopathic epiretinal membranes (iERMs). DESIGN: Retrospective, consecutive, and observational case series. METHODS: All patients examined between January 1, 2014, and December 31, 2019, for evaluation of epiretinal membrane with a CB lesion identified on spectral domain optical coherence tomography (SD-OCT) were included. Exclusion criteria included vitreoretinal comorbidities associated with secondary ERMs and an absence of CB lesions on SD-OCT. Patients were divided into two groups: those who were followed with observation (Group I) and those who received surgery (Group II). Each group had 3 different types of mechanical abnormalities of the CB previously described as cotton ball sign, subfoveal detachment, or acquired vitelliform lesion, without a subanalysis discrimination. MAIN OUTCOME MEASURES: Best-corrected visual acuity (BCVA) at baseline and last follow-up, subjective metamorphopsia, central retinal thickness (CMT), mechanical stress lesions of the CB, and resolution or evolution of the CB lesions during the follow-up interval. RESULTS: Two hundred seventy-six eyes with iERM were reviewed, and 46 eyes met the inclusion criteria. Among these, 21 of 46 (46%) were observed, and 25 of 46 (54%) underwent surgery. Metamorphopsia was identified in 61.9% of patients in Group I and 81.2% of patients in Group II, at baseline. The mean BCVA was 0.19 ± 0.17 (20/30) in Group I and 0.31 ± 0.33 (20/40) in Group II at presentation. At the final exam, patients in Group I achieved a mean BCVA of 0.24 ± 0.18 (20/30), while patients in Group II obtained a mean BCVA of 0.15 ± 0.21 (20/30). Spontaneous resolution of the CB sign occurred in 5 of 21 eyes (23.8%) that were observed, whereas, after surgery, the CB sign resolved in 16 of 25 eyes (61.5%). Mean CMT was 422 ± 84.2µm in Group I and 531 ± 143.9µm in Group II, at baseline, while at the latest follow-up, the mean CMT was 400 ± 40.8µm in the cases followed with observation and 454 ± 148.7µm in the surgical cases. CONCLUSION: The clinical course and surgical outcomes of CB findings in iERM are favorable in terms of visual acuity. However, those receiving surgery had an increase in visual acuity and resolution of the CB abnormality.

Treatment of Radiation Retinopathy with Intravitreal Injection of Ranibizumab (Lucentis®).

To report a treatment of radiation retinopathy in a patient exposed to ionizing radiation for a period of 2 years. A 26-year-old female patient with no comorbidities diagnosed with myelodysplasia confirmed by bone marrow biopsy. She presented a complaint of bilateral progressive visual acuity reduction. At the ophthalmologic examination, she presented alterations suggestive of radiation retinopathy as well as macular thickness to optical coherence tomography (OCT) of over 500 µm. The patient underwent intravitreal injection (0.05 mL) of ranibizumab (Lucentis®) monthly in both eyes and follow-up through visual acuity and OCT examination. She presented reduction of macular edema as well as a slight improvement of visual acuity. In this case, the treatment of radiation retinopathy with intravitreal injection of ranibizumab (Lucentis) was relatively useful, with a slight improvement of visual acuity, due to the regression of macular edema, not being curative.

The Clinical Course of Patients with Idiopathic Epiretinal Membranes and Good Visual Acuity Managed Without Surgery.

BACKGROUND/AIMS: To report the clinical course of patients with idiopathic epiretinal membranes (iERMs) and good baseline best-corrected visual acuity (BCVA) managed without surgical treatment. METHODS: Retrospective, observational case series of patients with iERMs and 20/50 or better BCVA who did not undergo surgery between January 2014 and December 2017 with a 1-year follow-up. Secondary epiretinal membranes were excluded. iERMs were stratified into two groups: Group I (BCVA 20/30 or better) and Group II (BCVA 20/40 to 20/50). The main outcome measures included baseline and final follow-up BCVA, central macular thickness (CMT) on OCT. RESULTS: The study included 174 eyes (145 patients): 139 eyes (79.8%) had typical iERMs and 35 eyes (18%) had LMH. For Group I typical iERMs, the logMAR baseline and final mean BCVA were 0.09 ± 0.1 (Snellen equivalent 20/25) and 0.10 ± 0.1 (20/25+) respectively (p = 0.22). In this group, the baseline and final mean CMT were 335 ± 73µm and 342 ± 78µm, respectively (p = 0.47). For Group II typical iERMs, the logMAR baseline and final mean BCVA were 0.3 ± 0.1 (20/44) and 0.4 ± 0.2 (20/45) respectively (p = 0.31). In this group, the baseline and final mean CMT were 386 ± 95µm and 391 ± 93µm, respectively (p = 0.84). CONCLUSION: The clinical course of patients with iERM and good baseline BCVA is generally favorable without surgery and includes stable BCVA and OCT measurements after at least one year.

Diathermy for 23-gauge sclerotomy: a functional and morphologic study to avoid ocular hypotony.

PURPOSE: To evaluate diathermy to minimize sclerotomy leakage during small-gauge vitrectomy and prevent ocular hypotony. METHODS: This observational prospective study included 327 patients (327 eyes) who underwent diathermy to close the sclerotomy sites during 23-gauge pars plana vitrectomy (PPV). All patients were operated by a single surgeon (ED) and evaluated at 30 and 60 days postoperatively. Patients with glaucoma, topical/systemic steroids use exceeding 30 days, ocular inflammation, or trauma were excluded. Chi-square, Kruskal-Wallis, Fisher Exact test, and multivariate statistical analyses were performed to evaluate potential risk factors. The primary outcomes were open sclerotomies, leakage, and ocular hypotony. RESULTS: Sclerotomies remained open in 12 (3.6%) and 2 (0.6%) patients, respectively, at 30 and 60 days postoperatively, revealing no case of ocular hypotony. Leakage only occurred in four patients (1.2%) during week 1 postoperatively. Multivariate analysis indicated that additional vitreoretinal surgeries and longer surgeries were risk factors for persistent sclerotomy opening. CONCLUSION: Diathermy was safe and feasible to close sclerotomies. Vitreoretinal surgery reoperations and longer surgeries were the most significant (P<0.05) risk factors for persistent sclerotomy opening, which may be functionally closed without evidence of leakage or ocular hypotony.

Comparative study of the clinical profile of chronic dacryocystitis and chronic rhinosinusitis after external dacryocystorhinostomy.

PURPOSE: To compare the clinical profile of patients with chronic dacryocystitis (CDC) with and without associated chronic rhinosinusopathies who had been submitted to external dacryocystorhinostomy (EDCR). METHODS: This was a retrospective, observational, and longitudinal study that included all patients diagnosed with CDC who were submitted to EDCR at the Antonio Pedro University Hospital. Patients were divided into two groups, with and without rhinosinusopathies (Group I and Group II, respectively). The following variables were assessed to compare the Group I and Group II: age, ethnicity, epiphora, discharge by expression of the lacrimal sac, duration of the CDC, and previous history of CDC exacerbation. RESULTS: The study included a total of 78 patients, 22 patients (28.2%) in Group I and 56 patients (71.8%) in Group II. The mean age was 64.3 (±19.7) years. In Group I and II predominated elderly, female, and White (p=0.93, p=0.38, p=0.77). In relation to the clinical characteristics, most of the patients presented epiphora and discharge by compression of the lacrimal sac in both Groups (p=0.61, p=0.44). In relation to a previous history of exacerbations of the CDC, six patients in Group I and four patients in Group II presented it as purulent discharge (p=0.04). CONCLUSION: Chronic rhinosinusopathies may favor episodes of exacerbations of chronic dacryocystitis in particular with the presence of purulent discharge.

Outer Retinal Tubulation and Neovascular Age-Related Macular Degeneration: A Review of the Pathogenesis and Clinical Implications.

Outer retinal tubulation (ORT) is a retinal finding that can mimic intraretinal fluid and has been identified with spectral-domain optical coherence tomography in patients with age-related macular degeneration (AMD). The purpose of this review is to summarize the findings related to the pathogenesis of ORT and its clinical implications. Studies reporting the pathogenesis and the clinical implications of ORT in patients with AMD were identified and summarized. A total of 18 studies were included in this review. The body of evidence to date regarding ORT in patients with AMD indicates that ORT is a structure associated with advanced macular diseases that does not require anti-vascular endothelial growth factor treatment. [Ophthalmic Surg Lasers Imaging Retina. 2018;49:870-876.].

Scleral wound healing with cross-link technique using riboflavin and ultraviolet A on rabbit eyes.

PURPOSE: The aim of study was to evaluate the cross-link using riboflavin and ultraviolet A (UVA) for improving scleral wound healing. MATERIALS AND METHODS: This was an experimental study involving four New Zealand rabbits (eight eyes). Therapy procedure was chosen for the right eye and control procedure for the left one. UVA irradiation of 365 nm with a surface irradiance of 3 mW/cm2 and a photosensitizer of riboflavin drops were applied for 30 minutes on the right eye at 2 mm from the limbus. Sclerotomy incision was performed at 2 mm from the limbus in both right (on the cross-link-treated area) and left eye. Then, 30 days after surgery, a morphological analysis and histological staining with hematoxylin-eosin and picrosirius red were performed, and the sclerotomy cicatrization of right and left eyes was compared. The variables investigated were as follows: sclerotomy incision pictures and measurements were made using the ImageJ Software. Scleral thickness was measured (employing the anterior optical coherence tomography and the digital caliper). Collagen fiber density stained with picrosirius red staining was measured using the Image Pro Plus software. RESULTS: The morphological analysis showed that in all samples, the right eye presented sclerotomy closure, and in two eyes, among them, there were no visible edges of the sclerotomies incision. The left eye presented sclerotomy closure and incision edges. The Image Pro demonstrated a higher density of collagen fibers in the right eye when compared to the one. The statistical analysis was significant when compared to the collagen fiber density in the treated eyes with the control eyes. CONCLUSION: The cross-link procedure resulted in a better sclerotomy wound healing.

Refração e síndrome de fadiga visual no uso de sistema de televisão ULTRA- HD-3D- 4K de tela curva / Refraction and visual fatigue syndrome on watching the ULTRA HD 4k television curved screen system

RESUMO Objetivo: Avaliar uma possível desordem de sensibilidade ocular (similar a glare), com sintomas de fadiga visual, através da observação de tela de televisão ULTRA HD- 3D- 4K de tela curva de 55 polegadas, em voluntários com exame oftalmológico normal. Métodos: Um estudo prospectivo, longitudinal, caso-controle, com formação de grupos por faixa etária e com critérios de inclusão e exclusão. Uma comparação de um vídeo documentário gravado com resolução HD 4K e o mesmo documentário gravado em FULL HD antes e após a tele-audiência anterior consistindo numa avaliação de três fases do estudo com os mesmos critérios. A fadiga visual foi analisada por meio de um questionário padronizado de queixas de síndrome de fadiga visual comuns e comparado a teste de sensibilidade ao contraste, teste de amplitude de acomodação e convergência, teste de frequência de piscar e teste de movimentos sacádicos conjugados oculares de grande amplitude. Equipamentos acessórios como tablets com câmara digitais serão utilizados para gravação de vídeos da frequência de piscar, e de movimentos oculares sacádicos durante toda a audiência televisiva. Analise estatística com Teste de Qui quadrado, teste t de Student, teste de Tukey e teste F com analise de Variância foram feitos para dados em tabelas de contingência e gráficos caixa em Box Plot. Nível de significância estimado em 5%. Resultados: Oitenta voluntários normais foram avaliados e avaliados como inferência de expressividade estatística alpha (α) de 10%, sem obter significância de 5% para as queixas de um questionário de Síndrome de Fadiga Visual. Outros testes estatísticos revelam dados de significância de 5% numa inferência global da pesquisa quanto à frequência de piscar e de movimentos sacádicos conjugados oculares de grande amplitude. Conclusão: Telas de televisão de alta resolução ULTRA HD 4K, podem provocar queixas de fadiga visual numa população de características pouco comuns (com baixa frequência de piscar palpebral e movimentos sacádicos conjugados), mas existentes. O baixo índice de estatística significativa poderá revelar-se de maior expressão no uso de uma amostragem de pesquisa mais numerosa. Os autores chamam a atenção para a possibilidade de incremento desse efeito de fadiga visual no futuro advento de Sistema de Televisão ULTRA HD 8K.

ABSTRACT Purpose: To evaluate eye sensitivity disorder (similar to glare), with symptoms of visual fatigue, through watching television ULTRA HD3D-55-inch 4K curved screen among volunteers with normal eye examination. Methods: A prospective, longitudinal, case-control study, with inclusion and exclusion criteria and groups formation enrolled by age range. A comparison of a video documentary presented with the ULTRA HD TV 4K and with the FULL HD TV before and after the previous tele-audience, consisting of an evaluation of three phases of the study regarding the case-control criteria. The main variable analyzed was a questionnaire of visual fatigue syndrome complaints which was compared with secondary variables as the contrast sensitivity test, amplitude of accommodation test, blink frequency test, and test of conjugated saccadic eye movements of big amplitude. Tablets with digital camera equipment were used for video recording of the blink frequency, and saccadic eye movements throughout the television audience. Statistical analysis with Chi Square test. Results: Eighty healthy volunteers were evaluated and assessed as expressiveness of statistical inference alpha (α) of 10%, without obtaining significance of 5% for complaints of a questionnaire Visual Fatigue Syndrome. Other statistical tests showed 5% of significance of data in a global inference research on the frequency of blinking and combined saccadic movements of great amplitude. Conclusion: High resolution television screens ULTRA HD 4K may cause complaints of eyestrain in a population with some uncommon characteristics (low eyelid blink frequency and conjugated saccades movements). The low statistical significant index could be increased in a research with a higher number of participants. The authors call attention to the possibility of increasing this visual fatigue effect in the future advent of Television System ULTRA HD 8K.

Fila cirúrgica digital como instrumento auxiliar de gestão hospitalar: Sugestões de adequações propostas por um serviço universitário de oftalmologia / The preoperative scheduling system as a secondary tool for hospital management: suggestions for adjustments proposed by a university ophthalmology unit

RESUMO Objetivo: Avaliar, através de busca na internet, quais os serviços públicos com atendimento oftalmológico no Brasil que possuem um pacote digital composto de página da instituição na rede digital, prontuário eletrônico, sistema de regulação de atendimento e fila de espera cirúrgica digital. Enfatizar a presença destes elementos de pesquisa com a condição de funcionamento de fila de espera cirúrgica digital com possibilidade de consulta publica pelo paciente usuário. Métodos: Estudo transversal através de busca na internet de serviços de oftalmologia com este pacote digital completo ou parcial em caráter nacional. Os dados foram pesquisados na internet no período de junho à julho de 2015. As instituições foram divididas em grupos de pesquisa, assim designados: hospitais multidisciplinares universitários, hospitais multidisciplinares assistenciais, hospitais uni-disciplinares assistenciais (somente oftalmologia) e banco de olhos (como entidade de atendimento público). Duas variáveis foram avaliadas: número total e parcial de serviços públicos de oftalmologia que possuem este sistema digital e como foi desenvolvido este pacote digital por cada instituição. Os dados foram avaliados através do teste Qui quadrado e prova exata de Fisher. O nível de significância do estudo foi 0,05. Resultados: Foram encontradas 48 instituições públicas oftalmológicas detentoras deste pacote digital, sendo: 24 universitárias, 15 assistenciais, 3 hospitalares uni-disciplinares (somente oftalmologia), 6 bancos de olhos. Somente 10,4 % destas instituições apresentaram uma fila de espera cirúrgica digital. Exclusivamente os bancos de olhos obtiveram dados significativos quanto a presença de fila cirúrgica digital, bem como a origem de seu desenvolvimento. Conclusão: Apenas algumas instituições apresentaram um pacote digital completo, porém a fila de espera cirúrgica digital é o componente mais raro destas instituições. Razões desta constatação são explanadas pelo estudo. Embora com pequena representação, em todo território nacional somente dois bancos de olhos apresentaram fila cirúrgica digital com possibilidade de consulta pública.

ABSTRACT Objective: To evaluate the incidence of a software program package at Brazilian public eye care institutions through an online survey. The package is made up of the institutions' websites, electronic medical records, regulatory assistance control system and the preoperative scheduling system. The aim is to analyze if this type of software facilitates the provisioning of eye care services, the patients' surgical procedure agenda, and access to information about the patients. Methods: Public health care institutions with eye care services were divided into multidisciplinary university hospitals, multidisciplinary health system hospitals, single discipline hospitals (only ophthalmology) and eye banks (when linked to public health care). Two kinds of data were evaluated on the Internet: I) ophthalmology institutions and the correlation with the presence of the software program, II) ophthalmology institutions and the correlation with the software source. A statistical analysis was performed using chi-square and Fisher's exact test. Significance levels were estimated at 0.05. Results: 48 public institutions were evaluated at 24 universities, 15 health care institutions, 3 single discipline hospital institutions (ophthalmology only), and 6 institutions specifically referred to as eye banks. In this survey, the digital preoperative scheduling system was only found in 10.4% of the institutions. After the statistical analysis, the eye bank was the only relevant institution that was significantly related to the presence of the digital preoperative scheduling system. Conclusion: Preoperative scheduling systems are expected to provide a good support tool for administrative management. However, this type of instrument as a software program is rarely found in public health care institutions in Brazil.