Syfte: Syftet med studien var att utvärdera NIBUT (Non-Invasive Break-Up Time) och TBUT (Tear Break-Up Time) hos heltidsstuderande vid Linnéuniversitetet samt bidra till en ökad förståelse av ögonhälsan hos denna grupp. Metod: Tårfilmens stabilitet kontrollerades med NIBUT och TBUT, tiden mättes direkt efter en blinkning till första uppsprickningen av tårfilmens yta eller ny blinkning. NIBUT utfördes icke invasivt i Sirius och TBUT mättes i biomikroskop med fluorescein. Deltagarna fick inledningsvis svara på en enkät som gjorde det möjligt att analysera insamlad data utifrån ålder, kön, termin, skärmtid och poäng på DEQ-5 (5-Item Dry Eye Questionnaire). Svaren från DEQ-5 möjliggjorde att resultaten från NIBUT och TBUT mätningarna kunde jämföras mot upplevda symtom på torra ögon. Resultat: Studien inkluderade 36 studenter i åldersspannet 18–39 år (medianålder 23 år, IQR 5,25 år). NIBUT och TBUT visade en positiv signifikant korrelation (p <0,001). En kortare TBUT korrelerade negativt med en högre totalpoäng på DEQ-5 (p = 0,004) samt antalet terminer som studerats (p = 0,025). NIBUT visade inte några liknande samband. Referensvärdet för torra ögon diagnostisering med hjälp av NIBUT och TBUT är en tid <10 sekunder. Över hälften av deltagarna i studien, NIBUT 58% och TBUT 53%, hade en nedsatt break-up time <10 sekunder. Vilket kan vara en indikation för torra ögon problematik. Slutsats: Denna studie visar att det finns ett signifikant samband mellan NIBUT och TBUT mätningarna. Kortare TBUT har visat en signifikant korrelation med högre totalpoäng på DEQ-5, likaså har signifikanta samband mellan TBUT och fler lästa terminer konstaterats. Trots korrelationen mellan NIBUT och TBUT påverkades resultaten av skillnader mellan de två mätmetoderna. / Purpose: The purpose of the studies was to evaluate NIBUT (Non-Invasive Break-Up Time) and TBUT (Tear Break-Up Time) in full-time students at Linnaeus University and to contribute to an increased understanding of the eye health of this group. Method: The stability of the tear film was checked with NIBUT and TBUT, the time was measured directly after a blink to the first break-up of the tear film surface or a new blink. NIBUT was performed non-invasively in Sirius and TBUT was measured in a biomicroscope with fluorescein. The participants initially had to answer a questionnaire that made it possible to analyze collected data based on age, sex, number of semesters studied, screen time and score on the DEQ-5 (5-Item Dry Eye Questionnaire). The responses from the DEQ-5 allowed the results from the NIBUT and TBUT measurements to be compared against perceived symptoms of dry eye. Results: The study included 36 students in the age range 18–39 years (median age 23 years, IQR 5.25 years). NIBUT and TBUT showed a positive significant correlation (p <0.001). A shorter TBUT correlated negatively with a higher DEQ-5 total score (p = 0.004) as well as the number of semesters studied (p = 0.025). NIBUT did not show any similar correlations. The reference value for dry eye diagnosis using NIBUT and TBUT is a time <10 seconds. Over half of the participants in the study, NIBUT 58% and TBUT 53%, had a reduced break-up time <10 seconds. Which can be an indication of dry eye problems. Conclusion: This study shows that there is a significant connection between the NIBUT and TBUT measurements. Shorter TBUT has shown a significant correlation with higher total scores on the DEQ-5, likewise significant connections between TBUT and more semesters read have been established. Despite the correlation between NIBUT and TBUT, the results were influenced by differences between the two measurement methods.

Orientador: Elenice Deffune / Resumo: Introdução: A Síndrome do Olho Seco (SOS) é uma doença multifatorial das lágrimas e da superfície ocular que resulta em desconforto, distúrbios visuais e instabilidade do filme lacrimal e afeta principalmente adultos com mais de 50 anos e mulheres. É uma doença que pode ter grande impacto negativo na qualidade de vida dos pacientes. A abordagem terapêutica com soro autólogo tem sido preconizada desde 1986 com prós e contras na literatura. Esta pesquisa teve como objetivo realizar uma revisão sistemática e metanálise para analisar a efetiva contribuição do Soro Autólogo segundo os protocolos, ensaios terapêuticos publicados nos últimos 10 anos e o atendimento dos pacientes portadores de Síndrome do olho seco (SOS) no Hospital das Clínicas da Faculdade de Medicina de Botucatu .Objetivos: 1) realizar revisão sistemática e metanálise para avaliar a eficácia do uso do soro autólogo em comparação com lágrimas artificiais comerciais no tratamento para adultos com olho seco. 2) realizar um trabalho retrospectivo da contribuição do soro autólogo de uso ocular no tratamento da SOS nos pacientes do ambulatório do Hospital das Clínicas de 2014-2018 comparando com o período anterior (2008-2013). Materiais e Métodos: Para a revisão sistemática e metanálise foi pesquisado na base de dados do Pubmed não usando restrições de língua, apenas trabalhos dos últimos 10 anos. Para os desfechos primários e secundários foi utilizado um intervalo de confiança de 95%. O levantamento de dados dos pacien... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Introduction: Dry Eye Syndrome is a multifactorial disease of tears and ocular surface that results into discomfort, visual disturbances and tear film instability and affects mainly female adults, over 50 years. It is a disease which may cause a great negative impact on the patients’ quality of life. The therapeutic approach employing autologous serum has been advocated in 1986, with pros and cons in the literature. This study aimed to perform a systematic review and a meta-analysis to investigate the effective contribution of Autologus Serum according to the protocols and clinical trials published in the last 10 years, and the SOS patients care at Hospital das Clínicas, during two periods: 2008-2013 and 2014- 2018.Objectives: 1) to perform a systematic review and meta-analysis to evaluate the efficacy of the autologous serum, in comparison to commercial artificial tears for the treatment of dry eye in adults. 2) to carry out a retrospective study of the ocular autologous serum contribution for SOS out patients’ treatment, at Hospital das Clínicas (2014 to 2018), comparing with the previous period (2008-2013).Materials and Methods: For the systematic review and meta-analysis, searches were realized in Pubmed databases, with no language restrictions, for papers published in the last 10 years, with full text availability, for researches dated until 10/12/2018. For the primary and secondary outcomes, a 95% confidence interval was used. For the outpatients’ data collection, each ... (Complete abstract click electronic access below) / Mestre

by Stefanie P.C. Czerwinski. / Thesis (M.S.)--Florida Atlantic University, 2013. / Includes bibliography. / Mode of access: World Wide Web. / System requirements: Adobe Reader. / Sjèogren's Syndrome (SS) is a chronic, inflammatory autoimmune disease affecting mostly the exocrine cells of lacrimal and salivary glands, leading to diminished secretory function and resulting in keratoconjunctivitis sicca (dry eye disease) and/or stomatitis sicca (dry mouth disease). Despite several decades of studies focusing on autoimmune diseases and dry eye diseases, the exact etiology and mechanisms of SS remain unknown. Besides the fact that SS is often unreported, unrecognized and untreated, today's therapies rely exclusively on treating the symptoms after disease progression; there exists neither prevention therapy nor cure for SS. In addition, SS has been diagnosed predominantly in post-menopausal women with the female to male ratio reaching 9:1, suggesting a role of ovarian sex hormones in the pathogenesis of SS. However, not all postmenopausal women develop SS, indicating the contribution of other factors such as a genetic background to the onset of SS. In the present study, ovariectomized (OVX) NOD.B10.H2b mice provide a model of menopause with a genetic predisposition to SS, as compared to non-predisposed C57BL/10 mice. Both strands of mice were either sham operated, OVX, OVX and treated with 17(Sb (Bestradiol (E2), or OVX and treated with dihydrotestosterone (DHT). Lacrimal glands were collected 3, 7, 21, and 30 days after surgery and processed for RNA analysis by rt-qPCR and protein assays by ELISA to evaluate cytokine expression and concentrations of IL- 1\U+fffd\, TNF-a, IFN-(Sd(B, IL-10, and IL-4 on a timeline. Overall, our results showed a significant increase in IL-1\U+fffd\ TNF-a, IL-10, and IL-4 expression and levels in the lacrimal glands of OVX NOD.B10.H2b mice as compared to sham operated animals, and treatment with E2 or DHT at time of OVX prevented the increase in cytokine expression and levels.

INTRODUÇÃO: A síndrome de Sjögren primária (SSp) é uma doença autoimune inflamatória crônica que afeta principalmente as glândulas exócrinas, levando aos sintomas de síndrome sicca. O olho seco é uma das características mais importantes dessa síndrome e um estudo recente relatou redução da atividade da DNase I em lágrimas de pacientes com olho seco de várias etiologias. Portanto, postulamos que pacientes com SSp possam ter anticorpos direcionados à DNase I. MÉTODOS: Avaliamos em um estudo de corte transversal 85 pacientes com SSp (conforme os critérios de classificação do American European Consensus Group Criteria, 2002), 50 pacientes com artrite reumatoide (AR) (American College of Rheumatology Criteria/ 1987) sem sintomas de síndrome sicca e 88 voluntários saudáveis. A reatividade IgG anti-DNase I foi detectada por ELISA utilizando a enzima de pâncreas bovino como antígeno e confirmada por Imunoblotting. RESULTADOS: A idade e sexo foram comparáveis nos três grupos (p > 0,05). A anti-DNase I foi detectada em 43,5% dos pacientes com SSp, conforme determinado por ELISA. Em contraste, essa reatividade estava ausente em todos os pacientes com AR (p= 0,0001). Comparações adicionais dos pacientes com SSp com (n= 37) e sem (n= 48) anti-DNase I revelaram que o primeiro grupo tinha níveis séricos de IgG mais altos (2293,2 ± 666,2 vs. 1483,9 ± 384,6 mg/dL, p= 0,0001) e uma frequência maior de leucopenia não induzida por drogas (43% vs. 19%, p= 0,02). A análise de regressão logística multivariada mostrou que apenas os níveis de IgG foram independentemente associados com o anti-DNase I. CONCLUSÃO: Descrevemos uma alta frequência de anticorpos anti-DNase I em pacientes com SSp associados a níveis séricos de IgG mais elevados. A falta dessa reatividade em pacientes com AR sem sintomas de sicca sugere que esse anticorpo pode ser útil no diagnóstico diferencial dessas doenças / INTRODUCTION: Primary Sjögren\'s syndrome (pSS) is a chronic inflammatory autoimmune disease that mainly affects exocrine glands. Dry eye is one of the most important features of this syndrome and a recent study reported reduced DNase I activity in tears of patients with dry eye of various etiologies. We therefore postulated that patients with pSS may have antibodies targeting DNase I. METHODS: We have evaluated in a cross-sectional study 85 pSS patients (American European Consensus Group Criteria/ 2002), 50 rheumatoid arthritis (RA) patients (American College of Rheumatology Criteria/ 1987) without sicca symptoms and 88 healthy volunteers. The IgG anti-DNase I reactivity was detected by ELISA using bovine pancreas enzyme as antigen and confirmed by Immunoblotting. RESULTS: Age/ gender were comparable in the three groups (p > 0.05). Anti-DNase I was detected in 43.5% of the pSS patients as determined by ELISA. In contrast, this reactivity was absent in all RA patients (p= 0.0001). Further comparison of pSS patients with (n= 37) and without (n= 48) anti-DNase I revealed that the former group had higher IgG serum levels (2293.2 ± 666.2 vs. 1483.9 ± 384.6 mg/dL, p= 0.0001) and a higher frequency of non-drug induced leukopenia (43% vs. 19%, p= 0.02). A multivariate logistic regression analysis identified that only IgG levels were independently associated with anti-DNase I. CONCLUSION: We describe a high frequency of anti-DNase I antibodies in pSS patients associated with higher serum IgG levels. The lack of this reactivity in RA patients without sicca symptoms suggests that this antibody may be helpful in the differential diagnosis of these diseases

This thesis investigates the feasibility of loading silicone hydrogel (SiHy) contact lenses with two different hydrophobic therapeutics, latanoprost and DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine), for treatment of glaucoma and hyperemia respectively. The two methods of loading were 1) thermal loading in an aqueous medium and 2) convective loading in a solution of n-propanol. Dailies Total1® lenses prepared in this manner were tested for their loading and their release into artificial tears. Continuous release over 1-4 days at therapeutic levels is achievable from thermal loading of DMPC, convective loading of DMPC, and convective loading of latanoprost. The DMPC loading processes can be naturally integrated into standard manufacturing lines for Dailies Total1®. Both DMPC and latanoprost release at rates proportional to the amount loaded into a contact lens. Latanoprost loads into a contact lens strictly proportionally to the loading concentration and the time of loading. The convective loading step represents a significant improvement on both the time of loading (reduced from days to minutes) and the loading capacity of silicone hydrogel contact lenses. This thesis also compares the loading and release of latanoprost in the convective loading procedure using the SiHy contact lenses of Acuvue Advance® (Johnson & Johnson Vision Care, Jacksonville, FL) , Air Optix® (Alcon, Copenhagen, Denmark), Biofinity® (CooperVision), PureVision® (Bausch & Lomb), and Dailies Total1® (Alcon), and the polyHEMA lens, SofLens 38® (Bausch & Lomb), finding that silicone hydrogels load an order of magnitude more drug than the polyHEMA lens and release into artificial tears for an order of magnitude longer. Overall, these experiments provide a quantitative understanding of the dynamics of loading and release for both DMPC and latanoprost.

Made available in DSpace on 2015-05-14T12:59:47Z (GMT). No. of bitstreams: 1 parte1.pdf: 1499360 bytes, checksum: 73a1a71524a39b1fbaa99614b57d192f (MD5) Previous issue date: 2009-11-10 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / The physiological and pharmacological effects of isotretinoin are yet to be completely understood despite its widespread use in the treatment of acne vulgaris and the known adverse effects that it may cause, dry eyes being one of the most common. The objective of this study was to evaluate the toxicity of oral isotretinoin on the conjunctiva of patients submitted to treatment with this drug, using impression cytology. A prospective cohort clinical trial was conducted at the Ophthalmological Referral Center of the Federal University of Paraíba and at the Laboratory of External Eye Diseases of the Federal University of São Paulo. Twentyeight patients with acne vulgaris were selected. A questionnaire on symptoms was applied and biomicroscopy, tear film break-up time (TBUT), fluorescein staining, Shirmer s test, rose bengal staining and impression cytology (IC) were performed prior to and after three months of treatment with oral isotretinoin. Samples for IC were collected from the temporal, superior, nasal and inferior bulbar conjunctiva of both eyes. The doses of isotretinoin varied from 0.35 to 0.88 mg/kg/day. Compared to pretreatment, burning, pruritus and gritty eye sensation were significantly more common during treatment with this drug, as were the biomicroscopic changes of hyperemia and blepharitis. The percentage of positive results for dry eyes according to TBUT and for rose bengal conjunctival staining was also greater during treatment. Regarding Shirmer s test and fluorescein staining of the cornea, no statistically significant changes were found with exposure to the drug. With respect to IC performed on the samples obtained from the superior and temporal quadrants, there was a reduction in the percentage of normal results from 100% to 82% and from 75% to 43%, respectively, and an increase in the percentage of borderline results from 0 to 14% and from 21% to 47%, respectively, during treatment compared to baseline results. For the samples from the nasal quadrant, an increase occurred in the percentage of abnormal findings from 0 to 11%, while in the samples taken from the inferior quadrant, no changes were found with the use of isotretinoin. The parameters affected by this treatment were cell-to-cell contact, nucleus-tocytoplasm ratio and the distribution of goblet cells, the scores of which increased significantly. No significant correlation was found between the results of IC, symptom score and tear function tests. Therefore, the present findings show that acne treatment with oral isotretinoin results in changes in the conjunctival epithelium in a significant percentage of patients. These changes are seen both in the exposed region of the bulbar conjunctiva (temporal and nasal) and in the unexposed conjunctiva (superior) and reflect a trend towards squamous metaplasia as an adaptive response of the conjunctival epithelium, which tends to become nonsecretory under the effect of the drug. / As ações fisiológicas e farmacológicas da isotretinoína ainda não são completamente conhecidas, apesar da sua ampla utilização no tratamento da acne vulgar e dos efeitos adversos que pode causar. Dentre esses, o quadro de olho seco é um dos mais frequentes. O objetivo deste estudo foi avaliar a toxicidade da isotretinoína oral sobre a conjuntiva de pacientes submetidos a tratamento com o fármaco, utilizando a citologia de impressão. Realizou-se estudo clínico prospectivo tipo coorte no Centro de Referência Oftalmológica da Universidade Federal da Paraíba e no Laboratório de Doenças Externas Oculares da Universidade Federal de São Paulo. Foram selecionados 28 pacientes portadores de acne vulgar. Realizou-se questionário de sintomas, biomicroscopia, teste do tempo de ruptura do filme lacrimal (TBUT), coloração por fluoresceína, teste de Shirmer, coloração por rosa bengala e citologia de impressão (CI) antes e aos 3 meses de tratamento com isotretinoína oral. Os espécimes para a CI foram coletados dos quadrantes temporal, superior, nasal e inferior da conjuntiva bulbar de ambos os olhos. As doses de isotretinoína variaram de 0,35 a 0,88 mg/kg/dia. Em relação ao pré-tratamento, os sintomas ardor ocular , prurido e sensação de areia nos olhos , assim como as alterações biomicroscópicas hiperemia e blefarite , ocorreram com uma frequência significantemente maior durante o tratamento com o fármaco. O percentual de resultados positivos para olho seco, para o TBUT e para a coloração conjuntival por rosa bengala também foi significantemente maior na vigência do tratamento. Para o teste de Shirmer e para a coloração da córnea por fluoresceína, não houve mudanças significantes com a exposição ao fármaco. Quanto à CI, para os espécimes obtidos dos quadrantes superior e temporal, houve diminuição do percentual de resultados normais (de 100 para 82 e de 75 para 43, respectivamente) e aumento do percentual de resultados limítrofes (de 0 para 14 e de 21 para 47, respectivamente) durante o tratamento, em relação aos resultados iniciais. Para os espécimes do quadrante nasal, houve aumento do percentual de resultados anormais (de 0 para 11), e para aqueles do quadrante inferior, não se observaram alterações com o uso de isotretinoína. Com o tratamento, foram afetados os parâmetros contato célula-célula , razão núcleo/citoplasma e distribuição das células caliciformes , que sofreram aumento significante em seus escores. Não houve uma correlação significante entre os resultados da CI, do escore de sintomas e dos testes da função lacrimal. Assim, de acordo com os resultados obtidos, o tratamento da acne com isotretinoína oral induz alterações no epitélio conjuntival de um percentual significante de pacientes. Essas alterações são observadas tanto na região exposta da conjuntiva bulbar (temporal e nasal), como na não exposta (superior) e representam uma tendência à metaplasia escamosa, como uma resposta adaptativa do epitélio conjuntival, que tende a se tornar não secretor sob efeito do fármaco.

Objetivo: descrever os achados de citologia de impressão em voluntários saudáveis e correlacioná-los com testes de olho seco e sintomatologia. Métodos: coleta de citologia de impressão (CI) da conjuntiva superior, inferior, nasal e temporal após anamnese, questionário de sintomas (QU) e exames clínicos biomicroscópicos, teste de Schirmer (TS), tempo de ruptura do filme lacrimal (TRFL), escores de fluoresceína (EF) e rosa bengala (ERB). Resultados: Foram examinados 78 olhos de 39 pacientes (30 mulheres, 85% brancos). Idade média foi de 36 anos (16-71 anos). Oitenta e cinco porcento dos pacientes eram assintomáticos no QU. TRFL médio foi de 13,6 segundos (70% ≥ 10 s), TS médio foi 19,2 mm (76% ≥ 6 mm), ERB foi 0-3 em 87%, EF foi zero em 75%. Biomicroscopia apresentou resultado normal em 65% dos olhos. CI foi normal em: 81% superior, 57% nasal, 87% inferior, 75% temporal. Foi encontrado padrão de cromatina snake-like em 15% das amostras superiores. Houve pouca correlação entre os testes clínicos, questionário e achados citológicos. A citologia de impressão do sítio nasal e a presença de cromatina snake-like associaram-se com alguns testes da superfície ocular, sintomas e com a idade dos pacientes. Conclusão: Nosso estudo encontrou 30% de testes clínicos anormais, sintomas e achados citológicos alterados (anormal e limítrofe) neste grupo de indivíduos normais. Os achados da conjuntiva bulbar da área de fenda e superior são os que mais apresentam alterações. Entretanto, apesar de algumas associações significativas, não houve correlação conclusiva entre testes, sintomas e citologia de impressão. / Purpose: To describe conjunctival findings of impression cytology in healthy volunteers and to correlate to dry eye tests and symptoms. Methods: superior, inferior, nasal and temporal bulbar conjunctivae impression cytology, symptoms questionnaire, slit lamp examination, Schirmer test (ST), tear film break-up time (TFBUT), fluorescein staining (FS) and rose Bengal staining (RBS) were evaluated. Results: 78 eyes of 39 patients (30 female, 85% white) were examined. Mean age was 36 years (16-71 years). Eighty-five percent of patients were asymptomatic in questionnaire. Mean TFBUT was 13.6 seconds (70% ≥ 10 sec), ST median was 19.2 mm (76% ≥ 6 mm), RBS grade was 0-3 in 87%, FS was 0 in 75%. Slit lamp examination did not reveal any alteration in 65% of the eyes. Impression cytology showed normal aspect in: 81% superior, 57% nasal, 87% inferior, and 75% temporal. Snake-like chromatin pattern was present in 15% of superior samples. There were few correlations among clinical tests, questionnaire result and cytological findings. Nasal impression cytology results and snake-like chromatin were associated with some ocular surface exams, symptoms and age of patients. Conclusion: Our study identified prevalence of 30% of abnormal clinical tests, symptoms, and altered cytological findings (abnormal and borderline) in this group of normal subjects. Impression cytology findings of exposed bulbar conjunctiva and superior conjunctiva are more often altered. Despite a few associations among tests, there was no conclusive correlation among these tests, symptoms and impression cytology results.

Objetivo: descrever os achados de citologia de impressão em voluntários saudáveis e correlacioná-los com testes de olho seco e sintomatologia. Métodos: coleta de citologia de impressão (CI) da conjuntiva superior, inferior, nasal e temporal após anamnese, questionário de sintomas (QU) e exames clínicos biomicroscópicos, teste de Schirmer (TS), tempo de ruptura do filme lacrimal (TRFL), escores de fluoresceína (EF) e rosa bengala (ERB). Resultados: Foram examinados 78 olhos de 39 pacientes (30 mulheres, 85% brancos). Idade média foi de 36 anos (16-71 anos). Oitenta e cinco porcento dos pacientes eram assintomáticos no QU. TRFL médio foi de 13,6 segundos (70% ≥ 10 s), TS médio foi 19,2 mm (76% ≥ 6 mm), ERB foi 0-3 em 87%, EF foi zero em 75%. Biomicroscopia apresentou resultado normal em 65% dos olhos. CI foi normal em: 81% superior, 57% nasal, 87% inferior, 75% temporal. Foi encontrado padrão de cromatina snake-like em 15% das amostras superiores. Houve pouca correlação entre os testes clínicos, questionário e achados citológicos. A citologia de impressão do sítio nasal e a presença de cromatina snake-like associaram-se com alguns testes da superfície ocular, sintomas e com a idade dos pacientes. Conclusão: Nosso estudo encontrou 30% de testes clínicos anormais, sintomas e achados citológicos alterados (anormal e limítrofe) neste grupo de indivíduos normais. Os achados da conjuntiva bulbar da área de fenda e superior são os que mais apresentam alterações. Entretanto, apesar de algumas associações significativas, não houve correlação conclusiva entre testes, sintomas e citologia de impressão. / Purpose: To describe conjunctival findings of impression cytology in healthy volunteers and to correlate to dry eye tests and symptoms. Methods: superior, inferior, nasal and temporal bulbar conjunctivae impression cytology, symptoms questionnaire, slit lamp examination, Schirmer test (ST), tear film break-up time (TFBUT), fluorescein staining (FS) and rose Bengal staining (RBS) were evaluated. Results: 78 eyes of 39 patients (30 female, 85% white) were examined. Mean age was 36 years (16-71 years). Eighty-five percent of patients were asymptomatic in questionnaire. Mean TFBUT was 13.6 seconds (70% ≥ 10 sec), ST median was 19.2 mm (76% ≥ 6 mm), RBS grade was 0-3 in 87%, FS was 0 in 75%. Slit lamp examination did not reveal any alteration in 65% of the eyes. Impression cytology showed normal aspect in: 81% superior, 57% nasal, 87% inferior, and 75% temporal. Snake-like chromatin pattern was present in 15% of superior samples. There were few correlations among clinical tests, questionnaire result and cytological findings. Nasal impression cytology results and snake-like chromatin were associated with some ocular surface exams, symptoms and age of patients. Conclusion: Our study identified prevalence of 30% of abnormal clinical tests, symptoms, and altered cytological findings (abnormal and borderline) in this group of normal subjects. Impression cytology findings of exposed bulbar conjunctiva and superior conjunctiva are more often altered. Despite a few associations among tests, there was no conclusive correlation among these tests, symptoms and impression cytology results.

Made available in DSpace on 2018-07-27T18:26:06Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-08-14. Added 1 bitstream(s) on 2018-07-27T18:30:15Z : No. of bitstreams: 1 000866549.pdf: 1249047 bytes, checksum: fb12f6b451fca36393121a26b2c8f5b5 (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / A ceratoconjuntivite seca (CCS) é uma afecção de caráter inflamatório, comum em cães. O uso do ômega 3 e 6 no tratamento de humanos e coelhos com CCS tem sido pesquisado devido ao potencial efeito imunomodulador desses ácidos graxos, porém não há relatos do seu uso em cães com essa afecção. Objetivou-se avaliar o efeito dos óleos de linho e peixe, produtos ricos em ômega 3 e 6, administrados por via oral, na produção lacrimal e inflamação ocular de cães com CCS. Foram utilizados 45 cães, sendo 15 sem CCS, constituindo o grupo controle (GC), e 30 com CCS. Estes foram divididos de forma randomizada e cega em dois grupos: grupo tratado com óleo de linho (GL) e grupo tratado com óleo de peixe (GP); cada animal recebeu, por via oral, uma cápsula a cada 24 horas durante 60 dias, de acordo com o seu grupo. Exame clínico, teste lacrimal de Schirmer 1, teste de ruptura do filme lacrimal e teste de fluoresceína foram realizados antes do início do tratamento (M0) e aos 15 (M15), 30 (M30), 45 (M45) e 60 (M60) dias de tratamento. A citologia de impressão de superfície ocular foi realizada no M0, M30 e M60, enquanto a biópsia conjuntival para histopatologia foi obtida antes do tratamento e no momento final de avaliação. Houve diminuição significativa da hiperemia conjuntival nos cães de ambos os grupos tratados aos 60 dias. Na análise histopatológica, detectou-se diminuição da espessura epitelial no GL e GP, diminuição da queratinização no GL e diminuição do infiltrado de células inflamatórias no GP ao final do tratamento. Não houve diferença significativa nas demais avaliações. Conclui-se que os óleos de linho e peixe não aumentam a produção lacrimal até 60 dias do tratamento, porém melhoram a qualidade da superfície ocular. O óleo de peixe reduz o quadro inflamatório. Desta forma, o tratamento com óleo de linho ou peixe pode ser indicado como terapia adjuvante para cães com CCS / The keratoconjunctivitis sicca (KCS) is inflammatory and a common disease in dogs. The use of omega 6 and 3 for treatment in humans and rabbits has been researched because of the potential immunomodulatory effect of these fatty acids, but there are no reports of its use in dogs with this condition. The aim of this study was to investigate the effect of linseed oil and fish oil, products rich in omega 3 and 6, administered orally on tear production and ocular inflammation in dogs with KCS. For this study we used 45 dogs: 15 without KCS, constituting the control group (CG) and 30 with KCS. A randomized, double-blind clinical study was performed in assigned to treatment orally with oil fish (FO) or linseed oil (LO), both once daily for 60 days. More 15 dogs with no KCS were evaluated for a control group (CG). Clinical examination of the eye, Schirmer tear tests I, tear film breakup time, fluorescein test were performed prior to treatment (M0) and at days 15 (M15), 30(M30), 45(M45) and 60(M60) after initiation of treatment. The impression cytology on ocular surface was performed at M0, M30 and M60. The conjunctival histopathological analysis was only performed prior to treatment and at day 60 after treatment. That was a significant decrease in conjunctival hyperemia in dogs of both treatments at day 60. The histopathological analysis revealed a decrease in the epithelial thickness both in FO and LO, a decrease on the degree of keratinization in LO and a decrease inflammatory cell infiltration in FO. There were no significant differences in the others evaluations in both groups. The analyzed results demonstrate that although both treatments administered orally do not increase tear production within 60 days of treatment, it improve the ocular surface. Thus, fish oil reduces eye inflammation. Therefore, treatment with linseed oil or fish may be indicated as adjunctive therapy for dogs with KCS

Objetivo: descrever os achados de citologia de impressão em voluntários saudáveis e correlacioná-los com testes de olho seco e sintomatologia. Métodos: coleta de citologia de impressão (CI) da conjuntiva superior, inferior, nasal e temporal após anamnese, questionário de sintomas (QU) e exames clínicos biomicroscópicos, teste de Schirmer (TS), tempo de ruptura do filme lacrimal (TRFL), escores de fluoresceína (EF) e rosa bengala (ERB). Resultados: Foram examinados 78 olhos de 39 pacientes (30 mulheres, 85% brancos). Idade média foi de 36 anos (16-71 anos). Oitenta e cinco porcento dos pacientes eram assintomáticos no QU. TRFL médio foi de 13,6 segundos (70% ≥ 10 s), TS médio foi 19,2 mm (76% ≥ 6 mm), ERB foi 0-3 em 87%, EF foi zero em 75%. Biomicroscopia apresentou resultado normal em 65% dos olhos. CI foi normal em: 81% superior, 57% nasal, 87% inferior, 75% temporal. Foi encontrado padrão de cromatina snake-like em 15% das amostras superiores. Houve pouca correlação entre os testes clínicos, questionário e achados citológicos. A citologia de impressão do sítio nasal e a presença de cromatina snake-like associaram-se com alguns testes da superfície ocular, sintomas e com a idade dos pacientes. Conclusão: Nosso estudo encontrou 30% de testes clínicos anormais, sintomas e achados citológicos alterados (anormal e limítrofe) neste grupo de indivíduos normais. Os achados da conjuntiva bulbar da área de fenda e superior são os que mais apresentam alterações. Entretanto, apesar de algumas associações significativas, não houve correlação conclusiva entre testes, sintomas e citologia de impressão. / Purpose: To describe conjunctival findings of impression cytology in healthy volunteers and to correlate to dry eye tests and symptoms. Methods: superior, inferior, nasal and temporal bulbar conjunctivae impression cytology, symptoms questionnaire, slit lamp examination, Schirmer test (ST), tear film break-up time (TFBUT), fluorescein staining (FS) and rose Bengal staining (RBS) were evaluated. Results: 78 eyes of 39 patients (30 female, 85% white) were examined. Mean age was 36 years (16-71 years). Eighty-five percent of patients were asymptomatic in questionnaire. Mean TFBUT was 13.6 seconds (70% ≥ 10 sec), ST median was 19.2 mm (76% ≥ 6 mm), RBS grade was 0-3 in 87%, FS was 0 in 75%. Slit lamp examination did not reveal any alteration in 65% of the eyes. Impression cytology showed normal aspect in: 81% superior, 57% nasal, 87% inferior, and 75% temporal. Snake-like chromatin pattern was present in 15% of superior samples. There were few correlations among clinical tests, questionnaire result and cytological findings. Nasal impression cytology results and snake-like chromatin were associated with some ocular surface exams, symptoms and age of patients. Conclusion: Our study identified prevalence of 30% of abnormal clinical tests, symptoms, and altered cytological findings (abnormal and borderline) in this group of normal subjects. Impression cytology findings of exposed bulbar conjunctiva and superior conjunctiva are more often altered. Despite a few associations among tests, there was no conclusive correlation among these tests, symptoms and impression cytology results.