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1.
BMC Ophthalmol ; 19(1): 41, 2019 Feb 04.
Artículo en Inglés | MEDLINE | ID: mdl-30717687

RESUMEN

BACKGROUND: To evaluate the safety and efficacy of using a lid hygiene brush prototype to wipe the lid margins with lid hygiene shampoo in subjects with normal meibomian glands. METHODS: Twelve eyes of 6 subjects were all evaluated just before and after wiping lid margins using 1) tap water alone, 2) Eye Shampoo, 3) Eye Brush, or 4) both products, each during a different week. The results after using both products twice daily for 1 month were also evaluated. Wiping efficacy was determined by post-wiping scores for the remaining fluorescein-stained 0.3% Tarivid ointment fully applied to eyelids and lid margins under microscopic view illuminated by blue light just after performing each of the four lid hygiene methods described above. RESULTS: No significant deterioration in ocular conditions occurred. Eyestrain, eye discharge, and dryness decreased with tap water (P = 0.020), Eye Shampoo (P = 0.036), and Eye Brush (P = 0.014), respectively. Sensations of eye discharge increased after 1 month of using both products (P = 0.042). The wiping efficacy of Eye Brush, Eye Shampoo or both was significantly greater than that of tap water alone (two-sided test, P = 0.003, 0.003, 0.002), and using both significantly increased efficacy above Eye Shampoo use alone (one-sided test, P = 0.009). CONCLUSIONS: Wiping lid margins using Eye Brush enhanced the cleansing power of Eye Shampoo. A daily healthcare routine using both products could be a safe and effective option for daily lid hygiene. TRIAL REGISTRATION: UMIN000016905 . Registration date: March 24, 2015; the study was prospectively registered.


Asunto(s)
Detergentes/uso terapéutico , Desinfección/instrumentación , Oftalmopatías/prevención & control , Enfermedades de los Párpados/prevención & control , Higiene , Agua/administración & dosificación , Adulto , Conjuntiva/patología , Córnea/patología , Dolor Ocular/diagnóstico , Humanos , Masculino , Persona de Mediana Edad , Proyectos Piloto , Estudios Prospectivos , Lágrimas/metabolismo
2.
Adv Ther ; 41(6): 2477-2485, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38709396

RESUMEN

INTRODUCTION: This study aimed to investigate the tolerability of high-viscosity diquafosol tetrasodium (DQS) ophthalmic solution (DIQUAS LX; DQSLX) and examine its usability and effect on clinical findings in patients with dry eye disease (DED). METHODS: This interventional retrospective study included 66 eyes of 66 patients with DED who switched from conventional DQS to DQSLX ophthalmic solution. Tear function assessments (tear film breakup time [BUT], keratoconjunctival vital staining [VS] score), evaluations of DED symptom relief, and a four-item usability questionnaire ("comfort upon instillation," "irritation upon instillation," "eye mucus discharge," "convenience of instillation frequency") assessed using a visual analog scale from 0 (worst) to 10 (best) were administered 4 weeks after switching to DQSLX. Factors associated with drug tolerability were assessed using multiple regression analysis. RESULTS: The symptoms improved by 64.2% after switching to DQSLX. The BUT value, VS score, and the questionnaire items "comfort upon instillation" and "convenience of instillation frequency" were significantly improved after switching to DQSLX. DQSLX tolerability was reported as acceptable in 56 (84.8%) and unacceptable in 10 (15.2%) patients. Overall, DQSLX tolerability was significantly associated with "comfort upon instillation" and "convenience of instillation frequency" and tended to be associated with a VS score ≥ 1. DQSLX tolerability depended on symptom and VS score improvements and absence of excessive "eye mucus discharge" in patients with a VS score ≥ 1 (39 patients), but on "comfort upon instillation" and absence of excessive "eye mucus discharge" in patients with a VS score = 0 (27 patients). CONCLUSION: The high-viscosity DQSLX ophthalmic solution was generally considered acceptable in the study population. However, drug tolerability seemingly differed between patients with DED with and without epithelial damage. The former were affected by improvements in symptoms and clinical findings, whereas the latter were affected by comfort upon instillation. TRIAL REGISTRATION: University Hospital Medical Information Network identifier, UMIN000051390.


Asunto(s)
Síndromes de Ojo Seco , Soluciones Oftálmicas , Polifosfatos , Nucleótidos de Uracilo , Humanos , Síndromes de Ojo Seco/tratamiento farmacológico , Masculino , Femenino , Nucleótidos de Uracilo/uso terapéutico , Nucleótidos de Uracilo/administración & dosificación , Soluciones Oftálmicas/uso terapéutico , Persona de Mediana Edad , Estudios Retrospectivos , Anciano , Polifosfatos/uso terapéutico , Polifosfatos/administración & dosificación , Lágrimas/efectos de los fármacos , Adulto , Preparaciones de Acción Retardada , Resultado del Tratamiento , Encuestas y Cuestionarios
3.
Ocul Surf ; 32: 139-144, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38458565

RESUMEN

PURPOSE: To evaluate stress levels extracted from prefrontal electroencephalogram (EEG) signals and investigate their relationship with dry eye symptoms. METHODS: This prospective, cross-sectional, comparative study included 25 eyes of 25 patients with aqueous tear-deficient dry eye (low Schirmer group), 25 eyes of 25 patients with short tear breakup time dry eye (short breakup time group), and 24 eyes of 24 individuals without dry eye. An EEG test, the Japanese version of the Ocular Surface Disease Index (OSDI), and a stress questionnaire were administered. EEG-detected stress levels were assessed under three conditions: eyes closed, eyes open, and eyes open under ocular surface anesthesia. RESULTS: Stress levels were significantly lower when the eyes were closed than when they were open in all groups (all P < 0.05). Stress levels during eyes open under ocular surface anesthesia were significantly lower than those during eyes open without anesthesia only in the low Schirmer group; no differences were found between the short breakup time and control groups. OSDI scores were associated with EEG-detected stress levels (P = 0.06) and vital staining score (P < 0.05) in the low Schirmer group; they were not associated with EEG-detected stress (P > 0.05), but with subjective stress questionnaire scores and breakup time values in the short breakup time group (P < 0.05). CONCLUSIONS: In the low Schirmer group, peripheral nerve stimulation caused by ocular surface damage induced stress reactions in the frontal lobe, resulting in dry eye symptoms. Conversely, in the short breakup time group, the stress response in the frontal lobe was not related to symptom development.


Asunto(s)
Síndromes de Ojo Seco , Electroencefalografía , Lóbulo Frontal , Lágrimas , Humanos , Síndromes de Ojo Seco/fisiopatología , Síndromes de Ojo Seco/metabolismo , Masculino , Femenino , Estudios Prospectivos , Estudios Transversales , Persona de Mediana Edad , Electroencefalografía/métodos , Lágrimas/metabolismo , Lóbulo Frontal/fisiopatología , Encuestas y Cuestionarios , Adulto , Anciano , Estrés Psicológico/fisiopatología
4.
J Refract Surg ; 29(1): 19-24, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23311738

RESUMEN

PURPOSE: To report the changes in functional visual acuity (FVA) in eyes with experimentally induced astigmatism. METHODS: This study included 26 right eyes from 26 healthy participants (mean age: 27.0±4.4 years). After confirming best correction under cycloplegia, the cylinder power ×90° and ×180° (against-the-rule [ATR] and with-the-rule [WTR] astigmatism, respectively) were added with 0.50-diopter (D) steps, from 0.50 to 2.50 D. Conventional visual acuity (VA), FVA as measured by the FVA Measurement System (NIDEK Co Ltd), and 10% low-contrast visual acuity (LCVA) were measured with 3-mm artificial pupil under each condition. RESULTS: The mean corrected logMAR VA, FVA, LCVA were -0.18±0.00 (20/13), -0.10±0.08 (20/16), and 0.06±0.06 (20/23), respectively. The VA, FVA, and LCVA had a significant linear negative correlation with the addition of cylinder irrespective of the axes. A significant decrease in FVA was noted on addition of ⩾0.50 D WTR astigmatism and ⩾1.00 D ATR astigmatism. With the addition of 1.00 D of cylindrical lens, 96% of eyes with WTR and ATR astigmatism could maintain 20/20 in VA testing, whereas only 50% and 62% of eyes with WTR and ATR astigmatism, respectively, could maintain 20/20 in FVA testing. CONCLUSIONS: Astigmatism may be associated with deterioration of visual function even when conventional VA of 20/20 is attained. Functional VA testing seems to be useful in evaluating the masked astigmatic visual impairment that cannot be detected by conventional VA testing.


Asunto(s)
Astigmatismo/fisiopatología , Agudeza Visual/fisiología , Adulto , Topografía de la Córnea , Femenino , Humanos , Masculino , Estudios Prospectivos , Adulto Joven
5.
Invest Ophthalmol Vis Sci ; 64(7): 19, 2023 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-37306988

RESUMEN

Purpose: The purpose of this study was to investigate the association between autonomic nerve activity and symptom intensity according to the type of dry eye (DE). Methods: This prospective, cross-sectional, comparative study included 25 eyes of 25 patients with short tear break-up time DE (sBUTDE; mean age = 57.4 ± 11.4 years, range = 30-74 years) and 24 eyes of 24 patients with aqueous tear-deficient DE (ADDE; mean age = 62.3 ± 10.7 years, range = 29-76 years) were studied. Autonomic nerve activity was examined, and the Japanese version of the Ocular Surface Disease Index (J-OSDI) and a stress check questionnaire were administered. Autonomic nerve activity was continuously measured for 10 minutes. The parameters were low-frequency (LF) and high-frequency (HF) components of heart rate variability, reflecting cardiac sympathetic and parasympathetic nerve activity, and parasympathetic nerve activity alone, respectively; and the coefficient of variation of R wave-to-R wave (RR) interval (cvRR), component coefficient of variation of LF (ccvLF), and component coefficient of variation of HF (ccvHF), reflecting fluctuation of RR interval, LF, and HF, respectively. Results: Higher J-OSDI scores were associated with higher HF, ccvHF, and subjective stress in sBUTDE, showing a significant correlation (r = 0.53, P < 0.01; r = 0.55, P = 0.01; and r = -0.66, P = 0.01); no correlations were observed between the J-OSDI score and autonomic parameters and stress in ADDE. Conclusions: DE symptoms were significantly associated with the magnitude and fluctuation of parasympathetic activity in sBUTDE. Thus, among the autonomic parameters, parasympathetic activity is involved in the development of symptoms in sBUTDE, whereas the involvement of the autonomic nervous system may be minimal in ADDE.


Asunto(s)
Vías Autónomas , Síndromes de Ojo Seco , Humanos , Adulto , Persona de Mediana Edad , Anciano , Estudios Transversales , Estudios Prospectivos , Sistema Nervioso Autónomo
6.
PLoS One ; 17(11): e0276945, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36383530

RESUMEN

The autonomic nervous system plays a crucial role in the maintenance of homeostasis. Neurogenic inflammation due to decreased stability of tear film may induce changes in autonomic nerve activity, which could be associated with symptom expression.This study aimed to measure biological parameters that represent autonomic nerve activity in dry eye (DE)s caused by tear film dysfunction and investigate their relationship with symptom intensity. This prospective, cross-sectional, comparative study evaluated 34 eyes of 34 participants (mean age: 52.5 ± 13.4 years; range: 20-81 years) without keratoconjunctival damage. Nineteen eyes in the DE group showed DE symptoms and tear break-up time (TBUT) of ≤5 seconds (short TBUT DE); the 15 eyes in the non-DE group showed no DE symptoms. Autonomic nerve activity was measured for 10 minutes-starting and ending 5 minutes before and after instilling ophthalmic solution-and evaluated using the low-frequency component (LF) to the high-frequency component (HF) ratio of heart rate variability (autonomic balance). The pre-ophthalmic solution administration LF/HF ratio was not significantly different (P = 0.59) between the two groups, however, the standard deviation of the LF/HF ratio (LF/HF-SD) tended to be higher in the DE group than that in the non-DE group (P = 0.086). The DE symptom intensity was significantly related to LF/HF-SD (P = 0.005), which significantly decreased after ophthalmic solution administration in the DE group (P = 0.04). The large fluctuations in autonomic balance may be key for the understanding of the mechanism underlying DE symptoms.


Asunto(s)
Vías Autónomas , Síndromes de Ojo Seco , Humanos , Adulto , Persona de Mediana Edad , Anciano , Estudios Prospectivos , Estudios Transversales , Soluciones Oftálmicas , Frecuencia Cardíaca/fisiología , Síndromes de Ojo Seco/diagnóstico
7.
Optom Vis Sci ; 88(9): 1112-8, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21705941

RESUMEN

PURPOSE: To evaluate the efficacy of surgical treatment for conjunctivochalasis using the Tear Film Stability Analysis System. METHODS: Fifteen eyes of 15 patients (74.5 ± 4.8 years; 14 females and 1 male) who had surgical reconstruction of the tear meniscus for conjunctivochalasis underwent evaluation with a symptom questionnaire, Schirmer I test, fluorescein tear film break-up time (FBUT), and break-up time index (BUI) measurement by Tear Film Stability Analysis System examinations that were performed preoperatively and 3 months after the surgery. Changes of these tear parameters were statistically analyzed using the paired t test. RESULTS: After the surgery, the mean FBUT and BUI values significantly improved from 5.7 ± 3.2 s and 42.8 ± 18.7, respectively, to 8.4 ± 2.5 s and 60.7 ± 16.5, respectively (FBUT, p = 0.0438; BUI, p = 0.0036). The mean Schirmer test value showed no significant changes before and after surgery (p = 0.9064). Fourteen eyes (93.3%) had improvement of ocular symptoms after surgery. One eye (6.7%) with no improvement of ocular symptoms, FBUT, and BUI after surgery appeared to have aqueous tear deficiency. CONCLUSIONS: Surgical treatment for conjunctivochalasis was associated with improvement of tear stability and clinical dry eye symptoms.


Asunto(s)
Enfermedades de la Conjuntiva/diagnóstico , Síndromes de Ojo Seco/diagnóstico , Procedimientos Quirúrgicos Oftalmológicos , Lágrimas/química , Anciano , Anciano de 80 o más Años , Enfermedades de la Conjuntiva/metabolismo , Enfermedades de la Conjuntiva/cirugía , Síndromes de Ojo Seco/metabolismo , Síndromes de Ojo Seco/cirugía , Femenino , Fluoresceína , Colorantes Fluorescentes , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Soluciones Oftálmicas , Periodo Posoperatorio , Reproducibilidad de los Resultados , Propiedades de Superficie , Encuestas y Cuestionarios , Resultado del Tratamiento
8.
Ocul Surf ; 19: 307-312, 2021 01.
Artículo en Inglés | MEDLINE | ID: mdl-33127598

RESUMEN

PURPOSE: To evaluate the role of transient receptor potential melastatin 8 (TRPM8) activity in menthol-induced cold sensitivity and its qualitative perception in patients with dry eye (DE). METHODS: This prospective, cross-sectional, comparative study included 52 eyes of 52 subjects (mean age: 66.8 ± 9.2 years; range: 44-86) with a tear break-up time (TBUT) of ≤5 s. The participants were classified into three groups: 17 patients with DE symptoms and keratoconjunctival (KC) staining scores of ≥3 points (positive KC-DE group), 18 patients with DE symptoms and KC staining scores of <3 points (negative KC-DE group), and 17 individuals with KC staining scores of <3 points and no symptoms (non-DE control group). The menthol-induced cool sensation (M-cool) and TBUT were measured after administration of 2 µl of 1.0 mM menthol eye drops. Furthermore, participants answered a questionnaire regarding their stimulus perception (pleasant, unpleasant, or neither). RESULTS: M-cool values were similar in the three groups. TBUT significantly increased in the negative KC-DE and control groups (P < 0.05) and remained unchanged in the positive KC-DE group (P > 0.05) after menthol administration. DE patients reported the sensation as pleasant or unpleasant, whereas most control participants were indifferent (P < 0.05). CONCLUSIONS: While M-cold sensitivity was similar in DE and control groups, its qualitative perception differed between these groups. Thus, TRPM8 activation at the peripheral level alone may not be sufficient to account for the manifestation of discomfort symptoms associated with DE.


Asunto(s)
Síndromes de Ojo Seco , Mentol , Anciano , Estudios Transversales , Síndromes de Ojo Seco/inducido químicamente , Humanos , Persona de Mediana Edad , Percepción , Estudios Prospectivos
9.
J Oleo Sci ; 70(6): 799-805, 2021 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-33967173

RESUMEN

INTRODUCTION: Demodex mites are microscopic arthropods that have been shown to be responsible for chronic blepharitis. Although many reports have demonstrated positive effects of lid hygiene on demodicosis, some have produced conflicting results. We retrospectively evaluated the effect of lid margin cleansing with a novel lid hygiene detergent, Eye Shampoo, in patients with ocular demodicosis. METHODS: Outpatient clinic notes recorded over a 24-month period between June 30, 2016, and June 29, 2018, at Keio University Hospital in Japan were reviewed to identify patients diagnosed with ocular demodicosis who started cleansing their lid margins with Eye Shampoo at least once daily as a lid hygiene therapy. RESULTS: Five patients diagnosed with ocular demodicosis who started cleansing their lid margins using Eye Shampoo for lid hygiene were identified. In four cases, Demodex mites were successfully eliminated, and ocular conditions were ultimately improved with no recurrence. Active Demodex mites were still noted after 3 months of lid hygiene therapy in one case; further observation of this case was not available. There were no adverse effects of Eye Shampoo in any of these cases. CONCLUSION: Lid hygiene therapy using Eye Shampoo successfully eliminated Demodex mites, a common pathogen of refractory obstructive meibomian gland dysfunction.


Asunto(s)
Detergentes/farmacología , Higiene , Disfunción de la Glándula de Meibomio/prevención & control , Glándulas Tarsales/parasitología , Ácaros/efectos de los fármacos , Adulto , Anciano , Animales , Femenino , Humanos , Masculino
10.
Curr Eye Res ; 45(7): 782-788, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-31899962

RESUMEN

PURPOSE: This study aimed to prospectively assess tear dynamics in soft contact lens-induced dry eye while wearing and after removing the soft contact lenses. MATERIALS AND METHODS: We analyzed 17 right eyes of soft contact lens users at Wada Eye Clinic (11 men, 6 women; mean age: 36.8 ± 8.3 years; range: 24-57 years). Participants were divided into two groups depending on presence of dry eye symptoms. Video interferometry was used to observe tear dynamics while wearing and after removing soft contact lenses. Interference images focusing on tear spread and interference fringe were compared between groups. RESULTS: This study included 10 symptomatic and 7 asymptomatic eyes. Considering the symptomatic eyes, while wearing soft contact lenses, 8 eyes showed poor tear spread and multicolor interference fringe, i.e., swift flow of multicolor interference waves after a grayish monochromatic band-color after a blink, but 8 and 10 eyes showed good tear spread and a grayish monochromatic interference fringe when soft contact lenses were removed, respectively. As for asymptomatic eyes, 6 eyes exhibited good tear spread and a grayish monochromatic interference fringe while wearing soft contact lenses and after removing soft contact lenses. CONCLUSIONS: soft contact lens-induced dry eye was associated with tear dynamics only while wearing soft contact lenses. Observation of tear film dynamics in eyes with soft contact lenses could facilitate the understanding of dry eye-related symptoms.


Asunto(s)
Lentes de Contacto Hidrofílicos/efectos adversos , Síndromes de Ojo Seco/metabolismo , Lágrimas/fisiología , Adulto , Parpadeo , Estudios Transversales , Síndromes de Ojo Seco/etiología , Femenino , Humanos , Interferometría , Metabolismo de los Lípidos/fisiología , Masculino , Persona de Mediana Edad , Adulto Joven
11.
PLoS One ; 15(5): e0233381, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32428010

RESUMEN

It has been suggested that functional visual acuity (VA) testing may be able to measure both the visual performance and cognitive ability needed for driving and help to reduce the number of road traffic accidents. The aim of this study was to investigate the relationship between visual ability and cognitive function in healthy elderly subjects. The study included 34 eyes with a decimal best-corrected visual acuity (VA) ≥1.0 in 34 subjects (16 men, 18 women; mean age 72.7 ± 6.1 [range, 61-83] years) with the same type of monofocal intraocular lens implant. Using the score on the Japanese version of the Mini-Mental State Examination (MMSE) questionnaire, the subjects were divided into a mild cognitive impairment (MCI) group (score <28) and a normal cognition (NC) group (score ≥28). Visual ability was evaluated by functional VA testing. Functional VA was significantly lower in the MCI group (n = 10) than in the NC group (n = 24; P<0.02). There was no significant difference in best-corrected VA between the two groups. High correlations were found between the MMSE score and the logMAR functional VA (r = -0.36, P = 0.04), standard deviation of functional VA (r = -0.39, P = 0.02), and the visual maintenance ratio (r = 0.34, P = 0.048). In summary, despite a good best-corrected VA, deterioration in visual ability was detected in elderly individuals with MCI when measured by the functional VA test. Functional VA could be used to evaluate the integrated visual ability associated with age-related cognitive decline and have applications that help to reduce the disproportionately high rate of road traffic accidents in the elderly.


Asunto(s)
Cognición/fisiología , Agudeza Visual/fisiología , Accidentes de Tránsito/prevención & control , Anciano , Anciano de 80 o más Años , Conducción de Automóvil/normas , Disfunción Cognitiva/diagnóstico , Disfunción Cognitiva/fisiopatología , Estudios Transversales , Femenino , Humanos , Masculino , Persona de Mediana Edad
12.
Ocul Surf ; 18(4): 620-626, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32712260

RESUMEN

PURPOSE: To evaluate transient receptor potential vanilloid 1 (TRPV1)-mediated pain sensitivity in patients with short tear break-up time (TBUT) dry eye (DE) by using the capsaicin stimulus test. METHODS: This prospective cross-sectional comparative study included 22 eyes of 22 patients with short TBUT DE and 11 eyes of 11 non-DE control subjects. Patients were divided into two groups based on response to standard DE treatments: 10 non-responders (intractable DE) and 12 responders (responsive DE). Mechanical touch (M-touch) and mechanical pain (M-pain) were measured using a Cochet-Bonnet esthesiometer. Capsaicin-induced pain (C-pain) and C-pain duration (C-pain DT) were measured using a capsaicin stimulus test. Psychological distress was also assessed. RESULTS: M-touch sensitivity was similar among all three groups. M-pain sensitivity was higher in the responsive DE group than in the intractable DE and control groups (P < .001). C-pain sensitivity was lower (P < .001) in the intractable DE group than in the responsive DE and control groups, and C-pain DT was shorter (P = .006) in the intractable DE group than in the responsive DE group. Psychological distress was higher in the intractable DE group than in the control group (P < .001). CONCLUSIONS: Patients with intractable short TBUT DE were less sensitive to the effects of capsaicin than patients with responsive short TBUT DE and controls. Altered neural activation may contribute to the development of DE symptoms in the short TBUT DE subjects. The capsaicin stimulus test may be used to better understand pain sensitivity in short TBUT DE patients.


Asunto(s)
Capsaicina/efectos adversos , Síndromes de Ojo Seco , Dolor/inducido químicamente , Estudios Transversales , Síndromes de Ojo Seco/inducido químicamente , Humanos , Estudios Prospectivos , Lágrimas
13.
Diagnostics (Basel) ; 10(4)2020 Mar 31.
Artículo en Inglés | MEDLINE | ID: mdl-32244289

RESUMEN

PURPOSE: The reported signs and symptoms of dry eye (DE) have been discordant. This study evaluated risk factors of DE-related symptoms and signs to explore their association with patient demographics, focusing on the age factor. METHODS: The study enrolled 704 consecutive patients visiting general eye clinics who complained of ocular discomfort, but had normal vision. The patients were asked about the presence of six common symptoms related to DE and, tear break-up time (TBUT). The severity of patients' keratopathy was also examined, and patients underwent Schirmer's test. RESULTS: Logistic regression analysis demonstrated that younger age (≤29 years) was associated with non-visual symptoms and keratopathy, while older age (≥60 years) was associated with short TBUT and low values on Schirmer's test. Middle age was associated with both severe symptoms and signs. CONCLUSIONS: Discrepancies in the signs and symptoms of DE may depend, in part, on age, with younger subjects showing severe non-visual symptoms with apparently normal tear function and severe keratopathy, and older subjects showing fewer symptoms and less severe keratopathy despite worse tear function.

14.
J Oleo Sci ; 68(1): 67-78, 2019 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-30542004

RESUMEN

PURPOSE: To investigate the efficacy of eyelid margin cleansing with lid hygiene detergent in patients with obstructive meibomian gland dysfunction (MGD). METHODS: As a pilot study, we investigated the safety and efficacy of lid hygiene using tap water and/or lid hygiene shampoo in fourteen eyes of 7 normal subjects. All subjects were instructed to cleanse the eyelid margin with tap water and/or lid hygiene shampoo. As a main prospective clinical study, thirty-four eyes of 34 patients with obstructive MGD were enrolled. All subjects were instructed to cleanse the eyelid margin with lid hygiene shampoo at least once daily for 1 month. Ocular surface conditions were observed before and 1 month after study initiation. RESULTS: A significant exacerbating change (p < 0.05) was not detected after either method in the pilot study. In the main study, significant improvements were observed in tear break-up time (TBUT), lid margin lissamine green staining scores, vascular dilatation, and meibum status (p < 0.05). No significant improvements in corneal or conjunctival fluorescein staining scores, the mucocutaneous junction, lid margin deformation, or plugging were observed (p ≥ 0.05). Subjective improvements were observed in 27 subjects. Meibography revealed that 28 subjects had normal meibomian glands, and 6 subjects had meibomian gland atrophy. Significant improvements were observed in TBUT, vascular dilatation, and meibum status only in the group with normal meibomian glands (p < 0.05), but subjective symptoms and lid margin lissamine green staining scores improved in both groups (p < 0.05). No subjects experienced any problems throughout the study. CONCLUSION: Daily routine use of lid hygiene detergent can alleviate the symptoms of MGD regardless of meibomian gland atrophy.


Asunto(s)
Detergentes/uso terapéutico , Enfermedades de los Párpados/tratamiento farmacológico , Enfermedades de los Párpados/prevención & control , Glándulas Tarsales/fisiopatología , Cuidados de la Piel/métodos , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proyectos Piloto , Estudios Prospectivos , Vasodilatación/efectos de los fármacos , Agua/química
15.
J Ophthalmol ; 2019: 8950418, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31583130

RESUMEN

The functional visual acuity test which is the average of the visual acuities measured during a specific time frame (standard, 60 seconds) has been used recently to assess the visual function in various conditions. The availability of a shorter version of the functional visual acuity test promises to be patient friendly in that it is a simple screening test performed in a shorter period of time than the standard test. The results of measurements of the FVA test between the 30-second measurement time (short-version FVA test) and the standard 60-second measurement are compared, and the feasibility of the short-version FVA test instead of the standard FVA test is investigated. Twenty-eight healthy volunteers (25 men and 3 women) were enrolled in this prospective observational study. All subjects underwent measurement of the binocular distance-corrected visual acuity and the binocular distance-corrected FVA with the 60-second and 30-second measurement times. The interchangeability of the corrected-distance FVA, maximal VA, visual maintenance ratio, and average response time in the short-version and the standard FVA tests was evaluated using the Bland-Altman method, and the results showed agreements of the two tests except for the minimal VA. The short-version FVA test is equivalent to the standard method except for evaluating the visual acuity fluctuations and promises to be a simple visual screening test that can be performed in a shorter time.

16.
Invest Ophthalmol Vis Sci ; 59(14): DES29-DES35, 2018 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-30481803

RESUMEN

Dry eye (DE) causes irregularity of the ocular surface and reduces the quality of vision. An intact, regular tear film is essential for high-quality retinal images; however, visual tasks requiring sustained gazing can disrupt the tear film, eventually degrading visual function. A functional visual acuity (FVA) measurement system has been uniquely developed in Japan to evaluate visual function related to tear stability in patients with DE. FVA has been shown to correlate with optical quality. The system measures the change in visual acuity (VA) over time automatically in aqueous-deficient DE and short tear breakup tear film DE characterized by decreased tear stability and minimal epithelial damage. It is also useful to detect minimal visual deterioration correlated with minimal ocular surface abnormality and vision-related quality of life otherwise undetectable by conventional VA testing, to assess and quantify vision-related symptomatology, and to determine the efficacy of treatments for DE disease. Recently, its use has been expanded, such as for the analysis of visual function accompanying refractive surgery, contact lens, cataract and cataract-related disease, retinal disease, glaucoma, amblyopia, presbyopia, and vehicle driving. Its use has revealed that FVA reflects not only visual function related to tear dynamics, but also visual function related to quick recognition of the target. This simple, noninvasive, and sensitive FVA measurement system may be expected to be used worldwide.


Asunto(s)
Síndromes de Ojo Seco/fisiopatología , Trastornos de la Visión/fisiopatología , Agudeza Visual/fisiología , Síndromes de Ojo Seco/diagnóstico , Síndromes de Ojo Seco/tratamiento farmacológico , Humanos , Japón , Soluciones Oftálmicas/administración & dosificación , Calidad de Vida , Encuestas y Cuestionarios , Lágrimas/fisiología , Trastornos de la Visión/diagnóstico , Trastornos de la Visión/tratamiento farmacológico
17.
Adv Ther ; 35(5): 697-706, 2018 May.
Artículo en Inglés | MEDLINE | ID: mdl-29671255

RESUMEN

INTRODUCTION: Complex mechanisms underlie dry eye (DE) symptom provocation. In particular, corneal hypersensitivity may provoke symptoms in short tear break-up time (BUT) DE characterized by tear film instability. We hypothesized that improved tear film stability may alleviate corneal sensitivity in patients with short tear BUT DE. Therefore, we investigated the effect of topical diquafosol tetrasodium (DQS) on corneal sensitivity in unstable tear film DE. METHODS: This prospective, randomized study included 27 subjects (age: 39.1 ± 8.4 years; range: 25-59 years) with short tear BUT DE, defined based on the presence of DE symptoms and tear film instability. Subjects were randomly divided into DQS (3% DQS, 12 subjects) and artificial tear (AT; preservative-free AT, 15 subjects) groups. Subjects applied the medication 6 times a day for 5 weeks. The perception of touch (S-touch) and pain (S-pain) sensitivity was measured using a Cochet-Bonnet esthesiometer. Tear evaluation, corneal sensitivity, and DE symptoms were compared before and after DQS or AT administration. The correlation between the improvement degrees of corneal sensitivity and DE symptoms following medication was analyzed. RESULTS: DQS significantly improved tear BUT and tear meniscus height (TMH) scores (p < 0.05), while AT significantly improved tear BUT (p < 0.05) but not TMH score. Mean S-pain and DE symptom scores were lower after medication use in the DQS (S-pain and DE symptoms: p  < 0.05) and AT groups (S-pain: p  = 0.05; DE symptoms: p  < 0.05). However, S-touch did not change significantly in either group. A positive correlation was observed between the improvement degrees of S-pain and DE symptoms in the overall subjects studied. CONCLUSION: Both DQS and AT alleviate corneal hypersensitivity and DE symptoms in eyes with short tear BUT DE. However, DQS seems to be more effective to adjust tear environment, leading to the normalization of corneal sensitivity and DE symptoms. TRIAL REGISTRATION: UMIN Clinical Trials Registry Identifier, UMIN000014536.


Asunto(s)
Síndromes de Ojo Seco , Polifosfatos , Lágrimas , Nucleótidos de Uracilo , Administración Tópica , Adulto , Córnea/efectos de los fármacos , Síndromes de Ojo Seco/diagnóstico , Síndromes de Ojo Seco/tratamiento farmacológico , Femenino , Humanos , Masculino , Persona de Mediana Edad , Soluciones Oftálmicas/administración & dosificación , Soluciones Oftálmicas/farmacocinética , Polifosfatos/administración & dosificación , Polifosfatos/farmacocinética , Estudios Prospectivos , Lágrimas/efectos de los fármacos , Lágrimas/fisiología , Factores de Tiempo , Resultado del Tratamiento , Nucleótidos de Uracilo/administración & dosificación , Nucleótidos de Uracilo/farmacocinética
18.
Ophthalmology ; 114(7): 1294-302, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17475335

RESUMEN

PURPOSE: To evaluate and grade the extent and severity of chronic ocular manifestations in Stevens-Johnson syndrome (SJS). DESIGN: Prospective multicenter case series. PARTICIPANTS: We enrolled 73 patients (138 eyes) with SJS seen between April 2003 and March 2005 at 3 tertiary referral centers. METHODS: Patients with a confirmed history of SJS and chronic ocular complications that persisted for at least 1 year from the onset of SJS were included. Their detailed medical history and ophthalmic examination results were recorded on an itemized data collection form. Complications were categorized as corneal, conjunctival, and eyelid complications, and 13 components were evaluated and graded on a scale from 0 to 3 according to their severity. MAIN OUTCOME MEASURES: These were broadly classified as corneal (superficial punctate keratopathy, epithelial defect, loss of the palisades of Vogt, conjunctivalization, neovascularization, opacification, keratinization), conjunctival (hyperemia, symblepharon formation), and eyelid (trichiasis, mucocutaneous junction involvement, meibomian gland involvement, punctal damage) complications. RESULTS: The most severely affected complication components were loss of the palisades of Vogt (114 eyes; 82.6%) and meibomian gland involvement (102 eyes; 73.9%). Visual acuity in 74 of the 138 eyes (53.6%) was worse than 20/200. The severity of corneal, conjunctival, and eyelid complications was significantly correlated with visual loss. All 13 complications were correlated significantly with logarithm of the minimum angle of resolution (logMAR) visual acuity; the correlation coefficient (R) ranged from 0.359 to 0.810 (P<0.0001); for corneal epithelial defects, R was 0.169 (P = 0.0473). Eyes with a higher total score for the 3 complication categories had poorer vision (R = 0.806; P<0.0001). Multivariate regression analysis showed that corneal neovascularization, opacification, keratinization, and cataracts significantly affected logMAR visual acuity (P<0.0001, P<0.0001, P = 0.0142, P = 0.0375, respectively). CONCLUSIONS: The authors describe a new method for grading the extent and severity of ocular involvement in patients with SJS and demonstrate that the severity of ocular involvement is correlated significantly with the final visual outcome. This new grading system provides a more objective method for evaluating SJS patients and may be adapted for use in other cicatricial ocular surface diseases.


Asunto(s)
Técnicas de Diagnóstico Oftalmológico , Oftalmopatías/diagnóstico , Oftalmopatías/etiología , Índice de Severidad de la Enfermedad , Síndrome de Stevens-Johnson/complicaciones , Adulto , Anciano , Catarata/diagnóstico , Catarata/etiología , Enfermedad Crónica , Enfermedades de la Conjuntiva/diagnóstico , Enfermedades de la Conjuntiva/etiología , Enfermedades de la Córnea/diagnóstico , Enfermedades de la Córnea/etiología , Oftalmopatías/fisiopatología , Enfermedades de los Párpados/diagnóstico , Enfermedades de los Párpados/etiología , Femenino , Glaucoma/diagnóstico , Glaucoma/etiología , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Análisis de Regresión , Trastornos de la Visión/etiología , Agudeza Visual
19.
Am J Ophthalmol ; 144(1): 81-85, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17509507

RESUMEN

PURPOSE: To reinvestigate tear evaporation rates in Sjögren syndrome (SS) and non-Sjögren (non-SS) dry eye patients with a recently reported ventilated chamber evaporimeter system. DESIGN: Prospective case-control study. METHODS: A ventilated chamber evaporimeter system was used to measure tear evaporation rates. A DR-1 camera (Kowa, Nagoya, Japan) was used for tear lipid layer interference image acquisition. The Yokoi severity grading system was used for DR-1 image evaluation. Twenty-four aqueous tear deficiency (ATD) eyes of 21 consecutive patients with SS were studied (SS ATD group). Twenty-one ATD eyes of 12 non-SS patients (non-SS ATD group) were examined as control subjects. RESULTS: Tear evaporation rates of the SS ATD group (5.9 +/- 3.5 [10(-7) g/cm(2) per second]) were significantly higher than those of the non-SS ATD group (2.9 +/- 1.8 [10(-7) g/cm(2) per second]; P = .0009). The severity grading of DR-1 tear interference images of the SS ATD group was significantly higher (P = .03), along with significantly worse meibomian gland expressibility and vital staining scores, compared with those of the non-SS ATD group. CONCLUSIONS: Tear evaporation rates were higher in eyes of the SS ATD group compared with the non-SS ATD group. Tear evaporation assessed in conjunction with tear lipid layer findings and meibomian gland expressibility provides an increased understanding in the differential diagnosis of dry eye states.


Asunto(s)
Síndrome de Sjögren/metabolismo , Lágrimas/metabolismo , Estudios de Casos y Controles , Síndromes de Ojo Seco/metabolismo , Femenino , Humanos , Interferometría , Metabolismo de los Lípidos , Masculino , Glándulas Tarsales/metabolismo , Persona de Mediana Edad , Fotograbar , Estudios Prospectivos
20.
Cornea ; 26(9 Suppl 1): S29-35, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17881912

RESUMEN

Functional visual acuity (FVA) has been suggested to reflect an individual's performance in relation to certain daily activities involving visual tasks. The concept of FVA has been thought applicable to the detection of masked impairment of visual function in patients with dry eye who complain of decreased visual acuity despite normal conventional visual acuity. A stable tear-film layer over the surface of the cornea is essential for a smooth ocular surface and the formation of clear visual images. In dry eye, the ocular surface tends to dry out when normal blinking is suppressed during gazing, and patients with dry eye may have problems maintaining clear vision while gazing. The FVA measurement system is a device to measure changes in continuous visual acuity over time. Visual maintenance ratio (VMR) is the ratio between FVA and baseline visual acuity. FVA and VMR are indices for the assessment of functional vision. FVA has been thought applicable to the detection of changes in functional vision in relation to the tear film over the ocular surface. It may also be useful for the assessment of subjective visual complaints in diseases that do not involve dry eye.


Asunto(s)
Síndromes de Ojo Seco/fisiopatología , Agudeza Visual/fisiología , Actividades Cotidianas , Humanos , Pruebas de Visión/métodos
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