Customary practices in the monitoring of dry eye disease in Sjogren's syndrome / Prácticas habituales en la supervisión de la enfermedad del ojo seco en el Síndrome de Sjogren

Purpose: Diagnostic testing for dry eye disease (DED) in Sjogren's syndrome (SS) is well described. Little is published about monitoring this systemic autoimmune DED. We analyzed the SS related DED tests used in North American optometric practices and compared academic settings to private practice settings. Methods: A retrospective chart review of 123 SS charts from 6 optometric practices in North America was conducted. Testing done during the first examination following a SS diagnosis was recorded on Research Electronic Data Capture (REDCap) database. The complete data file was reviewed and testing type and methodology were compared. Results: Symptoms of DED (98.4% of charts),meibomian gland dysfunction (76.4% of charts), corneal staining with fluorescein (75.6% of charts) and anterior blepharitis (73.2% of charts) were the most frequently recorded variables. Clinicians used different methodologies to measure and grade these variables. Private practitioners were more likely to use symptom questionnaires and grading scales and to describe anterior blepharitis. Academic settings were more likely to record TBUT and tear meniscus height. Conclusions: The monitoring of DED in SS is not uniform in optometric offices across North America. Creating accepted standards of testing will improve the ability of clinicians and researchers to communicate and understand the course of DED in SS

Objetivo: Las pruebas diagnósticas para la enfermedad del ojo seco en el síndrome de Sjogren (SS) están bien descritas. Se ha publicado poco acerca de la supervisión de este síndrome del ojo seco autoinmune sistémico. Analizamos el SS relacionado con las pruebas de ojo seco en las prácticas optométricas de Norte América, y comparamos los centros académicos con los centros de práctica privada. Métodos: Se realizó una revisión retrospectiva de 123 historias clínicas de SS procedentes de 6 centros optométricos de Norte América. Las pruebas realizadas durante el primer examen, tras el diagnóstico de SS, se registraron en la base de datos Research Electronic Data Capture (REDCap). Se revisó el archivo de datos completo y se compararon el tipo de prueba y la metodología. Resultados: Las variables más frecuentemente registradas fueron los síntomas de ojo seco (98,4% de las historias), disfunción de la glándula de Meibomio (76,4%), tinción corneal con fluoresceína (75,6%), y blefaritis anterior (73,2%). Los clínicos utilizaron diferentes metodologías para medir y clasificar dichas variables. Los facultativos privados tendieron a utilizar con mayor frecuencia los cuestionarios de síntomas y las escalas de clasificación, y a describir la blefaritis anterior. Los centros académicos tendieron a registrar con mayor frecuencia TBUT y la altura del menisco lagrimal. Conclusiones: La supervisión del ojo seco en el SS no es uniforme en los centros optométricos de Norte América. La creación de estándares de pruebas aceptados mejoraría la capacidad de comunicar y comprender el curso del ojo seco en el SS por parte de clínicos e investigadores

Sjogren's syndrome in optometric practices in North America.

PURPOSE: To describe the presentation of dry eye in Sjogren's syndrome (SS) in optometric practices, to report on the methodology used in dry eye monitoring and to explore the level of corneal staining versus age and time of disease. METHODS: Records of SS patients were reviewed in 6 optometric sites. A standardized abstraction tool was developed to collect data from the records including: health history, medications and symptoms and signs of dry eye. The methods of testing symptoms and signs of dry eye were recorded. Variables were recorded at each site and collated at the University of Waterloo. The first visit after January 1, 2000 was selected for description in this paper. RESULTS: 123 charts were included. The average time since diagnosis was 7.2 years ±5.1 years. Symptoms of dryness were present in 110/123 = 89.4% of charts. Corneal fluorescein staining was present in 96/123 = 78% of charts. MGD was present in 52% of charts. There were significant differences in the protocols and grading systems used in these 6 sites. Corneal staining levels did not change with greater age or length of disease. CONCLUSION: These 123 SS patients presented with a large variation in their symptoms and signs. Symptoms of dryness and corneal fluorescein staining were the most commonly recorded presentations. There was a great deal of inconsistency in dry eye protocols among offices. Future prospective research with standardized testing will contribute to our understanding of the best dry eye protocols for SS patients.

Customary practices in the monitoring of dry eye disease in Sjogren's syndrome.

PURPOSE: Diagnostic testing for dry eye disease (DED) in Sjogren's syndrome (SS) is well described. Little is published about monitoring this systemic autoimmune DED. We analyzed the SS related DED tests used in North American optometric practices and compared academic settings to private practice settings. METHODS: A retrospective chart review of 123 SS charts from 6 optometric practices in North America was conducted. Testing done during the first examination following a SS diagnosis was recorded on Research Electronic Data Capture (REDCap) database. The complete data file was reviewed and testing type and methodology were compared. RESULTS: Symptoms of DED (98.4% of charts),meibomian gland dysfunction (76.4% of charts), corneal staining with fluorescein (75.6% of charts) and anterior blepharitis (73.2% of charts) were the most frequently recorded variables. Clinicians used different methodologies to measure and grade these variables. Private practitioners were more likely to use symptom questionnaires and grading scales and to describe anterior blepharitis. Academic settings were more likely to record TBUT and tear meniscus height. CONCLUSIONS: The monitoring of DED in SS is not uniform in optometric offices across North America. Creating accepted standards of testing will improve the ability of clinicians and researchers to communicate and understand the course of DED in SS.

Comparison of anterior chamber depth of normal and keratoconus eyes using Scheimpflug photography.

OBJECTIVES: To compare the corneal anterior chamber depth (ACD) adjusted by age and sex in normal and keratoconus eyes. METHODS: Scheimpflug photography with the Oculus Pentacam was used to measure the ACD of 162 normal and 41 keratoconus patients. RESULTS: Univariate analysis showed that the mean ACD of 162 normal subjects (3.18 +/- 0.32 mm) was borderline significantly less than in 41 keratoconus patients (3.28 +/- 0.40 mm; P=0.079). However, we found that sex (P=0.001) and age (P<0.001) are significantly related to ACD in all patients. Women with normal eyes had a significantly lower mean ACD (3.13 +/- 0.34 mm) than men (3.27 +/- 0.28 mm, P=0.008). Women with keratoconus eyes also had a lower mean ACD (3.16 +/- 0.39 mm) than men with keratoconus (3.42 +/- 0.36 mm, P=0.032). Bivariate regression showed that with each additional year of aging, the ACD was decreased by an average of 0.012 mm in a normal eye (P<0.001) and by 0.014 mm in a keratoconus eye (P<0.001). Regression analysis showed that sex (P=0.003), age (P<0.001), and keratoconus (P=0.003) are all significant variables for determining ACD. After adjusting for age and sex, keratoconus eyes had a significantly higher mean ACD (3.34 +/- 0.34 mm) than normal eyes (3.18 +/- 0.28 mm) (P=0.003). CONCLUSIONS: Sex, age, and keratoconus are all significant variables for ACD. After adjusting for age, keratoconus eyes of both genders had a significantly higher ACD than normal eyes of both genders. Women showed lower mean ACD than men in both normal and keratoconus eyes.

Corneal endothelial cell count in keratoconus patients after contact lens wear.

PURPOSE: The influence of contact lenses on healthy corneal endothelium has been well documented, but little is known about the effect of contact lens wear on the corneal endothelial cells of patients with keratoconus. This cross-sectional comparative study was conducted to determine quantitative characteristics of corneal endothelial cells of 100 patients with keratoconus with or without contact lenses. METHODS: A Humphrey Atlas corneal topographer was used to map the keratoconic cornea. The corneal apex of the cone was located by using the axial topography map. The Konan SP-9000 Noncon Robo Pachy specular microscope and the Konan SP-400 specular microscopes were used to photograph the endothelium at the apex of the cone, and the average endothelial cell count was obtained. Patients were categorized into four groups based on the types of contact lenses worn: no contact lenses, SofLens 66 toric contact lenses, SoftPerm contact lenses, and FluoroPerm 30 aspheric rigid gas-permeable (RGP) contact lenses. Analysis of variance was used to determine differences in endothelial cell counts among groups. RESULTS: After controlling for age and severity of keratoconus, patients who wore SoftPerm contact lenses had 18% lower endothelial cell counts (2,157 +/- 442) than did patients without contact lenses (2,538 +/- 398). These patients also had 15% lower endothelial cell counts than did patients who wore soft toric disposable contact lenses (2,483 +/- 292). There was a 7% lower endothelial cell count in the group wearing aspheric RGP contact lenses than in the group that did not wear contact lenses, and a 5% lower endothelial cell count in the group wearing aspheric RGP contact lenses than in the group that wore soft toric contact lenses, but these differences were not statistically significant. CONCLUSIONS: Patients with keratoconus who wear SoftPerm contact lenses have a significantly lower endothelial cell count than those patients with keratoconus who do not wear lenses, or who wear soft toric disposable contact lenses or RGP contact lenses.

Clinical evaluation of an HP-guar gellable lubricant eye drop for the relief of dryness of the eye.

PURPOSE: To evaluate the efficacy of a new lubricant eye drop containing polyethylene glycol 400 and propylene glycol demulcents with hydroxypropyl-guar as a gelling agent (Test Product) to a system with carboxymethylcellulose (Control Product) for reducing dry eye signs and symptoms. METHODS: Eighty-seven dry eye volunteers were enrolled at seven sites for this six-week, concurrently controlled, double-masked clinical study. RESULTS: The Test Product significantly reduced conjunctival staining (p = 0.025) and temporal corneal staining (p = 0.024) compared to the Control. The Test Product also significantly reduced symptoms of dryness in the morning and evening, compared to the Control (p = 0.015 and p = 0.023, respectively). Subjects in the Test treatment group reported lower frequencies of foreign body sensation and felt their eyes were "refreshed longer" compared to those in the Control group (p = 0.033 and p = 0.037, respectively). CONCLUSIONS: The Test Product was more effective at reducing both the signs and symptoms of dry eye compared to the carboxymethylcellulose containing Control.