Impact of previous extended and daily wear schedules on signs and symptoms with high Dk lotrafilcon A lenses.

PURPOSE: This study measured the impact of previous contact lens wearing schedule on the resolution of signs and contact lens-related symptoms among wearers of lotrafilcon A lenses. METHODS: One hundred forty adapted low Dk daily wear (DW) and 140 adapted low Dk extended wear (EW) subjects were enrolled and examined for 1 year (overall study length is 3 years). All subjects wore lotrafilcon A lenses on a wearing schedule of up to 30 nights continuous wear with monthly replacement of lenses. Examinations were conducted at 1 week, 1, 6, and 12 months. RESULTS: The former EW wearers presented at baseline with significantly higher conjunctival staining and epithelial microcysts (p < 0.05) and lower ocular surface symptoms of end of day dryness than the former DW wearers. There were no significant differences in other ocular signs at baseline for the former DW and EW wearers. After use of lotrafilcon A, clinical signs of limbal, conjunctival redness, and neovascularization were significantly better by the 1-week visit for both groups of wearers. Regardless of former wearing schedule, symptoms of dryness (during and at the end of the day) and photophobia were significantly better after 1 week of lotrafilcon A use. The frequency and severity of symptoms of dryness during the day improved significantly among former low Dk DW and EW wearers within 1 week as did severity of dryness during the day for the former DW wearers, in part as a result of their higher prevalence at baseline in the DW group. Subjects reported redness improved significantly by the 1-month visit. CONCLUSIONS: Continuous wear of high Dk silicone hydrogel lenses resulted in an improvement in ocular redness and neovascularization and dryness symptoms among subjects in this trial, regardless of their previous low Dk lens-wearing schedule. All improvements in signs and symptoms were sustained through 12 months.     

Colonization of hydrogel lenses with Streptococcus pneumoniae: risk of development of corneal infiltrates.

PURPOSE: To report the association between colonization of contact lenses with Streptococcus pneumoniae and the observation of corneal infiltrative events in a group of patients wearing disposable hydrogel lenses on an extended-wear schedule. METHODS: In a prospective clinical trial, 330 patients wore disposable hydrogels on a 6-night extended-wear and replacement schedule. The contact lens, lid, and conjunctival microbiota of these subjects was analyzed at frequent intervals and at the time of an adverse event. RESULTS: Streptococcus pneumoniae was an uncommon isolate and was recovered from only one of the 3,763 conjunctival samples, five (0.1%) of the 3,764 lid samples, and 33 (0.8%) of the 4,315 contact lens samples. Of the 33 lens samples, 10 (30%) were associated with corneal infiltrative events. Many of the events were mild inflammatory responses and resolved rapidly on discontinuation of lens wear. The presence of S. pneumoniae on the contact lens was associated with a significant risk of development of corneal infiltrates (odds ratio, 3.0; p = 0.0227, logistic-regression analysis). CONCLUSIONS: Presence of S. pneumoniae on hydrogel lenses is a significant risk factor for the development of corneal infiltrates.     

The effect of degree of refractive error on hydrogel contact lens-induced complications and patient self-management behaviors.

INTRODUCTION: Although many aspects of hydrogel lens wear have been explored over the last 20 years, little attention has been paid to the role of refractive error magnitude in determining patients' ocular responses or associated contact lens behaviors. METHODS: A cross-sectional study was conducted in 32 optometric and ophthalmologic practices. We enrolled 2161 spherical soft contact lens-wearing patients. High ametropes were defined as those with at least +/- 5.00 D spherical equivalent refractive error in the right eye. Data on current contact lenses, prescribed care regimens, and slit lamp biomicroscopic signs were provided by the eye care practitioners, and information on actual lens care behaviors and attitudes toward contact lens wear were gathered by survey directly from the patients. All differences between high and low ametropes were compared using the chi-square test. RESULTS: Compared with low ametropes, high ametropes were more satisfied with their vision with contact lenses (p < 0.001). More high ametropes wore their lenses on an extended-wear schedule (p = 0.015). Both groups of patients reported a similar degree of lens awareness and lens-associated pain, but fewer high ametropes reported foreign body sensation (p = 0.002). In managing contact lens discomfort, high ametropes were more likely to use an old spare lens (p = 0.01) and more likely to continue wearing their lenses (p = 0.016)--indicators of a propensity for self-management. In response to a damaged lens, high ametropes were less likely to remove both of their lenses (p = 0.002). High ametropes showed more conjunctival staining (p = 0.001) and more corneal scars (p = 0.033). High ametropes also presented with more corneal fluorescein staining (p = 0.001) and more corneal vascularization (p < 0.001). These relations between the degree of ametropia and slit lamp signs of contact lens wear were not significantly affected by daily- vs. extended-wear status. CONCLUSIONS: In summary, practitioners should consider the implications of the patient's degree of ametropia when prescribing contact lenses. These results indicate the need for closer observation and specific advice concerning management of contact lens-related problems when caring for patients with high refractive errors.     

Influence of wearing schedule on extended-wear complications

The effect of wearing schedule on extended-wear (EW) success was evaluated over a nine-month period by assigning 36 subjects to 5 different wearing schedules (removal every 4, 7, 14, or 28 days, or daily wear [DW]). All but one EW patient required interruption of extended wear at least once; half of the DW patients completed the study without interruption. The most prevalent (100%) complication in the EW group was epithelial microcysts; 54% had to discontinue EW for 67 +/- 30 days while severe microcysts subsided. Evidence is given for a hypoxic etiology of microcysts. Other EW complications included: persistent punctate keratitis, infiltrative keratitis, infection, and idiopathic red eye. Neither the level of overnight corneal swelling nor the period between removals influenced the incidence or severity of complications. Data is given on the recovery of corneal parameters after EW is discontinued.     

Effects of daily and overnight wear of a novel hyper oxygen-transmissible soft contact lens on bacterial binding and corneal epithelium: a 13-month clinical trial

OBJECTIVE: To test prospectively a new biologic rationale for an advanced hyper oxygen-transmissible lens (HOTL) providing prospects for safer daily (DW) or extended (EW) contact lens wear. DESIGN: Prospective, randomized, double-masked, single-center, 13-month clinical trial. PARTICIPANTS: One hundred sixty-eight patients completed the DW study (1 month): control lens (n = 70); HOTL (n = 98). One hundred thirty-six patients finished 1 year of EW: controls (n = 56), HOTL (n = 25, 6 nights; n = 55, 30 nights). TESTING: Irrigation chamber to collect corneal surface cells, confocal microscopy, tear collection at baseline, 2, and 4, weeks of DW, and 24 hours, 1, 3, 6, 9, and 12 months of EW. MAIN OUTCOME MEASURES: (1) Pseudomonas aeruginosa (PA) binding to exfoliated corneal surface cells; (2) central epithelial thickness (CET); (3) superficial cell area (SCA); (4) epithelial surface cell exfoliation (DESQ); and (5) tear lactate dehydrogenase (LDH). RESULTS: Daily wear with control lens increased PA binding from 5.90 +/- 2.60 to 7.81 +/- 3.04 bacteria per cell (P < 0.01); HOTL wear increased PA binding significantly less (5.31 +/- 1.87-5.98 +/- 2.26; P < 0.01). Daily wear produced no significant changes in CET or SCA. Significant decreases in DESQ were seen with both lenses with no significant intergroup differences. Tear LDH increased significantly in DW with HOTL wear versus control (P = 0.0017), but not after 1 month of subsequent EW (P = 0.533). One to 3 months of EW with control lens showed significantly higher PA binding than HOTL wear (P < 0.01); binding adaptively decreased thereafter, returning to baseline at 9 to 12 months. Lens EW produced significantly enlarged SCA, thinning of CET (except 6-night HOTL wear), and decreased DESQ (P < 0.01). Some adaptive recovery was seen with CET and DESQ, but not SCA; importantly, the data indicated no significant difference between 6- or 30-night EW for all outcomes. CONCLUSIONS: Hyper oxygen-transmissible lens wear (DW or EW) produced significantly decreased PA binding compared with control lens wear, with no significant difference in wearing schedule (6 nights vs. 30 nights); additionally, there was a remarkable and unexpected adaptive recovery in the first 6 months of all soft lens wear, with a return to baseline PA binding levels and partial recovery for the other outcomes except SCA at 1 year. These results suggest that HOTL use should result in a decrease in the incidence of and risk(s) for lens-related microbial keratitis and that further epidemiologic studies should consider time in adapted EW in future risk and incidence analyses.     

The characteristics of corneal staining in successful daily and extended disposable contact lens wearers

Purpose : The aim of this investigation was to measure levels of corneal staining in successful daily and extended wearers of disposable hydrogel contact lenses. Methods : Twenty-four subjects on a daily wear (DW) schedule and 20 subjects on an extended wear (EW) schedule were examined at six-monthly intervals over a two-year period. Subjects wore two types of disposable hydrogel lenses. Measurements were taken from the eye wearing an etafilcon A contact lens only. The cornea was divided into five equally sized zones and the extent and depth of corneal staining were assessed on a zero to four scale. Results : The overall levels of corneal staining were low with median values below or equal to grade 0.5 in all groups. There was no difference in the extent, depth or geographical distribution of corneal staining between the DW and EW groups. Staining was more frequently recorded in the superior and inferior areas of the cornea than in the central, nasal or temporal regions (Pearson's Chi-Square, p < 0.10). Conclusions : The mode of wear with disposable contact lenses is not a contributing factor to the amount of corneal staining seen in successful wearers. Low levels of corneal staining should be expected in successful DW and EW wearers.     

Predicting extended wear complications from overnight corneal swelling.

PURPOSE: To examine the hypothesis that the corneal overnight swelling response (ONSR) is a predictor of ocular complications in contact lens extended wear (EW). METHODS: The Berkeley Contact Lens Extended Wear Study (CLEWS) was a randomized, concurrently controlled clinical trial in which more than 200 subjects in EW with rigid gas-permeable (RGP) lenses were observed for 1 year. After adapting to EW, subjects were randomized to either medium or high oxygen-permeable (Dk) RGP lenses and underwent clinical assessments, keratometry, and corneal pachometry at 3-month intervals. RESULTS: The ONSR was directly related to lens Dk (P = 0.01) and exhibited substantial variability across subjects. The probability of remaining free of complications over time was not significantly lower for subjects with a mild ONSR compared with those with greater edema (P = 0.84). The risk of development of keratopathy was not significantly related to the ONSR (relative risk = 1.00). CONCLUSIONS: The corneal ONSR is not a good predictor of ocular complications in 1 year of RGP EW. Lenses that cause little or no corneal edema are not necessarily safer for overnight wear.     

Effects of rigid and soft contact lens daily wear on corneal epithelium, tear lactate dehydrogenase, and bacterial binding to exfoliated epithelial cells.

OBJECTIVE: To determine the effects of lens type and oxygen transmissibility on human corneal epithelium during daily lens wear (DW). DESIGN: Prospective, randomized, double-masked, single-center, parallel treatment groups clinical trial. PARTICIPANTS: Two hundred forty-six patients fitted with: (1) high oxygen-transmissible soft lenses (n = 36), (2) hyper oxygen-transmissible soft lenses (n = 135), and (3) hyper oxygen-transmissible rigid gas-permeable (RGP) lenses (n = 75). INTERVENTION: Irrigation chamber to collect exfoliated epithelial surface cells, confocal microscopy, and tear collection at baseline, 2 weeks, and 4 weeks of DW. MAIN OUTCOME MEASURES: (1) Pseudomonas aeruginosa (PA) binding to exfoliated corneal epithelial surface cells, (2) central epithelial thickness, (3) superficial epithelial cell area, (4) epithelial surface cell exfoliation, and (5) tear lactate dehydrogenase (LDH). RESULTS: Four weeks of DW with the high oxygen-transmissible soft lens significantly increased PA binding from baseline 6.55 +/- 3.01 to 8.75 +/- 3.05 bacteria per epithelial cell (P < 0.01). By contrast, hyper oxygen-transmissible soft lens wear increased binding significantly less (6.13 +/- 2.45 to 7.62 +/- 3.06; P < 0.01), whereas hyper oxygen-transmissible RGP lens wear demonstrated no significant changes (5.91 +/- 2.40 to 6.13 +/- 2.17; P = 0.533). No significant change in central epithelial thickness was found after 4 weeks of DW in either soft lens; however, the epithelial thickness decreased by 9.8% (P < 0.001) with RGP lens wear. Epithelial cell surface area increased 3.3% and 4.1% with the high and hyper oxygen-transmissible soft lenses, respectively, and 10.5% with the hyper oxygen-transmissible RGP lens (P < 0.001). Epithelial desquamation significantly decreased in all groups (P < 0.001). Tear LDH levels increased for all test lenses (P < 0.001). CONCLUSIONS: Increased PA binding induced by wear of a conventional soft lens material is significantly greater than that induced by the new hyper oxygen-transmissible soft silicone hydrogel lens during DW. However, both soft materials showed significant increases in PA binding as compared with baseline controls. By contrast, hyper oxygen-transmissible RGP lens DW did not increase PA binding significantly. Taken together, these findings suggest for the first time both an oxygen effect as well as a difference between soft and rigid lens types on PA binding in DW.     

Defects in disposable contact lenses compromise ocular integrity

To ascertain the prevalence of defects in disposable contact lenses, an Optimec JFC contact lens analyser (× 16 magnification) was used to examine 150 Acuvue, 150 NewVues, and 150 SeeQuence lenses, all −3.00D in power. The percentage of each lens type found to be defective was: Acuvue 75%, NewVues 5%, and SeeQuence 9%. A single-center, simultaneously-controlled, double-masked, randomized study was conducted to determine whether such defects compromise ocular integrity. Each of 29 subjects wore a defective Acuvue lens in one eye and a non-defective Acuvue (control) lens in the other eye on an extended-wear basis for one week. Lenses with defects visible to the naked eye were excluded. Although there was no significant difference in vision, subjective sensation, or bulbar conjunctival hyperemia between eyes wearing defective vs. control lenses, a significantly greater ocular response was observed in eyes wearing defective lenses in the form of corneal epithelial microcysts (p = 0.04), corneal staining (p = 0.02), and conjunctival staining (p = 0.04). Two cases of peripheral corneal infiltrates were observed; both cases were unilateral and occurred in eyes wearing defective lenses. Such compromise may predispose the eye to more serious complications such as infection and corneal ulceration.     

Incidence of keratitis of varying severity among contact lens wearers

AIM: To determine the incidence of non-severe keratitis (NSK) and severe keratitis (SK) among wearers of current generation contact lenses. METHODS: A 12 month, prospective, hospital based epidemiological study was conducted by examining all contact lens wearers presenting with a corneal infiltrate/ulcer to a hospital centre in Manchester. A clinical severity matrix was used to differentiate between NSK and SK, based on the severity of signs and symptoms. The size of the hospital catchment population and the wearing modalities (daily wear (DW) or extended wear (EW)) and lens types being used were estimated from relevant demographic and market data. RESULTS: During the survey period, 80 and 38 patients presented with NSK and SK, respectively. The annual incidences (cases per 10,000 wearers) for each wearing modality and lens type were: DW rigid--NSK 5.7, SK 2.9; DW hydrogel daily disposable--NSK 9.1, SK 4.9; DW hydrogel (excluding daily disposable)--NSK 14.1, SK 6.4; DW silicone hydrogel--NSK 55.9, SK 0.0; EW rigid--NSK 0.0, SK 0.0; EW hydrogel--NSK 48.2, SK 96.4; EW silicone hydrogel--NSK 98.8, SK 19.8. The difference in SK between EW hydrogel and EW silicone hydrogel was significant (p = 0.04). CONCLUSIONS: A clinical severity matrix has considerable utility in assessing contact lens related keratitis. There is a significantly higher incidence of SK in wearers who sleep in contact lenses compared with those who only use lenses during the waking hours. Those who choose to sleep in lenses should be advised to wear silicone hydrogel lenses, which carry a five times decreased risk of SK for extended wear compared with hydrogel lenses.     

Incidence and morbidity of hospital‐presenting corneal infiltrative events associated with contact lens wear

Aim : To determine the incidence and morbidity (visual loss) of hospital‐presenting corneal infiltrative events (CIEs) associated with the wearing of current generation contact lenses. Methods : All contact lens wearers presenting with any form of corneal infiltrate/ulcer to a hospital centre in Manchester, UK, were surveyed in this 12‐month, prospective, hospital‐based epidemiological study. A clinical severity matrix was used to quantify the overall severity of presenting signs and symptoms. The size of the hospital catchment population and the wearing modalities (daily wear [DW] or extended wear [EW]) and lens types used in that population were estimated from relevant demographic and market data to facilitate the calculation of incidence. We also attempted to ascertain, from their eye care practitioners, the visual acuity (VA) of patients suffering from CIEs prior to and at about six months following attendance at the hospital. Results : During the survey period, 118 patients presented with CIEs of varying severity. The annual incidence (cases per 10,000 wearers) for all wearing modalities and lens types is 21.3 (95 per cent confidence interval 17.8 to 25.5). The incidence of CIEs for each wearing modality and lens type is: DW rigid, 8.6 (3.9 to 18.7); DW hydrogel daily disposable, 14.0 (9.3 to 21.0); DW hydrogel (excluding daily disposable), 20.4 (15.9 to 26.2); DW silicone hydrogel, 55.9 (9.9 to 309.6); EW rigid, zero (0.0 to 1758.8); EW hydrogel, 144.6 (66.4 to 311.8) and EW silicone hydrogel, 118.6 (75.2 to 186.7). The risk of developing a CIE with EW lenses was 8.1 (5.3 to 12.5) times greater than that with DW lenses (p < 0.0001). Although there was no difference between EW hydrogel and EW silicone hydrogel lenses with respect to the risk of developing CIEs, the clinical severity of CIEs was greater with EW hydrogel lenses (p = 0.04). Results of VA for pre‐and post‐hospital attendance were obtained from 38 patients, none of whom lost more than one line of VA. For the study population, zero patients (95 per cent CI: 0 to 9.2 per cent) suffered a significant loss of VA as a result of developing a CIE. Conclusions : Overall, there is an eight times higher incidence of CIEs in wearers who sleep in contact lenses compared with wearers who use lenses only during the waking hours. For those who choose to routinely or intermittently sleep in soft contact lenses, silicone hydrogels are the lens of first choice because CIEs are less clinically severe with this lens type compared with hydrogel lenses. The rate of significant visual loss as a result of developing a CIE is low.     

Contact lenses and corneal shields

Contact lens wear has been associated with a wide spectrum of corneal complications. Disposable contact lenses have not eliminated the problem of corneal ulcers associated with extended-wear contact lenses. Rigid, gas-permeable extended-wear lenses may be considered as an acceptable alternative to extended wear of soft contact lenses. Collagen corneal shields are a clinical indicator of collagenase activity on the ocular surface and serve as a collagenase inhibitor.     

Impact of contact lens material and design on the ocular surface

Background

To evaluate the impact on the ocular surface of a daily disposable hydrogel contact lens with high water content compared with two silicone hydrogel daily disposable lenses of lower water content.

Methods

The hydrogel lens assessed was made from nesofilcon A and the silicone hydrogel lenses were made of delefilcon A and stenfilcon A. Contact lens thickness was measured to assess material stability during daily wear, and ocular surface parameters such as tear film osmolarity, tear meniscus area and central corneal thickness were also assessed. Optical quality was analysed for all cases by means of wavefront aberrometry.

Results

The nesofilcon A was shown to be the thinnest lens (p < 0.001), while no differences in lens thickness were found between the two silicone hydrogel lenses (p = 0.495). No significant differences were found in tear film osmolarity, tear meniscus area, central corneal thickness or corneal aberrations, either as a function of the lens measured or time of use (p > 0.05).

Conclusion

In spite of having the thinnest lens and the highest water content, the hydrogel does not significantly impact on tear film and corneal swelling after one day of use in first‐time wearers.

     

Silicone hydrogel contact lenses and the ocular surface

For 30 years, contact lens research focused on the need for highly oxygen-permeable (Dk) soft lens materials. High Dk silicone hydrogel contact lenses, made available in 1999, met this need. The purpose of this review is to examine how silicone hydrogel lens wear affects the ocular surfaces and to highlight areas in which further research is needed to improve biocompatibility. Silicone hydrogel lenses have eliminated lens-induced hypoxia for the majority of wearers and have a less pronounced effect on corneal homeostasis compared to other lens types; however, mechanical interaction with ocular tissue and the effects on tear film structure and physiology are similar to that found with soft lens wear in general. Although the ocular health benefits of silicone hydrogel lenses have increased the length of time lenses can be worn overnight, the risk of infection is similar to that found with other soft lens types, and overnight wear remains a higher risk factor for infection than daily wear, regardless of lens material. Future contact lens research will focus on gaining a better understanding of the way in which contact lenses interact with the corneal surface, upper eyelid, and the tear film, and the lens-related factors contributing to infection and inflammatory responses.     

The effect of nonpreserved care solutions on 12 months of daily and extended silicone hydrogel contact lens wear

PURPOSE: To determine the effects of nonpreserved care solutions on human corneal epithelium in long-term daily wear (DW) compared with overnight (extended) wear (EW) of hyper-oxygen-permeable silicone hydrogel contact lenses. METHODS: This was a prospective, randomized, double-masked, single-center, parallel treatment group clinical trial (NCT 00344643). One hundred twenty-one patients completed the 13 month study: (1) Lotrafilcon A (30 night EW, n = 29; DW, n = 32); (2) Galyfilcon A (DW, n = 20); and (3) Lotrafilcon B (6 night EW, n = 20; DW, n = 21). Irrigation chamber collection of corneal surface cells (OD) and confocal microscopy (OS) were performed at baseline, 1 week; and 1, 3, 6, 9, and 12 months of EW. The main outcome measures were: (1) Pseudomonas aeruginosa (PA) binding to exfoliated corneal surface cells; (2) central epithelial thickness (CET); and (3) epithelial surface cell exfoliation rate (desquamation). RESULTS: DW had no significant effect on CET; there was a decrease in CET with EW that recovered (adapted) over 1 year (Lotrafilcon B, P < 0.05). All lens wear (DW, EW) decreased desquamation with adaptive effects over 1 year (P < 0.001). There was no significant difference in PA binding between lenses or modality of wear. CONCLUSIONS: PA binding to corneal epithelial cells is a prerequisite for infection, and no binding indicates no lens-enhanced risk of infection. In contrast to prior studies of preserved lens-care products, the absence of a change in the PA binding data results predict that the risk for PA CTL-keratitis should be similar for daily and extended silicone hydrogel lens wear over 1 year when preservative-free care solutions are used.     

Objective and subjective responses in patients refitted to daily-wear silicone hydrogel contact lenses.

PURPOSE: Silicone hydrogel (SiH) lenses offer many physiological advantages for daily wear (DW) in addition to the continuous-wear modality for which they were originally developed. The purpose of this study was to investigate the clinical performance and physiological responses in a group of successful long-term wearers of conventional hydrogel lenses when refitted with DW SiH contact lenses. METHODS: Eighty-seven successful soft lens wearers (8.4+/-4.7 years of prior lens wear) participated in this study. Bulbar and limbal hyperemia were subjectively graded and digitally photographed for subsequent masked objective evaluation. Subjective symptoms were scored using visual analog scales. In addition, refractive error, corneal curvature, and corneal thickness were measured. All subjects were refitted with Focus Night & Day (lotrafilcon A) SiH lenses; however, to reduce the potential for bias, they were informed that they were being randomly assigned to wear either low oxygen permeability (Dk) lenses or high Dk SiH lenses and were "masked" as to their lens assignment. Subjects returned after 1 week, 1 month, and 2 months of DW, at which time all gradings, photographs, and measurements were repeated. End-of-day subjective symptoms were also graded periodically during the study. RESULTS: Ninety-three percent of subjects were successfully refitted. Both objective and subjective evaluations showed that bulbar and limbal hyperemia decreased significantly in all quadrants during the study (p<0.001), particularly for those subjects with greater baseline hyperemia (p<0.001). Subjects reported a concurrent reduction in end-of-day dryness and improved end-of-day comfort compared with their habitual lenses (p<0.001). No significant changes in refractive error, tarsal papillary response, corneal curvature, or corneal thickness were found during the study. CONCLUSIONS: Hyperemia in contact lens wearers may be attributed to a number of factors, including hypoxia. Refitting existing low Dk lens wearers with SiH lenses on a DW basis can result in a decrease in hyperemia, which may be significant for some subjects and also results in improvements in symptoms of dryness and discomfort.     

Corneal ulcers associated with daily-wear and extended-wear contact lenses

Over a 21-month period, we treated corneal ulcers in 11 patients using daily-wear contact lenses and 29 patients using extended-wear contact lenses. Since more patients use daily-wear than extended-wear lenses, this suggests that patients using extended-wear lenses are at greater risk for the development of corneal ulcers. Positive bacterial cultures were obtained from the corneal scrapings of nine of 11 patients using daily-wear lenses and 20 of 29 patients using extended-wear lenses. In the daily-wear group, all 11 patients failed to exercise satisfactory care in using and disinfecting their contact lenses: three did not wash their hands before manipulating the contact lenses, eight wore them overnight, two did not use any disinfecting system, and four had contaminated contact lens cases, solutions, or drops. In the extended-wear group, 17 patients failed to exercise satisfactory care in using and disinfecting their contact lenses: 12 had contaminated contact lens care systems, two did not use any disinfection system, five reported not washing their hands before contact lens manipulation, and two disinfected their contact lenses at intervals of more than a month. We were unable to identify any defect in the way 12 patients took care of their extended-wear lenses, suggesting that there may be a problem with these contact lenses even when care is satisfactory.     

Hypoxic effects on the anterior eye of high-Dk soft contact lens wearers are negligible.

PURPOSE: To determine whether the eyes of high-Dk soft contact lens wearing subjects can be discriminated from non-contact lens wearing subjects. METHODS: This study was a prospective masked assessment of 32 subjects, 16 of whom wore experimental high-Dk soft contact lenses and 16 of whom did not wear contact lenses. Subjects wore high-Dk lenses on a 30-night replacement schedule for an average of 9 months. Tear film characteristics, staining and vascularization of the cornea, conjunctival staining, and the presence of microcysts in the corneal epithelium were assessed using slitlamp microscopy. The endothelium was examined for polymegethism. RESULTS: No differences were found between the two groups in any of the variables that were examined (p > 0.05) except that the high-Dk lens wearing group had about twofold more tear film debris and 2.5-fold more severe conjunctival staining (p < 0.05). CONCLUSIONS: Hypoxia-associated effects were not apparent in the eyes of subjects wearing experimental high-Dk soft contact lenses. Conjunctival staining can generally distinguish lens wearers from non-lens wearers and can be used to discriminate between high-Dk lens wearing subjects and non-lens wearing subjects.     

Mucin balls with wear of conventional and silicone hydrogel contact lenses.

PURPOSE: To compare the frequency of mucin balls in subjects wearing conventional and high-Dk silicone hydrogel lenses during 12 months of extended-wear and to determine whether mucin balls are associated with any lens or subject characteristics. METHODS: This study used data from a clinical trial where subjects wore either conventional hydrogel (N = 69, 6-night extended-wear) or silicone hydrogel (N = 70, 30-night extended-wear) contact lenses for 12 months. The number of mucin balls and other physiological responses, lens fit and performance, and subjective patient responses to lens wear were rated at each scheduled visit. RESULTS: Subjects in the silicone hydrogel group had significantly greater numbers of mucin balls compared with subjects in the conventional hydrogel group over time (p < 0.001), but there were no significant differences in the percentage of subjects with mucin balls between the two groups. Increasing lens wettability, back surface deposits, and time of lens wear were associated with higher numbers of mucin balls in the conventional hydrogel group (p < 0.05); steeper corneal curvature and increasing lens wettability, back surface deposits, and number of microcysts were associated with higher numbers of mucin balls in the silicone hydrogel group (p < 0.05). CONCLUSIONS: This study indicates that a subset of the population is predisposed to develop mucin balls irrespective of the soft contact lens type worn, but lens type influences the degree of mucin ball formation. The relationship between lens wettability, back surface deposits, and steeper corneal curvature with mucin balls supports the hypothesis that the mechanical interaction of a lens with the surface layer of the epithelium and the tear film in association with the blinking forces of the lid is involved in mucin ball formation.     

The risk of microbial keratitis with daily-wear and extended-wear use of disposable lenses

A pilot case-control study indicated an excess risk of microbial keratitis (MK) with disposable soft contact lenses (DSCL). A larger case-control study was conducted to separate the risks associated with daily-wear (DW) and extended-wear (EW) use of DSCL, and to determine whether there is an excess risk associated with the lenses after controlling for other variables.
Contact lens (CL) wearers presenting as new patients to Moorfields Eye Hospital Casualty over 12 months completed a questionnaire detailing CL use and hygiene practices. Cases were patients with presumed MK, according to established clinical criteria. Controls were patients attending with disorders unrelated to CL wear. Relative risks were calculated using conventional soft lenses (SCL) as the referent, and multivariable analysis was performed. DW and EW patients were analysed separately.
Among SCL wearers there were 89 cases, and 566 controls. Multivariable analysis confirmed a statistically significant increased risk with DSCL among both DW (×3.5) and EW patients (×4.8).
This study shows that, despite the proven reduction in less serious complications with the disposable regimen, there is an increased risk of MK with both DW and EW DSCL, even after controlling for other variables. Although patient and practitioner factors may contribute to these risks, it is likely that properties of some DSCL are partly responsible and require further investigation.