Does offering only the spherical contact lens trial to the low astigmats mislead the practitioners?

2021-08-16 09:56MonicaChaudhrySurendraPrasadSahIndraPrasadSharmaSoujanyaMondal

Monica Chaudhry, Surendra Prasad Sah, Indra Prasad Sharma, Soujanya Mondal

1Department of Optometry and Vision Science, Amity University, Haryana 122003, India

2School of Health Sciences, Ansal University, Gurugram,Haryana 122003, India

3Himalaya Eye Hospital, Gharinpatan, Pokhara 00977, Nepal 4Gyalyum Kesang Choeden Wangchuck National Eye Center,JDW National Referral Hospital, Thimphu 11001, Bhutan

5Optsight Eye Care, HCB Road, Amulapatti, Near MFC,Sivasagar, Assam 785640, India

Abstract

INTRODUCTION

Astigmatism is a common refractive error. Approximately 47% of astigmatic patients have an error of >0.75 diopters (D) cylinders and almost one-third of potential contact lens (CL) wearers require astigmatic correction[1]. However,eye care practitioner (ECP) prescribes soft toric contact lenses(TCL) only for approximately 25% of patients, ranging from 6% of lenses in Russia to 48% in Portugal[2]. Considering a cutoff of 0.75 D, 44.8% of patients would need TCL in India[3].For patients with low to moderate astigmatism, ECP prescribe astigmatic glasses. However, CL wearers are fitted with a soft spherical contact lens (SCL) in the form of a spherical equivalent. Shreds of evidence from industry sales records show that TCL constitutes less than 20% of CL sales in India.Possibly due to the easy availability of spherical trails, easy fitting procedures, relatively lower cost, the common practice is to first try a spherical equivalent and recommend spherical equivalent powers in low astigmatic patients. In the absence of large,randomized clinical studies, real-world, patient perspective and prospective studies could help ECPs choose between TCL and SCL for low astigmatic potential CL patients.

This study aimed to compare the subjective and objective responses of TCL and SCL trials in individuals with low astigmatism. The results were expected to give a better understanding of whether TCL trials are necessary to provide potential CL users with a better choice of refractive correction for low astigmatism.mean±SD

Table 1 Demographic and clinical characteristics of the subjects

SUBJECTS AND METHODS

Ethical ApprovalThis cross-sectional study was approved by the Institutional Ethical Committee of Amity University,Gurugram, India, and adhered to the tenets of the Declaration of Helsinki (2008). It was conducted between January and March 2016 at the Amity Optometry Clinic. Informed consent was obtained prior to the conduct of the study.

Patient Selection and ProcedureThe study enrolled 40(80 eyes) non-presbyopic neophytes (who had not used CL previously) participants aged 18 to 40y. Their non-cycloplegic ocular refraction at the corneal plane had to be between 0.75 to 1.25 D cylinders with/without spherical power up to±6.00 D. Eligible participants underwent a comprehensive eye examination, and participants contraindicated for CL wear were excluded.

For the subjects eligible, two sets of CLs are ordered based on empirical calculation: one set of SCL (Acuvue Oasys,Johnson and Johnson) and another set of TCL (Acuvue Oasys for astigmatism, Johnson and Johnson), and subjects were scheduled for two days trail visit. Block randomization was performed to select the type of lenses to be fitted on each visit.The subjects were blinded to the type of lens they wore on,the two different visits, but the examiner could not be blinded due to the nature of the study. The pre-fitting assessment,fitting (insertion and removal), and post fitting assessment were completed following a standardized protocol by a trained optometrist for consistency. After 20min of inserting the lens, the lens fitting was assessed by judging the coverage,centration, and movement in SCL and additionally rotation,and stability in the TCL. On achieving the ideal fit, subjects were asked to continue to wear the CLs for the day to carry out their routine activities and return to the clinic for evaluation after 4h of wear. On return to the clinic, visual acuity (VA) was tested with a high contrast logMAR chart and over-refraction was performed using the retinoscope(Heine beta 200).

Following the examination, a validated questionnaire was provided for each lens to the subjects in which they were asked to subjectively rate their quantity of vision (monocularly),quality of vision (satisfaction with vision), and comfort in each eye on a Likert scale of 1 (very good) to 5 (very bad). Subjects also rated fatigue/eyestrain after CL on a scale of 0 (no fatigue)to 10 (very fatigue). On completing the questionnaire, the lenses were removed and discarded. The crossover portion of the study with the other lens was completed on a different day depending on the subject’s convenience but within one week of the first trial. However, on both visits uniform procedures were followed.

Statistical AnalysisSensitivity power analysis using a computer program (Gpower 3.0) showed that the effect size between the two groups was 1.20 (large) with power (1‐β)set at 0.80 and α=0.05, two‐tailed. The sample size taken was considered adequate for the study. The statistical analysis was performed using Statistical Package for Social Science (SPSS)version 21. Descriptive test was performed for demographic data, and nonparametric Wilcoxon tests were used to compare the subjective and objective responses of the participants between the two lens trials.Pvalues of less than 0.05 were considered significant.

RESULTS

A total of 40 participants (80 eyes) were initially recruited for the study. With a response rate of 90%, the responses of 36 subjects (17 males and 19 females) with a mean age of 23.02±2.97y (18-33y) were evaluated. The characteristics of the subjects recruited are as shown in Table 1.

An average of 1.12±0.40 lenses was required to achieve an optimal fit for SCL, and took 1.42±0.33 lenses for TCL. A rotation of lesser than 5 degrees in the primary gaze with the TCL was considered acceptable. The monocular VA with SCL and TCL was 0.04±0.03 and -0.044±0.06 logMAR,respectively. The improvement in monocular VA with TCL compared to the SCL was approximately one line in the logMAR chart (P=0.01). However, the binocular VA remained similar: -0.14±0.04 and -0.12±0.07 logMAR for SCL and TCL,respectively (P=0.38). Over‐refraction revealed a significantly higher myopic spherical component of -0.08±0.10 D in SCL compared to 0.04±0.13 D in TCL (P<0.01). The mean difference between TCL and SCL on the monocular vision quantity rated was 0.683±0.051 (P=0.02). After four hour of CL wear, subject-reported responses for monocular vision quantity (clarity of vision monocularly) and vision quality(satisfaction) were analyzed and presented in Figure 1.

Subjects felt a noticeable difference in clarity when shifted to TCL as compared to the SCL. The satisfaction with vision(vision quality) was significantly better with TCL (P=0.03).Both the lenses were graded to be almost equally comfortable on wear (P=0.77; Figure 2). The fatigue with TCL was rated 2.5±0.6, while it was graded significantly higher with SCL at 4.6±1.3 (P=0.04). Thirty-three participants (91.6%) preferred to use CL for their refractive correction. Out of them, 26 participants (79%) reported a preference for TCL while the others choose SCL.

DISCUSSION

Anecdotal evidence reports that ECP and users are fairly satisfied with compensated spherical powers in low astigmatism. In India, it is a common practice to mask small cylindrical errors and prescribe SCL due to lesser cost. This study tried to assess the visual parameters and preference of TCL compared to SCL in low-to-moderate astigmatic subjects.In this study, both objective and subjective findings favoured the use of TCL in low astigmatism. While the SCL was tried,80% of the subjects ranked their vision as ‘very good’ and‘good’; however, this percentage shoot-up to 100% when they were fitted with TCL. The improvements in subjective vision reported here are consistent with previous reports that highlighted the vision benefits of prescribing TCL[4-6].Offering the SCL first gave a false impression that the quality is satisfactory. The subject realized the improvement only after he wore TCL. The reaction was immediate, and the subjects could appreciate it immediately on insertion of the CL.

VA improved monocularly by one-line logMAR with TCL as compared to the SCL, reporting similar outcomes to those studied elsewhere[7]. These findings justify the assumption of the acceptance of the spherical soft lens by practitioners. However, the findings after both CL trails reveal that the optimal vision should be reported only after trying TCL. The monocular response rate of patients was better with TCL as compared to SCL on vision quantity compared to the binocular quantity. The subjects also reported a better quality of vision (satisfaction with vision) with the TCL as compared to SCL as revealed in a previous study[8]. This could be attributed to improved vision with TCL and could be a determinant for TCL preference.

Subjective results showed no significant difference in the initial comfort between the two choices, consistent with previous literature[6]. Both TCL and SCL used in this study used the same material (senofilcon Α), water content (38%), and surface treatment of the lens. The study disagrees with the associations of TCL with discomfort due to lens rotation and complex fitting. The study found that the subjective response fatigue was more with SCL than TCL. Electromyography-measured eyestrain was also determined that TCL wearers have reduced eye strain than SCL users[9]. Squeezing of eyes and constant strain to focus best could be demonstrated in four hours of trial itself. This was the visual comfort that led to satisfaction.

Figure 1 Subject-reported responses rated for visual acuity A:Responses on vision quantity; B: Responses on vision quality.

Figure 2 Subjective response on comfort with SCL and TCL.

CL was the choice of refractive correction for 91.6% of participants. As expected, the preference of TCL over SCL 80%, however, higher than those reported elsewhere[6-7]. These higher preferences could be attributed to our study subjects(university students) where the visual requirements and acceptance are different from those of the older population.Overall results show that TCL provides better vision and less ocular fatigue for the first‐time CL users. ECP should perform TCL trials and not judge the acceptance of spherical equivalent lens trails. The spherical equivalent trial misleads ECP in low astigmatic CL recommendation. Use of TCL exhibit better overall driving performance and driving‐specific visual abilities compared to spherical lenses[10]. Moreover, correcting astigmatism with CL is associated with improved quality of life[7]. The complexity of fitting, high cost to patients, and poor availability of trials are perceived barriers in prescribing toric lenses and there is a need to address the barriers. Drop out in patients with residual astigmatism is evident and correct CL recommendation by ECP could prevent dropout.

The current study’s is limited using one type of lenses for the trails. The TCL designs and stabilization techniques may confound the subjective responses. The participants were not introduced to the use of CL solution, insertion and removal techniques and CL maintenance, which could interfere the CL preference. The other limitations include the number of participants and non-blinding of examiner. Future studies could be address these limitation with randomised contralled trails on a larger group of subjects.

The subjective and objective results suggest that VA and comfort are better with TCL as compared to SCL in lowto-moderate astigmatism. The acceptance of CL was high,and subjects preferred TCL over SCL. Practitioners should recommend TCL as the first option to astigmatic patients and not attempt spherical equivalent trial to judge the acceptance.Masking astigmatism and prescribing spherical equivalent trial can mislead ECPs in low astigmatic CL recommendation.

ACKNOWLEDGEMENTS

The authors acknowledge the management and faculties of the Department of Optometry and Vision Science, Amity University Gurugram for the technical support to conduct this study. We also thank Mr. Dhanapati Sharma, Lecturer, Royal University of Bhutan for reviewing our manuscript and editing language.

Conflicts of Interest:Chaudhry M,None;Sah SP,None;Sharma IP,None;Mondal S,None.