Abstract
Purpose
Long-standing prosthetic eye wearing induces ocular surface inflammation. We investigated the short-term effects of topical cyclosporine A 0.05% (Restasis) in patients with ocular discomfort resulting from long-standing prosthetic eye wearing.
Methods
This was a prospective, interventional case series. Patients who were unilateral prosthetic eye wearers over a period of 5 years were enrolled at a single institution from March to July 2013. The subjects were instructed to instill topical cyclosporine A 0.05% twice per day. Measurements were made pre-treatment and after 1 and 3 months of treatment. Outcome measures were the ocular symptom score, the lid margin abnormality score, the Schirmer test, and the tear meniscus amount, using Fourier-domain optical coherence tomography.
Results
In total, 20 consecutive patients (mean age: 60.1 years, 8 males, 12 females) were included. Ocular symptoms were improved after treatment for 1 month in all patients (ocular symptom score pre-treatment 76.83 vs 46.75 after treatment; P<0.001). There was no statistically significant difference in lid margin abnormality score or tear meniscus amount. The Schirmer test results were improved after treatment for 3 months (pre- and after treatment, 6.70 vs 11.40; P<0.001).
Conclusions
Topical cyclosporine A 0.05% showed a satisfactory effect in long-standing prosthetic eye wearers. Ocular symptoms were markedly relieved in all subjects after treatment for 1 month.
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Introduction
Patients wearing prosthetic eyes often complain of dryness, irritation, discomfort, and discharge. Indeed, there have been questionnaire-based investigations that reported that most prosthetic eye wearers are concerned about eye watering, crusting, and discharge.1, 2 Several studies have investigated the cause(s) of ocular discomfort in prosthetic eyes wearers.3 Allen et al4 suggested that most patients with anophthalmic socket have tear insufficiency and this may be a major cause of discomfort in these patients. In clinics, many prosthetic eye patients with ocular discomfort are prescribed artificial lubricants to relieve their ocular symptoms. However, some patients still continue to experience discomfort, even though they use artificial lubricants continuously over the long term.
Cyclosporine A 0.05% is a topical immunomodulatory compound with anti-inflammatory properties that has been demonstrated to have certain benefits in the treatment of dry-eye symptoms.5 Indeed, many clinical studies have found good results with topical cyclosporine A 0.05% treatment for dry-eye syndrome, through modulating ocular surface inflammation.6
To our knowledge, there is no reported study regarding the use of cyclosporine A 0.05% to treat patients with ocular prostheses who have dry eye symptoms or inflamed ocular surfaces. Thus, in the present study, we evaluated the effectiveness of treatment with cyclosporine A 0.05% in long-standing prosthesis wearers with ocular discomfort. We analyzed changes before and after cyclosporine A 0.05%, assessing Schirmer test results, tear meniscus amounts, lid margin abnormalities, and ocular symptom scores.
Materials and methods
Patients
In total, 20 patients with unilateral ocular prostheses for more than 5 years who visited Bucheon Soonchunhyang University Hospital between March 2013 and July 2013 were the subjects. Patients who had lid abnormalities, such as ectropion or entropion, were excluded. Patients who had socket problems, such as implant exposure or sac contracture, were also excluded. One of the authors (SYJ) prescribed cyclosporine A 0.05% (Restasis) to the subjects. All patients were advised to take one drop of cyclosporine A 0.05% twice per day for 3 months. The patients continued the treatment process over at least 3 months. They were asked questions regarding their demographic status and duration of eye prosthesis use. Furthermore, to assess the causes of ophthalmic surgery and type of surgery, such as evisceration or enucleation, we reviewed the chart of each patient.
This study adhered to the principles of the Declaration of Helsinki and was approved by the Institutional Review Board of Soonchunhyang University Hospital. Informed consent was obtained from all participants. Patients who did not agree to participate were excluded.
Outcome measures
A standard Schirmer test was performed on the prosthetic eyes at three points: (1) before the start of topical cyclosporine A 0.05%, (2) after 1 month of use, and (3) after 3 months of use. Sterile strips of filter paper were placed in the temporal one-third of the lower lid before closing the eyes for 5 min. Then, strips were removed and the lengths of the wet portion were measured (in mm) to determine the Schirmer test value.
Ocular symptoms, score measurements, and eyelid margin assessments were determined as described by Jang et al.7 Ocular symptoms were assessed using a five-point categorical scale: none (0), some of the time (1), half of the time (2), most of the time (3), and all the time (4). Patients were asked to assign the severity of their symptoms using this scale before the start, and after using topical cyclosporine A 0.05% for 1 and 3 months. Patients reported the frequency of symptoms related to dry eyes, such as ocular fatigue, discharge, foreign body sensation, pain, tearing, itching sensation, burning sensation, heavy sensation, excessive blinking, uncomfortable in windy conditions, and uncomfortable in very dry conditions. Each individual symptom score was added up, for a possible range between 0 and 60 points. We then converted the numbers to a score out of 100.
Eyelid margin abnormalities were scored to assess four items: lid margin irregularity, telangiectasis, mucocutaneous anterior displacement, and plugged orifices. Slit lamp examinations were used to assess the lid margin. If any of these signs were present, one point was assigned for each, with a total possible score range of 0–4 points. Lid margin abnormalities were also checked before the start and after using topical cyclosporine A 0.05% for 1 and 3 months.
Tear meniscus amount measurements were made as described by Kim et al.8 A high-speed, high-resolution, Fourier-domain optical coherence tomography (FD-OCT) device (RTVue; Optovue Inc., Fremont, CA, USA) was used to measure the tear meniscus height, depth, and angle; results were obtained using computer calipers. The tear meniscus area was calculated using a formula based on a triangular approximation (tear meniscus area=0.5 × tear meniscus height × tear meniscus depth). FD-OCT was performed before the start and after using topical cyclosporine A 0.05% for 1 and 3 months. OCT settings remained constant throughout the experiment for all subjects.
Data analysis
The PASW software (ver. 19.0; IBM Corp., Armonk, NY, USA) was used for data analysis. Wilcoxon’s signed rank test was used to compare ordinary categorical variables, such as the Schirmer test, lid margin abnormality scores, tear meniscus amounts, and ocular symptom scores.
Results
In total, 20 patients (8 males, 12 females) who had used an ocular prosthesis for longer than 5 years were treated with topical cyclosporine A 0.05%, one drop twice per day. Treatment was well tolerated, and no patient discontinued the study because of adverse events.
Patient demographic characteristics are summarized in Table 1. The mean patient age was 60.11±20.10 (range, 26–95) years and the mean duration of prosthesis usage was 10.89±5.18 (range, 5–25) years. The most common cause of ophthalmic surgery was trauma (50%) and evisceration was the most common type of eye removal surgery (65%).
The mean ocular symptoms score with an ocular prosthesis at baseline before the start of topical cyclosporine A 0.05% was 76.83±8.73. The mean ocular symptoms scores after treatment for 1 and 3 months were 54.37±9.47 (P<0.001) and 46.75±10.81 (P<0.001), respectively (Figure 1a). There was significant improvement in the ocular symptoms score after 1 month of cyclosporine A 0.05% treatment vs baseline (P<0.001; Table 2). For the symptoms listed in Table 3, all symptoms except excessive blinking showed significant improvements after 3 months of cyclosporine A 0.05% treatment.
The mean Schirmer test result before the start of topical cyclosporine A 0.05% was 6.70±2.96 mm. The mean Schirmer test results after 1 and 3 months of treatment were 7.10±3.16 (P=0.149) and 11.40±2.46 (P<0.001), respectively (Figure 1b). No significant difference was observed in the Schirmer test between the 1-month result and the initial evaluation (P=0.149). However, significant improvement was observed at 3 months compared with that at the initial evaluation (P<0.001; Table 2).
The mean lid margin score before using topical cyclosporine A 0.05% was 1.10±0.91. The mean lid margin scores after treatment for 1 and 3 months were 0.95±0.76 (P=0.180) and 0.85±0.67 (P=0.096), respectively. No significant changes were observed among the three values (Table 2).
Of the four criteria in Table 4, there was no significant change in the mean tear meniscus height, tear meniscus angle, or tear meniscus area after treatment for 1 or 3 months. In the case of tear meniscus depth, however, there was a significant improvement after cyclosporine A 0.05% treatment for 3 months (P=0.019; Table 4).
Discussion
Cyclosporine was originally developed to prevent solid organ graft rejection.9 In 1989, Kaswan et al10 first reported that topical cyclosporine was effective in the treatment of dry eye in dogs that had developed keratoconjunctivitis sicca. Since then, topical cyclosporine A 0.05% has been shown to be effective in the treatment of several ocular surface diseases, including vernal keratoconjunctivitis,11 immune-mediated keratitis,12 necrotizing scleritis,13 and corneal allograft rejection.14 There have been several clinical trials investigating the effect of cyclosporine in dry eye patients.15, 16, 17 In one, cyclosporine significantly reduced conjunctival Rose Bengal staining, superficial punctuate staining, and ocular irritation symptoms. Cyclosporine has been shown to decrease activated T cells,15 pro-inflammatory cytokines,18, 19 and epithelial cell apoptosis,20 and to increase goblet cell density in dry eye with an inflammatory component.21
In the present study, we investigated the short-term effects of cyclosporine A in patients with ocular discomfort resulting from long-standing prosthetic eye use. An anophthalmic socket has a different anatomical and physiological environment, as compared with a normal eye. It is characterized by the absence of a cornea and by continuous mechanical rubbing between the socket and prosthetic eye. As cyclosporine is known to be an effective treatment for controlling ocular surface inflammation, we hypothesized that topical cyclosporine might be effective for the relief of ocular symptoms resulting from the different environments in anophthalmic patients. In this study of subjects with prosthetic eyes, most symptoms showed improvement after 1 month of cyclosporine A 0.05% treatment. All patients showed satisfaction in terms of ocular symptom relief. Furthermore, there were statistically significant improvements in the Schirmer test after 3 months of cyclosporine A 0.05% treatment.
Prosthetic eye wearers tend to suffer from blepharitis and meibomian gland dysfunction. This is well documented in a recent report by Jang et al.7 It has been suggested that meibomian gland dysfunction can be treated effectively with cyclosporine A 0.05%.22, 23, 24 The ocular prosthesis causes mechanical trauma to the tarsal conjunctiva, thus altering the meibomian gland structure.3, 25 Furthermore, poor hygiene with the prosthetic eye can lead to inflammation of the anophthalmic socket. Discharge from inflammation of anophthalmic socket can also cause meibomian gland obstruction. Obstruction of the meibomian ducts can then cause accumulation of meibum, which may lead to inflammation and bacterial colonization.26, 27, 28, 29 These conditions may cause clinically apparent ocular discomfort to prosthetic eye wearers. Inflammatory cytokines, such as interleukin (IL)-1, IL-6, IL-8, IL-12, and epidermal growth factor, have been reported to be increased in patients with meibomian gland dysfunction.30, 31 Thus, topical cyclosporine A 0.05%, as a specific immunomodulator acting on T cells, may decrease the inflammation in meibomian gland dysfunction and improve the ocular symptoms.
Allen et al4 reported that prosthetic eye wearers did not produce as much tear fluid as people with normal eyes do. It was suggested that the mechanism of reduced tear production involved the absence of a corneal reflex. Reflex tears supply most of the aqueous components of tears. The aqueous component is important in the self-cleansing mechanism of the normal eye. Thus, with too little aqueous component in the prosthetic eye, excessive proportions of mucin and oily components result. The thick mucoid residue causes ocular discomfort to many patients. In the normal conjunctiva, mucus produced by goblet cells form networks of strands that are broken into coarser strands with each blink. The aqueous component, together with the blink mechanism, removes the mucus strands.32 Decreased aqueous production on the dry surface of the ocular prosthesis inhibits this self-cleansing mechanism in the anophthalmic socket, leading to mucoid discharge. This is why many prosthetic eye wearers use aqueous lubricants for comfort. We could not conclude whether cyclosporine is superior to lubricants. This is because we intended to investigate the effect of cyclosporine on patients with a unilateral prosthetic eye through an intra-individual comparison between pre- and post-cyclosporine treatment. We believe that this issue should be investigated to justify the use of cyclosporine. As cyclosporine is more expensive than lubricants, comparative double blinded investigations in which lubricants are compared with topical cyclosporine for treating symptomatic artificial eye wearers are necessary to evaluate cost-effectiveness.33
Kim et al34 reported that decreased goblet cell density and an increased nucleus-to-cytoplasm ratio associated with squamous metaplasia resulted in decreased mucus production in anophthalmic patients wearing an ocular prosthesis. They attributed these cytological changes to the constant irritation of prolonged prosthesis wear.34 One investigation reported that cyclosporine had a normalizing effect on conjunctival squamous metaplasia and caused an increase in conjunctival goblet cell density.21 We did not undertake histological examinations regarding inflammation of the conjunctiva or quantitative analyses of inflammation-mediating substances. As the main results were based on patient-reported outcome measurement (PROM), further investigation using objective variables is needed. However, the PROM data are still valuable because they were originally designed to assess treatment effectiveness in the context of clinical trials and are now more widely used to support decision making regarding the benefit of treatment.35
In conclusion, it was found that cyclosporine A 0.05% increased tear secretion and improved subjective symptoms in prolonged prosthesis wearers. However, due to the small sample and relatively short period of treatment (3 months), there are some limitations in demonstrating the clinical performance of cyclosporine A 0.05%. Nevertheless, this study is the first to report that cyclosporine A 0.05% can help long-standing prosthetic eye wearers in relieving ocular discomfort. These results could be utilized as a basis for a larger and longer-term follow-up clinical study in terms of usage of topical cyclosporine in anophthalmic patients.
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Acknowledgements
We gratefully acknowledge the statistical support of Ji Sung Lee, Biostatistician, Biostatistical Consulting Unit, and Soonchunhyang University Medical Center. This study was supported by the Soonchunhyang University Research fund.
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Han, J., Yoon, J. & Jang, S. Short-term effects of topical cyclosporine A 0.05% (Restasis) in long-standing prosthetic eye wearers: a pilot study. Eye 28, 1212–1217 (2014). https://doi.org/10.1038/eye.2014.174
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DOI: https://doi.org/10.1038/eye.2014.174
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