To our best knowledge, this is the first study to assess the real-life intraoperative central corneal epithelium thickness during alcohol-assisted PRK. Utilizing the OCP integrated in the SCWIND Amaris excimer laser platform, we found an overall high variability of the central corneal epithelium. In addition, the second operated eye had significantly thicker central epithelium than the first operated eye.
Several strategies have been reported in the literature for the measurement of epithelium thickness, including VHF digital ultrasound,[1, 3] optical pachymetry,[7, 17] anterior-segment OCT[4–6, 8–10, 18] and confocal microscopy.[19] The advances in imaging techniques enabled clinical applications of ET mapping. This tool is used in the preoperative evaluation of refractive surgery candidates and may provide data of the individual epithelium profile to diagnose subclinical disorders. However, these maps, obtained preoperatively, do not necessarily reflect intraoperative changes in the epithelium that may affect the ablation impact.
The OCP is used for continuous monitoring of the corneal thickness intraoperatively. OCP measurements have been previously reported to show a high reproducibility.[20–22] These reports are in agreement with our findings, in which the initial intraoperative OCP measurement of corneal thickness was significantly correlated to all preoperative corneal thickness measurements, both by US pachymetry and topography. Moreover, all measurements of corneal thickness in our study showed no difference between fellow eyes.
The calculated mean central ET in our study was 59.5 ± 19.9, similar to previous studies that reported a mean ET between 48 ± 5 μm[17] and 59.9 ± 5.9 μm.[7] However, in our study the high standard deviation (19.9 µm), reflecting the wide range of ET between 15-150 µm, supports the need for caution when referring intraoperatively to preoperative measurements, which may not reflect the intraoperative changes.
Our results did not show a difference in ET between genders and CL wear, nor did we find a correlation with age, refractive errors, or keratometry. The literature is controversial about whether age, gender, or refractive errors affect the corneal ET.[4–7] Several studies[8, 14, 17] showed a significant decrease in ET among CL-wear groups, with and an increase in thickness following discontinuation of the soft contact lenses.[8] It is important to note that our group of patients, seeking refractive surgery, were mostly young adults with varying degrees of myopia. All long-term CL wearers were requested to cease using CL at least 10 days prior to surgery. It may be partially for these reasons that we saw no age or CL-related ET differences, even though such differences have been observed in other publications.
When comparing consecutive eyes for each patient, we found that the corneal epithelium of the second operated eye was significantly thicker than that of the first operated eye (54.8 ± 17.6 compared to 64.1 ± 21.1, p=0.006). Studies assessing the preoperative epithelium, using VHF digital ultrasound[3] and OCT,[14, 23] showed no difference in epithelium thickness between the right and left eyes. It is possible that our findings can be explained by the time elapsed between the first and second operated eye.
Another factor that can affect the ET is the topical anesthesia. Several studies reported that the topical anesthetic agents proparacaine 0.5%[24–26] and oxybuprocaine 0.4%[24, 27] can cause a small transient increase in central corneal thickness. Mukhopadhyay et al.[26] found a large degree of interindividual variability in the amount of swelling, ranging from a decrease of more than 10 µm to an increase of over 30 µm in individual cases. Asensio et al.[27] reported a similar degree of variability, and concluded that topical anesthesia can affect corneal thickness by more than 10 µm in over 25% of the patients. Weekers et al.[28] revealed that cocaine, lidocaine, and benoxinate cause an alteration of the Na+/K+ endothelium pump on the corneal epithelium in rabbits, resulting in increased osmotic pressure and subsequent increased hydration of the epithelium and stroma. In our study, a drop of 0.4% oxybuprocaine was instilled in both eyes at the beginning of the surgery. The toxic effect of the anesthetic was probably greater in the second operated eye, in which more time elapsed between the installation of the anesthetic drops and the epithelial removal. This may support the high variability of ET and the difference between the first and the second operated eye.
Our study has several limitations. First, the values of ET were assessed indirectly by subtracting OCP measurements before and after epithelium removal. Second, although the toxic effect of the topical anesthesia could have also affected the stroma, affecting the epithelium calculation, our measurements of the total corneal thickness did not differ from the preoperative measurements.
Transepithelial PRK (SCHWIND eye-tech-solutions GmbH, Kleinostheim, Germany) is becoming a popular refractive procedure.[29–31] A single step standard epithelial ablation pattern of 55 μm centrally is performed followed immediately by the stromal ablation. Although many researchers showed the efficacy and safety of t-PRK,[29–31] concerns were raised about possible effect of interindividual epithelial thickness profile variability on the refractive outcomes.[32, 33] A recent study by Jun et al.[34] showed a significant difference in postoperative sphere and spherical equivalent between groups of ET undergoing t-PRK, with a mild hyperopic shift in the group of ET < 50 μm, and a slight myopic shift in the 60 μm or greater ET group. This phenomenon can be explained by less stromal ablation at the same ablation depth setting. Our intraoperative cohort showed that 45.7% of the eyes had an ET within the range between 40-60 μm, while 54.3% were below or above these values. The variation of ET found in our study can be similarly applicable to t-PRK and support the need of a real-life assessment of the ET and addressing the measurements in the excimer laser ablation profile.
In conclusion, the intraoperative OCP measurements during alcohol-assisted PRK showed a high variability of central corneal epithelium thickness, with the second operated eye being significantly thicker than the first operated eye. The intraoperative measurements may differ from the preoperative evaluation and may have potential implications (under- or overcorrections) on the refractive outcomes of surface keratorefractive surgery when not included in the surgical planning. Additional studies correlating between the preoperative epithelial profile and the real-life intraoperative measurements are warranted.