Purpose: The effect of residual astigmatism and its axis on distance and near visual acuities (VAs) with multifocal intraocular lenses (IOLs) has not been studied extensively. This study compared the tolerance to experimentally induced residual astigmatism among bifocal, trifocal, and extended depth-of-focus (EDOF) IOLs. Patients and Methods: This retrospective, comparative study included 70 eyes of 70 patients implanted with bifocal, trifocal, or EDOF IOLs. Distance and near VAs were assessed with experimentally induced astigmatism by placing positive cylindrical lenses in increments of 0.50 diopters to 2.00 diopters at 90° and 180° axes over the best distance correction. Results: Both distance and near VAs worsened with increasing magnitudes of experimentally induced astigmatism except in the EDOF group, in which the near VA remained within a clinically acceptable limit, ie, within one line from the best corrected VA under all ranges of experimentally induced astigmatism. Furthermore, the EDOF group showed the highest astigmatic threshold for losing VA lines following experimental astigmatic induction at both distance and near. The distance VA was generally better at with-the-rule (WTR) than against-the-rule (ATR) astigmatism for all three IOL groups. On the other hand, the near VA was generally better at WTR than ATR astigmatism in the bifocal group, comparable between WTR and ATR astigmatism in the trifocal group, and generally better at ATR than WTR astigmatism in the EDOF group. Conclusion: The EDOF IOL demonstrated the highest tolerance to experimentally induced astigmatism at both distance and near. VA was generally less affected by WTR astigmatism than ATR astigmatism, especially at distance. We proposed the residual astigmatism thresholds for clinically acceptable VA reduction in all three IOL groups.
Keywords: residual astigmatism; bifocal; extended depth-of-focus; trifocal
John So Min Chang,
Correspondence: John So Min Chang, Department of Ophthalmology, Hong Kong Sanatorium & Hospital, Hong Kong, Tel +852 2835 8884, Fax +852 2835 8887, Email [email protected]
Due to their good visual outcomes and high possibilities of spectacle independence, leading to high patient satisfaction,[
For patients with low or moderate corneal astigmatism, the use of toric MIOLs may be too costly, whereas clear corneal incision could be less effective. In addition, it has been suggested that mild postoperative astigmatism may be beneficial to near vision while preserving acceptable distance vision in eyes implanted with monofocal IOLs.7–10 To make an informed decision, surgeons should understand the tolerance to residual astigmatism of different types of MIOLs and EDOF IOLs so as to achieve acceptable vision at various distances.
In comparative studies that assessed the distance vision in eyes implanted with MIOLs, EDOF IOLs provided greater tolerance to astigmatism than bifocal or trifocal IOLs,[
The astigmatic axis might also play a role. Studies have suggested that with-the-rule (WTR) astigmatism is generally more favorable than against-the-rule (ATR) astigmatism for distance vision in virgin eyes,[
Besides, these results may not be generalized to eyes implanted with MIOLs. One study reported that ATR astigmatism resulted in greater reduction in distance visual acuity (VA) than WTR astigmatism for trifocal IOL.[
Given that few comparative studies of MIOLs have simultaneously evaluated the effect of residual astigmatism on distance and near vision and that they have focused only on ATR astigmatism,[
This retrospective, comparative case series included patients who underwent cataract surgery or refractive lens exchange with unilateral or bilateral implantation of one of the following MIOLs at the Hong Kong Sanatorium & Hospital: TECNIS ZMB00 (Johnson & Johnson Vision, Santa Ana, CA, USA) [bifocal group]; FineVision Pod F (Physiol, Liége, Belgium) and FineVision Pod FT (Physiol) [trifocal group]; LENTIS Comfort (LS-313 MF15) (Teleon Surgical BV, Spankeren, the Netherlands), LENTIS Comfort Toric (LS-313 MF15Tx) (Teleon Surgical BV), and LENTIS Mplus toric (LU-313 MF15T) (Teleon Surgical BV) [EDOF group].
The inclusion criteria were age of 40 years or older, postoperative corrected distance VA of 20/25 or better, and postoperative follow-up period of 28 days or longer. The exclusion criteria were the presence of any systemic or ocular disease that might affect vision, use of systemic or ocular medications that might affect vision, history of corneal refractive surgery, and presence of intraoperative complications.
The bifocal IOL used in this study is diffractive and provides +4.00 diopters (D) of near addition (~ +3.20 D at the spectacle plane). Light energy is distributed symmetrically between the distance and near foci and is independent of pupillary size.
The trifocal IOL is diffractive and provides a near addition of +3.50 D (~ +2.80 D at the spectacle plane) and an intermediate addition of +1.75 D (~ +1.40 D at the spectacle plane). The light energy is distributed to the distance, intermediate, and near foci by 42%, 15%, and 29%, respectively. The toric version was also included.
The EDOF IOL is rotationally asymmetric and refractive. It contains an aspheric distance zone and a sector-shaped near zone of +1.50 D near addition (~ +1.20 D at the spectacle plane) with a transition zone for intermediate vision. The two toric versions were also included in this study, with one allowing spherical and cylindrical power being customized to the nearest 0.01 D.
One surgeon performed all surgeries. A keratome was used to create a 2.25-mm clear corneal incision either superiorly or temporally. DisCoVisc ophthalmic viscosurgical device (Alcon Laboratories Inc., Fort Worth, TX, USA) was injected into the anterior chamber, and a manual continuous curvilinear capsulorhexis was made. Coaxial phacoemulsification was performed after hydrodissection and nuclear splitting. The residual cortex was irrigated and aspirated. Posterior capsule was polished using a coaxial system. All IOLs were placed into the capsular bag.
Preoperatively, all patients underwent a comprehensive ophthalmic assessment, including history taking, VA, biometry, and ocular health examination.
Follow-up visits were scheduled for postoperative 1 day, 1 week, 1 month, and 3 months. The outcome measures included uncorrected distance and near VAs, non-cycloplegic subjective refraction, and distance-corrected VA with and without experimentally induced astigmatism at distance and near. The near viewing distance was 30 cm for the bifocal and trifocal groups, and 40 cm for the EDOF group.
Near VA was measured using the SLOAN Two-Side Early Treatment Diabetic Retinopathy Study Format Near Vision Chart (Precision Vision, La Salle, IL, USA). Because this chart is designed for a viewing distance at 40 cm, the actual near VAs for the bifocal and trifocal groups were calculated by the visual angle subtended. All vision tests were performed under photopic condition at 85 candelas/m
Older patients usually have ATR astigmatism.[
In general, one eye was randomly chosen for analysis for patients with bilateral implantation. However, due to the lower implantation rate of trifocal IOLs compared to other IOL types, the eye implanted with trifocal IOL was chosen for analysis when the other eye was implanted with a bifocal or EDOF IOL.
All VAs were converted to the logarithm of minimum angle of resolution (logMAR) for statistical analysis.
Normality of data was checked using Shapiro–Wilk test. Patient demographics between IOL groups were compared using one-way analysis of variance with Bonferroni-corrected independent t-test, except for IOL cylindrical power with independent t-test, which involved only two IOL groups. The differences in VA between experimentally induced ATR and WTR astigmatism for each DC for each IOL group and the difference in VA reduction for each condition of experimentally induced astigmatism between distance and near were assessed using paired t-test. The differences in VA reduction from plano for each condition of experimentally induced astigmatism among the three IOL groups were assessed using one-way analysis of variance and post-hoc pairwise analysis using the Bonferroni-corrected independent t-test.
A corresponding alternative statistical test was used when there was a violation in statistical assumption.
A p-value <0.05 was considered statistically significant. All statistical analyses were performed using SPSS (version 25.0, SPSS Inc.).
The research ethics committee of Hong Kong Sanatorium & Hospital approved the study, which adhered to the tenets of the Declaration of Helsinki. Patient consent was waived due to the retrospective nature of the study. Patient's personal information was maintained with confidentiality.
This study included 70 eyes of 70 patients (31 men [44%]; mean age, 59.6±7.0 years; range, 47 to 78 years). The bifocal, trifocal, and EDOF groups comprised 25, 23, and 22 eyes, respectively.
Table 1 shows the patient demographics overall and by IOL group. Patients in the EDOF group were significantly older at surgery than those in the bifocal and trifocal groups. The EDOF group had a greater proportion of men than the bifocal group. The follow-up period was significantly longer in the bifocal group than the trifocal and EDOF groups.
Table 2 shows the postoperative refraction and distance-corrected VAs overall and by IOL group. The postoperative refractions (sphere, cylinder, and spherical equivalent) and corrected distance VAs did not differ significantly among the groups. The distance-corrected near VAs were significantly better in the bifocal and trifocal groups than the EDOF group.
Figure 1 shows the comparison of the reduction in VA from plano under different conditions of experimentally induced astigmatism among the IOL groups. The distance VA worsened with increasing magnitude of experimentally induced astigmatism in all three IOL groups, with more remarkable VA reduction in the bifocal group than the EDOF group (Figure 1A). The near VA worsened with increasing magnitude of experimentally induced astigmatism in the bifocal and trifocal groups only (Figure 1B). The near vision in the EDOF group remained within the clinically acceptable reduction in VA for all ranges of experimentally induced astigmatism magnitudes and axes. In all three IOL groups, the VA reduction for all experimentally induced astigmatism magnitudes was more pronounced at distance than near (p<0.05) except with WTR astigmatism of 0.50 DC in the bifocal group, and WTR astigmatism of 0.50 DC and 1.00 DC in the trifocal group.
The distance VA was generally better with WTR than ATR astigmatism for all three IOL groups (Figure 2A-C). The near VA was generally better with WTR than ATR astigmatism in the bifocal group (Figure 2D), comparable between WTR and ATR astigmatism in the trifocal group (Figures 2E), and generally better with ATR than WTR astigmatism in the EDOF group (Figure 2F).
Table 3 and Table 4 show the astigmatic thresholds for clinically acceptable reduction in VA by IOL group and the axis of experimentally induced astigmatism. The EDOF group showed the highest astigmatic thresholds at distance (Table 3) and near (Table 4), with a higher threshold at near than distance.
Our study showed that experimentally induced residual astigmatism had a clinically significant impact on the distance VA in all three IOL groups. In contrast, residual astigmatism adversely affected the near VA mainly in the bifocal and trifocal IOL groups but improved the near VA in the EDOF IOL group. ATR astigmatism had a greater adverse effect than WTR astigmatism on distance VA with all IOL types and on near VA with bifocal IOL only. An opposite trend was observed for near vision with the EDOF IOL.
The overall better distance visual performance with WTR than ATR astigmatism in all three IOL groups in our study agrees with previous studies of virgin eyes,[
For near vision, our results showed that VA with WTR astigmatism was significantly better than ATR astigmatism with bifocal IOL. However, no previous study has assessed the impact of astigmatism axis on near vision in eyes implanted with bifocal IOLs. On the other hand, near VA was similar between WTR and ATR astigmatism with trifocal IOLs, which is in line with studies on virgin eyes[
The greater VA reduction with experimentally induced astigmatism at distance than at near in all three IOL groups was consistent with the findings reported in virgin eyes,[
The tolerance to astigmatism was the highest with the EDOF IOL at both distance and near. This is consistent with the findings reported by Carones.[
The astigmatic thresholds for different types of MIOLs have been reported previously.[
Our results may aid preoperative planning if surgeons wish to leave mild residual WTR or ATR astigmatism according to patients' visual demands and the type of MIOL being implanted.
When the IOL cylindrical power is unavailable in precise increments or if different IOL formulas or biometers give different results, targeting mild postoperative residual WTR astigmatism (≤0.50 DC) would be more desirable for bifocal and trifocal IOLs because it could offer better distance vision and similar or better near vision compared to mild ATR astigmatism. For EDOF IOLs, surgeons may consider targeting mild ATR astigmatism (≤0.50 DC) especially when the patient has a greater visual demand at near than distance, because it provided better near VA while offering similar distance vision when compared to mild WTR astigmatism.
If monovision is planned for bilateral implantation with an EDOF IOL, surgeons may allow more postoperative astigmatism (especially ATR astigmatism) in eyes targeting myopia. Although this can lead to worsened distance VA in the eye targeting myopia, the binocular distance VA should only be minimally affected.31–33
Surgeons should also take into account the type of MIOL when deciding whether to leave the corneal astigmatism untreated (ie, using a non-toric IOL). Due to the higher tolerance to residual astigmatism with EDOF IOL, surgeons may offer a non-toric IOL to candidates for implantation of EDOF IOL even if they have moderate corneal astigmatism. However, the possible advantages and disadvantages of the non-toric option should be thoroughly explained to patients preoperatively.
Our study has several limitations. First, the increment of the astigmatic simulation was 0.50 DC, which might have yielded a less precise astigmatic threshold. However, a finer step with 0.25 DC would significantly lengthen the examination time, causing patient fatigue. Second, not all the bifocal, trifocal, or EDOF IOLs have the same design. Our results may not be generalized to other IOLs of the same type. Third, oblique astigmatism was not evaluated because it was less commonly seen in cataract surgery planning[
In conclusion, at both distance and near, the EDOF IOL provided the highest tolerance to experimentally induced astigmatism, whereas the bifocal and trifocal IOLs performed similarly. The EDOF IOL provided a slight improvement in near vision, especially with ATR astigmatism. For all three IOL types, the distance vision was generally less affected by WTR astigmatism than ATR astigmatism. The near vision was less adversely affected by WTR astigmatism for the bifocal IOL, but less adversely affected by ATR astigmatism for the EDOF IOL, and affected in a similar extent by WTR and ATR astigmatisms for the trifocal IOL. The distance vision was generally more affected by astigmatism than the near vision with all three IOL types. Our study reported the astigmatic threshold for clinically acceptable vision for all three IOLs. Surgeons may target mild-to-moderate residual WTR or ATR astigmatism based on the patients' visual demand and the type of MIOL being implanted.
By John So Min Chang; Sylvia Chui Ting Liu; Nadine Tsz Ching Ma and Jack Chun Man Ng
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