The present study indicated that 45.1% of patients presented for bilateral cataract surgery in a public hospital were considered as proper candidates for a MIOL implantation. Furthermore, if we add the patients who were excluded because of the presence of regular astigmatism more than half of cataract patients (60.7%) may be benefited from a toric or a non toric MIOL. This compares with a previous study by Desphande et al who reported the feasibility of implantation of a multifocal IOL in 54.4% of their patients [13]. Their patient population, however, was significantly younger (mean age 59.4 years) than the patient population in the present study. This fact may explain why in their study an increased number of suitable candidates among patients without astigmatism was observed.
A significant burden for the implantation of MIOL is indisputably ocular comorbidities. According to results of the present study excluding patients with regular astigmatim and dementia thirty-nine percent of patients had an eye disease along with cataract in either or both eyes. The 39% prevalence of comorbidities in our patient population is within the range of 26–49% previously reported [14,15]. The present study, however, differs from previous studies as the exclusion criteria were applied in either one of the eyes.
The most prevalent contraindication for the implantation of a MIOL according to the present study was retinal pathology, which was the sole contraindication in 121 of 768 patients (15.8%). This compares well with a more than 20% of patients having macular disease or diabetic retinopathy reported recently in Swedish cataract registry [15]. Similarly, to the present study Desphande et al [13] reported that retinal pathology was the most common reason for non-feasibility of MIOL implantation in their patient population. More than half of the patients had ARMD and 20% an epiretinal membrane that most of the times was detected only by the OCT examination of the fundus. This fact underlies the importance of macular examination with an OCT before the implantation of a premium IOL. A recent study has shown that in 13% of cataract cases scheduled for a premium IOL implantation macular pathology was not detected by biomicroscopic examination [16].
All patients with retinal pathology were considered unsuitable candidates for the purpose of the current study. This is because MIOLs apart from reducing contrast sensitivity make problematic the visualization of the fundus for retinal surgery [7]. There is no unanimity among the experts however, regarding this subject. Although most experts would not implant a multifocal IOL in a patient with wet ARMD or diabetic retinopathy with macular edema a significant minority would not object to the implantation of a multifocal IOL in a patient with a non-proliferative diabetic retinopathy without macular edema or resolved central serous chorioretinopathy [17]. Furthermore, a recent review failed to find convincing evidence that patients with retinal disease should be advised against multifocal IOL [18]..
Two hundred and six patients in our sample (26.8%) had more than 1 diopter of astigmatism. Previous studies reported that the percentage of eyes that had astigmatism of 1 diopter or higher ranged between 23 and 47%. [19]. For the one hundred and twenty of 768 patients (15.6%) astigmatism was the sole contraindication for the implantation of a multifocal IOL. The presence of astigmatism, however, is not considered an absolute contraindication for the implantation of a multifocal IOL as there are various methods for the correction of astigmatism during or after cataract surgery. Among them implantation of toric multifocal IOLs resulted in excellent visual outcomes [20].
Seven-point five percent of patients were considered bad candidates due to PEX. The prevalence of PEX varies in different parts of the world. Previous studies in Greece reported a prevalence of 11.3%. [21].Pseudoexfoliation is associated with loose zonules, and it is the most common risk factor for spontaneous IOL dislocation, accounting for more than 50% of cases [22].The detrimental effect of PEX to the zonules is a continuously evolving process that may affect IOL centration long after cataract surgery. The quality of vision in cases of MIOLs is greatly affected by even small amounts of decentration (> 0.25mm) so the contraindication of MIOLs implantation in PEX eyes seems reasonable [23,24].
Seven-point one percent (7.1%) of patients were considered unsuitable candidates because of glaucoma or ocular hypertension. This fact likewise underlies the importance of optic nerve examination with biomicroscopy or OCT as a significant percentage of patients in the present study were unaware of glaucoma and had normal IOP at the time of preoperative examination. The percentage of undiagnosed glaucoma is high and in Greek population may well reach 50% [25].Similarly to what happens with retinal disease most experts would agree that moderate or advanced glaucoma is an absolute contraindication for the implantation of MIOL. There is uncertainty however, regarding the implantation of MIOLs in patients with early glaucoma or ocular hypertension [26,27].Although these patients may not exhibit any significant visual disability [28] there is always the concern of progression of disease and treatment effects to ocular surface and quality of vision.
In this study, we excluded a priori all patients who had a monofocal IOL implanted in one eye at the time they presented for evaluation for possible MIOL implantation in the second eye as well as patients not eligible for bilateral cataract surgery. Applying these rigid exclusion criteria resulted in 432 out of 1200 tested patients (36%) not being given the option of benefiting from a MIOL implantation. For years, literature has been advocating bilateral MIOL implantation [7] and there is extensive literature on symmetrical or mix and match techniques for bilateral MIOL implantation.
“Hybrid” monovision, though, ie implantation of a monofocal IOL in the dominant eye and a multifocal in the other eye has not been tested in a large scale study; however there are studies [29] addressing this clinical scenario reported encouraging results.
A significant result of the present study is that the only characteristic that differentiated suitable from unsuitable candidates was age. This finding was not unexpected as comorbidities increase with age. This pairs with an earlier finding that younger patients have higher gain and higher self-assessed visual function than older patients after cataract surgery probably from the same reason [30].
The present study indicated that three quarters of the Greek cataract patients who were qualified for the MIOL implantation would prefer a MIOL to a monofocal IOL if the procedure was carried out in a public hospital and the cost was covered by the insurance. Results of the present study contrast those of a recent survey conducted in public sector in Great Britain. According to this survey 85.8% of cataract patients did not mind wearing glasses after cataract surgery, most patients (75.3%) were not familiar with premium IOLs, and 58.9% of patients were not willing to consider them because of associated risks [10].There are several reasons for this contrast: Our patient population was familiar with premium IOLs as toric IOLs have been used for several years in our institution with excellent results. Furthermore, our patients devoted increase time to near activities as almost all used either smart phone or tablet. This necessity of MIOLs becomes apparent by a very recent study conducted in Switzerland which found that most patients who achieve perfect bilateral emmetropia after implantation of monofocal aspheric lenses have bought varifocal spectacles within 6 months of surgery [31].This preference of the patients should be taken in account by policy makers. Although several previous studies have shown that implantation of a multifocal IOL is more cost effective than the implantation of monofocal IOL paired with the use of glasses [32,33], the National Health systems do not cover or partly cover the extra cost of multifocal IOLs. This is one of the major restrains for the widespread use of MIOLs.
Recently, extended depth of focus (EDOF) lenses came into practice. Instead of diverging the light to more than one focus as do MIOLs these IOLs split the light in an elongated area of focus [34].They provide good far and intermediate vision with a supposedly reduced risk of photic phenomena compared to MIOLs. It is not clear to us if results of the present study apply to EDOF lenses as it was based on exclusion criteria summarized in the consensus paper that referred only to MIOLs. A very recent metanalysis failed to detect significant differences in the contrast sensitivity between multifocal and EDOF IOLs [34] Although reports in the literature [35] indicated favorable results with EDOF IOLs in cases were MIOLs may be contraindicated more data are necessary.
There are various limitations in the present study. First it was conducted in a predominantly urban population with specific demographic and socioeconomic characteristics that may prevent generalizations. Second, strict exclusion criteria were applied during screening that as we have already mentioned are not universally accepted. Furthermore, advances in the optical design of MIOLs may ameliorate some of these contraindications especially in early stages of ocular diseases. Finally, in the setting of a busy public hospital. personality traits that could made some patients unsuitable candidates for MIOLs may not have been adequately assessed.
In conclusion the present study illustrates the relative frequency of contraindications of MIOL implantation in the Greek population and provides an insight into
the percentage of well-informed eligible candidates that would consent to it.