The aim of this study was to present the detailed procedure of a modified approach and initially evaluate the efficacy and safety of IOL repositioning in this manner. In general, the clinical outcomes were favorable for all patients, and no severe complications occurred after surgery. All IOLs were stable with no significant lens tilt, and the mean BCVA of all patients improved significantly from 0.49 ± 0.26 to 0.29 ± 0.17 (logMAR, p < 0.05, t = 2.204) by the most recent follow-up visit. Surgical complications in this research included elevated lOP (2 eyes) and CME (1 eye), which all could be resolved by the topical use of eyedrops. Serious complications, such as UGH syndrome, IOL redislocation, retinal detachment, choroidal expulsive hemorrhage, endophthalmitis, and suture breakage or erosion, were not observed in this research. The modified scleral suturing technique repositioning the IOL with two 9 − 0 polypropylene sutures is considered to be safe and effective for late in-the-bag IOL dislocation.
Dislocated intraocular lenses (IOLs) are one of the most feared but treatable complications after cataract surgery. The rate of in-the-bag IOL dislocations has been reported to increase yearly over the past decade. The frequency of IOL dislocation after cataract surgery has been reported to be 0.2–3%[2, 3, 11]. The wide variability in reported incidence rates has been suggested to arise from a number of reasons, such as unequal distribution of predisposing conditions across populations and varying follow-up lengths. Different conditions are associated with late in-the-bag IOL dislocation. Previous studies have established pseudoexfoliation syndrome (PEX) as one of the most important predisposing factors[3, 12, 13]. Other associated conditions include previous vitreoretinal surgery, myopia/increased axial length, uveitis, retinitis pigmentosa, certain connective tissue disorders, and trauma—that is, both direct blunt trauma and indirect trauma, the latter in the form of head injuries or working with vibrating machines[2, 3, 12, 14]. Recent research suggests that the different types of materials and designs of IOL used in cataract surgery may be another cause. Plate–haptic silicone IOLs have been associated with an increased risk of anterior capsule opacification with secondary capsule contraction, which may subsequently increase the risk for dislocation[15, 16]. The possible preventive role of CTR should also be discussed. However, no prospective comparative studies specifically addressing this issue have been published. One prospective cohort study found a higher proportion of late dislocation in eyes with CTR. The probable reason is that the implantation of CTR may induce some damage to the zonular fibers, which may increase the vulnerability for later dislocation. Thus, no final conclusion regarding a possible preventive role of CTR has been reached thus far[17, 18]. The etiological distribution of the 11 patients included in this research was as follows: 3 eyes undergoing prior vitrectomy, 3 eyes with high myopia, 2 eyes implanted with a CTR, 1 eye with trauma and 2 eyes with unknown etiologies. This is slightly different from what has been reported in the literature. No cases were associated with PEX, which may be attributed to the varying incidence of PEX among different ethnic groups.
A variety of methods to manage dislocated IOLs have been reported, all in principle variants of either repositioning the existing IOL or exchanging it for a new IOL. However, no definite clinical recommendations have been made in terms of the choice between IOL repositioning and IOL exchange[6, 19]. The choice to manage dislocated IOLs is highly dependent on the surgeon’s preference and individual case features, such as the integrity of the capsule, type of IOL and coexisting ocular pathologies. Although some researchers have reported that there were no significant differences in visual acuity or complication rates between eyes undergoing IOL repositioning and those undergoing IOL exchange, IOL repositioning by scleral suturing is mentioned in a number of articles as the recommended operation method for most cases of IOL dislocation. The reason may be that IOL exchange is inherently more traumatic, with a larger incision required and an increased risk for vitreous loss, iris trauma, corneal endothelial damage, and postoperative astigmatism[5, 6]. The dislocated IOLs are always repositioned by iris fixation or scleral fixation. In both approaches, the scleral fixation of the IOLs at the ciliary sulcus allows the anchoring of the haptics to secure and stabilize the structure, and the IOLs are localized closer to the original anatomic location. Therefore, most of the time, a dislocated IOL was fixed in situ at the ciliary sulcus by scleral fixation sutures to secure the haptic(s). Numerous methods of scleral fixation have been reported in previous studies[3, 4, 7, 20]. The step that involves looping the suture around the IOL haptic(s) is the largest variable and most technically difficult between different scleral fixation methods. In this study, all subjects received Rayner aspheric monofocal IOL (920H, Hove, UK) implantation in their primary cataract surgery; the device is a one-piece hydrophilic acrylic IOL with closed-loop haptics. The haptics of the dislocated IOLs were fixated in situ with a slipknot tied to the haptic loop by passing the needle through the loop at the end of a suture. There are several advantages to the minimally invasive and scleral fixation technique used in this study. The IOP during the procedure was more stable, and the surgery process was less traumatic with the small scleral and corneal puncture sites, thus reducing the risk for serious complications such as retinal detachment or choroidal expulsive hemorrhage. All needle passes were guided by docking into a 27-gauge needle. As a result, there was no blind needle passage under the iris, and the fixation was at the exact scleral position identified externally. Suture passes were made at an orientation that led the IOL to obtain optimal centration. All IOLs remained stable with no significant lensing tilt at the most recent follow-up visit. We have found that a slipknot passed around the haptic loop through the stiff fibrotic capsule is sufficient to prevent slippage of the suture. In this way, we reduced the amount of manipulation required to tie the knot around the haptic, which can reduce the intraoperative risk caused by extra manipulation. As a result, there were no serious complications, such as retinal detachment, choroidal expulsive hemorrhage, endophthalmitis, and suture breakage or erosion, in the present study.
One-piece IOLs were used in this study. Several researchers have debated whether a 1-piece IOL is suitable for repositioning because of the potential risk of UGH syndrome due to iris chaffing from thick haptics. Although, in principle, any IOL in the AC or sulcus could cause UGH syndrome, the disease triad has been reported to be associated with a 1-piece IOL inside the capsular bag. In recent studies, UGH syndrome was identified as an important long-term complication that may mimic several different pathologies and, therefore, represent a diagnostic challenge[8, 9]. This reminds us to pay extra attention to UGH syndrome after surgery. Fortunately, none of the patients in this study had UGH syndrome, suggesting that 1-piece IOLs are as good as other types of IOLs. This result is in agreement with a recent prospective cohort study reported by Marius Dalby et al.[4]. In conclusion, this technique is a simple, effective, and safe way to reposition dislocated 1-piece IOLs. Although this technique has only been used for one-piece hydrophilic acrylic IOLs with a closed loop in the haptics, we believe that it is also suitable for other types of IOLs with similar structures. This will be explored in our future research.
There are several limitations to our study. First, this retrospective study was subject to potential inherent limitations related to the study design. Second, the follow-up was not long enough. The mean follow-up time was 14.55 ± 5.34 months, and a long-term follow-up is needed to evaluate complaints such as stability of the IOL and suture breakage or erosion. Third, a relatively small population was included in this study due to the particular type of IOL enrolled. Thus, additional randomized trial studies with a higher number of subjects and a longer follow-up period are needed to further confirm our findings.
In summary, repositioning 1-piece IOLs in this modified manner is a simple, effective, and safe method. As long as the IOLs are similar in structure to the type of IOL used in this study, this surgical technique appears to be well suited for the treatment of IOL dislocations.