- Original article
- Open Access
Net technique for intraocular lens support in aphakia without capsular support
International Journal of Retina and Vitreousvolume 3, Article number: 32 (2017)
This paper describes a modified surgical technique for intraocular lens implantation in aphakic eyes with no capsular support.
Retrospective case series. Seventeen eyes of 17 aphakic patients with no capsule support underwent intraocular lens (IOL) implantation using a standardized technique in which a net was created at the ciliary sulcus plane with two threads forming a net pattern. The net was used as support for the IOL. Follow-up ranged from 6 to 38 months, with an average of 23 months.
In all cases, the IOL was safely implanted and remained stable during the follow-up. In 16 eyes, the IOL remained well centered; in one eye, slight decentration was observed. Distance-corrected visual acuity improved by a mean of 4 lines, from 1.13 (LogMAR) to 0.52 (P = 0.01).
This technique might be especially useful in cases of insufficient capsular support associated with tissue loss or iris atrophy. In these cases, iris fixation is not feasible; thus, the only surgical alternative is IOL scleral fixation.
Several options are available for the correction of aphakia in cases with absence of support of the posterior crystalline lens capsule. The most conservative nonsurgical options are correction with glasses or contact lenses. Glasses are rarely used because the corrective power required for aphakia results in relative loss of visual acuity, significant anisometropia and unsatisfactory esthetical results. One surgical option is intraocular lens implantation in the sclera through sutures or stabilization in a scleral groove [1,2,3,4,5]. Other options include iris-suture fixated lenses or iris fixation by enclavation and angle-supported anterior chamber phakic intraocular lenses [6, 7].
In this retrospective study, we describe a modified surgical technique that enables the implantation of an intraocular lens in the posterior chamber through a reproducible, relatively low-cost suture that provides safe support for the IOL, as well as good centralization and stability.
Patients and methods
Following approval by an institutional review board, this retrospective cohort study was carried out from April 2014 to April 2016, according to the principles of the Declaration of Helsinki. All study participants provided written informed consent.
The study was carried out at the Sadalla Amin Ghanem Eye Hospital, and Garrido’s Eye Clinic, operations were conducted from April 2014 to April 2016. Seventeen patients underwent operation and were followed-up for at least 6 months. All surgeries were carried out by two surgeons (FJN and TLG).
Post-op follow-up ranged from 6 to 38 months, with an average of 23 months. A full ophthalmologic examination was performed at all consultations, including best-corrected visual acuity, biomicroscopy, fundoscopy and intraocular pressure measurement.
Posterior pars plana vitrectomy (PPV) was performed due to cases of retinal detachment or displacement of the lens into the vitreous cavity (4 patients). In such cases, vitrectomy should be performed regardless of the type of IOL implantation.
Topical 1% mydriacyl was applied twice 15 min before peribulbar anesthesia. Standard asepsis was achieved with periocular 10% povidone-iodine solution and 5% povidone-iodine instillation.
A peritomy was performed in the 4 quadrants, and an initial 5-mm-long groove was created 2.0 mm from the limbus (Fig. 1a).
One straight 16-mm needle of a doubled-armed 9-0 polypropylene suture (Ethicon, Inc.) was inserted into the anterior chamber. A 25-gauge needle was inserted 180° away in the contralateral groove to serve as a docking guide. The needle was passed through the guide, exiting on the opposite side (Fig. 1b). This procedure was repeated with the same technique and needle 180° away. The standard distance between the 2 parallel threads was 4 mm. The knot was secured in the initial groove, thus protected by the sclera and preventing conjunctival erosion (Fig. 1c).
The threads formed an efficient support in a netting-shaped structure in which the IOL may be placed and positioned according to the surgeon’s discretion (Fig. 1d).
The IOL was inserted on the top of the net. Centration was easy, and no tilt was observed (Fig. 2). A 3-piece foldable IOL was implanted with better stabilization. In some cases, repositioning of a previously implanted IOL (single-piece foldable) was performed.
Additional file 1 shows the surgical technique.
Seventeen eyes of seventeen patients (9 males and 8 females) were enrolled in the study. The mean age was 67 years (range 33–86 years). Preoperative diagnoses included retinal detachment in 1 patient, surgical aphakia in 6 patients, trauma in 4 patients, posterior PPV due to diabetic retinopathy in 1 patient, lens subluxation in 3 patients and IOL explant due to endophthalmitis in 2 patients (Table 1). Follow-up ranged from 6 to 38 months, with an average of 23 months.
Postoperative best-corrected visual acuity (BCVA) was counting fingers in 3 patients (18%), 20/200 in 1 patient (6%), 20/80 in 2 patients (12%), 20/60 in 1 patient (6%), 20/30 in 2 patients (12%), 20/25 in 4 patients (23%), and 20/20 in 4 patients (23%) (Table 1). In all cases, the IOL was safely implanted. No intraoperative complications were observed. After a mean follow-up of 23 months, the lens remained well centered in 95% of cases. Slight dislocation occurred in 1 eye without the need for surgical repositioning. One case presented with pigmented dispersion. No increased pressure, glaucoma or uveitis was observed.
Distance-corrected visual acuity improved by a mean of 4 lines, from 20/200 (1.1 LogMAR) to 20/70 (0.54 LogMAR) (P = 0.01) (we used the LogMAR table from The Journal of Cataract and Refractive Surgery).
A 34-year-old male (Patient 3, Table 1) was seen on July 1st, 2014 after left eye trauma caused by a screwdriver. The patient underwent a corneo-scleral suture and hyphema wash for 5 days, which were performed at another health service. Upon examination, the patient presented with hand motion vision, cataract, phacodonesis, and retinal and choroidal detachment diagnosed by ultrasound.
The patient underwent phacoemulsification, IOL implantation in the ciliary sulcus, posterior vitrectomy and silicone oil implantation. The patient progressed to 20/400 vision and presented with an applied retina and a nasally dislocated IOL, which was supported on the ciliary sulcus, with a temporal haptic under the iris.
After 15 months, silicone oil removal was carried out with IOL repositioning according to the netting-shaped structure technique described above, which enabled positioning of the temporal haptic in the ciliary sulcus and IOL centralization.
Visual acuity increased to 20/80; 6 months post-op, the IOL remained well positioned and well centered.
A 56-year-old male patient (Patient 6, Table 1) presented with 5-day-old trauma in the right eye due to splitting wood with an ax. The patient reported loss of vision and pain immediately after the trauma. At our service, the patient presented with increased intraocular pressure, 2 mm hyphema, +/+++ corneal edema, cataract, phacodonesis and visual acuity with light perception. The patient was treated with anti-inflammatory and anti-hypertensive medications. After complete absorption of the hyphema and absence of intraocular inflammation, removal of the crystalline lens was performed.
With an estimated 270° zonular rupture, cataract removal was difficult, with dislocation of a crystalline lens fragment to the vitreous. Pars plana vitrectomy was performed. We chose to perform the netting-shaped structure technique described above for IOL implantation.
The patient progressed to 20/80 visual acuity with a well-positioned lens (Fig. 2a). Vision failed to fully recover due to the formation of an epiretinal membrane and optic disc color change, possibly resulting from trauma.
There are several options for the management of aphakia in the absence of capsular support. Among the definitive surgical options, lens implantation in the anterior or posterior segment is a potential option.
Among lenses implanted in the anterior chamber, the options include iris-suture-fixated lenses or iris fixation by enclavation [6, 8] and angle-supported anterior chamber phakic intraocular lenses , which are rarely used due to complications, such as endothelial loss, pupil distortion and secondary glaucoma .
In 1980, Van der Pol and Worst  described iris-fixated IOLs for the correction of aphakia in congenital cataract. Compared with earlier designed lenses, the Artisan lens, an iris-fixated polymethyl methacrylate IOL, has been considerably improved and is currently used in many countries for the correction of aphakia and high myopia in patients without capsular support. However, the Artisan lens must be iris-fixated.
Scleral fixation, whether by suture or enclavation through the ciliary sulcus, offers the advantage of maintaining a clear anterior chamber without interfering with the anatomy of the region. However, the surgical technique for this approach is more complex. Transscleral lens fixation may be performed with haptic suturing through the ciliary sulcus or pars plana [1, 3, 5] or without suturing [11–14].
In 2013, Samuel Masket described a technique that involves the creation of safety netting with a double-armed 10-0 polypropylene suture at the ciliary sulcus, which would act as support for handling IOLs lacking adequate capsular support for post-vitrectomy eyes and repositioning of IOLs. He also used this technique for secondary IOL implantation with intrascleral fixation. In this case, the netting acted as scaffolding for IOL implantation. In both situations, the polypropylene netting was removed after IOL fixation or repositioning . The creation of netting at the ciliary sulcus had been previously published in papers reporting silicone oil retention sutures performed to prevent silicone oil migration to the anterior chamber in aphakic eyes [16, 17].
The technique in our study is based on secondary IOL implantation at the ciliary sulcus with the lens supported by a 9.0 polypropylene suture without additional sutures or haptic fixation. Our netting provides full support for both the IOL body and the haptics. Follow-up revealed that the lenses implanted with our technique remained steady and centralized in nearly all cases. This netting provides several support points for the IOL; in addition, since the netting is created 2.0 mm away from the limbus, tilting, a frequent cause of complications in transscleral fixation , does not occur.
Another major advantage of this technique is IOL fixation even when iris fixation is not feasible, either due to iris tissue loss or atrophy. This technique could be useful in cases of absence of capsular support in patients with thin sclera; in these cases, scleral fixation is very technically challenging. One disadvantage of using a polypropylene suture for IOL support is that this suture may degrade , mainly when it is subjected to ultraviolet rays. An alternative for lessening this complication is the use of Gore-Tex® suture threads; this monofilament material is non-absorbable and has recently shown good results for IOL scleral fixation . Table 2 compares the results of our study with the results of other studies in the literature [21,22,23,24,25].
The intraocular lens implantation technique in which an IOL is placed anterior to the netting is a relatively low-cost and reproducible option. This technique might be especially useful in cases of insufficient capsular support associated with tissue loss or iris atrophy. In these cases, iris fixation is not feasible; thus, the only correction alternative is scleral fixation of intraocular lenses. The findings of this study demonstrate that the net technique for IOL support is a reproducible, safe and effective option for surgical treatment of aphakia with no capsular support.
The limitations of our study include the small sample size, short follow-up period and absence of a control group. Further comparative studies and longer follow-up periods are essential to assess the safety and effectiveness of this technique.
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All the authors significantly contributed to this research. FJN and TLG were the surgeons. All authors designed the study, participated in data acquisition and drafted the manuscript. RCG, GSR and FJN reviewed the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
The dataset supporting the conclusion of this article is included within Additional file 2 of the article.
Consent to participate
Included patients provided written informed consent.
Consent to publication
The material submitted in this manuscript has not been published nor simultaneously submitted for publication elsewhere. All authors consent to this statement. Consent for the publication of figures was obtained from the patients.
An institutional review committee approved this study, which followed the principles of the Declaration of Helsinki. This retrospective cohort study was carried out from April 2014 to April 2016.
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