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Refractive Surgery | Oct 2009

Corneal Remodeling Using the Keraring

A variety of thicknesses, arc lengths, and optical zone sizes allows tailoring of the procedure to the individual patient.

Keratoconus is one of the most challenging corneal pathologies faced by ophthalmologists. The onset of the disease during puberty and its often progressive course can have a potentially devastating impact on the patient's vision and overall quality of life.

Keratoconus treatment options were, until recently, limited to spectacles, contact lenses, and corneal transplantation. However, over the past few years, new diagnostic and therapeutic tools have greatly expanded our options to address keratoconus and other corneal ectatic disorders. Advanced contact lens materials and designs, ultraviolet (UV) collagen crosslinking (CXL), intrastromal corneal ring segments (ICRS), phakic IOLs, conductive keratoplasty, and modern wavefront- or topography-guided photoablative procedures have all been proposed for treatment of keratoconus.

Techniques that allow us to reshape the cornea for therapeutic purposes may collectively be called corneoplastics, a term coined by Arun C. Gulani, MD. Corneoplastics is spreading rapidly and becoming a new subspecialty allied to refractive and corneal surgery. But with so many treatment options now available, which is best? I believe there is not one best solution for all cases; our job is to select the best corneoplastic treatment or combination of treatments for each patient. Herein, I present my preferred option, Keraring ICRS (Mediphacos, Belo Horizonte, Brazil). Two articles to follow present other intrastromal corneal ring options.

In my personal practice at the Clinique de la Vision in Paris, femtosecond–laser-assisted implantation of the Keraring has been an important corneoplastic option for most of our keratoconic patients since 2004. The Keraring is an implantable device designed to correct corneal surface irregularities, improve UCVA and BCVA, and reduce refractive errors associated with keratoconus and other corneal ectatic disorders (Figure 1).

Our main indications for Keraring implantation are keratoconus with reduced BCVA and contact lens intolerance, progressing keratoconus, pellucid marginal degeneration, post-LASIK ectasia, and high amounts of regular or irregular astigmatism after penetrating keratoplasty.

In my experience with many eyes treated, post-LASIK ectasia is an excellent indication for Keraring implantation and probably one of the best options as it not only treats the ectatic cornea and reduces higher-order aberrations but also corrects refractive error in patients who desire a refractive procedure. I exclude patients presenting with keratometry readings greater than 60.00 D, extensive central corneal opacity, severe atopic disease, or unrealistic expectations regarding refractive result. I believe that it is extremely important to take time to properly educate patients about keratoconus and the objectives of the Keraring procedure so that they have realistic expectations.

The Keraring system is quite versatile, offering 40 combinations of ring segment thicknesses, arc lengths, and optical zones (Figure 2). The segments are available with thicknesses from 150 to 350 µm in 50 µm steps; arc lengths from 90° to 210° in 30° steps; and optical zones of 5, 5.5, and 6 mm. Depending on the case, one or two Keraring segments of the same or different sizes may be implanted. The implant is delivered with one ring segment per box so the surgeon can mix and match the sizes and number of segments implanted as desired.

Each Keraring size can be compared with a unique structural building block with specific properties of action on the corneal dome. By increasing the thickness we can increase the segment's effect; by varying the arc length we can independently modulate the sphere and cylinder correction; and by using different optical zones we can address variations in corneal pachymetry, pupil diameter, and stage of the disease. With an understanding of these properties, we can design a truly customized approach to corneal remodeling and refractive effect according to the individual case.

The refractive component of Keraring implantation improves UCVA. This is crucial for keratoconic patients, who are usually contraindicated for corneal refractive treatments and often intolerant of any optical correction.

Unlike other ICRS originally developed for myopic correction, which are mostly astigmatically neutral, the Keraring was designed specifically for keratoconus to intentionally induce high degrees of astigmatism. This mechanism allows us to position the implant in such a way that it corrects preexisting astigmatism by producing cylinder at the complementary axis. I find this ability to correct cylinder especially helpful in addressing advanced keratoconus and high astigmatism after penetrating keratoplasty. Asymmetric implantation allows us to treat irregular astigmatism and to decrease large amounts of higher-order aberrations, especially coma.

In my experience, the design of the Keraring and its variable optical zone of 5 to 6 mm produce greater effect than other ICRS that are implanted more peripherally. This is especially important to allow us to more effectively treat the severe corneal surface irregularities and high refractive errors that often accompany keratoconus.1 A smaller optical zone also prevents corneal neovascularization, which can sometimes be observed with other ICRS implanted closer to the limbus.

The incidence of glare and halos, which one would expect with the smaller optical zone, is reduced due to the Keraring's design. Its triangular cross-sectional shape produces a prismatic effect and mitigates visual disturbances in low light (Figure 3).

Although my clinical observations support the benefits of the prismatic design, for patients with mesopic pupil diameters greater than 5 mm and mild disease we have the option to implant the new Keraring SI-6 model at a 6-mm optical zone and further avoid glare (Figure 4). I also choose the SI-6 when I plan a secondary procedure such as topography-guided PRK or posterior chamber phakic IOL implantation. The SI-6 has a wide base, scalene triangular cross-section, and truncated apex design that provides 25% more implant volume compared with the SI-5 Keraring of similar thickness. This increased volume offsets the loss of effect expected from the larger optical zone.

Good surgical outcomes depend largely on careful patient selection, choice of implant size and location, and surgical technique. As a starting point for my surgical plans, I use the Keraring calculation guidelines and nomograms available from the manufacturer. These nomograms assist me in selecting the implant based on shape, extent, and distribution of the corneal ectasia; visual acuity; and aberrometric and manifest refraction values. However, as every ectatic cornea is unique, often I extrapolate the nomograms and design a more customized surgical plan. The technical help desk service offered by the manufacturer provides advice for surgical plan customization that I find useful for complex cases.

The surgical technique begins with construction of an intrastromal tunnel at a depth equivalent to 75% of the corneal thickness followed by implantation of the Keraring segments. The implantation tunnel can be dissected mechanically using special surgical instrumentation or created with a femtosecond laser such as the IntraLase2,3 (Abbott Medical Optics Inc., Santa Ana, California). We prefer to use a femtosecond–laser-assisted technique as we find it to be faster, less invasive, and more consistent than the mechanical technique. The IntraLase allows safe dissection of the stromal tunnel with the exact dimensions desired and consistent centration on the visual axis.

The entire procedure takes a few minutes and is performed under topical anesthesia on an outpatient basis. The technique is minimally invasive and sutureless. Patients receive a bandage contact lens for 24 hours and a prescription regimen with antibiotics and antiinflammatory drugs as in other corneal procedures. Most patients notice visual improvement by a few days after the procedure. Topographic and refraction changes can fluctuate during the first 3 months, and then they tend to stabilize.

Although the corneoplastic effects of implantation have been shown to be stable for several years in most cases, we can in cases of unstable cornea and progressive disease synergistically combine the Keraring with UV CXL to further stabilize the cornea and lock in the achieved result (Figure 5).

We prefer to first reshape the cornea with the Keraring and then perform CXL once a good result is obtained, usually 3 months or less after the first procedure. However, we prefer not to perform CXL unless we document progression of the disease or fluctuation of the refractive results.

Other interesting and potentially synergistic combinations include Keraring implantation followed by phakic IOL implantation or PRK plus UV CXL, when indicated. These techniques can often enhance the corneoplastic result and correct residual refractive error, further improving the overall result and patient satisfaction.

ICRS procedures are also reversible and adjustable. Topographic and refractive results may be adjusted by implant exchange or by changing the implant location. If necessary, explantation allows the cornea to revert to its preoperative shape with no sequelae. If the implant fails to provide acceptable results, or in the event of major complications, penetrating or lamellar keratoplasty can be performed without being affected by the implant's presence. The implant is removed with the host graft (Figure 6).

Complications are relatively rare and mostly related to poor surgical technique or wrong implant selection. Implant extrusion has been reported in rare cases and is often related to superficial implantation, excessive implant thickness, or implant position too close to the incision. Extrusion usually requires explantation with possible reimplantation after 90 days.4 Migration of the segment, usually caused by frequent eye rubbing, has also been occasionally described.4 It requires surgical repositioning of the implant and treatment of the associated atopic condition.

Infection is fortunately rare (0.2%), most often caused by poor patient compliance to the prescription drug regimen or an implant left too close to the incision. Depending on the severity of the infection, explantation or corneal transplantation may be required.

We have observed loss of BCVA in 2% of cases, attributable to poor surgical planning or technique. In such cases the implant size or position can be adjusted to improve the outcome. Persistent glare and halos were reported by 3% of patients, often related to poor centration of the implant or to patient susceptibility. Over time, most patients adjust to such symptoms, and for extreme cases miotic drops at dusk or even explantation are possible alternatives.

Case 1 (Figure 7) illustrates the evolution of the corneal topographic pattern over time. The initial effect of Keraring implantation is not complete at day 1. Stabilization of the cornea is achieved at 3 months after Keraring implantation. Preoperatively, this ectatic cornea had a maximal keratometric value of 53.00 D and BCVA of 20/32. At 3 months postop, UCVA was 20/20, even with the small amount of residual irregular astigmatism.

Case 2 (Figure 8) illustrates the effect induced by implantation of a pair of Keraring segments on the Orbscan (Bausch & Lomb, Rochester, New York) differential map. The effect on the cornea is clearly an induced cylindrical bowtie pattern when implantation is symmetrical.

Case 3 (Figures 9 and 10) is an incidence of post-LASIK ectasia after initial microkeratome LASIK probably performed on a cornea with pellucid marginal degeneration. BCVA is still 20/20, but the patient did not tolerate the optical correction and complained of poor quality of vision. After uneventful femtosecond–laser-assisted Keraring implantation, UCVA improved to 20/20, restoring the initial postoperative result. This patient was crosslinked in a secondary procedure, as ectasia showed recent progression.

Case 4 (Figure 11) illustrates how combining treatments can improve results. The Keraring always provides the main improvement in vision, and its effect can be enhanced by a secondary procedure such as topography-guided PRK, in this case allowing a central ablation of 36 µm and a gain of three lines of BCVA.

Modern corneoplastic techniques are dramatically changing the way we treat corneal ectatic disorders. Implantation of the Keraring either as a standalone or combined procedure can enhance our ability to deliver a customized approach to corneal remodeling and improve outcomes, potentially avoiding the need for corneal transplantation and improving patients' quality of life5 in many cases.

Dominique Pietrini, MD, practices at the Clinique de la Vision, Paris. He did not disclose financial interest. He may be reached at tel: +33 1 58 05 2000; fax: +33 1 58 05 2001; e-mail: dpietrini@club.fr.

Tony Guedj is an optometrist at the Clinique de la Vision, Paris. He did not disclose financial interest. He may be reached at e-mail: tony.guedj@yahoo.fr.

  1. Uceda-Montanes A, Tomás JD, Alió JL. Correction of severe ectasia after LASIK with intracorneal ring segments. J Refract Surg. 2008;24(4):408-411.
  2. Shabayek MH, Alió JL. Intrastromal corneal ring segment implantation by femtosecond laser for keratoconus correction. Ophthalmology. 2007;114(9):1643-1652.
  3. Coskunseven E, Kymionis GD, Tsiklis NS, et al. One-year results of intrastromal corneal ring segment implantation (KeraRing) using femtosecond laser in patients with keratoconus. Am J Ophthalmol. 2008;145(5):775-779.
  4. Coskunseven E, Kymionis GD, Tsiklis NS, et al. Complications of intrastromal corneal ring segment implantation using a femtosecond laser for channel creation: a survey of 850 eyes with keratoconus. Acta Ophthalmol. 2009 Aug 14 [Epub ahead of print].
  5. Paranhos JF, Avila MP, Paranhos A Jr, Schor P. Evaluation of the impact of intracorneal ring segments implantation on the quality of life of patients with keratoconus using the NEI-RQL (National Eye Institute Refractive Error Quality of life) instrument. Br J Ophthalmol. 2009 Sep 11 [Epub ahead of print].