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Visual prognosis of crosslinking for kearatoconus based on preoperative corneal tomography

Abstracts

Purpose:

To verify pre-operative tomographic indices as predictive parameters for the improvement in best corrected visual acuity (BCVA) in one year after corneal collagen crosslinking (CXL) procedure for keratoconus.

Methods:

Retrospective study that included 63 eyes of 53 patients with progressive keratoconus submitted to CXL following the Dresden’s protocol: topical anesthesia, 9.0 mm of epithelial abrasion, riboflavin 0.1% drops for 30 minutes and ultraviolet-light A (UVA) with an irradiance of 3mW/cm2 for 30 minutes. Corneal tomography taken by Scheimplug rotational system (Pentacam, Oculus) before CXL was evaluated along with pre and 1 year post-operative BCVA. Statistical analysis was accomplished with the Kolmogorov-Smirnov test, student’s t-test and Receiver Operating Characteristic (ROC) curve.

Results:

There were statistically significant differences (p<0.05) between patients who improved BCVA in one year after CXL and those who did not experienced improvement in BCVA in the same period of time in the pre-operative tomographic indices related to corneal volume and thickness. Among those who had its BCVA improved all of them had a corneal volume in 6.0mm grater then 14.55mm3 and 97.2% of them had corneal volume in 6.5mm grater then 17.76mm3. So with 94.29% of them hadthickness in 4.0mm grater then 487μm and 82.86% had thickness on the thinnest point grater then 421μm.

Conclusion:

Patients with less advanced keratoconus (grater corneal volume and thickness) in the pre-operative had more chances to improve its BCVA in one year after CXL. Prospective studies involving others variables related to total aberrometry and corneal biomechanics are relevant to increase the prognostic capability of CXL result.


Objetivo:

Verificar índices tomográficos do pré-operatório de pacientes com ceratocone submetidos à crosslinking corneano (CXL) como fatores preditivos para a melhora na acuidade visual corrigidas (AVc) após um ano.

Métodos:

Estudo retrospectivo que incluiu 63 olhos de 53 pacientes com ceratocone progressivo submetidos à CXL segundo o protocolo de Dresden: deseptelização corneana, riboflavina 0,1% por 30 minutos e luz ultra-violeta A (UVA) a uma irradiância de 3mW/cm2 por 30 minutos. Foram avaliados exames de tomografia corneana com sistema de Scheimpflug rotacional (Pentacam, Oculus) antes do CXL e a acuidade visual corrigida antes e após a cirurgia. A análise estatística foi feita com o teste de Kolmorov-Smirnov, teste t de student e curvas de característica operador-receptor (ROC).

Resultados:

Houve diferença estatisticamente significante (p<0,05) entre os pacientes que obtiveram melhora de AVc em um ano e os que não experimentaram melhora na AVc nesse período nos índices tomográficos pré-operatórios relacionados com espessura e volume corneano. Entre os pacientes que obtiveram melhora na AVc todos possuíam volume corneano em 6,0mm maior que 14,55mm3 e 97,2% deles possuíam volume corneano em 6,5mm maior que 17,76mm3. Assim como, 94,29% desses pacientes apresentavam paquimetria média em 4,0mm maior que 487 μm e 82,86% paquimetria no ponto mais fino maior de 421 μm.

Conclusão:

Pacientes com ceratocone menos avançado (volume e espessura da córnea maiores) no período pré-operatório obtiveram mais chances de ter melhora da AVc um ano após CXL. Estudos prospectivos envolvendo outras variáveis relacionadas com a aberrometria total e o estudo biomecânico da córnea são relevantes para se aumentar a capacidade prognóstica do resultado após CXL.

Ceratocone; Tomografia da córnea; Prognóstico; Acuidade visual


INTRODUCTION

Keratoconus is a progressive, usually bilateral corneal ectasia whose treatment has changed in recent years. Until the past decade, treatments such as hard contact lenses, intrastromal corneal ring segment implantation, and corneal transplantation aimed to improve visual performance [1Rabinowitz YS. Keratoconus. SurvOphthalmol. 1998;42(4):297-319. Review.,2Siganos D, Ferrara P, Chatzinikolas K, Bessis N, Papastergiou G. Ferrara intrastromal corneal rings for the correction of keratoconus. J Cataract Refract Surg. 2002;28(11):1947-51.]. In the late 1990s and early 21st century [3Wollensak G, Spoerl E, Seiler T. Riboflavin/ultraviolet-a-induced collagen crosslinking for the treatment of keratoconus.Am J Ophthalmol. 2003;135(5):620-7.], the University of Dresden, Germany, began to study a new conservative treatment for keratoconus in human corneas based on the formation of covalent bonds in corneal collagen, called crosslinking (CXL). Its primary goal is to prevent the progression of ectasia by increasing the biomechanical stiffness of the cornea [4Spoerl E, Huhle M, Seiler T. Induction of cross-links in corneal tissue. Exp Eye Res. 1998;66(1):97-103.,5Wollensak G, Spoerl E, Seiler T. Stress-strain measurements of human and porcine corneas after riboflavin-ultraviolet-A-induced cross-linking. J Cataract Refract Surg. 2003;29(9):1780-5.].

In its original protocol [3Wollensak G, Spoerl E, Seiler T. Riboflavin/ultraviolet-a-induced collagen crosslinking for the treatment of keratoconus.Am J Ophthalmol. 2003;135(5):620-7.], CXL was induced by ultraviolet A radiation and riboflavin (vitamin B2), a water-soluble photosensitiser that penetrates the stroma in the absence of epithelium. Several studies have demonstrated its safety, stability, and ability to improve corneal topography and tomography indices, as well as corrected visual acuity (CVA) [7Spoerl E, Mrochen M, Sliney D,Trokel S, Seiler T. Safety of UVA-riboflavin cross-linking of the cornea. Cornea. 2007;26(4):385-9. Review.

Vinciguerra P,Albè E,Trazza S, Rosetta P,Vinciguerra R, Seiler T, et al. Refractive, topographic, tomographic, and aberrometric analysis of keratoconic eyes undergoing corneal cross-linking. Ophthalmology. 2009;116(3):369-78.

Koller T, Pajic B,Vinciguerra P, Seiler T. Flattening of the cornea after collagen crosslinking for keratoconus. J Cataract Refract Surg. 2011;37(8):1488-92.

10 Greenstein SA, Shah VP,Fry KL, Hersh PS. Corneal thickness changes after corneal collagen crosslinking for keratoconus and corneal ectasia: one-year results. J Cataract Refract Surg. 2011;37(4):691-700.
-1111 Raiskup-Wolf F, Hoyer A, Spoerl E, Pillunat LE. Collagen crosslinking with riboflavin and ultraviolet-A light in keratoconus: long-term results. J Cataract Refract Surg. 2008;34(5):796-801.]. CXL has also been suggested as an adjunctive therapy to rigid contact lenses and intrastromal corneal ring segment implantation [1212 AlmodinE,Arschinoff S,Almodin J,Ferrara P. [Addictive treatment of keratoconus with collagen crosslinking after Ferrara ring implant]. Rev BrasOftalmol.2009;68(3):138-45. Portuguese.]. However, complications related to the procedure, although infrequent, have been observed; they include scars and corneal opacities, persistent epithelial defect and, more rarely, bacterial keratitis [1313 Koller T, Mrochen M, Seiler T. Complication and failure rates after corneal crosslinking. J Cataract Refract Surg. 2009;35(8):1358-62.,1414 Pérez-Santonja JJ, Artola A, Javaloy J, Alió JL, Abad JL. Microbial keratitis after corneal collagen crosslinking. J Cataract Refract Surg. 2009;35(6):1138-40.].

Because CXL is not an innocuous treatment, prognostic factors able to predict the stability or improvement of patients submitted to the procedure are very important to refine its indication criteria. The present study aimed to identify preoperative corneal tomography indices that may predict whether the CVA of patients subjected to the procedure is likely to improve in one year.

METHODS

Data from patients with progressive keratoconus submitted to CXL were analysed retrospectively. Inclusion criteria were progressive ectasia followed up for at least six months and characterised by an increase in maximum keratometry (Kmax) by 1.00 D (equivalent to 3 standard deviations [SD] of the device repeatability) [1515 Koller T, Iseli HP, Hafezi F,Vinciguerra P, Seiler T. Scheimpflug imaging of corneas after collagen cross-linking. Cornea. 2009;28(5):510-5.] and Kmax <65.00 D. Exclusion criteria were preoperative superficial corneal opacities, as Scheimpflug images are unreliable in these cases; corneal pachymetry <400 µm even after instillation of hypotonic riboflavin; pregnancy; and other eye diseases, especially endothelial disease, history of recurrent erosion, and connective tissue disorders.

CXL was performed after topical anaesthesia with oxybuprocaine alternated with tetracaine eye drops every 3 minutes for 15 minutes. Corneal abrasion with a diameter of 9 mm was then performed. Riboflavin 0.1%, prepared immediately before treatment by diluting 0.5% aqueous riboflavin into a 20% dextran T-500 solution, was instilled every 3 minutes for 30 minutes. Central corneal ultrasonic pachymetry was then performed. In eyes where corneal thickness after epithelial removal was less than 400 ìm, 0.1% hypotonic riboflavin without dextran was added until the thickness reached 400 ìm; this was carefully monitored in all cases prior to the procedure. The presence of riboflavin in the anterior chamber was observed by slit lamp examination with a cobalt blue filter. The eye was then irradiated for 30 minutes using UVA light with an irradiance of 3 mW/cm2 (UV-X, Peschke Meditrade). During irradiation, riboflavin 0.1% was administered every 3 minutes and oxybuprocaine was administered as needed. At the end of the procedure, a 0.3% ofloxacin solution and bandage contact lenses were applied. The antibiotic was maintained for two days; after epithelial healing, patients used topical fluorometholone twice a day for one week.

CVA, tested with optotypes on a logarithmic scale, was assessed preoperatively and one year after treatment. Pre- and postoperative corneal tomography data were obtained with a rotating Scheimpflug system (Pentacam 70700™, Oculus).

Statistical analysis was done using BioEstatTM 5.3 software. The Kolmogorov-Smirnov test was used to assess whether the study population was normally distributed. Student's t-test was used to compare patients with and without improvement in CVA. ROC curves were calculated to determine the best cut-off values for parameters with statistically-significant differences. p-values <0.05 were considered statistically significant.

RESULTS

Of the 53 patients (63 eyes), 21 were female and 32 were male. Mean age was 29.4 ± 9.4 years (range: 15 to 56 years). After one year, CVA had improved in 35 eyes (55.6%), remained stable in 12 eyes (19%), and worsened in 16 eyes (25.4%).

Table 1 presents the differences in CVA, indices of central keratometry, and corneal thickness and volume before and one year after CXL. Statistically-significant differences were observed, with CVA improvement, flattening of the flattest corneal meridian (K1), reduction of corneal volume between the 2 mm and 4.5 mm diameters, and corneal thinning at the thinnest point and at the 2 mm diameter.

Table 1
Tomographic indices before and after CXL

Patients whose CVA improved in one year had a statistically higher (p<0.05) preoperative corneal volume at the 2.0 to 7.0 mm diameters, as shown by 11 tomographic indexes (Table 2, Figure 1). Among the indices that performed better (largest area under the ROC curve), corneal volumes at 6.0 and 6.5 mm presented a sensitivity of 100% and 97.14% at the 14.55 and 17.76 mm3 cut-off points, respectively. In addition to the good sensitivity, only 12% of patients with these characteristics presented a decrease in CVA. The corneal volume at 7 mm had a specificity of 60.7% at the 21.43 mm3 cut-off point (Table 3, Figure 1).

Table 2
Preoperative tomographic indexes
Table 3
Receiver operating characteristic (ROC) curve analysis
Figure 1
Box-plot presenting the comparison of corneal volume between patients with or without CVA improvement.

C. Vol.: Corneal volume


Patients whose CVA improved in one year (p<0.05) also showed better preoperative corneal thickness values in five tomographic indexes: pachymetry at the thinnest point and at the 2, 4, 6, and 8 mm diameters (Table 2, Figure 2). Of these, pachymetry at 4 mm and at the thinnest point had a sensitivity of 94.29% and 82.86% at the 487 µm and 421 µm cut-off points, respectively (Table 3). For these pachymetry values at 4 mm and at the thinnest point, 12.8% and 13.6% of patients, respectively, presented a decrease in CVA.

Figure 2
Box-plot comparing corneal thickness among patients with or without CVA improvement.

Min. Pach.: pachymetry at the thinnest point; Pach.: pachymetry


DISCUSSION

CXL was initially proposed as a method to increase the biomechanical stiffness of the cornea and slow the progression of ectasia; however, as the method started to be used, in many patients corneal ectasia not only stabilised, but also improved. In CVA: Best corrected visual acuity expressed as LogMAR; K1: Central corneal curvature at the flattest meridian; K2: Central corneal curvature at the steepest meridian;Astig.: central corneal astigmatism;C.Vol.: corneal volume; Min. Pach.: pachymetry at the thinnest point; Pach.: corneal pachymetry particular, the procedure improves high-contrast CVA, which is an objective measure visual function widely used in the ophthalmic practice.

In the present sample, flattening at K1 and reduced corneal volume and thickness were observed. These results are in agreement with the literature and may indicate compression of corneal collagen fibres and increased corneal resistance.

CVA improved in 55.6% of patients submitted to CXL - slightly less than the 65% observed by Wollensak et al. [3Wollensak G, Spoerl E, Seiler T. Riboflavin/ultraviolet-a-induced collagen crosslinking for the treatment of keratoconus.Am J Ophthalmol. 2003;135(5):620-7.]. The CVA of patients with greater corneal volume and thickness was more likely to improve in one year.

Our results presented high sensitivity, suggesting that the less advanced the ectasia, the greater the chance of CVA improvement and the lesser the chance of CVA worsening one year after CXL. Conversely, patients with more advanced ectasia are unlikely to achieve CVA improvement in one year. These results can help refine the indications for the procedure, so as to avoid its indication to patients who are unlikely to improve.

Prospective studies involving other variables related to total aberrometry and biomechanical studies of the cornea are important to improve our ability to accurately predict the outcomes of CXL. Further studies involving other means of assessing visual function, such as contrast sensitivity [1616 Ginsburg AP. Contrast sensitivity: determining the visual quality and function of cataract, intraocular lenses and refractive surgery. CurrOpinOphthalmol. 2006;17(1):19-26. Review.] and assessment of brain neuroplasticity, may help clarify how visual quality improves in these patients and how this affects their daily activities [1717 Braddick O, Atkinson J. Development of human visual function. Vision Res. 2011;51(13):1588-609. Review.,1818 Li R,Polat U, Makous W, Bavelier D. Enhancing the contrast sensitivity function through action video game training. Nat Neurosci. 2009;12(5):549-51.].

In the present study, patients with less advanced keratoconus (higher volume and corneal thickness) preoperatively were more likely to achieve CVA improvement one year after CXL. Prospective studies involving other variables related to total aberrometry and biomechanical studies of the cornea would help improve our ability to predict the outcomes of CXL.

  • Study conducted at the Renato Ambrósio Eye Institute, Rio de Janeiro/RJ, Brazil.

REFERÊNCIAS

  • 1
    Rabinowitz YS. Keratoconus. SurvOphthalmol. 1998;42(4):297-319. Review.
  • 2
    Siganos D, Ferrara P, Chatzinikolas K, Bessis N, Papastergiou G. Ferrara intrastromal corneal rings for the correction of keratoconus. J Cataract Refract Surg. 2002;28(11):1947-51.
  • 3
    Wollensak G, Spoerl E, Seiler T. Riboflavin/ultraviolet-a-induced collagen crosslinking for the treatment of keratoconus.Am J Ophthalmol. 2003;135(5):620-7.
  • 4
    Spoerl E, Huhle M, Seiler T. Induction of cross-links in corneal tissue. Exp Eye Res. 1998;66(1):97-103.
  • 5
    Wollensak G, Spoerl E, Seiler T. Stress-strain measurements of human and porcine corneas after riboflavin-ultraviolet-A-induced cross-linking. J Cataract Refract Surg. 2003;29(9):1780-5.
  • 6
    Renesto Ada C, Sartori M, Campos M. [Cross-linking and intrastromal corneal ring segment]. Arq Bras Oftalmol. 2011;74(1):67-74. Review. Portuguese.
  • 7
    Spoerl E, Mrochen M, Sliney D,Trokel S, Seiler T. Safety of UVA-riboflavin cross-linking of the cornea. Cornea. 2007;26(4):385-9. Review.
  • 8
    Vinciguerra P,Albè E,Trazza S, Rosetta P,Vinciguerra R, Seiler T, et al. Refractive, topographic, tomographic, and aberrometric analysis of keratoconic eyes undergoing corneal cross-linking. Ophthalmology. 2009;116(3):369-78.
  • 9
    Koller T, Pajic B,Vinciguerra P, Seiler T. Flattening of the cornea after collagen crosslinking for keratoconus. J Cataract Refract Surg. 2011;37(8):1488-92.
  • 10
    Greenstein SA, Shah VP,Fry KL, Hersh PS. Corneal thickness changes after corneal collagen crosslinking for keratoconus and corneal ectasia: one-year results. J Cataract Refract Surg. 2011;37(4):691-700.
  • 11
    Raiskup-Wolf F, Hoyer A, Spoerl E, Pillunat LE. Collagen crosslinking with riboflavin and ultraviolet-A light in keratoconus: long-term results. J Cataract Refract Surg. 2008;34(5):796-801.
  • 12
    AlmodinE,Arschinoff S,Almodin J,Ferrara P. [Addictive treatment of keratoconus with collagen crosslinking after Ferrara ring implant]. Rev BrasOftalmol.2009;68(3):138-45. Portuguese.
  • 13
    Koller T, Mrochen M, Seiler T. Complication and failure rates after corneal crosslinking. J Cataract Refract Surg. 2009;35(8):1358-62.
  • 14
    Pérez-Santonja JJ, Artola A, Javaloy J, Alió JL, Abad JL. Microbial keratitis after corneal collagen crosslinking. J Cataract Refract Surg. 2009;35(6):1138-40.
  • 15
    Koller T, Iseli HP, Hafezi F,Vinciguerra P, Seiler T. Scheimpflug imaging of corneas after collagen cross-linking. Cornea. 2009;28(5):510-5.
  • 16
    Ginsburg AP. Contrast sensitivity: determining the visual quality and function of cataract, intraocular lenses and refractive surgery. CurrOpinOphthalmol. 2006;17(1):19-26. Review.
  • 17
    Braddick O, Atkinson J. Development of human visual function. Vision Res. 2011;51(13):1588-609. Review.
  • 18
    Li R,Polat U, Makous W, Bavelier D. Enhancing the contrast sensitivity function through action video game training. Nat Neurosci. 2009;12(5):549-51.

Publication Dates

  • Publication in this collection
    Jul-Aug 2014

History

  • Received
    06 June 2013
  • Accepted
    09 Apr 2014
Sociedade Brasileira de Oftalmologia Rua São Salvador, 107 , 22231-170 Rio de Janeiro - RJ - Brasil, Tel.: (55 21) 3235-9220, Fax: (55 21) 2205-2240 - Rio de Janeiro - RJ - Brazil
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