Printer Friendly

Simultaneous Noncentered Photoactivated Chromophore for Keratitis-Corneal Collagen Cross-Linking and Penetrating Keratoplasty for Treatment of Severe Marginal Fusarium spp. Keratitis: A Description of a New Surgical Technique.

1. Introduction

Fungal keratitis is a major concern for cornea surgeons, especially those in developing nations. Although topical antifungal therapy continues to be the gold-standard for treatment worldwide, photoactivated chromophore for keratitis-corneal collagen cross-linking (PACK-CXL) has been explored as an option for decreasing the likelihood of complications, specially corneal perforation.

When a corneal perforation does occur, an emergent tectonic penetrating keratoplasty (PK) is indicated. Nevertheless, a marginal keratitis with limbal involvement and a perforated central defect can represent a real challenge for the corneal surgeon. A regular PK leaves a small amount of infected receptor cornea in place, in which infectious agents can survive and infect the corneal graft, despite intensive topical antifungal treatment. A penetrating sclerokeratoplasty is not an easy option either, as it is a difficult-to-perform surgery, with a high rate of complications, including chronic glaucoma.

Studies in humans have demonstrated the ability of crosslinking to control corneal infections and stop melting in those patients in whom pharmacological management is ineffective. It could also decrease the probability of corneal perforation and the need for an emergent penetrating keratoplasty. Nevertheless, so far no paper has described PACKCXL surgery immediately after PK once corneal perforation has ensued. In this paper, the authors present, to the best of their knowledge, the first published instance in which simultaneous PK and PACK-CXL were performed as treatment for a central corneal perforation with a marginal corneal compromise. This case highlights the possibility of PACKCXL to help in the management of patients undergoing emergency PK in a context in which not all infectious burden can be removed. It also serves as a support to suggest that CXL could be safely undertaken immediately following PK, an approach which maybe used for many other applications.

2. Case Report

A 39-year-old male patient, with no relevant personal history, presented to our cornea clinic complaining of a week duration of severe pain, tearing, redness, and blurred vision in the right eye. He worked as a farmer and janitor in a rural potato plantation in Colombia and had a history of working with soil and plants. On physical examination, his vision on the right eye was 20/400 (0.05, LogMAR 1.3). His right cornea had a 2 x 2 mm inferotemporal ulcer surrounded by a dense infiltrate that compromised all the way but 1.5 mm before the corneal limbus. Corneal thinning at the site of ulcer was about 50%. Clinical examination of his left eye was completely unremarkable. The patient was instructed to start hourly gatifloxacin 0.5% and hourly natamycin 5%. Sodium hyaluronate 4 mg/mL was also ordered. The patient presents to our clinic a week after medications were ordered. The patient had not started medication yet, due to his very poor socioeconomic status (which hindered his option of buying the medicines himself) and his nearly nonfunctional health insurance which refused to pay for the drops. He complained of increased eye redness and pain. On clinical examination, there was a 2 x 2 mm descemetocele overlying a large infectious infiltrate with featheryborders that compromised all the way to the sclerocorneal limbus. There was a localized limbal insufficiency. There was an almost complete shallowing of the anterior chamber and a cataract (Figure 1). Due to a complete perforation of the cornea, a standard PACK-CXL was not considered possible, so an emergent, "a chaud," PK was ordered. Simultaneous noncentered PACK-CXL was also ordered for treatment of the peripheral infiltrate, due to the patient's poor access to medications.

Surgery (Figure 2) was performed by one of the authors (K.B.) under general anesthesia: donor and receptor corneas were cut with an 8.50 mm and 8.00 mm trephine, respectively. The cut was centered on the receptor cornea, which was sent for culture. Open-Sky lensectomy was performed with a cystotome, as well as hydrodissection. Aspiration of cortical material was performed with bimanual irrigation/aspiration cannulas, with intraocular lens implantation in the ciliary sulcus, followed by intracameral acetylcholine. Donor cornea was sutured with 10-0 nylon. Then, the eye was impregnated with a solution containing riboflavin 0.1% and dextran 500 (Keralynx[R], Nanosigma Biotech Ltd, New Taipei City, Taiwan) at a dose of one application every three minutes for 30 minutes before ultraviolet light exposure. Irradiation with ultraviolet was performed with a CXL machine (UV-X 2000[R], Avedro Inc., Waltham, United States) (Figure 3) for ten minutes, aiming for an energy dose of 9 mW/[cm.sup.2]. During irradiation, riboflavin irrigation was continued at a rate of one drop every three minutes. An irradiation spot size of 7 mm was used. The patient's eye was grasped superiorly with a 0.30 mm forceps and pulled upwards so the infected area of cornea and limbus was exposed. UV irradiation beam was positioned so that it included part of the donor cornea, the whole infected receptor cornea, affected limbus, and a small part of sclera (Figure 4). After the irradiation, riboflavin was flushed with copious irrigation of balanced salt solution.

Corneal culture was positive for Fusarium spp. Due to the patient's economic status and insurance, he could only start antibiotic and antifungal treatment about 21 days after surgery (Figure 5). His regimen consisted of hourly natamycin, hourly fortified vancomycin, and sodium hyaluronate every two hours. The dose of the drops was slowly tampered.

During the follow-up period (over four months) the patient has shown an excellent recovery; his eye inflammation has been as expected for a penetrating keratoplasty, and no clinical signs of infection recurrence have been noted (Figure 6). On last clinical evaluation, his pinhole visual acuity was 20/60 (LogMAR 0.47), and he was pain-free, with a clear corneal graft.

3. Discussion

The current cross-linking (CXL) technique was first described by Sporl et al. in 1997 [1]; however the antimicrobial properties of riboflavin in combination with UVA light were reported much earlier in 1965 1965 by Tsugita et al. [2]. Since then, it is used for the eradication of microorganisms in water, food, and blood products. Designating the name of photoactivated chromophore for keratitis-corneal collagen cross-linking (PACK-CXL) to the applications of the technique focused on the management of infectious keratitis has been proposed [3, 4]. The mechanism that explains the antimicrobial action is the release of reactive oxygen species and the damage to DNA and RNA of pathogens [5-7]. This effect has been studied in in vitro experiments for both bacterial and fungal keratitis, being higher if riboflavin is combined with UVA light [8]. The cross-linking strengthens corneal collagen degradation by collagenolytic enzymes induced by microorganisms [9]. In addition to these properties, possible nociceptive and anti-inflammatory effects have been reported [10, 11]. Studies in humans have demonstrated the ability of cross-linking to control corneal infections and stop melting in those patients in whom pharmacological management is ineffective. It could also decrease the possibility of a corneal perforation and the need for an emergent penetrating keratoplasty [12-17]. The use of PACK-CXL without antimicrobial agents has also been proposed and its efficacy has been demonstrated in small-sized keratitis [18]. The fungicidal effect has been demonstrated in vitro and in animals for Candida albicans, Fusarium sp. [19], and Aspergillus fumigatus [20], in addition to potentiating the effect of antifungal agents such as amphotericin-B [21]. Studies performed in humans have also demonstrated the effectiveness against fungi [22]. However, there are studies that question its fungicidal effect on deep stromal keratitis [23, 24]. The PACK-CXL protocol has been variable, but most of the studies have used the conventional protocol with irradiation of 365 nm and 3mW/[cm.sup.2]. Some authors have also used an accelerated protocol with irradiation of 365 nm and 9mW/[cm.sup.2] for 10 minutes [6, 25]. The use of PACK-CXL has been reported in corneas with penetrating keratoplasties with infectious keratitis due to Staphylococcus aureus, 12 months after the procedure, with good results [26]. The use of CXL in penetrating keratoplasty has also been reported as a safe method, in addition to hypothetically decreasing the rate of graft rejection [27, 28] and causing a stronger adhesion between donor tissue and receptor [29].

In our case, combining simultaneous noncentered PACKCXL with centered tectonic penetrating keratoplasty was carried out to treat the fungal marginal keratitis with corneal perforation, in which regular penetrating keratoplasty alone would leave fungal elements in the receptor corneal tissue, which would predispose to infection of the graft. To our knowledge, it is the first reported case worldwide in which the two procedures are done simultaneously, one immediately after the other. PACK-CXL was performed in an decentered way to cover the infiltrates in the lower periphery that could not be removed during the keratoplasty, first performing the keratoplasty to remove the thinned tissue containing the infection, preventing the adverse effects of the UV light on the endothelium [30]. The limbal insufficiency in the inferior zone observed in our case was caused as a consequence of the infection and was present before the surgical procedure. Therefore we can conclude that combining simultaneous noncentered PACK-CXL with centered penetrating keratoplasty appears to be a safe and effective way of treating patients with fungal marginal keratitis with corneal perforation, in which regular penetrating keratoplasty alone would leave fungal elements in the receptor corneal tissue, which would predispose to infection of the graft.

4. Conclusions

(i) Studies in humans have demonstrated the ability of cross-linking to control corneal infections and stop melting in those patients in whom pharmacological management is ineffective. It can also be used to decrease the possibility of requiring an emergent penetrating keratoplasty.

(ii) Combining simultaneous noncentered PACK-CXL with centered penetrating keratoplasty appears to be a safe and effective way of treating patients with fungal marginal keratitis with corneal perforation.

Conflicts of Interest

The authors declare no financial or proprietary interest.


The authors wish to thank Paula Upegui, B.S., and Sandra Patricia Hernandez, B.S. (Clinica de Oftalmologia Sandiego, Medellin, Colombia), for their valuable theoretical assistance and insight into cross-linking application in atypical cases.


[1] E. Sporl, M. Huhle, M. Kasper, and T. Seiler, "Increased rigidity of the cornea caused by intrastromal cross-linking," Der Ophthalmologe, vol. 94, no. 12, pp. 902-906, 1997.

[2] A. Tsugita, Y. Okada, and K. Uehara, "Photosensitized inactivation of ribonucleic acids in the presence of riboflavin," Biochimica et Biophysica Acta, vol. 103, no. 2, pp. 360-363,1965.

[3] F. Hafezi and J. Bradley Randleman, "PACK-CXL: Defining CXL for infectious keratitis," Journal of Refractive Surgery, vol. 30, no. 7, pp. 438-439, 2014.

[4] D. Tabibian, O. Richoz, and F. Hafezi, "PACK-CXL: Corneal cross-linking for treatment of infectious keratitis," Journal of Ophthalmic & Vision Research, vol. 10, no. 1, pp. 77-80, 2015.

[5] G. P. Pfeifer, "Formation and processing of UV photoproducts: Effects of DNA sequence and chromatin environment," Photochemistry and Photobiology, vol. 65, no. 2, pp. 270-283,1997.

[6] Prashant Garg and Aravind Roy, "Collagen cross-linking for microbial keratitis," Middle East African Journal of Ophthalmology, vol. 24, pp. 18-23, 2017.

[7] A. L. Santos, V. Oliveira, I. Baptista et al., "Wavelength dependence of biological damage induced by UV radiation on bacteria," Archives of Microbiology, vol. 195, no. 1, pp. 63-74, 2013.

[8] S. A. R. Martins, J. C. Combs, G. Noguera et al., "Antimicrobial efficacy of riboflavin/UVA combination (365 nm) in vitro for bacterial and fungal isolates: a potential new treatment for infectious keratitis," Investigative Ophthalmology & Visual Science, vol. 49, no. 8, pp. 3402-3408, 2008.

[9] E. Spoerl, G. Wollensak, and T. Seiler, "Increased resistance of crosslinked cornea against enzymatic digestion," Current Eye Research, vol. 29, no. 1, pp. 35-40, 2004.

[10] G. D. Kymionis, D. G. Mikropoulos, D. M. Portaliou, I. C. Voudouragkaki, V. P. Kozobolis, and A. G. P. Konstas, "An overview of corneal collagen cross-linking (CXL)," Advances in Therapy, vol. 30, no. 10, pp. 858-869, 2013.

[11] R. Shetty, H. Nagaraja, C. Jayadev, Y. Shivanna, and T. Kugar, "Collagen crosslinking in the management of advanced nonresolving microbial keratitis," British Journal of Ophthalmology, vol. 98, no. 8, pp. 1033-1035, 2014.

[12] H. P. Iseli, M. A. Thiel, F. Hafezi, J. Kampmeier, and T. Seiler, "Ultraviolet a/riboflavin corneal cross-linking for infectious keratitis associated with corneal melts," Cornea, vol. 27, no. 5, pp. 590-594, 2008.

[13] K. Makdoumi, J. Mortensen, and S. Crafoord, "Infectious keratitis treated with corneal crosslinking," Cornea, vol. 29, no. 12, pp. 1353-1358, 2010.

[14] D. G. Said, M. S. Elalfy, Z. Gatzioufas et al., "Collagen crosslinking with photoactivated riboflavin (PACK-CXL) for the treatment of advanced infectious keratitis with corneal melting," Ophthalmology, vol. 121, no. 7, pp. 1377-1382, 2014.

[15] A. Panda, S. N. Krishna, and S. Kumar, "Photo-activated riboflavin therapy of refractory corneal ulcers," Cornea, vol. 31, no. 10, pp. 1210-1213, 2012.

[16] M. O. Price, L. R. Tenkman, A. Schrier, K. M. Fairchild, S. L. Trokel, and F. W. Price Jr., "Photoactivated riboflavin treatment of infectious keratitis using collagen cross-linking technology," Journal of Refractive Surgery, vol. 28, no. 10, pp. 706-713, 2012.

[17] S. Bamdad, H. Malekhosseini, and A. Khosravi, "Ultraviolet A/riboflavin collagen cross-linking for treatment of moderate bacterial corneal ulcers," Cornea, vol. 34, no. 4, pp. 402-406, 2015.

[18] K. Makdoumi, J. Mortensen, O. Sorkhabi, B.-E. Malmvall, and S. Crafoord, "UVA-riboflavin photochemical therapy of bacterial keratitis: A pilot study," Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 250, no. 1, pp. 95-102, 2012.

[19] G. Galperin, M. Berra, J. Tau, G. Boscaro, J. Zarate, and A. Berra, "Treatment of fungal keratitis from fusarium infection by corneal cross-linking," Cornea, vol. 31, no. 2, pp. 176-180, 2012.

[20] R. T. Kashiwabuchi, F. R. S. Carvalho, Y. A. Khan, F. Hirai, M. S. Campos, and P. J. McDonnell, "Assessment of fungal viability after long-wave ultraviolet light irradiation combined with riboflavin administration," Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 251, no. 2, pp. 521-527, 2013.

[21] A. Sauer, V. Letscher-Bru, C. Speeg-Schatz et al., "In vitro efficacy of antifungal treatment using riboflavin/UV-A (365 nm) combination and amphotericin B," Investigative Ophthalmology & Visual Science, vol. 51, no. 8, pp. 3950-3953, 2010.

[22] Z. Li, V. Jhanji, X. Tao, H. Yu, W. Chen, and G. Mu, "Riboflavin/ultravoilet light-mediated crosslinking for fungal keratitis," British Journal of Ophthalmology, vol. 97, no. 5, pp. 669-671, 2013.

[23] M. Uddaraju, J. Mascarenhas, M. R. Das et al., "Corneal crosslinking as an adjuvant therapy in the management of recalcitrant deep stromal fungal keratitis: A randomized trial," American Journal of Ophthalmology, vol. 160, no. 1, pp. 131-134, 2015.

[24] R. B. Vajpayee, S. N. Shafi, P. K. Maharana, N. Sharma, and V. Jhanji, "Evaluation of corneal collagen cross-linking as an additional therapy in mycotic keratitis," Clinical & Experimental Ophthalmology, vol. 43, no. 2, pp. 103-107, 2015.

[25] L. Papaioannou, M. Miligkos, and M. Papathanassiou, "Corneal Collagen Cross-Linking for Infectious Keratitis: A Systematic Review and Meta-Analysis," Cornea, vol. 35, no. 1, pp. 62-71, 2015.

[26] G. Labiris, A. Giarmoukakis, R. Larin, H. Sideroudi, and V. P. Kozobolis, "Corneal collagen cross-linking in a late-onset graft infectious ulcer: a case report," Journal of Medical Case Reports, vol. 8, article 180, 2014.

[27] G. Wollensak, E. Spoerl, M. Wilsch, and T. Seiler, "Keratocyte apoptosis after corneal collagen cross-linking using riboflavin/UVA treatment," Cornea, vol. 23, no. 1, pp. 43-49, 2004.

[28] F. Wang, "UVA/riboflavin-induced apoptosis in mouse cornea," Ophthalmologica, vol. 222, no. 6, pp. 369-372, 2008.

[29] G. Rocha, M. Butler, A. Butler, and J. M. Hackett, "Femtosecond-UVA-riboflavin (FUR) cross-linking approach to penetrating keratoplasty and anterior lamellar keratoplasty," Saudi Journal of Ophthalmology, vol. 25, no. 3, pp. 261-267, 2011.

[30] G. Wollensak, E. Sporl, F. Reber, L. Pillunat, and R. Funk, "Corneal endothelial cytotoxicity of riboflavin/UVA treatment in vitro," Ophthalmic Research, vol. 35, no. 6, pp. 324-328, 2003.

Kepa Balparda, (1) Juan Carlos Mejia-Turizo, (2) and Tatiana Herrera-Chalarca (3)

(1) Department of Cornea and Refractive Surgery, Clinica de Oftalmologia Sandiego, Medellin, Colombia

(2) Department of Ophthalmology, Clinica de Oftalmologia Sandiego, Medellin, Colombia

(3) Universidad de Antioquia, Medellin, Colombia

Correspondence should be addressed to Kepa Balparda;

Received 16 September 2017; Revised 17 November 2017; Accepted 23 November 2017; Published 14 December 2017

Academic Editor: Maurizio Battaglia Parodi

Caption: Figure 1: Clinical appearance of the patient before surgery. Please note a corneal perforation surrounded by a dense infiltrate (A) associated with inferior neovascularization (B).

Caption: Figure 2: Simultaneous noncentered photoactivated chromophore for keratitis-corneal collagen cross-linking (PACK-CXL) and penetrating keratoplasty. (a) Corneal trephination. (b) Cornea removal. (c) Open-sky cataract removal. (d) Intraocular lens implantation. (e) Donor cornea suturing. (f) Riboflavin impregnation.

Caption: Figure 3: Cross-linking lamp used for the treatment of the patient (UV-X 2000, Avedro Inc., Waltham, United States).

Caption: Figure 4: Schematic representation of the areas of the eye covered by the penetrating keratoplasty procedure (blue circle, 8 mm) and the noncentered PACK-CXL (green circle, 7 mm).

Caption: Figure 5: Clinical appearance of the patient three weeks after surgery. Note some natamycin over the eye.

Caption: Figure 6: Clinical appearance of the patient two months after surgery, showing a complete resolution of infection, with conjunctivalization replacing the area that was infected in the receptor rim.
COPYRIGHT 2017 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Case Report
Author:Balparda, Kepa; Mejia-Turizo, Juan Carlos; Herrera-Chalarca, Tatiana
Publication:Case Reports in Ophthalmological Medicine
Date:Jan 1, 2017
Previous Article:Atypical Presentation of Idiopathic Bilateral Optic Perineuritis in a Young Patient.
Next Article:Optical Coherence Tomography Angiography of Macular Telangiectasia Type 2 with Associated Subretinal Neovascular Membrane.

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |