A serious adverse surgical event

Herpes simplex keratitis (HSK) is one of the major causes of corneal inflammation and corneal blindness, rated just second to trauma in most developed countries [1‐3]. Clinical reports support the possible transmission of herpes simplex virus type 1 (HSV-1) via donor corneas and its role in graft failure [4]. Cleator et al. reported a case of primary graft failure due to presumed donor-to-host transmission of HSV following organ culture in a patient who underwent a penetrating keratoplasty for keratoconus [5]. It has also been reported that the HSV-1 may remain viable in stored corneal tissue at 4° [6]. There are reports of post-keratoplasty HSV-1 infection in patients with no history of an herpetic infection [7, 8] and evidence of donor-to-host transmission of the virus has also been demonstrated in animal studies. In rabbits, latently infected donor tissue can induce HSV-1 infection in naive recipients after penetrating keratoplasty [9]. HSV-1 inoculation in the anterior chamber of one eye has been shown to lead to the spread of virus to the brain, contralateral optic nerve and then posterior segment of contralateral eye [10, 11]. We report a case of clinically suspected HSK in the donor cornea following organ culture and subsequently in the recipient following penetrating keratoplasty and the perioperative management to reduce the infection risk and development of disease of the central nervous system.

A 68-year-old man underwent penetrating keratoplasty for aphakic bullous keratopathy and corneal scarring. He had no history of herpetic disease. The donor cornea originated from a 71-year-old female who died due to chronic pulmonary disease. The time interval between death and transfer of the corneoscleral button into organ culture medium was 36 h. The endothelial count was 2400cell/mm² with mild polymegethism and pleomorphism. A 8.5 mm Hessberg–Barron trephine was used to prepare the donor cornea and a 8 mm trephine for the recipient. After placement of the donor onto the aphakic eye a large dendritic-geographic epithelial ulcer was noted (Fig. 1). The graft was removed, all surgical instruments were changed and the surgical staff regowned. Fortunately, a second donor corneoscleral disc was available, which was then used to complete the operation instead of resuturing the patient’s own cornea back into place. The second donor originated from a 69-year-old male who died from a myocardial infarction. The time interval between death and transfer of the corneoscleral button into organ culture medium was 40 h. The endothelial count was 2600cell/mm² with some variation in cell size and shape.

Perioperative intravenous aciclovir was administered intravenously (5 mg/kg). Postoperatively, the patient was commenced on systemic and local antiviral therapy for 1 week (valaciclovir 1 g three times a day, acyclovir ointment five times per day) and local antibiotic treatment (chloramphenicol four times a day). Topical steroids were withheld for 48 h. At 1 week the graft was clear and had re-epithelialized. Long term prophylactic acyclovir 400 mg twice a day was commenced but 6 months later the patient developed a geographic corneal ulcer involving the graft-host interface (Fig. 2) with keratic precipitates and corneal oedema (central corneal thickness 710 μm). The patient was treated with acyclovir 400 mg and topical aciclovir both five times a day for 2 weeks with resolution of the ulcer and residual scarring. Although the patient had HSV IgG serum antibodies, evidence of HSV-1 DNA was not detected in the first donor cornea or following sampling of the corneal ulcer via PCR and culture methods.

The potential transmission of HSV-1 from donor to host has been recognized by clinical and laboratory studies [12‐14]. Viral particles have been found in keratocytes and endothelial cells [15] of corneal grafts with postoperative keratitis. HSV-1 is known to induce endothelial cell necrosis during organ culture, consistent with reports of postoperative keratitis [5, 16]. A rate of 1.2 per 1000 person-years has been reported for newly acquired herpetic keratitis in the early postoperative period [12]. Borderie et al. reported that HSV-1 was responsible for 3 out of 4 primary graft failures among 586 consecutive grafts performed [17]. Evidence of HSV-1 has been found in 10% of patients with diseased corneas with no history of HSK undergoing corneal transplantation [16] and also in cell pellets obtained from donor cornea culture medium in (%) (3 out of 80) donor corneas [18, 19]. Currently, however, screening assays are not undertaken by eye banks to identify HSV-1 in the donor cornea or medium during storage.

We describe a case of clinically suspected HSK in the donor cornea and subsequently in the recipient. Biswas et al. [20] described the development of primary graft failure and ulcerative keratitis in two patients, respectively [20]. Similar to our patient, they suggested transmission of HSV-1 through organ-cultured corneal graft in two patients in spite of negative results of PCR performed on both recipient corneas, based on the presence of endothelial cell necrosis in the fellow donor cornea in one of the cases. In the presented case HSV-1 originating from the host cannot be ruled out as the source of the described viral keratitis, but is deemed highly unlikely given the absence of previous herpetic disease. Although we were not able to isolate HSV-1 either from the donor or host, the clinical appearances were typical in both the donor and host. Intraoperative and perioperative antiviral treatment may have prevented potential intraocular spread to the posterior segment as described by Atherton and Streilein [10, 11] following anterior chamber inoculation and subsequent disease of the central nervous system in a similar mechanism to oronasal and vomeronasal spread [21‐23]. This case highlights the issue of being able to adequately examine the donor corneoscleral disc prior to use. Adequate biomicroscopic visualization of the donor cornea is not possible in the storage transport containers currently used for organ cultured corneas. This problem could be addressed by redesigning the transport chamber used for organ cultured corneas, or the use of hypothermic transport containers, which allow assessment of donor tissue by slit lamp biomicroscopy or the operating microscope before use [24].