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TitlePeripheral Ulcerative Keratitis: Clinical Outcomes at a Tertiary Academic Center
PurposePeripheral ulcerative keratitis is an inflammatory condition of the peripheral cornea resulting in thinning, stromal destruction, and eventual perforation. We evaluated the clinical course of patients with PUK to determine risk factors for perforation.
MethodsRetrospective study of 66 PUK patients seen at the Wilmer Eye Institute from January 2003 to August 2022. Data collected included demographics, immunosuppressive medications and doses, and whether perforation occurred.
ResultsThe median age was 54 years. 55% of patients were male, and 48% were caucasian. The median duration of ocular symptoms prior to presentation was 3 months. A systemic disease was present in 39 patients (59%); the most common was rheumatoid arthritis. At baseline, 55 eyes (42%) had corneal thinning, and 8 (6%) had perforated prior to presentation. During follow-up, 5 eyes (4%) perforated in a median time of 82 days. Surgical management consisted of a patch-graft (PG) in 3 eyes and a penetrating keratoplasty (PK) in 3 eyes. Two eyes required multiple surgical interventions: one with a PG then subsequent PK, and one with 2 successive PKs. At the time of perforation 3 of 5 patients were on corticosteroids, with a median dose of 60mg daily. Only one patient was taking a systemic immunosuppressive medication (mycophenolate mofetil dosed at 1 gram daily). Of all patients who experienced perforation 58% (N=7) had an underlying systemic illness.

ConclusionThe percentage of patients with PUK requiring PG or PK for corneal perforation decreases with aggressive initiation of prednisone with combination immunosuppressive therapy. Long term immunosuppressive therapy may be especially useful in those with an underlying autoimmune disorder.
Conflict of interestNo
Authors 1
Last nameMALLEM
Initials of first name(s)K
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States
Authors 2
Last nameChaon, MD
Initials of first name(s)B
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States
Authors 3
Last nameBurkholder, MD
Initials of first name(s)B
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States
Authors 4
Last nameWalsh, MD, PhD
Initials of first name(s)J
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States
Authors 5
Last nameThorne, MD, PhD
Initials of first name(s)J
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States
Authors 6
Last nameBerkenstock, MD
Initials of first name(s)M
Department Division of Ocular Immunology, Wilmer Eye Institute, Johns Hopkins School of Medicine,
CityBaltimore, MD
CountryUnited States