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. 2021 Sep;10(3):565-580.
doi: 10.1007/s40123-021-00351-4. Epub 2021 Jun 12.

Noninfectious Intermediate, Posterior, or Panuveitis: Results from the Retrospective, Observational, International EyeCOPE Study

Collaborators, Affiliations

Noninfectious Intermediate, Posterior, or Panuveitis: Results from the Retrospective, Observational, International EyeCOPE Study

Michal Kramer et al. Ophthalmol Ther. 2021 Sep.

Abstract

Introduction: The EyeCOPE study characterized noninfectious intermediate posterior, or panuveitis (NIIPPU) before biologic agents were widely available.

Methods: This retrospective, observational study included adults with NIIPPU attending a routine ophthalmological visit. Data were collected from the study visit and medical records.

Results: Of 565 patients, 58.8% were female, and the mean age was 41.3 years; 33.8% had idiopathic uveitis and 45.8% had panuveitis. The median time from symptom onset to diagnosis and treatment was 27.0 and 30.5 days, respectively. Patients received immunosuppressants and systemic/local corticosteroids. Most patients experienced substantial decline in ocular function (mean best corrected visual acuity, 0.4 logMAR). Mean total work productivity impairment among employed patients was 31.0%. Most patients reported ocular complications (70.8%) such as vision loss and cataracts.

Conclusions: Despite treatment, most patients with NIIPPU experienced a decline in ocular function and ocular complications. There is an unmet need for additional NIIPPU treatment, such as targeted monoclonal antibodies.

Keywords: Corticosteroid disease burden; Disease characteristics; Immunosuppressants; Noninfectious uveitis; Patient-reported outcomes.

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Figures

Fig. 1
Fig. 1
Summary of AC cell gradea (a), VH gradeb (b), and presence of active inflammatory chorioretinal and/or inflammatory retinal vascular lesionsb (c). MAS population with left (n = 559) and right (n = 558) eye. Patients with valid data were included and percentages were calculated based on non-missing values. aMissing data from one left eye. bMissing data from two left eyes. AC anterior chamber, MAS main analysis set, NEI National Eye Institute, SUN Standardization of Uveitis Nomenclature, VH vitreous haze
Fig. 2
Fig. 2
Summary of treatment patterns in NIIPPU patients (MAS population). Systemic therapies (a) and topical and injectable corticosteroid therapies (b). Methods of application were eye drops, subtenon and subconjunctival injection, intravitreal injection, and intravitreal implant. Prednisone was used as topical only. Participants previously using systemic therapies, n = 565; local corticosteroid therapies, n = 565. Participants currently using systemic therapies, n = 565; local corticosteroid therapies, n = 565. a“Other” includes immunosuppressants (including immunobiologicals, e.g., monoclonal antibodies), corticosteroids for systemic use, immunostimulants, anti-inflammatory and anti-rheumatic products, anti-anemic preparations, anti-diarrheals, intestinal anti-inflammatory/anti-infective agents, anti-gout preparations, ophthalmologicals, anti-bacterials for systemic use, drugs for acid-related disorders, anti-neoplastic agents, and anti-protozoals. b“Other” includes ophthalmologicals (prednisolone acetate, triamcinolone acetonide, triamcinolone, fluorometholone, betamethasone diproprionate, betamethasone and chloramphenicol, loteprednol etabonate, prednisolone, rimexolone, dexamethasone, loteprednol, difluprednate, betabioptal, dexamethasone sodium phosphate, methylprednisolone acetate). MAS main analysis set; NIIPPU noninfectious intermediate, posterior, or panuveitis
Fig. 3
Fig. 3
Summary of ocular complications in NIIPPU patients. Patients with previous ocular complications, n = 439. Patients with current ocular complications, n = 400. MAS main analysis set, NIIPPU noninfectious intermediate, posterior, or panuveitis

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