Table 1

Summary of the characteristics of patients treated with topical ciclosporin (Ikervis) in Nottingham, UK

ParametersTotal n=463
n (%)
Age, years
 0–1834 (7.3)
 >18 to 3044 (9.5)
 >31 to 5098 (21.2)
 >51 to 70152 (32.8)
 >70135 (29.2)
Gender
 Female273 (59.0)
 Male190 (41.0)
Diagnosis
 Dry eye diseases322 (69.5)
 AED53 (11.4)
 OMMP28 (6.0)
 Post-corneal graft14 (3.0)
 SJS10 (2.2)
 Others*36 (7.8)
CDVA, logMAR
 Baseline0.24±0.45
 Final0.23±0.47
Clinical outcome†
 Resolved119 (25.7)
 Stable224 (48.4)
 Active44 (9.5)
 Intolerant to Ikervis76 (16.4)
Treatment frequency
 Once a day286 (61.8)
 Twice a day173 (37.4)
 >Twice a day4 (0.9)
Follow-up duration, months14.6±9.2
  • *Included cases of inflammatory keratitis (n=9), non-specific chronic conjunctivitis (n=7), scleritis/episcleritis (n=4), limbal stem cell deficiency (n=3), neurotrophic keratopathy (n=2), pseudopterygium (n=2), peripheral ulcerative keratitis (n=2), superior limbic keratoconjunctivitis (n=2), uveitis (n=2), epithelial ingrowth (n=1), conjunctival granuloma (n=1) and giant papillary conjunctivitis (n=1).

  • †Clinical outcome is defined as: (1) resolved: resolution of disease without further need of Ikervis; (2) stable: stable disease with ongoing Ikervis; (3) active: active disease requiring additional treatment such as topical steroids and (4) intolerant: Ikervis discontinued due to intolerable side effects.

  • AED, allergic eye disease (which included vernal keratoconjunctivitis and atopic keratoconjunctivitis; CDVA, corrected distance visual acuity; OMMP, ocular mucous membrane pemphigoid; SJS, Steven-Johnson syndrome.