Table 4

Comparison of characteristics and clinical findings between patients having a poor visual prognosis (BCVA≤20/50) and patients with a preserved visual prognosis (BCVA >20/50)

CharacteristicPoor visual prognosis (BCVA ≤20/50)
n=9
Preserved visual prognosis (BCVA >20/50)
n=74
p Value
Age (years)*59 (50; 67)51 (34; 62)0.062
Gender (female)9 (100%)55 (74.3%)0.11
Follow-up period (months)*91 (48; 110)60 (43; 98)0.40
Ethnicity0.87
 Caucasian7 (78.8%)54 (73%)
 Non-Caucasian2 (22.2%)20 (26.3%)
 Maghrebin2 (22.2%)12 (16.2%)
 African06 (8.1%)
 Asian02 (2.7%)
Familial history of sarcoidosis1 (11.1%)4 (5.4%)0.45
Ophthalmological findings
Intraocular manifestations
  Anterior017 (23%)
  Anterior intermediate1 (11.1%)10 (13.5%)
  Intermediate1 (11.1%)3 (4.1%)
  Posterior011 (14.9%)
  Panuveitis7 (77.8%)33 (44.6%)
Chronic form7 (77.8%)49 (66.2%)0.14
Bilateral involvement7 (77.8%)56 (75.7%)0.71
Granulomatous uveitis5 (55.6%)40 (57.1%)1.00
Elevated IOP010 (13.9%)1.00
CME8 (88.9%)28 (39.4%)0.59
PMC2 (22.2%)22 (31%)0.009
Other eye involvement
  Conjunctival node1 (11.1%)6 (8.2%)0.72
  Episcleritis01 (1.4%)0.71
  Scleritis02 (2.7%)1.00
Treatment
Local treatment
  Eye drops6 (66.7%)51 (70.8%)0.002
  Injections6 (66.7%)11 (15.5%)0.11
Systemic therapy9 (100%)54 (73%)0.10
  Oral steroids9 (100%)52 (71.2%)0.097
  Methotrexate4 (44.4%)14 (18.9%)0.54
  Other immunosuppressant014 (18.9%)0.030
Oral corticoid dependence4 (44.4%)9 (12.2%)0.061
Systemic therapy duration (months)*36 (24; 74)18 (0; 36)0.0004
Systemic therapy at last report9 (100%)28 (37.8%)0.0005
Persistent ocular inflammation5 (55.6%)4 (5.4%)
Indication for systemic therapy0.41
 Ocular8 (88.9%)37 (68.5%)
 Extraocular06 (11.1%)
 Both1 (11.1%)11 (20.4%)
  • Data are expressed as number and percentage, n (%); or * median (1st; 3rd quartile).

  • BCVA, best-corrected visual acuity; CME, chronic macular oedema; elevated IOP, chronically elevated intraocular pressure >21 mm Hg resulting from damage of angle; PMC, peripheral multifocal choroiditis.