Table 1.

McGill University Health Centre SLE patients with retinal toxicity (cases) versus matched SLE controls without retinal toxicitya.

VariableCases, n = 18Controlsb, n = 5495% CI for Difference
Females, n (%)16 (88.9)50 (92.6)−10.9 to 29.2f
White, n (%)11 (61.1)40 (74.1)−12.0 to 40.1f
Abnormal GFR or endstage renal disease, n (%)4 (22.2)8 (14.8)−12.2 to 34.4f
Mean daily dose > 5 mg/kg HCQ or > 2.3 mg/kg CQc, n (%)12 (66.7)26 (48.2)−10.5 to 41.9f
Ever exposed to > 5 mg/kg HCQ or > 2.3 mg/kg CQ, n (%)17 (94.4)44 (81.5)−12.4 to 27.3f
Ever exposed to > 6.5 mg/kg HCQ or > 3 mg/kg CQ, n (%)11 (61.1)24 (44.4)−12.0 to 41.2f
Missing ≥ 1 ophthalmology assessment, n (%)d9 (50.0)35 (64.8)–12.4 to 41.0f
Median age at SLE diagnosis (IQR)e29 (23–35)29 (24–38)−4.2 to 6.7g
Median HCQ/CQ use, yrs (IQR)e19 (14–20)16 (11–22)−6.0 to 2.0g
  • a Based on the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index recorded at yearly SLE assessments.

  • b Controls were matched 3:1 on age at SLE diagnosis (within 5 yrs), and SLE duration.

  • c Daily dose of antimalarial agents per actual body weight averaged for the entire course of treatment.

  • d Adherence to annual ophthalmology assessments recorded over the last 5 years preceding discontinuation of antimalarial therapy for patients with retinal toxicity (cases) and recorded over the last 5 years of antimalarial therapy for patients without retinal complications (controls).

  • e IQR: interquartile range.

  • f 95% CI for difference in percentage.

  • g 95% CI for difference in mean. SLE: systemic lupus erythematosus; GFR: glomerular filtration rate; HCQ: hydroxychloroquine; CQ: chloroquine.