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. 2011 Sep 16;6:467–476. doi: 10.2147/COPD.S14247

Table 4.

Crude and adjusted OR and 95% CI of the association between FSC use and incident glaucoma between 2003 and 2006

FSC Crude OR 95% CI Adjusted OR 95% CI
Ever use in the last year
 No use Reference Reference
 Use 0.84 (0.62–1.15) 0.68 (0.45–1.01)
Last use prior to index date (days)
 No use Reference Reference
 12 days 1.02 (0.61–1.71) 1.00 (0.53–1.89)
 13–25 days 0.92 (0.52–1.62) 0.67 (0.34–1.30)
 26–52 days 0.54 (0.3–0.97) 0.55 (0.28–1.09)
 53–365 days 0.98 (0.58–1.65) 0.81 (0.44–1.52)
Duration of use (days)
 No use Reference Reference
 1–90 1.14 (0.66–1.97) 1.02 (0.54–1.90)
 91–180 0.62 (0.36–1.08) 0.50 (0.26–0.96)
 181–270 0.68 (0.36–1.28) 0.52 (0.25–1.08)
 ≥271 0.99 (0.61–1.59) 0.75 (0.42–1.34)
Number of prescriptions
 No prescriptions in last year Reference Reference
 1–3 1.14 (0.66–1.97) 1.01 (0.54–1.89)
 4–6 0.63 (0.36–1.10) 0.49 (0.26–0.93)
 7–9 0.70 (0.38–1.30) 0.50 (0.24–1.03)
 ≥10 0.96 (0.59–1.56) 0.72 (0.39–1.30)

Notes: Population includes patients with COPD in the GPRD between 2003 and 2006. Controls matched to cases on gender, age within 2 years, general practice, and number of years in the cohort prior to the event of interest. Model adjusted for other inhaled corticosteroids, asthma, long-acting beta agonists, short-acting bronchodilators, oral corticosteroids, BMI, smoking status, statin use, depression, diabetes, oxygen, nebulizer, and count of antibiotic prescriptions.

Abbreviations: BMI, body mass index; CI, confidence interval; FSC, fluticasone propionate/salmeterol fixed-dose combination; GPRD, General Practice Research Database OR, odds ratio.