Table 1

Selected baseline characteristics according to adherence during the first adherence ascertainment year

 Non-adherers (PDC <80%)
(n=20 120)
Adherers (PDC ≥80%)
(n=22 687)
nPer centnPer centSD
Age, years
 45–49242312.022389.90.070
 50–54528626.3540923.80.056
 55–59662132.9794935.00.045
 60–64579028.8709131.30.054
Statin at baseline
 Simvastatin780138.8876838.70.003
 Lovastatin3731.93371.50.029
 Pravastatin14217.110464.60.105
 Fluvastatin14857.418188.00.024
 Atorvastatin714735.5809535.70.003
 Rosuvastatin18939.4262311.60.070
Intensity of statin therapy
 Low*595429.6711431.40.038
 Moderate†14 05769.915 51268.40.032
 High‡1090.5610.30.043
Diabetes204010.1273212.00.061
Insulin6053.07653.40.021
Hypertensive diseases524626.1648528.60.056
Number of concurrent CVD medications
 010 44351.910 81247.70.085
 1547027.2668229.50.050
 2307815.3378116.70.037
 3–611295.614126.20.026
Depression262413.0308913.60.017
Respiratory diseases341817.0350215.40.042
Hormone therapy765438.0939841.40.069
Total number of concurrent medications
 1–2708535.2728932.10.065
 3–5720235.8803735.40.001
 6–31583329.0736132.50.077
Number of in-hospital days
 012 19360.614 22262.70.043
 1–2390219.4409918.10.034
 3–7265613.2282512.50.022
 8–32113696.815416.80.000
Charlson Comorbidity Index
 ≥113076.515837.00.019
  • *Fluvastatin 20–40 mg, lovastatin 20 mg, pravastatin 10–20 mg, simvastatin 5–10 mg.

  • †Atorvastatin 10–20 mg, fluvastatin 80 mg, lovastatin 40 mg, pravastatin 40 mg, rosuvastatin 10 mg, simvastatin 20–40 mg.

  • ‡Atorvastatin 40–80 mg, rosuvastatin 20–40 mg, simvastatin 80 mg.

  • CVD, cardiovascular disease; PDC, proportion of days covered; SD, standardised difference.