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. 2007 Jan 3;63(6):698–708. doi: 10.1111/j.1365-2125.2006.02828.x

Table 1.

Characteristics of patients starting a new statin treatment in the Régie de l'assurance maladie du Québec database in 1998–2000

Entire cohort Atorvastatin Fluvastatin Lovastatin Pravastatin Simvastatin
No. patients 20 543 10 208 1254 442 4850 3789
Nonfatal CAD events (%) 1 535 (7.5) 647 (6.0) 95 (7.6) 44 (10) 421 (8.7) 328 (8.7)
Mean age (continuous)* 58 (±5) 58 (±5) 58 (±5) 58 (±5) 58 (±5) 58 (±5)
Mean dose 18 (±11) 12 (±5) 27 (±9) 21 (±4) 19 (±7) 15 (±7)
Follow-up time (days) (continuous) 586 (±322) 510 (±278) 688 (±349) 700 (±367) 660 (±345) 649 (±340)
Sex (male vs. female) (%) 37 39 33 37 35 36
Social assistance (yes vs. no) (%)* 29 31 33 33 26 26
Diabetes mellitus (yes vs. no) (%) 19 20 16 14 17 20
Hypertension (yes vs. no) (%) 45 45 48 41 45 46
Dose distribution (mg) (%)*
 5 1 0 0 0 6
 10 79 0 6 19 52
 20 19 66 89 75 39
 40 1 34 5 6 3
 80 0 0 0 0 0
*

At treatment initiation.

Statins equivalent to simvastatin dose during follow-up [46].Simvastatin 10 mg = lovastatin 20 mg = pravastatin 20 mg = fluvastatin 40 mg = atorvastatin 5 mg.

ICD-9 or pharmacological treatment before the index date.