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Pravachol
Clinical Pharmacology
Pravachol
A double-blind, placebo-controlled study in 214 patients (100 boys and 114 girls) with heterozygous familial hypercholesterolemia (HeFH), aged 8-18 years was conducted for two (2) years. The children (aged 8-13 years) were randomized to placebo (N=63) or 20 mg of pravastatin daily (N=65) and the adolescents (aged 14-18 years) were randomized to placebo (N=45) or 40 mg of pravastatin daily (N=41). Inclusion in the study required an LDL-C level > 95th percentile for age and sex and one parent with either a clinical or molecular diagnosis of familial hypercholesterolemia. The mean baseline LDL-C value was 239 mg/dL and 237 mg/dL in the pravastatin (range: 151-405 mg/dL) and placebo (range: 154-375 mg/dL) groups, respectively.
Pravastatin significantly decreased plasma levels of LDL-C, Total-C, and apolipoprotein B in both children and adolescents (see Table 6). The effect of pravastatin treatment in the two age groups was similar.
Table 6: Lipid-Lowering Effects of Pravastatin in Pediatric Patients with Heterozygous Familial Hypercholesterolemia: Least-Squares Mean Percent Change from Baseline at Month 24 (Last Observation Carried Forward: Intent-to-Treat)*
| Pravastatin 20 mg (Aged 8-13 years) N=65 |
Pravastatin 40 mg (Aged 14-18 years) N=41 |
Combined Pravastatin (Aged 8-18 years) N=106 |
Combined Placebo (Aged 8-18 years) N=108 |
95% CI of the Difference Between Combined Pravastatin and Placebo |
|
| LDL-C | -26.04** | -21.07** | -24.07** | -1.52 | (-26.74, -18.86) |
| TC | -20.75** | -13.08** | -17.72** | -0.65 | (-20.40, -13.83) |
| HDL-C | 1.04 | 13.71 | 5.97 | 3.13 | (-1.71, 7.43) |
| TG | -9.58 | -0.30 | -5.88 | -3.27 | (-13.95, 10.01) |
| ApoB (N) |
-23.16** (61) | -18.08** (39) | -21.11** (100) | -0.97 (106) | (-24.29, -16.18) |
| * The above least-squares mean values were
calculated based on log-transformed lipid values. ** Significant at p≤ 0.0001 when compared with placebo |
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The mean achieved LDL-C was 186 mg/dL (range: 67-363 mg/dL) in the pravastatin group compared to 236 mg/dL (range: 105-438 mg/dL) in the placebo group.
The safety and efficacy of pravastatin doses above 40 mg daily have not been studied in children. The long-term efficacy of pravastatin therapy in childhood to reduce morbidity and mortality in adulthood has not been established.
REFERENCES
1 Shepherd J, et al. Prevention of Coronary Heart Disease with Pravastatin in Men with Hypercholesterolemia (WOS). N Engl J Med 1995;333:1301-7.
2 The Long-term Intervention with Pravastatin in Ischemic Disease Group. Prevention of Cardiovascular Events and Death with Pravastatin in Patients with Coronary Heart Disease and a Broad Range of Initial Cholesterol Levels (LIPID). N Engl J Med 1998;339:1349-1357.
3 Sacks FM, et al. The Effect of Pravastatin on Coronary Events After Myocardial Infarction in Patients with Average Cholesterol Levels (CARE). N Engl J Med 1996;335:1001-9.
4 Pitt B, et al. Pravastatin Limitation of Atherosclerosis in the Coronary Arteries (PLAC I): Reduction in Atherosclerosis Progression and Clinical Events. J Am Coll Cardiol 1995;26:1133-9.
5 Jukema JW, et al. Effects of Lipid Lowering by Pravastatin on Progression and Regression of Coronary Artery Disease in Symptomatic Man With Normal to Moderately Elevated Serum Cholesterol Levels. The Regression Growth Evaluation Statin Study (REGRESS). Circulation 1995;91:2528-2540.
6 Crouse JR, et al. Pravastatin, Lipids, and Atherosclerosis in the Carotid Arteries: Design Features of a Clinical Trial with Carotid Atherosclerosis Outcome (PLAC II). Controlled Clinical Trials 1992;13:495.
7 Salonen R, et al. Kuopio Atherosclerosis Prevention Study (KAPS). A Population-based Primary Preventive Trial of the Effect of LDL Lowering on Atherosclerotic Progression in Carotid and Femoral Arteries. Research Institute of Public Health, University of Kuopio, Finland. Circulation 1995;92:1758.
Generic Name: Pravastatin Sodium
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