TY - JOUR
T1 - Treatment of patients with elevated plasma levels of low-density lipoproteins with a cholestyramine tablet compared with cholestyramine powder
AU - Kwiterovich, Peter O.
AU - Zavoral, James H.
AU - Kafonek, Stephanie D.
AU - Bullemer, Faye
AU - Kittner, Bert
N1 - Funding Information:
The authors wish to acknowledge Norman R. Marquis, Ph.D., for his help in the conduct of the study, and Gary D. Hutton, M.S., for performing the statistical analyses. The study was supported by a grant from Bristol-Myers Squibb Company.
PY - 1992/8
Y1 - 1992/8
N2 - A primary elevation of plasma low-density lipoproteins (LDL) is a common cause of coronary artery disease. Cholestyramine powder is often used to treat such patients, but compliance can be less than optimal. This study was designed to assess the efficacy of a wax-coated tablet form of cholestyramine resin (1 gm per tablet). Ninety-six male and female subjects with total and LDL cholesterol concentrations above the 90th percentile, after an American Heart Association step I diet, were randomized to receive either the tablet or powder formation (dose of 16 gm per day). Forty-three subjects in each group completed a minimum of 6 weeks of treatment. Similar reductions in total (20% powder, 21% tablet) and LDL cholesterol (29% powder, 31% tablet) concentrations occurred in each group. Compliance in the two groups was identical (91% powder, 92% tablet). Gastrointestinal side effects were reported by 97% of the subjects from both groups. The cholestyramine tablet was as effective as cholestyramine powder in the treatment of hypercholesterolemia and can provide an alternate and more convenient dosage form.
AB - A primary elevation of plasma low-density lipoproteins (LDL) is a common cause of coronary artery disease. Cholestyramine powder is often used to treat such patients, but compliance can be less than optimal. This study was designed to assess the efficacy of a wax-coated tablet form of cholestyramine resin (1 gm per tablet). Ninety-six male and female subjects with total and LDL cholesterol concentrations above the 90th percentile, after an American Heart Association step I diet, were randomized to receive either the tablet or powder formation (dose of 16 gm per day). Forty-three subjects in each group completed a minimum of 6 weeks of treatment. Similar reductions in total (20% powder, 21% tablet) and LDL cholesterol (29% powder, 31% tablet) concentrations occurred in each group. Compliance in the two groups was identical (91% powder, 92% tablet). Gastrointestinal side effects were reported by 97% of the subjects from both groups. The cholestyramine tablet was as effective as cholestyramine powder in the treatment of hypercholesterolemia and can provide an alternate and more convenient dosage form.
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U2 - 10.1016/S0011-393X(05)80484-9
DO - 10.1016/S0011-393X(05)80484-9
M3 - Article
AN - SCOPUS:0026656981
SN - 0011-393X
VL - 52
SP - 330
EP - 337
JO - Current Therapeutic Research
JF - Current Therapeutic Research
IS - 2
ER -