TY - JOUR
T1 - Hyperlipidemia after heart transplantation
T2 - Report of a 6-year experience, with treatment recommendations
AU - Ballantyne, Christie M.
AU - Radovancevic, Branislav
AU - Farmer, John A.
AU - Frazier, O. Howard
AU - Chandler, Linda
AU - Payton-Ross, Charlotte
AU - Cocanougher, Beth
AU - Jones, Peter H.
AU - Young, James B.
AU - Gotto, Antonio M.
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1992/5
Y1 - 1992/5
N2 - Mean plasma lipid values in 100 patients who survived >3 months after heart transplantation increased significantly at 3 months over pretransplantation values: total cholesterol from 168 ± 7 to 234 ± 7 mg/dl, low density lipoprotein (LDL) cholesterol from 111 ± 6 to 148 ± 6 mg/dl, high density lipoprotein (HDL) cholesterol from 34 ± 1 to 47 ± 1 mg/dl and triglycerides from 107 ± 6 to 195 ± 10 mg/dl. There were no significant increases after this time. The LDL cholesterol values remained ≥130 mg/dl in 64% of patients and triglyceride values remained ≥200 mg/dl in 41% of patients 6 months after postoperative dietary instructions. Beginning in 1985, select patients whose total cholesterol values remained >300 mg/dl despite 6 months of dietary intervention were treated with lovastatin given alone in a high dose (40 to 80 mg/day) or in combination with another hypolipidemic agent. Four of the five patients so treated developed rhabdomyolysis; two of the four had acute renal failure. Beginning in 1988, a second protocol-lovastatin at 20 mg/day as monotherapy-was used in patients who despite dietary intervention had total cholesterol > 240 mg/dl (mean follow-up 13 months). In the 15 patients so treated, mean total cholesterol decreased from 299 ± 10 mg/dl before treatment with lovastatin to 235 ± 9 mg/dl during treatment (21% reduction, p < 0.001) and mean LDL cholesterol was reduced from a baseline value of 190 ± 10 to 132 ± 12 mg/dl during treatment (31% reduction, p < 0.001). In this study, lovastatin at a dose of ≤29 mg/day as monotherapy was a well tolerated, effective treatment for hyperlipidemia after heart transplantation. It did not result in rhabdomyolysis and required no alteration in immunosuppressive therapy. However, the dose should not exceed 20 mg/day and combination therapy with either gemfibrozil or nicotinic acid should be avoided, even if the target LDL cholesterol value is not reached.
AB - Mean plasma lipid values in 100 patients who survived >3 months after heart transplantation increased significantly at 3 months over pretransplantation values: total cholesterol from 168 ± 7 to 234 ± 7 mg/dl, low density lipoprotein (LDL) cholesterol from 111 ± 6 to 148 ± 6 mg/dl, high density lipoprotein (HDL) cholesterol from 34 ± 1 to 47 ± 1 mg/dl and triglycerides from 107 ± 6 to 195 ± 10 mg/dl. There were no significant increases after this time. The LDL cholesterol values remained ≥130 mg/dl in 64% of patients and triglyceride values remained ≥200 mg/dl in 41% of patients 6 months after postoperative dietary instructions. Beginning in 1985, select patients whose total cholesterol values remained >300 mg/dl despite 6 months of dietary intervention were treated with lovastatin given alone in a high dose (40 to 80 mg/day) or in combination with another hypolipidemic agent. Four of the five patients so treated developed rhabdomyolysis; two of the four had acute renal failure. Beginning in 1988, a second protocol-lovastatin at 20 mg/day as monotherapy-was used in patients who despite dietary intervention had total cholesterol > 240 mg/dl (mean follow-up 13 months). In the 15 patients so treated, mean total cholesterol decreased from 299 ± 10 mg/dl before treatment with lovastatin to 235 ± 9 mg/dl during treatment (21% reduction, p < 0.001) and mean LDL cholesterol was reduced from a baseline value of 190 ± 10 to 132 ± 12 mg/dl during treatment (31% reduction, p < 0.001). In this study, lovastatin at a dose of ≤29 mg/day as monotherapy was a well tolerated, effective treatment for hyperlipidemia after heart transplantation. It did not result in rhabdomyolysis and required no alteration in immunosuppressive therapy. However, the dose should not exceed 20 mg/day and combination therapy with either gemfibrozil or nicotinic acid should be avoided, even if the target LDL cholesterol value is not reached.
UR - http://www.scopus.com/inward/record.url?scp=0026552691&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026552691&partnerID=8YFLogxK
U2 - 10.1016/0735-1097(92)90340-S
DO - 10.1016/0735-1097(92)90340-S
M3 - Article
C2 - 1564233
AN - SCOPUS:0026552691
SN - 0735-1097
VL - 19
SP - 1315
EP - 1321
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 6
ER -