Long-term effects of low-density lipoprotein apheresis using an automated dextran sulfate cellulose adsorption system

被引:80
作者
Gordon, BR [1 ]
Kelsey, SF [1 ]
Dau, PC [1 ]
Gotto, AM [1 ]
Graham, K [1 ]
Illingworth, DR [1 ]
Isaacsohn, J [1 ]
Jones, PH [1 ]
Leitman, SF [1 ]
Saal, SD [1 ]
Stein, EA [1 ]
Stern, TN [1 ]
Troendle, A [1 ]
Zwiener, RJ [1 ]
机构
[1] New York Hosp, Cornell Med Ctr, Rogosin Inst, New York, NY USA
关键词
D O I
10.1016/S0002-9149(97)00947-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The short-term effectiveness of low-density lipoprotein (LDL) apheresis using a dextran sulfate cellulose adsorption column technique was previously examined in a 9-center, 22-week controlled trial in 64 patients with familial hypercholesterolemia (FH) who did not adequately respond to diet and drug therapy. Forty-nine patients (40 treatment, 9 controls) subsequently received LDL apheresis procedures as part of an optional follow-up phase. This study reports on the long-term safety, lipid lowering, and clinical efficacy of LDL apheresis for the 5-year period that includes both the initial controlled study and follow-up phase. During this time, patients received a total of 3,902 treatments bf which 3,314 treatments were given during the follow-vp phase. Adverse events were infrequent, occurring in 142 procedures (3.6%). Immediate reduction in LDL cholesterol was 76% both in homozygotes and in heterozygotes. Patients with homozygous FH had a progressive decrease in pretreatment LDL cholesterol level along with an increase in high-density lipoprotein (HDL) cholesterol level. There wets no appreciable change in pretreatment lipoprotein level over time in heterozygotes. The rate of cardiovascular events during therapy with LDL apheresis and lipid-lowering drugs was 3.5 events per 1,000 patient-months of treatment compared with 6.3 events per 1,000 patient-months for the 5 years before LDL apheresis therapy. These findings support the long-term safety and clinical efficacy of LDL apheresis in patients with heterozygous and homozygous FH who are inadequately controlled with drug therapy. (C) 1998 by Excerpta Medica, Inc.
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页码:407 / 411
页数:5
相关论文
共 14 条
[1]  
Borberg H, 1988, Prog Clin Biol Res, V255, P317
[2]   TREATMENT OF REFRACTORY FAMILIAL HYPERCHOLESTEROLEMIA BY LOW-DENSITY-LIPOPROTEIN APHERESIS USING AN AUTOMATED DEXTRAN SULFATE CELLULOSE ADSORPTION SYSTEM [J].
GORDON, BR ;
KELSEY, SF ;
BILHEIMER, DW ;
BROWN, DC ;
DAU, PC ;
GOTTO, AM ;
ILLINGWORTH, DR ;
JONES, PH ;
LEITMAN, SF ;
PRIHODA, JS ;
STEIN, EA ;
STERN, TN ;
ZAVORAL, JH ;
ZWIENER, RJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 70 (11) :1010-1016
[3]   INDICATIONS FOR LOW-DENSITY-LIPOPROTEIN APHERESIS [J].
GORDON, BR ;
STEIN, E ;
JONES, P ;
ILLINGWORTH, DR .
AMERICAN JOURNAL OF CARDIOLOGY, 1994, 74 (11) :1109-1112
[4]   HOW EFFECTIVE IS DRUG-THERAPY IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA [J].
ILLINGWORTH, DR .
AMERICAN JOURNAL OF CARDIOLOGY, 1993, 72 (10) :D54-D58
[5]   LDL-apheresis atherosclerosis regression study (LAARS) - Effect of aggressive versus conventional lipid lowering treatment on coronary atherosclerosis [J].
Kroon, AA ;
Aengevaeren, WRM ;
vanderWerf, T ;
Uijen, GJH ;
Reiber, JHC ;
Bruschke, AVG ;
Stalenhoef, AFH .
CIRCULATION, 1996, 93 (10) :1826-1835
[6]   A NEW LOW-DENSITY-LIPOPROTEIN APHERESIS SYSTEM USING 2 DEXTRAN SULFATE CELLULOSE COLUMNS IN AN AUTOMATED COLUMN REGENERATING UNIT (LDL CONTINUOUS APHERESIS) [J].
MABUCHI, H ;
MICHISHITA, I ;
TAKEDA, M ;
FUJITA, H ;
KOIZUMI, J ;
TAKEDA, R ;
TAKADA, S ;
OONISHI, M .
ATHEROSCLEROSIS, 1987, 68 (1-2) :19-25
[7]   THE HELP-LDL-APHERESIS MULTICENTER STUDY, AN ANGIOGRAPHICALLY ASSESSED TRIAL ON THE ROLE OF LDL-APHERESIS IN THE SECONDARY PREVENTION OF CORONARY HEART-DISEASE .2. FINAL EVALUATION OF THE EFFECT OF REGULAR TREATMENT ON LDL-CHOLESTEROL PLASMA-CONCENTRATIONS AND THE COURSE OF CORONARY HEART-DISEASE [J].
SCHUFFWERNER, P ;
GOHLKE, H ;
BARTMANN, U ;
BAGGIO, G ;
CORTI, MC ;
DINSENBACHER, A ;
EISENHAUER, T ;
GRUTZMACHER, P ;
KELLER, C ;
KETTNER, U ;
KLEOPHAS, W ;
KOSTER, W ;
OLBRICHT, CJ ;
RICHTER, WO ;
SEIDEL, D ;
SCHOPPENTHAU, M ;
SCHLIERF, G ;
MARBURGER, C ;
ZOLLNER, N ;
SUHLER, K ;
SCHWANDT, P ;
SCHOTTENFELDNAOR, J ;
LESCHKE, M ;
GRIES, FA ;
GOHLKE, W ;
BESTEHORN, HP ;
BRAUNAGEL, K ;
BAUER, M ;
HORL, WH ;
JUST, H ;
MEINERTZ, T ;
SCHOLLMEYER, P ;
WIELAND, H ;
PREVIATO, L ;
CREPALDI, G ;
ARMSTRONG, VW ;
SCHOEPPE, W ;
MUCHE, R ;
REXER, H ;
HILGERS, R .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1994, 24 (11) :724-732
[8]  
SCHUFFWERNER P, 1988, CONTRIB INFUS THER, V23, P118
[9]  
STOFFEL W, 1981, LANCET, V2, P1005
[10]   Single LDL apheresis improves endothelium-dependent vasodilatation in hypercholesterolemic humans [J].
Tamai, O ;
Matsuoka, H ;
Itabe, H ;
Wada, Y ;
Kohno, K ;
Imaizumi, T .
CIRCULATION, 1997, 95 (01) :76-82