DOES THE NEW ANGIOTENSIN CONVERTING-ENZYME-INHIBITOR CILAZAPRIL PREVENT RESTENOSIS AFTER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY - RESULTS OF THE MERCATOR STUDY - A MULTICENTER, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED TRIAL

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作者
BALCON, R
TIMMINS, J
SPRINGINGS, DC
BRECKER, SJD
DAVIES, SW
BONNET, JL
DHOUDAIN, F
BUIS, B
BAKX, ALM
SEDNEY, MI
CAMPOLO, L
DANZI, GB
DEBIASE, AM
CHAPPUIS, F
RUTISHAUSER, W
URBAN, P
MEIER, B
DANCHIN, N
JUILLIERE, Y
VOILQUINTHOMAS, V
EMANUELSSON, H
ALBERTSSON, P
SELIN, K
EKSTROM, L
VONESSEN, R
NEBELSIECK, H
UBERREITER, A
IGERL, K
HEYNDRICKX, GR
NELLENS, P
DEBRUYNE, B
GOETHALS, M
ISCHINGER, T
FISCHER, M
COPPENRATH, K
JUST, HJ
WOLLSCHLAGER, H
DREXLER, H
ELIAS, G
KRAYENBUHL, HP
HESS, O
AMANN, FW
SCHLAPFER, R
BUCHI, M
KUNKEL, B
FURSTE, T
LABLANCHE, JM
JORIS, JM
EEMAN, T
HENRY, M
机构
[1] THORAX CTR ROTTERDAM, CATHETERIZAT LAB, POSTBOX 1738, 3000 DR ROTTERDAM, NETHERLANDS
[2] LONDON CHEST HOSP, LONDON, ENGLAND
[3] HOP LA TIMONE, MARSEILLE, FRANCE
[4] LEIDEN UNIV HOSP, 2333 AA LEIDEN, NETHERLANDS
[5] OSPIDALE NUGUARDA CA GRANDA, MILAN, ITALY
[6] HOP CANTONAL GENEVA, CH-1211 GENEVA 4, SWITZERLAND
[7] GOTHENBURG UNIV, S-41124 GOTHENBURG, SWEDEN
[8] CHU BRABOIS, F-54500 Vandoeuvre Les Nancy, FRANCE
[9] MED KLIN MUNCHEN, MUNICH, GERMANY
[10] WALSGRAVE GEN HOSP, COVENTRY CV2 2DY, W MIDLANDS, ENGLAND
[11] MED KLIN 1, AACHEN, GERMANY
[12] ST LUC UNIV HOSP, BRUSSELS, BELGIUM
[13] F HOFFMANN LA ROCHE & CO LTD, CH-4002 BASEL, SWITZERLAND
[14] SOCAR SA, GIVINS, SWITZERLAND
[15] ONZE LIEVE VROUW HOSP, AALST, BELGIUM
[16] STADT KRANKENHAUS BOGENHAUSEN, MUNICH, GERMANY
[17] UNIV FREIBURG, W-7800 FREIBURG, GERMANY
[18] MED POLIKLIN, ZURICH, SWITZERLAND
[19] UNIV ERLANGEN NURNBERG, W-8520 ERLANGEN, GERMANY
[20] CTR HOSP REG & UNIV LILLE, HOP CARDIOL, LILLE, FRANCE
[21] KANTONSSPITAL BASEL, BASEL, SWITZERLAND
[22] HANNOVER MED SCH, W-3000 HANNOVER 61, GERMANY
[23] HOP TROUSSEAU, TOURS, FRANCE
[24] FREEMAN RD HOSP, Newcastle Upon Tyne NE7 7DN, TYNE & WEAR, ENGLAND
[25] HERZZENTRUM HIRSLANDEN, ZURICH, SWITZERLAND
[26] FREE UNIV BERLIN, KLINIKUM VIRCHOW, W-1000 BERLIN 33, GERMANY
[27] UNIV KLIN KIEL, KIEL, GERMANY
[28] UNIV CATHOLIQUE LOUVAIN, CLIN MT GODINNE, YVOIR, BELGIUM
关键词
CLINICAL TRIALS; CILAZAPRIL; ANGIOTENSIN CONVERTING ENZYME; PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Cilazapril is a novel angiotensin converting enzyme inhibitor with antiproliferative effects in the rat model after balloon injury. Methods and Results. We conducted a randomized, double-blind placebo-controlled trial to assess the effect of cilazapril in angiographic restenosis prevention after percutaneous transluminal coronary angioplasty (PTCA). Patients received cilazapril 2.5 mg in the evening after successful PTCA and 5 mg b.i.d. for 6 months or matched placebo. In addition, all patients received aspirin for 6 months. Coronary angiograms before PTCA, after PTCA, and at 6-month follow-up were quantitatively analyzed. In 94% of 735 recruited patients, PTCA was successful and all inclusion and exclusion criteria were met. For the per-protocol analysis, quantitative angiography after PTCA and at follow-up was available in 595 patients who complied with the treatment regimen (309 control, 286 cilazapril). The mean difference in minimal coronary lumen diameter between post-PTCA and follow-up angiogram (primary end point) was -0.29+/-0.49 mm in the control group and -0.27+/-0.51 mm in the cilazapril group. Clinical events during 6-month follow-up, analyzed on an intention-to-treat basis, were ranked according to the most serious clinical event ranging from death (control, two; cilazapril, three), nonfatal myocardial infarction (control, eight; cilazapril, 5), coronary revascularization (control, 51; cilazapril, 53), or recurrent angina requiring medical therapy (control, 67; cilazapril, 68) to none of the above (control, 224; cilazapril, 212). There were no significant differences in ranking. Conclusions. Long-term angiotensin converting enzyme inhibition with cilazapril in a dose of 5 mg b.i.d. does not prevent restenosis and does not favorably influence the overall clinical outcome after PTCA.
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页码:100 / 110
页数:11
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