Platelet aggregability and occurrence of restenosis following coronary angioplasty

被引:13
作者
Goel, PK [1 ]
Shahi, M [1 ]
Agarwal, AK [1 ]
Srivastava, S [1 ]
Seth, PK [1 ]
机构
[1] IND TOXICOL RES CTR,LUCKNOW 226001,UTTAR PRADESH,INDIA
关键词
platelet aggregability; biological risk factors; adenosine di-phosphate; restenosis; predictors of;
D O I
10.1016/S0167-5273(97)00085-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Restenosis following percutaneous coronary angioplasty (PTCA) is a complex medical problem occurring in nearly a third of the patients undergoing PTCA with no single definite predictor demonstrated in an individual patient. Platelets are known to play an important role in the pathogenesis of the restenotic process. However, no known parameter of platelet function or activity has been studied as a risk factor predicting the occurrence of restenosis. We prospectively assessed platelet activation in twenty two consecutive patients with stable angina who underwent a successful PTCA for single vessel coronary artery disease. Platelet activation levels were measured using aggregability curves derived from unclotted blood samples on a platelet aggregometer using varying concentrations of adenosine di-phosphate (ADP) in the following time sequence: (1) Basal i.e. pre-PTCA, (2) post-PTCA day 1, (3) post-PTCA day 7, and (4) post-PTCA day 28. Occurrence of restenosis was studied using angiographic follow-up in all patients. At follow-up, seven of the twenty two patients studied developed restenosis. There was no significant difference or any specific trend noted over time in the levels of platelet aggregability in the study group as a whole (basal: 30.0+/-15.4%, post-PTCA day 1: 32.5+/-16.1%, post-PTCA day 7: 34.6+/-15.4% and post-PTCA day 28: 32.6+/-16.1%). However, when the patients were subgrouped into those with and without restenosis, the patients with restenosis had a significantly higher basal platelet aggregability (38.7+/-16.3%) versus those who did not develop restenosis (25.0+/-12.1%), p=0.0128. We conclude that patients developing restenosis after PTCA have a significantly higher basal platelet aggregability and this could be used as a marker for its occurrence in an individual patient. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:227 / 231
页数:5
相关论文
共 31 条
[1]  
ABUKHALIL J, 1990, AM HEART J, V119, P178
[2]  
AUSTIN GE, 1987, ARCH PATHOL LAB MED, V111, P1158
[3]   BIOLOGICAL RISK-FACTORS FOR RESTENOSIS AFTER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY [J].
BENCHIMOL, D ;
BONNET, J ;
BENCHIMOL, H ;
DROUILLET, F ;
DUPLAA, C ;
COUFFINHAL, T ;
DESGRANGES, C ;
BRICAUD, H .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1993, 38 (01) :7-18
[4]   CLINICAL, PHYSIOLOGICAL, ANATOMIC AND PROCEDURAL FACTORS PREDICTIVE OF RESTENOSIS AFTER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY [J].
BOURASSA, MG ;
LESPERANCE, J ;
EASTWOOD, C ;
SCHWARTZ, L ;
COTE, G ;
KAZIM, F ;
HUDON, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 18 (02) :368-376
[5]  
CALIFF RM, 1991, J AM COLL CARDIOL, V17, pB2
[6]   RESTENOSIS AFTER ARTERIAL INJURY CAUSED BY CORONARY STENTING IN PATIENTS WITH DIABETES-MELLITUS [J].
CARROZZA, JP ;
KUNTZ, RE ;
FISHMAN, RF ;
BAIM, DS .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (05) :344-349
[7]   PERCUTANEOUS TRANS-LUMINAL CORONARY ANGIOPLASTY IN 1985-1986 AND 1977-1981 - THE NATIONAL-HEART-LUNG-AND-BLOOD-INSTITUTE REGISTRY [J].
DETRE, K ;
HOLUBKOV, R ;
KELSEY, S ;
COWLEY, M ;
KENT, K ;
WILLIAMS, D ;
MYLER, R ;
FAXON, D ;
HOLMES, D ;
BOURASSA, M ;
BLOCK, P ;
GOSSELIN, A ;
BENTIVOGLIO, L ;
LEATHERMAN, L ;
DORROS, G ;
KING, S ;
GALICHIA, J ;
ALBASSAM, M ;
LEON, M ;
ROBERTSON, T ;
PASSAMANI, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (05) :265-270
[8]   A PARADIGM FOR RESTENOSIS BASED ON CELL BIOLOGY - CLUES FOR THE DEVELOPMENT OF NEW PREVENTIVE THERAPIES [J].
FORRESTER, JS ;
FISHBEIN, M ;
HELFANT, R ;
FAGIN, J .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 17 (03) :758-769
[9]  
Gruentzig A, 1978, LANCET, V1, P263
[10]  
HAUDENSCHILD CC, 1993, AM J MED, V94, pS40