Vascular closure devices and the risk of vascular complications after percutaneous coronary intervention in patients receiving glycoprotein IIb-IIIa inhibitors

被引:72
作者
Resnic, FS
Blake, GJ
Ohno-Machado, L
Selwyn, AP
Popma, JJ
Rogers, C
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Cardiovasc Div, Boston, MA 02116 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Decis Syst Grp, Boston, MA 02116 USA
关键词
D O I
10.1016/S0002-9149(01)01725-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular closure devices offer advantages over traditional means of obtaining hemostasis after percutaneous coronary intervention (PCI) in terms of patient comfort and time to ambulation. We investigate whether such devices also reduce the risk of vascular complications in selected patient populations. We conducted a retrospective analysis of all patients who underwent PCI at our institution between January 1998 and December 1999. Of 3,151 consecutive patients, 3,027 were eligible tio receive vascular closure devices. Of these, 1,485 received a closure device and 1,409 received glycoprotein IIIb-IIIa antagonists. The overall vascular complication rate, as defined by the need for surgical repair or transfusion, or the development of arteriovenous fistula, pseudoaneurysm, or large hematoma, was 4.20%. By univariate analysis, the use of closure devices was associated with a lower vascular complication rate (3.03% vs 5.52%; p = 0.002) and a shorter length of hospital stay (2.77 vs 3.97 days, p <0.001). Multivariate analysis showed a significant reduction in vascular complications with closure devices (odds ratio 0.59, p = 0.007). For the subgroup of patients receiving glycoprotein IIb-IIIa antagonists, the use of closure devices was associated with an even more pronounced reduction in the risk of vascular complications (odds ratio 0.45, p <0.008). Thus, the use of closure devices in selected patients undergoing PCI is associated with a low rate of vascular complications and decreased length of stay. This benefit was most marked for patients receiving glycoprotein IIb-IIIa antagonists. (C) 2001 by Excerpta Medica, Inc.
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页码:493 / 496
页数:4
相关论文
共 15 条
[1]   Suture-mediated closure of the femoral access site after cardiac catheterization: Results of the suture to ambulate and discharge (STAND I and STAND II) trials [J].
Baim, DS ;
Knopf, WD ;
Hinohara, T ;
Schwarten, DE ;
Schatz, RA ;
Pinkerton, CA ;
Cutlip, DE ;
Fitzpatrick, M ;
Ho, KKL ;
Kuntz, RE .
AMERICAN JOURNAL OF CARDIOLOGY, 2000, 85 (07) :864-869
[2]   Vascular access site complications after percutaneous coronary intervention with abciximab in the evaluation of c7E3 for the prevention of ischemic complications (EPIC) trial [J].
Blankenship, JC ;
Hellkamp, AS ;
Aguirre, FV ;
Demko, SL ;
Topol, EJ ;
Califf, RM .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 81 (01) :36-40
[3]  
Chamberlin JR, 1999, CATHETER CARDIO INTE, V47, P143, DOI 10.1002/(SICI)1522-726X(199906)47:2<143::AID-CCD1>3.0.CO
[4]  
2-M
[5]  
Kussmaul WG, 1996, CATHETER CARDIO DIAG, V37, P362, DOI 10.1002/(SICI)1097-0304(199604)37:4<362::AID-CCD3>3.0.CO
[6]  
2-9
[7]  
Lunney L, 1999, J INVASIVE CARDIOL, V11, p2B
[8]   A MULTICENTER RANDOMIZED TRIAL COMPARING A PERCUTANEOUS COLLAGEN HEMOSTASIS DEVICE WITH CONVENTIONAL MANUAL COMPRESSION AFTER DIAGNOSTIC ANGIOGRAPHY AND ANGIOPLASTY [J].
SANBORN, TA ;
GIBBS, HH ;
BRINKER, JA ;
KNOPF, WD ;
KOSINSKI, EJ ;
ROUBIN, GS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1993, 22 (05) :1273-1279
[9]  
Sesana M, 2000, J INVASIVE CARDIOL, V12, P395
[10]  
Silber S, 1999, J INVASIVE CARDIOL, V11, p19B