RESTENOSIS AFTER CORONARY ANGIOPLASTY - A MULTIVARIATE STATISTICAL-MODEL TO RELATE LESION AND PROCEDURE VARIABLES TO RESTENOSIS

被引:338
作者
HIRSHFELD, JW
SCHWARTZ, JS
JUGO, R
MACDONALD, RG
GOLDBERG, S
SAVAGE, MP
BASS, TA
VETROVEC, G
COWLEY, M
TAUSSIG, AS
WHITWORTH, HB
MARGOLIS, JR
HILL, JA
PEPINE, CJ
机构
[1] UNIV PENN,PHILADELPHIA,PA 19104
[2] CORDIS CORP,MIAMI,FL
[3] DALHOUSIE UNIV,HALIFAX B3H 4H2,NS,CANADA
[4] THOMAS JEFFERSON UNIV,PHILADELPHIA,PA 19107
[5] UNIV HOSP JACKSONVILLE,JACKSONVILLE,FL 32209
[6] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,RICHMOND,VA 23298
[7] CENT FLORIDA CARDIOL GRP,ORLANDO,FL
[8] S MIAMI HOSP,MIAMI,FL
[9] UNIV FLORIDA,GAINESVILLE,FL 32611
[10] VET ADM MED CTR,GAINESVILLE,FL 32602
关键词
D O I
10.1016/0735-1097(91)90783-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Multi-Hospital Eastern Atlantic Restenosis Trial group obtained follow-up angiography in 510 patients with 598 successfully dilated coronary lesions who were enrolled in a controlled trial of the effects of a single dose of 1 g of methylprednisolone on restenosis after coronary angioplasty. The overall restenosis rate was 39.6%. The strongest univariate relations to the restenosis rate were found for lesion location (saphenous vein graft, 68%; left anterior descending artery, 45%; left circumflex artery and right coronary artery, 32%; p = 0.002); lesion length (less-than-or-equal-to 4.6 mm, 33%; > 4.6 mm, 45%; p = 0.001); percent stenosis before angioplasty (less-than-or-equal-to 73%, 25%; > 73%, 43%; p = 0.005), percent stenosis after angioplasty (less-than-or-equal-to 21%, 33%; > 21%, 46%; p = 0.017) and arterial diameter (< 2.9 mm, 44%; greater-than-or-equal-to 2.9 mm, 34%; p = 0.036). Two multivariate models to predict restenosis probability were developed with use of stepwise logistic regression. The preprocedural model, which included only variables whose values were known before angioplasty, entered lesion length, vein graft location, left anterior descending artery location, percent stenosis before angioplasty, eccentric lesion and arterial diameter. The postprocedural model, which also included variables whose values were known after angioplasty was performed, was similar to the preangioplasty model except that it also entered postangioplasty percent stenosis and "optimal" balloon sizing but did not enter eccentric lesion. These data indicate that the probability of restenosis after angioplasty is determined predominantly by the characteristics of the lesion being dilated. They are consistent with the known intimal proliferative mechanism of restenosis, offer a means of identifying lesions at unusually high or low risk of restenosis, and of predicting the likelihood that a particular lesion will restenose after angioplasty and provide a rationale for stratification by restenosis probability in the design of future studies of restenosis.
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页码:647 / 656
页数:10
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