Lesion-to-lesion independence of restenosis after treatment by conventional angioplasty, stenting, or directional atherectomy. Validation of lesion-based restenosis analysis.

BACKGROUND Since many restenosis trials include patients in whom more than one lesion is treated, analysis of the angiographic data on a "per lesion" basis might be confounded by potential correlations of restenosis among multiple treated lesions within each patient. The goals of this study were: 1) to determine whether there was any correlation in the rate of restenosis among multiple lesions that underwent conventional angioplasty, stenting, or directional atherectomy within the same patient and 2) to determine whether lesions treated in a multilesion intervention experience a different magnitude of restenosis than lesions undergoing single-lesion procedures. METHODS AND RESULTS Of 441 patients treated by Palmaz-Schatz stenting (n = 114), directional atherectomy (n = 100), or conventional balloon angioplasty (n = 227), 67 underwent multilesion procedures involving treatment of 146 lesions. A general linear model with intraclass correlation (GLIMIC) was used to calculate the coefficient of correlation (rho) of the change in the measured minimum luminal diameter (late loss) from the time of the initial procedure to 6-month angiogram among the multiple lesions within the same patient for all 441 patients. This showed no correlation among multiple lesions within the same patient for the late loss in minimum luminal diameter (rho = -0.12 [95% CI: -0.40, 0.12]), among lesions in the same vessel (rho = 0.14 [95% CI: -0.34, 0.62]), or among different vessels (rho = -0.18 [95% CI: -0.52, 0.16]), suggesting that the magnitude of late loss is independent among multiple lesions within the same patient. There was no difference (p = 0.96) between the observed incidence of zero-, one-, and two-vessel restenosis (> or = 50% diameter stenosis at follow-up) for patients with multiple-lesion treatment and that predicted assuming lesion-to-lesion independence. Similarly, there was no difference in late loss or in the overall binary restenosis rate when single-lesion procedures were compared with multilesion procedures. Multivariable analysis of the late loss in lumen diameter (which adjusted for the effects of the acute result and the device used) demonstrated no independent effect (p = 0.20) of single-lesion versus multilesion status. CONCLUSIONS Luminal encroachment appears to occur at independent rates among multiple lesions treated in a single patient. The observed incidence of restenosis for patients with multiple treated lesions is accurately predicted assuming independent probabilities of restenosis. Lesion-based analysis, even when including multiple treated lesions within the same patient, is thus valid for evaluating conventional angioplasty, stenting, or directional atherectomy.

[1]  D. Baim,et al.  Novel approach to the analysis of restenosis after the use of three new coronary devices. , 1992, Journal of the American College of Cardiology.

[2]  T Sandor,et al.  Quantitative angiographic and statistical methods to assess serial changes in coronary luminal diameter and implications for atherosclerosis regression trials. , 1992, The American journal of cardiology.

[3]  P. Serruys,et al.  Relative Risk Analysis of Angiographic Predictors of Restenosis Within the Coronary Wallstent , 1991, Circulation.

[4]  J. Webb,et al.  Coronary angioplasty in young adults: initial results and late outcome. , 1990, Journal of the American College of Cardiology.

[5]  C. Lambert,et al.  Videodensitometry versus digital calipers for quantitative coronary angiography. , 1990, The American journal of cardiology.

[6]  W. Wijns,et al.  Detection of restenosis after successful coronary angioplasty: improved clinical decision making with use of a logistic model combining procedural and follow-up variables. , 1990, Journal of the American College of Cardiology.

[7]  J J Albers,et al.  Regression of coronary artery disease as a result of intensive lipid-lowering therapy in men with high levels of apolipoprotein B. , 1990, The New England journal of medicine.

[8]  D. Baim,et al.  Clinical and angiographic results of balloon-expandable intracoronary stents in right coronary artery stenoses. , 1990, Journal of the American College of Cardiology.

[9]  R D Safian,et al.  Coronary atherectomy. Clinical, angiographic, and histological findings and observations regarding potential mechanisms. , 1990, Circulation.

[10]  P. Serruys,et al.  Restenosis after coronary angioplasty: new standards for clinical studies. , 1990, Journal of the American College of Cardiology.

[11]  P. Whitlow,et al.  Percutaneous transluminal angioplasty of saphenous vein graft stenosis: long-term follow-up. , 1989, Journal of the American College of Cardiology.

[12]  D. Faxon,et al.  One-year follow-up results of the 1985-1986 National Heart, Lung, and Blood Institute's Percutaneous Transluminal Coronary Angioplasty Registry. , 1989, Circulation.

[13]  J. Popma,et al.  In vivo assessment of a digital angiographic method to measure absolute coronary artery diameters. , 1989, The American journal of cardiology.

[14]  Bernard Rosner,et al.  Multivariate Methods for Clustered Binary Data with More than One Level of Nesting , 1989 .

[15]  S. Ellis,et al.  Importance of stenosis morphology in the estimation of restenosis risk after elective percutaneous transluminal coronary angioplasty. , 1989, The American journal of cardiology.

[16]  D. Waters,et al.  Multiple coronary angioplasty: a model to discriminate systemic and procedural factors related to restenosis. , 1988, Journal of the American College of Cardiology.

[17]  L Schwartz,et al.  Aspirin and dipyridamole in the prevention of restenosis after percutaneous transluminal coronary angioplasty. , 1988, The New England journal of medicine.

[18]  M. Brand Incidence ofrestenosis after successful coronary angioplasty: a time-related phenomenon , 1988 .

[19]  M. Nobuyoshi,et al.  Restenosis after successful percutaneous transluminal coronary angioplasty: serial angiographic follow-up of 229 patients. , 1988, Journal of the American College of Cardiology.

[20]  P. Esser,et al.  Quantitative analysis of coronary arteriograms by microprocessor cinevideodensitometry. , 1987, Catheterization and cardiovascular diagnosis.

[21]  B. Chaitman,et al.  Multilesion coronary angioplasty: clinical and angiographic follow-up. , 1987, Journal of the American College of Cardiology.

[22]  D. Ku,et al.  Pulsatile Flow and Atherosclerosis in the Human Carotid Bifurcation: Positive Correlation between Plaque Location and Low and Oscillating Shear Stress , 1985, Arteriosclerosis.

[23]  B Rosner,et al.  Multivariate methods in ophthalmology with application to other paired-data situations. , 1984, Biometrics.

[24]  E L Bolson,et al.  A new digital electronic caliper for measurement of coronary arterial stenosis: comparison with visual estimates and computer-assisted measurements. , 1984, The American journal of cardiology.

[25]  P D Esser,et al.  Quantification of relative coronary arterial stenosis by cinevideodensitometric analysis of coronary arteriograms. , 1984, Circulation.

[26]  C. Zarins,et al.  Carotid Bifurcation Atherosclerosis: Quantitative Correlation of Plaque Localization with Flow Velocity Profiles and Wall Shear Stress , 1983, Circulation research.

[27]  A. Donner,et al.  Randomization by cluster. Sample size requirements and analysis. , 1981, American journal of epidemiology.

[28]  C. Zarins,et al.  Local Effects of Stenoses: Increased Flow Velocity Inhibits Atherogenesis , 1981, Circulation.

[29]  E. Bolson,et al.  Quantitative Coronary Arteriography: Estimation of Dimensions, Hemodynamic Resistance, and Atheroma Mass of Coronary Artery Lesions Using the Arteriogram and Digital Computation , 1977, Circulation.