Skip to main content

Advertisement

ADVERTISEMENT

Reduction of Early Elastic Recoil by Cutting Balloon Angioplasty as Compared to Conventional Balloon Angioplasty

Katsuhiro Kawaguchi, MD, Taizo Kondo, MD, Takanori Shumiya, MD, Tomohiro Uchikawa, MD, Tomomichi Suzuki, MD, Yoshifumi Awaji, MD, Mitsuhiro Mochizuki, MD
September 2002
Percutaneous transluminal coronary angioplasty (PTCA) by conventional balloon is the primary technique used for percutaneous coronary revascularization. However, restenosis after successful coronary balloon angioplasty remains a problem. Although neointimal proliferation is important in restenosis, early elastic behavior after balloon angioplasty may also play a significant role. Early elastic recoil after conventional balloon angioplasty was observed to be a luminal diameter loss of 17–50% immediately after balloon deflation.1–7 Restenosis was significantly greater in patients with early elastic recoil.6 The cutting balloon apparatus contains 3–4 longitudinal microminiaturized microtome blades, or “atherotomes”. “Controlled” sharp, longitudinal incisions in the diseased arterial segment result in less severe arterial injury and fewer major dissections than conventional balloon angioplasty.8 Theoretically, the mechanisms of cutting balloon angioplasty may lead to less elastic recoil and less late restenosis. Angiographic restenosis rates are lower in cutting balloon angioplasty than in conventional balloon angioplasty.9,10 This study was undertaken to compare early elastic recoil within 10 minutes after successful angioplasty and early lumen loss at 24 hours after angioplasty in cutting balloon and conventional balloon groups. Methods Patient population. From a total of 924 patients undergoing percutaneous coronary intervention at Komaki City Hospital between September 1994 and January 1998, we identified 121 patients with 133 lesions that were suitable for cutting balloon angioplasty and matched the criteria defined below. We performed cutting balloon angioplasty in 73 patients with 82 lesions, and conventional balloon angioplasty in 48 patients with 51 lesions. All patients underwent repeat coronary angiography 24 hours after successful angioplasty. In the cutting balloon group, coronary angioplasty was performed only by cutting balloon. Adjunctive conventional balloon angioplasty was not considered. Exclusion criteria included total occlusions, significant left main coronary artery disease, ostial lesions, lesions containing extensive calcification, tortuous lesions proximal to the target lesion, angiographically visible thrombus, bypass graft lesions, in-stent restenotic lesions, vessel diameters Coronary angioplasty procedure. Percutaneous coronary angioplasty was performed by the femoral approach. During catheterization, a bolus of 10,000 IU of intravenous heparin and 5 mg of intracoronary isosorbide dinitrate were given immediately before the angioplasty procedure. The ratio of dilating balloon to the reference vessel diameter used was visually estimated to be between 1.1 and 1.3. Inflation time and pressure were left to the discretion of the operators. Balloon inflations were repeated until there was an acceptable gain in lumen diameter, and during each inflation a film sequence of the contrast-filled balloon was obtained. Medications after angioplasty (up to the 24-hour repeat angiogram) consisted of a continuous infusion of intravenous heparin, intravenous nitroglycerin, aspirin and a calcium channel blocker. Quantitative coronary analysis. Patients were examined angiographically before, 10 minutes after, and 24 hours after angioplasty. Five mg of intracoronary isosorbide dinitrate were administered prior to performing coronary angiogram. The percent diameter stenosis, reference diameter, minimal luminal diameter and lesion length were determined using an automated edge detection system (Cardiovascular Measurement System, Medis Medical Imaging Systems, Nuenen, The Netherlands). The basic method of analysis was described in a previous report.11 The mean balloon diameter at the highest inflation pressure was also determined. Acute coronary recoil after angioplasty was calculated as the mean balloon diameter at the maximal inflation pressure minus the minimal luminal diameter after angioplasty. The percent acute recoil was also calculated as (acute recoil/inflated balloon diameter at the maximal inflation pressure) x 100. Statistical analysis. Individual quantitative data were used to calculate mean values and standard deviations. Comparisons between groups for continuous data were performed with Mann-Whitney’s U-test. Differences between proportions were assessed by Chi-square analysis. A p-value Baseline clinical characteristics are shown in Table 1. Clinical presentations and risk factor prevalences were not different between the cutting balloon group and the conventional balloon group. Table 2 shows baseline angiographic and procedural angiographic data. There were no significant differences in the distribution and ACC/AHA classification of lesions between the two groups. The balloon diameter to reference artery ratio was 1.19 ± 0.11 in the cutting balloon group and 1.19 ± 0.13 in the conventional balloon group (p = NS). Maximal inflation pressure was lower in the cutting balloon group (6.5 ± 0.9 atm vs. 7.3 ± 2.4 atm in the conventional balloon group; p = 0.004). Both the longest inflation time (159 ± 61 seconds vs. 204 ± 72 seconds; p = 0.004) and the total inflation time (220 ± 119 seconds vs. 529 ± 316 seconds; p Angiographic analysis. The results of reference diameter, minimal luminal diameter, diameter stenosis and lesion length at baseline, 10 minutes after, and 24 hours after angioplasty are shown in Table 2. At baseline, there were no differences in reference diameter and in stenotic severity between groups. Lesion calcification was observed in 18% of the cutting balloon group and in 22% of the conventional balloon group (p = NS). There were no significant minimal luminal diameter differences at baseline (0.87 ± 0.36 mm vs. 0.79 ± 0.24 mm) or at 10 minutes after angioplasty (2.03 ± 0.44 mm vs. 1.90 ± 0.52 mm), but there was a significant difference in minimal luminal diameter 24 hours after the procedure (1.94 ± 0.41 mm vs. 1.64 ± 0.41 mm; p = 0.001) between the cutting balloon group and the conventional balloon group, respectively. There was no significant difference in percent diameter stenosis at baseline (70.8 ± 9.2% vs. 71.8 ± 8.9%), but there were significant differences in percent stenosis 10 minutes after (29.1 ± 10.6% vs. 33.1 ± 12.5%; p = 0.04) and 24 hours after angioplasty (31.4 ± 11.5% vs. 39.8 ± 12.8%; p = 0.0003) between the cutting balloon group and the conventional balloon group, respectively. There were no total occlusions at 24-hour follow-up angiograms in either group. Acute gain and acute coronary recoil. There was no significant difference in the acute gain between the cutting balloon group and the conventional balloon group (1.15 ± 0.49 mm vs. 1.08 ± 0.60 mm, respectively). The early recoil within 10 minutes after angioplasty was significantly smaller in the cutting balloon group than in the conventional balloon group (0.96 ± 0.40 mm vs. 1.12 ± 0.37 mm, respectively; p = 0.04). Also, acute recoil at 24 hours after angioplasty was significantly smaller in the cutting balloon group than in the conventional balloon group (1.05 ± 0.41 mm vs. 1.32 ± 0.44 mm, respectively; p = 0.0007). Percent acute recoil 10 minutes and 24 hours after angioplasty was significantly lower in the cutting balloon group than in the conventional balloon group (32.0 ± 11.9% vs. 37.4 ± 11.6%, p = 0.02; 34.7 ± 11.6% vs. 43.6 ± 12.4%, p 0.3 mm loss in minimal luminal diameters and/or > 10% increase in diameter stenosis at 24-hour angiography after successful PTCA.6 Implantation of Palmaz-Schatz stent eliminated the decrease in vessel dimensions caused by elastic recoil after balloon angioplasty.4 Therefore, coronary stenting in such a high-risk group with early minimal luminal diameter loss after successful angioplasty reduced the incidence of restenosis.17 Cutting balloons contain 3–4 longitudinal microminiaturized microtome blades which are used to make sharp, longitudinal incisions in the diseased arterial segment before dilating. This results in less severe arterial injury and fewer major dissections than conventional balloon angioplasty.8 Honye et al. observed a higher restenosis rate in concentric plaques without dissection, suggesting that limited wall dissection can be beneficial for long-term lumen patency.18 Controlled incision of plaques by cutting balloon might lead to less late restenosis. We previously reported a 23% angiographic restenosis rate in the cutting balloon group and 42% in the conventional balloon group.9 Ergene et al. similarly reported 27% angiographic restenosis rate for the cutting balloon and 47% for the conventional balloon procedures.10 Our results revealed that early elastic recoil within 10 minutes after angioplasty was significantly smaller in the cutting balloon group (0.96 ± 0.40 mm vs. 1.12 ± 0.37 mm in the conventional balloon group; p = 0.04). In addition, the mean amount of lumen loss during the first 24 hours after angioplasty was also significantly smaller in the cutting balloon group (0.08 ± 0.28 mm vs. 0.20 ± 0.33 mm in the conventional balloon group; p = 0.02). Greater arterial stretching during angioplasty was associated with more recoil; that is, the most important predictor of absolute and relative recoil was the balloon to artery ratio.1,5,7 As the balloon to artery ratio was similar between the cutting balloon group and the conventional balloon group (1.19 ± 0.11 vs. 1.19 ± 0.13, respectively; p = NS), the influence of the balloon to artery ratio on acute recoil was negligible in this study. The underlying mechanism of less elastic recoil with cutting balloon than with conventional balloon is unknown. “Controlled” incision with the cutting balloon may result in plaque compression or cutting through some of the smooth muscle layer rather than stretching of the disease-free wall. This may lead to less elastic recoil. Reducing early elastic recoil with cutting balloon might be one of the important factors inhibiting restenosis. Study limitations. This study has several limitations. First, it was an uncontrolled retrospective observational study limited to a subset of patients who underwent successful coronary intervention. By protocol, vessels with significant dissections were not included in the analysis. Second, coronary angiograms were obtained in several projections taking into account the asymmetry of stenotic lesions. However, views of the inflated balloon were obtained in a single projection, with a balloon cross-section that was assumed to be circular at maximal inflation pressure. Although balloons appeared fully expanded without visible indentation, it is possible that constraints provided by eccentric stenoses would have limited the expansion of the balloon in some directions. Third, although vessel wall and lumen areas are more objectively quantifiable by intravascular ultrasound, we didn’t perform this procedure in our analysis. Finally, late follow-up data were not assessed, so the relationship between acute elastic recoil and late restenosis was not clearly evident in this population. Conclusion Our data demonstrated that the magnitude of early elastic recoil after balloon angioplasty is smaller in cutting balloon angioplasty than in conventional balloon angioplasty. “Controlled” incision with cutting balloon may result in plaque compression or cutting through some of the smooth muscle layer rather than a stretching of a disease-free wall, and this may lead to less elastic recoil. Less elastic recoil by cutting balloon will probably result in reduced late angiographic restenosis.
1. Rensing BJ, Hermans WRM, Beatt KJ, et al. Quantitative angiographic assessment of elastic recoil after percutaneous transluminal coronary angioplasty. Am J Cardiol 1990;66:1039–1044. 2. Rensing BJ, Hermans WR, Strauss BH, Serruys PW. Regional differences in elastic recoil after percutaneous transluminal coronary angioplasty: A quantitative angiographic study. J Am Coll Cardiol 1991;17:34B–38B. 3. Hanet C, Wijns W, Michel X, Schroeder E. Influence of balloon size and stenosis morphology on immediate and delayed elastic recoil after percutaneous transluminal coronary angioplasty. J Am Coll Cardiol 1991;18:506–511. 4. Haude M, Erbel R, Issa H, Meyer J. Quantitative analysis of elastic recoil after balloon angioplasty and after intracoronary implantation of balloon-expandable Palmaz-Schatz stents. J Am Coll Cardiol 1993;21:26–34. 5. Rozenman Y, Gilon D, Welber S, et al. Clinical and angiographic predictors of immediate recoil after successful coronary angioplasty and relation to late restenosis. Am J Cardiol 1993;72:1020–1025. 6. Rodriguez A, Santaera O, Larribeau M, et al. Early decrease in minimal luminal diameter after successful percutaneous transluminal coronary angioplasty predicts late restenosis. Am J Cardiol 1993;71:1391–1395. 7. Ardissino D, Di Somma S, Kubica J, et al. Influence of elastic recoil on restenosis after successful coronary angioplasty in unstable angina pectoris. Am J Cardiol 1993;71:659–663. 8. Barath P, Fishbein MC, Vari S, Forrester JS. Cutting balloon: A novel approach to percutaneous angioplasty. Am J Cardiol 1991;68:1249–1252. 9. Kondo T, Kawaguchi K, Awaji Y, Mochizuki M. Immediate and chronic results of cutting balloon angioplasty: A matched comparison with conventional angioplasty. Clin Cardiol 1997;20:459–463. 10. Ergene O, Seyithanoglu BY, Tastan A, et al. Comparison of angiographic and clinical outcome after cutting balloon and conventional balloon angioplasty in vessels smaller than 3 mm in diameter: A randomized trial. J Invas Cardiol 1998;10:70–75. 11. Hausleiter J, Nolte CWT, Jost S, et al. Comparison of different quantitative coronary analysis system: ARTREK, CAAS, and CMS. Cathet Cardiovasc Diagn 1996;37:14–22. 12. Waller BF. “Crackers, breakers, stretchers, drillers, scrapers, shavers, burners, welders and melters” — The future treatment of atherosclerotic coronary artery disease? A clinical-morphologic assessment. J Am Coll Cardiol 1989;13:969–987. 13. Baptista J, Di Mario C, Ozaki Y, et al. Impact of plaque morphology and composition on the mechanisms of lumen enlargement using intracoronary ultrasound and quantitative angiography after balloon angioplasty. Am J Cardiol 1996;77:115–121. 14. Potkin BN, Keren G, Mintz GS, et al. Arterial responses to balloon coronary angioplasty: An intravascular ultrasound study. J Am Coll Cardiol 1992;20:942–951. 15. Gerber TC, Erbel R, Görge G, et al. Classification of morphologic effects of percutaneous transluminal coronary angioplasty assessed by intravascular ultrasound. Am J Cardiol 1992;70:1546–1554. 16. Rodríguez AE, Santaera O, Larribau M, et al. Coronary stenting decreases restenosis in lesions with early loss in luminal diameter 24 hours after successful PTCA. Circulation 1995;91:1397–1402. 17. Rodríguez AE, Palacios IF, Fernández MA, et al. Time course and mechanism of early luminal diameter loss after percutaneous transluminal coronary angioplasty. Am J Cardiol 1995;76:1131–1134. 18. Honye J, Mahon DJ, Jain A, et al. Morphological effects of coronary balloon angioplasty in vivo assessed by intravascular ultrasound imaging. Circulation 1992;85:1012–1025.

Advertisement

Advertisement

Advertisement