Skip to main content

Advertisement

ADVERTISEMENT

Original Contribution

Clinical Experience with Rotational Atherectomy in Patients with Severe Left Ventricular Dysfunction

Ravi K. Ramana, DO, Dominique Joyal, MD, Dinesh Arab, MD, Robert S. Dieter, MD, RVT, Lowell Steen, MD, Bruce Lewis, MD, Ferdinand Leya, MD
November 2006
Over the past decade there have been tremendous advancements in the technique and procedural success rates in the field of interventional cardiology. Many of these advancements have addressed percutaneous coronary interventions (PCI) on lesions with high-risk characteristics.1,2 For example, high-speed rotational atherectomy (RA), first described in 1989,3 is performed using a rotating abrasive burr that is designed to debulk atherosclerotic plaque by producing small particles (approximately 7–15 microns in diameter) that are washed away across the capillary bed and filtered by the reticuloendothelial system.4 Early studies evaluating the efficacy of RA revealed very high procedural success rates with low complication rates.5 But more recent data regarding RA have been unable to replicate these early clinical successes; although the clinical practice in these studies6–12 (e.g., RA followed by low-pressure balloon inflation without stent implantation) is strikingly different from the current practice of RA use.5 Presently, RA is being used in patients with complex coronary lesions,13 such as those with severely calcified, diffuse coronary artery lesions or diffuse, severe in-stent restenosis that may prove difficult to cross or dilate,14 and is followed by high-pressure inflation with stent implantation. Further studies have suggested that RA diminishes plaque volume with abrasion, as opposed to fracturing plaque, and therefore has the potential to minimize acute vessel injury and avoid disruption of soft elastic tissue.15 Therefore, RA can possibly reduce some types of complications including restenosis in smaller vessels,8 heavily calcified or diffuse high-risk lesions. However, RA is not without its dangers: previous research suggests that specific procedural complications including myocardial infarction via direct platelet activation16 and coronary artery perforation may occur more frequently with RA.17,18 Also, in patients undergoing RA (compared to balloon angioplasty), wall motion abnormalities occurred with similar severity (mean wall motion abnormality ~30%), but with much higher frequency and persisted much longer.19 In fact (according to the device manufacturer), RA is not recommended to be used in patients with severe left ventricular dysfunction (defined as LVEF 20 Procedural success was defined as: (1) asymptomatic and hemodynamically stable patient at the conclusion of the procedure; (2) successful crossing of the lesion with the rotational atherectomy burr; (3) no evidence of coronary artery dissection or perforation; and (4) residual diameter stenosis e.g., as evidenced by pulmonary edema) or left ventricular systolic function (e.g., as evidenced by reduced ejection fraction by transthoracic echocardiography), acute renal insufficiency, and length of hospital stay were also noted. The interventional cardiologist performed the RA procedure according to standard practice at our institution: All patients received periprocedural intravenous glycoprotein IIb/IIIa inhibitors (GP IIb/IIIa); all patients who were undergoing intervention to a right coronary artery or dominant left circumflex artery lesion received a temporary pacemaker; all patients deemed hemodynamically unstable had preprocedural intraaortic balloon pump placement. All patients, who were not taking clopidogrel prior to the procedure were given 300 mg of clopidogrel at the start of the case. During the procedure, unfractionated heparin was administered in all patients in order to maintain a partial prothrombin time (PTT) > 300 seconds. All patients received sirolimus drug-eluting stents. Following the procedure, the patient was monitored on telemetry for at least 12 hours for signs of ischemia, congestive heart failure or other procedural complications. Electrocardiographic evaluation of all patients was completed postprocedure, and serum cardiac biomarkers were drawn only when clinically indicated by the patient’s symptoms and clinical presentation. If no complications arose, the patient was discharged home in stable condition with standard 2-week cardiology outpatient follow up. Clopidogrel (75 mg/daily) and aspirin were prescribed to all patients for at least 3 months following the procedure unless contraindicated. Results During the 4-year period, 27 lesions were treated with RA in 23 patients (17 males) with a LVEF 1 mm ST-segment elevation in 2 contiguous leads, and 1 with > 2 mm ST-segment depression in at least 2 contiguous leads) — none of whom required repeat revascularization. The average postprocedural troponin was 4.12 ng/mL (range 0–27) in the 10 patients whose clinical presentation dictated serum biomarker evaluation. No patients necessitated emergency coronary artery bypass. There were no in-hospital mortalities related to the procedure. Only 1 patient died during hospitalization; this patient initially was admitted with AML blast crisis, underwent cardiac catheterization with RA solely for relief of refractory angina and died after all medical therapy and life-support for the hematologic emergency were withdrawn. Therefore, in-hospital MACE were observed in 4 patients (17.4%). There were no postdischarge deaths or MACE after 30 days. Further endpoints included 1 patient with significant bleeding requiring transfusions (4.3%) and another with acute renal insufficiency (4.3%). There were no patients with worsening dyspnea or congestive heart failure (e.g., as evidenced by pulmonary edema) or progressive decline of left ventricular function assessed by transthoracic or transesophageal echocardiography, and the average length of hospital stay was 3.2 days (range 1–15 days). Discussion Presently, RA is being used with more frequency in patients with complex coronary lesions. RA is designed to debulk complex atherosclerotic plaque by producing small particles of atheromatous debris which initially was proposed to pass harmlessly through the coronary capillary bed and then be filtered from the bloodstream by the reticuloendothelial system.21–23 However, Friedman et al disputed this claim by demonstrating histological evidence of myocardial microinfarctions after intracoronary infusion of atherectomized debris.24 Other studies have investigated the clinical consequences of the “shower” of debris by performing simultaneous echocardiography during and following RA. A study showed in patients undergoing RA that wall motion abnormalities occurred with much higher frequency, developed in predictable territories related to the target artery, and were unrelated to cardiac biomarker release or electrocardiographic changes. More importantly, these wall motion abnormalities persisted much longer than in those patients undergoing balloon angioplasty (153 minutes compared to 3 minutes).19 This prolonged segmental LV dysfunction can possibly be explained by the distal embolization of atherosclerotic debris,24,25 production of microcavitation with microbubbles26 in the target coronary artery, induction of coronary artery spasm at the site of RA and resultant low-flow1,27 and/or increased platelet activation and aggregation.28 Therefore, it seems reasonable to suggest that patients with severe LV dysfunction may have a higher likelihood of hemodynamic instability during RA. And although in our small case series there were no detected coronary artery perforations or dissections, it seems reasonable to also assume that this patient subgroup would have little cardiac function reserve to tolerate significant coronary artery damage. In our experience, this was not necessarily the case: controversy still exists on predicting hemodynamic instability during PCI, therefore no formal clinical guidelines exist on intra-aortic balloon pump (IABP) placement during PCI.29 Elective high-risk PCI often can be performed without placement of an IABP.29 However, it is appropriate to consider elective IABP placement prior to the intervention in patients who have high-risk characteristics: ejection fraction 50% myocardium at risk, PTCA performed on the last remaining vessel or cardiogenic shock.29–31 IABP placement preceding or during PCI in these patient populations have been shown to improve clinical outcomes.32,33 Specifically, recent literature has suggested RA is feasible in patients with varying degrees of LV dysfunction (only 31% of these patients had a LVEF 34 However, no study to date has specifically addressed the role of RA and its clinical efficacy and safety in patients with severe LV dysfunction. The current study is a small, retrospective study reporting our clinical experience with RA in patients with severe LV dysfunction undergoing PCI. Our results support the notion that RA in patients with severe LV dysfunction is a safe and feasible technique for revascularization when no other therapeutic options are available and when performed by experienced operators at medical centers with on-site surgical backup. Study limitations. Although these data are encouraging, there are a few limitations that must be acknowledged. First, this study was completed at only one tertiary medical center, which makes the accuracy of extrapolating these conclusions to community hospitals unknown. Second, there was not a standard protocol for cardiac biomarker assessment for postprocedural MI. Instead, cardiac biomarker evaluation was only done when the clinical scenario or patients’ symptoms suggested ischemia or infarction. Although this may underestimate the total number of postprocedural MIs, it may not affect the reported event rate of clinically significant infarctions. Conclusions It is certain that in the era of drug-eluting stents, we are intervening on more complex coronary lesions and treating sicker patients who previously were deemed poor candidates for any revascularization. Recent reviews of patient registries have revealed no decrease in procedural success with RA, despite increasing complexity in patients’ medical illness or coronary lesions.13 This suggests that RA may allow PCI in patients who were previously deemed poor candidates for revascularization. However, it is crucial to evaluate a patient’s likelihood of tolerating a time-consuming procedure while lying supine and receiving moderate-to-large amounts of intravenous fluids and nitrates prior to undergoing RA. Therefore, it is imperative that we have a clear understanding of the subset of patients in which RA is effective and when concomitant IABP use is necessary. Our small, retrospective study suggests that RA is safe and effective in patients with severe LV dysfunction when performed by experienced operators (with extensive knowledge in determining burr size, burr speed, number of runs and number of vessels to be safely treated) and at centers with on-site surgical backup and IABP support. Further studies involving a larger patient population are needed to validate our clinical experience with a standard protocol involving postprocedure cardiac biomarker assessment and objective evaluation with postprocedure LV systolic function (e.g., cardiac magnetic resonance imaging or multiple gated acquisition [MUGA] testing). Also, studies are needed to evaluate the long-term clinical outcomes of RA with patients who have severe LV dysfunction to further confirm the importance of the use of this interventional technique in high-risk patient populations.
REFERENCES 1. Teirstein PS, Warth DC, Hag N, et al. High-speed rotational coronary atherectomy for patients with diffuse coronary artery disease. J Am Coll Cardiol 1991;18:1694–1701. 2. Ellis SG, Popma JJ, Buchbinder M, et al. Relation of clinical presentation, stenosis morphology, and operator technique to the procedural results of rotational atherectomy and rotational atherectomy-facilitated angioplasty. Circulation 1994;89:882–892. 3. Fourrier JL, Bertrand ME, Auth DC, et al. Percutaneous coronary rotational angioplasty in humans: A preliminary report. J Am Coll Cardiol 1989;14:1278–1282. 4. Rubartelli P, Niccoli L, Alberti A, et al. Coronary rotational atherectomy in current practice. Cath and CV Inter 2004;61:463–471. 5. Levin TN, Holloway S, Feldman T. Acute and late clinical outcome after rotational atherectomy for complex coronary disease. Cathet Cardiovasc Diagn 1998;45:122–130. 6. VonDahl J, Dietz U, Haager PK, et al. Rotational atherectomy does not reduce recurrent in-stent restenosis (ARTIST). Circulation 2002;105:583–588. 7. Dill T, Dietz U, Hamm CW, et al. A randomized comparison of balloon angioplasty versus rotational atherectomy in complex coronary lesions (COBRA). Eur Heart J 2000;21:1759–1766. 8. Mauri L, Reisman, M, Buchbinder M, et al. Comparison of rotational atherectomy with conventional balloon angioplasty in the prevention of restenosis of small coronary arteries (DART). Am Heart J 2003;145:847–854. 9. Reifart N, Vandormael M, Krajcar M, et al. Randomized comparison of angioplasty of complex lesions at a single center. (ERBAC). Circulation 1997;19:91–98. 10. Buchbinder M, Fortuna R, Sharma SK, et al. Debulking prior to stenting improves acute outcomes: Early results from the SPORT trial. J Am Coll Cardiol 2000;35(A):9A. 11. Goldberg SL, Berger P, Cohen DJ, et al. Rotational atherectomy or balloon angioplasty in the treatment of intra-stent restenosis: BARASTER Multicenter Registry. Cath and CV Inter 2000;51:407–413. 12. Sharma SK, Kini A, Mehran R, et al. Randomized trial of rotational atherectomy versus balloon angioplasty for diffuse in-stent restenosis (ROSTER). Am Heart J 2004;147:16–22. 13. Reisman M, Harms V, Whitlow P, et al. Comparison of early and recent results with rotational atherectomy. J Am Coll Cardiol 1997;29:353–357. 14. Borgan WC, Popma JJ, Pichard AD, et al. Rotational coronary atherectomy after unsuccessful coronary balloon angioplasty. Am J Cardiol 1993;71:794–798. 15. Hoffman R, Mintz GS, Kent KM, et al. Comparative early and nine-month results of rotational atherectomy, stents and the combination of both for calcified lesions in large coronary arteries. J Am Coll Cardiol 1998;81:552–557. 16. Dehmer GJ, Nichols TC, Bode AP, et al. Assessment of platelet activation by coronary sinus blood sampling during balloon angioplasty and directional coronary atherectomy. Am J Cardiol 1997;80:871–877. 17. Ellis SG, Ajluni S, Arnold AZ, et al. Increased coronary perforation in the new device era: Incidence, classification, management and outcome. Circulation 1994;90:2725–2730. 18. Ajluni SC, Glazier S, Blankenship L, et al. Perforations after percutaneous coronary interventions: Clinical, angiographic, and therapeutic observations. Cathet Cardiovasc Diagn 1994;32:206–212. 19. Williams MJ, Dow CJ, Newell JB, et al. Prevalence and timing of regional myocardial dysfunction after rotational coronary atherectomy. J Am Coll Cardiol 1996;28:861–869. 20. Ellis SG, Vandormael MG, Cowley MJ, et al. Coronary morphologic and clinical determinants of procedural outcome with angioplasty for multivessel coronary disease: Implications for patient selection. Circulation 1990;82:1193–1202. 21. Hansen DD, Auth DC, Vracko R, et al. Rotational atherectomy in atherosclerotic rabbit iliac arteries. Am Heart J 1988;115:160–165. 22. Ahn SS, Auth D, Marcus DR, et al. Removal of focal atheromatous lesions by angioscopically guided high-speed rotational atherectomy. J Vasc Surg 1988;7:292–300. 23. Hansen DD, Auth DC, Hall M, et al. Rotational endarterectomy in normal canine coronary arteries. J Am Coll Cardiol 1988;11:1073–1077. 24. Friedman HZ, Elliot MA, Gottleib GJ, et al. Mechanical rotational atherectomy: The effects of microparticle embolization on myocardial blood flow and function. J Interv Cardio 1989;2:77–83. 25. Safian RD, Niazi KA, Strzelecki M, et al. Detailed angiographic analysis of high-speed rotational atherectomy in human coronary arteries. Circulation 1993;88:961–968. 26. Zotz RJ, Erbel R, Phillip A, et al. High-speed rotational angioplasty-induced echo contrast in vivo and in vitro optical analysis. Cathet Cardiovasc Diagn 1992;26:98–109. 27. Bertrand ME, Lablanche JM, Leroy F, et al. Percutaneous transluminal coronary rotary ablation with Rotablator. Am J Cardiol 1992 ;69:470–474. 28. Nunez BD, Keelan ET, Lerman A, et al. Coronary hemodynamics after rotational atherectomy. J Am Coll Cardiol 1995;25:95A. 29. Smith S, Feldman T, Hirshfeld J, et al. ACC/AHA/SCAI 2005 Guideline update for percutaneous coronary intervention. J Am Coll Cardiol 2006. 30. Hartzler GO, Rutherford BD, McConahay DR, et al. High-risk coronary artery angioplasty. J Am Coll Cardiol 1989;13:283–288. 31. Bergelson BA, Jacobs AK, Cupples LA, et al. Prediction of risk for hemodynamic compromise during percutaneous transluminal coronary angioplasty. Am J Cardiol 1992;70:1540–1545. 32. Kreidieh I, Davis DW, Lim R, et al. High-risk coronary angioplasty with elective intra-aortic balloon pump support. Int J Cardiol 1989;64:967–970. 33. Anwar A, Mooney MR, Stertzer SH, et al. Intra-aortic balloon counterpulsation support for elective coronary angioplasty in the setting of poor left ventricular function: A two center study. J Invasive Cardiol 1990;2:175–180. 34. O’Murchu B, Foreman R, Shaw R, et al. Role of intraaortic balloon pump counterpulsation in high-risk coronary rotational atherectomy. J Am Coll Cardiol 1995;26:1270–1275.

Advertisement

Advertisement

Advertisement