Improvement in Hemodynamics with a New, Larger-Volume (50 cc) Intra-Aortic Balloon for High-Risk Percutaneous Coronary Intervention
The development of adverse outcomes among high-risk patients undergoing percutaneous coronary intervention (PCI) is often multifactorial. A primary cause, however, may be a diminished capacity to tolerate the hemodynamic and ischemic insults that can occur during the procedure. Thus in selected high-risk patients undergoing PCI, mechanical support, including the intra-aortic balloon pump (IABP), is sometimes used periprocedurally to prevent the potential for hemodynamic instability or ischemic compromise. Although studies have reported improved outcomes with IABP support among high-risk patients undergoing PCI,1–6 a recent randomized trial of elective versus no planned IABP use showed no significant differences in major adverse cardiac events (MACE) at discharge or in all-cause mortality 6 months after PCI in 301 patients in the U.K. who had severe left ventricular dysfunction and extensive coronary disease.7
IABP technology has now evolved such that smaller patients now might safely receive the benefits presumed to accrue from insertion of larger balloon catheters. We describe the successful augmentation of left heart function and reduction in right and left heart pressures achieved with the use of a novel 50 cc IABP for support in a patient with both severe left ventricular dysfunction and severe coronary arteriosclerosis, for whom PCI with stenting was indicated.
Case Presentation
A 75-year-old man with chronic ischemic cardiomyopathy (ejection fraction 25%), noninsulin-dependent diabetes mellitus, hypertension and dyslipidemia was referred to our institution after several weeks of worsening shortness of breath and fatigue. His breathing became labored with minimal activity (New York Heart Association Class III). He reported no chest discomfort. Additional medical history included 3-vessel coronary artery bypass grafting after myocardial infarction and left carotid endarterectomy, both 20 years previously, and an implantable defibrillator placed 10 years previously. His outpatient medical regimen included warfarin for left ventricular dysfunction, furosemide, fenofibrate, digoxin, enalapril, metoprolol, rosiglitazone and simvastatin. Electrocardiography revealed sinus bradycardia and left anterior fascicular block. His body mass index was 20.6 kg/m2 (height: 162.6 cm; weight: 54.5 kg). He had an elevated jugular venous pressure (10 cm), clear lung fields, regular bradycardic rhythm, 2/6 holosystolic murmur at the apex, no edema of the lower extremities and bilateral femoral bruits. Laboratory assessment revealed a mildly abnormal glomerular filtration rate (59 ml/min/1.73 m2), hypoalbuminemia (3.0 gm/dl), mildly abnormal liver function tests (total bilirubin, 1.4 mg/dl; aspartate aminotransferase, 75 IU/l), and pancytopenia with marked thrombocytopenia (white cell count, 3.4 × 109/l; hematocrit, 31%; platelet count, 47 × 109/l). Troponin levels were within normal limits; however, the brain natriuretic peptide level was markedly elevated (3160 pg/ml).






Discussion
Factors that can increase the risk of in-hospital complications of PCI include advanced age, shock, renal insufficiency, urgency of the procedure, heart failure, the presence of thrombus, peripheral arterial disease, recent myocardial infarction and left main or multivessel coronary disease.8,9 Patients with congestive heart failure and left ventricular systolic dysfunction are at particularly increased risk for adverse in-hospital and long-term outcomes after PCI.10–12 Although the cause of adverse outcomes among these patients is often multifactorial, these outcomes may partially relate to a reduced capacity to tolerate the hemodynamic or ischemic insults that can occur with PCI. Thus, selected patients with high-risk features undergoing PCI also receive mechanical support periprocedurally. IABP is often used for this purpose. The IABP was first used clinically in 1968 in patients who developed cardiogenic shock after acute myocardial infarction.13 The three primary goals of IABP use remain to increase coronary perfusion, reduce left ventricular afterload and increase cardiac output. Balloon inflation during early diastole and deflation during end-diastole each provide their own beneficial hemodynamic effects (Table 1). Deflation during end-diastole actively draws blood from the central aorta and thus reduces aortic systolic pressure and left ventricular end-diastolic pressure by an estimated 8.9–26.6% and 25–40%, respectively.14,15 Diastolic augmentation occurring with balloon inflation can improve coronary perfusion by 5–15%, and, in association with reduced afterload, result in improved myocardial contractility.16,17 As a consequence, cardiac output can increase by as much as 50%.15,18,19 IABs have long been used electively during high-risk PCI and emergently in cases of periprocedural hemodynamic instability.1–6 However, although prophylactic IABP support for high-risk PCI has been independently associated with higher 6-month survival5 and reduced intraprocedural complications6 in selected series, a recent randomized trial showed no benefit in terms of MACE at hospital discharge or all-cause mortality at 6 months.7 Elective IABP in high-risk PCI has consistently been associated with comparable or reduced rates of major procedural complications, major or minor bleeding and access-site complications.5–7 Thus, the role of prophylactic IABP in high-risk PCI remains unclear. In our patient, the use of a new, larger-volume IAB, which provides 25% greater blood volume displacement compared with the 40 cc balloon,20 produced remarkable diastolic augmentation that resulted in improved hemodynamics. Despite the patient’s severe pulmonary hypertension, within 1 hour after beginning IABP support, his transpulmonary gradient had improved from 17 mmHg to 10 mmHg. In our patient’s case, the decision for IABP support was driven by the extent of coronary artery disease and amount of myocardium at risk. If flow in the LAD had become compromised during PCI, the risk of hemodynamic collapse would have been substantial because of reduced perfusion, not only in the LAD territory, but also in the RCA territory supplied by LAD collateral flow.

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