STATE-OF-THE-ART PAPER
Aarush Manchanda, MD,* Ozlem Soran, MD, MPH, FACC, FESC†
Washington, DC; and Pittsburgh, Pennsylvania
J Am Coll Cardiol 2007; : 1523–31) © 2007 by the American College of Cardiology Foundation
Between 25,000 and 75,000 new cases of angina refractory to maximal medical therapy and standard coronary revascularization procedures are diagnosed each year. In addition, heart failure also places an enormous burden on the U.S. health care system, with an estimated economic impact ranging from $20 billion to more than $50 billion per year. The technique of counterpulsation, studied for almost one-half century now, is considered a safe, highly beneficial, low-cost, noninvasive treatment for these angina patients, and now for heart failure patients as well. Recent evidence suggests that enhanced external counterpulsation (EECP) therapy may improve symptoms and decrease long-term morbidity via more than 1 mechanism, including improvement in endothelial function, promotion of collateralization, enhancement of ventricular function, improvement in oxygen consumption (VO2), regression of atherosclerosis, and peripheral training effects similar to exercise. Numerous clinical trials in the last 2 decades have shown EECP therapy to be safe and effective for patients with refractory angina with a clinical
response rate averaging 70% to 80%, which is sustained up to 5 years. It is not only safe in patients with coexisting heart failure, but also is shown to improve quality of life and exercise capacity and to improve left ventricular function long-term. Interestingly, EECP therapy has been studied for various potential uses other than heart disease, such as restless leg syndrome, sudden deafness, hepatorenal syndrome, erectile dysfunction, and so on. This review summarizes the current evidence for its use in stable angina and heart failure and its future directions.
An estimated 6.4 million patients in the U.S. suffer from symptomatic coronary artery disease (CAD), and about 400,000 new cases develop each year (1). Despite optimal medical therapy and invasive procedures, such as angioplasty and cardiac bypass surgery, there are an estimated 300,000 to 900,000 patients in the U.S. who have refractory angina pectoris (RAP). About 25,000 to 75,000 new cases of RAP are diagnosed each year (1). Daily tasks such as climbing a flight of stairs, walking a dog, or mowing the lawn become impossible without experiencing chest pain for these difficult-to-treat patients. In addition, despite advances in medical therapy for the treatment of heart failure (HF) over the past decade, substantial unmet needs remain, particularly in patients with moderate to severe HF. Heart failure is the number 1 diagnosis in Medicare patients and approximately 5 million Americans experience HF, with 550,000 new cases per year reported (1). It has been estimated that in 2005, the total direct and indirect cost of HF in the U.S. will be equal to $27.9 billion, and approximately $2.9 billion annually is spent on drugs for the treatment of HF (1). Only a few consensus therapies exist to treat HF beyond medical management, and many patients now are left to suffer their symptoms and restrict their activities chronically, and anticipate a reduced life expectancy. Current nonpharmacological options available for these patients with RAP with or without underlying HF include neurostimulation (transcutaneous electrical nerve stimulation and spinal cord stimulation), enhanced external counterpulsation (EECP) therapy, laser revascularization techniques, gene therapy, and newer interventional procedures such as percutaneous in situ coronary venous arterialization or percutaneous in situ coronary artery bypass (2). Of these modalities, EECP therapy represents the only truly noninvasive technique for which both a reduction of angina symptoms, improvement in objective measures of myocardial ischemia, and improvement in left ventricular function (both systolic and diastolic) have been shown (3–5).
From the *Department of Internal Medicine, The George Washington University, Washington, DC; and the †Cardiovascular Institute, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania. Dr. Soran serves on the Speakers’ Bureau of Vasomedical, Inc. Manuscript received April 2, 2007; revised manuscript received May 25, 2007, accepted July 17, 2007.
Journal of the American College of Cardiology Vol. 50, No. 16, 2007 © 2007
The American College of Cardiology Foundation ISSN 0735-1097/07/$32.00
Published by Elsevier Inc. doi:10.1016/j.jacc.2007.07.024
Downloaded from content.onlinejacc.org by on May 10, 2011
Historical Perspective
Almost one-half century ago, researchers at Harvard Universityconducted experiments with counterpulsation showing that this technique markedly reduces the workload, and thus oxygen consumption, of the left ventricle. In 1953, Kantrowitz and Kantrowitz (6) described diastolic augmentation as a means of improving coronary blood flow. Birtwell et al. (7) did pioneering work toward the development of this technique and were first to apply this concept by developing the initial arterial counterpulsator in the U.S. Zheng et al. (8) were the first to report the benefits of external counterpulsation in the 1980s by using the first
pneumatic counterpulsation device. Lawson et al. (9–13) at the State University of New York, Stony Brook, undertook a number of open-label studies with the enhanced system, EECP, between 1989 and 1998 using both objective and subjective end points. These studies, although open and nonrandomized, showed statistical improvement in exercise tolerance by patients as evidenced by thallium-stress testing and partial or complete resolution of coronary perfusion defects as evidenced by radionuclide imaging studies. In
1999, Arora et al. (14) reported results of the first double blind randomized placebo-controlled multicenter trial (MUST-EECP [Multicenter Study of Enhanced External Counterpulsation]) (14). Since then, EECP therapy has emerged as an effective, noninvasive, and durable therapeutic option for patients not only with angina but also with HF.
Technique
The technique of EECP therapy consists of electrocardiogram-gated rapid, sequential compression of the lower extremities taking place during diastole, followed by simultaneous decompression during systole. These actions produce hemodynamic effects similar to those of an intraaortic balloon pump, but unlike an intra-aortic balloon pump, EECP therapy also increases venous return (Fig. 1). Cuffs resembling oversized blood pressure cuffs—on the calves, the lower thighs, and the upper thighs, including the buttocks, inflate rapidly and sequentially—via computer interpreted electrocardiogram signals—starting from the calves and proceeding upward to the buttocks (Fig. 1) during the resting phase of each heartbeat (diastole). This
has the effect of creating a strong retrograde counterpulse in the arterial system, forcing freshly oxygenated blood toward the heart and coronary arteries, while simultaneously increasing the volume of venous blood return to the heart under increased pressure. Just before the next heartbeat, before the systole, all 3
cuffs simultaneously deflate, significantly reducing the workload of the heart. This is achieved because the vascular beds in the lower extremities are relatively empty when the cuffs are deflated, significantly lowering the resistance to blood ejected by the heart, reducing the amount of work the heart must do to pump oxygenated blood to the rest of the body. The inflation-deflation activity is monitored with the help of a finger plethysmogram and coordinated by a microprocessor that interprets electrocardiogram signals
from the patient’s heart and actuates the inflation and deflation cycles. The end result of this sequential squeezing of the legs is to create a pressure wave that significantly increases peak diastolic pressure, benefiting circulation to the heart muscle and other organs, while also reducing systolic pressure and systemic vascular resistance to the general benefit of the vascular system. A typical treatment
course consists of 35 outpatient treatments administered as 1 h per day over 7 weeks.
Three pairs of pneumatic cuffs are applied to the calves, lower thighs, and upper thighs. The cuffs are inflated sequentially during diastole, distal to proximal. The compression of the lower-extremity vascular bed increases diastolic pressure and flow and increases venous return. The pressure is then released at the onset of systole. Inflation and deflation are timed according to the R-wave on the patient’s cardiac monitor. The pressures applied and the inflation– deflation timing can be altered by using the pressure waveforms and electrocardiogram on the enhanced external counterpulsation (EECP) therapy monitor.
Mechanism of Action of EECP
Recent advances in the understanding of coronary arterial physiology and response to EECP therapy have provided some insight into possible modes of effect and an explanation for the benefits seen with EECP therapy (Fig. 2.) However, most of the experience is from small animal or human uncontrolled studies, and the mechanism of the sustained antianginal benefit with EECP remains unclear. Development of new functional collateral vessels by increasing nitric oxide and decreasing endothelin-1 levels to the ischemic myocardium was postulated as the mechanism of action for EECP therapy by many early studies conducted.
Masuda et al. (15) reported that the development of functional collateral vessels is one of the mechanisms of
EECP therapy using ammonia positron emission tomography. Endothelial shear stress from increased diastolic augmentation after EECP therapy was shown to augment endothelium-derived relaxing factor/nitric oxide production (16) and to cause down-regulation of endothelin-1 levels, thereby recruiting more collateral vessels (17). Akhtar et al. (18) recently showed that EECP therapy has a sustained, dose-related effect in stimulating endothelial cell production of the vasodilator nitric oxide and in decreasing production of endothelin-1. However, an increase in myocardial perfusion on nuclear stress tests was inconsistent with improvement in symptoms (Table 1), making it unlikely as a sole mechanism of benefit. In recent studies by Tao et al. (19,20), EECP therapy demonstrated stabilization of coronary endothelium, an effect very similar to that of athletic training. These recent studies confirm the earlier results by Bonetti et al. (21); they
had seen improvement in the peripheral endothelial function (RH-PAT) in their patients after 35 h of EECP
treatment. Zhang et al. (22) also showed retardation of the atherosclerosis process by the metabolic effects of external counterpulsation therapy on the NF-kappa signaling pathways. Recently Levenson et al. (23) postulated that an increase in cyclic guanosine monophosphate (cGMP) acutely after EECP therapy might in part be responsible for the improved peripheral arterial function. Cyclic guanosine monophosphate regulates vascular smooth muscle tone, which may improve arterial function. Fifty-five subjects were randomized into 2 groups to receive either sham (control) or active EECP therapy during 1 h. Plasma and platelet cGMP were measured immediately before and after EECP therapy by radioimmunoassay. One hour of EECP
therapy increased cGMP plasma concentration by 52% and platelet content by 19%. This theory of endothelial stabilization has attracted the most attention in the recent past as one of the primary mechanisms of action, with more clinical trials needed to further understand it completely. Arora et al. (24) showed a trend toward increased vascular endothelial growth factor levels after EECP therapy in human subjects, thereby confirming the findings of Chen et al. (25) in the canine model. Vascular endothelial growth factor, along with other growth factors such as fibroblast growth factor, is the most widely studied in gene therapy for RAP. It is considered important in promoting angiogenesis or neorevascularization of the ischemic myocardium. However, failure to show consistent improvement in myocardial perfusion as discussed above makes neorevascularization unlikely, an argument similar to the one against collateralization. Ochoa et al. (26) recently reported the acute effects of EECP therapy on oxygen uptake: VO2 at rest in adults with symptomatic CAD compared with healthy volunteers using sham control group. They measured VO2 continuously in 20 adults during a single treatment session of EECP therapy, including 10 subjects with previous coronary revascularization who were referred for EECP therapy for refractory angina and 10 healthy, sedentary volunteers. Both groups showed a small, sustained increase in VO2 during EECP
Possible Mechanisms Responsible for the Clinical Benefit Associated With EECP Therapy
Acute afterload reduction decreases myocardial demand. By increasing coronary blood flow, enhanced external counterpulsation (EECP) therapy is thought to promote myocardial collateralization via opening of preformed collateral vessels, arteriogenesis, and angiogenesis. Increased blood flow and shear stress also may improve coronary endothelial function, favoring vasodilation and myocardial perfusion. In addition, improvement in endothelial function may further
promote collateral formation by arteriogenesis and angiogenesis. In addition to a peripheral training effect, a minor placebo effect is considered to contribute to the symptomatic benefit of
Treatment Duration (h) Angina Relief (% >1 CCS Class1) Nitroglycerine Use Versus Frequency
Exercise Capacity (%) Time to ST-Segment Depression on Stress Test Cardiac Perfusion
(% of Patients) Other Findings Zheng et al. (8) 1983 200 12 2(97%) NA NA NA NA — Lawson et al. (10) 1992 18 36 2(100%) 2 167 NA 1(78%) — Lawson et al. (11,12) 1996 27 35 NA NA 181 NA 1(78%) In addition, EECP therapy seemed to decrease PVR and HR response to exercise, the so-called training effect Lawson et al. (13) 1998 60 35 2 NA 1 NA 1(75%) Benefit sustained at 2-yr
follow-up Arora et al. (14) 1999 139 35 2 2 1 1 NA Only double-blind trial to date using sham
controls Lawson et al. (27) 2000 33 35 2(100%) 2 NA NA 1(79%) Benefit sustained at 5-yr
follow-up Lawson et al. (28) 2000 2,289 35 2(74%) NA NA NA NA EECP consortium.
Efficacy was independent of provider setting or experience Masuda et al. (29)
2001 11 35 NA NA 1 1 1 Coronary perfusion increased both at baseline and during dipyridamole
Provocation Stys et al. (30) 2001 395 35 2(88%) NA NA NA NA EECP was equally effective in men and women and young and elderly (65 yrs) Barsness et al. (31) 2001 978 35 2 (81%) 2 NA NA NA EECP therapy can be used for those who prefer noninvasive treatment to avoid revascularization Stys et al. (32) 2002 175 35 2 (85%) NA 1 NA 1(83%) — Fitzgerald et al.
(33) 2003 4,454 35 2* 2* NA NA 1 *Comparable benefit seen for both previously revascularized and PUMPERS Tartaglia et al. (34) 2003 25 35 2 (93%) NA 1 1(80%) NA — Lawson et al.
(35) 2006 363 35 2 (72%)* 2 52* NA NA NA *Benefit sustained at 2 yrs Lawson et al.
(36) 2005 746 32 2 (72%) 2 NA NA NA Equal benefit in both systolic and diastolic heart failure
Novo et al. (37) 2006 25 35 2 (84%) NA NA NA 1(36%) dobutamine stress if possible echocardiography Maximal benefit seen in patients with worst systolic failure Lawson et al.
(38) 2006 1,458 35 2 2 1 NA NA EECP therapy was found to be equally beneficial in mild vs.
severe anginal symptoms Loh et al. (39) 2006 58 35 2 (86%)* 2 1 NA NA *Sustained improvement in 78% at 1-yr follow-up treatment. Because VO2 is an independent predictor of increased exercise capacity, it led them to conclude that increase in VO2 may also in part be one of the mechanisms
by which EECP therapy increases exercise tolerance in stable angina patients (26). In summary, further studies are needed to elucidate both the mechanism of action and the overall effects of EECP therapy, or a combination of the above mechanisms may explain the sustained benefit from EECP therapy in the
clinical trials (27).
EECP and Angina
Several nonrandomized and randomized trials have shown a consistently positive clinical response among patients of RAP treated with EECP therapy (Table 1) (8 –14,28 –39). Benefits associated with EECP therapy include reduction of angina and nitrate use, increased exercise tolerance, favourable psychosocial effects and enhanced quality of life, as well as prolongation of the time to exercise-induced ST-segment depression and an accompanying resolution of myocardial perfusion defects (Table 1). Patients with severely disabling
angina at baseline and those without a history of smoking are more likely to improve their angina class after EECP therapy (40). Most of the studies on EECP therapy cannot be double blind and lack good control groups because of technical limitations, which have frequently raised questions of operator bias in the past. But the MUST-EECP study, a randomized, double-blind, sham-controlled trial, also showed the clinical benefit of EECP therapy in patients with chronic stable angina and positive exercise stress tests (14). In this study, 139 patients (mean age 63 years, range 35 years to 81 years) with angina pectoris (typical Canadian
Cardiovascular Society classes I, II, and III angina) and documented coronary ischemia were equally randomized to hemodynamically inactive counterpulsation with EECP versus active counterpulsation. Patients in the active EECP therapy group showed a statistically significant increase in time to exercise-induced ST-segment depression when compared with sham and baseline, and reported a statistically
significant decrease in the frequency of angina episodes when compared with sham and baseline. Exercise duration increased significantly in both groups; however, the increase was greater in the active EECP group. Moreover, a MUSTEECP sub-study showed a significant improvement in quality-of-life parameters in patients assigned to active treatment, which was sustained during a 12-month follow-up period (41).
Results from the International EECP Patient Registry (31,33,35) and the EECP Clinical Consortium (28) have shown that the symptomatic benefit observed in controlled studies also translates to the heterogeneous patient population seen in clinical practice. Moreover, follow-up data indicate that the clinical benefit may be maintained for up to 5 years in patients with a favorable initial clinical response (27,35). One of the ongoing debates with most of the published trials discussed earlier (Table 1) is that the increased exercise tolerance reported after EECP therapy may, at least in part, be attributed to a training effect.
EECP in Angina with Left Ventricular Dysfunction
When providing EECP therapy to the HF population, the primary concern of the initial researchers was that the increased venous return resulting from EECP therapy could precipitate pulmonary edema in angina patients with severe left ventricular dysfunction (LVD). Soran et al. (42,43) evaluated the safety and efficacy of EECP therapy in patients with angina and severe LVD (ejection fraction [EF] _35%). The outcomes of EECP treatment were followed up in 363 patients enrolled in the International EECP Patient Registry, an international multicenter study of EECP therapy for the treatment of patients with chronic angina. The EECP therapy was observed to be a safe and effective treatment of angina in patients with severe LVD
who were not considered good candidates for revascularization by coronary artery bypass graft or percutaneous coronary intervention (43). After completion of treatment, there was a significant reduction in severity of angina: 72% improved from severe angina to no angina or mild angina. Fifty-two percent of patients discontinued nitroglycerin use. Quality of life showed a significant increase. At 2-year follow-up, this angina reduction was maintained in 55%, 83% survived, and event-free (death/myocardial infarction/
percutaneous coronary intervention/coronary artery bypass graft) survival rate was 70%. Forty-three percent had no cardiac hospitalization; 81% had no congestive HF event (43). Lawson et al. (44) also evaluated RAP patients with preserved left ventricular function (EF _35%) and with severe left ventricular dysfunction (EF _35%) who were treated with a 35-h course of EECP therapy. Bioimpedance measurements of cardiovascular function were obtained before the first and again after the 35th hour of EECP therapy. Twenty-five patients were enrolled, 20 with preserved left ventricular function and 5 with severe left
ventricular dysfunction. Angina class improved similarly in both groups. The severe left ventricular dysfunction group, in contrast to the preserved left ventricular function group, increased cardiac power, stroke volume, and cardiac index and decreased systemic vascular resistance with treatment. This study suggests that EECP could benefit patients experiencing CAD with severe left ventricular dysfunction
directly by improving cardiac power and indirectly by decreasing systemic vascular resistance (44).
EECP Therapy in HF
Most of the data to date on the efficacy and safety of EECP therapy in HF are from small studies (45,46). In a pilot study of clinically stable patients diagnosed with mild to moderate HF (New York Heart Association [NYHA] JACC Vol. 50, No. 16, 2007 Manchanda and Soran 1527 October 16, 2007:1523–31 EECP and Future Directions Downloaded from content.onlinejacc.org by on May 10, 2011
functional class II or III) and a left ventricular EF _35%, Soran et al. (45) found EECP treatment to be safe with no unexpected adverse events during the application of EECP treatment. Soran et al. (45) also conducted a multicenter feasibility study in which stable HF (New York Heart Association functional class II to III, ischemic and nonischemic etiology) patients with left ventricular EF _35% were treated with 35 1-h sessions of EECP therapy over a 7-week period and followed up over a 6-month period. The mean EF for the ischemic and nonischemic groups was 25.6 _ 7.1% and 18.7 _ 7.4%, respectively. Mild to moderate
valvular heart disease was the most common etiology for the group with nonischemic etiology. Study results showed that EECP therapy was safe and well-tolerated in this group of patients (46). In addition, EECP therapy was associated with significant improvements in exercise capacity as measured by peak oxygen uptake and exercise duration and in quality of life at 1 week and 6 months after EECP treatment. Although safety was the primary end point of this feasibility study, the efficacy results suggest that EECP therapy can increase peak oxygen uptake, improve exercise capacity and functional status, as well as improve the
patient’s quality of life, for both the short term and long term (6 months) after the completion of EECP therapy. Although study subjects benefited from EECP therapy to a similar degree regardless of ischemic or nonischemic etiology of their HF, because of a small number of patients in the nonischemic group, further studies need to be conducted to evaluate the effectiveness of EECP in patients with a nonischemic etiology (46). Based on these results, a larger, controlled study of EECP therapy in patients with stable HF (NYHA
functional classes II and III) and LVD was undertaken called the PEECH (Prospective Evaluation of EECP in Heart Failure) trial (47), results of which were recently published. It was a controlled, randomized, single-blind, parallel-group, multicenter study of 187 patients with symptomatic but stable HF (NYHA functional classes II and III, ischemic and nonischemic etiology) and a left ventricular EF _35% was designed to assess the efficacy of EECP therapy in patients with stable HF. Medical therapy is optimized in all patients based on the recommendations of the Heart Failure Society of America (usual care), and then randomized between 2 treatment groups, usual care or EECP therapy (35 h over 7 weeks). The EECP therapy improved exercise tolerance, quality of life, and NYHA functional class without an accompanying increase in peak VO2. Investigators also assessed whether differences existed in response to EECP therapy in patients with HF secondary to either ischemic or nonischemic dilated cardiomyopathy. Albeit in a relatively small sample size, subgroup analysis based on etiology of disease showed benefit in patients with ischemic cardiomyopathy, whereas this difference was not seen in the small number of patients with nonischemic
disease. Because patients were not blinded to therapy, these benefits of EECP therapy may be attributable to a placebo effect. However, the usefulness of EECP therapy by physicians must be individualized based on their assessment of the totality of EECP therapy data. Further studies may help elucidate both the mechanism of action and the overall effects of EECP therapy.
Limitations of the Technique
It is important to point out that EECP therapy is not for everyone. This noninvasive outpatient procedure can be somewhat uncomfortable for patients because of the high pressure sequential compression of the cuffs. It is not recommended for certain types of valvular heart disease
Side Effects and Contraindications of Enhanced External Counterpulsation
Side Effects of Enhanced External Counterpulsation
Leg or waist pain
Skin abrasion or ecchymoses
Bruises in patients using Coumadin when INR dosage is not adjusted
Paresthesias
Worsening of heart failure in patients with severe arrhythmias (especially aortic insufficiency), or for those with recent cardiac catheterization, an irregular heart rhythm, severe hypertension, significant blockages in the leg arteries, or a history of deep venous thrombosis (Table 2). For anyone else, however, the procedure seems to be quite safe.
Contraindications of Enhanced External Counterpulsation
Coagulopathy with an INR of prothrombin time _2.5 Arrhythmias that may interfere with triggering of EECP system (uncontrolled atrial fibrillation, flutter, and very frequent premature ventricular contractions)
Within 2 weeks after cardiac catheterization or arterial puncture (risk of bleeding at femoral puncture site)
Decompensated heart failure
Moderate to severe aortic insufficiency (regurgitation would prevent diastolic augmentation)
Severe peripheral arterial disease (reduced vascular volume and muscle mass may prevent effective counterpulsation, increased risk of thromboembolism)
Severe hypertension _180/110 mm Hg (the augmented diastolic pressure may exceed safe limits)
Aortic aneurysm (_5 mm) or dissection (diastolic pressure augmentation may be deleterious)
Pregnancy or women of childbearing age (effects of EECP therapy on fetus have not been studied)
Venous disease (phlebitis, varicose veins, stasis ulcers, prior or current deep vein thrombosis or pulmonary embolism)
Severe chronic obstructive pulmonary disease (no safety data in pulmonary hypertension)
Future Directions and Potential Uses of EECP
Future Directions and Potential Uses of EECP
Potential Uses of EECP Therapy in Conditions Other Than RAP and HF Remarks Werner et al. (48) 2005/Germany 19 2
Hepatorenal syndrome
Safety: EECP therapy was tolerated by healthy and cirrhotic patients alike
Efficacy: EECP therapy increased MAP and increased urinary production (urinary flow rate) in patients with end-stage cirrhosis and hepatorenal syndrome. Potential role of EECP therapy in diuresis and increased urinary flow in patients with end-stage liver disease who
are awaiting transplant Rajaram et al. (49) 2005/U.S. 6 35
Restless leg syndrome
Relief of symptoms and change in the IRLS score from 28.8 to 6.0 after EECP therapy
Benefit sustained for 6 months; IRLS score was 3.3 at the end of 6 months It was a small, uncontrolled case series Hilz et al. (50) 2004/Germany 38 1 Peripheral vasodilatation and skin effects similar to those during exercise Potential role of EECP therapy in improving vascular flow
in mild nonulcerative peripheral vascular disease Nike Sports Research Lab (51) 2004/U.S. 19 vigorously active men in training 35 Improvement in postural instability and ataxia in
EECP treatment group as compared with control EECP therapy had no significant effect on the physiological parameters considered to be the best for predicting
performance in endurance-type sportsmen: VO2, lactate levels, work tolerance time
Erectile dysfunction
Froschermaier et al. (52) 1998/Germany 13 35 Increase in the penile artery flow by 200%, and
11 of 13 reported improved erectile function Case series looking at EECP therapy and erectile
Sudden deafness and tinnitus (vascular in origin)
Dysfunction Offergeld et al. (53) 1998/Germany 30 5–10 Treatment of sudden deafness and tinnitus (vascular in origin) Hearing threshold increased in 28%, on average by 19 dB Tinnitus decreased in 47% of the patients by an average of 16 dB Improvement persisted at 1-year follow-up
Future Directions and Conclusions
Throughout the world, EECP therapy has been studied for various potential uses other than heart disease (48 –53) (Table 3). Its role in improving endothelial function might be beneficial in the treatment of patients with Cardiac Syndrome X, which is marked by severe chest pain caused by myocardial dysfunction, often without detectable atherosclerosis. Mayo Clinic investigators have reported successful treatment of Cardiac Syndrome X with severely symptomatic coronary endothelial dysfunction in the absence of obstructive CAD with standard 35-h course of EECP therapy (54). However, it is important to realize that EECP therapy is an option for patients with angina refractory to medical treatment who are not candidates for interventional
or surgical revascularization. The American Heart Association recommends it as a Class IIb (Level of Evidence: B) intervention for treatment of RAP, among other nonpharmacological approaches such as neurostimulation (Class IIb, Level of Evidence: B) and transmyocardial laser revascularization
(Class IIa, Level of Evidence: A) (55). The European Society of Cardiology views EECP therapy as an
interesting modality available for treatment of RAP with more clinical trials needed to define its role in treating RAP (56). Enhanced external counterpulsation therapy is a valuable outpatient procedure providing acute and long-term relief of anginal symptoms and improved quality of life among a group of patients with symptomatic ischemic heart disease with or without congestive HF.
Reprint requests and correspondence: Dr. Ozlem Soran, University
of Pittsburgh Cardiovascular Institute, 200 Lothrop Street,
UPMC, Presbyterian Hospital, F-748, Pittsburgh, Pennsylvania
15213. E-mail: soranzo@upmc.edu.
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J. Am. Coll. Cardiol. 2007;50;1523-1531; originally published online Oct 1, 2007;
Aarush Manchanda, and Ozlem Soran
Medical Management for Patients With Angina and Heart Failure
Enhanced External Counterpulsation and Future Directions: Step Beyond
This information is current as of May 10, 2011
CORRECTION
Manchanda A, Soran O. Enhanced external counterpulsation and future directions: step beyond medical management
for patients with angina and heart failure. J Am Coll Cardiol 2007;50:1523–31.
Figure 2 from this article on page 1525 had previously appeared in a 2003 article in the Journal. The final line of this figure
caption should have contained the following credit line:
Reproduced with permission from Bonetti et al. Enhanced external counterpulsation for ischemic heart disease: what’s
behind the curtain? J Am Coll Cardiol 2003;41:1918 –25.
The authors apologize for this omission.
doi:10.1016/j.jacc.2007.11.023
Journal of the American College of Cardiology Vol. 50, No. 25, 2007
© 2007 by the American College of Cardiology Foundation ISSN 0735-1097/07/$32.00
Published by Elsevier Inc.
Downloaded from content.onlinejacc.org by on May 10, 2011
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