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MP 2.02.06 Enhanced External Counterpulsation (EECP)

Medical Policy    
Original Policy Date
Last Review Status/Date
Reviewed with literature search/2:2015
  Return to Medical Policy Index


Our medical policies are designed for informational purposes only and are not an authorization, or an explanation of benefits, or a contract.  Receipt of benefits is subject to satisfaction of all terms and conditions of the coverage.  Medical technology is constantly changing, and we reserve the right to review and update our policies periodically. 


EECP uses timed, sequential inflation of pressure cuffs on the calves, thighs, and buttocks to augment diastolic pressure, decrease left ventricular (LV) afterload, and increase venous return. Augmenting diastolic pressure displaces a volume of blood backward into the coronary arteries during diastole when the heart is in a state of relaxation and the resistance in the coronary arteries is at a minimum. The resulting increase in coronary artery perfusion pressure may enhance coronary collateral development or increase flow through existing collaterals. In addition, when the LV contracts, it faces a reduced aortic pressure to work against, because the counterpulsation has somewhat emptied the aorta. EECP has been primarily investigated as a treatment for chronic stable angina.

Intra-aortic balloon counterpulsation is a more familiar, invasive form of counterpulsation that is used as a method of temporary circulatory assistance for the ischemic heart, often after an acute myocardial infarction (MI). In contrast, EECP is thought to provide a permanent effect on the heart by enhancing the development of coronary collateral development. A full course of therapy usually consists of 35 one-hour treatments, which may be offered once or twice daily, usually 5 days per week. The multiple components of the procedure include the use of the device itself, finger plethysmography to follow the blood flow, continuous electrocardiograms to trigger inflation and deflation, and optional use of pulse oximetry to measure oxygen saturation before and after treatment.

Regulatory Status

While EECP has been primarily researched as a treatment of chronic stable angina, it has also been used in patients with heart failure. The Vasomedical EECP® Therapy System Model has the following labeled indication under 510(k) clearance from the U.S. Food and Drug Administration (FDA):

"The EECP Therapy System Model TS3 with Pulse Oximetry is a noninvasive external counterpulsation device intended for the use in the treatment of patients with heart failure, stable or unstable angina pectoris, acute myocardial infarction, or cardiogenic shock."

Cardiomedics Inc. has FDA 510(k) clearance to market the CardiAssist™ Counterpulsation System (K022107) and the CardiAssist ECP System (K010261) for the same indications as the Vasomedical EECP® systems.




Enhanced external counterpulsation is considered investigational for all indications, including but not limited to, treatment of chronic stable angina pectoris, heart failure, erectile dysfunction, or ischemic stroke.

Policy Guidelines


This policy only addresses the outpatient uses of enhanced external counterpulsation (EECP), ie, for the treatment of chronic stable angina or heart failure. This policy does not address its use for unstable angina pectoris, acute myocardial infarction, or cardiogenic shock.

EECP may be coded for by using a series of CPT codes describing the individual components involved in the procedure (see the coding section below). In the year 2000, the following HCPCS code was introduced, which also describes EECP:

G0166: External counterpulsation, per treatment session. 

Benefit Application
BlueCard/National Account Issues


State or federal mandates (e.g., FEP) may dictate that all FDA-approved devices may not be considered investigational, and thus these devices may be assessed only on the basis of their medical necessity.


This policy was created in 1998 and has been updated regularly with searches of the MEDLINE database. The most recent literature review was performed for the period of November 10, 2013 through December 18, 2014.

Randomized controlled trials (RCTs) that report on relevant clinical outcomes are required to determine whether enhanced external counterpulsation (EECP) is efficacious and whether it is at least as good as alternative treatments. Observational data are of limited utility given the variable natural history of disorders such as angina and/or heart failure, the presence of many potential confounders of cardiac outcomes, and the potential for a placebo effect.

The literature base consists of a small number of RCTs, some of which report relevant clinical outcomes and others that report intermediate, or physiologic, outcome measures. In addition to the small number of RCTs, there are a large number of observational studies, including publications from EECP registries and case series, which generally report pre- and posttreatment measures of EECP effectiveness.

Chronic Stable Angina

The original literature review for this policy was based on a 1999 TEC Assessment on EECP for chronic stable angina and updated with 2002 and 2005 TEC Assessments. These assessments concluded that the evidence was insufficient to determine whether EECP improved the net health outcome or is as beneficial as any established alternatives in patients with chronic stable angina.

Specifically, the 2005 TEC Assessment offered the following observations and conclusions regarding EECP for chronic stable angina(1,2):

  • There is insufficient evidence to draw conclusions about the benefits of EECP.
  • The results of the single RCT, the Multicenter Study of Enhanced External Counterpulsation (MUST-EECP) must be interpreted with caution, in view of the high subject dropout rate and uncertainty regarding the clinical significance of the reported improvement in physiologic measures, especially when intent-to-treat analysis is applied.(3,4)
  • Comparative studies of EECP do not address the hard outcomes of cardiac death or recurrent cardiac events such as myocardial infarction and revascularization procedures.(5,6)
  • Several case series and registry-based studies have reported the outcomes of large numbers of patients treated in a number of different institutions. There are several problems with this kind of evidence. These studies, while contributing to the body of knowledge of EECP, do little to address the efficacy or durability of EECP treatment. The lack of comparison groups makes it impossible to rule out either placebo effect or spontaneous recovery among patients with milder disease.

In 1999, Arora et al presented results of the MUST-EECP trial. MUST-EECP applied a randomized controlled, double-blinded protocol that compared active treatment to placebo (inactive counterpulsation [CP] sham treatment) among 139 patients with Canadian Cardiovascular Society (CCS) Classification Scales (a functional assessment tool based on the level of exertion that elicits symptoms) class I–III chronic, stable angina.(3) Four outcomes were examined:

  • Self-reported frequency of angina, analyzed 2 ways;
  • Self-reported use of on-demand nitroglycerin;
  • Exercise duration tolerance testing; and
  • Time to exercise-induced ischemia (defined as time to depression of ≥1mm in the ST segment on electrocardiogram).

All patients underwent the same 35-hour protocol, followed by an exercise tolerance test within 1 week of completion of therapy. Follow-up beyond the treatment period was not conducted. Intention-to-treat analyses were reported for the angina count and nitroglycerin usage outcomes only. There was a statistically significant difference (p=0.01) between groups in the change in time to 1 mm or greater ST segment depression. Patients in the EECP group had an average difference of 37 seconds longer time to ST segment depression compared with the sham-treated group. There was no significant difference between treatment groups in the change in exercise duration from baseline to the posttreatment period (p<0.31). In addition, there were no statistically significant differences between groups with respect to angina counts (p<0.09) or nitroglycerin use (p>0.1).

In addition to a number of methodologic limitations found in the design, execution, and reporting of this study, the magnitude of the benefit reported is not large. Of the 4 end points of interest, only the time to ST segment depression was statistically different in the EECP group compared with the sham-treated group. The clinical significance of a 37-second improvement in time to ST segment depression is unknown, but given that it occurred while the other 3 end points were statistically unchanged with therapy, does not suggest a marked improvement. That both groups showed increased exercise duration suggests a degree of placebo effect; exercise duration possesses a motivational component that time to ST segment depression does not.

In 2002, Arora et al published a 12-month follow-up study to the MUST-EECP trial.(4) However, only 71 (54%) of the original 139 subjects were included in the study. Subjects treated with EECP reported greater improvement in several quality-of-life scales. However, such findings could not be correlated with treatment response reported in the first study (because of data limitations). The findings are further limited by the small sample size and potentially biased sample of the original subject pool.

A small unblinded RCT published in 20127 addressed 1 health outcome, change after 7 weeks in CCS angina class, along with multiple intermediate outcomes. Twenty patients with refractory angina (CCS class III) were randomized to EECP or no EECP. Mean CCS class was significantly improved in the EECP group but not in the no EECP group. At 7-week follow-up, soluble interleukin-2 receptor measurements significantly increased in the EECP group and significantly decreased in the no EECP
group. There were no differences between groups at 7 weeks in resting cutaneous microvascular blood flow or response to acetylcholine, sodium nitroprusside or local heating.

Some small RCTs have reported on intermediate, or physiologic, outcomes. One such RCT (n=20) was published in 2010 comparing intracoronary blood flows in patients treated with EECP against those treated with a sham procedure.(8) This trial was designed to detect statistically significant differences in collateral flow rates by angiography, not anginal symptoms. After 7 weeks of treatment, collateral flow index increased significantly in the EECP group compared with sham treatment. Similar findings were noted in a comparative study by Buschmann et al of 23 patients published in 2009.(9)

Two publications from a single study reported on blood flow and other measures of arterial function.(10,11) This study randomized 42 patients with coronary artery disease and chronic angina to EECP or sham EECP. EECP improved flow-mediated dilation in the brachial and femoral arteries and improved numerous serum markers of blood flow and inflammation. The same study also reported that measures of arterial stiffness were improved in the EECP group. Martin et al(12) randomized 18 patients with abnormal glucose tolerance to EECP or standard care and reported that measures of glucose tolerance, as well as measures of arterial function, were improved in the EECP group.

A number of systematic reviews of the literature have been performed evaluating EECP for chronic stable angina. In 2010, Amin et al published a Cochrane review of major databases through 2008 on evidence of the effectiveness of EECP for chronic angina pectoris.(13) The solitary RCT identified was the MUST-EECP trial. The authors of this review highlighted patient selection for this study. They comment that limiting the study population to patients with CCS class below IV diminishes the study’s generalizability to patients of interest, that is, patients with the most severe symptoms of chronic angina pectoris.

Also in 2010, Shah et al published a meta-analysis of prospective studies, not limited to RCTs, of EECP in stable angina in which CCS class was adequately reported before and after treatment.(14) The MUST-EECP RCT was not included, as change in CCS class was not one of the reported outcomes. A total of 13 studies met these inclusion criteria (n=949 patients). Overall, improvement of at least 1 level of angina class occurred in 86% of patients (95% confidence interval, 82% to 90%; p=0.008). No conclusions can be drawn from this analysis given the lack of randomization (comparison group) for most studies in this analysis.

In a 2009 paper, McKenna et al report on a systematic review and economic analysis of EECP for the treatment of stable angina and heart failure.(15) Four studies (1 RCT and 3 nonrandomized comparative studies) comparing EECP treatment with no treatment in adults with chronic stable angina were included in the analysis.(3-6) The systematic review included a study by Barsheshet et al in which 25 patients (15 EECP and 10 controls) were evaluated at the end of treatment.(16) Similar to the previously reviewed Schechter et al study,(6) “CCS classification improved with EECP but not with usual care, however statistical analysis of between group differences was not reported and, for CCS classification, the data were treated as continuous data which is inappropriate for this four-category classification.”

Registry-based studies have been published that report on relatively large numbers of patients. In a registry-based study, 450 patients with left ventricular dysfunction (ejection fraction, ≤40) and refractory angina had 0.7 fewer emergency department visits and 0.8 fewer hospitalizations 6 months after treatment with EECP compared with the 6 months before EECP; 6-month data were available on only 81 patients.(17) Drawing conclusions from this study is not possible due to lack of a comparison group.

Another registry-based study (the International Enhanced External Counterpulsation Patient [IECP] Registry) reported long-term (3-year) results on patients with chronic refractory angina for patients in this registry.(18) The registry enrolled 5000 patients from 99 U.S. and 9 international centers between 1999 and 2001. However, analysis was completed only for those centers who had at least 80% compliance with follow-up data submission; the study reported results on 1427 patients. In this selective group, 220 patients (15.4%) died, while 1061 patients (74.4%) completed their follow-up. Immediately post-EECP, the proportion of patients with severe angina (CCS class III/IV) were reduced from 89% to 25% (p<0.001). This was sustained in 74% of the patients during follow-up. More severe baseline angina and a history of heart failure or diabetes were independent predictors of unfavorable outcome. Again, the lack of a control group precludes drawing conclusions about this technology based on this study.

The IECP data have also been examined to determine the safety and efficacy of the use of this device in patients with peripheral arterial disease (PAD). PAD, while a common comorbidity of CAD, has been regarded as a relative contraindication to EECP due to concerns of compression on peripheral blood flow and a potentially greater risk of aortic rupture. Thakker et al compared registry data in patients with PAD to those without.(19) Based on a reduction of 1 or more CCS angina classes, patients with PAD had a similar rate of improvement (76.6% vs 79.0%, respectively; p=0.27), as did the group without PAD. Rates of hospitalization for all cardiac causes (6.1% vs 4.4%, respectively; p=0.17) and for unstable angina (5.4% vs 3.5%, respectively; p=0.25) were also similar between groups.

Numerous individual observational studies have been detailed in previous reviews and are included in systematic reviews previously described.(4-6,9,16,20) For example, 2 prospective cohort studies (n=55 and n=61) with 1-year outcomes have been reported.(21,22) Improved CCS classification was the main reported outcome, which persisted for 1 year in 79% and 78% of patients in the respective studies. Both studies had higher rates of treatment completion and follow-up than the previously reported (registry) studies of long-term outcomes. These studies address the need for data regarding treatment durability, but their single-arm design does not change policy conclusions.

Section Summary

The data for use of EECP in chronic stable angina are insufficient to form conclusions on the efficacy of this treatment. The single randomized trial (MUST-EECP) that included relevant clinical outcomes reported a benefit on 1 of 4 main angina-related outcomes, and the magnitude of this benefit was of uncertain clinical significance. The RCTs that report on intermediate outcomes offer evidence on possible physiologic mechanisms underlying EECP treatment but do not themselves provide evidence of health outcome benefits. Observational studies, such as registry data and case series, offer little evidence on the efficacy of this procedure due to the variable natural history of angina, the multiple confounders of cardiac outcomes, and the potential for a placebo effect.

Heart Failure

The 510(k) approval of the Vasomedical devices states that objective measures such as peak oxygen consumption, exercise duration, and preload-adjusted maximal left ventricular (LV) power are improved following EECP therapy, as well as subjective measures of patient response to therapy, such as quality of life and functional ability measures. However, no clinical details of these studies are provided in the U.S. Food and Drug Administration (FDA) summary, and these data are not from controlled trials.

The 2005 TEC Assessment included heart failure in the analysis and concluded the evidence supporting the role of EECP as an effective treatment for heart failure is lacking in both quantity and quality. A single randomized, multicenter study of EECP compared with usual care in 187 optimally medically managed patients with New York Heart Association (NYHA) functional class II/III heart failure with an ejection fraction of 35% or less of ischemic or idiopathic etiology, the “Prospective Evaluation of EECP in Congestive Heart Failure” (PEECH trial), was mostly inconclusive.(24) The design and methods of the PEECH trial were published by Feldman et al.(23) The results of the PEECH trial found statistically improved, but modest, changes in exercise duration and improved functional classification but not in quality of life or peak oxygen uptake (VO2).(24)

A subgroup analysis from the PEECH trial for heart failure was published.(2) It showed that subjects aged 65 years and older treated with EECP (n=41) were more likely to meet the exercise duration (35% vs 25% increased by ≥60 seconds) and peak VO2 (30% vs 11% increased by ≥1.25 mL/kg/min) improvement thresholds compared with those undergoing sham treatment (n=45); there was no difference at 6 months in NYHA class. This poststudy analysis must be viewed as a preliminary result.

Registry studies for heart failure use angina outcomes and contribute little to the body of evidence.(25-28) The single-arm study by Soran et al(29) indicates that patients respond with some improvements, but the lack of a comparison arm precludes inference about the true effects of therapy. Treatment durability for either angina or heart failure has yet to be addressed with long-term studies. Therefore, the evidence is insufficient to determine whether EECP improves the net health outcome or is as beneficial as any established alternatives in patients with chronic stable heart failure.

The previously described 2009 review by McKenna et al15 included the single trial of EECP for heart failure included in the systematic review, the PEECH study.(24) The authors conclude that the studies do not provide firm evidence of the clinical effectiveness of EECP in refractory stable angina or in heart failure and that high-quality studies are required to investigate the benefits of EECP and whether these outweigh the common adverse effects.

Section Summary

Evidence for the use of EECP in heart failure is insufficient to form conclusions on efficacy. The single RCT that includes clinical outcomes reported modest improvements on some outcomes and no improvement on others. The observational studies add little to the evaluation of efficacy due to the variable natural history of heart failure, the multiple confounding variables for cardiac outcomes, and the potential for a placebo effect. Further high-quality RCTs are needed to determine whether EECP is a useful treatment for heart failure.

Other Indications

The use of EECP for other conditions of ischemia has been investigated. In 2009, Fraser and Adams produced a Cochrane review on interventions for central retinal artery occlusion (CRAO).(30) One of the 2 RCTs identified compared hemodilution with EECP against hemodilution without further intervention. In this case, the EECP intervention was a single, 2-hour treatment. According to the reviewers, in this study (n=20), patients were randomized but not blinded; no sham treatment was given. Primary outcomes were Doppler flowmetry of retinal perfusion and visual acuity.(31) While acknowledging the relative safety of the technique, the authors remark: “The small size of the stud[y], potential for bias and the lack of data on final vision means that we do not have convincing evidence at present to support the routine use of …
EECP in patients with CRAO.”

Published registry studies also demonstrated improvements in erectile function.(32) Erectile function was improved in a study of 120 men prospectively enrolled from 16 centers. Three of 5 domains of the International Index of Erectile Function were statistically improved with EECP treatment (erectile function, intercourse satisfaction, overall satisfaction), and the total score improved from 28 to 32, a statistically significant improvement.(32) The noncomparative design of this study makes it difficult to draw conclusions on treatment efficacy. This indication is added as investigational due to lack of adequate data on clinical outcomes. Preliminary studies from Asia are also reporting early results on use of EECP to the lower extremities in the treatment of acute ischemic stroke.(33) A 2012 Cochrane review of 2 RCTs of EECP in acute ischemic stroke34 concluded that the methodologic quality of the studies was poor and reliable conclusions could not be reached from this evidence. Thus, this indication is considered as investigational due to inadequate evidence concerning impact on outcomes.

Ongoing and Unpublished Clinical Trials

A search of online in November 2014 found no ongoing trials.

Clinical Input Received From Physician Specialty Societies and Academic Medical Centers

In response to requests, input was received from 3 academic medical centers while this policy was under review, one during review in April 2008, one during review in October 2008, and one during review in 2009. While the various physician specialty societies and academic medical centers may collaborate with and make recommendations during this process, through the provision of appropriate reviewers, input received does not represent an endorsement or position statement by the physician specialty societies or academic medical centers, unless otherwise noted. Reviewers agreed with the conclusion that this was investigational. Some reviewers commented about potential use in those with angina not amenable to surgical interventions.

Summary of Evidence

Enhanced external counterpulsation (EECP) is a noninvasive treatment used to augment diastolic pressure, decrease left ventricular afterload, and increase venous return. It has been studied primarily as a treatment for patients with refractory angina and heart failure, as well as for other indications such as erectile dysfunction and ischemic stroke.

The evidence on the efficacy of EECP for treatment of chronic angina is insufficient to form conclusions. There is only 1 blinded RCT that includes clinical outcomes, and this trial reported benefit on only 1 of 4 main angina outcomes. Additional small randomized controlled trials (RCTs) report changes in physiologic measures associated with EECP but do not provide relevant evidence on clinical efficacy. The evidence from observational studies, including registry studies with large numbers of patients, adds little to determinations of efficacy. This is because of the variable natural history of angina, the multiple confounding variables for cardiac outcomes, and the potential for a placebo effect.

For the treatment of heart failure, the evidence is of a similar nature. There is 1 RCT that includes clinical outcomes, and this trial reports modest benefits on some outcomes and no benefit on others. The observational studies on EECP in heart failure have the same limitations as do the studies on chronic angina. There is very limited evidence on the use of EECP for indications other than chronic angina or heart failure. For these reasons, the use of EECP is considered investigational for all indications.

Practice Guidelines and Position Statements

The 2012 American College of Cardiology/American Heart Association guidelines on the management of patients with stable ischemic heart disease indicate EECP “may be considered for relief of refractory angina.” This recommendation is based on Class IIb, Level of Evidence: B, which indicates the efficacy of the intervention is not well established and further studies would be helpful.(35) In 2014, ACC/AHA issued a Focused Update on the 2012 guideline on the diagnosis and management of patients with stable ischemic heart disease in which they specifically reviewed their recommendation on EECP. Based on their review, the recommendation on EECP remains unchanged from the 2012 guideline.

U.S. Preventive Services Task Force Recommendations
The U.S. Preventive Services Task Force has not addressed enhanced external counterpulsation.

Medicare National Coverage
Medicare has published a national coverage decision regarding EECP that mandates coverage for the following indications(36):

“Coverage is provided for the use of EECP for patients who have been diagnosed with disabling angina who, in the opinion of a cardiologist or cardiothoracic surgeon, are not readily amenable to surgical intervention, such as percutaneous transluminal coronary angioplasty or cardiac bypass because: 1) Their condition is inoperable, or at high risk of operative complications or post-operative failure; 2) Their coronary anatomy is not readily amendable to such procedures; or 3) They have comorbid states which create excessive risk.”

Medicare’s coverage policy also notes that while the U.S. Food and Drug Administration has cleared EECP “for use in treating a variety of cardiac conditions, including stable or unstable angina pectoris, acute myocardial infarction and cardiogenic shock, the use of this device to treat cardiac conditions other than stable angina pectoris is not covered….”

This Medicare NCD differs from the BCBSA determination of medical necessity. The discrepancy primarily arises from different interpretations of the MUST-EECP trial. In the original CMS NCD issued in 11/1999,37 the conclusion was that, based on the results of MUST-EECP, EECP was reasonable and necessary for patients with severe angina refractory to medical and/or surgical intervention. Subsequent reanalyses of this decision in 2001 and 200636 did not result in any changes to the coverage position. In contrast, a TEC Assessment performed in 1999 concluded that evidence from the MUST-EECP trial was not sufficient to permit conclusions on the impact of the technology (see Rationale for detailed discussion of TEC conclusions regarding the MUST-EECP trial). Subsequent TEC Assessments in 2002 and 20051 , which considered the MUST-EECP trial together with additional evidence, also concluded that the evidence was not sufficient to permit conclusions.


  1. Blue Cross and Blue Shield Association Technology Evaluation Center (TEC). External Counterpulsation for Treatment of Chronic Stable Angina Pectoris and Chronic Heart Failure. TEC Assessments. 2005;20(Tab 12). PMID
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  3. Arora RR, Chou TM, Jain D, et al. The multicenter study of enhanced external counterpulsation (MUST-EECP): effect of EECP on exercise-induced myocardial ischemia and anginal episodes. J Am Coll Cardiol. Jun 1999;33(7):1833-1840. PMID 10362181
  4. Arora RR, Chou TM, Jain D, et al. Effects of enhanced external counterpulsation on Health-Related Quality of Life continue 12 months after treatment: a substudy of the Multicenter Study of Enhanced External Counterpulsation. J Investig Med. Jan 2002;50(1):25-32. PMID 11813825
  5. Holubkov R, Kennard ED, Foris JM, et al. Comparison of patients undergoing enhanced external counterpulsation and percutaneous coronary intervention for stable angina pectoris. Am J Cardiol. May 15 2002;89(10):1182-1186. PMID 12008172
  6. Shechter M, Matetzky S, Feinberg MS, et al. External counterpulsation therapy improves endothelial function in patients with refractory angina pectoris. J Am Coll Cardiol. Dec 17 2003;42(12):2090-2095. PMID 14680732
  7. Bondesson SM, Edvinsson ML, Pettersson T, et al. Reduced peripheral vascular reactivity in refractory angina pectoris: Effect of enhanced external counterpulsation. J Geriatr Cardiol. Dec 2011;8(4):215-223. PMID 22783308
  8. Gloekler S, Meier P, de Marchi SF, et al. Coronary collateral growth by external counterpulsation: a randomised controlled trial. Heart. Feb 2010;96(3):202-207. PMID 19897461
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  10. Braith RW, Conti CR, Nichols WW, et al. Enhanced external counterpulsation improves peripheral artery flow-mediated dilation in patients with chronic angina: a randomized sham-controlled study. Circulation. Oct 19 2010;122(16):1612-1620. PMID 20921442
  11. Casey DP, Beck DT, Nichols WW, et al. Effects of enhanced external counterpulsation on arterial stiffness and myocardial oxygen demand in patients with chronic angina pectoris. Am J Cardiol. May 15 2011;107(10):1466-1472. PMID 21420062
  12. Martin JS, Beck DT, Aranda JM, Jr., et al. Enhanced External Counterpulsation (EECP) Improves Peripheral Artery Function and Glucose Tolerance in Subjects with Abnormal Glucose Tolerance. J Appl Physiol. Dec 22 2011. PMID 22194326
  13. Amin F, Al Hajeri A, Civelek B, et al. Enhanced external counterpulsation for chronic angina pectoris. Cochrane Database Syst Rev. 2010(2):CD007219. PMID 20166092
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  15. McKenna C, McDaid C, Suekarran S, et al. Enhanced external counterpulsation for the treatment of stable angina and heart failure: a systematic review and economic analysis. Health Technol Assess. Apr 2009;13(24):iii-iv, ix-xi, 1-90. PMID 19409154
  16. Barsheshet A, Hod H, Shechter M, et al. The effects of external counter pulsation therapy on circulating endothelial progenitor cells in patients with angina pectoris. Cardiology. 2008;110(3):160-166. PMID 18057883
  17. Soran O, Kennard ED, Bart BA, et al. Impact of external counterpulsation treatment on emergency department visits and hospitalizations in refractory angina patients with left ventricular dysfunction. Congest Heart Fail. Jan-Feb 2007;13(1):36-40. PMID 17268208
  18. Loh PH, Cleland JG, Louis AA, et al. Enhanced external counterpulsation in the treatment of chronic refractory angina: a long-term follow-up outcome from the International Enhanced External Counterpulsation Patient Registry. Clin Cardiol. Apr 2008;31(4):159-164. PMID 18404725
  19. Thakkar BV, Hirsch AT, Satran D, et al. The efficacy and safety of enhanced external counterpulsation in patients with peripheral arterial disease. Vasc Med. Feb 2010;15(1):15-20. PMID 19841026
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  27. Lawson WE, Silver MA, Hui JC, et al. Angina patients with diastolic versus systolic heart failure demonstrate comparable immediate and one-year benefit from enhanced external counterpulsation. J Card Fail. Feb 2005;11(1):61-66. PMID 15704066
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  30. Fraser SG, Adams W. Interventions for acute non-arteritic central retinal artery occlusion. Cochrane Database Syst Rev. 2009(1):CD001989. PMID 19160204
  31. Werner D, Michalk F, Harazny J, et al. Accelerated reperfusion of poorly perfused retinal areas in central retinal artery occlusion and branch retinal artery occlusion after a short treatment with enhanced external counterpulsation. Retina. Aug 2004;24(4):541-547. PMID 15300074
  32. Lawson WE, Hui JC, Kennard ED, et al. Effect of enhanced external counterpulsation on medically refractory angina patients with erectile dysfunction. Int J Clin Pract. May 2007;61(5):757-762. PMID 17493089
  33. Han JH, Leung TW, Lam WW, et al. Preliminary findings of external counterpulsation for ischemic stroke patient with large artery occlusive disease. Stroke. Apr 2008;39(4):1340-1343. PMID 18309160
  34. Lin S, Liu M, Wu B, et al. External counterpulsation for acute ischaemic stroke. Cochrane Database Syst Rev. 2012;1:CD009264. PMID 22259001
  35. Fihn SD, Gardin JM, Abrams J, et al. 2012 ACCF/AHA/ACP/AATS/PCNA/SCAI/STS Guideline for the diagnosis and management of patients with stable ischemic heart disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, and the American College of Physicians, American Association for Thoracic Surgery, Preventive Cardiovascular Nurses Association, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons. Journal of the American College of Cardiology. Dec 18 2012;60(24):e44-e164. PMID 23182125
  36. Center for Medicare and Medicaid Services (CMS). National Coverage Determination for external counterpulsation (ECP) thereapy fo severe angina (20.20). Updated March 2006. Accessed December 18, 2014.
  37. (CMS) CfMaMS. National Coverage Analysis (NCA) for External Counterpulsation (ECP) Therapy (CAG-00002N). 1999; Accessed 1/29/15.




CPT  92971  Cardio-assist-method of circulatory assist; external 
  93041 Rhythm EKG, one to three leads; tracing only without interpretation and reports
  93922  Non-invasive physiologic studies of upper or lower extremity arteries, single level, bilateral (e.g., volume plethysmography) 
  94761  Non-invasive ear or pulse oximetry for oxygen saturation; multiple determinations 
  99354 Prolonged physician services (outpatient) with direct (face-to-face) patient contact; first hour
  99355 Prolonged physician services (outpatient) with direct (face-to-face) patient contact; each additional 30 minutes
  99356 Prolonged physician services (inpatient) with direct (face-to-face) patient contact; first hour
  99357 Prolonged physician services (inpatient) with direct (face-to-face) patient contact; each additional 30 minutes
  99358 Prolonged physician services without direct (face-to-face) contact; first hour
  99359 Prolonged physician services without direct (face-to-face) contact; each additional 30 minutes
  99211  Office or outpatient visit for the evaluation of an established patient by non-physician  
ICD-9 Procedure  No Code   
ICD-9 Diagnosis    Investigational for all codes 
HCPCS  G0166  External counterpulsation, per treatment session 
ICD-10-CM (effective 10/1/15)    Investigational for all codes
   I20.1-I20.9 Angina pectoris code range (I20.0 is unstable angina pectoris)
   I50.1-I50.9 Heart failure code range
ICD-10-PCS (effective 10/1/15)    ICD-10-PCS is for use only on inpatient services. There is no specific ICD-10-PCS code for this procedure.
Type of Service  Cardiology 
Place of Service  Office 


Counterpulsation, Enhanced External
Enhanced External Counterpulsation

Policy History


Date Action Reason
01/30/1998 Add to Medicine section New policy
02/18/2000 Replace policy Policy updated to include reference to TEC Assessment; policy statement unchanged
07/12/2002 Replace policy Policy updated and retitled to reflect focus on chronic stable angina; policy statement unchanged; new reference to 2002 TEC Assessment
04/29/03 Replace policy New policy statement added regarding EECP for congestive heart failure; considered investigational. Policy statement unchanged regarding chronic stable angina; still considered investigational
04/1/05 Replace policy Updated with literature search; no change to policy statements
12/14/05 Replace policy Policy updated with 2005 TEC Assessment; policy statement unchanged
12/12/06 Replace policy Policy updated with literature search; policy statement unchanged. Reference numbers 6,7, and15 added; references renumbered
04/09/08 Replace policy  Policy updated with literature search; policy statement unchanged. Reference numbers 16-18 added.
10/07/08 Replace policy Policy updated with literature search and clinical input; reference numbers 18 and 20 added, other references renumbered. Current policy statements unchanged, treatment of ischemic stroke added as investigational indication
01/14/10 Replace policy Policy updated with literature search, clinical input reviewed; policy statement unchanged. Reference numbers 21 and 22 added.
02/10/11 Replace policy Policy updated with literature search; policy statement unchanged. Rationale revised. Reference numbers 6 - 9, 14, 15, 27, 28 and 31 - 33 added; references 18 and 34 updated
2/09/12 Replace policy Policy updated with literature search, references 8, 9, 10 added. Policy statement unchanged.
2/14/13 Replace policy Policy updated with literature search. Title of policy changed to indicate it applies to more indications than only chronic stable angina and heart failure. References 6, 34 added. Policy statement unchanged.
1/09/14 Replace policy Policy updated with literature search through November 10, 2013. Reference 36 added. Previous references 36 and 37 deleted. Policy statement unchanged.
2/12/15 Replace policy Policy updated with literature review through December 18, 2014. No references added. Policy statement unchanged.

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