archived

Exercise Tolerance Testing to Screen for Coronary Heart Disease: A Systematic Review

Coronary Heart Disease (Electrocardiography): Screening (2004)

February 03, 2004

Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.

By Angela Fowler-Brown, MD; Michael Pignone, MD, MPH; Mark Pletcher, MD, MPH; Jeffrey A. Tice, MD; Sonya F. Sutton, BSPH; Kathleen N. Lohr, PhD

Return to Table of Contents

Background: Coronary heart disease is the leading cause of morbidity and mortality in the United States. Exercise tolerance testing has been proposed as a means of better identifying asymptomatic patients at high risk for coronary heart disease events.

Purpose: To review the evidence on the use of exercise tolerance testing to screen adults with no history of cardiovascular disease for coronary heart disease.

Data Sources: The MEDLINE® database from 1966 through February 2003, hand-searching of bibliographies, and expert input.

Study Selection: Eligible studies evaluated the benefits or harms of exercise tolerance testing when added to traditional risk assessment for adults with no known history of cardiovascular events.

Data Extraction: One reviewer extracted information from eligible articles into evidence tables, and another reviewer checked the tables. Disagreements were resolved by consensus.

Data Synthesis: No study has directly examined the effect of screening asymptomatic patients with exercise tolerance testing on coronary heart disease outcomes or risk-reducing behaviors or therapies. Multiple cohort studies demonstrate that screening exercise tolerance testing identifies a small proportion of asymptomatic persons (up to 2.7 percent of those screened) with severe coronary artery obstruction who may benefit from revascularization. Several large prospective cohort studies, conducted principally in middle-aged men, suggest that exercise tolerance testing can provide independent prognostic information about the risk for future coronary heart disease events (relative risk with abnormal exercise tolerance testing, 2.0 to 5.0).

However, when the risk for coronary heart disease events is low, most positive findings will be false and may result in unnecessary further testing or worry. The risk level at which the benefits of additional prognostic information outweigh the harms of false-positive results is unclear and requires further study.

Conclusions: Although screening exercise tolerance testing detects severe coronary artery obstruction in a small proportion of persons screened and can provide independent prognostic information about the risk for coronary heart disease events, the effect of this information on clinical management and disease outcomes in asymptomatic patients is unclear.

Return to Table of Contents

Coronary heart disease is the leading cause of death in the United States. Each year, more than 1 million Americans experience nonfatal or fatal myocardial infarction or sudden death from coronary heart disease. Coronary heart disease can also present as angina, but only 20 percent of acute coronary events are preceded by long-standing angina.1 An estimated 1 to 2 million middle-aged men have asymptomatic but physiologically significant coronary artery obstruction, which puts them at increased risk for coronary heart disease events.2,3 The economic burden of coronary heart disease is also substantial. The direct and indirect costs of coronary heart disease in the United States are projected to total $129.9 billion for 2003.1 The clinical and economic impact of coronary heart disease is the basis for considerable public health interest in the development of effective strategies to reduce the incidence of coronary heart disease events.

In 1996, the U.S. Preventive Services Task Force considered use of resting electrocardiography or exercise tolerance testing to detect asymptomatic coronary artery disease and prevent coronary heart disease events.4 The Task Force found insufficient evidence to recommend for or against using these tests to screen middle-aged and older men and women. They recommended against screening children, adolescents, or young adults.

To update the evidence review and recommendations on screening for asymptomatic coronary artery disease, the Task Force and the Agency for Healthcare Research and Quality (AHRQ) requested that the RTI International-University of North Carolina Evidence-based Practice Center perform an updated evidence review beginning in 2001.

The complete review considers resting electrocardiography, exercise tolerance testing, and electron-beam computed tomography for coronary calcium and is available at Available at: http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=es22.5 This article describes the findings on exercise tolerance testing only. The recommendations and rationale of the Task Force on screening for asymptomatic coronary artery disease are available at http://www.uspreventiveservicestaskforce.org/Page/Document/RecommendationStatementFinal/coronary-heart-disease-electrocardiography-screeni.6

Clinicians can use 2 general approaches to prevention of morbidity and mortality from coronary heart disease. The first approach involves screening for and treating the traditional modifiable risk factors for coronary heart disease, such as hypertension, abnormal blood levels of lipids, diabetes, cigarette smoking, physical inactivity, and diet. Such an approach may incorporate explicit calculations of the patient's risk for coronary heart disease events by using risk prediction equations derived from the Framingham Heart Study or other cohort studies.7 The second strategy involves supplementation of screening based on traditional risk factors with additional tests to provide further information about future risk for coronary heart disease or to detect severe blockages of the coronary arteries that might warrant treatment.

Detection of increased risk for future coronary heart disease events may lead to intensified use of risk-reducing treatments. Some risk-reducing treatments are directed at traditional risk factors (for example, therapy with statins for hyperlipidemia), whereas others are not (for example, aspirin therapy). Revascularization by using coronary artery bypass graft surgery or percutaneous coronary intervention seeks to treat blockages of the coronary arteries. Whether revascularization will reduce the risk for coronary heart disease events in persons identified by screening is unknown.

Exercise tolerance testing is widely used as a diagnostic test in the initial evaluation of patients with symptoms suggestive of myocardial ischemia and in persons with previously recognized coronary heart disease. Although exercise tolerance testing has been applied and studied as a screening or prognostic test in asymptomatic persons, its utility in this group is controversial. The best measure of the value of screening exercise tolerance testing would come from studies that examined whether patients randomly assigned to undergo such tests had fewer coronary heart disease events or received more appropriate risk-reducing therapies than did patients assigned to receive treatments after standard risk factor assessment.

Such direct evidence is not available. However, indirect evidence suggests that screening exercise tolerance testing may be helpful in guiding medical management.8 In the Multiple Risk Factor Intervention Trial Research study, high-risk male participants were randomly assigned to receive a multimodal intervention to reduce cardiovascular risk or usual care. Among participants with an abnormal baseline result on exercise tolerance testing, those who received the intervention had a significantly lower rate of mortality from coronary heart disease during followup than did the group that received usual care. No effect was seen among men with a normal baseline result on exercise tolerance testing. It is not clear from the report of this post-hoc analysis whether the cardiovascular risk profiles of participants with an abnormal result on exercise tolerance testing at baseline differed significantly from those of participants with a normal result.

Because direct evidence on possible benefits of screening exercise tolerance testing is lacking, we used data from observational cohort studies to examine whether screening exercise tolerance testing could detect clinically significant asymptomatic obstructions of the coronary arteries or provide greater independent prognostic information about the risk for future coronary heart disease events than would be obtained solely by standard history, physical examination, and measurement of traditional risk factors. We also sought information about harms of screening, including the likelihood of false-positive results and the effect of labeling a person as being "at high risk."

Return to Table of Contents

Literature Review

To identify the relevant literature, we searched the MEDLINE® database from 1966 through February 2003 by using the exploded Medical Subject Headings coronary heart disease, exercise test, and mass screening and the keywords asymptomatic and screening. We limited the search to English-language articles on human subjects. To supplement our literature searches, we hand-searched the bibliographies of key articles, used other recent systematic reviews when available, and included references provided by expert reviewers that had not been identified by other mechanisms.

Study Eligibility and Data Abstraction

Two reviewers examined the abstracts of the articles identified in the initial MEDLINE® search and selected a subset for a full-text review. The same reviewers examined the full text of the selected articles to determine final eligibility. One reviewer extracted information from eligible articles into evidence tables, and another reviewer checked the tables. They resolved disagreements by consensus.

To be eligible, studies had to have been performed in participants with no history of cardiovascular disease or provide subset analysis for this group. Included studies on the detection of severe coronary artery obstruction reported the total number of persons screened to obtain the sample of persons with an abnormal result on exercise tolerance testing and the proportion of persons who were found to have coronary heart disease on angiography. The yield of exercise tolerance testing screening was determined by dividing the number of participants found to have abnormal results on angiography by the total number screened.

For the prognostic benefit of exercise tolerance testing, included studies reported the independent value of the test for predicting coronary heart disease events. We included studies that examined the prognostic benefit of exercise testing by using several variables, including ST-segment depression, functional capacity, chronotropic incompetence, heart rate recovery, and development of exercise-induced premature ventricular contractions. We also included studies that used nuclear medicine imaging to detect ischemia.

We excluded studies that did not use statistical methods to control for the effect of other risk factors (such as age or systolic blood pressure) on the estimate of the prognostic strength of a positive result of exercise tolerance testing. Table 1 shows information on excluded studies.

The studies used different means of characterizing the prognostic benefit of screening with exercise tolerance testing. Many studies reported outcomes in terms of independent relative risk associated with a positive (versus a negative) screening test. Others used diagnostic test terminology, such as "sensitivity and specificity" or "positive predictive value." In such cases, the terms are used to indicate test accuracy over the entire followup period rather than at 1 point in time.

To assess whether a relationship exists between sensitivity of exercise tolerance testing for future coronary heart disease and duration of followup, we examined the correlation between reported sensitivity and mean duration of followup by using STATA® statistical software, version 7.0 (Stata® Corp., Chicago, Illinois).

Data Summary and Quality Assessment

We rated the quality of the included articles according to criteria developed by the USPSTF Methods Work Group.9  Tables 3 and 4 show information only from studies judged "good." For the studies shown in Table 2, we considered several factors that affect quality, chiefly the percentage of patients with a positive exercise tolerance testing who underwent catheterization and how completely outcomes were assessed. We used the final set of eligible articles to create evidence tables and produce the larger evidence report, which also included evaluation of resting electrocardiography and electron-beam computed tomography to detect coronary calcium. The full evidence report was subjected to external peer review and revised on the basis of the comments received; we used the revised report as the basis for this article.

Role of the Funding Agency

This evidence report was funded through a contract to the RTI-University of North Carolina Evidence-based Practice Center from AHRQ. Staff of the funding agency contributed to the study design, reviewed draft and final manuscripts, and made editing suggestions.

Return to Table of Contents

We identified 713 articles for review. We reviewed the abstracts and retained 55 articles that examined the diagnostic or prognostic significance of screening with exercise tolerance testing. After full article review, we kept 31 articles representing 29 studies that met the inclusion criteria.10-40 We identified another 11 articles for inclusion through review of reference lists and input of expert reviewers.8,41-50 Table 1 lists articles excluded during review of the full articles and the reason for exclusion.51-74

We found no studies that directly tested whether screening asymptomatic persons with exercise tolerance testing improves coronary heart disease and mortality. Similarly, we found no studies that examined the effect of screening with exercise tolerance testing on the subsequent use of risk-reducing interventions and behaviors. However, we identified fair- or good-quality observational cohort studies of asymptomatic adults that prospectively evaluated the value of exercise tolerance testing in detecting asymptomatic coronary artery obstruction14-18,22,23,25,27,28,30,31,38,75 and predicting future coronary heart disease events, such as angina, myocardial infarction, and sudden death.8,10-13,19-21,26,29,32-36,38-50 We also identified 3 good-quality studies that estimated the cost effectiveness of exercise tolerance testing to identify asymptomatic, severe, prevalent coronary heart disease.24,28,37

Exercise Tolerance Testing To Detect Asymptomatic Prevalent Disease

We identified 13 studies in 14 articles that examined the utility of exercise tolerance testing to detect asymptomatic coronary artery obstruction (Table 2).14,15,18,22,23,25,27,28,30,31,38,75 In these studies, the prevalence of abnormal exercise tolerance testing, usually defined as exercise-induced ST-segment depression of 1 mm or more, ranged from about 3 percent among aviators who were presumed healthy16 to 29 percent in a sample of diabetic persons in Finland.15,75 A portion of the participants with a positive exercise tolerance testing in each study (1 percent to 60 percent) proceeded to evaluation with cardiac catheterization. Screening with exercise tolerance testing yielded angiographically demonstrable coronary heart disease, usually defined as greater than 50 percent stenosis of a major coronary artery, in a minority of the screened patients.

The yield of screening exercise tolerance testing was greater in higher-risk groups. Five studies in 6 articles evaluated diabetic persons,15,75 those with multiple risk factors,18,31 those with siblings with coronary heart disease17 and those who were prescreened by using a chest pain questionnaire.25 In these studies, the yield of screening for angiographically demonstrable coronary heart disease ranged from 1.2 percent31 to 9 percent.15,18 Most cases of coronary artery obstruction identified by screening were single-vessel disease, but up to 2.7 percent of screened participants had significant left main or three-vessel disease18 and as many as 1.7 percent proceeded to revascularization after screening.25 Eight studies screened unselected, low-risk patients.14,16,22,23,27,28,30,38 These studies demonstrated a yield of 0.06 percent to 1.6 percent for asymptomatic coronary heart disease on angiography.

Cost Effectiveness

Three studies attempted to estimate the cost-effectiveness of screening to identify prevalent coronary artery obstruction. Sox and colleagues24 used a decision-analysis model to estimate the clinical effectiveness and cost-effectiveness of exercise testing in asymptomatic adults. Their model was structured so that the benefit of screening was achieved through detection of patients with severe disease who would benefit from revascularization. Only direct costs were considered. Levels were based on reimbursement rates at the time of the study (late 1980s): $165 for exercise testing, $3,595 for angiography, and $31,178 for coronary artery bypass surgery. No discounting rate was given. Screening 60-year-old men had a cost per life-year saved of $24,600; for 60-year-old women, the cost was $47,606. For persons 40 years of age, the cost-effectiveness ratios were much higher: $80,349 per life-year saved for men and $216,496 per life-year saved for women.

The presence or absence of risk factors for coronary heart disease affected the cost-effectiveness ratios. The cost per life-year saved was $44,332 for 60-year-old men with no risk factors and $20,504 for those with 1 or more risk factors. The investigators concluded that routine screening was not warranted in general but that it may be beneficial for persons at increased risk for coronary heart disease (for example, older men with 1 or more risk factors). An earlier cost-effectiveness analysis of screening exercise tolerance testing had similar findings.37

Pilote and colleagues28 performed a cost analysis of data from their study of the clinical yield of screening exercise tolerance testing to detect unsuspected severe coronary artery obstruction. They sampled more than 4,000 persons referred to the Cleveland Clinic for screening exercise tolerance testing. Data on cost were obtained from 1994 Medicare reimbursement rates: $110 for exercise testing, $1,780 for angiography, and $27,270 for coronary artery bypass surgery. Screening identified 19 patients with severe coronary artery obstruction (0.44 percent of the cohort); of these, 14 had subsequent coronary artery bypass graft surgery. The investigators estimated a cost of $39,623 to identify 1 case of severe coronary artery disease by screening exercise tolerance testing. The estimated cost per year of life saved was $55,274.

On the basis of these studies, it appears that screening with exercise treadmill testing and performing bypass surgery on persons with severe obstructions is relatively cost effective compared with other, better-accepted types of preventive care, such as mammography in women 50 to 69 years of age.76

Exercise Tolerance Testing as a Prediction Tool for Risk for Coronary Heart Disease Events

Exercise tolerance testing can be used to provide information about a person's risk for a future coronary heart disease event that may augment the predictive ability of traditional risk assessment. Better risk assessment may help clinicians and patients make better decisions about interventions for intermediate- and long-term risk reduction.

ST-segment Response

Traditionally, studies of the predictive value of exercise tolerance testing on future coronary heart disease have examined ST-segment response to exercise as the risk predictor. Most of these studies reported the total number of coronary heart disease events (fatal and nonfatal myocardial infarction, new-onset stable or unstable angina, and coronary death) as their main outcome. Others reported death from coronary heart disease or from all causes as the main outcome or as secondary outcomes. The mortality rate from coronary heart disease, and particularly the total mortality rate, may be less subject to ascertainment bias than is the total number of coronary heart disease events and, hence, may be more valid measures. However, whether from coronary heart disease or other causes, death is uncommon in the generally healthy, asymptomatic patients enrolled in these studies, making it difficult to estimate the ability of exercise tolerance testing to predict such events.

We identified 15 studies in 18 articles that examined the relationship between ST-segment response to exercise and risk for future coronary heart disease events (Table 3).8,11-13,19-21,26,29,32,33,36,39-42,45,50 Thirteen of these studies (in 16 articles) found that ST-segment response during exercise predicted future coronary heart disease events.8,11-13,19-21,26,29,33,36,39-41,45,50 In 1 of these studies, only coronary heart disease events occurring during exercise was considered as the outcome;12 we therefore excluded it from analysis of the predictive utility for coronary heart disease events. Two studies found that ST-segment response to exercise alone did not predict future coronary heart disease events.32,42

Of the studies that found ST-segment response to be predictive of future coronary heart disease events, 6 (published in 8 articles) selected persons for participation on the basis of the presence of 1 or more risk factors: diabetes,13 multiple risk factors,8,33,39,50 hyperlipidemia,26,41 and sedentary lifestyle and obesity.29 The prevalence of an abnormal exercise tolerance testing, usually defined as ST-segment depression of 1 mm or more, ranged from 12 percent to 52 percent. After adjustment for other risk factors, the independent relative risk for coronary heart disease events associated with an abnormal ST-segment response to exercise in these higher-risk groups ranged from 3.58,50 to 21.0.13 Sensitivity for occurrence of coronary heart disease events over the duration of the studies (3 to 8 years) ranged from 30 percent to 100 percent. The positive predictive value of an abnormal exercise tolerance testing ranged from 7.1 percent26,41 to 46 percent.29

Seven studies (published in 8 articles) found ST-segment response to exercise to be predictive of future coronary heart disease events in an unselected, low-risk sample.11,19-21,33,36,40,45 The prevalence of an abnormal test tended to be lower than that in the higher-risk sample, ranging from 3 percent33 to 20 percent.11,21 The independent relative risk for coronary heart disease events associated with an abnormal exercise tolerance testing ranged from 1.640 to 21,33 with the majority of the values between 2.0 and 5.0. Gibbons and colleagues33 reported a higher relative risk in low-risk persons (21.0) than did the other investigators; however, the absolute event rate was low (0.08 to 2.8 events/1000 person-years) and the confidence interval was wide (6.9 to 63.3). The sensitivity of exercise tolerance testing for coronary heart disease events was 10 percent45 to 70 percent.11,21 The positive predictive values ranged from 2.2 percent33 to 24 percent.19

Two of the studies added nuclear perfusion imaging to exercise electrocardiography.19,32 These studies reported positive predictive values of about 50 percent. However, imaging is likely to increase screening program costs.19,32 As might be expected, the sensitivity of an abnormal exercise tolerance testing decreased as the duration of followup increased (r = -0.56). Data from these cohort studies suggest that the majority of asymptomatic persons with an abnormal exercise tolerance testing do not go on to have coronary heart disease events, at least within the time frame of followup. Persons who do have events often develop angina rather than experience myocardial infarction or sudden death. The prevalence of an abnormal result on exercise tolerance testing and its predictive value among asymptomatic persons is greater in those at higher risk. These data are consistent with those of other investigators and policymakers who have suggested that the value of exercise tolerance testing is greater when it is applied to patients with 1 or more risk factors for coronary heart disease because selection of a higher-risk cohort for screening increases the prevalence of disease and positive predictive value.10 Bruce and associates10 reported that in the Seattle Heart Watch Study of 4158 asymptomatic men and women, a positive result on exercise tolerance testing in the absence of risk factors provided little predictive value. However, among patients with 1 or more other risk factors for coronary heart disease, the occurrence of 2 different types of abnormal response to exercise tolerance testing (exercise risk predictors) was associated with a 15-fold increase in risk compared with patients who had a normal result.

Other Exercise Predictors

More recent studies of the value of exercise testing in asymptomatic persons have examined the utility of other exercise-associated risk markers, including functional capacity, chronotropic incompetence, heart rate recovery, and development of exercise-induced premature ventricular contractions, for predicting patients' risk for coronary heart disease events or death (Table 4).21,34,35,42-49 In contrast to ST-segment response, these exercise indicators may not directly detect ischemic myocardium, but they probably indicate other cardiovascular derangements, such as abnormal autonomic regulation, that predict coronary heart disease events. In general, these findings are associated with moderate increases in risk for coronary heart disease after adjustment for other risk factors for coronary heart disease (relative risk, 1.7 to 3.5). Some factors are common: For example, failure to achieve target heart rate was noted in 21 percent of patients in the Framingham Offspring Study.44

Exercise Tolerance Testing in Women

Two recent studies contribute important information on the predictive value of exercise tolerance testing in asymptomatic women.42,43 The majority of other studies that we identified did not include women or did not provide subgroup analysis of the predictive value of screening exercise tolerance testing for women. Mora and colleagues42 analyzed data from the female participants in the Lipid Research Clinics Prevalence Study, many of whom had hyperlipidemia. They found that unlike in studies whose samples comprised predominantly men, ST-segment response did not predict future risk for coronary heart disease events (relative risk, 0.88 [95 percent CI, 0.48 to 1.61]) in women.42 Low exercise capacity, along with low heart-rate recovery after exercise, was an independent predictor of death from coronary heart disease (relative risk, 3.52 [95% CI, 1.57 to 7.86) and of all-cause death (relative risk, 2.11 [95% CI, 1.47 to 3.04]) in women.

Gulati and coworkers43 sampled asymptomatic female volunteers living in the Chicago area. They found that exercise capacity predicts risk for all-cause death in women. For every increase in exercise capacity of 1 metabolic equivalent, the relative risk for death was 0.83 (95% CI, 0.78 to 0.89). The predictive utility of exercise markers other than ST-segment response in these 2 studies of women is consistent with the results of similar studies in which most participants were men.

Exercise Tolerance Testing Before Beginning an Exercise Program

Exercise tolerance testing is frequently used as part of an evaluation of middle-aged persons before they begin an exercise program. Few data are available to determine the effectiveness of this approach in reducing the risk for activity-related coronary heart disease events. Siscovick and colleagues12 analyzed the effectiveness of exercise tolerance testing to predict activity-related coronary heart disease events in the Lipid Research Clinics cohort of asymptomatic hypercholesterolemic men. After an initial exercise tolerance test, the cohort was followed for an average of 7.4 years; during that time, the investigators used retrospective record review to identify coronary heart disease events that were associated with moderate or intense activity. The cumulative incidence of activity-related coronary heart disease events during followup was 2 percent. An abnormal ST-segment response to exercise at the time of entry into the study was associated with a relative risk of 2.6 (95% CI, 1.3 to 5.2) for activity-related coronary heart disease events. The sensitivity of exercise testing for predicting the events was 18 percent, and the predictive value of a positive test for coronary heart disease events during exercise was 4 percent. Of the persons who had an activity-associated coronary heart disease event, 80 percent had an initially normal ST-segment response to exercise; 94 percent of persons with abnormal ST-segment response to exercise did not have an activity-associated event during followup. Thus, exercise testing appears to have limited ability to detect persons who will have exercise-related coronary heart disease events.

Adverse Effects of Screening Exercise Tolerance Testing

Other than information on the frequency of false-positive results, we found no studies that examined the potential harms of screening. No study reported rates of complications from angiography of asymptomatic persons, measures of anxiety from knowledge of an abnormal test result, or adverse events from medical therapy initiated because of an abnormal test result.

Return to Table of Contents

We identified no randomized trials that examined the effect of screening exercise tolerance testing to guide management and improve health outcomes of coronary heart disease or affect the use of risk-reducing treatments in asymptomatic adults. Exercise tolerance testing of asymptomatic persons rarely detects previously unrecognized, clinically important coronary artery obstruction (up to 2.7 percent of screened persons). It does provide some independent prognostic information in at least some persons (relative risk of about 2.0 to 5.0 for coronary heart disease events associated with an abnormal result) above and beyond the prognostic information that can be gained from traditional assessment of risk factors. The effect of this additional information on clinical decision making, however, has not been studied. The potential benefits of screening exercise tolerance testing are likely to be small for groups in which the prevalence of the disease is low, such as young adults; such screening would also produce many cases of false-positive results. In such cases, the costs and harms associated with additional testing may exceed any benefits from screening.

The value of screening exercise tolerance testing rests in large part on the underlying incidence of coronary heart disease events and the prevalence of serious artery obstructions in the screened sample. Exercise tolerance testing will probably perform better when applied to higher-risk groups, such as persons with 1 or more risk factors for coronary heart disease. Selection of a higher-risk group for screening increases the prevalence of disease in those screened and, thus, the predictive value of a positive test result. Whether the benefits of such tests exceed the disadvantages, including costs, in higher-risk groups is still unclear at present and requires investigation.

For persons at low risk for coronary heart disease events, a positive result on exercise tolerance testing is much more likely to be false positive than true positive. False-positive results in this context are concerning because they can lead to unnecessary, and possibly injurious, additional procedures.

Screening has been advocated for people with high-risk occupations, but we did not identify new studies on the effect of screening such patients. Data from studies of patients with known coronary heart disease but no ischemic symptoms suggest that treatment with medications, such as beta-blockers, or revascularization can improve outcomes over no treatment, but whether patients with no history of coronary heart disease would have the same results is unclear.77 Exercise tolerance testing can be normal or nondiagnostic in an important proportion of patients who will experience a coronary heart disease event, as evidenced by the sensitivity values of 10 percent to 74 percent in the studies that evaluated ST-segment depression as a risk marker (Table 3). In a defined cohort of low-risk patients, a larger absolute number of coronary heart disease events occurs among those with an initially normal result on exercise tolerance testing than among those with an initially abnormal result. The suboptimal sensitivity of ST-segment response for predicting coronary heart disease events may be explained in part by the fact that ST-segment depression on exercise tolerance testing detects ischemia from obstructed coronary arteries, but many acute coronary heart disease events result from sudden occlusion of a previously nonobstructed segment of artery.78 Use of other measures than the exercise test that are not as dependent on identification of atherosclerotic obstructions may mitigate this dilemma.79

The primary tangible harm of screening exercise tolerance testing is the potential for medical complications related to cardiac catheterization done to further evaluate a positive result. Coronary angiography is generally considered a safe procedure. Of all persons undergoing outpatient coronary angiography, however, an estimated 0.08 percent will die as a result of the procedure and 1.8 percent will experience a complication.80 Complications of coronary angiography include myocardial infarction, stroke, arrhythmia, dissection of the aorta and coronary artery, retroperitoneal bleeding, femoral artery aneurysm, renal dysfunction, and systemic infection. Rates of complications are likely to be somewhat lower in asymptomatic persons, but no good data are available. A positive result on exercise tolerance testing may also be an impetus to initiate risk-reducing therapy; hence, another potential harm of screening is use of therapies such as aspirin or statins to over-treat persons who would not otherwise require treatment (that is, would be considered low risk) if they did not have an abnormal result on exercise tolerance testing. Other potential harms, including the psychological consequences of a false-positive test result, also have not been well studied.

Our findings are consistent with those of the American Heart Association/American College of Cardiology expert panel, which also examined the effectiveness of screening exercise tolerance testing.33 They recommended against routine exercise tolerance testing in asymptomatic adults because of concerns about the positive and negative predictive value of screening exercise tolerance testing and the potential harms of false-positive results. The American Heart Association/American College of Cardiology found that screening exercise tolerance testing for persons with multiple risk factors to guide to risk-reduction therapy or for sedentary middle-aged adults who wish to start a vigorous exercise program is controversial but potentially beneficial.

Further studies are required to determine the balance of benefits and harms of screening exercise tolerance testing for patients with different degrees of risk for coronary heart disease. An adequately powered randomized trial of screening exercise tolerance testing compared with management based on traditional risk factors would greatly inform clinical decision making. Such a study should compare a traditional global coronary heart disease risk assessment tool to a screening strategy that also incorporates exercise tolerance testing. A broad spectrum of patients should be enrolled, including a sufficient number of women. Studies examining how providers and patients actually apply the additional information from exercise tolerance testing will also be helpful. Finally, better information about the adverse effects of screening is required if researchers are to perform well-informed cost-effectiveness analyses of exercise tolerance testing screening plus risk-factor-based decision making compared with risk-factor-based decisionmaking alone.

Return to Table of Contents

Source: Originally published in Annals of Internal Medicine on 17 February 2004 (Ann Intern Med. 2004;140:W9-W24).

Acknowledgments: The authors thank Jacqueline Besteman, JD, Director of the Agency for Healthcare Research and Quality EPC Programs; David Atkins, MD, MPH, Chief Medical Officer of the Agency for Healthcare Research and Quality Center for Practice Technology and Assessment; Jean Slutsky, PA, MSPH, Agency for Healthcare Research and Quality Task Order Officer, for their assistance. They also thank
Paul Frame, MD, Tri-County Family Medicine, Cohocton, New York, and Carolyn Westhoff, MD, MPH, Department of Obstetrics and Gynecology, Columbia University, New York, New York, who were the liaisons for the U.S. Preventive Services Task Force. Finally, they thank Tammeka Swinson, BA, and Loraine Monroe of RTI International.

Grant Support: By contract 290-97-0011, Task Order 3, from the U.S. Preventive Services Task Force, Agency for Healthcare Research and Quality.

Potential Financial Conflicts of Interest: Consultancies: M. Pignone (Bayer, Inc.); Honoraria: M. Pignone (Bayer, Inc.); Expert testimony: M. Pignone (Bayer, Inc.); Grants received: M. Pignone (Bayer, Inc.); Royalties: M. Pignone (Bayer, Inc.).

Return to Table of Contents

1. American Heart Association. Heart Disease and Stroke Statistics—2003 Update. Dallas, TX, American Heart Association; 2002.
2. Thaulow E, Erikssen J, Sandvik L, Erikssen G, Jorgensen L, Cohn PF. Initial clinical presentation of cardiac disease in asymptomatic men with silent myocardial ischemia and angiographically documented coronary artery disease (the Oslo Ischemia Study). Am J Cardiol 1993;72:629-33.
3. Cohn PF. Detection and prognosis of the asymptomatic patient with silent myocardial ischemia. Am J Cardiol 1988;61:4B-6B.
4. U.S. Preventive Services Task Force. Guide to Clinical Preventive Services, 2nd ed. Washington, DC: Office of Disease Prevention and Health Promotion; 1996.
5. Fowler-Brown A, Pignone M, Pletcher M, Tice JA, Sutton SF, Lohr KN. Screening for Asymptomatic Coronary Artery Disease: A Systematic Review for the U.S. Preventive Services Task Force. Systematic Evidence Review No. 22 (Prepared by the Research Triangle Institute-University of North Carolina Evidence-based Practice Center under Contract No. 290-97-0011). Rockville, MD: Agency for Healthcare Research and Quality. February 2004. (Available at: Available at: http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=es22.)
6. U.S. Preventive Services Task Force. Screening for coronary heart disease: recommendation statement. February, 2004. Rockville, MD: Agency for Healthcare Research and Quality. Ann Intern Med February 2004. Available at http://www.acponline.org/journals/annals/series/uspstf/screening-for-coronary-heart-disease.pdf.
7. Wilson PW, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation 1998;97:1837-47.
8. Exercise electrocardiogram and coronary heart disease mortality in the Multiple Risk Factor Intervention Trial. Multiple Risk Factor Intervention Trial Research Group. Am J Cardiol 1985;55:16-24.
9. Harris RP, Helfand M, Woolf SH, Lohr KN, Mulrow CD, Teutsch SM, et al. Current methods of the U.S. Preventive Services Task Force: a review of the process. Am J Prev Med 2001;20:21-35.
10. Bruce RA, Hossack KF, DeRouen TA, Hofer V. Enhanced risk assessment for primary coronary heart disease events by maximal exercise testing: 10 years' experience of Seattle Heart Watch. J Am Coll Cardiol 1983;2:565-73.
11. Josephson RA, Shefrin E, Lakatta EG, Brant LJ, Fleg JL. Can serial exercise testing improve the prediction of coronary events in asymptomatic individuals? Circulation 1990;81:20-4.
12. Siscovick DS, Ekelund LG, Johnson JL, Truong Y, Adler A. Sensitivity of exercise electrocardiography for acute cardiac events during moderate and strenuous physical activity. The Lipid Research Clinics Coronary Primary Prevention Trial. Arch Intern Med 1991;151:325-30.
13. Rutter MK, Wahid ST, McComb JM, Marshall SM. Significance of silent ischemia and microalbuminuria in predicting coronary events in asymptomatic patients with type 2 diabetes. J Am Coll Cardiol 2002;40:56-61.
14. Boyle RM, Adlakha HL, Mary DA. Diagnostic value of the maximal ST segment/heart rate slope in asymptomatic factory populations. J Electrocardiol 1987;20 Suppl:128-34.
15. Koistinen MJ. Prevalence of asymptomatic myocardial ischaemia in diabetic subjects. BMJ 1990;301:92-5.
16. Piepgrass SR, Uhl GS, Hickman JR Jr, Hopkirk JA, Plowman K. Limitations of the exercise stress test in the detection of coronary artery disease in apparently healthy men. Aviat Space Environ Med 1982;53:379-82.
17. Blumenthal RS, Becker DM, Yanek LR, Aversano TR, Moy TF, Kral BG, et al. Detecting occult coronary disease in a high-risk asymptomatic population. Circulation 2003;107:702-7.
18. Massie BM, Szlachcic Y, Tubau JF, O'Kelly BF, Ammon S, Chin W. Scintigraphic and electrocardiographic evidence of silent coronary artery disease in asymptomatic hypertension: a case-control study. J Am Coll Cardiol 1993;22:1598-606.
19. Fleg JL, Gerstenblith G, Zonderman AB, Becker LC, Weisfeldt ML, Costa PT Jr, et al. Prevalence and prognostic significance of exercise-induced silent myocardial ischemia detected by thallium scintigraphy and electrocardiography in asymptomatic volunteers. Circulation 1990;81:428-36.
20. Laukkanen JA, Kurl S, Lakka TA, Tuomainen TP, Rauramaa R, Salonen R, et al. Exercise-induced silent myocardial ischemia and coronary morbidity and mortality in middle-aged men. J Am Coll Cardiol 2001;38:72-9.
21. Rywik TM, O'Connor FC, Gittings NS, Wright JG, Khan AA, Fleg JL. Role of nondiagnostic exercise-induced ST-segment abnormalities in predicting future coronary events in asymptomatic volunteers. Circulation 2002;106:2787-92.
22. Livschitz S, Sharabi Y, Yushin J, Bar-On Z, Chouraqui P, Burstein M, et al. Limited clinical value of exercise stress test for the screening of coronary artery disease in young, asymptomatic adult men. Am J Cardiol 2000;86:462-4.
23. Davies B, Ashton WD, Rowlands DJ, El-Sayed M, Wallace PC, Duckett K, et al. Association of conventional and exertional coronary heart disease risk factors in 5,000 apparently healthy men. Clin Cardiol 1996;19:303-8.
24. Sox HC Jr, Littenberg B, Garber AM. The role of exercise testing in screening for coronary artery disease. Ann Intern Med 1989;110:456-69.
25. Cameron JD, Jennings GL, Kay S, Wahi S, Bennett KE, Reid C, et al. A self-administered questionnaire for detection of unrecognised coronary heart disease. Aust NZ J Public Health 1997;21:545-7.
26. Ekelund LG, Suchindran CM, McMahon RP, Heiss G, Leon AS, Romhilt DW, et al. Coronary heart disease morbidity and mortality in hypercholesterolemic men predicted from an exercise test: the Lipid Research Clinics Coronary Primary Prevention Trial. J Am Coll Cardiol 1989;14:556-63.
27. Caralis DG, Bailey I, Kennedy HL, Pitt B. Thallium-201 myocardial imaging in evaluation of asymptomatic individuals with ischaemic ST segment depression on exercise electrocardiogram. Br Heart J 1979;42:562-7.
28. Pilote L, Pashkow F, Thomas JD, Snader CE, Harvey SA, Marwick TH, et al. Clinical yield and cost of exercise treadmill testing to screen for coronary artery disease in asymptomatic adults. Am J Cardiol 1998;81:219-24.
29. Katzel LI, Sorkin JD, Goldberg AP. Exercise-induced silent myocardial ischemia and future cardiac events in healthy, sedentary, middle-aged and older men. J Am Geriatr Soc 1999;47:923-9.
30. Dunn RL, Matzen RN, VanderBrug-Medendorp S. Screening for the detection of coronary artery disease by using the exercise tolerance test in a preventive medicine population. Am J Prev Med 1991;7:255-62.
31. Okin PM, Kligfield P, Milner MR, Goldstein SA, Lindsay J Jr. Heart rate adjustment of ST-segment depression for reduction of false positive electrocardiographic responses to exercise in asymptomatic men screened for coronary artery disease. Am J Cardiol 1988;62:1043-7.
32. Blumenthal RS, Becker DM, Moy TF, Coresh J, Wilder LB, Becker LC. Exercise thallium tomography predicts future clinically manifest coronary heart disease in a high-risk asymptomatic population. Circulation 1996;93:915-23.
33. Gibbons LW, Mitchell TL, Wei M, Blair SN, Cooper KH. Maximal exercise test as a predictor of risk for mortality from coronary heart disease in asymptomatic men. Am J Cardiol 2000;86:53-8.
34. Cole CR, Foody JM, Blackstone EH, Lauer MS. Heart rate recovery after submaximal exercise testing as a predictor of mortality in a cardiovascularly healthy cohort. Ann Intern Med 2000;132:552-5.
35. Ekelund LG, Haskell WL, Johnson JL, Whaley FS, Criqui MH, Sheps DS. Physical fitness as a predictor of cardiovascular mortality in asymptomatic North American men. The Lipid Research Clinics Mortality Follow-up Study. N Engl J Med 1988;319:1379-84.
36. Giagnoni E, Secchi MB, Wu SC, Morabito A, Oltrona L, Mancarella S, et al. Prognostic value of exercise EKG testing in asymptomatic normotensive subjects. A prospective matched study. N Engl J Med 1983;309:1085-9.
37. Stason WB, Fineberg HV. Implications of alternative strategies to diagnose coronary artery disease. Circulation 1982;66:III80-6.
38. Hollenberg M, Zoltick JM, Go M, Yaney SF, Daniels W, Davis RC Jr, et al. Comparison of a quantitative treadmill exercise score with standard electrocardiographic criteria in screening asymptomatic young men for coronary artery disease. N Engl J Med 1985;313:600-6.
39. Okin PM, Grandits G, Rautaharju PM, Prineas RJ, Cohen JD, Crow RS, et al. Prognostic value of heart rate adjustment of exercise-induced ST segment depression in the multiple risk factor intervention trial. J Am Coll Cardiol 1996;27:1437-43.
40. Okin PM, Anderson KM, Levy D, Kligfield P. Heart rate adjustment of exercise-induced ST segment depression. Improved risk stratification in the Framingham Offspring Study. Circulation 1991;83:866-74.
41. Gordon DJ, Ekelund LG, Karon JM, Probstfield JL, Rubenstein C, Sheffield LT, et al. Predictive value of the exercise tolerance test for mortality in North American men: the Lipid Research Clinics Mortality Follow-up Study. Circulation 1986;74:252-61.
42. Mora S, Redberg RF, Cui Y, Whiteman MK, Flaws JA, Sharrett AR, et al. Ability of exercise testing to predict cardiovascular and all-cause death in asymptomatic women: a 20-year follow-up of the lipid research clinics prevalence study. JAMA 2003;290:1600-7.
43. Gulati M, Pandey DK, Arnsdorf MF, Lauderdale DS, Thisted RA, Wicklund RH, et al. Exercise capacity and the risk of death in women: the St. James Women Take Heart Project. Circulation 2003;108:1554-9.
44. Lauer MS, Okin PM, Larson MG, Evans JC, Levy D. Impaired heart rate response to graded exercise. Prognostic implications of chronotropic incompetence in the Framingham Heart Study. Circulation 1996;93:1520-6.
45. Jouven X, Ducimetière P. Recovery of heart rate after exercise [Letter]. N Engl J Med 2000;342:662-3.
46. Frolkis JP, Pothier CE, Blackstone EH, Lauer MS. Frequent ventricular ectopy after exercise as a predictor of death. N Engl J Med 2003;348:781-90.
47. Morshedi-Meibodi A, Larson MG, Levy D, O'Donnell CJ, Vasan RS. Heart rate recovery after treadmill exercise testing and risk for cardiovascular disease events (The Framingham Heart Study). Am J Cardiol 2002;90:848-52.
48. Wei M, Kampert JB, Barlow CE, Nichaman MZ, Gibbons LW, Paffenbarger RS Jr, et al. Relationship between low cardiorespiratory fitness and mortality in normal-weight, overweight, and obese men. JAMA 1999;282:1547-53.
49. Blair SN, Kampert JB, Kohl HW 3rd, Barlow CE, Macera CA, Paffenbarger RS Jr, et al. Influences of cardiorespiratory fitness and other precursors on cardiovascular disease and all-cause mortality in men and women. JAMA 1996;276:205-10.
50. Rautaharju PM, Prineas RJ, Eifler WJ, Furberg CD, Neaton JD, Crow RS, et al. Prognostic value of exercise electrocardiogram in men at high risk for future coronary heart disease: Multiple Risk Factor Intervention Trial experience. J Am Coll Cardiol 1986;8:1-10.
51. Allen WH, Aronow WS, Goodman P, Stinson P. Five-year follow-up of maximal treadmill stress test in asymptomatic men and women. Circulation 1980;62:522-7.
52. Aronow WS, Allen WH, De Cristofaro D, Ungermann S. Follow-up of mass screening for coronary risk factors in 1817 adults. Circulation 1975;51:1038-45.
53. Aronow WS, Allen WH, De Cristofaro D, Ungermann S, Wan MK, Chun GM, et al. Mass screening for coronary risk factors in 2,524 asymptomatic adults. J Am Geriatr Soc 1975;23:121-6.
54. Cumming GR, Samm J, Borysyk L, Kich L. Electrocardiographic changes during exercise in asymptomatic men: 3-year follow-up. Can Med Assoc J 1975;112:578-81.
55. Elamin MS, Boyle R, Kardash MM, Smith DR, Stoker JB, Whitaker W, et al. Accurate detection of coronary heart disease by new exercise test. Br Heart J 1982;48:311-20.
56. Fadayomi MO, Akinroye KK. Implications of positive treadmill exercise tests in asymptomatic adult African blacks. Eur Heart J 1987;8:611-7.
57. Froelicher VF Jr, Thomas MM, Pillow C, Lancaster MC. Epidemiologic study of asymptomatic men screened by maximal treadmill testing for latent coronary artery disease. Am J Cardiol 1974;34:770-6.
58. Froelicher VF Jr, Thompson AJ, Wolthuis R, Fuchs R, Balusek R, Longo MR Jr, et al. Angiographic findings in asymptomatic aircrewmen with electrocardiographic abnormalities. Am J Cardiol 1977;39:32-8.
59. Gerson MC, Khoury JC, Hertzberg VS, Fischer EE, Scott RC. Prediction of coronary artery disease in a population of insulin-requiring diabetic patients: results of an 8-year follow-up study. Am Heart J 1988;116:820-6.
60. Gianrossi R, Detrano R, Mulvihill D, Lehmann K, Dubach P, Colombo A, et al. Exercise-induced ST depression in the diagnosis of coronary artery disease. A meta-analysis. Circulation 1989;80:87-98.
61. Goodman S, Rubler S, Bryk H, Sklar B, Glasser L. Arm exercise testing with myocardial scintigraphy in asymptomatic patients with peripheral vascular disease. Chest 1989;95:740-6.
62. Gupta R, Gupta S. Value of maximal treadmill exercise test to screen asymptomatic persons for coronary artery disease. J Assoc Physicians India 1983;31:783-5.
63. Hopkirk JA, Uhl GS, Hickman JR Jr, Fischer J, Medina A. Discriminant value of clinical and exercise variables in detecting significant coronary artery disease in asymptomatic men. J Am Coll Cardiol 1984;3:887-94.
64. MacIntyre NR, Kunkler JR, Mitchell RE, Oberman A, Graybiel A. Eight-year follow-up of exercise electrocardiograms in healthy, middle-aged aviators. Aviat Space Environ Med 1981;52:256-9.
65. Manca C, Barilli AL, Dei Cas L, Bernardini B, Bolognesi R, Visioli O. Multivariate analysis of exercise ST depression and coronary risk factors in asymptomatic men. Eur Heart J 1982;3:2-8.
66. Mark DB, Hlatky MA, Califf RM, Morris JJ Jr, Sisson SD, McCants CB, Lee KL, Harrell FE Jr, Pryor DB. Painless exercise ST deviation on the treadmill: long-term prognosis. J Am Coll Cardiol 1989;14:885-92.
67. McHenry PL, O'Donnell J, Morris SN, Jordan JJ. The abnormal exercise electrocardiogram in apparently healthy men: a predictor of angina pectoris as an initial coronary event during long-term follow-up. Circulation 1984;70:547-51.
68. Melin JA, Piret LJ, Vanbutsele RJ, Rousseau MF, Cosyns J, Brasseur LA, et al. Diagnostic value of exercise electrocardiography and thallium myocardial scintigraphy in patients without previous myocardial infarction: a Bayesian approach. Circulation 1981;63:1019-24.
69. Pedersen F, Sandoe E, Laerkeborg A. Prevalence and significance of an abnormal exercise ECG in asymptomatic males. Outcome of thallium myocardial scintigraphy. Eur Heart J 1991;12:766-9.
70. Roger VL, Jacobsen SJ, Pellikka PA, Miller TD, Bailey KR, Gersh BJ. Prognostic value of treadmill exercise testing: a population-based study in Olmsted County, Minnesota. Circulation 1998;98:2836-41.
71. Rubler S, Gerber D, Reitano J, Chokshi V, Fisher VJ. Predictive value of clinical and exercise variables for detection of coronary artery disease in men with diabetes mellitus. Am J Cardiol 1987;59:1310-3.
72. Selvester RH, Ahmed J, Tolan GD. Asymptomatic coronary artery disease detection: update 1996. A screening protocol using 16-lead high-resolution ECG, ultrafast CT, exercise testing, and radionuclear imaging. J Electrocardiol 1996;29 Suppl:135-44.
73. Tubau JF, Szlachcic J, Hollenberg M, Massie BM. Usefulness of thallium-201 scintigraphy in predicting the development of angina pectoris in hypertensive patients with left ventricular hypertrophy. Am J Cardiol 1989;64:45-9.
74. Uhl GS, Kay TN, Hickman JR Jr. Computer-enhanced thallium scintigrams in asymptomatic men with abnormal exercise tests. Am J Cardiol 1981;48:1037-43.
75. Koistinen MJ, Huikuri HV, Pirttiaho H, Linnaluoto MK, Takkunen JT. Evaluation of exercise electrocardiography and thallium tomographic imaging in detecting asymptomatic coronary artery disease in diabetic patients. Br Heart J 1990;63:7-11.
76. Salzmann P, Kerlikowske K, Phillips K. Cost-effectiveness of extending screening mammography guidelines to include women 40 to 49 years of age. Ann Intern Med 1997;127:955-65.
77. Conti CR, Bourassa MG, Chaitman BR, Geller NL, Knatterud GL, Pepine CJ, et al. Asymptomatic cardiac ischemia pilot (ACIP). Trans Am Clin Climatol Assoc 1994;106:77-83.
78. Coplan NL, Fuster V. Limitations of the exercise test as a screen for acute cardiac events in asymptomatic patients. Am Heart J 1990;119:987-90.
79. Ashley EA, Myers J, Froelicher V. Exercise testing in clinical medicine. Lancet 2000;356:1592-7.
80. Bashore TM, Bates ER, Berger PB, Clark DA, Cusma JT, Dehmer GJ, et al. American College of Cardiology/Society for Cardiac Angiography and Interventions Clinical Expert Consensus Document on cardiac catheterization laboratory standards. A report of the American College of Cardiology Task Force on Clinical Expert Consensus Documents. J Am Coll Cardiol 2001;37:2170-214.

Return to Table of Contents

Author, Year (Reference) Reason for Exclusion
Allen et al., 198051 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Aronow et al., 197552,53 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Cumming et al., 197554 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Elamin et al., 198255 Diagnostic use in symptomatic patients
Fadayomi et al., 198756 Unclear ascertainment of end points
Froelicher et al., 197457 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Froelicher et al., 197758 Did not report the total number of persons screened
Gerson et al., 198859 Did not report the independent risk for a positive result on exercise tolerance testing
Gianrossi et al., 198960 Diagnostic use in symptomatic patients
Goodman et al., 198961 Participants had history of cardiovascular disease
Gupta et al., 198362 Did not report independent risk for a positive result on exercise tolerance testing
Hopkirk et al., 198463 Did not report the total number of persons screened
MacIntyre et al., 198164 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Manca et al., 198265 Did not report the independent risk for a positive result on exercise tolerance testing
Mark et al., 198966 Participants had history of cardiovascular disease
McHenry et al., 198467 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Melin et al., 198168 Diagnostic use in symptomatic patients
Pedersen et al., 199169 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Roger et al., 199870 Included symptomatic patients without sub-analysis
Rubler et al., 198771 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Selvester et al., 199672 Used a screening protocol that employed multiple technologies
Tubau et al., 198973 No adjustment for the effect of other risk factors on the relative risk for an abnormal result on exercise tolerance testing.
Uhl et al., 198174 Did not report the total number of persons screened
Return to Table of Contents

Author, Year (Reference) Sample Exclusion Criteria Test Definition of Abnormal Exercise Electrocardiography Result Prevalence of Abnormal Exercise Tolerance Test Result Definition of Abnormal Cardiac Catheterization Result Abnormal Catheterizations/Total Catheterizations* Abnormal Catheterizations/ Abnormal Exercise Tolerance Test Result* Abnormal Exercise Tolerance Test Result and Abnormal Catheterizations/ All Screened Persons* Quality Grade
Caralis et al., 197927 3,496 men and women

Mean age: NR

% men NR

NR Maximal exercise and thallium scintigraphy ≥2 mm of horizontal ST-segment depression 22/3496
(0.6%)
NR 10/15
(66.7%)
10/22
(45.5%)
10/3,496
(0.3%)
Fair
Piepgrass et al., 198216 771 men in U.S. Air Force flight crew

Mean age ±SD, 42 ±5.2 y
100% men

Resting electrocardio-graphic abnormalities, history of chest pain, cardiovascular disease, marked hypertension Maximal treadmill or two-step double Master's ≥0.1 mV of ST-segment depression 80 ms from the J point or exercise induced arrhythmia 27/771
(3.5%)
NR 4/19
(21%)
4/27
(14.8%)
4/771
(0.5%)
all cases were mild to moderate disease
Fair
Hollenberg et al., 198538 377 U.S. Army officers

Mean age 37y

% men NR

Known CHD Maximal treadmill - U.S. Air Force School Aerospace Medicine Protocol ≥1 mm ST depression during or after exercise or treadmill exercise score <5 units 45/377
(12%)
≥50% narrowing of the luminal diameter of major epicardial artery 1/10
(10%)
1/45
(2%)
1/377
(0.3%)
1 had 1- vessel disease
Fair
Boyle et al., 198714 1,174 employees from 2 factories in the United Kingdom

Mean age: NR
Age range: 19-64y

95% men

Symptoms of angina, orthopedic problems, hypertension with retinopathy, fainting, fibrillation Treadmill Maximal ST/heart rate slope value of >13
mm·beats-1 min 10-3
68/1,174
(5.8%)
≥75% stenosis of epicardial artery 9/24
(37.5%)
9/68
(13.2%)

9/1,174
(0.8%)

1 patient had coronary artery bypass graft surgery

Fair
Okin et al.,198831 606 men in the Army Reserve at moderate to high risk by Framingham Risk score

Mean age: NR
Age: >40 years

100% male

Known or suspected CHD or angina Modified Balke-Ware with radionuclide scintigram for an abnormal exercise ECG ≥1 mm ST depression 10/606 (1.7)
positive—abnormal exercise electro-cardiogram and scintigram;
52/606 (8.6)
inconclusive—abnormal exercise electrocard-iogram and normal scintigram)
≥50% narrowing of the luminal diameter 7/10
(70%)
7/10
(70%)
7/606
(1.2%)

2 patients had 3-vessel disease,
2 had 2-vessel disease,
3 had 1-vessel disease

Good
Koistinen 199015,75 136 diabetic patients in Finland

Mean age: 49 y

62% men

Clinical evidence of CHD, use of lipid lowering agents, diabetes mellitus for less than 5 y, retinopathy, renal failure Maximal bicycle ergometry and thallium scintigraphy ≥1 mm horizontal or downsloping ST-segment depression 40/136
(29%)
Significant (≥50%) narrowing of the luminal diameter 12/34
(35%)
12/40
(30%)
12/136
(9%)

2 patients had 3-vessel disease, 5-had 2-vessel disease, 5 had 1-vessel disease

Fair
Dunn et al., 199130 1,930 patients referred to Cleveland Clinic Foundation for screening exercise tolerance testing in 1987-1988(5.6% had history of chest pain)

Mean age: 49 y

85% men

Known CAD Symptom-limited exercise electrocardiography, then thallium scintography if results were abnormal ≥1 mm of horizontal or downsloping ST-segment depression, or arrhythmia 155/1,930
(8%)
≥50% blockage of any major vessel 25/41
(61%)
25/155
(16.1%)
25/1,930
(1.3%)

6 patients had coronary artery bypass graft surgery

Fair
Massie et al., 199318 226 men from the San Francisco Veteran's Medical Center, all of whom had hypertension and at least 1 other cardiovascular risk factor

Mean age ± SD, 61 ± 8 y

100% men

Known cardiac disease history or symptoms, resting electrocardio-graphy abnormalities, paced rhythm, noncardiac limitation to exercise Standard Bruce with thallium scintigraphy ≥0.1 mV of additional horizontal or downsloping ST-segment depression at 80 ms after the J point Abnormal exercise electrocardiogram 67/226 (30%)

Abnormal scintigram 41/226 (18%)

Intraluminal lesion of =50% diameter of vessel in 2 projections 14/26
(54%)

18/21
(86%)

14/67
(21%)

18/29
(62%)

20/226
(9%)

6 patients had left main disease or 3-vessel disease; 5 had 2-vessel disease; 7 had 1-vessel disease

Fair
Davies et al., 199623 5,000 men from the United Kingdom

Mean age: NR

100% men

NR Modified Balke 1 mV of horizontal or downsloping depression persisting for ≥5 complexes 162/5,000
(3.2%)
≥75% stenosis epicardial artery 67/86
(78%)
67/162
(41.4%)
67/5,000
(1.3%)

26 patients had coronary artery bypass graft surgery

Fair
Cameron et al., 199725 229 Australians who responded to questionnaire about chest pain

Mean age: NR

43% men

Known CAD or negative screening questionnaire Modified Bruce Flat ST- segment depression ≥0.15 mV Men
15/98 (15.3%)
women
17/131 (13%)
NR 10/13
(77%)
10/32
(31%)
10/229
(4%)

4 patients had coronary artery bypass graft surgery

Fair
Pilote et al., 199828 4,334 patients referred to Cleveland Clinic Foundation for screening exercise tolerance testing in 1990-1993

Median age: 51 y

89% men

History of chest pain, heart failure, valvular or congenital heart disease, arrhythmia or digitalis use Bruce or modified Bruce ≥1 mm horizontal or downsloping ST-segment depression, ≥1 mm ST elevation in leads other than aVR or V1, decrease in blood pressure ≥10 mmHg, typical chest pain, failure to reach target heart rate 633/4,334
(15%)
Coronary artery disease ≥1 coronary segment with ≥50% stenosis 71/126
(56%)
71/633
(11%)
71/4,334
(1.6%)

19 patients had left main disease or 3-vessel disease

Fair
Livschitz et al., 200022 4,900 male soldiers in the Israeli army ≥39 years of age

Mean age ±SD 43 + -3 y

100% men

Angina, heart failure, valvular disease, congenital heart disease, arrhythmia Bruce ≥1 mV of horizontal or downsloping ST-segment depression or ≥1.5 mV upsloping ST-segment depression 299/4,900
(6.1%)
NR 3/4
(75%)
3/299
(1%)
3/4900
(0.06%)

1 patient had coronary artery bypass graft surgery

2 had 1-vessel disease

Good
Blumenthal et al., 200317 734 primarily white healthy siblings of persons with CAD diagnosed before age 60 in Baltimore

Mean age: NR
but <60 y

"Primarily male"

Known CAD, limitations that precluded testing Modified Bruce and thallium scintigraphy NR for exercise tolerance testing 153/734
(21%)

(Abnormal exercise electrocardio-gram, scan, or both)

Clinically significant CAD: intraluminal lesion of ≥50% diameter 41/105
(39%)
41/153
(27%)
41/734
(5.5%)
Good

*Percentages were calculated by the authors of this report.
CAD = coronary artery disease; CHD = coronary heart disease; NR = not reported

Return to Table of Contents

Author, Year (Reference) Sample Exclusion Criteria Mean Years of Followup Test Abnormal Test Result Cumulative Event Rate Adjusted Relative Risk (95% CI) for CHD Events with Abnormal ST-Segment Response Sensitivity for CHD Events Positive Predictive Value of Abnormal T Response Variables for Which Relative Risk Was Adjusted
Definition Prevalence
Giagnoni et al., 198336 514 factory workers in Italy

Age range: 18-65 y

73% men

Positive history and physical exam for CVD, resting blood pressure ≥160/95 mm Hg, abnormal resting electocardiogram 6 y Submaximal supine cycle ergometry ≥1 mm of horizontal/downsloping ST-segment depression during or after exercise NR Normal exercise test 3.4%
Abnormal exercise test result 15.6%*
5.5
(2.8-11.2)
62 15 Age, systolic blood pressure, smoking, coronary risk index
MRFIT Trial Research Group, 19858

Rautaharju et al., 198650

6,205 men in the upper 10% to 15% Framingham risk score distribution

Age range: 35-57

100% men

Clinical heart disease, life-limiting conditions, diastolic blood pressure ≥115 mm Hg, cholesterol ≥350 mg/dL 7 y Submaximal Computer code ST- segment depression 16 muV-s or more in leads CS5, aVL, aVF, V5 during or after exercise (in electrocardiogram with less than 6 muV-s depression at rest) 12.2% Normal exercise test result 2/1,000 person years*

Abnormal exercise test result 7.6/1,000 person years*

3.5
(P <0.05)*

1.61
(P <0.01)

NR 36 Age, diastolic blood pressure, cholesterol, number of cigarettes smoked daily
Gordon et al., 198641

Ekelund et al., 198926

3,640 white men in Lipid Research Clinics Prevalence Survey in United States and Canada

Mean age: 47

Age range: 35-59 y

100% men

Evidence of CHD by history, resting electrocardiogram, and physician exam. Secondary hyperlipidemia, BMI >32.1 kg/m2, blood pressure ≥165/105 mm Hg with antihypertensive or cardiovascular medication; diabetes mellitus. 8.1 y Submaximal modified Bruce ≥1 mm of ST-segment depression or elevation or computer- ST integral decreased or increased ≥10 muV-s from resting value 8.3% Placebo group

Normal exerciser test result 13/1,000 person years*

Abnormal exercise test result 1.9/1,000 person years*

Placebo group
5.7
(2.7-12.2)*
 

3.3
(1.8-5.9)

30 7.1 Age, LDL cholesterol level, HDL cholesterol level, systolic blood pressure, smoking, family history
Cholestyramine group

Normal exercise test result 7.2/1,000 person years*

Abnormal exercise test result 1.5/1,000 person years*

Cholestyramine group

4.9
(2.2-10.8)*

 

2.9
(1.6-5.2)

Fleg et al., 199019 407 residents of Baltimore, Maryland (mainly white)

Mean age ±SD 60 ±11 y

Range: 40-90 y

71% men

NR 4.6 y Maximal treadmill with thallium modified Balke ≥1 mm of horizontal/ downsloping ST-segment during or after exercise Abnormal electro-cardiogram only 16.0%

Abnormal thallium scan only 14%

Both tests abnormal 6.0%

Both test results normal, 7%


Abnormal electrocardiogram only, 12%

Abnormal thallium scan, only 3%

Both tests abnormal, 48%

1.0
 


2.4
(P <0.05)

 
1.4
(NS)

3.6
(1.6-8.1)

 

 

40

 

N/A

28

 

 

24

 

N/A

48

Age, sex, hypertension, fasting blood glucose, total cholesterol, BMI, smoking, exercise duration
Okin et al., 199140 3,168 participants in the Framingham Offspring Study

Mean age ±SD, 44 ±10 y Age range: 17-70 y

48% male

Medical contraindications to exercise, history of myocardial infarction, CHF, valvular disease, syncope, conduction abnormalities, digoxin use, atrial fibrillation 4.3 y Standard Bruce ST segment corrected for heart rate index >1.6 muV per beat per min or abnormal rate recovery loop 416/3168
13%

(either test abnormal)

Both tests normal 1.6%

Either test abnormal 4.1%

Both tests abnormal 9.8%

1.0
 

1.6
(1.1-2.5)

2.7
(1.8-4.0)

 

23%

8%

 

4%

10%

Age, sex, smoking, diastolic blood pressure, total cholesterol level, fasting blood glucose, left ventricular hypertrophy on electrocardiography
Siscovick et al., 199112 3,617 white men in the Lipid Research Clinics Prevalence Survey

Mean age: NR
Age range: 35-59 y

100% male

Clinical evidence of CHD or CHF on history, various resting electrocardiogram abnormalities 7.4 y Submaximal modified Bruce Visual code ≥1 mm ST-segment depression or elevation or computer code ≥10 muV 1/N s 6.6% Overall 2% 2.6 (1.3 - 5.2) 18% 5% Age, LDL cholesterol level, HDL cholesterol level, smoking, physical activity, workload achieved, family history of CHD, BMI, alcohol consumption
Blumenthal et al., 199632 264 healthy siblings of individuals with CAD before age 60 in Baltimore, Maryland

Mean age ±SD, 46 ± 8
Age range: 37-59 y

69% men

Known CAD, corticosteriods, collagen vascular disease, decreased life expectancy, functional status limitations 6.2 y Modified Bruce and thallium scintigraphy ≥1 mm (≥2 mm for women) of horizontal or downsloping depression in 3 consecutive beats during exercise or first 3 min of recovery Abnormal exercise electrocardiogram 5.4%

Abnormal plus thallium scan 18.1%

Abnormal exercise electrocardiogram and scan 4.6%

Normal 3% 1.0     Age, sex
Abnormal exercise electrocardiogram 7% 1.5
(0.2-12.5)
N/A N/A
Abnormal thallium scan 13% 3.6
(1.1-11.4)
63% 20%
Abnormal exercise electrocard-iogram and scan 50% 14.5
(4.2-50.2)
32% 50%
Okin et al., 199639 5,940 men in the usual care group of MRFIT

Mean age: NR
Age range: 35-57 y

100% men

No evidence of CHD by history, physical examination, or resting electrocardiography 7 y Submaximal treadmill ST segment corrected for heart rate index >1.6 muV per beats per min 729/5,940
(12.3%)
Normal exercise test result 1.3%*

Abnormal exercise test result 5.4%*

3.6
(2.4-5.4)*
36% 5% Age. Diastolic blood pressure, cholesterol level, smoking
Katzel et al., 199929 170 healthy sedentary obese men living in the Baltimore-Washington, DC area (96% white)

Mean age: NR
Age range: 45-79 y

100% men

History or laboratory evidence of CAD, diabetes mellitus, hypertension, hyperlipidemia 7.3 y Maximal Bruce ≥1 mm of horizontal or downsloping ST-segment depression in 2 or more leads 37/170
(22%)
Overall 18% 4.23
(2.03-8.83)
55% 46% Age, BMI, maximal VO2, fasting glucose level
Gibbons et al., 200033 25,927 patients of a preventive medicine clinic in Texas (mainly white)

Mean age: 42.9
Age range 20-82 y

100% men

Evident CHD, severe aortic stenosis, acute systemic illness, uncontrolled atrial or ventricular arrhythmias, pericarditis, myocarditis, thrombophlebitis or exercise-limiting orthopedic problems 8.4 y Maximal treadmill modified Blake Chest pain and ≥1mm ST-segment depression or elevation, exercise induced-decrease ≥10 mm in systolic blood pressure, systolic blood pressure >250 mm Hg, diastolic blood pressure >120 mm Hg, ventricular tachycardia, left bundle-branch block, right bundle branch block, super-ventricular tachycardia No risk factors, 3.0% No risk factors
Normal exercise test result 0.08/1000 person years*

Abnormal ETT 2.8/1000 person years*

21
(6.9-63.3)*
60 2.2 Age
>1 risk factor,
7.1%
>1 risk factor
Normal ETT 0.5/1000 person years*

Abnormal exercise test result 7.6/1000 person years*

9* 61 7.7  
Josephson et al., 199011

Rywik et al., 200221

1,083 participants in the Baltimore Longitudinal Study of Aging

Mean age ±SD, 52 ±18 y

57% men

History of angina or heart failure, Q wave on resting electrocardiography, valvular disease, use of anti-arrhythmic drugs, inability to achieve 85% of maximal heart rate 7.9 Modified Balke Normal Men 4%
Women 3%
1.0§ Men 74
Women 68
Men 16
Women 7
Age, cholesterol, sex, exercise duration
Minnesota Code 11.1§ 20% Men 17%
Women 8%
2.7
(1.6-4.7)
Minnesota Code 11.5§ 5.5% Men 17%
Women 11%
2.7
(1.05-7.10)
Minnesota Code 11.2§ 7% Men 10%
Women 5%
OR 1.8
(0.6-5.4)
Minnesota Code 11.4§ 11.5% Men 17%
Women 3%
OR 1.3
(0.6-2.9)
Jouven and Ducimetiere, 200045 6,101 Frenchmen in Paris Civil Service

Age range: 42-53 y

100% men

Known or suspected CVD, resting systolic blood pressure ±180 mm Hg, resting Electrocardiographic abnormality 23 Bicycle ergometry J-point depression of at least 1 mm with a flat or downsloping ST segment during exercise or recovery 4.4% Normal exercise test result, 6.4%

Abnormal exercise test result 16.7%*

2.6
(1.93-3.59)*
10 17-25 Age, BMI, heart rate at rest, smoking, physical activity, diabetes mellitus, total cholesterol level, premature ventricular complex
Laukkanen et al., 200120 1,769 participants, population in Kupio Ischemic Heart Disease Study base sample of Finnish men

Mean age ±SD,
52 ±5.2 y
100% men

Known CHD or symptoms suggestive of CHD 10 Maximal Bicycle ergometry >1 mm ST-segment depression during exercise 10.7% Normal exercise test result 9.2%
2.4%*

Abnormal 15.3%
7.9%*

1.7
(1.1-2.6)
 

3.5
(1.9-6.5)*

16 15 Age, examination year, smoking, systolic blood pressure, alcohol consumption, BMI, max oxygen uptake, diabetes mellitus, LDL cholesterol level, HDL cholesterol level
Rutter et al., 200213 86 diabetic patients in the United Kingdom

Mean age ±SD,
62 ±7 y
Age range: 46-74 y

72% men

History of CAD 2.8 Treadmill >1 mm of horizontal or downsloping ST-segment depression for 3 consecutive beats 52% Both normal and abnormal exercise test results
17%
21
(2-204)
100% 20% Ankle brachial index, microalbuminuria, Framingham 10-y CHD risk >30%, fibrinogen level
Mora et al., 200342 2994 women enrolled in the Lipid Research Clinics Prevalence Study

Age range 30-80

0% men

Pregnancy or significant cardiovascular disease 20.3 Maximal Bruce ≥1mm horizontal or downsloping ST-segment depression at 0.08 seconds after the J point during recovery or exercise 4.7% Both normal and abnormal exercise tolerance test results

5%*

14%

0.88
(0.48-1.61)*

0.69
(0.45-1.04)

 

 

Age, smoking, diabetes, family history of premature heart disease, obesity, HDL cholesterol level, LDL cholesterol level, triglyceride level, hypertension

*CHD death.
All-cause death.
For CHD events occurring during exercise.
§ Minnesota code 11.1 = ≥1 mm J-point depression with flat or downsloping ST segment in most complexes in any lead except aVR; Minnesota code 11.2 = horizontal or downsloping ST-segment depression of 0.5-1.0 mm; Minnesota code 11.4 = J-point depression of ≥1 mm with upsloping ST; Minnesota code 11.5 = ST-segment depression at rest that worsens to 11.1 during exercise.
Values are odds ratios (95% CI).

Note: Events are CHD events unless otherwise indicated.
BMI = body mass index; CAD = coronary heart disease; CVD = cardiovascular disease; HDL = high-density lipoprotein; LDL = low-density lipoprotein; MRFIT = Multiple Risk Factor Intervention Trial Research Group; NA = not applicable; NR = not reported.

Return to Table of Contents

Author, Year
(Reference)
Sample Exclusion Criteria Mean Years of Followup Test Definition of Abnormal Test Result Prevalence of Predictor Cumulative Event Rate Relative Risk for CHD Events with Positive Test Sensitivity for CHD Events Positive Predictive Value of Abnormal Test Relative Risk Adjusted for the Following Variables
Ekelund et al., 198835 3,106 (healthy white men) in Lipid Research Clinics Prevalence Survey in united States and Canada

Age range: 30-69 y

100% men

Men with CVD symptoms or hypertension were analyzed separately 8.5 Modified submaximal Bruce Heart rate during stage 2 of exercise tolerance test and exercise time Increase of 2 SD in stage 2 heart rate

 
Decrease of 2 SD in time on the treadmill

0.26-1.69%* 3.2 (1.5-6.7)
for abnormal heart rate recovery

2.8 (1.3-6.1)
for decrease in exercise time

NR NR Age, smoking, HDL cholesterol level, LDL cholesterol level, systolic blood pressure
Lauer et al., 199644 1,575 subjects in Framingham Offspring Study (predominantly white)

Mean age: 43 y

100% men

Prevalent CAD, inability to reach stage 2 in Bruce protocol, use of beta-blockers at time of exercise tolerance test 7.7 Submaximal Bruce Failure to achieve age- and sex-predicted target heart rate on exercise tolerance test 21% 3% for those who reached target heart rate (all cause death)

6% for those who failed to reach heart rate

No significant association of predictor with all cause death

1.75
(1.11-2.74)*

46% 14% Age, ST-segment response, physical activity, BMI, smoking, hypertension, hypertension medication, diabetes mellitus, total cholesterol level/HDL cholesterol level
Wei et al., 199948

Blair et al., 199649

25,714 patients at a preventive med clinic in Texas Aerobics Center Longitudinal Study (>95% white), 10% of men with known CVD

Mean age: 43.8 y

100% men

History of cancer, BMI <18.5 kg/m2, age <20 y, or <1 y of follow-up 24 Maximal treadmill Low fitness using age-based MET cut points on exercise tolerance test Normal weight: 10%

Overweight: 19% 

Obese: 51%

Overall 1.7/1,000 person years* Normal Weight
1.7 (1.1-2.5)*
1.6 (1.3-2.1)

Overweight
1.9 (1.4-2.5)*
1.7 (1.4-2.6)

Obese
2.0 (1.2-3.6)*
2.3 (1.5-3.4)

36%

52%

79%

4.6%

5.4%

3.4%

Diabetes mellitus, cholesterol level, hypertension, current smoking, history of CVD, abnormal electrocardiogram at rest, age, BMI parental history of CVD, examination year
Cole et al., 200034 5,234 in Lipid Research Clinics Prevalence Survey in United States and Canada

Mean age: >30 y

39% men

Age <30 y, use of beta-blockers, digoxin, antiarrhythmic agents or nitrates, history of cardiovascular disease, unable to reach stage 2 12 Bruce or modified submaximal Bruce Abnormal heart rate recovery defined as heart rate change of 42 beats/min or less from peak exercise to that measured 2 min later 33% Normal heart rate recovery 4% died

Abnormal heart rate recovery 10% died

1.95
(1.11-3.42)*

1.55
(1.22-1.98)

54% 10% Age, sex, BMI, ethnicity, systolic blood pressure, hypertension medication, exercise habits, physical fitness, smoking, diabetes mellitus, lipids, ST-segment response, heart rate, chronotropic index, socioeconomic status
Jouven and Ducimetier 200045 6,101 French men in Paris civil service

Age range: 42-53 y

100% men

Known or suspected CVD, systolic blood pressure =180 at rest, or resting electrocardiographic abnormality 23 Bicycle ergometry Premature ventricular complex constituting more than 10% of all ventricular depolarizations during exercise 2.3% Normal exercise tolerance test result 6.4%

Abnormal exercise tolerance test result 16.1%*

2.53
(1.65-3.88)*

 

1.1 (0.8-1.5)

5%* 17%* Age, BMI, heart rate, systolic blood pressure, tobacco use, level of physical activity, diabetes mellitus, total cholesterol, presence or absence of premature ventricular depolarizations before or after exercise
Morshedi-Meibodi et al., 200247 2,967 participants in Framingham Offspring Study

Mean age ±SD: 43 ±10 y

47% men

Prevalent CVD, chronic obstructive pulmonary disease, use of digoxin or beta-blockers, resting electrocardiographic abnormalities, inability to complete stage 1 of exercise 15 Submaximal Bruce Heart rate recovery index - decrease in peak heart rate to 2 min of <42 beats/min N/A Overall 7.2% 0.8 (0.5-1.1) NA NA Age, BMI, smoking, SBP, diastolic blood pressure, anti-hypertensive medication, diabetes mellitus, total cholesterol level, HDL cholesterol level, resting heart rate and peak heart rate
Rywik et al., 200221 1,083 participants in the Baltimore Longitudinal Study of Aging

Mean age ±SD: 52 ±18 y

57% men

History of angina or heart failure, Q wave on rest electrocardiogram, valvular disease, use of antiarrhythmic drugs, inability to achieve 85% of max heart rate 7.9 Modified Balke Duration of exercise N/A Overall 7% 0.87 (0.79-0.96)
(For CHD event for 1 minute increase in exercise duration)
NR NR Age, cholesterol, sex, ST-segment changes
Frolkis et al., 200346 29,244 persons referred to Cleveland Clinic for exercise tolerance testing

Mean age ±SD: 56 ±11 y

70% men

Age <30 y, symptomatic heart failure, use of digoxin, valvular disease, end-stage renal disease, pacer, atrial fibrillation, heart block, frequent ventricular ectopic arrhythmia at rest, heart transplant, concurrent evaluation for an arrhythmia 5.3 Submaximal Bruce Frequent ventricular ectopic arrhythmia (>7 ventricular premature contractions/min), ventricular bigeminy or trigeminy, ventricular couplets or triplets, ventricular tachycardia, ventricular flutter, torsade de pointes, or ventricular fibrillation No ventricular ectopic arrhythmia

Frequent ventricular ectopic arrhythmia during recovery 2%

Frequent ventricular ectopic arrhythmia during exercise 3%

5%

11% 

9%

1.0

1.5 (1.1-1.9) 

1.1 (0.9-1.3)


3%

 

4%


12%

 

 9%

Age, sex, diabetes mellitus, hypertension, smoking, previous CAD, medication use, BMI, resting heart rate, systolic blood pressure, ST- segment changes, chronotropic incompetence, abnormal heart rate recovery, peak exercise capacity
Mora et al., 200342 2994 women enrolled in the Lipid Research Clinics Prevalence Study

Age range 30-80 y

0% men

Pregnancy or significant cardiovascular disease 20.3 Maximal Bruce Low exercise capacity (<7.5 METS) and low heart rate recovery (<55 beats/minute) 31% Normal and abnormal results on exercise tolerance test

5%*

14%

 

 

3.52 (1.57-7.86)*

2.11 (1.47-3.04)

71% 11% Age, smoking, diabetes, family history of premature heart disease, obesity, HDL cholesterol level, LDL cholesterol level, triglycerides, hypertension
Gulati et al., 200343 5721 women from the Chicago area (86% white)

Mean age 52 y

0% men

Self reported CHD, Percutaneous coronary intervention, coronary bypass surgery, congestive heart failure 9 Maximal Bruce Exercise capacity, in METS N/A 3.2% 0.83 (0.78-0.89)
for each 1 MET increase in exercise capacity
- - Framingham Risk Score

Note: Events are CHD events unless otherwise indicated. BMI = body mass index; CAD = coronary artery disease; CHD = coronary heart disease; CVD = cardiovascular disease; HDL = high-density lipoprotein cholesterol; LDL = low-density lipoprotein cholesterol; MET = metabolic equivalent; NA = not applicable; NR = not reported
* CHD death.
† All-cause death

Return to Table of Contents