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Pre-hospital ECG for acute coronary syndrome in urban India: A cost-effectiveness analysis
© Schulman-Marcus et al; licensee BioMed Central Ltd. 2010
Received: 21 May 2009
Accepted: 12 March 2010
Published: 12 March 2010
Patients with acute coronary syndrome (ACS) in India have increased pre-hospital delay and low rates of thrombolytic reperfusion. Use of ECG could reduce pre-hospital delay among patients who first present to a general practitioner (GP). We assessed whether performing ECG on patients with acute chest pain would improve long-term outcomes and be cost-effective.
We created a Markov model of urban Indian patients presenting to a GP with acute chest pain to compare a GP's performing an ECG versus not performing one. Variables describing the accuracy of a GP's referral decision in chest pain and ACS, ACS treatment patterns, the effectiveness of thrombolytic reperfusion, and costs were derived from Indian data where available and other developed world studies. The model was used to estimate the incremental cost-effectiveness ratio (ICER) of the intervention in 2007 US dollars per quality adjusted life years (QALY) gained.
Under baseline assumptions, the ECG strategy cost an additional $12.65 per QALY gained compared to no ECG. Sensitivity analyses around the cost of the ECG, cost of thrombolytic, and referral accuracy of the GP yielded ICERs for the ECG strategy ranging between cost-saving and $1124/QALY. All results indicated the intervention is cost-effective under current World Health Organization recommendations.
While direct presentation to the hospital with acute chest pain is preferable, in urban Indian patients presenting first to a GP, an ECG performed by the GP is a cost-effective strategy to reduce disability and mortality. This strategy should be clinically studied and considered until improved emergency transport services are available.
Ischemic heart disease is already the leading cause of mortality in India , and the magnitude of this disease's impact is expected to grow over the next two decades . It is projected that ischemic heart disease will result in two and one-half million Indian deaths by 2020 . Acute coronary syndrome (ACS), including both ST-elevation myocardial infarction (STEMI) and non-ST elevation ACS (NSTE-ACS), is an important manifestation of ischemic heart disease. Rapid diagnosis and treatment with appropriate reperfusion therapies has been proven to increase survival for patients with STEMI. This benefit of reperfusion diminishes as the interval from time of symptom onset to initiation of therapy increases . Current ACS guidelines emphasize the importance of rapid hospital care, especially for STEMI patients who may be eligible for thrombolytic reperfusion within the first twelve hours [4, 5].
A recent multi-center Indian registry found only a mean of 58.5% of Indian STEMI patients received thrombolytics, (6% of eligible patients undergo percutaneous revascularization) with an average interval between symptom onset and hospital arrival (pre-hospital delay) of five hours . This was twice as long as the median delay seen in the second Euro Heart survey . Increased pre-hospital delay in India has been attributed to poor patient knowledge about ACS, lack of emergency medical services (EMS) infrastructure, and transportation difficulties [1, 6, 8, 9].
In developed countries, pre-hospital electrocardiography (ECG) performed by EMS technicians is associated with faster access to reperfusion therapies for STEMI patients . As urban EMS systems are often lacking in India, ACS patients have been reported as likely to first present to a general practitioner (GP), which has generally been associated with increased pre-hospital delay [8, 9]. However, one retrospective Indian study of hospitalized ACS patients observed that although overall pre-hospital presentation to a GP doubled the risk of significant pre-hospital delay , a subgroup in which the GP performed an electrocardiogram (ECG) had reduced delay compared to patients who did not have an ECG and even to those who presented to the hospital directly. This finding was attributed to improved diagnosis of ACS and more prompt referral of patients to a hospital (unpublished data - with permission from Dr. Rajagopalan 5/25/08). These data were obtained under current urban transportation conditions.
It is therefore plausible that a pre-hospital ECG performed by a GP will have an analogous effect in increasing timely access to reperfusion through quicker and more accurate referral to a hospital. Such a strategy could be useful until improvements are made to India's EMS infrastructure. We modeled the hypothesis that compared to an urban GP not performing an ECG, a GP performing one leads to decreased pre-hospital delay, and consequentially increased eligibility for thrombolytics and improved long-term outcomes. Subsequently, we assessed the cost-effectiveness of this ECG strategy compared to not performing one.
Costs and quality adjusted survival were calculated based on estimates derived from prior studies of a GP's accuracy in referring patients with chest pain to either an appropriate medical facility or home. In both arms, we modeled that STEMI patients incorrectly sent home (false negatives) would be delayed in presenting to a hospital, and consequently would be ineligible for thrombolytic treatment. Patients incorrectly referred to a hospital without ACS (false positives) would incur costs of further medical evaluation. We modeled a cohort of adult patients with the median age of sixty years old, which is the median age of ACS in India .
Baseline values for input variables and costs
Chest pain is caused by ACS
GP Sensitivity with ECG
GP Sensitivity without ECG
Unpublished data from 
GP Specificity with ECG
GP Specificity without ECG
Correctly referred STEMI patients receiving thrombolysis (%)
Relative risk reduction of thrombolytics
Costs (2007 US$)
Emergency department visit
Annual secondary prevention
Specificity of the GP's referral decision was derived from studies performed in developed countries, as no Indian data were available. The specificity of the referral decision when an ECG was administered was estimated from the approximate mean specificity of admission decisions for patients with acute chest pain in the emergency department [12–16]. The specificity of the decision without an ECG was lower owing to decreased diagnostic certainty based on a study of physicians diagnosing acute myocardial infarction without the use of an ECG . We modeled among patients without ACS incorrectly referred to the hospital by the GP (false positives), a fraction equal to one minus the specificity of GP with the ECG would be admitted for 24 hours to "rule-out" ACS.
We adhered to recommendations of the US Panel on Cost-Effectiveness in Health and Medicine in choosing a societal perspective for the baseline analysis . The entire chest pain cohort was modeled until death, either from cardiovascular disease or other causes. No ethics approval was required, because no patients were used for data collection. All analyses were performed with TreeAge Pro Suite 2008 (TreeAge Software Inc., Williamstown, MA). All authors had full access to all the data and had final responsibility for the decision to submit for publication.
Chest Pain and ACS Data
ACS is the diagnosis in 10-20% of acute chest pain patients in developed world studies [19–22]. This percentage is unknown in India, so we elected to use the lower bound of 10% for our baseline analysis. This decision was based on the knowledge that the overall prevalence of coronary disease is likely lower and the prevalence of other causes of acute chest pain (e.g. tuberculosis) likely greater compared to developed countries. However, we tested the entire range of values in the sensitivity analysis. Based on the recent CREATE registry, which is the largest reported source of ACS data specific to urban India, we modeled 60.6% as having STEMI and the remainder having NSTE-ACS .
The model assumed that 58.5% of patients with STEMI correctly referred by the GP received thrombolytics, which is the Indian average . As Rajagopalan and colleagues observed a median delay of 24 hours for ACS patients who were misdiagnosed by a GP (unpublished data), we modeled that none of the STEMI patients incorrectly sent home by the GP received thrombolytics regardless of eventual hospitalization status. The short- and long-term effectiveness and risks of thrombolytics were derived from the overall effects reported in the Second International Study of Infarct Survival (ISIS-2) and Fibrinolytic Therapy Trialists (FTT) studies [23–25]. All patients who were treated in a hospital received early aspirin therapy, which had a relative risk reduction derived from ISIS-2.
Mortality to 35 days was estimated from ISIS-2 for STEMI patients [23, 24], and from the CREATE registry for NSTE-ACS patients . Patients with STEMI who were incorrectly sent home by the GP but later returned to the hospital were modeled to have a twelve-hour pre-hospital delay conveying an additional 0.9% mortality, which is half the first-day STEMI mortality rate in the FTT and Clopidogrel and Metoprolol in Myocardial Infarction (COMMIT) studies [25, 26]. All ACS patients who were incorrectly sent home by the GP and did not return to the hospital had double the 35-day mortality of those admitted, a hazard determined from developed world studies of ACS patients incorrectly sent home from the emergency department [11, 21].
Mortality after 35 days for chest pain patients without ACS was derived from World Health Organization (WHO) life tables for India . We assumed that patients without ACS did not have ischemic heart disease, so we adjusted the annual mortality probabilities to decrease the influence of heart disease for the first ten years. In the patients who had ACS, for the first ten years we used mortality and reinfarction data derived from Law and colleagues , with adjustments for the effects of secondary prevention. After ten years, the annual mortality for ACS patients was equivalent to the sum of fatal reinfarction and the yearly mortality in the WHO life tables.
For secondary prevention after 35 days, we considered a regimen of aspirin, a beta-blocker, a statin, and an angiotensin converting enzyme (ACE) inhibitor. As an international survey showed that the actual population of patients taking secondary prevention in India is well below those eligible , we modeled the relative risk reduction of secondary prevention only for the percentage of Indian patients taking the individual drugs. The relative risk reductions of the secondary prevention regimen were derived from the reported literature [30–33]. In accordance with evidence that has suggested a diminishing effect of beta-blockers over time , the beta-blocker was only included in the secondary prevention regimen for the first six years of the model. We assumed that the relative risk reductions of the drugs were independent, and therefore we calculated the overall effect by multiplying the individual relative risks associated with each drug.
Outcomes and Costs
Outcomes in the analyses were measured in quality adjusted life-years (QALYs) gained and net health costs. QALYs were obtained by using the disability weights of the WHO Global Burden of Disease Project as used in the 2nd edition of the Disease Control Priorities (DCP) Project [35, 36].
Costs of hospital admission, salaries, office visits, and laboratory fees were derived from regional estimates done for the Disease Control Priorities Project . As the median duration of hospitalization for ACS in India is five days , we modeled a five day admission to a secondary hospital with the pro-rated labor costs of a cardiologist, junior doctor, nursing care, and an administrative worker. For patients who needed a blood transfusion or stroke care owing to the adverse effects of thrombolytics, additional days of hospitalization were added. Drug costs were calculated from the International Drug Price Indicator Guide  and local costing data where available. All secondary prevention drug costs were computed as a year's supply, though covering only the proportion of Indian patients taking medical therapy as reported in the WHO-PREMISE survey .
The baseline cost of an ECG was estimated as the current reimbursement rate to private hospitals by India's Central Government Health Scheme (CGHS) in large metropolitan areas . An additional $0.08 cost was added based on a 500 rupee training cost  spread over an estimated 30 annual ECGs performed over a five year period. We did not model the direct costs of transportation to the hospital, time lost from work, or rehabilitation. Initial costs obtained in India rupees prior to 2007 were inflated to 2007 rupees using the Indian wholesale price index  and then converted to 2007 US dollars with the midyear exchange rate. The costs are modest but the Gross National Income (GNI) per capita was approximately $800 in 2006, reflecting the relatively cheap labor supply in India and as a result lower costs.
All costs and benefits were tallied at mid-cycle increments. Those dying during a cycle were assumed to incur one half of the utilities and costs of that cycle. All costs as well as health outcomes were discounted at 3% per year, which is consistent with guidelines . Incremental cost-effectiveness ratios (ICERs) were calculated as the difference in costs between the ECG intervention and no intervention divided by the increase in QALYs gained.
One-way sensitivity analyses on the "sensitivity" and "specificity" of the GP's referral decision relied on studies of admission decisions for emergency department patients with acute chest pain [12–16]. Analyses of the effectiveness of the thrombolytics relied on the standard deviations reported in ISIS-2. As the efficacy of therapy in real Indian settings may be substantially lower than that in developed world controlled trials, we also assessed reduction in thrombolytic efficacy of up to 50%. Sensitivity analyses of the costs of health-care delivery relied on the ranges reported in the DCP working paper , except for the cost of an ECG which was estimated from selected Indian price schedules as well as one developed world reimbursement schedule for comparison [42–44]. Analysis of the price of thrombolytic relied on a lower bound from an online Indian database of drug prices  and an upper bound from the International Drug Price Indicator Guide. In our sensitivity analyses, we use the term "cost-saving" to mean that the ECG intervention cost less and resulted in more QALYs gained than not performing an ECG. We also performed a probabilistic sensitivity analysis with second-order Monte Carlo simulation of 1000 randomly selected sets of parameters in which we simultaneously sampled values from the distributions with corresponding logit-means and logit-standard deviations.
Results with baseline assumptions
GP without ECG
GP with ECG
Results of one-way sensitivity analysis
Chest pain is caused by ACS
0.01 -- 0.2
Cost-saving† -- 119
GP sensitivity with ECG
0.7 -- 0.98
Cost-saving -- 103
GP sensitivity without ECG
0.667 -- 0.818
13 -- cost-saving
GP specificity with ECG
0.44 -- 0.67
76 -- cost-saving
GP specificity without ECG
0.3 -- 0.5
57 -- 351
Relative risk reduction of thrombolytics
0.71 -- 0.875
13 -- 12
Costs (2007 US$)
1.00 -- 15.00
Cost-saving -- 1124
68.74 -- 162.38
Cost-saving -- 33
99.71 -- 459.39
Cost-saving -- 73
We performed a probabilistic sensitivity analysis (PSA) on the main variables of uncertainty, including the sensitivity and specificity, the efficacy of thrombolytics in India, the cost of ECGs in India. The PSA using the variables in Table 3 resulted in a mean ICER of $154/QALY (95% confidence interval, -$1790/QALY., $1830/QALY). Greater than 97.5% of the values were less than a willingness to pay threshold of $3000.
Discussion and Conclusions
We modeled a cohort of urban Indian patients with acute chest pain presenting to a general practitioner to compare the lifelong cost-effectiveness of a GP performing an ECG versus not performing one. Our model found that it cost only $12.65 to gain an additional quality adjusted life year for this cohort. The relatively cheap cost for a life year results from the ECG facilitating a GP's decision in the early and appropriate referral of STEMI to a hospital where thrombolysis is administered, as well as a reduction in unnecessary referrals of patients without ACS to hospitals in order to "rule-out" an event. One-way sensitivity analyses around uncertain variables and assumptions demonstrated that this finding is robust, especially for the values most commonly found in contemporary Indian settings.
WHO considers interventions to be cost-effective if they have ICERs that are less than three times gross national income (GNI) per head . In 2006, India's GNI per capita was $820, or $2460 after adjustment for purchasing power parity . As the baseline findings of our model and all sensitivity analyses suggest the ICER of the GP's performing an ECG compared to not performing one is under $1200, the ECG strategy is certainly cost-effective under current WHO definitions. Furthermore, the results of the probabilistic sensitivity analyses suggest the findings are robust with a 95% confidence interval that is well below the likely willingness to pay threshold for India based on WHO recommendations. Also, since we did not model the direct costs of missed work owing to unnecessary hospitalization of chest pain patients without ACS, it is likely that the ECG strategy is even more cost-effective than our results indicate.
Current guidelines recommend that all patients with acute chest pain should be educated to directly present to a hospital emergency department, and that any such patients presenting to an outpatient practitioner should be urgently referred . We did not model a direct presentation strategy in this study owing to inadequate data, though we think it would be interesting to compare its cost-effectiveness to pre-hospital GP strategies in the future. While such a direct presentation strategy is likely to further increase the population eligible for thrombolysis, it may also cost substantially more owing to increased chest pain patients without ACS presenting to crowded emergency rooms. Still, in the absence of further evidence, we emphasize that direct presentation with acute chest pain is preferable.
In the meantime, while the Indian public undergoes public education regarding the association of chest pain with serious conditions such as myocardial ischemia and the possibility of myocardial infarction and the need to present to an appropriate facility in a timely fashion; the use of ECG machines by general practitioners may facilitate a timely presentation to an appropriate hospital where acute treatments such as thrombolytics can be applied. Training to use the ECG machine and interpret results can be obtained for as little as $10 and machines can be purchased for under $300. Many private based GPs already may have them. Government based clinics could consider their purchase if not already available. The policy of using ECG machines may not be feasible in rural areas however, given the access to facilities where thrombolysis can be safely be administered may not available.
We did not model a strategy whereby a GP would use a point-of-care troponin assay to make a referral decision. Troponins are frequently negative early in ACS  and it is unclear how useful a pre-hospital troponin assay would be when compared to or combined with an ECG. A pre-hospital troponin test's impact on mortality is also uncertain, as troponin assays mostly increase the sensitivity for NSTE-ACS , for which thrombolytics are not indicated. We think this is an area that deserves additional research
Sensitivity analyses around the "sensitivity" and "specificity" of the GP's referral decisions with and without the ECG robustly support our baseline findings. We performed these analyses using an especially broad range of possible values for two reasons. First, most data regarding physicians' performance in the diagnosis and referral of ACS patients using ECG are from emergency departments; it is unknown if outpatient GPs perform similarly. Second, there is very limited knowledge about how real physicians perform in the diagnosis and referral of patients with ACS when there is no ECG available. Therefore, in the sensitivity analysis of the GP's referral decision without the ECG, we extended the tested range of values up to the baseline values for the GP with the ECG. This is a very conservative assumption, for it is the equivalent of stating that the ECG is not helpful in referral decision-making, which is at odds with published guidelines . Even so, these one-way analyses did not greatly affect the calculated cost-effectiveness of the ECG strategy
There are several limitations to our study. First, our baseline estimates of the "sensitivity" of a GP's referral decision are based on supplementary observations of a small single-center study that had of mainly urban middle-class patients with confirmed ACS . No confidence intervals were reported in that study. The primary study itself was retrospective, and it was not designed to evaluate a GP's pre-hospital decision making. However, these are the only Indian data available studying a scenario common to urban India. Sensitivity analysis using a wide range of values derived from developed world studies for the sensitivity of GP's referral decision demonstrates that our findings are robust.
Second, owing to limited data on the ultimate diagnosis of acute chest pain across different age groups in India, we only modeled a cohort of sixty-year old patients. We assumed that ACS was the cause of chest pain in 10% of the cohort, which was the lower end of the reported range in developed world studies [19–22]. However, sensitivity analysis supports our finding that the ECG strategy is cost-effective throughout the entire reported range. We found that when ACS as a cause of chest pain was less prevalent, as might be expected in younger cohorts, the ECG strategy was actually cost-saving. When ACS was the cause of acute chest pain in 20% of the modeled cohort, which may be true in older cohorts of patients, the ECG strategy still had an ICER still well beneath the WHO threshold for cost-effectiveness. Further, a previous study has shown that the use of thrombolytics in the elderly led to an cost-effectiveness ratio for those over the age of 75 what was double of that for those under the age of 70 Given that women present at a later age and over all with lower prevalence this would tend to make the ratios in general lower for women than men, especially since case-fatality is higher for females.
Third, owing to limited Indian data, our model did not study the hour-dependent differential effects of thrombolytics on mortality. Major international studies suggest that the subgroup receiving thrombolytics within three hours of ACS onset benefits more than the subgroups receiving them from 3-6 and 6-12 hours after onset [23, 25]. Our model treated receiving thrombolytics as a binary variable, and the risk reduction in mortality was the average reported from a large international trial. We predict that modeling thrombolytic administration as a time-dynamic variable would lead to even greater reductions in mortality, which would further favor the ECG strategy. This is a topic that deserves further research once Indian data are available.
A recent study in the United States suggests that pre-hospital ECG performed by emergency medical services increase the frequency and rapidity of reperfusion therapies for patients with STEMI . Given that many Indian ACS patients present first to a GP and the current absence of emergency systems, it is reasonable to study whether a GP performing pre-hospital ECG could yield analogous benefits. We modeled such a GP-based strategy and found it to be robustly cost-effective compared to a GP not performing an ECG for urban patients with acute chest pain. This finding should be considered a strong rationale for clinical trials. Meanwhile, our findings also suggest that it is sensible for GPs in urban India to perform an ECG in patients with acute chest pain until improvements to India's emergency medical services are put in place.
Sources of support
Sarnoff Cardiovascular Research Foundation (J Schulman-Marcus) Fogarty International Center, National Institutes of Health: K01TW007141-01 (TA Gaziano)
This study was funded through a Sarnoff Cardiovascular Research Foundation fellowship to JSM. The sponsor of the study had no role in study design, data analysis, or the writing of the report. We wish to thank Dr. R Rajagopalan (Chennai) for providing supplementary data.
- Karthikeyan G, Xavier D, Prabhakaran D, Pais P: Perspectives on the management of coronary artery disease in India. Heart. 2007, 93 (11): 1334-1338. 10.1136/hrt.2007.131193.View ArticlePubMedPubMed CentralGoogle Scholar
- Reddy KS: India wakes up to the threat of cardiovascular diseases. J Am Coll Cardiol. 2007, 50 (14): 1370-1372. 10.1016/j.jacc.2007.04.097.View ArticlePubMedGoogle Scholar
- Ezzati M, Lopez AD, Rodgers A, Murray CJL: Comparative quantification of health risks. Global and regional burden of disease attributable to major risk factors. 2004, Geneva: World Health OrganizationGoogle Scholar
- Antman EM, Anbe DT, Armstrong PW, Bates ER, Green LA, Hand M, Hochman JS, Krumholz HM, Kushner FG, Lamas GA, et al: ACC/AHA guidelines for the management of patients with ST-elevation myocardial infarction: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Revise the 1999 Guidelines for the Management of Patients with Acute Myocardial Infarction). Circulation. 2004, 110 (9): e82-292.PubMedGoogle Scholar
- API expert consensus document on management of ischemic heart disease. J Assoc Physicians India. 2006, 54: 469-480.Google Scholar
- Xavier D, Pais P, Devereaux PJ, Xie C, Prabhakaran D, Reddy KS, Gupta R, Joshi P, Kerkar P, Thanikachalam S, et al: Treatment and outcomes of acute coronary syndromes in India (CREATE): a prospective analysis of registry data. Lancet. 2008, 371 (9622): 1435-1442. 10.1016/S0140-6736(08)60623-6.View ArticlePubMedGoogle Scholar
- Mandelzweig L, Battler A, Boyko V, Bueno H, Danchin N, Filippatos G, Gitt A, Hasdai D, Hasin Y, Marrugat J, et al: The second Euro Heart Survey on acute coronary syndromes: Characteristics, treatment, and outcome of patients with ACS in Europe and the Mediterranean Basin in 2004. Eur Heart J. 2006, 27 (19): 2285-2293. 10.1093/eurheartj/ehl196.View ArticlePubMedGoogle Scholar
- Rajagopalan RE, Chandrasekaran S, Pai M, Rajaram R, Mahendran S: Pre-hospital delay in acute myocardial infarction in an urban Indian hospital: a prospective study. Natl Med J India. 2001, 14 (1): 8-12.PubMedGoogle Scholar
- Malhotra S, Gupta M, Chandra KK, Grover A, Pandhi P: Prehospital delay in patients hospitalized with acute myocardial infarction in the emergency unit of a North Indian tertiary care hospital. Indian Heart J. 2003, 55 (4): 349-353.PubMedGoogle Scholar
- Diercks DB, Kontos MC, Chen AY, Pollack CV, Wiviott SD, Rumsfeld JS, Magid DJ, Gibler WB, Cannon CP, Peterson ED, et al: Utilization and impact of pre-hospital electrocardiograms for patients with acute ST-segment elevation myocardial infarction: data from the NCDR (National Cardiovascular Data Registry) ACTION (Acute Coronary Treatment and Intervention Outcomes Network) Registry. J Am Coll Cardiol. 2009, 53 (2): 161-166. 10.1016/j.jacc.2008.09.030.View ArticlePubMedGoogle Scholar
- Lee TH, Rouan GW, Weisberg MC, Brand DA, Acampora D, Stasiulewicz C, Walshon J, Terranova G, Gottlieb L, Goldstein-Wayne B, et al: Clinical characteristics and natural history of patients with acute myocardial infarction sent home from the emergency room. Am J Cardiol. 1987, 60 (4): 219-224. 10.1016/0002-9149(87)90217-7.View ArticlePubMedGoogle Scholar
- Pozen MW, D'Agostino RB, Selker HP, Sytkowski PA, Hood WB: A predictive instrument to improve coronary-care-unit admission practices in acute ischemic heart disease. A prospective multicenter clinical trial. N Engl J Med. 1984, 310 (20): 1273-1278.View ArticlePubMedGoogle Scholar
- Karlson BW, Herlitz J, Wiklund O, Richter A, Hjalmarson A: Early prediction of acute myocardial infarction from clinical history, examination and electrocardiogram in the emergency room. Am J Cardiol. 1991, 68 (2): 171-175. 10.1016/0002-9149(91)90739-8.View ArticlePubMedGoogle Scholar
- Ting HH, Lee TH, Soukup JR, Cook EF, Tosteson AN, Brand DA, Rouan GW, Goldman L: Impact of physician experience on triage of emergency room patients with acute chest pain at three teaching hospitals. Am J Med. 1991, 91 (4): 401-408. 10.1016/0002-9343(91)90158-T.View ArticlePubMedGoogle Scholar
- Selker HP, Beshansky JR, Griffith JL, Aufderheide TP, Ballin DS, Bernard SA, Crespo SG, Feldman JA, Fish SS, Gibler WB, et al: Use of the acute cardiac ischemia time-insensitive predictive instrument (ACI-TIPI) to assist with triage of patients with chest pain or other symptoms suggestive of acute cardiac ischemia. A multicenter, controlled clinical trial. Ann Intern Med. 1998, 129 (11): 845-855.View ArticlePubMedGoogle Scholar
- Mant J, McManus RJ, Oakes RA, Delaney BC, Barton PM, Deeks JJ, Hammersley L, Davies RC, Davies MK, Hobbs FD: Systematic review and modelling of the investigation of acute and chronic chest pain presenting in primary care. Health Technol Assess. 2004, 8 (2): iii-1-158View ArticlePubMedGoogle Scholar
- Herlitz J, Karlson BW, Karlsson T, Dellborg M, Hartford M, Luepker R: Diagnostic accuracy of physicians for identifying patients with acute myocardial infarction without an electrocardiogram. Experiences from the TEAHAT Trial. Cardiology. 1995, 86 (1): 25-27. 10.1159/000176831.View ArticlePubMedGoogle Scholar
- Gold M, Siegel J, Russell L, M W, eds: Cost-effectiveness in health and medicine. 1996, New York: Oxford University PressGoogle Scholar
- Davie AP, Caesar D, Caruana L, Clegg G, Spiller J, Capewell S, Starkey IR, Shaw TR, McMurray JJ: Outcome from a rapid-assessment chest pain clinic. QJM. 1998, 91 (5): 339-343. 10.1093/qjmed/91.5.339.View ArticlePubMedGoogle Scholar
- Burt CW: Summary statistics for acute cardiac ischemia and chest pain visits to United States EDs, 1995-1996. Am J Emerg Med. 1999, 17 (6): 552-559. 10.1016/S0735-6757(99)90195-X.View ArticlePubMedGoogle Scholar
- Pope JH, Aufderheide TP, Ruthazer R, Woolard RH, Feldman JA, Beshansky JR, Griffith JL, Selker HP: Missed diagnoses of acute cardiac ischemia in the emergency department. N Engl J Med. 2000, 342 (16): 1163-1170. 10.1056/NEJM200004203421603.View ArticlePubMedGoogle Scholar
- Herlitz J, Karlson BW, Karlsson T, Stensdotter L, Sjolin M: Rate of admission and long-term prognosis among patients with acute chest pain in the 1990s compared with the 1980s. Cardiology. 2005, 104 (1): 51-56. 10.1159/000086525.View ArticlePubMedGoogle Scholar
- ISIS-2 (Second International Study of Infarct Survival) Collaborative Group: Randomised trial of intravenous streptokinase, oral aspirin, both, or neither among 17,187 cases of suspected acute myocardial infarction: ISIS-2. Lancet. 1988, 2 (8607): 349-360.Google Scholar
- Baigent C, Collins R, Appleby P, Parish S, Sleight P, Peto R: ISIS-2: 10 year survival among patients with suspected acute myocardial infarction in randomised comparison of intravenous streptokinase, oral aspirin, both, or neither. The ISIS-2 (Second International Study of Infarct Survival) Collaborative Group. BMJ. 1998, 316 (7141): 1337-1343.View ArticlePubMedPubMed CentralGoogle Scholar
- Fibrinolytic Therapy Trialists' (FTT) Collaborative Group: Indications for fibrinolytic therapy in suspected acute myocardial infarction: collaborative overview of early mortality and major morbidity results from all randomised trials of more than 1000 patients. Lancet. 1994, 343 (8893): 311-322.Google Scholar
- Chen ZM, Pan HC, Chen YP, Peto R, Collins R, Jiang LX, Xie JX, Liu LS: Early intravenous then oral metoprolol in 45,852 patients with acute myocardial infarction: randomised placebo-controlled trial. Lancet. 2005, 366 (9497): 1622-1632. 10.1016/S0140-6736(05)67661-1.View ArticlePubMedGoogle Scholar
- Rodriguez T, Malvezzi M, Chatenoud L, Bosetti C, Levi F, Negri E, La Vecchia C: Trends in mortality from coronary heart and cerebrovascular diseases in the Americas: 1970-2000. Heart. 2006, 92 (4): 453-460. 10.1136/hrt.2004.059295.View ArticlePubMedPubMed CentralGoogle Scholar
- Law MR, Watt HC, Wald NJ: The underlying risk of death after myocardial infarction in the absence of treatment. Arch Intern Med. 2002, 162 (21): 2405-2410. 10.1001/archinte.162.21.2405.View ArticlePubMedGoogle Scholar
- Mendis S, Abegunde D, Yusuf S, Ebrahim S, Shaper G, Ghannem H, Shengelia B: WHO study on Prevention of REcurrences of Myocardial Infarction and StrokE (WHO-PREMISE). Bull World Health Organ. 2005, 83 (11): 820-829.PubMedPubMed CentralGoogle Scholar
- Antithrombotic Trialists' Collaboration: Collaborative meta-analysis of randomised trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients. BMJ. 2002, 324 (7329): 71-86. 10.1136/bmj.324.7329.71.View ArticleGoogle Scholar
- Dagenais GR, Pogue J, Fox K, Simoons ML, Yusuf S: Angiotensin-converting-enzyme inhibitors in stable vascular disease without left ventricular systolic dysfunction or heart failure: a combined analysis of three trials. Lancet. 2006, 368 (9535): 581-588. 10.1016/S0140-6736(06)69201-5.View ArticlePubMedGoogle Scholar
- Freemantle N, Cleland J, Young P, Mason J, Harrison J: Beta Blockade after myocardial infarction: systematic review and meta regression analysis. BMJ. 1999, 318 (7200): 1730-1737.View ArticlePubMedPubMed CentralGoogle Scholar
- The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group: Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. N Engl J Med. 1998, 339 (19): 1349-1357. 10.1056/NEJM199811053391902.View ArticleGoogle Scholar
- Yusuf S, Peto R, Lewis J, Collins R, Sleight P: Beta blockade during and after myocardial infarction: an overview of the randomized trials. Prog Cardiovasc Dis. 1985, 27 (5): 335-371. 10.1016/S0033-0620(85)80003-7.View ArticlePubMedGoogle Scholar
- Jamison D, Breman J, Measham A, Alleyne G, Claeson M, Evans DB, et al: Disease control priorities in developing countries. 2006, New York: Oxford University Press and the World Bank, 2Google Scholar
- Mathers CD, Lopez AD, Murray CJL: The burden of disease and mortality by condition: data, methods, and results for 2001. Global Burden of Disease and Risk Factors. 2006, New York: Oxford University Press, 45-93.Google Scholar
- Mulligan J, Fox-Rushby J, Taghreed A: Unit costs of health care inputs in low and middle income regions. Disease Control Priorities Project Working Paper 9, Bethesda (MD). 2004Google Scholar
- Fyre J, ed: International drug price indicator guide. 2008, Cambridge (MA): Management Sciences for HealthGoogle Scholar
- Ghaffar A, Reddy KS, Singhi M: Burden of non-communicable diseases in South Asia. BMJ. 2004, 328 (7443): 807-810. 10.1136/bmj.328.7443.807.View ArticlePubMedPubMed CentralGoogle Scholar
- Shafey O, Eriksen M, Ross H, Mackay J: The Tobacco Atlas, Third Edition. 2009, Atlanta: American Cancer SocietyGoogle Scholar
- Ahmad N, Bhopal R: Is coronary heart disease rising in India? A systematic review based on ECG defined coronary heart disease. Heart. 2005, 91 (6): 719-725. 10.1136/hrt.2003.031047.View ArticlePubMedPubMed CentralGoogle Scholar
- Goyal A, Yusuf S: The burden of cardiovascular disease in the Indian subcontinent. Indian J Med Res. 2006, 124 (3): 235-244.PubMedGoogle Scholar
- Jafar TH, Qadri Z, Chaturvedi N: Coronary artery disease epidemic in Pakistan: more electrocardiographic evidence of ischaemia in women than in men. Heart. 2008, 94 (4): 408-413. 10.1136/hrt.2007.120774.View ArticlePubMedGoogle Scholar
- Joshi R, Chow CK, Raju PK, Raju R, Reddy KS, MacMahon S, Lopez AD, Neal B: Fatal and Nonfatal Cardiovascular Disease and the Use of Therapies for Secondary Prevention in a Rural Region of India. Circulation. 2009, 119 (14): 1950-1955. 10.1161/CIRCULATIONAHA.108.819201.View ArticlePubMedGoogle Scholar
- Yusuf S, Hawken S, Ounpuu S, Dans T, Avezum A, Lanas F, McQueen M, Budaj A, Pais P, Varigos J, et al: Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004, 364 (9438): 937-952. 10.1016/S0140-6736(04)17018-9.View ArticlePubMedGoogle Scholar
- Doubilet P, Begg CB, Weinstein MC, Braun P, McNeil BJ: Probabilistic sensitivity analysis using Monte Carlo simulation. A practical approach. Med Decis Making. 1985, 5 (2): 157-177. 10.1177/0272989X8500500205.View ArticlePubMedGoogle Scholar
- Macroeconomics and health: investing in health for economic development. 2001, Geneva: World Health OrganizationGoogle Scholar
- S Mauss FB, Schmutz G, Henke J, Richter WO: Lipoprotein(a) in patients initiating antiretroviral therapy. HIV Medicine. 2008, 9 (6): 415-420. 10.1111/j.1468-1293.2008.00574.x.View ArticleGoogle Scholar
- Roger VL, Killian JM, Weston SA, Jaffe AS, Kors J, Santrach PJ, Tunstall-Pedoe H, Jacobsen SJ: Redefinition of myocardial infarction: prospective evaluation in the community. Circulation. 2006, 114 (8): 790-797. 10.1161/CIRCULATIONAHA.106.627505.View ArticlePubMedGoogle Scholar
- Gaziano TA: Cardiovascular Disease in the Developing World and Its Cost-Effective Management. Circulation. 2005, 112 (23): 3547-3553. 10.1161/CIRCULATIONAHA.105.591792.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/10/13/prepub
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