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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Arch Intern Med. Author manuscript; available in PMC 2012 July 25.
Published in final edited form as:
PMCID: PMC3164860

The Impact of New Cardiovascular Device Technology on Health Care Costs

Peter W. Groeneveld, MD, MS,1,2,3 Daniel Polsky, PhD,2,3 Feifei Yang, MS,2 Lin Yang, MS,2 and Andrew J. Epstein, PhD1,2,3


Drug-eluting coronary stents (DES) are widely used1 and entail sizeable Medicare hospital expenditures.2 However, the overall cost impact of DES has not been well quantified. Clear understanding of how new technologies like DES affect healthcare expenditures can provide insight into national trends in healthcare cost growth, of which new technology is presumably the leading driver.3 New technology may not only increase costs by being more expensive than previous treatments, but also by changing the patterns of care for chronic disease.4 Accordingly, we sought to assess the overall impact of DES on Medicare expenditures in a nationally-representative cohort of Medicare beneficiaries with coronary artery disease (CAD).


Because DES were introduced in 2003, we calculated average annual payer-perspective costs among CAD patients during 2002–2006 (including 2002 costs as a baseline), in each U.S. Hospital Referral Region (HRR)6 using a 5% random sample of fee-for-service Medicare beneficiaries, excluding patients younger than 66 and older than 85 (DES use declines markedly at older ages).5 Calculations were separately performed on each of three CAD sub-cohorts categorized annually by clinical events: patients with acute myocardial infarction (AMI), patients with acute coronary syndrome (ACS) but no AMI, and patients without ACS. We did not assume DES-associated healthcare cost growth was confined solely to DES recipients, thus cohorts included all CAD patients regardless of treatments received. Costs included all facility and provider Medicare payments, including non-cardiovascular costs, inflated to 2006 dollars using the consumer price index. This design captured costs downstream of major cardiovascular procedures and events, as patients were retained in the cohort through 12/31/2006 or until death. Annual DES rates within each HRR and subcohort were also calculated.

Substantial geographic variation in DES use across HRRs enabled measurement of the relationship between higher DES use and higher healthcare costs. Multivariable regression models were estimated predicting annual HRR-level healthcare costs among CAD patients as a function of the local DES rate, HRR “fixed effects” that controlled for time-invariant differences in costs across HRRs, and time varying controls such as an annual HRR-specific medical cost index (controlling for geographic variability in healthcare inflation), patients’ average DxCG Risk Score (predicting comorbidity-associated costs), and general time trend controls. Models were estimated separately for each subcohort.

To fully describe the national expenditure implications of the per-patient DES cost increases estimated by regression models, we computed the total change in national expenditures attributable to DES by multiplying the total number of Medicare beneficiaries nationwide in each CAD subgroup by the per-patient 2002–2006 cost increase predicted by the models.


Calculations were derived from 1,981,088 Medicare beneficiaries with CAD, of whom 4.5% had a recent AMI, 3.4% had a recent non-infarction ACS, and 92% had no recent ACS. Between 2002–2006, DES use increased from 0% in all subcohorts to 23% among AMI, 29% among non-infarction ACS, and 1.1% among non-ACS patients. Inflation-adjusted cost increases during 2002–2006 among CAD subcohorts ranged from 4.7% to 11.7%. Multivariable regressions indicated that each 1% increase in DES use was associated with a $28 average per-patient cost increase (p=0.009) among AMI patients, a $35 increase (p<0.001) among non-infarct ACS patients, and a $133 increase (p=0.003) among non-ACS patients. These estimates implied a DES-attributable increase in annual expenditures on AMI patients of $657, on non-infarct ACS patients of $999, and on non-ACS patients of $146 (Table 1). Because the vast majority of CAD patients were non-ACS, this subgroup comprised the largest portion of DES-attributable national cost growth.

Patient-level and Subgroup-level Costs Attributable to DES


Drug-eluting stents substantially increased costs for Medicare beneficiaries with CAD. The fraction of DES cost growth attributable to non-ACS patients (68%) was much larger than the proportion of DES received by this subcohort (33%), suggesting DES use among non-ACS patients was particularly cost-amplifying (i.e., DES introduction changed patterns of care for non-ACS patients in a more costly manner than for ACS patients). This is troubling, as the limited efficacy of PCI among non-ACS patients, whether or not DES is utilized, would not justify sizeable DES-related cost increases among non-ACS patients.7, 8

This analysis contributes to understanding the cost-increasing effects of technology because the cost effects of DES were measured beyond the price of the new technology itself. By measuring “global” costs among stable groups of patients over time, we captured temporal changes in both direct and indirect costs related to changing rates of DES use that occurred among patients who actually received the technology as well as non-recipients.

This observational study could not establish whether the association between increased DES use and cost growth was causal. Use of DES may be appropriate in selected non-ACS patients and could deliver benefits at acceptable cost.9 Outpatient pharmaceutical costs were not included; these may have amplified or attenuated the DES-associated cost increase.

Drug-eluting stents added $1.57 billion in annual Medicare expenditures among beneficiaries ages 66–85, with the largest cost increase occurring among non-ACS patients.


Research support: This research was supported by the National Heart, Lung, and Blood Institute (1R01HL086919) and by the Agency for Healthcare Research and Quality (1R01HS018403). Dr. Groeneveld was additionally supported by a Career Development Transition Award from the Department of Veterans Affairs’ Health Services Research and Development Service, Washington, DC. This project was also funded, in part, under a grant from the Pennsylvania Department of Health, which specifically disclaims responsibility for any analyses, interpretations, or conclusions.


Presented at the American Heart Association Quality of Care and Outcomes Forum (oral presentation) on May 20, 2010 in Washington, DC.

None of the authors had any personal or financial conflicts of interest in regard to this study.


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