Abstract
Background:
Healthcare spending for coronary artery disease (CAD)–related services is higher than for other chronic conditions. Diagnosis of incident cancer may impede management of CAD, thereby increasing the risk of CAD-related complications and associated healthcare expenditures. This study examined the relationship between incident cancer and CAD-related expenditures among elderly Medicare beneficiaries.
Patients and Methods:
A retrospective longitudinal study was conducted using the SEER-Medicare linked registries and a 5% noncancer random sample of Medicare beneficiaries. Elderly fee-for-service Medicare beneficiaries with preexisting CAD and with incident breast, colorectal, or prostate cancer (N=12,095) or no cancer (N=34,237) were included. CAD-related healthcare expenditures comprised Medicare payments for inpatient, home healthcare, and outpatient services. Expenditures were measured every 120 days during the 1-year preindex and 1-year postindex periods. Adjusted relationship between incident cancer and expenditures was analyzed using the generalized linear mixed models.
Results:
Overall, CAD-related mean healthcare expenditures in the preindex period accounted for approximately 32.6% to 39.5% of total expenditures among women and 41.5% to 46.8% among men. All incident cancer groups had significantly higher CAD-related expenditures compared with noncancer groups (P<.0001). Men and women with colorectal cancer (CRC) had 166% and 153% higher expenditures, respectively, compared with their noncancer counterparts. Furthermore, men and women with CRC had 57% and 55% higher expenditures compared with those with prostate or breast cancer, respectively.
Conclusions:
CAD-related expenditures were higher for elderly Medicare beneficiaries with incident cancer, specifically for those with CRC. This warrants the need for effective programs and policies to reduce CAD-related expenditures. Close monitoring of patients with a cancer diagnosis and preexisting CAD may prevent CAD-related events and expenditures.
Background
Cardiovascular disease, including coronary artery disease (CAD) and cerebrovascular disease, has the highest healthcare expenditures (~$231.1 billion in 2013).1 Healthcare spending for CAD-related services is higher than that for other chronic conditions.2–4 Furthermore, CAD-related healthcare expenditures in the United States are projected to increase 198% by 2030 because of the aging population.2
Evidence also suggests that individuals with CAD have many preexisting conditions or may develop new conditions. The most common preexisting or existing conditions in patients with CAD include cancer, hyper-tension, diabetes, and other cardiovascular diseases.5 For these individuals, CAD-related expenditures can be higher than for those who only have CAD.4,6 Specifically, CAD-related expenditures may be higher among individuals with incident cancer (and CAD) during the period immediately after cancer diagnosis, because cardiotoxicity from specific cancer treatments can exacerbate preexisting CAD,7,8 and diagnosis of incident cancer may impede management of CAD, thereby increasing the risk of CAD-related complications, given that cancer is considered a dominant condition.9
However, there is a dearth of studies on the impact of incident cancer diagnosis on CAD-related expenditures. It is important to analyze CAD-related expenditures among Medicare beneficiaries because there are significant differences in healthcare expenditures directly attributed to CAD and total expenditures associated with CAD.2 Specifically, published studies suggest that inpatient spending accounts for nearly 43% of total expenditures for cardiovascular diseases.10 Furthermore, CAD-related expenditures may be higher among elderly individuals (aged ≥65 years) as a result of comorbidities related to aging. For example, Dieleman et al1 reported that 65.2% of expenditures for CAD and related diseases were for elderly individuals, suggesting that these individuals account for most of the expenditures associated with CAD care. Because nearly 84% of elderly patients are covered by Medicare,11 payments made by Medicare for CAD are substantial, suggesting that it is important to estimate Medicare payments for CAD care. In 2012, Medicare paid $273 billion for heart disease–related expenditures, with a per-person cost of $10,345.12
Estimating the extent to which incident cancer affects CAD-related expenditures can help payers with emerging healthcare delivery reform initiatives. These initiatives are focused on financial incentives to improve healthcare quality with lower expenditures. For example, new payment models from the Centers for Medicare & Medicaid Services (CMS) support bundled payments for episodes of care. One experimental initiative will support bundled payments for clinicians providing care to patients with CAD.13 Such models have the potential to be extended to individuals who develop cancer after CAD. For example, the Medicare Access and CHIP Reauthorization Act of 2015 (MACRA) created alternative payment models,13 providing value-based care and penalties for poor quality of care. These models require risk adjustment for patients,14–16 and therefore identifying those at risk for high cost is important.
The present study examined the impact of incident cancer on CAD-related expenditures using data from a cohort of elderly fee-for-service (FFS) Medicare beneficiaries with and without cancer. The cancer cohort consisted of elderly patients with incident breast, colorectal, or prostate cancer. These cancers were selected because they have a higher prevalence among the elderly population,17 and preexisting CAD is highly prevalent in this population diagnosed with these cancers.18–23
Patients and Methods
Conceptual Framework
The conceptual framework of this study was adapted based on Andersen’s Behavioral Model of Health Service Use for understanding CAD-related healthcare expenditures and a priori selection of independent variables.24,25 This model posits that an individual’s predisposing, enabling, and need factors; personal health practices; healthcare use; and external environment may influence healthcare expenditures.26
Study Design
A retrospective observational longitudinal cohort design with 12-month preindex and postindex periods was used. Index date was defined as the date of incident cancer diagnosis for the cancer cohort and pseudo-diagnosis date for the noncancer cohort. Pseudo-diagnosis dates were randomly selected from the dates of service. Each individual was observed for 48 months (Figure 1).
Data Sources
Data were derived from claims in the SEER-Medicare linked registries, 5% noncancer random sample of Medicare beneficiaries in the SEER region (living in the same SEER areas as those in the cancer registry), American Community Survey (census tract information),27 and the Area Health Resources Files (county-level healthcare environment factors).28
Study Population
The study population comprised beneficiaries with preexisting CAD, who were further categorized into those with incident breast, colorectal, or prostate cancer and those without cancer. The cancer cohort comprised the total number of incident cases and not the random sample. CAD was identified using a validated algorithm developed by CMS29 that used ICD-9-CM codes. Individuals with at least 2 inpatient, outpatient, and carrier claims (clinician encounters only), or home healthcare agency (HHA) service Medicare claims with a primary or secondary diagnosis of CAD during the baseline were classified as preexisting CAD. Incident cancer, defined as new cancer diagnosis during the study period (January 2008 through December 2011), was identified using the ICD-O-3 codes from the SEER registries.
Other inclusion criteria were age ≥68 years, alive with continuous FFS Medicare Parts A and B enrollment during the entire study period, continuous Part D enrollment during the preindex and postindex periods, no missing information on county, and total expenditures >$0 during the preindex and postindex periods. In the cancer cohort, individuals with missing data on cancer type and stage and those diagnosed postmortem were excluded (Figure 2).
Measures
Dependent Variable: CAD-Related Expenditures
CAD-related healthcare and total expenditures consisted of Medicare payments for inpatient, HHA, and out-patient services for CAD-related care, measured every 120 days (t1, t2, t3, t4, t5, and t6). CAD-related services were identified using ICD-9-CM primary and secondary diagnosis codes for CAD.30,31 Prescription medication and durable medical equipment (DME) expenditures were not included because of the challenges in identifying CAD-related expenditures in DME and prescription drug claims. Short-term healthcare expenditures >12 months in the postindex period were examined. Healthcare expenditures were adjusted by the Consumer Price Index for medical services32 and expressed in 2012 USD.
Key Independent Variables: Sex and Cancer Type
Because the study included women with breast cancer and men with prostate cancer, the key time-invariant independent variable accounted for both sex and cancer type and was categorized into 6 mutually exclusive groups: women with breast cancer, women with colorectal cancer (CRC), women with no cancer, men with prostate cancer, men with CRC, and men with no cancer.
Other Independent Variables
Predisposing Factors
Age measured at index month of incident cancer diagnosis and race/ethnicity were time-invariant independent variables.
Enabling Factors
Medicare Part D coverage gap (measured every 120 days) and census tract–level education attainment and poverty status (based on income threshold that varied by family size and composition; measured at baseline).
Need-Based Factors
Physical health conditions were measured at baseline and categorized into concordant (cardiac arrhythmias, congestive heart failure, diabetes, hyperlipidemia, hypertension, and stroke) and discordant (dementia, asthma, chronic obstructive pulmonary disease, arthritis, hepatitis, HIV, and osteoporosis). Mental health conditions included severe mental illness (schizophrenia, bi-polar disorder, and psychoses; measured at baseline), anxiety, and depression (measured every 120 days). For CAD severity, a proxy measure, which was measured at baseline, was constructed based on the CMS hierarchical condition category (HCC) classification system, in which each of the HCC codes for CAD was assigned a specific score based on the risk and severity, ranging from 0.231 to 0.349. Higher scores represented severe manifestations of CAD.33
Personal Healthcare Practices
Tobacco and alcohol abuse34,35 were measured every 120 days.
Healthcare Use
Primary care visits, cardiologist visits, and adherence to statins or angiotensin converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers (ARBs), or β-blockers measured every 120 days. Adherence was defined as proportion of days covered (PDC), calculated among those who filled ≥2 prescriptions for either statins or any 2 prescriptions of ACEIs/ARBs/b-blockers. Individuals with PDC ≥80% were considered adherent and those with PDC <80% were considered non-adherent.36 PDC measure is recommended by the Pharmacy Quality Alliance37 and used by CMS in its rating of an insurance plan.38 Adherence was classified into 5 mutually exclusive groups (supplemental eAppendix 1, available with this article at JNCCN.org).
External Environment Factors
These time-invariant external environment factors were measured at baseline. This domain included SEER region, county metropolitan status, and percentage of cardiologists and oncologists in the county. This study also controlled for time (t1–t6) to better reflect changes associated with time in treatment practices.
Statistical Analyses
Unadjusted subgroup differences in time-invariant characteristics between cancer and noncancer categories by sex (6 groups) were tested with chi-square statistics. Our preliminary analyses indicated that there were significant group differences in age, race/ethnicity, concordant and discordant physical health conditions, mental health conditions, SEER region, and index year between the categories. Therefore, inverse probability treatment weights (IPTWs) were derived using the multinomial logistic regression on cancer and noncancer categories, with sex, age, race/ethnicity, SEER region, and index year as independent variables; these weights were used when modeling expenditures to adjust for the differences in these variables between cancer and non-cancer cohorts. The weighting enabled us to balance the differences among cancer and noncancer cohorts. Supplemental eAppendix 2 summarizes the findings from the multinomial logistic regression used to calculate IPTW.
Because CAD-related healthcare expenditures were measured every 120 days during the preindex and postindex periods, each individual had 6 observations. These observations were not independent, and therefore the authors used generalized linear mixed models (GLMMs) with gamma distribution and log-link to analyze adjusted relationships between cancer and noncancer groups and CAD-related healthcare expenditures. This is the most commonly used approach in previous cost analyses.39,40 These GLMMs included predisposing, enabling and need factors, external environmental characteristics, and time.
Results
Characteristics of the Study Cohorts Before and After IPTW Adjustment
The study cohort comprised 46,332 elderly FFS Medicare beneficiaries with preexisting CAD (12,095 with cancer and 34,237 without cancer). After adjusting with IPTW, no significant differences were seen in independent variables between cancer diagnoses (Table 1).
Table 1.
Characteristics | Before IPTW (%) for Cancer Groups | After IPTW (Weighted %) for Cancer Groups | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Breast | Colorectal (Women) | Colorectal (Men) | Prostate | None (Women) | None (Men) | Siga | Breast | Colorectal (Women) | Colorectal (Men) | Prostate | None (Women) | None (Men) | Siga | |
Age, y | *** | NS | ||||||||||||
68–70 | 13.8 | 9.2 | 14.7 | 21.4 | 13.7 | 22.4 | 17.0 | 16.6 | 16.7 | 16.5 | 16.8 | 16.9 | ||
71–74 | 19.8 | 14.5 | 23.4 | 30.5 | 17.2 | 23.8 | 20.7 | 20.8 | 20.7 | 20.6 | 20.6 | 20.6 | ||
75–79 | 26.0 | 22.2 | 25.0 | 27.8 | 21.2 | 23.4 | 22.8 | 23.5 | 23.4 | 23.0 | 23.1 | 22.9 | ||
≥80 | 40.4 | 54.1 | 36.9 | 20.3 | 47.9 | 30.4 | 39.5 | 39.2 | 39.2 | 39.9 | 39.5 | 39.6 | ||
Race/Ethnicity | *** | NS | ||||||||||||
White | 82.5 | 78.7 | 82.8 | 82.7 | 75.0 | 77.6 | 77.5 | 77.0 | 77.1 | 76.0 | 77.2 | 77.1 | ||
African American | 9.4 | 11.2 | 4.9 | 7.6 | 10.4 | 5.7 | 8.7 | 8.8 | 8.7 | 9.0 | 8.7 | 8.7 | ||
Hispanic | 2.9 | 2.3 | 2.1 | 2.6 | 4.3 | 4.0 | 3.7 | 3.6 | 4.1 | 4.2 | 3.9 | 4.0 | ||
Other | 5.2 | 7.8 | 10.2 | 7.1 | 10.3 | 12.7 | 10.0 | 10.6 | 10.0 | 10.8 | 10.2 | 10.2 | ||
Concordant PHCb | *** | NS | ||||||||||||
Yes | 95.5 | 96.4 | 95.4 | 94.6 | 94.0 | 92.4 | 93.8 | 93.4 | 94.0 | 94.3 | 93.9 | 93.9 | ||
No | 4.5 | 3.6 | 4.6 | 5.4 | 6.0 | 7.6 | 6.2 | 6.6 | 6.0 | 5.7 | 6.1 | 6.1 | ||
Discordant PHCb | *** | |||||||||||||
Yes | 48.1 | 51.4 | 37.5 | 31.7 | 50.1 | 33.9 | 43.2 | 43.9 | 43.4 | 43.9 | 43.5 | 43.8 | ||
No | 51.9 | 48.6 | 62.5 | 68.3 | 49.9 | 66.1 | 56.8 | 56.1 | 56.6 | 56.1 | 56.5 | 56.2 | ||
MHCb | *** | |||||||||||||
Yes | 13.0 | 13.1 | 8.9 | 5.7 | 15.2 | 9.3 | 12.1 | 12.6 | 12.4 | 12.6 | 12.2 | 12.6 | ||
No | 87.0 | 86.9 | 91.1 | 94.3 | 84.8 | 90.7 | 87.9 | 87.4 | 87.6 | 87.4 | 87.8 | 87.4 | ||
SEER region | *** | NS | ||||||||||||
Northeast | 24.1 | 26.3 | 24.0 | 20.0 | 22.7 | 18.9 | 21.9 | 21.6 | 21.7 | 20.1 | 21.6 | 21.7 | ||
South | 25.1 | 25.4 | 22.2 | 24.6 | 25.6 | 23.8 | 24.9 | 24.5 | 24.7 | 25.2 | 24.7 | 24.5 | ||
North-Central | 13.9 | 14.5 | 12.8 | 14.2 | 11.8 | 10.5 | 12.1 | 11.5 | 12.1 | 12.8 | 12.0 | 11.9 | ||
West | 36.9 | 33.8 | 41.0 | 41.1 | 39.9 | 46.8 | 41.1 | 42.3 | 41.5 | 41.9 | 41.6 | 41.9 | ||
Index year | ** | NS | ||||||||||||
2008 | 24.0 | 25.1 | 24.9 | 24.6 | 23.9 | 23.4 | 24.1 | 25.9 | 23.7 | 22.8 | 23.9 | 24.7 | ||
2009 | 24.5 | 23.9 | 23.8 | 25.1 | 23.8 | 24.7 | 23.8 | 23.7 | 24.9 | 23.6 | 24.2 | 24.2 | ||
2010 | 25.4 | 25.6 | 25.3 | 23.8 | 26.1 | 24.8 | 26.0 | 25.7 | 25.6 | 25.5 | 25.4 | 25.2 | ||
2011 | 26.1 | 25.3 | 25.9 | 26.5 | 26.3 | 27.1 | 26.2 | 24.7 | 25.7 | 28.1 | 26.6 | 25.9 |
Time-invariant characteristics included cancer diagnosis categories, age, race/ethnicity, poverty status, high school education, concordant and discordant physical health conditions, severe mental illness, SEER region, and county-level characteristics. Time-variant characteristics included tobacco use, alcohol use, depression, anxiety, routine follow-up with primary care physician and/or cardiologist, and donut hole.
Abbreviations: CAD, coronary artery disease; IPTW, inverse probability treatment weighting; MHC, mental health conditions; NS, nonsignificant; PHC, physical health conditions; sig, significance.
Asterisks represent significant differences in time-invariant patient-level characteristics based on chi-square tests.
Concordant physical health conditions consisted of diabetes, hyperlipidemia, hypertension, stroke, cardiac arrhythmia, and congestive heart failure. Discordant physical health conditions consisted of arthritis, asthma, chronic obstructive pulmonary disease, osteoporosis, dementia, human immunodeficiency virus, and hepatitis. Mental health conditions included anxiety, depression, severe mental illness (schizophrenia, bipolar disorder, psychoses).
P<.001
.001≤P<.01
.01≤P<05. Column percentages are reported
Expenditures for t1, t2, and t3 were aggregated to represent the preindex period, and expenditures for t4, t5, and t6 were aggregated to represent the postindex period (Table 2). CAD-related expenditures in the postindex period were approximately 3 times higher for men and women with CRC, 2 times higher for women with breast cancer, and 1.5 times higher for ment with prostate cancer. The postindex CAD-related expenditures for the noncancer group, in comparison, were similar to those in the preindex period.
Table 2.
Cancer and Noncancer Groups | Preindex | Postindex | Significancea | ||||
---|---|---|---|---|---|---|---|
Total | CAD-Related | % CAD-Relatedc | Total | CAD-Related | % CAD-Relatedc | ||
Wt Mean (SD)b | Wt Mean (SD)b | Wt Mean (SD)b | Wt Mean (SD)b | ||||
Women | |||||||
Breast | 10,493 (18,644) | 3,423 (10,504) | 32.6 | 29,596 (27,749) | 6,154 (14,419) | 20.8 | |
Colorectal | 14,504 (27,138) | 5,722 (15,071) | 39.5 | 55,895 (45,829) | 18,916 (27,102) | 33.8 | *** |
None (Ref) | 12,099 (22,579) | 4,662 (13,670) | 38.5 | 10,656 (22,379) | 4,164 (13,370) | 39.1 | |
Men | |||||||
Colorectal | 17,548 (31,452) | 8,220 (19,298) | 46.8 | 56,849 (48,323) | 23,021 (28,781) | 40.5 | *** |
Prostate | 11,089 (18,689) | 4,603 (12,063) | 41.5 | 28,040 (27,099) | 7,022 (16,316) | 25.0 | * |
None (Ref) | 13,943 (26,758) | 6,380 (16,668) | 45.8 | 11,659 (26,681) | 5,377 (15,594) | 46.1 |
Abbreviations: CAD, coronary artery disease; Wt, weighted.
Asterisks represent significant differences in cancer and noncancer categories. Significance was derived from unadjusted generalized linear model with gamma distribution and log-link. The analysis included 6 repeated observations.
All expenditures reported in 2012 USD.
Percentage .
P<.001
.001≤P<.01
.01≤P<.05.
CAD-Related Expenditures Over Time by Cancer and Noncancer Status
When time was included as an adjuster, the time coefficient was positive across all cancer groups, suggesting that CAD-related expenditures increased over time for all cancer groups (Figure 3). However, no such differences were observed for noncancer groups.
Adjusted Relationships Between Cancer and CAD-related Healthcare Expenditures
Total CAD-related expenditures are presented in Table 3 and inpatient and outpatient CAD-related expenditures are presented in Table 4. CAD-related healthcare expenditure comparisons by cancer status, sex, and cancer type are detailed as follows.
Table 3.
Cancer Diagnosis Categories | Coefficient | SE | P Value | % Changea |
---|---|---|---|---|
Cancer vs noncancer (Ref: none [women]) | ||||
Breast | 0.13 | 0.04 | .002 | 14% |
Colorectal (women) | 0.92 | 0.05 | .000 | 151% |
Intercept | 4.01 | 0.14 | ||
Cancer vs noncancer (Ref: none [men]) | ||||
Colorectal (men) | 0.97 | 0.05 | .000 | 164% |
Prostate | 0.11 | 0.04 | .008 | 12% |
Intercept | 4.25 | 0.14 | ||
Sex differences (Ref: none [men]) | ||||
None (women) | −0.24 | 0.03 | .000 | −21% |
Intercept | 4.25 | 0.14 | ||
Sex differences (Ref: colorectal [men]) | ||||
Colorectal (women) | −0.29 | 0.07 | .000 | −25% |
Intercept | 5.22 | 0.15 | ||
Cancer type differences (Ref: breast) | ||||
Colorectal (women) | 0.79 | 0.06 | .000 | 55% |
Intercept | 4.93 | 0.15 | ||
Cancer type differences (Ref: prostate) | ||||
Colorectal (men) | 0.85 | 0.06 | .000 | 57% |
Intercept | 5.22 | 0.15 |
Abbreviations: CAD, coronary artery disease; GLMMs, generalized linear mixed models.
Percent change for GLMMs was calculated as (e(intercept + β) – eintercept)/eintercept.
Table 4.
Cancer Diagnosis Categories | Inpatient CAD-Related Expenditures | Outpatient CAD-Related Expenditures | ||||||
---|---|---|---|---|---|---|---|---|
Coefficient | SE | P Value | % Changea | Coefficient | SE | P Value | % Changea | |
Cancer vs noncancer (Ref: none [women]) | ||||||||
Breast | 0.11 | 0.08 | .15 | 12% | 0.43 | 0.04 | .000 | 54% |
Colorectal (women) | 1.22 | 0.08 | .000 | 239% | 0.39 | 0.05 | .000 | 48% |
Intercept | 2.36 | 0.20 | 3.13 | 0.12 | ||||
Cancer vs noncancer (Ref: none [men]) | ||||||||
Colorectal (men) | 1.25 | 0.08 | .000 | 249% | 0.41 | 0.06 | .000 | 51% |
Prostate | 0.10 | 0.07 | .152 | 11% | 0.27 | 0.04 | .000 | 31% |
Intercept | 2.71 | 0.20 | 3.47 | 0.11 | ||||
Sex differences (Ref: none [men]) | ||||||||
None (women) | −0.35 | 0.06 | .000 | −30% | −0.35 | 0.03 | .000 | −30% |
Intercept | 2.71 | 0.20 | 3.47 | 0.11 | ||||
Sex differences (Ref: colorectal [men]) | ||||||||
Colorectal (women) | −0.38 | 0.10 | .000 | −32% | −0.37 | 0.07 | .000 | −31% |
Intercept | 3.96 | 0.21 | 3.89 | 0.13 | ||||
Cancer type differences (Ref: breast) | ||||||||
Colorectal (women) | 1.11 | 0.1 | .000 | 67% | −0.04 | 0.06 | .522 | −4% |
Intercept | 3.58 | 0.21 | 3.52 | 0.13 | ||||
Cancer type differences (Ref: prostate) | ||||||||
Colorectal (men) | 1.14 | 0.09 | .000 | 68% | 0.14 | 0.09 | .056 | 13% |
Intercept | 3.96 | 0.21 | 3.89 | 0.13 |
Abbreviations: CAD, coronary artery disease; GLMMs, generalized linear mixed models.
Percent change for GLMM was calculated as (e(intercept + β) – eintercept)/eintercept.
Cancer Versus No Cancer
Patients with breast, colorectal, or prostate cancer had higher outpatient and total CAD-related expenditures compared with their noncancer counterparts. Inpatient expenditures were significantly higher for CRC, but not for breast or prostate cancer, compared with their noncancer counterparts.
Men Versus Women
Women with CRC or no cancer had lower total inpatient, outpatient, and CAD-related expenditures compared with men with CRC or no cancer, respectively.
Cancer Type
Both men and women with CRC had higher inpatient and total CAD-related expenditures compared with men with prostate cancer and women with breast cancer, respectively.
Relationship Between Other Independent Variables and Expenditures
Factors associated with significantly increased expenditures included age ≥80 years, concordant and discordant physical health conditions, mental health conditions, higher CAD severity, tobacco use, alcohol use, visit to primary care physician or cardiologist, and nonadherence to one or both medication classes (for those using both medication classes; supplemental eAppendix 1).
Discussion
This is the first study to estimate short-term CAD-related expenditures among cancer and noncancer FFS Medicare beneficiaries with preexisting CAD. In general, CAD accounted for a substantial portion of total expenditures before and after cancer diagnosis, and these expenditures were higher for those with cancer compared with those without. The authors speculate that part of the CAD-related expenditures among patients with cancer may result from cancer treatments.7,8 For patients undergoing cancer surgery, CAD may need to be stabilized using medical management,7 further adding to their overall CAD-related expenditures. Moreover, it is plausible that cancer may take precedence over CAD management and impede the recommended care for CAD, thereby increasing CAD-related complications9 and leading to higher CAD-related expenditures.
Notably, CAD-related expenditures were highest among patients with CRC compared with those with breast, prostate, or no cancer. Furthermore, CAD-related expenditures were highest during the 120-day interval immediately after CRC diagnosis. Most patients in our study had advanced-stage CRC (63.0%), treatment of which consists of surgery and adjuvant chemotherapy (eg, 5-fluorouracil and capecitabine).41 This suggests that CAD-related expenditures may be higher among those with CRC due to chemotherapy-related cardiotoxicity. Additionally, nonadherence to statins and ACEIs/ARBs/β-blockers was significantly higher in patients with CRC who had undergone surgery (81%). Nonadherence to these medications may increase the risk of CAD-related complications and hospitalizations, thereby increasing inpatient expenditures.42
Another noteworthy finding was that women had lower CAD-related expenditures compared with men. Chiha et al43 assessed the differences in CAD severity among men and women and noted that women were more likely to have normal coronary arteries or less severe disease than age-matched men. Although we controlled for severity of CAD with HCC, future research needs to explore whether the lower expenditures among women are because of sex-related differences in severity of CAD.
Finally, CAD-related expenditures increased over time for all cancer groups. Our findings indicated that expenditures were highest during the 120-day interval immediately after cancer diagnosis, suggesting that the period after cancer diagnosis may be crucial for CAD management.
Policy Implications
New bundled payment models and the Medicare Shared Savings Program use risk adjustment to calculate expenditure benchmarks needed to provide care and obtain shared savings from the CMS.13,44 These value-based frameworks have been designed to improve the quality and affordability of care. These frameworks aim to ensure that the cost of overall care, including treatment, interventions, and prescriptions, reflect the benefits for better quality of life. There are few notable value frameworks in oncology that account for each stake-holder’s perspective. Collectively, our findings can help payers calculate these benchmark expenditures by adjusting for case mix of Medicare beneficiaries, specifically those with preexisting CAD and incident cancer.14–16 In addition, our findings can help capture the episode-specific contribution of individual risk factors (eg, age, sex, comorbidities, episode severity) to resource use, similar to risk models implemented by the PROMETHEUS Payment model.16,45 PROMETHEUS is a bundled payment model that uses algorithms to create episodes with relevant services. It helps determine appropriate reimbursement rates for payment for multiple medical conditions and procedures in an episode-of-care system. Currently, no specific payment models account for cancer and CAD, but available models such as PROMETHEUS can be tailored to specific patterns of resource use within CAD. Therefore, it is crucial to understand the extent to which a specific cancer contributes to CAD-related expenditures to implement these models. Based on our study findings, it is apparent that resource allocation for CAD-related expenditures should be higher for patients with CRC, followed by prostate and breast cancer.
The authors also found that CAD-related inpatient expenditures accounted for two-thirds of the overall CAD-related healthcare expenditures. Heart failure as a comorbidity can greatly diminish the patient’s quality of life, limit the therapeutic dose of anticancer treatment, and significantly affect the patient’s use of healthcare services, with frequent hospital readmissions. Although CMS has imposed penalties for potential hospital readmissions and preventable hospitalizations, such as inpatient admissions for angina without procedures,46 these may not be effective in patients with complex conditions such as CAD and cancer. In this context, future research needs to focus on collaborative care models, such as the patient-centered medical home, because such models have been shown to reduce inpatient use.47,48
Strengths and Limitations
This study adopted a longitudinal design and compared expenditures over time between cancer and noncancer groups. We also used statistical adjustment for selection bias in observed and unobservable characteristics. Use of Medicare FFS claims data enabled us to track individuals across various providers and settings, and calculate expenditures and measure variables for specific periods. The study also adjusted for a comprehensive list of factors that can influence CAD-related expenditures and included individuals with significant medical comorbidities.
Our findings cannot be generalized to all Medicare beneficiaries, because the study population is restricted to those residing in SEER regions and those with FFS Medicare plans. Furthermore, SEER-Medicare data are not developed for research purposes, and therefore have limitations associated with their use for estimating healthcare expenditures. There might be underestimation of CAD-related diagnosis, which in turn may undermine CAD-related expenditures for several reasons. It is possible that CAD diagnosis may be undercoded or misclassified in claims data, because these data are dependent on professional ICD coding. Furthermore, 1 year of follow-up may not be long enough to assess advanced-stage incident cancer, which might influence the link between increased spending and incidence cases. In addition, SEER-Medicare data do not capture all procedures performed. The overall cost burden of CAD in incident cancer cases might be an underestimate as a result of not including end-of-life care and broader expenditures, such as out-of-pocket costs or productivity issues. Finally, we were not able to control for family history, patient-level lifestyle health behaviors, knowledge, attitude, and preferences, or number of cancer-related complications, treatment-related adverse effects, and cost-related factors that may affect CAD-related expenditures.
Conclusions
Our findings showed that incident cancer diagnosis was associated with higher short-term CAD-related expenditures compared with patients without cancer. Specifically, inpatient expenditures for patients with CRC were considerably higher than outpatient expenditures, suggesting the need for greater emphasis on preventing cardiac events in the outpatient setting to reduce more expensive inpatient encounters. Future studies are needed to explore whether the emerging payment reforms and collaborative care models can lower costs while maintaining high-quality CAD care for patients with and without cancer.
Supplementary Material
Acknowledgments
Disclaimer: Research reported in this publication was supported by the National Institute of General Medical Sciences of the NIH (U54GM104942). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Footnotes
Disclosures: The authors have not received any financial consideration from any person or organization to support the preparation, analysis, results, or discussion of this article.
References
- 1.Dieleman JL, Baral R, Birger M, et al. US spending on personal health care and public health, 1996–2013. JAMA 2016;316:2627–2646. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Druss BG, Marcus SC, Olfson M, et al. Comparing the national economic burden of five chronic conditions. Health Aff (Millwood) 2001; 20:233–241. [DOI] [PubMed] [Google Scholar]
- 3.Tarride JE, Lim M, DesMeules M, et al. A review of the cost of cardiovascular disease. Can J Cardiol 2009;25:e195–202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Gerteis J, Izrael D, Deitz D, et al. Multiple chronic conditions chartbook: 2010 medical expenditure panel survey data Rockville, MD: Agency for Healthcare Research and Quality: 2014. [Google Scholar]
- 5.Fillenbaum GG, Pieper CF, Cohen HJ, et al. Comorbidity of five chronic health conditions in elderly community residents: determinants and impact on mortality. J Gerontol A Biol Sci Med Sci 2000;55:M84–89. [DOI] [PubMed] [Google Scholar]
- 6.Koene RJ, Prizment AE, Blaes A, et al. Shared risk factors in cardiovascular disease and cancer. Circulation 2016;133:1104–1114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Krone RJ. Managing coronary artery disease in the cancer patient. Prog Cardiovasc Dis 2010;53:149–156. [DOI] [PubMed] [Google Scholar]
- 8.Herrmann J, Lerman A, Sandhu NP, et al. Evaluation and management of patients with heart disease and cancer: cardio-oncology. Mayo Clin Proc 2014;89:1287–1306. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Piette JD, Kerr EA. The impact of comorbid chronic conditions on diabetes care. Diabetes Care 2006;29:725–731. [DOI] [PubMed] [Google Scholar]
- 10.Nichols GA, Bell TJ, Pedula KL, et al. Medical care costs among patients with established cardiovascular disease. Am J Manag Care 2010;16:e86–93. [PubMed] [Google Scholar]
- 11.Distribution of Medicare Beneficiaries by Eligibility Category. Henry J Kaiser Family Foundation website; Available at: http://kff.org/medicare/state-indicator/distribution-of-medicare-beneficiaries-by-eligibility-category-2/. Accessed May 27, 2016. [Google Scholar]
- 12.Wakim R, Ritchey M, Hockenberry J, et al. Geographic variations in incremental costs of heart disease among Medicare beneficiaries, by type of service, 2012. Prev Chronic Dis 2016;13:E180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Episode Payment Models: General Information. Centers for Medicare & Medicaid Services website Available at: https://innovation.cms.gov/initiatives/epm. Accessed January 20, 2017.
- 14.A Framework for Alternative Payment Models. Center for Health-care Quality & Payment Reform website Available at: http://www.chqpr.org/. Accessed January 8, 2017.
- 15.CMS’ Value-Based Programs Available at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Value-Based-Programs/Value-Based-Programs.html. Accessed January 6, 2017.
- 16.O’Byrne TJ, Shah ND, Wood D, et al. Episode-based payment: evaluating the impact on chronic conditions. Medicare Medicaid Res Rev 2013;3:pii: mmrr.003.03.a07. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Cancer Stat Facts. National Cancer Institute. Surveillance, Epidemiology, and End Results Program website Available at: http://seer.cancer.gov/statfacts. Accessed March 18, 2016.
- 18.Doyle JJ, Neugut AI, Jacobson JS, et al. Radiation therapy, cardiac risk factors, and cardiac toxicity in early-stage breast cancer patients. Int J Radiat Oncol Biol Phys 2007;68:82–93. [DOI] [PubMed] [Google Scholar]
- 19.Gross CP, McAvay GJ, Guo Z, et al. The impact of chronic illnesses on the use and effectiveness of adjuvant chemotherapy for colon cancer. Cancer 2007;109:2410–2419. [DOI] [PubMed] [Google Scholar]
- 20.Hall HI, Satariano WA, Thompson T, et al. Initial treatment for prostate carcinoma in relation to comorbidity and symptoms. Cancer 2002;95:2308–2315. [DOI] [PubMed] [Google Scholar]
- 21.Jagsi R, Griffith KA, Koelling T, et al. Stroke rates and risk factors in patients treated with radiation therapy for early-stage breast cancer. J Clin Oncol 2006;24:2779–2785. [DOI] [PubMed] [Google Scholar]
- 22.Otto SJ, Schro¨ der FH, de Koning HJ. Risk of cardiovascular mortality in prostate cancer patients in the Rotterdam randomized screening trial. J Clin Oncol 2006;24:4184–4189. [DOI] [PubMed] [Google Scholar]
- 23.Al-Kindi SG, Oliveira GH. Prevalence of preexisting cardiovascular disease in patients with different types of cancer: the unmet need for onco-cardiology. Mayo Clin Proc 2016;91:81–83. [DOI] [PubMed] [Google Scholar]
- 24.Andersen RM. Revisiting the behavioral model and access to medical care: does it matter? J Health Soc Behav 1995;36:1–10. [PubMed] [Google Scholar]
- 25.Andersen R, Newman JF. Societal and individual determinants of medical care utilization in the United States. Milbank Mem Fund Q Health Soc 1973;51:95–124. [PubMed] [Google Scholar]
- 26.Engels EA, Pfeiffer RM, Ricker W, et al. Use of Surveillance, Epidemiology, and End Results-Medicare data to conduct case-control studies of cancer among the US elderly. Am J Epidemiol 2011;174:860–870. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.American Community Survey. Summary File Data. United States Census Bureau website Available at: https://www.census.gov/programs-surveys/acs/data/summary-file.html. Accessed March 30, 2016.
- 28.Area Health Resource Files (AHRF). Data.HRSA.gov website Available at: https://data.hrsa.gov/topics/health-workforce/ahrf. Accessed March 2, 2016.
- 29.Condition Categories. Chronic Conditions Data Warehouse website Available at: https://www.ccwdata.org/web/guest/condition-categories. Accessed May 18, 2016.
- 30.Whellan DJ, Greiner MA, Schulman KA, et al. Costs of inpatient care among Medicare beneficiaries with heart failure, 2001 to 2004. Circ Cardiovasc Qual Outcomes 2010;3:33–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Hall AE, Highfill T. Calculating Disease-Based Medical Care Expenditure Indexes for Medicare Beneficiaries: a Comparison of Method and Data Choices Available at: http://www.nber.org/papers/w19720. Accessed June 17, 2016.
- 32.Consumer Price Index. Bureau of Labor Statistics website Available at: https://www.bls.gov/cpi/. Accessed January 24, 2017.
- 33.Pope GC, Kautter J, Ingber MJ, et al. Evaluation of the CMS-HCC Risk Adjustment Model: Final Report Available at: https://www.cms.gov/Medicare/Health-Plans/MedicareAdvtgSpecRateStats/downloads/Evaluation_Risk_Adj_Model_2011.pdf. Accessed December 2, 2018.
- 34.Huxley RR, Woodward M. Cigarette smoking as a risk factor for coronary heart disease in women compared with men: a systematic review and meta-analysis of prospective cohort studies. Lancet 2011;378:1297–1305. [DOI] [PubMed] [Google Scholar]
- 35.Djoussé L, Gaziano JM. Alcohol consumption and heart failure: a systematic review. Curr Atheroscler Rep 2008;10:117–120. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Choudhry NK, Shrank WH, Levin RL, et al. Measuring concurrent adherence to multiple related medications. Am J Manag Care 2009; 15:457–464. [PMC free article] [PubMed] [Google Scholar]
- 37.Nau DP. Proportion of Days Covered (PDC) as a Preferred Method of Measuring Medication Adherence Available at: https://sep.yimg.com/ty/cdn/epill/pdcmpr.pdf?t51544201383&. Accessed March 20, 2016.
- 38.Medicare 2016 Part C & D Star Rating Technical Notes: First Plan Preview Available at: https://www.cms.gov/Medicare/Prescription-Drug-Coverage/PrescriptionDrugCovGenIn/Downloads/2016-Technical-Notes-Preview-1-v2015_08_05.pdf. Accessed October 17, 2016.
- 39.Pagano E, Petrelli A, Picariello R, et al. Is the choice of the statistical model relevant in the cost estimation of patients with chronic diseases? An empirical approach by the Piedmont Diabetes Registry. BMC Health Serv Res 2015;15:582. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Mihaylova B, Briggs A, O’Hagan A, et al. Review of statistical methods for analysing healthcare resources and costs. Health Econ 2011;20: 897–916. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Floyd J, Morgan JP. Cardiotoxicity of Nonanthracycline Cancer Chemotherapy Agents Available at: https://www.uptodate.com/contents/cardiotoxicity-of-nonanthracycline-cancer-chemotherapy-agents?search=cardiotoxicity-of-nonanthracycline-cancer-chemotherapy-agent&source=search_result&selectedTitle=1~150&usage_type=default&display_rank=1. Accessed December 30, 2015.
- 42.Bitton A, Choudhry NK, Matlin OS, et al. The impact of medication adherence on coronary artery disease costs and outcomes: a systematic review. Am J Med 2013;126:357.e7–357.e27. [DOI] [PubMed] [Google Scholar]
- 43.Chiha J, Mitchell P, Gopinath B, et al. Gender differences in the severity and extent of coronary artery disease. Int J Cardiol Heart Vasc 2015;8:161–166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Shared Savings Program. CMS.gov Available at: https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/sharedsavingsprogram/index.html?redirect5/SharedSavingsProgram/. Accessed February 4, 2017.
- 45.Hussey PS, Ridgely MS, Rosenthal MB. The PROMETHEUS bundled payment experiment: slow start shows problems in implementing new payment models. Health Aff (Millwood) 2011;30:2116–2124. [DOI] [PubMed] [Google Scholar]
- 46.Hospital Readmissions Reduction Program (HRRP). CMS.gov Available at: https://www.cms.gov/medicare/medicare-fee-for-service-payment/acuteinpatientpps/readmissions-reduction-program.html. Accessed February 4, 2017.
- 47.Maeng DD, Khan N, Tomcavage J, et al. Reduced acute inpatient care was largest savings component of Geisinger Health System’s patient-centered medical home. Health Aff (Millwood) 2015;34:636–644. [DOI] [PubMed] [Google Scholar]
- 48.Neilsen M, Beult L, Patel K, Nichols LM. The patient-centered medical home’s impact on cost and quality Available at: https://www.pcpcc.org/sites/default/files/resources/The%20Patient-Centered%20Medical%20Home%27s%20Impact%20on%20Cost%20and%20Quality%2C%20Annual%20Review%20of%20Evidence%2C%202014-2015.pdf. Accessed February 4, 2017.
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.