Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2017 Feb 22.
Published in final edited form as: Cancer Epidemiol. 2016 Jul 7;43:63–69. doi: 10.1016/j.canep.2016.06.011

Racial and Socio-Economic Disparities in Breast Cancer Hospitalization Outcomes by Insurance Status

Tomi Akinyemiju 1,2,*, Swati Sakhuja 1, Neomi Vin Raviv 3,4
PMCID: PMC5321053  NIHMSID: NIHMS851332  PMID: 27394678

Abstract

Background

Breast cancer remains a major cause of morbidity and mortality among women in the US, and despite numerous studies documenting racial disparities in outcomes, the survival difference between Black and White women diagnosed with breast cancer continues to widen. Few studies have assessed whether observed racial disparities in outcomes vary by insurance type e.g. Medicare/Medicaid versus private insurance. Differences in coverage, availability of networked physicians, or cost-sharing policies may influence choice of treatment and treatment outcomes, even after patients have been hospitalized, effects of which may be differential by race.

Purpose

The aim of this analysis was to examine hospitalization outcomes among patients with a primary diagnosis of breast cancer and assess whether differences in outcome exist by insurance status after adjusting for age, race/ethnicity and socio-economic status.

Methods

We obtained data on over 67,000 breast cancer patients with a primary diagnosis of breast cancer for this cross-sectional study from the 2007-2011 Healthcare Cost and Utilization project Nationwide Inpatient Sample (HCUP-NIS), and examined breast cancer surgery type (mastectomy vs. breast conserving surgery or BCS), post-surgical complications and in-hospital mortality. Multivariable regression models were used to compute estimates, odds ratios and 95% confidence intervals.

Results

Black patients were less likely to receive mastectomies compared with White women (OR: 0.80, 95% CI: 0.71 - 0.90), regardless of whether they had Medicare/Medicaid or Private insurance. Black patients were also more likely to experience post-surgical complications (OR: 1.41, 95% CI: 1.12-1.78) and higher in-hospital mortality (OR: 1.57, 95%: 1.21-2.03) compared with White patients, associations that were strongest among women with Private insurance. Women residing outside of large metropolitan areas were significantly more likely to receive mastectomies (OR: 1.89, 95% CI: 1.54-2.31) and experience higher in-hospital mortality (OR: 1.74, 95% CI: 1.40-2.16) compared with those in metropolitan areas, regardless of insurance type.

Conclusion

Among hospitalized patients with breast cancer, racial differences in hospitalization outcomes existed and worse outcomes were observed among Black women with private insurance. Future studies are needed to determine factors associated with poor outcomes in this group of women, as well as to examine contributors to low BCS adoption in non-metropolitan areas.

Keywords: Race/Ethnicity, Socio-Economic Status, Insurance type, mortality, post-surgical complications

INTRODUCTION

Breast cancer is a leading cause of loss of more potential life years in women under 65 years of age compared to any other non-traumatic condition in the U.S [1]. Even though it is the most commonly diagnosed cancer among both Black and White women in the United States [2], significant racial disparities are evident both in breast cancer incidence and mortality [3], as well as in receipt of adequate treatment and outcomes [4-9]. Black women continue to experience significantly lower five-year survival rates despite decades of research in this area [10-12], and while numerous reasons have been presented to account for survival disparity, the root cause of the disparity and potential strategies to eliminate them remain elusive. Racial differences in breast cancer outcomes have been attributed to racial differences in access to and utilization of high-quality screening and treatment [10, 11, 13], primary risk factors such as breastfeeding and obesity that are differentially distributed by race [12-15], socioeconomic status [14, 16-20], and biological differences such as tumor aggressiveness [21, 22].

Differences in healthcare outcomes based on access to healthcare have been a subject of considerable debate in the United States. According to the Centers for Disease control, approximately 36 million people in the United States do not have health insurance, leading to either significant delay or lack of necessary medical care due to significant out of pocket costs [23]. Ayanian et al. showed that women who did not have private insurance, most often obtained through an employer, were more likely to experience adverse outcomes of breast cancer [1]. A few other studies demonstrated treatment differences based on type of insurance; for instance, women with private insurance were more likely to undergo breast conserving surgery compared with those who were uninsured or had Medicaid or Medicare insurance [24-26]. Furthermore, mastectomy rates have also been shown to vary by insurance payer status, with patients on Medicaid insurance more likely to receive mastectomy [27]. National guidelines for breast cancer treatment in the US recommends breast conservation therapy plus radiation in lieu of mastectomy as the preferable treatment option for most women with early stage breast cancer [25]. However, since both treatment modalities are associated with similar survival rates, the decision to have BCS versus mastectomy is likely based on issues of cost as well as individual and physician preference.

Although the influence of insurance status and type of insurance on treatment options have been extensively studied [25, 28], it is still not clear whether differences exist in terms of hospitalization outcomes based on insurance type. These differences may be driven by policy-specific differences in allowable procedures, hospital length of stay before discharge, or it may be due to demographic-related differences since patients with private insurance through an employer tend to be younger, healthier and of higher SES compared with patients on Medicare or Medicaid [29]. The aim of this analysis was to examine hospitalization outcomes among patients with a primary diagnosis of breast cancer and assess whether differences in outcome exist by insurance status after adjusting for age, race/ethnicity and socio-economic status.

METHODS

Study Design And Data Source

We obtained data for this cross-sectional study from the Healthcare Cost and Utilization project Nationwide Inpatient Sample (HCUP-NIS). The HCUPNIS discharge database includes administrative claims on hospital inpatient stays representing a 20% of stratified sample of hospitals in the United States, including public hospitals and academic medical centers [1]. This dataset is widely considered the most valid and reliable source of epidemiological data on inpatient care and outcomes in the US. Currently, HCUP covers about 1000 US hospitals with data on over seven million hospital stays. The dataset includes claims on all diagnoses and procedures performed during admission, captured with ICD-9 codes, and also includes non-clinical variables assessed upon admission such as race/ethnicity, residential region, and median household income in the patient’s zip code. Further details about NIS can be obtained from: http://www.hcupus.ahrq.gov/nisoverview.jsp.

Clinical Variables

We used the International Classification of Diseases, 9th Revision or the ICD-9 diagnostic and primary procedure codes to identify patients admitted with a primary diagnosis of breast cancer for this analysis. As cancer stage data is not captured in the dataset, a proxy breast cancer stage variable was created using the clinical criteria of disease staging. Patients with breast cancer were assigned into metastatic stage when ICD-9 code indicated metastatic disease to other organs (196.0), non-metastatic stage when those codes were absent, and in-situ stage was defined using ICD-9 code 2330. Multiple previous studies have used similar staging criteria using the HCUP-NIS database [30]. To determine the presence of other comorbid conditions among patients, a modified Deyo Comorbidity Index was created using ICD-9 codes to identify major comorbid conditions including: congestive heart failure, chronic pulmonary disease, cerebrovascular disease, diabetes mellitus with or without chronic complications, dementia, myocardial infarctions, rheumatic disease, peripheral vascular disease, mild, moderate or severe liver disease, peptic ulcer disease, renal disease, hemiplegia or paraplegia, and HIV/AIDS. The presence of each condition within each patient was identified and summed up to get a single comorbidity score per patient. The modified Deyo Comorbidity Index was previously used in several studies utilizing the HCUP-NIS database [2-4].

Other Covariates

Our main predictor for this analysis was race/ethnicity (categorized into: White, Black, Hispanic and Other) and area-level income (based on median household income at the zip-code level, divided into quartiles ranging from lowest income zip-code to the highest income zip-code). The aim of this analysis was to determine whether racial and socio-economic disparities in breast cancer hospitalization outcomes differed by insurance status. We defined insurance status using the HCUP insurance variable [1], classified as: Medicaid/Medicare, private (this includes private commercial carriers, Health Maintenance Organizations or HMOs and Preferred Provider Organizations or PPOs) and others (includes self-insured and Worker’s Compensation, Title V, and other government programs). We adjusted for a priori specified confounders, including age at admission and residential region. Residential region was based on the 2003 version of the Urban Influence Codes [5], and categorized into: large metropolitan areas with 1 million residents or more), small metropolitan areas (metropolitan areas with less than 1 million residents), micropolitan areas (non-metropolitan areas adjacent to metropolitan areas) and non-metropolitan or micropolitan areas (noncore areas with or without its own town).

Outcome Variable

We focused on three sets of breast cancer hospitalization outcomes in our analysis: first, receipt of surgery (Mastectomy vs Breast conserving surgery or BCS) among patients with a primary diagnosis of breast cancer; second, post-surgical complications among breast cancer patients who received surgery; and third, in-hospital mortality among all women with a primary diagnosis of breast cancer. To address these questions, we created two analytic datasets; the full dataset with all women diagnosed with breast cancer, and a restricted dataset with only patients who received breast cancer surgery. Receipt of surgery was defined based on ICD-9 diagnosis and procedure codes for mastectomy (ICD-9 codes 85.41-85.48), and BCS (ICD-9 codes 85.21, 85.22, 85.23). In-hospital mortality was based on deaths occurring during hospitalization. The presence of post-surgical complications was determined by using ICD-9 codes to identify infections, mechanical wounds, pulmonary, gastrointestinal, urinary cardiovascular and intra-operative complications. HCUP-NIS does not contain information on patient outcomes such as mortality or complications after discharge and so those outcomes were not included in our analysis.

Statistical Analysis

Descriptive statistics was used to examine the differences between baseline study characteristics including race/ethnicity and residential income, stratified by insurance status using chi-square for categorical variables and ANOVA for continuous variables. The association between race/ethnicity and residential income on each study outcome (1. receipt of surgery, 2. post-surgical complications, and 3. In-hospital mortality) stratified by insurance status and adjusted for stage of presentation, residential region, age, and comorbidities was analyzed using multivariable logistic regression analysis. The models examining receipt of the surgery and post-surgical complication outcomes was based on the restricted dataset containing only breast cancer patients who received mastectomy or BCS. All analysis was conducted using SAS 9.4 (Cary, NC).

RESULTS

There were 67,084 women ages 40 years and older who were hospitalized with a primary diagnosis of breast cancer between 2007 and 2011. Of these, 34,653 (51.7%) received mastectomy and 2,762 (4.12%) received BCS as a treatment for breast cancer, and 1,206 (1.8%) died during hospitalization (Table 1). About 48.1% of women had Medicare or Medicaid insurance, 47.6% had a private insurance, and the remaining 4.3% were classified as having any other type of insurance-these include self-insured, Veteran’s Affairs or other types of insurance coverage. Patients with Medicaid/Medicare (mean age: 69.8 years) were older at the time of admission compared to those with Private (mean age: 54.2 years) or other (mean age: 56.1 years) insurance. About 50.4% of patients with metastatic disease were covered under Medicare/Medicaid, compared with 44.1% with Private insurance Patients with Private insurance had had significantly lower average number of comorbidities (0.13) compared with those on Medicare/Medicaid (0.34) and Other (0.16) insurance types (p-value <0.0001), while patients on Medicare/Medicaid were more likely to experience in-hospital mortality (p-value <.0001). About 46% of women with private insurance received mastectomies, compared with 50% of those with Medicaid/Medicare, while 54.34% of women with private insurance had BCS treatment, compared with 40.33% of those with Medicaid/Medicare (p-value < 0.0001). White patients were more likely to have Private health insurance (49.3%) relative to other types of health insurance, while most of the Black (53.2%) and Hispanic (50%) patients had Medicaid/Medicare insurance. Women with Private insurance were mostly from large metropolitan areas as compared with those having other types of health insurance (50.81% with Private, 44.6% with Medicare/ Medicaid and 4.6% with other). About 60% of patients with Medicaid/ Medicare insurance resided in low area-level income areas, compared to 34% of patients with private insurance and 5.8% of patients with Other insurance types.

Table 1.

Baseline characteristics by insurance among hospitalized breast cancer patients, Nationwide Inpatient Sample, 2007-2011

Insurance Status N(%)

Allβ
67084
Medicare/Medicaid
32262(48.09)
Private
31923(47.59)
Other
2899(4.32)
p-
value*

Race <.0001
 White 48978 (73.01) 23285(47.54) 24143 (49.29) 1550 (3.16)
 Blacks 8617 (12.85) 4585(53.21) 3440 (39.92) 592 (6.87)
 Hispanic 5132 (7.65) 2566(50.00) 2047 (39.89) 519 (10.11)
 Other 4357 (6.49) 1826(41.91) 2293 (52.63) 238 (5.46)
Area-level Income <.0001
 Q4-Highest 20185 (30.09) 7351 (36.42) 12253 (60.70) 581 (2.88)
 Q3 16043 (23.91) 7369(45.93) 8006 (49.90) 668 (4.16)
 Q2 15313 (22.83) 8183(53.44) 6376 (41.64) 754 (4.92)
 Q1-Lowest 15543 (23.17) 9359(60.21) 5288 (34.02) 896 (5.76)
Region <.0001
 Large metro 40017(59.65) 17852(44.61) 20332(50.81) 1833(4.58)
 Small metro 16741(24.96) 8459(50.53) 7662(45.77) 620(3.70)
 Micropolitan 6160(9.18) 3424(55.58) 2476(40.19) 260(4.22)
 Not metro or micro 4166(6.21) 2527(60.66) 1453(34.88) 186(4.46)
Disease stage <.0001
 Non-metastatic 46866(69.86) 22081(47.12) 23006(49.09) 1779(3.80)
 Metastatic 20218(30.14) 10181(31.56) 8917(44.10) 1120(5.54)
Mastectomy <.0001
 No 32431 (48.34) 14901(45.95) 15918(49.08) 1612(4.97)
 Yes 34653 (51.66) 17361(50.10) 16005(46.19) 1287(3.71)
Breast Conserving <.0001
 No 64322 (95.88) 30761(47.82) 30809(47.90) 2752(4.28)
 Yes 2762 (4.12) 1501(54.34) 1114(40.33) 147(5.32)
Died During
Hospitalization
<.0001
 No 65878 (98.20) 31740(48.18) 31405(47.67) 2733(4.15)
 Yes 1206(1.80) 522(43.28) 518(42.95) 166(13.76)
Complications 0.2872
 0 64196 (95.69) 30829(48.02) 30585(47.64) 2782(4.33)
 1 2689 (4.01) 1336(49.68) 1248(46.41) 105(3.90)
 >=2 199 (0.30) 97(48.74) 90(45.23) 12(6.03)
Age at admission-years 61.76(13.00) 69.79(11.96) 54.16(8.69) 56.14(10.31) <.0001
Number of
Comorbidities
0.23(0.52) 0.34(0.62) 0.13(0.38) 0.16(0.44) <.0001

Mean (Standard Deviation)

*

Estimated using ANOVA or Chi-square test

β

Column percentage

Row percentage

Racial and socio-economic differences in the receipt of mastectomy compared with BCS was evaluated, overall and stratified by insurance status among patients who received surgery (Table 2). After adjusting for age, number of comorbidities, stage of presentation, and residential region, the odds of receiving mastectomy compared to BCS was significantly lower among Black (OR: 0.80, 95% CI: 0.71 – 0.90) and Hispanic (OR: 0.77, 95% CI: 0.67 – 0.88) patients in the entire sample compared with White patients, with similar findings for patients on Medicaid/Medicare (Black OR=0.82, 95% CI: 0.70 - 0.97; Hispanics OR=0.78, 95% CI: 0.64-0.95). However, among patients with Private insurance, only Black patients still had lower odds of receiving mastectomies compared with White patients (OR: 0.80, 95% CI: 0.66 – 0.97). In addition, the odds of mastectomy compared to BCS were lower among patients in lower area-level income in the entire sample (OR: 0.86, 95% CI: 0.77 – 0.97), and among patients with Private insurance (OR=0.82, 95% CI: 0.69-0.98) compared with patients in highest area-level income areas. Residing outside of large metropolitan areas significantly increased the odds of receiving mastectomies in the overall sample and especially among patients on Medicare/Medicaid (OR=1.90, 95%CI: 1.48-2.44) and Other (OR: 3.84, 95% CI: 1.16 – 12.64) insurance. Finally, women with higher number of comorbidities had significantly lower odds of mastectomy compared to BCS in the total sample and all insurance types except Other, although the association was non-significant in this group.

Table 2.

Multivariable adjusted odds ratios for mastectomy vs. BCS stratified by insurance Status among surgically treated breast cancer patients, Nationwide Inpatient Sample, 2007-2011.

All Medicaid/Medicare Private Other

n AOR(95%CI) α n AOR(95%CI) α n AOR(95%CI) α n AOR(95%CI) α

Race/Ethnicity
 White 27350 Ref 13809 Ref 12814 Ref 727 Ref
 Black 4651 0.80(0.71- 0.90) 2493 0.82(0.70-0.97) 1889 0.80(0.66-0.97) 269 0.76(0.47-1.25)
 Hispanic 2873 0.77(0.67- 0.88) 1451 0.78(0.64-0.95) 1127 0.88(0.69-1.12) 295 0.66(0.42-1.05)
 Other 2541 0.86(0.74- 1.00) 1109 0.91(0.73-1.14) 1289 0.87(0.70-1.10) 143 0.60(0.34-1.06)
Area-level Income
 Q4-Highest 10975 Ref 4204 Ref 6490 Ref 281 Ref
 Q3 8831 0.97(0.87- 1.08) 4215 1.07(0.91-1.25) 4299 0.95(0.81-1.12) 317 0.59(0.34-1.06)
 Q2 8728 0.86(0.77- 0.97) 4896 0.96(0.82-1.13) 3465 0.82(0.69-0.98) 367 0.64(0.36-1.15)
 Q1-Lowest 8881 0.95(0.84- 1.08) 5547 1.07(0.91-1.26) 2865 0.96(0.78-1.17) 469 0.59(0.34-1.04)
Region
 Large metro 21877 Ref 10124 Ref 10841 Ref 912 Ref
 Small metro 9398 1.37(1.24- 1.51) 5037 1.50(1.31-1.72) 4066 1.23(1.05-1.44) 295 1.07(0.68-1.68)
 Micropolitan 3702 1.44(1.24-1.68) 2167 1.62(1.32-1.98) 1402 1.18(0.93-1.51) 133 1.50(0.74-3.03)
 Not metro or micro 2438 1.89(1.54- 2.31) 1534 1.90(1.48-2.44) 810 1.75(1.22-2.52) 94 3.84(1.16-12.64)
Stage at Presentation
 Non-metastatic/in-situ 27066 Ref 13617 Ref 12446 Ref 1003 Ref
 Metastatic 10349 0.85(0.78- 0.93) 5245 1.06(0.94-1.19) 4673 0.65(0.57-0.74) 431 0.93(0.64-1.34)
Age at admission-years 37415 0.99(0.99- 0.99) 18862 0.99(0.99-1.00) 17119 0.99(0.98-0.99) 1434 0.99(0.98-1.01)
Number of Co-
morbidities
37415 0.84(0.78-0.90) 18862 0.83(0.77-0.90) 17119 0.83(0.71-0.96) 1434 1.04(0.68-1.60)
α

Adjusted for race, age, area-level income, region, stage of presentation and number of comorbidities.

AOR= Adjusted Odds Ratio

Among patients who received surgery, odds of post-operative complications were assessed overall and stratified by insurance status (Table 3). Overall, Black patients were significantly more likely to experience post-operative complications compared with Whites (OR: 1.21, 95% CI: 1.03 – 1.42), however this association was only observed among Black patients with Private insurance (OR=1.41, 95%CI: 1.12-1.78). There were no other racial differences in post-operative complications, although patients with more comorbid conditions experienced significantly more complications in both Medicaid/Medicare (OR= 1.45, 95%CI: 1.32-1.60) as well as Private (OR= 1.34, 95%CI: 1.12-1.60) insurance holders.

Table 3.

Multivariable adjusted odds ratios for post-operative complications stratified by insurance status among surgically treated breast cancer patients, Nationwide Inpatient Sample, 2007-2011.

All Medicaid/Medicare Private Other

n AOR(95%CI) α n AOR(95%CI) α n AOR(95%CI) α n AOR(95%CI) α

Race/Ethnicity
 White 27350 Ref 13809 Ref 12814 Ref 727 Ref
 Black 4651 1.21(1.03-1.42) 2493 1.09(0.87- 1.37) 1889 1.41(1.12-1.78) 269 0.69(0.25- 1.88)
 Hispanic 2873 0.96(0.78-1.19) 1451 0.90(0.67- 1.22) 1127 0.88(0.63-1.25) 295 2.01(1.00- 4.05)
 Other 2541 0.93(0.74-1.15) 1109 0.84(0.60- 1.17) 1289 0.93(0.68-1.29) 143 2.10(0.93- 4.74)
Area-level Income
 Q4-Highest 10975 Ref 4204 Ref 6490 Ref 281 Ref
 Q3 8831 1.08(0.94-1.25) 4215 0.91(0.74- 1.12) 4299 1.22(0.99-1.49) 317 1.36(0.62- 2.98)
 Q2 8728 0.99(0.85-1.15) 4896 0.86(0.69- 1.07) 3465 1.13(0.90-1.42) 367 1.03(0.45- 2.37)
 Q1-Lowest 8881 0.86(0.73-1.02) 5547 0.76(0.60- 0.95) 2865 1.03(0.80-1.33) 469 0.56(0.22- 1.41)
Region
 Large metro 21877 Ref 10124 Ref 10841 Ref 912 Ref
 Small metro 9398 0.96(0.84-1.09) 5037 0.77(0.64- 0.93) 4066 1.21(1.00-1.45) 295 1.11(0.53- 2.29)
 Micropolitan 3702 1.06(0.88-1.28) 2167 1.07(0.84- 1.37) 1402 1.02(0.75-1.38) 133 1.04(0.35- 3.14)
 Not metro or micro 2438 1.12(0.89-1.40) 1534 0.97(0.64- 0.93) 810 1.31(0.91-1.88) 94 1.86(0.59- 5.88)
Stage at Presentation
 Non-metastatic 27066 Ref 13617 Ref 12446 Ref 1003 Ref
 Metastatic 10349 0.89(0.79-1.00) 5245 0.84(0.71- 1.00) 4673 0.95(0.80-1.13) 431 0.70(0.37- 1.32)
Age at admission-years 37415 1.00(1.00-1.01) 18862 1.00(0.99- 1.01) 17119 1.01(1.00-1.02) 1434 1.01(0.99- 1.04)
Number of Co-morbidities 37415 1.39(1.28-1.51) 18862 1.45(1.32- 1.60) 17119 1.34(1.12-1.60) 1434 0.65(0.28- 1.52)
α

Adjusted for race, age, area-level income, region, stage of presentation and number of comorbidities.

AOR= Adjusted Odds Ratio

Among the entire sample of hospitalized breast cancer patients during the study period (Table 4), in-hospital mortality outcomes were evaluated overall and stratified by insurance status. After adjusting for age, disease stage, residential region and comorbidities, Black (OR: 1.37, 95% CI: 1.17 – 1.62) and Hispanic (OR: 1.25, 95% CI: 1.01 – 1.56) patients experienced significantly higher in-hospital mortality compared with White patients, as did patients residing in the lowest areal-level income areas (OR: 1.34, 95% CI: 1.11 – 1.62) compared with patients in the highest area-level income areas. Similar results were observed by race among patients with Medicare/Medicare insurance, however Black patients with Private insurance experienced even higher odds of in-hospital mortality than those on Medicare/Medicaid (OR=1.57, 95%CI: 1.21-2.03) compared with Whites, while the association for Hispanics became non-significant. The association between area-level income and in-hospital mortality was attenuated and non-significant among patients with Medicare/Medicaid, but remained among patients with Private insurance (OR: 1.63, 95% CI: 1.27 – 2.10).

Table 4.

Multivariable adjusted odds ratios for in-hospital mortality stratified by Insurance status among all breast cancer patients, Nationwide Inpatient Sample, 2007-2011.

All Medicaid/Medicare Private Other

n AOR(95%CI)α n AOR(95%CI)α n AOR(95%CI)α n AOR(95%CI)α

Race/Ethnicity
 White 48978 Ref 23285 Ref 24143 Ref 1550 Ref
 Black 8617 1.37(1.17-1.62) 4585 1.32(1.03-1.68) 3440 1.57(1.21-2.03) 592 0.68(0.42-1.08)
 Hispanic 5132 1.25(1.01-1.56) 2566 1.38(1.01-1.89) 2047 1.37(0.96-1.96) 519 0.38(0.21-0.69)
 Other 4357 0.92(0.70-1.21) 1826 1.14(0.77-1.69) 2293 0.88(0.57-1.34) 238 0.38(0.16-0.90)
Area-level Income
 Q4-Highest 20185 Ref 7351 Ref 12253 Ref 581 Ref
 Q3 16043 1.35(1.13-1.60) 7369 1.13(0.84-1.50) 8006 1.63 (1.27-2.10) 668 0.67(0.39-1.16)
 Q2 15313 1.20(1.00-1.45) 8183 0.99(0.74-1.32) 6376 1.30 (0.99-1.72) 754 0.95(0.57-1.60)
 Q1-Lowest 15543 1.34(1.11-1.62) 9359 1.20(0.90-1.59) 5288 1.30 (0.97- 1.75) 896 1.02(0.60-1.73)
Region
 Large metro 40017 Ref 17852 Ref 20332 Ref 1833 Ref
 Small metro 16741 1.09(0.94-1.26) 8459 1.05(0.84-1.32) 7662 1.26(1.02- 1.57) 620 0.88(0.56-1.37)
 Micropolitan 6160 1.27(1.03-1.56) 3424 1.30(0.96-1.77) 2476 1.43(1.04- 1.98) 260 0.99(0.54-1.82)
 Not metro or micro 4166 1.74(1.40-2.16) 2527 2.01(1.48-2.72) 1453 1.62(1.10- 2.39) 186 1.36(0.73-2.52)
Stage at Presentation
 Non-metastatic 46866 Ref 22081 Ref 23006 Ref 1779 Ref
 Metastatic 20218 14.25(12.12-16.76) 10181 11.52(9.09-14.60) 8917 18.48(14.21-24.03) 1120 10.20(6.58-15.81)
Age at admission-years 67084 1.01(1.00-1.01) 32262 0.99(0.98-1.00) 31923 1.06(1.05-1.07) 2899 1.05(1.03-1.06)
Number of Co-
morbidities
67084 1.45(1.33-1.59) 32262 1.49(1.32-1.67) 31923 1.65(1.40-1.95) 2899 1.39(1.04-1.85)
α

Adjusted for race, age, area-level income, region, stage of presentation and number of comorbidities.

AOR= Adjusted Odds Ratio

DISCUSSION

In this large dataset of patients hospitalized with a primary diagnosis of breast cancer, only about 4% received BCS and 52% received mastectomies, in line with recommendations by the National Institutes of Health regarding the use of BCS plus radiation as the preferred treatment for early-stage breast cancer [6]. Other US studies have shown higher rates of BCS, with estimates ranging from 50% to 70% [8-10]. Although both BCS and mastectomies are associated with similar survival rates [11-14], BCS is less invasive, and associated with less disfigurement, with superior quality of life outcomes related to body image and sexual functioning [15-17]. Thus, there are likely other factors such as socio-economic status and health insurance, in addition to individual or physician preferences that may influence treatment type. Health insurance coverage has been well studied as an important factor in determining the timing and quality of breast cancer treatment among US women [25, 31], but access to health insurance does not fully account for the notable racial/ethnic disparities in care. By utilizing the data from the large Nationwide Inpatient Sample database and focusing on hospitalized patients who had theoretically accessed the healthcare successfully, we are able to determining whether type of insurance made a difference in post-operative complications, hospital length of stay and inhospital mortality. This information may help to further shed light on persistent disparities in breast cancer outcomes, and possibly highlighting areas where targeted efforts may be focused to improve survival for all women with breast cancer.

We observed that after adjusting for clinical factors such as stage at presentation and number of comorbidities, Black and Hispanic patients were less likely to receive Mastectomies, however patients residing outside of large metropolitan areas were almost twice as likely to receive Mastectomies compared with BCS. The observed association was consistent across insurance types (private insurance or Medicare/Medicaid), but strongest among patients with Other insurance types, with those patients almost four times more likely to receive mastectomies compared with BCS. This finding may be driven by other aspects of healthcare access beyond insurance status, such as distance and availability of radiation therapy (RT) in non-metropolitan areas, which has been shown to influence cancer treatment and utilization of radiation therapy. Several studies have demonstrated that patients living greater distance from the RT facility statistically significant lower probability of receiving BCS [32-35]. Many patients choose mastectomy over BCS and RT to avoid the protracted course of daily treatment involved with RT, which consists of daily radiotherapy to the whole breast followed by a boost to the tumor bed, delivered over the course of 6–7.5 weeks [32].

We also observed that upon adjusting for clinical factors including stage and comorbidities, racial disparities persisted in in-hospital mortality among patients, with Black patients at 37% higher odds of dying during hospitalization compared with Whites in the overall sample, and 32% higher odds among patients with Medicaid/Medicare. The association was stronger among patients with Private insurance, with Black patients at 57% higher odds of dying during hospitalization compared with White patients, but no significant difference among patients with Other insurance types. There were also significant differences by region, with patients residing outside of large metropolitan areas more likely to die during hospitalization across insurance types, although the strongest association was among patients with Medicare/Medicaid. Similarly, Black patients experienced significantly higher odds of post-surgical complications, and this appeared to be driven mainly by the association among patients with Private insurance. Our results suggest that although Black patients were more likely to receive BCS according to national recommendations, they were more likely to experience negative hospitalization outcomes, and these negative outcomes were more likely among those with private insurance. Our observation of strong regional differences in surgery type and in-hospital mortality requires further investigation to determine whether this is driven by lack of healthcare resources in rural areas where hospitals may lack trained medical personnel or equipment to perform the newer BCS procedures, and/or to provide necessary post-surgical care. However, the regional differences do not fully explain racial differences in hospitalization outcomes, since Blacks tend to reside in urban, metropolitan areas [36].

Private insurance is most often obtained through employment, implying that private insurance holders are likely younger [37] and of higher socio-economic status [38]. These trends were observed in our study population, with 61% of women at the highest area-level income category on Private insurance, compared with 36% on Medicare/Medicaid and 2.8% on Other insurance types. In addition, the average age at admission for women on Private insurance was 54 years, compared with 70 years among women on Medicare/Medicaid and 56 years among women on Other insurance. In addition, women on Private insurance likely have better access to high-quality healthcare resources, as Private insurance tends to provide higher reimbursements to physicians compared to Medicare/Medicaid [39]. The observation of worse hospitalization outcomes among women with Private insurance warrants further study for several reasons: 1) we adjusted for stage at presentation and number of comorbidities at admission, reducing the possibility of confounding due to disease severity; 2) the established higher prevalence of aggressive (hormone-receptor negative) sub-types of breast cancer among Black women does not explain the stronger association with Private insurance as similar distribution of sub-types would be expected among Black women with other insurance types. Yet women on Private insurance still experienced much higher in-hospital mortality, and post-surgical complications compared with Black women with other insurance types. Future studies may be needed to examine the quality of cancer care among Black women, especially for younger, higher SES women with Private insurance. In addition, previous studies have shown that patient-physician interactions vary by race [40]. To the extent that such variations result in worse health outcomes for Black patients, interventions at both the patient and physician level will be critical to ensuring that patient-physician communication is improved, and guideline-adherent treatment is offered and received. Despite increased access to coverage, cost sharing continues to be a concern, particularly in the Medicare and privately insured populations [41]. Out-of pocket expenses have risen to a degree that is often thought to be unmanageable by many patients, and having insurance is not enough to alleviate the considerable burden posed by the high cost of treatment [42]. More research is also needed to better understand factors associated with realized vs. potential access [43] for those with insurance coverage as well as improved patient education regarding health insurance benefits and coverage for women with breast cancer.

There are several limitations of this study that should be noted. First, we were unable to conduct detailed assessment of non-surgical treatment, e.g. chemotherapy and hormonal therapy, as those are often outpatient procedures. Second, we were limited in our ability to adjust for aggressiveness of disease using variables such as ER, PR, and HER2 status as those are not available in the HCUP dataset. These variables are critical in determining the treatment modalities for breast cancer, including targeted therapy in women testing positive for any one of these measures, and may influence choice of surgery. In addition, our analyses include only inpatient stays and do not capture outpatient care or mortality occurring after discharge.

CONCLUSION

There were significant regional differences in the receipt of BCS compared with mastectomies among hospitalized women in the HCUP dataset, however significant racial differences existed in mortality and post-surgical complications, especially among women with Private insurance. Future studies are required to identify factors associated with low BCS adoption in non-metropolitan areas, and to determine whether biological factors, individual preference, patient-provider communication or lack of awareness of insurance benefits/coverage is responsible for poor breast cancer hospitalization outcomes among Black women with Private insurance.

Supplementary Material

01

Supplementary Table 1. ICD9 Codes

Acknowledgements

Dr. Akinyemiju was supported by grant U54 CA118948 from the NIH. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.

Footnotes

Conflicts of Interest: None

REFERENCES

  • [1].Ayanian JZ, Kohler BA, Abe T, Epstein AM. The relation between health insurance coverage and clinical outcomes among women with breast cancer. The New England journal of medicine. 1993;329(5):326–31. doi: 10.1056/NEJM199307293290507. [DOI] [PubMed] [Google Scholar]
  • [2].Jemal A, Murray T, Ward E, Samuels A, Tiwari RC, Ghafoor A, Feuer EJ, Thun MJ. Cancer Statistics, 2005. CA: A Cancer Journal for Clinicians. 2005;55(1):10–30. doi: 10.3322/canjclin.55.1.10. [DOI] [PubMed] [Google Scholar]
  • [3].Baquet CR, Commiskey P. Socioeconomic factors and breast carcinoma in multicultural women. Cancer. 2000;88(5 Suppl):1256–64. doi: 10.1002/(sici)1097-0142(20000301)88:5+<1256::aid-cncr13>3.0.co;2-3. [DOI] [PubMed] [Google Scholar]
  • [4].Smigal C, Jemal A, Ward E, Cokkinides V, Smith R, Howe HL, Thun M. Trends in breast cancer by race and ethnicity: update 2006. CA Cancer J Clin. 2006;56(3):168–83. doi: 10.3322/canjclin.56.3.168. [DOI] [PubMed] [Google Scholar]
  • [5].Glass AG, Lacey JV, Jr., Carreon JD, Hoover RN. Breast cancer incidence, 1980-2006: combined roles of menopausal hormone therapy, screening mammography, and estrogen receptor status. Journal of the National Cancer Institute. 2007;99(15):1152–61. doi: 10.1093/jnci/djm059. [DOI] [PubMed] [Google Scholar]
  • [6].Martin JA, Hamilton BE, Sutton PD, Ventura SJ, Menacker F, Kirmeyer S. Births: final data for 2004, National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics. National Vital Statistics System. 2006;55(1):1–101. [PubMed] [Google Scholar]
  • [7].Krieger N, Chen JT, Waterman PD. Decline in US breast cancer rates after the Women's Health Initiative: socioeconomic and racial/ethnic differentials. American journal of public health. 2010;100(Suppl 1):S132–9. doi: 10.2105/AJPH.2009.181628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [8].Jemal A, Ward E, Thun MJ. Recent trends in breast cancer incidence rates by age and tumor characteristics among U.S. women. Breast cancer research : BCR. 2007;9(3):R28. doi: 10.1186/bcr1672. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [9].Hausauer AK, Keegan TH, Chang ET, Clarke CA. Recent breast cancer trends among Asian/Pacific Islander, Hispanic, and African-American women in the US: changes by tumor subtype. Breast cancer research : BCR. 2007;9(6):R90. doi: 10.1186/bcr1839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [10].Balasubramanian BA, Demissie K, Crabtree BF, Ohman Strickland PA, Kohler B, Rhoads GG. Racial differences in adjuvant systemic therapy for early breast cancer among Medicaid beneficiaries. The breast journal. 2010;16(2):162–8. doi: 10.1111/j.1524-4741.2009.00877.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [11].Celaya MO, Berke EM, Onega TL, Gui J, Riddle BL, Cherala SS, Rees JR. Breast cancer stage at diagnosis and geographic access to mammography screening (New Hampshire, 1998-2004) Rural and remote health. 2010;10(2):1361. [PMC free article] [PubMed] [Google Scholar]
  • [12].Du XL, Lin CC, Johnson NJ, Altekruse S. Effects of individual-level socioeconomic factors on racial disparities in cancer treatment and survival: findings from the National Longitudinal Mortality Study, 1979-2003. Cancer. 2011;117(14):3242–51. doi: 10.1002/cncr.25854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [13].Newman LA. Breast cancer in African-American women. The oncologist. 2005;10(1):1–14. doi: 10.1634/theoncologist.10-1-1. [DOI] [PubMed] [Google Scholar]
  • [14].Freedman RA, Virgo KS, He Y, Pavluck AL, Winer EP, Ward EM, Keating NL. The association of race/ethnicity, insurance status, and socioeconomic factors with breast cancer care. Cancer. 2011;117(1):180–9. doi: 10.1002/cncr.25542. [DOI] [PubMed] [Google Scholar]
  • [15].Deshpande AD, Jeffe DB, Gnerlich J, Iqbal AZ, Thummalakunta A, Margenthaler JA. Racial disparities in breast cancer survival: an analysis by age and stage. The Journal of surgical research. 2009;153(1):105–13. doi: 10.1016/j.jss.2008.05.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [16].Booth CM, Li G, Zhang-Salomons J, Mackillop WJ. The impact of socioeconomic status on stage of cancer at diagnosis and survival: a population-based study in Ontario, Canada. Cancer. 2010;116(17):4160–7. doi: 10.1002/cncr.25427. [DOI] [PubMed] [Google Scholar]
  • [17].Du XL, Fang S, Meyer TE. Impact of treatment and socioeconomic status on racial disparities in survival among older women with breast cancer. American journal of clinical oncology. 2008;31(2):125–32. doi: 10.1097/COC.0b013e3181587890. [DOI] [PubMed] [Google Scholar]
  • [18].Harper S, Lynch J, Meersman SC, Breen N, Davis WW, Reichman MC. Trends in area-socioeconomic and race-ethnic disparities in breast cancer incidence, stage at diagnosis, screening, mortality, and survival among women ages 50 years and over (1987-2005) Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2009;18(1):121–31. doi: 10.1158/1055-9965.EPI-08-0679. [DOI] [PubMed] [Google Scholar]
  • [19].Komenaka IK, Martinez ME, Pennington RE, Jr., Hsu CH, Clare SE, Thompson PA, Murphy C, Zork NM, Goulet RJ., Jr. Race and ethnicity and breast cancer outcomes in an underinsured population. Journal of the National Cancer Institute. 2010;102(15):1178–87. doi: 10.1093/jnci/djq215. [DOI] [PubMed] [Google Scholar]
  • [20].Niu X, Pawlish KS, Roche LM. Cancer survival disparities by race/ethnicity and socioeconomic status in New Jersey. Journal of health care for the poor and underserved. 2010;21(1):144–60. doi: 10.1353/hpu.0.0263. [DOI] [PubMed] [Google Scholar]
  • [21].Martin DN, Boersma BJ, Yi M, Reimers M, Howe TM, Yfantis HG, Tsai YC, Williams EH, Lee DH, Stephens RM, Weissman AM, Ambs S. Differences in the tumor microenvironment between African-American and European-American breast cancer patients. PloS one. 2009;4(2):e4531. doi: 10.1371/journal.pone.0004531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [22].Braun KL, Fong M, Gotay C, Pagano IS, Chong C. Ethnicity and breast cancer in Hawaii: increased survival but continued disparity. Ethnicity & disease. 2005;15(3):453–60. [PubMed] [Google Scholar]
  • [23].Weissman JS, Stern R, Fielding SL, Epstein AM. Delayed access to health care: risk factors, reasons, and consequences. Annals of internal medicine. 1991;114(4):325–31. doi: 10.7326/0003-4819-114-4-325. [DOI] [PubMed] [Google Scholar]
  • [24].Roetzheim RG, Gonzalez EC, Ferrante JM, Pal N, Van Durme DJ, Krischer JP. Effects of health insurance and race on breast carcinoma treatments and outcomes. Cancer. 2000;89(11):2202–13. doi: 10.1002/1097-0142(20001201)89:11<2202::aid-cncr8>3.0.co;2-l. [DOI] [PubMed] [Google Scholar]
  • [25].Coburn N, Fulton J, Pearlman DN, Law C, DiPaolo B, Cady B. Treatment variation by insurance status for breast cancer patients. The breast journal. 2008;14(2):128–34. doi: 10.1111/j.1524-4741.2007.00542.x. [DOI] [PubMed] [Google Scholar]
  • [26].Lautner M, Lin H, Shen Y, Parker C, Kuerer H, Shaitelman S, Babiera G, Bedrosian I. Disparities in the Use of Breast-Conserving Therapy Among Patients With Early-Stage Breast Cancer. JAMA surgery. 2015;150(8):778–86. doi: 10.1001/jamasurg.2015.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [27].Adepoju L, Wanjiku S, Brown M, Qu W, Williams M, Redfern RE, Sferra JJ. Effect of insurance payer status on the surgical treatment of early stage breast cancer: data analysis from a single health system. JAMA surgery. 2013;148(6):570–2. doi: 10.1001/jamasurg.2013.61. [DOI] [PubMed] [Google Scholar]
  • [28].Lukavsky R, Sariego J. Insurance status effects on stage of diagnosis and surgical options used in the treatment of breast cancer. Southern medical journal. 2015;108(5):258–61. doi: 10.14423/SMJ.0000000000000281. [DOI] [PubMed] [Google Scholar]
  • [29].Young GJ, Cohen BB. The process and outcome of hospital care for Medicaid versus privately insured hospital patients. Inquiry : a journal of medical care organization, provision and financing. 1992;29(3):366–71. [PubMed] [Google Scholar]
  • [30].Akinyemiju TF, Vin-Raviv N, Chavez-Yenter D, Zhao X, Budhwani H. Race/ethnicity and socio-economic differences in breast cancer surgery outcomes. Cancer epidemiology. 2015;39(5):745–51. doi: 10.1016/j.canep.2015.07.010. [DOI] [PubMed] [Google Scholar]
  • [31].Kuzmiak CM, Haberle S, Padungchaichote W, Zeng D, Cole E, Pisano ED. Insurance status and the severity of breast cancer at the time of diagnosis. Acad Radiol. 2008;15(10):1255–8. doi: 10.1016/j.acra.2008.04.011. [DOI] [PubMed] [Google Scholar]
  • [32].Nattinger AB, Kneusel RT, Hoffmann RG, Gilligan MA. Relationship of distance from a radiotherapy facility and initial breast cancer treatment. Journal of the National Cancer Institute. 2001;93(17):1344–6. doi: 10.1093/jnci/93.17.1344. [DOI] [PubMed] [Google Scholar]
  • [33].Punglia RS, Weeks JC, Neville BA, Earle CC. Effect of distance to radiation treatment facility on use of radiation therapy after mastectomy in elderly women. Int J Radiat Oncol Biol Phys. 2006;66(1):56–63. doi: 10.1016/j.ijrobp.2006.03.059. [DOI] [PubMed] [Google Scholar]
  • [34].Voti L, Richardson LC, Reis IM, Fleming LE, Mackinnon J, Coebergh JW. Treatment of local breast carcinoma in Florida: the role of the distance to radiation therapy facilities. Cancer. 2006;106(1):201–7. doi: 10.1002/cncr.21557. [DOI] [PubMed] [Google Scholar]
  • [35].Athas WF, Adams-Cameron M, Hunt WC, Amir-Fazli A, Key CR. Travel distance to radiation therapy and receipt of radiotherapy following breast-conserving surgery. Journal of the National Cancer Institute. 2000;92(3):269–71. doi: 10.1093/jnci/92.3.269. [DOI] [PubMed] [Google Scholar]
  • [36].Liff JM, Chow WH, Greenberg RS. Rural-urban differences in stage at diagnosis. Possible relationship to cancer screening. Cancer. 1991;67(5):1454–9. doi: 10.1002/1097-0142(19910301)67:5<1454::aid-cncr2820670533>3.0.co;2-k. [DOI] [PubMed] [Google Scholar]
  • [37].Fronstin P. Sources of health insurance and characteristics of the uninsured: analysis of the March 2007 Current Population Survey. EBRI Issue Brief. 2007;310:1–33. [PubMed] [Google Scholar]
  • [38].Becker G, Newsom E. Socioeconomic status and dissatisfaction with health care among chronically ill African Americans. American journal of public health. 2003;93(5):742–8. doi: 10.2105/ajph.93.5.742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [39].Zuckerman S, McFeeters J, Cunningham P, Nichols L. Changes in medicaid physician fees, 1998-2003: implications for physician participation. Health Aff (Millwood) Suppl Web Exclusives. 2004 doi: 10.1377/hlthaff.w4.374. W4-374-84. [DOI] [PubMed] [Google Scholar]
  • [40].Bird ST, Bogart LM. Perceived race-based and socioeconomic status(SES)-based discrimination in interactions with health care providers. Ethnicity & disease. 2001;11(3):554–63. [PubMed] [Google Scholar]
  • [41].Stockdale H, Guillory K. Lifeline: Why Cancer Patients Rely on Medicare for Critical Coverage. American Cancer Society Cancer Action Network. 2013 [Google Scholar]
  • [42].Zafar SY, Peppercorn JM, Schrag D, Taylor DH, Goetzinger AM, Zhong X, Abernethy AP. The financial toxicity of cancer treatment: a pilot study assessing out-of-pocket expenses and the insured cancer patient's experience. The oncologist. 2013;18(4):381–90. doi: 10.1634/theoncologist.2012-0279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [43].Alegria M, Lin J, Chen CN, Duan N, Cook B, Meng XL. The impact of insurance coverage in diminishing racial and ethnic disparities in behavioral health services. Health Serv Res. 2012;47(3 Pt 2):1322–44. doi: 10.1111/j.1475-6773.2012.01403.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [44].Dehal A, Abbas A, Johna S. Comorbidity and outcomes after surgery among women with breast cancer: analysis of nationwide in-patient sample database. Breast Cancer Research and Treatment. 2013;139(2):469–476. doi: 10.1007/s10549-013-2543-9. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

01

Supplementary Table 1. ICD9 Codes

RESOURCES