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1.
Annu Rev Public Health ; 37: 295-311, 2016.
Article in English | MEDLINE | ID: mdl-26989830

ABSTRACT

Over the past two decades, there has been growing interest in improving black men's health and the health disparities affecting them. Yet, the health of black men consistently ranks lowest across nearly all groups in the United States. Evidence on the health and social causes of morbidity and mortality among black men has been narrowly concentrated on public health problems (e.g., violence, prostate cancer, and HIV/AIDS) and determinants of health (e.g., education and male gender socialization). This limited focus omits age-specific leading causes of death and other social determinants of health, such as discrimination, segregation, access to health care, employment, and income. This review discusses the leading causes of death for black men and the associated risk factors, as well as identifies gaps in the literature and presents a racialized and gendered framework to guide efforts to address the persistent inequities in health affecting black men.


Subject(s)
Black or African American/statistics & numerical data , Health Status Disparities , Men's Health/ethnology , Social Determinants of Health/ethnology , Age Factors , Cause of Death , Environment , Exercise , Gender Identity , Health Behavior/ethnology , Health Services Accessibility , Humans , Life Expectancy/ethnology , Male , Racism/ethnology , Sex Factors , Socioeconomic Factors , United States
2.
Am J Public Health ; 106(6): 1086-91, 2016 06.
Article in English | MEDLINE | ID: mdl-27077346

ABSTRACT

OBJECTIVES: To evaluate African American-White differences in medical debt among older adults and the extent to which economic and health factors explained these. METHODS: We used nationally representative data from the 2007 and 2010 US Health Tracking Household Survey (n = 5838) and computed population-based estimates of medical debt attributable to economic and health factors with adjustment for age, gender, marital status, and education. RESULTS: African Americans had 2.6 times higher odds of medical debt (odds ratio = 2.62; 95% confidence interval = 1.85, 3.72) than did Whites. Health status explained 22.8% of the observed disparity, and income and insurance explained 19.4%. These factors combined explained 42.4% of the observed disparity. In addition, African Americans were more likely to be contacted by a collection agency and to borrow money because of medical debt, whereas Whites were more likely to use savings. CONCLUSIONS: African Americans incur substantial medical debt compared with Whites, and more than 40% of this is mediated by health status, income, and insurance disparities. Public health implications. In Medicare, low-income beneficiaries, especially low-income African Americans with poor health status, should be protected from the unintended financial consequences of cost-reduction strategies.


Subject(s)
Black or African American/statistics & numerical data , Insurance, Health/statistics & numerical data , Patient Credit and Collection/statistics & numerical data , White People/statistics & numerical data , Aged , Cross-Sectional Studies , Female , Health Services/economics , Health Status , Health Surveys , Humans , Income , Male , Socioeconomic Factors , United States
3.
Matern Child Health J ; 20(9): 1911-22, 2016 09.
Article in English | MEDLINE | ID: mdl-27126445

ABSTRACT

Objectives To examine correlates of lifetime mental health services (MHS) use among pregnant women reporting prenatal depressive symptoms by race/ethnicity. Methods This cross-sectional population-based study included 81,910 pregnant women with prenatal depressive symptoms using data from the Florida Healthy Start prenatal screening program (2008-2012). Multivariable logistic regression was conducted to ascertain adjusted odds ratios and corresponding 95Ā % confidence intervals for racial/ethnic differences in the correlates of lifetime MHS use. Results Findings of this study revealed racial/ethnic differences in MHS use among women with prenatal depressive symptoms, the highest rates being among non-Hispanic Whites and the lowest rates among Mexicans and other Hispanics. Most need for care factors, including illness, tobacco use, and physical or emotional abuse, consistently predicted MHS use across racial/ethnic groups after adjusting for covariates. Adjusted associations between predisposing and enabling/restricting factors and MHS use were different for different racial/ethnic groups. Conclusions Racial/ethnic differences in MHS use were found, with pregnant Hispanic women reporting prenatal depressive symptoms being the least likely to use MHS. Our study findings have significant public health implications for targeted intervention for pregnant women with prenatal depressive symptoms.


Subject(s)
Depression/ethnology , Healthcare Disparities , Hispanic or Latino/psychology , Mental Health Services/statistics & numerical data , Pregnant Women/psychology , White People/psychology , Adolescent , Adult , Cross-Sectional Studies , Depression/psychology , Female , Florida/epidemiology , Health Care Surveys , Hispanic or Latino/statistics & numerical data , Humans , Maternal Age , Pregnancy , Pregnant Women/ethnology , Prenatal Care , Prevalence , Socioeconomic Factors , White People/statistics & numerical data , Young Adult
4.
Ethn Dis ; 25(3): 295-304, 2015 Aug 07.
Article in English | MEDLINE | ID: mdl-26673460

ABSTRACT

PURPOSE: Studies have demonstrated the effects of segregated social and physical environments on the development of chronic diseases for African Americans. Studies have not delineated the effects of segregated environments specifically on the health of African American men over their lifetime. This study examines the relationship between life course measures of racial composition of social environments and diagnosis of hypertension among African American men. DESIGN: We analyzed cross-sectional data from a convenience sample of African American men seeking health care services in an outpatient primary care clinic serving a medically underserved patient population (N=118). Multivariable logistic regression analyses were used to examine associations between racial composition of multiple environments across the life course (eg, junior high school, high school, neighborhood growing up, current neighborhood, place of employment, place of worship) and hypertension diagnosis. RESULTS: The majority (86%) of participants were not currently in the workforce (retired, unemployed, or disabled) and more than half (54%) reported an annual household income of <$9,999; median age was 53. Results suggest that African American men who grew up in mostly Black neighborhoods (OR=4.3; P=.008), and worked in mostly Black environments (OR=3.1; P=.041) were more likely to be diagnosed with hypertension than those who did not. CONCLUSION: We found associations between mostly Black residential and workplace settings and hypertension diagnoses among African American men. Findings suggest exposure to segregated environments during childhood and later adulthood may impact hypertension risk among African American men over the life course.


Subject(s)
Black or African American , Heart Diseases/ethnology , Racial Groups , Chronic Disease , Cross-Sectional Studies , Humans , Male , Middle Aged , Morbidity/trends , Social Environment , Socioeconomic Factors , United States/epidemiology
5.
Front Public Health ; 11: 1142603, 2023.
Article in English | MEDLINE | ID: mdl-37483922

ABSTRACT

Introduction: Little is known about food insecurity among Americans with chronic diseases, one of the vulnerable groups in health care. Factors influencing food insecurity among this population group are especially poorly understood. Methods: Using data from the COVID Impact Survey, this cross-sectional study sought to examine food insecurity among adults with chronic diseases in the United States and to identify factors associated with their risks for food insecurity during the COVID-19 pandemic. Results: Nearly 28% of the national and 32% of the regional samples from the COVID Impact Survey were at risk for food insecurity. The logistic regressions show that chronically ill US adults with one of the following characteristics have higher odds of being at risk for food insecurity: younger than 60 years, having financial stress, unemployed, having received food from a food pantry, without health insurance, having a household income lower than $100,000, and without a college degree. Discussion: Targeted policies and programs are warranted to address underlying determinants of food insecurity that adults with chronic illnesses experience.


Subject(s)
COVID-19 , Adult , Humans , United States/epidemiology , COVID-19/epidemiology , Cross-Sectional Studies , Pandemics , Food Supply , Food Insecurity , Chronic Disease
6.
Am J Public Health ; 102(12): 2242-5, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22698017

ABSTRACT

We examined the relationship between trust in the medical system, medication adherence, and hypertension control in Southern African American men. The sample included 235 African American men aged 18 years and older with hypertension. African American men with higher general trust in the medical system were more likely to report better medication adherence (odds ratio [OR] = 1.06), and those with higher self-efficacy were more likely to report better medication adherence and hypertension control (OR = 1.08 and OR = 1.06, respectively).


Subject(s)
Black or African American/statistics & numerical data , Hypertension/drug therapy , Medication Adherence/psychology , Trust , Adult , Black or African American/psychology , Aged , Alabama/epidemiology , Humans , Male , Medication Adherence/statistics & numerical data , Middle Aged , Self Efficacy , Young Adult
7.
J Natl Med Assoc ; 104(9-10): 441-8, 2012.
Article in English | MEDLINE | ID: mdl-23342818

ABSTRACT

PURPOSE: To assess women's attitudes, beliefs, characteristics, the perception of risks, and their relationships with not utilizing human immunodeficiency virus (HIV) testing services. METHODS: This study is a retrospective study and secondary data analysis of the 2006 National Health Interview Survey. Parametric testing using univariate, bivariate, and multivariate analyses was performed to examine perception of HIV acquisition and the relationship with not utilizing HIV testing services among women in the United States. RESULTS: More than half of the women in this study had never been tested for HIV (52.26%). In the multivariate analysis, using SAS callable SUDAAN, women who had not been tested for HIV that believed they had no risk of getting HIV were more likely to have never been married (odds ratio [OR], 0.37; 95% CI, 0.31-28.73; p = .0013). In addition, women who had never been tested for HIV that believed they had no risk of getting HIV were more likely to have less than a high school diploma (OR, 0.35; 95% CI, 0.15-0.78; p = .0022). CONCLUSION: Findings from this study can lend themselves to the development of more efficient and sustainable interventions to prevent HIV infection and decrease high-risk behaviors among more susceptible populations and for the development of HIV testing policy.


Subject(s)
Attitude to Health , Culture , HIV Infections/psychology , HIV , Health Surveys/methods , Women's Health , Adolescent , Adult , Female , HIV Infections/diagnosis , HIV Infections/epidemiology , Humans , Middle Aged , Morbidity/trends , Retrospective Studies , Risk Factors , United States/epidemiology , Young Adult
8.
J Aging Soc Policy ; 24(3): 271-90, 2012.
Article in English | MEDLINE | ID: mdl-22720887

ABSTRACT

Middle-aged adults are becoming an increasing share of the nursing home population. Minimum Data Set assessment data for 2000 and 2008 are used to explore similarities and differences in sociodemographic, residential, medical, and psychiatric characteristics of newly admitted middle-aged adults (31-64) compared to their older counterparts (65+). Relative to their share of the state population, Black middle-aged adults are overrepresented in nursing homes across 45 states and the District of Columbia. Chronic conditions, including diabetes, renal failure, chronic obstructive pulmonary disease, asthma, and circulatory/heart disorders, appeared to contribute to the increasing presence of middle-aged adults. There were substantial increases in diagnoses of psychiatric disorders at admission; psychiatric diagnoses were significantly higher among middle-aged adults. Middle-aged adults were also more likely to have residential histories of prior stays in psychiatric facilities relative to older adults. States' rebalancing efforts need to attend to the increasing presence of disability associated with chronic medical and psychiatric conditions among middle-aged adults.


Subject(s)
Nursing Homes/statistics & numerical data , Residence Characteristics/statistics & numerical data , Adult , Age Distribution , Aged , Centers for Medicare and Medicaid Services, U.S./statistics & numerical data , Chronic Disease/epidemiology , Female , Geriatric Assessment , Humans , Insurance Claim Review/statistics & numerical data , Male , Mental Disorders/epidemiology , Middle Aged , Sex Distribution , Socioeconomic Factors , United States
9.
J Ambul Care Manage ; 45(2): 114-125, 2022.
Article in English | MEDLINE | ID: mdl-35202028

ABSTRACT

This study examined satisfaction with and confidence in understanding health insurance use among Blacks and Hispanic Americans with ambulatory care-sensitive conditions. Using the 2013-2016 Health Reform Monitoring Survey data sets, descriptive statistics and ordinary least-square regressions estimated the association between satisfaction and confidence scores and racial or ethnic groups with ambulatory care-sensitive conditions. Compared with their White counterparts, Black (Ɵ = -.13; 95% confidence interval [CI], -0.19 to -0.06) and Hispanic (Ɵ = -0.41; 95% CI, -0.48 to -0.33) participants' standardized confidence scores were significantly lower. Research is needed to identify factors that may enhance this population's confidence level.


Subject(s)
Black or African American , Health Care Reform , Ambulatory Care , Hispanic or Latino , Humans , Insurance, Health , United States , White People
10.
Cancer Causes Control ; 22(11): 1597-606, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21877121

ABSTRACT

OBJECTIVE: To assess social and clinical influences of prostate cancer treatment decisions among white and black men in the Midlands of South Carolina. METHODS: We linked data collected on treatment decision making in men diagnosed with prostate cancer from 1996 through 2002 with clinical and sociodemographic factors collected routinely by the South Carolina Central Cancer Registry (SCCCR). Unconditional logistic regression was used to assess social and clinical influences on treatment decision. RESULTS: A total of 435 men were evaluated. Men of both races who chose surgery (versus radiation) were more likely to be influenced by their physician and by family/friends. Black men who chose surgery also were ~5 times more likely to make independent decisions (i.e., rather than be influenced by their doctor). White men who chose surgery were twice as likely to be influenced by the desire for cure and less likely to consider the side effects of impotence (odds ratio (OR)Ā =Ā 0.40; 95% confidence interval (CI): 0.18, 0.88) and incontinence (ORĀ =Ā 0.27; 95% CI: 0.12, 0.63); by contrast, there was a suggestion of an opposite effect in black men, whose decision regarding surgery tended to be more strongly influenced by these side effects. CONCLUSION: Results suggest that both clinical and social predictors play an important role for men in choosing a prostate cancer treatment, but these influences may differ by race.


Subject(s)
Decision Making , Prostatic Neoplasms/psychology , Prostatic Neoplasms/therapy , Black or African American , Aged , Cohort Studies , Humans , Male , Middle Aged , Prostatic Neoplasms/ethnology , Social Environment , South Carolina , Surveys and Questionnaires , White People
12.
Health Lit Res Pract ; 5(4): e319-e332, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34905430

ABSTRACT

BACKGROUND: Health insurance literacy (HIL) may influence medical financial burden among people who are sick and the most vulnerable. OBJECTIVE: This study examined the relationships between HIL, health insurance factors, and medical debt among middle-age Americans, a population with an increasing prevalence of illnesses. METHODS: Linear and generalized linear regression analyses were conducted on data drawn from the 2015-2016 waves of the Health Reform Monitoring Survey, a national, internet-based sample of Americans age 18 to 64 years. The analytical sample included 8,042 people age 50 to 64 years. KEY RESULTS: Adjusted mean HIL scores did not differ by private versus public insurance or by out-of-pocket costs. Mean HIL scores were lower with higher deductibles; however, differences in mean scores were small. Higher HIL was associated with lower medical debt (odds ratio = 0.97; 95% confidence interval [0.96, 0.98]), but at the highest HIL score, the risk of having medical debt was still 13.8%. Public coverage, higher annual deductibles, and out-of-pocket costs were associated with higher risks of having medical debt. CONCLUSIONS: The findings suggest that HIL plays an important role in medical debt burden. However, with the shift toward high cost-sharing insurance plans, addressing health care affordability issues along with HIL are critical to eliminate medical debt problems. [HLRP: Health Literacy Research and Practice. 2021;5(4):e319-e332.] Plain Language Summary: Understanding and using health insurance (also defined as health insurance literacy) may influence the ability to pay medical bills among people who are sick and vulnerable. This study examined the relationships among health insurance literacy, health insurance factors, and difficulty paying medical bills (i.e., medical debt) in Americans age 50 to 64 years using data from the Health Reform Monitoring Survey. People with higher health insurance literacy reported lower medical debt. Type of insurance coverage did not influence medical debt. Those with annual deductibles and out-of-pocket health care costs were more likely to report having medical debt.


Subject(s)
Health Literacy , Adolescent , Adult , Health Care Reform , Health Expenditures , Humans , Insurance Coverage , Insurance, Health , Middle Aged , United States , Young Adult
13.
Med Care ; 48(10): 915-22, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20733530

ABSTRACT

BACKGROUND: Black prostate cancer patients are less likely to receive aggressive therapy (AT) than Whites: reported rates for patients ≥ 65 years old are about 55% versus 65%. Little is known about treatment rates in socioeconomically deprived states with large Black populations like Alabama. STUDY DESIGN: Medicare claims and Alabama Statewide Cancer Registry records were linked for Alabamian men in Medicare fee-for-service diagnosed with loco-regional prostate cancer in 2000-2002. The association between race and likelihood of: (1) AT (prostatectomy or external beam radiation therapy [EBRT] or brachytherapy); (2) hormone therapy (primary androgen deprivation therapy [ADT] or orchiectomy); (3) <30 days of EBRT; and (4) <6 months of ADT, was investigated adjusting for age, clinical tumor stage, grade, Comorbidity Index, and census tract proportion of Black residents, of persons living below poverty and with ≤ high school. RESULTS: Of 3561 patients, 71.2% received AT and 38.3% hormone therapy. Blacks were less likely to receive AT (64.3% vs. 73.0%, adjusted [adj.] OR: 0.80, CI: 0.67-0.96). There was no difference between Blacks and Whites in the likelihood of receiving hormone therapy (40.8% vs. 37.7%, adj. OR: 1.10, CI: 0.91-1.34), <30 days of EBRT (30.5% vs. 31.5%, adj. OR: 0.98, CI: 0.72-1.32) or <6 months of ADT (50.7% vs. 54.0%, adj. OR: 0.84, CI: 0.63-1.12). CONCLUSIONS: In Alabama, there were racial differences in utilization of aggressive treatment for locoregional prostate cancer. Research should investigate factors associated with prostate cancer treatment among older men, such as patient behavior and access to care.


Subject(s)
Attitude to Health/ethnology , Black or African American/statistics & numerical data , Health Services Accessibility/statistics & numerical data , Prostatic Neoplasms/ethnology , Prostatic Neoplasms/therapy , White People/statistics & numerical data , Aged , Aged, 80 and over , Alabama/epidemiology , Confidence Intervals , Health Behavior , Health Status Disparities , Humans , Male , Odds Ratio , Prostatic Neoplasms/diagnosis , Socioeconomic Factors
14.
J Natl Med Assoc ; 102(7): 556-61, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20690318

ABSTRACT

Asthma is a chronic illness among children. Minority children may be vulnerable to asthma complications since more than half are from households that are poor or near poor, and some have no health insurance. Asthma management plans are important for the long-term treatment of asthma and beneficial for self-management. This study analyzed insurance type and the relationship between having an asthma management plan among children across all races with asthma. This study utilized the 2002 and 2003 National Health Interview Survey. Findings showed that whites were significantly more likely than Non-Hispanic blacks and Hispanics to have an asthma management plan (OR, 1.66; p = .0031). In this study, children who reported Children's Health insurance Program (CHIP) coverage were twice as likely to have an asthma management plan (OR, 2.67; p = .0004). Mandating all insurers to provide an asthma management plan to children with asthma may reduce the race-based inequities and differences in asthma management plan status.


Subject(s)
Asthma/therapy , Disease Management , Health Status Disparities , Insurance, Health/statistics & numerical data , Adolescent , Child , Child Health Services , Child, Preschool , Female , Health Surveys , Humans , Male , Racial Groups/statistics & numerical data , State Health Plans , United States
15.
Am J Mens Health ; 14(4): 1557988320943359, 2020.
Article in English | MEDLINE | ID: mdl-32693654

ABSTRACT

Although the number of men with health insurance has increased, men are less likely to utilize health services than females, and experience difficulty in paying medical bills. Understanding the details of health insurance can be challenging and the lack of understanding can have financial consequences. This study, guided by Andersen's model of health-care utilization, assessed the relationship between confidence level in understanding health insurance terms and difficulty in paying medical bills among American men. Data were drawn from the Health Reform Monitoring Survey, 2015-2016. The study included 6,643 men aged between 18 and 64. Descriptive statistics examined participants' difficulty in paying medical bills by predisposing, enabling, and need characteristics, and by confidence in understanding health insurance terms. A modified Poisson regression analysis examined the association between difficulty in paying medical bills, confidence in understanding health insurance terms score, and predisposing, enabling, and need characteristics. An increase in confidence in understanding health insurance terms score was associated with significantly lower reported difficulty in paying medical bills (PR = .98; 95% CI = [.97-.99]; p = .002). Participants with a college degree or higher were less likely to report difficulty in paying their medical bills compared to participants with less than a high school degree (PR = .72; 95% CI = [.56-.92]; p = .009). A better understanding of health insurance might prevent men from experiencing difficulties in paying medical bills. Additional research should be performed to understand the relationship between the level of confidence in understanding health insurance, knowledge level of health insurance terms, use of health insurance, and their impact on difficulty in paying medical bills.


Subject(s)
Cost of Illness , Health Expenditures/statistics & numerical data , Health Services Accessibility/economics , Insurance, Health/economics , Men's Health/economics , Adult , Health Services Accessibility/statistics & numerical data , Humans , Insurance Coverage/economics , Insurance, Health/statistics & numerical data , Male , Men's Health/statistics & numerical data , Middle Aged , Socioeconomic Factors , United States , Young Adult
18.
Med Care Res Rev ; 65(3): 338-55, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18182483

ABSTRACT

States' use of Medicaid 1915(c) waiver services for persons living with HIV/AIDS (PLWHA) has been limited. The authors examine state-level factors related to the decision to offer waiver services, as well as waiver use and expenditures in states offering waivers for PLWHA. They use fixed effects cross-sectional time series models to explore these state factors. States with Democratic governors were more likely to offer waiver services and were found to have higher rates of use and greater expenditures and to devote a larger share of long-term care dollars to waiver services for PLWHA. State supply of both institutional and residential care beds was negatively related to use and expenditures. Medicaid community-based care has been found to be related to improved outcomes and reduced costs of care. Ways to foster 1915(c) waiver expansion are important so as to increase access to care for PLWHA.


Subject(s)
Community Health Services/economics , HIV Infections/therapy , Health Expenditures/statistics & numerical data , Home Care Services/economics , Medicaid/statistics & numerical data , State Health Plans/economics , Community Health Services/statistics & numerical data , Female , Health Services Accessibility/economics , Health Services Accessibility/standards , Home Care Services/statistics & numerical data , Humans , Long-Term Care/economics , Long-Term Care/legislation & jurisprudence , Male , Medicaid/legislation & jurisprudence , State Health Plans/legislation & jurisprudence , United States
19.
J Rural Health ; 24(1): 24-31, 2008.
Article in English | MEDLINE | ID: mdl-18257867

ABSTRACT

CONTEXT: Community Health Centers (CHCs) and Critical Access Hospitals (CAHs) play a significant role in providing health services for rural residents across the United States. PURPOSE: The overall goal of this study was to identify the CAHs that have collaborations with CHCs, as well as to recognize the content of the collaborations and the barriers and facilitators to collaborations. METHODS: The target population was CAHs within 60 miles of CHCs. Surveys were mailed to 386 chief executive officers of CAHs in 41 states who met the study criteria. The response rate was 40.9%. A descriptive analysis using chi-square tests compared the status of partnerships along with factors identified as barriers and facilitators to collaboration. FINDINGS: Out of the 161 CAH respondents, 24 (14.9%) reported having a collaborative agreement with a CHC, and 2 indicated that they planned to develop a collaborative agreement. A common reason given for not collaborating was lack of awareness of a CHC within the service area. Other barriers identified were competition with CHCs and organizational differences. External funding to start a collaborating service was the most frequently cited factor to facilitate collaborations. CONCLUSIONS: The findings indicate that collaborations between CAHs and CHCs are a largely untapped resource. The rural health care services continuum may benefit from increased collaborations.


Subject(s)
Community Health Centers , Continuity of Patient Care/organization & administration , Cooperative Behavior , Health Care Surveys , Hospitals, Rural , Emergency Service, Hospital , Humans , United States
20.
Ethn Dis ; 18(2): 225-7, 2008.
Article in English | MEDLINE | ID: mdl-18507278

ABSTRACT

OBJECTIVE: To examine the influence of race and having an asthma management plan on the impact of experiencing asthmatic episodes. METHODS: This study utilized the 2002 and 2003 National Health Interview Survey to conduct a retrospective study and secondary data analysis. Univariate, bivariate, and multivariate analysis was performed to examine physician asthma management plan recommendations among minority and non-minority children in the United States. RESULTS: Most of the study participants (59%) reported not having an asthma management plan. Children who experienced an asthma episode in the past 12 months were less likely to have an asthma management plan (OR .51, P<.0001). In the multivariate analysis, Whites were significantly more likely than were Blacks and Hispanics to have an asthma management plan (OR 1.66, P=.0031). CONCLUSIONS: Findings from this study indicate that Black and Hispanic children with asthma are less likely to have an asthma management plan, and children with an asthma management plan are less likely to have had asthma episodes in the past 12 months. Requiring all insurers to provide an asthma management plan to children with asthma may reduce these race-based inequities.


Subject(s)
Asthma/therapy , Black or African American/statistics & numerical data , Hispanic or Latino/statistics & numerical data , Patient Care Planning/statistics & numerical data , Self Care/statistics & numerical data , White People/statistics & numerical data , Adolescent , Asthma/epidemiology , Asthma/ethnology , Child , Child, Preschool , Disease Management , Emergency Service, Hospital , Female , Health Surveys , Healthcare Disparities , Humans , Male , Multivariate Analysis , Patient Acceptance of Health Care/ethnology , Patient Acceptance of Health Care/statistics & numerical data , Retrospective Studies , United States/epidemiology
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