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1.
Rheumatology (Oxford) ; 51(9): 1697-706, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22653381

ABSTRACT

OBJECTIVES: To determine whether there are racial/ethnic differences in the willingness of SLE patients to receive CYC or participate in clinical trials, and whether demographic, psychosocial and clinical characteristics contribute to these differences. METHODS: Data from 120 African-American and 62 white lupus patients were evaluated. Structured telephone interviews were conducted to determine treatment preferences, as well as to study characteristics and beliefs that may affect these preferences. Data were analysed using serial hierarchical multivariate logistic regression and deviances were calculated from a saturated model. RESULTS: Compared with their white counterparts, African-American SLE patients expressed less willingness to receive CYC (67.0% vs 84.9%, P = 0.02) if their lupus worsened. This racial/ethnic difference remained significant after adjusting for socioeconomic and psychosocial variables. Logistic regression analysis showed that African-American race [odds ratio (OR) 0.29, 95% CI 0.10, 0.80], physician trust (OR 1.05, 95% CI 1.00, 1.12) and perception of treatment effectiveness (OR 1.40, 95% CI 1.22, 1.61) were the most significant determinants of willingness to receive CYC. A trend in difference by race/ethnicity was also observed in willingness to participate in a clinical trial, but this difference was not significant. CONCLUSION: This study demonstrated reduced likelihood of accepting CYC in African-American lupus patients compared with white lupus patients. This racial/ethnic variation was associated with belief in medication effectiveness and trust in the medical provider, suggesting that education about therapy and improved trust can influence decision-making among SLE patients.


Subject(s)
Antirheumatic Agents/therapeutic use , Cyclophosphamide/therapeutic use , Decision Making , Lupus Erythematosus, Systemic , Minority Groups , Patient Care Planning , Patient Preference/ethnology , Adult , Black or African American/ethnology , Attitude to Health/ethnology , Female , Health Knowledge, Attitudes, Practice , Humans , Illinois/ethnology , Lupus Erythematosus, Systemic/drug therapy , Lupus Erythematosus, Systemic/ethnology , Lupus Erythematosus, Systemic/psychology , Male , Middle Aged , Minority Groups/psychology , Patient Education as Topic , Patient Preference/psychology , Physician-Patient Relations , White People/ethnology
2.
Sci Rep ; 11(1): 18443, 2021 09 16.
Article in English | MEDLINE | ID: mdl-34531435

ABSTRACT

Prior research has well established the association of ethno-racial and economic inequality with COVID-19 incidence and mortality rates across counties in the US. In this ecological study, a similar association was found between ethno-racial and economic inequality and COVID-19 full vaccination rates across the 102 counties in the American state of Illinois in the early months of vaccination. Among the counties with income inequality below the median, a county's poverty rate had a negative association with the proportion of population fully vaccinated. However, among the counties with income inequality above the median, a higher percentage of Black or Hispanic population was persistently associated with a lower proportion of fully vaccinated population over the two-month period from early February to early April of 2021.


Subject(s)
Black or African American/statistics & numerical data , COVID-19/epidemiology , COVID-19/prevention & control , Hispanic or Latino/statistics & numerical data , Vaccination Coverage/statistics & numerical data , Aged , Aged, 80 and over , COVID-19/mortality , Female , Health Status Disparities , Humans , Illinois/ethnology , Incidence , Male , Mass Vaccination/statistics & numerical data , Mortality/ethnology , Socioeconomic Factors
3.
Am J Psychiatry ; 165(1): 15-20, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18086748

ABSTRACT

Many people who struggle with psychotic disorder often refuse offers of help, including housing, extended by mental health services. This article uses the ethnographic method to examine the reasons for such refusal among women who are homeless and psychiatrically ill in the institutional circuit in an urban area of Chicago. It concludes that such refusals arise not only from a lack of insight but also from the local culture's ascription of meaning to being "crazy." These data suggest that offers of help-specifically, diagnosis-dependent housing-to those on the street may be more successful when explicit psychiatric diagnosis is downplayed.


Subject(s)
Ill-Housed Persons/psychology , Psychotic Disorders/psychology , Treatment Refusal/psychology , Anthropology, Cultural/methods , Attitude to Health , Ethnicity/psychology , Ethnicity/statistics & numerical data , Female , Ill-Housed Persons/statistics & numerical data , Humans , Illinois/ethnology , Psychiatric Status Rating Scales , Psychotic Disorders/diagnosis , Psychotic Disorders/ethnology , Residential Treatment , Sex Factors , Terminology as Topic , Treatment Refusal/ethnology , United States/ethnology , Urban Population/statistics & numerical data
4.
Child Abuse Negl ; 76: 561-572, 2018 02.
Article in English | MEDLINE | ID: mdl-28941983

ABSTRACT

While all children deserve a stable living environment, national data illustrate that many states struggle to achieve placement stability for youth in the child welfare system as a significant number of children in foster care continue to experience multiple placements while in state custody. Prior research has not considered the impact of youth protective factors or strengths on the frequency of placement changes that youth experience while in the child welfare system. This study examined the association between strengths measured at multiple levels (i.e., individual, family, and community) and placement stability among 4022 minority youth (aged 10-18) using administrative and clinical data from the Illinois child welfare system. Negative binomial regressions at the family level revealed that youth with at least one loving and supportive family member experienced 16% fewer placement changes than youth without family strengths. At the community level, youth attending schools that work to create an environment that meets its students' needs experienced 13% fewer placement changes than youth without educational supports. These findings can inform the quality of treatment and services provided to minority youth in the child welfare system.


Subject(s)
Child Protective Services , Child Welfare/psychology , Foster Home Care/psychology , Adolescent , Child , Child Welfare/ethnology , Ethnicity , Female , Foster Home Care/statistics & numerical data , Humans , Illinois/ethnology , Longitudinal Studies , Male , Minority Groups , Racial Groups/ethnology , Risk Factors
5.
JAMA Netw Open ; 1(5): e182497, 2018 09 07.
Article in English | MEDLINE | ID: mdl-30646169

ABSTRACT

Importance: There is a genetic predisposition to early-onset atrial fibrillation (EOAF) in European American individuals. However, the role of family history in the pathogenesis of EOAF in racial and ethnic minorities remains unclear. Objective: To determine whether probands with EOAF across racial and ethnic groups have a higher rate of AF in first-degree family members than racially and ethnically matched control patients with non-early-onset AF (non-EOAF). Design, Setting, and Participants: In this cohort study, patients prospectively enrolled in a clinical and genetic biorepository were administered baseline questionnaires that included questions about family history of AF. Early-onset AF was defined as AF occurring in probands aged 60 years or younger in the absence of structural heart disease. All other forms were categorized as non-EOAF. Recruitment took place from July 2015 to December 2017. Analysis was performed in January 2018. Main Outcomes and Measures: Primary analysis of reported family history of AF in first-degree relatives with sensitivity analysis restricted to those in whom a family history was confirmed by medical record review and electrocardiogram. Results: Of 664 patients enrolled (mean [SD] age, 62 [12] years; 407 [61%] male), 267 (40%) were European American; 258 (39%), African American; and 139 (21%), Hispanic/Latino. There was a family history of AF in 36 probands with EOAF (49%) compared with 128 patients with non-EOAF (22%) (difference, 27%; 95% CI, 14%-40%; P < .001). On multivariable analysis, the adjusted odds of a proband with EOAF who was of African descent (odds ratio [OR], 2.69; 95% CI, 1.06-6.91; P < .001) or Hispanic descent (OR, 9.25; 95% CI, 2.37-36.23; P = .002) having a first-degree relative with AF were greater than those of European descent (OR, 2.51; 95% CI, 1.29-4.87; P = .006). Overall, probands with EOAF were more likely to have a first-degree relative with AF compared with patients with non-EOAF (adjusted OR, 3.02; 95% CI, 1.82-4.95; P < .001) across the 3 racial and ethnic groups. Atrial fibrillation in a first-degree family member was confirmed in 32% of probands with EOAF vs 11% of those with non-EOAF (difference, 21%; 95% CI, 11%-33%; P < .001). Furthermore, African American (28% vs 5%; difference, 23%; 95% CI, 4%-43%; P = .001), European American (35% vs 20%; difference, 15%; 95% CI, 1%-30%; P = .03), and Hispanic/Latino (30% vs 5%; difference, 25%; 95% CI, 4%-54%; P = .02) probands with EOAF were more likely to have a first-degree relative with confirmed AF vs racially and ethnically matched control patients with non-EOAF. The positive and negative predictive values for a family history of confirmed AF were both 89%. Conclusions and Relevance: Probands of African or Hispanic/Latino descent with EOAF were more likely to have a first-degree relative with AF when compared with European American individuals. These findings support genetic predisposition to EOAF across all 3 races.


Subject(s)
Atrial Fibrillation/diagnosis , Ethnicity/statistics & numerical data , Medical History Taking/statistics & numerical data , Adult , Atrial Fibrillation/epidemiology , Atrial Fibrillation/ethnology , Black People/ethnology , Black People/statistics & numerical data , Cohort Studies , Female , Genetic Predisposition to Disease/epidemiology , Genetic Predisposition to Disease/ethnology , Hispanic or Latino/statistics & numerical data , Humans , Illinois/epidemiology , Illinois/ethnology , Male , Middle Aged , Odds Ratio , Prospective Studies , Registries/statistics & numerical data , Time Factors , White People/ethnology , White People/statistics & numerical data
6.
J Gen Intern Med ; 22(9): 1239-45, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17594131

ABSTRACT

BACKGROUND: Racial and socioeconomic disparities have been identified in osteoporosis screening. OBJECTIVE: To determine whether racial and socioeconomic disparities in osteoporosis screening diminish after hip fracture. DESIGN: Retrospective cohort study of female Medicare patients. SETTING: Entire states of Illinois, New York, and Florida. PARTICIPANTS: Female Medicare recipients aged 65-89 years old with hip fractures between January 2001 and June 2003. MEASUREMENTS: Differences in bone density testing by race/ethnicity and zip-code level socioeconomic characteristics during the 2-year period preceding and the 6-month period following a hip fracture. RESULTS: Among all 35,681 women with hip fractures, 20.7% underwent bone mineral density testing in the 2 years prior to fracture and another 6.2% underwent testing in the 6 months after fracture. In a logistic regression model adjusted for age, state, and comorbidity, women of black race were about half as likely (RR 0.52 [0.43, 0.62]) and Hispanic women about 2/3 as likely (RR 0.66 [0.54, 0.80]) as white women to undergo testing before their fracture. They remained less likely (RR 0.66 [0.50, 0.88] and 0.58 [0.39, 0.87], respectively) to undergo testing after fracture. In contrast, women residing in zip codes in the lowest tertile of income and education were less likely than those in higher-income and educational tertiles to undergo testing before fracture, but were no less likely to undergo testing in the 6 months after fracture. CONCLUSIONS: Racial, but not socioeconomic, differences in osteoporosis evaluation continued to occur even after Medicare patients had demonstrated their propensity to fracture. Future interventions may need to target racial/ethnic and socioeconomic disparities differently.


Subject(s)
Black People/ethnology , Bone Density , Diagnostic Tests, Routine , Hip Fractures/ethnology , Hispanic or Latino/ethnology , White People/ethnology , Aged , Aged, 80 and over , Bone Density/physiology , Cohort Studies , Diagnostic Tests, Routine/statistics & numerical data , Female , Florida/ethnology , Hip Fractures/diagnosis , Hip Fractures/economics , Humans , Illinois/ethnology , New York/ethnology , Retrospective Studies , Socioeconomic Factors
7.
Clin Lymphoma Myeloma Leuk ; 16(6): 350-7, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27052852

ABSTRACT

BACKGROUND: The Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs) are characterized by an increased risk of thrombotic and hemorrhagic complications. Large retrospective studies have demonstrated racial disparities in MPN outcomes and attributed this to differences in access to health care. Utilizing a single institution experience, we report outcomes in patients with polycythemia vera (PV), essential thrombocythemia (ET), and myelofibrosis in relation to ethno-racial background. PATIENTS AND METHODS: A total of 127 Caucasian (56%) and non-Caucasian (44%) adult patients with MPNs consecutively treated at the University of Illinois between 1990 and 2012 were examined in this retrospective study. Relationships between ethno-racial background and vascular complications, and disease transformation were evaluated using multivariate logistic regression models. RESULTS: Non-Caucasian PV patients had an increased risk of vascular complications including cardiovascular thrombosis and hemorrhagic events, while Caucasian patients with PV and ET had a higher risk of progression to myelofibrosis. In a Cox proportional hazard regression analysis, Caucasian race emerged as an independent prognostic factor protective against cardiovascular thrombosis in PV and ET patients (hazard ratio, 0.2; 95% confidence interval, 0.03-0.9; P = .04) while age > 60 years and prior thrombosis were significant risk factors in univariate analysis. Non-Caucasian race was also a significant risk factor in univariate analysis of hemorrhagic complications of PV and ET, and this was largely driven by African American ethnicity. CONCLUSION: This study shows for the first time that race can influence clinical outcomes in myeloproliferative neoplasms. Our findings highlight the need for greater representation of non-Caucasian patients in studies investigating vascular risk factors in MPNs.


Subject(s)
Ethnicity , Myeloproliferative Disorders/epidemiology , Outcome Assessment, Health Care , White People , Adult , Female , Humans , Illinois/epidemiology , Illinois/ethnology , Kaplan-Meier Estimate , Male , Middle Aged , Mutation , Myeloproliferative Disorders/diagnosis , Myeloproliferative Disorders/genetics , Myeloproliferative Disorders/mortality , Retrospective Studies
9.
Plan Perspect ; 25(4): 433-55, 2010.
Article in English | MEDLINE | ID: mdl-20857602

ABSTRACT

In 1913, the Illinois Legislature enacted the Forest Preserve District Act. After adoption of the Act by voters in Cook County, the Chicago metropolitan area became among the first in the USA to establish a park system with an outer ring of nature preserves. This article chronicles the story of how the Cook County Forest Preserve District was established, its historical context and its influence on planning practice. It contends that although Chicago was not the originator of the idea of outer parks, it added significantly to development of the concept of comprehensive park system planning. The article contends that the paradigm of park management changed from conservation of the native landscape to multiple use management during the 20-year struggle to establish the district, and that passage of the Act was largely the result of the efforts of two individuals - Dwight Perkins and Jens Jensen.


Subject(s)
Conservation of Natural Resources , Forestry , Legislation as Topic , Public Health , Recreation , Activities of Daily Living/psychology , Conservation of Natural Resources/economics , Conservation of Natural Resources/history , Conservation of Natural Resources/legislation & jurisprudence , Forestry/economics , Forestry/education , Forestry/history , Forestry/legislation & jurisprudence , Government Programs/economics , Government Programs/education , Government Programs/history , Government Programs/legislation & jurisprudence , History, 20th Century , Illinois/ethnology , Legislation as Topic/economics , Legislation as Topic/history , Public Health/economics , Public Health/education , Public Health/history , Public Health/legislation & jurisprudence , Recreation/economics , Recreation/physiology , Recreation/psychology , Social Change/history
10.
Soc Serv Rev ; 84(3): 403-35, 2010.
Article in English | MEDLINE | ID: mdl-20873020

ABSTRACT

Placement instability remains a vexing problem for child welfare agencies across the country. This study uses child welfare administrative data to retrospectively follow the entire placement histories (birth to age 17.5) of 474 foster youth who reached the age of majority in the state of Illinois and to search for patterns in their movement through the child welfare system. Patterns are identified through optimal matching and hierarchical cluster analyses. Multiple logistic regression is used to analyze administrative and survey data in order to examine covariates related to patterns. Five distinct patterns of movement are differentiated: Late Movers, Settled with Kin, Community Care, Institutionalized, and Early Entry. These patterns suggest high but variable rates of movement. Implications for child welfare policy and service provision are discussed.


Subject(s)
Child Advocacy , Child Welfare , Foster Home Care , Public Policy , Social Work , Child , Child Advocacy/economics , Child Advocacy/education , Child Advocacy/history , Child Advocacy/legislation & jurisprudence , Child Advocacy/psychology , Child Care/economics , Child Care/history , Child Care/legislation & jurisprudence , Child Care/psychology , Child Welfare/economics , Child Welfare/ethnology , Child Welfare/history , Child Welfare/legislation & jurisprudence , Child Welfare/psychology , Child, Preschool , Foster Home Care/economics , Foster Home Care/history , Foster Home Care/legislation & jurisprudence , Foster Home Care/psychology , Government Agencies/economics , Government Agencies/history , Government Agencies/legislation & jurisprudence , History, 20th Century , Humans , Illinois/ethnology , Public Assistance/economics , Public Assistance/history , Public Assistance/legislation & jurisprudence , Public Policy/economics , Public Policy/history , Public Policy/legislation & jurisprudence , Social Responsibility , Social Work/economics , Social Work/education , Social Work/history , Social Work/legislation & jurisprudence
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