Second roundtable conference on health care reform, the Health Security Act, and Indian health care a consensus statement final report

Authors: IHS-
Publication Year: 1994
Last Updated: 2010-01-21 08:14:08
Journal: Indian Health Service, Staff Office of Planning, Evaluation, and Research
Keywords: Consensus Development Conferences/Publication Type/); Community Health Planning; Community Networks; Clinical Competence; Comprehensive Health Care; Consumer Participation; Efficiency, Organizational; Eligibility Determination; Financial Management; Financing, Government; Financing, Organized; Health Care Quality, Access, and Evaluation; Health Care Reform; Health Services Accessibility; Health Planning Support; Medicare Part B; Organizational Innovation; Professional Competence; Quality Assurance, Health Care; Regional Health Planning; Social Responsibility

Short Abstract: This Roundtable on Health Care Reform was the second Indian Health Service (IHS)-sponsored Roundtable on the topic of Health Care Reform and its impact on Indian health.  This second Roundtable was held to provide tribal leaders, urban health care providers, and national Indian organizations with the opportunity to contribute their perspectives on detailed substance of the Health Security Act and other reform proposals, and to provide the IHS with Consensus Statements from which further policy analysis can occur.

Abstract: This Roundtable on Health Care Reform was the second Indian Health Service (IHS)-sponsored Roundtable on the topic of Health Care Reform and its impact on Indian health. This second Roundtable was held to provide tribal leaders, urban health care providers, and national Indian organizations with the opportunity to contribute their perspectives on detailed substance of the Health Security Act and other reform proposals, and to provide the IHS with Consensus Statements from which further policy analysis can occur. The Consensus Statements reflected in this document were developed through a process which allowed for presentation of most current information, deliberation, and discussion by Roundtable participants, and formulation of Consensus Statements which best projected the breadth of positions. The Consensus Statements developed by the Roundtable participants focused on the following major issue areas: 1) tribal sovereignty; 2) comprehensive and supplemental benefits; 3) governance and structure; 4) eligibility and enrollment; 5) financing; and 6) transition and competition. A major overriding concern expressed by Roundtable participants that influenced the discussion of every major aspect of Health Care Reform were the cutbacks to the IHS in fiscal years 1994 and 1995. These cuts will cause devastating and potentially irreparable harm to the Indian health care delivery structure nationally. The Roundtable participants stated repeatedly, that it will be impossible for the Indian health care system to withstand the magnitude of proposed staffing and budget cuts, and still compete under the new Health Care reform system

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Code: 3090
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Racial misidentification of American Indians/Alaska Natives in the HIV/AIDS Reporting Systems of five states and one urban health jurisdiction, U.S., 1984-2002

Authors: Bertolli J, Lee LM, Sullivan PS
Publication Year: 2007
Last Updated: 2010-01-21 08:14:08
Journal: Public Health Reports
Keywords: Acquired Immunodeficiency Syndrome/ethnology; Disease Notification/statistics and numerical data; HIV infections; homosexuality; male; humans; Indians; North American; Inuits; Male Residence Characteristics; Substance Abuse; Intravenous/ethnology; United States/epidemiology; Indian Health Service

Short Abstract: Objectives: We examined racial misidentification of American Indians/Alaska Natives (AI/AN) reported to the human immunodeficiency virus (HIV)/acquired immunodeficiency sydrome (AIDS) Reporting Systems (HARS) of five U.S. States and one county.

Abstract: OBJECTIVES: We examined racial misidentification of American Indians/Alaska Natives (AI/AN) reported to the human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS) Reporting Systems (HARS) of five U.S. states and one county. METHODS: To identify AI/AN records with misidentified race, we linked HARS data from 1984 through 2002 to the Indian Health Service National Patient Information and Reporting System (NPIRS), excluding non-AI/AN dependents, using probabilistic matching with clerical review. We used chi-square tests to examine differences in proportions and logistic regression to examine the associations of racial misidentification with HARS site, degree of AI/AN ancestry, mode of exposure to HIV, and urban or rural location of residence at time of diagnosis. RESULTS: A total of 1,523 AI/AN individuals was found in both NPIRS and HARS; race was misidentified in HARS for 459 (30%). The percentages of racially misidentified ranged from 3.7% (in Alaska) to 55% (in California). AI/AN people were misidentified as white (70%), Hispanic (16%), black (11%), and Asian/Pacific Islander (2%); for 0.9%, race was unspecified. Logistic regression results (data from all areas, all variables) indicated that urban residence at time of diagnosis, degree of AI/AN ancestry, and mode of exposure to HIV were significantly associated with racial misidentification of AI/AN people reported to HARS. CONCLUSIONS: Our findings add to the evidence that racial misidentification of AI/AN in surveillance data can result in underestimation of AI/AN HIV/AIDS case counts. Racial misidentification must be addressed to ensure that HIV/ AIDS surveillance data can be used as the basis for equitable resource allocation decisions, and to inform and mobilize public health action.

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Code: 3002
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PRIME-MD: its utility in detecting mental disorders in American Indians

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Positioning and Networking – CPG Needs Assessment Survey

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Patterns and predictors of HIV risk among urban American Indians.

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High school students’ misuse of over-the-counter drugs: a population-based study in an urban county

Authors: Steinman, Kenneth J.
Publication Year: 2005
Last Updated: 2010-01-21 08:14:08
Journal: Journal of Adolescent Health
Keywords: Substance Abuse; Adolescents; Over the counter

Short Abstract: A survey of high school students (n=~ 39,345) found 4.7% occasionally misuse over-the-counter drugs (i.e., to get high) and an additional 2.1% reported misuse during the past month. Misuse more common among older white and Native American youths and was associated with depressive affect and other substance use, especially alcohol and illicit drugs.

Abstract: A survey of high school students (n=39,345) found 4.7% occasionally misuse over-the-counter drugs (i.e., to get high) and an additional 2.1% reported misuse during the past month. Misuse was more common among older white and Native American youths and was associated with depressive affect and other substance use, especially alcohol and illicit drugs.

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Code: 2015
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What can the IHS clinical support center do for you?

Authors: Indian Health Service, IHS
Publication Year: 1994
Last Updated: 2010-01-21 08:14:08
Journal: IHS Primary Care Provider
Keywords: Education, Continuing; Education, Medical, Continuing; Health Occupations; Health Planning Support; Health Services Administration; Information Services

Short Abstract: This article is a brief description of some of the services available through the Clinical Support Center (CSC) to Indian Health Service (IHS), Tribal, and Urban Indian health programs. The CSC directs the planning, implementation, and evaluation of continuing education activities for health care providers; enhances communication for health care providers and educators; and facilitates special initiatives and activities for IHS clinical programs.

Abstract: This article is a brief description of some of the services available through the Clinical Support Center (CSC) to Indian Health Service (IHS), Tribal, and Urban Indian health programs. The CSC directs the planning, implementation, and evaluation of continuing education activities for health care providers; enhances communication for health care providers and educators; and facilitates special initiatives and activities for IHS clinical programs.

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Funding:
Code: 3086
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Trends in incidence and treatment for ductal carcinoma in situ in Hispanic, American Indian, and non-Hispanic white women in New Mexico, 1973-1994.

Authors: Adams-Cameron M, Gilliland FD, Hunt WC, Key CR
Publication Year: 1999
Last Updated: 2010-01-21 08:14:08
Journal: Cancer
Keywords: breast carcinoma, epidemiology, breast-conserving surgery, Hispanics, American Indians, ductal carcinoma in situ, population-based New Mexico Tumor Registry, multiple logistic regression, incidence rates, geographic location, ethnicity, rural/urban residency, socioeconomic status

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Background:  Incidence rates of ductal carcinoma in situ (DCIS) breast carcinoma and the use of breast-conserving surgery (BCS) for its treatment show substancial geographic and ethnic variations nationwide.  To the authors' knowledge, few studies have investigated incidence rates and treatment patterns in Hispanics and American Indians.

Abstract: BACKGROUND: Incidence rates of ductal carcinoma in situ (DCIS) breast carcinoma and the use of breast-conserving surgery (BCS) for its treatment show substantial geographic and ethnic variations nationwide. To the authors' knowledge, few studies have investigated incidence rates and treatment patterns in Hispanics and American Indians. METHODS: The authors used data from the population-based New Mexico Tumor Registry to describe trends in DCIS incidence rates between 1973-1994 and investigate patient and physician characteristics related to BCS in a multiethnic population between 1985-1994. Multiple logistic regression was used to evaluate patient and physician factors related to receiving BCS. RESULTS: Incidence rates for DCIS in Hispanics were approximately 50% lower compared with non-Hispanic whites. American Indians had the lowest incidence rate. Beginning in 1985, incidence rates for Hispanics and non-Hispanic whites showed a 21% annual increase. Between 1990-1994, incidence rates in American Indians increased more than twofold. BCS increased 5.8% per year between 1985-1994, with 50% of Hispanic and non-Hispanic white patients treated with BCS in 1994. The strongest factor associated with receiving BCS was geographic location of treatment (P < 0.001). The odds of receiving BCS were 5.8 times higher in the northern third of the state compared with the southern third. No significant variation in BCS was found by ethnicity, rural/urban residency, socioeconomic status, or physician characteristics. CONCLUSIONS: Incidence rates for DCIS increased substantially in all three ethnic groups. The use of BCS was associated most strongly with the location of treatment, most likely reflecting differences in physician practices and treatment recommendations. Further research is needed to investigate the increasing incidence rates of DCIS and the determinants of BCS for the treatment of DCIS. 

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Funding: Supported in part by Contract N01-67007, Division of Cancer Control and Population Sciences, national Cancer Institute.
Code: 173
Source: Na

The Great Smoky Mountains Study of Youth. Goals, design, methods, and the prevalence of DSM-III-R disorders.

Authors: Costello EJ, Angold A, Stangl DK, Tweed, DL, Erkanli A, Worthman CM, Burns BJ
Publication Year: 1996
Last Updated: 2010-01-21 08:14:08
Journal: Archives of General Psychiatry
Keywords: youth, psychiatric disorder, mental health, behavioral health, anxiety, hyperactivity, tic disorder, oppositional defiant disorder, conduct disorder, poverty

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BACKGROUND:  The Great Smoky Mountains Study of youth focuses on the relationship between the development of psychiatric disorder and the need for and use of mental health services.

Abstract: BACKGROUND: The Great Smoky Mountains Study of youth focuses on the relationship between the development of psychiatric disorder and the need for and use of mental health services. METHODS: A multistage, overlapping cohorts design was used, in which 4500 of the 11758 children aged 9, 11, and 13 years in an 11-county area of the southeastern United States were randomly selected for screening for psychiatric symptoms. Children who scored in the top 25% on the screening questionnaire, together with a 1 in 10 random sample of the rest, were recruited for 4 waves of intensive, annual interviews (n = 1015 at wave 1). In a parallel study, all American Indian children aged 9, 11, and 13 years were recruited (N = 323 at wave 1). RESULTS: The 3-month prevalence (+/-SE) of any DSM-III-R axis I disorder in the main sample, weighted to reflect population prevalence rates, was 20.3% +/- 1.7%. The most common diagnoses were anxiety disorders (5.7% +/- 1.0%), enuresis (5.1% +/- 1.0%), tic disorders (4.2% +/- 0.9%), conduct disorder (3.3% +/- 0.6%), oppositional defiant disorder (2.7% +/- 0.4%), and hyperactivity (1.9% +/- 0.4%). CONCLUSIONS: The prevalence of psychiatric disorder in this rural sample was similar to rates reported in other recent studies. Poverty was the strongest demographic correlate of diagnosis, in both urban and rural children. 

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Funding: This project was supported by grant MH48085 from the National Institute of Mental Health, Bethesda, MD. Additional support was provided through a project grant (Dr Worthman) and a Faculty Scholars award (Drs Costello, Angold and Worthman) from the William T. Grant Foundation and a Center grant from the Leon Lowenstein Foundation, New York, NY (Dr Angold).We gratefully acknowledge support of the psychometric studies of the Child and Adolescent Psychiatric Assessment from the William T Grant Found
Code: 199
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Successful strategies for increasing breast and cervical cancer screening: lessons learned from tribal programs

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