ABSTRACT
INTRODUCTION: To improve services and assure predictable costs of care for Children and Youth with Special Health Care Needs (CYSHCN), state Title V and Medicaid programs are cooperating to reconceive care systems including contracting arrangements with managed care organizations (MCOs). This article describes how a consensus-based framework, the National Standards for Systems of Care for CYSHCN, influenced the redesign of two state Medicaid managed care programs: a statewide managed care plan for children with medical complexity in Florida and a regional accountable care program serving children and adults in Colorado. METHODS: Data are drawn from a recent evaluation of the National Standards, which define the core components of a comprehensive, coordinated, and family-centered system of care for CYSHCN. The authors synthesized insights from documents and semi-structured interviews with national and state stakeholders. RESULTS: The states used the National Standards in different ways. Florida translated the Standards into contract provisions and holds its MCO accountable to performance targets specific to CYSHCN. In Colorado, the Standards had an indirect influence on contract provisions with regional accountable entities (RAEs) and the state's oversight of EPSDT, which helps ensure that RAEs meet their obligations to CYSHCN. Managed care leaders viewed the Standards as an impetus to sharpen quality improvement and foster whole-person care. DISCUSSION: The National Standards offer a flexible framework to help states design Medicaid managed care programs and improve systems of care for CYSHCN. States can learn from one another's experiences applying the Standards in the context of their policy environments.
Subject(s)
Managed Care Programs , Medicaid , Accountable Care Organizations , Adolescent , Adult , Child , Colorado , Florida , Health Facilities , Humans , Standard of Care , United StatesABSTRACT
Health care delivery systems, including academic medical centers (AMCs), are increasingly focused on improving care for vulnerable, high-need, high-cost patients, in part because value-based payment models offer the promise of financial returns, or the avoidance of losses, for doing so. AMCs and other providers that have participated in Medicare and Medicaid demonstrations and value-based payment programs have important insights to offer about the features of successful and promising programs for high-need, high-cost patients. As more AMCs embrace value-based payment, they may have greater flexibility to provide services that address the medical and nonmedical needs of clinically complex patients and thereby reduce avoidable health care utilization. AMCs have many opportunities to create high-performing health systems, establish operational evidence for how to transform delivery systems, and train the next generation of providers to better address the care of high-need, high-cost individuals.
Subject(s)
Academic Medical Centers/economics , Delivery of Health Care/economics , Health Expenditures/trends , Cost-Benefit Analysis , Humans , Medicaid , Medicare , Quality of Health Care , United StatesABSTRACT
Issue: Given uncertainty about the future of the Affordable Care Act, it is useful to examine the progress in coverage and access made under the law. Goal: Compare state trends in access to affordable health care between 2013 and 2016. Methods: Analysis of recent data from the U.S. Census Bureau and the Behavioral Risk Factor Surveillance System. Findings and Conclusions: Between 2013 and 2016, the uninsured rate for adults ages 19 to 64 declined in all states and the District of Columbia, and fell by at least 5 percentage points in 47 states. Among children, uninsured rates declined by at least 2 percentage points in 33 states. There were reductions of at least 2 percentage points in the share of adults age 18 and older who reported skipping care because of costs in the past year in 36 states and D.C., with greater declines, on average, in Medicaid expansion states. The share of at-risk adults without a recent routine checkup, and of nonelderly individuals who spent a high portion of income on medical care, declined in at least of half of states and D.C. These findings offer evidence that the ACA has improved access to health care for millions of Americans. However, actions at the federal level including a shortened open enrollment period for marketplace coverage, a failure to extend CHIP funding, and a potential repeal of the individual mandate's penalties could jeopardize the gains made to date.
Subject(s)
Health Services Accessibility/statistics & numerical data , Health Services Accessibility/trends , Insurance Coverage/statistics & numerical data , Insurance Coverage/trends , Medically Uninsured/statistics & numerical data , Adolescent , Adult , Child , Child, Preschool , Forecasting , Humans , Infant , Infant, Newborn , Medicaid , Middle Aged , Patient Protection and Affordable Care Act/statistics & numerical data , Patient Protection and Affordable Care Act/trends , Poverty , State Government , United States , Young AdultABSTRACT
ISSUE: Prior to the Affordable Care Act (ACA), blacks and Hispanics were more likely than whites to face barriers in access to health care. GOAL: Assess the effect of the ACA's major coverage expansions on disparities in access to care among adults. METHODS: Analysis of nationally representative data from the American Community Survey and the Behavioral Risk Factor Surveillance System. FINDINGS AND CONCLUSIONS: Between 2013 and 2015, disparities with whites narrowed for blacks and Hispanics on three key access indicators: the percentage of uninsured working-age adults, the percentage who skipped care because of costs, and the percentage who lacked a usual care provider. Disparities were narrower, and the average rate on each of the three indicators for whites, blacks, and Hispanics was lower in both 2013 and 2015 in states that expanded Medicaid under the ACA than in states that did not expand. Among Hispanics, disparities tended to narrow more between 2013 and 2015 in expansion states than nonexpansion states. The ACA's coverage expansions were associated with increased access to care and reduced racial and ethnic disparities in access to care, with generally greater improvements in Medicaid expansion states.
Subject(s)
Black People/statistics & numerical data , Black or African American/statistics & numerical data , Ethnicity/statistics & numerical data , Health Services Accessibility/legislation & jurisprudence , Health Services Accessibility/statistics & numerical data , Healthcare Disparities/legislation & jurisprudence , Healthcare Disparities/statistics & numerical data , Hispanic or Latino/statistics & numerical data , Insurance Coverage/statistics & numerical data , Medically Uninsured/statistics & numerical data , Patient Protection and Affordable Care Act/statistics & numerical data , White People/statistics & numerical data , Adult , Ethnicity/legislation & jurisprudence , Forecasting , Health Services Accessibility/trends , Healthcare Disparities/trends , Humans , Insurance Coverage/legislation & jurisprudence , Insurance Coverage/trends , Medicaid , Medically Uninsured/legislation & jurisprudence , Middle Aged , Minority Groups , Patient Protection and Affordable Care Act/trends , Patient-Centered Care/legislation & jurisprudence , Patient-Centered Care/statistics & numerical data , United StatesABSTRACT
ISSUE: Homebound and functionally limited individuals are often unable to access office-based primary care, leading to unmet needs and increased health care spending. GOAL: Show how home-based primary care affects outcomes and costs for Medicare and Medicaid beneficiaries with complex care needs. METHODS: Qualitative synthesis of expert perspectives and the experiences of six case-study sites. FINDINGS AND CONCLUSIONS: Successful home-based primary care practices optimize care by: fielding interdisciplinary teams, incorporating behavioral care and social supports into primary care, responding rapidly to urgent and acute care needs, offering palliative care, and supporting family members and caregivers. Practices participating in Medicare's Independence at Home Demonstration saved $3,070 per beneficiary on average in the first year, primarily by reducing hospital use under this shared-savings program. The experience of a risk-based medical group that contracts with health plans and health systems to provide home-based care suggests similar potential to reduce health care spending under capitated or value-based payment arrangements. Making effective home-based primary care more widely available would require a better-prepared workforce, appropriate financial incentives to encourage more clinicians to provide house calls to their home-limited patients, and relevant quality measures to ensure that value-based payment is calibrated to meet the needs of patients and their families.
Subject(s)
Home Care Services/organization & administration , Primary Health Care/organization & administration , Caregivers , Cost Savings , Fee-for-Service Plans , Humans , Independent Living , Insurance, Health, Reimbursement , Palliative Care , Patient Care Team , Social Support , WorkforceABSTRACT
Issue: Finding ways to improve outcomes and reduce spending for patients with complex and costly care needs requires an understanding of their unique needs and characteristics. Goal: Examine demographics and health care spending and use of services among adults with high needs, defined as people who have three or more chronic diseases and a functional limitation in their ability to care for themselves or perform routine daily tasks. Methods: Analysis of data from the 20092011 Medical Expenditure Panel Survey. Key findings: High-need adults differed notably from adults with multiple chronic diseases but no functional limitations. They had average annual health care expenditures that were nearly three times higherand which were more likely to remain high over two years of observationand out-of-pocket expenses that were more than a third higher, despite their lower incomes. Rates of hospital use for high-need adults were more than twice those for adults with multiple chronic conditions only; high-need adults also visited the doctor more frequently and used more home health care. Costs and use of services also varied widely within the high-need group. Conclusion: These findings suggest that interventions should be targeted and tailored to high-need individuals most likely to benefit.
Subject(s)
Chronic Disease/economics , Comorbidity , Health Expenditures/statistics & numerical data , Health Resources/statistics & numerical data , Health Services Needs and Demand/economics , Health Services Needs and Demand/statistics & numerical data , Adult , Demography , Disabled Persons , Emergency Medical Services/statistics & numerical data , Financing, Personal , Humans , United StatesABSTRACT
Issue: Achieving a high-performing health system will require improving outcomes and reducing costs for high-need, high-cost patients--those who use the most health care services and account for a disproportionately large share of health care spending. Goal: To compare the health care experiences of adults with high needs--those with three or more chronic diseases and a functional limitation in the ability to care for themselves or perform routine daily tasks--to all adults and to those with multiple chronic diseases but no functional limitations. Methods: Analysis of data from the 2009--2011 Medical Expenditure Panel Survey. Key findings: High-need adults were more likely to report having an unmet medical need and less likely to report having good patient-provider communication. High-need adults reported roughly similar ease of obtaining specialist referrals as other adults and greater likelihood of having a medical home. While adults with private health insurance reported the fewest unmet needs overall, privately insured high-need adults reported the greatest difficulties having their needs met. Conclusion: The health care system needs to work better for the highest-need, most-complex patients. This study's findings highlight the importance of tailoring interventions to address their needs.
Subject(s)
Health Expenditures/statistics & numerical data , Health Services Accessibility/economics , Health Services Accessibility/statistics & numerical data , Health Services Needs and Demand/economics , Health Services Needs and Demand/statistics & numerical data , Adult , Chronic Disease , Communication , Comorbidity , Disabled Persons , Humans , Insurance, Health , Patient-Centered Care , Physician-Patient Relations , Private Sector , United StatesABSTRACT
Issue: The Affordable Care Act's policy reforms sought to expand health insurance coverage and make health care more affordable. As the nation prepares for policy changes under a new administration, we assess recent gains and challenges. Goal: To compare access to affordable health care across the U.S. between 2013 and 2015. Methods: Analysis of most recent publicly available data from the U.S. Census Bureau and the Behavioral Risk Factor Surveillance System. Key findings and conclusions: Between 2013 and 2015, uninsured rates for adults ages 19 to 64 declined in all states and by at least 3 percentage points in 48 states and the District of Columbia. For children, uninsured rates declined by at least 2 percentage points in 28 states. The share of adults age 18 and older who reported forgoing a visit to the doctor when needed because of costs dropped by at least 2 percentage points in 38 states and D.C. In contrast, there was little progress in expanding access to dental care for adults, which is not a required benefit under the ACA. These findings illustrate the impact that policy can have on access to care and offer a focal point for assessing future policy changes.
Subject(s)
Health Services Accessibility/statistics & numerical data , Insurance Coverage/statistics & numerical data , Medically Uninsured/statistics & numerical data , Patient Protection and Affordable Care Act , Adolescent , Adult , Black or African American/statistics & numerical data , Child , Child, Preschool , Forecasting , Healthcare Disparities/statistics & numerical data , Hispanic or Latino/statistics & numerical data , Humans , Infant , Infant, Newborn , Insurance Coverage/trends , Middle Aged , Poverty , State Government , United States , White People/statistics & numerical dataABSTRACT
This brief analyzes experts' reviews of evidence about care models designed to improve outcomes and reduce costs for patients with complex needs. It finds that successful models have several common attributes: targeting patients likely to benefit from the intervention; comprehensively assessing patients' risks and needs; relying on evidence-based care planning and patient monitoring; promoting patient and family engagement in self-care; coordinating care and communication among patients and providers; facilitating transitions from the hospital and referrals to community resources; and providing appropriate care in accordance with patients' preferences. Overall, the evidence of impact is modest and few of these models have been widely adopted in practice because of barriers, such as a lack of supportive financial incentives under fee-for-service reimbursement arrangements. Overcoming these challenges will be essential to achieving a higher-performing health care system for this patient population.
Subject(s)
Health Care Costs , Health Services Needs and Demand , Health Services/economics , Health Services/statistics & numerical data , Models, Theoretical , Humans , United StatesABSTRACT
This historical analysis shows that in the years just prior to the Affordable Care Act's expansion of health insurance coverage, black and Hispanic working-age adults were far more likely than whites to be uninsured, to lack a usual care provider, and to go without needed care because of cost. Among insured adults across all racial and ethnic groups, however, rates of access to a usual provider were much higher, and the proportion of adults going without needed care because of cost was much lower. Disparities between groups were narrower among the insured than the uninsured, even after adjusting for income, age, sex, and health status. With surveys pointing to a decline in uninsured rates among black and Hispanic adults in the past year, particularly in states extending Medicaid eligibility, the ACA's coverage expansions have the potential to reduce, though not eliminate, racial and ethnic disparities in access to care.
Subject(s)
Health Services Accessibility/trends , Healthcare Disparities/trends , Adolescent , Adult , Black People , Forecasting , Health Care Costs , Health Care Surveys , Health Services Accessibility/economics , Healthcare Disparities/economics , Healthcare Disparities/statistics & numerical data , Hispanic or Latino , Humans , Insurance Coverage/statistics & numerical data , Insurance Coverage/trends , Insurance, Health , Medically Uninsured/statistics & numerical data , Middle Aged , Minority Health , Patient Protection and Affordable Care Act , United States , White PeopleABSTRACT
This analysis compares access to affordable health care across U.S. states after the first year of the Affordable Care Act's major coverage expansions. It finds that in 2014, uninsured rates for working-age adults declined in nearly every state compared with 2013. There was at least a three-percentage-point decline in 39 states. For children, uninsured rates declined by at least two percentage points in 16 states. The share of adults who said they went without care because of costs decreased by at least two points in 21 states, while the share of at-risk adults who had not had a recent checkup declined by that same amount in 11 states. Yet there was little progress in expanding access to dental care for adults, which is not a required insurance benefit under the ACA. Wide variation in insurance coverage and access to care persists, highlighting many opportunities for states to improve.
Subject(s)
Health Services Accessibility/trends , Insurance Coverage/trends , Insurance, Health/trends , Patient Protection and Affordable Care Act , Adolescent , Adult , Child , Child, Preschool , Dental Care/statistics & numerical data , Health Care Costs , Health Services Accessibility/economics , Health Services Accessibility/legislation & jurisprudence , Health Services Accessibility/statistics & numerical data , Humans , Infant , Insurance Benefits/legislation & jurisprudence , Insurance Coverage/economics , Insurance Coverage/legislation & jurisprudence , Insurance Coverage/statistics & numerical data , Insurance, Health/economics , Insurance, Health/legislation & jurisprudence , Insurance, Health/statistics & numerical data , Medically Uninsured/legislation & jurisprudence , Medically Uninsured/statistics & numerical data , Middle Aged , Poverty , United StatesABSTRACT
As health care providers adopt and make "meaningful use" of health information technology (health IT), communities and delivery systems must set up the infrastructure to facilitate health information exchange (HIE) between providers and numerous other stakeholders who have a role in supporting health and care. By facilitating better communication and coordination between providers, HIE has the potential to improve clinical decision-making and continuity of care, while reducing unnecessary use of services. When implemented as part of a broader strategy for health care delivery system and payment reform, HIE capability also can enable the use of analytic tools needed for population health management, patient engagement in care, and continuous learning and improvement. The diverse experiences of seven communities that participated in the three-year federal Beacon Community Program offer practical insight into factors influencing the technical architecture of exchange infrastructure and its role in supporting improved care, reduced cost, and a healthier population. The case studies also document challenges faced by the communities, such as significant time and resources required to harmonize variations in the interpretation of data standards. Findings indicate that their progress developing community-based HIE strategies, while driven by local needs and objectives, is also influenced by broader legal, policy, and market conditions.
ABSTRACT
The Commonwealth Fund and the Institute for Healthcare Improvement convened 15 experts in May 2013 to help address the current controversy over the measurement of hospital readmissions. Experts agreed that Medicare should, through payment and other means, be encouraging greater coordination of care, improvement in care transitions, and mitigation of risks that leave patients vulnerable to readmission. While the current readmissions metric is undoubtedly an imperfect proxy for broader health system failures, it also provides a valuable foundation on which to build a better policyone that is useful for improvement, fair for accountability, and above all, relevant to patients.
Subject(s)
Continuity of Patient Care/legislation & jurisprudence , Medicare/legislation & jurisprudence , Patient Readmission/legislation & jurisprudence , Continuity of Patient Care/economics , Continuity of Patient Care/statistics & numerical data , Humans , Medicare/economics , Medicare/statistics & numerical data , Patient Readmission/economics , Patient Readmission/statistics & numerical data , Quality Improvement , United StatesSubject(s)
Hospitals/standards , Outcome Assessment, Health Care/methods , Patient Readmission/statistics & numerical data , Reimbursement, Incentive , Risk Adjustment , Causality , Chronic Disease , Delivery of Health Care, Integrated , Health Policy , Health Status , Humans , Medicare/economics , Models, Theoretical , Patient Care/standards , Patient Protection and Affordable Care Act , Quality Improvement , Social Conditions , United StatesABSTRACT
The largest mucosal surface in the body is in the gastrointestinal tract, a location that is heavily colonized by microbes that are normally harmless. A key mechanism required for maintaining a homeostatic balance between this microbial burden and the lymphocytes that densely populate the gastrointestinal tract is the production and transepithelial transport of poly-reactive IgA (ref. 1). Within the mucosal tissues, B cells respond to cytokines, sometimes in the absence of T-cell help, undergo class switch recombination of their immunoglobulin receptor to IgA, and differentiate to become plasma cells. However, IgA-secreting plasma cells probably have additional attributes that are needed for coping with the tremendous bacterial load in the gastrointestinal tract. Here we report that mouse IgA(+) plasma cells also produce the antimicrobial mediators tumour-necrosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS), and express many molecules that are commonly associated with monocyte/granulocytic cell types. The development of iNOS-producing IgA(+) plasma cells can be recapitulated in vitro in the presence of gut stroma, and the acquisition of this multifunctional phenotype in vivo and in vitro relies on microbial co-stimulation. Deletion of TNF-α and iNOS in B-lineage cells resulted in a reduction in IgA production, altered diversification of the gut microbiota and poor clearance of a gut-tropic pathogen. These findings reveal a novel adaptation to maintaining homeostasis in the gut, and extend the repertoire of protective responses exhibited by some B-lineage cells.
Subject(s)
Immunoglobulin A/immunology , Intestine, Small/cytology , Intestine, Small/immunology , Plasma Cells/cytology , Plasma Cells/immunology , Animals , Bone Marrow Cells/cytology , Cell Lineage , Cells, Cultured , Chimera/immunology , Citrobacter rodentium/immunology , Coculture Techniques , Female , Germ-Free Life , Granulocytes/cytology , Granulocytes/metabolism , Immunity, Innate/immunology , Immunoglobulin A/biosynthesis , Intestinal Mucosa/cytology , Intestinal Mucosa/immunology , Intestine, Small/microbiology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Monocytes/cytology , Monocytes/metabolism , Nitric Oxide Synthase Type II/biosynthesis , Nitric Oxide Synthase Type II/deficiency , Nitric Oxide Synthase Type II/metabolism , Phenotype , Plasma Cells/metabolism , Spleen/cytology , Stromal Cells/cytology , Tumor Necrosis Factor-alpha/biosynthesis , Tumor Necrosis Factor-alpha/deficiency , Tumor Necrosis Factor-alpha/immunology , Tumor Necrosis Factor-alpha/metabolismABSTRACT
B cell activation factor of the TNF family (BAFF) is a potent B cell survival factor. BAFF overexpressing transgenic mice (BAFF-Tg mice) exhibit features of autoimmune disease, including B cell hyperplasia and hypergammaglobulinemia, and develop fatal nephritis with age. However, basal serum IgA levels are also elevated, suggesting that the pathology in these mice may be more complex than initially appreciated. Consistent with this, we demonstrate here that BAFF-Tg mice have mesangial deposits of IgA along with high circulating levels of polymeric IgA that is aberrantly glycosylated. Renal disease in BAFF-Tg mice was associated with IgA, because serum IgA was highly elevated in nephritic mice and BAFF-Tg mice with genetic deletion of IgA exhibited less renal pathology. The presence of commensal flora was essential for the elevated serum IgA phenotype, and, unexpectedly, commensal bacteria-reactive IgA antibodies were found in the blood. These data illustrate how excess B cell survival signaling perturbs the normal balance with the microbiota, leading to a breach in the normal mucosal-peripheral compartmentalization. Such breaches may predispose the nonmucosal system to certain immune diseases. Indeed, we found that a subset of patients with IgA nephropathy had elevated serum levels of a proliferation inducing ligand (APRIL), a cytokine related to BAFF. These parallels between BAFF-Tg mice and human IgA nephropathy may provide a new framework to explore connections between mucosal environments and renal pathology.
Subject(s)
B-Cell Activating Factor/genetics , B-Cell Activating Factor/immunology , Glomerulonephritis, IGA/etiology , Animals , Antibodies, Antinuclear/blood , Antibodies, Bacterial/blood , B-Cell Activating Factor/blood , DNA-Binding Proteins/blood , Disease Models, Animal , Female , Gene Expression , Glomerulonephritis, IGA/genetics , Glomerulonephritis, IGA/immunology , Glomerulonephritis, IGA/pathology , Humans , Immunoglobulin A/blood , Immunoglobulin G/blood , Kidney/immunology , Kidney/pathology , Male , Mice , Mice, Transgenic , Transcription Factors/bloodABSTRACT
Between 2004 and 2008, North Carolina's Assuring Better Child Health and Development (ABCD) program quintupled the number of screening tests administered during Medicaid well-child visits to identify young children at risk for developmental disabilities and delays. Referrals to Early Intervention programs quadrupled, helping to increase the percentage of infants and toddlers receiving Early Intervention services statewide--from an estimated 3.0 percent in 2003 to 4.3 percent in 2008. As a result, fewer North Carolina children are entering school with unrecognized or untreated developmental problems. Key elements of the ABCD program include identifying standardized screening tools and training physicians on how to implement them without disrupting the workflow of their practices; building providers' knowledge of referral agencies; helping their practices develop processes for tracking cases; and establishing working relationships with community agencies to enhance communication and bridge gaps in understanding.
Subject(s)
Child Development , Child Health Services/organization & administration , Community Health Services/organization & administration , Community Networks/organization & administration , Developmental Disabilities/diagnosis , Early Intervention, Educational/organization & administration , Neonatal Screening/organization & administration , Referral and Consultation/organization & administration , Child , Child, Preschool , Community-Institutional Relations , Humans , Infant , Infant, Newborn , Medicaid , North Carolina , State Government , United StatesABSTRACT
During an immune response, activated antigen (Ag)-specific T cells condition dendritic cells (DCs) to enhance DC function and survival within the inflamed draining lymph node (LN). It has been difficult to ascertain the role of the tumor necrosis factor (TNF) superfamily member lymphotoxin-alphabeta (LTalphabeta) in this process because signaling through the LTbeta-receptor (LTbetaR) controls multiple aspects of lymphoid tissue organization. To resolve this, we have used an in vivo system where the expression of TNF family ligands is manipulated only on the Ag-specific T cells that interact with and condition Ag-bearing DCs. We report that LTalphabeta is a critical participant required for optimal DC function, independent of its described role in maintaining lymphoid tissue organization. In the absence of LTalphabeta or CD40L on Ag-specific T cells, DC dysfunction could be rescued in vivo via CD40 or LTbetaR stimulation, respectively, suggesting that these two pathways cooperate for optimal DC conditioning.