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1.
J Public Health Dent ; 82 Suppl 1: 140-143, 2022 03.
Article in English | MEDLINE | ID: mdl-35014051

ABSTRACT

Like other areas of health, structural racism has a deep impact on oral health and is a key driver of racial inequities in access to care and outcomes. Racism also structures the relationship between oral health and access to economic opportunities. As a result, communities of color, American Indian/Alaska Native (AI/AN) communities, and low-income populations experience the highest rates of the health, social, and economic costs of dental disease. This is compounded by issues of community-level dental fear/trauma resulting from receiving itinerate care. Dentistry has long struggled to equitably distribute care and diversify its overwhelmingly white and affluent workforce, resulting in many communities not having access to providers who represent their identity and/or live in their community. While multi-generational lack of access to dental care is not unique to Alaska, Alaska Native communities are the home to a reimagined, community-centered care delivery system that is improving health outcomes. For almost two decades, AI/AN leaders have recruited and trained community members to serve as dental therapists-dental team members who offer routine and preventive care responsive to local geographic and cultural/community norms. As members of the communities they serve, dental therapists are fluent in the language and cultural norms of their patients, improving patient-provider trust, access to care, and oral health outcomes. The communities that dental therapists serve are also now investing money and training in their community members, building educational opportunities, and professional wage jobs and directly countering the economic impact structural racism has on oral health.


Subject(s)
Racism , Dental Care , Health Services Accessibility , Humans , Oral Health , Systemic Racism
2.
J Child Health Care ; 23(1): 6-19, 2019 03.
Article in English | MEDLINE | ID: mdl-29772924

ABSTRACT

Children with disabilities utilize more health-care services and incur higher costs than other children do. Medicaid Buy-In programs for children with disabilities have the potential to increase access to benefits while reducing out-of-pocket costs for families whose income exceeds Medicaid eligibility. This study sought to understand how parents and caregivers of Massachusetts children with disabilities perceive access to care under CommonHealth, Massachusetts's Medicaid Buy-In program. Parents and caregivers ( n = 615) whose children were enrolled in CommonHealth participated in a survey assessing the impact of the program. Qualitative data were coded across five access domains-availability, accessibility, accommodation, affordability, and acceptability. Data suggest that CommonHealth improves access to care for children with disabilities by providing the benefits that were limited in scope or unavailable through other insurance before enrollment and by making available services more affordable. Policy and administrative changes could improve the program and further increase access to care for children with complex, costly conditions. Adopting a Medicaid Buy-In program may be an effective way for states to create a pathway to Medicaid for children with disabilities whose family income is too high for Medicaid and who have unmet needs and/or whose families incur high out-of-pocket costs for their care.


Subject(s)
Caregivers/economics , Child Health Services , Disabled Children/statistics & numerical data , Health Expenditures , Health Services Accessibility/trends , Insurance Coverage/economics , Adolescent , Caregivers/psychology , Child , Child, Preschool , Employment/economics , Female , Health Services Accessibility/statistics & numerical data , Humans , Infant , Infant, Newborn , Male , Massachusetts , Medicaid/economics , Qualitative Research , Surveys and Questionnaires , United States
3.
Soc Work Health Care ; 54(6): 547-58, 2015.
Article in English | MEDLINE | ID: mdl-26186425

ABSTRACT

Older adults with Alzheimer's/dementia have high health care costs; they may benefit from home-based care, but few have home visits. This article describes a home-based care program for frail elders, including those with Alzheimer's/dementia. Descriptive statistics are provided for Medicare-enrolled program participants and matched controls with Alzheimer's/dementia on expenditures along six services: skilled nursing facility, inpatient acute, physician, home health, hospice, and social services. Cases with dementia were significantly more likely to have home health and hospice expenditures than controls, suggesting potential for the program to improve end-of-life care. Very few cases or controls had any social service expenditures. Social workers should advocate for the expanded role of home-based care for older adults with dementia and for increased Medicare reimbursement of social work services.


Subject(s)
Dementia/economics , Frail Elderly , Home Care Services/organization & administration , House Calls/economics , Aged , Aged, 80 and over , Alzheimer Disease/economics , Costs and Cost Analysis , Female , Home Care Services/economics , Hospices/economics , Humans , Male , Medicare/statistics & numerical data , Skilled Nursing Facilities/economics , Social Work/economics , United States
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