Welcome to the December Edition of the Catalyst Center E-Newsletter!
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Recent Media Highlights
We took a break...but the world of health care coverage and financing did not!
As you may have noticed, due to the Thanksgiving Holiday there was no Week In Review on Monday. But news still happened! Here are links to some interesting articles that may be important to CYSHCN:Abstract: Identifying children with lifelong chronic conditions for care coordination by using hospital discharge data Neff, J., Clifton, H., Park, K., Goldenberg, C., Popalisky, J., Stout, J., & B. Danielson, Academic Pediatrics Children with lifelong chronic conditions are expensive to care for, and make up a high proportion of the patients at children's hospitals. Using hospital discharge data, this study demonstrates a unique way to identify children with lifelong chronic conditions for care coordination. Abstract: Primary health care quality in a national sample of children and youth with mental health impairment
Bell, J., Johnson, M., Myers, K., & P. Donald, Journal of Developmental and Behavioral Pediatrics This study sought to examine the primary health care quality experience of children aged 5 to 17 years with mental health needs and their families. The analysis focused specifically on provider communication, access to care, and timeliness of service delivery. The results indicated that these health care experiences were rated unfavorably by parents, and that interventions are needed to improve the health care systems currently in place for children and youth with mental health needs. Perceived effects of paid family leave among parents of CSHCN: California's Experience
The RAND Corporation: Health Children with chronic illness make up half of all child hospital days nationwide, require many more medical visits than other children, and miss many more days of school. The parents of this population of CYSHCN often struggle to balance work and the needs of their child. With the intention to minimize the challenges to parents, California implemented a Paid Family Leave Insurance (PFLI) program in 2004, providing parents of chronically ill children up to 6 weeks annually of leave to care for their children, at 55% of salary. This assessment provides an analysis of the program's impact. Exchanges and Advocates: Helping Your State Create a Successful Exchange
By Christine Barber, Health Policy Hub: The Community Catalyst Blog HHS recently released its first guidance on states' creation of insurance Exchanges under the Affordable Care Act - this link to Community Catalyst lists their top ten priorities for advocates in helping to create an effective health insurance Exchange.
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New Digital Story: Working Hard Isn't Enough
When her daughter was born with a complex genetic disorder, Meg Comeau (director of the Catalyst Center) and her family found it difficult to keep up with all the expenses associated with her care, despite having what they thought was adequate insurance.
| Meg and her daughter Sarah in 1987. | Watch Meg's story: "Working Hard Isn't Enough" on our website.
Interested in learning more? Additional stories from the field can be accessed here.
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New Digital Story: Bridging the Gaps for Families of Children with Special Health Care Needs
The Rhode Island Pediatric Practice Enhancement Project (PPEP) places and supports trained Parent Consultants in pediatric primary and specialty care practices. They work as part of the medical home team by assisting families and providers in accessing community-based resources and specialty services. They also help identify barriers to effective care coordination.
This nationally recognized program is a model for cost-effective, parent/professional partnership in the medical home and provides a real-life illustration of the inter-connectedness of the six Healthy People 2010 performance outcome measures for children and youth with special health care needs. Click the image below to view a video story that describes the development of PPEP and the role of the Parent Consultants. View the video to learn more.
| At Federal Hill House in Providence, RI, a parent consultant supports a parent in caring for her child with special health care needs. |
Watch "Bridging the Gaps for Families of Children with Special Health Care Needs"
Interested in learning more? Additional stories from the field can be accessed here.
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Issue Highlight: States seek alternatives to Medicaid spending when families of CYSHCN can least afford them
Many families of children and youth with special health care needs (CYSHCN) depend on public benefit programs like Medicaid and the Children's Health Insurance Program (CHIP) to pay for their child's health-related services. Medicaid and CHIP both provide coverage with little or no cost-sharing for families. Medicaid is particularly important to CYSHCN because enrollees under the age of 21 are entitled to Early Periodic Screening, Diagnosis and Treatment (EPSDT), which is designed to assure preventive treatment and to promote early diagnosis and treatment of identified health needs. In addition to EPSDT, Medicaid offers a wide array of services to CYSHCN, such as Home- and Community-Based Service (HCBS) waivers which allow CYSHCN who meet an institutional level of care to live at home with the right supports.
As our nation slowly recovers from the worst recession since the 1930s, many families continue to face financial challenges after becoming unemployed. In October of 2010, the national unemployment rate was 9.6 percent - up from 6.6 percent in 2008.[1] Many adults who lose their jobs also lose access to their family's employer-sponsored health insurance, putting families at risk for uninsurance at a time when they are less able to afford out-of-pocket health care costs. Fortunately, need-based public benefit programs such as Medicaid were created as a vital safety net to help pay for health care in the wake of economic challenge. This safety net appears to be working for children in general and CYSHCN in particular. While the percentage of people under the age of 65 without health insurance increased from 17.3 percent in 2008 to 18.8 percent in 2009, uninsurance rates for children under 18 remained stable[2] - with much of the credit going to public benefit programs like Medicaid and CHIP.[3] Thanks to these programs, the risk to would-be uninsured families that their child's health status would worsen because of delayed or missed care was lowered.
...Continue reading "States seek alternatives to Medicaid spending" on our website.
[1] Bureau of Labor Statistics. October 2010. "News Release: The Employment Situation - October 2010." Accessed November 29, 2010 at http://www.bls.gov/news.release/pdf/empsit.pdf. [2] DeNavas-Walt, Proctor, & Smith. 2009. Income, Poverty, and Health Insurance Coverage in the U.S.: 2009. US Census Bureau. Accessed November 29, 2010 at http://www.census.gov/prod/2010pubs/p60-238.pdf. [3] Sell, Zlotnik, Noonan, & Rubin. November 2010. The Effect of the Recession on Child Well-Being. First Focus. Accessed November 30, 2010 at http://www.firstfocus.net/library/reports/the-effect-of-the-recession-on-child-well-being.
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COMING SOON
A New Catalyst Center White Paper:
Financing the Mental Health Care of
Children with Serious Mental Health Treatment Needs
Children with serious mental health treatment needs comprise a special population of CYSHCN.[1] Like other CYSHCN, they often face significant barriers to accessing affordable health care but coverage for treatment and services related to mental health can be particularly scarce. As a result, the mental health care they need to play, learn and grow to their fullest potential frequently goes unmet or unreimbursed, putting their families at risk for significant financial hardship.
In an upcoming white paper, the Catalyst Center will examine the barriers faced by children with serious mental health treatment needs and their families in accessing affordable mental health care, and the resultant negative consequences these barriers have on the health and well-being of these children and on the financial stability of their families. The paper will map out the various public options states can offer to expand coverage of mental health services, and discuss the advantages and drawbacks of each. In addition, the white paper will include a section on the potential impact of the Patient Protection and Affordable Care Act (ACA), also known as federal health reform, on children with mental health treatment needs and their families.
While important legislation like the Mental Health Parity and Addiction Equity Act of 2008 has worked to make a difference, historically children with serious mental health treatment needs have been underrepresented in efforts to expand and improve both private and public health insurance options. It is critical that the unique needs of this population of CYSHCN not be forgotten as our nation moves forward with a revamped health insurance system. We hope the Catalyst Center's upcoming white paper will shed some light on these issues and serve as a conversation starter for both policymakers and advocates in their work to improve coverage and financing of care for CYSHCN. Look for the announcement of this paper's publication in an upcoming issue of the E-newsletter and on our website!
Call for perspectives "from the field"
Have you encountered policy issues related to coverage and financing of care for children and youth with serious mental health treatment needs that you think should be addressed in our white paper?
Do you know of successful best practices in coverage and financing for children's mental health services that we should be aware of?
If so, we want to hear from you! Please e-mail your comments and suggestions to Emily Winter, Catalyst Center Research Assistant at ewinter@bu.edu by December 15. Thank you!
[1] As defined by Maternal and Child Health Bureau, children and youth with special health care needs (CYSHCN) are those from birth to age 21 who have, or are at increased risk for, chronic physical, developmental, behavioral, or emotional conditions and need health and related services of a type or amount beyond that required by children generally.
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The Catalyst Center is a national technical assistance and research center
dedicated to working with states and stakeholder groups on
improving health care insurance and financing for
Children and Youth with Special Health Care Needs (CYSHCN).
For more information please visit us at www.catalystctr.org or
contact Meg Comeau, Project Director at mcomeau@bu.edu.
The Catalyst Center is funded under grant #U41MC13618 from the
Maternal and Child Health Bureau, Health Resources and Services Administration
US Department of Health and Human Services.
The Catalyst Center Health & Disability Working Group Boston University School of Public Health 715 Albany Street Boston, MA 02118-2526
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