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Quote of the Week "The greater danger for most of us lies not in setting our aim too high and falling short; but in setting our aim too low, and achieving our mark. " - Michelangelo |
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Health Care Reform
'Grandfathered' Plans: Keep it in the Family?
Robert Wood Johnson Foundation
November 1, 2010
New brief examines what grandfathered health plans mean for consumers, employers and insurers.
...Read More
State steps up as insurers curb policies for sick kids (New Mexico)
By: Trip Jennings
The New Mexico Independent
October 26, 2010
State opens high-risk pool to children with preexisting conditions.
...Read More
HHS announces availability of $3.9 million to support families of children with special health care needs through the state-based Family-to-Family Health Information Centers
HHS
October 26, 2010
HHS Secretary Kathleen Sebelius has announced $3.9 million in funding to continue support for Family-to-Family Health Information Centers.
...Read More
NAIC Rebuffs Insurance on Rule Setting Minimum Medical Payouts for Insurance Policies
By: John Reichard
The Commonwealth Fund
October 21, 2010
The National Association of Insurance Commissioners (NAIC) on Thursday concluded months of intense deliberations on a key rule establishing minimum medical payouts under the health care overhaul law by rejecting arguments that would have given insurers much greater flexibility to meet the standards.
...Read More
Federal Funds to Help Consumers Combat Insurers Roll into States
By: Jane Norman
The Commonwealth Fund
October 19, 2010
Consumers will get help resolving disputes with insurance companies and better information before enrolling in health plans under $30 million in grants awarded to states Tuesday by the Department of Health and Human Services (HHS).
...Read More
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Medicaid
Idaho to cut $8 million in Medicaid services
Associated Press
October 27, 2010
Cuts in Medicaid budget will greatly impact children with special health care needs. ...Read More |
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Events
2011 AMCHP and Family Voices National Conferences
Date: February 12 - 15, 2010
Location: Washington, DC
Registration is now open for the 2011 AMCHP and Family Voices National Conferences.
...Read More
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Catalyst Picks
Many children not receiving needed mental health services
HRSA
October 19, 2010
New HRSA report released on mental and emotional health of US kids.
...Read More The Case for Inclusion: An Analysis of Medicaid for Americans with Intellectual and Development Disabilites
By: United Cerebral Palsy 2010 Report
United Cerebral Palsy has released it's annual report looking at where states stood before the recession in providing community-based Medicaid services for people with intellectual and developmental disabilities.
...Read More |
'Grandfathered' Plans: Keep it in the Family?
Robert Wood Johnson Foundation
November 1, 2010
Policy-makers took care during deliberations over the Affordable Care Act (ACA) to stress that Americans could keep the health insurance they already have, if they wanted to, in a post-reform world. The law 'grandfathered' health plans that were already in effect on that date, and exempted them from many changes the law requires of new health plans. An employer or insurer offering coverage when the ACA took effect in March may elect to-but is not required to-have the plan grandfathered and continue to operate it even after 2014. These grandfathered plans are then subject to some regulations, including that they are generally not permitted to enroll new applicants in the plan. There are also several other permitted exemptions for grandfathered plans, leaving employers and employees alike wondering whether a grandfathered plan or newly established plan is their best option.
A new policy brief from Health Affairs and the Robert Wood Johnson Foundation examines what grandfathered plans mean, and explores just how much a grandfathered plan may change over time and still retain its grandfathered status-such as altering the list of preferred providers or changing the prescription drug formulary. The authors conclude that there are no clear indicators about whether sticking with a grandfathered plan is the best option-and therefore these decisions must be evaluated on a case-by-case basis.
Read the policy brief. ...Back |
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State steps up as insurers curb policies for sick kids (New Mexico)
By: Trip Jennings
The New Mexico Independent
October 26, 2010
Four of the state's major health insurers plan to limit the number of new insurance policies they write for children with preexisting conditions, prompting the state to take action earlier this month to ensure youngsters potentially affected won't go without health coverage.
New Mexico threw open the doors of its high-risk pool to youngsters upon learning that the insurers were, in effect, largely walking away from writing new child-only insurance policies.
The nation's new health care law prohibits insurers from denying coverage to children under 19 with preexisting conditions, but insurance companies fear that means families with sick kids could sign up for policies right before extremely expensive treatments, leaving them with no choice but to cover the sky-high bills.
The board for the New Mexico Medical Insurance Pool voted to waive a rule requiring applicants show proof, usually in the form of rejection notices, that they are uninsurable. The action was taken to ensure the children get coverage, Deborah Armstrong, the pool's executive director, said Monday.
"We saw the children as a class of individuals who wouldn't get insurance coverage," Jason Sandel, acting board chairman of the high-risk pool, told The Independent.
The insurers' decision to severely limit new child-only policies provoked disappointment, even indignation, in some corners Monday.
"While we are proud to be offering coverage to the state's uninsured children at this time, the current neglect of children within the private market is very unfortunate," Sandel is quoted as saying in a news release issued late Friday.
One health care advocate had even stronger words.
"It's hard to hear this in a country that prides itself on equality that we would fight over children with preexisting conditions," said Barbara Webber of Health Action New Mexico, which advocates for affordable and accessible health care.
State doesn't know how many kids will be affected
Lovelace, Presbyterian, United and Blue Cross and Blue Shield all notified the state that they intend to limit how often they will take applications for health coverage for children with preexisting conditions to once or twice a year in open enrollment periods, state officials said Monday. The notifications came during a meeting of the high-risk pool's board Oct. 14 and 15, Sandel said.
That change is a sharp deviation from past practice in which insurers allowed enrollment all year long, and would severely limit how many child-only policies are written.
Presbyterian and Blue Cross Blue Shield could not be reached for comment Monday afternoon. The Independent previously reported on Lovelace Health Plan and its plans to allow parents to apply for child-only health policies only to one month every year.
It is unclear how many children might be affected by their decision. But state officials said the number didn't matter.
"Whether we're talking about one child or 1,000 children up to the age of 19 who aren't being provided services as the Patient Protection and Affordable Care Act (PPACA) intended - these young people will be allowed access to our pool - that's what we do," the state's insurance superintendent, John Franchini, is quoted as saying in last week's news release.
Currently, premium rates for children at the New Mexico Medical Insurance Pool are $142 per month for a $500 deductible plan, according to last week's news release. Premiums are lower for higher deductibles.
Policies will still be available in New Mexico-but parents will only be able to apply during one or two months per year
It's unclear when the health insurers will hold their open enrollment periods. "All of them apparently want to hold their respective open enrollment periods at different times of year," Gerald Garnder, a spokesman for the New Mexico Public Regulation Commission, told The Independent via e-mail Monday.
Franchini and members of the Insurance Division will meet with these companies next week to discuss the particulars, Garner said.
At heart in the insurers' decision is the tug of war inherent in the insurance industry between balancing costs and spreading the risk around of pay outs due to unexpected medical costs.
Insurance is at its core based on the concept of shared risk, meaning the more people who are insured reduces the risk of catastrophic medical costs an insurer is required to pay out in certain situations. A requirement to cover already sick children could expose insurers to large medical costs, industry officials have said.
A health insurance industry representative has described the new federal provision as a powerful incentive to parents to wait until their child becomes sick before they buy insurance, potentially costing insurers money.
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HHS announces availability of $3.9 million to support families of children with special health care needs
HHS
October 26, 2010
HHS Secretary Kathleen Sebelius today announced $3.9 million in funding to continue support for Family-to-Family Health Information Centers, non-profit organizations run by families and for families with children with special health care needs. Funding for the centers was extended through 2012 by the Affordable Care Act.
Created in 2005, Family-to-Family Information Centers provide information, education, training, outreach, and peer support to families of children and youth with special health care needs and the professionals who serve them. The centers are operated by family leaders who have children with special health care needs and expertise in federal and state public and private health care systems, as well as by health professionals. HHS' Health Resources and Services Administration (HRSA) oversees the program.
"These centers take a unique approach to helping families make more informed health care choices for their children with special health care needs, leading to better treatment decisions and improved outcomes," said Secretary Sebelius.
"This program is a model for effective collaboration between families and health care professionals," said HRSA Administrator Mary Wakefield, Ph.D., R.N. "By working together, we can ensure that children with special health care needs get the best care and treatment available."
"The Family-to-Family Information Centers are making a significant contribution to enhancing the lives of children with disability and special health care needs by giving them and their families trusted information and support from families managing similar disability related circumstances everyday," said HHS Office on Disability Director Henry Claypool.
Since its inception, Family-to-Family Health Information Centers have served hundreds of thousands of families and health care providers.
The funding will continue support for Family-to-Family Health Information Centers located in 40 states and the District of Columbia. Centers in the remaining ten states (Alaska, Alabama, Arkansas, Iowa, Idaho, Kentucky, Ohio, South Carolina, West Virginia and Wyoming) were funded during fiscal year 2009. Because they are in their second year of three-year funding, they are not eligible for this funding opportunity.
For more information on the program, and other HRSA maternal and child health programs, visit www.mchb.hrsa.gov/. To view this funding announcement, visit www.grants.gov and enter announcement number "HRSA-11-035." For more information on finding health coverage options for children, visit www.InsureKidsNow.gov. For more information about the Affordable Care Act, visit www.HealthCare.gov.
The Health Resources and Services Administration (HRSA), part of the U. S. Department of Health and Human Services, is the primary Federal agency for improving access to health care services for people who are uninsured, isolated, or medically vulnerable. For more information about HRSA and its programs, visit www.hrsa.gov.
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NAIC Rebuffs Insurance on Rule Setting Minimum Medical Payouts for Insurance Policies
By: John Reichard
The Commonwealth Fund
October 21, 2010
The National Association of Insurance Commissioners (NAIC) on Thursday concluded months of intense deliberations on a key rule establishing minimum medical payouts under the health care overhaul law by rejecting arguments that would have given insurers much greater flexibility to meet the standards.
The recommendations agreed to by the NAIC were hailed by the Obama administration and blasted by the insurance industry.
The nation's largest health insurance lobby-America's Health Insurance Plans (AHIP)-issued a statement predicting that a number of insurers would be forced to drop out of the market as a result of NAIC's action and that others would pare back their spending to improve the quality of care and prevent fraud.
The recommendations, which NAIC will forward to Health and Human Services (HHS) early next week, "will reduce competition, disrupt coverage, and threaten patients' access to health plans' quality improvement services," said AHIP President Karen Ignagni.
HHS Secretary Kathleen Sebelius hailed the NAIC recommendations as a victory for consumers. She said they would not imperil the availability of coverage.
"Not only do they ensure consumers receive better value for their health care dollar, they recognize special circumstances in different markets to preserve market stability and employee coverage," Sebelius said in a statement on NAIC's unanimous vote.
NAIC was responsible under the law for recommending how various types of spending by insurers should be counted-whether as "medical" or "administrative"-under a "medical loss ratio" (MLR) rule setting minimum percentages of premium income insurers must pay for medical care.
The law requires that policies sold to individuals and small groups pay out at least 80 percent of premiums for medical care. In the case of policies sold to larger groups, the minimum is 85 percent. To the extent insurers fall short of the standards, they must issue rebates to purchasers of the policies.
HHS is expected to issue a regulation within weeks based on the NAIC recommendations. The standards take effect Jan. 1. Insurers will have to issue rebates in 2012 in the amount they fall short of the standards in 2011.
Aggregation Rejected
Insurers had hoped to persuade NAIC that their medical payouts could be "aggregated" across the various states in which they operate to calculate a national average. That would have made it easier to meet the standards than having to meet them in each state in which they do business.
But the NAIC rejected the idea of having a national average.
Another issue that the NAIC tackled was compensation of insurance agents. Agents did not want their commissions treated as administrative expenses because insurers likely would trim those payments if they were counted that way. But NAIC decided it did not have the flexibility under the law to count commissions as anything other than administrative spending.
Commissioners did agree, however, to ask HHS to establish a working group to address agent compensation. The National Association of Insurance and Financial Advisors issued a statement praising the commissioners for that action.
NAIFA President Terry K. Headley said that "while disappointed the NAIC did not believe it has the authority to modify the MLR definition to accommodate agent commissions, NAIFA is hopeful that the NAIC and HHS will side with consumers by recognizing that agents need to be compensated for the vital assistance they provide consumers in managing day-to-day health care issues."
Insurers Wanted Transition
Ignagni said that the recommendations would undermine the key goal of the overhaul law, improving access to insurance while minimizing disruption to the existing insurance market. "We are concerned that the current draft proposal will create unintended consequences," she said.
AHIP also emphasized the importance of having NAIC suggest regulations establishing transition periods to ease compliance burdens and complained that the recommendations took too narrow a view of what constitutes quality improvement spending that can be counted under the MLR rule as medical care.
At a press briefing after the vote, one key commissioner said the NAIC knows fully that some insurers may have a tough time meeting the standards being set.
"This is placing on [insurers] some pretty stringent requirements," Kansas Insurance Commissioner Sandy Praeger said. Praeger chaired one of two main NAIC committees overseeing the development of the recommendations.
"There are some companies that probably in the current environment operate below these new established standards," Praeger added. "I think that most [commissioners] feel that the large group market is not going to have much difficulty complying with the 85 percent, but in the individual and small group market where you have a really small book of business there might be some difficulty."
A longtime health insurance executive who requested anonymity in order to speak more freely predicted that Sebelius, who earlier in her career served as the insurance commissioner in Kansas, would ease the impact of the rule on markets where a it looked like a significant number of insurers would drop out.
NAIC "did not issue transition regs, but on the other hand, the secretary has flexibility to issue waivers," the executive said. "It's highly unlikely she would ignore waiver requests where the insurance commissioner or the governor said: 'We need a waiver or the market could be severely disrupted.'"
"She's a former insurance commissioner and really understands these issues, the source said. "On the other hand, she's going to make states justify such requests."
Praise for ruling
Sen. John D. Rockefeller IV, who authored the MLR portion of the overhaul law, and Health Care for America Now (HCAN), a consumer group, praised the NAIC decision.
"Because of this strong standard, health insurance companies across the country will not be able to take advantage of people in states with weaker consumer protections,'' Rockefeller, D-W.Va., said in a statement. "And, those companies that fail to meet the benchmark will be held accountable-if they are overcharging, they will be required to increase benefits, lower premiums, or pay rebates directly to consumers.''
The senator pointed to a report last week by Citigroup Investment Research health analyst Carl McDonald who estimated that had just the minimum MLR rule been in effect for 2010, consumer rebates would have totaled nearly $900 million.
HCAN Executive Director Ethan Rome called the NAIC decision "an important milestone in the implementation of the Affordable Care Act.
"After HHS adopts the commissioners' recommendations, the formal rule will end the insurance companies' practice of spending too few premium dollars on actual medical services even as they deny people the health care they need and charge us more and more."
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Federal Funds to Help Consumers Combat Insurers Roll into States
By: Jane Norman
The Commonwealth Fund
October 19, 2010
Consumers will get help resolving disputes with insurance companies and better information before enrolling in health plans under $30 million in grants awarded to states Tuesday by the Department of Health and Human Services (HHS).
HHS Secretary Kathleen Sebelius announced the grants to 35 states, four territories and the District of Columbia at a news conference at HHS. She said that for years, consumers and small businesses have been left to fend for themselves in the complex and often confusing insurance market. But help is on the way via the new health care law.
"When insurance companies rejected a claim people felt they had nowhere to go," Sebelius said. Now states will use the grant money to educate consumers about their new rights and consumer protections under the law (PL 111-148, PL 111-152).
Karen Pollitz, deputy director for consumer support at HHS's Office of Consumer Information and Insurance Oversight, said many of the programs receiving awards will be at state insurance departments. Congress wanted to provide direct assistance to consumers who have complaints or need to make appeals, Pollitz said. Many of the grantees already have track records recovering money for their state residents, she said.
"These programs are also important because they'll have a sentinel effect," she added. The law requires grantees to collect data and report on problems consumers are encountering. "That will help us to strengthen oversight" and dig deeper into the sources of common problems, she explained.
"Because there will be a watchdog in the marketplace I think everyone will be a little more accountable and a little more careful to provide the coverage consumers are entitled to," she said.
For example, New York will receive $1.76 million to "provide consumer assistance to at least 8,000 New Yorkers with their enrollment in coverage and/or their navigation and disputes with insurance carriers," said an HHS statement. The money will also pay for expanded walk-in services and public education about the state's high-risk pool.
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Idaho to cut $8 million in Medicaid services
Associated Press
October 27, 2010
BOISE, Idaho (AP) - The state is poised to make $8 million worth of cuts to Medicaid programs and services that cater to low-income adults with severe mental illness or children with disabilities like Autism.
The Idaho Department of Health and Welfare has drafted a new set of rules that would authorize cuts designed to save the agency about $1.6 million. The state cuts, however, would also trigger the loss of another $6.5 million in Medicaid matching money used to pay for those services.
Advocates for the mentally ill and disabled say the rules unfairly target a group that can ill afford rollbacks in services and programs.
Set to go in effect in January, the reductions or elimination of some services target programs for adults diagnosed with severe depression and schizophrenia, or children with Asperger's syndrome or other developmental challenges.
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2011 AMCHP and Family Voices National Conferences
Date: February 12 - 15, 2010
Location: Washington, DC
Online registration is now open. Early-bird rates are in effect through Jan. 3. Regular rates will be in effect starting Jan. 4.
Click here to view the AMCHP/Family Voices 2011 Registration Fees Chart.
Schedule and Sessions
Take a look at the AMCHP and Family Voices events that you'll be attending!
The conference will begin on Saturday, Feb. 12, with the AMCHP Annual Conference Training Institute - one and a half days of in-depth skills-building sessions and events. Don't miss these exceptional opportunities for professional growth and understanding - all are included with your full conference registration.
The general conference program kicks off mid-day Sunday, Feb. 13 with a Warm Welcome Coffee Reception and the Welcome Plenary - including the MacQueen Memorial Lecture - followed by a packed agenda of sessions and networking opportunities.
Certain events and sessions will be shared between the conferences and open to all attendees. Shared events begin on Monday, Feb. 14 and include most meals, breaks, and receptions, access to the AMCHP exhibit hall, the Tuesday Plenary session, and Tuesday workshops.
Click here to download our Schedule-at-a-Glance.
Click here to download our Session List.
Click here for more information on the AMCHP/Family Voices Conference!
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Many children not receiving needed mental health services
HRSA
October 19, 2010
Of nearly 7.4 million children in the United States diagnosed with emotional, behavioral, or developmental conditions, a disproportionate number do not get the mental health services they need because they are underinsured, according to a new report released by the Health Resources and Services Administration (HRSA). The study also finds that boys, adolescents, and children from low-income families are affected by conditions such as depression or Attention Deficit Disorder at higher rates than other children, but that adequate health services for these children remain an unmet need.
The report, "The Mental and Emotional Well-Being of Children: A Portrait of States and the Nation 2007," identified seven emotional, behavioral, or developmental conditions: depression, anxiety, Attention Deficit Disorder/Attention Deficit Hyperactivity Disorder, conduct disorders, autism spectrum disorders, developmental delay and Tourette Syndrome. Children with these conditions can benefit from a variety of therapies including counseling and medication.
Additional findings include:
- 11.3 percent (nearly 7.4 million) of children in the United States are reported by their parents to have been diagnosed with emotional, behavioral, or developmental conditions.
- Nearly two-thirds (65.7 percent) are boys
- More than half (51.1 percent) are between the ages of 12 and 17 years
- Nearly one-quarter (24.8 percent) have family incomes below the Federal poverty level
- One-third of these children have also been diagnosed with a chronic physical condition
- 29.4 percent of diagnosed children with insurance were reported by their parents to have insurance that did not usually or always meet their needs.
- 40.3 percent of diagnosed children have more than one emotional, behavioral, or developmental condition.
- 45.8 percent of children with one or more emotional, behavioral, or developmental conditions also had learning disabilities, compared to 2.7 percent of children without these conditions.
More in-depth information about the survey and its findings can be found at:
http://www.mchb.hrsa.gov/nsch/07emohealth/index.html.
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The Case for Inclusion: An Analysis of Medicaid for Americans with Intellectual and Development Disabilities
By: United Cerebral Palsy
2010 Report
The 2010 Case for Inclusion report (medicaid.ucp.org) ranks all 50 states and the District of Columbia (DC) for Medicaid services provided to persons with intellectual and developmental disability (ID/DD). The fifth annual rankings reveal:
- Despite significant progress, all states have room to improve outcomes and services for individuals with ID/DD, particularly in the current economic climate.
- Too many Americans with ID/DD still do not live in the community, although real and notable progress have been made since last year.
- Certain states are making substantial progress.
- Too much money is still spent isolating people in large institutions, with nominal change since 2009.
- Waiting lists have increased dramatically, but performance is quite mixed by state; most are not serving everyone in need.
Top/bottom ten states in terms of quality of Medicaid service provided:
1) Arizona; 42) Virginia;
2) Vermont; 43) Ohio;
3) New Hampshire; 44) Indiana;
4) Washington; 45) Tennessee;
5) California; 46) Utah;
6) Massachusetts; 47) DC;
7) Michigan; 48) Illinois;
8) Connecticut; 49) Texas;
9) Colorado; 50) Arkansas;
10) Hawaii; 51) Mississippi
Seventeen states shifted by at least five places in the rankings from 2009 to 2010, and 21 states shifted at least six places in the rankings from 2007 to 2010. Highlights include:
- An impressive 22 states (up by three) from 2009 and an increase from 16 states in 2007 have more than 80% of those served living in home-like settings.
- From 2005 to 2008, an impressive 13 states reduced the number of Americans living in large institutions by 20% or more.
- Overall the number of Americans with ID/DD on waiting lists for residential services has increased 56% from 2005 to 2008.
This report focuses on what is being achieved; not how much or how little money is being spent. While current Federal Stimulus funds have alleviated Medicaid spending pressures at the state level to a large extent, Medicaid shortfalls are projected to come roaring back in 2011, if the temporary increase in Medicaid funds run out.
Click on this link to access the full report.
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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).
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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