Posts Tagged ‘Department of Health and Human Services’

Cross-Post: A Disappointing Rollback of Consumer Protections on Appeals

Friday, June 24th, 2011

June 23, 2011

The Affordable Care Act (ACA) established many consumer protections, but it was only the first step.  As decisions are made about implementation and regulations, the need for consumer engagement is critical. As an example of where protections could have been stronger, the Department of Health and Human Services just released regulations that relax a number of requirements on health plans and insurers, making it more difficult for consumers to successfully pursue appeals against them.

This is just a reminder that there will be many opportunities in the coming months and years to weigh in on federal regulations as the ACA is implemented – and it’s important for consumers to respond.  Community Catalyst will continue to provide updates about these opportunities and to work with consumer advocates to ensure consumer voices are heard, and state experiences inform the federal debate.

This blog was originally posted on Georgetown Center for Children and Families’ Say Ahh!

Imagine you’re a parent and your child has been diagnosed with cancer and is going through painful, debilitating treatment. You can imagine the sleepless nights, the worry, the exhaustion, the fear. Now imagine that your insurance company denies some of the claims for your child’s treatment – treatment that the doctors assure you are essential to saving your child’s life. If not paid by the insurer, the bills amount to tens of thousands of dollars – putting you at risk of bankruptcy. At a time when your sole focus should be – has to be – your child’s health, you are forced to spend hours on the phone, fighting with health plan bureaucrats.

For President Obama, it was exactly this type of situation that sparked his passion for health care reform. He watched his mother, dying of ovarian and uterine cancer, battle the insurance company from her hospital bed to get insurance coverage for which she’d faithfully been paying premiums. As he said in a 2009 speech to AARP: “That happens all across the country. We are going to put a stop to that.”

And he did. With passage of the Affordable Care Act, for the first time consumers across the country, no matter what plan they’re in, are empowered to appeal their health plans’ decisions to an independent, external review panel. This critical consumer protection is designed to stop the worst of insurance company abuses and was a great win for consumers. In fact, a recent study by the General Accounting Office found that when consumers appeal denied claims, the health plan has to reverse its decision as much as 50% of the time.

Yet, as with everything health reform related, the devil is in the details. And how the appeals provision is implemented matters just as much – if not more – than having the right in the first place. Unfortunately, in a regulation quietly released late yesterday, the Administration relaxed a number of requirements on health plans and insurers, making it more difficult for consumers to successfully pursue appeals. Here are a few specifics:

• Scope of Review. The Administration has significantly narrowed the range of issues consumers can appeal. Originally the rules allowed consumers to seek external review of any adverse benefit decision (except eligibility for the plan). In the new version, consumers can only seek review for claims that involve “medical judgment” or a rescission of coverage. This means that any decision that’s considered “contractual” cannot be appealed to the external reviewer. For example, a plan’s determination that a particular service, drug, or supply is not covered would probably be considered contractual. Unfortunately, according to a recent AMA study, that’s one of the top reason patients’ claims are denied.
•Urgent Care Claims. Originally insurers were required to make a decision on an emergency care claim within in 24 hours of receiving it. In this latest rule, in response to complaints from industry that the time frame was too “burdensome,” the Administration is giving plans up to 72 hours to make a decision. This, in spite of many comments from consumer groups and providers highlighting the need for fast turnaround in emergency situations.
•Translations for Patients with Limited English. The law is clear: plans must provide enrollees with information about their appeal rights in a “culturally and linguistically appropriate manner.” Yet the Administration has significantly weakened this requirement. First, in only 6 counties in the country will plans be required to translate materials into any language other than Spanish. Second, plans only need to provide translations orally. If an enrollee wants translated materials in writing (kind of important if you’re going through the legalistic process of pursuing an appeal), they must proactively request them. Third, the Administration eliminated a requirement that plans keep a record of an enrollee’s language preference. That was, you guessed it, deemed too “burdensome” for the plans.
•Allowing Plans to Forum Shop. Perhaps the craziest part of the new rules is that they allow plans to choose their own judge and jury. Thankfully, this won’t be true in all states. State laws that already have strong laws that ensure an independent, impartial review will not be preempted by the federal rules However, a significant number of states do not have adequate external review laws, and will be preempted by a federal process. The problem is, under the new rules, plans in states subject to the federal process will be allowed to choose their own external reviewer. This is at odds with the recommendations of the National Association of Insurance Commissioners (NAIC), whose model state law on external review requires that external reviewers be randomly assigned (not handpicked by plans) to ensure and independent, impartial process.
•Giving Patients Less Time to File an Appeal. The earlier rule allowed consumers to have 120 days before filing the appeal. In response to complaints from insurance companies that this was too long, the new rule gives consumers only 60 days. Yet for someone struggling with pain, a recent surgery, rehabilitation, or other after-effects of an injury or illness, this time can pass in the blink of an eye. Many patients are likely to miss the deadline, and thereby miss their opportunity to correct an insurer’s bad decision.
•Delaying Implementation. Finally, many of the new appeals protections were to have gone into effect next week.  But in March new rules gave plans until January 1, 2012 (some even later), to comply. For consumers, these delays effectively deny them access to an impartial, fair review of their claim.

Sadly, all of these changes add up to some unfortunate administrative hurdles that will prove challenging for those parents fighting with their health plan to pay for the care essential to cure their child’s illness. Or for sons who must watch their mother battle cancer and her insurance company at the same time. On the other hand, the health reform law provides many of these same families with rights they didn’t have before. I hope that as we transition to 2014, and people gain more experience with their new appeal rights, we can convince policymakers to enact the necessary rules to make them real.

- Sabrina Corlette, Research Professor
Health Policy Institute, Georgetown University

Consumers Win on MLRs!

Thursday, October 21st, 2010

In the final showdown at the NAIC meeting, Insurance Commissioners listened to consumer advocates and took a firm stand on medical loss ratios (MLRs). After a furious week of lobbying by both the insurance industry and consumer advocates, the MLR definition passed without any amendments. This is a critical win that underscores the importance and influence of consumer advocacy on implementation decisions.

The amendments were filed on two issues — national aggregation (filed by Florida) and broker fees (by Ohio) — but were withdrawn after discussion among the Commissioners. An amendment on the most contested issue of late, credibility adjustments (also filed by Ohio), failed to pass by a vote of 34 to 19 (with one abstention).

The final vote to support the MLR definition was unanimous — thanks in large part to the hard work of consumer representatives on the NAIC and advocates around the country who supported them and reached out to their Commissioners on these issues.

Congratulations to all who worked to ensure this victory. It is a great example of how a concerted effort by consumers can have great impact! Next step: HHS approval!

– Christine Barber, Senior Policy Analyst

Consumer Assistance Programs grants, an important victory

Wednesday, October 20th, 2010

Yesterday marked an important victory for health consumers and consumer advocates as the Department of Health and Human Services (HHS) announced nearly $30 million in grants to consumer assistance programs (CAPs) in 35 states, four territories and the District of Columbia.

Community Catalyst has, throughout our history, championed consumer involvement in health care. CAPs are critical to making consumer involvement effective, and as such was one of the primary features of health care reform that we worked hard to see succeed.

The federal funds to create CAPs will establish a range of essential services for consumers to educate them about the new law, aide them with enrollment in health care plans and help them navigate their care options. CAPs are also required to provide feedback to policymakers about any problems with existing laws and regulations. For these reasons, Community Catalyst sees CAPs as a way of linking consumers to the health care system and a vital ingredient to the success of the Affordable Care Act.

While the grants are awarded to states, many will partner with non-profit organizations to provide this assistance, and we continue to urge states to work with consumer advocacy organizations, even in an advisory and oversight role. Community Catalyst has seen the proven consumer assistance work of organizations like Community Service Society of New York and Maine Consumers for Affordable Health Care (CAHC) guide thousands of consumers through the health care process, and know how vital this assistance is to consumers.

In fact, Joe Ditré, executive director of Maine CAHC and a Community Catalyst board member, was recognized by HHS and was one of the featured speakers at yesterday’s press conference announcing the grant awards. He spoke about how CAPs can help all sectors of a community from consumers to health care providers, businesses and insurers. Maine CAHC will contract through their state grant to strengthen its current consumer assistance program.

As many consumers remain confused about how the ACA will affect them, CAPs are one tool to clear up this confusion and educate individuals about changes in health care. The support these programs provide, from outreach to the newly insured to help filling out paperwork, is vital to the success of health reform. And, importantly, the actual impact of these grants will be felt on the ground where individuals and their families will get real help.

— Christine Lindberg, Communications Associate

Insurers behaving badly

Friday, October 1st, 2010

You may have heard that many health insurers across the country (including several major insurers such as WellPoint, UnitedHealth Group, Aetna, Cigna, and Humana) have been announcing the discontinuation of new child-only policies. These are insurance products sold in the individual market to children under age 19 that comprise approximately 8 percent of all individual policies. This is a relatively small group of children to be sure but it’s also a particularly vulnerable one. Parents who work for employers that do not offer insurance plans with dependent coverage and grandparents enrolled in Medicare who act as the primary caregiver for children often rely on these policies.

So, why are insurers saying that they will stop selling these products?

Insurers are discontinuing the sale of new child-only policies to avoid having to comply with a provision in the Affordable Care Act (ACA) that prohibits new group and individual plans from denying coverage for pre-existing conditions for children under age 19. This provision applies to all new plans except grandfathered individual plans (those in existence prior to September 23, 2010). Insurers claim that they are afraid families will only purchase insurance for their children when they are already sick or have significant health expenses (known to health policy wonks as “adverse selection”).

While the concern about adverse selection is not entirely unreasonable, the decision of insurers to address it by ceasing to sell new child-only policies is unnecessary. There are solutions available to insurers that can help to mitigate the risk of adverse selection, as outlined by Secretary of Health and Human Services (HHS) Kathleen Sebelius in this letter to Karen Ignagni, President and CEO of America’s Health Insurance Plans (AHIP). Measures permitted by HHS include (to the extent allowed under state law): allowing insurers to establish open enrollment periods, allowing insurers to adjust rates based on health status, permitting child-only rates to be different from rates for dependent children, and allowing a surcharge to be assessed for dropping coverage and subsequently reapplying.

However, many of AHIP’s members don’t seem to believe that these measures are adequate. Advocates should contact their state insurance departments to explore what creative policy options can be pursued that will result in the continued sale of new child-only policies. For example, the New Hampshire Insurance Department recently issued a bulletin warning insurers that New Hampshire state insurance law and the ACA taken together “require all health insurance carriers to take an application for any of their individual products from any New Hampshire resident, regardless of that person’s age. For an applicant under age 19, a health carrier must guarantee issue any of its individual products.” In other words, insurers offering coverage in the individual market in New Hampshire must offer child-only policies and can’t deny coverage based on a pre-existing condition to a child who applies for such a policy.

Children in New Hampshire are fortunate that advocates and regulators there are working together to require insurers to continue to offer child-only policies. In some states, policy options may be more limited due differences in state insurance laws but it remains important that advocates and regulators across the country work together to ensure that child-only policies remain as widely available as possible.

—Patrick Tigue, Children’s Health Care Coordinator, New England Alliance for Children’s Health

Accepting the Challenge

Friday, September 3rd, 2010

Today is an exciting day in children’s health! As this press release explains, Secretary of Health and Human Services Sebelius is urging leaders from across government and the private sector to join the Connecting Kids to Coverage Challenge. The Challenge issued by the Secretary is to enroll the nearly five million uninsured children eligible for Medicaid and the Children’s Health Insurance Program (CHIP) over the next five years. For additional information about these children, please see this new study published in the journal Health Affairs today and find out your state’s Medicaid/CHIP participation rate on an interactive map by clicking here.

At the New England Alliance for Children’s Health, an initiative of Community Catalyst, we enthusiastically support the Secretary’s efforts and have formally accepted the Challenge. We’ve done this because we believe, just as the Secretary does, that as the nation moves forward with health insurance reform for all Americans, children do not have to wait. Medicaid and CHIP together provide a vital opportunity to extend coverage to millions of eligible but enrolled children today. Will you accept the Challenge?

—Patrick Tigue, Children’s Health Care Coordinator, New England Alliance for Children’s Health

Cross Post: Consumer Assistance: A Guided Tour to Your New Health Care Choices

Thursday, July 29th, 2010

Everyone has heard about some aspect of the Affordable Care Act (ACA), however many people are still confused about the new law. At Community Catalyst, we think Consumer Assistance Programs (CAPs) are vital to ensuring people understand what the changing health care system means for them, and will help people get clear, accurate information about their health care. The ACA set aside $30 million in 2010 to provide grants for state CAPs and ombudsman programs, and last week the Department of Health and Human Services Office of Consumer Information and Insurance Oversight (OCIIO) released the grant guidelines. Today on Say Ahhh! A Children’s Health Policy Blog, one of our senior policy analysts, Christine Barber, explains some of the provisions of the guidelines:

-The grant criteria take steps to ensure that the selected programs are independent. In particular, we are happy to see that the guidelines clearly welcome states to contract with non-profit organizations to provide consumer assistance.

-CAPs must assist people with all types of coverage and provide assistance that is culturally appropriate. In addition, programs must collect data about any problems and questions, which we hope will provide real-time, on-the-ground information about what’s working and what’s not. Regular feedback to state and local policymakers can help improve health reform implementation.

-Each state is eligible for one grant award. Therefore, it is important that states know about this grant program, so consumers can get help, no matter their zip code.

We applaud the guidelines, and have created a summary with the Community Service Society to further explain the grant criteria. Check out the rest of Barber’s post here, or read the full grant guidelines. Applications are due September 10.

– Christine Lindberg, Communications Associate