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Issue Brief May 2001 A Patient's Bill of Rights |
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I.
Introduction So why haven't they passed anything yet?
The answer lies in one simple word - LIABILITY.
So why don't they stop trying? The answer lies in another simple word - POLITICS. All recent polling data -- before, during, and after
the last campaign -- show that the public feels very strongly about this
particular issue. In fact, a post-election survey conducted by the Kaiser
Family Foundation and Harvard School of Public Health last January shows
that 76 percent of the voting population favors some form of Patients'
Rights Legislation. And,
unlike many other health care issues, this one garners strong support from
voters of all political persuasions with 71 percent of Republicans, 81
percent of Democrats and 76 percent of Independents supporting the idea of
a patients' bill of rights. So what are the issues?
What problems have been solved?
And, more importantly, what problems remain? II. The
Issues in Agreement A.
Information Disclosure B.
Access to Specialists C.
Access to Emergency Services D.
Prohibition of Gag Rules E.
Grievance Appeals Process While there are still many possible areas of
disagreement within these issues, committees in both houses of Congress
and members in both parties have come a long way to resolving most of the
issues and could very likely pass a bill on these issues.
III.
Major Unresolved Areas of Disagreement A. ERISA The act established an elaborate regulatory system to
ensure that employees receive the benefits their employers promise them.
It tried to create a uniform set of requirements that would govern
the administration of pension and benefit plans.
The intention of the act's sponsors was twofold:
first to prevent the type of fraud and mismanagement that had
occurred in the past, and second, to allow employers doing business in
more than one state to design benefit plans that could operate nationwide
and would not face conflicting state requirements.
In order to accomplish the second goal, Congress incorporated broad
language in ERISA that preempted state laws regulating benefit plans. The sponsors of ERISA were
responding to pension benefit abuses and could not have foreseen the
effect its preemptions of state law would have on the future delivery of
health care. They intended
their legislation to protect plan assets and ensure fiduciary propriety
and prudence. Remedies
included under the law were geared toward accomplishing that goal not
designed to protect beneficiaries needing services such as medical care. When ERISA passed, the health
care delivery system was quite different from what it is today.
In 1974, almost all employer-sponsored health plans were
traditionally insured, fee-for-service plans. In those systems, if an
individual believed his or her doctor had injured or harmed him, he could
pursue legal remedies under state medical malpractice laws.
This is still true for individuals who receive their medical care
under non-ERISA health plans. Under ERISA governed health
insurance plans or HMO's, individuals who are denied treatment or
otherwise injured must pursue the plan for remedy.
Because of ERISA preemptions, these patients are often denied the
"right to sue" under state medical malpractice laws. (The
federal court system has neither the remedies nor the established
infrastructure to provide justice to them.)
Medical malpractice cases
have traditionally been the purview of the states.
When ERISA passed, no one anticipated it being used to protect
health care providers from legitimate claims in the event of injury or
death due to medical malpractice. But
that is what has happened in many instances when employer-sponsored
managed care entities have successfully argued that their decisions were
fiduciary decisions and, therefore, were protected from state purview
under ERISA's preemption provisions. There is no evidence that
Congress intended ERISA to regulate the clinical quality of medical care
or medical malpractice and the courts have been wrestling with this
problem for several years. Case
law has evolved and last year the United States Supreme Court reaffirmed
the primacy of state law in the case of Pegrim v Herdrich.
In this case the Court distinguished between medical decisions and
fiduciary decisions. Here the
court noted that decisions often claimed to be fiduciary are actually
mixed eligibility and treatment decisions.
It stated that Congress did not intend "...to federalize
malpractice litigation in the name of fiduciary duty ...."
Because of the many
difficulties involved in sorting out these cases, several judges have
asked Congress to pass legislation clarifying the situation.
And, that is where today's conflict lies. IV.
Proposals for Reform On another side of the issue,
doctors, trial lawyers, and patient advocates argue that amending ERISA to
include a "right to sue" for injured plan participants need not
increase costs significantly if it is done properly. Further they argue that this is a fundamental right people
should have and all other protections provided by a patients' bill of
rights become meaningless if they are not backed up by the ultimate remedy
of a "right to sue". After
all, what good does it do people to have a bunch of contractual rights if
they cannot be enforced in court? These conflicts are further
illuminated when compromise solutions are offered. For instance, the employers are most adamantly opposed to
exposing health plans to both federal and state tort liability as some of
the bills propose. Employers
argue that the medical tort liability system is broken and subjecting
group health plans to a broken tort system will only hurt plan
participants and their dependents as more and more employers opt out of
the system all together. They instead favor a more
limited approach that would rely on binding independent external review to
resolve disputes over benefit determinations. And if they have to live
with any liability exposure they want it to be very limited, in federal
court, and subject to caps. (Currently,
federal remedies only allow a patient to recover the value of treatment
that was denied. There is no
ability to receive economic damages or awards for other damages such as "pain and suffering".) The doctors and patient
advocates argue for a much stronger liability protection. They want a basic federal standard that sets a floor on
consumer protections in health care.
If states want to go beyond the federal floor and provide more
protections that would be fine with them but all consumers throughout the
country would have a clear set of basic rights that do not change
regardless of where they live. And,
they want these protections to be enforceable in court. On February 6. Senators John
McCain, Edward Kennedy and John Edwards introduced a bill that would allow
patients harmed by treatment denials or delays to sue their managed care
plans in state court, subject only to the damage caps in their state.
They would also allow civil assessments of up to $5 million in
federal court "if clear and convincing evidence of bad faith and
flagrant disregard for a patient's safety is proven."
In other provisions of the bill they would require federal courts
to deal with contract questions while state courts would handle medical
questions. The following day, President
Bush laid out his principles for a bipartisan patients' bill of rights.
In that statement he proposed that patients be allowed to sue their
health plans for denial of needed medical care in federal court after an
extended review process. To discourage excessive litigation he recommended capping the
damage awards. On May 15, the President gave
his support to legislation introduced by Senators Bill Frist, John Breaux,
and Jim Jeffords that would not expand patients' rights to sue in state
court but would give them a limited right to sue in federal court and win
more money than is currently possible.
As I noted earlier, today patients with successful federal lawsuits
can only win the value of the medical care they were denied.
Under the Frist proposal, injured patients could also recover
damages to reimburse them for lost earnings, medical expenses and related
costs. The bill would
prohibit punitive damages and limit pain and suffering awards to $500,000. Patients who want to sue
would have two basic kinds of constraints.
In most cases they would have to bring their complaint to a new
outside review panel and then they could only sue if the panel rejected
their complaint. The bill
would also not expand their right to sue in state court.
Since the state court system has a much more developed
infrastructure for dealing with medical malpractice issues and is usually
more convenient and closer to most people, the requirement that patients
take their complaints to federal court is also a "de facto"
impediment to litigation. V.
Conclusion It looks like after eight
long years the public may have to wait a while longer to see some
resolution of this issue. Nevertheless,
having the President endorse a specific bill breathes new life into the
issue and there will probably be further action in this area soon. It remains to be seen whether
the deep ideological and practical problems posed by the liability
provisions can be solved this year. And
it also remains to be seen whether we will ever get national legislation
to reform the whole medical liability tort system even though Senator Jack
Danforth and I proposed national tort reform years ago.
Our efforts were opposed by some of the people who are currently
supporting this bill including the American Trial Lawyers Association and
Public Citizen. While
there is general agreement that the tort system needs to be reformed, it
has been agreed by the major actors working on the Patient's Bill of
Rights that they are not going to be able to take on that problem in this
legislation. The
Institute of Medicine reports have stimulated the search for safe and
error-free medical systems including the need for reporting of adverse
events and comparative performance data.
Purchaser-payors and lawyers obviously see great advantage in this
while the medical professions strongly resist.
It is imperative that policymakers take some of the energy they are
devoting to the patients’ bill of rights and turn their attention to
enacting those public policies that improve system performance.
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