What Doctors and Patients Have to Lose Under ObamaCare
Changes to Medicare will give the feds
control of surgical decisions.
Democrats are touting the American Medical Association's endorsement of
President Obama's health plan. But there's an important reason why the American
College of Surgeons and 18 other specialty groups are opposed.
The plan's most tangible efforts to restrain medical costs are through its
controls on specialist physicians. Based on the government's premise that they
often make wasteful treatment decisions, the health-care legislation in Congress
will subject doctors to a mix of financial penalties and regulations to
constrain their use of the most costly clinical options. The penalties and
regulations are aimed first and foremost at surgeons and the medical devices
that they use, largely because that's where the bulk of spending is.
It all starts with the sweeping power that the Senate bill gives to the
Centers for Medicare and Medicaid Services. The agency will be given the
authority to unilaterally write new rules on when medical devices and drugs can
be used, and how they should be priced. In particular, the Obama team wants to
give the agency the power to decide when a cheaper medical option will suffice
for a given problem and, in turn, when Medicare only has to pay for the least
costly alternative.
The government has already sought to acquire this same power
administratively. But on Tuesday the Obama Justice department got swatted down
by the U.S. Court of Appeals for the D.C. Circuit, in what the judges described
in their opinion as an attempt by Mr. Obama's legal team to "end-run around the
statute [Medicare]."
Hays v. Sebelius involved a patient who said Medicare unfairly
denied her a prescribed treatment for her serious lung disease. Medicare decided
instead to pay for a different drug that bureaucrats argued was a suitable but
cheaper alternative.
Now the Obama team will use murky provisions embedded in the Senate bill to
subtly attain in law those powers they couldn't more artfully acquire in court.
In fact, the bill lets Medicare seek almost any restrictive payment authority it
wants from a Medicare Commission established for the purposes of cost control.
If Congress believes Medicare has overreached, it has to pass a separate law
to explicitly block the agency's newly acquired powers. These provisions are
deliberately designed to leverage Congress's inability to act in a timely
fashion.
The Senate health-care bill also exempts Medicare's actions from judicial
review, taking away the right of patients to sue the government. Unlike existing
Medicare coverage laws, patients won't have the ability to appeal any of the
decisions of this new Medicare Commission.
Ironically, private health insurers must comply with new patient appeals
rights under the Senate bill. The government has exempted itself from the same
sort of protections.
Thus Medicare will have the power to control which medical devices surgeons
use. But clamping down on expensive procedures also means the agency will need
to have authority over the specialists themselves. The organization of doctors
into mostly small, disaggregated practices always made it hard for a central
bureaucracy to control individual physicians. ObamaCare tries to fix this by
putting doctors on the financial hook for their treatment decisions.
Primary-care doctors who refer patients to specialists will face financial
penalties under the plan. Doctors will see 5% of their Medicare pay cut when
their "aggregated" use of resources is "at or above the 90th percentile of
national utilization," according to the chairman's mark of Section 3003 of the
bill. Doctors will feel financial pressure to limit referrals to costly
specialists like surgeons, since these penalties will put the referring
physician on the hook for the cost of the referral and perhaps any resulting
procedures.
Next, the plan creates financial incentives for doctors to consolidate their
practices. The idea here is that Medicare can more easily apply its regulations
to institutions that manage large groups of doctors than it can to individual
physicians. So the Obama plan imposes new costs on doctors who remain solo,
mostly by increasing their overhead requirements—such as requiring three years
of medical records every time a doctor orders routine medical equipment like
wheelchairs.
The plan also offers doctors financial carrots if they give up their small
practices and consolidate into larger medical groups, or become salaried
employees of large institutions such as hospitals or "staff model" medical plans
like Kaiser Permanente. One provision, laid out in Section 3022, allows doctors
to share with the government any savings to the government they achieve by
delivering less care—but only if physicians are part of groups caring for more
than 5,000 Medicare patients and "have in place a leadership and management
structure, including with regard to clinical and administrative systems."
While these payment reforms are structured as pilot programs in the
legislation, this distinction has little practical meaning. Medicare is being
given broad authority, for the first time, to roll these demonstration programs
out nationally without the need for a second authorization by Congress.
Regulation of medicine has always been a local endeavor, and it's mostly the
province of medical journals and professional medical societies to set clinical
standards. This is for good reason. Medical practice evolves more quickly than
even the underlying technologies that doctors use. This is especially true in
surgery, where advances flow from experimentation by good doctors to try
different surgical approaches.
The regulation of medical devices and their pricing will also have
consequences for patients by discouraging innovation. Most improvements in
medical devices come incrementally, with each generation of a device having
small but clinically relevant advance over prior versions. This owes to the
underlying hardware, which turns on embedded software and microprocessors that
themselves undergo constant upgrades.
But if Medicare starts pricing similar devices off one another—a form of the
same "reference" pricing schemes used in Europe—manufacturers will start holding
back the small changes. Instead, they will introduce new models every four or
five years that are sufficiently unique to fall outside of Medicare's pricing
scheme. Meanwhile, patients will have lost the benefit of regular improvements
and annual upgrades that characterize medical devices today.
The impact of these provisions won't be confined to Medicare. Private
insurance sold in the federally regulated "exchanges" will take cues from
Medicare, since they're both managed from the same bureaucracy. Medicare will
set the standard for medical care across the entire marketplace.
Mr. Obama promised that under his plan people wouldn't have to change their
doctors. But it's clear that doctors will be forced to change how they make
their medical decisions.
Dr. Gottlieb, an internist and a resident fellow at the American
Enterprise Institute, is a former senior official at the Centers for Medicare
and Medicaid Services. He is partner to a firm that invests in health-care
companies.
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