House
Approves Medicare Reform Package
In a mostly party-line vote, the House approved the "Medicare
Modernization and Prescription Drug Act of 2002," H.R. 4954.
The ACC endorsed H.R. 4954 on the grounds that it would provide
an approximate 6 percent increase in Medicare physician payments2
percent each year from 2003 to 2005. The College commends
those members who responded to the ACC's legislative
alert and contacted their U.S. representative. Most Democrats
were strongly opposed to the legislation because they believe
the centerpiece of H.R. 4954, the $310 billion prescription
drug benefit, is inadequate. The prescription drug benefit
is a key issue for both parties in this election year. It
is anticipated that the Senate will debate Medicare legislation
in July. The ACC is working with other physician organizations
to ensure that physician payment is addressed in any legislation.
For more information on the effort to prevent future reductions,
members should visit the "Fight
Medicare Fee Cuts" section on the ACC Web site.
Proposed
Rule on 2003 Medicare Fee Schedule Offers Some Good News
Under the proposed Medicare Physician
Payment rule for 2003 released on June 28, physician payments
would be reduced by 4.4 percent in 2003 as opposed to the
earlier estimates of a 5.7 percent reduction. However, if
the physician payment provisions of the "Medicare Modernization
and Prescription Drug Act of 2002" passed by the House are
enacted and the final rule is similar to the proposed rule,
the average physician will see a 2.7 percent increase in 2003,
and cardiologists will see a 3.7 percent increase. Cardiovascular
specialists are projected in the proposed rule to fair better
than the average physician with a 3.4 percent reduction-due
in large part to ACC efforts to persuade the CMS to propose
some technical changes in its practice expense methodology.
Changes in the legislation and in the final regulation could
affect the final payment numbers significantly. The impacts
will vary according to the mix of services each physician
provides. A more detailed
summary of the proposed rule is available on the ACC Web
site.
FDA
Approves InSync ICD System, Extended-Release Lovastatin
The FDA last week approved Medtronic's
InSync ICD system for the treatment of heart failure patients
who have ventricular dysynchrony and who are also at risk
for ventricular arrhythmias that could lead to sudden cardiac
arrest. The approval follows close on the heels of the publication
of the MIRACLE
ICD trial, in which the InSync ICD system improved quality
of life measures and exercise capacity, and improved patients'
functional status. The FDA also approved Andrx Corp.'s Altocor,
an extended-release lovastatin. Altocor is Andrx's first internally
developed drug. Up to this point, the company had only produced
generics. According to an Andrx statement, the extended-release
drug achieves "sustained blood levels of the active drug,
resulting in LDL choleseterol lowering of 24 to 41 percent
for the 10 mg to 60 mg dosing ranges approved."
AMA
HOD Votes to Form Organization of Organizations
At the recent AMA House of Delegates meeting, the House voted
to create a committee to develop a plan to transform the AMA
into an organization of organizations. The committee will
bring together interested state medical societies, national
medical specialty societies, and other appropriate components
of the Federation to develop a business plan for the transition.
The plan will be presented to the House of Delegates at the
2003 annual meeting. The House also voted to form an Advocacy
Coordinating Forum (ACF), which will include state and specialty
societies, to better allow medicine to speak with a unified
voice; launch a medical liability reform initiative; and endorse
an 80-hour work week for residents.
CMS
Addresses ACC Concerns Surrounding NCCI Edits
The Administar Federal/CMS has responded to the ACC's letter
of appeal concerning several upcoming edits in the most recent
version of the National Correct Coding Initiative (NCCI),
effective July 1, 2002. As was reported
last week, the ACC had expressed concerns about new edits
that require a modifier when an ECG was performed on the same
day as Microvolt t-wave alternans, 3-D mapping, and electrophysiology
studies. The Administar Federal/CMS clarified that an ECG
can be billed and paid if done on the same date of service
using modifier -59, as long as it is separately performed
on the patient for a reason unrelated to the other procedure.
For example, it is a misuse to report the ECG code when only
3-D mapping is performed on the patient and an ECG has not
been performed for a separate reason. The edits were not meant
to imply that the ECGs were a component code of the other
procedure being performed, Administar Federal/CMS explained.
It was also clarified that new edits affecting anesthesia
codes and cardiology will not affect cardiologists because
they do not bill anesthesia codes.
Florida
Physicians Groups Protest Expansion of "Board-Certified" Designation
State specialty societies in Florida are protesting the state
Board of Medicine's recent decision to allow physicians who
are certified by the American Association of Physician Specialists
(AAPS) to say that they are "board-certified" specialists.
According to a report in the Palm Beach Post, prior
to this decision, only physicians who have completed an American
Board of Medical Specialties-approved residency program could
advertise themselves as board certified. The expansion was
made in February when AAPS, based on a 725-page report that
assessed its certification process, successfully petitioned
the Board to recognize as board-certified specialists those
who had met the AAPS criteria. "One can conclude that such
a change will result in a decrease in the quality of medical
care provided our citizens, a change that is unacceptable
to the profession and our citizens," the state specialty groups
argued in a letter to the Board of Medicine.
FDA
Approves Skin-Based Cholesterol Test
The FDA has approved a new skin-based laboratory test to measure
cholesterol levels. The test-Cholesterol 1,2,3, made by International
Medical Innovations Inc. of Toronto, Canada-is only to be
used in people suspected of having severe coronary artery
disease (defined as 50 percent closure of two or more arteries)
and those with a history of heart attack. The FDA noted in
a statement that the Cholesterol 1,2,3 test "is intended to
be used along withnot as a substitute forthe
standard blood tests." The agency based its approval on a
review of clinical studies that showed, in patients with severe
disease or previous heart attack, it could provide 4 to 15
percent more information about the risk of severe coronary
artery disease beyond that already available with blood cholesterol
and other risk factors.
More
Than 1 Percent of Hospitals Closed in 2000, OIG Reports
In its 13th annual report on hospital closures, the HHS Office
of Inspector General reported last week that 64 general, short-term,
and acute care hospitals closed in 20001.4
percent of all hospitals. Although the same number of hospitals
closed in 2000 as in 1999, 29 hospitals opened or reopened
in 2000, while only 22 opened or reopened in 1999. According
to the
report, the average daily patient load in the year prior
to closure was 23 in rural hospitals and 69 in urban hospitals.
Although residents of a few communities had to travel greater
distances for hospital care, the OIG found, most had emergency
and inpatient medical care available within 10 miles of a
closed hospital. After closure, 31 percent of the hospitals
were being used for other health-related services.
Because
of the July 4 holiday, Advocacy Weekly will not be published
next week.
Advocacy
Weekly is a product of the Advocacy Division of the American
College of Cardiology. Questions or comments regarding this
publication should be directed to the Advocacy Division
at 800-435-9203 or to advocacydiv@acc.org.
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