[House Hearing, 109 Congress]
[From the U.S. Government Publishing Office]
THE MEDICARE VALUE-BASED PURCHASING FOR PHYSICIANS ACT
=======================================================================
HEARING
before the
SUBCOMMITTEE ON HEALTH
COMMITTEE ON WAYS AND MEANS
U.S. HOUSE OF REPRESENTATIVES
ONE HUNDRED NINTH CONGRESS
FIRST SESSION
__________
SEPTEMBER 29, 2005
__________
Serial No. 109-42
__________
Printed for the use of the Committee on Ways and Means
_____
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COMMITTEE ON WAYS AND MEANS
BILL THOMAS, California, Chairman
E. CLAY SHAW, JR., Florida CHARLES B. RANGEL, New York
NANCY L. JOHNSON, Connecticut FORTNEY PETE STARK, California
WALLY HERGER, California SANDER M. LEVIN, Michigan
JIM MCCRERY, Louisiana BENJAMIN L. CARDIN, Maryland
DAVE CAMP, Michigan JIM MCDERMOTT, Washington
JIM RAMSTAD, Minnesota JOHN LEWIS, Georgia
JIM NUSSLE, Iowa RICHARD E. NEAL, Massachusetts
SAM JOHNSON, Texas MICHAEL R. MCNULTY, New York
PHIL ENGLISH, Pennsylvania WILLIAM J. JEFFERSON, Louisiana
J.D. HAYWORTH, Arizona JOHN S. TANNER, Tennessee
JERRY WELLER, Illinois XAVIER BECERRA, California
KENNY C. HULSHOF, Missouri LLOYD DOGGETT, Texas
RON LEWIS, Kentucky EARL POMEROY, North Dakota
MARK FOLEY, Florida STEPHANIE TUBBS JONES, Ohio
KEVIN BRADY, Texas MIKE THOMPSON, California
THOMAS M. REYNOLDS, New York JOHN B. LARSON, Connecticut
PAUL RYAN, Wisconsin RAHM EMANUEL, Illinois
ERIC CANTOR, Virginia
JOHN LINDER, Georgia
BOB BEAUPREZ, Colorado
MELISSA A. HART, Pennsylvania
CHRIS CHOCOLA, Indiana
DEVIN NUNES, California
Allison H. Giles, Chief of Staff
Janice Mays, Minority Chief Counsel
______
SUBCOMMITTEE ON HEALTH
NANCY L. JOHNSON, Connecticut, Chairman
JIM MCCRERY, Louisiana FORTNEY PETE STARK, California
SAM JOHNSON, Texas JOHN LEWIS, Georgia
DAVE CAMP, Michigan LLOYD DOGGETT, Texas
JIM RAMSTAD, Minnesota MIKE THOMPSON, California
PHIL ENGLISH, Pennsylvania RAHM EMANUEL, Illinois
J.D. HAYWORTH, Arizona
KENNY C. HULSHOF, Missouri
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C O N T E N T S
Page______
Advisory of September 22, 2005 announcing the hearing............ 2
WITNESSES
Centers for Medicare and Medicaid Services, Hon. Mark McClellan,
Administrator.................................................. 7
______
American Medical Association, John H. Armstrong, M.D............. 52
America's Health Insurance Plans, Karen Ignagni.................. 43
Jevon, Thomas, M.D., Practicing Family Physician................. 39
Urban Institute, Robert Berenson................................. 32
SUBMISSIONS FOR THE RECORD
California Medical Association, San Francisco, CA, joint letter.. 67
Ebeler, Jack, Alliance of Community Health Plans, statement...... 71
EmCare, Inc., Dallas, TX, statement.............................. 75
Griskewicz, Mary, Healthcare Information and Management Systems
Society, Alexandria, VA, statement............................. 77
Johnson, Michele, Medical Group Managment Association, statement. 78
Mennuti, Michael, American College of Obstetricians and
Gynecologists, Washington, DC, letter.......................... 80
Moore, Justin, American Physical Therapy Association, Alexandria,
VA, statement.................................................. 81
Wojcik, Steven, National Business Group on Health, statement..... 84
THE MEDICARE VALUE-BASED PURCHASING FOR PHYSICIANS ACT
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THURSDAY, SEPTEMBER 29, 2005
U.S. House of Representatives,
Committee on Ways and Means,
Subcommittee on Health
Washington, DC.
The Subcommittee met, pursuant to notice, at 3:00 p.m., in
room 1100, Longworth House Office Building, Hon. Nancy L.
Johnson (Chairman of the Subcommittee) presiding.
[The advisory announcing the hearing follows:]
ADVISORY
FROM THE
COMMITTEE
ON WAYS
AND
MEANS
SUBCOMMITTEE ON HEALTH
CONTACT: (202) 225-3943
FOR IMMEDIATE RELEASE
September 22, 2005
No. HL-9
Johnson Announces Hearing on the Medicare Value-Based Purchasing for
Physicians Act
Congresswoman Nancy L. Johnson (R-CT), Chairman, Subcommittee on
Health of the Committee on Ways and Means, today announced that the
Subcommittee will hold a hearing on H.R. 3617, the ``Medicare Value-
Based Purchasing for Physicians' Services Act of 2005.'' The hearing
will take place on Thursday, September 29, 2005, in the main Committee
hearing room, 1100 Longworth House Office Building, beginning at 3:00
p.m., or immediately following the full Committee hearing.
In view of the limited time available to hear witnesses, oral
testimony at this hearing will be from invited witnesses only. However,
any individual or organization not scheduled for an oral appearance may
submit a written statement for consideration by the Committee and for
inclusion in the printed record of the hearing.
BACKGROUND:
H.R. 3617, introduced by Congresswoman Johnson on July 29, 2005,
would repeal the Sustainable Growth Rate formula and replace it with a
stable and predictable annual update based on changes in the costs of
providing care. Such payments would be linked to health care quality
and efficiency.
This legislation would provide a differential payment update to
practitioners meeting pre-established thresholds of quality or pre-
established levels of improvement, equal to the Medicare Economic Index
(MEI). Practitioners not meeting these thresholds would receive an
update of MEI, minus 1 percent.
Measures of quality and efficiency would include a mix of outcome,
process and structural measures. Clinical care measures must be
evidence-based. Practitioners would be directly involved in determining
the measures used for assessing their performance.
The Centers for Medicare & Medicaid Services would be required to
analyze volume and spending growth annually, and make recommendations
on regulatory or legislative changes to respond to inappropriate
growth. The Medicare Payment Advisory Commission would review this
report and recommendations.
In announcing the hearing, Chairman Johnson stated, ``I introduced
the Medicare Value-Based Purchasing Act in response to testimony at our
three Subcommittee hearings on physician payments and value-based
purchasing this year. Many of my colleagues on this Subcommittee and in
the House support this bill, and I thank them for that support. For
several years, I have argued that the current Medicare payment system
for physicians is unsustainable. I believe that this legislation
represents an important step in our efforts to move Medicare into the
twenty-first century. We have the ability to vary payment based on the
quality and efficiency of care delivered to our seniors under Medicare,
and we should use it. This hearing will offer the Subcommittee an
opportunity to hear from witnesses about this important legislation.''
FOCUS OF THE HEARING:
The hearing will focus on the provisions in H.R. 3617.
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Chairman JOHNSON. Good afternoon, everyone. I am going to
call the hearing to order. Pete is on his way, but I am going
to start with my opening statement, assuming that he will
survive not hearing it. We are going to have five votes in an
hour, so we are going to try to hear all of our witnesses
before we do have to vote because it is such a long recess, and
after that, of course, people are flying off to planes. Let me
just open by saying I am very pleased to be holding this
hearing on actually a legislative initiative that we introduced
and a series of amendments that we have circulated. I want to
thank many of my colleagues on the Subcommittee for
cosponsoring the legislation and for many others for taking an
intense interest in it, because I think this initiative
represents an attempt to move into the 21st century. It is not
going to be perfect, but it is a serious start. There are 80
pay-for-performance systems out there already, and I think it
is very important that the Federal Government set a model of
how you do this and try to make sure that as the Nation moves
in this development--in this direction, there is some
homogeneity in both process and criteria.
Today's legislative hearing on H.R. 3617 follows a series
of hearings by this Subcommittee to explore ways to address
physician reimbursement under the Medicare Program. This
legislation incorporates the many ideas brought to the
Subcommittee by government agencies, physician and other
practitioner organizations, purchasers with experience in
value-based purchasing in the private market, and
representatives of Medicare beneficiaries. To promote health
care quality, as well as efficiency in Medicare, the bill would
no longer pay providers the same amount regardless of the
quality of the care they provide. Payment updates would be
linked to health care quality and efficiency. Under this
legislation, Medicare would provide a differential update for
physician services. All practitioners would receive a 1.5-
percent update in 2006 instead of the 4.4-percent decrease
projected under the current law, and in 2007 and thereafter--
2007, 2008, practitioners who report quality and efficiency
measures would receive an update equal to the medical economic
index (MEI). Those who do not report will receive a lower but
still positive update equal to the MEI minus 1 percentage
point. This is similar to how we currently pay hospitals under
Medicare.
Beginning in 2009, practitioners who meet pre-established
thresholds of quality or show pre-established levels of
improvement would receive a payment update equal to the MEI.
Those who do not meet this threshold would receive a positive
but lower update equal to MEI minus 1 percentage point. The
legislation provides a structure for a value-based program. It
outlines characteristics that quality measures must satisfy.
For example, measures must include a mix of outcome, process
and structural measures; be evidence-based if they are related
to clinical care; be consistent, valid, practical and not
overly burdensome to collect. So, there are a number of
criteria in the bill that measures must meet to assure that
they are objective and quality-oriented. The program must
address issues of fairness by adjusting measures and ratings to
account for very sick patients, those who cannot or do not
comply with directives or who are located in neighborhoods
where traditions delay entry into the health care system. It is
critically important that the value-based program not encourage
patient selection or de-selection. The legislation outlines a
process for selecting measures that ensures that practitioners
would be directly involved in the measures used to gauge their
performance.
Practitioners would submit clinical care--I am going to cut
short my opening statement and not go through the whole
process. It is laid out in the bill. But I do want to note that
I believe it is terribly important that clinicians have control
over clinical measures. So, in the bill, they do make the
proposals, and while the consensus-building body builds
consensus around which measures are most important to use, the
government actually cannot invent clinical measures. The
government can initiate on its own process and structural
measures and goes through the rulemaking process to assure that
they receive public input in the process of identifying
measures in those categories.
Our witnesses provide their thoughts on this legislation
and on the amendments that we have circulated. On our first
panel we have Dr. Mark McClellan, the Centers for Medicare and
Medicaid Services (CMS) Administrator. Our second panel
includes Dr. Robert Berenson of the Urban Institute and a
former CMS official who brings us a wealth of knowledge about
physician payments. Dr. Thomas Jevon is a family physician in
solo practice located in Wakefield, Massachusetts, who will
provide input from that perspective. Dr. Jevon also will share
his experiences with the Bridges to Excellence quality
improvement program as a solo practitioner. Karen Ignagni, from
America's Health Insurance Plans, will provide us with a
purchaser's point of view and give us examples of value-based
purchasing programs from her member companies. Our last
witness, Dr. John Armstrong from the American Medical
Association (AMA), will present the views of physicians of the
AMA, many of which have had experience with physician payment
systems similar to that recommended in the legislation. Mr.
Stark, welcome, and would you like to make an opening
statement?
Mr. STARK. I would love to. Thank you, Madam Chair. This is
our fourth hearing this year on this physician payment system
or problem, and we still haven't focused in on the underlying
issues that got us to where we are today. The administration,
majority, organized medicine and, I suppose, us by acquiescence
all know full well what the temporary increases in the Medicare
Modernization Act (MMA), would exacerbate the cliff or the drop
that we now face, yet we have done nothing to craft a solution.
We have had a lot of hearings, but no solutions. Organized
medicine and many in Congress have proposed to just repeal the
sustainable growth rate (SGR) with little or no discussion or
options as to what we could replace it with. I am not going to
defend the SGR, but--I will let Chairman Thomas do that--but in
my view, simply repealing it isn't an option. I think you told
us, Dr. McClellan, sometime in previous testimony that we are
talking $180 billion to do it, and that is a little scarce
right now. People are quite enchanted, if not overly focused,
on the this notion of pay for performance. Done properly, that
would show me some promise. But I don't believe it can be done
without a decent information technology plan in place.
I would be willing to look, but I just don't--I think that
particular issue--and I don't think until we are able to have
complete electronic recordkeeping and universal recordkeeping
that we can track pay for performance. Even then I suspect it
would take several years, if not 10, to get the whole system
going. I think the best thing we have now are the
demonstrations that CMS has for hospitals and physicians, and I
think we could watch those and evaluate those and have a better
idea then of how to expand from the demonstrations that are now
going forth. To rush to embrace this, is a fad as I call it,
has diverted our attention from underlying problems in
physician reimbursement, a system that needs to have these
problems addressed; RBS utilization, Committee process, coding
issues, perverse incentives, a whole host of things that I
think we have to straighten out. The critical component of fee-
for-service Medicare has been ignored. The current system
allows abusive providers to profit while the prudent providers
pay the price in terms of reduced fees. We have to keep in mind
that physician increases lead to premium increases unless we
prevent it. Our beneficiaries are going to have record high
increases, the next year increase again significant. We need to
protect these premiums, and I share AARP's stand on this.
I want to remind everyone--and although I would not be so
skeptical as to suggest it was intentional--increased physician
spending will get us very quickly toward this arbitrary 45-
percent cap on Medicare's general revenue support. That to me
is the sword of Damocles hanging over our head, and if that
drops, we are in the soup. That, in effect, destroys Medicare
as we know it. If that is the intention of the administration
and the majority, fine, let's talk about it; but the idea that
we hit the 45-percent cap and then we no longer have an
entitlement to me is something that I think should be repealed
or else addressed with some replacement for Medicare as an
entitlement. I would be willing to, as I discussed with the
Chair and with Dr. McClellan, to support--whether you care
whether I support it or not--but I would be willing to
negotiate to support some kind of a 2-year override in the plan
cuts, provided that we have some concrete steps for a new
mechanism, whether it is geographic or specialty-specific
targets, that would keep some control on overall expenditures.
The best way, of course, to pay for this all would be to bring
the plan payment down to fee-for-service rates, which is what
we always intended, and nobody has ever shown me that the plans
deserve this outrageous bonus that they are getting. In the
meantime, I would support starting with pay for performance in
the private plans. Let us start with these plans as MedPAC has
recommended. They already have the data. They claim they
deliver high-quality care. Let us hold them accountable, and,
as they say, let us see if they can walk the walk as well as
they talk the talk. Thanks.
Chairman JOHNSON. Thank you very much, Pete. I would like
to just acknowledge the presence of two of the Republican
physicians who have been very actively interested in the health
care legislation that we have been working on, Dr. Burgess of
Texas and Dr. Gingrey of Georgia. Welcome to sitting with us
this afternoon. All of the issues that Pete raised will be a
part of our discussion as we move forward. There are two sides
to every matter, and I hope that we can come to an
understanding that allows my colleague from California to work
with me on this legislation, because I certainly respect his
concerns. Dr. McClellan.
STATEMENT OF THE HONORABLE MARK MCCLELLAN, M.D., PH.D.,
ADMINISTRATOR, CENTERS FOR MEDICARE AND MEDICAID SERVICES, U.S.
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Dr. MCCLELLAN. Madam Chairman, Congressman Stark,
distinguished Subcommittee Members and other distinguished
Members, thank you for the opportunities to be with you here
this afternoon. In recent weeks we have seen once again the
critical role that physicians play in helping people recover
and stay well. We saw this in the response to Hurricane Katrina
where when evacuees needed care all through the gulf coast and
around the country, local physicians did not ask, how is this
going to be paid for, what are the rules? They asked, what kind
of care and assistance do evacuees need? They started providing
it. We responded by supporting those efforts through
modifications in our rules in Medicare and Medicaid and setting
up a new waiver program that is already now available to most
evacuees in our payment systems. In addition, I want to thank
the physician community for being one of our most critical
partners as we work to bring new drug coverage to Medicare
beneficiaries on schedule and nationwide. Physician
organizations and physicians all over the country have taken
steps, like making available brochures and other information on
where their patients can get the support they need to take
advantage of the new coverage.
On average, seniors are going to see their out-of-pocket
costs fall by many hundreds of dollars next year, and I truly
appreciate the effort physicians are taking to ensure that
their patients have access to the medicines they need in this
new program. As you well know, physician participation and
leadership are also critical in providing care to beneficiaries
in Medicare. We need to ensure that physicians are adequately
compensated for this care in the Medicare Program, but how we
pay also matters. Medicare's payment system for physicians
should be set up to encourage and support them in providing
quality care and preventing avoidable health care costs. After
all, physicians are in the best position to know what can work
best to improve their practice. Updates in the current payment
system for physician services are now projected to be negative
for the next 7 years. Continued negative updates for many years
are not sustainable in terms of assuring access to quality care
for Medicare beneficiaries. At the same time, simply increasing
spending by adding larger updates into the current payment
system is also not sustainable from the standpoint of
Medicare's costs or beneficiary premiums and cost sharing, so
it is critical now for Medicare to support physicians in
achieving better care for our beneficiaries at a lower overall
cost.
I would like to thank you, Madam Chairman, for your
leadership on this issue. I would like to thank the Ranking
Member for his continued efforts to make sure that Medicare and
our beneficiaries are getting the most value. There is also
bipartisan interest in the Senate. We intend to continue
working closely with you to consider changes to increase the
effectiveness of how Medicare compensates physicians and to
take new steps to avoid unnecessary costs. That is the best
path to a sustainable payment system. I also want to thank the
Nation's physician organizations for their leadership on issues
of quality and performance. Thanks in part to the leadership
and hard work of many physician organizations, substantial
progress has been made to develop quality measures for most
physician specialties. In fact, they have identified 66
evidence-based quality measures for 29 specialties, as I detail
in my written testimony. Those specialties represent 80 percent
of Medicare physician spending. This is tremendous progress
working together, and physician leadership has helped make it
possible. We are also developing the infrastructure needed to
support the reporting of measures like these on existing
physician claims as soon as 2006. While we are still analyzing
the issues, we are working out the details so that voluntary
reporting can be accomplished under existing statutory
authorities.
Our collaborative work on identifying and measuring quality
care so that we can better support it has been guided by some
widely accepted principles. Quality measures should be
evidence-based, valid, reliable and relevant to a significant
part of a physician's actual practice. It is always important
that quality measures do not discourage physicians from
treating high-risk or difficult cases, as you mentioned. In
addition, quality measures should be implemented in a realistic
manner that is most relevant for quality improvements in all
types of practices and patient populations while being least
burdensome for physicians and other stakeholders. To make sure
that these principles are met, quality measures should be
developed in conjunction with open and transparent processes
that promote consensus from a broad range of health care
stakeholders.
To achieve these goals, CMS joined in a process with the
National Committee of Quality Assurance (NCQA), the AMA's
Physician Consortium For Performance Improvement, other
physician organizations and stakeholders to develop measures
that would be appropriate for the ambulatory setting. We
supported the National Quality Forum (NQF) endorsement of
ambulatory care measures developed by the NCQA and the
Physician Consortium. More recently we have also been working
with the Ambulatory Care Quality Alliance, the American College
of Physicians, the American Academy of Family Practitioners,
the Nation's health plans and many other stakeholders to expand
these efforts, and we are building on this progress--that I
have already noted--with additional primary care quality
measures as well as measures in other specialties. Activity is
under way to prepare the other measures for NQF endorsement. As
a result of this activity, we have 66 measures, as I mentioned,
and 30 have already been endorsed or a part of the NQF process.
The bottom line is that quality measures or indicators have
been developed or are well along in the development process for
most physician specialties. There are strong collaborations
among health care providers and other stakeholders to build on
this rapid progress to improve quality and avoid unnecessary
costs. This is very good news for achieving our shared goal of
supporting the best efforts of physicians to keep seniors well
and to keep health care costs down. Madam Chairman, Mr. Stark,
thanks again for the opportunity to testify. I would be happy
to answer any of your questions.
[The prepared statement of Dr. McClellan follows:]
Statement of The Honorable Mark McClellan, M.D., Ph.D., Administrator,
Centers for Medicare and Medicaid Services, U.S. Department of Health
and Human Services
Madam Chairman Johnson, Congressman Stark, distinguished
Subcommittee members, thank you for inviting me to testify on value-
based purchasing for physicians under Medicare.
I want to take this opportunity to thank the physician community
for their heroic efforts on behalf of evacuees of hurricanes Katrina
and Rita. Physicians rushed to provide care for those in need without
even considering payments or program requirements. Providers who were
personally affected by the hurricanes as well as those in areas
sheltering evacuees have provided extensive medical services under the
most challenging conditions. We have acted expeditiously to provide
effective support for these efforts. We've done this through
administrative adjustments to our Medicare and Medicaid payment rules.
And we've implemented a new Medicaid waiver that provides for
immediate, temporary Medicaid coverage as well as financial support for
needed medical services that fall outside of standard Medicaid
benefits, all using existing systems in the affected states so that
they can be implemented quickly and effectively. Within just ten
business days CMS reviewed and approved waivers for the states housing
the vast majority of evacuees, including Texas, Arkansas, Mississippi,
Alabama, Georgia, Florida, Idaho, and the District of Columbia. And we
are working closely with all other states that need financial support.
Through these efforts, we are helping all evacuees get the care they
need as they get back on their feet, we are making sure that the health
care providers get reimbursed for providing that care, and we are
making sure that the states hosting the evacuees are covered for any
substantial expenses that they incur.
In addition, the physician community is one of our key partners as
we work to implement the Medicare Modernization Act (MMA). As you well
know, we are rapidly approaching the implementation date for Medicare's
new prescription drug coverage. As physicians have known for many
years, adequate access to medications is more important today than ever
before. Physician organizations have worked closely with us to help
inform their membership about the new benefits coming in Medicare to
help their patients get access to up to date care. Physicians all over
the country are helping beneficiaries take advantage of the new
coverage, for example by providing materials in their offices about the
basics of Medicare's prescription drug coverage, and letting them know
where to go to get the information and support they need to make a
confident decision. The new Medicare drug coverage will be available on
time, nationwide, at a lower cost and with more benefits available than
many people had expected. As a result, on average seniors will save
many hundreds of dollars next year in their total out of pocket costs.
I truly appreciate the time and effort physicians are taking to ensure
their Medicare patients have access to the medications they need.
As I testified in July, continued improvement of the Medicare
program requires the successful participation of physicians and we need
to ensure they are adequately compensated for the care they provide to
people with Medicare. But how we pay also matters. In addition to
providing adequate payments, Medicare's payment system for physicians
should encourage and support them to provide quality care and prevent
avoidable health care costs. After all, physicians are in the best
position to know what can work best to improve their practices, and
physician expertise coupled with their strong professional commitment
to quality means that any solution to the problems of health care
quality and affordability must involve physician leadership.
Updates to the current payment system for physicians' services are
projected to be negative for the next seven years. Such continued
negative updates raise real concerns about this payment system in terms
of assuring access to quality care for Medicare beneficiaries. At the
same time, simply increasing spending by adding larger updates into the
current volume-based payment system that is already experiencing
increases of 12 to 13 percent or more per year would have an adverse
effect from the standpoint of Medicare's finances or beneficiary
premiums and cost-sharing, and does not promote better quality care.
However, it is clear, under our current system, there is much
potential for physicians to improve the value of our health care
spending. Under the current system, there are substantial variations in
resources and in spending growth for the same medical condition in
different practices and in different parts of the country, without
apparent difference in quality and outcomes, and without a clear basis
in existing medical evidence. A study published in 2003 looked at
regional variations in the number of services received by Medicare
patients who were hospitalized for hip fractures, colorectal cancer,
and acute myocardial infraction. The researchers found that patients in
higher spending areas received approximately 60 percent more care, but
that quality of care in those regions was no better on most measures
and was worse for several preventive care measures. \1\ Further, there
are many examples of steps that physicians have taken to improve
quality while helping to keep overall costs down.
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\1\ Fisher, Elliott S., MD, MPH; David E. Wennberg, MD, MPH;
Therese A. Stukel, Ph.D.; Daniel J. Gottlieb, MS; F.L. Lucas, Ph.D.;
and Etoile L. Pinder, MS, ``The Implications of Regional Variations in
Medicare Spending. Part 1: The Content, Quality, and Accessibility of
Care,'' in The Annals of Internal Medicine, February 18, 2003, Vol.
138, Issue 4.
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Because it is critical for CMS payment systems to support better
outcomes for our beneficiaries at a lower cost, CMS is working closely
and collaboratively with medical professionals and Congress to consider
changes to increase the effectiveness of how Medicare compensates
physicians for providing services to Medicare beneficiaries. I am
engaging physicians on issues of quality and performance with the goal
of supporting the most effective clinical and financial approaches to
achieve better health outcomes for people with Medicare. We are
committed to developing reporting and payment systems that enable us to
support and reward quality, to improve care without increasing overall
Medicare costs. When clear, valid and widely accepted quality measures
are in place, pay-for-performance is a tool that could enable our
reimbursement to better support efforts to improve quality and avoid
unnecessary costs.
Currently, hospitals and physicians are paid under separate
systems. Under these systems, physicians do not receive credit for
avoiding unnecessary hospitalizations by providing better care to their
patients. However, in our physician group practice demonstration
project, physicians could receive performance based payments derived
from savings from preventing chronic disease complications, avoiding
hospitalizations, and improving quality of care.
The evidence is increasing that when we provide an incentive for
reporting and achieving better quality, health care providers respond
by using payments to take a range of steps from the simple to the high-
tech to make it happen. This should not really be surprising--our
health professionals are dedicated, and they want to do everything in
their power to get the best care to their patients. So when we support
better quality, we enable them to do what they do best.
We've seen this approach work first-hand with hospital payments
where we have tied the annual hospital payment update to quality
measure reporting. It has had a positive impact on the availability of
quality information, with about 70 percent of hospitals reporting
quality data.
Reporting clinically valid quality measures is an important step
toward making it easier to achieve major improvements in quality--if
you cannot measure it, it is hard to take steps to improve it. We have
been working hard in close collaboration with health professionals and
other stakeholders to promote the development of better measures.
Voluntary Reporting of Quality Measures Can Be Implemented Soon
Thanks to the leadership and hard work of many physician
organizations, we have made considerable progress creating consensus
around a set of primary care quality measures. In addition, we have
made substantial progress to develop quality measures for the majority
of physician specialties. We now have 66 quality measures for 29
specialties. Those 29 specialties represent about 80 percent of
Medicare physician spending. We are also developing the infrastructure
so that the reporting of these measures on existing physician claims
could begin as soon as 2006. While we are still analyzing the issues,
we are working out the details so that reporting can be accomplished
under existing statutory authorities.
CMS Works with Partners to Develop, Endorse, and Implement Quality
Measures
The ability to evaluate and measure quality is an important
component in delivering high quality care. For several years, CMS has
been collaborating with a variety of stakeholders to develop and
implement uniform, standardized sets of performance measures for
various health care settings. In recent months, thanks to the
leadership of many physician organizations, these efforts have
accelerated even further.
Our work on the quality measures has been guided by the following
widely-accepted principles. Quality measures should be evidence-based.
They should be valid and reliable. They should be relevant to a
significant part of medical practice. And to assure these features,
quality measures should be developed in conjunction with open and
transparent processes that promote consensus from a broad range of
health care stakeholders. It also is important that quality measures do
not discourage physicians from treating high-risk or difficult cases,
for example, through a risk adjustment mechanism. In addition, quality
measures should be implemented in a realistic manner that is most
relevant for quality improvement in all types of practices and patient
populations, while being least burdensome for physicians and other
stakeholders.
More than two years ago, CMS initiated a process with the National
Committee for Quality Assurance (NCQA), the American Medical
Association's (AMA) Physician Consortium for Performance Improvement,
and other stakeholders to develop measures that would be appropriate
for the ambulatory setting. As part of this endeavor, CMS took the lead
in supporting the National Quality Forum (NQF) endorsement of
ambulatory care measures developed by the NCQA and the Physician
Consortium. The NCQA is a private, not-for-profit organization
dedicated to improving health care quality by providing information
about health care quality to help inform consumer and employer choice.
The NQF is a private, not-for-profit membership organization created to
develop and implement a national strategy for healthcare quality
measurement and reporting. The result of this activity has been the
recent endorsement by the NQF of 36 ambulatory quality measures.
Examples of three ambulatory quality measures are the results of
the hemoglobin A1C and LDL and blood pressure tests for diabetic
patients. The clinical evidence suggests that patients who have a
hemoglobin A1C test below 9 percent, an LDL less than or equal to 100
mg/dl, and blood pressures less than or equal to 140/90 mmHg have
better outcomes. These measures are evidence-based, reliable and valid,
widely accepted and supported, and were developed in an open and
transparent manner. Evidence indicates that reaching these goals can
lead to fewer hospitalizations by avoiding complications from diabetes
such as amputation, renal failure, and heart disease.
Two quality measures endorsed by NQF for heart failure patients
include placing the patient on blood pressure medications and beta
blocker therapy. Here too, these therapies have been shown to lead to
better health outcomes and reduce preventable complications. Together,
diabetes and heart failure account for a large share of potentially
preventable complications.
In addition to primary care quality measures, other specialties are
developing measures. For example, measures of effectiveness and safety
of some surgical care at the hospital level have been developed through
collaborative programs like the Surgical Care Improvement Program
(SCIP), which includes the American College of Surgeons. Preventing or
decreasing surgical complications can result in a decrease in avoidable
hospital expenditures and use of resources. For example, use of anti-
biotic prophylaxis has been shown to have a significant effect in
reducing post-operative complications at the hospital level. This
measure is well developed and there is considerable evidence that its
use could not only result in better health but also avoid unnecessary
costs. These post-operative complication measures, which are in use in
our Hospital Quality Initiative, are being adapted for use as physician
quality measures. Application of this type of post-operative
complication measure at the physician level has the potential to help
avoid unnecessary costs as well as improve quality.
We also are collaborating with other specialty societies, such as
the Society of Thoracic Surgeons (STS), to implement quality measures
that reflect important aspects of the care of specialists and sub-
specialists. The STS has already developed a set of 21 measures at the
hospital level that are risk adjusted and track many common
complications as outcome measures. STS is also conducting a national
pilot program to measure cost and quality simultaneously, while
communicating quality and efficiency methods across regional hubs with
the objective of reducing unnecessary complications and their
associated cost. The STS measures have been adapted to a set of five
quality measures for physicians, such as for a patient who receives by-
pass surgery with use of internal mammary artery.
Many other specialties have also taken steps to develop evidence-
based quality measures. On July 14, 2005, I sent a letter to many
specialty societies, summarizing some of the work to date and
requesting an update on their efforts to develop quality and
performance measures.
I want to thank the AMA and specialty societies for their very
positive response to this effort. Six months ago few specialties had
quality measures. Today the majority of specialties have quality
measures. Many specialties have created quality task forces and are
participating in the quality measurement process. As a result, a total
of 66 quality measures now exist covering 29 specialties. These
specialties represent about 80 percent of Medicare physician spending.
NQF has endorsed 36 of the measures. Activity is underway to prepare
the other measures for NQF endorsement. The latest version of all 66
quality measures is attached to this statement.
CMS has had productive exchanges with most medical specialty
organizations. I would encourage organizations that have not entered
into discussions with us to initiate a dialogue as soon as possible so
we can work together to develop clinically valid measures. In certain
areas, compliance with evidence-based practice guidelines has the
potential to be a quality measure.
The process we have used with the medical profession to develop
quality measures beyond ambulatory care should greatly expedite and
facilitate the development, acceptance and implementation of quality
measures for additional specialties and services. By working in
collaboration with the societies, there has been considerable progress
in the measure development process. This preparation will facilitate
the NQF endorsement process. However, measures that have not yet gone
through the NQF endorsement process are still of great value. Physician
reporting of these measures will help foster their acceptance in the
medical community and help prepare physicians for their eventual
adoption. Moreover, since there is likely to be reporting of the
quality measures for a period of time before payment based on
performance, NQF consensus is not required to begin reporting of such
measures. The rapid progress to develop quality measures for the
majority of specialties is a clear indication that quality measures are
gaining acceptance as an important element in achieving better
performance in our health care system.
Our experience with hospital quality measures is that after a
measure is endorsed additional work with stakeholders is necessary to
assure successful implementation. The Hospital Quality Alliance played
an important role in implementation of the hospital quality measures by
facilitating hospital adoption and understanding of technical concerns.
The Ambulatory Care Quality Alliance (AQA) can serve a similar role to
help with physician adoption of the ambulatory quality measures. The
AQA is a consortium led by the American Academy of Family Physicians,
the American College of Physicians, America's Health Insurance Plans
and the Agency for Healthcare Research and Quality, CMS and other
stakeholders, including the AMA and other physician groups, as well as
representatives of private sector purchasers and consumers.
CMS is Developing a System to Simply Reporting of Quality Measures
The development, endorsement, and consensus process is not
sufficient to implement measures successfully. Detailed specifications
are needed about such items as the associated diagnosis codes and the
rules for reporting (e.g., the ordering vs. performing physician).
There is also a key issue about how a payor like Medicare can obtain
information on the quality measures. For this reason, while the rapid
development of quality measures is ongoing, CMS also has been working
on the technical methods for supporting effective, simple, and the
least burdensome reporting and payment based on these measures.
In the years ahead, it is expected that electronic record systems
can be developed that would provide information that is needed to
measure and report on quality while fully protecting patient
confidentiality. However, while electronic health records would greatly
facilitate the accurate and efficient use of information on quality
measures and quality improvement, progress on supporting quality
improvement should not be delayed until electronic health records are
widely used. Indeed, taking steps now to promote quality reporting and
improvement also could promote the adoption of and investment by
physicians in electronic records, which would facilitate more efficient
quality reporting and quality improvement activities. In the short
term, there is considerable evidence that information on a broad range
of quality measures can be obtained adequately via information
transmitted on existing claims. In particular, with adequate guidance
for appropriate coding practices by physician offices, the so-called G-
codes, HCPCS codes established by Medicare and reportable on existing
claims forms, can be the vehicle to report the information on claims.
While HCPCS codes generally represent services furnished, the G-codes
would report information on the quality measures, and could potentially
be a basis for payment based on the report of such information.
We are in the process of converting all the quality measures into a
series of G-codes that could then be reported by a physician on a claim
in a way that is simple and does not burden physicians. This reporting
mechanism has several advantages. It allows collection of information
on the quality measures via an existing system familiar to the
physician community. It makes reporting of the information simple for
physicians. Furthermore, it allows collection of the quality measures
to begin very soon--possibly as early as 2006.
Many changes in Medicare involve changes in the systems used by our
contractors to pay claims. We are currently assessing whether changes
in our contractor systems might be necessary to implement the reporting
of information on the quality measures on claims. We are also assessing
implementation issues under a scenario where reporting and subsequent
performance could result in a payment differential for physicians.
Many believe that a trial period of a year or two might be
appropriate where physicians would report on the quality measures,
including quality measures that have broad endorsement and support but
that have not yet fully completed a formal consensus process. The bill
you introduced, Madam Chairman, H.R. 3617, would begin with reporting
and move to performance. Some believe that Medicare could establish a
payment differential where physicians who report on the measures get a
different payment from physicians who do not report. Many believe that
after a trial period for reporting Medicare would then move to a system
where the payment differential would be based on performance for the
measures.
In many ways, where we are today with reporting quality measures
for physicians is analogous to where we were before the MMA enacted
section 501, the 0.4 percentage point payment differential for
reporting of 10 quality measures. Prior to MMA, mechanisms had been
established so that hospitals could voluntarily report information on
the quality measures. When MMA was enacted, hospitals quickly responded
and most of those institutions that had not previously reported the
measures did so. Today there are a total of 20 hospital quality
measures. Hospitals can voluntarily report information on the
additional 10 measures and such reporting does not have a payment
consequence. About 70 percent of hospitals are already reporting on 17
of the measures. Information on all measures reported by hospitals is
available on the CMS Hospital Compare website.
The bottom line is that quality measures or indicators have been
developed or are well along in the development process for most
physicians' specialties. We are currently developing G-codes to report
information on these measures on existing claims. We are sorting
through systems issues for our contractors. While we still have much
work to do, at this point, we believe that we can make rapid progress
in very short order so that broad initial reporting of measures that
are very relevant to the quality and cost of care for our beneficiaries
could begin as soon as 2006.
CMS Works to Ensure Resources are Utilized Appropriately
In many cases, quality measures may help us get more value for our
health care dollars. We need to build on this by examining appropriate
resource use. The well documented wide variation in resource use among
areas for treating the same medical condition raises questions about
whether Medicare is getting good value in all areas.
In my June 24 letter to you and Chairman Thomas, I indicated that
we supported and were preparing to implement MedPAC's March
recommendation to Congress that: ``The Secretary should use Medicare
claims data to measure fee-for-service physicians' resource use and
share results with physicians confidentially to educate them about how
they compare with aggregated peer performance.''
Measures of physician resource use have been used and are being
developed by a number of public and private entities. The most widely
used measure of physician resource use is total expenditures per case.
Total expenditures include all resources involved in furnishing the
case, including physicians' services, laboratory services and other
diagnostic tests, hospital services, other facilities, drugs, durable
medical equipment, etc.
The measures of resource use are generally applied to episodes of
care. The beginning of an episode may be defined by a new diagnosis or
treatment, such as hospitalization. Such episodes usually end after
claims related to the episode are not present for a defined period of
time. Such episodes could include heart attacks or broken hips. For
surgeons, coronary bypass surgery and hip replacements would be
considered episodes. Episodes also may occur for a full year in the
case of chronic diseases, such as diabetes, heart failure, and chronic
pulmonary disease.
We are working to implement the MedPAC recommendation using
information derived from claims data. We are developing resource use
measures that target particular tests and procedures that may be over--
or under-used, as overuse is inefficient and under-use raises quality
concerns. We also are developing pilot projects that will use software
programs created by a number of private sector entities. These programs
group services into episodes using claims data. The episodes are then
assigned to physicians so average resource use can be computed. We plan
to pilot test resource use for a few selected conditions in two states.
We are assessing measurement issues such as case-mix/severity
adjustment and identification of appropriate comparison groups. Our
goal would be to share results with physicians confidentially to
educate them about how they compare to peers and ultimately to
incorporate measures related to services, resources, and expenditures
into the payment system as envisioned in your bill, H.R. 3617.
Conclusion
Madam Chairman, thank you again for this opportunity to testify on
improving how Medicare pays for services. We look forward to working
with Congress and the medical community to develop a system that
ensures appropriate payments while also promoting the highest quality
of care, without increasing overall Medicare costs. As a growing number
of stakeholders now agree, we must increase our emphasis on payment
based on improving quality and avoiding unnecessary costs to solve the
problems with the current physician payment system. Thanks to the
leadership of many private-sector organizations working together, and
especially thanks to the leadership of physicians, we have made rapid
progress in developing quality measures and indicators as well as in
building an infrastructure to allow the reporting of such measures. I
would be happy to answer any of your questions.
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Conversion of Clinial Measures to G-Codes
Physicians Pay-for-Performance
As of: September 26, 2005
Internal Medicine, Family Practice, General Practice
Diabetic patient with most recent HbA1c level (within the
last 6 months) documented as less than or equal to 9%
Diabetic patient with most recent HbA1c level (within the
last 6 months) documented as greater than 9%
Clinician documented that diabetic patient was not
eligible candidate for HbA1c measure
Clinician has not provided care for the diabetic patient
for the required time for HbA1c measure (within the last 6 months)
Diabetic patient with most recent LDL (within the last 12
months) documented as less than or equal to 100 mg/dl
Diabetic patient with most recent LDL (within the last 12
months) documented as greater than 100 mg/dl
Clinician documented that diabetic patient was not
eligible candidate for LDL measure
Clinician has not provided care for the diabetic patient
for the required time for LDL measure (within the last 12 months)
Diabetic patient with most recent blood pressure (within
the last 6 months) documented as less than or equal to 140/90 mmHg
Diabetic patient with most recent blood pressure (within
the last 6 months) documented as greater than 140/90 mmHg
Clinician documented that the diabetic patient was not
eligible candidate for blood pressure measure
Clinician has not provided care for the diabetic patient
for the required time for blood measure (within the last 6 months)
HF patient with LVSD documented to be on either ACE-I or
ARB therapy
HF patient with LVSD not documented to be on either ACE-I
or ARB therapy
Clinician documented that HF patient was not eligible
candidate for either ACE-I or ARB therapy measure
HF patient with LVSD documented to be on B-blocker therapy
HF patient with LVSD not documented to be on B-blocker
therapy
Clinician documented that HF patient was not eligible
candidate for B-blocker therapy measure
AMI-CAD patient documented to be on B-blocker therapy
AMI-CAD patient not documented to be on B-blocker therapy
Clinician documented that AMI-CAD patient was not eligible
candidate for B-blocker therapy measure
AMI-CAD patient documented to be on antiplatelet therapy
AMI-CAD patient not documented to be on antiplatelet
therapy
Clinician documented that AMI-CAD patient was not eligible
candidate for antiplatelet therapy measure
Patient documented to have received influenza vaccination
during the flu season
Patient not documented to have received influenza
vaccination during the flu season
Clinician documented that patient was not eligible
candidate for influenza vaccination measure
Internal Medicine--Cardiology
HF patient with LVSD documented to be on either ACE-I or
ARB therapy
HF patient with LVSD not documented to be on either ACE-I
or ARB therapy
Clinician documented that HF patient was not eligible
candidate for either ACE-I or ARB therapy measure
HF patient with LVSD documented to be on B-blocker therapy
HF patient with LVSD not documented to be on B-blocker
therapy
Clinician documented that HF patient was not eligible
candidate for B-blocker therapy measure
AMI-CAD patient documented to be on B-blocker therapy
AMI-CAD patient not documented to be on B-blocker therapy
Clinician documented that AMI-CAD patient was not eligible
candidate for B-blocker therapy measure
AMI-CAD patient documented to be on antiplatelet therapy
AMI-CAD patient not documented to be on antiplatelet
therapy
Clinician documented that AMI-CAD patient was not eligible
candidate for antiplatelet therapy measure
CAD--with LDL documented to be less than or equal to
100mg/dl
CAD--with LDL documented to be greater than 100mg/dl
Clinician documented that CAD patient was not eligible
candidate for LDL measure
Counseling on the importance of blood sugar control and
monitoring of HgA1c documented to have been provided to patient with
diabetes mellitus
Counseling on the importance of blood sugar control and
monitoring of HgA1c not documented to have been provided to patient
with diabetes mellitus
Counseling on the use of antioxidants documented to have
been provided to patient with intermediate age-related macular
degeneration (AMD), or advanced AMD in one eye, based on data from the
Age-Related Eye Disease Study
Counseling on the use of antioxidants not documented to
have been provided to patient with intermediate age-related macular
degeneration (AMD), or advanced AMD in one eye, based on data from the
Age-Related Eye Disease Study
Clinician documented that patient with intermediate age-
related macular degeneration (AMD), or advanced AMD in one eye (based
on data from the Age-Related Eye Disease Study) was not eligible
candidate for antioxidant measure
Central corneal thickness measurement documented for a
patient who is primary open angle glaucoma suspect
Central corneal thickness measurement not documented for a
patient who is primary open angle glaucoma suspect
Clinician documented that patient who is primary open
angle glaucoma suspect was not eligible candidate for central corneal
thickness measure
Cataract surgery candidate documented to have been
questioned about his/her visual function, including a review of the
patient's self-assessment of visual status and visual needs
Cataract surgery candidate not documented to have been
questioned about his/her visual function, including a review of the
patient's self-assessment of visual status and visual needs
A 5% solution of povidone-iodine documented to have been
provided as an infection prophylaxis in the pre-operative period for
intraocular surgery
A 5% solution of povidone-iodine not documented to have
been provided as an infection prophylaxis in the pre-operative period
for intraocular surgery
Clinician documented that patient at the pre-operative
period for intraocular surgery was not an eligible candidate for 5%
solution of povidone-iodine infection prophylaxis measure
Surgery--Ophthalmology
Chronic open angle glaucoma patient documented to have
received optic nerve assessment
Chronic open angle glaucoma patient not documented to have
received optic nerve assessment
Surgery--Orthopedic
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for the antibiotic prophylaxis one hour prior to incision
time (two hours for vancomycin) measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboemoblism prophylaxis measure
Surgery--General
ESRD Patient requiring hemodialysis vascular access
documented to have received autogenous AV fistula
ESRD Patient requiring hemodialysis documented to have
received vascular access other than autogenous AV fistula
Clinician documented that ESRD patient requiring
hemodialysis was not a candidate for autogenous AV fistula (or other
autogenous AV fistula) evaluation measure
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for the antibiotic prophylaxis one hour prior to incision
time (two hours for vancomycin) measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboembolism prophylaxis measure
Internal Medicine--Hematology
Patient with multiple myeloma not in remission documented
to be treated with a bisphophonate
Patient with multiple myeloma not in remission not
documented to be treated with a bisphophonate
Clinician documented that patient with multiple myeloma
not in remission was not an eligible candidate for bisphophonate
treatment measure
MDS patient presenting with anemia (Hb < 11 g/dl)
documented to have received bone marrow examination, including iron
stain, prior to receiving erythropoietin therapy
MDS patient presenting with anemia (Hb < 11 g/dl) not
documented to have received bone marrow examination, including iron
stain, prior to receiving erythropoietin therapy
Clinician documented that MDS patient presenting with
anemia (Hb < 11 g/dl) was not an eligible candidate for bone marrow
examination, including iron stain, measure prior to receiving
erythropoietin therapy
CLL patient documented to have received confirmation of
CLL diagnosis by flow cytometry as part of initial diagnostic
evaluation
CLL patient not documented to have received confirmation
of CLL diagnosis by flow cytometry as part of initial diagnostic
evaluation
Clinician documented that CLL patient was not eligible
candidate for flow cytometry as part of initial CLL diagnostic
evaluation measure
MDS and acute leukemia patient documented to have received
cytogenic testing on bone marrow or peripheral blood (as appropriate)
as part of initial diagnostic evaluation
MDS and acute leukemia patient not documented to have
received cytogenic testing on bone marrow or peripheral blood (as
appropriate) as part of initial diagnostic evaluation
Clinician documented that MDS and acute leukemia patient
was not an eligible candidate for cytogenic testing on bone marrow or
peripheral blood (as appropriate) as part of initial diagnostic
evaluation measure
Emergency Medicine
AMI: Patient documented to have received aspirin at
arrival
AMI: Patient not documented to have received aspirin at
arrival
Clinician documented that AMI patient was not an eligible
candidate aspirin at arrival measure
AMI: Patient documented to have received B-blocker at
arrival
AMI: Patient not documented to have received B-blocker at
arrival
Clinician documented that AMI patient was not an eligible
candidate for B-blocker at arrival measure
PNE: Patient documented to have received antibiotic within
4 hours of presentation
PNE: Patient not documented to have received antibiotic
within 4 hours of presentation
Clinician documented that PNE patient was not an eligible
candidate for antibiotic within 4 hours of presentation measure
Internal Medicine--Gastroenterology
Clinician documented that patient received conscious
sedation consistent with guidelines, including procedural monitoring
(ASGE Guidelines)
Patient received conscious sedation in a manner that was
not outlined in the guideline specifications, including procedural
monitoring (ASGE Guidelines)
Clinician documented that patient was not an eligible
candidate for conscious sedation measure
Patient documented to have serum HCV RNA performed prior
to initiating HCV antiviral therapy
Patient not documented to have serum HCV RNA performed
prior to initiating HCV antiviral therapy
Internal Medicine--Pulmonology
COPD patient with documented spirometry evaluation in last
12 months
COPD patient without documented spirometry evaluation in
last 12 months
COPD patient documented to have received, at least
annually, smoking cessation intervention
COPD patient no documented to have received, at least
annually, smoking cessation intervention
COPD patient documented to have received annual influenza
vaccination
COPD patient not documented to have received annual
influenza vaccination
Anesthesiology
Patient who underwent general anesthesia for greater than
60 minutes documented to have immediate post-operative normothermia
Patient who underwent general anesthesia for greater than
60 minutes not documented to have immediate post-operative normothermia
Clinician documented that patient who underwent general
anesthesia for greater than 60 minutes was not an eligible candidate
for immediate post-operative normothermia measure
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for the antibiotic prophylaxis one hour prior to incision
time (two hours for vancomycin) measure
Patient treated with chronic pain management with
documented comprehensive history and physical consistent with
guidelines (ASA Guidelines)
Patient treated with chronic pain management without
documented comprehensive history and physical consistent with
guidelines (ASA Guidelines)
Internal Medicine--Neurology
Patient with acute ischemic stroke documented to be on
anti-thrombotic therapy (aspirin, ticlopidine, clopidogrel,
dipyridamole, and warfarin)
Clinician documented that patient with acute ischemic
stroke was not an eligible candidate for anti-thrombotic therapy
(aspirin, ticlopidine, clopidogrel, dipyridamole, and warfarin) measure
Patient with acute ischemic stroke and nonvalvular atrial
fibrillation documented to be on warfarin therapy
Clinician documented that patient with acute ischemic
stroke and nonvalvular atrial fibrillation was not an eligible
candidate for warfarin therapy measure
Non-ambulatory patient with acute ischemic stroke
documented to have received DVT prophylaxis within the first 24 hours
of admission
Clinician documented that non-ambulatory patient with
acute ischemic stroke was not an eligible candidate for DVT prophylaxis
measure within the first 24 hours of admission
Patient with mild to moderate Alzheimer's disease
documented to have received centrally acting cholinesterase inhibitors
Clinician documented that patient with mild to moderate
Alzheimer's disease was not an eligible candidate for centrally acting
cholinesterase inhibitor measure
Psychiaty
For patients with a newly diagnosed episode of major depressive
disorders:
Patient documented as being treated with antidepressant
medication during the entire 12 week Acute Treatment Phase
Patient not documented as being treated with
antidepressant medication during the entire 12 week Acute Treatment
Phase
Clinician documented that patient was not an eligible
candidate for antidepressant medication during the entire 12 week Acute
Treatment Phase measure
Patient documented as being treated with antidepressant
medication for at least 6 months Continuous Treatment Phase
Patient not documented as being treated with
antidepressant medication for at least 6 months Continuous Treatment
Phase
Clinician documented that patient was not an eligible
candidate for antidepressant medication for Continuous Treatment Phase
Internal Medicine--Nephrology
ESRD patient with documented dialysis dose of URR greater
than or equal to 65% (or Kt/V greater than or equal to 1.2)
ESRD patient with documented dialysis dose of URR less
than 65% (or Kt/V less than 1.2)
Clinician documented that ESRD patient was not an eligible
candidate for URR or Kt/V measure
ESRD patient with documented hematocrit greater than or
equal to 35
ESRD patient with documented hematocrit less than 35
Clinician documented that ESRD patient was not an eligible
candidate for hematocrit measure
ESRD Patient requiring hemodialysis vascular access
documented to have been evaluated for autogenous AV fistula
ESRD Patient requiring hemodialysis documented to have
been evaluated for vascular access other than autogenous AV fistula
Clinician documented that ESRD patient requiring
hemodialysis was not a candidate for autogenous AV fistula (or other
autogenous AV fistula) evaluation measure
Internal Medicine and Rehabilitation
Patient with acute ischemic stroke documented to be on
anti-thrombotic therapy (aspirin, ticlopidine, clopidogrel,
dipyridamole, and warfarin)
Clinician documented that patient with acute ischemic
stroke was not an eligible candidate for anti-thrombotic therapy
(aspirin, ticlopidine, clopidogrel, dipyridamole, and warfarin) measure
Patient with acute ischemic stroke and nonvalvular atrial
fibrillation documented to be on warfarin therapy
Clinician documented that patient with acute ischemic
stroke and nonvalvular atrial fibrillation was not an eligible
candidate for warfarin therapy measure
Non-ambulatory patient with acute ischemic stroke
documented to have received DVT prophylaxis within the first 24 hours
of admission
Clinician documented that non-ambulatory patient with
acute ischemic stroke was not an eligible candidate for DVT prophylaxis
within the first 24 hours of admission measure
Internal Medicine--Rheumatology
Patient with established diagnosis of rheumatoid arthritis
documented to be treated with a DMARD
Clinician documented that patient with established
diagnosis of rheumatoid arthritis was not an eligible candidate for
DMARD treatment measure or patient refuses
Osteoporosis patient documented to have been prescribed
calcium and vitamin D supplements
Clinician documented that osteoporosis patient was not an
eligible candidate for calcium and vitamin D supplement measure
Newly diagnosed osteoporosis patients documented to have
been treated with antiresorptive therapy and/or PTH within 3 months of
diagnosis
Clinician documented that newly diagnosed osteoporosis
patient was not an eligible candidate for antiresorptive therapy and/or
PTH treatment measure within 3 months of diagnosis
Within 6 months of suffering a nontraumatic fracture,
female patient 65 years of age or older documented to have undergone
bone mineral density testing or to have been prescribed a drug to treat
or prevent osteoporosis
Clinician documented that female patient 65 years of age
or older who suffered a nontraumatic fracture within the last 6 months
was not an eligible candidate for measure to test bone mineral density
or drug to treat or prevent osteoporosis
Patients diagnosed with symptomatic osteoarthritis with
documented annual assessment of function and pain
Clinician documented that symptomatic osteoarthritis
patient was not an eligible candidate for annual assessment of function
and pain measure
Surgery--Neurological
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for the antibiotic prophylaxis one hour prior to incision
time (two hours for vancomycin) measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboembolism prophylaxis measure
Surgery--Vascular
ESRD Patient requiring hemodialysis vascular access
documented to have received autogenous AV fistula
ESRD Patient requiring hemodialysis documented to have
received vascular access other than autogenous AV fistula
Clinician documented that ESRD patient requiring
hemodialysis was not a candidate for autogenous AV fistula (or other
autogenous AV fistula) evaluation measure
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for the antibiotic prophylaxis one hour prior to incision
time (two hours for vancomycin) measure
Patient documented to have required surgical re-
exploration
Patient did not require surgical re-exploration
Patient undergoing carotid endarterectomy, aortic aneurysm
repair, or lower extremity bypass surgery documented to have received
pre-operative beta-blockade
Patient undergoing carotid endarterectomy, aortic aneurysm
repair, or lower extremity bypass surgery not documented to have
received pre-operative beta-blockade
Clinician determined that patient undergoing carotid
endarterectomy, aortic aneurysm repair or lower extremity bypass was
not an eligible candidate to receive pre-operative beta-blockade
Patient undergoing carotid endarterectomy or lower
extremity bypass surgery documented to have received aspirin or
clopidogrel within 24 hours
Patient undergoing carotid endarterectomy or lower
extremity bypass surgery not documented to have received aspirin or
clopidogrel within 24 hours
Clinician determined that patient undergoing carotid
endarterectomy or lower extremity bypass surgery not a candidate for
aspirin or clopidogrel within 24 hours
Patient undergoing carotid endarterectomy documented to
have received heparin during surgery
Patient undergoing carotid endarterectomy documented not
to have received heparin during surgery
Clinician determined that patient undergoing carotid
endarterectomy was not eligible candidate for heparin during surgery
Patient undergoing carotid stent documented to have
received clopidogrel within 24 hours
Patient undergoing carotid stent documented not to have
received clopidogrel within 24 hours
Clinician determined that patient undergoing carotid stent
was not eligible for clopidogrel within 24 hours
Surgey--Thoracic, Cardiac
Patient documented to have received CABG with use of IMA
Patient documented to have received CABG without use of
IMA
Clinician documented that patient was not an eligible
candidate for CABG with use of IMA measure
Patient with isolated CABG documented to have received
pre-operative beta-blockade
Patient with isolated CABG not documented to have received
pre-operative beta-blockade
Clinician documented that patient with isolated CABG was
not an eligible candidate for pre-operative beta-blockade measure
Patient with isolated CABG documented to have prolonged
intubation
Patient with isolated CABG not documented to have
prolonged intubation
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for antibiotic prophylaxis one hour prior to incision time
(two hours for vancomycin) measure
Patient with isolated CABG documented to have required
surgical re-exploration
Patient with isolated CABG did not require surgical re-
exploration
Obsterics/Gynecology
Patient documented to have received antibiotic prophylaxis
one hour prior to hysterectomy
Patient not documented to have received antibiotic
prophylaxis one hour prior to hysterectomy
Clinician documented that patient was not an eligible
candidate for antibiotic prophylaxis one hour prior to hysterectomy
measure
Patient documented to have received management of initial
abnormal cervical cytology consistent with guideline (ACOG Guidelines)
Patient documented to have received management of initial
abnormal cervical cytology in a manner that was not outlined in the
guideline (ACOG Guidelines)
Clinician documented that patient was not an eligible
candidate for management of initial abnormal cervical cytology measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboembolism prophylaxis measure
Surgey--Plastic & Reconstructive
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for antibiotic prophylaxis one hour prior to incision time
(two hours for vancomycin) measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboembolism prophylaxis measure
Internal Medicine Endocrinology/Diabetes/ Metalbolism
Diabetic patient with most recent HbA1c level (within the
last 6 months) documented as less than or equal to 9%
Diabetic patient with most recent HbA1c level (within the
last 6 months) documented as greater than 9%
Clinician documented that diabetic patient was not
eligible candidate for HbA1c measure
Clinician has not provided care for the diabetic patient
for the required time for HbA1c measure (within the last 6 months)
Diabetic patient with most recent LDL (within the last 12
months) documented as less than or equal to 100 mg/dl
Diabetic patient with most recent LDL (within the last 12
months) documented as greater than 100 mg/dl
Clinician documented that diabetic patient was not
eligible candidate for LDL measure
Clinician has not provided care for the diabetic patient
for the required time for LDL measure (within the last 12 months)
Diabetic patient with most recent blood pressure (within
the last 6 months) documented as less than or equal to 140/90 mmHg
Diabetic patient with most recent blood pressure (within
the last 6 months) documented as greater than 140/90 mmHg
Clinical has not provided care for the diabetic patient
for the required time for HbA1c measure (within the last 6 months)
Critical Care
Prevention of catheter-related infection
Patient with documented catheter insertion including the
use of sterile barrier precautions in a manner consistent with
guidelines for prevention of IV catheter-related infections (CDC
Guidelines)
Catheter insertion performed in a manner that was not
outlined in the guideline specifications for prevention of IV catheter-
related infections (CDC Guidelines)
Management of catheter-related infection
Management of patient for catheter-related infection
(i.e., staphylococcus A and candida A), including removal of catheter,
blood cultures and empiric antibiotics was performed in a manner
consistent with guidelines for management of IV catheter-related
infections and is documented in chart (IDSA/ACCCM/SHEA/SCCM Guidelines)
Management of patient for catheter-related infection
(i.e., staphylococcus A and candida A), including removal of catheter,
blood cultures and empiric antibiotics was performed in a manner that
was not outlined in the guideline specifications for management of IV
catheter-related infections and is documented in chart (IDSA/ACCCM/
SHEA/SCCM Guidelines)
Internal Medicine--Geratic Medicine
For patients 75 years of age or older:
Patient documented to have received influenza vaccination
during flu season
Patient not documented to have received influenza
vaccination during flu season
Clinician documented that patient was not an eligible
candidate for influenza vaccination measure
Patient documented to have received pneumococcal
vaccination
Patient not documented to have received pneumococcal
vaccination
Clinician documented that patient was not an eligible
candidate for pneumococcal vaccination measure
Patient (female) documented to have been screened for
osteoporosis
Patient (female) not documented to have been screened for
osteoporosis
Clinician documented that patient was not an eligible
candidate for osteoporosis screening measure
Patient documented for the assessment for falls within
last 12 months
Patient not documented for the assessment for falls within
last 12 months
Clinician documented that patient was not an eligible
candidate for the falls assessment measure within the last 12 months
Patient documented to have received hearing screening
Patient not documented to have received hearing screening
Clinician documented that patient was not an eligible
candidate for hearing screening measure
Patient documented for the assessment of urinary
incontinence
Patient not documented for the assessment of urinary
incontinence
Clinician documented that patient was not an eligible
candidate for urinary incontinence assessment measure
Surgey--Colorectal
Patient documented to have received antibiotic prophylaxis
one hour prior to incision time (two hours for vancomycin)
Patient not documented to have received antibiotic
prophylaxis one hour prior to incision time (two hours for vancomycin)
Clinician documented that patient was not an eligible
candidate for antibiotic prophylaxis one hour prior to incision time
(two hours for vancomycin) measure
Patient with documented receipt of thromboemoblism
prophylaxis
Patient without documented receipt of thromboemoblism
prophylaxis
Clinician documented that patient was not an eligible
candidate for thromboembolism prophylaxis measure
Nuclear Medicine
Patient documented to have received myocardial perfusion
imaging examination in a manner consistent with the guidelines,
including determination of proper patient preparation (SNM Guidelines)
Patient documented to have received myocardial perfusion
imaging in a manner that was not outlined in the guideline
specifications, including determination of proper patient preparation
(SNM Guidelines)
Clinician documented that patient was not an eligible
candidate for myocardial perfusion imaging measure
Patient documented to have received SPECT MPI for an
indication rated as appropriate/may be appropriate as outlined in the
ACC/ASNC SPECT MPI appropriateness criteria
Patient documented to have received SPECT MPI
appropriateness rating in a manner that was not outlined in the ACC/
ASNC SPECT MPI appropriateness criteria or for an indication not
specified
Preventive Medicine
Patient documented to have received influenza vaccination
during the flu season
Patient not documented to have received influenza
vaccination during the flu season
Clinician documented that patient was not an eligible
candidate for influenza vaccination measure