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House Passes Bill to Require Medicare Drug Price Negotiations
New Law
Transfers Public Health Preparedness to HHS; Authorizes Grants for Health
IT, Other Provisions
CMS Waives Late Enrollment Penalty for Low Income
Beneficiaries
AHRQ Releases National Healthcare Quality Report; Improvements
in Hospital Care Attributed to QIO Program
Adding Lab Data and Refining
Secondary Diagnosis Information Improves Measurement of Hospital Quality
CMS
Funds Medicaid Demo Aimed at Keeping Seniors in
Medicaid Commission Releases
Final Recommendations to Modernize Program
Wanted: Public Comment on
Anti-Fraud Guidelines for EHRs
NIH Site Offers Information on Depression
for Seniors
National Campaign to Reduce Avoidable Hospitalization in
Home Health Patients Kicks Off at CMS Headquarters
SAVE THE DATE
New Weekly News Report on Disparities Available for Free
Spanish Health
Resource Available
AHRQ Database Provides Health Insurance Cost Data
for Large US Cities
NIH Plan Aims to Transform Clinical Research
Commonwealth: Using Research
Effectively in State Policymaking
House Passes Bill to Require Medicare Drug Price Negotiations
The U.S. House of Representatives passed, by a vote of 255-170, a measure
to amend Medicare’s Part D prescription drug program to require
the Secretary of Health and Human Services to negotiate lower drug prices
on behalf of Medicare beneficiaries. The bill has been referred to the
Senate Finance Committee.
“The ability to negotiate the cost of prescription drugs purchased
through the Medicare program has the potential to constitute a tremendous
savings to taxpayers,” said Representative Jo Ann Emerson (R-MO)
in a press release announcing the bill’s introduction. Representative
Emerson joined Representatives John Dingell (D-MI), Chairman of the Committee
on Energy and Commerce; Charles Rangel (D-NY), Chairman of Ways and Means;
and Carol Shea-Porter (D-NH) in sponsoring H.R. 4.
In a statement, HHS Secretary Michael Leavitt said he was “disappointed
that a majority of House members discounted the overwhelming success of
the Medicare Part D program over the last year and voted to pass H.R.
4.” “Despite statements from the nonpartisan Congressional
Budget Office and the independent Centers for Medicare & Medicaid
Services’ actuaries that this legislation would not result in savings,
this legislation was hastily adopted without hearings in the House,” Leavitt’s
statement continued.
“Although the bill would require the Secretary to negotiate with
drug manufacturers regarding drug prices, the inability to drive market
share via the establishment of a formulary or development of a preferred
tier significantly undermines the effectiveness of this negotiation,” explained
Paul Spitalnic, Director of the Parts C and D Actuarial Group in the Office
of the Actuary.
If enacted, the bill would require the Secretary to negotiate prices
for plan years beginning on January 1, 2008. By June 1, 2007, and every
six months thereafter, the bill requires the Secretary to submit a report
to Congress on negotiations conducted, “and the prices and price
discounts achieved.”
In a statement on the bill’s passage, Speaker of the House Nancy
Pelosi (D-CA) called the vote “a resounding victory for America’s
seniors.”
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New Law Transfers Public Health Preparedness to HHS; Authorizes Grants
for Health IT, Other Provisions
President Bush has signed into law the Pandemic and All-Hazards Preparedness
Act, which calls for the Secretary of Health and Human Services to lead
federal public health and medical responses to public health emergencies – previously
a responsibility of the Department of Homeland Security. The new law was
introduced as Senate Bill 3678 by Senator Richard Burr (R-NC) in July
2006.
The law reauthorizes the Public Health Security and Bioterrorism Preparedness
and Response Act of 2002, which was signed into law following the terrorist
attacks of September 11th, and builds on the Project BioShield Act of
2004 to accelerate advanced research and development of drugs and vaccines
to protect the United States from health emergencies. The legislation
also authorizes grant funds to help entities meet requirements set out
in the law.
“This bill will help improve our preparedness and response to emergencies
and disasters be they a terrorist attack, or caused by Mother Nature,” Burr
said in a press release. “It will also help improve our ability
to create new drugs and vaccines to fight against emergencies like a flu
pandemic.”
The legislation charges HHS with developing a national information network
to coordinate federal and state response to public health emergencies
such as pandemic influenza, natural disasters, or terrorist attacks. It
also enables HHS to partner with universities, research institutions,
and industry to bring more and better medical countermeasures to the public
faster in case of emergency and establishes the position of Assistant
Secretary for Preparedness and Response within HHS. Beginning in 2009
and every four years thereafter, the Secretary is tasked with creating
a “National Health Security Strategy” report for Congress.
Within the next two years, the law calls for the establishment of “a
near real-time electronic nationwide public health situational awareness
capability through an interoperable network of systems to share data and
information” to support early detection and response to public health
emergencies. The network is expected to include public and voluntarily
provided private data from such diverse sources as: federal, state, and
local entities; health care systems and providers; disease monitoring
systems and poison control centers. Grant funds are authorized to help
states and consortia of states establish this network. HHS Secretary Leavitt
must submit a plan for developing the network to Congress within 180 days.
Read the law at: http://thomas.loc.gov/cgi-bin/query/C?c109:./temp/~c109VsJZ1m
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CMS Waives Late Enrollment Penalty for Low Income Beneficiaries
Last week CMS Acting Administrator Leslie Norwalk announced the elimination
of a late enrollment penalty for low income beneficiaries who failed to
sign up for a Part D plan by the program deadline.
“It is very important that we remove whatever barriers may be preventing
low-income beneficiaries from taking advantage of this great, cost-saving
program,” said Ms. Norwalk. “This is our most difficult population
to reach and the one for which we continue to focus our efforts. By continuing
to remove the fear of a late enrollment penalty for those who may not
be able to pay, we are taking a positive step aimed at broader coverage
for everyone.”
Low income beneficiaries who think they may qualify for subsidized coverage
should first check with the Social Security Administration to determine
if they are eligible. All eligible beneficiaries can than sign up for
drug coverage any time during 2007 without fear of a late enrollment penalty.
If a low income beneficiary does not enroll on their own, Medicare will
enroll them in an appropriate plan.
AHRQ Releases National Healthcare Quality Report; Improvements in
Hospital Care Attributed to QIO Program
The recently released Agency for Healthcare Research and Quality
(AHRQ) 2006 National Healthcare Quality Report (NHQR) indicates that care in
hospitals improved at a greater rate than care in other settings – an
advance that AHRQ attributed CMS efforts through the work of QIOs and
public reporting of quality performance.
Both the NHQR and its companion 2006 National Healthcare Disparities
Report (NHDR) provide congressionally mandated annual snapshots of the
U.S. health care system in four key areas: effectiveness of health care,
patient safety, timeliness of care, and patient centeredness. The reports
represent the “broadest analysis of the quality of health care undertaken
in the United States,” authors state.
While the quality of U.S. health care continues to improve, “the
pace of change is slow overall, there is a high degree of variation among
States on many measures, and there is a long way to go to achieve the
best quality possible across most measures” the report said.
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Hospital Care Improves
According to the report, hospital care improved at a significantly higher
rate than care in other settings – 7.8 percent versus 3.2 percent
in ambulatory settings and 1 percent in nursing homes. In a news release
AHRQ attributed this significant improvement “to initiatives sponsored
by HHS’ Centers for Medicare & Medicaid Services (CMS). Quality
Improvement Organizations under contract with CMS, for example, work
with hospitals, consumers, doctors and other caregivers to foster appropriate
and timely care. The Hospital Quality Alliance, a public-private collaboration
that includes hospital organizations and CMS, provides quality measurement
information to consumers and others as an incentive for hospitals to
improve care.”
“Quality improvement programs initiated by HHS are clearly enhancing
health care in the nation, particularly within hospitals,” said
AHRQ Director Carolyn Clancy, MD. “Everyone is benefiting—the
professionals who provide care, the insurers who help pay for care and
the patients who receive care.”
QIO “measures for good heart attack care showed the greatest improvement
of all core measures at 15.0% per year,” noted the report. “This
rate of improvement is markedly better than the 9.2% rate reported last
year and more than 5 times the 2.6% overall rate of improvement for all
non-hospital core measures.”
“QIO measures of the quality of hospital care for pneumonia care
and for heart failure also showed high rates of improvement compared with
all other measures—11.7% and 8.4%, respectively,” the report
said. Avoidance of post-operative complications improved by 7.3 percent.
NHQR Findings
Overall, acute care measures are improving about twice as fast as preventive
or chronic care measures (4.3 percent versus 2.4 percent and 1.8 percent
respectively). The report noted a few exceptions -- vaccinations for
children, teens, and the elderly, which improved 58 percent overall
and chronic care for diabetes, end stage renal disease, and pediatric
asthma, which improved more than three times faster than chronic care
in nursing homes and home health (3.6 percent versus 1 percent).
Care among states varies greatly, the NHQR found. While the all-state
average improved for the percentage of chronic nursing home patients who
were physically restrained, for instance, the variance among states ranged
from 1.7 percent to 14.6 percent.
NHQR includes data from the QIO program, Hospital Compare, OASIS, and
HEDIS, among other data sources. This year’s report also includes
new measure including data from the CAHPS Hospital Survey and the QIO
measure, timing of antibiotics to prevent postoperative wound infection.
The findings seem to indicate that “sustained focus, public reporting,
and active and persistent interventions seem to make a significant difference
in the quality of health care,” the report said. Programs that “appear
to be making an impact” include the Institute for Healthcare Improvement’s
100,000 Lives Campaign, public and private endorsement of hospital quality
measures, implementation of voluntary public reporting programs, and private
sector pay-for-performance efforts to align reimbursements with high quality
care.
NHDR Findings
“It’s encouraging to learn that overall quality continues to
improve,” said AHRQ Director Carolyn M. Clancy, MD. “At the
same time, the message is clear: Much more can be done to prevent illness
from occurring or progressing.”
The 2006 NHDR identified prevention as a key area in which health care
efforts have much room for improvement. Access to care varies widely among
racial, ethnic, and economically disparate groups. As compared to whites,
African Americans received poorer quality of care in 73 percent of core
measures; Hispanics in 77 percent of measures. Low income individuals
received poorer quality of care than higher-income individuals for 71
percent of the measures. Among people 65 and older, blacks, Hispanics
and those in lower income groups were less likely to have ever received
a vaccine to prevent pneumonia.
Overall, findings in the 2006 NHDR indicate that disparities remain prevalent;
improvement in disparities is inconsistent – some measures are diminishing
while others are increasing; and opportunities for raising awareness of
and reducing disparities continue to exist.
The National Healthcare Quality Report is available online at: http://www.ahrq.gov/qual/nhqr06/nhqr06.htm;
the National Healthcare Disparities Report is available at: http://www.ahrq.gov/qual/nhdr06/nhdr06.htm.
Print copies of the reports also can be obtained by calling 1-800-358-9295
or by sending an E-mail to ahrqpubs@ahrq.gov.
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Adding Lab Data and Refining Secondary Diagnosis Information Improves
Measurement of Hospital Quality
In a January 3 JAMA study, researchers found that using new billing codes
taking into account diagnoses present on admission and readily available
numerical laboratory data improves the accuracy of risk-adjusted inpatient
mortality by 24 percent. The study, “Enhancement of Claims Data
to Improve Risk-Adjustment of Hospital Mortality,” was funded by
the Agency for Healthcare Research and Quality.
The accuracy and integrity
of clinical performance data used in determining the quality of care
provided by hospitals and providers is critical in successful implementation
of pay-for-performance and quality improvement initiatives. “This
analysis strongly supports the value of enhancing administrative claims
data with POA codes and a limited set of numerical laboratory values obtained
at admission. These data provide information required to avoid errors
in the designation of hospitals and their medical staffs as delivering
better than average or worse than average care,” said
the authors.
The researchers looked at risk-adjusted mortality rates
for five health conditions: acute myocardial infarction, congestive
heart failure, acute cerebrovascular accident, gastrointestinal tract
hemorrhage, and pneumonia; and three surgical procedures: abdominal aortic
aneurysm repair, coronary artery bypass graft surgery, and craniotomy.
By supplementing claims data with easy to obtain information -- numerical
results of 20 common laboratory tests performed on admission and present
on admission diagnoses -- the authors achieved levels of accuracy only
five percent lower than using complete but difficult and costly to obtain
clinical data.
Read the abstract at: http://jama.ama-assn.org/cgi/content/abstract/297/1/71
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CMS Funds Medicaid Demo Aimed at Keeping Seniors in
Community, Home Setting
In a recent announcement, CMS’ Acting Administrator Leslie Norwalk
said the agency awarded the first round of more than $23 million in grants
for demonstration programs in 17 states designed to help build Medicaid
long-term care programs to keep people in the community and out of institutions.
The new awards are the first round of grants totaling $1.75 billion over
five years (2007-2011) to help states shift Medicaid’s traditional
emphasis on institutional care to a system offering greater choices and
a full range of home- and community-based services. The funds allow states
to do away with waiver programs previously used to fund home and community-based
services. These services will now become a permanent part of the states’ Medicaid
benefits.
Known as Money Follows the Person (MFP), the effort is part of the New
Freedom Initiative, a nationwide effort launched in 2001 to remove barriers
to community living for people of all ages with disabilities and long-term
illnesses. CMS defines MFP as “a system of flexible financing for
long-term services and supports that enables available funds to move with
the individual to the most appropriate and preferred setting as the individual’s
needs and preferences change.” MFP grant funds are expected to help
states expand coverage for individuals with disabilities; increase access
to community supports; and promote personal responsibility, independence,
and choice.
“States will also get more for their money by giving the elderly
and people with disabilities more control over how and where they get
the Medicaid services they need. With these grants, the states propose
to transition over 20,000 individuals from institutions and into community
settings,” said Norwalk. “Because experience shows that money
following the person’s own preferences improves satisfaction and
can reduce Medicaid costs too, we intend to continue taking steps, such
as those taken through these grants, to remove barriers, real or perceived,
that prevent them from participating fully in community life.”
All states are eligible for the grant funds, which require a commitment
to participate in the demonstration services for at least two consecutive
years. A second round of state grants may be announced later this year
using 2007 grant money. Grant amounts varied by state but total more than
$23 million. The 17 states are: Arkansas, California, Connecticut, Iowa,
Indiana, Maryland, Michigan, Missouri, Nebraska, New Hampshire, New York,
Ohio, Oklahoma, South Carolina, Texas, Washington and Wyoming.
More details on the New Freedom Initiative are available at: http://www.cms.hhs.gov/newfreedom/.
More information on the demonstration project is available at: http://www.cms.hhs.gov/NewFreedomInitiative/downloads/MFP_2007_Announcement.pdf
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Medicaid Commission Releases Final Recommendations to Modernize Program
The Medicaid Commission, headed by former Tennessee governor Don Sundquist
and former Maine governor Angus King, Jr., recently presented its final
report and recommendations to Department of Health and Human Services
Secretary Michael Leavitt. The Commission’s recommendations call
for changes in policy that would, among other things, provide better care
coordination, quality reporting, and measurement; break down administrative
barriers; and institute a payment system that rewards care quality versus
quantity.
Quality
In noting that “quality must be brought to the forefront of any
discussion about reforming the Medicaid program,” the Commission
called for transparency in Medicaid payments to providers as well as data
collection on “how Medicaid money is being spent to determine which
programs, providers, and services are effective and which need improvement.” Payments
to providers should be “tied to objective measures of risk- and
case-adjusted medical outcomes” to ensure patients are getting the
care they need.
The Commission also suggests that CMS establish a National Health Care
Innovations Program “1) support the implementation of state-led,
system-wide demonstrations in health care reform and 2) make data design
specifications available to all other states for possible adoption.” “CMS
and Congress should support state innovation to deliver value for taxpayer
dollars by purchasing quality health care outcomes as opposed to simply
reimbursing for health care processes,” the report continues.
A medical home, defined by the Commission as “a source of primary
health care that provides accessible, comprehensive, coordinated care,” is
also recommended for each beneficiary to improve care coordination. Existing
barriers to the creation of medical homes should be eliminated.
Health IT
The Commission calls for all Medicaid beneficiaries to have an electronic
health record by 2012 and for HHS to continue supporting the implementation
of health IT from the federal level. Congressional initiatives to support
health IT are “hampered,” the report said, by the current
Congressional Budget Office scoring process used to determine the cost
of legislation because CBO does not take into account future savings.
The Commission suggested that costs be amortized over five years and
long-term savings be counted.
To ensure interoperability, the report says that Medicaid agencies should
require participating providers to adopt health IT systems that meet recognized
standards.
Long term care
The Commission recommends the adoption of public policy that supports
individual planning for long term care and respects beneficiary preference
to “stay at home in their communities in the least restrictive
or most integrated setting appropriate to their long-term care needs.”
However, in a dissenting opinion, Medicaid Commission member Gwen Gillenwater
of the American Association of People with Disabilities said that the
report fails to “deal with Medicaid’s institutional bias” and
that it “would do nothing to give Medicaid beneficiaries a true
choice between HCBS [home- and community-based services] and nursing homes
and do nothing to address the myriad of state policies and programs that
determine who can and cannot qualify for HCBS.”
The Medicaid Commission was established by Secretary Leavitt under Public
Law 92-463, Federal Advisory Committee Act to provide recommendations
on modernizing the Medicaid program. The first report, submitted in September
2005, included recommendations for achieving $10 billion in Medicaid savings
over five years as well as meaningful program changes to enhance beneficiary
care. This second and final report addresses longer-term changes to ensure
the future of the Medicaid program.
Read the report at: http://www.aspe.hhs.gov/medicaid/122906rpt.pdf
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Wanted: Public Comment on Anti-Fraud Guidelines for EHRs
RTI International, under contract with the Office of the National Coordinator
for Health Information Technology, is seeking comment from industry leaders,
practitioners and the general public on model recommendations to prevent
medical claims errors and detect health care fraud in electronic health
record systems (EHRs).
The standards aim to improve claims accuracy and to reduce the ability
of individuals to create fraudulent claims and other improper payments
against public and private health care plans.
“Currently, most billing errors or fraud is detected after payment
is made, which makes dealing with the claims very inefficient for both
the provider and the payer,” said Colleen McCue, PhD, a senior research
scientist at RTI and project manager. “EHR systems will allow for
the opportunity to correctly bill from the very beginning, which will
help physicians to receive accurate payments and ultimately will reduce
fraud.”
Once finalized, the model anti-fraud requirements will be submitted to
the Certification Commission for Health Information Technology as potential
EHR anti-fraud certification criteria.
The recommendations are available for review and comment at: http://ehrantifrauddev.rti.org.
Comments must be submitted by January 22, 2007.
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NIH Site Offers Information on Depression for Seniors
Information on depression was recently added to NIHSeniorHealth.gov,
an award-winning Web site designed to provide accessible, easy to understand
aging-related health information especially for adults age 60 to 88.
The Web site and materials were developed by the National Institutes
of Health’s National Institute on Aging and the National Library
of Medicine. The depression materials, which were contributed by the National
Institute of Mental Health, include segments titled “About Depression;” “Causes
and Risk Factors;” “Symptoms and Diagnosis;” “ Treatment
and Research;” “Frequently Asked Questions;” and a link
to Medline Plus for more information. Read more at: http://nihseniorhealth.gov/depression/toc.html
Other topics available include common senior health problems such as
diabetes, medication administration, falls, heart failure, and heart attack.
Design of the Web site ensures that information is easy for seniors to
see, understand, and navigate. An audio button allows text to be read
aloud; other buttons can increase text size and/or contrast to improve
readability.
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National Campaign to Reduce Avoidable Hospitalization in
Home Health Patients Kicks Off at CMS Headquarters
At the Centers for Medicare & Medicaid Services’ (CMS) headquarters
in Baltimore, national home care and health care leaders kicked off the
2007 Home Health Quality Improvement (HHQI) National Campaign, an initiative
that unites the home care community under a shared vision of reducing
avoidable hospitalizations to improve patient quality of care. To date,
more than 3000 agencies have signed up to participate – with more
than 1200 doing so within the first hours of the Campaign.
Patients would prefer to stay at home whenever possible while recuperating
from an injury or illness. Being hospitalized can create financial and
emotional burdens for patients and their families, and can negatively
impact the health care delivery system. Currently, more than one in four
home health patient episodes will result in a hospitalization. HHQI seeks
to change that by bringing the home care community together to share tools,
resources, guidelines, information, and best practices among agencies
across the country.
“Providing quality post acute care is a high priority for CMS,” said
Barry Straube, MD, Chief Medical Officer and Director of the Office of
Clinical Standards and Quality. “To help achieve our vision for
the right care for every person every time, we are pleased to have a broad
array of stakeholders working together in the home care setting to reduce
avoidable hospitalizations that will improve patient satisfaction, outcomes,
and save Medicare dollars.”
The Campaign
Similar in structure to the national nursing home campaign (Advancing
Excellence in America’s Nursing Homes) launched last September,
HHQI is a 12-month campaign led by CMS and the Home Health QIOSC (Quality
Insights of Pennsylvania) and includes key home health, hospital, physician,
and managed care stakeholders. The goal is to increase the number of
home care patients able to remain in their home and avoid hospitalizations.
Success will be measured by a reduction in the average acute care hospitalization
rate across all participating home health agencies by a five percent relative
improvement from baseline to the end of the Campaign.
Participants will be assisted by local area networks of excellence, or
LANEs. “We started planning this campaign in September 2006 and
already 95 percent of states and territories have LANEs,” said Marian
Essey, RN, BSN, Director, Home Health Quality Improvement at Quality Insights
of Pennsylvania. The primary role of LANEs will be ongoing communication
with participating agencies in their states. “We have been very
pleased with the response from QIOs and state home care associations in
their willingness to act as a LANE in their states or territories. A very
high number of QIOs have committed to act as a LANE. The stakeholder enthusiasm
for this campaign has been tremendous. We attribute the large number of
early home health agency participants to the outreach and enthusiasm of
the stakeholders and QIOs,” continued Ms. Essey.
Home health agencies wishing to join the campaign can register online.
Each will receive a welcome packet with information on the Campaign as
well as a logo and certificate of participation. The early adopters that
signed up within the first 24 hours will receive a special logo and recognition
as a “premier agency.” Participation is free and no additional
data collection will be required.
Each state’s QIO will provide participating agencies with data
comparing individual agency performance with all Medicare home health
agencies. The Home Health QIOSC will provide each LANE with a monthly
eBulletin to assist in their efforts to act as champions for the Campaign
and support ongoing communications with participating agencies. Beginning
in March and monthly thereafter, a new Best Practice Intervention Package
will be available on the HHQI website (www.homehealthquality.org). Each
package focuses on one of the 12 top best practices available to reduce
hospitalization.
The Summit
More than 200 people representing QIOs, health care industry leaders,
home health agencies, CMS, and AHQA attended the kick-off event held
in Baltimore. After welcome remarks from Cynthia Pamon, RN, BSN, CCM,
CPUM, Home Health Government Task Leader for CMS, Ms. Essey, who moderated
the event, introduced the Campaign and its overall goals.
The Campaign “seeks to unite the home care community under a shared
vision” for improved care explained Dr. Straube in his presentation,
which explained how the Campaign fit in CMS’ overall goals to improve
care for all Medicare beneficiaries.
Presenting the physician perspective, Steve Winbery, PhD, MD, Medical
Director at QSource, the Tennessee QIO, stressed that good, coordinated
communication between the physician and home care provider is critical
to improving care. Pursuing support or advocacy from a medical director
who can participate in peer-to-peer communication with providers might
help, he suggested Dr. Winbery also called for more frequent review and
updating of OASIS measures to ensure that the measurement accurately reflects
performance.
Interspersed throughout the day-long event were taped vignettes featuring
home health patients and their providers discussing the importance of
receiving care at home and how it has impacted their health and improved
their quality of life. These vignettes and other information from the
event are available online at: http://www.homehealthquality.org/hh/summit/default.aspx.
The home health care provider is the “hub of a lot of different
settings,” said Robyn Stone, DrPH, Executive Director of the Institute
for the Future of Aging Services at the American Association of Homes
and Services for the Aging. Dr. Stone presented an integrated model for
care improvement, which includes person-centeredness, staff improvement,
and continuous quality improvement. Good communications and personal interactions
are integral to the clinical aspects of home care, she said.
On December 13, 2006, CMS announced a home health demonstration pay-for-performance
program designed to improve quality of care without increasing cost, said
James Coan, Office of Research Development and Information at CMS. Mr.
Coan said that two-year voluntary program scheduled to begin in October
2007, would use existing quality measures and compensate both the top
performers and those showing the most improvement over time. Proposed
measures for the demo include: acute care hospitalization, emergent care,
bathing, ambulation, transferring, incontinence, oral medications, and
surgical wounds. More information on the demo is available at www.hhp4p.info.
Members of the Home Health QIO Executive Steering Committee rounded out
the event with comments about how their respective organizations would
support the campaign and provided resources available to HHQI participants.
Founding stakeholders of HHQI include: National Association for Home
Care and Hospice; American Association for Homecare; Visiting Nurse Association
of America; American Telemedicine Association; Hospice and Palliative
Nurses Association; Care Transitions Program, University of Colorado Health
Sciences Center; American Occupational Therapy Association; American Physical
Therapy Association; American Speech-Language-Hearing Association; Gentiva
Health Services; Visiting Nurse Service of New York, Center for Home Care
Policy and Research; The Remington Report; CMS and QIOs.
The HHQI official Web site is: www.homehealthquality.org.
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SAVE
THE DATE
Health Affairs Briefing
Health Information Technology And Rapid Learning
HHS Secretary Michael Leavitt To Kick Off Discussion On
How Electronic Health Records Can Speed Advances In Medical Care
WHEN: Friday,
January 26, 2007 – Washington, D.C.
9:30 a.m. – 11:30 a.m.
WHERE: Columbus Club
Union Station [Union Station metro stop]
WHO: Michael O. Leavitt, Health & Human Services Secretary
John Lumpkin, M.D., Senior Vice President and Health Care Group Director, Robert
Wood Johnson Foundation
Lynn Etheredge, consultant, Health Insurance Reform Project at the George Washington
University
David Eddy, M.D., Medical Director and Founder, Archimedes
Joel Kupersmith, M.D., Chief Research & Development Officer, Veterans Health
Administration
Paul Wallace, M.D., Medical Director, Health and Productivity Management Programs,
Kaiser Permanente
John Iglehart, Founding Editor, Health Affairs
RSVP: Please RSVP for this event online at www.burnesscommunications.com/new.
For more information about this event, contact Erin Kerr at ekerr@burnesscommunications.com
or 301-652-1558.
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New Weekly News Report on Disparities Available for Free
The Kaiser Family
Foundation (KFF) recently launched a free weekly email news report on
racial and ethnic disparities. The Kaiser Health Disparities Report:
A Weekly Look at Race, Ethnicity and Health summarizes and synthesizes
news coverage of minority health issues from hundreds of print and broadcast
news sources, including outlets serving racial and ethnic communities.
The report will also highlight studies, initiatives and journal articles
that don’t receive mainstream news coverage, and provide a calendar
of upcoming events on health disparities.
KFF will also expand its
coverage to include webcasts of policy-oriented conferences and events
on racial and ethnic health issues and provide related original broadcast
programming such as interviews and interactive panel discussions. “With
this new report, our aim is to bring news and developments on health
disparities on a real-time basis to people working in the field, especially
outside the beltway,” said Drew
Altman, president and CEO of the Kaiser Family Foundation.
To sign up
and get more information, visit: http://www.kff.org/profile/subscriptions.cfm?site=kaisernetwork
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Spanish Health Resource Available
A Spanish version of the 290-page Alliance
for Health Reform book, “Covering
Health Issues,” is now available free for downloading at www.allhealth.org/sourcebookTOC.asp?SBID=2
Although the resource was developed to educate news reporters covering
health care issues, much of the material is relevant to the general
public. The publication includes basic but thorough information on Medicaid,
Medicare, children’s health coverage, disparities, mental health,
the uninsured and an array of other topics. It also includes a complete
glossary of health coverage terms in Spanish.
“La cobertura periodística
de temas de salud 2006 – 2007” is
the latest in a series of guides produced at the Alliance, with a grant
from the Robert Wood Johnson Foundation. To download the publication (by
chapter), visit www.allhealth.org/sourcebookTOC.asp?SBID=2.
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AHRQ Database Provides Health Insurance Cost Data for Large US Cities
A new federal database developed by the Agency for Healthcare Research
and Quality (AHRQ) offers companies, consumers, health care analysts and
others the ability to compare health insurance costs among the nation’s
largest cities.
The database, based on information from AHRQ’s Medical Expenditure
Panel Survey for 2004, provides comparable statistics on average annual
costs for companies and workers contributing to private-sector health
insurance. It is available at:
http://www.meps.ahrq.gov/mepsweb/survey_comp/Insurance.jsp.
Large geographical variations are evident in how much Americans pay for
family and individual coverage as well as how much employers contribute
to workers’ health insurance premiums. The data include statistical
averages from the following cities and surrounding areas: New York, Los
Angeles, Chicago, Philadelphia, Dallas-Fort Worth, Miami, Houston, Washington,
DC, Atlanta, Detroit, Boston, San Francisco, Riverside, Phoenix, Seattle,
Minneapolis, San Diego, St. Louis, Baltimore and Tampa.
“We already know that the quality of health care can vary significantly
according to geography,” said AHRQ Director Carolyn M. Clancy, MD
in a press release. “These new data highlight local cost variations
and may help employers make annual benefit plan decisions.”
NIH Plan Aims to Transform Clinical Research
The Journal Clinical Pharmacology & Therapeutics recently published
the article “Translational Research: Moving Discovery to Practice” by
Dr. Elias Zerhouni, Director of the National Institutes of Health, which
outlines plans to change the nation’s approach to clinical research.
Drawing from the NIH Roadmap, an ongoing plan developed in consultation
with scientists and clinicians, the NIH recently awarded the first 12
of about 60 total Clinical and Translational Science Awards (CTSAs) to
academic health centers throughout the nation. When fully implemented
in 2012, the institutions will be linked together to become a national
research consortium that increase the efficiency of clinical research
and allow patients quicker, more widespread access to new treatments and
processes that can improve care. “Working together, these sites
will serve as discovery engines that will improve medical care by applying
new scientific advances to real-world practice,” writes Dr. Zerhouni.
In addition to “Re-engineering the Clinical Research Enterprise,” under
which the CTSA grants fall, the NIH Roadmap also includes plans for “New
Pathways to Discovery,” and “Research Teams of the Future.” Read
the roadmap at: http://nihroadmap.nih.gov/
The NIH has issued a second
request for applications for CTSAs grants with a submission deadline
of January 17, 2007; awards are expected to be made in fall 2007. The
Request for Applications is available at http://grants.nih.gov/grants/guide/rfa-files/RFA-RM-07-002.html.
For
more information about this initiative, visit http://www.ncrr.nih.gov/clinicaldiscipline.asp.
The
full text of Dr. Zerhouni’s article is available free at: http://www.nature.com/clpt/journal/v81/n1/full/6100029a.html
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Commonwealth: Using Research Effectively in State Policymaking
The Commonwealth
Fund recently released “Toward More Effective Use
of Research in State Policymaking,” a publication to help state
policymakers turn health services research into action through a conceptual
framework.
The report uses the creation and launch of Massachusetts statewide
health plan as a case study to demonstrate the four stages if its
framework: understanding the scope and extent of the problem; developing
options; implementing a program/policy; and evaluating the program/policy.
Practical lessons and communication strategies are gleaned from interviews
with researchers working on state issues and state health policymakers.
Recommendations are presented as targeted tools for researchers and
policymakers separately, to address their unique roles.
The full report
is available free at: http://www.cmwf.org/usr_doc/Meyer_towardmoreeffectiveusestatepolicymaking_980.pdf
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