NIH Consensus Development Conference: Management of Hepatitis B; Notice, 47199 [E8-18656]
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Federal Register / Vol. 73, No. 157 / Wednesday, August 13, 2008 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
ebenthall on PRODPC60 with NOTICES
NIH Consensus Development
Conference: Management of Hepatitis
B; Notice
Notice is hereby given of the National
Institutes of Health (NIH) ‘‘NIH
Consensus Development Conference:
Management of Hepatitis B’’ to be held
October 20–22, 2008, in the NIH
Natcher Conference Center, 45 Center
Drive, Bethesda, Maryland 20892. The
conference will begin at 8:30 a.m. on
October 20 and 21, and at 9 a.m. on
October 22, and will be open to the
public.
Hepatitis B is a major cause of liver
disease worldwide, ranking as a
substantial cause of cirrhosis and liver
cancer. In the United States, about 1.25
million people are chronically infected
with the virus, resulting in 3,000 to
5,000 deaths each year. However, this
condition occurs more frequently in
high risk groups, including Asian
Americans, emigrants from areas of the
world where hepatitis B is common
(China, Korea, Southeast Asia, the
Indian Subcontinent, Africa, and
Micronesia), men who have sex with
men, injection drug users, and
recipients of blood and blood products
before screening procedures with
enhanced sensitivity were implemented
in 1986. Since routine hepatitis B
vaccination of U.S. children began in
1991, new cases of acute hepatitis B
among children and adolescents have
dropped by more than 95 percent—and
by 75 percent across all age groups. In
nonprotected individuals, transmission
can result from exposure to infectious
blood or body fluids containing blood.
A major impediment to diagnosis is that
many infected individuals are either
asymptomatic or experience only
nonspecific symptoms of disease, such
as fatigue or muscle ache.
For approximately 90 percent of
adults, acute infection with the hepatitis
B virus is resolved by the body’s
immune system and does not cause
long-term problems. The transition from
acute to chronic infection appears to
occur when the immune system does
not effectively destroy and clear virusinfected cells. This leads to high blood
levels of both hepatitis B DNA and
antigens, as well as antibodies produced
by the body in an attempt to combat the
infection. The natural history of the
disease is not well understood,
however, which makes management of
this complex disease challenging.
VerDate Aug<31>2005
15:38 Aug 12, 2008
Jkt 214001
Many factors can influence treatment
decisions for an individual patient,
including age, ALT (alanine
aminotransferase, a liver enzyme) level,
viral load, liver biopsy results, and the
presence of a co-infecting virus (i.e.,
HIV). Treatment decisions require indepth analysis of multiple blood test
results, which are typically repeated at
regular intervals to monitor the disease
course. There are currently six approved
therapeutic agents: interferon-alpha,
lamivudine, adefovir dipivoxil,
entecavir, pegylated interferon, and
telbivudine, which are often used in
combination. Generally, these drugs act
to decrease the risk of liver damage from
hepatitis B by slowing or stopping the
replication of the virus.
Questions remain as to which groups
of patients benefit from therapy and at
which point in the course of their
disease. Specific recommendations for
hepatitis B therapy are limited by a lack
of reliable long-term safety and efficacy
information. This is a difficult decision
for physicians and patients, as
treatments are expensive and may have
bothersome, if not harmful, effects on
patients. Left untreated, however,
chronic hepatitis B can lead to liver
failure and other serious liver problems.
To examine these important issues, the
National Institute of Diabetes and
Digestive and Kidney Diseases and the
Office of Medical Applications of
Research of the National Institutes of
Health will convene a Consensus
Development Conference from October
20 to 22, 2008, to assess the available
scientific evidence related to the
following questions:
• What is the current burden of
hepatitis B?
• What is the natural history of
hepatitis B?
• What are the benefits and risks of
the current therapeutic options for
hepatitis B?
• Which persons with hepatitis B
should be treated?
• What measures are appropriate to
monitor therapy and assess outcomes?
• What are the greatest needs and
opportunities for future research on
hepatitis B?
An impartial, independent panel will
be charged with reviewing the available
published literature in advance of the
conference, including a systematic
literature review commissioned through
the Agency for Healthcare Research and
Quality. The first day and a half of the
conference will consist of presentations
by expert researchers and practitioners
and open public discussions. On
Wednesday, October 22, the panel will
present a statement of its collective
assessment of the evidence to answer
PO 00000
Frm 00074
Fmt 4703
Sfmt 4703
47199
each of the questions above. The panel
will also hold a press conference to
address questions from the media. The
draft statement will be published online
later that day, and the final version will
be released approximately six weeks
later. The primary sponsors of this
meeting are the NIH National Institute
of Diabetes and Digestive and Kidney
Diseases and the NIH Office of Medical
Applications of Research.
Advance information about the
conference and conference registration
materials may be obtained from
American Institutes for Research of
Silver Spring, Maryland, by calling 888–
644–2667, or by sending e-mail to
consensus@mail.nih.gov. American
Institutes for Research’s mailing address
is 10720 Columbia Pike, Silver Spring,
MD 20901. Registration information is
also available on the NIH Consensus
Development Program Web site at
https://consensus.nih.gov.
Please Note: The NIH has instituted
security measures to ensure the safety of NIH
employees and property. All visitors must be
prepared to show a photo ID upon request.
Visitors may be required to pass through a
metal detector and have bags, backpacks, or
purses inspected or x-rayed as they enter NIH
buildings. For more information about the
security measures at NIH, please visit the
Web site at https://www.nih.gov/about/
visitorsecurity.htm.
Dated: August 4, 2008.
Raynard S. Kington,
Deputy Director, National Institutes of Health.
[FR Doc. E8–18656 Filed 8–12–08; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
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National Institutes of Health’s Senior
Executive Service 2008 Performance
Review Board
The National Institutes of Health
(NIH) announces the persons who will
serve on the National Institutes of
Health’s Senior Executive Service 2008
Performance Review Board. This action
is being taken in accordance with Title
5, U.S.C., Section 4314(c)(4), which
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review boards be appointed in a manner
to ensure consistency, stability, and
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The following persons will serve on
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E:\FR\FM\13AUN1.SGM
13AUN1
Agencies
[Federal Register Volume 73, Number 157 (Wednesday, August 13, 2008)]
[Notices]
[Page 47199]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-18656]
[[Page 47199]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
NIH Consensus Development Conference: Management of Hepatitis B;
Notice
Notice is hereby given of the National Institutes of Health (NIH)
``NIH Consensus Development Conference: Management of Hepatitis B'' to
be held October 20-22, 2008, in the NIH Natcher Conference Center, 45
Center Drive, Bethesda, Maryland 20892. The conference will begin at
8:30 a.m. on October 20 and 21, and at 9 a.m. on October 22, and will
be open to the public.
Hepatitis B is a major cause of liver disease worldwide, ranking as
a substantial cause of cirrhosis and liver cancer. In the United
States, about 1.25 million people are chronically infected with the
virus, resulting in 3,000 to 5,000 deaths each year. However, this
condition occurs more frequently in high risk groups, including Asian
Americans, emigrants from areas of the world where hepatitis B is
common (China, Korea, Southeast Asia, the Indian Subcontinent, Africa,
and Micronesia), men who have sex with men, injection drug users, and
recipients of blood and blood products before screening procedures with
enhanced sensitivity were implemented in 1986. Since routine hepatitis
B vaccination of U.S. children began in 1991, new cases of acute
hepatitis B among children and adolescents have dropped by more than 95
percent--and by 75 percent across all age groups. In nonprotected
individuals, transmission can result from exposure to infectious blood
or body fluids containing blood. A major impediment to diagnosis is
that many infected individuals are either asymptomatic or experience
only nonspecific symptoms of disease, such as fatigue or muscle ache.
For approximately 90 percent of adults, acute infection with the
hepatitis B virus is resolved by the body's immune system and does not
cause long-term problems. The transition from acute to chronic
infection appears to occur when the immune system does not effectively
destroy and clear virus-infected cells. This leads to high blood levels
of both hepatitis B DNA and antigens, as well as antibodies produced by
the body in an attempt to combat the infection. The natural history of
the disease is not well understood, however, which makes management of
this complex disease challenging.
Many factors can influence treatment decisions for an individual
patient, including age, ALT (alanine aminotransferase, a liver enzyme)
level, viral load, liver biopsy results, and the presence of a co-
infecting virus (i.e., HIV). Treatment decisions require in-depth
analysis of multiple blood test results, which are typically repeated
at regular intervals to monitor the disease course. There are currently
six approved therapeutic agents: interferon-alpha, lamivudine, adefovir
dipivoxil, entecavir, pegylated interferon, and telbivudine, which are
often used in combination. Generally, these drugs act to decrease the
risk of liver damage from hepatitis B by slowing or stopping the
replication of the virus.
Questions remain as to which groups of patients benefit from
therapy and at which point in the course of their disease. Specific
recommendations for hepatitis B therapy are limited by a lack of
reliable long-term safety and efficacy information. This is a difficult
decision for physicians and patients, as treatments are expensive and
may have bothersome, if not harmful, effects on patients. Left
untreated, however, chronic hepatitis B can lead to liver failure and
other serious liver problems. To examine these important issues, the
National Institute of Diabetes and Digestive and Kidney Diseases and
the Office of Medical Applications of Research of the National
Institutes of Health will convene a Consensus Development Conference
from October 20 to 22, 2008, to assess the available scientific
evidence related to the following questions:
What is the current burden of hepatitis B?
What is the natural history of hepatitis B?
What are the benefits and risks of the current therapeutic
options for hepatitis B?
Which persons with hepatitis B should be treated?
What measures are appropriate to monitor therapy and
assess outcomes?
What are the greatest needs and opportunities for future
research on hepatitis B?
An impartial, independent panel will be charged with reviewing the
available published literature in advance of the conference, including
a systematic literature review commissioned through the Agency for
Healthcare Research and Quality. The first day and a half of the
conference will consist of presentations by expert researchers and
practitioners and open public discussions. On Wednesday, October 22,
the panel will present a statement of its collective assessment of the
evidence to answer each of the questions above. The panel will also
hold a press conference to address questions from the media. The draft
statement will be published online later that day, and the final
version will be released approximately six weeks later. The primary
sponsors of this meeting are the NIH National Institute of Diabetes and
Digestive and Kidney Diseases and the NIH Office of Medical
Applications of Research.
Advance information about the conference and conference
registration materials may be obtained from American Institutes for
Research of Silver Spring, Maryland, by calling 888-644-2667, or by
sending e-mail to consensus@mail.nih.gov. American Institutes for
Research's mailing address is 10720 Columbia Pike, Silver Spring, MD
20901. Registration information is also available on the NIH Consensus
Development Program Web site at https://consensus.nih.gov.
Please Note: The NIH has instituted security measures to ensure
the safety of NIH employees and property. All visitors must be
prepared to show a photo ID upon request. Visitors may be required
to pass through a metal detector and have bags, backpacks, or purses
inspected or x-rayed as they enter NIH buildings. For more
information about the security measures at NIH, please visit the Web
site at https://www.nih.gov/about/visitorsecurity.htm.
Dated: August 4, 2008.
Raynard S. Kington,
Deputy Director, National Institutes of Health.
[FR Doc. E8-18656 Filed 8-12-08; 8:45 am]
BILLING CODE 4140-01-P