| Issue Number
75, September 16, 2008 |
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| Contents of this Issue |
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ABBREVIATIONS: ACIP, Advisory Committee on Immunization Practices; CDC, Centers
for Disease Control and Prevention; DVH, Division of Viral Hepatitis; HAV,
hepatitis A virus; HBV, hepatitis B virus; HCV, hepatitis C virus; IAC,
Immunization Action Coalition; IDU, injection drug user; MMWR, Morbidity and
Mortality Weekly Report; MSM, men who have sex with men; STD, sexually
transmitted disease; VIS, Vaccine Information Statement; WHO, World Health
Organization.
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(1 of 11)
September 16, 2008
2006 NIS DATA INDICATE 50 PERCENT OF NEWBORNS BORN BETWEEN JANUARY 2003-JUNE
2005 RECEIVED THE HEPATITIS B BIRTHDOSE BY AGE 3 DAYS
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/4/08.]
CDC published "Newborn Hepatitis B Vaccination Coverage Among Children Born
January 2003-June 2005--United States" in the August 1 issue of MMWR. It is
reprinted below in its entirety, excluding one table and references.
IAC Express editor's note: We have included links to several relevant resources
at the end of this IAC Express article.
***********************
Hepatitis B vaccine was first recommended for administration to all infants in
1991 by the Advisory Committee on Immunization Practices (ACIP) as the primary
focus of a strategy to eliminate hepatitis B virus (HBV) transmission in the
United States. The recommended timing of administration of the first dose of
hepatitis B vaccine to infants has evolved since then to optimize prevention of
perinatal and early childhood HBV infections. In 1991, the first dose was
recommended to be administered at birth before hospital discharge or at age 1-2
months. In 2002, ACIP indicated a preference for the first dose to be
administered to newborns before hospital discharge. In December 2005, ACIP
issued revised recommendations specifying that all medically stable newborns who
weigh >=2,000 g (4.4 lbs) receive their first dose of hepatitis B vaccine before
hospital discharge. To measure hepatitis B vaccination coverage during the
neonatal period, CDC analyzed data from the 2006 National Immunization Survey (NIS).
This report summarizes the results of this analysis and provides national,
state, and local data on vaccination coverage for infants who received the
hepatitis B vaccine during the first days of life. The findings reveal that,
during January 2003-June 2005, before implementation of the 2005 ACIP hepatitis
B vaccine recommendation, the national newborn hepatitis B vaccination coverage
estimate was 42.8% at age 1 day and 50.1% at age 3 days, with substantial
variation by states and local areas. To comply with ACIP recommendations and
increase coverage, delivery hospitals should provide hepatitis B vaccination of
newborns as a standard of care.
NIS provides estimates of vaccination coverage among noninstitutionalized
children aged 19-35 months for each of the 50 states and selected local areas.
To collect vaccination data, NIS conducts a random-digit-dialed telephone survey
of households and a mail survey of children's vaccination providers identified
by household respondents. Data are weighted to adjust for households with
multiple telephone lines, household nonresponse, and exclusion of households
without landline telephones. Infant age at vaccination was calculated by
subtracting birth date from vaccination date. Children included in the 2006 NIS
were born during January 2003-June 2005.
Household response rate for the survey was 64.5%, based on Council of American
Survey and Research Organizations guidelines (CASRO); 21,044 children with
provider-verified vaccination records were included in this report and represent
70.4% of all children with completed household interviews. National newborn
hepatitis B vaccination coverage was 42.8% at age 1 day, 48.5% at 2 days, 50.1%
at 3 days, 51.1% at 4 days, 51.8% at 5 days, and 52.5% at 6 days. State and
local area rates showed substantial variability, with hepatitis B vaccination
coverage at age 1 day ranging from 8.2% in Fresno County, California, to 77.5%
in Detroit, Michigan. Among all states and local areas surveyed, the median
coverage estimate was 50.3% at age 1 day and 58.7% at 3 days.
Editorial Note:
The analysis in this report indicates that, for the January 2003-June 2005 birth
cohort, 42.8% of newborns had received hepatitis B vaccine by age 1 day and
50.1% had received hepatitis B vaccine by age 3 days. These data provide a
baseline for assessing implementation of the December 2005 ACIP recommendation
to administer hepatitis B vaccine to all newborns before hospital discharge. The
2009 NIS will be the first to include all survey-eligible children who were born
after the December 2005 recommendation was made. Therefore, that survey will be
the first to provide full estimates of national newborn vaccination coverage to
evaluate the effect of the 2005 ACIP recommendation.
Newborn hepatitis B vaccination coverage estimates varied substantially among
and within states. Administration of hepatitis B vaccine to newborns is
dependent on hospital policies and procedures and on provider and parent
preferences.
Although NIS does not distinguish whether hepatitis B vaccine was given before
or after hospital discharge, National Hospital Discharge Survey data indicate
that the average length of hospital stay for all newborns in 2004 was 3.3 days,
with an average stay of 2.1 days for well newborns and an average stay of 5.0
days for ill newborns; 85.6% of all newborns were discharged by age 3 days.
The findings in this report are subject to at least four limitations. First, NIS
is a telephone survey; although results are statistically adjusted to account
for nonresponse and households without telephones, some bias might remain.
Second, vaccination coverage is confirmed using provider-verified records.
Although clinic providers might not always have records of a
hospital-administered hepatitis B vaccine dose, this does not appear to result
in substantial under-ascertainment of vaccination. A 2004 study in eight
locations matched provider-reported vaccination records for the children sampled
in NIS to their vaccination histories reported by the state Immunization
Information Systems (IIS). NIS data underestimated birth dose coverage by no
more than 5% at any one location when compared with the combined NIS and IIS
coverage among children who had vaccination histories from both sources (M Khare,
CDC, personal communication, February 2008). Third, estimates from state and
local areas should be interpreted with caution because of smaller sample size
and wider confidence intervals compared with the national estimate. Finally,
infants who were not recommended to receive hepatitis B vaccine until age 1
month or after hospital discharge because their birth weights were <2,000 g and
they were born to HBsAg-negative mothers could not be excluded from the coverage
estimates. Inclusion of those infants in the denominator might result in an
underestimate of newborn coverage, but the effect should be minimal because
infants at this birth weight account for only 3% of births.
Infants infected with HBV typically are asymptomatic and have a 90% likelihood
of remaining chronically infected. Up to 25% of chronically infected children
die prematurely of cirrhosis or liver cancer. Two primary modes of HBV
transmission occur during infancy and early childhood: (1) from an infected
mother to her infant during delivery, and (2) from infected household contacts
to infant or child. Both modes of transmission can be prevented by immunization
of newborn infants. For infants born to mothers identified as hepatitis B
surface antigen (HBsAg)-positive (i.e., HBV-infected), administration of
hepatitis B vaccine and hepatitis B immune globulin within 12 hours of birth is
85%-95% effective as postexposure prophylaxis in preventing HBV infection in the
infant. In addition, hepatitis B vaccine alone is 70%-95% effective in
preventing perinatal HBV transmission when the first dose is given within 24
hours of birth. Thus, administration of hepatitis B vaccine soon after birth
provides timely postexposure prophylaxis to infants born to HBsAg-positive
mothers who were not screened prenatally, or were not identified as HBsAg-positive
because of testing errors or lapses in reporting or documentation of test
results. Hepatitis B vaccination of all newborns also provides early preexposure
protection to infants born to uninfected women during a period when the risk for
developing chronic HBV infection is greatest.
The 2005 ACIP recommendation to administer the first dose of hepatitis B vaccine
to all newborns before hospital discharge will increase hepatitis B vaccination
coverage during the first days of life. Delivery hospitals play a key role in
the national strategy to eliminate HBV transmission. The 2005 ACIP statement
recommends that delivery hospitals have policies and procedures in place,
including appropriate standing orders, to ensure (1) administration of hepatitis
B vaccine to all newborns with birth weights >=2,000 g before hospital discharge
and (2) identification of all infants born to HBsAg-positive mothers and infants
born to mothers with unknown HBsAg status to allow initiation of postexposure
prophylaxis within 12 hours of birth. State and local information on prevention
of HBV infection in infants and children, including information on
hospital-based policies and procedures to prevent HBV infection, is available
through CDC-funded perinatal hepatitis B prevention coordinators based in state
health departments. Contact information for those coordinators is available at
http://www.cdc.gov/vaccines/vpd-vac/hepb/perinatal-contacts.htm
***********************
To access a web-text (HTML) version of the complete article, go to:
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5730a3.htm
To access a ready-to-print (PDF) version of this issue of MMWR, go to:
http://www.cdc.gov/mmwr/PDF/wk/mm5730.pdf
To receive a FREE electronic subscription to MMWR (which includes new ACIP
recommendations), go to:
http://www.cdc.gov/mmwr/mmwrsubscribe.html
Relevant resources:
"A Comprehensive Immunization Strategy to Eliminate Transmission of Hepatitis B
Virus Infection in the United States. Recommendations of the Advisory Committee
on Immunization Practices (ACIP). Part 1: Immunization of Infants, Children and
Adolescents":
http://www.cdc.gov/mmwr/PDF/rr/rr5416.pdf
"AAP Endorsed Policy Statement: A Comprehensive Immunization Strategy to
Eliminate Transmission of Hepatitis B Virus Infection in the United States":
http://aappolicy.aappublications.org/cgi/content/full/pediatrics;118/1/404
"Guidelines for Standing Orders in Labor & Delivery & Nursery Units to Prevent
Hepatitis B (HBV) Transmission to Newborns":
http://www.immunize.org/catg.d/p2130.pdf
"Hepatitis B Shots Are Recommended for All New Babies":
http://www.immunize.org/catg.d/p4110.pdf
"States Report Hundreds of Medical Errors in Perinatal Hepatitis B Prevention":
http://www.immunize.org/catg.d/p2062.pdf
"Unprotected Babies: Two More Infants Chronically Infected with Hepatitis B
Virus . . . the Medical Errors Continue":
http://www.immunize.org/catg.d/p2127.pdf
"Medical Errors Put Infants at Risk for Chronic Hepatitis B Virus Infection--Six
Case Reports":
http://www.immunize.org/catg.d/p2128.pdf
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September 16, 2008
CDC CORRECTS AN "ASK THE EXPERTS" ANSWER THAT APPEARED IN RECENT ISSUES OF
NEEDLE TIPS, VACCINATE ADULTS, AND VACCINATE WOMEN
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/4/08.]
IAC was informed by a careful reader that an incorrect answer was published in
"Ask the Experts" in Needle Tips (March 2008, page 22), Vaccinate Adults (March
2008, page 10), and Vaccinate Women (June 2008, page 10). The question concerned
pre-exposure prophylaxis for travelers to protect them from hepatitis A virus
infection. The question and its corrected answer follow.
QUESTION:
What are the new recommendations for vaccination of travelers to protect them
from hepatitis A virus (HAV) infection?
ANSWER:
The new recommendations (www.cdc.gov/mmwr/preview/mmwrhtml/mm5641a3.htm)
state that (1) hepatitis A vaccine is recommended for healthy susceptible
persons ages 1 through 40 years who travel to or work in regions where hepatitis
A is endemic and (2) hepatitis A vaccine should be given as soon as travel is
considered, but it can be given any time prior to departure. For optimal
protection, persons older than age 40 years, immunocompromised persons, and
persons with diagnosed chronic liver disease or other chronic medical
conditions, if departure will take place within two weeks, should also receive
IG simultaneously with the first dose of hepatitis A vaccine but at a different
anatomic injection site. For travelers younger than age 1 year, IG alone is
recommended because hepatitis A vaccine is not licensed for use in this age
group. Hepatitis A is endemic in all regions except the United States, Western
Europe, New Zealand, Australia, Canada, and Japan.
IAC regrets the confusion the initial Q&A may have caused readers of Needle
Tips, Vaccinate Adults, and Vaccinate Women.
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September 16, 2008
CDC LAUNCHES ONLINE FORUM FOR EXCHANGING IDEAS ABOUT HIV, HEPATITIS, STD, AND TB
PREVENTION
You are invited to exchange ideas on HIV/AIDS, viral hepatitis, STD, and TB
prevention research and programs on Health Protection Perspectives, the new blog
by Dr. Kevin Fenton, Director of CDC's National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention.
To access this new resource, go to
http://www.cdc.gov/nchhstp/blog
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September 16, 2008
IAC UPDATES EIGHT PIECES RELATED TO HEPATITIS B OR GENERAL IMMUNIZATION
IAC made the following changes to eight of its educational pieces related to
hepatitis B or general immunization:
(1) In the piece "Guide to Contraindications and Precautions to Commonly Used
Vaccines," changes were made to the sections on rotavirus vaccine; diphtheria,
tetanus, pertussis (DTaP) vaccine; tetanus, diphtheria (DT, Td) vaccines; and
zoster vaccine.
To access this revised resource, go to:
http://www.immunize.org/catg.d/p3072a.pdf
(2) In the piece "It's Federal Law! You must give your patients current Vaccine
Information Statements (VISs)," the issue dates were changed for the VISs for
trivalent inactivated influenza vaccine (TIV; injectable) and live attenuated
influenza vaccine (LAIV; nasal spray).
To access this revised resource, go to:
http://www.immunize.org/catg.d/p2027.pdf
NOTE: To access continually updated information on the issue dates for VISs, see
the chart on IAC's Vaccine Information Statement web section at
http://www.immunize.org/vis
(3) "Suggestions to Improve Your Immunization Services" was reviewed and minor
revisions were made.
To access the revised "Suggestions to Improve Your Immunization Services," go
to:
http://www.immunize.org/catg.d/p2045.pdf
(4) Newly licensed vaccines Pentacel, Kinrix, and Rotarix were added to
"Notification of Vaccination Letter."
To access this revised resource, go to:
http://www.immunize.org/catg.d/p3060.pdf
(5) The title was changed, and Tdap, zoster, and HPV vaccines were added to
"Before you vaccinate adults, consider their 'H-A-L-O!'"
To access this revised resource, go to:
http://www.immunize.org/catg.d/p3070.pdf
(6) National statistics were updated and other minor changes made to "Hepatitis
B: Questions and Answers."
To access this revised resource, go to:
http://www.immunize.org/catg.d/p4205.pdf
Sarah Jane Schwarzenberg, MD, recently reviewed two of her print materials on
childhood hepatitis B virus infection and revised one of them, as follows:
(7) "Brief Introduction to Hepatitis B for Parents of Adopted Children" was
reviewed and found to be still accurate.
To access this resource, go to:
http://www.immunize.org/catg.d/p4150.pdf
(8) Minor changes were made to "What the Physician Can Do to Help the Child with
Chronic Hepatitis B Virus Infection."
To access this revised resource, go to:
http://www.immunize.org/catg.d/p2170.pdf
IAC's Print Materials web section has more than 175 FREE, ready-to-print
English-language resources for healthcare professionals and the public--as well
as many in translation. To access all of IAC's print resources, go to:
http://www.immunize.org/printmaterials
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September 16, 2008
TWO OF IAC'S REVISED VIRAL-HEPATITIS SCREENING QUESTIONNAIRES ARE NOW AVAILABLE
IN SPANISH
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/25/08.]
The screening questionnaires "Should You Be Vaccinated Against Hepatitis B? A
screening questionnaire for adults" and "Should You Be Vaccinated Against
Hepatitis A? A screening questionnaire for adults" were updated in June 2008.
The updated versions are now available in Spanish.
To access the Spanish version of "Should You Be Vaccinated Against Hepatitis B?
A screening questionnaire for adults," go to:
http://www.immunize.org/catg.d/p2191-01.pdf
To access the English version of "Should You Be Vaccinated Against Hepatitis B?
A screening questionnaire for adults," go
to:
http://www.immunize.org/catg.d/p2191.pdf
To access the Spanish version of "Should You Be Vaccinated Against Hepatitis A?
A screening questionnaire for adults," go
to:
http://www.immunize.org/catg.d/p2190-01.pdf
To access the English version of "Should You Be Vaccinated Against Hepatitis A?
A screening questionnaire for adults," go
to:
http://www.immunize.org/catg.d/p2190.pdf
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September 16, 2008
FDA APPROVES USE OF THE HIV DRUG VIREAD FOR TREATMENT OF CHRONIC HEPATITIS B
VIRUS INFECTION IN ADULTS
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/18/08.]
On August 11, FDA issued a supplement to its approval of tenofovir disoproxil
fumarate (Viread; Gilead). The drug is now indicated for use in treating chronic
hepatitis B virus infection in adults. Previously, it was approved only for
treating HIV infection.
To access the approval letter, go to:
http://www.fda.gov/cder/foi/appletter/2008/021356s025ltr.pdf
To access the package insert posted on the Gilead website, go to:
http://www.gileadhiv.com/pdf/VireadFPI.pdf
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September 16, 2008
CDC PRESENTS INFECTION-CONTROL REQUIREMENTS FOR DIALYSIS FACILITIES AND GIVES
GUIDANCE ON PARENTERAL MEDICATION VIALS
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/18/08.]
CDC published "Infection Control Requirements for Dialysis Facilities and
Clarification Regarding Guidance on Parenteral Medication Vials" in the August
15 issue of MMWR. A summary made available to the press is reprinted below in
its entirety.
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In dialysis and other healthcare settings, injected medications that are labeled
for single-use should be used one time for one patient only. To avoid
contamination and potential spread of infection in dialysis settings,
medications and solutions must be handled using proper infection control
precautions as described in CDC guidelines and now mandated through the new CMS
Conditions for Coverage. This includes injection preparation using only new
sterile needles/syringes in a clean area separate from patient treatment areas
and contaminated items. Beginning in October 2008, outpatient dialysis
facilities will be required by the Centers for Medicare and Medicaid Services
(CMS) to follow CDC infection control guidelines that pertain to hemodialysis
settings. These guidelines include recommendations for correct handling and use
of injected medications. To prevent transmission of both bacteria and bloodborne
viruses in hemodialysis settings, all injectable medications labeled as
"single-use" should be used for one patient and be entered one time only.
Medications packaged as multidose should be assigned to a single patient
whenever possible. All parenteral medications should be prepared using sterile
injection equipment in a clean area that is removed from the patient treatment
area and separate from potentially contaminated items and surfaces.
***********************
To access a web-text (HTML) version of the MMWR article, go to:
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5732a3.htm
To access a ready-to-print (PDF) version of this issue of MMWR, go to:
http://www.cdc.gov/mmwr/PDF/wk/mm5732.pdf
To receive a FREE electronic subscription to MMWR (which includes new ACIP
recommendations), go to:
http://www.cdc.gov/mmwr/mmwrsubscribe.html
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September 16, 2008
CDC ISSUES RECOMMENDATIONS FOR POSTEXPOSURE INTERVENTIONS TO PREVENT INFECTION
WITH HEPATITIS B VIRUS, HEPATITIS C VIRUS, OR HIV VIRUS AND TETANUS IN PERSONS
WOUNDED DURING BOMBINGS AND OTHER MASS-CASUALTY EVENTS
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/4/08.]
On August 1, CDC published "Recommendations for Postexposure Interventions to
Prevent Infection with Hepatitis B Virus, Hepatitis C Virus, or Human
Imunodeficiency Virus, and Tetanus in Persons Wounded During Bombings and Other
Mass-Casualty Events--United States, 2008: Recommendations of the Centers for
Disease Control and Prevention (CDC)" in MMWR Recommendations and Reports. The
recommendations' Summary is reprinted below.
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Summary
This report outlines recommendations for postexposure interventions to prevent
infection with hepatitis B virus, hepatitis C virus, or human immunodeficiency
virus, and tetanus in persons wounded during bombings or other events resulting
in mass casualties. Persons wounded during such events or in conjunction with
the resulting emergency response might be exposed to blood, body fluids, or
tissue from other injured persons and thus be at risk for bloodborne infections.
This report adapts existing general recommendations on the use of immunization
and postexposure prophylaxis for tetanus and for occupational and
nonoccupational exposures to bloodborne pathogens to the specific situation of a
mass-casualty event. Decisions regarding the implementation of prophylaxis are
complex, and drawing parallels from existing guidelines is difficult. For any
prophylactic intervention to be implemented effectively, guidance must be
simple, straightforward, and logistically undemanding. Critical review during
development of this guidance was provided by representatives of the National
Association of County and City Health Officials, the Council of State and
Territorial Epidemiologists, and representatives of the acute injury care,
trauma and emergency response medical communities participating in CDC's
Terrorism Injuries: Information, Dissemination and Exchange (TIIDE) project. The
recommendations contained in this report represent the consensus of U.S. federal
public health officials and reflect the experience and input of public health
officials at all levels of government and the acute injury response community. .
. .
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To access a ready-to-print (PDF) version of the recommendations, go to:
http://www.cdc.gov/mmwr/PDF/rr/rr5706.pdf
To access a web-text (HTML) version of the recommendations, go to:
http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5706a1.htm
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September 16, 2008
VIET HEP B FREE PROJECT OFFERS CULTURALLY APPROPRIATE INFORMATION ON ITS WEBSITE
The Vietnamese Community Health Promotion Project has launched a program called
the Viet Hep B Free Project which aims to increase knowledge about hepatitis B
and receipt of hepatitis B testing in the Vietnamese community in Northern
California.
The Viet Hep B Free Project's website has information about hepatitis B testing,
vaccination, and treatment in English and Vietnamese at
http://www.suckhoelavang.org/VietHepB
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September 16, 2008
REMINDER: NIH CONSENSUS DEVELOPMENT CONFERENCE ON THE MANAGEMENT OF HEPATITIS B
TO BE HELD OCTOBER 20-22 IN BETHESDA
[The following is cross posted from the Immunization Action Coalition's "IAC
Express" electronic newsletter, 8/18/08.]
The National Institute of Health's (NIH) Consensus Development Conference on the
Management of Hepatitis B will be held October 20-22, in Bethesda, MD. This
conference is sponsored by the National Institute of Diabetes and Digestive and
Kidney Diseases and the Office of Medical Applications of Research.
Speakers and attendees at this conference will discuss issues related to the
benefits and risks of current therapeutic options for HBV infection, including
which persons should be treated, what measures are appropriate to monitor
therapy and assess outcomes, and what the greatest needs are for future
research.
For more information, including the preliminary agenda, go to:
http://consensus.nih.gov/2008/2008HepatitisBCDC120main.htm
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September 16, 2008
JOURNAL ARTICLES YOU MAY HAVE MISSED
The following recent journal articles present research related to viral
hepatitis prevention or treatment.
"Hepatitis B and C among Veterans on a Psychiatric Ward"
Source: Dig Dis Sci, June 2008, Vol. 53(6):1693-8
Authors: Tabibian JH, Wirshing DA, Pierre JM, et al.
Click
here.
"Excellent Response Rate to a Double Dose of the Combined Hepatitis A and B
Vaccine in Previous Nonresponders to Hepatitis B Vaccine"
Source: The Journal of Infectious Diseases, September 1, 2008,
Vol. 198:299–304
Authors: Cardell K, Akerlind B, Sallberg M, Fryden A
http://www.hivandhepatitis.com/hep_b/news/2008/082908_a.html
"Has the Time Come to Control Hepatitis A Globally? Matching Prevention to the
Changing Epidemiology"
Source: Journal of Viral Hepatitis, August 27, 2008, Vol. 15 (Suppl2):1-15
Authors: Hendrickx G, Van Herck K, Vorsters A, et al.
http://www3.interscience.wiley.com/journal/121388614/abstract
"Characteristics of Persons and Jobs with Needlestick Injuries in a National
Data Set"
Source: Am J Infect Control, August 2008, Vol. 36(6):414-20
Authors: Leigh JP, Wiatrowski WJ, Gillen M, Steenland NK
Click
here.
"Greater Drug Injecting Risk for HIV, HBV, and HCV Infection in a City Where
Syringe Exchange and Pharmacy Syringe Distribution Are Illegal"
Source: J Urban Health, May 2008, Vol. 85(3):309-22
Authors: Neaigus A, Zhao M, Gyarmathy VA, Cisek L, Friedman SR, Baxter RC
Click
here.
"Injecting Drug Users' Understanding of Hepatitis C"
Source: Addict Behav, July 22, 2008 ePrint
Authors: O'Brien S, Day C, Black E, Dolan K
Click
here.
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