1.
Tetanus, diphtheria, and acellular pertussis (Td/Tdap)
vaccination
Tdap should replace a single dose of Td for adults aged
<65 years who have not previously received a dose of
Tdap. Only one of two Tdap products (Adacel®
[Sanofi Pasteur]) is licensed for use in adults.
Adults with uncertain
histories of a complete primary vaccination series with
tetanus and diphtheria toxoid--containing vaccines
should begin or complete a primary vaccination series. A
primary series for adults is 3 doses of tetanus and
diphtheria toxoid--containing vaccines; administer the
first 2 doses at least 4 weeks apart and the third dose
6--12 months after the second. However, Tdap can
substitute for any one of the doses of Td in the 3-dose
primary series. The booster dose of tetanus and
diphtheria toxoid--containing vaccine should be
administered to adults who have completed a primary
series and if the last vaccination was received >10
years previously. Tdap or Td vaccine may be used, as
indicated.
If the person is
pregnant and received the last Td vaccination >10
years previously, administer Td during the second or
third trimester; if the person received the last Td
vaccination in <10 years, administer Tdap during the
immediate postpartum period. A one-time administration
of 1 dose of Tdap with an interval as short as 2 years
from a previous Td vaccination is recommended for
postpartum women, close contacts of infants aged <12
months, and all health-care workers with direct patient
contact. In certain situations, Td can be deferred
during pregnancy and Tdap substituted in the immediate
postpartum period, or Tdap can be administered instead
of Td to a pregnant woman after an informed discussion
with the woman.
Consult the ACIP
statement for recommendations for administering Td as
prophylaxis in wound management.

2.
Human
papillomavirus (HPV) vaccination
HPV vaccination is recommended for all females aged <26
years who have not completed the vaccine series. History
of genital warts, abnormal Papanicolaou test, or
positive HPV DNA test is not evidence of prior infection
with all vaccine HPV types; HPV vaccination is still
recommended for these persons.
Ideally, vaccine should
be administered before potential exposure to HPV through
sexual activity; however, females who are sexually
active should still be vaccinated. Sexually active
females who have not been infected with any of the HPV
vaccine types receive the full benefit of the
vaccination. Vaccination is less beneficial for females
who have already been infected with one or more of the
HPV vaccine types.
A complete series
consists of 3 doses. The second dose should be
administered 2 months after the first dose; the third
dose should be administered 6 months after the first
dose.
Although HPV
vaccination is not specifically recommended for females
with the medical indications described in
"Vaccines that might be indicated for
adults based on medical and other indiations,
"Vaccines that might be indicated for adults based on
medical and other indications," it is not a live-virus
vaccine and can be administered. However, immune
response and vaccine efficacy might be less than in
persons who do not have the medical indications
described or who are immunocompetent.
3.
Measles, mumps, rubella (MMR) vaccination
Measles component:
adults born before 1957
can be considered immune to measles. Adults born during
or after 1957 should receive >1 dose of MMR
unless they have a medical contraindication,
documentation of >1 dose, history of measles
based on health-care provider diagnosis, or laboratory
evidence of immunity.
A
second dose of MMR is recommended for adults who 1) have
been recently exposed to measles or are in an outbreak
setting; 2) have been previously vaccinated with killed
measles vaccine; 3) have been vaccinated with an unknown
type of measles vaccine during 1963--1967; 4) are
students in postsecondary educational institutions; 5)
work in a health-care facility; or 6) plan to travel
internationally.
Mumps component:
adults born before 1957 can
generally be considered immune to mumps. Adults born
during or after 1957 should receive 1 dose of MMR unless
they have a medical contraindication, history of mumps
based on health-care provider diagnosis, or laboratory
evidence of immunity.
A
second dose of MMR is recommended for adults who 1) are
in an age group that is affected during a mumps
outbreak; 2) are students in postsecondary educational
institutions; 3) work in a health-care facility; or 4)
plan to travel internationally. For unvaccinated
health-care workers born before 1957 who do not have
other evidence of mumps immunity, consider administering
1 dose on a routine basis and strongly consider
administering a second dose during an outbreak.
Rubella component:
administer 1 dose of MMR vaccine to women whose rubella
vaccination history is unreliable or who lack laboratory
evidence of immunity. For women of childbearing age,
regardless of birth year, routinely determine rubella
immunity and counsel women regarding congenital rubella
syndrome. Women who do not have evidence of immunity
should receive MMR vaccine on completion or termination
of pregnancy and before discharge from the health-care
facility.
4.
Varicella
vaccination
All adults without evidence
of immunity to varicella should receive 2 doses of
single-antigen varicella vaccine unless they have a
medical contraindication. Special consideration should
be given to those who 1) have close contact with persons
at high risk for severe disease (e.g., health-care
personnel and family contacts of immunocompromised
persons) or 2) are at high risk for exposure or
transmission (e.g., teachers; child care employees;
residents and staff members of institutional settings,
including correctional institutions; college students;
military personnel; adolescents and adults living in
households with children; nonpregnant women of
childbearing age; and international travelers).
Evidence of immunity to varicella in adults includes any
of the following: 1) documentation of 2 doses of
varicella vaccine at least 4 weeks apart; 2) U.S.-born
before 1980 (although for health-care personnel and
pregnant women, birth before 1980 should not be
considered evidence of immunity); 3) history of
varicella based on diagnosis or verification of
varicella by a health-care provider (for a patient
reporting a history of or presenting with an atypical
case, a mild case, or both, health-care providers should
seek either an epidemiologic link with a typical
varicella case or to a laboratory-confirmed case or
evidence of laboratory confirmation, if it was performed
at the time of acute disease); 4) history of herpes
zoster based on health-care provider diagnosis; or 5)
laboratory evidence of immunity or laboratory
confirmation of disease.
Assess pregnant women for evidence of varicella
immunity. Women who do not have evidence of immunity
should receive the first dose of varicella vaccine upon
completion or termination of pregnancy and before
discharge from the health-care facility. The second dose
should be administered 4--8 weeks after the first dose.

5.
Influenza
vaccination
Medical indications: chronic disorders of the
cardiovascular or pulmonary systems, including asthma;
chronic metabolic diseases, including diabetes mellitus,
renal or hepatic dysfunction, hemoglobinopathies, or
immunosuppression (including immunosuppression caused by
medications or human immunodeficiency virus [HIV]); any
condition that compromises respiratory function or the
handling of respiratory secretions or that can increase
the risk of aspiration (e.g., cognitive dysfunction,
spinal cord injury, or seizure disorder or other
neuromuscular disorder); and pregnancy during the
influenza season. No data exist on the risk for severe
or complicated influenza disease among persons with
asplenia; however, influenza is a risk factor for
secondary bacterial infections that can cause severe
disease among persons with asplenia.
Occupational indications: health-care personnel and
employees of long-term--care and assisted-living
facilities.
Other
indications: residents of nursing homes and other
long-term--care and assisted-living facilities; persons
likely to transmit influenza to persons at high risk
(e.g., in-home household contacts and caregivers of
children aged 0--59 months, or persons of all ages with
high-risk conditions); and anyone who would like to be
vaccinated. Healthy, nonpregnant adults aged <49
years without high-risk medical conditions who are not
contacts of severely immunocompromised persons in
special care units can receive either intranasally
administered live, attenuated influenza vaccine (FluMist®)
or inactivated vaccine. Other persons should receive the
inactivated vaccine.
6.
Pneumococcal polysaccharide vaccination
Medical indications: chronic pulmonary disease
(excluding asthma); chronic cardiovascular diseases;
diabetes mellitus; chronic liver diseases, including
liver disease as a result of alcohol abuse (e.g.,
cirrhosis); chronic alcoholism, chronic renal failure,
or nephrotic syndrome; functional or anatomic asplenia
(e.g., sickle cell disease or splenectomy [if elective
splenectomy is planned, vaccinate at least 2 weeks
before surgery]); immunosuppressive conditions; and
cochlear implants and cerebrospinal fluid leaks.
Vaccinate as close to HIV diagnosis as possible.
Other
indications: Alaska Natives and certain American
Indian populations and residents of nursing homes or
other long-term--care facilities.
7.
Revaccination with pneumococcal polysaccharide
vaccine
One-time revaccination after 5 years for persons with
chronic renal failure or nephrotic syndrome; functional
or anatomic asplenia (e.g., sickle cell disease or
splenectomy); or immunosuppressive conditions. For
persons aged >65 years, one-time revaccination if
they were vaccinated >5 years previously and were
aged <65 years at the time of primary vaccination.
8.
Hepatitis A
vaccination
Medical indications: persons with chronic liver
disease and persons who receive clotting factor
concentrates.
Behavioral indications: men who have sex with men
and persons who use illegal drugs.
Occupational indications: persons working with
hepatitis A virus (HAV)-infected primates or with HAV in
a research laboratory setting.
Other
indications: persons traveling to or working in
countries that have high or intermediate endemicity of
hepatitis A (a list of countries is available at
http://wwwn.cdc.gov/travel/contentdiseases.aspx) and
any person seeking protection from HAV infection.
Single-antigen vaccine formulations should be
administered in a 2-dose schedule at either 0 and 6--12
months (Havrix®), or 0 and 6--18 months (Vaqta®).
If the combined hepatitis A and hepatitis B vaccine (Twinrix®)
is used, administer 3 doses at 0, 1, and 6 months.
9.
Hepatitis B
vaccination
Medical indications: persons with end-stage renal
disease, including patients receiving hemodialysis;
persons seeking evaluation or treatment for a sexually
transmitted disease (STD); persons with HIV infection;
and persons with chronic liver disease.
Occupational indications: health-care personnel and
public-safety workers who are exposed to blood or other
potentially infectious body fluids.
Behavioral indications: sexually active persons who
are not in a long-term, mutually monogamous relationship
(e.g., persons with more than one sex partner during the
previous 6 months); current or recent injection-drug
users; and men who have sex with men.
Other
indications: household contacts and sex partners of
persons with chronic hepatitis B virus (HBV) infection;
clients and staff members of institutions for persons
with developmental disabilities; international travelers
to countries with high or intermediate prevalence of
chronic HBV infection (a list of countries is available
at
http://wwwn.cdc.gov/travel/contentdiseases.aspx);
and any adult seeking protection from HBV infection.
Settings
where hepatitis B vaccination is recommended for all
adults: STD treatment facilities; HIV testing and
treatment facilities; facilities providing drug-abuse
treatment and prevention services; health-care settings
targeting services to injection-drug users or men who
have sex with men; correctional facilities; end-stage
renal disease programs and facilities for chronic
hemodialysis patients; and institutions and
nonresidential day care facilities for persons with
developmental disabilities.

Special formulation indications: for adult patients
receiving hemodialysis and other immunocompromised
adults, 1 dose of 40 µg/mL (Recombivax HB®)
or 2 doses of 20 µg/mL (Engerix-B®),
administered simultaneously.
10.
Meningococcal
vaccination
Medical indications: adults with anatomic or
functional asplenia or terminal complement component
deficiencies.
Other
indications: first-year college students living in
dormitories; microbiologists who are routinely exposed
to isolates of Neisseria meningitidis; military
recruits; and persons who travel to or live in countries
in which meningococcal disease is hyperendemic or
epidemic (e.g., the "meningitis belt" of sub-Saharan
Africa during the dry season [December--June]),
particularly if their contact with local populations
will be prolonged. Vaccination is required by the
government of Saudi Arabia for all travelers to Mecca
during the annual Hajj.
Meningococcal conjugate vaccine is preferred for adults
with any of the preceding indications who are aged <55
years, although meningococcal polysaccharide vaccine
(MPSV4) is an acceptable alternative. Revaccination
after 3--5 years might be indicated for adults
previously vaccinated with MPSV4 who remain at increased
risk for infection (e.g., persons residing in areas in
which disease is epidemic).
11. Herpes zoster
vaccination
A
single dose of zoster vaccine is recommended for adults
aged >60 years regardless of whether they report
a prior episode of herpes zoster. Persons with chronic
medical conditions may be vaccinated unless a
contraindication or precaution exists for their
condition.
Report
all clinically significant postvaccination reactions to
the Vaccine Adverse Event Reporting System (VAERS).
Reporting forms and instructions on filing a VAERS
report are available at
http://www.vaers.hhs.gov or by telephone,
800-822-7967.
Information on how to file a Vaccine Injury Compensation
Program claim is available at
http://www.hrsa.gov/vaccinecompensation or by
telephone, 800-338-2382. To file a claim for vaccine
injury, contact the U.S. Court of Federal Claims, 717
Madison Place, N.W., Washington, D.C. 20005; telephone,
202-357-6400.
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