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Immunizations and Tuberculosis Screening
Printable version of this page
Texas
A&M University no longer requires the submission of immunization
records as a requirement for class registration. However, Student Health
Services strongly recommends that every student, and their family members,
review our updated list of immunizations most appropriate for the
university student. This list of recommended vaccines was compiled by the
American College Health Association (ACHA) with assistance from the
Advisory Committee on Immunization Practices (ACIP) of the Centers for
Disease Control and Prevention (CDC).
Health
science majors and some international students will be an exception to this recommendation.
International students should review the recommended immunizations below
as well as the TB Screening information at the bottom on the page.
Health
science majors are
required by state law to be compliant with certain immunization
requirements prior to the beginning of their clinical rotations. Assuring
that health science students comply with state laws regarding required
immunizations is the responsibility of the health science department or
college.
All of the recommended
vaccines are available to students at Student Health Services. If you have
any questions regarding recommended vaccines, please contact Student
Health Services at 979-458-8345.
You are welcome to
continue to submit immunization records voluntarily in order to assure the
availability of a more complete medical record while you are a student at
Texas A&M University.
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VACCINE |
AGE INDICATED |
MAJOR INDICATIONS |
MAJOR PRECAUTIONS |
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Measles, Mumps, Rubella (MMR) |
Two doses of MMR at least 28
days apart after 12 months
of age. |
All college students born
after 1956 without lab evidence of disease or physician diagnosed
disease. |
Pregnancy; history of hypersensitivity
or anaphylaxis to any of the components in the vaccine. Guidelines
exist for vaccination of persons with altered immunocompentence |
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Tetanus,
Diphtheria, Pertussis
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DT: pediatric (< age 7
years) preparation of diphtheria and tetanus toxoids.
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DTaP: pediatric preparation of diphtheria, tetanus toxoid, and
acellular pertussis.
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DTP (also known as DTwP): pediatric preparation of diphtheria, tetanus
toxoid, and whole cell pertussis (no longer available in the
U.S.).
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Td: 7 years and older preparation of tetanus toxoid and diphtheria
toxoid.
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Tdap: adolescent and older preparation of tetanus toxoid, diphtheria,
and acellular pertussis. |
Primary series with DT, DTaP DTP or Td; booster at age 11-64 years
with Tdap.
For adolescents age 11-18, at least 5 years should have elapsed since
the last dose of tetanus and diphtheria toxoid-containing vaccine,
prior to receiving Tdap. For adults 19-64 years, Tdap to replace a
single dose of Td for booster immunization against tetanus,
diphtheria, and pertussis if they received their last dose of Td > 10
years earlier. Tetanus prophylaxis in wound management: For both age
groups above, patients who require a tetanus toxoid containing vaccine
as part of wound management should receive Tdap instead of Td if they
have not previously received Tdap. If Tdap is not available or was
administered previously, Td should be administered. Pertussis
prophylaxis: For both age groups above, intervals shorter than 10
years since the last Td may be used to protect against pertussis.
Particularly in settings with increased risk from
pertussis or its complications or for those who have or who anticipate
having close contact with an infant < 12 months of age (parents,
childcare providers, healthcare providers), a single dose of Tdap
should be administered. The benefits of using a single dose of Tdap at
a shorter interval to protect against pertussis generally outweighs
the risk of local and systemic reactions after
vaccination. The safety of intervals as short as 2 years between Td
and Tdap are supported by studies from
Canada.
Routine
booster dose intervals: Adults should receive decennial Td boosters,
beginning 10 years after receiving Tdap, until guidance on subsequent
Tdap booster doses is available.
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Tdap for the decennial booster dose for all college students.
Any student in
the setting of: pertussis outbreaks, close contact with infants less
than 12 months of age, or wound management, as appropriate. |
History of hypersensitivity to any of
the components in the vaccine.
There is a theoretical
risk of increased rates of local or systemic reactions when two
diphtheria toxoid containing vaccines are
administered within a short interval (i.e., on different days).
Efforts should be made to administer Tdap and tetravalent
meningococcal conjugate (MCV4) vaccines simultaneously if both are
indicated. If simultaneous vaccination is not feasible, Tdap and MCV4
vaccines (which contain diphtheria toxoid) can be administered in any
sequence. |
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Polio Vaccine
-Inactive (IPV)
-Oral poliovirus (OPV) |
Primary series in childhood with IPV
alone, OPV alone, or IPV/OPV sequentially; booster only if needed for
travel after age 18 years |
IPV for certain international
travelers. |
History of hypersensitivity to any of
the components of the vaccine. |
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Varicella (Chickenpox)
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Childhood, adolescence, young adulthood
(two doses at least one month apart, if 13 years of age or older). |
All entering college students without
history of the disease or without age appropriate immunization or with
a negative antibody titer (two doses at least one month apart, if over
age 13 years). |
Pregnancy, history of hypersensitivity
or anaphylaxis to any of the components in the vaccine. Guidelines
exist for vaccination of persons with altered immunocompentence. |
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Hepatitis B Vaccine |
Series of 3 doses (given at 0, 1-2 mo.,
and 6-12 mo.) prior to college entry. A series of 2 adult doses may
be given to adolescents 11-15 years of age (given at 0 and 4-6mo).
Combined hepatitis A and B vaccines may be given as a series of 3
doses (given at 0, 1-2 mo., and 6-12 mo.). |
All college students |
History of hypersensitivity to any of
the components in the vaccine. |
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Hepatitis A Vaccine |
Series of 2 doses
(given at 0, 6-12 mo.) prior to college entry. Combined hepatitis A
and B vaccines may be given as a series of 3 doses (given at 0, 1-2
mo., and 6-12 mo.).
Over 2 years,
repeat every 3-5 yrs.
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Recommended for routine use in
adolescents through the age of 18 in some states and regions and for
certain high risk groups (i.e., persons traveling to countries where
hepatitis A is moderately or highly endemic, men who have sex with
men, users of injectable and noninjectable drugs, persons who have
clotting-factor disorders, persons working with nonhuman primates, and
persons with chronic liver disease). |
History of hypersensitivity to any of
the components in the vaccine. |
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Pneumococcal Polysaccharide
Vaccine-23 valent |
Childhood, adolescence, adulthood |
Young adults with diabetes, heart
disease, chronic pulmonary or liver disease. Revaccinate every 5
years for immunodeficiency states, renal failure, recipients of
clotting factor concentrates, asplenia, terminal complement component
deficiencies, and HIV infection. |
History of hypersensitivity to any of
the components in the vaccine. |
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Meningococcal
quadrivalent
Conjugate (Preferred)
Polysaccharide (Acceptable alternative if conjugate not available)
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11-55 years (data for
revaccination pending)
Over 2 years of age, repeat
every 3-5 years |
Certain high-risk groups including
persons with terminal complement deficiencies or those with asplenia.
Research or laboratory personnel who may be exposed to aerosolized meningococci.
Travelers to hyperendemic or endemic areas of the world.
College freshmen living in dormitories are at modestly
increased risk for disease and may wish to consider vaccination. |
History of hypersensitivity to any of
the components in the vaccine.
Avoid vaccinating
persons who are known to have experienced Guillain-Barre (GBS)
syndrome
There is a theoretical risk of increased rates of local or systemic
reactions when two diphtheria toxoid-containing vaccines are
administered within a short interval (i.e., on different days).
Efforts should be made to administer Tdap and tetravalent
meningococcal
conjugate (MCV4) vaccines simultaneously if both are indicated. |
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Influenza Vaccine |
Annually |
All college students particularly those
at high risk of complications from the flu such as diabetics or
asthmatics or patients with certain immunodeficiencies, and any
student who wants to minimize disruption of routine activities during
epidemics) |
History of hypersensitivity to any of
the components in the vaccine. |
Tuberculosis Screening
Tuberculosis (TB) skin testing, utilizing the Mantoux test, is
required for all incoming, high-risk students, domestic or international, who
have arrived from countries where TB is endemic. As it is easier to identify
countries of low, rather than high TB prevalence, please review the following
list of exceptions. Students should undergo TB screening if they have arrived
from any country EXCEPT those on the following list:
EXCEPTION LIST (countries where TB is not
endemic):
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American Region: |
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Canada |
Jamaica |
Saint Lucia |
Saint Kitts and Nevis |
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USA |
Virgin Islands |
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European Region: |
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Belgium |
Greece |
Luxembourg |
San Marino |
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Denmark |
Iceland |
Malta |
Sweden |
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Finland |
Ireland |
Monaco |
Switzerland |
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France |
Italy |
Netherlands |
United Kingdom |
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Germany |
Liechtenstein |
Norway |
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Western Pacific Region: |
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American Samoa |
Australia |
New Zealand |
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In addition, other categories of
individuals who may be at increased risk for TB infection or disease, and should
consider TB screening include:
- Persons who have been close contacts of
a person with infectious TB
- Persons with signs or symptoms of active
TB
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Persons with HIV
infection
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Persons who inject
drugs
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Persons who have
resided in, have been employed by, or volunteered in the following
high-risk congregate settings: prisons and jails, nursing homes and
other long-term facilities for the elderly, hospitals and other health
care facilities, residential facilities for patients with acquired
immunodeficiency syndrome (AIDS), and homeless shelters
- Persons with the
following clinical conditions that place them at high risk: silicosis,
diabetes mellitus, chronic renal failure, some hematologic disorders
(e.g. leukemias and lymphomas), other specific malignancies (e.g.
carcinoma of the head or neck and lung), low body weight (10% or more
below the ideal), gastrectomy and jejunoileal bypass, prolonged
corticosteroid therapy (e.g. prednisone 15 mg/d for 1 month), other
immunosuppressive therapy, pulmonary fibrotic lesions seen on chest
radiographs (presumed to be from prior, untreated TB)
Please note that all
countries in the African Region, Eastern Mediterranean Region, and
Southeast Asia Region as well as Russia are considered high risk.
Detailed information
about screening and treatment for tuberculosis can be found at the
following website:
http://www.cdc.gov/nchstp/tb/pubs/corecurr/
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