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| Quick reference medical handouts used
by Pediatric offices |

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Immunizations: Not just for Kids!
Summary
of Recommendations for Adult Immunization
Adapted from the
recommendations of the Advisory Committee on Immunization Practices (ACIP)*
by the Immunization Action Coalition, September 2006
|
Vaccine name
and route |
For whom vaccination is recommended |
Schedule for vaccine administration
(any vaccine can be given with another) |
Contraindications and precautions
(mild illness is not a contraindication) |
Influenza
Trivalent inactivated
influenza vaccine
(TIV)
Give IM |
•
Persons age 50yrs and older.
• Persons with medical problems (e.g., heart disease, lung disease,
diabetes, renal dysfunction, hemoglobinopathy, immunosuppression) and/or
people living in chronic-care facilities.
• Persons with 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, seizure
disorder, or other neuromuscular disorder).
• Persons working or living with at-risk people.
• Women who will be pregnant during the influenza season (December–March).
• All healthcare workers and other persons who provide direct care to
at-risk people.
• Household contacts and out-of-home caregivers of children ages 0–59m.
• Travelers at risk for complications of influenza who go to areas where
influenza activity exists or who may be among people from areas of the
world where there is current influenza activity (e.g., on organized
tours).
• Persons who provide essential community services.
• Students or other persons in institutional settings (e.g., dormitory
residents).
• Anyone wishing to reduce the likelihood of becoming ill with influenza. |
• Given every year in the fall or winter.
• October and November are the ideal months to give TIV.
• LAIV may be given as early as August.
• Continue to give TIV and LAIV through the influenza season from December
through March (including when influenza activity is present in the
community) and at other times when the risk of influenza exists. |
Contraindication
Previous anaphylactic reaction to this vaccine, to any of its components,
or to eggs.
Precautions
• Moderate or severe acute illness.
• History of Guillain-Barré syndrome within 6wks of previous TIV. |
Influenza
Live
attenuated
influenza
vaccine
(LAIV)
Give
intranasally |
•
Healthy, non-pregnant persons age 49yrs and younger who meet any of the
conditions listed below.
- Working or living
with at-risk people as listed in the section above.
- Healthcare workers or other persons who provide direct care to
at-risk people (except persons in close contact with severely
immunosuppressed persons).
- Household contacts and out-of-home caregivers of children ages
0–59m.
- Travelers who may be among people from areas of the world where
there is current influenza activity (e.g., on organized tours).
- Persons who provide essential community services.
- Students or other persons in institutional settings (e.g.,
dormitory residents).
- Anyone wishing to reduce the likelihood of becoming ill with
influenza. |
|
Contraindications
• Previous anaphylactic reaction to this vaccine, to any of its
components, or to eggs.
• Pregnancy, asthma, reactive airway disease or other chronic disorder of
the pulmonary or cardiovascular system; an underlying medical condition,
including metabolic disease such as diabetes, renal dysfunction, and
hemoglobinopathy; a known or suspected immune deficiency disease or
receiving immunosuppressive therapy; history of Guillain-Barré syndrome.
Precaution
Moderate or severe acute illness. |
Pneumococcal
poly-
saccharide
(PPV)
Give IM or SC |
• Persons age
65yrs and older.
• Persons who have chronic illness or other risk factors, including
chronic cardiac or pulmonary disease, chronic liver disease, alcoholism,
diabetes, CSF leak, as well as people living in special environments or
social settings (including Alaska Natives and certain American Indian
populations). Those at highest risk of fatal pneumococcal infection are
persons with anatomic asplenia, functional asplenia, or sickle cell
disease; immunocompromised persons including those with HIV infection,
leukemia, lymphoma, Hodgkin’s disease, multiple myeloma, generalized
malignancy, chronic renal failure, or nephrotic syndrome; persons
receiving immunosuppressive chemotherapy (including corticosteroids);
those who received an organ or bone marrow transplant; and candidates for
or recipients of cochlear implants. |
• Routinely given
as a one-time dose; administer if previous vaccination history is unknown.
• One-time revaccination is recommended 5yrs later for persons at highest
risk of fatal pneumococcal infection or rapid antibody loss (e.g., renal
disease) and for persons age 65yrs and older if the 1st dose was given
prior to age 65 and 5yrs or more have elapsed since the prior dose. |
Contraindication
Previous anaphylactic reaction to this vaccine or to any of its
components.
Precaution
Moderate or severe acute illness.
|
Hepatitis B
(Hep B)
Give IM
Brands may
be used
interchangeably. |
• All
adolescents; any adult wishing to obtain immunity.
• High-risk persons, including household contacts and sex partners of
HBsAg-positive persons; injecting drug users; heterosexuals with more than
one sex partner in 6 months; men who have sex with men; persons with
recently diagnosed STDs; patients receiving hemodialysis and patients with
renal disease that may result in dialysis; recipients of certain blood
products; healthcare workers and public safety workers who are exposed to
blood; clients and staff of institutions for the developmentally disabled;
inmates of long-term correctional facilities; and certain international
travelers.
• Persons with chronic liver disease.
Note: Provide serologic screening for immigrants from endemic
areas. When HBsAg-positive persons are identified, offer appropriate
disease management. In addition, screen their sex partners and household
members, and give the first dose of vaccine at the same visit. If found
susceptible, complete the vaccine series. |
• Three doses are
needed on a 0, 1, 6m schedule.
• Alternative timing options for vaccination include 0, 2, 4m and 0, 1,
4m.
• There must be 4wks between doses #1 and #2, and 8wks between doses #2
and #3. Overall, there must be at least 16wks between doses #1 and #3.
• Schedule for those who have fallen behind: If the series is
delayed between doses, DO NOT start the series over. Continue from where
you left off. |
Contraindication
Previous anaphylactic reaction to this vaccine or to any of its
components.
Precaution
Moderate or severe acute illness. |
| For
Twinrix®
(hepatitis A and B combination vaccine [GSK]), three doses are needed on a
0, 1, 6m schedule. Recipients must be age 18yrs or older. |
Hepatitis A
(Hep A)
Give IM
Brands may be used interchangeably. |
•
Persons who travel or work anywhere except the U.S., Western Europe, New
Zealand, Australia, Canada, and Japan.
• Persons with chronic liver disease, including persons with hepatitis B
and C; injecting and non-injecting drug users; men who have sex with men;
people with clotting-factor disorders; persons who work with hepatitis A
virus in experimental lab settings (not routine medical laboratories); and
food handlers when health authorities or private employers determine
vaccination to be cost effective.
• Anyone wishing to obtain immunity to hepatitis A.
Note: Prevaccination testing is likely to be cost effective for
persons older than age 40yrs, as well as for younger persons in certain
groups with a high prevalence of hepatitis A virus infection. |
Contraindication
Previous anaphylactic reaction to this
vaccine or to any of its components.
Precautions
• Moderate or severe acute illness.
• Safety during pregnancy has not been determined, so benefits must be
weighed against potential risk. |
• Two doses are
needed.
• The minimum interval between doses #1 and #2 is 6m.
• If dose #2 is delayed, do not repeat dose #1. Just give dose #2. |
Td, Tdap
(Tetanus, diphtheria, pertussis)
Give IM |
• All adults who lack a
history of a primary series consisting of at least 3 doses of tetanus- and
diphtheria-containing vaccine.
• A booster dose of tetanus- and diphtheria-containing toxoid may be
needed for wound management as early as 5yrs after receiving a previous
dose, so consult ACIP recommendations.*
• Using tetanus toxoid (TT) instead of Td or Tdap is not recommended.
• In pregnancy, when indicated, give Td or Tdap in 2nd or 3rd trimester.
If not administered during pregnancy, give Tdap in immediate postpartum
period.
For Tdap (tetanus- and
diphtheria-toxoids with acellular pertussis vaccine) only:
• All adults younger than age 65yrs who have not received Tdap.
• Healthcare workers who work in hospitals or ambulatory care settings and
have direct patient contact and who have not received Tdap.
• Adults in contact with infants younger than age 12m (e.g., parents,
grandparents younger than age 65yrs, childcare providers, healthcare
workers) who have not received a dose of Tdap. |
• For persons who
are unvaccinated or behind, complete the primary series with Td (spaced at
0, 1–2m, 6–12m intervals). One dose of Tdap may be used for any dose if
ages
19–64yrs.
• Give Td booster every 10yrs after the primary series has been completed.
For adults ages 19–64yrs, a 1-time dose of Tdap is recommended to replace
the next Td.
• Intervals of 2yrs or less between Td and Tdap may be used if needed.
Note: The 2 Tdap products are licensed for different age groups:
Adacel (sanofi) for use in persons ages 11–64yrs and Boostrix (GSK) for
use in persons ages 10–18yrs. |
Contraindications
• Previous anaphylactic reaction to this
vaccine or to any of its components.
• For Tdap only, history of encephalopathy within 7 days following
DTP/DTaP.
Precautions
• Moderate or severe acute illness.
• Guillain-Barré syndrome within 6wks of
receiving a previous dose of tetanus
toxoid-containing vaccine.
• Unstable neurologic condition.
• Note: Use of Td or Tdap is not contraindicated in pregnancy. At the
provider’s discretion, either vaccine may be administered during the 2nd
or 3rd trimester. |
Polio
(IPV)
Give IM or SC |
Not
routinely recommended for persons age 18yrs and older.
Note: Adults living in the U.S. who never received or completed a
primary series of polio vaccine need not be vaccinated unless they intend
to travel to areas where exposure to wild-type virus is likely (i.e.,
India, Pakistan, Afghanistan, and certain countries in Africa). Previously
vaccinated adults can receive one booster dose if traveling to polio
endemic areas. |
•
Refer to ACIP recommendations* regarding unique situations, schedules, and
dosing information. |
Contraindication
Previous anaphylactic or neurologic reaction to this vaccine or to any of
its components.
Precautions
• Moderate or severe acute illness.
• Pregnancy |
Varicella
(Var)
(Chickenpox)
Give SC |
All
adults without evidence of immunity. Immunity is defined as any one of the
following:
• a history of two doses of Var
• born in the U.S. before 1980
• history of varicella disease or herpes zoster based on healthcare
provider diagnosis
• laboratory evidence of immunity or laboratory confirmation of disease. |
•
Two doses are needed.
• Dose #2 is given 4–8wks after dose #1.
• If Var and either MMR, LAIV, and/or yellow fever vaccine are not given
on the same day, space them at least 28d apart.
• If the second dose is delayed, do not repeat dose #1. Just give dose #2. |
Contraindications
• Previous anaphylactic reaction to this vaccine or to any of its
components.
• Pregnancy or possibility of pregnancy within 4wks.
• Persons immunocompromised because of malignancies and primary or
acquired cellular immunodeficiency including HIV/AIDS. (See MMWR
1999, Vol. 48, No. RR-6.) Note: For those on high-dose
immunosuppressive therapy, consult ACIP recommendations regarding delay
time.*
Precautions
• If blood, plasma, and/or immune globulin (IG or VZIG) were given in past
11m, see ACIP statement General Recommendations on Immunization*
regarding time to wait before vaccinating.
• Moderate or severe acute illness. |
Meningococcal
Conjugate vaccine
(MCV4)
Give IM
---------
Polysaccharide
vaccine
(MPSV4)
Give SC |
•
College freshmen living in dormitories.
• Adolescents and adults with anatomic or functional asplenia or with
terminal complement component deficiencies.
• Persons who travel to or reside in countries in which meningococcal
disease is hyperendemic or epidemic (e.g., the “meningitis belt” of
Sub-Saharan Africa).
• Microbiologists who are routinely exposed to isolates of
N. meningitidis. |
•
One dose is needed.
• If previous vaccine was MPSV4, revaccinate after 5yrs if risk continues.
• Revaccination after MCV4 is not recommended.
• MCV4 is preferred over MPSV4 for persons age 55yrs and younger, although
MPSV4 is an acceptable alternative. |
Contraindication
Previous anaphylactic or neurologic reaction to this vaccine or to any of
its components, including diphtheria toxoid (for MCV4).
Precautions
• Moderate or severe acute illness.
• For MCV4 only, history of Guillain-Barré syndrome |
MMR
(Measles, mumps,
rubella)
Give SC |
• Persons born in
1957 or later (especially those born outside the U.S.) should receive at
least one dose of MMR if there is no serologic proof of immunity or
documentation of a dose given on or after the first birthday.
• Persons in high-risk groups, such as healthcare workers, students
entering college and other post–high school
educational institutions, and international travelers, should receive a
total of two doses.
• Persons born before 1957 are usually considered immune, but proof of
immunity (serology or vaccination) may be desirable for healthcare
workers.
• Women of childbearing age who do not have acceptable evidence of rubella
immunity or vaccination. |
One or two doses
are needed.
• If dose #2 is recommended, give it no sooner than 4wks after dose #1.
• If MMR and either Var, LAIV, and/or yellow fever vaccine are not given
on the same day, space them at least 28d apart.
• If a pregnant woman is found to be rubella susceptible, administer MMR
postpartum. |
Contraindications
• Previous anaphylactic reaction to this vaccine or to any of its
components.
• Pregnancy or possibility of pregnancy within 4wks.
• Persons immunocompromised because of cancer, leukemia, lymphoma,
immunosuppressive drug therapy, including high-dose steroids or radiation
therapy. Note: HIV positivity is NOT a contraindication to MMR
except for those who are severely immunocompromised.
Precautions
• If blood, plasma, and/or immune globulin were given in past 11m, see
ACIP statement General Recommendations on Immunization* regarding
time to wait before vaccinating.
• Moderate or severe acute illness.
• History of thrombocytopenia or thrombocytopenic purpura.
Note: If PPD (tuberculosis skin test) and MMR are both needed but
not given on same day, delay PPD for 4–6wks after MMR. |
Human-papillomavirus
(HPV)
Give IM |
All previously
unvaccinated women through age 26yrs. |
• Three doses are
needed.
• Dose #2 is given 4–8wks after dose #1, and dose #3 is given 6m after
dose #1 (at least 12wks after dose #2). |
Contraindication
Previous anaphylactic reaction to this vaccine or to any of its
components.
Precaution
Data on vaccination in pregnancy are limited; therefore, vaccination
during pregnancy should be delayed until after completion of the
pregnancy. |
Zoster
(shingles)
(Zos)
Give SC |
A herpes zoster
(shingles) vaccine was licensed in May 2006 for use in persons age 60yrs
and older. ACIP recommendations for its use are pending. Refer to the
package insert for details on its use. |
The above article used with the permission of the
Immunization Action Coalition.
The mission of the nonprofit Immunization Action Coalition is to boost
immunization rates and prevent disease. The Coalition promotes physician,
community, and family awareness of, and responsibility for, appropriate
immunization of all children and adults against all vaccine-preventable
diseases.
Revised 01-17-07
As a reminder, this information should not be relied on as
medical advice and is not intended to replace the advice of your childs pediatrician.
Please read our full disclaimer.
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