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64 Cards in this Set
- Front
- Back
Incubation period of the influenza virus in an immunocompetent adult |
-Range of 1-4 days (average of 2 days) |
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Efficacy of the influenza vaccines in preventing in preventing influenza or reducing the severity of the disease
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- 70% to 80% effective in preventing influenza or reducing the severity of disease |
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The Injectable vaccine
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-does not contain live virus and is not shed |
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Influenza vaccine recommended for use in pregnant women
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-the injectable trivalent influenza vaccine (TIV)
-recommended for all pregnant women |
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Timing of TIV administration
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-based largely on the vaccines availability b/c a formulation based on predicted influenza strains is produced annually
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Appropriate age group for TIV administration
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-can be given to infants 6 months old and older |
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Immunization rates are typically the highest in what group?
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-Immunization rates against influenza for individuals with chronic illness are typically the highest, although with considerable room for improvement |
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Certain groups have very low immunization rates and should be targeted for improvement. These groups include: |
-persons who live with or care for persons at high risk for influenza-related mortality and morbidity |
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What is the current rate of immunization for health care providers? |
-40%
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Nasal spray flu vaccine (FluMist) |
-aka live attenuated influenza vaccine (LAIV) |
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For what ages is administration of the LAIV approved for use? |
-approved for use in healthy people 2 to 49 years old |
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What individuals should not receive LAIV?
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-children < 2 yrs old |
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What are adverse effects of LAIV? |
-nasal irritation and discharge |
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In the northern hemisphere when is the optimal time to receive any influenza vaccine? |
-usually in October or November, about 1 month before the anticipated onset of the flu season |
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What are the four antiviral drugs approved by the FDA for use against influenza? |
-amantadine (Symmetrel) |
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The adamantane derivatives (amantadine and rimantidine are approved for only treatment and prevention of which type(s) of influenza? |
- amantadine and rimantidine are approved only for treatment and prevention of influenza type A |
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For which type(s) of influenza are the neuraminidase inhibitor drugs (zanamivir and oseltamivir approved? |
-zanamivir and oseltamivir are approved for use in influenza A and influenza B |
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CDC viral surveillance has shown high levels of resistance of influenza A viruses to what drugs? |
-amantadine and other similar medications |
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CDC viral surveillance has shown high levels of resistance of influenza A viruses to what drugs? |
-amantadine and other similar medications |
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Zanamivir and oseltamivir |
-are used to treat influenza A and B infections caused by susceptible viral strains |
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CDC viral surveillance has shown high levels of resistance of influenza A viruses to what drugs? |
-amantadine and other similar medications |
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Zanamivir and oseltamivir
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-are used to treat influenza A and B infections caused by susceptible viral strains |
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What is the preferred method for immunization against influenza A and B? |
-although many antiviral meds carry indications for the post exposure prevention of influenza, all have a less favorable adverse reaction profile then the influenza vaccine; active immunization against influenza A and B by administering the flu shot or intranasal spray is the preferred method of disease prevention. |
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Which of the following is true about the MMR Vaccine?
A. It contains inactivated virus
B. Its use is contraindicated in patients w/ a h/o egg allergy
C. Revaccination of an immune person is associated w/ risk of allergic reaction
D. Two doses at least 1 month apart are recommended for young adults who have not been previously immunized |
D is the correct answer. Two doses at least 1 month apart are recommended for young adults who have not been previously immunized
A is false. The MMR vaccine contains live but weakened (attenuated) virus
B is false. In the past, a h/o egg allergy was considered a C/I to receiving MMR vaccine. The vaccine now seems to be safe in people w/ egg allergy
C is false. Revaccination of an immune person is not assoc. w/ risk of allergic reaction. As with all vaccines, giving additional doses to patients w/ unclear immunization history is safe
-Two immunizations 1 month apart are recommended for adults born after 1957 because adults born before then are considered immune as a result of having had these diseases (native or wild infection)
Vaccine against these three formerly common illnesses was unavailable until the 1960's |
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Who should not receive the MMR? |
-Patients w/ a h/o life-threatening allergic reaction to neomycin or gelatin should not receive MMR
-The MMR vaccine is safe to use during lactation, but its use during pregnancy is discouraged b/c of the theoretical but unproven risk of congenital rubella syndrome from the live virus contained in the vaccine
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What adverse reactions may occur with administration of the MMR Vaccine? |
-The MMR is well-tolerated; there have been rare reports of mild, transient adverse reactions such as rash and sore throat |
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Does evidence support an associated between autism and the MMR vaccine? |
No. Evidence gathered by the NIH (at the request of the CDC) does not support an association between autism and the MMR vaccine
-Although the preservative thimerosal, a mercury derivative, has been mentioned as a possible autism contributor, the MMR vaccine licensed for use in the U.S. does not contain this preservative |
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What risk of complication does Rubella carry for the infected person? |
-Rubella typically causes a relatively mild, 3- to 5-day illness w/ little risk of complication to the person infected
-When rubella is contracted during pregnancy however, the effects on the fetus can be devastating
-Immunizing the entire population against rubella protects unborn children from the risk of contracting congenital rubella syndrome |
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What are the sequellae of measles? |
-Measles can cause severe illness with serious sequellae, including encephalitis and pneumonia |
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What is a sequella of mumps? |
-Sequellae of mumps include orchitis |
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Examples of Primary Prevention |
Prevent Disease/Injury/Condtion
Examples: -Youth violence prevention -Bullying prevention -Personal safety promotion (e.g., seatbelts, airbags, helmets) -Disease prevention (e.g., immunizations, using sunscreen) -Healthy lifestyle promotion -Promotion of OSHA laws (e.g., workplace safety) and EPA laws (e.g., clean water, anti-pollution laws) |
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Examples of Secondary Prevention |
Detect Disease/Condition as early as possible to minimize bodily damage
Examples: -Any lab test to screen for a disease (e.g., CBC for anemia, TSH for thyroid disease)
-USPSTF screening recommendations (e.g., mammograms, PSA, purified protein derivative [PPD])
-Screening for high-risk behavior (e.g., asking a pt about the # of sexual partners), screening for suicide risk (e.g., assess suicide risk, check for signs and sxs of depression)
-Personal actions to detect cancer (e.g., BSE, GSE) |
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Examples of Tertiary Prevention |
Limiting further harm and disability (Rehabilitation, Support groups, Education or Equipment)
Examples: -All types of rehab (e.g., cardiac rehab, PT, OT, speech therapy, addiction/drug rehab)
-Support groups (e.g., breast cancer patients, AA)
-Exercise for an obese person (if the person is healthy, then it is primary prevention) |
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Screening Tests -
Sensitivity |
-Detect individuals who have the disease
-Highly sensitive tests have higher risk of "false positives"
-For example, the HIV ELISA test has a 99% sensitivity for HIV antibodies, but it is too sensitive and can be "false positive" (especially in low-risk populations
The next step is the Western Blot test, which is very specific for HIV (the confirmatory test) |
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Screening Tests -
Specificity |
-Detect individuals who do not have the disease
-For example, a positive HIV ELISA result is always "confirmed" w/ the Western Blot test, which is very specific for HIV antibodies
The Western Blot is the "confirmatory test" for HIV. It is better at ruling out a person who does not have the disease |
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Screening for Breast Cancer (USPSTF, 2009) |
Baseline mammogram: start at age 50 yrs, then every 2 years (biennially) until the age of 74
Age 75 yrs and older: insufficient evidence for routine mammogram. Individualize
*Age 40-49 years (individualize based on risk factors, biennial schedule if done
Against teaching BSE (Grade D rec) **The American Cancer Society recommends starting routine screening at age 40 yrs |
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Screening for Cervical Cancer |
-start at age 21 years
-Every 3 years (Pap Smear) until age 65
*Against routine screening if < 21 yrs old
**Age 65 or older or Hysterectomy w/ removal of cervix (benign disease) --> Stop routine screening if h/o adequate screening (and not high risk for cervical cancer); can stop routine pap smear screening |
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Screening for Colon/Colorectal Cancer |
-Start at age 50
-High-sensitivity FOBT (every year), or sigmoidoscopy (every 5 years), or colonoscopy (every 10 years)
-Age 76-85 years: individualize
-Age older than 85 years: Stop routine screening |
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Against routine screening for: |
Lung cancer Skin cancer (insufficient evidence) Ovarian cancer Testicular cancer (adolescents or adult males) Pancreatic cancer |
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What are contraindications for Live Attenuated Inactivated Virus (LAIV) Influenza vaccine? |
-Pregnancy
-Chronic diseases (i.e., asthma, COPD, renal failure, DM)
-C/I in children on aspirin therapy (age 2 to 17 yrs)
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What is the youngest age at which flu vaccine (injection) can be given?
LAIV vaccine? |
TIV: At the age of 6 months
LAIV: 2 to 49 years |
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What types of medications are avoided after receiving the LAIV flu vaccine (nasal form)? |
-Some antivirals (amantadine, rimantadine, zanamivir, osletamivir) should be avoided 48 hours before and 14 days after vaccination b/c they interfere w/ antibody production |
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Tetanus Vaccine: |
-Give every 10 years for lifetime
-Boosters: for "dirty"/Contaminated wounds, give a booster if the last dose was more than 5 years prior
-Age 7 yrs and older: Use only tetanus and diptheria (Td) and tetanus, diptheria, and acellular pertussis (Tdap) forms of the vaccine
-Td: Given by IM route. Start using this form at age 7 years
-Tdap: Given by IM route
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When can the Tdap be used as a booster in adolescents and adults? |
The Tdap can be substituted for a single dose of Td (once in a lifetime) |
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What is done if a patient has a tetanus-prone wound and vaccination status is unknown? |
Administer immediate dose of Td vaccine and the tetanus immunoglobulin (TIG) injection |
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Which wounds are considered as highest risk for tetanus infection? |
Puncture wounds, wounds w/ devitalized tissue, soil-contaminated wounds, crush injuries, others... |
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What vaccine is recommended for persons who are 65 years of age? |
Give one dose of Pneumovax (lifetime). No booster is needed |
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If a person is vaccinated with the Pneumovax vaccine before the age of 65, what is recommended? |
-Give a booster dose of Pneumovax 5 years after the initial dose |
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When should the Zoster Vaccine (Zostavax) be given? |
-Zostavax is a live attenuated virus vaccine
-Administer at age 60 years; one-time dose SC (even if the pt has already had shingles)
-The youngest the age that Zostavax can be given is 50 years of age
*Do not use vaccine if no h/o chickenpox or shingles (seronegative). The patient will become ill w/ chickenpox.
However, if a person had shingles before, the vaccine can still be administered.
*Certain antivirals (acyclovir, famciclovir, valacyclovir) can decrease immunologic response if take 24 hours before or 14 days after vaccination.
**May cause exacerbation of asthma and PMR
C/I: -pregnancy and breastfeeding -Leukemia, lymphomas, or other malignancies of the bone/bone marrow -Immunocompromise (high-dose steroids > 2 wks, anti-TNF meds such as etanercept |
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Varicella Vaccine |
-Varicella live attenuated virus (Varivax): given by SC route; health teenagers to adults w/ no h/o chickenpox; health care workers
-Need 2 doses (4 to 8 weeks apart)
-Exposure to chickenpox: give w/in 5 days after incident for post-exposure prophylaxis
-Acceptable evidence of varicella infection
-Written documentation of two doses of varicella vaccine (at least 28 days apart)
-Written diagnosis of chickenpox or shingles based on health care provider diagnosis
-Positive laborary varicella titer
-Born in the US before 1980 |
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Meningococcal conjugate vaccine quadrivalent (MCV4) |
Schedule - depends: for adults, give one or two doses (at least 2 months apart)
-First-year college students through age 21 years who will be living in residence halls (give one dose) |
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What is the follow-up if a person w/ a history of Bacille-Calmette-Guerin (BCG) immunization has a positive PPD? |
-Evaluate the person for S&S of TB
-Rule out latent infection
-Order a CXR and check for S&S of TB such as "chronic" cough, weight loss, and night sweats
-Do not assume the reaction is from the BCG vaccine since the effect of the vaccine declines over time
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Hepatitis B |
Schedule: Total of 3 doses
-Hepatitis B titers should be checked w/in 60 days of the third dose.
*If incomplete series do not restart. If had one dose, give the second dose during the visit. If had two doses, give the 3rd dose
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Health Care Personnel Vaccination Recommendations |
Td or Tdap: give one-time dose of Tdap for all health care personnel who have not received the Tdap when due for tetanus booster. Continue giving Td boosters every 10 years for a lifetime
MMR: Proof of immunity necessary (born before 1957, laboratory confirmation such as positive titers). If not vaccinated for MMR, need two doses (at least 4 weeks apart)
Varicella: Proof of immunity necessary (positive varicella titer, documentation of two doses of varicella vaccine or diagnosis of varicella by physician/HCP
Hepatitis B: Hep B titers should be checked w/in 60 days of the 3rd dose. If incomplete hep B series (fewer than 3 doses), complete the series (do not restart) and check the titer as recommended
Influenza: all health care personnel should have annual flu shot during the fall/winter |
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What is active immunity? |
Resistance developed in response to an antigen (infecting agent or vaccine) and usually characterized by the presence of an antibody produced by the host
Onset of protection: Usually w/in 1 month of dose
Duration of protection: Usually years or lifelong |
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What is passive immunity? |
Immunity conferred by an antibody produced in another host, acquired naturally by an infant from mother, or artificially by administration of an antibody-containing preparation (antiserum or immune globulin [IG])
Onset of protection: usually w/in hours of dose
Duration of protection: time-limited, usually 6-9 mos |
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What is a C/I to Hepatitis B vaccination? |
Anaphylactic reaction hx to Baker's yeast |
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What are C/I's to varicella vaccination? |
Anaphylactic reaction hx to Gelatin & Neomycin |
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What are C/I's to MMR vaccination? |
Anaphylactic reaction hx to Neomycin & Gelatin |
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What are C/I's to IPV vaccination? |
Anaphylactic reaction hx to Neomycin, polymixin B, streptomycin |
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What is a C/I to vaccinia (smallpox) vaccination? |
Anaphylactic reaction hx to Neomycin, polymixin B, streptomycin |
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True or False -
While the PPD tuberculin skin test (TST) can be applied before or on the same day that MMR vaccine is given, if MMR vaccine is given on the previous day or earlier, the PPD TST test should be delayed for at least one month |
True |
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True or False -
A 55-year old woman w/ Asthma is an ideal candidate for live attenuated influenza vaccine (LAIV, FluMist) against seasonal influenza |
False |
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Calculating Pack-Year History to Quantify Tobacco Use |
Number of packs-per-day (PPD) x the number of years smoked
Example:
2 PPD x 30 years = 60 pk-yr hx
0.5 PPD x 10 years = 5 pk-yr hx |