- •Abbreviations
- •1 Overview of Antimicrobial Therapy
- •Factors in Antibiotic Selection
- •Factors in Antibiotic Dosing
- •Microbiology and Susceptibility Testing
- •PK/PD and Other Considerations in Antimicrobial Therapy
- •Antibiotic Failure
- •Pitfalls in Antibiotic Prescribing
- •References and Suggested Readings
- •2 Empiric Therapy Based on Clinical Syndrome
- •Empiric Therapy of CNS Infections
- •Empiric Therapy of HEENT Infections
- •Empiric Therapy of Lower Respiratory Tract Infections
- •Empiric Therapy of GI Tract Infections
- •Empiric Therapy of Genitourinary Tract Infections
- •Empiric Therapy of Sexually Transmitted Diseases
- •Empiric Therapy of Bone and Joint Infections
- •Empiric Therapy of Skin and Soft Tissue Infections
- •Sepsis/Septic Shock
- •Febrile Neutropenia
- •Transplant Infections
- •Toxin-Mediated Infectious Diseases
- •Bioterrorist Agents
- •References and Suggested Readings
- •Gram Stain Characteristics of Isolates
- •Parasites, Fungi, Unusual Organisms in Blood
- •Parasites, Fungi, Unusual Organisms in CSF/Brain
- •Parasites, Fungi, Unusual Organisms in Lungs
- •Parasites, Fungi, Unusual Organisms in Heart
- •Parasites, Fungi, Unusual Organisms in the Liver
- •References and Suggested Readings
- •5 HIV Infection
- •HIV Infection Overview
- •Stages of HIV Infection
- •Acute (Primary) HIV Infection
- •Initial Assessment of HIV Infection
- •Indications for Treatment of HIV Infection
- •Antiretroviral Treatment
- •Treatment of Other Opportunistic Infections in HIV
- •HIV Coinfections (HBV/HCV)
- •References and Suggested Readings
- •6 Prophylaxis and Immunizations
- •Surgical Prophylaxis
- •Post-Exposure Prophylaxis
- •Chronic Medical Prophylaxis
- •Endocarditis Prophylaxis
- •Travel Prophylaxis
- •Tetanus Prophylaxis
- •Immunizations
- •References and Suggested Readings
- •Empiric Therapy of CNS Infections
- •Empiric Therapy of HEENT Infections
- •Empiric Therapy of Lower Respiratory Tract Infections
- •Empiric Therapy of Vascular Infections
- •Empiric Therapy of Gastrointestinal Infections
- •Empiric Therapy of Bone and Joint Infections
- •Empiric Therapy of Skin and Soft Tissue Infections
- •Common Pediatric Antimicrobial Drugs
- •References and Suggested Readings
- •8 Chest X-Ray Atlas
- •References and Suggested Readings
- •9 Infectious Disease Differential Diagnosis
- •11 Antimicrobial Drug Summaries
- •Appendix
- •Malaria in Adults (United States)
- •Malaria in Children (United States)
- •Index
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Chapter 6. Prophylaxis and Immunizations |
377 |
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Table 6.15. Malaria Prophylaxis (cont’d) |
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Area of |
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Drug |
Exposure |
Adult Dose |
Comments |
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Primaquine |
Used for |
30 mg base (52..6 |
Indicated for persons who have had |
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presumptive |
mg salt) orally, once/ |
prolonged exposure to P.. vivax and |
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antirelapse |
day for 14 days after |
P.. ovale or both.. |
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therapy (terminal |
departure from the |
Contraindicated in persons |
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prophylaxis) to |
malarious area.. |
with G6PD† deficiency.. Also |
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decrease the risk |
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contraindicated during pregnancy |
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for relapses of |
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and lactation unless the infant being |
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P.. vivax and |
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breastfed has a documented normal |
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P.. ovale |
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G6PD level.. |
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HDCV = human diploid cell vaccine, PCEC = purified chick embryo cell vaccine, RVA = rabies vaccine absorbed, RIG = rabies immune globulin.
†Glucose-6-phosphate dehydrogenase. . Those who take primaquine should have a normal G6PD level before starting the medication..
TETANUS PROPHYLAXIS
Current information suggests that immunity lasts for decades/life-time after tetanus immunization. A tetanus booster should not be routinely given for minor wounds, but is recom-
mended for wounds with high tetanus potential (e..g.., massive crush wounds, soil-contaminated wounds, or deep puncture wounds)..
Table 6.16. Tetanus Prophylaxis in Routine Wound Management
History of Adsorbed |
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Tetanus Toxoid |
Wound Type |
Recommendations |
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Unknown or < 3 doses |
Clean, minor wounds |
Td‡ or Tdap‡ |
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Tetanus-prone wounds† |
(Td‡ or Tdap‡) plus TIG |
≥ 3 doses |
Clean, minor wounds |
No prophylaxis needed |
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Tetanus-prone wounds† |
Td‡ if > 10 years since last dose* |
DT = diphtheria and tetanus toxoids adsorbed (pediatrics), DTP = diphtheria and tetanus toxoids and pertussis vaccine adsorbed, Td = tetanus and diphtheria toxoids adsorbed (adult), TIG = tetanus immune globulin, Tdap = tetanus and diphtheria toxoids and pertussis vaccine absorbed.
†For example, massive crush wounds; wounds contaminated with dirt, soil, feces, or saliva; deep puncture wounds; or significant burn wounds or frostbite..
‡For children < 7 years, DTP (DT if pertussis is contraindicated) is preferred to tetanus toxoid alone. . For children ≥ 7 years old and adults, Tdap is preferred to Td or tetanus toxoid alone..
*More frequent booster doses are unnecessary and can increase side effects. . Protection lasts > 20 yrs Adapted from: Centers for Disease Control and Prevention.. MMWR Rep 40 (RR-10):1–28.. 1991..
378 |
A n t i b i o t i c E s s e n t i a l s |
IMMUNIZATIONS
Immunizations are designed to reduce infections in large populations, and may prevent/ decrease the severity of infection in non-immunized individuals. Compromised hosts with altered immune systems may not develop protective antibody titers to antigenic components of various vaccines.. Immunizations are not fully protective, but are recommended (depending on the vaccine) for most normal hosts, since some protection is better than none..
Table 6.17. Adult Immunizations
Vaccine |
Indications |
Dosage |
Comments |
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Bacille |
Possibly beneficial for |
Primary: 1 dose |
Live attenuated vaccine induces |
Calmette |
adults at high-risk of |
(intradermal).. |
a positive PPD which may |
Guérin |
multiple-drug resistant |
Booster not |
remain positive for years/life.. |
(BCG) |
tuberculosis.. |
recommended.. |
Contraindicated in immuno- |
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compromised hosts.. Injection |
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site infection or disseminated |
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infection are rare.. |
Hemophilus |
For those at increased |
Primary: 0..5 mL dose |
Capsular polysaccharide |
influenzae |
risk for invasive disease, |
(IM).. Booster not |
conjugated to diphtheria toxoid.. |
(type B) |
e..g.., functional or |
recommended.. |
Benefit uncertain.. Safety in |
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anatomic asplenia, |
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pregnancy unknown.. Mild local |
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HIV, immunoglobulin |
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reaction in 10%.. |
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deficiency, complement |
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deficiency (C1-3), stem cell |
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transplants, chemotherapy |
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or radiation therapy.. |
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Hepatitis A |
All children beginning |
Primary: 1 mL dose |
Inactivated whole virus.. |
(HAV) |
age 12 to 23 months and |
(IM).. One-time |
Pregnancy risk not fully |
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adults at increased risk |
booster ≥ 6 months |
evaluated.. Mild soreness at |
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of HAV.. |
later.. Booster |
injection site.. Occasional |
|
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not routinely |
headache/malaise.. |
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recommended.. |
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Hepatitis B |
Household/sexual |
Primary (3 dose |
Recombinant vaccine comprised |
(HBV) |
contact with carrier, IV |
series): Recombivax |
of hepatitis B surface antigen.. For |
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drug use, multiple sex |
10 mcg (1 mL) |
compromised hosts (including |
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partners (heterosexual), |
or Engerix-B 20 |
dialysis patients), use specially |
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homosexual male |
mcg (1 mL) IM |
packaged Recombivax 40-mcg |
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activity, blood product |
in deltoid at 0, 1, |
doses (1 mL vial containing 40 |
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recipients, hemodialysis, |
and 6 months.. |
mcg/mL).. HBsAb titers should be |
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occupational exposure |
Alternate schedule |
obtained 6 months after 3-dose |
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to blood, |
for Engerix-B: 4 dose |
primary series.. Those with non- |
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series at 0, 1, 2, and |
protective titers (≤10 mIU/mL) |
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12 months.. Booster |
should receive 1 dose monthly |
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Chapter 6. Prophylaxis and Immunizations |
379 |
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Table 6.17. Adult Immunizations (cont’d) |
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Vaccine |
Indications |
Dosage |
Comments |
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residents/staff of |
not routinely |
up to a maximum of 3 doses and |
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institutions for |
recommended.. |
retest for HbsAb titers.. Pregnancy |
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developmentally disabled, |
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not a contraindication in high- |
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prison inmates, residence |
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risk females.. Mild local reaction |
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≥ 6 months in areas of |
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in 10–20%.. Occasional fever, |
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high endemicity, others at |
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headache, fatigue, nausea.. Twinrix |
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high risk.. |
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1 mL (IM) (combination of Hepatitis |
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A inactivated vaccine and Hepatitis |
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B recombinant vaccine) is available |
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for adults on a 0, 1, and 6-month |
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schedule or 0, 7 days, 21–30 days, |
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and 12 month schedules.. |
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Herpes |
Adults ≥60 years to reduce |
Primary: 0..65 mL |
Duration of protection is at least |
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zoster (VZV) |
the frequency of shingles/ |
(SC).. Need for |
4 years.. Injection site reactions |
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prevent post-herpetic |
revaccination not |
in 48%.. Contraindicated in |
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neuralgia.. Use in those with |
yet defined.. Vaccine |
immunocompromised hosts |
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previous H.. zoster is not yet |
must be stored |
(with immunosuppressive |
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defined.. Protection best in |
frozen and used |
disorder or receiving |
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60–69 year group; efficacy |
within 30 minutes |
immunosuppressive drug) or |
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decreases with increasing |
after thawing.. |
untreated TB.. Not indicated for |
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age.. |
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therapy of H.. zoster or post- |
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herpetic neuralgia.. |
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Influenza |
All adults.. |
Annual vaccine.. |
High dose (HD) vaccine has 4 × |
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Single 0..5 mL dose |
the antigen content as the |
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(IM) before flu |
standard dose (SD) vaccine.. |
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season is optimal, |
Quadrivalent (2 A strains + 2 B |
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but can be given |
strain) and trivalent inactivated |
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anytime during flu |
whole and split virus vaccines |
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season.. (2 A strains + |
available.. Contraindications |
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1 B strain) |
include anaphylaxis to eggs or |
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sensitivity to thimerosal.. Mild |
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local reaction common.. Malaise/ |
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myalgias in some.. For pregnancy, |
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administer in 2nd or 3rd trimester |
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during flu season.. High titer (HD) |
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inactivated vaccine indicated for |
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adults ≥65 years, but enhanced |
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protective efficacy (vs.. SD) not |
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yet demonstrated.. |
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380 |
A n t i b i o t i c E s s e n t i a l s |
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Table 6.17. Adult Immunizations (cont’d) |
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Vaccine |
Indications |
Dosage |
Comments |
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Measles |
Adults born after 1956 |
Primary: 0..5 mL dose |
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Live virus vaccine (usually given |
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without live-virus |
(SC).. A second dose |
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in MMR).. Contraindicated in |
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immunization or measles |
(≥ 1 month later) |
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compromised hosts, pregnancy, |
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diagnosed by a physician |
is recommended |
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history of anaphylaxis to eggs |
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or immunologic test.. Also |
for certain adults |
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or neomycin.. Ineffective if |
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indicated for revaccination |
at increased |
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given 3–11 months after blood |
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of persons given killed |
risk of exposure |
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products.. Side effects include |
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measles vaccine between |
(e..g.., healthcare |
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low-grade fever 5–21 days |
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1963–67.. |
workers, travelers |
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after vaccination, rash, and |
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to developing |
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local reactions in if previously |
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countries).. No |
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immunized with killed vaccine |
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routine booster.. |
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(1963–67).. |
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Meningo- |
Patients with splenic |
Meningococcal |
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Also used in epidemic control |
coccus |
dysfunction or with |
conjugate vaccine |
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of N.. meningitides serogroups A, |
(invasive |
complement defects |
0..5 mL (IM).. Primary: |
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C, Y, and W-135.. For sero- |
disease) |
(C7-9) laboratory workers.. |
0..5 mL (IM) then |
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group B use meningococcal |
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May be given to 1st year |
again at months 2 |
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group B vaccine.. |
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college students living in |
and 6 (3 dose series) |
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dormitories.. |
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Mumps |
Non-immune adults.. |
Primary: 0..5 mL dose |
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Live attenuated vaccine (usually |
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(SC).. No routine |
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given in MMR).. Contraindicated |
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booster.. |
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in immunocompromised hosts, |
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pregnancy, history of anaphylaxis |
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to eggs or neomycin.. |
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Papilloma |
Females up to 26 years |
Primary: 0..5 mL |
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Quadrivalent HPV vaccine to |
(human) |
of age.. Contraindicated |
(IM).. Second dose: |
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prevent cervical, vulvar, vaginal |
Virus (HPV) |
in pregnancy.. Suggested |
2 months after 1st |
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and cancers caused by HPV types |
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for males up to 26 years |
dose.. Third dose: |
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6, 11, 16, 18.. 9 valent HPV vaccine |
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of age.. |
6 months after 1st |
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includes HPV types 52, 58, 31, 33, |
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dose.. |
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45, 6, 11, 16, 18.. |
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Pertussis |
Use Tdap instead of Td in |
A Single Tdap |
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Recommended since adults may |
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booster dose.. |
booster dose 0..5 |
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get pertussis or transmit it to |
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mL (IM).. |
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susceptible infants.. |
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Chapter 6. Prophylaxis and Immunizations |
381 |
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Table 6.17. Adult Immunizations (cont’d) |
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Vaccine |
Indications |
Dosage |
Comments |
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Pneumo- |
Immunocompetent hosts |
PPSV-23 |
Pneumococcal vaccine naïve |
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coccus |
≥ 65 years old, or > 19 |
PCV-13 |
persons aged ≥ 65.. Give PCV-13, |
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(S.. Pneumo |
years old with diabetes, |
Primary: 0..5 mL dose |
then give PPSV-23 6-12 months |
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niae) |
CSF leaks, or chronic |
(IM).. No booster.. |
later (minimal interval 8 weeks).. |
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cardiac, pulmonary or |
Primary: 0..5 |
Persons who previously received |
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liver disease.. Also for |
mL dose (SC or |
PPSV-23 at age ≥ 65.. Give PCV-13 |
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immunocompromised |
IM).. A one-time |
>1 year later after PPSV-23 given.. |
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hosts > 19 years old with |
booster at 5 years |
Persons who previously received |
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functional/anatomic |
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is recommended |
PPSV-23 before age 65 years who |
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asplenia,* leukemia, |
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for immuno – |
are now age ≥ 65.. Give PCV-13 |
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lymphoma, multiple |
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compromised hosts |
when ≥ 65 years give > 1 year |
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myeloma, widespread |
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> 2 years old and for |
later (minimum interval between |
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malignancy, chronic renal |
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failure, bone marrow/ |
those who received |
sequential administration of |
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the vaccine before |
PCV-13 and PPSV-23 is 8 weeks).. |
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organ transplant, or on |
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age 65 for high-risk |
If this window is missed, PPSV-23 |
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immunosuppressive/ |
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conditions.. |
can be given 6-12 months after |
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steroid therapy.. |
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PCV-13.. |
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Rubella |
Non-immune adults, |
Primary: 0..5 mL dose |
Live virus (RA 27/3 strain) |
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particularly women of |
(SC).. No routine |
vaccine (usually given in MMR).. |
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childbearing age.. |
booster.. |
Contraindicated in immuno- |
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compromised hosts, pregnancy, |
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history of anaphylactic reaction |
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to neomycin.. Joint pains and |
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transient arthralgias in up to |
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40%, beginning 3–25 days after |
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vaccination and lasting 1–11 days; |
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arthritis in < 2%.. |
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Tetanus- |
Adults |
Primary: Td two 0..5 |
Adsorbed toxoid vaccine.. |
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diphtheria |
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mL doses (IM), 1–2 |
Contraindicated if |
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months apart; third |
hypersensitivity/neurological |
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dose 6–12 months |
reaction or severe local |
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after second dose.. |
reaction to previous doses.. Side |
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Booster: a single |
effects include local reactions, |
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Tdap 0..5 mL (IM) |
occasional fever, systemic |
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is recommended.. |
symptoms, Arthus-like reaction |
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Tdap should be |
in persons with multiple previous |
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substituted for one of |
boosters, and systemic allergy |
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the three Td doses.. |
(rare).. |
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PCV-13 = 13 valent pneumococcal conjugate vaccine (contains strains: 1, 3, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F)
PPSV-23 = 23 valent pneumococcal polysaccharide vaccine (contains strains: 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19F, 19A, 20, 22F, 23F, 33F)..
*Pneumococcal polysaccharide vaccine may be given before splenectomy, but is in effective post-splenectomy, the conjugate vaccine is more effective..