Immunization: Difference between revisions
From IDWiki
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==Passive and Active== |
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* |
*'''Passive''' immunization refers to the transfer of antibodies to confer protection |
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** |
**Mother-to-child transfer and immunoglobulins are examples |
||
** |
**Hepatitis B |
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** |
**Chicken pox, that cannot recieve vaccine (in pregnant women, immunocompromised, baby exposed by mom at birth) |
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** |
**Measles, that cannot recieve vaccine |
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** |
**Hepatitis A, that cannot recieve vaccine or are high risk (liver disease) |
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** |
**Rabies |
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** |
**Tetanus |
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* |
*'''Active''' immunization refers to a vaccine intended to provoke an immune response and therefore confer protection |
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== |
==Components== |
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* |
*Immunogen |
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** |
**'''Live attenuated:''' a weakened version of a pathogen that provokes an immune response without causing disease |
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** |
**'''Inactivated:''' killed pathogens, often provoking a weaker immune response than live, and may have problems with injection of unwanted proteins |
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** |
**'''Subunit:''' include proteins, polysaccharides and protein-polysaccharide conjugates |
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* |
*Adjuvant |
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** |
**Additional compound that stimulates immune response |
||
** |
**Canada only uses aluminum salts (aluminum hydroxide, aluminum phosphate or potassium aluminum sulfate) |
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*** |
***Rare side effects include subcutaneous nodules, granulomatous inflammation or contact hypersensitivity |
||
* |
*Preservatives |
||
** |
**Prevent the vaccine from being contaminated with bacteria |
||
** |
**Includes thimerosal, phenol, and 2-phenoxyethanol |
||
* |
*Additives |
||
** |
**May contain trace amount of substances required during the purification process or to confirm vaccine quality |
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== |
==List of Vaccines== |
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{| class="wikitable" |
{| class="wikitable" |
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!Vaccine |
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!Notes |
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|Bacille Calmette-GuΓ©rin Vaccine |
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|Cholera and Enterotoxigenic Escherichia Coli |
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|Diphtheria Toxoid |
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|Haemophilus Influenzae Type B Vaccine |
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|Hepatitis A Vaccine |
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|Hepatitis B Vaccine |
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|Herpes Zoster (Shingles) Vaccine |
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|Human Papillomavirus Vaccine |
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|Influenza Vaccine |
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|Japanese Encephalitis Vaccine |
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|Measles Vaccine |
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|Meningococcal Vaccine |
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|Mumps Vaccine |
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|Pertussis Vaccine |
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|Pneumococcal Vaccine |
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|Poliomyelitis Vaccine |
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|Rabies Vaccine |
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|Rotavirus Vaccine |
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|Rubella Vaccine |
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|Smallpox Vaccine |
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|Tetanus Toxoid |
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|Typhoid Vaccine |
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|Toxoid vaccine. |
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|Varicella (Chickenpox) Vaccine |
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|Yellow Fever Vaccine |
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|} |
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* |
*Live attenuated |
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** |
**MMR |
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** |
**Varicella (Zostavax) |
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** |
**Smallpox |
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** |
**Oral polio |
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** |
**Nasal spray influenza |
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* |
*Killed |
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** |
**Hep A |
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** |
**Injectable influenza |
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** |
**Injectable polio |
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** |
**Rabies |
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* |
*Subunit |
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** |
**Hib |
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** |
**Hep B |
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** |
**HPV |
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** |
**Pertussis, TdAP |
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** |
**Varicella (Shingrix) |
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== |
==Pathophysiology== |
||
* |
*Depends on the specific vaccine |
||
* |
*Generally work by inducing specific IgG serum antibodies |
||
** |
**BCG is the only T-cell-specific vaccine, although T-cell response may contribute to others |
||
* |
*Generally do not elicit a mucosal antibody response, so infection may only be stopped after already infecting a mucosal surface |
||
** |
**Therefore, they do not induce sterilizing immunity |
||
* |
*Antigen-presenting cells are activated by a pathogen and in turn stimulate B and T cell response in the local lymph node |
||
** |
**Live vaccines may travel throughout the body, activating multiple lymph nodes in different sites |
||
** |
**Non-live vaccines only activate APCs that travel to the local lymph node, explaining why they may be given in multiple limbs at once |
||
* |
*Protein antigens trigger T-cells to help to activate B-cells in germinal centres |
||
** |
**It can take a few weeks to produce IgG antibodies |
||
** |
**IgG peaks within 4-6 weeks of primary immunization |
||
* |
*Polysaccharide antigens travel to lymphoid tissue where they bind B cells directly and trigger maturation into plasma cells |
||
** |
**Without germinal centres, memory B cells are not produced |
||
** |
**Need to be coupled to a carrier protein in order to generate a memory response |
||
* |
*Memory B cells require several days to redifferentiate into plasma cells upon reexposure |
||
=== |
===T-cells=== |
||
* |
*Th1: IFN-gamma and TNF-alpha to activate response against intracellular pathogens |
||
* |
*Th2: IL-4, IL-5, and IL-13 to activate response against extracellular pathogens such as helminths |
||
== |
==Vaccination Schedule== |
||
* |
*[https://www.canada.ca/en/public-health/services/provincial-territorial-immunization-information/provincial-territorial-routine-vaccination-programs-infants-children.html Canada's Provincial and Territorial Routine (and Catch-up) Vaccination Routine Schedule Programs for Infants and Children] |
||
* |
*[https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-1-key-immunization-information/page-13-recommended-immunization-schedules.html Canadian Immunization Guide: Recommended Immunization Schedules] |
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* |
*[https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-3-vaccination-specific-populations/page-10-immunization-persons-new-canada.html Canadian Immunization Guide: Immunization of Persons New to Canada] |
||
=== |
===Adult Vaccination=== |
||
==== |
====Pneumococcus==== |
||
* |
*Conjugate better than polysaccharide |
||
** |
**Prevnar: PC-7, then PC-10 and PC-13 |
||
*** |
***Conjugated with diphtheria CRM197 |
||
*** |
***Incremental benefit of vaccinating adults over and above vaccinating children is not high enough to warrant funding the vaccine |
||
** |
**Pneumovax: PS-23 |
||
* |
*In age >65 years or other high-risk groups, PC first, then PS 8 weeks later (recommended), though only PS is paid for in Ontario |
||
* |
*For high-risk groups, add a PS booster at 5 years |
||
* |
*If PS-23 already given, wait a year before giving PC-13 |
||
==== |
====Influenza==== |
||
* |
*Trivalent has H1N1 and H2N3 (both flu A) and a flu B strain |
||
* |
*The quadrivalent adds a second flu B, for children who get more flu B |
||
** |
**The first time someone receives the vaccine, they need a second booster |
||
* |
*The high dose is more effective but more expensive (Fluzone) |
||
** |
**Trivalent vaccine |
||
** |
**24% increase in efficacy in the elderly (brings up to normal population) |
||
* |
*Ensure that higher risk patients are vaccinated as well as their household |
||
==== |
====Shingles/Varicella-zoster==== |
||
* |
*Live attenuated zoster vaccine (Zostavax) |
||
** |
**Can be given if pred <20 mg/d or <14 days, low-dose methotrexate, azathioprine, 6MP, hydroxychloroquine, sulfasalazine, etc. |
||
* |
*Recombinatnt glycoprotein vaccine (Shingrix), 2 doses IM 2 months apart |
||
** |
**Protection is at least 3-4 years, possibly longer |
||
==== |
====Asplenia==== |
||
* |
*Risk factor for encapsulated organisms: ''Streptococcus pneumoniae'', ''Haemophilus influenzae'' type B, and ''Neisseria meningitidis'' |
||
* |
*Splenectomy, indications include trauma, cancer, ITP |
||
* |
*Also beware functional asplenia as in sickle cell disease and Howell-Jolly bodies |
||
* |
*Highest risk in the first 5 years, but can be up to 20 years out |
||
* |
*2 weeks before elective or 2 weeks after unplanned emergent |
||
* |
*Recommended vaccines |
||
** |
**Menactra (conjugate ACYW-135) + Bexsero (Men B, but not covered) |
||
*** |
***Second dose at 8 weeks, or later if given after splenectomy |
||
** |
**HiB once |
||
** |
**Pill-in-pocket amox/clav or levoflox to take on the way to ED if they get a fever |
||
* |
*Travel precautions: be careful about babesia in New England (fulminant sepsis and die), as well as malaria |
||
* |
*Dog bites are very high risk for severe ''Capnocytophaga'' |
||
** |
**Prophylaxis with amox/clav x5 days |
||
=== Close Contacts of Immunocompromised Patients === |
|||
== Contraindications == |
|||
* In general, close contacts should receive all routine vaccines, including rotavirus and annual influenza |
|||
* Anaphylaxis to the vaccine or a component of the vaccine |
|||
* Specific vaccines do have some caveats, however: |
|||
* GBS within 6 weeks of immunization not attributable to other cause |
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** [[Rotavirus]]: the immunocompromised patient should not change diapers for 4 weeks after the infant receives their vaccine |
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* Usually deferred in cases of |
|||
** [[Varicella-zoster virus]] (live): avoid contact only if the vaccinated household member develops a rash (rare) |
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** Acute febrile illness |
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** [[Influenza]] (live, annual): avoid close contact for 2 weeks after the household member receives their vaccine |
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** Immunosuppressive therapy |
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** [[Poliovirus]] (live, oral): do ''not'' immunize close contacts with the live oral polio vaccine |
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*** Prednisone β₯20 mg and duration >14 days |
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** [[Smallpox]]: avoid vaccinating close contacts if at all possible |
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*** Inactivated given 3 mo after immunosuppression stops (since they're less immunogenic) |
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* Of note, the strains in the MMR vaccine are not transmitted person-to-person, so it is safe for close contacts to be vaccinated with MMR |
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*** Live given 1-3 mo after immunosuppression stops |
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** Pregnancy (live vaccines) |
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* Live vaccines |
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** Immunocompromised |
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** Suspicious family or personal history of immunodeficiency |
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** Pregnancy (as a precaution) |
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** Live influenza: severe asthma |
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* Rotavirus: congenital GI malformation or history of intussusception |
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* MMR/MMRV/VZV/HZV: active, untreated tuberculosis |
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* BCG or yellow fever: infant with signs and symptoms of AIDS |
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==Contraindications== |
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=== Acute illness === |
|||
*Anaphylaxis to the vaccine or a component of the vaccine |
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* If significant nasal congestion is present that might impede delivery of LAIV to the nasopharyngeal mucosa, TIV can be administered or LAIV could be deferred until resolution of the illness. |
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*GBS within 6 weeks of immunization not attributable to other cause |
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* In infants with moderate-to-severe gastroenteritis, rotavirus vaccine should be deferred until the condition improves unless deferral will result in scheduling of the first dose beyond the recommended age limit. |
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*Usually deferred in cases of |
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* Administration of oral cholera and travellers' diarrhea vaccine should be postponed in persons with acute gastrointestinal illness. |
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**Acute febrile illness |
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**Immunosuppressive therapy |
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***Prednisone β₯20 mg and duration >14 days |
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***Inactivated given 3 mo after immunosuppression stops (since they're less immunogenic) |
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***Live given 1-3 mo after immunosuppression stops |
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**Pregnancy (live vaccines) |
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*Live vaccines |
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**Immunocompromised |
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**Suspicious family or personal history of immunodeficiency |
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**Pregnancy (as a precaution) |
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**Live influenza: severe asthma |
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*Rotavirus: congenital GI malformation or history of intussusception |
|||
*MMR/MMRV/VZV/HZV: active, untreated tuberculosis |
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*BCG or yellow fever: infant with signs and symptoms of AIDS |
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=== |
===Acute illness=== |
||
*If significant nasal congestion is present that might impede delivery of LAIV to the nasopharyngeal mucosa, TIV can be administered or LAIV could be deferred until resolution of the illness. |
|||
* IVIg at 2 g/kg, wait 11 months before giving live vaccines |
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*In infants with moderate-to-severe gastroenteritis, rotavirus vaccine should be deferred until the condition improves unless deferral will result in scheduling of the first dose beyond the recommended age limit. |
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* Even pRBC, should wait 4-5 months |
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*Administration of oral cholera and travellers' diarrhea vaccine should be postponed in persons with acute gastrointestinal illness. |
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====IVIg and Transfusion==== |
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== Side Effects == |
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*IVIg at 2 g/kg, wait 11 months before giving live vaccines |
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* Common to very common AEFI |
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*Even pRBC, should wait 4-5 months |
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** Vaccination site pain and swelling |
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** Fever |
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** Fever/rash a week after MMR |
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** Large local reactions |
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*** Giant red swollen injection site or arm (not cellulitis, just watch and wait) |
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*** Commonly recur, especially tetanus-containing vaccines |
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* Uncommon AEFI |
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** Hypotonic-hyporesponsive events (HHE) after infant vaccines (especially pertussis-containing vaccines) |
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** Lymphadenopathy (MMR) |
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* Rare AEFI |
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** Febrile seizure after MMR vaccine |
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* Very rare AEFI |
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** Anaphylaxis after any vaccine |
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** BCG can cause all sorts of things: lymphadenopathy, abscesses, disseminated |
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==Side Effects== |
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== Vaccine Hesitancy == |
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*Common to very common AEFI |
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* Stay engaged with the patient/parent |
|||
**Vaccination site pain and swelling |
|||
* Use presumptive language (e.g. "it's time to give you your immunizations today") |
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**Fever |
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* Use motivational interviewing |
|||
**Fever/rash a week after MMR |
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** Open-ended question about specific question |
|||
**Large local reactions |
|||
** Affirmation |
|||
***Giant red swollen injection site or arm (not cellulitis, just watch and wait) |
|||
** Reflective listening |
|||
***Commonly recur, especially tetanus-containing vaccines |
|||
* Use clear language to present risks and benefits fairly |
|||
*Uncommon AEFI |
|||
** Use framing: "If you decide not to get the HPV vaccine, you increase your risk of getting HPV and cervical cancer" (instead of getting it decreases your risk); "the vaccine is 99% safe" (instead of 1% risk) |
|||
**Hypotonic-hyporesponsive events (HHE) after infant vaccines (especially pertussis-containing vaccines) |
|||
* Address pain and fear of pain (for children) |
|||
**Lymphadenopathy (MMR) |
|||
* Emphasize that herd immunity is not a guarantee, especially if there is an outbreak |
|||
*Rare AEFI |
|||
**Febrile seizure after MMR vaccine |
|||
*Very rare AEFI |
|||
**Anaphylaxis after any vaccine |
|||
**BCG can cause all sorts of things: lymphadenopathy, abscesses, disseminated |
|||
==Vaccine Hesitancy== |
|||
=== Further Reading === |
|||
*Stay engaged with the patient/parent |
|||
* WHO: [http://www.who.int/vaccine_safety/initiative/detection/immunization_misconceptions/en/ Six common misconceptions about immunization] |
|||
*Use presumptive language (e.g. "it's time to give you your immunizations today") |
|||
* CPS: [https://www.cps.ca/en/documents/position/working-with-vaccine-hesitant-parents Working with vaccine-hesitant parents: An update] |
|||
*Use motivational interviewing |
|||
**Open-ended question about specific question |
|||
**Affirmation |
|||
**Reflective listening |
|||
*Use clear language to present risks and benefits fairly |
|||
**Use framing: "If you decide not to get the HPV vaccine, you increase your risk of getting HPV and cervical cancer" (instead of getting it decreases your risk); "the vaccine is 99% safe" (instead of 1% risk) |
|||
*Address pain and fear of pain (for children) |
|||
*Emphasize that herd immunity is not a guarantee, especially if there is an outbreak |
|||
== |
===Further Reading=== |
||
*WHO: [http://www.who.int/vaccine_safety/initiative/detection/immunization_misconceptions/en/ Six common misconceptions about immunization] |
|||
* [https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-2-vaccine-safety/page-3-contraindications-precautions-concerns.html Canadian Immunization Guide: Contraindications, Precautions and Concerns] |
|||
*CPS: [https://www.cps.ca/en/documents/position/working-with-vaccine-hesitant-parents Working with vaccine-hesitant parents: An update] |
|||
==Further Reading== |
|||
*[https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-2-vaccine-safety/page-3-contraindications-precautions-concerns.html Canadian Immunization Guide: Contraindications, Precautions and Concerns] |
|||
[[Category:Vaccination]] |
[[Category:Vaccination]] |
Revision as of 19:03, 19 August 2020
Passive and Active
- Passive immunization refers to the transfer of antibodies to confer protection
- Mother-to-child transfer and immunoglobulins are examples
- Hepatitis B
- Chicken pox, that cannot recieve vaccine (in pregnant women, immunocompromised, baby exposed by mom at birth)
- Measles, that cannot recieve vaccine
- Hepatitis A, that cannot recieve vaccine or are high risk (liver disease)
- Rabies
- Tetanus
- Active immunization refers to a vaccine intended to provoke an immune response and therefore confer protection
Components
- Immunogen
- Live attenuated: a weakened version of a pathogen that provokes an immune response without causing disease
- Inactivated: killed pathogens, often provoking a weaker immune response than live, and may have problems with injection of unwanted proteins
- Subunit: include proteins, polysaccharides and protein-polysaccharide conjugates
- Adjuvant
- Additional compound that stimulates immune response
- Canada only uses aluminum salts (aluminum hydroxide, aluminum phosphate or potassium aluminum sulfate)
- Rare side effects include subcutaneous nodules, granulomatous inflammation or contact hypersensitivity
- Preservatives
- Prevent the vaccine from being contaminated with bacteria
- Includes thimerosal, phenol, and 2-phenoxyethanol
- Additives
- May contain trace amount of substances required during the purification process or to confirm vaccine quality
List of Vaccines
Vaccine | Notes |
---|---|
Bacille Calmette-GuΓ©rin Vaccine | |
Cholera and Enterotoxigenic Escherichia Coli | |
Diphtheria Toxoid | |
Haemophilus Influenzae Type B Vaccine | |
Hepatitis A Vaccine | |
Hepatitis B Vaccine | |
Herpes Zoster (Shingles) Vaccine | |
Human Papillomavirus Vaccine | |
Influenza Vaccine | |
Japanese Encephalitis Vaccine | |
Measles Vaccine | |
Meningococcal Vaccine | |
Mumps Vaccine | |
Pertussis Vaccine | |
Pneumococcal Vaccine | |
Poliomyelitis Vaccine | |
Rabies Vaccine | |
Rotavirus Vaccine | |
Rubella Vaccine | |
Smallpox Vaccine | |
Tetanus Toxoid | |
Typhoid Vaccine | Toxoid vaccine. |
Varicella (Chickenpox) Vaccine | |
Yellow Fever Vaccine |
- Live attenuated
- MMR
- Varicella (Zostavax)
- Smallpox
- Oral polio
- Nasal spray influenza
- Killed
- Hep A
- Injectable influenza
- Injectable polio
- Rabies
- Subunit
- Hib
- Hep B
- HPV
- Pertussis, TdAP
- Varicella (Shingrix)
Pathophysiology
- Depends on the specific vaccine
- Generally work by inducing specific IgG serum antibodies
- BCG is the only T-cell-specific vaccine, although T-cell response may contribute to others
- Generally do not elicit a mucosal antibody response, so infection may only be stopped after already infecting a mucosal surface
- Therefore, they do not induce sterilizing immunity
- Antigen-presenting cells are activated by a pathogen and in turn stimulate B and T cell response in the local lymph node
- Live vaccines may travel throughout the body, activating multiple lymph nodes in different sites
- Non-live vaccines only activate APCs that travel to the local lymph node, explaining why they may be given in multiple limbs at once
- Protein antigens trigger T-cells to help to activate B-cells in germinal centres
- It can take a few weeks to produce IgG antibodies
- IgG peaks within 4-6 weeks of primary immunization
- Polysaccharide antigens travel to lymphoid tissue where they bind B cells directly and trigger maturation into plasma cells
- Without germinal centres, memory B cells are not produced
- Need to be coupled to a carrier protein in order to generate a memory response
- Memory B cells require several days to redifferentiate into plasma cells upon reexposure
T-cells
- Th1: IFN-gamma and TNF-alpha to activate response against intracellular pathogens
- Th2: IL-4, IL-5, and IL-13 to activate response against extracellular pathogens such as helminths
Vaccination Schedule
- Canada's Provincial and Territorial Routine (and Catch-up) Vaccination Routine Schedule Programs for Infants and Children
- Canadian Immunization Guide: Recommended Immunization Schedules
- Canadian Immunization Guide: Immunization of Persons New to Canada
Adult Vaccination
Pneumococcus
- Conjugate better than polysaccharide
- Prevnar: PC-7, then PC-10 and PC-13
- Conjugated with diphtheria CRM197
- Incremental benefit of vaccinating adults over and above vaccinating children is not high enough to warrant funding the vaccine
- Pneumovax: PS-23
- Prevnar: PC-7, then PC-10 and PC-13
- In age >65 years or other high-risk groups, PC first, then PS 8 weeks later (recommended), though only PS is paid for in Ontario
- For high-risk groups, add a PS booster at 5 years
- If PS-23 already given, wait a year before giving PC-13
Influenza
- Trivalent has H1N1 and H2N3 (both flu A) and a flu B strain
- The quadrivalent adds a second flu B, for children who get more flu B
- The first time someone receives the vaccine, they need a second booster
- The high dose is more effective but more expensive (Fluzone)
- Trivalent vaccine
- 24% increase in efficacy in the elderly (brings up to normal population)
- Ensure that higher risk patients are vaccinated as well as their household
Shingles/Varicella-zoster
- Live attenuated zoster vaccine (Zostavax)
- Can be given if pred <20 mg/d or <14 days, low-dose methotrexate, azathioprine, 6MP, hydroxychloroquine, sulfasalazine, etc.
- Recombinatnt glycoprotein vaccine (Shingrix), 2 doses IM 2 months apart
- Protection is at least 3-4 years, possibly longer
Asplenia
- Risk factor for encapsulated organisms: Streptococcus pneumoniae, Haemophilus influenzae type B, and Neisseria meningitidis
- Splenectomy, indications include trauma, cancer, ITP
- Also beware functional asplenia as in sickle cell disease and Howell-Jolly bodies
- Highest risk in the first 5 years, but can be up to 20 years out
- 2 weeks before elective or 2 weeks after unplanned emergent
- Recommended vaccines
- Menactra (conjugate ACYW-135) + Bexsero (Men B, but not covered)
- Second dose at 8 weeks, or later if given after splenectomy
- HiB once
- Pill-in-pocket amox/clav or levoflox to take on the way to ED if they get a fever
- Menactra (conjugate ACYW-135) + Bexsero (Men B, but not covered)
- Travel precautions: be careful about babesia in New England (fulminant sepsis and die), as well as malaria
- Dog bites are very high risk for severe Capnocytophaga
- Prophylaxis with amox/clav x5 days
Close Contacts of Immunocompromised Patients
- In general, close contacts should receive all routine vaccines, including rotavirus and annual influenza
- Specific vaccines do have some caveats, however:
- Rotavirus: the immunocompromised patient should not change diapers for 4 weeks after the infant receives their vaccine
- Varicella-zoster virus (live): avoid contact only if the vaccinated household member develops a rash (rare)
- Influenza (live, annual): avoid close contact for 2 weeks after the household member receives their vaccine
- Poliovirus (live, oral): do not immunize close contacts with the live oral polio vaccine
- Smallpox: avoid vaccinating close contacts if at all possible
- Of note, the strains in the MMR vaccine are not transmitted person-to-person, so it is safe for close contacts to be vaccinated with MMR
Contraindications
- Anaphylaxis to the vaccine or a component of the vaccine
- GBS within 6 weeks of immunization not attributable to other cause
- Usually deferred in cases of
- Acute febrile illness
- Immunosuppressive therapy
- Prednisone β₯20 mg and duration >14 days
- Inactivated given 3 mo after immunosuppression stops (since they're less immunogenic)
- Live given 1-3 mo after immunosuppression stops
- Pregnancy (live vaccines)
- Live vaccines
- Immunocompromised
- Suspicious family or personal history of immunodeficiency
- Pregnancy (as a precaution)
- Live influenza: severe asthma
- Rotavirus: congenital GI malformation or history of intussusception
- MMR/MMRV/VZV/HZV: active, untreated tuberculosis
- BCG or yellow fever: infant with signs and symptoms of AIDS
Acute illness
- If significant nasal congestion is present that might impede delivery of LAIV to the nasopharyngeal mucosa, TIV can be administered or LAIV could be deferred until resolution of the illness.
- In infants with moderate-to-severe gastroenteritis, rotavirus vaccine should be deferred until the condition improves unless deferral will result in scheduling of the first dose beyond the recommended age limit.
- Administration of oral cholera and travellers' diarrhea vaccine should be postponed in persons with acute gastrointestinal illness.
IVIg and Transfusion
- IVIg at 2 g/kg, wait 11 months before giving live vaccines
- Even pRBC, should wait 4-5 months
Side Effects
- Common to very common AEFI
- Vaccination site pain and swelling
- Fever
- Fever/rash a week after MMR
- Large local reactions
- Giant red swollen injection site or arm (not cellulitis, just watch and wait)
- Commonly recur, especially tetanus-containing vaccines
- Uncommon AEFI
- Hypotonic-hyporesponsive events (HHE) after infant vaccines (especially pertussis-containing vaccines)
- Lymphadenopathy (MMR)
- Rare AEFI
- Febrile seizure after MMR vaccine
- Very rare AEFI
- Anaphylaxis after any vaccine
- BCG can cause all sorts of things: lymphadenopathy, abscesses, disseminated
Vaccine Hesitancy
- Stay engaged with the patient/parent
- Use presumptive language (e.g. "it's time to give you your immunizations today")
- Use motivational interviewing
- Open-ended question about specific question
- Affirmation
- Reflective listening
- Use clear language to present risks and benefits fairly
- Use framing: "If you decide not to get the HPV vaccine, you increase your risk of getting HPV and cervical cancer" (instead of getting it decreases your risk); "the vaccine is 99% safe" (instead of 1% risk)
- Address pain and fear of pain (for children)
- Emphasize that herd immunity is not a guarantee, especially if there is an outbreak
Further Reading
- WHO: Six common misconceptions about immunization
- CPS: Working with vaccine-hesitant parents: An update