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Immunizations June 5, 2015 Brenda Ormesher, MD Infectious Disease - PowerPoint PPT Presentation

Immunizations June 5, 2015 Brenda Ormesher, MD Infectious Disease Peacehealth Medical Group Springfield, OR Disclosures None Goals Understand basic public health impact of immunization Recognize types of vaccinations available


  1. Immunizations June 5, 2015 Brenda Ormesher, MD Infectious Disease Peacehealth Medical Group Springfield, OR

  2. Disclosures  None

  3. Goals  Understand basic public health impact of immunization  Recognize types of vaccinations available  Identify resources available for identifying CDC recommended immunizations  Discuss differences and rationale for use of specific vaccination formulations in practice

  4. Introduction

  5. Vaccine vac·cine /vakˈsēn/ (Noun) a substance used to stimulate the production of antibodies and provide immunity against one or several diseases, prepared from the causative agent of a disease, its products, or a synthetic substitute, treated to act as an antigen without inducing the disease.

  6. History  One of the great public health achievements in human history  Inoculation against smallpox was practiced 2000 years ago but modern concept credited to Edward Jenner (1796)  Now 23 FDA approved vaccine-preventable diseases

  7. http://www.immunize.org/catg.d/p4037.pdf

  8. General Characteristics of Vaccines

  9. Components of Vaccine  Antigens  component derived from disease- causing organism which trigger protective immune response  Stabilizers  Maintain effectiveness during storage  Factors affecting stability include temperature and pH  Include magnesium chloride (OPV), magnesium sulfate (RSV, measles), lactose-sorbitol and sorbitol- gelatin  Adjuvants  Added to vaccines to stimulate production of antibodies  Several hundred different types  Antibiotics  Trace amounts used in manufacturing to prevent bacterial contamination of tissue growth cells for viruses  Trace amounts (25 micrograms neomycin in MMR and IPV)  Preservatives  Multidose vaccines to prevent bacterial and fungal growth  Include thiomersal, formaldehyde (purification process removes almost all formaldehyde, <0.02% per dose)

  10. Routes of Administration http://vaccine-safety-training.org/adverse-events-causes.html

  11. Types of Vaccines  Live, attenuated  Inactivated/ killed  Toxoid (inactivated toxin)  Subunit/ conjugate  DNA vaccine  Recombinant vector

  12. Live, attenuated • Living microbe that has been weakened in the lab • Should not be given in immunocompromised host • Closest to natural infection • Elicit strong cell-mediated and antibody response • Life long immunity with only 1 or 2 doses (similar immunogenicity as wild-type pathogen)  Examples:  MMR (measles, mumps, rubella)  Varicella (chickenpox)  Influenza nasal spray  Rotavirus  Zoster (shingles)  Yellow fever  Tuberculosis (BCG)  Oral polio vaccine (OPV)

  13. Live, attenuated Vaccines http://vaccine-safety-training.org/live-attenuated-vaccines.html

  14. Inactivated, killed  Produce inactivated vaccine by killing the microbe with chemicals, heat, or radiation  More stable and safe than live vaccines (dead microbes cannot mutate)  Stimulate a weaker immune system response than live vaccines  Requires booster shots to maintain immunity  Examples:  Polio (IPV)  Hepatitis A  Whole-cell pertussis (wP)  Rabies

  15. Inactivated, killed Vaccines http://vaccine-safety-training.org/inactivated-whole-cell-vaccines.html

  16. Toxoid (inactivated toxin)  For bacteria that secrete toxins (toxin must be main cause of illness)  Inactivate toxins by treating with formalin  To increase immune response the toxoid is absorbed to aluminum or calcium salts (serve as adjuvant)  Produces antibodies that lock onto & block the toxin  Examples:  Diphtheria, tetanus (part of DTaP)

  17. Toxoid Vaccines http://vaccine-safety-training.org/toxoid-vaccines.html

  18. Subunit Protein-based, Polysaccharide, Conjugate  Use only part of a target pathogen (no live components)  Protein or polysaccharide- Uses part of target pathogen to provoke a response from the immune system Conjugate- Link antigens or toxins that immune system will recognize to the polysaccharide coating of bacteria  No guarantee that immunological memory will be formed in correct manner  Examples:  Influenza (injection)  Haemophilus influenza type b (Hib)  Pertussis (part of DTaP)  Pneumococcal  Meningococcal  Human papillomavirus (HPV)

  19. Subunit: Polysaccharide versus Conjugate Polysaccharide Conjugate  Little or short-lived impact on  Enhances the immune carriage of bacteria response and long term recognition  Decreasing immune response with time (needs boosters)  Protective immune response in infants  Limited ability to protect children under 2 years  Minimizes hyporesponsiveness  Harder to design/ develop

  20. Polysaccharide vs Conjugate Vaccines http://www.nature.com/nri/journal/v9/n3/fig _tab/nri2494_F1.html

  21. Subunit (purified antigen) Vaccines http://vaccine-safety-training.org/subunit-vaccines.html

  22. CDC Immunization Recommendations

  23. Recommended adult immunization schedule, by vaccine and age group CDC 2015 Adult Immunization Schedule

  24. Vaccines that might be indicated for adults based on medical or other indications CDC 2015 Adult Immunization Schedule

  25. “There’s an app for that” • Free! • Available from App store for iOS 5.0 or later or Google Play for Android 2.1 • http://www.cdc.gov/vaccines/s chedules/hcp/schedule- app.html#download

  26. Vaccine Specific Information

  27. Vaccine-Preventable Diseases  Adenovirus type 4 & 7  Mumps  Anthrax  Pertussis (Whooping cough)   Chickenpox (Varicella) Pneumococcal  Diphtheria  Poliovirus  Hepatitis A  Rabies  Hepatitis B  Rotavirus   Hib ( Haemophilis influenza type b) Shingles (Herpes zoster, varicella)   HPV (Human Papillomavirus) Tetanus  Influenza  Tuberculosis  Japanese encephalitis  Typhoid fever  Measles  Yellow fever  Meningococcal

  28. Influenza http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/us-vaccines.pdf

  29. Which influenza vaccine is right for my patient?  That depends….

  30. Does your patient have an egg allergy? Cost $32/ dose http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm#Tab

  31. Is your patient a pediatric patient?  In pediatrics demonstrated superior efficacy in live attenuated vaccine  reduction of 55% in culture confirmed influenza cases in ages 6 to 59 months  52% increased protection in children age 6 to 71 months) http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm

  32. Is your patient age 6 months to 2 years?  Give Fluzone  In a previously unvaccinated child (< 8 years old) give 2 doses of influenza vaccine at least 4 weeks apart http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm

  33. Is your patient age 2 to 49 years old and have special medical conditions?  Pregnant?  Immunosuppressed?  Egg allergy?  Children age 2 to 17 years receiving aspirin?  Children age 2 to 4 years who have asthma with wheezing in past 12 months?  Influenza antiviral medications in past 48 hours?  Care for severely immunosuppressed person who require a protective environment? http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm

  34. Is your patient age 2 to 49 years old and have special medical conditions?  Yes: do not give live attenuated vaccine (FluMist), give inactivated influenza vaccine  No: give FluMist (cost $22 per dose) http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm

  35. Is your patient over 65 years old?  Inactivated influenza vaccine high dose (60 m g of hemagglutinin per strain) induced a significantly higher antibody response and provider better protection against lab-confirmed illness than standard inactivated influenza vaccine (15 m g of hemagglutinin per strain)  Cost of high dose influenza vaccine $30 vs $10 for standard dose DiazGranados , C. Et al. “Efficacy of High -Dose versus Standard- Dose Influenza Vaccine in Older Adults.” NEJM 2014; 371:635 -645.

  36. Vaccine Effectiveness  Vaccine effectiveness decline post-vaccination  By age: Vaccine effectiveness in < 65 years estimated at 44%, vaccine effectiveness > 65 years estimated at 19%  By time: Vaccine effectiveness in first 100 days 61%, between 100 and 119 days was 42%, after 120 days was 0% Castilla J, et al. “Decline in Vaccine Effectiveness with Time After Vaccination, Navarre, Spain, Season 2011/12.” Eurosurveillance, Volume 18, Issue 5, 31Jan2013.

  37. Quadrivalent versus Trivalent  Rationale for quadrivalent: historically influenza vaccines contain only one strain of B virus although though there are two different lineages of B strains that circulate most seasons  Benefit: improved coverage of B strain which could account for 1-44% of influenza cases (based on data from preceding 10 years)  Negative: Cost ($15 for quad vs $10 for tri), supply

  38. Pneumococcal ₊ Pneumovax (PPSV23)- Pneumococcal polyvalent ( polysaccharide ) vaccine covering 23 serotypes, cost $85/ dose ₊ Prevnar (PCV13)- Pneumococcal conjugate vaccine covering 13 serotypes, cost $150/ dose http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/us-vaccines.pdf

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