Kenneth McCall, BSPharm, PharmD Associate Professor | UNE President | Maine Pharmacy Association Objectives Discuss the gap between current rates and Healthy People 2020 goals for vaccinations. Categorize each of the CDC recommended flu vaccines based upon live/inactivated, route, prep., and storage. Discuss the influenza vaccines for 2014 including the new quadrivalent and mammalian cell vaccines. Identify vaccine contraindications and recommend vaccines based upon age and medical history. Apply ACIP recommendations and FDA approved indications for the CDC recommended vaccines. Outline Background & Principles of Vaccination Influenza Vaccines Quadrivalent inactivated Quadrivalent live Mammalian High Dose Intradermal Classification of Vaccines Live attenuated Weakened form of the “wild” virus or bacteria Inactivated Whole viruses or bacteria Fractions of viruses or bacteria *Epidemiology and Prevention of Vaccine-Preventable Diseases, 12th Edition Classification of Vaccines Live attenuated: Measles, mumps, rubella, varicella, zoster, intranasal influenza Inactivated: hepatitis A, hepatitis B, influenza, pneumonia, diphtheria, tetanus, pertussis, HPV, meningicoccal *Epidemiology and Prevention of Vaccine-Preventable Diseases, 12th Edition 8 2014 Recommended Adult Immunization Schedule, by vaccine and age group www.cdc.gov/vaccines/schedules/hcp/adult.html Vaccines that might be indicated for adults based on medical and other indications www.cdc.gov/vaccines/schedules/hcp/adult.html 2014 Influenza Vaccination Recommendations Annual vaccination against influenza is recommended for all persons aged 6 months or older. Adults aged 18 to 49 years can receive the recombinant or mammalian vaccine. Healthy, nonpregnant persons aged 2 to 49 years without high-risk medical conditions can receive either intranasal, live vaccine or inactivated vaccine. Health care personnel who care for severely immunocompromised persons should receive inactivated vaccine. Adults 18 to 64 years can receive either the intramuscular or intraderm. Adults 65+ years can receive either the standard-dose or the high-dose. www.cdc.gov/vaccines/schedules/hcp/adult.html What is the Healthy People 2020 goal for annual flu vaccination for adults 65 and older? 25% 25% 25% 25% 100% 2. 90% 3. 70% 4. 50% 1. 14 Influenza Virus Strains Influenza A virus Moderate to severe illness All age groups Humans and other animals Influenza B virus Milder disease Primarily affects children Humans only Influenza C virus Rarely reported in humans No epidemics 15 2013-14 Influenza Surveillance CDC has antigenically characterized 2,110 influenza viruses Influenza A 2009 H1N1 [1,657]: 99.9% of the 2009 H1N1 viruses tested were characterized as A/California/7/2009-like, the influenza A (H1N1) component of the 2013-2014 Northern Hemisphere influenza vaccine. Influenza A (H3N2) [269]: 98.1% of the influenza A (H3N2) viruses tested have been characterized as A/Texas/50/2012-like, the influenza A (H3N2) component of the 2013-2014 Northern Hemisphere influenza vaccine. Influenza B [184]: 124 (67%) of the 184influenza B viruses tested belong to B/Yamagata/16/88-lineage and the remaining 60 (33%) influenza B viruses tested belong to B/Victoria/02/87 lineage. Yamagata Lineage [124]: 124 influenza B/Yamagata-lineage viruses were characterized as B/ Massachusetts/2/1012-like, which is included as an influenza B component of the 2013-2014 Northern Hemisphere trivalent and quadrivalent influenza vaccines. Victoria Lineage [60]: 60 influenza B/Victoria-lineage viruses were characterized as B/Brisbane/60/2008-like, which is included as an influenza B component of the 2013-2014 Northern Hemisphere quadrivalent influenza vaccine. US Influenza Vaccines: 2014 Vaccine Inactivated, Trivalent Standard Dose Age Group Dosage Schedule Route 6-35 mos 0.25 ml 1 or 2 shots IM 3-8 years 0.5 ml 1 or 2 shots IM >9 years 0.5 ml 1 shot IM Inactivated, Quadrivalent Standard Dose 3-8 years 0.5 ml 1 or 2 shots IM >9 years 0.5 ml 1 shot IM Inactivated, Mammalian Trivalent Standard Dose >18 years 0.5 ml 1 shot IM 18-49 years 0.5 ml 1 shot IM Inactivated, Trivalent High Dose >65 years 0.5 ml 1 shot IM Inactivated, Trivalent Intra-dermal 18-64 years 0.1 ml 1 shot ID 2-8 years 0.2 ml 1 or 2 Nasal 9-49 years 0.2 ml 1 dose Nasal Inactivated, Recombinant Trivalent Standard Dose Live, Quadrivalent Intranasal New Influenza Vaccines: 2013-14 Fluarix ® (GlaxoSmithKline) – inactivated, quadrivalent vaccine FDA approved December 2012 People ages 3 years and older Fluzone® (Sanofi Pasteur) – inactivated, quadrivalent vaccine. FDA approved March 2013 People ages 6 months and older Flumist® Quadrivalent (MedImmune)– live, attenuated, quadrivalent vaccine FDA approved March, 2012 People ages 2 through 49 years Flucelvax® (Novartis)– trivalent inactivated vaccine grown in mammalian cells. FDA approved November, 2012 Adults 18 years and older Doesn’t list “severe allergic reaction to egg protein” in the contraindications Flublok® (Protein Sciences Corp.) – inactivated, trivalent, recombinant vaccine. FDA approved March 2013 People ages 6 months and older Doesn’t list “severe allergic reaction to egg protein” in the contraindications Which of the following was the predominant flu strain of 2013-14? 25% 1. Type B strain in trivalent vaccine 25% 2. Type B strain not in trivalent vaccine 25% 3. Type A H1N1 strain 25% 4. Type A H3N2 strain 21 New Influenza Vaccines: 2013-14 Fluarix ® (GlaxoSmithKline) – inactivated, quadrivalent vaccine which contains two type A and two type B strains FDA approved December 2012 People ages 3 years and older Fluzone ® (Sanofi Pasteur) – inactivated, quadrivalent vaccine which contains two type A and two type B strains FDA approved March 2013 People ages 6 months and older Quadrivalent vs. Trivalent: Local Side Effects Local Side Effect Fluarix Quadrivalent N=3,015 Trivalent Influenza Vaccine (TIV) TIV-1 (B Victoria) N=1,003 TIV-2 (B Yamagata) N=607 Pain 36 37 31 Redness 2 2 2 Swelling 2 2 1 Fluarix [package insert]. Dresden, Germany: GlaxoSmithKline Inc; 2013. Quadrivalent vs. Trivalent: Systemic Side effects Systemic Side Effect Fluarix Quadrivalent N=3,015 Trivalent Influenza Vaccine (TIV) TIV-1 (B Victoria) N=1,003 TIV-2 (B Yamagata) N=607 Muscle Aches 16 19 16 Headache 16 16 13 Fatigue 16 18 15 Arthralgia 8 10 9 GI Symptoms 7 7 6 Shivering 4 5 4 Fever ≥99.5°F 2 1 2 Fluarix [package insert]. Dresden, Germany: GlaxoSmithKline Inc; 2013. Quadrivalent vs. Placebo: Vaccine Efficacy Attack Rates (n/N) N N % Vaccine Efficacy % LL UL Antigenically Matched Strains FLUARIX 5,103 49 1.0 66.9 51.9 77.4 placebo 2,549 74 2.9 - - - All Cultured-Confirmed Influenza (Matched, Unmatched, and Untyped) FLUARIX 5,103 63 1.2 61.6 46.0 72.8 placebo 2,549 82 3.2 - - - Fluarix [package insert]. Dresden, Germany: GlaxoSmithKline Inc; 2013. Administration Fluarix®: 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 26 Quadrivalent Influenza Vaccines contain which of the following? 25% 1. Four type A strains 25% 2. Two type A strains, 1 type B, & 1 type C 25% 3. Two type A strains & 2 type B strains 25% 4. Four type B strains 28 New Influenza Vaccines: 2013-14 Flumist® Quadrivalent (MedImmune)– live attenuated vaccine which contains two type A and two type B strains FDA approved March, 2012 People ages 2 through 49 years Live Attenuated Influenza Vaccine Indication Healthy people 2 through 49 years of age Contraindications I pick my nose! Pregnant women People who have long-term health problems with: heart disease kidney or liver disease lung disease metabolic disease, such as diabetes asthma anemia, and other blood disorders Anyone with a weakened immune system Severe egg allergy 30 Immune Response Studies of FluMist Quadrivalent in Children and Adults A multicenter, randomized, double-blind study was performed to assess the immunogenicity of FluMist Quadrivalent compared to FluMist Trivalent in 2,312 children and adolescents 2 through 17 years of age. A multicenter, randomized, double-blind study was performed to assess the immunogenicity of FluMist Quadrivalent compared to FluMist Trivalent in 1,800 adults 18 through 49 years of age. Conclusion: In both studies, the addition of the second B strain did not result in immune interference to other strains included in the vaccine. FluMist Quadrivalent [package insert]. Gaithersburg, MD: MedImmune Inc; 2012. Summary of solicited adverse reactions observed within 14 days after FluMist in Children 2-17 years FluMist Quadrivalent [package insert]. Gaithersburg, MD: MedImmune Inc; 2012. Summary of solicited adverse reactions observed within 14 days after FluMist in Adults 18-49 years FluMist Quadrivalent [package insert]. Gaithersburg, MD: MedImmune Inc; 2012. Administration Flumist®: 0.1-mL dose in each nostril Intranasal 34 Intranasal Administration Active inhalation (sniffing) by the patient is not required Which of the following patients is a candidate for the live influenza vaccine? 20% 1. 45 yo man with severe egg allergy 20% 2. 27 yo healthy woman 20% 3. 38 yo man with diabetes 20% 4. 54 yo healthy man 20% 5. 19 yo pregnant woman 37 New Influenza Vaccines: 2013-14 Flucelvax® (Novartis)– trivalent inactivated vaccine grown in mammalian cells rather than chicken embryo cells. FDA approved November, 2012 Adults 18 years and older Doesn’t list “severe allergic reaction to egg protein” in the contraindications Head-to-Head Comparison: Flucelvax vs. Placebo Barrett PN, et al. Lancet 2011;377:751-59 Flucelvax vs. Placebo Local & Systemic Adverse Reactions Flucelvax [package insert]. Cambridge, MA: Novartis Vaccines & Diagnostics Inc; 2012. Flucelvax Compared to Agriflu Local Adverse Reactions **Agriflu Flucelvax [package insert]. Cambridge, MA: Novartis Vaccines & Diagnostics Inc; 2012. Flucelvax Compared to Agriflu Systemic Adverse Reactions **Agriflu Administration Flucelvax®: 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 43 Which of the following influenza vaccines does not include “severe egg allergy” as a contraindication? 20% 1. Inactivated quadrivalent 20% 2. Live quadrivalent 20% 3. Inactivated trivalent intradermal 20% 4. Inactivated trivalent high dose 20% 5. Inactivated trivalent mammalian 45 New Influenza Vaccines: 2013-14 Flublock® (Protein Sciences Corporation)– trivalent inactivated vaccine grown in insect cells rather than chicken embryo cells. FDA approved November, 2013 Adults 18 through 49 years of age. Doesn’t list “severe allergic reaction to egg protein” in the contraindications Vaccine Efficacy against Culture-Confirmed Influenza in Healthy Adults 18-49 years Frequency of Local and Systemic Reactions within 7 days of Flublok or Placebo in Adults 18-49 years Administration Flucelvax®: 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 49 ACIP Recommendations for flu vaccination of person who report egg allergy. Select an influenza vaccine for a healthy 37year-old woman with severe egg allergy. 25% 1. Flublok 25% 2. Flumist 25% 3. Fluzone 25% 4. Fluarix 52 Methods: Multicenter, randomized, double-blind controlled study HD vaccine (60 mcg of hemagglutinin per strain): N=2,575 SD vaccine (15 mcg of hemagglutinin per strain): N=1,262 in adults 65 years of age and older. J Infect Dis. 2009;200(2):172-80 53 antibody titer level Comparison of responses to high-dose (HD) and standard-dose (SD) influenza vaccine 140 700 120 600 100 500 80 400 60 300 40 200 20 100 0 0 SD A/H1N1 B J Infect Dis. 2009;200(2):172-80 HD A/H3N2 54 Comparison of systemic side effects to HD and SD influenza vaccine 25 Percent 20 15 SD HD 10 5 0 Fever Headache Malaise J Infect Dis. 2009;200(2):172-80 Myalgia 55 Administration Fluzone HD®: 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 56 Intradermal Influenza Vaccine Indication Persons 18 through 64 years of age Contraindications Severe egg allergy 58 Intradermal vs Traditional IM needle Length 30 Gauge Needle and Less Volume Methods: Multicenter, randomized, double-blind controlled study ID vaccine (9 mcg of hemagglutinin per strain) N=1,803 IM vaccine (15 mcg of hemagglutinin per strain): N=452 in adults 18 to 60 years of age. Human Vaccines. 2010;6:346-54. Seroprotection Rate Comparison of responses to Intradermal (ID) and Intramuscular (IM) influenza vaccine 100 100 90 90 80 80 70 70 60 60 50 50 IM 15 mcg 40 40 ID 9 mcg 30 30 20 20 10 10 0 0 A/H1N1 B A/H3N2 Human Vaccines. 2010;6:346-54. 62 Comparison of systemic side effects to ID and IM influenza vaccine 35 30 Percent 25 20 IM 15 mcg 15 ID 9 mcg 10 5 0 Fever Headache Malaise Myalgia Human Vaccines. 2010;6:346-54. 63 Comparison of local side effects to ID and IM influenza vaccine 90 80 70 Percent 60 50 IM 15 mcg 40 ID 9 mcg 30 20 10 0 Erythema Swelling Induration Pain Human Vaccines. 2010;6:346-54. 64 Intradermal Injection Technique 1. Remove needle cap 2. Hold microinjection system between thumb and middle finger Do not place fingers on the windows 3. Insert needle rapidly perpendicular to the skin 4. Inject using the index finger 5. Remove needle from the skin and activate the needle shield by pushing firmly on the plunger Which side effect is more common with the intradermal influenza vaccine than the IM influenza vaccine? 0% 1. Injection site pain 0% 2. Headache 0% 3. Fever 0% 4. Injection site swelling 0% 5. Malaise Influenza Vaccines and Age Indications Vaccine Age Indications 6-23m 2-3y 3-17y 18-49y Inactivated Trivalent (Fluzone©, Afluria©, Fluvirin©) Inactivated Quadrivalent (Fluarix©, FluLaval©, Fluzone©) Inactivated Mammalian Trivalent (Flucelvax©) Recombinant Influeza Vaccine, Trivalent (FluBlok©) Live Quadrivalent (Flumist©) Intradermal Trivalent (Fluzone ID©) High Dose Trivalent (Fluzone HD©) Indicated for those meeting age requirements and without contraindications 50-64y 65+y Influenza Vaccine Indications Vaccine Indication Pregnant Severe Egg Allergy Patients with high risk medical conditions** Inactivated Trivalent (Fluzone©, Afluria©, Fluvirin©) Inactivated Quadrivalent (Fluarix©) Inactivated Mammalian & Recombinant Trivalent (FluBlok©, Flucelvax©) Live Quadrivalent (Flumist©) Intradermal Trivalent (Fluzone ID©) High Dose Trivalent (Fluzone HD©) Indicated for individuals meeting age requirements. contraindicated **Patients with high risk medical conditions: including immunocompromised, chronic cardiovascular disease, Diabetes Mellitus, pulmonary disease, or metabolic disease. Which of the following influenza vaccine(s) is/are appropriate for a healthy 16-year-old boy. 20% 1. Fluzone 20% 2. Fluzone ID 20% 3. Fluzone HD 20% 4. Flucelvax 20% 5. 1 and 2 Which of the following influenza vaccines is NOT indicated for a 72-year old woman? 25% 1. Inactivated trivalent IM vaccine 25% 2. Inactivated quadrivalent vaccine 25% 3. Inactivated high dose vaccine 25% 4. Inactivated trivalent intradermal vaccine A 35-year-old woman requests an annual flu shot. She has ulcerative colitis and is taking Prednisone 40 mg QD. Which flu vaccine(s) is/are appropriate? 14% 1. Influenza intradermal vaccine 14% 2. Influenza intramuscular vaccine 14% 3. Influenza high dose vaccine 14% 4. Flumist nasal spray 0.2 ml nasal 14% 5. Either 1 or 2 14% 6. Either 2 or 3 14% 7. Either 2 or 4 2014 ACIP Recommendations for Pneumococcal Vaccination in Adults Immunocompromised? no Age > 65? no Lung, liver, kidney, heart disease, diabetes, smoking, nursing home? yes yes Previously received Pneumovax? no Administer Pneumovax yes no Vaccine not recommended Administer Prevnar followed by Pneumovax 8 weeks later yes Administer Prevnar one or more years after last Pneumovax 2014 ACIP Recommendations on Revaccination with Pneumovax in Adults Age > 65? Renal disease, Immunocompromised? no yes Vaccine not recommended no yes no Previous Pneumovax > 5 years ago? no yes Vaccine not recommended Previous Pneumovax > 5 years ago and prior to age 65? Vaccine not recommended Administer Pneumovax yes Administer Pneumovax Administration Pneumovax® / Prevnar ® : 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 81 A 54-year-old man is immuno-compromised due to asplenia. No prior pneumonia vaccination. What pneumonia vaccine(s) is/are recommended? 25% 1. Pneumovax only 25% 2. Prevnar only 25% 3. Both; Pneumovax prior to Prevnar 25% 4. Both; Prevnar prior to Pneumovax A 67-year-old woman has a history of type 2 diabetes. No prior pneumonia vaccination. What pneumonia vaccine(s) is/are recommended? 25% 1. Pneumovax only 25% 2. Prevnar only 25% 3. Both; Pneumovax prior to Prevnar 25% 4. Both; Prevnar prior to Pneumovax Which of the following statements about the administration of influenza and pneumonia vaccines is true? 0% 1. Same day, opposite arm, separate syringe 0% 2. Same day, same arm, mixed in 1 syringe 0% 3. Must be separated by at least 7 days 0% 4. Must be separated by at least 4 weeks Which of the following vaccines is a live vaccine? 20% 1. Pneumovax 20% 2. Flumist 20% 3. Prevnar 20% 4. Fluarix 20% 5. Fluzone HD 88 89 Clinical Presentation of Herpes Zoster1–3 Herpes Zoster Rash Follows a Dermatomal Distribution © Phototake. © Phototake. © Dr. P. Marazzi / Photo Researchers, Inc. Prodrome Acute HZ Rash Evolution of Rash Complications? Abnormal Skin Sensations Headache Photophobia Malaise Unilateral Dermatomal Rash Maculopapules/Vesicles Altered Sensitivity to Touch Unbearable Itching Cessation of New Vesicles Pustulation Scabbing Cutaneous Healing Neurologic Cutaneous Ophthalmic Visceral (rare) Pain (varying severity) “Aching”, “burning”, “stabbing”, “shock-like” 1. Oxman MN. In: Arvin AM et al, eds. Varicella-Zoster Virus: Virology and Clinical Management. Cambridge, UK: Cambridge University Press; 2000:246–275. 2. Weaver BA. J Am Osteopath Assoc. 2007;107(suppl 1):S2–S7. 3. Harpaz R et al. MMWR Morb Mortal Wkly Rep. 2008;57(RR-5):1–30. Zoster Incidence by Age Group1 12 Number of Cases Rate per person-years 1,800 10 1,600 1,400 8 1,200 1,000 6 800 4 600 400 Rate per 1,000 Person-Years Number of Cases of Zoster (n = 9,152) 2,000 2 200 0 0 0-14 15-29 30-39 40-49 50-59 60-69 70-79 80+ Age 1. Insinga RP et al. J Gen Intern Med. 2005;20:748–753. 55 Zoster Vaccination Rates are Low1–3 50 % Vaccinated in (cumulative) Individuals Aged ≥60 Years 45 40 35 30 25 20 15 14% 7% 15.8% 10% 10 5 2008 2008 2009 2009 2010 2011 0 Year More than 99.5% of US adults ≥40 years of age have serologic evidence of previous infection of varicella zoster virus; therefore, all older adults are at risk of zoster infection4 1. Centers for Disease Control and Prevention (CDC). cdc.gov/vaccines/stats-surv/nhis/2009-nhis.htm. Accessed January 19, 2011. 2. Centers for Disease Control and Prevention (CDC). Morbid Mortal Wkly Rep. 2012;61(4):66–72. 3. Centers for Disease Control and Prevention (CDC). MMWR. 2013;62(4):61–76. 4. Harpaz R et al. Morbid Mortal Wkly Rep. 2008;57(RR-5):1–30. Zoster Vaccine Indication ACIP recommends routine vaccination of all persons aged >60 years with 1 dose of zoster vaccine. NEW FDA LABELING: “ZOSTAVAX is a live attenuated virus vaccine indicated for prevention of herpes zoster (shingles) in individuals 50 years of age and older.” Persons who report a previous episode of zoster and persons with chronic medical conditions can be vaccinated unless those conditions are contraindications or precautions. Zoster vaccination is not indicated to treat acute zoster. Zostavax® [package insert]. Whitehouse Station, NJ: Merck; April 2011. Recommendations of the Advisory Committee on Immunization Practices (ACIP) http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5705a1.htm?s_cid=rr5705a1_e 93 Vaccine Contraindications Allergy to neomycin or any vaccine component Pregnancy Immunocompromised status AIDS or other clinical manifestations of HIV, including persons with CD4+ T-lymphocyte values <200 per mm3 malignant neoplasms affecting the bone marrow chemotherapy or radiation within the last 3 months Persons on immunosuppressive therapy, including highdose corticosteroids (>20 mg/day of prednisone or equivalent) lasting two or more weeks 94 Efficacy of ZOSTAVAX® (Zoster Vaccine Live) on Incidence of Herpes Zoster in Adults Aged 60 Years Based on the results of the Shingles Prevention Study (SPS)a OVERALL LOWER INCIDENCE OF ZOSTERa RESULTS BY AGE GROUPS (YEARS) 60–69 in subjects 70–79 in subjects [95% CI: 28–52] 334 122 Placebo ZOSTAVAX (n=10,356) (n=10,370) Number of Zoster Cases [95% CI: 56–71] Number of Zoster Cases 18% 51% 80 in subjects [95% CI: –29–48; NS] 261 156 Placebo ZOSTAVAX (n=7,559) (n=7,621) 47 Placebo (n=1,332) 60 [95% CI: 44–58] Number of Zoster Cases in subjects 41% Number of Zoster Cases 64% 642 315 37 ZOSTAVAX (n=1,263) Placebo ZOSTAVAX (n=19,247) (n=19,254) CI=confidence interval; NS=not significant. aIn the Shingles Prevention Study, efficacy was evaluated in a placebo-controlled, double-blind clinical trial of ZOSTAVAX. 38,546 subjects 60 years of age or older were randomized to receive a single dose of either ZOSTAVAX (n=19,270) or placebo (n=19,276) and were monitored for the development of zoster for a median of 3.1 years (range, 31 days to 4.90 years). Efficacy of ZOSTAVAX® (Zoster Vaccine Live) on Incidence of PHN in Adults Aged 60 Years Who Developed Zoster Post-Vaccination Based on the results of the Shingles Prevention Study (SPS)a % of Zoster Cases With PHN 30 Placebo 39%b 20 ZOSTAVAX (95% CI: 7–59) 10 12.5 8.6 0 Number of PHN Cases Number of HZ Cases 80 642 27 315 Overall The benefit of ZOSTAVAX in the prevention of PHN can be primarily attributed to the effect of the vaccine on the prevention of herpes zoster. HZ=herpes zoster; PHN=postherpetic neuralgia. aPHN was defined as herpes zoster-associated pain rated as ≥3 on a 10-point scale and occurring or persisting at least 90 days after rash onset. Efficacy of ZOSTAVAX® (Zoster Vaccine Live) on Incidence of Herpes Zoster in Adults Aged 50–59 Years Based on the results of the ZOSTAVAX Efficacy and Safety Trial (ZEST)1,a Number of Zoster Cases 70% in subjects 50–59 [95% CI: 54–81] 99 30 Placebo (n=11,228) aStudy Design ZOSTAVAX (n=11,211) for ZEST: In the ZOSTAVAX Efficacy and Safety Trial, efficacy was evaluated in a placebocontrolled, double-blind study of ZOSTAVAX. 22,439 subjects 50 to 59 years of age were randomized to receive a single dose of either ZOSTAVAX (n=11,211) or placebo (n=11,228) and were monitored for the occurrence of shingles for a median of 1.3 years postvaccination (range, 0 to 2 years). 1. Schmader KE et al. Clin Infect Dis. 2012;54:922–928. Storage and Handling zoster vaccine must be stored frozen The vaccine must be discarded if not used within 30 minutes after reconstitution. New labeling: Zostavax may be stored and/or transported at fridge temp for up to 72 hours prior to reconstitution. Any unused vaccine at fridge temp should be discarded. Zostavax® [package insert]. Whitehouse Station, NJ: Merck; April 2011. 98 Administration Zostavax: 0.65-mL dose (reconstituted) SQ – upper, outer tricep 5/8 inch, 25 gauge needle 100 Which of the following statements about the administration of influenza and zoster vaccines is true? 0% 1. Same day, opposite arm, separate syringe. 0% 2. Same day, same arm, mixed in 1 syringe. 0% 3. Must be separated by at least 7 days. 0% 4. Must be separated by at least 4 weeks. RR is a 70-year-old woman with COPD. She has no allergies. Her meds include albuterol, Pulmicort and Spiriva. She has an 80-pack-year history of smoking. She quit smoking 5 years ago. Her last pneumonia shot was 8 years ago. Which vaccine(s) is/are appropriate for her? 11% 1. Pneumovax 0.5 ml IM 11% 2. Influenza SD shot 0.25 ml IM 11% 3. Influenza HD shot 0.5 ml IM 11% 4. Flumist nasal spray 0.1 ml in each nostril 11% 5. Zostavax 0.65 ml SQ 11% 6. Both 1 and 2 11% 7. 1, 2 and 5 11% 8. 1, 3 and 5 11% 9. 1, 4 and 5 Pathogen (Common name) Table Pathogen Tetanus (lockjaw) Diphtheria Pertussis (whooping cough) Classification Gram + Bacteriatoxin Gram + Bacteriatoxin Gram – Bacteria Transmission Wound Complication Respiratory failure Respiratory Myocarditis/Neuritis Respiratory Pneumonia Comparison of 20th Century and current US Morbidity of VPDs Diseases 20th Century 2010 Reported Annual Morbidity Cases Percent Decrease Smallpox 29,005 0 100% Polio (paralytic) 16,316 0 100% Measles 530,217 61 >99% Mumps 162,344 2,528 98% Pertussis 200,752 21,291 89% Diphtheria 21,053 0 100% Rubella 47,745 6 >99% Congenital Rubella Syndrome 152 0 100% Tetanus 580 8 99% 20,000 270 99% Haemophilus influenzae New FDA Approval – July 8, 2011 US FDA has expanded the age indication for Boostrix® vaccine to prevent tetanus, diphtheria, and pertussis (whooping cough) to people ages 65 and older. Boostrix® is the first vaccine approved to prevent all three diseases in people 65 and older. Adacel® is approved for persons 11 through 64 years. Boostrix® [package insert]. Rixensart, Belgium: GlaxoSmithKline; July 2011. Adacel® [package insert]. Swiftwater, PA: Sanofi Pasteur Inc.; February 2012. Tetanus, diphtheria, and pertussis (Td/Tdap) Vaccination Administer a one-time dose of Tdap to adults younger than age 65 years who have not received Tdap previously or for whom vaccine status is unknown to replace one of the 10-year Td boosters. Tdap is specifically recommended for the following persons: pregnant women more than 20 weeks’ gestation, adults, regardless of age, who are close contacts of infants younger than age 12 months (e.g., parents, grandparents, or child care providers), and health-care personnel. Tdap can be administered regardless of interval since the most recent tetanus or diphtheria containing vaccine. Pregnant women not vaccinated during pregnancy should receive Tdap immediately postpartum. Adults 65 years and older may receive Tdap. Administration Boostrix®/Adacel®: 0.5-mL dose IM - deltoid 1 inch, 25 gauge needle 108 AB is a 52-year-old woman with hypertension. She has no allergies. Her meds include amlodipine 10 mg PO QD. She smokes 1 PPD. Her newborn grandson lives with her. Which vaccine(s) is/are appropriate for her? 11% 1. Pneumovax 0.5 ml IM 11% 2. Influenza SD shot 0.5 ml IM 11% 3. Influenza HD shot 0.5 ml IM 11% 4. Flumist nasal spray 0.1 ml in each nostril 11% 5. Zostavax 0.65 ml SQ 11% 6. Tdap 0.5 ml IM 11% 7. 1, 2 and 5 11% 8. 1, 3 and 5 11% 9. 1, 2, 5 and 6 Pathogen (Common name) Table Pathogen Classification Transmission Complication Influenza (flu) virus Respiratory Pneumonia Pneumococcus Gram + Bacteria Respiratory Meningitis/Bacteremia Varicella (chicken pox) virus Respiratory Bacterial infection Zoster (shingles) virus Latent varicella Neuralgia HPV (genital warts) virus Sexual contact Cervical cancer Meningococcus Gram - Bacteria Respiratory Invasive disease Tetanus (lockjaw) Gram + Bacteria-toxin wound Respiratory failure Diphtheria Gram + Bacteria-toxin Respiratory Myocarditis/Neuritis Pertussis (whooping cough) Gram - Bacteria Respiratory Pneumonia Measles virus Respiratory Diarrhea, pneumonia Mumps virus Respiratory Meningitis Rubella virus Respiratory Arthritis Hepatitis A virus Fecal-oral Acute/chronic hepatitis Hepatitis B virus Blood-serous fluids Acute hepatitis Adult Vaccine Table Vaccine Vaccine Type Route / Reconstitute Series Storage Influenza IIV Inactivated IM / No 1x annually Fridge Flumist Live Intranasal / No 1x annually Fridge Pneumovax Inactivated IM or SQ / No 1-2 doses Fridge Zostavax Live SQ / Yes 1 dose Freezer Gardasil (HPV4) Cervarix (HPV2) Inactivated IM / No 3 doses Fridge Td Inactivated IM / No 1 q 10 years Fridge Tdap Inactivated IM / No 1x, then Td Fridge Varivax Live SQ / Yes 2 doses Freezer MMR Live SQ / Yes 1-2 doses Fridge or Freezer Menactra, Menveo Menomune (MPSV4) Inactivated IM / No 1-2+ doses Fridge Havrix, Vaqta Inactivated IM / No 2 doses Fridge Recombivax-HB Engerix-B Inactivated IM / No 3 doses Fridge