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HomeMy WebLinkAboutinfluenza-and-pertussis-pediatric-moldonado-01242018-archivePrevention and Treatment of Pertussis and Influenza Yvonne (Bonnie) Maldonado, MD, FAAP Professor of Pediatrics and of Health Research and Policy Chief, Division of Pediatric Infectious Diseases Stanford University School of Medicine 2 The problem with influenza Failure to vaccinate Variable circulating strains impact on vaccine performance Variable populations at risk each season 4 "Influenza has been around for a long time, and is remarkable both for the rapidity of its spread, the brevity of the immunity it confers, and the instability of the virus that causes the disease.” William McNeill Plagues and Peoples 1977 5 Influenza was a key factor in the ultimate defeat of the German army. Historical perspective Four out of five American casualties in WWI were attributable to influenza. 6 Influenza Key Points •Yearly epidemics •Marked seasonality •Emerging/re-emerging pathogen •Pandemics secondary to antigenic shift (genetic reassortment) •Characteristic (and uncharacteristic) age distributions 7 RNA Hemagglutinin Neuraminidase Antibodies Sialic acid Antigenic Drift 8 Antigenic Shift 9 and Epidemics Introduction of hypothetical A HxNx virus Significant minor variation A HxNx may occur at any of these points. Epidemics may or may not beassociated with such variations Introduction of hypothetical A HyNy major (new subtype) variant A HxNx disappears Di s e a s e I n c i d e n c e Me a n P o p u l a t i o n A n t i b o d y L e v e l Pandemic EpidemicEpidemic Pandemic Interpandemic Period Epidemic Time in Years 1 2 3 4 5 6 7 8 9 10 11 12 Incidence of clinically manifest influenza Mean level of population antibody vs A HxNx Mean level of population antibody vs A HyNy 10 11 12 13 14 How Does Influenza Spread? Droplet (e.g. coughing, sneezing, speaking) Contact (touching a contaminated surface) 15 To Prevent Spreading of Flu Droplet (e.g. coughing, sneezing, speaking) ALWAYS: Good Personal Hygiene- habits via a)covering of mouth when coughing or sneezing b)Washing or cleaning hands with soap or alcohol based gel CLINCIAL SETTING: Appropriate Screening and Isolation Personal Protective Equipments/PPE a)Masks -for those who are well b)Gowns -for those who are well c)Protective goggles or faceshields d)Gloves 16 17 18 National Early-Season Flu Vaccination Coverage, United States, November 2017 19 National Early-Season Flu Vaccination Coverage, United States, November 2017 •~2 of of every 5 children and adults in the United States had received an influenza (flu) vaccination by early November 2017: –38.6% of all persons 6 months and older –38.8% of children 6 months through 17 years –38.5% of adults 18 years and older •Early 2017–18 flu season vaccination coverage was similar to coverage at the same time last flu season for children, adults, and all persons 6 months and older •Among children, flu vaccination coverage was similar across all racial/ethnic groups with one exception—non-Hispanic children of other or multiple races had higher flu vaccination coverage than non-Hispanic black children. •Among adults, flu vaccination coverage among adults 18-49 years decreased by 3.7 percentage points compared with the same time last season. •Flu vaccination coverage among Hispanic adults decreased by 7.7 percentage points compared with the same time last season. •Among adults, non-Hispanic persons of other or multiple races had higher flu vaccination coverage this early season than non-Hispanic whites, non-Hispanic blacks, and Hispanics. •Among both adults and children, the most common places reported for receiving flu vaccination were medical locations (children: 86.5%, adults: 49.2%). Retail settings (28.2%) and workplaces (17.0%) were other important venues for adults. 20 21 22 The problem with pertussis Failure to vaccinate Adverse events following vaccination Acellular vaccine performance Prevention of neonatal pertussis 24 Resurgence of Epidemic Pertussis •Pertussis outbreaks will continue to occur because neither infection nor immunization produce lifelong immunity •Pertussis increases gradually began in 1982 and have continued since then •Initially, increases were likely to increased physician awareness and diagnosis •More recently, it is clear that DTaP vaccines are less potent that the DTP vaccines •There is also evidence of waning vaccine-induced immunity 25 Pertussis Background •Pertussis is the most poorly controlled vaccine-preventable disease –Incidence increasing since the 1990s –Cyclical: peaks every 2-5 years as numbers of susceptible people increase enough to allow sustained transmission; last prior peak year 2005 with 25,616 U.S. cases, a 45 year high •Adults are vulnerable to pertussis –27% of reported cases in 2004 were among adults –Pertussis immunity is not lifelong and wanes 4-12 years after the DTaP series and 4-20 years after natural infection* –~20% of cough illness lasting >2 weeks is pertussis •First pertussis vaccines (Tdap)†for adolescents and adults licensed in 2005, but uptake suboptimal –in 2008, ~40% of adolescents and ~6% of adults were estimated to have ever received Tdap *Wendleboe et al. Infect Dis J 2005;24 (Suppl 5):S58-61. 26 Pertussis Background, continued •Bordetella pertussis bacteria are inhaled and attach to cilia of respiratory epithelium where they attach to the cilia* •In a study of fatal cases,B. pertussis was frequently isolated from alveoli and less commonly from the trachea or bronchi* •Pertussis toxin exerts its biological effects on systemic sites via the bloodstream •HIGHLY contagious: basic reproduction number (Ro) estimate is 12-17 (similar to measles and in contrast with influenza, which has an Ro of 1-2); approximately 90% of susceptible household contacts become infected •MINIMUM PROPORTION of population that must be immune to eliminate transmission estimated to be 92-95%; achieving this level of population immunity will difficult without a vaccine that confers lifelong immunity * Weiss and Hewlett. Ann Rev Microbiol. 1986;40:661-86 27 Age-Group 1980-19891 1990-19991 2000-20102 0-1 month 38 68 170 2-3 month 11 16 28 4-5 month 5 5 2 6-11 month 7 4 1 1-4 years 13 2 3 5-10 years 1 6 3 11-18 years 0 0 3 >18 years 1 2 11 Total 77±103 221 1 Vitek CR, et al. Pediatr Infect Dis J 2003; 22(7):628-34. 2 National Notifiable Diseases Surveillance System, CDC, *Provisional 2010 data ±Includes one case with unknown age Reported Pertussis-related Deaths by Age Groups, US, 1980-2010* 28 Source of Pertussis Transmission to Infants •Household members responsible for 75%–83% •Parents and siblings were common sources –Parents (55%) –Siblings (16%-20%) –Aunts/uncles (10%) –Friends/cousins/others (10%-24%) –Grandparents (6%) –Caretakers (2%) Wendelboe AM., et al. Transmission of Bordetella pertussis to Young Infants. Pediatr Infect Dis J 2007;26: 293–299 Bisgard KM, Pascual FB, Ehresmann KR, Miller CA, Cianfrini C, Jennings CE et al. Infant pertussis: who was the source? Pediatr Infect Dis J 2004; 23(11):985-989. 29 CDC DTaP and Tdap Recommendations •DTaP for those younger than 7 years of age, and Tdap or Td for those 7 years or older across the lifespan •Infants and children should receive 5 doses of DTaP, usually administered at 2, 4, and 6 months, 15 through 18 months, and 4 through 6 years of age. DT can be used for infants and children who should not receive acellular pertussis- containing vaccines. •Adolescents should receive a single dose of Tdap, preferably at 11 to 12 years of age. •Pregnant women should receive a single dose of Tdap during every pregnancy, preferably at 27 through 36 weeks gestation. Tdap is recommended only in the immediate postpartum period before discharge from the hospital or birthing center for new mothers who have never received Tdap before or whose vaccination status is unknown. •Adults should receive a single dose of Td every 10 years. For adults who did not receive Tdap as an adolescent, a dose of Tdap can replace one of the 10-year Td booster doses. 30 Tetanus, Diphtheria, and Pertussis (Tdap) Vaccines •There are two Tdap vaccines used in the United States: Adacel® and Boostrix®. •Each 0.5-mL dose of Adacel® (Sanofi Pasteur) contains 5 Lf tetanus toxoid, 2 Lf diphtheria toxoid, and acellular pertussis antigens (2.5 µg detoxified PT, 5 µg FHA, 3 µg pertactin, 5 µg FIM). Other ingredients per 0.5-mL dose include 1.5 mg aluminum phosphate (0.33 mg aluminum) as the adjuvant, ≤5 µg residual formaldehyde, <50 ng residual glutaraldehyde, and 3.3 mg (0.6% v/v) 2- phenoxyethanol (not as a preservative). •Each 0.5-mL dose of Boostrix® (GlaxoSmithKline) is formulated to contain 5 Lf of tetanus toxoid, 2.5 Lf of diphtheria toxoid, 8 µg of inactivated PT, 8 µg of FHA, and 2.5 µg of pertactin (69 kiloDalton outer membrane protein). Each 0.5-mL dose contains aluminum hydroxide as adjuvant (not more than 0.39 mg aluminum by assay), 4.5 mg of sodium chloride, ≤100 µg of residual formaldehyde, and ≤100 µg of polysorbate 80 (Tween 80). 31 Pertussis Surveillance •Pertussis is nationally-notifiable and clinicians should notify the appropriate health department of all patients with suspected pertussis. •Diagnostic laboratories should notify health departments of all positive pertussis laboratory results and state health departments then report confirmed and probable pertussis cases to CDC through the National Notifiable Diseases Surveillance System (NNDSS). •Although many pertussis cases are not diagnosed and therefore not reported, the surveillance system is useful for monitoring epidemiologic trends. 32 33 34 DTP DTaP Tdap 35 Pertussis immunization landmarks •1948 DTP becomes commercially available •1980’s DTP required for school entry •1993 DTP reformulated as DTaP (attenuated pertussis) to reduce adverse events –Reformulation is less immunogenic and immunity wanes more readily •2005 Tdap recommended for adolescents and adults •2015 Tdap recommended for pregnant women in third trimester to prevent deaths in infancy 36 Whole-cell pertussis vaccine Adverse events HHE, hypotonic, hyporepsonsive episodes Olin P, Rasmussen F, Gustasffson L, et al. Randomized controlled trial of two-component, three-component and five-component acellular pertussis vaccines compared to whole-cell pertussis vaccine. Lancet 1997; 350:1569-77. Cody CL, Baraff LJ, Cherry JD, Marcy SM, Manclark CR. Pediatrics 1981; 68:650-60. 37 Annual rate of pertussis and pertussis vaccine type received during the first 2 years of life in the entire KPNC population from January 2010 to December 2011, by birth year Klein NP, BartlettJ, Fireman B, Rowhani-Rahbar A, Baxter R. Comparative effectiveness of acellular versus whole-cell pertussis vaccines in teenagers. Pediatrics 2013; 131:e1716-22. ©2013 by American Academy of Pediatrics 38 What you can do to manage a suspected or confirmed Infectious Disease Outbreak Goals: Identify and eliminate the source of infection For example, separate waiting room area for coughing children Prevent additional cases Screening questions regarding symptoms at the front desk Ongoing surveillance and communication essential to confirm cessation of outbreak Track disease trends and advice through AAP, CDC, local county public health officials, local disease experts 39 Managing a suspected or confirmed Infectious Disease Outbreak General Principles: Establish a plan for evaluating suspected or confirmed infectious disease outbreaks in your office setting Prompt and consistent ongoing evaluation so that transmission to healthcare workers, patients and visitors is prevented or minimized The source(s) and route(s) of exposure must be determined To understand why an outbreak occurred How to prevent similar outbreaks in the future Treat exposed individuals Prevent others from being exposed to the source(s) of infection. 40 What the Public Health System Will Do: 1)Establish case definition(s) 2)Confirm that cases represent true infections 3)Establish the background rate of disease 4)Find cases, decide if there is an outbreak, define scope of the outbreak 5)Examine the descriptive epidemiologic features of the cases 6)Generate and test hypotheses 7)Collect and test environmental samples if appropriate 8)Assist providers and others in implementation of infection control measures in accordance with CDC, State or local public health recommendations 9)Communicate with other organizations or individuals as necessary 10)Report when outbreak has been contained 41 What the Public Health System Will Do: Determine whether the control measures are effective. 1.No new cases have occurred after the control measures were implemented. The time period for new cases will vary depending on the nature of the infection but will likely be days to weeks 2. Continue to conduct ongoing prospective surveillance to ensure the outbreak has been terminated. 3. Notify providers and public health agencies at various levels that the outbreak has terminated 42 •NNII (www.immunizationinfo.org) •VEC (www.vaccine.chop.edu) •IAC (www.immunize.org) •CDC/NIP (www.cdc.gov/nip) •AAP (www.aap.org) •AAFP (www.aafp.org/) •IVS (www.vaccinesafety.edu) •Vaccine Page (www.vaccines.org) •Every Child by Two (www.ecbt.org) •PKIDS (www.pkids.org/) References/Resources http://www.cdc.gov/vaccines/acip/meetings/slides-2014-06.html http://www.cdc.gov/measles/travelers.html Questions? Thank you