influenza update 2009 100109

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    Influenza Update 2009

    Tim Gieseke MD, CMD

    Assistant Clinical Professor, UCSF

    Multi-facility Medical Director

    Associate Medical Director, Sutter VNA Hospice

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    Objectives

    H1N1 2009 update

    LTC Outbreak

    Manifestations & Diagnosis Management

    Immunization Programs

    Patient Education

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    H1N1 2009 Pandemic Declared

    June 11, 2009

    New Influenza A outbreak in Mexico lateMarch 2009

    First identified in a Wisconsin, 17 y/o teenager

    in 2005 Combination of parts of known Flu viruses

    from: Human, Avian, and 2 Swine strains.

    > 65 y/o - less impacted then expected

    1/3 of > 60 y/o may be partially immuneAs of July 24, 2009, only 4% of hospitalized

    cases were in > 65 y/o

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    Disaster Preparedness Indicated

    Previous Pandemics had initial Spring minor outbreak& then major Winter outbreak.

    In Sonoma County as of 9/30/09: 60 hospitalizations (Pneumonia & Dehydration)

    9 deaths 3 HCW hospitalized

    8 pregnant women hospitalized

    In the USA as of 9/3/09: ~ 9,000 Hospitalizations

    ~ 600 Deaths

    If 33% attack rate this winter in Sonoma County: ~ 1,470 Hospitalizations

    ~ 355 deaths

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    High Risk Groups, to Date

    Pregnant women 4X > risk of hospitalization

    Spontaneous abortion

    Pre-term delivery

    Obese 2X > risk of hospitalization

    Increased mortality

    Middle Aged Increased mortality mainly because more susceptible to

    getting the flu than > 60 y/o

    Young Children (2-9 y/o) 2X more susceptible then older ages

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    Presentation

    Influenza like illness (IFL): abrupt onset Temp > 100 or 37.8

    Cough &/or sore Throat

    Absence of alternative cause

    Other common symptoms: Malaise

    Headaches, Nasal & sinus congestion

    Myalgias & arthralgias

    Elderly & Children may lack fever H1N1 Distinctive

    Nausea & vomiting with dehydration (25-30%)

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    Case Definition by CPDH for H1N1

    2009

    Highly Suspected Case

    ILI with lab confirmed influenza A by real-

    time RT-PCR

    All + specimens have been H1N1

    Viral culture sub-typing will only be done for

    Fatalities

    ICU Cases Index case (s) in HCW (Health Care Worker)

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    Lab Testing for H1N1

    Rapid Antigen tests have not been reliable

    PHD does real-time RT-RCP testing whichidentifies Influenza A.

    CPDH requires SNFs to report to countysuspected H1N1 cases Reporting form available on www.calpan.org.

    Direct health care workers (HWCs) with IFL

    illnesses should be tested. Most outpatients with IFL do not need to be

    tested.

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    Outbreak of Seasonal Flu Jan 2008

    85 y/o with intermediate stage AlzheimerDementia, HBP, Osteoporosis &Diastolic CHF

    Sudden onset of lethargy, weakness,cough, low grade fevers, the prior day &had spent the past day in bed

    Worse then usual confusion, shortattention span, & reversion to nativeGerman language.

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    Assessment

    PE 126/80 80 36.7 22 94% on RA

    Weak, delirious, but neg. HEENT, Neck, Chest,Cardiac, Abd., Extr., and Skin Exams

    Lab: WBC 7.2 Hct 37.4 UA: neg. CXR: neg.

    Dx: Possible Influenza, Pertussis, RSV, SARS (Corona

    Virus) Other viruses

    Pneumonia (D. Pneumo, or Aspiration)

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    Outbreak Management

    4th IFL illness in facility

    Outbreak declared and PHD notified

    Oseltamivir (Tamiflu) prescribed

    Respiratory Viral Culture of Nose and Naso-pharynx sent to PHD.

    Facility Quarantined Canceled: admissions, visitors, activities programs

    Residents encouraged to stay in their rooms Meals in rooms on paper plates, etc.

    Same staffing for each station (Cohorting)

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    Management

    Isolation Measures:

    Staff wore masks, gowns, gloves

    Infected patients wore masks

    Spray and Splatter control measures.

    30 sec hand washing( Happy Birthday twice), &/or

    Alcohol hand cleansers.

    Other measures:

    New cases promptly given Tamiflu

    Attending physicians notified by faxed letter of

    suspected outbreak.

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    Whats Changed for H1N1 2009?

    Use of goggles if suctioning or delivering Nebulizer Tx.

    Use of N 95 masks for all HCWs with direct contactwith known N1H1 cases. May be reused until wet.

    Store in brown bag Are effective in preventing Flu, whereas regular surgical

    masks are not effective

    If N1H1 cases must leave their room, they must: wear reg. mask, wash hands, & give 6 ft. spacing from

    others, if possible

    Housekeeping protocols to daily (?) cleanse infectedrooms, bathrooms, & door knobs. Use 1:10 diluted bleach & designated stethoscopes.

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    Other Changes?

    Aerosol Precautions sign on door.

    All HCWs hospitalized today had some non-compliance with PPE procedures.

    Mandatory hand cleansing prior & immediately aftereach patient physical contact. Patients taught to expect it.

    Easy access to Kleenex, Disposable hand towels, &sinks / or Alcohol gels. Quick disposal of kleenix.

    Cough or Sneeze into Sleeves or Kleenex,no

    t hands. Visitors must use Alcohol Hand Cleanser or Hand

    washing on arrival in facility. Education on importance of following hand cleansing protocol.

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    Other Changes?

    No sick employees or visitors permitted infacility.

    Encourage families to call, rather then visit aresident with IFL illness.

    Quarantine H1N1 case & facility until 7 dayspost onset of of last case, Unless still still sick, then continue until 24 hrs

    asymptomatic.

    Direct contact HCWs should keep finger nailswell trimmed Forbid use artificial nails.

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    Chemo-Prophylaxis for H1N1 2009

    Because of concern about the potential fordeveloping resistance, Chemo-prophylaxisshould be rare, with most use reserved for

    those who have become sick enough to behospitalized:

    Exceptions: Congregate living facility for frail persons (eg. SNF),

    with an outbreak in facility.

    Household case, with a child < 6 mo/o.

    Exposed person with at risk co-morbid conditions, Start at the first onset of illness symptoms.

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    Typing of Influenza

    H (Hemaglutinin) Antigen

    A surface glycoprotein

    Binds to sialic acid residues on the respiratory

    epithelium Permits penetration of these cells

    N (Neuraminidase) Antigen

    Cleaves intracellular viral progeny so they can be

    released. Reduces entrapment of the virus in the respiratory

    secretions

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    High mutation rate of H & N

    antigens

    Antigenic Drifts Minor changes that produce local outbreaks annually

    Antigenic Shifts Are associated with Pandemics

    Occur about every 10-30 years

    Last pandemic in 1977

    Influenza A in humans 3 major subtypes (H1, H2, H3)

    Only 2 N subtypes (N1, N2)

    Influenza B Much less propensity for antigenic change

    Only drifts in H have been described

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    Characteristics ofOutbreaks

    Almost exclusively in the Winter time in the Northernand Southern Hemispheres Occurs year around in the tropics

    Influenza A may occur throughout the year

    Attack rates: 10-20% of population in an outbreak

    ~ 25-50% in a pandemic

    Time Course ofOutbreaks: Abrupt onset with multiple cases

    Peak incidence by 2-3 weeks

    Duration usually 4-8 weeks First indicator usually IFL illness in Children with high

    absenteeism from school.

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    Morbidity & Mortality of Seasonal

    Flu

    20-50 K excess deaths annually in USA

    Disproportionately effects the elderly (> 64 y/o)and the young (< 5 y/o)

    20% increased rate of pneumoniahospitalizations in the winter secondary to Flu.

    50% higher mortality for pneumonia occurringin the winter months.

    Risk of Pneumonia greatest in the Elderly with: Diabetes, Chronic Pulmonary, Dysphagia, immuno-

    compromised or Cardiac diseases.

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    Morbidity & Mortality

    During Flu season, >

    hospitalization rates for acute cardiopulmonary

    events

    Mortality

    Mortality in Pandemics

    Illness Severity index:

    10X > for 1918 strain, then H1N1 2009

    20-50 million deaths worldwide in 1918

    ~ 50% of deaths occur in low risk groups, since:

    more susceptible with high dIsease prevalence

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    Usual Illness Clinical Course

    Contagious from:

    1 day prior to illness onset

    Until 24 hrs afebrile Incubation Time: 1-4 days

    Viral Shedding (?): < 7 days

    Duration of illness: 2-5 days Post Influenza Asthenia: 1-6 weeks

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    Transmission

    Viral replication only occurs in the respiratorytract

    Transmitted by droplet and aerosolized:

    Coughing Sneezing Talking Survives on surfaces for hours

    Viral shedding: Peaks at 24-48 hrs

    Rapidly becomes negligible by day 6 May still shed in the Elderly, High risk patients, or

    Children for up to 5 weeks

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    Complications

    Pneumonia is most common complication High Risk patients have greatest risk

    Primary Pneumonia may be diffuse and

    severe (ARDS) Secondary Bacterial Pneumonia

    25% of all Influenza deaths Strep Pneumonia in 48%

    Staph (19%, MRSA)

    Suspect when exacerbation of fever & resp.symptoms occur days after initial clinicalimprovement.

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    Complications

    Dehydration

    Myositis predominantly in children

    CNS

    Encephalitis, Aseptic meningitis, Reyes Syndrome

    Transverse myelitis

    Guillian-Barre syndrome

    Other Myocarditis & pericarditis

    MI & Strokes

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    Diagnosis

    In SNF Outbreaks, cultures of nose and nasal-pharynxfor virus to PHD Real-time RT-PCR

    Culture takes 48-72 hrs, but report may take 1 wk.

    In outbreaks, IFL illness highly predictive of Flu

    For usual seasonal outbreak, rapid diagnostic tests Quick-vue A & B test (Clia waiver)

    ~ 75% sensitivity

    Many other similar test kits

    Rapid: 15-30 min.

    Not recommended this year, since not reliable for H1N12009

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    Mode of Spread

    Cough and Spray of large droplets Aerosolizes up to 3-4 feet

    Keep > 6 foot away from other residents &

    roommate (s). Consider chemo-prophylaxis for roommates.

    Virus may survive on surfaces for hours

    Hands spread it to eyes, nose, and mouth &may precipitate illness. Discourage this habit.

    Clean surfaces with 1/10 diluted bleach.

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    Treatment (Supportive measures)

    Isolation measures Spray & Splatter Control

    Fever & pain control (Tylenol or Advil) Avoid Aspirin to reduce risk Reyes Syndrome & GI Bleed.

    Pulmonary supportive measures O2, O2 Sats, Suction, HOB elevation > 15 degrees

    Dysphagia measures Diet consistency appropriate?

    Swallow therapy Evaluation

    Fall risk & Delirium management Hydration measures considerIV fluids

    Acute hospitalization? (Advanced Directives, POLST)

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    Neuraminidase Inhibitors

    Work by reducing rate of Viral Shedding

    from Respiratory cells

    Most effective when given within 30 hrsof symptom onset or for prophylaxsis.

    Reduce duration of illness by 2-3 days

    Reduce severity of illness &

    hospitalization rate

    Effective for H1N1 2009

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    Neuraminidase Inhibitors

    Side Effects Oseltamivir (Tamiflu)

    Nausea (rarely vomiting), but is rarely severe enough tostop it

    Zanamivir (Relenza) has been associated with Broncho-spasm

    Decline in respiratory function in patients with Asthma

    Contraindicated in Asthmatics

    Acute Illness Dosing Oseltamivir: 75 mg bid X 5 days

    Zanamivir: 10 mg (2 puffbid) X 5 days

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    Chemo-Prophylaxis in 2009

    Zanamivir (Relenza) Household contacts: 10 mg daily X 10 days

    Only if < 6 mo/o or severe immuno-compromised person

    SNF Community Outbreak: Start within 48 hrs of identified outbreak Continue until 7 days post onset of last case in facility.

    Oseltamivir (Tamiflu) 75 mg daily X 10 days or 7 days post last case.

    Renal Dosing required forOseltamivir Cr.Cl. 30-60: 75 mg daily X 5 days for acute illness

    Cr.Cl. < 30 not defined ask SC PHD

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    Seasonal Flu Vaccines

    Development

    Based on Worldwide Flu surveillance by theCDC and the WHO

    Vaccine chosen to cover the 3 most prevalentstrains anticipated for the coming season Targets are H & N proteins

    Future targets of more conserved viral proteins likeMatrix Protein 2 & the Intersubunit of Hemaglutinin

    Production starts about in Jan or Feb withdelivery of manufactured vaccine in lateSeptember

    Similar manufacturing process for H1N1 2009

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    2009-2010 Seasonal Flu Vaccine for

    Northern Hemisphere

    4 Manufacturers of Inactivated vaccine

    Only 1 manufacturer of the live

    attenuated vaccine Contains following virus strains:

    A/Brisbane/59/2007-like virus (H1N1)

    A/Brisbane/10/2007-like virus (H3N2)

    B/Brisbane/60/2008(only change this yr)

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    Vaccine Types same for Seasonal

    and H1N1 2009

    TIV (Trivalent Inactivated Vaccine) Dead can not cause influenza

    IM route only

    Whole virus form not available in USA Split virus ( subvirion components) fewer adverse

    reactions in children The only TIV available in USA

    Only vaccine for < 2 y/o & > 50 y/o

    Side effects Soreness at injection site

    Myalgias and sl. fever ~ 12-36 hr < 5% of vaccinated

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    FluMist = LAIV (Live Attenuated

    Vaccine) - Intranasal

    Approved for 2-49 y/o who do not have Asthma

    HCW may receive it if: not taking care of severely immuno-compromised patients

    Stored 2-8 degrees C and thawed just prior to use

    Less protective then TIV in 2007-2008 season.

    Side Effects: Runny nose, nasal congestion, HA, and sore throat < 12-36 hr

    No anaphylaxis, GB Syndrome, Asthma or Bells palsy yet

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    Efficacy of Seasonal Vaccine

    Greatest in < 65 y/o

    ~ 80% protected if good vaccine match

    ~ 60% poor

    Protective Vaccine levels > 4 mo. aftervaccination in most Seniors

    Probably reduces mortality in frail Seniors

    especially in Seniors annually vaccinated

    TIV safe in all phases of Pregnancy

    Pregnancy is a high risk state for Mom / baby

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    Vaccination & Herd Effect

    If most of population vaccinated, the risk of an

    outbreak is much less.

    When elementary students vaccinated,

    Household adults had less missed work that winter.

    When Acute Hospital HCWs vaccinated (51%

    vs. 5%)

    Acute Hospital Mortality was reduced significantly

    (13.6 vs. 22.4%) over the next 6 months.

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    Seasonal Vaccine Indicated for:

    > 50 y/o (29% with one or more high risk conditions)

    < 5 y/o (increased morbidity)

    SNF Direct HCWs

    Women pregnant during influenza season Adults with serious co-morbid chronic illnesses:

    Chronic Pulm dz, CV dz, CRD, Liver dz, D.M., Asplenia,Immunosuppression, CNS disorders (Seizures, Dementia,Neuromuscular disorders with dysphagia)

    Consider forspouses and all visitors to SNFs

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    Who shouldnt have it?

    Acute illness more then trivial URI or medicallyunstable

    Serious Allergies to eggs Grown on egg medium

    Egg intolerance is not a contraindication

    New vaccine grown on insect media in development

    Allergy to preservative Thimersol Commonly used Mercury preservative in eye drops

    Omitted in vaccine given to < 3 y/o and pregnant women

    Previous Guillian-Barre syndrome

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    2009 Vaccine Recommendations

    Give usual Trivalent seasonal vaccine as soon asavailable this September. TIV may given simultaneously with H1N1, but not LAV.

    Give H1N1 2009 vaccine (TIV or LAIV forms) when it

    becomes available in Mid-October per CDC guidelines A.California/07/2009 mono-valent vaccine

    Not initially available for SNF residents.

    Initially give 1 dose for > 10 y/o, & 2nd dose 4 weeks later if