influenza update 2009 100109
TRANSCRIPT
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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