H1N1 Diagnosis, Management and Treatment
H1N1 Diagnosis, Management and Treatment
H1N1 Diagnosis, Management and Treatment
DEFINITION
A virus responsible for a flu pandemic in 2009 that was
originally referred to as swine flu" because many of the
genes in this new virus were very similar to influenza
viruses that normally occur in pigs in North America.
However, the virus is actually a novel influenza A (H1N1)
virus. This virus first caused illness in Mexico and the
United States in March and April, 2009 that spread to
pandemic status over the following months.
H1N1 flu is spread from person to person, unlike typical
swine flu, although it is not clear how easily the virus is
able to spread among people.
Type A
Typeavian,
A
(Seasonal,
swine
influenza,.)
(Seasonal,
a\ian, swine
influenza,.)
Type B
Type B
(Seasonal influenza)
Limited to humans
H1N1
The 2009 H1N1 virus is a hybrid of
swine, avian and human strains
India and Pakistan currently
experiencing outbreaks.
MODE OF TRANSMISSION
How does H1N1 Influenza spread?
Fever
Cough
Runny or stuffy nose
Body aches
Headache
Chills
Fatigue
In addition, vomiting (25%) and diarrhea (25%) have
been reported. (Higher rate than for seasonal flu.)
Sudden dizziness
Confusion
INVESTIGATIONS
If swine flu is suspected, clinicians should
obtain a respiratory swab for swine
influenza testing and place it in a
refrigerator (not a freezer)
once collected, the clinician should contact
their state or local health department to
facilitate transport and timely diagnosis at a
state public health laboratory
INVESTIGATIONS
The Human Influenza Virus Real-Time RT-PCR
Detection and Characterization Panel (rRT-PCR Flu
Panel) is an in vitro laboratory diagnostic test that can
provide results within 4 hours. It is the only in vitro
diagnostic test for influenza that is cleared by the FDA
for use with lower respiratory tract specimens .
The kit utilizes a 3-module design and can:
Identify and distinguish between influenza A and B
viruses,
Classify influenza A viruses by subtype, and
Detect highly pathogenic avian influenza A (H5N1) virus
infection in human respiratory tract specimens.
TREATMENT
NON PHARMACEUTICAL
INTERVENTIONS
1. Delay disease transmission and
outbreak peak
2. Decompress peak burden on
healthcare infrastructure
3. Diminish overall cases and health
impacts
VOLUNTARY ISOLATION
Separation and restricted movement of ill
persons with contagious disease (often in a
hospital setting and Primarily individual
level)
Isolate severe and mild cases
Location of isolation (home, hospital) depends on
several factors (severity of illness, the number of
affected persons, the domestic setting)
Do not wait for lab confirmation
Plan for large number of severe cases
Provide medical and social care
VOLUNTARY ISOLATION
Infection Control of Ill Persons in a Healthcare Setting
Patients with suspected or confirmed case-status should be placed in
a single-patient room with the door kept closed. If available, an
airborne infection isolation room (AIIR) with negative pressure air
handling with 6 to 12 air changes per hour can be used. Air can be
exhausted directly outside or be recirculated after filtration by a high
efficiency particulate air (HEPA) filter. For suctioning, bronchoscopy,
or intubation, use a procedure room with negative pressure air
handling.
The ill person should wear a surgical mask when outside of the
patient room, and should be encouraged to wash hands frequently
and follow respiratory hygiene practices. Cups and other utensils
used by the ill person should be washed with soap and water before
use by other persons. Routine cleaning and disinfection strategies
used during influenza seasons can be applied to the environmental
management of swine influenza.
VOLUNATARY QUARANTINE
Separation and restricted movement of well
persons presumed exposed
Identification of contacts
Hand Washing
Wet hands with clean (not hot) water
Apply soap
Rub hands together for at least 20 seconds
Rinse with clean water
Dry with disposable towel or air dry
Use towel to turn off faucet
Alcohol based hand rubs can be used, more
costly than hand washing
ISOLATION PRECAUTIONS
PERSONAL PROTECTIVE
EQUIPMENT
PERSONAL PROTECTIVE
EQUIPMENT
For specific work activities that involve contact with people who
have ILI(influenza like illness), such as escorting a person with ILI,
interviewing a person with ILI, providing assistance to an individual
with ILI, the following are recommended:
workers should try to maintain a distance of 6 feet or more from the
person with ILI;
workers should keep their interactions with ill persons as brief as
possible;
the ill person should be asked to follow good cough etiquette and
hand hygiene and to wear a facemask, if able, and one is available;
workers at increased risk of severe illness from influenza infection
(see footnote 3 of table 1) should avoid people with ILI (possibly by
temporary reassignment); and,
where workers cannot avoid close contact with persons with ILI,
some workers may choose to wear a facemask or N95 respirator on
a voluntary basis.
Management
Co Morbid conditions
Those considered vulnerable to severe outcomes & should be a focus
of early identification, assessment and treatment, include the
following:
Chronic respiratory conditions, eg asthma, COPD, OSA
Pregnant women, esp. in second or third trimester
Obesity (BMI > 30) & morbid obesity (BMI > 40)
Other predisposing conditions, such as chronic cardiac disease, and
chronic illnesses including diabetes mellitus, renal failure,
haemoglobinopathies, immunosuppression.
Adults > 65 years of age esp. those with other chronic diseases
.
Severe illness following influenza occurs in at least 3
ways:
1. severe 1 viral infection with ARDS occurring relatively
early in illness related to viral pneumonia (within 1 st 4
days)
2. bacterial pneumonia,
pneumonia complicating initial bronchitis
caused by influenza
3. destabilization of pre-existing chronic condition. This
may present as respiratory distress related to
exacerbations of COPD, asthma or CCF. Influenza can
also cause acute destabilization of diabetes, CRF,
chronic liver disease etc
Home assessment
1
Lab Test
Who needs to be tested?
What test?
How about rapid test
a) RT-PCR
b) Viral culture
Rapid test
Rapid test : use to detect the presence of Influenza A
virus in respiratory specimens.
A positive rapid test means-presence of Flu A virus.
Does not differentiate between seasonal flu or Influenza
A-H1N1.
Detection rate varies from one test kit to another.
A negative test does not rule out Influenza virus
infection
Treatment
RECOMMENDATION:
Antiviral Treatment is recommended for:
All hospitalized patients (ie. those with moderate
to severe disease) with confirmed or suspected
novel influenza A H1N1. Empirical therapy for
suspected patients with severe disease should be
considered if the turnaround time for H1N1 confirmation
is prolonged. The antiviral treatment maybe stopped if
the results are negative.
All individual with co-morbid factors whether they are
admitted or not.
Drugs
Zanamivir dosage:
10mg (2 puffs) bd for 5days (Adults & children)
(Children < 5 yrs may have difficulty with Diskhaler )
In patients with bronchospasm: Zanamivir is not
recommended for the treatment of patients with
underlying airways disease (eg. asthma or COPD).
Patients with pulmonary dysfunction should always
have a fast-acting bronchodilator available and
discontinue zanamivir if respiratory difficulty develops.
No dosage adjustment is required in patients with renal
impairment
If NO moderate/severe illness;
Does patient have a comorbidity associated with
increased risk of influenza
complications?
Prevention
The best way for people to protect
themselves
Handwashing and using disinfectants
Taking antivirals Tamiflu or Relenza
Getting a vaccine
Preexposure chemoprophylaxis
Preexposure antiviral chemoprophylaxis
should be used only for persons who are
at very high risk (e.g., severely
immunosuppressed patients) for
influenza-related complications who
cannot otherwise be protected during
times when a high risk for exposure exists
Postexposure
chemoprophylaxis
Decisions on whether to administer
antivirals for chemoprophylaxis should
take into account the exposed person's
risk for influenza complications, the type
and duration of contact,and clinical
judgment
Postexposure
chemoprophylaxis
Generally, postexposure chemoprophylaxis
for persons should be only used when
antivirals can be started within 48 hours of
the most recent exposure.
Chemoprophylaxis with antiviral
medications is not a substitute for
influenza vaccination when influenza
vaccine is available
Masks
Facemasks help stop
droplets from being
spread by the person
wearing them. They also
keep splashes or sprays
from reaching the mouth
and nose of the person
wearing the facemask.
They are not designed to
protect you against
breathing in very small
particles and viruses.
A respirator (for
example, an N95 or
higher filtering
facepiece respirator)
is designed to protect
you from breathing in
very small particles,
which might contain
viruses.
Obesity and H1 N1