Lesson 2:ย
#๐ฆ Influenza
Parajuli SB, 2025
๐ www.suryaparajuli.com.np
๐ฅ Community Medicine (Kathmandu University) | MBBS 6th Semester |
#๐ฏ Specific Learning Outcomes (SLOs)
At the end of the session, the learner will be able to:
๐น State the โGolden 3โ basics of Influenza โ the causative agent, mode of transmission, and period of communicability.
๐น Describe the problem statement and public health importance of seasonal and pandemic influenza.
๐น Explain the epidemiological determinants of influenza including host, agent, and environmental factors.
๐น Identify the clinical features, diagnostic approaches, and treatment options for influenza, including use of antivirals.
๐น Discuss the prevention and control measures, including types of influenza vaccines, their schedules, contraindications, and adverse effects.
๐น Describe the principles and importance of influenza surveillance in controlling outbreaks and informing vaccine policy.
#๐ฅ Golden 3 Basics of Influenza
๐ฆ Influenza is an acute respiratory tract infection caused by the influenza virus, which is classified into four types:
๐น Influenza A
๐น Influenza B
๐น Influenza C
๐น Influenza D
๐ Important Points
๐น Influenza A and B are responsible for epidemics in humans.
๐น The disease is characterized by sudden onset of symptoms such as:
๐ก๏ธ Chills
๐ซ Malaise
๐ฅ Fever
๐ช Muscle pain
๐ฎโ๐จ Cough
#๐ Problem Statement
๐ Influenza is a global disease, capable of affecting populations worldwide, regardless of geography.
๐ Pandemics occur every 10โ40 years, driven by major antigenic changes in the virus.
๐ Historical Pandemics include:
๐๏ธ 1918 โ Spanish influenza
๐๏ธ 1957 โ Asian influenza
๐๏ธ 1968 โ Hong Kong influenza
๐ Global Burden
๐น Annual influenza epidemics result in an estimated:
๐งโโ๏ธ 3โ5 million cases of severe illness
โฐ๏ธ 290,000 to 650,000 deaths globally
๐ฆ Influenza A is the predominant strain, accounting for approximately 59% of all detected influenza viruses worldwide.
#๐งฌ Types of Influenza
๐น ๐ฆ๏ธ Seasonal Influenza
๐น ๐ฆ Avian Influenza (Bird Flu)
๐น ๐ Pandemic Influenza A (Swine Flu)
#๐ฆ๏ธ Seasonal Influenza
#๐ฆ Epidemiological Determinants โ Agent Factors
#(a) ๐งช Agent
๐ท๏ธ Family: Orthomyxoviridae
๐งฌ Types: Four viral subtypes
๐น Influenza A
๐น Influenza B
๐น Influenza C
๐น Influenza D
๐ซ Cross-immunity:
No cross-immunity exists between the types.
#๐ฆ Key Characteristics
#Influenza A Virus
Has two distinct surface antigens:
๐น Haemagglutinin (H)
โก๏ธ Enables virus to attach and enter host cells.
๐น Neuraminidase (N)
โก๏ธ Facilitates release of new viral particles from infected cells.
๐งฌ Subtypes:
๐น 18 HA
๐น 11 NA
๐จโโ๏ธ Humans are mostly infected with:
๐น H1, H2, H3
๐น N1, N2
#๐ Antigenic Variation
#๐ด Antigenic Shift
โก Sudden, major change
๐งฌ Due to genetic reassortment
(e.g., humanโavian virus mix)
๐ Leads to pandemics
#๐ก Antigenic Drift
๐ข Gradual change
๐งฌ Due to point mutations
๐ Leads to seasonal epidemics
#๐ฆ Influenza B Virus
๐น Does not undergo antigenic shift
๐น Not divided into subtypes
๐น Minor antigenic drift may occur
#๐ฆ Influenza C Virus
๐น Antigenically stable
๐น Causes mild illness
๐น Does not contribute to epidemics
#๐๐๐ Reservoir of Infection
A major reservoir of influenza viruses exists in animals and birds.
๐ฆ Influenza viruses have been isolated from:
๐ Swine
๐ Horses
๐ Dogs
๐ Cats
๐ Domestic poultry
๐ฆ Wild birds
#๐งซ Source of Infection
The source is usually:
๐งโโ๏ธ Clinical case
๐คง Subclinical/asymptomatic case
๐ During epidemics, many mild or asymptomatic infections occur and play a major role in transmission.
๐ซ Respiratory tract secretions
(droplets, aerosols) are infective.
#โณ Period of Infectivity
The virus is present in the nasopharynx:
๐๏ธ From 1 to 2 days before symptom onset
๐๏ธ Up to 1 to 2 days after symptom onset
#๐ง Epidemiological Determinants โ Host Factors
#(a) ๐ถ Age and Sex
๐น Influenza affects all age groups and both sexes.
๐น Children have a higher attack rate and play a significant role in transmission.
๐น Adults tend to have a lower attack rate.
#(b) ๐ Human Mobility
๐ถ Movement of people contributes significantly to the spread of infection, especially during outbreaks and epidemics.
#(c) ๐ก๏ธ Immunity
๐น Immunity is subtype-specific
(no cross-protection between types A, B, and C)
๐งช Antibodies against:
๐น Haemagglutinin (HA)
๐น Neuraminidase (NA)
are key for protection.
๐ Timeline of antibody response:
๐๏ธ Appears ~7 days after infection
๐ Peaks in ~2 weeks
๐ Declines to pre-infection level in 8โ12 months
#๐ Epidemiological Determinants โ Environmental Factors
#(a) ๐ฆ๏ธ Season
๐ Northern Hemisphere:
๐น Epidemics commonly occur during winter months.
๐ Southern Hemisphere:
๐น Occurs during winter or rainy season.
๐ด Tropical regions:
๐น Influenza circulates year-round, with 1 or 2 peaks typically during the rainy season.
#(b) ๐ซ Overcrowding
๐น Facilitates transmission of the virus.
๐ High attack rates observed in densely populated settings, such as:
๐ซ Schools
๐ Hostels
๐ข Institutions
๐ข Ships
๐ช Military camps
#๐ถโโ๏ธ Mode of Transmission
๐ฆ Influenza primarily spreads from person to person via:
๐ง Droplet infection
๐ซ๏ธ Droplet nuclei
๐น These droplets are generated when an infected person:
๐คง Sneezes
๐ฎโ๐จ Coughs
๐ฃ๏ธ Talks
๐ Portal of entry:
๐ซ Respiratory tract
#โณ Incubation Period
๐๏ธ Ranges from 1 to 4 days after exposure to the virus.
#๐งฌ Pathogenesis and Clinical Features
๐ฆ The virus enters through the respiratory tract, causing:
๐น Inflammation
๐น Necrosis of the tracheal and bronchial mucosa
โก๏ธ Followed by secondary bacterial invasion
โ No viraemia observed
#๐ค Common Symptoms (Influenza A & B)
๐ก๏ธ Fever
๐ฅถ Chills
๐ Body aches and pains
๐ฎโ๐จ Cough
๐ซ Generalized weakness
๐ Fever duration:
๐น 1โ5 days
๐น Average 3 days in adults
#โ ๏ธ Frequent Complications
๐ Acute sinusitis
๐ Otitis media
๐ค Purulent bronchitis
๐ซ Pneumonia โ Most serious complication
#๐จ Suspect Pneumonia If:
๐ก๏ธ Fever persists >4โ5 days
๐ Fever recurs abruptly after initial recovery
#๐จ Reye Syndrome (Rare but Severe)
๐ง Encephalopathy with fatty liver (hepatic failure)
๐ง Seen mainly in children aged 2โ16 years
๐ Associated with aspirin use during viral infections
โ ๏ธ Mortality rate:
๐น 10โ40%
โ Exact pathogenesis unknown
#๐ฆ Avian Influenza (Bird Flu)
#๐ Golden 5 Basics of Bird Flu
๐ฆ Primary Host:
Birds, especially wild waterfowl and domestic poultry.
๐ Transmission:
Mainly bird-to-bird; rare bird-to-human transmission.
๐ค Symptoms in Humans:
Range from mild flu-like illness to severe respiratory disease.
๐ Pandemic Risk:
Mutation or reassortment can lead to human-to-human transmission.
๐ก๏ธ Prevention:
Surveillance, poultry control, and public health preparedness.
#๐ฆ Avian Influenza (Bird Flu) (Birdโs EYE View)
๐ฆ Avian influenza refers to a large group of influenza viruses that primarily infect birds.
๐น Occasionally, some avian influenza viruses can infect other species such as:
๐ Pigs
๐จ Humans
โฆbut this is rare.
๐ The vast majority of avian influenza viruses do not infect humans.
๐ฆ The H5N1 strain is notable for its pandemic potential because it might adapt to become contagious among humans.
๐ When such an adaptation happens:
โก๏ธ The virus transitions from a bird virus to a human influenza virus.
๐ Influenza pandemics occur when new influenza viruses adapt to human transmission.
๐จโโ๏ธ Health experts have been closely monitoring the H5N1 virus for almost 15 years due to its severity.
๐ Currently:
๐น Does not easily jump from birds to humans
๐น Does not spread efficiently among humans
โ ๏ธ However:
Once a fully contagious virus emerges, its global spread is considered inevitable.
#๐ Transmission of Avian Influenza
๐จ Human infections with avian influenza viruses are rare but sporadically reported.
๐ฆ Infection usually occurs through direct contact with:
๐ Infected live or dead poultry birds
OR
๐ช Contaminated environments
(e.g., live bird markets)
#โณ Incubation Period
๐๏ธ Typically ranges from 2 to 5 days after exposure.
#๐ฌ Diagnosis
โ Confirmed by:
๐งช RT-PCR
(Reverse Transcriptase Polymerase Chain Reaction)
โ ๏ธ Rapid Influenza Diagnostic Tests (RDTs):
๐น Available
๐น Have lower sensitivity compared to RT-PCR.
#๐ Treatment
๐ฆ Antiviral drugs such as:
๐ Oseltamivir
๐ Zanamivir
can:
๐น Reduce the duration of viral replication
๐น Improve chances of survival
#๐ก๏ธ Prevention
๐งผ Regular hand washing with proper drying
๐ท Good respiratory hygiene
(cover mouth and nose when coughing or sneezing)
๐ Early self-isolation if sick
๐ซ Avoid close contact with infected individuals
๐ซ Avoid touching the eyes, mouth, and nose
#๐ Vaccine
๐ In 2007, a vaccine for bird flu was licensed for people 18 to 64 years old.
๐ It is an inactivated influenza vaccine administered in:
๐น Two doses
๐น 28 days apart
#โ ๏ธ Common Side Effects
๐ Pain and tenderness at injection site
๐ค Headache
๐ช Muscle pain
๐ซ General malaise
๐ Other vaccines have been approved, but because H5N1 mutates continuously, existing vaccines may not always be effective during a pandemic.
#๐ Pandemic Influenza A (H1N1) 2009 (Swine Flu)
#๐ Golden 5 Basics of Pandemic Influenza A (H1N1) 2009
๐งฌ Origin:
Swine-origin influenza virus with novel genetic makeup.
๐ฅ Population Impact:
Mainly affects children, young and middle-aged adults due to low immunity.
๐ซ Pathogenicity:
Ability to infect lower respiratory tract causing severe pneumonia.
๐ Global Spread:
Rapid worldwide dissemination; declared pandemic in 2009.
๐ Current Status:
Now circulates as a seasonal virus with ongoing surveillance.
#๐ Pandemic Influenza A (H1N1) 2009 (Swine Flu) (Birdโs EYE View)
๐น The H1N1 2009 virus differs from seasonal influenza in two key ways:
1๏ธโฃ Low pre-existing immunity in most people led to infection across a wider age range, especially in children and young adults.
2๏ธโฃ The virus can infect the lower respiratory tract, causing rapidly progressive pneumonia, notably in children and young to middle-aged adults.
๐ The virus emerged in March 2009 and spread quickly worldwide.
๐ On 11th June 2009, WHO declared it a pandemic.
๐ The world is now in the post-pandemic period.
๐ In India, the virus causes local outbreaks; in 2020, India reported:
๐น 2,752 cases
๐น 44 deaths
๐น Case fatality rate of 1.6%
๐ Based on past pandemics, H1N1 2009 is expected to circulate seasonally for years.
โ ๏ธ Though current concern has diminished, national health vigilance remains critical due to unpredictable virus behavior.
๐ On 26th September 2011, WHO renamed it Influenza A (H1N1) pdm09.
#โณ Incubation Period
๐๏ธ Typically 1 to 4 days
๐ Can range up to 7 days
#๐ Case Definitions for Influenza A (H1N1) 2009
#๐งโโ๏ธ 1. Suspected Case
A person with acute febrile respiratory illness (fever โฅ 38โ) with onset:
(a) Within 7 days of close contact with a confirmed influenza A (H1N1) 2009 case, or
(b) Within 7 days of travel to areas with confirmed cases, or
(c) Residing in a community with confirmed influenza A (H1N1) 2009 cases.
#๐งช 2. Probable Case
A person with acute febrile respiratory illness who:
(1) Tests positive for influenza A, but subtyping for H and N is not possible by RT-PCR or reagents for seasonal influenza, or
(2) Tests positive for influenza A by rapid test or immunofluorescence assay (IFA) and meets suspected case criteria, or
(3) Has a clinically compatible illness and died of unexplained acute respiratory illness epidemiologically linked to a probable or confirmed case.
#โ 3. Confirmed Case
A person with acute febrile respiratory illness with laboratory confirmation of influenza A (H1N1) 2009 infection by WHO-approved tests:
๐น Real-Time PCR
๐น Viral culture
๐น Four-fold rise in influenza A (H1N1) specific neutralizing antibodies
#๐ฉบ Clinical Features of Influenza A (H1N1) 2009
The disease presents a wide clinical spectrum, ranging from:
๐น Mild, non-febrile upper respiratory illness
๐น Febrile influenza-like illness (ILI)
๐น Severe or fatal complications, including rapidly progressive pneumonia.
๐ Case fatality rate:
Approximately 0.5%, though this may vary.
#๐งพ (a) Uncomplicated Influenza
#๐ค Influenza-Like Illness (ILI) Symptoms
๐ก๏ธ Fever
๐ฎโ๐จ Cough
๐ฃ Sore throat
๐ Rhinorrhoea (runny nose)
๐ค Headache
๐ช Muscle pain
๐ซ Malaise (general discomfort)
๐ซ No shortness of breath or dyspnoea (difficulty breathing)
๐ Patients may have some or all of these symptoms.
#๐ฝ๏ธ Gastrointestinal Illness
๐น Diarrhoea and/or vomiting, especially common in children
๐น Occurs without evidence of dehydration
#โ ๏ธ (b) Complicated or Severe Influenza
#๐ฉบ Clinical and Radiological Signs
๐ฎโ๐จ Shortness of breath (dyspnoea)
๐จ Rapid breathing (tachypnea)
๐ฉธ Low oxygen levels (hypoxia)
๐ซ Radiological evidence of lower respiratory tract disease (e.g., pneumonia)
๐ง Central nervous system involvement
(e.g., encephalopathy, encephalitis)
๐ง Severe dehydration
๐ฆ Secondary complications such as:
๐น Renal failure
๐น Multi-organ failure
๐น Septic shock
Other complications:
๐ช Rhabdomyolysis (muscle breakdown)
โค๏ธ Myocarditis (heart inflammation)
#๐ฅ Exacerbation of Underlying Chronic Diseases
Includes:
๐ซ Asthma
๐ซ Chronic Obstructive Pulmonary Disease (COPD)
๐งซ Chronic liver or kidney failure
๐ฌ Diabetes
โค๏ธ Cardiovascular conditions
๐ Any clinical condition requiring hospital admission for management.
โ ๏ธ Presence of signs indicating progressive disease.
#๐จ Signs Requiring Urgent Medical Review
Patients with initially uncomplicated influenza may rapidly (within 24 hours) develop severe illness.
#๐ซ (a) Oxygen Impairment or Cardiopulmonary Insufficiency
๐ฎโ๐จ Shortness of breath (with activity or at rest)
๐ฐ Difficulty breathing
๐ต Cyanosis (turning blue)
๐ฉธ Bloody or discolored sputum
๐ Chest pain
๐ Low blood pressure
๐ถ In children: fast or labored breathing
๐ Hypoxia detected by pulse oximetry
#๐ง (b) Central Nervous System (CNS) Complications
๐ง Altered mental status
๐ด Unconsciousness or drowsiness
โ ๏ธ Difficulty awakening
โก Recurring or persistent seizures (convulsions)
๐ต Confusion
๐ช Severe weakness or paralysis
#๐ฆ (c) Sustained Virus Replication or Secondary Bacterial Infection
๐ก๏ธ Persistent high fever
โณ Symptoms lasting beyond 3 days
๐งช Laboratory evidence or clinical signs indicating ongoing viral or bacterial infection
#โ ๏ธ Risk Factors for Severe Disease
The risk factors for severe disease from pandemic influenza A (H1N1) 2009 are similar to those for seasonal influenza complications, including:
๐ถ Infants and young children, especially those under 2 years
๐คฐ Pregnant women
๐ซ Persons of any age with chronic pulmonary diseases
(e.g., asthma, COPD)
โค๏ธ Persons of any age with chronic cardiac diseases
(e.g., congestive heart failure)
๐ฌ Persons with metabolic disorders
(e.g., diabetes)
๐งซ Persons with:
๐น Chronic renal or hepatic disease
๐น Certain neurological conditions
(neuromuscular, neurocognitive, seizure disorders)
๐ฉธ Haemoglobinopathies
๐ก๏ธ Immunosuppression
(due to HIV, immunosuppressive medication, malignancy, etc.)
๐ Children on chronic aspirin therapy
๐ด Persons aged 65 years and older
โ๏ธ Individuals who are obese, especially those who are morbidly obese
#๐งช Laboratory Diagnosis of Pandemic Influenza A (H1N1) 2009
#โญ Importance
๐ฌ Early and accurate lab diagnosis is crucial for:
โ๏ธ Proper case management
โ๏ธ Infection control
โ๏ธ Antiviral treatment decisions
โ๏ธ Avoiding unnecessary antibiotics
#๐งซ Diagnostic Tests
#๐งช RT-PCR (Reverse Transcriptase Polymerase Chain Reaction)
โ๏ธ Most sensitive and timely test for detecting infection.
#โก Rapid Influenza Diagnostic Tests (RIDTs)
โ๏ธ Widely available
โ ๏ธ Less sensitive
โ Negative results do not rule out infection and should not delay treatment or infection control.
#๐งด Specimen Collection
๐ Respiratory samples are required.
#Upper respiratory tract samples:
๐ Nasal swabs
๐ Nasopharyngeal swabs
๐ Throat swabs
#Lower respiratory tract samples:
๐ซ Tracheal aspirates
๐ซ Bronchial aspirates
โ๏ธ Provide higher diagnostic yield in patients with lower respiratory symptoms.
#๐ฉบ Clinical Diagnosis
๐ When influenza is widespread:
โ๏ธ Uncomplicated cases can be diagnosed clinically and epidemiologically.
#๐ Follow-Up Advice
Patients should be advised to:
๐ Seek follow-up if symptoms worsen
โณ Or do not improve within 72 hours
#๐ฏ Testing Prioritization
Testing should be prioritized for:
โ ๏ธ At-risk groups
โ ๏ธ Severe or progressive illness
๐ Results guide:
โ๏ธ Infection control
โ๏ธ Management of close contacts
#โ ๏ธ Important Note
๐ซ Diagnostic testing should never delay:
โ๏ธ Infection control measures
โ๏ธ Initiation of antiviral treatment
If clinical and epidemiological suspicion is high.
#๐ฆ Infection Control Measures
#๐ Transmission
Pandemic H1N1 spreads similarly to:
๐ฆ Seasonal influenza A and B viruses.
#๐งผ Standard Precautions
โ๏ธ Practice strict hand hygiene with soap and water or alcohol-based sanitizer.
โ๏ธ Cover mouth and nose with tissue or handkerchief when coughing or sneezing.
โ๏ธ Ill persons should wear a face mask when going out in public
(e.g., to seek medical care) to reduce virus spread.
#๐ซ Aerosol-Generating Procedures
Examples:
๐น Bronchoscopy
๐น Respiratory tract aspiration
Required protection:
๐ท Use particulate respirators
(N95, FFP2, or equivalent)
๐ Wear eye protection
๐งฅ Wear gown
๐งค Wear gloves
๐ฌ๏ธ Perform procedures in well-ventilated rooms
(natural or mechanical ventilation).
#๐ฅ Isolation Precautions for Hospitalized Patients
๐ Continue isolation for:
โ๏ธ 7 days after illness onset
OR
โ๏ธ At least 24 hours after fever and respiratory symptoms resolve, whichever is longer.
#โ ๏ธ Special Cases
For prolonged or complicated illness (e.g., pneumonia):
โ๏ธ Maintain precautions until clinical improvement.
๐ก๏ธ Immunosuppressed patients require special attention
Because:
๐น They may shed virus longer
๐น Higher risk of antiviral resistance
#๐ Influenza Vaccine
There are currently three main technologies used to produce influenza vaccines:
#๐ฅ Egg-Based Vaccines
โ๏ธ Inactivated influenza vaccines (IIVs)
Prepared from:
๐ฅ Virus particles grown in embryonated chicken eggs.
Process:
๐ฌ Virus particles are inactivated
๐งช Detergent-solubilized
โก๏ธ To isolate:
๐น Haemagglutinin (HA)
๐น Neuraminidase (NA) proteins
#๐ก๏ธ Live Attenuated Influenza Vaccine (LAIV)
โ๏ธ Made from weakened virus strains grown in eggs.
#๐งซ Cell-Cultured Vaccines
Produced by:
๐งฌ Growing influenza viruses in animal cell cultures instead of eggs.
Advantages:
โก Faster manufacturing process.
โ ๏ธ Note:
Although no hen's eggs are used, trace amounts of egg protein might still be present.
#๐งฌ Recombinant Influenza Vaccines
Method:
๐ฌ Isolates the HA gene and proteins
โก๏ธ Stimulates immune response without using chicken eggs.
Produced in:
๐ฆ Insect cell cultures.
Feature:
๐ Contain about three times more HA than standard-dose vaccines.
โ๏ธ Recombinant vaccine is the only completely egg-free influenza vaccine.
#๐งฌ Vaccine Composition
Influenza vaccines include components from:
๐ฆ Human influenza A viruses
๐ฆ Influenza B viruses
#๐ Vaccine Update Process
Formulation is reviewed and updated annually based on:
๐น The viruses currently circulating in the population
๐น How widely these viruses are spreading
๐น Effectiveness of the previous yearโs vaccine
๐ The World Health Organization (WHO) provides recommendations on which specific virus strains should be included each year.
#๐ Inactivated Influenza Vaccine (IIVs)
#๐ Overview
๐ Available since the 1940s
#๐งฌ Trivalent IIVs contain:
๐น Influenza A (H1N1)
๐น Influenza A (H3N2)
๐น One Influenza B strain
#๐งฌ Quadrivalent Vaccines
๐ Introduced in 2013โ2014
โ๏ธ Add:
๐น A second B strain
โก๏ธ Provide broader protection.
#๐ Administration
๐ Given via:
๐ Intramuscular (IM) injection
๐ Intradermal (ID) injection
#๐ Doses
๐ถ Pediatric: 0.25 ml
๐จ Adult: 0.5 ml
#๐ Dosage Schedule
โ๏ธ One dose annually for persons 9 years and older
๐ถ Children 6 months to 8 years receiving vaccine for first time:
๐ Two doses
๐ 28 days apart
โ๏ธ Annual immunization is recommended.
#๐ Inactivated Influenza Vaccine (IIVs)
#๐ Effectiveness
โ๏ธ Approximately 60% effective among healthy persons under 65 years.
โณ Protection starts about 14 days after vaccination.
๐ก๏ธ Immunity lasts 6โ12 months.
โ ๏ธ Vaccinated individuals can still get infected:
๐น Shortly before vaccination
๐น Shortly after vaccination
๐น By influenza strains not covered by the vaccine.
#๐ด Effectiveness in Elderly Persons
โ๏ธ 50โ60% effective in preventing hospitalization
โ๏ธ 80% effective in preventing death
#๐ฆ Storage
๐ก๏ธ Store at 2โ8โ
๐ซ Do not freeze
#๐ด Special Vaccines for Older Adults (65+ years)
Two vaccines designed to improve immune response:
#๐ High-Dose IIV (HD-IIV)
๐ Contains four times the HA antigen of standard vaccines.
#๐ Adjuvanted IIV (aIIV)
๐งช Contains an adjuvant to boost immune response.
โ๏ธ Both are trivalent vaccines.
๐ HD-IIV shown to be 24% more effective than standard vaccines in preventing lab-confirmed influenza in older adults.
#โ ๏ธ Side Effects
#Common Side Effects
๐ Local soreness
๐ Swelling
๐ Redness at injection site
๐ก๏ธ Mild fever
๐ช Muscle/joint aches
๐ค Headache
โณ Usually mild and last 1โ2 days.
๐ Children tend to have these side effects more often than elderly.
#Rare Side Effects
โ ๏ธ Allergic reactions such as:
๐น Hives
๐น Swelling
๐น Asthma
๐น Severe systemic hypersensitivity
#๐ซ Contraindications โ Inactivated Influenza Vaccine (IIVs)
IIVs should NOT be given to:
โ People with severe allergy to chicken eggs
โ Those with history of:
๐น Anaphylactic reaction
๐น Severe allergic reaction to any vaccine component
โ Persons who had severe reaction to prior influenza vaccine.
โ People who developed Guillain-Barrรฉ Syndrome (GBS) within 6 weeks after influenza vaccination.
โ Children under 6 months of age
(vaccine not approved for this age)
โ People with moderate to severe illness with fever
(vaccination should wait until recovery).
#๐ก๏ธ Live Attenuated Influenza Vaccine (LAIV)
#๐ Overview
๐ Approved for use in 2003.
Contains:
๐ฆ Same influenza viruses as inactivated vaccines
But:
๐งฌ Cold-adapted to replicate in nasopharyngeal mucosa
#๐งช Production
โ๏ธ Grown in chicken eggs
โ ๏ธ Contains residual egg protein
#๐ Administration
๐ Delivered as:
๐ Single-dose nasal spray
Method:
๐ Half sprayed into each nostril
#๐งด Composition
๐ซ Does not contain:
โ Thimerosal
โ Other preservatives
#๐ฅ Approved Age Group
โ๏ธ Healthy, non-pregnant persons aged:
๐ 2 to 49 years
#๐งซ Virus Shedding
๐ถ Vaccinated children may shed vaccine virus in:
๐ Nasal secretions
โณ For up to 3 weeks
#๐ Effectiveness of LAIV
โ๏ธ 87% effective against culture-confirmed influenza in children aged 60โ84 months.
โ๏ธ Reduces:
๐ Febrile otitis media by 27%
๐ Otitis media requiring antibiotics by 28%
#โ ๏ธ Side Effects โ LAIV
#Common Side Effects
๐ Runny nose
๐ Nasal congestion
๐ฎโ๐จ Cough
#Less Common Side Effects
๐ฃ Sore throat
๐ก๏ธ Low-grade fever
๐ Irritability
๐ช Muscle aches
๐ค Headache
#Reported in Some Children
โ ๏ธ Wheezing
โ ๏ธ Vomiting episodes
#๐ซ Contraindications โ LAIV
LAIV should not be given to:
โ Children under 2 years
โ Persons 50 years and older
#โ Persons with Chronic Medical Conditions
Including:
๐ซ Asthma
๐ฌ๏ธ Recent wheezing
๐ซ Reactive airway disease
โค๏ธ Chronic pulmonary or cardiovascular diseases
๐ฌ Metabolic diseases (e.g., diabetes)
๐งซ Renal disease
๐ฉธ Hemoglobinopathies
(e.g., sickle cell disease)
#โ Additional Contraindications
๐ Children/adolescents on long-term aspirin therapy
(due to risk of Reye syndrome)
๐ก๏ธ Immunosuppressed persons
(HIV, immunosuppressive therapy)
๐คฐ Pregnant women
๐ฅ Persons with severe allergy to eggs
โ ๏ธ Persons with history of Guillain-Barrรฉ Syndrome (GBS) within 6 weeks of prior influenza vaccine
(precaution)
๐ Note
Persons in these groups should receive:
๐ Inactivated influenza vaccine instead
#๐ WHO Recommendations on Influenza Vaccination Priorities
#๐ฅ Vaccinate Health Care Workers First
Purpose:
โ๏ธ Protect health infrastructure
โ๏ธ Prevent hospital outbreaks
#๐ฅ Recommended Groups by Priority
๐คฐ Pregnant women
๐งซ Individuals >6 months old with chronic medical conditions
๐ง Healthy young adults (15โ49 years)
๐ถ Healthy children
๐จ Healthy adults (49โ65 years)
๐ด Healthy adults >65 years
#๐ COVID-19 Vaccine Interaction
โณ Wait at least 7 days between:
๐ COVID-19 vaccine
AND
๐ Influenza vaccine
#๐ Treatment of Pandemic Influenza A (H,N) 2009
#๐งพ Key Principles of Clinical Management:
โ๏ธ Provide basic symptomatic care (e.g., fever and pain relief).
๐งฌ Use antiviral drugs early, especially for high-risk populations.
๐ฆ Administer antimicrobials to treat or prevent co-infections.
๐ Maintain proactive monitoring for signs of disease progression.
#๐ฅ Hospital Care:
๐ซ Early supplemental oxygen therapy to correct hypoxemia, with continuous monitoring of oxygen saturation during triage and hospitalization, if possible.
๐ง Careful fluid replacement to maintain hydration.
๐ Use of antimicrobials for other infections causing severe respiratory distress.
๐ซ Severely ill patients may require mechanical ventilation and intensive care support due to respiratory distress.
#๐งฌ Antiviral Therapy for Pandemic Influenza A (H,N) 2009
#๐ฆ Virus Susceptibility:
#โ๏ธ Susceptible to neuraminidase inhibitors (NAIs):
๐ Oseltamivir
๐ Zanamivir
#โ Resistant to M2 inhibitors:
๐ซ Amantadine
๐ซ Rimantadine
#๐ Antiviral Therapy โ Treatment Recommendations
#๐จ Severe or Progressive Illness:
โ๏ธ Treat all patients with oseltamivir as soon as possible
๐ Includes:
๐คฐ Pregnant women
๐ถ Children under 2 years (including neonates)
#โ ๏ธ If Severe Illness Not Responding:
Consider:
๐ Higher doses (e.g., 150 mg twice daily in adults)
โณ Longer treatment duration
#๐ If Oseltamivir Unavailable or Resistant Virus:
๐ Use zanamivir
#๐งโโ๏ธ High-Risk Patients with Uncomplicated Illness:
โ๏ธ Treat early with:
๐ Oseltamivir OR
๐ Zanamivir
#๐ง Patients Not at High Risk with Uncomplicated Illness:
๐ซ Antiviral treatment is generally not necessary.
โ๏ธ If used, start early for best outcomes.
#โ ๏ธ Additional Notes on Antivirals
๐ Start antiviral treatment immediately based on clinical suspicion
๐ซ Do NOT wait for laboratory confirmation
#๐ If Persistent Severe Illness Despite Oseltamivir:
Alternative options (with caution):
๐ Intravenous zanamivir
๐ Peramivir
๐ Ribavirin
โ ๏ธ Should NOT be used alone and NOT in pregnant women
โ ๏ธ Zanamivir powder for inhalation should NOT be nebulized due to lactose content affecting ventilator function.
#๐ Standard Oseltamivir Antiviral Treatment Regimens
#๐ถ Infants (<1 year)
Age Group | Dose | Frequency | Duration |
|---|---|---|---|
0โ1 month | 2 mg/kg | Twice daily | 5 days |
1โ3 months | 2.5 mg/kg | Twice daily | 5 days |
3โ12 months | 3 mg/kg | Twice daily | 5 days |
#๐ง Children (1โ12 years by weight)
Weight | Dose | Frequency | Duration |
|---|---|---|---|
โค15 kg | 30 mg | Twice daily | 5 days |
15โ23 kg | 45 mg | Twice daily | 5 days |
24โ40 kg | 60 mg | Twice daily | 5 days |
>40 kg | 75 mg | Twice daily | 5 days |
#๐ง Adults
๐ 75 mg orally
๐ Twice daily
โณ 5 days
#๐งช Zanamivir Dosing for Influenza Treatment
๐ Indication: Treatment of influenza in adults and children aged โฅ5 years
๐จ Route: Inhalation (Diskhaler)
#๐ Recommended Dose:
๐ง Adults & children (โฅ5 years):
๐จ 2 inhalations (2 ร 5 mg = 10 mg)
๐ Twice daily (morning and evening)
โณ Duration: 5 days
#๐ก๏ธ Chemoprophylaxis Regimen with Oseltamivir
๐ Indication:
โ๏ธ Healthcare personnel
โ๏ธ Close contacts of suspected, probable, or confirmed cases
โณ Duration:
๐๏ธ Once daily for 10 days after last exposure
#๐ถ Infants (<1 year)
Age | Dose |
|---|---|
<3 months | Not recommended (unless critical) |
3โ5 months | 20 mg once daily |
6โ11 months | 25 mg once daily |
#๐ง Children โฅ1 year (by weight)
Weight | Dose |
|---|---|
<15 kg | 30 mg once daily |
15โ23 kg | 45 mg once daily |
24โ40 kg | 60 mg once daily |
>40 kg | 75 mg once daily |
#๐ Influenza Surveillance
#๐ฏ Purpose of Surveillance:
#๐งฌ Monitor Circulating Strains
๐ Track prevalence and types of influenza viruses in circulation
๐งฌ Detect emergence of new or variant strains important for vaccine formulation
#๐ Estimate Impact
๐ Assess burden of disease in terms of:
๐งโโ๏ธ Morbidity (illness rates)
โฐ๏ธ Mortality (death rates)
๐ฐ Economic losses (healthcare costs, lost productivity)
#๐จ Early Outbreak Detection
โ ๏ธ Identify and respond promptly to influenza outbreaks
#๐ก๏ธ Guide Control Measures
๐ Enable timely public health action including:
๐ Vaccination campaigns
๐ Antiviral distribution
๐ข Public advisories
#๐ Key Takeaways
๐ฆ Influenza is a contagious respiratory virus with seasonal and pandemic forms.
๐ง Transmission is via droplets and contact; incubation is 1โ4 days.
๐ค Symptoms include fever, cough, sore throat; severe disease in high-risk groups.
๐ Treatment includes supportive care and antivirals (oseltamivir/zanamivir).
๐ Vaccination (IIV/LAIV) is key prevention; annual doses recommended.
๐ก๏ธ Chemoprophylaxis for exposed high-risk individuals and healthcare workers.
๐ Surveillance tracks virus trends and informs vaccine updates.
#๐ References
WHO. Weekly Epidemiological Record, No. 47, 23 Nov 2012.
Papadakis MA, McPhee SJ. Current Medical Diagnosis and Treatment, 53rd ed. 2014. Lange Publication.
WHO. Fact Sheet, March 14, 2018.
WHO. Technical Report Series, No. 642, 1980.
WHO. Bulletin of the World Health Organization, 1985; 63(1): 51.
Jawetz E, et al. Medical Microbiology, 22nd ed. Lange Medical Publication, 2001.
Jawetz E, et al. Medical Microbiology, 28th ed. Lange Medical Publication, 2019.
WHO. Weekly Epidemiological Record, No. 49/50, Oct 14, 2005.
WHO. Weekly Epidemiological Record, No. 41, 9 Oct 2009.
Government of India. National Health Profile 2021. Central Bureau of Health Intelligence, Ministry of Health and Family Welfare, New Delhi.
WHO. Recommendations for the Post-Pandemic Period: Pandemic (H1N1) 2009 Briefing Note 23, 2010.
WHO. Weekly Epidemiological Record, No. 43, 21 Oct 2011.
Government of India. Guidelines for Swine Flu (Influenza A H1N1). Ministry of Health and Family Welfare, New Delhi, 2010.
WHO. Clinical Management of Human Infection with Pandemic (H1N1) 2009: Revised Guidance, November 2009.
McPhee SJ, et al. Current Medical Diagnosis and Treatment, 49th ed. Lange Medical Publication, 2010.
Carter A. Flu Vaccine. Medically reviewed, 8 Sept 2020.
Yung AD, et al. U.S. Pharmacist: The Pharmacist Resource for Clinical Excellence, Nov 12, 2019; 44(11): 18โ22.
CDC. Epidemiology and Prevention of Vaccine-Preventable Diseases, April 15, 2019.
WHO. Safety of Pandemic (H1N1) 2009 Vaccines, Oct 30, 2009.