Influenza

Influenza

Influenza Uncovered: From Virus to Vaccine

Dr. Surya Parajuli
Dr. Surya Parajuli 13 Jan 2026

Lesson 2:ย 

#๐Ÿฆ  Influenza

Parajuli SB, 2025
๐ŸŒ www.suryaparajuli.com.np
๐Ÿฅ Community Medicine (Kathmandu University) | MBBS 6th Semester |


#๐ŸŽฏ Specific Learning Outcomes (SLOs)

At the end of the session, the learner will be able to:

๐Ÿ”น State the โ€œGolden 3โ€ basics of Influenza โ€” the causative agent, mode of transmission, and period of communicability.

๐Ÿ”น Describe the problem statement and public health importance of seasonal and pandemic influenza.

๐Ÿ”น Explain the epidemiological determinants of influenza including host, agent, and environmental factors.

๐Ÿ”น Identify the clinical features, diagnostic approaches, and treatment options for influenza, including use of antivirals.

๐Ÿ”น Discuss the prevention and control measures, including types of influenza vaccines, their schedules, contraindications, and adverse effects.

๐Ÿ”น Describe the principles and importance of influenza surveillance in controlling outbreaks and informing vaccine policy.


#๐Ÿฅ‡ Golden 3 Basics of Influenza

๐Ÿฆ  Influenza is an acute respiratory tract infection caused by the influenza virus, which is classified into four types:

๐Ÿ”น Influenza A
๐Ÿ”น Influenza B
๐Ÿ”น Influenza C
๐Ÿ”น Influenza D

๐Ÿ“Œ Important Points

๐Ÿ”น Influenza A and B are responsible for epidemics in humans.

๐Ÿ”น The disease is characterized by sudden onset of symptoms such as:

๐ŸŒก๏ธ Chills
๐Ÿ˜ซ Malaise
๐Ÿ”ฅ Fever
๐Ÿ’ช Muscle pain
๐Ÿ˜ฎโ€๐Ÿ’จ Cough


#๐ŸŒ Problem Statement

๐ŸŒŽ Influenza is a global disease, capable of affecting populations worldwide, regardless of geography.

๐Ÿ”„ Pandemics occur every 10โ€“40 years, driven by major antigenic changes in the virus.

๐Ÿ“œ Historical Pandemics include:

๐Ÿ—“๏ธ 1918 โ€” Spanish influenza

๐Ÿ—“๏ธ 1957 โ€” Asian influenza

๐Ÿ—“๏ธ 1968 โ€” Hong Kong influenza

๐Ÿ“Š Global Burden

๐Ÿ”น Annual influenza epidemics result in an estimated:

๐Ÿง‘โ€โš•๏ธ 3โ€“5 million cases of severe illness

โšฐ๏ธ 290,000 to 650,000 deaths globally

๐Ÿฆ  Influenza A is the predominant strain, accounting for approximately 59% of all detected influenza viruses worldwide.


#๐Ÿงฌ Types of Influenza

๐Ÿ”น ๐ŸŒฆ๏ธ Seasonal Influenza

๐Ÿ”น ๐Ÿฆ Avian Influenza (Bird Flu)

๐Ÿ”น ๐Ÿ– Pandemic Influenza A (Swine Flu)


#๐ŸŒฆ๏ธ Seasonal Influenza

#๐Ÿฆ  Epidemiological Determinants โ€“ Agent Factors

#(a) ๐Ÿงช Agent

๐Ÿท๏ธ Family: Orthomyxoviridae

๐Ÿงฌ Types: Four viral subtypes

๐Ÿ”น Influenza A
๐Ÿ”น Influenza B
๐Ÿ”น Influenza C
๐Ÿ”น Influenza D

๐Ÿšซ Cross-immunity:
No cross-immunity exists between the types.


#๐Ÿฆ  Key Characteristics

#Influenza A Virus

Has two distinct surface antigens:

๐Ÿ”น Haemagglutinin (H)
โžก๏ธ Enables virus to attach and enter host cells.

๐Ÿ”น Neuraminidase (N)
โžก๏ธ Facilitates release of new viral particles from infected cells.

๐Ÿงฌ Subtypes:
๐Ÿ”น 18 HA
๐Ÿ”น 11 NA

๐Ÿ‘จโ€โš•๏ธ Humans are mostly infected with:

๐Ÿ”น H1, H2, H3
๐Ÿ”น N1, N2


#๐Ÿ”„ Antigenic Variation

#๐Ÿ”ด Antigenic Shift

โšก Sudden, major change

๐Ÿงฌ Due to genetic reassortment
(e.g., humanโ€“avian virus mix)

๐ŸŒ Leads to pandemics


#๐ŸŸก Antigenic Drift

๐Ÿข Gradual change

๐Ÿงฌ Due to point mutations

๐Ÿ“ˆ Leads to seasonal epidemics


#๐Ÿฆ  Influenza B Virus

๐Ÿ”น Does not undergo antigenic shift

๐Ÿ”น Not divided into subtypes

๐Ÿ”น Minor antigenic drift may occur


#๐Ÿฆ  Influenza C Virus

๐Ÿ”น Antigenically stable

๐Ÿ”น Causes mild illness

๐Ÿ”น Does not contribute to epidemics


#๐Ÿ–๐ŸŽ๐Ÿ• Reservoir of Infection

A major reservoir of influenza viruses exists in animals and birds.

๐Ÿฆ  Influenza viruses have been isolated from:

๐Ÿ– Swine

๐ŸŽ Horses

๐Ÿ• Dogs

๐Ÿˆ Cats

๐Ÿ” Domestic poultry

๐Ÿฆ… Wild birds


#๐Ÿงซ Source of Infection

The source is usually:

๐Ÿง‘โ€โš•๏ธ Clinical case

๐Ÿคง Subclinical/asymptomatic case

๐Ÿ“Œ During epidemics, many mild or asymptomatic infections occur and play a major role in transmission.

๐Ÿซ Respiratory tract secretions
(droplets, aerosols) are infective.


#โณ Period of Infectivity

The virus is present in the nasopharynx:

๐Ÿ—“๏ธ From 1 to 2 days before symptom onset

๐Ÿ—“๏ธ Up to 1 to 2 days after symptom onset


#๐Ÿง Epidemiological Determinants โ€“ Host Factors

#(a) ๐Ÿ‘ถ Age and Sex

๐Ÿ”น Influenza affects all age groups and both sexes.

๐Ÿ”น Children have a higher attack rate and play a significant role in transmission.

๐Ÿ”น Adults tend to have a lower attack rate.


#(b) ๐ŸŒ Human Mobility

๐Ÿšถ Movement of people contributes significantly to the spread of infection, especially during outbreaks and epidemics.


#(c) ๐Ÿ›ก๏ธ Immunity

๐Ÿ”น Immunity is subtype-specific
(no cross-protection between types A, B, and C)

๐Ÿงช Antibodies against:

๐Ÿ”น Haemagglutinin (HA)
๐Ÿ”น Neuraminidase (NA)

are key for protection.

๐Ÿ“Š Timeline of antibody response:

๐Ÿ—“๏ธ Appears ~7 days after infection

๐Ÿ“ˆ Peaks in ~2 weeks

๐Ÿ“‰ Declines to pre-infection level in 8โ€“12 months

#๐ŸŒ Epidemiological Determinants โ€“ Environmental Factors

#(a) ๐ŸŒฆ๏ธ Season

๐ŸŒ Northern Hemisphere:
๐Ÿ”น Epidemics commonly occur during winter months.

๐ŸŒ Southern Hemisphere:
๐Ÿ”น Occurs during winter or rainy season.

๐ŸŒด Tropical regions:
๐Ÿ”น Influenza circulates year-round, with 1 or 2 peaks typically during the rainy season.


#(b) ๐Ÿซ Overcrowding

๐Ÿ”น Facilitates transmission of the virus.

๐Ÿ“Š High attack rates observed in densely populated settings, such as:

๐Ÿซ Schools

๐Ÿ  Hostels

๐Ÿข Institutions

๐Ÿšข Ships

๐Ÿช– Military camps


#๐Ÿšถโ€โ™‚๏ธ Mode of Transmission

๐Ÿฆ  Influenza primarily spreads from person to person via:

๐Ÿ’ง Droplet infection

๐ŸŒซ๏ธ Droplet nuclei

๐Ÿ”น These droplets are generated when an infected person:

๐Ÿคง Sneezes
๐Ÿ˜ฎโ€๐Ÿ’จ Coughs
๐Ÿ—ฃ๏ธ Talks

๐Ÿ“ Portal of entry:
๐Ÿซ Respiratory tract


#โณ Incubation Period

๐Ÿ—“๏ธ Ranges from 1 to 4 days after exposure to the virus.


#๐Ÿงฌ Pathogenesis and Clinical Features

๐Ÿฆ  The virus enters through the respiratory tract, causing:

๐Ÿ”น Inflammation
๐Ÿ”น Necrosis of the tracheal and bronchial mucosa

โžก๏ธ Followed by secondary bacterial invasion

โŒ No viraemia observed


#๐Ÿค’ Common Symptoms (Influenza A & B)

๐ŸŒก๏ธ Fever

๐Ÿฅถ Chills

๐Ÿ˜– Body aches and pains

๐Ÿ˜ฎโ€๐Ÿ’จ Cough

๐Ÿ˜ซ Generalized weakness

๐Ÿ•’ Fever duration:
๐Ÿ”น 1โ€“5 days
๐Ÿ”น Average 3 days in adults


#โš ๏ธ Frequent Complications

๐Ÿ‘ƒ Acute sinusitis

๐Ÿ‘‚ Otitis media

๐Ÿ˜ค Purulent bronchitis

๐Ÿซ Pneumonia โ€“ Most serious complication


#๐Ÿšจ Suspect Pneumonia If:

๐ŸŒก๏ธ Fever persists >4โ€“5 days

๐Ÿ” Fever recurs abruptly after initial recovery


#๐Ÿšจ Reye Syndrome (Rare but Severe)

๐Ÿง  Encephalopathy with fatty liver (hepatic failure)

๐Ÿง’ Seen mainly in children aged 2โ€“16 years

๐Ÿ’Š Associated with aspirin use during viral infections

โ˜ ๏ธ Mortality rate:
๐Ÿ”น 10โ€“40%

โ“ Exact pathogenesis unknown


#๐Ÿฆ Avian Influenza (Bird Flu)

#๐ŸŒŸ Golden 5 Basics of Bird Flu

๐Ÿฆ Primary Host:
Birds, especially wild waterfowl and domestic poultry.

๐Ÿ”„ Transmission:
Mainly bird-to-bird; rare bird-to-human transmission.

๐Ÿค’ Symptoms in Humans:
Range from mild flu-like illness to severe respiratory disease.

๐ŸŒ Pandemic Risk:
Mutation or reassortment can lead to human-to-human transmission.

๐Ÿ›ก๏ธ Prevention:
Surveillance, poultry control, and public health preparedness.


#๐Ÿฆ Avian Influenza (Bird Flu) (Birdโ€™s EYE View)

๐Ÿฆ  Avian influenza refers to a large group of influenza viruses that primarily infect birds.

๐Ÿ”น Occasionally, some avian influenza viruses can infect other species such as:

๐Ÿ– Pigs
๐Ÿ‘จ Humans

โ€ฆbut this is rare.

๐Ÿ“Š The vast majority of avian influenza viruses do not infect humans.

๐Ÿฆ  The H5N1 strain is notable for its pandemic potential because it might adapt to become contagious among humans.

๐Ÿ”„ When such an adaptation happens:

โžก๏ธ The virus transitions from a bird virus to a human influenza virus.

๐ŸŒ Influenza pandemics occur when new influenza viruses adapt to human transmission.

๐Ÿ‘จโ€โš•๏ธ Health experts have been closely monitoring the H5N1 virus for almost 15 years due to its severity.

๐Ÿ“Œ Currently:

๐Ÿ”น Does not easily jump from birds to humans

๐Ÿ”น Does not spread efficiently among humans

โš ๏ธ However:

Once a fully contagious virus emerges, its global spread is considered inevitable.


#๐Ÿ”„ Transmission of Avian Influenza

๐Ÿ‘จ Human infections with avian influenza viruses are rare but sporadically reported.

๐Ÿฆ  Infection usually occurs through direct contact with:

๐Ÿ” Infected live or dead poultry birds

OR

๐Ÿช Contaminated environments
(e.g., live bird markets)


#โณ Incubation Period

๐Ÿ—“๏ธ Typically ranges from 2 to 5 days after exposure.


#๐Ÿ”ฌ Diagnosis

โœ… Confirmed by:

๐Ÿงช RT-PCR
(Reverse Transcriptase Polymerase Chain Reaction)

โš ๏ธ Rapid Influenza Diagnostic Tests (RDTs):

๐Ÿ”น Available
๐Ÿ”น Have lower sensitivity compared to RT-PCR.


#๐Ÿ’Š Treatment

๐Ÿฆ  Antiviral drugs such as:

๐Ÿ’Š Oseltamivir

๐Ÿ’Š Zanamivir

can:

๐Ÿ”น Reduce the duration of viral replication

๐Ÿ”น Improve chances of survival


#๐Ÿ›ก๏ธ Prevention

๐Ÿงผ Regular hand washing with proper drying

๐Ÿ˜ท Good respiratory hygiene
(cover mouth and nose when coughing or sneezing)

๐Ÿ  Early self-isolation if sick

๐Ÿšซ Avoid close contact with infected individuals

๐Ÿšซ Avoid touching the eyes, mouth, and nose


#๐Ÿ’‰ Vaccine

๐Ÿ“… In 2007, a vaccine for bird flu was licensed for people 18 to 64 years old.

๐Ÿ’‰ It is an inactivated influenza vaccine administered in:

๐Ÿ”น Two doses
๐Ÿ”น 28 days apart


#โš ๏ธ Common Side Effects

๐Ÿ’‰ Pain and tenderness at injection site

๐Ÿค• Headache

๐Ÿ’ช Muscle pain

๐Ÿ˜ซ General malaise


๐Ÿ“Œ Other vaccines have been approved, but because H5N1 mutates continuously, existing vaccines may not always be effective during a pandemic.

#๐Ÿ– Pandemic Influenza A (H1N1) 2009 (Swine Flu)

#๐ŸŒŸ Golden 5 Basics of Pandemic Influenza A (H1N1) 2009

๐Ÿงฌ Origin:
Swine-origin influenza virus with novel genetic makeup.

๐Ÿ‘ฅ Population Impact:
Mainly affects children, young and middle-aged adults due to low immunity.

๐Ÿซ Pathogenicity:
Ability to infect lower respiratory tract causing severe pneumonia.

๐ŸŒ Global Spread:
Rapid worldwide dissemination; declared pandemic in 2009.

๐Ÿ“Œ Current Status:
Now circulates as a seasonal virus with ongoing surveillance.


#๐Ÿ– Pandemic Influenza A (H1N1) 2009 (Swine Flu) (Birdโ€™s EYE View)

๐Ÿ”น The H1N1 2009 virus differs from seasonal influenza in two key ways:

1๏ธโƒฃ Low pre-existing immunity in most people led to infection across a wider age range, especially in children and young adults.

2๏ธโƒฃ The virus can infect the lower respiratory tract, causing rapidly progressive pneumonia, notably in children and young to middle-aged adults.

๐Ÿ“… The virus emerged in March 2009 and spread quickly worldwide.

๐Ÿ“… On 11th June 2009, WHO declared it a pandemic.

๐ŸŒ The world is now in the post-pandemic period.

๐Ÿ“Š In India, the virus causes local outbreaks; in 2020, India reported:

๐Ÿ”น 2,752 cases
๐Ÿ”น 44 deaths
๐Ÿ”น Case fatality rate of 1.6%

๐Ÿ“Œ Based on past pandemics, H1N1 2009 is expected to circulate seasonally for years.

โš ๏ธ Though current concern has diminished, national health vigilance remains critical due to unpredictable virus behavior.

๐Ÿ“… On 26th September 2011, WHO renamed it Influenza A (H1N1) pdm09.


#โณ Incubation Period

๐Ÿ—“๏ธ Typically 1 to 4 days

๐Ÿ“Œ Can range up to 7 days


#๐Ÿ“‹ Case Definitions for Influenza A (H1N1) 2009


#๐Ÿง‘โ€โš•๏ธ 1. Suspected Case

A person with acute febrile respiratory illness (fever โ‰ฅ 38โ„ƒ) 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.


#๐Ÿงช 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.


#โœ… 3. Confirmed Case

A person with acute febrile respiratory illness with laboratory confirmation of influenza A (H1N1) 2009 infection by WHO-approved tests:

๐Ÿ”น Real-Time PCR

๐Ÿ”น Viral culture

๐Ÿ”น Four-fold rise in influenza A (H1N1) specific neutralizing antibodies


#๐Ÿฉบ Clinical Features of Influenza A (H1N1) 2009

The disease presents a wide clinical spectrum, ranging from:

๐Ÿ”น Mild, non-febrile upper respiratory illness

๐Ÿ”น Febrile influenza-like illness (ILI)

๐Ÿ”น Severe or fatal complications, including rapidly progressive pneumonia.

๐Ÿ“Š Case fatality rate:
Approximately 0.5%, though this may vary.


#๐Ÿงพ (a) Uncomplicated Influenza

#๐Ÿค’ Influenza-Like Illness (ILI) Symptoms

๐ŸŒก๏ธ Fever

๐Ÿ˜ฎโ€๐Ÿ’จ Cough

๐Ÿ˜ฃ Sore throat

๐Ÿ‘ƒ Rhinorrhoea (runny nose)

๐Ÿค• Headache

๐Ÿ’ช Muscle pain

๐Ÿ˜ซ Malaise (general discomfort)

๐Ÿšซ No shortness of breath or dyspnoea (difficulty breathing)

๐Ÿ“Œ Patients may have some or all of these symptoms.


#๐Ÿฝ๏ธ Gastrointestinal Illness

๐Ÿ”น Diarrhoea and/or vomiting, especially common in children

๐Ÿ”น Occurs without evidence of dehydration


#โš ๏ธ (b) Complicated or Severe Influenza

#๐Ÿฉบ Clinical and Radiological Signs

๐Ÿ˜ฎโ€๐Ÿ’จ Shortness of breath (dyspnoea)

๐Ÿ’จ Rapid breathing (tachypnea)

๐Ÿฉธ Low oxygen levels (hypoxia)

๐Ÿซ Radiological evidence of lower respiratory tract disease (e.g., pneumonia)

๐Ÿง  Central nervous system involvement
(e.g., encephalopathy, encephalitis)

๐Ÿ’ง Severe dehydration

๐Ÿฆ  Secondary complications such as:

๐Ÿ”น Renal failure

๐Ÿ”น Multi-organ failure

๐Ÿ”น Septic shock

Other complications:

๐Ÿ’ช Rhabdomyolysis (muscle breakdown)

โค๏ธ Myocarditis (heart inflammation)


#๐Ÿฅ Exacerbation of Underlying Chronic Diseases

Includes:

๐Ÿซ Asthma

๐Ÿซ Chronic Obstructive Pulmonary Disease (COPD)

๐Ÿงซ Chronic liver or kidney failure

๐Ÿฌ Diabetes

โค๏ธ Cardiovascular conditions

๐Ÿ“Œ Any clinical condition requiring hospital admission for management.

โš ๏ธ Presence of signs indicating progressive disease.


#๐Ÿšจ Signs Requiring Urgent Medical Review

Patients with initially uncomplicated influenza may rapidly (within 24 hours) develop severe illness.


#๐Ÿซ (a) Oxygen Impairment or Cardiopulmonary Insufficiency

๐Ÿ˜ฎโ€๐Ÿ’จ Shortness of breath (with activity or at rest)

๐Ÿ˜ฐ Difficulty breathing

๐Ÿ”ต Cyanosis (turning blue)

๐Ÿฉธ Bloody or discolored sputum

๐Ÿ’” Chest pain

๐Ÿ“‰ Low blood pressure

๐Ÿ‘ถ In children: fast or labored breathing

๐Ÿ“Ÿ Hypoxia detected by pulse oximetry


#๐Ÿง  (b) Central Nervous System (CNS) Complications

๐Ÿง  Altered mental status

๐Ÿ˜ด Unconsciousness or drowsiness

โš ๏ธ Difficulty awakening

โšก Recurring or persistent seizures (convulsions)

๐Ÿ˜ต Confusion

๐Ÿ’ช Severe weakness or paralysis


#๐Ÿฆ  (c) Sustained Virus Replication or Secondary Bacterial Infection

๐ŸŒก๏ธ Persistent high fever

โณ Symptoms lasting beyond 3 days

๐Ÿงช Laboratory evidence or clinical signs indicating ongoing viral or bacterial infection


#โš ๏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:

๐Ÿ‘ถ Infants and young children, especially those under 2 years

๐Ÿคฐ Pregnant women

๐Ÿซ Persons of any age with chronic pulmonary diseases
(e.g., asthma, COPD)

โค๏ธ Persons of any age with chronic cardiac diseases
(e.g., congestive heart failure)

๐Ÿฌ Persons with metabolic disorders
(e.g., diabetes)

๐Ÿงซ Persons with:

๐Ÿ”น Chronic renal or hepatic disease

๐Ÿ”น Certain neurological conditions
(neuromuscular, neurocognitive, seizure disorders)

๐Ÿฉธ Haemoglobinopathies

๐Ÿ›ก๏ธ Immunosuppression
(due to HIV, immunosuppressive medication, malignancy, etc.)

๐Ÿ’Š Children on chronic aspirin therapy

๐Ÿ‘ด Persons aged 65 years and older

โš–๏ธ Individuals who are obese, especially those who are morbidly obese

#๐Ÿงช Laboratory Diagnosis of Pandemic Influenza A (H1N1) 2009

#โญ Importance

๐Ÿ”ฌ Early and accurate lab diagnosis is crucial for:

โœ”๏ธ Proper case management
โœ”๏ธ Infection control
โœ”๏ธ Antiviral treatment decisions
โœ”๏ธ Avoiding unnecessary antibiotics


#๐Ÿงซ Diagnostic Tests

#๐Ÿงช RT-PCR (Reverse Transcriptase Polymerase Chain Reaction)

โœ”๏ธ Most sensitive and timely test for detecting infection.


#โšก Rapid Influenza Diagnostic Tests (RIDTs)

โœ”๏ธ Widely available
โš ๏ธ Less sensitive

โ— Negative results do not rule out infection and should not delay treatment or infection control.


#๐Ÿงด Specimen Collection

๐Ÿ“Œ Respiratory samples are required.

#Upper respiratory tract samples:

๐Ÿ‘ƒ Nasal swabs

๐Ÿ‘ƒ Nasopharyngeal swabs

๐Ÿ‘„ Throat swabs


#Lower respiratory tract samples:

๐Ÿซ Tracheal aspirates

๐Ÿซ Bronchial aspirates

โœ”๏ธ Provide higher diagnostic yield in patients with lower respiratory symptoms.


#๐Ÿฉบ Clinical Diagnosis

๐Ÿ“Œ When influenza is widespread:

โœ”๏ธ Uncomplicated cases can be diagnosed clinically and epidemiologically.


#๐Ÿ“… Follow-Up Advice

Patients should be advised to:

๐Ÿ”„ Seek follow-up if symptoms worsen

โณ Or do not improve within 72 hours


#๐ŸŽฏ Testing Prioritization

Testing should be prioritized for:

โš ๏ธ At-risk groups

โš ๏ธ Severe or progressive illness

๐Ÿ“Œ Results guide:

โœ”๏ธ Infection control

โœ”๏ธ Management of close contacts


#โš ๏ธ Important Note

๐Ÿšซ Diagnostic testing should never delay:

โœ”๏ธ Infection control measures

โœ”๏ธ Initiation of antiviral treatment

If clinical and epidemiological suspicion is high.


#๐Ÿฆ  Infection Control Measures

#๐Ÿ”„ Transmission

Pandemic H1N1 spreads similarly to:

๐Ÿฆ  Seasonal influenza A and B viruses.


#๐Ÿงผ Standard Precautions

โœ”๏ธ Practice strict hand hygiene with soap and water or alcohol-based sanitizer.

โœ”๏ธ Cover mouth and nose with tissue or handkerchief when coughing or sneezing.

โœ”๏ธ Ill persons should wear a face mask when going out in public
(e.g., to seek medical care) to reduce virus spread.


#๐Ÿซ Aerosol-Generating Procedures

Examples:

๐Ÿ”น Bronchoscopy

๐Ÿ”น Respiratory tract aspiration

Required protection:

๐Ÿ˜ท Use particulate respirators
(N95, FFP2, or equivalent)

๐Ÿ‘“ Wear eye protection

๐Ÿงฅ Wear gown

๐Ÿงค Wear gloves

๐ŸŒฌ๏ธ Perform procedures in well-ventilated rooms
(natural or mechanical ventilation).


#๐Ÿฅ Isolation Precautions for Hospitalized Patients

๐Ÿ“… Continue isolation for:

โœ”๏ธ 7 days after illness onset

OR

โœ”๏ธ At least 24 hours after fever and respiratory symptoms resolve, whichever is longer.


#โš ๏ธ Special Cases

For prolonged or complicated illness (e.g., pneumonia):

โœ”๏ธ Maintain precautions until clinical improvement.

๐Ÿ›ก๏ธ Immunosuppressed patients require special attention

Because:

๐Ÿ”น They may shed virus longer

๐Ÿ”น Higher risk of antiviral resistance


#๐Ÿ’‰ Influenza Vaccine

There are currently three main technologies used to produce influenza vaccines:


#๐Ÿฅš Egg-Based Vaccines

โœ”๏ธ Inactivated influenza vaccines (IIVs)

Prepared from:

๐Ÿฅš Virus particles grown in embryonated chicken eggs.

Process:

๐Ÿ”ฌ Virus particles are inactivated

๐Ÿงช Detergent-solubilized

โžก๏ธ To isolate:

๐Ÿ”น Haemagglutinin (HA)

๐Ÿ”น Neuraminidase (NA) proteins


#๐ŸŒก๏ธ Live Attenuated Influenza Vaccine (LAIV)

โœ”๏ธ Made from weakened virus strains grown in eggs.


#๐Ÿงซ Cell-Cultured Vaccines

Produced by:

๐Ÿงฌ Growing influenza viruses in animal cell cultures instead of eggs.

Advantages:

โšก Faster manufacturing process.

โš ๏ธ Note:

Although no hen's eggs are used, trace amounts of egg protein might still be present.


#๐Ÿงฌ Recombinant Influenza Vaccines

Method:

๐Ÿ”ฌ Isolates the HA gene and proteins

โžก๏ธ Stimulates immune response without using chicken eggs.

Produced in:

๐Ÿฆ  Insect cell cultures.

Feature:

๐Ÿ“Š Contain about three times more HA than standard-dose vaccines.

โœ”๏ธ Recombinant vaccine is the only completely egg-free influenza vaccine.


#๐Ÿงฌ Vaccine Composition

Influenza vaccines include components from:

๐Ÿฆ  Human influenza A viruses

๐Ÿฆ  Influenza B viruses


#๐Ÿ“… Vaccine Update Process

Formulation is reviewed and updated annually based on:

๐Ÿ”น The viruses currently circulating in the population

๐Ÿ”น How widely these viruses are spreading

๐Ÿ”น Effectiveness of the previous yearโ€™s vaccine


๐ŸŒ The World Health Organization (WHO) provides recommendations on which specific virus strains should be included each year.


#๐Ÿ’‰ Inactivated Influenza Vaccine (IIVs)

#๐Ÿ“˜ Overview

๐Ÿ“… Available since the 1940s


#๐Ÿงฌ Trivalent IIVs contain:

๐Ÿ”น Influenza A (H1N1)

๐Ÿ”น Influenza A (H3N2)

๐Ÿ”น One Influenza B strain


#๐Ÿงฌ Quadrivalent Vaccines

๐Ÿ“… Introduced in 2013โ€“2014

โœ”๏ธ Add:

๐Ÿ”น A second B strain

โžก๏ธ Provide broader protection.


#๐Ÿ’‰ Administration

๐Ÿ“ Given via:

๐Ÿ’‰ Intramuscular (IM) injection

๐Ÿ’‰ Intradermal (ID) injection


#๐Ÿ“ Doses

๐Ÿ‘ถ Pediatric: 0.25 ml

๐Ÿ‘จ Adult: 0.5 ml


#๐Ÿ“… Dosage Schedule

โœ”๏ธ One dose annually for persons 9 years and older

๐Ÿ‘ถ Children 6 months to 8 years receiving vaccine for first time:

๐Ÿ’‰ Two doses

๐Ÿ“… 28 days apart


โœ”๏ธ Annual immunization is recommended.

#๐Ÿ’‰ Inactivated Influenza Vaccine (IIVs)

#๐Ÿ“Š Effectiveness

โœ”๏ธ Approximately 60% effective among healthy persons under 65 years.

โณ Protection starts about 14 days after vaccination.

๐Ÿ›ก๏ธ Immunity lasts 6โ€“12 months.

โš ๏ธ Vaccinated individuals can still get infected:

๐Ÿ”น Shortly before vaccination

๐Ÿ”น Shortly after vaccination

๐Ÿ”น By influenza strains not covered by the vaccine.


#๐Ÿ‘ด Effectiveness in Elderly Persons

โœ”๏ธ 50โ€“60% effective in preventing hospitalization

โœ”๏ธ 80% effective in preventing death


#๐Ÿ“ฆ Storage

๐ŸŒก๏ธ Store at 2โ€“8โ„ƒ

๐Ÿšซ Do not freeze


#๐Ÿ‘ด Special Vaccines for Older Adults (65+ years)

Two vaccines designed to improve immune response:


#๐Ÿ’‰ High-Dose IIV (HD-IIV)

๐Ÿ“Š Contains four times the HA antigen of standard vaccines.


#๐Ÿ’‰ Adjuvanted IIV (aIIV)

๐Ÿงช Contains an adjuvant to boost immune response.


โœ”๏ธ Both are trivalent vaccines.

๐Ÿ“Š HD-IIV shown to be 24% more effective than standard vaccines in preventing lab-confirmed influenza in older adults.


#โš ๏ธ Side Effects

#Common Side Effects

๐Ÿ’‰ Local soreness

๐Ÿ’‰ Swelling

๐Ÿ’‰ Redness at injection site

๐ŸŒก๏ธ Mild fever

๐Ÿ’ช Muscle/joint aches

๐Ÿค• Headache

โณ Usually mild and last 1โ€“2 days.

๐Ÿ“Œ Children tend to have these side effects more often than elderly.


#Rare Side Effects

โš ๏ธ Allergic reactions such as:

๐Ÿ”น Hives

๐Ÿ”น Swelling

๐Ÿ”น Asthma

๐Ÿ”น Severe systemic hypersensitivity


#๐Ÿšซ Contraindications โ€” Inactivated Influenza Vaccine (IIVs)

IIVs should NOT be given to:

โŒ People with severe allergy to chicken eggs

โŒ Those with history of:

๐Ÿ”น Anaphylactic reaction

๐Ÿ”น Severe allergic reaction to any vaccine component

โŒ Persons who had severe reaction to prior influenza vaccine.

โŒ People who developed Guillain-Barrรฉ Syndrome (GBS) within 6 weeks after influenza vaccination.

โŒ Children under 6 months of age
(vaccine not approved for this age)

โŒ People with moderate to severe illness with fever
(vaccination should wait until recovery).


#๐ŸŒก๏ธ Live Attenuated Influenza Vaccine (LAIV)

#๐Ÿ“˜ Overview

๐Ÿ“… Approved for use in 2003.

Contains:

๐Ÿฆ  Same influenza viruses as inactivated vaccines

But:

๐Ÿงฌ Cold-adapted to replicate in nasopharyngeal mucosa


#๐Ÿงช Production

โœ”๏ธ Grown in chicken eggs

โš ๏ธ Contains residual egg protein


#๐Ÿ’‰ Administration

๐Ÿ“ Delivered as:

๐Ÿ‘ƒ Single-dose nasal spray

Method:

๐Ÿ‘ƒ Half sprayed into each nostril


#๐Ÿงด Composition

๐Ÿšซ Does not contain:

โŒ Thimerosal

โŒ Other preservatives


#๐Ÿ‘ฅ Approved Age Group

โœ”๏ธ Healthy, non-pregnant persons aged:

๐Ÿ“… 2 to 49 years


#๐Ÿงซ Virus Shedding

๐Ÿ‘ถ Vaccinated children may shed vaccine virus in:

๐Ÿ‘ƒ Nasal secretions

โณ For up to 3 weeks


#๐Ÿ“Š Effectiveness of LAIV

โœ”๏ธ 87% effective against culture-confirmed influenza in children aged 60โ€“84 months.

โœ”๏ธ Reduces:

๐Ÿ‘‚ Febrile otitis media by 27%

๐Ÿ‘‚ Otitis media requiring antibiotics by 28%


#โš ๏ธ Side Effects โ€” LAIV

#Common Side Effects

๐Ÿ‘ƒ Runny nose

๐Ÿ‘ƒ Nasal congestion

๐Ÿ˜ฎโ€๐Ÿ’จ Cough


#Less Common Side Effects

๐Ÿ˜ฃ Sore throat

๐ŸŒก๏ธ Low-grade fever

๐Ÿ˜  Irritability

๐Ÿ’ช Muscle aches

๐Ÿค• Headache


#Reported in Some Children

โš ๏ธ Wheezing

โš ๏ธ Vomiting episodes


#๐Ÿšซ Contraindications โ€” LAIV

LAIV should not be given to:

โŒ Children under 2 years

โŒ Persons 50 years and older


#โŒ Persons with Chronic Medical Conditions

Including:

๐Ÿซ Asthma

๐ŸŒฌ๏ธ Recent wheezing

๐Ÿซ Reactive airway disease

โค๏ธ Chronic pulmonary or cardiovascular diseases

๐Ÿฌ Metabolic diseases (e.g., diabetes)

๐Ÿงซ Renal disease

๐Ÿฉธ Hemoglobinopathies
(e.g., sickle cell disease)


#โŒ Additional Contraindications

๐Ÿ’Š Children/adolescents on long-term aspirin therapy
(due to risk of Reye syndrome)

๐Ÿ›ก๏ธ Immunosuppressed persons
(HIV, immunosuppressive therapy)

๐Ÿคฐ Pregnant women

๐Ÿฅš Persons with severe allergy to eggs

โš ๏ธ Persons with history of Guillain-Barrรฉ Syndrome (GBS) within 6 weeks of prior influenza vaccine
(precaution)


๐Ÿ“Œ Note

Persons in these groups should receive:

๐Ÿ’‰ Inactivated influenza vaccine instead


#๐ŸŒ WHO Recommendations on Influenza Vaccination Priorities

#๐Ÿฅ Vaccinate Health Care Workers First

Purpose:

โœ”๏ธ Protect health infrastructure

โœ”๏ธ Prevent hospital outbreaks


๐Ÿคฐ Pregnant women

๐Ÿงซ Individuals >6 months old with chronic medical conditions

๐Ÿง‘ Healthy young adults (15โ€“49 years)

๐Ÿ‘ถ Healthy children

๐Ÿ‘จ Healthy adults (49โ€“65 years)

๐Ÿ‘ด Healthy adults >65 years


#๐Ÿ’‰ COVID-19 Vaccine Interaction

โณ Wait at least 7 days between:

๐Ÿ’‰ COVID-19 vaccine

AND

๐Ÿ’‰ Influenza vaccine

#๐Ÿ’Š Treatment of Pandemic Influenza A (H,N) 2009

#๐Ÿงพ Key Principles of Clinical Management:

โœ”๏ธ Provide basic symptomatic care (e.g., fever and pain relief).

๐Ÿงฌ Use antiviral drugs early, especially for high-risk populations.

๐Ÿฆ  Administer antimicrobials to treat or prevent co-infections.

๐Ÿ“Š Maintain proactive monitoring for signs of disease progression.


#๐Ÿฅ Hospital Care:

๐Ÿซ Early supplemental oxygen therapy to correct hypoxemia, with continuous monitoring of oxygen saturation during triage and hospitalization, if possible.

๐Ÿ’ง Careful fluid replacement to maintain hydration.

๐Ÿ’Š Use of antimicrobials for other infections causing severe respiratory distress.

๐Ÿซ Severely ill patients may require mechanical ventilation and intensive care support due to respiratory distress.


#๐Ÿงฌ Antiviral Therapy for Pandemic Influenza A (H,N) 2009

#๐Ÿฆ  Virus Susceptibility:

#โœ”๏ธ Susceptible to neuraminidase inhibitors (NAIs):

๐Ÿ’Š Oseltamivir

๐Ÿ’Š Zanamivir


#โŒ Resistant to M2 inhibitors:

๐Ÿšซ Amantadine

๐Ÿšซ Rimantadine


#๐Ÿ’Š Antiviral Therapy โ€” Treatment Recommendations


#๐Ÿšจ Severe or Progressive Illness:

โœ”๏ธ Treat all patients with oseltamivir as soon as possible

๐Ÿ“Œ Includes:

๐Ÿคฐ Pregnant women

๐Ÿ‘ถ Children under 2 years (including neonates)


#โš ๏ธ If Severe Illness Not Responding:

Consider:

๐Ÿ’Š Higher doses (e.g., 150 mg twice daily in adults)

โณ Longer treatment duration


#๐Ÿ”„ If Oseltamivir Unavailable or Resistant Virus:

๐Ÿ’Š Use zanamivir


#๐Ÿง‘โ€โš•๏ธ High-Risk Patients with Uncomplicated Illness:

โœ”๏ธ Treat early with:

๐Ÿ’Š Oseltamivir OR
๐Ÿ’Š Zanamivir


#๐Ÿง Patients Not at High Risk with Uncomplicated Illness:

๐Ÿšซ Antiviral treatment is generally not necessary.

โœ”๏ธ If used, start early for best outcomes.


#โš ๏ธ Additional Notes on Antivirals

๐Ÿ“Œ Start antiviral treatment immediately based on clinical suspicion

๐Ÿšซ Do NOT wait for laboratory confirmation


#๐Ÿ” If Persistent Severe Illness Despite Oseltamivir:

Alternative options (with caution):

๐Ÿ’‰ Intravenous zanamivir

๐Ÿ’‰ Peramivir

๐Ÿ’Š Ribavirin
โš ๏ธ Should NOT be used alone and NOT in pregnant women


โš ๏ธ Zanamivir powder for inhalation should NOT be nebulized due to lactose content affecting ventilator function.


#๐Ÿ’‰ Standard Oseltamivir Antiviral Treatment Regimens

#๐Ÿ‘ถ Infants (<1 year)

Age Group

Dose

Frequency

Duration

0โ€“1 month

2 mg/kg

Twice daily

5 days

1โ€“3 months

2.5 mg/kg

Twice daily

5 days

3โ€“12 months

3 mg/kg

Twice daily

5 days


#๐Ÿ‘ง Children (1โ€“12 years by weight)

Weight

Dose

Frequency

Duration

โ‰ค15 kg

30 mg

Twice daily

5 days

15โ€“23 kg

45 mg

Twice daily

5 days

24โ€“40 kg

60 mg

Twice daily

5 days

>40 kg

75 mg

Twice daily

5 days


#๐Ÿง‘ Adults

๐Ÿ’Š 75 mg orally

๐Ÿ” Twice daily

โณ 5 days


#๐Ÿงช Zanamivir Dosing for Influenza Treatment

๐Ÿ“Œ Indication: Treatment of influenza in adults and children aged โ‰ฅ5 years

๐Ÿ’จ Route: Inhalation (Diskhaler)


๐Ÿง‘ Adults & children (โ‰ฅ5 years):

๐Ÿ’จ 2 inhalations (2 ร— 5 mg = 10 mg)

๐Ÿ” Twice daily (morning and evening)

โณ Duration: 5 days


#๐Ÿ›ก๏ธ Chemoprophylaxis Regimen with Oseltamivir

๐Ÿ“Œ Indication:

โœ”๏ธ Healthcare personnel
โœ”๏ธ Close contacts of suspected, probable, or confirmed cases

โณ Duration:

๐Ÿ—“๏ธ Once daily for 10 days after last exposure


#๐Ÿ‘ถ Infants (<1 year)

Age

Dose

<3 months

Not recommended (unless critical)

3โ€“5 months

20 mg once daily

6โ€“11 months

25 mg once daily


#๐Ÿ‘ง Children โ‰ฅ1 year (by weight)

Weight

Dose

<15 kg

30 mg once daily

15โ€“23 kg

45 mg once daily

24โ€“40 kg

60 mg once daily

>40 kg

75 mg once daily


#๐Ÿ“Š Influenza Surveillance

#๐ŸŽฏ Purpose of Surveillance:


#๐Ÿงฌ Monitor Circulating Strains

๐Ÿ“Š Track prevalence and types of influenza viruses in circulation

๐Ÿงฌ Detect emergence of new or variant strains important for vaccine formulation


#๐Ÿ“ˆ Estimate Impact

๐Ÿ“Š Assess burden of disease in terms of:

๐Ÿง‘โ€โš•๏ธ Morbidity (illness rates)

โšฐ๏ธ Mortality (death rates)

๐Ÿ’ฐ Economic losses (healthcare costs, lost productivity)


#๐Ÿšจ Early Outbreak Detection

โš ๏ธ Identify and respond promptly to influenza outbreaks


#๐Ÿ›ก๏ธ Guide Control Measures

๐Ÿ“Œ Enable timely public health action including:

๐Ÿ’‰ Vaccination campaigns

๐Ÿ’Š Antiviral distribution

๐Ÿ“ข Public advisories


#๐Ÿ”‘ Key Takeaways

๐Ÿฆ  Influenza is a contagious respiratory virus with seasonal and pandemic forms.

๐Ÿ’ง Transmission is via droplets and contact; incubation is 1โ€“4 days.

๐Ÿค’ Symptoms include fever, cough, sore throat; severe disease in high-risk groups.

๐Ÿ’Š Treatment includes supportive care and antivirals (oseltamivir/zanamivir).

๐Ÿ’‰ Vaccination (IIV/LAIV) is key prevention; annual doses recommended.

๐Ÿ›ก๏ธ Chemoprophylaxis for exposed high-risk individuals and healthcare workers.

๐Ÿ“Š Surveillance tracks virus trends and informs vaccine updates.


#๐Ÿ“š References

  1. WHO. Weekly Epidemiological Record, No. 47, 23 Nov 2012.

  2. Papadakis MA, McPhee SJ. Current Medical Diagnosis and Treatment, 53rd ed. 2014. Lange Publication.

  3. WHO. Fact Sheet, March 14, 2018.

  4. WHO. Technical Report Series, No. 642, 1980.

  5. WHO. Bulletin of the World Health Organization, 1985; 63(1): 51.

  6. Jawetz E, et al. Medical Microbiology, 22nd ed. Lange Medical Publication, 2001.

  7. Jawetz E, et al. Medical Microbiology, 28th ed. Lange Medical Publication, 2019.

  8. WHO. Weekly Epidemiological Record, No. 49/50, Oct 14, 2005.

  9. WHO. Weekly Epidemiological Record, No. 41, 9 Oct 2009.

  10. Government of India. National Health Profile 2021. Central Bureau of Health Intelligence, Ministry of Health and Family Welfare, New Delhi.

  11. WHO. Recommendations for the Post-Pandemic Period: Pandemic (H1N1) 2009 Briefing Note 23, 2010.

  12. WHO. Weekly Epidemiological Record, No. 43, 21 Oct 2011.

  13. Government of India. Guidelines for Swine Flu (Influenza A H1N1). Ministry of Health and Family Welfare, New Delhi, 2010.

  14. WHO. Clinical Management of Human Infection with Pandemic (H1N1) 2009: Revised Guidance, November 2009.

  15. McPhee SJ, et al. Current Medical Diagnosis and Treatment, 49th ed. Lange Medical Publication, 2010.

  16. Carter A. Flu Vaccine. Medically reviewed, 8 Sept 2020.

  17. Yung AD, et al. U.S. Pharmacist: The Pharmacist Resource for Clinical Excellence, Nov 12, 2019; 44(11): 18โ€“22.

  18. CDC. Epidemiology and Prevention of Vaccine-Preventable Diseases, April 15, 2019.

  19. WHO. Safety of Pandemic (H1N1) 2009 Vaccines, Oct 30, 2009.

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