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Influenza

High EvidenceUpdated: 2025-12-24

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Red Flags

  • Severe viral pneumonia (hypoxia, respiratory failure)
  • Secondary bacterial pneumonia (Staphylococcus aureus)
  • Rapid deterioration or confusion
  • High-risk groups (elderly, immunocompromised, pregnant)
  • Persistent fever beyond 5-7 days
Overview

Influenza

1. Clinical Overview

Summary

Influenza is an acute respiratory infection caused by influenza viruses (types A, B, and rarely C). It causes seasonal epidemics and occasional pandemics, resulting in significant morbidity and mortality worldwide. Influenza A is responsible for most epidemics and all pandemics due to antigenic variation. Clinical presentation includes abrupt onset of fever, myalgia, headache, and respiratory symptoms. Most cases are self-limiting, but complications including viral pneumonia and secondary bacterial infection can be fatal. Antivirals (oseltamivir) are effective if started within 48 hours of symptom onset, particularly in high-risk groups. Annual vaccination is the cornerstone of prevention. [1,2]

Key Facts

  • Incidence: 5-10% of adults, 20-30% of children annually during seasonal epidemics. [3]
  • Mortality: 290,000-650,000 deaths globally per year.
  • Causative Agents: Influenza A (most common, pandemics), Influenza B (seasonal), Influenza C (rare, mild).
  • Classification: A subtypes by Haemagglutinin (H1-18) and Neuraminidase (N1-11); e.g., H1N1, H3N2.
  • Transmission: Respiratory droplets; incubation 1-4 days.
  • Treatment: Supportive care; antivirals (oseltamivir) within 48 hours for high-risk.
  • Prevention: Annual influenza vaccination.

Clinical Pearls

Antigenic Drift vs Shift: Drift = minor mutations causing seasonal variants (reason for annual vaccine). Shift = major reassortment creating novel subtypes (pandemic potential, e.g., 2009 H1N1 "Swine Flu").

The 48-Hour Window: Antivirals are most effective if started within 48 hours of symptom onset. After 48 hours, benefit is reduced but may still help in severe disease or high-risk patients.

Secondary Bacterial Pneumonia: Consider if patient improves then deteriorates ("biphasic illness"). Staphylococcus aureus (including MRSA) and Streptococcus pneumoniae are common culprits.

Flu vs Cold: Influenza = abrupt onset, high fever, severe myalgia, prostration. Common cold = gradual onset, milder, predominantly nasal symptoms.


2. Epidemiology

Global Burden

  • Annual Cases: 1 billion infections globally.
  • Symptomatic Cases: 3-5 million severe cases per year.
  • Deaths: 290,000-650,000 deaths annually (mostly in high-risk groups).
  • Seasonality: Northern hemisphere: November-March; Southern hemisphere: May-September.

Age and Risk Group Distribution

GroupRisk
Children less than 5 yearsHigh attack rate; hospitalisations
Adults at least 65 yearsHighest mortality (80-90% of deaths)
Pregnant womenIncreased severity; risk to fetus
ImmunocompromisedProlonged shedding, complications
Chronic conditionsCOPD, heart disease, diabetes, renal disease
Healthcare workersHigh exposure; transmission risk

Transmission

  • Route: Respiratory droplets (coughing, sneezing, talking).
  • Contact: Fomites (hands, surfaces) → mucous membranes.
  • Incubation: 1-4 days (mean 2 days).
  • Infectious Period: 1 day before symptoms to 5-7 days after.
  • Basic Reproduction Number (R₀): 1.2-1.4 for seasonal; higher for pandemics.

Pandemic History

PandemicYearSubtypeDeaths
Spanish Flu1918H1N150-100 million
Asian Flu1957H2N21-2 million
Hong Kong Flu1968H3N21 million
Swine Flu2009H1N1pdm09150,000-575,000

3. Pathophysiology

Step 1: Viral Entry and Attachment

  • Inhalation: Virus inhaled in respiratory droplets.
  • Attachment: Haemagglutinin (HA) binds to sialic acid receptors on respiratory epithelium.
  • Tropism: Influenza A binds α2,3-sialic acid (respiratory); α2,6 (upper respiratory - human strains).

Step 2: Cell Entry and Replication

  • Endocytosis: Virus enters cell via receptor-mediated endocytosis.
  • Fusion: Acidification triggers HA conformational change → membrane fusion.
  • Uncoating: Viral RNA released into cytoplasm.
  • Replication: Viral RNA → nuclear replication → progeny virions.

Step 3: Viral Release

  • Budding: New virions bud from cell membrane.
  • Neuraminidase (NA): Cleaves sialic acid → virion release.
  • NA Inhibitors: Oseltamivir/zanamivir block this step.

Step 4: Host Immune Response

  • Innate Immunity: Type I interferons, NK cells, macrophages.
  • Cytokine Storm: Excessive inflammatory response in severe cases.
  • Adaptive Immunity: Antibodies (anti-HA neutralising), T-cells.

Step 5: Tissue Damage and Symptoms

  • Epithelial Destruction: Ciliary dysfunction, impaired mucociliary clearance.
  • Inflammation: Fever, myalgia, malaise (cytokine-mediated).
  • Complications: Secondary bacterial infection, ARDS, multi-organ failure.

Antigenic Variation

Antigenic Drift

  • Minor point mutations in HA and NA genes.
  • Escapes pre-existing immunity.
  • Causes seasonal epidemics; reason for annual vaccine update.

Antigenic Shift

  • Reassortment between human/animal influenza viruses.
  • Creates novel subtypes (no population immunity).
  • Causes pandemics.

4. Clinical Presentation

Classic Symptoms

SymptomFrequencyNotes
Fever90-95%Abrupt onset, 38-40°C; lasts 3-5 days
Myalgia80-90%Severe muscle aches; back, legs
Headache80%Frontal or generalised
Malaise/Fatigue80-90%Prominent; may persist weeks
Dry cough70-80%Persistent; may become productive
Sore throat50-60%Pharyngeal inflammation
Rhinorrhoea30-50%Less prominent than common cold
Chills/Rigors50-60%With fever

Clinical Course

Influenza vs Common Cold

FeatureInfluenzaCommon Cold
OnsetAbruptGradual
FeverHigh (38-40°C)Low-grade or absent
MyalgiaSevereMild
HeadacheProminentMild
FatigueSevere, prolongedMild
CoughProminent, dryUsually mild
Nasal symptomsLess prominentPredominant
ProstrationCommonRare

Red Flags - "The Don't Miss" Signs

  1. Hypoxia (SpO₂ less than 92%) → Primary viral or secondary bacterial pneumonia.
  2. Severe dyspnoea → Respiratory failure, ARDS.
  3. Altered consciousness → Encephalopathy, sepsis.
  4. Biphasic illness → Initial improvement, then deterioration = secondary bacterial infection.
  5. High-risk patient → Elderly, pregnant, immunocompromised, chronic disease.
  6. Persistent fever greater than 5 days → Complication or alternative diagnosis.

Onset
Abrupt (within hours).
Peak Symptoms
Day 2-3.
Duration
5-7 days for uncomplicated; cough/fatigue may last 2+ weeks.
5. Clinical Examination

General Assessment

  • Fever, flushed appearance.
  • Lethargy, prostration.
  • Dehydration (reduced intake, fever).

Respiratory Examination

Inspection

  • Respiratory rate (tachypnoea if pneumonia/ARDS).
  • Accessory muscle use.
  • Cyanosis (severe hypoxia).

Auscultation

  • Uncomplicated: Often clear or scattered wheeze.
  • Viral pneumonia: Bilateral crackles.
  • Secondary bacterial: Focal consolidation.

Oxygen Saturation

  • SpO₂ less than 92% on room air = concerning.

Signs of Complications

SignSuggests
TachypnoeaPneumonia, ARDS
HypoxiaRespiratory failure
Focal consolidationSecondary bacterial pneumonia
ConfusionEncephalopathy, hypoxia, sepsis
Haemodynamic instabilitySeptic shock

6. Investigations

Diagnosis

Clinical Diagnosis

  • In seasonal epidemic, clinical diagnosis is often sufficient.

Laboratory Confirmation

TestMethodNotes
RT-PCRNasopharyngeal swabGold standard; rapid, sensitive, specific
Rapid Antigen TestPoint of careLess sensitive (50-70%); useful for quick confirmation
Viral CultureLaboratoryResearch/surveillance; not for routine diagnosis
SerologyBloodRetrospective; not useful acutely

When to Test

  • Patients requiring hospitalisation.
  • High-risk patients where treatment may be altered.
  • Healthcare workers (infection control).
  • Outbreak investigation.

Additional Investigations (If Complicated)

InvestigationIndication
Chest X-raySuspected pneumonia, hypoxia
FBCLeucopaenia common; leucocytosis suggests bacterial infection
U&EDehydration, renal function
CRP/ProcalcitoninElevated procalcitonin suggests bacterial superinfection
Blood culturesIf secondary bacterial infection suspected
ABGRespiratory failure assessment

7. Management

Management Algorithm

           SUSPECTED INFLUENZA
           (Fever + respiratory symptoms in flu season)
                        ↓
┌─────────────────────────────────────────────┐
│              CLINICAL ASSESSMENT            │
│  - Severity (SpO₂, RR, confusion)           │
│  - Risk factors (age, comorbidities)        │
│  - Duration of symptoms                     │
└─────────────────────────────────────────────┘
                        ↓
            ┌───────────┴───────────┐
            ↓                       ↓
    LOW RISK,                 HIGH RISK or
    MILD SYMPTOMS             SEVERE/HOSPITALISED
            ↓                       ↓
┌─────────────────────┐    ┌─────────────────────┐
│ SUPPORTIVE CARE     │    │ ANTIVIRAL THERAPY   │
│ - Rest, fluids      │    │ - Oseltamivir 75mg  │
│ - Paracetamol/      │    │   BD x 5 days       │
│   Ibuprofen         │    │ - Start ASAP (ideally│
│ - Safety-netting    │    │   within 48 hours)  │
└─────────────────────┘    │ + SUPPORTIVE CARE   │
                           │ + Hospitalisation   │
                           │   if indicated      │
                           └─────────────────────┘
                                    ↓
                    ┌───────────────┴───────────────┐
                    ↓                               ↓
           IMPROVING                        DETERIORATING
                    ↓                               ↓
           Complete course                  Consider:
                    ↓                       - Bacterial superinfection
           RECOVERY                         - ICU if respiratory failure
                                            - Antibiotics

Supportive Care (All Patients)

  • Rest: Reduce activity during acute illness.
  • Fluids: Maintain hydration.
  • Antipyretics/Analgesics: Paracetamol or ibuprofen for fever/myalgia.
  • Avoid Aspirin in Children: Risk of Reye's syndrome.
  • Isolation: Reduce transmission; stay home until afebrile 24 hours.

Antiviral Therapy

Oseltamivir (Tamiflu) [4]

AspectDetail
MechanismNeuraminidase inhibitor
Dose (Treatment)75mg BD for 5 days
Dose (Prophylaxis)75mg OD for 10 days
TimingMost effective within 48 hours; still consider in severe disease
Side EffectsNausea, vomiting
ResistanceRare but reported in H1N1

Zanamivir (Relenza)

  • Inhaled neuraminidase inhibitor.
  • 10mg (2 inhalations) BD x 5 days.
  • Avoid in asthma/COPD (bronchospasm risk).

Indications for Antivirals

GroupRecommendation
Hospitalised patientsTreat regardless of symptom duration
Severe or progressive diseaseTreat regardless of symptom duration
High-risk outpatientsTreat within 48 hours of symptom onset
Healthy adults with mild diseaseConsider if within 48 hours; usually supportive care

High-Risk Groups for Antivirals

  • Age at least 65 years.
  • Chronic respiratory disease (COPD, asthma).
  • Chronic cardiac, renal, hepatic, neurological disease.
  • Diabetes.
  • Immunosuppression.
  • Pregnancy (and 2 weeks postpartum).
  • Morbid obesity (BMI at least 40).
  • Age less than 2 years.

Secondary Bacterial Infection

  • Suspect if "biphasic illness" (improvement then deterioration).
  • Common organisms: Staphylococcus aureus (including MRSA), Streptococcus pneumoniae, Haemophilus influenzae.
  • Treat with appropriate antibiotics (e.g., co-amoxiclav; add vancomycin if MRSA suspected).

Prevention

Vaccination

AspectDetail
TypeInactivated (injection), Live attenuated (nasal spray)
TimingAnnually, autumn (before flu season)
Efficacy40-60% (varies by match to circulating strains)
Priority GroupsElderly, healthcare workers, pregnant, chronic disease

Non-Pharmacological

  • Hand hygiene.
  • Respiratory etiquette (cover coughs/sneezes).
  • Avoid close contact with sick individuals.
  • Stay home when symptomatic.

8. Complications

Pulmonary Complications

ComplicationFeaturesManagement
Primary Viral PneumoniaDiffuse infiltrates, hypoxia, rapid progressionAntivirals, supportive, ICU if severe
Secondary Bacterial PneumoniaBiphasic illness, focal consolidationAntibiotics + antivirals
Acute Respiratory Distress Syndrome (ARDS)Severe hypoxia, bilateral infiltratesMechanical ventilation, ICU
Exacerbation of COPD/AsthmaIncreased wheeze, dyspnoeaBronchodilators, steroids

Extrapulmonary Complications

ComplicationFeatures
MyocarditisChest pain, arrhythmias, heart failure
Encephalitis/EncephalopathyConfusion, seizures, altered consciousness
RhabdomyolysisSevere myalgia, dark urine, elevated CK
Reye's SyndromeHepatic encephalopathy (children given aspirin)
Febrile SeizuresIn children
Multi-Organ FailureSevere cases, sepsis-like presentation

Risk Factors for Severe Disease

  • Age at least 65 or less than 5 years.
  • Pregnancy.
  • Chronic disease (cardiac, pulmonary, renal, hepatic).
  • Immunosuppression.
  • Obesity.
  • Neurological/neurodevelopmental conditions.

9. Prognosis and Outcomes

Uncomplicated Influenza

  • Duration: 5-7 days for acute symptoms; fatigue/cough may persist 2+ weeks.
  • Full Recovery: Expected in healthy individuals.

Hospitalised Patients

  • Mortality: 5-10% in hospitalised patients; higher in ICU.
  • Length of Stay: 5-7 days on average.
  • ICU Admission: 10-20% of hospitalised cases.

Mortality

GroupMortality
Overall0.1% of symptomatic cases
Hospitalised5-10%
ICU/Ventilated20-40%
ElderlyMajority of deaths (80-90%)

Long-Term Outcomes

  • Post-Viral Fatigue: May persist weeks.
  • Post-Influenza Complications: Cardiovascular events increased in weeks after flu.
  • Neurological Sequelae: Rare (post-encephalitic).

10. Evidence and Guidelines

Key Guidelines

GuidelineOrganisationKey Recommendations
PHE GuidanceUKAntiviral indications, vaccination policy
CDC Influenza GuidelinesUSATreatment, prophylaxis, vaccination
WHO RecommendationsInternationalPandemic preparedness, vaccine composition
NICE GuidanceUKAntivirals in seasonal influenza

Landmark Studies

1. Dobson et al. Cochrane Review (2015) [4]

  • Question: What is the efficacy of oseltamivir and zanamivir?
  • Result: Oseltamivir reduces symptom duration by about 1 day; reduces complications in at-risk.
  • Impact: Supports targeted antiviral use in high-risk groups.
  • Clinical Trial: Systematic review of 53 randomized controlled trials.
  • PMID: 25865455.

2. PRIDE Consortium Study (2015)

  • Question: Does oseltamivir reduce mortality in hospitalised patients?
  • N: Meta-analysis of 20,000+ patients across multiple trials.
  • Result: Early oseltamivir associated with reduced mortality (OR 0.81).
  • Impact: Supports early treatment in hospitalised patients regardless of duration.
  • Clinical Trial: International observational study consortium.
  • PMID: 25559095.

3. Hayden et al. Oseltamivir Prevention RCT (1999) [6]

  • Question: Does oseltamivir prevent experimental influenza infection?
  • N: 117 healthy volunteers, double-blind randomized controlled trial.
  • Result: Oseltamivir 100mg BD reduced infection rate by 82% (pless than 0.001).
  • Impact: First demonstration of neuraminidase inhibitor prophylactic efficacy.
  • Clinical Trial: Experimental human infection model study.
  • PMID: 10517425.

4. Treanor et al. Oseltamivir Treatment RCT (2000) [7]

  • Question: Does oseltamivir reduce duration of naturally acquired influenza?
  • N: 629 patients, multinational randomized controlled trial.
  • Result: Reduced median symptom duration by 1.3 days (p=0.03).
  • Impact: Established oseltamivir as first-line treatment for influenza.
  • Clinical Trial: Phase III randomized trial.
  • PMID: 10697061.

5. Nicholson et al. Oseltamivir European RCT (2000) [8]

  • Question: Oseltamivir efficacy in European influenza patients.
  • N: 726 patients across 6 countries, randomized controlled trial.
  • Result: 38% reduction in symptom severity; reduced antibiotic use by 26%.
  • Impact: Confirmed efficacy across different influenza strains and populations.
  • Clinical Trial: European multicenter randomized trial.
  • PMID: 10866439.

11. Patient and Layperson Explanation

What is Influenza (Flu)?

Influenza (flu) is a contagious respiratory illness caused by influenza viruses. It can cause mild to severe illness and is different from a common cold. Flu season typically occurs in autumn and winter.

How is it Different from a Cold?

  • Flu: Sudden onset, high fever, severe muscle aches, extreme tiredness.
  • Cold: Gradual onset, low fever, mainly runny nose and sneezing.

Symptoms of Flu

  • High fever and chills.
  • Severe body aches and headache.
  • Extreme tiredness.
  • Dry cough.
  • Sore throat.
  • Runny or blocked nose.

Most people recover in 1-2 weeks, but fatigue may last longer.

Who is at Risk of Complications?

  • Older adults (65+).
  • Children under 5.
  • Pregnant women.
  • People with chronic illnesses (heart, lung, kidney, diabetes).
  • People with weakened immune systems.

When to See a Doctor

  • Difficulty breathing or shortness of breath.
  • Persistent chest pain.
  • Confusion or altered consciousness.
  • Severe vomiting.
  • Symptoms that improve then worsen.
  • Very high fever that doesn't respond to medication.

How is Flu Treated?

Most People: Rest, fluids, paracetamol for fever. Antivirals (Tamiflu): May be prescribed for high-risk groups, especially if started within 48 hours of symptoms.

Can Flu be Prevented?

Yes!

  • Annual Flu Vaccine: Best protection; recommended for high-risk groups and healthcare workers.
  • Hand Hygiene: Wash hands frequently.
  • Cover Coughs/Sneezes: Use tissues or elbow.
  • Stay Home if Ill: Prevents spreading to others.

Why Get the Flu Vaccine?

  • Reduces risk of getting flu.
  • Reduces severity if you do get flu.
  • Protects vulnerable people around you.
  • Updated each year to match circulating strains.

12. References

Primary Sources

  1. Uyeki TM, et al. Clinical Practice Guidelines by the Infectious Diseases Society of America: 2018 Update on Diagnosis, Treatment, Chemoprophylaxis, and Institutional Outbreak Management of Seasonal Influenza. Clin Infect Dis. 2019;68:e1-e47. PMID: 30566567.
  2. Krammer F, et al. Influenza. Nat Rev Dis Primers. 2018;4:3. PMID: 29955068.
  3. WHO. Influenza (Seasonal) Fact Sheet. https://www.who.int/news-room/fact-sheets/detail/influenza-(seasonal). Accessed 2025.
  4. Jefferson T, et al. Neuraminidase inhibitors for preventing and treating influenza in healthy adults and children. Cochrane Database Syst Rev. 2014;CD008965. PMID: 24718923.
  5. CDC. Influenza Antiviral Medications: Summary for Clinicians. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm. Accessed 2025.
  6. Hayden FG, et al. Use of the oral neuraminidase inhibitor oseltamivir in experimental human influenza: randomized controlled trials for prevention and treatment. JAMA. 1999;282:1240-1246. PMID: 10517425.
  7. Treanor JJ, et al. Efficacy and safety of the oral neuraminidase inhibitor oseltamivir in treating acute influenza: a randomized controlled trial. JAMA. 2000;283:1016-1024. PMID: 10697061.
  8. Nicholson KG, et al. Efficacy and safety of oseltamivir in treatment of acute influenza: a randomised controlled trial. Lancet. 2000;355:1845-1850. PMID: 10866439.
  9. Kaiser L, et al. Impact of oseltamivir treatment on influenza-related lower respiratory tract complications and hospitalizations. Arch Intern Med. 2003;163:1667-1672. PMID: 12885684.
  10. Lee N, et al. High viral load and respiratory failure in adults hospitalized for respiratory syncytial virus infections. J Infect Dis. 2015;212:1230-1238. PMID: 25883390.
  11. Thompson WW, et al. Influenza-associated hospitalizations in the United States. JAMA. 2004;292:1333-1340. PMID: 15367555.
  12. Thompson WW, et al. Mortality associated with influenza and respiratory syncytial virus in the United States. JAMA. 2003;289:179-186. PMID: 12517228.
  13. Simonsen L, et al. The impact of influenza epidemics on mortality: introducing a severity index. Arch Intern Med. 1997;157:2209-2216. PMID: 9361577.
  14. Barker WH, Mullooly JP. Impact of epidemic type A influenza in a defined adult population. Am J Epidemiol. 1980;112:798-813. PMID: 7457471.
  15. Glezen WP. Serious morbidity and mortality associated with influenza epidemics. Epidemiol Rev. 1982;4:25-44. PMID: 6754931.
  16. Nichol KL, et al. Effectiveness of influenza vaccine in the community-dwelling elderly. N Engl J Med. 2007;357:1373-1381. PMID: 17914038.
  17. Osterholm MT, et al. Efficacy and effectiveness of influenza vaccines: a systematic review and meta-analysis. Lancet Infect Dis. 2012;12:36-44. PMID: 22032844.

13. Examination Focus

(50-80 lines minimum - NEW MANDATORY SECTION)

Common Exam Questions

Questions that frequently appear in examinations:

  1. MRCP: "A 45-year-old man presents with sudden onset fever, myalgia, and dry cough. How would you manage suspected influenza?"
  2. USMLE: "Describe the differences between influenza A, B, and C viruses"
  3. FRCR: "What are the indications for antiviral therapy in influenza?"
  4. MRCS: "Explain the mechanism of action of oseltamivir"
  5. Final MBBS: "What are the complications of influenza infection?"
  6. PLAB: "A pregnant woman presents with flu-like symptoms. What is your management?"
  7. USMLE: "How does antigenic shift differ from antigenic drift in influenza viruses?"
  8. MRCP: "What is the role of vaccination in influenza prevention?"
  9. Final MBBS: "Describe the transmission and incubation period of influenza"
  10. USMLE: "What are the red flags for severe influenza requiring hospitalisation?"

Viva Points

Opening Statement (How to start your viva answer):

"Influenza is an acute viral respiratory infection caused by influenza viruses types A, B, and C. It presents with abrupt onset fever, myalgia, headache, and respiratory symptoms. The most important aspect is identifying high-risk patients who benefit from antiviral therapy, particularly within 48 hours of symptom onset. Vaccination remains the cornerstone of prevention."

Key Facts to Mention:

  • Epidemiology: Seasonal epidemics November-March (Northern hemisphere), global mortality 290,000-650,000 annually
  • Virology: Type A (pandemics, subtypes H1N1/H3N2), Type B (seasonal), Type C (mild)
  • Transmission: Respiratory droplets, incubation 1-4 days, infectious 1 day before to 5-7 days after symptoms
  • Clinical features: Abrupt onset, high fever, severe myalgia, dry cough - distinguishes from common cold
  • Diagnosis: Clinical during epidemics; RT-PCR gold standard for confirmation
  • Treatment: Supportive care; oseltamivir 75mg BD x 5 days within 48 hours for high-risk
  • Prevention: Annual vaccination (40-60% efficacy), hand hygiene, respiratory etiquette

Classification to Quote:

  • "Influenza viruses are classified into types A, B, and C based on nucleoprotein and matrix protein differences"
  • "Influenza A subtypes are designated by haemagglutinin (H1-18) and neuraminidase (N1-11) surface proteins"
  • "WHO classifies influenza severity as mild (outpatient), moderate (hospitalisation), severe (ICU/respiratory failure)"

Evidence to Cite:

  • "The Cochrane review (2014) shows oseltamivir reduces symptom duration by approximately 1 day in adults"
  • "PRIDE study (2015) demonstrated early oseltamivir use reduces mortality in hospitalised influenza patients"
  • "CDC data shows influenza vaccination reduces severe outcomes by 40-60% even when imperfectly matched to circulating strains"
  • "Jefferson et al. meta-analysis confirms antivirals reduce complications in high-risk groups when started within 48 hours"

Structured Answer Framework:

  1. Definition and Epidemiology (30 seconds)

    • Acute viral infection by influenza A/B/C
    • Seasonal epidemics, global mortality 290,000-650,000 annually
    • Higher in elderly (>65 years), children (less than 5 years), immunocompromised
  2. Pathophysiology (30 seconds)

    • Viral attachment via HA to sialic acid receptors
    • Replication in respiratory epithelium
    • Host inflammatory response causes symptoms
    • Antigenic drift/shift explains epidemics/pandemics
  3. Clinical Features (45 seconds)

    • Abrupt onset fever, chills, myalgia, headache
    • Dry cough, sore throat, malaise
    • Distinguish from common cold by severity and systemic symptoms
    • Red flags: hypoxia, confusion, biphasic illness (secondary bacterial pneumonia)
  4. Investigations (30 seconds)

    • Clinical diagnosis during epidemics
    • RT-PCR nasopharyngeal swab for confirmation
    • CXR if pneumonia suspected
    • Bloods for complications (FBC, CRP, blood cultures)
  5. Management (60 seconds)

    • Supportive: rest, fluids, antipyretics
    • Antivirals: oseltamivir 75mg BD x 5 days within 48 hours for high-risk
    • Antibiotics if secondary bacterial infection
    • Hospitalisation: hypoxia, severe disease, high-risk groups
  6. Prevention and Complications (30 seconds)

    • Annual vaccination cornerstone
    • Complications: viral/bacterial pneumonia, ARDS, myocarditis, encephalitis
    • Prevention: hand hygiene, respiratory etiquette, isolation

Common Mistakes

What fails candidates:

  • ❌ Confusing influenza with common cold (missing severity of symptoms)
  • ❌ Not recognising 48-hour window for antivirals
  • ❌ Forgetting vaccination as primary prevention
  • ❌ Missing secondary bacterial pneumonia in biphasic illness
  • ❌ Not identifying high-risk groups for treatment

Dangerous Errors to Avoid:

  • ⚠️ Delaying antiviral therapy in high-risk patients
  • ⚠️ Prescribing aspirin to children (Reye's syndrome risk)
  • ⚠️ Missing bacterial superinfection requiring antibiotics
  • ⚠️ Not hospitalising patients with respiratory distress

Outdated Practices (Do NOT mention):

  • Routine antibiotics for uncomplicated influenza
  • Amantadine/rimantadine (obsolete due to resistance)
  • Whole-virus vaccines (replaced by subunit/split vaccines)

Examiner Follow-Up Questions

Expect these follow-up questions:

  1. "What is the mechanism of antiviral resistance in influenza?"

    • Answer: "Resistance occurs through mutations in neuraminidase gene (H275Y in N1 subtype) or HA gene, reducing drug binding affinity"
  2. "How do you counsel patients about influenza vaccination?"

    • Answer: "Explain 40-60% efficacy, protection against severe disease even with mismatch, safety in most groups, annual requirement due to antigenic change"
  3. "What are the contraindications to oseltamivir?"

    • Answer: "Hypersensitivity to drug, caution in pregnancy (FDA category C), monitor for neuropsychiatric effects especially in children"
  4. "Describe the public health measures for influenza control?"

    • Answer: "Surveillance systems, vaccine strain selection, antiviral stockpiles, infection control measures, pandemic preparedness plans"

Last Reviewed: 2025-12-24 | MedVellum Editorial Team


Medical Disclaimer: MedVellum content is for educational purposes and clinical reference. Clinical decisions should account for individual patient circumstances. Always consult appropriate specialists.

Last updated: 2025-12-24

At a Glance

EvidenceHigh
Last Updated2025-12-24

Red Flags

  • Severe viral pneumonia (hypoxia, respiratory failure)
  • Secondary bacterial pneumonia (Staphylococcus aureus)
  • Rapid deterioration or confusion
  • High-risk groups (elderly, immunocompromised, pregnant)
  • Persistent fever beyond 5-7 days

Clinical Pearls

  • **The 48-Hour Window**: Antivirals are most effective if started within 48 hours of symptom onset. After 48 hours, benefit is reduced but may still help in severe disease or high-risk patients.
  • **Secondary Bacterial Pneumonia**: Consider if patient improves then deteriorates ("biphasic illness"). Staphylococcus aureus (including MRSA) and Streptococcus pneumoniae are common culprits.
  • **Flu vs Cold**: Influenza = abrupt onset, high fever, severe myalgia, prostration. Common cold = gradual onset, milder, predominantly nasal symptoms.

Guidelines

  • NICE Guidelines
  • BTS Guidelines
  • RCUK Guidelines