Influenza
Overview
•Highly contagious acute respiratory illness caused by influenza A or B viruses
•Influenza A - responsible for most seasonal epidemics and all recorded pandemics
•Incubation period 1-4 days (typically 2 days); contagious from ~1 day before symptoms until 5-7 days after onset
Presentation
•Abrupt onset - hallmark feature (patient well in morning, floored by afternoon)
•Fever - sudden onset, 38-40°C, almost universal
•Myalgia - severe, particularly legs and back; defining feature
•Headache - prominent and early
•Dry cough - persistent
•Sore throat and coryza - present but less prominent than common cold
•Fatigue and malaise - can be severe and prolonged (weeks)
•Febrile convulsions - in young children with rapid temperature rise
Influenza vs common cold
| Feature | Influenza | Common cold |
|---|---|---|
| Onset | Sudden (hours) | Gradual |
| Fever | High (38-40°C), almost universal | Low-grade or absent |
| Myalgia | Severe | Mild or absent |
| Nasal symptoms | Minor | Prominent |
| Systemic illness | Prominent | Absent/mild |
Investigations
•Clinical diagnosis - sufficient in community settings during seasonal circulation; no testing needed to start antivirals in at-risk patients
•Rapid influenza diagnostic test (RIDT) / point-of-care PCR - used in hospitals and care homes for infection control
🏆 Gold standard
•RT-PCR of nasopharyngeal swab - highest sensitivity and specificity; differentiates A from B; identifies subtype; used for public health surveillance
•Chest X-ray - if pneumonia suspected (consolidation; bilateral interstitial infiltrates in viral pneumonia)
•FBC, U&E, CRP, LFTs - in hospitalised patients to assess severity
Management
•Healthy adults: supportive care - rest, hydration, paracetamol or ibuprofen for fever/myalgia; full recovery in 1-2 weeks
•At-risk patients: oseltamivir 75 mg twice daily for 5 days - start within 48 hours of symptom onset without waiting for confirmation
•Zanamivir (inhaled) - alternative if oseltamivir not tolerated or resistance suspected
Prevention
•Annual influenza vaccination - vaccine reformulated yearly due to antigenic drift; typically includes 2 influenza A subtypes and 1-2 influenza B strains
•Eligible groups: all adults ≥65; all pregnant women; chronic respiratory, cardiac, renal, hepatic, neurological, or metabolic conditions; immunosuppressed; BMI ≥40; residents of long-stay care facilities; carers; all healthcare workers
•Children (2-17 years): live attenuated intranasal influenza vaccine (LAIV) as part of routine childhood immunisation
•Inactivated injectable vaccine instead in children with severe asthma or who are immunosuppressed
•Adults ≥65: adjuvanted quadrivalent inactivated vaccine (QIVe) - produces stronger immune response given age-related immunosenescence
Complications
•Primary viral pneumonia - bilateral interstitial infiltrates; can progress to ARDS; higher mortality than secondary bacterial pneumonia
•Secondary bacterial pneumonia - occurs 5-10 days after initial improvement; caused by Streptococcus pneumoniae, Staphylococcus aureus (including MRSA), or Haemophilus influenzae; presents with recurrence of fever and productive cough
•Exacerbation of chronic conditions - COPD, asthma, heart failure, ischaemic heart disease
•Reye syndrome - rare hepatic encephalopathy in children; associated with aspirin use during influenza
•Influenza encephalitis/encephalopathy, myocarditis, pericarditis - rare
Virology - Key Concepts
•Haemagglutinin (HA) - mediates viral attachment to sialic acid receptors on respiratory epithelium
•Neuraminidase (NA) - cleaves receptors to allow release of new viral particles
•Antigenic drift - gradual point mutations in HA/NA; partially evades existing immunity; reason vaccine must be reformulated annually
•Antigenic shift - reassortment of whole gene segments between two influenza A strains; produces novel subtype with no population immunity; mechanism behind pandemic influenza