Influenza
Acute respiratory infection caused by influenza A or B viruses, characterised by fever, myalgia, cough, and headache. Seasonal epidemics cause significant morbidity and mortality, particularly in the elderly and high-risk groups. Annual vaccination is the primary prevention strategy.
Key Facts
Influenza A and B cause seasonal epidemics; influenza A causes pandemics due to antigenic shift (reassortment of genome segments) Annual UK vaccination programme: offered to all aged ≥65, pregnant women, chronic disease, healthcare workers, children aged 2–10 (nasal spray) Oseltamivir (Tamiflu) 75mg BD for 5 days: neuraminidase inhibitor — effective if started within 48 hours of symptom onset (NICE TA168) Complications: secondary bacterial pneumonia (S. aureus, S. pneumoniae), myocarditis, encephalitis, Guillain-Barré syndrome, Reye syndrome (aspirin in children) UK burden: ~10,000–25,000 excess deaths/year in severe influenza seasons Antigenic drift: minor mutations → seasonal epidemics; antigenic shift: major reassortment → pandemics (1918, 1957, 1968, 2009) High-risk groups for complications: >65, <2 years, pregnancy, chronic respiratory/cardiac/renal/liver disease, immunocompromised, diabetes, BMI >40 Diagnosis: nasopharyngeal swab for influenza PCR (rapid point-of-care tests also available)
Overview
Key Facts
Influenza is a major cause of morbidity and mortality in the UK, particularly during winter months. Vaccination remains the most effective preventive strategy. Antiviral treatment should be initiated promptly in at-risk patients.
Epidemiology
- UK: ~10,000–25,000 excess winter deaths attributable to influenza in severe seasons
- Global: 3–5 million severe cases/year; 290,000–650,000 deaths/year (WHO)
- Seasonal peaks: November–March in Northern Hemisphere
- Attack rate: 5–10% of adults, 20–30% of children annually
- Pandemics: H1N1 (2009), H3N2 (1968), H2N2 (1957), H1N1 (1918 — 50 million deaths)
Aetiology
- Influenza A: subtypes defined by haemagglutinin (H1–18) and neuraminidase (N1–11); infects humans, birds, pigs
- Influenza B: two lineages (Victoria, Yamagata); humans only; typically milder
- Influenza C: mild, sporadic
- Transmission: respiratory droplets, aerosols, fomites; incubation 1–4 days; infectious from 1 day before to 5–7 days after symptom onset
Pathophysiology
- Virus binds sialic acid residues on respiratory epithelial cells via haemagglutinin
- Neuraminidase cleaves sialic acid → release of progeny virions → spread
- Epithelial cell death → mucosal inflammation → susceptibility to secondary bacterial infection
- Systemic inflammatory response: cytokine release → fever, myalgia, malaise
- Severe disease: viral pneumonitis → ARDS; secondary bacterial pneumonia (S. aureus, S. pneumoniae)
- Antigenic drift: point mutations in HA/NA genes → seasonal epidemics (need annual vaccine update)
- Antigenic shift: reassortment between human and animal influenza A strains → novel virus → pandemic
Clinical Presentation
Typical Presentation
- Sudden onset high fever (>38.5°C), rigors
- Severe myalgia and arthralgia
- Headache
- Dry cough
- Sore throat
- Prostration and malaise (often more severe than common cold)
- Duration: 5–7 days (cough may persist 2 weeks)
Complications
- Primary viral pneumonia: progressive dyspnoea, bilateral infiltrates → ARDS
- Secondary bacterial pneumonia: classically S. aureus (rapid onset, cavitation) or S. pneumoniae (after initial improvement)
- Myocarditis/pericarditis: chest pain, troponin elevation
- Encephalitis/encephalopathy: rare, confusion, seizures
- Rhabdomyolysis: myalgia, raised CK, AKI
- Reye syndrome: hepatic encephalopathy in children given aspirin
- Exacerbation of chronic disease: COPD, asthma, heart failure
Red Flags
- Dyspnoea, tachypnoea, SpO2 <92%
- Haemoptysis
- Persistent fever >5 days (secondary infection)
- Confusion or altered consciousness
- Dehydration, unable to tolerate oral fluids
- High-risk patient with typical influenza symptoms
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| COVID-19 | Similar presentation, anosmia, endemic | SARS-CoV-2 PCR |
| RSV | Bronchiolitis (children), elderly | RSV PCR |
| Common cold (rhinovirus) | Milder, coryzal symptoms predominate, no prostration | Clinical diagnosis |
| Bacterial pneumonia | Productive cough, focal consolidation, higher CRP | CXR, sputum culture |
| Mycoplasma pneumoniae | Younger adults, dry cough, gradual onset, erythema multiforme | Mycoplasma PCR/serology |
| Meningitis | Neck stiffness, photophobia, rash | LP, blood cultures |
Diagnosis / Investigation
Bedside
- Nasopharyngeal swab: influenza PCR (gold standard) — also tests for COVID-19 and RSV (multiplex PCR)
- Point-of-care rapid influenza test: less sensitive (~60–70%) but fast (15 min)
- SpO2: assess severity
- NEWS2: escalation tool
Bloods
- FBC: lymphopenia, relative leucopenia (high WCC suggests secondary bacterial infection)
- CRP/procalcitonin: CRP moderately raised; procalcitonin low in viral, high if bacterial superinfection
- U&Es, LFTs: assess organ function
- CK: if rhabdomyolysis suspected
- Blood cultures: if secondary bacterial infection suspected
- Blood gas: if respiratory compromise
Imaging
- CXR: if pneumonia suspected — bilateral interstitial infiltrates (viral) or lobar consolidation (bacterial)
- CT chest: if complicated pneumonia, ARDS
Special Tests
- Viral typing/subtyping: for surveillance (PHE/UKHSA)
- Sputum culture: if secondary bacterial pneumonia suspected
Management
Non-pharmacological
- Rest and hydration: adequate oral fluid intake
- Isolation: respiratory droplet precautions; stay home for ≥5 days from symptom onset
- Infection control in hospital: surgical mask, hand hygiene, single room if possible
Pharmacological
Antivirals (NICE TA168):
- Oseltamivir (Tamiflu) 75mg BD for 5 days: indicated in at-risk patients within 48 hours of symptoms
- Zanamivir (Relenza) 10mg BD inhaled for 5 days: alternative if oseltamivir contraindicated
- Consider in hospitalised patients even if >48 hours from onset (may still reduce duration)
- Post-exposure prophylaxis: oseltamivir 75mg OD for 10 days for close contacts of confirmed cases who are at risk
Symptomatic treatment:
- Paracetamol/ibuprofen for fever and myalgia
- Avoid aspirin in children <16 (Reye syndrome risk)
Secondary bacterial pneumonia:
- Treat per NICE NG138 (community-acquired pneumonia guidelines)
- Co-amoxiclav 625mg TDS or doxycycline 200mg loading then 100mg OD
- If severe/S. aureus suspected: flucloxacillin 1g QDS IV ± gentamicin
Vaccination (annual):
- Quadrivalent inactivated vaccine: ≥65 (adjuvanted — aQIV), pregnant women, at-risk adults
- Live attenuated nasal spray (LAIV): children aged 2–10
- Healthcare workers: annual vaccination recommended
- Timing: September–November (before flu season peak)
Surgical/Interventional
- Not applicable for uncomplicated influenza
- Ventilatory support (NIV/invasive) for ARDS
- ECMO: in refractory ARDS (specialist centres)
Referral Criteria
- Hospital admission: severe symptoms, SpO2 <92%, dehydration, complications
- ICU: ARDS, septic shock, multi-organ failure
- Public health notification: not individually notifiable but outbreaks are reportable
Prognosis
- Uncomplicated influenza: self-limiting in 5–7 days in most healthy adults
- Hospitalisation rate: ~1% overall, much higher in elderly and high-risk groups
- UK excess winter deaths attributable to influenza: 10,000–25,000 in severe seasons
- Secondary bacterial pneumonia mortality: 10–30%
- ARDS from influenza: ICU mortality ~30–40%
- Vaccination reduces hospitalisation by 40–60% (higher in well-matched seasons)
- Oseltamivir: reduces symptom duration by ~1 day and reduces complications in at-risk groups
- Pandemic influenza (e.g. 1918 H1N1): case-fatality rate was ~2–3% (50 million deaths globally)
- Children: generally good prognosis; rare fulminant cases with encephalopathy
Other Relevant Information
UK Influenza Vaccination Programme
| Group | Vaccine Type |
|---|---|
| Age ≥65 | Adjuvanted QIV (aQIV) |
| Age 50–64 | QIV |
| Pregnant women | QIV (any trimester) |
| Chronic disease (heart, lung, kidney, liver, diabetes) | QIV |
| Immunosuppressed | QIV (avoid LAIV) |
| Healthcare workers | QIV |
| Children 2–10 years | LAIV (nasal spray) |
| Carers and household contacts of immunocompromised | QIV |
Influenza vs Common Cold
| Feature | Influenza | Common Cold |
|---|---|---|
| Onset | Sudden | Gradual |
| Fever | High (>38.5°C) | Low-grade/absent |
| Myalgia | Severe | Mild |
| Cough | Dry, prominent | Mild |
| Prostration | Marked | Rare |
| Duration | 5–7 days | 3–5 days |