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haematology infectious-disease

4C Mortality Score for COVID-19

Validated prognostic score predicting in-hospital mortality in adults hospitalised with COVID-19. Uses 8 readily available clinical variables at admission. Validated in multiple national and international cohorts.

Score interpretation

Low Risk -- 4C Score 0-3 (~1.2% in-hospital mortality) 0–3

4C low risk -- very low probability of in-hospital mortality from COVID-19

→ Consider outpatient or early discharge pathway (with safety netting); monitor SpO2 at home (alert return if SpO2 < 94% or rapid decline); antipyretics and symptomatic management; ensure vaccination status reviewed; antivirals: nirmatrelvir-ritonavir (Paxlovid) or sotrovimab if high-risk immunocompromised patient (NICE COVID therapeutics; refer via COVID Medicines Delivery Unit); no specific antiviral for low-risk admitted patients; dexamethasone NOT indicated unless requiring supplemental O2.

Intermediate Risk -- 4C Score 4-8 (~9.9% mortality) 4–8

4C intermediate risk -- moderate mortality probability; active inpatient management

→ Inpatient admission; supplemental O2 if SpO2 < 92%; dexamethasone 6 mg OD x10 days if requiring supplemental oxygen (RECOVERY: deaths reduced by about one fifth on oxygen and one third on invasive ventilation); remdesivir 200 mg IV day 1 then 100 mg IV days 2-5 if SpO2 <= 94% requiring supplemental O2 (EMA approved); baricitinib 4 mg OD x14 days if on O2 + dexamethasone (RECOVERY, COV-BARRIER trials); VTE prophylaxis (therapeutic or prophylactic based on D-dimer/risk); prone awake positioning if tolerated; NEWS2 monitoring; escalation criteria pre-agreed (ICU if RR > 30, SpO2 < 90 on O2, or haemodynamic compromise).

High Risk -- 4C Score 9-14 (~31.4% in-hospital mortality) 9–14

4C high risk -- in-hospital mortality 31.4% in the validation cohort (Knight 2020); intensive management and escalation planning

→ Senior review and ICU/HDU consideration; high-flow nasal oxygen (HFNO) 40-60 L/min or CPAP 5-10 cmH2O for moderate-severe hypoxaemic respiratory failure (CPAP reduced intubation or death in RECOVERY-RS); dexamethasone 6 mg OD x10 days; baricitinib 4 mg OD; remdesivir if within 10 days of symptom onset and not on invasive ventilation; intubation and invasive ventilation if: RR > 35, PaO2/FiO2 < 100, signs of fatigue; lung-protective ventilation (6 mL/kg IBW, plateau pressure < 30 cmH2O); prone ventilation > 12 hours/day (PROSEVA); VTE: standard prophylactic-dose anticoagulation for patients on high-flow oxygen, CPAP, NIV or invasive ventilation (therapeutic-dose heparin benefited only non-critically ill patients -- ATTACC/ACTIV-4a/REMAP-CAP; NICE NG191); ECMO if severe refractory ARDS; goals of care discussion; DNACPR consideration; palliative care early involvement for very high risk patients.

Very High Risk -- 4C Score >= 15 (~61.5% in-hospital mortality) 15–21

4C very high risk -- in-hospital mortality 61.5% in the validation cohort (Knight 2020)

→ Senior review and ICU/HDU consideration; high-flow nasal oxygen (HFNO) 40-60 L/min or CPAP 5-10 cmH2O for moderate-severe hypoxaemic respiratory failure (CPAP reduced intubation or death in RECOVERY-RS); dexamethasone 6 mg OD x10 days; baricitinib 4 mg OD; remdesivir if within 10 days of symptom onset and not on invasive ventilation; intubation and invasive ventilation if: RR > 35, PaO2/FiO2 < 100, signs of fatigue; lung-protective ventilation (6 mL/kg IBW, plateau pressure < 30 cmH2O); prone ventilation > 12 hours/day (PROSEVA); VTE: standard prophylactic-dose anticoagulation for patients on high-flow oxygen, CPAP, NIV or invasive ventilation (therapeutic-dose heparin benefited only non-critically ill patients -- ATTACC/ACTIV-4a/REMAP-CAP; NICE NG191); ECMO if severe refractory ARDS; goals of care discussion; DNACPR consideration; palliative care early involvement for very high risk patients.

Interpretation bands for the 4C Mortality Score. Apply clinical judgement and local guidance.

References

Related

Curated clinical cross-links plus same-class fallbacks.

Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.