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emergency-medicine respiratory

Pulmonary Embolism Severity Index (PESI)

Predicts 30-day mortality in acute pulmonary embolism. Guides decision between inpatient vs outpatient management.

How to use & interpret

The PESI (and simplified sPESI) estimates 30-day mortality after acute pulmonary embolism and is used to identify low-risk patients who may be suitable for outpatient or early-discharge management. PESI sorts patients into classes I–V; classes I–II (or an sPESI of 0) indicate low risk.

It supports — but does not replace — assessment of haemodynamic stability, right-heart strain (echo/CT, troponin, BNP) and social factors before deciding on ambulatory care.

Score interpretation

Class I — Very low 30-day mortality (<1.6%)

→ Outpatient treatment or early discharge; DOAC

Class II — Low mortality (1.7-3.5%)

→ Short inpatient stay or outpatient with close follow-up

Class III — Moderate mortality (3.2-7.1%)

→ Inpatient treatment; monitor closely

Class IV — High mortality (4-11.4%)

→ Inpatient; ICU consideration; assess for thrombolysis

Class V — Very high mortality (10-24.5%)

→ ICU; consider systemic thrombolysis or catheter-directed therapy

Interpretation bands for the PESI. Apply clinical judgement and local guidance.

Frequently asked questions

Can a low PESI alone justify outpatient PE treatment?

No. Confirm haemodynamic stability, absence of right-ventricular dysfunction, adequate home circumstances and follow-up, and check for contraindications before ambulatory management.

References

Related

Curated clinical cross-links plus same-class fallbacks.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

The PESI is covered in detail — with RCEM/NICE evidence base, indications and pitfalls — in the following exam-focused pathways on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.

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