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Tertiary survey and missed injury prevention

Essential points for quick revision.

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New deterioration reopens the primary survey

A tertiary survey prevents delayed diagnosis but must never postpone immediate reassessment when airway, breathing, perfusion, consciousness, neurology or limb status worsens.

Action: Return at once to CABCDE, treat any life threat, compare with previous findings and interventions, call senior trauma support, and use targeted imaging or operative review before resuming the planned head-to-toe tertiary process.

Synopsis

Use repeated structured assessment, definitive report reconciliation and closed-loop handover to detect injuries obscured by resuscitation, altered consciousness, distracting pain or transfers.

  • Schedule a documented tertiary survey after initial resuscitation and imaging, commonly within 24 hours, and repeat when the patient is awake, sober or able to cooperate.
  • Start with interval events and another CABCDE review; any deterioration takes priority over completing the checklist and triggers immediate treatment.
  • Rebuild the mechanism and AMPLE history from patient, witnesses, ambulance and records, including anticoagulants, baseline function, pregnancy and pre-existing deficits.

Key red flags

New hypoxia, shock, falling GCS, focal deficit, escalating pain or loss of distal perfusion after admission represents active deterioration, not a routine tertiary-survey finding.

Investigation priorities

01
First-line record reconciliationFirst stepFirst line

Identify incomplete assessments, pending results and discrepancies across transitions.

Management branches

TimingPrepare a reliable tertiary survey

Initial resuscitation and urgent treatment are complete enough for systematic reassessment.

  1. Schedule the survey within the trauma pathway and identify which regions or history remain unreliable because of sedation, pain, intoxication or urgent intervention.
  2. Collect ambulance, emergency, operative and transfer records, preliminary and final imaging reports, laboratory trends and current device lists before bedside review.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom