A brief resolved unexplained event (BRUE) is a sudden, transient episode of altered breathing, colour, tone or responsiveness in an infant under 1-year-old, which resolves spontaneously and has no clear explanation after clinical assessment. BRUE is not a diagnosis but rather a clinical presentation, requiring careful evaluation to determine underlying causes. The term BRUE replaces the older term apparent life-threatening event (ALTE), refining the definition and introducing a risk-stratification approach..

 

Definition of BRUE 

The American Academy of Pediatrics (AAP) 2016 Criteria defines BRUE as a sudden, brief, and unexplained event in an infant under 1 year old that has completely resolved and meets all of the following criteria:

1. Occurs in an infant <12 months old

2. Brief duration (<1 minute, typically 2–30 seconds)

3. Resolves spontaneously with a return to baseline

4. No identifiable medical cause after thorough history and examination

5. At least one of the following features is present:

  • Cyanosis or pallor
  • Absent, decreased, or irregular breathing
  • Marked change in muscle tone (hypotonia or hypertonia)
  • Altered level of responsiveness

Key point: A BRUE should only be diagnosed when a complete clinical evaluation fails to identify a specific cause for the event.

 

 

Risk factors for BRUE

Certain factors increase the likelihood of BRUE episodes:

  • Prematurity (<32 weeks gestation)
  • Age <10 weeks
  • Recent anesthesia exposure
  • Airway abnormalities (e.g., laryngomalacia)
  • Gastroesophageal reflux disease (GERD)
  • Previous apneic episodes
  • Respiratory syncytial virus (RSV) infection
  • Feeding difficulties

 

Differentiating low-risk vs. high-risk BRUE

The AAP stratifies BRUE into low-risk and high-risk groups based on recurrence risk and association with serious conditions.

 

A low-risk BRUE is identified if all of the following apply:

  • Age >60 days.
  • Gestational age ≥32 weeks and postconceptional age ≥45 weeks.
  • Event duration <1 minute.
  • First BRUE episode (not recurrent).
  • No CPR was required by a trained healthcare provider.
  • No concerning historical features or physical exam findings.

 

A high-risk BRUE is identified if any of the following apply:

  • Age <60 days.
  • Gestational age <32 weeks.
  • Event duration >1 minute.
  • Recurrent episodes.
  • CPR required.
  • Concerning history or abnormal physical exam.

 

 

Differential diagnosis 

BRUE is a diagnosis of exclusion. Other serious conditions must be ruled out:

Category

Potential causes

 

Respiratory

Pertussis, bronchiolitis, aspiration, airway obstruction

 

Cardiac

Arrhythmias (e.g. long QT syndrome, SVT), congenital heart disease

 

Gastrointestinal

Gastroesophageal reflux disease (GORD), milk protein allergy

 

Neurological

 

Seizures, breath-holding spells, intracranial haemorrhage

 

Metabolic

 

Hypoglycaemia, inborn errors of metabolism

 

Infectious

 

Sepsis, meningitis, RSV, UTI

 

Non-accidental injury (NAI)

 

Child abuse, suffocation, poisoning

 

Clinical assessment

History:

  • Event details: Duration, colour change, breathing pattern, tone, seizure-like movements.
  • Preceding events: Fever, vomiting, feeding issues, infections.
  • Post-event behaviour: Normal vs. lethargic, irritable.
  • Positioning: Prone/supine, risk of airway obstruction.
  • Family history: Sudden infant death syndrome (SIDS), arrhythmias, metabolic disorders.
  • Social history: Co-sleeping, smoking, substance exposure.

 

Examination:

  • Vital signs: Temperature, HR, RR, BP, oxygen saturation.
  • General appearance: Alert vs. lethargic.
  • Respiratory: Stridor, nasal flaring, chest retractions.
  • Cardiac: Murmurs, femoral pulses (coarctation of the aorta).
  • Neurological: Hypotonia, hypertonia, abnormal reflexes.
  • Skin exam: Bruising, signs of non-accidental trauma.

 

 

Investigations in BRUE

Low-risk BRUE:

  • No investigations are required in most cases.
  • Some units may perform:
    • Capillary blood gas (CBG): Assess blood glucose, bicarbonate, and lactate for metabolic abnormalities.
    • ECG: Evaluate for arrhythmias, particularly prolonged QT interval.
  • There is no need for prolonged observation or monitoring.

 

High-risk BRUE:

  • Minimum required investigations:
    • CBG: Assess blood glucose, bicarbonate, and lactate to screen for metabolic disease.
    • ECG: Evaluate for arrhythmias (QT interval assessment).
    • Continuous cardiorespiratory monitoring during observation.
  • Additional investigations (guided by local protocols and clinical suspicion):
  • Blood tests: Full blood count, U&Es, CRP.
  • Nasopharyngeal aspirate (NPA): Assess for pertussis and/or RSV if infection suspected.

 

 

Management 

Low-risk BRUE:

  • Brief period of monitoring in ED (1–4 hours) with pulse oximetry.
  • Provide parental education and CPR training.
  • Discharge with reassurance.
  • Organise follow-up within 24 hours.

 

High-risk BRUE:

  • Admit for continuous monitoring and targeted investigations.
  • Investigate underlying causes based on suspected aetiology (e.g. infection, cardiac, metabolic or neurological causes).
  • Consider blood tests, ECG, brain imaging and polysomnography if clinically indicated.
  • Speciality referral (neurology, cardiology, respiratory) if required.

 

Parental counselling:

  • Educate on safe sleep practices (supine sleeping, no soft bedding).
  • Reassure that low-risk BRUE is unlikely to recur.
  • Provide clear guidance on when to seek medical attention.

 

 

Thank you to the joint editorial team of MRCEM Exam Prep for this article.