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peds.brue.v1

Brief Resolved Unexplained Event (BRUE)

pediatricsacutepediatricacuteinpatientoutpatient

NEW pediatric dossier — promoted PLANNED->INTEGRATED 2026-05-25: seed routing manifest authored (prisma/seed/manifests/peds.brue.v1.ts), workups[] repointed to 3 registry-resolving entries (workup.pediatric_fever, workup.bronchiolitis, workup.airway_distress), all 6 evidence PMIDs live-verified (4 fabricated codes corrected), all 4 regimen RxCUIs RxNav-confirmed. package/atoms authoring deferred to a future pass. NEXT STEPS (for SCAFFOLDED promotion): (1) author manifest at prisma/seed/manifests/peds.brue.v1.ts; (2) register calc.brue_risk_stratification (lower-risk vs higher-risk per AAP 2016 6-criterion checklist) in clinical-tools-registry.ts; (3) register BRUE-specific workups (workup.brue_lower_risk_observation, workup.brue_higher_risk_tailored, workup.brue_cardiac_evaluation, workup.brue_seizure_evaluation, workup.brue_abuse_evaluation, workup.brue_metabolic_evaluation); (4) RxCUI validation for ampicillin, gentamicin, acyclovir, azithromycin, lorazepam (already in regimen_axes). AAP 2016 Tieder replaced ALTE with BRUE — terminology shift drove the lower-risk algorithm reducing unnecessary admissions and workups by ~30-50% in implementation studies (Mittal Pediatrics 2020 validation). Lower-risk classification (6 criteria) is highly conservative: age >60 d AND GA ≥32 wk AND PMA ≥45 wk AND first event AND duration <60 s AND no trained-CPR AND no concerning history/exam → ALL must apply for lower-risk; any one failing → higher-risk. Sibling differentiation from peds.febrile-infant.core.v1 (fever-centric), peds.bronchiolitis.v1 (URI-prodrome), and peds.status_epilepticus.v1 (active seizure) documented across 3 sibling rows. Authored 2026-05-15 (shard-5-obped-id Phase C wave 12 NEW dossier): 3-file set (peds.brue.v1.ts + _briefs/peds.brue.v1.md + _research-bundles/peds.brue.v1.md). Backbone: AAP 2016 Tieder PMID 27244835 + AAP 2020 Christian abusive head trauma + AAP 2021 Pantell febrile infant (cross-ref) + AAP 2022 Moon safe sleep + Red Book 2021 (pertussis) + NASPGHAN 2018 Rosen (GERD) + AES 2016 (seizure). 10 severity_triggers: higher_risk_brue_full_workup (severe), lower_risk_brue_discharge_with_education (mild), suspected_child_abuse_in_brue (life_threatening — skeletal survey + ophthalmology + social work + CPS), seizure_in_brue (severe — EEG + neuro), cardiac_workup_brue (severe — ECG + echo + cardiology), gerd_with_brue (moderate — peds GI; avoid empiric PPI), metabolic_disorder_screen_brue (severe — ammonia/lactate/acylcarnitine/organic acids/amino acids), repeat_brue_higher_risk_evaluation (severe — intensified workup), pertussis_test_in_unexplained_brue (severe — PCR + azithromycin + public health), apnea_of_prematurity_overlap (moderate — <44 wk PMA different entity). 3 setting_playbooks (ed / inpatient / outpatient). 2 regimen_axes (lower_risk_supportive + higher_risk_etiology_specific). _registry.ts NOT touched per §5 refined pattern. Status PLANNED; manifest field blank per §5.5 pragmatic policy. Phenotype matrix (age band × GA × PMA × event-features × first-vs-recurrent × trained-CPR × concerning history-exam → lower-risk vs higher-risk) encoded indirectly via severity_triggers + setting_playbook logic. First-class TS field for phenotype matrix is schema-blocked. Bayesian linkage (pre-test serious-illness prior in BRUE ~ 0.4-2.5% lower-risk per Mittal Pediatrics 2020 validation cohort; ~ 5-15% higher-risk depending on criterion violated; LRs: age ≤60 d LR+ ~ 3-5 for serious illness; duration ≥60 s LR+ ~ 2-3; CPR by trained provider LR+ ~ 5-8; recurrent event LR+ ~ 4-6; bruising in non-mobile infant LR+ ~ 30-50 for abuse; T_treat ~ 5% post-test for admission + workup; T_test ~ 1% post-test for targeted workup without admission; cross-dossier routing to peds.febrile-infant.core.v1 / peds.bronchiolitis.v1 / peds.status_epilepticus.v1 / id.sepsis.peds.v1) documented in _research-bundles/peds.brue.v1.md. ROS/DDx LR seed data audited by npm run audit:ros-ddx-coverage (cross-cutting; not touched by this shard). All 6 evidence PMIDs live-verified vs PubMed E-utilities 2026-05-25; 4 prior fabricated codes corrected: 27095103->27244835 (Tieder 2016 BRUE CPG), 24127022->23359576 (Kimberlin neonatal HSV Pediatrics 2013), 32820067->34168059 (Tieder 2021 multicenter BRUE risk study), 26952506->19403508 (Christian abusive head trauma Pediatrics 2009). Prehospital recognition is currently encoded implicitly via flow.entry_points; a first-class "prehospital" DossierSetting value is schema-blocked.

Entry points (5)

  • symptom
    Brief (<1 min) resolved episode in infant <1 yr with cyanosis/pallor, breathing change, tone change, or altered responsiveness (AAP 2016 Tieder PMID 27244835)
    brief_resolved_unexplained_event_infant
  • symptom
    Cyanotic or pallid spell in infant <1 yr — caregiver report (AAP 2016 Tieder)
    cyanotic_or_pallid_spell_infant
  • symptom
    Apneic or breathing-irregularity episode in infant <1 yr, now well (AAP 2016 Tieder)
    apneic_episode_infant_now_well
  • symptom
    Altered tone (hyper-/hypotonia) or altered responsiveness episode, resolved (AAP 2016 Tieder)
    altered_tone_or_responsiveness_resolved
  • history
    Caregiver-initiated CPR or rescue breathing for an infant <1 yr (AAP 2016 Tieder — concerning history feature)
    caregiver_initiated_cpr_infant

Required inputs (19)

  • age_daysrequired
    demographic • used at FRAME
    Age >60 d is a lower-risk gate (AAP 2016 Tieder); <60 d → higher-risk by definition
  • gestational_age_weeksrequired
    demographic • used at FRAME
    GA ≥32 wk AND PMA ≥45 wk required for lower-risk classification (AAP 2016 Tieder)
  • postconceptional_age_weeksrequired
    demographic • used at FRAME
    PMA ≥45 wk required for lower-risk classification; <44 wk PMA overlaps with apnea of prematurity (AAP 2016 Tieder)
  • event_duration_secondsrequired
    symptom • used at FRAME
    Duration <60 s required for lower-risk classification; ≥60 s → higher-risk (AAP 2016 Tieder)
  • event_features_cyanosis_pallorrequired
    symptom • used at FRAME
    Cyanosis or pallor is one of the 4 defining BRUE features (AAP 2016 Tieder)
  • event_features_breathing_changerequired
    symptom • used at FRAME
    Absent / decreased / irregular breathing is a defining BRUE feature (AAP 2016 Tieder)
  • event_features_tone_changerequired
    symptom • used at FRAME
    Marked tone change (hyper- or hypotonia) is a defining BRUE feature (AAP 2016 Tieder)
  • event_features_altered_responsivenessrequired
    symptom • used at FRAME
    Altered level of responsiveness is a defining BRUE feature (AAP 2016 Tieder)
  • first_event_vs_recurrentrequired
    history • used at RISK_STRATIFICATION
    First event required for lower-risk; recurrent → higher-risk + workup intensification (AAP 2016 Tieder)
  • trained_cpr_requiredrequired
    history • used at RISK_STRATIFICATION
    CPR by trained provider during event → higher-risk by definition (AAP 2016 Tieder)
  • concerning_history_featuresrequired
    history • used at CONTEXT
    Family history of sudden unexplained death, parental concern for abuse, prior similar events, social-risk concerns (AAP 2016 Tieder)
  • concerning_exam_featuresrequired
    symptom • used at CONTEXT
    Abnormal vital signs, bruising, retinal hemorrhages, abnormal neurologic exam, cardiopulmonary findings (AAP 2016 Tieder)
  • temperaturerequired
    vital • used at RED_FLAGS
    Fever in infant <60 d routes to peds.febrile-infant.core.v1 sibling pathway (AAP 2016 Tieder; AAP 2021 Pantell)
  • spo2required
    vital • used at CONTEXT
    Persistent hypoxemia after event → higher-risk + admit (AAP 2016 Tieder)
  • hrrequired
    vital • used at CONTEXT
    Tachycardia / bradycardia at presentation → higher-risk (AAP 2016 Tieder)
  • rrrequired
    vital • used at CONTEXT
    Tachypnea or apnea at presentation → higher-risk (AAP 2016 Tieder)
  • ecg_12_lead
    imaging • used at INITIAL_WORKUP
    ECG MAY be obtained even in lower-risk BRUE per AAP 2016 (weak recommendation) to screen for long-QT, WPW, hypertrophic cardiomyopathy; required in higher-risk (AAP 2016 Tieder)
  • pertussis_pcr_if_under_4mo
    lab • used at BRANCHING_WORKUP
    Pertussis screen for unexplained BRUE especially <4 mo (AAP 2016 Tieder weak recommendation)
  • cyanosis_pallor_distinction
    history • used at FRAME
    Caregiver perception of color change must be assessed carefully — distinguish true central cyanosis from perioral cyanosis with crying, pallor with fright (AAP 2016 Tieder)

12-phase flow (12)

  1. 1FRAME
    Confirm BRUE definition: infant <1 yr + sudden brief (<1 min) resolved episode + ≥1 of cyanosis-pallor / breathing change / tone change / altered responsiveness + no explanation after history-exam (AAP 2016 Tieder PMID 27244835)
    inputs: age_days, event_duration_seconds, event_features_cyanosis_pallor, event_features_breathing_change, event_features_tone_change, event_features_altered_responsiveness
    advance: BRUE definition confirmed; episode resolved at presentation; no alternative diagnosis from history-exam
  2. 2ENTRY
    Caregiver-reported cyanotic / pallid / breathing / tone / responsiveness event in infant <1 yr; now well-appearing (AAP 2016 Tieder)
    inputs: age_days
    advance: Entry trigger captured + infant currently well
  3. 3CONTEXT
    Birth history (GA, perinatal complications, NICU stay), feeding history (GERD symptoms, choking with feeds), family history (sudden unexplained death, channelopathy, metabolic disease), social history (caregiver stress, prior CPS involvement), prior similar events, vaccination status, sleep environment, current medications, exposure to medications-toxins (AAP 2016 Tieder)
    inputs: gestational_age_weeks, postconceptional_age_weeks, concerning_history_features, concerning_exam_features, spo2, hr, rr
    advance: Complete history + exam documented
  4. 4RED_FLAGS
    Fever in infant <60 d → route to peds.febrile-infant.core.v1; persistent hypoxemia or hemodynamic instability or seizure activity → resuscitate + admit + full workup; bruising / retinal hemorrhages / abnormal neuro exam → child abuse pathway (AAP 2016 Tieder)
    inputs: temperature, concerning_exam_features
    advance: Red flags screened; any positive → bypass to higher-risk workup + admit
  5. 5INITIAL_WORKUP
    Lower-risk: NO routine labs / imaging / EEG / CXR / echo; ECG may be obtained per AAP 2016 weak recommendation; pertussis PCR may be obtained if <4 mo; brief monitored observation (1-4 h continuous pulse-ox); CPR teaching for caregivers (AAP 2016 Tieder). Higher-risk: tailored workup based on clinical concern (AAP 2016 Tieder)
    inputs: ecg_12_lead, pertussis_pcr_if_under_4mo
    actions: workup.brue_lower_risk_observation, workup.brue_higher_risk_tailored
    advance: Initial workup completed per risk tier
  6. 6BRANCHING_WORKUP
    Higher-risk subtype-specific workup: (1) sepsis if febrile or ill-appearing → blood/urine/CSF cultures per peds.febrile-infant.core.v1; (2) seizure → EEG + neuro consult; (3) cardiac → echo if structural CHD suspected from ECG/exam; (4) GERD → pediatric GI consult, trial of management; (5) child abuse → skeletal survey + ophthalmology retinal exam + social work + CPS notification; (6) inborn errors of metabolism → ammonia, lactate, glucose, acylcarnitine profile, urine organic acids, plasma amino acids if recurrent / family history; (7) pertussis → PCR if <4 mo or unvaccinated; (8) apnea of prematurity → if <44 wk PMA, consider as different entity (AAP 2016 Tieder)
    inputs: concerning_history_features, concerning_exam_features
    actions: workup.pediatric_fever, workup.brue_cardiac_evaluation, workup.brue_seizure_evaluation, workup.brue_abuse_evaluation, workup.brue_metabolic_evaluation
    advance: Subtype workup launched as clinically indicated
  7. 7DIFFERENTIAL
    BRUE (idiopathic — most common) vs sepsis vs seizure vs GERD with apnea vs congenital heart disease (long-QT, WPW, hypertrophic cardiomyopathy, anomalous coronary, ductal-dependent lesion) vs metabolic / inborn error vs child abuse (abusive head trauma, suffocation) vs pertussis vs apnea of prematurity (if <44 wk PMA) vs breath-holding spell (typically >6 mo with trigger) vs vasovagal-equivalent vs medication / toxin exposure (AAP 2016 Tieder)
    advance: Differential narrowed; idiopathic BRUE is diagnosis of exclusion after risk-stratified evaluation
  8. 8RISK_STRATIFICATION
    Apply AAP 2016 lower-risk criteria (ALL must be met): age >60 d AND GA ≥32 wk AND PMA ≥45 wk AND first event AND duration <60 s AND no CPR by trained provider AND no concerning history-exam features → lower-risk BRUE. Any criterion failing → higher-risk BRUE. Calculator: calc.brue_risk_stratification (deferred to future SCAFFOLDED+ pass)
    inputs: age_days, gestational_age_weeks, postconceptional_age_weeks, event_duration_seconds, first_event_vs_recurrent, trained_cpr_required, concerning_history_features, concerning_exam_features
    advance: Risk tier (lower-risk vs higher-risk) assigned
  9. 9TREATMENT
    Lower-risk BRUE — NO routine medications; supportive observation; caregiver CPR teaching; reassurance; shared decision-making about brief admission for monitoring vs discharge with close follow-up (AAP 2016 Tieder). Higher-risk — etiology-specific treatment: empiric antibiotics if sepsis suspected (route to peds.febrile-infant.core.v1), antiepileptics if seizure confirmed (route to peds.status_epilepticus.v1 if recurrent), GERD management (lifestyle + acid suppression per peds GI), cardiac management (route to peds cardiology), metabolic management (route to peds metabolism). Treat the underlying cause, not the BRUE itself (AAP 2016 Tieder)
    advance: Treatment plan documented per risk tier + suspected etiology
  10. 10DISPOSITION
    Lower-risk BRUE: shared decision-making with caregivers — option A) brief observation (1-4 h continuous pulse-ox) + discharge with close (24 h) PCP follow-up + CPR teaching + return precautions; option B) brief admission for cardiorespiratory monitoring if caregiver anxiety high or social-risk concerns (AAP 2016 Tieder). Higher-risk BRUE: admit for monitored observation + targeted workup; PICU if respiratory failure, seizure activity, or hemodynamic instability (AAP 2016 Tieder)
    advance: Disposition documented per risk tier + caregiver preference
  11. 11MONITORING
    Lower-risk: continuous pulse-ox during brief observation; vitals q1h; recheck before discharge. Higher-risk: continuous cardiorespiratory monitoring + apnea alarm; vitals q4h; serial neuro exam if seizure suspected; EEG monitoring if epileptiform activity captured (AAP 2016 Tieder)
    advance: Monitoring orders documented
  12. 12FOLLOWUP
    Lower-risk: PCP follow-up within 24 h (telephone + in-person at 24-72 h); reinforce CPR teaching; review return precautions (any new event, color change, breathing concern, feeding difficulty, lethargy → ED); discuss safe sleep (back-to-sleep, room-sharing not bed-sharing, smoke-free home) and breastfeeding promotion (AAP 2016 Tieder; AAP 2022 Moon safe sleep). Higher-risk: outpatient pediatric subspecialist follow-up based on workup findings (cardiology, neurology, GI, metabolism, child abuse / CPS); developmental surveillance (AAP 2016 Tieder)
    advance: Follow-up plan + return precautions + safe sleep + CPR teaching documented