• Episode 216: BRUE (Brief Resolved Unexplained Event)
    Dec 1 2025
    We review BRUEs (Brief Resolved Unexplained Events). Hosts: Ellen Duncan, MD, PhD Noumi Chowdhury, MD https://media.blubrry.com/coreem/content.blubrry.com/coreem/BRUE.mp3 Download Leave a Comment Tags: Pediatrics Show Notes What is a BRUE? BRUE stands for Brief Resolved Unexplained Event.It typically affects infants <1 year of age and is characterized by a sudden, brief, and now resolved episode of one or more of the following: Cyanosis or pallor Irregular, absent, or decreased breathing Marked change in tone (hypertonia or hypotonia) Altered level of responsiveness Crucial Caveat: BRUE is a diagnosis of exclusion. If the history and physical exam reveal a specific cause (e.g., reflux, seizure, infection), it is not a BRUE. Risk Stratification: Low Risk vs. High Risk Risk stratification is the most important step in management. While only 6-15% of cases meet strict “Low Risk” criteria, identifying these patients allows us to avoid unnecessary invasive testing. Low Risk Criteria To be considered Low Risk, the infant must meet ALL of the following: Age: > 60 days old Gestational Age: GA > 32 weeks (and Post-Conceptional Age > 45 weeks) Frequency: This is the first episode Duration: Lasted < 1 minute Intervention: No CPR performed by a trained professional Clinical Picture: Reassuring history and physical exam Management for Low Risk: Generally do not require extensive testing or admission. Prioritize safety education/anticipatory guidance. Ensure strict return precautions and close outpatient follow-up (within 24 hours). High Risk Criteria Any infant not meeting the low-risk criteria is automatically High Risk. Additional red flags include: Suspicion of child abuse History of toxin exposure Family history of sudden cardiac death Abnormal physical exam findings (trauma, neuro deficits) Management for High Risk: Requires a more thorough evaluation. Often requires hospital admission. Note: Serious underlying conditions are identified in approx. 4% of high-risk infants. Differential Diagnosis: “THE MISFITS” Mnemonic T – Trauma (Accidental or Non-accidental/Abuse) H – Heart (Congenital heart disease, dysrhythmias) E – Endocrine M – Metabolic (Inborn errors of metabolism) I – Infection (Sepsis, meningitis, pertussis, RSV) S – Seizures F – Formula (Reflux, allergy, aspiration) I – Intestinal Catastrophes (Volvulus, intussusception) T – Toxins (Medications, home exposures) S – Sepsis (Systemic infection) Workup & Diagnostics Step 1: Stabilization ABCs (Airway, Breathing, Circulation) Point-of-care Glucose Cardiorespiratory monitoring Step 2: Diagnostic Testing (For High Risk/Symptomatic Patients) Labs: VBG, CBC, Electrolytes. Imaging: CXR: Evaluate for infection and cardiothymic silhouette. EKG: Evaluate for QT prolongation or dysrhythmias. Neuro: Consider Head CT/MRI and EEG if there are concerns for trauma or seizures. Clinical Pearl: Only ~6% of diagnostic tests contribute meaningfully to the diagnosis. Be judicious—avoid “shotgunning” tests in low-risk patients. Prognosis & Outcomes Recurrence: Approximately 10% (lower than historical ALTE rates of 10-25%). Mortality: < 1%. Nearly always linked to an identifiable cause (abuse, metabolic disorder, severe infection). BRUE vs. SIDS: These are not the same. BRUE: Peaks < 2 months; occurs mostly during the day. SIDS: Peaks 2–4 months; occurs mostly midnight to 6:00 AM. Take-Home Points Diagnosis of Exclusion: You cannot call it a BRUE until you have ruled out obvious causes via history and physical. Strict Criteria: Stick strictly to the Low Risk criteria guidelines. If they miss even one (e.g., age < 60 days), they are High Risk. Education: For low-risk families, the most valuable intervention is reassurance, education, and arranging close follow-up. Systematic Approach: For high-risk infants, use a structured approach (like THE MISFITS) to ensure you don’t miss rare but reversible causes. Read More
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  • Episode 215: Marburg Virus and Global EM
    Nov 1 2025

    Lessons from Rwanda’s Marburg Virus Outbreak and Building Resilient Systems in Global EM.

    Hosts:
    Tsion Firew, MD
    Brian Gilberti, MD

    https://media.blubrry.com/coreem/content.blubrry.com/coreem/Marburg_Virus.mp3 Download Leave a Comment Tags: Global Health, Infectious Diseases Show Notes Context and the Rwanda Marburg Experience
    • The Threat: Marburg Virus Disease is from the same family as Ebola and has historically had a reported fatality rate as high as 90%.
    • The Outbreak (Sept. 2024): Rwanda declared an MVD outbreak. The initial cases involved a miner, his pregnant wife (who fell ill and died after having a baby), and the baby (who also died).
    • Healthcare Worker Impact: The wife was treated at an epicenter hospital. Eight HCWs were exposed to a nurse who was coding in the ICU; all eight developed symptoms, tested positive within a week, and four of them died.
    • The Turning Point: The outbreak happened in city referral hospitals where advanced medical interventions (dialysis, mechanical ventilation) were available.
      • Rapid Therapeutics Access: Within 10 days of identifying Marburg, novel therapies (experimental drugs and monoclonal antibodies) and an experimental vaccine were made available through diplomacy with the US government/CDC and agencies like WHO, Africa CDC, CEPI and more.
    • The Outcome: This coordinated effort—combini...
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  • Episode 214: Acute Pulmonary Embolism
    Oct 2 2025

    We review the diagnosis, risk stratification, & management of acute pulmonary embolism in the ED.

    Hosts:
    Vivian Chiu, MD
    Brian Gilberti, MD

    https://media.blubrry.com/coreem/content.blubrry.com/coreem/Acute_Pulmonary_Embolism.mp3 Download One Comment Tags: Pulmonary Show Notes Core Concepts and Initial Approach
    • Definition: Obstruction of pulmonary arteries, usually from a DVT in the proximal lower extremity veins (iliac/femoral), but may be tumor, air, or fat emboli.
    • Incidence & Mortality: 300,000–370,000 cases/year in the USA, with 60,000–100,000 deaths annually.
    • Mantra: “Don’t anchor on the obvious. Always risk stratify and resuscitate with precision.”
    • Risk Factors: Broad, including older age, inherited thrombophilias, malignancy, recent surgery/trauma, travel, smoking, hormonal use, and pregnancy.
    Clinical Presentation and Risk Stratification
    • Presentation: Highly variable, showing up as anything from subtle shortness of breath to collapse.
    • Acute/Subacute: Dyspnea (most common), pleuritic chest pain, cough, hemoptysis, and syncope. Patients are likely tachycardic, tachypneic, hypoxemic on room air, and may have a low-grade fever.
    • Chronic: Can mimic acute symptoms or be totally asymptomatic.
    • Pulmonary Infarction Signs: Pleuritic pain, hemoptysis, and an effusion.
    • High-Risk Red Flags: Signs of hypotension (systolic blood pressure < 90 mmHg for over 15...
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  • Episode 213: Pneumothorax
    Sep 1 2025

    We break down pneumothorax: risks, diagnosis, and management pearls.

    Hosts:
    Christopher Pham, MD
    Brian Gilberti, MD

    https://media.blubrry.com/coreem/content.blubrry.com/coreem/Pneumothorax.mp3 Download Leave a Comment Tags: Chest Trauma, Pulmonary, Trauma Show Notes Risk Factors for Pneumothorax
    • Secondary pneumothorax
      • Trauma: rib fractures, blunt chest trauma (as in the case).
      • Iatrogenic: central line placement, thoracentesis, pleural procedures.
    • Primary spontaneous pneumothorax
      • Young, tall, thin males (10–30 years).
      • Connective tissue disorders: Marfan, Ehlers-Danlos.
      • Underlying lung disease: COPD with bullae, interstitial lung disease, CF, TB, malignancy.
    • Technically, anyone is at risk.
    Symptoms & Differential Diagnosis
    • Typical PTX presentation: Dyspnea, chest pain, pleuritic discomfort.
    • Exam clues: unilateral decreased breath sounds, focal tenderness/crepitus.
    • Red flags (suggest tension PTX):
      • JVD
      • Tracheal deviation
      • Hypotension, shock physiology
      • Severe tachycardia, hypoxia
    • Differential diagnoses:
      • Pulmonary: asthma, COPD, pneumonia, pulmonary edema (SCAPE), ILD, infections.
      • Cardiac: ACS, CHF, pericarditis.
      • PE and other acute causes of dyspnea.
    Diagnostics
    • Bloodwork: limited role, except type & screen if intervention likely.
    • EKG: reasonable given chest pain/shortness of br...
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  • Episode 212: Angioedema
    Aug 2 2025

    Angioedema – Recognition and Management in the ED

    Hosts:
    Maria Mulligan-Buckmiller, MD
    Brian Gilberti, MD

    https://media.blubrry.com/coreem/content.blubrry.com/coreem/Angioedema.mp3 Download Leave a Comment Tags: Airway Show Notes Definition & Pathophysiology

    Angioedema = localized swelling of mucous membranes and subcutaneous tissues due to increased vascular permeability.

    Triggers increased vascular permeability → fluid shifts into tissues.

    Etiologies
    • Histamine-mediated (anaphylaxis)
      • Associated with urticaria/hives, pruritus, and redness.
      • Triggered by allergens (foods, insect stings, medications).
      • Rapid onset (minutes to hours).
    • Bradykinin-mediated
      • Hereditary angioedema (HAE): C1 esterase inhibitor deficiency (autosomal dominant).
      • Acquired angioedema: Associated with B-cell lymphoma, autoimmune disease, MGUS.
      • Medication-induced: Most commonly ACE inhibitors; rarely ARBs.
      • Typically lacks urticaria and itching.
      • Gradual onset, can last days if untreated.
    • Idiopathic angioedema
      • Unknown cause; diagnosis of exclusion.
    Clinical Presentations
    • Swelling
      • Asymmetric, non-pitting, usually non-painful.
      • May involve lips, tongue, face, extremities, GI tract.
    • Respiratory compromise
      • Upper airway swelling → stridor, dyspnea, sensation of throat closure.
      • Airway obstruction is the most feared complication.
    • Abdominal manifestations
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    • Episode 211: Granulomatosis with Polyangiitis
      Jul 1 2025

      Granulomatosis with Polyangiitis (GPA) – Recognition and Management in the ED

      Hosts:
      Phoebe Draper, MD
      Brian Gilberti, MD

      https://media.blubrry.com/coreem/content.blubrry.com/coreem/GPA.mp3 Download One Comment Tags: Rheumatology Show Notes Background
      • A vasculitis affecting small blood vessels causing inflammation and necrosis
      • Affects upper respiratory tract (sinusitis, otitis media, saddle nose deformity), lungs (nodules, alveolar hemorrhage), and kidneys (rapidly progressive glomerulonephritis)
      • Can lead to multi-organ failure, pulmonary hemorrhage, renal failure
      Red Flag Symptoms:
      • Chronic sinus symptoms
      • Hemoptysis (especially bright red blood)
      • New pulmonary complaints
      • Renal dysfunction
      • Constitutional symptoms (fatigue, weight loss, fever)
      Workup in the ED:
      • CBC, CMP for anemia and AKI
      • Urinalysis with microscopy (hematuria, RBC casts)
      • Chest imaging (CXR or CT for nodules, cavitary lesions)
      • ANCA testing (not immediately available but important diagnostically)
      Management:
      • Stable patients: Outpatient workup, urgent rheumatology consult, prednisone 1 mg/kg/day
      • Unstable patients: High-dose IV steroids (methylprednisolone 1 g daily x3 days), consider plasma exchange, cyclophosphamide or rituximab initiation, ICU admission
      Conditions that Mimic GPA:
      • Goodpasture syndrome (anti-GBM antibodies)
      • TB, fungal infections
      • Lung malignancy
      • Other vasculitides (EGPA, MPA, lupus)
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    • Episode 210: Capacity Assessment
      Jun 2 2025

      We discuss capacity assessment, patient autonomy, safety, and documentation.

      Hosts:
      Anne Levine, MD
      Brian Gilberti, MD

      https://media.blubrry.com/coreem/content.blubrry.com/coreem/Capacity_Assessment.mp3 Download One Comment Show Notes The Importance of Capacity Assessment
      • Arises frequently in the ED, even when not formally recognized
      • Carries both legal implications and ethical weight
      • Failure to appropriately assess capacity can result in:
        • Forced treatment without justification
        • Missed opportunities to respect autonomy
        • Increased risk of litigation and poor patient outcomes
      Defining Capacity
      • Capacity is:
        • Decision-specific: varies based on the medical choice at hand
        • Time-specific: can fluctuate due to medical conditions, intoxication, delirium
      • Distinct from competency, which is a legal determination
      • Relies on a patient’s ability to:
        • Understand relevant information
        • Appreciate the consequences
        • Reason through options
        • Communicate a clear choice
      Real-World ED Examples
      • Intoxicated patient with head trauma refusing CT
        • Unreliable neuro exam
        • Potentially time-sensitive intracranial injury
      • Elderly patient with sepsis refusing admission due to caregiving responsibilities
        • Balancing autonomy vs. beneficence
      • Patient with gangrenous diabetic foot refusing surgery
        • Demonstrates logic and consistency despite high-risk decision
      The 4 Pillars of Capacity Assessment
      • Understanding
        • Can the patient explain:
        • Their condition
        • Recommended treatments
        • Risks and benefits
        • Alternatives and outcomes?
      • Sample prompts:
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      • Episode 209: Blast Crisis
        May 1 2025
        We dive into the recognition and management of blast crisis. Hosts: Sadakat Chowdhury, MD Brian Gilberti, MD https://media.blubrry.com/coreem/content.blubrry.com/coreem/Blast_Crisis.mp3 Download 2 Comments Tags: Hematology, Oncology Show Notes Topic Overview Blast crisis is an oncologic emergency, most commonly seen in chronic myeloid leukemia (CML).Defined by: >20% blasts in peripheral blood or bone marrow.May include extramedullary blast proliferation. Without treatment, median survival is only 3–6 months. Pathophysiology & Associated Conditions Usually occurs in CML, but also in: Myeloproliferative neoplasms (MPNs)Myelodysplastic syndromes (MDS) Transition from chronic to blast phase often reflects disease progression or treatment resistance. Risk Factors 10% of CML patients progress to blast crisis.Risk increased in: Patients refractory to tyrosine kinase inhibitors (e.g., imatinib).Those with Philadelphia chromosome abnormalities.WBC >100,000, which increases risk for leukostasis. Clinical Presentation Symptoms often stem from pancytopenia and leukostasis: Anemia: fatigue, malaise.Functional neutropenia: high WBC count, but increased infection/sepsis risk.Thrombocytopenia: bleeding, bruising. Leukostasis/hyperviscosity effects by system: Neurologic: confusion, visual changes, stroke-like symptoms.Cardiopulmonary: ARDS, myocardial injury.Others: priapism, limb ischemia, bowel infarction. Rapid deterioration is common — early recognition is critical. Diagnostic Workup CBC with differential: assess blast % and cytopenias.Peripheral smear and manual diff: confirm immature blasts.CMP: screen for tumor lysis syndrome: Elevated potassium, phosphate, uric acid.Low calcium. LDH & uric acid: markers of high cell turnover.Coagulation studies (PT, PTT): assess for DIC.Definitive tests (done inpatient): bone marrow biopsy, flow cytometry. Emergency Department Management Resuscitation & ABCs: oxygen, IV fluids, vitals monitoring.Avoid aggressive transfusions: Risk of hyperviscosity with PRBCs and platelets. Initiate broad-spectrum antibiotics early: High suspicion for sepsis in functionally neutropenic patients. Consider antifungals for prolonged febrile neutropenia.Cytoreduction strategies: Hydroxyurea to lower WBCs quickly.Tyrosine kinase inhibitors (TKIs).High-dose chemotherapy. Early consultation with hematology/oncology is essential.Mutation testing may guide targeted therapy. Prognosis Without treatment: median survival ~3 months.With treatment: Potential survival >1 year.Best outcomes in patients who enter a second chronic phase and undergo allogeneic stem cell transplant. Ethical & Logistical Considerations Treatment may involve aggressive interventions with serious side effects.Important to assess: Patient goals of care.Capacity for informed consent. Resource limitations: Not all hospitals have oncology services.Patients may require transfer over long distances. Emphasize early, transparent discussions with patients and families. Top 3 Take-Home Points Recognize early: Look for cytopenias, leukostasis, and rapid clinical decline.Resuscitate appropriately: Start antibiotics; be cautious with transfusions.Call for help: Early hematology/oncology involvement is essential for definitive care. Read More
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