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Eduovisual

Special Senses & Otolaryngology

Epistaxis: anterior and posterior management

Clinical Overview and When to Suspect Epistaxis

Anterior (90%): bleeding from Kiesselbach's plexus on the anterior nasal septum (Little's area), confluence of branches from the anterior ethmoidal, sphenopalatine, greater palatine, and superior labial arteries

Posterior (10%): bleeding from the sphenopalatine artery branches in the posterior nasal cavity (Woodruff's plexus), more brisk, often bilateral, blood seen draining down the posterior pharynx

— Failure of anterior packing to control bleeding

— Hemorrhage from both nares

— Persistent posterior pharyngeal blood drainage with anterior packing in place

— Hemodynamic instability or hemoptysis/hematemesis from swallowed blood

Local: digital trauma (nose-picking), dry air/winter, intranasal steroids, cocaine, septal deviation, neoplasm (squamous cell, juvenile nasopharyngeal angiofibroma in adolescent males)

Systemic: hypertension (correlation, not direct cause), anticoagulants/antiplatelets, liver disease, uremia, hereditary hemorrhagic telangiectasia (HHT/Osler-Weber-Rendu), von Willebrand disease, leukemia

Epistaxis = bleeding from the nasal cavity; one of the most common ENT emergencies, with a bimodal age distribution (children 2–10, adults >50)
Anatomic classification drives management:
When to suspect posterior epistaxis:
Common precipitants:
Step 3 management: Anticoagulation use is the single most important modifier — always ask about warfarin, DOACs, dual antiplatelets, NSAIDs, and herbal supplements (ginkgo, garlic, fish oil) before deciding on disposition
Board pearl: Recurrent unilateral epistaxis in an adolescent male = juvenile nasopharyngeal angiofibroma until proven otherwise — do not biopsy in clinic (catastrophic bleeding); obtain contrast imaging and ENT referral
Epistaxis is usually self-limited, but 5–10% require medical intervention, and posterior bleeds carry mortality up to 3–6% in elderly anticoagulated patients
Solid White Background
Presentation Patterns and Key History

— Unilateral bleeding from one naris, often after nose-blowing, sneezing, or trauma

— Patient leaning forward, blood visible at the nasal vestibule

— Self-limited or stops with simple pressure

— Bleeding from both nares OR brisk unilateral bleed not controlled by anterior measures

Blood dripping down the oropharynx with patient swallowing/spitting blood

— Hematemesis or coffee-ground emesis from swallowed blood (mimics UGIB)

— Older patient on anticoagulation, often hypertensive on arrival

Duration and estimated volume — soaked tissues vs. cups of blood

— Laterality and whether bilateral

— Trauma, foreign body (especially pediatrics), recent surgery

— Prior episodes and prior interventions (cautery, packing, embolization)

— Atrial fibrillation, mechanical valve, recent DVT/PE → anticoagulation

— Coronary stents → DAPT

— Cirrhosis, ESRD on dialysis (uremic platelet dysfunction)

— Hematologic disorders, HHT, recurrent mucocutaneous bleeds

— Hypertension, especially uncontrolled

— Warfarin (check INR), apixaban/rivaroxaban/dabigatran, aspirin, clopidogrel/ticagrelor

— Intranasal steroids, oxymetazoline overuse

— Cocaine, methamphetamine (septal perforation)

— NSAIDs, SSRIs (mild platelet effect), supplements

Classic anterior presentation:
Classic posterior presentation:
Critical history elements (HPI):
Past medical history red flags:
Medications to elicit:
Family history: HHT (autosomal dominant — recurrent epistaxis + telangiectasias + AVMs in lung/brain/liver + family history = Curaçao criteria)
Key distinction: Hematemesis from swallowed posterior epistaxis vs. true UGIB — clarify whether the patient saw nasal bleeding first and whether the emesis is bright red (recent swallowing) vs. coffee-ground; nasal exam clarifies
Step 3 management: Always document last anticoagulant dose, indication, and time-since-last-dose — drives reversal decisions and disposition
Solid White Background
Physical Exam Findings and Hemodynamic Assessment

— Vital signs: tachycardia, hypotension, orthostatics

— Airway compromise from posterior bleed or aspiration in obtunded patients

— Establish two large-bore IVs if bleeding is brisk or patient is on anticoagulation

— Headlamp or head mirror, nasal speculum, Frazier suction, bayonet forceps

— Topical anesthetic + vasoconstrictor (lidocaine 4% + oxymetazoline, or lidocaine + epinephrine)

— PPE: gown, face shield, gloves — high splash risk

— Have patient blow nose to clear clots

— Apply topical vasoconstrictor on cotton pledgets for 10–15 minutes

— Reexamine after vasoconstriction — often reveals the bleeding source

— Discrete bleeding point or oozing on the anterior septum (Kiesselbach's)

— Bleeding stops with pinching the cartilaginous portion of the nose (NOT the bony bridge)

— No identifiable anterior source despite good visualization

— Blood streaming down posterior pharyngeal wall on oral exam

— Persistent bleeding after well-placed anterior pack

— Bilateral bleeding

— Telangiectasias on lips/tongue/fingers → HHT

— Petechiae, ecchymoses → thrombocytopenia or coagulopathy

— Hepatomegaly, jaundice, spider angiomas → cirrhotic coagulopathy

— Lymphadenopathy, pallor → hematologic malignancy

Initial priority = ABCs and hemodynamics:
Position the patient: upright, leaning forward (not back — prevents aspiration and accurate assessment of volume swallowed)
Equipment for exam:
Sequence:
Anterior bleed signs:
Posterior bleed signs:
Systemic exam clues:
Board pearl: Pinch the soft cartilaginous nose (not the nasal bridge) firmly for 15 continuous minutes — most anterior bleeds stop with this maneuver alone; premature release is the #1 reason for "failure"
CCS pearl: Order CBC, type & screen, PT/INR, PTT early in any patient on anticoagulation or with hemodynamic changes — don't wait for packing failure
Solid White Background
Diagnostic Workup — Initial Labs and Imaging

— Anticoagulant or antiplatelet use

— Suspected coagulopathy (cirrhosis, ESRD, hematologic disease)

— Heavy or prolonged bleeding requiring packing

— Hemodynamic instability

— Recurrent epistaxis without clear local cause

CBC: hemoglobin/hematocrit (may underestimate acute loss), platelet count

PT/INR, aPTT: essential if on warfarin or unexplained bleeding

Type and screen if transfusion may be needed or posterior bleed suspected

BMP: renal function (uremic platelet dysfunction; also dosing for reversal agents)

LFTs if cirrhosis suspected

Fibrinogen if DIC or massive transfusion considered

— Routine PT/PTT are unreliable for DOACs

Anti-Xa level (calibrated for apixaban/rivaroxaban) — limited availability

Dilute thrombin time or ecarin clotting time for dabigatran

— In practice: rely on time since last dose and renal function

— Trauma with suspected facial fracture → CT face/maxillofacial

— Recurrent unilateral epistaxis with suspected mass → CT or MRI with contrast

— Adolescent male with recurrent unilateral bleed → CT with contrast for juvenile nasopharyngeal angiofibroma (do NOT biopsy)

— Pre-embolization planning → CT angiography

Most epistaxis is a clinical diagnosis — labs are selective, not routine
Indications for laboratory workup:
Initial labs:
DOAC-specific testing:
Imaging — generally NOT needed acutely for routine epistaxis
Imaging indications:
ECG: in elderly patients with significant blood loss, tachycardia, chest pain, or known CAD — assess demand ischemia
Board pearl: Hemoglobin in acute hemorrhage lags real blood loss by hours; don't be falsely reassured by a normal initial Hgb in a brisk posterior bleed
Step 3 management: In a warfarin patient with INR >3 and active epistaxis, do not wait for bleeding to fail conservative measures — start reversal planning while applying initial hemostatic measures
Solid White Background
Diagnostic Workup — Advanced and Confirmatory Studies

— Performed by ENT (or trained EM in some centers) with flexible or rigid endoscope

— Allows direct visualization of posterior bleeding sites including sphenopalatine artery branches and Woodruff's plexus

— Enables targeted electrocautery or chemical cautery under direct vision

— Should be considered before blind posterior packing when ENT is available

— Indicated when planning endovascular embolization

— Identifies vascular anomalies, tumors, traumatic pseudoaneurysm

— Evaluates aberrant internal carotid contributions (important to avoid catastrophic embolization complications)

— Both diagnostic and therapeutic for refractory posterior epistaxis

— Maps internal maxillary artery distribution and identifies bleeding source

von Willebrand panel (VWF antigen, ristocetin cofactor, factor VIII) — most common inherited bleeding disorder

Platelet function testing (PFA-100) if platelet dysfunction suspected

Peripheral smear if thrombocytopenia or hematologic malignancy suspected

Genetic testing for HHT (ENG, ACVRL1 mutations) — confirms diagnosis when Curaçao criteria suggest

— Pulmonary AVMs: contrast echocardiography (bubble study), then CT chest if positive

— Cerebral AVMs: MRI brain

— Hepatic AVMs: abdominal Doppler US if symptomatic

Nasal endoscopy is the definitive diagnostic and often therapeutic tool when source unclear or bleeding persists:
CT angiography (CTA):
Conventional angiography:
Workup for underlying systemic cause (in recurrent/severe cases):
HHT screening when diagnosed:
Key distinction: Workup of a first uncomplicated anterior bleed in a healthy adolescent or adult does not require imaging or extensive labs — vs. recurrent unilateral, family history, or severe presentations which mandate further evaluation
Board pearl: In confirmed/suspected HHT, screen for pulmonary AVMs — they cause paradoxical embolic stroke and brain abscess, and are treatable with embolization
Step 3 management: Refer recurrent epistaxis without identifiable local cause to hematology for bleeding disorder workup before assuming it is idiopathic
Solid White Background
Risk Stratification and First-Line Management Logic

Step 1: ABCs, IV access, hemodynamic stabilization, suction

Step 2: Have patient blow nose to evacuate clots

Step 3: Direct pressure — pinch cartilaginous nose firmly for 15 continuous minutes, leaning forward

Step 4: If continues, apply topical vasoconstrictor (oxymetazoline) on cotton pledget + topical anesthetic (lidocaine 4%) for 10–15 minutes

Step 5: Inspect with nasal speculum and headlamp; identify bleeding point

Step 6: Silver nitrate cautery if discrete anterior bleeding point is visualized after hemostasis (do NOT cauterize both sides of septum simultaneously → septal perforation risk)

Step 7: Anterior nasal packing if bleeding persists despite above (Merocel/Rapid Rhino balloon catheter or ribbon gauze with petrolatum)

Step 8: If anterior pack fails, blood still draining posteriorly, or bilateral → posterior pack + ENT consult + admit

Step 9: Refractory posterior bleeding → endoscopic sphenopalatine artery ligation or endovascular embolization

— Treat severe HTN (SBP >180 or DBP >110) after initial hemostatic measures

— Use short-acting agents (labetalol, nicardipine); avoid aggressive lowering

— Balance bleeding severity vs. thrombotic risk (mechanical valve, recent stent)

Anterior pack only, stable patient, no comorbidities → discharge with ENT follow-up in 48–72 hours

Posterior packadmit, often to monitored bed/ICU (risk of nasopulmonary reflex, hypoxia, dysrhythmia)

— Significant blood loss, ongoing anticoagulation → admit

Stepwise algorithm for acute epistaxis:
Hypertension management:
Anticoagulant reversal decisions (see chunk 7):
Disposition logic:
Board pearl: Posterior packing requires admission — historically associated with the "nasopulmonary reflex" causing bradycardia/hypoxia, plus continuous monitoring for re-bleeding and airway compromise
CCS pearl: Order BP control, hold anticoagulants, give appropriate reversal agent, type and screen, ENT consult, and admit to telemetry/ICU — all early in the encounter, not sequentially
Solid White Background
Pharmacotherapy — Hemostatic Agents and Anticoagulant Reversal

Oxymetazoline 0.05% — 2–3 sprays or on cotton pledget; alpha-1 agonist

Phenylephrine 0.25–1% — alternative

Cocaine 4% (topical) — combines vasoconstriction + anesthesia; rarely used today

— Caution in uncontrolled HTN, CAD, MAOI use

Lidocaine 4% spray or pledget

— Often combined with vasoconstrictor: lidocaine + oxymetazoline soaked pledgets for 10–15 minutes

Tranexamic acid (TXA) 500 mg soaked on gauze applied intranasally — increasing evidence for benefit

Floseal, Surgicel, gelfoam — absorbable hemostatic matrices

— Silver nitrate sticks for chemical cautery of discrete anterior bleeding points

— IV TXA may be considered in significant or refractory bleeding, especially with antiplatelet use

Warfarin:

— Severe bleed: 4-factor PCC (Kcentra) + IV vitamin K 5–10 mg

— FFP if PCC unavailable

Dabigatran: Idarucizumab (Praxbind) 5 g IV

Apixaban/Rivaroxaban: Andexanet alfa (expensive, limited availability) or 4-factor PCC 50 units/kg

Heparin: protamine sulfate

Antiplatelets: platelet transfusion only for life-threatening bleeding; DDAVP for uremic platelet dysfunction

— Minor anterior bleed, controlled with packing: hold anticoagulant 24–48 hours, no reversal

— Major or posterior bleed with hemodynamic compromise: reverse

— Mechanical mitral valve, recent PE, recent coronary stent → consult cardiology before full reversal

Topical vasoconstrictors (first-line adjunct):
Topical anesthetics:
Topical hemostatics:
Systemic TXA:
Anticoagulant reversal (when bleeding severe):
Hold vs. reverse decision:
Step 3 management: Resume anticoagulation as soon as hemostasis is durable (typically 24–72 hours post-packing removal) — thrombotic risk often exceeds re-bleeding risk in high-risk patients
Board pearl: Andexanet alfa has a short half-life and rebound anti-Xa activity; coordinate timing with hemostatic intervention
Solid White Background
Procedures — Packing, Cautery, Ligation, and Embolization

— Apply for 5–10 seconds to bleeding point AFTER hemostasis achieved

— Never cauterize both sides of septum at the same visit → septal perforation

— Avoid in bleeding diathesis or large bleeds (ineffective)

Merocel sponge: insert dry, then hydrate with saline; expands to tamponade

Rapid Rhino: carboxymethylcellulose-coated balloon, soak in water first, inflate with air; less mucosal trauma

Petrolatum/bismuth ribbon gauze: layered packing for experienced operators

— Leave 24–72 hours; provide prophylactic antibiotics to cover S. aureus (cephalexin, augmentin) — concerns for toxic shock syndrome historically (evidence weak but practice persists)

Foley catheter (12–14 Fr): pass into nasopharynx, inflate balloon with 7–10 mL saline, pull anteriorly to seat against posterior choana, secure with umbilical clamp (protect ala with padding)

Epistat or double-balloon devices: dedicated posterior packs

— Classic gauze posterior pack (rarely used now)

Admit all patients with posterior packs — monitor for hypoxia, dysrhythmia, pressure necrosis

— First-line surgical management of refractory posterior epistaxis

— Performed by ENT; high success rate (>95%); lower morbidity than embolization

— Performed by interventional radiology

— Targets internal maxillary artery branches

— Reserved for failed ligation, surgical contraindications, or massive bleeding

— Risks: stroke, facial pain, skin necrosis, ophthalmoplegia (avoid internal carotid territory)

Silver nitrate cautery (anterior, discrete source):
Anterior nasal packing:
Posterior nasal packing:
Endoscopic sphenopalatine artery ligation (ESPAL):
Endovascular embolization:
External carotid artery ligation: rarely performed today
CCS pearl: For refractory posterior epistaxis — ENT consult, transfer to OR for endoscopic sphenopalatine artery ligation; if unavailable or unstable, IR consult for embolization
Board pearl: Patients with posterior packs need continuous pulse oximetry and cardiac monitoring; supplemental O2 is reasonable
Solid White Background
Special Populations — Elderly and Renal/Hepatic Impairment

— Higher anticoagulation prevalence (afib, valves, VTE)

— Atherosclerotic, friable vessels less responsive to vasoconstrictors

— Higher incidence of posterior bleeds (sphenopalatine territory)

— Hypertension often poorly controlled

— Reduced physiologic reserve → faster decompensation with blood loss

— Lower threshold for admission even with anterior packing if frail, on AC, or living alone

— Cautious BP lowering (avoid cerebral hypoperfusion)

Cardiac monitoring with posterior packs (high rate of demand ischemia, AFib triggers)

— Avoid cocaine-containing topicals (CV risk)

— Use lower doses of sedatives if needed for packing

Uremic platelet dysfunction (GFR <30, especially dialysis-dependent)

— Treat with DDAVP 0.3 mcg/kg IV/SC, cryoprecipitate, or conjugated estrogens

— Consider dialysis if uremia severe

Apixaban is the preferred DOAC in CKD; dabigatran is contraindicated in severe renal impairment (renally cleared, accumulates)

— Adjust reversal agent dosing per renal function

— Decreased clotting factor synthesis (II, VII, IX, X), thrombocytopenia (hypersplenism), platelet dysfunction

— Check INR and platelets; consider FFP or 4-factor PCC + vitamin K

— Avoid NSAIDs entirely

— Cirrhotic patients are often rebalanced — hemostatic resuscitation should be guided by active bleeding, not just abnormal labs

Elderly patients carry disproportionate epistaxis morbidity:
Management modifications in elderly:
Renal impairment:
Hepatic impairment:
Polypharmacy: review for redundant antiplatelets, supplements (ginkgo, fish oil, garlic, vitamin E)
Step 3 management: In an elderly patient on apixaban with controlled anterior epistaxis — hold apixaban 24–48 hours, do NOT routinely reverse; resume after hemostasis confirmed and ENT follow-up arranged
Board pearl: DDAVP is the go-to for uremic bleeding — works by releasing endogenous vWF and factor VIII from endothelium
Solid White Background
Special Populations — Pregnancy, Pediatrics, and HHT

— Almost always anterior from Kiesselbach's plexus

— Triggers: digital trauma, dry air, allergic rhinitis, foreign body (suspect with unilateral foul-smelling discharge)

— Treatment: pressure, humidification, saline spray, petroleum jelly to vestibule, treat underlying allergic rhinitis

Avoid silver nitrate cautery in young children when possible; if needed, very limited application

— Recurrent pediatric epistaxis → consider von Willebrand disease (most common inherited bleeding disorder; ask about easy bruising, menorrhagia in adolescents, family history)

— Recurrent unilateral epistaxis in adolescent malejuvenile nasopharyngeal angiofibroma — imaging, ENT, do NOT biopsy

— Increased epistaxis frequency due to estrogen-driven mucosal vascularity and edema (rhinitis of pregnancy)

— Usually self-limited, anterior

— Treatment: humidification, saline, gentle pressure

Avoid oxymetazoline overuse; safe for short-term use but rebound congestion concerns

Avoid cocaine topicals

— Silver nitrate and packing safe

— Severe bleeding: TXA considered safe in pregnancy

— Autosomal dominant; Curaçao criteria: spontaneous recurrent epistaxis, mucocutaneous telangiectasias, visceral AVMs, first-degree relative — 3 of 4 = definite

— Epistaxis is the most common presentation (90%+)

— Management: humidification, nasal moisturizers, ablative therapy (laser, sclerotherapy, bevacizumab intranasal/IV), septodermoplasty, Young's procedure (nasal closure for severe cases)

— Systemic anti-angiogenics (bevacizumab) for severe/refractory bleeding

— Screen for pulmonary, cerebral, hepatic AVMs

Pediatric epistaxis:
Pregnancy:
Hereditary Hemorrhagic Telangiectasia (HHT):
Board pearl: Pediatric recurrent epistaxis + heavy menses + family history = von Willebrand disease — order vWF antigen, ristocetin cofactor, factor VIII
Step 3 management: Counsel HHT patients to avoid NSAIDs and aspirin; iron deficiency anemia is common — supplement and monitor
Solid White Background
Complications and Adverse Outcomes

Hypovolemic shock — uncommon but more frequent with posterior bleeds and anticoagulation

Acute anemia requiring transfusion

Aspiration of blood → pneumonitis, pneumonia, hypoxia

Hematemesis from swallowed blood, may trigger unnecessary UGIB workup

Septal hematoma (after trauma or packing) → must drain to prevent septal abscess and saddle-nose deformity

Septal perforation from bilateral simultaneous cautery or pressure necrosis

Synechiae (adhesions) from prolonged packing

Sinusitis, otitis media (eustachian tube obstruction) with packing

Pressure necrosis of ala from improperly secured posterior pack/Foley

Vasovagal/bradycardic reflex during nasal manipulation

— Hypoxia, hypoventilation

— Bradycardia, dysrhythmias

— Sleep apnea exacerbation

— Demand cardiac ischemia in CAD patients

Toxic shock syndrome (TSS) — historically associated with packing; rare but reportable; mandates prophylactic antibiotics in most practices (cephalexin, amoxicillin-clavulanate)

— Sinusitis, bacteremia

— Stroke (inadvertent ICA territory embolization)

— Facial pain, trismus, mucosal/skin necrosis

— Ophthalmoplegia, blindness (rare)

— Chronic anemia, iron deficiency (especially HHT)

— Recurrent epistaxis, anxiety, reduced quality of life

— Psychological impact in pediatric patients

Hemorrhagic complications:
Procedure-related complications:
Posterior packing-specific risks ("nasopulmonary reflex"):
Infectious complications:
Embolization complications:
Long-term:
Board pearl: Septal hematoma = boggy, fluctuant septal swelling after trauma — emergent incision and drainage to prevent cartilage necrosis (septum is avascular and depends on perichondrium)
Step 3 management: Any patient with prolonged anterior or posterior packing should receive prophylactic antibiotics (anti-staphylococcal) and have packing removed within 72 hours to minimize TSS and necrosis risk
Solid White Background
When to Escalate Care — ICU, Consult, and Inpatient Triage

— Anterior bleeding not controlled with cautery and packing

— Suspected or confirmed posterior bleed

— Recurrent epistaxis despite outpatient management

— Suspicion of nasal mass, neoplasm, or foreign body

— Trauma with possible septal hematoma

— HHT patients with severe bleeding

Posterior nasal pack (mandatory admission)

— Hemodynamic instability or significant blood loss requiring transfusion

— Anticoagulated patient requiring reversal

— Severe comorbidities (CAD, CHF, COPD) with significant bleeding

— Failure of outpatient management

— Inability to manage at home, frailty, lack of follow-up access

Posterior packs — telemetry minimum; ICU if elderly, OSA, CAD, or hypoxia

— Active or recently controlled massive bleeding

— Ongoing transfusion requirement

— Significant anticoagulation reversal

— Airway concerns

— Failed surgical ligation

— Surgical contraindication

— Massive uncontrolled bleeding

— HHT with refractory bleeding

— Suspected bleeding disorder (vWD, hemophilia, platelet dysfunction)

— Recurrent unexplained epistaxis

— Anticoagulation management in complex patients (mechanical valves, recent VTE)

— Anticoagulation reversal in mechanical valve, recent stent

— Demand ischemia from blood loss

Indications for ENT consult:
Admission criteria:
ICU/monitored bed criteria:
Interventional radiology consult:
Hematology consult:
Cardiology consult:
CCS pearl: Patient with posterior pack — admit to telemetry/ICU, continuous pulse oximetry, supplemental O2 as needed, ENT consult for definitive management (endoscopic ligation in next OR window), hold AC, BP control, IV fluids/transfusion as needed
Step 3 management: Do not discharge a patient with a posterior pack — this is a tested decision point; even hemodynamically stable patients require monitored admission
Solid White Background
Key Differentials — Same-Category (Otolaryngologic) Causes

Anterior septal bleed (Kiesselbach's) — most common, easily visualized, responds to pressure

Posterior bleed (sphenopalatine/Woodruff's) — brisk, bilateral, posterior drainage

Septal perforation — chronic crusting and intermittent bleeding; causes: trauma, cocaine, surgery, GPA (Wegener's), syphilis

Septal deviation — turbulent airflow → mucosal drying and bleeding

Allergic rhinitis — clear rhinorrhea, sneezing, congestion, pale boggy mucosa; treat underlying

Viral URI — vasodilation, friable mucosa

Acute bacterial sinusitis — purulent rhinorrhea, facial pain

Granulomatosis with polyangiitis (GPA) — chronic sinusitis, crusting, septal perforation, saddle-nose; check c-ANCA/PR3

Juvenile nasopharyngeal angiofibroma — adolescent male, unilateral recurrent epistaxis, nasal obstruction; vascular, do NOT biopsy

Squamous cell carcinoma — chronic smoker, unilateral mass, recurrent bleeding

Inverted papilloma — unilateral nasal mass, malignant potential

Nasopharyngeal carcinoma — Asian/Mediterranean ancestry, EBV-associated, cervical lymphadenopathy

Esthesioneuroblastoma — rare, anosmia, epistaxis

Nasal bone fracture — periorbital ecchymosis, crepitus, deformity

Septal hematoma — examine after any nasal trauma

CSF rhinorrhea with basilar skull fracture — clear fluid with halo sign or beta-2 transferrin positive

— Post-septoplasty, sinus surgery, nasogastric/nasotracheal tube placement

— Intranasal steroid sprays (direct septal trauma — direct nozzle laterally)

— Pediatric, unilateral foul-smelling purulent rhinorrhea

Local mucosal causes of epistaxis to distinguish:
Inflammatory/infectious:
Neoplastic:
Traumatic:
Iatrogenic:
Foreign body:
Key distinction: Adolescent male + recurrent unilateral epistaxis + nasal obstruction = JNA, not idiopathic — contrast imaging mandatory, biopsy contraindicated due to massive hemorrhage risk
Solid White Background
Key Differentials — Other-Category (Systemic) Causes

von Willebrand disease — most common inherited bleeding disorder; mucocutaneous bleeding, menorrhagia, family history; vWF antigen, ristocetin cofactor, factor VIII

Hemophilia A/B — X-linked; deep tissue bleeding more typical, but mucosal bleeding possible

Immune thrombocytopenia (ITP) — petechiae, isolated thrombocytopenia

Leukemia — pancytopenia, fatigue, infections, bleeding

Disseminated intravascular coagulation (DIC) — sepsis, malignancy, OB emergencies; ↑PT/PTT, ↓fibrinogen, ↑D-dimer, ↓platelets

Platelet dysfunction — uremia, medications, Glanzmann's, Bernard-Soulier

Hereditary hemorrhagic telangiectasia (HHT) — Curaçao criteria

Ehlers-Danlos (vascular type, type IV) — fragile vessels, easy bruising

Warfarin, DOACs, heparin — primary culprits

Aspirin, clopidogrel, ticagrelor

NSAIDs — both gastric and mucosal bleeding

SSRIs — mild platelet effect, additive with other agents

Cocaine, methamphetamine — vasoconstriction → necrosis → bleeding; septal perforation

Topical steroids with poor technique

— Herbal: ginkgo, garlic, ginseng, fish oil, vitamin E

— Low humidity (winter heating, high altitude, supplemental O2)

— Occupational chemical exposure

Hemoptysis from lower airway

Hematemesis from UGIB

— Post-tonsillectomy bleed presenting as oral/posterior blood

Hematologic disorders:
Vascular/structural:
Pharmacologic causes:
Hepatic disease: cirrhosis-related coagulopathy and thrombocytopenia
Renal disease: uremic platelet dysfunction (treat with DDAVP, dialysis)
Hypertensive crisis: severe HTN may be associated but rarely sole cause; treat both
Environmental:
Mimics of epistaxis (blood appearing to come from nose):
Board pearl: Recurrent epistaxis + telangiectasias on lips/tongue/fingers + family history of bleeding/strokes/lung AVMs = HHT — initiate Curaçao criteria assessment and AVM screening
Solid White Background
Secondary Prevention, Discharge Medications, and Long-Term Plan

Avoid nose-blowing for at least 12 hours

— Sneeze with mouth open

— Avoid heavy lifting, straining, bending for 24–48 hours

— Avoid hot beverages, spicy foods, alcohol initially (vasodilation)

— No smoking, no nasal picking

— Humidified air, saline nasal spray, petroleum jelly or bacitracin ointment to vestibule 2–3× daily for 1–2 weeks

Cephalexin 500 mg QID or amoxicillin-clavulanate — covers S. aureus

— Continue until packing removed (typically 48–72 hours)

— Theoretical TSS prevention; evidence modest

— Anterior packs: 24–72 hours, in ENT clinic or by trained provider

— Soak with saline before removal to ease extraction

Hold for 24–48 hours after hemostasis in most cases

Resume when hemostasis durable — typically within 72 hours

— Coordinate with cardiology/hematology for high-risk patients (mechanical valves, recent VTE, recent stent)

— For DAPT after recent PCI: avoid stopping if at all possible; consult cardiology

Blood pressure control — long-term target <130/80

— Treat allergic rhinitis (intranasal steroids — teach proper technique, direct nozzle laterally away from septum)

— Smoking cessation, cocaine cessation

— Environmental: humidifier in winter, especially with home O2

— Ferrous sulfate 325 mg daily; IV iron if oral intolerant or severe deficiency

— vWD: desmopressin prophylaxis for known triggers

— HHT: bevacizumab considerations, AVM management

Discharge instructions after anterior packing/cautery:
Antibiotic prophylaxis while packing in place:
Pack removal:
Anticoagulation management:
Risk factor modification:
Iron supplementation for chronic/recurrent bleeders (HHT especially):
Bleeding disorder management:
Step 3 management: Always document anticoagulation hold and restart plan at discharge — failure to bridge or restart appropriately is a major source of post-discharge thrombotic events and malpractice risk
Board pearl: Teach proper intranasal steroid spray technique — angled away from the nasal septum — prevents the most common iatrogenic epistaxis cause
Solid White Background
Follow-Up, Monitoring Parameters, and Counseling

— Anterior packing → 48–72 hours for pack removal and nasal exam

— Cautery only → 1–2 weeks to assess healing

— Posterior packing/surgical intervention → admission with inpatient ENT care, then outpatient follow-up 1–2 weeks

— Recurrent epistaxis without clear etiology → ENT evaluation with nasal endoscopy

— Within 1–2 weeks for medication reconciliation (AC restart), BP optimization, anemia recheck

— CBC at 1–2 weeks if significant blood loss occurred

— Recurrent epistaxis without local cause

— Family history of bleeding disorder

— Personal history of mucocutaneous bleeding, easy bruising, menorrhagia

— HHT diagnosis or suspicion

— Patient/family education on recognizing re-bleeding

— Counsel on return precautions: bleeding lasting >20 min despite pressure, lightheadedness, syncope, large clots, hematemesis, melena

First-aid technique: sit upright, lean forward, pinch soft part of nose firmly for 15 minutes continuously, breathe through mouth

— Saline spray 2–4× daily

— Petrolatum or mupirocin/bacitracin ointment to anterior septum nightly (HHT and recurrent bleeders)

— Avoid digital trauma; trim children's nails

— Maintain home humidity (40–50%)

— Address nose-picking habit

— Treat underlying allergic rhinitis

— Reassurance — usually benign and self-limited

— Annual screening for new symptoms

— Periodic re-evaluation of pulmonary/cerebral/hepatic AVMs

— Iron status monitoring (CBC, ferritin)

ENT follow-up:
Primary care follow-up:
Hematology referral:
Monitoring parameters at home:
Counseling and self-management (key for prevention):
Pediatric counseling:
HHT longitudinal care:
CCS pearl: Order outpatient CBC and ferritin in 2 weeks for any patient who lost significant blood; iron deficiency anemia often emerges after the acute event
Step 3 management: Schedule ENT follow-up before discharge — patients with packs cannot remove their own packing safely; lack of follow-up = repeat ED visit
Solid White Background
Ethical, Legal, and Patient Safety Considerations

— Posterior packing, cautery, and embolization require explanation of risks: pain, septal perforation, infection, hypoxia (posterior packs), stroke (embolization)

— Document discussion of alternatives and risks

Capacity assessment in intoxicated, hypoxic, or hypovolemic patients — proceed with emergency exception if life-threatening

— Document the risk-benefit analysis: severity of bleed, indication for AC, thrombotic risk

— Discuss with the patient (or surrogate) whenever feasible

— In mechanical mitral valves and recent stents, reversal carries significant thrombotic risk — multidisciplinary input documented

— High-risk transition: ED discharge of anticoagulated patient with packed nose

Closed-loop communication: ED → ENT → primary care

— Written instructions on pack removal date, anticoagulation restart, return precautions

— Confirm patient can read instructions; provide translation services as needed

Pack tracking: document number and type of packs placed; failure to remove packing has caused toxic shock syndrome and death

— Some institutions use checklists or wristbands for indwelling nasal packs

— Verify removal at follow-up; if missed appointment, contact the patient

— Recurrent epistaxis in a child should prompt evaluation for abuse if accompanied by other suspicious findings (bruising patterns, inconsistent histories)

— Foreign body epistaxis — explore non-accidental causes when context suggests

— Suspected child or elder abuse with associated injuries

— Cocaine use as cause of severe epistaxis — does not require reporting in adults but document and offer counseling/treatment for substance use

— Ensure access to humidifiers, ointments, follow-up — barriers disproportionately affect low-income patients with recurrent epistaxis

Informed consent issues:
Anticoagulation reversal decisions:
Transitions of care:
Patient safety:
Pediatric considerations:
Mandatory reporting:
Health equity:
Step 3 management: Always document pack placement and removal plan in the chart and on after-visit summary — undocumented/forgotten packing is a sentinel patient-safety event with regulatory implications
Board pearl: A patient discharged with an indwelling nasal pack who does not follow up requires active outreach — this is a tested transitions-of-care safety scenario
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High-Yield Associations and Rapid-Fire Clinical Facts
Anterior bleed = Kiesselbach's plexus (Little's area) = 90% of cases
Posterior bleed = sphenopalatine artery (Woodruff's plexus) = 10%, but disproportionate morbidity
Pinch the soft cartilaginous nose, not the bony bridge — for 15 minutes continuously
Lean forward, not back — prevents aspiration and accurate volume assessment
Adolescent male + recurrent unilateral epistaxis = juvenile nasopharyngeal angiofibroma — do NOT biopsy
Recurrent epistaxis + telangiectasias + AVMs + family history = HHT (Osler-Weber-Rendu) — Curaçao criteria
HHT AVMs: screen pulmonary (bubble echo), cerebral (MRI), hepatic (US)
Recurrent pediatric epistaxis + menorrhagia in teen + family history = von Willebrand disease
Cocaine → septal perforation, recurrent epistaxis
GPA (Wegener's) → saddle nose, septal perforation, c-ANCA/PR3
Septal hematoma after trauma → emergent I&D to prevent cartilage necrosis and saddle deformity
Never cauterize both sides of the septum simultaneously → perforation
Posterior packadmit (telemetry/ICU) → endoscopic sphenopalatine artery ligation or embolization for refractory cases
Idarucizumab = dabigatran reversal; andexanet alfa = apixaban/rivaroxaban reversal; PCC = universal option
DDAVP = uremic platelet dysfunction
Topical TXA has emerging evidence for reducing rebleed
Antibiotic prophylaxis with packing → cover S. aureus → prevent TSS
Intranasal steroid spray technique = nozzle aimed away from septum (laterally)
Acute Hgb in active bleeding lags real loss — don't be falsely reassured
Hypertension during acute epistaxis is often reactive — treat the bleed first, then BP
Most epistaxis is self-limited — only 5–10% require medical intervention
Embolization targets internal maxillary artery branches; avoid internal carotid territory
Board pearl: Memorize the algorithm: pressure → vasoconstrictor → cautery → anterior pack → posterior pack + admit → endoscopic ligation → embolization
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Board Question Stem Patterns

— Young adult, anterior bleeding, BP normal, no anticoagulation → direct pressure for 15 min on the cartilaginous portion → likely answer choice

— Distractor: leaning the head back, pinching the bony bridge

— Persistent bleeding despite pressure and vasoconstrictor → silver nitrate cautery if discrete source, otherwise anterior packing

— Elderly anticoagulated patient, blood from both nares, persistent oropharyngeal blood despite anterior pack → posterior packing + admit + ENT consult

— Warfarin patient with INR 4.5, hypotensive, brisk posterior bleed → 4-factor PCC + IV vitamin K

— Dabigatran patient with massive epistaxis → idarucizumab

— Apixaban patient → andexanet alfa or 4-factor PCC

— Adolescent male with recurrent unilateral epistaxis, nasal obstruction → CT with contrast for JNA — do NOT biopsy

— Young child with unilateral foul-smelling discharge → foreign body

— Recurrent pediatric epistaxis + menorrhagia + family history → vWD workup

— Recurrent epistaxis, telangiectasias on lips/tongue, sibling with epistaxis → HHT → screen for pulmonary AVMs with bubble echo

— Post-trauma, boggy septal swelling → incision and drainage

— Anterior pack placed → antibiotic prophylaxis + ENT follow-up in 48–72 hours

— Don't forget to hold anticoagulation and arrange restart

— Posterior pack fails → endoscopic sphenopalatine artery ligation (first surgical option) or embolization if unstable/surgical contraindication

— ESRD on HD, mucosal bleeding → DDAVP

Stem 1 — Anterior epistaxis basics:
Stem 2 — Failed anterior management:
Stem 3 — Posterior bleed identification:
Stem 4 — Anticoagulant reversal:
Stem 5 — Pediatric patient:
Stem 6 — HHT:
Stem 7 — Septal hematoma:
Stem 8 — Discharge planning:
Stem 9 — Refractory bleed:
Stem 10 — Uremic patient:
Step 3 management: Stems often hinge on disposition — recognizing that posterior pack = admit is high-yield
Board pearl: When asked "next best step," follow the algorithm strictly: pressure → vasoconstrictor → cautery → anterior pack → posterior pack/admit → procedural intervention
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One-Line Recap

Epistaxis management follows a stepwise algorithm — pressure and vasoconstriction first, anterior cautery or packing next, and posterior packing with admission plus ENT-guided ligation or embolization for refractory bleeds — while always identifying and addressing anticoagulation, hypertension, and underlying bleeding diatheses.

Anatomy drives management: anterior (90%, Kiesselbach's plexus) responds to pressure/cautery/anterior pack; posterior (10%, sphenopalatine artery) requires posterior pack and admission with consideration of endoscopic sphenopalatine artery ligation or endovascular embolization
The algorithm: 15 minutes of pressure on the cartilaginous nose while leaning forward → topical oxymetazoline + lidocaine pledget → silver nitrate cautery of discrete source → Merocel or Rapid Rhino anterior pack → posterior pack (Foley balloon) + ENT consult + admit → ESPAL or embolization
Anticoagulation is the dominant modifier: hold all AC, reverse only for severe/life-threatening bleeds (4-factor PCC + vitamin K for warfarin, idarucizumab for dabigatran, andexanet alfa or PCC for Xa inhibitors, DDAVP for uremia/vWD), and plan timely restart to balance thrombotic risk
High-yield associations: adolescent male + recurrent unilateral bleed = JNA (image, don't biopsy); recurrent epistaxis + telangiectasias + family history = HHT (screen AVMs); post-trauma boggy septum = septal hematoma (drain emergently); never cauterize bilateral septum (perforation); posterior packs mandate admission with telemetry and antibiotic prophylaxis to prevent TSS
Step 3 disposition pearls: anterior pack → discharge with ENT follow-up in 48–72 hours and antibiotic prophylaxis; posterior pack → admit to monitored bed; always document anticoagulation hold/restart plan and arrange closed-loop ENT follow-up to prevent retained packing and re-bleeding
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