Rosen & Barkin's 5-Minute Emergency Medicine Consult (748 page)

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Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
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PRE HOSPITAL
  • Cautions:
    • Systemic allergic reactions can rapidly progress if not treated with early epinephrine
  • Severe reaction:
    • Manage airway, oxygen
    • IM epinephrine
    • Parenteral or inhaled β-agonist for bronchospasm
    • IV crystalloid and vasopressors as needed
INITIAL STABILIZATION/THERAPY

Remove offending agent if possible

ED TREATMENT/PROCEDURES
  • Largely symptomatic except in severe reactions
  • Treatment aimed at stimulus, effector cells, inflammatory mediators, and target receptors
  • β-Agonist (parenteral or inhaled):
    • Severe hives, angioedema, systemic features
  • H
    1
    -receptor antagonist (1st or 2nd generation):
    • Mainstay of treatment
  • H
    2
    -receptor antagonist:
    • May be beneficial as adjunct to H
      1
      blocker when no response to H
      1
      blocker alone
  • Corticosteroid (oral):
    • S
      evere or refractory cases
  • Avoid NSAIDs and opiates:
    • May exacerbate condition
  • Concurrent use of ketoconazole or macrolides alters hepatic metabolism of antihistamine; use with caution
MEDICATION
  • β-Agonists:
    • Epinephrine (1:1,000 solution): 0.1–0.5 mg IM q10–15min PRN (peds: 0.01 mg/kg, IM [max. single dose not to exceed 0.3 mg] q15min PRN)
    • IV epinephrine 0.1–0.25 mg (1:10,000 sol) IV over 5–10 min q5–15min then 1–4 μg/min IV ONLY if anaphylactic shock
    • Albuterol (0.5% solution): 0.5 mL nebulized q20min PRN (peds: 0.01–0.05 mL/kg per dose [max. 0.5 mL/dose] nebulized q20min PRN bronchospasm)
    • Terbutaline: 0.25 mg SC q15–30min PRN (max. 0.5 mg q4h); (peds: <12 yr old; 0.005–0.01 mg/kg [max. 0.4 mg/dose] SC q15–20min × 3 PRN bronchospasm)
  • H
    1
    -receptor antagonist (1st generation—lipophilic and sedating)
    • Diphenhydramine: 25–50 mg PO, IV, or IM q6h (peds: 1 mg/kg q6h [max. 300 mg/24 h])
    • Hydroxyzine: 25–50 mg PO or IM q6h (peds: 2 mg/kg/24 h PO div. q8h or 0.5–1 mg/kg IM q4–6h PRN)
  • H
    1
    -receptor antagonist (2nd generation—less sedating and preferred):
    • Cetirizine: Adult and peds ≥6 yr old: 5–10 mg PO QD (peds 2–6 yr old: 2.5 mg QD to BID)
    • Loratadine: 10 mg PO BID (peds 2–6 yr old: 5 mg PO QD
    • Fexofenadine: 60 mg PO BID or 180 mg PO QD (peds 6–12 yr old: 30 mg PO BID)
  • H
    2
    -receptor antagonist (suggested dosage):
    • Famotidine: 20 mg IV q12h or 20–40 mg PO QHS (peds: 1 mg/kg/d div. QID [max. 40 mg/24 h])
    • Ranitidine: 150 mg PO BID (peds: Neonate: 2–4 mg/kg/24 h PO div. q8–12h or 2 mg/kg/24 h IV div. q6–8h; infants and children: 4–5 mg/kg/24 h PO div. q8–12h or 2–4 mg/kg/24 h IV or IM div. q6–8h)
  • Corticosteroid:
    • Methylprednisolone: 125 mg IV (peds: Start at 2 mg/kg × 1)
    • Prednisolone: 50 mg PO QD for 3 days (peds: 0.5–2 mg/kg/24 h [max. 80 mg/24 h] div. QD to BID for 3–5 days)
    • Prednisone: 40 mg PO QD or 20 mg PO BID for 3–5 days (peds: 1–2 mg/kg/24 h [max. 80 mg/24 h] div. QD to BID for 3–5 days)
  • Antileukotrienes:
    • Montelukast: 10 mg PO QD
    • Zafirlukast: 20 mg PO BID
First Line
  • H
    1
    -receptor antagonist, 2nd generation
  • Corticosteroids
  • β-Agonists:
    • Albuterol if bronchospasm present
    • Epinephrine for severe or systemic signs
Second Line
  • Antileukotrienes
  • H
    1
    -receptor antagonist, 1st generation
  • H
    2
    -receptor antagonist, data weak
FOLLOW-UP
DISPOSITION
Admission Criteria
  • Systemic allergic reaction with:
    • Respiratory distress or failure
    • Refractory hypotension or shock
  • Severe case with dysfunction of health-related quality of life
  • Other comorbidities
Discharge Criteria
  • Normal vitals
  • Absence of other condition requiring admission
  • Adequate ability of caregivers at home to monitor for further exacerbations
FOLLOW-UP RECOMMENDATIONS

Follow with PCP, especially if lasting >6 wk

PEARLS AND PITFALLS
  • If severe presentation, there is often a biphasic course. Rebound may occur in 4–6 hr
  • Chronic urticaria often has a systemic cause
ADDITIONAL READING
  • Kropfl L, Mauer M, Zuberbier T. Treatment strategies in urticaria.
    Expert Opin. Pharmacother.
    2010;11:1445–1450.
  • Nichols K, Cook-Bolden F. Allergic skin disease: Major highlights and recent advances.
    Med Clin N Am.
    2009;93:1211–1224.
  • Ricci G, Giannetti A, Belotti T, et al. Allergy is not the main trigger of urticaria in children referred to the emergency room.
    J Eur Acad Dermatol Venereol.
    2010;24:1347–1348.
  • Wolfson AB, Hendey GW, Ling LJ, et al. (eds)
    Harwood-Nuss’ Clinical Practice of Emergency Medicine.
    5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2010.
  • Zuberbier T. A summary of the new international EAACI/GA(2)LEN/EDF/WAO guidelines in urticaria.
    WAO J.
    2012;5(suppl 1):S1–S5.
  • Zuberbier T, Asero R, Bindslev-Jensen C, et. al. EAACI/GA2LEN/EDF/WAO guideline: definition, classification, and diagnosis of urticaria.
    Allergy.
    2009;64:1417–1426.
See Also (Topic, Algorithm, Electronic Media Element)
  • Angioedema
  • Erythema Multiforme
  • Vasculitis
CODES
ICD9
  • 708.0 Allergic urticaria
  • 708.1 Idiopathic urticaria
  • 708.9 Unspecified urticaria
ICD10
  • L50.0 Allergic urticaria
  • L50.1 Idiopathic urticaria
  • L50.9 Urticaria, unspecified
UVULITIS
James P. Brewer
BASICS
DESCRIPTION

Uvulitis refers to any inflammatory condition involving the uvula. Uvulitis can be separated into 2 broad categories:

  • Infectious:
    • Bacterial
    • Viral
    • Candidal
  • Traumatic or noninfectious
EPIDEMIOLOGY
Incidence and Prevalence Estimates
  • Exact incidence is unknown owing to limited reporting
  • Once thought to be rare but may in fact be more common (e.g., viral etiologies)
  • Children (age 5–15) more often affected than adults due to prevalence of group A streptococcal infections in this age group
  • Noninfectious causes more common than infectious causes in adult population
ETIOLOGY
  • Infectious:
    • Bacterial:
      • Group A streptococcal infection (GAS), most common
      • Haemophilus influenzae
        type b (Hib)
      • Other bacterial infections (
        Fusobacterium nucleatum, Provetella intermedia, Streptococcus pneumonia
        )
    • Viral:
      • Not well reported but suspected in mild/transient cases
      • Known to cause uvular lesions however rare in isolation
      • Coxsackie virus (other enteroviruses)
      • Herpes simplex virus
      • Varicella-zoster virus
      • Epstein–Barr virus
    • Candidal infections
  • Noninfectious:
    • Trauma/procedure related
    • Inhalation/ingestion of chemical or thermal irritants
    • Vasculitis
    • Allergic
    • Angioedema:
      • Hereditary
      • Medication induced (e.g., Angiotensin-converting enzyme inhibitor [ACEi], Angiotensin receptor blocker [ARB])
DIAGNOSIS
SIGNS AND SYMPTOMS

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