Rosen & Barkin's 5-Minute Emergency Medicine Consult (429 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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Pediatric Considerations
  • Kawasaki disease
  • PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis)
TREATMENT
INITIAL STABILIZATION/THERAPY

Ensure airway, breathing, and circulation management and hemodynamic stability

ED TREATMENT/PROCEDURES
  • General principles:
    • Antibiotics based on involved primary organ/suspected pathogen (see also “Cellulitis”)
    • Consider local prevalence of MRSA and other resistant pathogens in addition to usual causes
    • Usual outpatient treatment: 7–10 days
    • Elevation
    • Application of moist heat
    • Analgesics
  • Drainage of abscesses if present:
    • Obtain culture if drainage performed, especially to help identify resistant pathogens
  • Skin origin:
    • Outpatient:
      • Oral cephalexin plus trimethoprim/sulfamethoxazole (TMP/SMX) (to cover CA-MRSA)
      • Alternatives to cephalexin: Oral dicloxacillin, macrolide, or levofloxacin
      • Alternatives to TMP/SMX: Clindamycin or doxycycline
    • Inpatient:
      • IV nafcillin or equivalent, plus IV vancomycin (to cover CA-MRSA)
  • Pharyngeal or periodontal origin:
    • Outpatient:
      • Oral penicillin VK
      • Alternatives: Oral clindamycin or amoxicillin/clavulanate
    • Inpatient:
      • IV penicillin G (aqueous) and IV metronidazole
      • Alternatives: IV ampicillin/sulbactam or IV clindamycin
  • Axillary lymphadenitis:
    • Outpatient:
      • Oral penicillin VK
      • Alternatives: Oral macrolide or amoxicillin/clavulanate
    • Inpatient:
      • IV penicillin G (aqueous)
      • Alternatives: IV ampicillin/sulbactam
  • Acute unilateral cervical suppurative lymphadenitis:
    • Outpatient:
      • Oral penicillin VK
      • Alternatives: Oral clindamycin or amoxicillin/clavulanate
  • MRSA:
    • Nosocomial MRSA:
      • IV vancomycin or PO or IV linezolid
    • CA-MRSA:
      • PO: TMP/SMX, clindamycin or doxycycline
      • IV: Vancomycin or clindamycin
MEDICATION
  • Amoxicillin/clavulanate: 500–875 mg (peds: 45 mg/kg/24 h) PO BID or 250–500 mg (peds: 40 mg/kg/24 h) PO TID
  • Ampicillin/sulbactam: 1.5–3 g (peds: 100–300 mg/kg/24 h up to 40 kg; >40 kg, give adult dose) IV q6h
  • Cephalexin: 500 mg (peds: 50–100 mg/kg/24 h) PO QID
  • Clindamycin: 450–900 mg (peds: 20–40 mg/kg/24 h) PO or IV q6h
  • Dicloxacillin: 125–500 mg (peds: 12.5–25 mg/kg/24 h) PO q6h
  • Doxycycline: 100 mg PO BID for adults
  • Erythromycin base: (adult) 250–500 mg PO QID
  • Linezolid: 600 mg PO or IV q12h (peds: 30 mg/kg/d divided q8h)
  • Metronidazole: (adult) 15 mg/kg IV once, followed by 7.5 mg/kg IV q6h
  • Nafcillin: 1–2 g IV q4h (peds: 50–100 mg/kg/24 h divided q6h); max. 12 g/24 h
  • Penicillin VK: 250–500 mg (peds: 25–50 mg/kg/24 h) PO q6h
  • Penicillin G (aqueous): 4 mIU (peds: 100,000–400,000 U/kg/24 h) IV q4h
  • Rifampin: 600 mg PO BID for adults
  • TMP/SMX: 2 DS tabs PO q12h (peds: 6–10 mg/kg/24 h TMP divided q12h)
  • Vancomycin: 1 g IV q12h (peds: 10 mg/kg IV q6h, dosing adjustments required age <5 yr); check serum levels
FOLLOW-UP
DISPOSITION
Admission Criteria
  • Toxic appearing
  • History of immune suppression
  • Concurrent chronic medical illnesses
  • Unable to take oral medications
  • Unreliable patients
Discharge Criteria
  • Mild infection in a nontoxic-appearing patient
  • Able to take oral antibiotics
  • No history of immune suppression or concurrent medical problems
  • Has adequate follow-up within 24–48 hr
Issues for Referral
  • If not found in context of acute infection and not quick to resolve with course of antibiotics, evaluate for more serious underlying causes (e.g., malignancy)
  • Lymph node biopsy may be helpful in the following circumstances:
    • Clinical findings indicate likely malignancy
    • Lymph node size >1 cm
    • Supraclavicular location
FOLLOW-UP RECOMMENDATIONS
  • Follow-up within 24–48 hr for response to treatment
  • If symptoms worsen—including new or worsening lymphangitis, new or increasing area of redness over the node, worsening fever—patient should be instructed to return sooner
PEARLS AND PITFALLS
  • Staph species are the most common cause of acute regional lymphadenitis due to pyogenic bacteria
  • Empiric antibiotic coverage must extend to include CA-MRSA, in addition to coverage for other staph species and strep
ADDITIONAL READING
  • Abrahamian FM, Talan DA, Moran GJ. Management of skin and soft-tissue infections in the emergency department.
    Infect Dis Clin North Am
    . 2008;22:89–116.
  • Boyce JM. Severe streptococcal axillary lymphadenitis.
    N Engl J Med
    . 1990;323:655–658.
  • Henry PH, Longo DL. Enlargement of lymph nodes and spleen. In: LongoDL, Kasper DL, JamesonJL, et al., eds.
    Harrison’s Principles of Internal Medicine
    . 18th ed. New York, NY: McGraw-Hill;2012:465–471.
  • Pasternack MS, Swartz MN. Lymphadenitis and lymphangitis. In: Mandell GL, BennettJE, Dolin R, eds.
    Mandell, Douglas and Bennett’s Principlesand Practice of Infectious Diseases
    . 7th ed. New York, NY: Elsevier/ChurchillLivingstone; 2010:1323–1333.
  • Thomas KT, Feder HM Jr,Lawton AR, et al. Periodic fever syndrome in children.
    JPediatr
    .1999;135:15–21.
See Also (Topic, Algorithm, Electronic Media Element)
  • Cellulitis
  • Lymphangitis
  • MRSA
CODES
ICD9
  • 289.1 Chronic lymphadenitis
  • 289.3 Lymphadenitis, unspecified, except mesenteric
  • 683 Acute lymphadenitis
ICD10
  • I88.9 Nonspecific lymphadenitis, unspecified
  • L04.0 Acute lymphadenitis of face, head and neck
  • L04.2 Acute lymphadenitis of upper limb
LYMPHANGITIS
John Mahoney
BASICS
DESCRIPTION
  • Lymphangitis is the infection of lymphatics that drain a focus of inflammation
  • Histologically, lymphatic vessels are dilated and filled with lymphocytes and histiocytes:
    • Inflammation frequently extends into perilymphatic tissues and may lead to cellulitis or abscess formation
ETIOLOGY
  • Acute lymphangitis:
    • Likely caused by bacterial infection
    • Most commonly group A β-hemolytic Streptococcus
    • Less commonly due to other strep groups, and occasionally
      Staphylococcus aureus,
      including resistant strains such as community-associated methicillin-resistant
      S. aureus
      (CA-MRSA):
      • CA-MRSA risk factors: Prior MRSA infection, household contact of CA-MRSA patient, military personnel, incarcerated persons, athletes in contact sports, IV drug users, men who have sex with men
      • Different antibiotic susceptibility than nosocomial MRSA
      • CA-MRSA now sufficiently prevalent to warrant empiric treatment
      • Suspect CA-MRSA in unresponsive infections or if multiple or recurrent abscesses
    • Other organisms:
      • Pasteurella multocida
        (cat or dog bite)
      • Spirillum minus
        (rat-bite fever)
      • Wuchereria bancrofti
        (filariasis): Consider in immigrants from Africa, Southeast Asia/Pacific, and tropical South America with lower-extremity involvement
  • Chronic lymphangitis:
    • Usually caused by mycotic, mycobacterial, and filarial infections
    • Sporothrix schenckii
      (most common cause of chronic lymphangitis in US):
      • Inoculation occurs while gardening or farming (rose thorn)
      • Organism is present on some plants and in sphagnum moss
      • Multiple SC nodules appear along course of lymphatic vessels
      • Typical antibiotics and local treatment fail to cure lesion
    • Mycobacterium marinum:
      • Atypical Mycobacterium
      • Grows optimally at 25–32°C in fish tanks and swimming pools
      • May produce a chronic nodular, single wart-like or ulcerative lesion at site of abrasion
      • Additional lesions may appear in distribution similar to sporotrichosis
    • Nocardia brasiliensis
    • Mycobacterium kansasii
    • W. bancrofti

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