Brain abscess medical therapy: Difference between revisions

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==Overview==
==Overview==
The treatment of brain abscess involves the reduction of [[intracranial pressure]], localization of the infection spread, and administration of antimicrobial therapy. Empiric antimicrobial therapy among otherwise healthy individuals includes [[Metronidazole]] and either [[Cefotaxime]] or [[Ceftriaxone]]. Patients with co-morbidities may require alternative antimicrobial therapies.
The treatment of brain abscess includes prompt administration of antimicrobial therapy upon suspicion and occasionally drainage to reduce the mass effect. Empiric antimicrobial therapy among otherwise healthy individuals includes [[metronidazole]] and either [[cefotaxime]] or [[ceftriaxone]]. Patients with co-morbidities may require alternative antimicrobial therapies. Administration of steroid therapy is generally not recommended and is only indicated among patients who have brain abscesses with mass effect.


==Medical Therapy==
==Medical Therapy==
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==Antimicrobial Regimen==
==Antimicrobial Regimen==
{{ID-Brain abscess}}


{{ID-Brain abscess}}
==Other Pharmacologic Agents==
===Steroids===
*Administration of glucocorticoids is generally not recommended. However, glucorticoids are only indicated when the brain abscess has a mass effect, as suggested by findings on imaging.
*Steroid regimen:
:*Preferred regimen: [[Dexamethasone]] 10 mg IV loading dose {{then}} 4 mg q6h until the mass effect is no longer observed on imaging.


==References==
==References==
{{reflist|2}}
{{reflist|2}}


[[Category:Infectious Disease Project]]
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[[Category:Neurosurgery]]
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[[Category:Infectious disease]]
[[Category:Infectious disease]]
[[Category:Neurosurgery]]

Latest revision as of 20:40, 29 July 2020

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sheng Shi, M.D. [2]

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Overview

The treatment of brain abscess includes prompt administration of antimicrobial therapy upon suspicion and occasionally drainage to reduce the mass effect. Empiric antimicrobial therapy among otherwise healthy individuals includes metronidazole and either cefotaxime or ceftriaxone. Patients with co-morbidities may require alternative antimicrobial therapies. Administration of steroid therapy is generally not recommended and is only indicated among patients who have brain abscesses with mass effect.

Medical Therapy

  • Prompt administration of antimicrobial therapy is indicated among all patients with brain abscesses.
  • Neurosurgery should always be consulted upon diagnosis. The decision of whether to surgically drain, aspirate, or simply administer antimicrobial therapy depends on the number of abscesses, their size, and their location. To learn more about indications of surgical vs. aspiration drainage, click here.
  • Stereotactic needle biopsy can be performed to obtain tissues for cultures.
  • A follow-up head CT scan or MRI is usually indicated at 2-4 weeks of follow-up. The improvement on imaging is often delayed compared to clinical improvement.

Antimicrobial Regimen

  • 1. Empiric antimicrobial therapy[1][2]
Note: The optimal duration of antimicrobial therapy remains unclear. A 4- to 6-week course of treatment is usually required.
  • 1.1 Brain abscess in otherwise healthy patients
  • 1.2 Brain abscess with comorbidities
  • 1.2.1 Otitis media, mastoiditis, or sinusitis
  • 1.2.2 Dental infection
  • 1.2.3 Penetrating trauma or post-neurosurgy
  • 1.2.4 Lung abscess, empyema, or bronchiectasis
  • 1.2.5 Bacterial endocarditis
  • 1.2.6 Congenital heart disease
  • 1.2.7 Transplant recipients
  • 1.2.8 Patients with HIV/AIDS
  • 1.2.9 Staphylococcus aureus coverage
  • Preferred regimen: Vancomycin 30–45 mg/kg/day q8–12h
  • 1.2.10 Mycobacterium tuberculosis coverage
  • 2. Pathogen-directed antimicrobial therapy[3][4][5]
Note: The optimal duration of antimicrobial therapy remains unclear. A 4- to 6-week course of treatment is usually required.
  • 2.1 Bacteria
  • 2.1.1 Actinomyces
  • 2.1.2 Bacteroides fragilis
  • 2.1.3 Enterobacteriaceae
  • Preferred regimen (1): Cefotaxime 2 g IV q4-6h
  • Preferred regimen (2): Ceftriaxone 2 g IV q12h
  • Preferred regimen (3): Cefepime 2 g IV q12h
  • Alternative regimen (1): Aztreonam 6–8 g/day IV q6–8h
  • Alternative regimen (2): TMP-SMZ 10–20 mg/kg/day q6–12h
  • Alternative regimen (3): Ciprofloxacin 800–1200 mg/day IV q8–12h
  • Alternative regimen (4): Meropenem 2 g IV q8h
  • 2.1.4 Fusobacterium
  • 2.1.5 Haemophilus
  • Preferred regimen (1): Cefotaxime 2 g IV q4-6h
  • Preferred regimen (2): Ceftriaxone 2 g IV q12h
  • Preferred regimen (3): Cefepime 2 g IV q12h
  • Alternative regimen (1): Aztreonam 6–8 g/day IV q6–8h
  • Alternative regimen (2): TMP-SMZ 10–20 mg/kg/day q6–12h
  • 2.1.6 Listeria monocytogenes
  • Preferred regimen (1): Ampicillin 12 g/day q4h
  • Preferred regimen (2): Penicillin G 4 MU IV q4h
  • Alternative regimen (1): TMP-SMZ 10–20 mg/kg/day q6–12h
  • 2.1.7 Nocardia
  • Preferred regimen (1): TMP-SMZ 10–20 mg/kg/day q6–12h
  • Preferred regimen (2): Sulfadiazine 4–6 g/day q6h
  • Alternative regimen (1): Meropenem 2 g IV q8h
  • Alternative regimen (2): Cefotaxime 2 g IV q4-6h
  • Alternative regimen (3): Ceftriaxone 2 g IV q12h
  • Alternative regimen (4): Amikacin 15 mg/kg/day IV q8h
  • 2.1.8 Prevotella melaninogenica
  • 2.1.9 Pseudomonas aeruginosa
  • Preferred regimen (1): Ceftazidime 6 g/day q8h
  • Preferred regimen (2): Cefepime 6 g/day q8h
  • Alternative regimen (1): Aztreonam 6–8 g/day IV q6–8h
  • Alternative regimen (2): Ciprofloxacin 800–1200 mg/day IV q8–12h
  • Alternative regimen (3): Meropenem 2 g IV q8h
  • 2.1.10 Staphylococcus aureus, methicillin-resistant (MRSA)
  • Preferred regimen: Vancomycin 30–45 mg/kg/day IV q8–12h for 4–6 weeks
  • Alternative regimen (1): Linezolid 600 mg PO/IV q12h for 4–6 weeks
  • Alternative regimen (2):TMP-SMX 5 mg/kg/dose PO/IV q8–12h for 4–6 weeks
  • Pediatric dose (1): Vancomycin 15 mg/kg/dose IV q6h
  • Pediatric dose (2): Linezolid 10 mg/kg/dose PO/IV q8h
  • Note: Consider the addition of Rifampin 600 mg qd or 300–450 mg bid to vancomycin.
  • 2.1.11 Staphylococcus aureus, methicillin-susceptible (MSSA)
  • Preferred regimen (1): Nafcillin 2 g IV q4h
  • Preferred regimen (2): Oxacillin 2 g IV q4h
  • Alternative regimen: Vancomycin 30–45 mg/kg/day IV q8–12h
  • 2.1.12 Streptococcus
  • 2.2 Fungi
  • 2.2.1 Aspergillus
  • Preferred regimen: Voriconazole 8 mg/kg/day q12h
  • Alternative regimen (1): Amphotericin B deoxycholate 0.6–1.0 mg/kg/day IV q24h
  • Alternative regimen (2): Amphotericin B lipid complex 5 mg/kg/day IV q24h
  • Alternative regimen (3): Itraconazole 400–600 mg/day IV q12h
  • Alternative regimen (4): Posaconazole 800 mg/kg/day IV q6–12h
  • 2.2.2 Candida
  • 2.2.3 Cryptococcus neoformans
  • 2.2.4 Mucorales
  • 2.2.5 Pseudallescheria boydii (Scedosporium apiospermum)
  • 2.3 Protozoa
  • 2.3.1 Toxoplasma gondii

Other Pharmacologic Agents

Steroids

  • Administration of glucocorticoids is generally not recommended. However, glucorticoids are only indicated when the brain abscess has a mass effect, as suggested by findings on imaging.
  • Steroid regimen:
  • Preferred regimen: Dexamethasone 10 mg IV loading dose THEN 4 mg q6h until the mass effect is no longer observed on imaging.

References

  1. Bennett, John (2015). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  2. Bartlett, John (2012). Johns Hopkins ABX guide : diagnosis and treatment of infectious diseases. Burlington, MA: Jones and Bartlett Learning. ISBN 978-1449625580.
  3. Bennett, John (2015). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
  4. Bartlett, John (2012). Johns Hopkins ABX guide : diagnosis and treatment of infectious diseases. Burlington, MA: Jones and Bartlett Learning. ISBN 978-1449625580.
  5. Liu, Catherine; Bayer, Arnold; Cosgrove, Sara E.; Daum, Robert S.; Fridkin, Scott K.; Gorwitz, Rachel J.; Kaplan, Sheldon L.; Karchmer, Adolf W.; Levine, Donald P.; Murray, Barbara E.; J Rybak, Michael; Talan, David A.; Chambers, Henry F.; Infectious Diseases Society of America (2011-02-01). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (3): –18-55. doi:10.1093/cid/ciq146. ISSN 1537-6591. PMID 21208910.