eMedicine Specialties > Infectious Diseases > Skin and Soft-Tissue Infections
Epidural Abscess: Treatment & Medication
Updated: Apr 20, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
Treatment
Medical Care
Spinal epidural abscess
A combined medical-surgical approach, with emergent surgical decompression and drainage of purulent material, has been the traditional approach to spinal epidural abscess. Antibiotic-based therapy, sometimes combined with CT-directed needle aspiration, has traditionally been used only in patients who are determined to be at prohibitively high risk of surgery or who have a fixed paralysis that lasts more than 72 hours and that is presumed to be irreversible.
Wider use of the antibiotic-based therapy for spinal epidural abscess has been advocated,11,12 condemned,13,14 and cautiously discussed.8,15 The current literature on the subject consists largely of small case series and is inadequate to resolve the controversy.1,2
If medical therapy is to be used as initial therapy for spinal epidural abscess and surgery held in reserve, a number of caveats apply, as follows:
- The patient should have no neurological deficits.
- A culture-proven microbiological diagnosis should be available (from blood culture or aspiration).
- Stringent follow-up by both the primary team and neurosurgeons must be available and emergent surgery available, if needed.
- The physicians caring for the patient must be aware that rapid deterioration may occur at any time (the first 72 hours being most risky) and that even prompt rescue surgery may leave the patient with a neurological deficit that might have been avoided with surgery at first diagnosis.
- A follow-up MRI is necessary within 2-4 weeks to evaluate for improvement with medical therapy.
Empirical antibiotic therapy should include coverage of gram-positive cocci, particularly staphylococci (including MRSA), and gram-negative bacilli. Vancomycin has been the standard agent for gram-positive infections, although linezolid, daptomycin, or tigecycline could be considered. The third- and fourth-generation cephalosporins and meropenem offer excellent gram-positive (except MRSA) and gram-negative coverage in addition to CNS penetration. Additional coverage may be needed if some of the less-common etiologic agents (see Causes) are suspected. Always tailor coverage once culture data are available; for example, nafcillin is a much better drug for MSSA infections than vancomycin.
Intracranial epidural abscess
A combined medical-surgical approach is used for intracranial epidural abscess. A craniotomy is usually performed. Empiric antibiotic therapy is similar to that described for spinal epidural abscess; since many of these infections result from prior interventions, the possibility of more-resistant nosocomial organisms must be considered. Vancomycin plus cefepime or meropenem would be good starting choices, with metronidazole added to the cefepime if anaerobes are a major concern.
Surgical Care
- Prompt decompression is used to manage intracranial epidural abscess, as it is uniformly considered a neurosurgical emergency.
- As discussed in detail above, most patients with spinal epidural abscess require urgent decompressive laminectomy; other surgical techniques may be preferred in certain situations.16 In some patients without neurologic deficits, medical therapy might be cautiously attempted, recognizing that disastrous outcomes may ensue from this conservative approach (see Medical Therapy). CT-guided drainage might be helpful in some cases of posterior spinal epidural abscess, but the literature on this is scant.
Consultations
Emergent consultation with a neurosurgeon is mandatory for surgical decompression and drainage of purulent material in patients with intracranial epidural abscess. Emergent surgical intervention is needed in most patients with spinal epidural abscess, and prompt consultation and tight follow-up are mandatory in those in whom surgery is deferred (see Treatment). Consultation with an infectious disease specialist is strongly recommended for both diagnostic and therapeutic assistance.
Medication
The course of medication therapy is not well defined, but 4-12 weeks is generally considered adequate. Concomitant osteomyelitis requires a 6- to 12-week course. A transition to highly bioavailable oral agents might be appropriate in some cases. Rely on an infectious disease specialist consultant for guidance. (See Medical Treatment for empiric selections.)
Antibiotics
Empiric antimicrobial therapy must be comprehensive and cover all likely pathogens. Antibiotic combinations, usually vancomycin or another MRSA agent plus a broad gram-negative agent, are recommended in both intracranial epidural abscess and spinal epidural abscess while awaiting culture data. This approach ensures coverage for a broad range of organisms and polymicrobial infections. Once organisms and sensitivities are known, antibiotic monotherapy is recommended.
Ceftriaxone (Rocephin)
Third-generation cephalosporin with fair gram-negative and gram-positive activity. Superior CNS penetration. Arrests bacterial growth by binding to one or more penicillin-binding proteins. Does not cover MRSA, Pseudomonas species, or resistant nosocomial enterics.
Adult
2 g IV q12-24h
Pediatric
100 mg/kg/d given IM/IV divided q12-24h (infants and children-not neonates)
Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Caution in breastfeeding women and patients with allergy to penicillin; excreted in bile and may cause sludging in gall bladder or biliary tree. Pseudomembranous colitis may occur, requiring discontinuation of medication; superinfection is possible with long courses of therapy; adjust dose in severe renal impairment
Ceftazidime (Ceptaz, Fortaz)
Third-generation cephalosporin with broad-spectrum, gram-negative activity (including Pseudomonas species). Poor efficacy against gram-positive organisms and some resistant gram-negative organisms. Arrests bacterial growth by binding to one or more penicillin-binding proteins.
Adult
2 g IV q8h
Pediatric
50 mg/kg IV q8h (1 month-12 years old)
Nephrotoxicity may increase with aminoglycosides, furosemide, and ethacrynic acid; probenecid may increase levels
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Pseudomembranous colitis may occur, requiring discontinuation of medication; superinfection is possible with long courses of therapy; adjust dose in renal impairment
Meropenem (Merrem IV)
Bactericidal broad-spectrum carbapenem antibiotic that inhibits cell wall synthesis. Effective against most gram-positive and gram-negative bacteria, with excellent CNS penetration. Has slightly increased activity against gram-negative bacteria and slightly decreased activity against staphylococci and streptococci compared with imipenem, but much less likely than imipenem to cause seizures.
Adult
1-2 g IV q8h
Pediatric
<3 months: Not established
>3 months: 40 mg/kg IV q8h
Probenecid may inhibit renal excretion, increasing levels
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Pseudomembranous colitis may occur, requiring discontinuation of medication; superinfection is possible with long courses of therapy; adjust dose in renal impairment
Metronidazole (Flagyl, Protostat)
Imidazole ring-based antibiotic active against various anaerobic bacteria and protozoa. Not active against any aerobes. Must be used in combination for most bacterial infections.
Adult
500 mg PO/IV q8h or 1 g IV q12-24h
Pediatric
30 mg/kg/d PO/IV usually divided q6h
Cimetidine may increase toxicity; may increase effects of anticoagulants; may increase toxicity of lithium and phenytoin; disulfiramlike reaction may occur with orally ingested ethanol
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
May be contraindicated during first trimester of pregnancy; adjust dose in hepatic disease; monitor for seizures and development of peripheral neuropathy; metallic taste and nausea may occur
Vancomycin (Lyphocin, Vancocin)
Potent antibiotic directed against most gram-positive organisms and active against most Enterococcus species. Indicated in patients who cannot receive or have failed to respond to penicillins and cephalosporins or who have infections with MRSA or another susceptible gram-positive organism.
Adult
1 g IV q12h traditional, but many patients will require higher doses to achieve optimal AUC/MIC ratios; consult ID or pharmacy for dosing assistance
Pediatric
10-15 mg/kg IV q6-8h for ages 1 month-12 years
Erythema, histaminelike flushing, and anaphylactic reactions may occur ; when taken concurrently with aminoglycosides, risk of nephrotoxicity increases above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Caution in renal failure and neutropenia; red man syndrome is caused by too rapid IV infusion (dose administered over a few min) but rarely happens when dose is administered over 2 h or as PO or IP administration; red man syndrome is an anaphylactoid reaction caused by histamine release
Nafcillin (Nafcil, Unipen)
A penicillin used almost exclusively for MSSA. Is not effective against MRSA infections. Do not use empirically when MRSA infection is possible.
Adult
2 g IV q4h
Pediatric
>1 month: 25 mg/kg/d IV q6h
Associated with warfarin resistance when administered concurrently; effects may decrease with bacteriostatic action of tetracycline derivatives; probenecid can increase effects
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Only use for MSSA. May cause interstitial nephritis, cytopenias.
More on Epidural Abscess |
| Overview: Epidural Abscess |
| Differential Diagnoses & Workup: Epidural Abscess |
Treatment & Medication: Epidural Abscess |
| Follow-up: Epidural Abscess |
| References |
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References
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Darouiche RO. Spinal epidural abscess. N Engl J Med. Nov 9 2006;355(19):2012-20. [Medline].
Tsiodras S, Falagas ME. Clinical assessment and medical treatment of spine infections. Clin Orthop Relat Res. Mar 2006;444:38-50. [Medline].
Tang HJ, Lin HJ, Liu YC, Li CM. Spinal epidural abscess--experience with 46 patients and evaluation of prognostic factors. J Infect. Aug 2002;45(2):76-81. [Medline].
Reihsaus E, Waldbaur H, Seeling W. Spinal epidural abscess: a meta-analysis of 915 patients. Neurosurg Rev. Dec 2000;23(4):175-204; discussion 205. [Medline].
Tunkell, AR. Subdural empyema, epidural abscess, and suppurative intracranial thrombophlebitis. In: Mandell GL, Bennet JE, Dolin R, eds. Mandell, Douglas, and Bennett's Principles and Practices of Infectious Diseases. 2005:1165-8.
Hlavin ML, Kaminski HJ, Fenstermaker RA. Intracranial suppuration: a modern decade of postoperative subdural empyema and epidural abscess. Neurosurgery. Jun 1994;34(6):974-80; discussion 980-1. [Medline].
Chen WC, Wang JL, Wang JT, Chen YC, Chang SC. Spinal epidural abscess due to Staphylococcus aureus: clinical manifestations and outcomes. J Microbiol Immunol Infect. Jun 2008;41(3):215-21. [Medline].
Lury K, Smith JK, Castillo M. Imaging of spinal infections. Semin Roentgenol. Oct 2006;41(4):363-79. [Medline].
An HS, Seldomridge JA. Spinal infections: diagnostic tests and imaging studies. Clin Orthop Relat Res. Mar 2006;444:27-33. [Medline].
Siddiq F, Chowfin A, Tight R. Medical vs surgical management of spinal epidural abscess. Arch Intern Med. Dec 13-27 2004;164(22):2409-12. [Medline].
Sørensen P. Spinal epidural abscesses: conservative treatment for selected subgroups of patients. Br J Neurosurg. Dec 2003;17(6):513-8. [Medline].
Curry WT, Hoh BL, Amin-Hanjani S. Spinal epidural abscess: clinical presentation, management, and outcome. Surg Neurol. Apr 2005;63(4):364-71; discussion 371. [Medline].
Pereira CE, Lynch JC. Spinal epidural abscess: an analysis of 24 cases. Surg Neurol. 2005;63 Suppl 1:S26-9. [Medline].
Savage K, Holtom PD, Zalavras CG. Spinal epidural abscess: early clinical outcome in patients treated medically. Clin Orthop Relat Res. Oct 2005;439:56-60. [Medline].
Löhr M, Reithmeier T, Ernestus RI, Ebel H, Klug N. Spinal epidural abscess: prognostic factors and comparison of different surgical treatment strategies. Acta Neurochir (Wien). Feb 2005;147(2):159-66; discussion 166. [Medline].
Kowalski TJ, Layton KF, Berbari EF, Steckelberg JM, Huddleston PM, Wald JT. Follow-up MR imaging in patients with pyogenic spine infections: lack of correlation with clinical features. AJNR Am J Neuroradiol. Apr 2007;28(4):693-9. [Medline].
Davis DP, Wold RM, Patel RJ. The clinical presentation and impact of diagnostic delays on emergency department patients with spinal epidural abscess. J Emerg Med. Apr 2004;26(3):285-91. [Medline].
Further Reading
Keywords
epidural abscess, spinal epidural abscess, SEA, intracranial epidural abscess, IEA, increased intracranial pressure, ICP, diabetes mellitus, subdural empyema
Treatment & Medication: Epidural Abscess