Updated: Aug 13, 2009
A spinal epidural abscess threatens the spinal cord or cauda equina by compression and also by vascular compromise (see Media files 1-2). If untreated, an expanding suppurative infection in the spinal epidural space impinges on the spinal cord, producing sensory symptoms and signs, motor dysfunction, and, ultimately, paralysis and death. Intervention early in the course of the disease undoubtedly improves the outcome. Frequently, diagnosis is understandably delayed because the initial presentation may be only back pain. One half of cases are estimated to be misdiagnosed or have a delayed diagnosis.1 At times, radicular symptoms may lead to a chief complaint of chest pain or abdominal pain2 , mimicking a myocardial infarction or an acute abdomen.3
The spinal epidural space is not a uniform space. Posteriorly, the epidural space contains fat, small arteries, and the venous plexus. Infections in this space may spread over several vertebral levels. Anteriorly, the epidural space is a potential space with the dura tightly adherent to the vertebral bodies and ligaments. Abscesses occur more frequently in the larger posterior epidural space. Most spinal epidural abscesses occur in the thoracic area, which is anatomically the longest of the spinal regions.
Hematogenous spread with seeding of the epidural space is the suspected source of infection in most children and is thought to occur in many adults as well. Reported sources of infection are numerous and include bacterial endocarditis, infected indwelling catheters, urinary tract infection, peritoneal and retroperitoneal infections, and others.
Direct extension of infection from vertebral osteomyelitis occurs in adults and rarely in children.
Epidural catheters and injections may lead to direct innoculation of the epidural space. The source of infection is not identified in many patients.
The more clinically significant effects of the epidural abscess may be from involvement of the vascular supply to the spinal cord and subsequent infarction rather than direct compression. Staphylococcus aureus is the most commonly reported pathogen4 , though many other bacteria have been implicated, including Staphylococcus and Pseudomonas species, Escherichia coli, Brucella, and Mycobacterium tuberculosis. Methicillin-resistant Staphylococcus aureus (MRSA) is increasingly reported particularly in patients with spinal surgery or implanted devices.
The frequency in large tertiary care centers is estimated to be about 2.8 cases per 10,000 admissions. The incidence is suspected to be increasing in relation to intravenous (IV) drug abuse.5
Because these abscesses occur rarely, the frequency is unknown. It probably parallels the US experience of rarity, although limited diagnostic capabilities in medically underserved countries might increase its importance as a health risk.
If untreated, spinal epidural abscess causes progressive paraplegia and death.
Older studies found an equal sex ratio; more recent data indicate a male predominance, likely reflecting the pattern of IV drug use.
The average age is older than 50 years, but spinal epidural abscess can occur at any age.
Clinical presentation may be quite variable. The clinical triad of fever, back pain, and neurologic deficit is not present in most patients.4,6 Early presentations may be subtle, and atypical presentations are not unusual. A 4-phase sequential evolution has been described, with (1) localized spinal pain, (2) radicular pain and paresthesias, (3) muscular weakness, sensory loss, and sphincter dysfunction, and finally (4) paralysis.1
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Cervical disk syndromes
Lumbosacral disk syndromes
Lumbosacral spondylosis
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Psoas abscess
Retropharyngeal abscess
Transverse myelitis
Urinary tract infection
Vertebral osteomyelitis
Back pain
Cat scratch disease8
Lumbar puncture (LP) is relatively contraindicated if spinal epidural abscess is suspected. However, LP may be essential to exclude meningitis from the differential diagnosis. Lumbar puncture runs the risk of introducing purulent material into the subarachnoid space. Some advocate slowly advancing the needle with gentle syringe aspiration if spinal epidural abscess is suspected; if purulent material is encountered, it should be aspirated gently to obtain laboratory specimens, and the needle should not be advanced further.
Antibiotic treatment should be initiated as soon as possible and in conjunction with surgical therapy. The usual duration of the therapy is 3-4 weeks, but it may be prolonged in the presence of osteomyelitis.
Because S aureus is a common pathogen, antistaphylococcal drugs should be included in the treatment regimen. An antistaphylococcal penicillin, a cephalosporin, or vancomycin may be used. If the patient has undergone a neurosurgical procedure recently, the penicillin should be combined with a third-generation cephalosporin and an aminoglycoside. Gram-stain and culture results are used to guide therapy.
Third-generation cephalosporin that has broad gram-negative spectrum, lower efficacy against gram-positive organisms, and higher efficacy against resistant organisms. By binding to penicillin-binding proteins, arrests bacterial cell wall synthesis and inhibits bacterial growth.
2 g IV q12-24h
Not established
Probenecid may decrease clearance and increase serum levels; ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in patients with renal impairment and use with caution in breastfeeding women and patients allergic to penicillin
Treats infections caused by penicillinase-producing staphylococci. Used to initiate therapy in any patient in whom penicillin G-resistant staphylococcal infection suspected. Should not be used for treatment of penicillin G-susceptible staphylococci.
Parenteral therapy used initially in severe infections. Very severe infections may require very high doses. As condition improves, parenteral therapy should be changed to oral therapy.
Because of occasional occurrence of thrombophlebitis associated with parenteral route, particularly in the elderly, parenteral route should be used only for short term (24-48 h) and changed to oral route, if clinically possible.
2 g IV q4h
37.5 mg/kg IV q6h
Associated with warfarin resistance; bacteriostatic action of tetracycline derivatives may impair bactericidal effects
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Bacteriologic studies should be performed to determine causative organisms and their susceptibility so that appropriate therapy administered; duration of therapy must be sufficient to eliminate organism (minimum of 10 d), otherwise sequelae (eg, endocarditis, rheumatic fever) may ensue
Cultures should be taken after treatment to confirm eradication of pathogens
First-generation semisynthetic cephalosporin, which by binding to penicillin-binding proteins arrests bacterial cell wall synthesis and inhibits bacterial growth. Active primarily against skin flora, including S aureus. Total daily dosage is same for both IV and IM routes.
2 g IV q8h
20 mg/kg IV/IM q8-12h
Probenecid decreases renal clearance and prolongs effect; aminoglycosides may increase renal toxicity; may yield false-positive urine dip for glucose
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in patients with renal impairment; prolonged use of antibiotics associated with superinfections and promotion of nonsusceptible organisms—however, complications usually reversible
Used in combination with other antibiotics in epidural abscess following neurosurgical procedures. Active against various anaerobic bacteria and protozoa. Appears to be absorbed into cells, and intermediate-metabolized compounds formed bind DNA and inhibit protein synthesis, causing cell death.
500 mg IV q6-12h
15 mg/kg IV q12h
Potentiates anticoagulant effect of warfarin; agents that alter hepatic P450 system also affect clearance—phenytoin and phenobarbital may decrease half-life; orally ingested ethanol may cause disulfiramlike reaction—although risk for most patients is slight, caution advised
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Avoid in patients with hypersensitivity to parabens; adjust dose in patients with severe hepatic disease since they may metabolize drug slowly; monitor patients for seizures and development of peripheral neuropathy
Used in combination with other antibiotics for epidural abscess following neurosurgical procedures. Aminoglycoside antibiotic used for gram-negative bacterial coverage. Commonly used in combination with both an agent against gram-positive organisms and one that covers anaerobes. Dosing regimens are numerous and are adjusted based on CrCl and changes in volume of distribution. May be administered IV or IM.
1.5 mg/kg IV q8h
May adjust dosage in patients with renal impairment
Neonates and infants: 7.5 mg/kg/d IV
Children: 6-7.5 mg/kg/d IV
Other aminoglycosides, cephalosporins, penicillins, and amphotericin B may increase nephrotoxic potential; enhances effects of neuromuscular blocking agents, which may result in prolonged respiratory depression
Loop diuretics appear to increase auditory toxicity—hearing loss of varying degrees may occur and may be irreversible; important to monitor patients regularly
Documented hypersensitivity; non–dialysis-dependent renal insufficiency
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Due to narrow therapeutic index and toxicity associated with extended administration, not intended for long-term therapy
Adjust dose in patients with renal impairment; improper dosing (without regard to serum levels) may lead to ototoxicity or nephrotoxicity; use caution in patients with renal failure (not on dialysis), hypocalcemia, myasthenia gravis, and conditions that depress neuromuscular transmission
Often used when MRSA or other resistant organisms are suspected. Potent antibiotic directed against gram-positive organisms and active against enterococci species. Useful in the treatment of septicemia and skin structure infections. Indicated for patients who cannot receive or whose conditions have failed to respond to penicillins and cephalosporins, or those who have infections with resistant staphylococci. For abdominal penetrating injuries, it is combined with an agent active against enteric flora and/or anaerobes.
To avoid toxicity, current recommendation is to assay vancomycin trough levels after third dose drawn 0.5 h prior to next dosing. Use creatinine clearance to adjust dose in patients with renal impairment.
Used in conjunction with gentamicin for prophylaxis in penicillin-allergic patients undergoing gastrointestinal or genitourinary procedures.
500 mg to 2 g/d IV divided tid/qid 7-10 d
40 mg/kg/d IV divided tid/qid 7-10 d
Erythema, histaminelike flushing, and anaphylactic reactions may occur when administered with anesthetic agents; taken concurrently with aminoglycosides, risk of nephrotoxicity may increase above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in renal failure and neutropenia; red man syndrome is caused by too rapid IV infusion (dose given over a few min) but rarely happens when dose given IV over 2 h administration or as PO or IP administration; red man syndrome is not an allergic reaction
Transfer to a facility with spinal cord imaging and care facilities may be necessary.
The many complications of spinal cord injury include bladder dysfunction, decubiti, supine hypertension, recurrent sepsis, and other problems.
For excellent patient education resources, visit eMedicine's Infections Center and Brain and Nervous System Center. Also, see eMedicine's patient education articles Brain Infection and Antibiotics.
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Gerberding JL, Romero JM, Ferraro MJ. Case records of the Massachusetts General Hospital. Case 34-2008. A 58-year-old woman with neck pain and fever. N Engl J Med. Oct 30 2008;359(18):1942-9. [Medline].
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Uchida K, Nakajima H, Yayama T, Sato R, Kobayashi S, Chen KB, et al. Epidural abscess associated with pyogenic spondylodiscitis of the lumbar spine; evaluation of a new MRI staging classification and imaging findings as indicators of surgical management: a retrospective study of 37 patients. Arch Orthop Trauma Surg. Jun 30 2009;[Medline].
spinal cord compression, vertebral osteomyelitis, epidural space infection, Staphylococcus aureus, Staphylococcus species, Pseudomonas species, Escherichia coli, Mycobacterium tuberculosis, brucellosis, spinal cord dysfunction, localized spinal pain, radicular pain and paresthesias, muscular weakness, sensory loss, sphincter dysfunction, paralysis
J Stephen Huff, MD, Associate Professor, Emergency Medicine and Neurology, Department of Emergency Medicine, University of Virginia Health Sciences Center
J Stephen Huff, MD is a member of the following medical societies: American Academy of Emergency Medicine, American Academy of Neurology, American College of Emergency Physicians, and Society for Academic Emergency Medicine
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Edward L Hogan, MD, Professor, Department of Neurology, Medical College of Georgia; Emeritus Professor and Chair, Department of Neurology, Medical University of South Carolina
Edward L Hogan, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Neurology, American Neurological Association, American Society for Biochemistry and Molecular Biology, Phi Beta Kappa, Sigma Xi, Society for Neuroscience, and Southern Clinical Neurological Society
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Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
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Florian P Thomas, MD, MA, PhD, Drmed, Director, Spinal Cord Injury Unit, St Louis Veterans Affairs Medical Center; Director, National MS Society Multiple Sclerosis Center; Professor, Department of Neurology and Psychiatry, Associate Professor, Institute for Molecular Virology, and Department of Molecular Microbiology and Immunology, St Louis University
Florian P Thomas, MD, MA, PhD, Drmed is a member of the following medical societies: American Academy of Neurology, American Paraplegia Society, and National Multiple Sclerosis Society
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Matthew J Baker, MD, Consulting Staff, Collier Neurologic Specialists, Naples Community Hospital
Matthew J Baker, MD is a member of the following medical societies: American Academy of Neurology
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Nicholas Y Lorenzo, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Neurology
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