Spinal Column Infections
Barrett Boody, MD
Cristian A. Balcescu, MD
Dr. Boody or an immediate family member serves as a paid consultant to or is an employee of Medtronic and Relievant Medsystems and has received research or institutional support from Biom’edUp. Neither Dr. Balcescu nor any immediate family member has received anything of value from or has stock or stock options held in a commercial company or institution related directly or indirectly to the subject of this chapter.
ABSTRACT
Infections involving the spinal column and neural elements can lead to serious illness or death. Chronic or untreated infections can lead to deformity and instability as well as neurologic deficits. It is important for the orthopaedic surgeon to understand the etiology of various infection types, including osteomyelitis and diskitis, spinal epidural abscesses, and postoperative spinal infections, and be aware of prevention strategies for postoperative spinal infections.
Keywords: diskitis; osteomyelitis; postoperative spinal infection; spinal epidural abscess
Introduction
Spinal column infections are associated with a substantial risk of morbidity and mortality. Gaining an understanding of the different types of infections that can occur in the spinal column as well as obtaining prompt diagnosis and treatment are crucial to minimizing the risk of significant long-term consequences.
Osteomyelitis/Osteodiskitis
Epidemiology
Osteomyelitis refers to an infection of the osseous aspects of the spinal column, whereas osteodiskitis refers to an infection of the intervertebral disk space. Because the vascular supply of the disk space is relatively limited with most of its blood supply originating from the vertebral body and occurring via diffusion across the end plate, infection of the disk space usually originates from the vertebral body. Osteomyelitis typically involves the anterior column and is rarely seen in the posterior column.1 Significant morbidity and mortality can occur if this condition is left untreated. The incidence of osteomyelitis has been reported at 2.2 per 100,000 people per year and appears to be increasing to 5.8 per 100,000 people per year.2
The risk factors for osteomyelitis of the spine are similar to those found for osteomyelitis of the appendicular skeleton. Conditions that affect the immune system such as diabetes, smoking, HIV, and hepatitis C are among the more common risk factors associated with osteomyelitis. Other factors include the presence of another infection, previous spine surgery, and skin compromise. A systematic review of 14 studies with a total of 1,008 patients who had pyogenic vertebral osteomyelitis (PVO) was conducted. The authors found that the median age of the patients was 59 years, and 62% of affected individuals were male.3 Comorbidities in this study included diabetes mellitus in 24% and intravenous drug use in 11%.3 The lumbar spine was affected in 59% of patients followed by the thoracic spine in 30% and cervical spine in 11%3 (Figure 1).
Pathogenesis
Osteomyelitis and diskitis typically occur either from direct inoculation or hematogenous spread from another site.4 Hematogenous spread accounts for most cases as the multiple vascular supplies to the spine provide an avenue for bacteria to readily seed the vertebrae.1,4 Direct inoculation typically requires skin compromise, such as following spinal surgery or in the setting of chronic ulcers.5 After bacteria have been introduced to the vertebral body, they may spread through diffusion and lead to diskitis of the adjacent disk spaces.
Staphylococcus aureus is the most common bacterial cause of osteomyelitis/osteodiskitis. The second most common pathogen isolated in cases of PVO is another gram-positive bacteria, Streptococcus. Gramnegative bacteria are also a frequent cause of spinal
infections, with the most common species including Escherichia coli and Klebsiella pneumoniae.6 In patients with a history of intravenous drug abuse, Pseudomonas aeruginosa also has been described as a common bacterial cause.7,8
infections, with the most common species including Escherichia coli and Klebsiella pneumoniae.6 In patients with a history of intravenous drug abuse, Pseudomonas aeruginosa also has been described as a common bacterial cause.7,8
In a 2020 study of 586 patients with PVO over a 12-year period, S aureus was found to be the most common pathogen at 43.5%, followed by gram-negative infection at 22.2% and Streptococcus at 20.1%.9 A total of 64% of patients underwent echocardiography and 11.2% of these patients had infective endocarditis. Gram-negative infections were found more commonly in older patients, females, and those with cirrhosis or a solid tumor. S aureus was more common in males and younger patients. MRSA was more common in those with chronic renal disease.9
Diagnosis
Patients with osteomyelitis/osteodiskitis most frequently present with back pain that worsens over the course of weeks to months, followed by fevers.3,10 As the infection progresses, bony retropulsion or abscess formation in the epidural space can occur and lead to neurologic deficits.3 A systematic review found that 34% of patients presented with some form of neurologic deficit, including symptoms ranging from radiculopathy to urinary incontinence.3
Initial laboratory workup may show either an elevated or normal white blood cell (WBC) count. The erythrocyte sedimentation rate (ESR) and the C-reactive protein (CRP) levels are typically elevated and reflect the body’s inflammatory response to the infection. On diagnosis, blood cultures should be obtained to help identify the offending pathogen and guide antibiotic management.1
Radiographic changes associated with osteomyelitis/osteodiskitis typically are seen in the vertebral body and rarely involve the posterior elements. Changes to the architecture of the vertebral body including sclerosis of the subchondral bone and scalloping of the end plates may be found.1 In acute cases, these radiographic changes may not be observed as they take several weeks to develop. In chronic cases, deformity and focal kyphosis caused by the bony erosion may be present. Standing full-length radiographs can help assess for changes in alignment.1
These bony changes can further be assessed using noncontrast CT, which can more clearly delineate the extent of vertebral end-plate erosion and other bony changes.1
MRI with and without contrast enhancement most clearly evaluates the soft-tissue structures and should be performed in all patients in whom osteomyelitis/osteodiskitis is suspected to evaluate for associated epidural abscess, to evaluate local spread of the infection, and to determine the chronicity of the infectious process. In patients with vertebral osteomyelitis/osteodiskitis, T1-weighted imaging will reveal a hypointense signal at the affected end plate and disk, whereas T2-weighted imaging will show a corresponding hyperintense signal in
the vertebral body and disk.1 Contrast-enhanced studies provide improved visualization of these processes and more clearly delineate the affected areas where the contrast is taken up at the site of the infection.1
the vertebral body and disk.1 Contrast-enhanced studies provide improved visualization of these processes and more clearly delineate the affected areas where the contrast is taken up at the site of the infection.1
Treatment
In the absence of neurologic deficits, vertebral osteomyelitis/osteodiskitis can be managed without surgery. This typically consists of culture-directed intravenous antibiotics. Blood cultures obtained before the initiation of antibiotics can help identify the organism. CT-guided bone biopsies are often obtained, although the efficacy of this treatment modality has been called into question. In one study, 323 patients with possible PVO underwent image-guided biopsies. Of the 92 patients highly suspected to have infection before the biopsy, the biopsy was only positive for a bacterial pathogen 30.4% of the time.11 Intermediate and low prebiopsy probability groups had positive biopsies in 16.1% and 5%, respectively.11
When a high suspicion for PVO exists despite a negative CT-guided biopsy, the biopsy may be repeated. One study of 136 patients with suspected PVO found that 44.1% of patients had initial biopsy results that identified the pathogen, whereas pathology was identified in 79.6% of patients who had an additional biopsy when biopsy findings were negative the first time.12
Infectious disease specialists should be consulted to help guide the antibiotic treatment course for these patients. Intravenous antibiotics are typically continued for 6 weeks and then transitioned to oral antibiotics if necessary.1 Serial laboratory evaluation (WBC count, ESR, CRP level) should be conducted during this treatment to monitor for improvement. Intravenous cefazolin is the most commonly used antibiotic in the setting of gram-positive non-methicillin-resistant S aureus (MRSA) infections, whereas intravenous vancomycin is the treatment of choice in most cases of MRSA osteomyelitis.10
Brace treatment can also be implemented in the management of vertebral osteomyelitis.1 A lumbosacral orthosis is used in cases of lumbar osteomyelitis, whereas a thoracolumbar orthosis or Jewett extension is used for thoracic infections. Although there are no long-term studies on the benefits of brace treatment, braces help support the spinal column when it has been weakened by the infectious process.1
Indications for surgical management of vertebral osteomyelitis include failure of nonsurgical treatment, development of an associated epidural abscess with neurologic deficit, and development of bony instability or significant kyphotic deformity. Surgical management of osteodiskitis with a small epidural abscess without neurologic deficit is controversial. The primary goals of surgical management are débridement of the infection, stabilization of the spine, and preservation of neurologic function. Coronal or sagittal plane deformities that occur following infection can also be corrected with surgery.1
When a significant portion of the vertebral body is involved results in deformity or failure of medical management, surgical management often consists of a subtotal or total corpectomy depending on the amount of the vertebral body affected. Reconstruction is subsequently performed with autograft, allograft, or cage placement.1 Although iliac crest autograft is preferred when feasible, allograft or cages can be used with similar efficacy and have been demonstrated to be safe despite local infection. The approach used is dictated by the level affected and surgeon preference and can include anterior, lateral, or posterior approaches.1 Pedicle screws are typically used to help stabilize the affected levels. In cases where an associated epidural abscess has formed, a laminectomy may also be performed for evacuation.1
Even with appropriate management, there is significant morbidity associated with PVO. In a retrospective review of 65 patients with osteomyelitis/osteodiskitis related to recent spinal surgery, the overall 1-year mortality rate was 6%. At final follow-up, these patients were noted to have significantly lower Oswestry Disability Index and lower quality of life scores measured by the EuroQol five-dimension questionnaire compared with unaffected individuals.13 A retrospective cohort analysis of 1,505 patients with osteomyelitis/osteodiskitis found that these patients had a 1.47 mortality rate ratio relative to unaffected individuals.14
Spinal Epidural Abscess
Epidemiology
Spinal epidural abscess (SEA) is an infection of the epidural space in the spinal canal. If left untreated, this infection is associated with high morbidity and mortality, and it can have devastating neurologic complications due to the proximity of the infection to the neural elements.1,15 SEA is most common in males ages 50 to 70 years and rarely is seen in the pediatric population. The incidence of SEA has been reported to range from 2 to 5 cases per 10,000 hospital admissions.15,16,17
Risk factors for SEA include intravenous drug use, recent trauma, and alcohol use.18 Procedures involving direct inoculation such as spinal epidural or facet injections also increase the risk of SEA. Patients with
medical comorbidities including diabetes and immunocompromising conditions are also at increased risk.18 In a review of 128 patients with SEA, the most common risk factor was intravenous drug use (39.1%) followed by diabetes (21.9%).19
medical comorbidities including diabetes and immunocompromising conditions are also at increased risk.18 In a review of 128 patients with SEA, the most common risk factor was intravenous drug use (39.1%) followed by diabetes (21.9%).19
S aureus is the most common bacterial cause of SEA; methicillin-susceptible S aureus is more common than MRSA. Other pathogens that have been reported include coagulase-negative Staphylococcus species, Streptococcus species, and gram-negative bacteria.18 The lumbar spine has been found to be the most frequent location for SEA in multiple studies. One study reported that 54.7% of cases were in the lumbar spine, with 39.1% in the thoracic spine.19
Pathogenesis
SEA can result from either direct inoculation or hematogenous spread.1 In a review of all SEA cases at one tertiary care hospital over 10 years, hematogenous spread was the most common source, with recent surgeries/procedures being the second most common.17
Neurologic dysfunction in the setting of SEA can occur due to either direct compression or secondary to spinal cord ischemia.15 This ischemia may be caused by mass effect of the abscess on the cord or through bacterial occlusion of the vasculature.15 The abscess may be located either ventrally or dorsally. Ventral SEA most commonly occurs in the setting of vertebral osteomyelitis/osteodiskitis, whereas dorsal SEA more commonly can be from a de novo process.1
Diagnosis
The classic presentation of SEA involves four stages of increasing disability.16,20 Initially the patient experiences focal back pain, followed by the development of radicular pain. This subsequently evolves into motor and sensory deficits with possible bowel and bladder incontinence. In the last stage, patients may present with paralysis. A systematic review of 1,099 patients found that 66.8% of patients initially presented with back pain, 52% with motor weakness, 40% with sensory abnormalities, 27.1% with bowel/bladder incontinence, and 43.7% with fever.18

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