1. Introduction
Spondylodiscitis is a potentially life-threatening infection that has high morbidity rates [
1]. While vertebral osteomyelitis is rare, at a rate of 3–5%, it is the third most common form of osteomyelitis at >50 years of age [
2,
3]. Spondylodiscitis is usually a monobacterial infection and more than 50% of cases in Europe are caused by Staphylococcus aureus, followed by Gram-negative pathogens such as Escherichia coli (11–25%) [
4,
5]. The most common pathogen worldwide is
Mycobacterium tuberculosis [
4]. Brucellosis is endemic in the Mediterranean [
6]. Rare causes include fungal infections like Coccidioidomycosis [
7] and secondary syphilis [
8]. While the literature has reported a low incidence of approximately 5–6/100,000 patient years, recent data are clearly higher at an age-standardized rate of approximately 30/250,000 [
9]. The rate of surgical procedures in older, polymorbid patients is rising, and patients aged over 65 years are affected up to 3.5 times more frequently, while women are affected 0.82 times less frequently [
10]. Other risk factors include diabetes mellitus, immunosuppression, a history of infections, intravenous drug abuse, and HIV infection [
9]. Lethal outcomes occur almost exclusively in the older age group [
11].
Spontaneous and iatrogenic spondylodiscitis are becoming more frequent, yet there are no definite treatment guidelines [
12,
13]. Diagnosis is based on history and physical examinations, laboratory data, proper imaging, and culture. In the past, most infections were treated with an appropriate course of antibiotics and bracing if needed. An operative treatment of spondylodiscitis may be favorable in certain conditions, but it is not undisputedly to be performed in each case [
9,
14]. Neurologic deficits, sepsis, intraspinal empyema, the failure of conservative treatment, and spinal instability are all indications that surgical treatment is suitable [
9]. While surgical treatment of spondylodiscitis has its advantages, conservative therapy with immobilization, bracing, and intravenous antibiotic therapy, followed by a course of oral antibiotic therapy for six weeks, is still considered to be an effective therapy [
14], at least for patients with mild to moderate symptoms, with an absence of spinal instability and empyema or sepsis, as well as for patients with monosegmental infection. An image-guided or intraoperative aspiration or biopsy of a disc space or vertebral endplate sample often establishes the microbiological and pathological diagnosis of native vertebral osteomyelitis [
15]. Surgical treatment of spondylodiscitis allows for rapid mobilization and shortened hospital stays [
16], which leads to a paradigm change in the treatment and has made surgical treatment the first-line therapy. Complete healing of the infection with a normalization of the laboratory infection parameters, and with the application of antibiotic therapy for a minimum of six weeks, is the second pillar in the treatment of spondylodiscitis [
17]. Screening for associated infectious diseases in patients with spondylodiscitis has been recently advocated [
18]. With increasing experience in spinal instrumentation and fusion techniques, surgical management needs to be revisited [
19]. This retrospective study aims to assess the effectiveness of surgical treatment, as well as to identify prognostic parameters, which correlate with mid and long-term outcomes.
2. Materials and Methods
A retrospective review of patients who underwent surgical treatment in our department in the period between January 2010 and December 2018 was performed. Two hundred and thirty-seven consecutive cases were identified, and data were collected through review of patient’s electronic records and relevant imaging. In all the cases, Gadolinium contrast-enhancing MRI from the infected region of the spine was obtained. Leukocyte count and C-reactive protein concentrations (CRP) were determined in all patients using routine laboratory techniques. The leukocyte count and CRPs were standardly measured prior to surgery, as well as every 2–3 days following surgery, in order to discharge. These parameters were also obtained up to the follow-up in ambulatory setting for infection control assessment. A normal leukocyte count was defined as <10 G/L and a normal CRP value was defined as <5 mg/L. For the final assessment, CRP values prior to surgery, at the time of the switch from intravenous to oral antibiotic therapy, as well as at the last follow-up, were taken into consideration for statistical analysis.
Indications for surgery included the presence of pain, neurological deficits, sepsis, radiological signs of compression of the spinal cord, spinal instability, and the presence of empyema. In cases of instability, instrumentation surgery was performed. Furthermore, in cases without instability of the spine, stabilization surgery for segmental immobilization was performed as an analogue to immobilization with a corset in non-surgical treatment. CT scans were regularly obtained for all the patients who underwent spinal stabilization with screws, rods, and cages following surgery. Conservative treatment with immobilization was advised to patients as an alternative therapy option. Application of antibiotic therapy was performed in coordination with microbiologists. Broad-spectrum antibiotic therapy, which covers Gram-positive (Vancomycin), multiresistant Gram-positive (Linezolid), Gram-negative (Meropenem), and multiresistant Gram-negative pathogens (Fosfomycin) with solid bone and liquor accessibility, was initially used. Antibiotic therapy was initially performed intravenously (IV) as a broad-spectrum therapy (standard use of Vancomycin 3 × 1 g IV or Linezolid 2 × 600 mg IV, +Meropenem 3 × 1 g i.v + Fosfomycin 3 × 5 g IV), followed by targeted therapy tailored according to the antibiogram in cases where pathogens could be isolated. Antibiotic therapy was switched to oral administration (oral antibiotics tailored to antibiogram or broad spectrum antibiotics in cases where the pathogen was not isolated) after clear improvement to the clinical and laboratory parameters and applied until clinical improvement and significant regression of infection parameters occurred. Screening for further foci was performed using contrast-enhancing computer tomography (CT) of the thorax and abdomen, trans-esophageal echocardiography (TEE), urinary status, as well as a clinical examination of the nasal cavities, dental status, and craniofacial sinuses. Complete regression of the infection was defined as a significant decline in the infection parameters (leukocyte count and CRP concentration) without clinical and/or radiological signs of infection at the follow-up and at a minimum of four months after surgery. In addition, the neurological status was determined postoperatively at a minimum of four months following surgery. The neurological status of patients with spine diseases at our clinic is standardized and contains an examination of motoric deficits, which are defined into grades of muscle strength 1–5 for muscles of the upper and lower extremity (0 = complete paralysis, 1 = flicker of contraction, 2 = contraction with gravity eliminated alone, 3 = contraction against gravity alone, 4 = contraction against gravity and some resistance, and 5 = contraction against powerful resistance for deltoid, biceps, and triceps muscle, iliopsoas, quadriceps, as well as foot dorsiflexion, plantar flexion, eversion and inversion and toe plantar flexion and dorsiflexion. Furthermore, examination of the spinal ataxia in patients who were able to walk (tightrope and blind walk), examination of the coordination of upper and lower extremities using a finger nose test and knee heel try, the sensory exam with a comparing of tactile sensations between the left and right upper and lower extremities and the trunk, and an assessment of deep tendon reflexes (biceps, triceps, quadriceps knee jerk, and ankle jerk) were performed. In patients who reported urinary or stool incontinency, perianal, and perigenital sensory exams were performed with a digital rectal examination, as well as an assessment of residual urine with ultrasound or catheterization. The neurological outcome was measured in means of improvement, and unchanged or worsened neurological status following surgery, as compared to recorded neurological deficits prior to surgery.
Pain assessment was performed using Visual Analogue Score scale (VAS scale). VAS was routinely obtained prior to surgery and at discharge from the hospital. All statistical computations were performed using SPSS Statistics 23 (IBM, Hamburg, Germany). In descriptive statistics, for parametric variables, such as gender, infection parameters, including the WBC count of CRP, hospital stay or duration of antibiotic therapy, minimal and maximal value with a mean and standard deviation (STD) were calculated. For non-parametric variables (favorable or non-favorable outcomes and the influence of the presence or absence of empyema in the outcome), calculation of frequencies in distinct classes and their percentage were defined, as well as the cross-product and Pearson’s Chi-Squared test and Fisher’s Exact test for defining the significance of the differences in the frequencies in the classes or groups (for example, determination of significance of differences between patients with improved, unchanged or worsened neurological statuses following surgery or the determination of a significance between patients with favorable and non-favorable outcomes, as well as the influence of certain parameters on outcomes, such as smoking, diabetes mellitus and duration of antibiotic therapy). A t-test was used to measure statistically significant differences between the means. To calculate the differences between standard deviations, Leven’s Test for the equality of variances was performed before the t-test. If there was a statistically significant difference between the SDs, the t-test was not performed. An independent sample t-test was used to compare the different mean values between the two groups (favorable and non-favorable outcomes) and paired sample t-tests to compare the variables of two dependent samples for the same patients in different settings (e.g., comparison of parameters before and after surgery), which was used to determine the statistical significance. A correlation analysis was used to determine the correlation variables in the form of a parameter with strength correlation measured as a coefficient between 0 and 1. If the correlation coefficient is higher, i.e., more near to 1, correlation of variables is stronger. Regression analysis showed a quantitative correlation and provided the possibility of prediction of a value of the dependent variable from one or more independent variables. An ANOVA test was used where several variables in the parametric form were tested to determine the difference in significances.
3. Results
3.1. General Characteristics of the Patients
The general characteristics of the patients are summarized in
Table 1. Spondylodiscitis of the cervical spine was defined as an infection of one or more segments from C1/2 to C7/T1; spondylodiscitis of thoracic spine was defined as an infection in the segments T1/T2 to T12/L1, and spondylodiscitis of the lumbosacral spine was defined as an infection in segments from L1/2 to S4 with an infection of psoas muscle. Twenty-six patients had an infection of more than one segment of the spine. These patients were classified as cervical, lumbar, or thoracic according to the predominant site of pathology. Single level spondylodiscitis was defined as an infection of one intervertebral disc.
3.2. Symptoms and Neurological Status
Symptoms and neurological statuses are summarized in
Table 2. Pain was the most common symptom, present in 225 (94.9%) of patients. One hundred and seventy-two patients, or 72.6%, had neurological deficits. Time from onset of symptoms to diagnosis ranged from one to 67 days, with mean value of 17.9 days (SD: 14.8). Patients with epidural abscess had significantly higher rates of neurological deficits than the patients without abscess (
p < 0.05).
3.3. Laboratory Findings and Microbiology
All patients had increased values of laboratory infection parameters in the blood analysis. Forty-six patients, or 19.4%, had sepsis with multiple organ failures. In 180 patients (76%), microorganisms were isolated from the intraoperative specimen. The most common pathogen was
Staphylococcus aureus (77 patients, or 32.5%; of which 13 patients, or 5.5%, were diagnosed with
Methicillin-resistant Staphylococcus aureus (MRSA). Positive blood culture with an isolation of the pathogen was found in 55 patients (23.2%), and the most common pathogen was
Staphylococcus aureus (26 patients). There were no cases of multiple pathogens. In 57 patients (24%), the pathogen could not have been isolated from the intraoperative specimen. The diagnosis of the infectious disease in these cases was set in accordance with clinical findings, elevated infection parameters in the blood analysis, neuroradiological diagnosis of spondylodiscitis and neuropathological findings from the intraoperative specimen confirming an inflammation reaction in the tissue. The laboratory and microbiological findings are summarized in
Table 3.
3.4. Operative Therapy
Details of the operative treatment are summarized in
Table 4.
All patients with spondylodiscitis of the cervical spine received instrumentation, and of these, 23 patients received dorsoventral stabilization (360° fusion). In patients with spondylodiscitis of the thoracic and lumbar spine, decompression surgery with empyema evacuation was initially performed in 54 patients (in 26 patients as immediate surgery in less than 12 h following admission and in a further 28 patients following admission in 12–24 h). One hundred and thirty-eight patients in thoracic and lumbar spine groups received dorsal instrumentation. Illustrative cases are demonstrated in
Figure 1,
Figure 2 and
Figure 3.
Surgical complications occurred in 51 patients (21.5%). Twenty-eight patients (11.8%) underwent revision surgery due to hardware failure (screw correction and dislocation of the implant). In 44 cases, wound healing deficits occurred (18.6%), 5 patients had cerebrospinal fluid leaks (2.1%), and 8 patients had postoperative hematoma (3.4%). Eighteen patients (7.6%) required three or more surgeries due to complications.
Recurrent spondylodiscitis occurred in 18 patients (7.6%), and of these, 9 cases had treated and adjacent segments and another 9 cases had adjacent segments only. Adjacent segment disease, which required further stabilization surgery, occurred in 11 patients during the follow-up (4.7%), and 7 patients were treated conservatively for recurrent spondylodiscitis.
3.5. Etiology and Concomitant Infections
Sixty-two (26.2%) patients had postoperative spondyodiscitis following surgery on the spine to address degenerative disease with localization of the infection on the operated segment of the spine. All of these patients received a nucleotomy in the initial surgery. From this number, 18 patients underwent prior surgery at our department and 44 at other institutions. In 175 (73.8%) patients, there were no previous surgeries on the spine.
One hundred and forty-eight patients (62.4%) had isolated spondylodiscitis, and from this number, 45 patients had spondylodiscitis following spine surgery, and 89 patients, or 37.6%, had concomitant infections other than infection of the psoas muscle (
n = 35), which were counted as infectious diseases of the lumbar spine, together with spondylodiscitis. Concomitant infections are summarized in
Table 5.
One hundred seventy or 71.7% of patients who did not develop adequate remission of infection following initial operative and antibiotic therapy, or where the pathogen could not have been isolated, were fully screened for further infection foci. In 81 patients (34.2%), screening was negative, in 89 patients, one or more concomitant infection sites were found. Fifteen patients had one or more infection foci in the oral cavity, 8 patients in the nasal cavity, 10 patients with endocarditis, 40 patients had urinary tract infection, 48 patients had pneumonia, and 8 patients had other infections.
In 10 patients, endocarditis was diagnosed with trans-esophageal echocardiography. Eight patients with endocarditis were treated with IV antibiotics only and an additional two patients underwent surgery for valve reconstruction with antibiotic therapy.
3.6. Antibiotic Therapy
Broad spectrum antibiotic therapy was applied in all patients following surgery with the standard use of Vancomycin 3 × 1 g IV or Linezolid 2 × 600 mg IV, +Meropenem 3 × 1 g i.v + Fosfomycin 3 × 5 g IV Specific antibiotic therapy directed to the pathogen could then be applied in 180 patients (76%) after isolation of the microorganisms from the intraoperative specimen. In all other cases, broad spectrum IV antibiotic therapy was applied continuously until the antibiotic therapy could be switched to oral application.
Ninety-eight patients, or 41.4%, received antibiotic therapy at other hospitals prior to the diagnosis of spondylodiscitis due to the symptoms of the infection. From this number, in 57 patient microorganisms could not have been isolated from the intraoperative specimen or blood culture. Details of the duration of antibiotic therapy are summarized in
Table 6. Ninety-one patients received cumulative antibiotic therapy for a period longer than 6 weeks (42 days).
3.7. Outcome
3.7.1. Healing of Infection and Recovery of Infection Parameters
Complete healing was defined as normalization of the infection parameters (normalization of leukocyte count and significant fall of C-reactive protein) was achieved in 211 (89%) of cases. The mean postoperative leucocyte count at follow-up was 8.03 G/L (SD: 4.05) and was statistically significant compared to the preoperative value of 11.66 (SD: 5.27) (match paired t test, t = 11.071;
p < 0.001). The mean time of normalization of the leukocyte count (<10 G/L) was 9.5 days (SD: 44.56). Mean postoperative CRP was 45.4 mg/L (SD: 68.85) and was statistically significantly reduced in comparison to the preoperative value of 160.8 (SD: 159.52) (t = 15.107;
p < 0.001). In 96 patients, CRP was normal (<5 mg/L) at the follow-up (40.5%). The mean CRP value at the point of switch of antibiotic therapy from IV to oral was 76.5 mg/L (SD ± 48.35) for all patients. The mean CRP value at the start of oral antibiotic therapy in patients with favorable outcomes was 64.3 mg/L, as compared to 98 mg/L in patients with unfavorable outcomes without statistical significance. Antibiotic therapy was switched to oral use when the initial CRP fell to an average of 53.1% of the initial value (54.5% for patients with favorable and 52% for patients with unfavorable outcomes). Mean postoperative CRP for patients with unfavorable outcomes was 71.8 mg/L/SD: 96.71) and mean postoperative CRP for patients with favorable outcomes was 31.2 (SD: 42.81) (
Figure 4). Thirteen patients, or 5.5%, had infections with methicillin-resistant
Staphylococcus aureus (MRSA), 10 of them had unfavorable outcomes, with 5 dying during their primary hospital stay. All 21 patients who died during the hospital stay had sepsis with multiple organ failures and two or more concomitant infections.
3.7.2. Pain Reduction and Neurological Status
Postoperative pain reduction was significant, with a mean postoperative VAS of 2.03 (SD: 0.19) (Pearson Chi Square χ2 = 0.262, p < 0.001, ANOVA Regression Coefficient R = 0.778). Immediately following surgery, the neurological status improved in 38 of 211 patients, in 160 it remained unchanged, and in 13 it worsened. At follow-up, the neurological status improved in 101 patients (42.6%), remained unchanged in 95 patients (40%) and worsened in 15 patients (6.3%). One hundred and fifty-six patients (65.8%) were able to walk at the last follow-up. The number of patients with an improved neurological status was significant (χ2 = 9.981, p = 0.002).
3.7.3. Outcome Measurement
Significant outcome parameters are summarized in
Table 7. A favorable outcome was defined as a complete regression of infection (significant decline of C-reactive protein), significant reduction of pain symptoms (VAS Score), improved neurological status or unchanged neurological status in patients without deficits prior to surgery, with ability to walk. One hundred and fifty-six patients (65.8%) had favorable outcomes. Favorable outcomes were shown in patients without concomitant infections (
n = 148, χ
2 = 7.948,
p = 0.005), with a completely normalized CRP value (
n = 96, χ
2 = 5.410;
p = 0.02) and in patients who received antibiotic therapy over a period of more than six weeks (
n = 91 or 38.4%, Corr = −0.159, χ
2 = 5.733
p = 0.017). The number of patients with favorable outcomes vs. number of patients with unfavorable outcomes was significant (χ
2 = 18.941,
p < 0.01).
An unfavorable outcome was defined as an incomplete regression of infection (decline of C-reactive protein concentration not significant) with or without recurrent spondylodiscitis and/or unchanged or worsened neurological status without the ability to walk. Eighty-one patients (34.2%) had an unfavorable outcome, including 26 patients who died (21 in the initial hospital stay and 5 up to two years following surgery) and 15 patients with worsened neurological outcomes. Unfavorable outcomes were shown in patients with higher preoperative CRP values (mean CRP of 174.35 mg/L vs. 131. 84 mg/L compared to patients with favorable outcome), with postoperative spondylodiscitis (corr = −0.155; χ2 = 5.724, p < 0.02) and with recurrent spondylodiscitis (Corr = −0.184, χ2 = 0.004, p < 0.01).
The preoperative leucocyte count, age and gender, microbiological diagnosis (isolation of pathogen in operative specimen or blood culture), presence of empyema and risk factors such as diabetes mellitus or smoking, presence of neurological deficits, as well as operative approach (ventral vs. dorsal) did not show a correlation with the outcome (
p < 0.05). Patients with unfavorable outcomes had more frequent postoperative complications, as compared to patients with favorable outcomes, but this was not statistically significant (
p < 0.05) (
Table 7).
5. Conclusions
Our conclusion supports the current guideline facts. Spondylodiscitis should be included in the differential diagnosis of every unclear infectious disease associated with neck or back pain, especially in elderly multimorbid patients. Indications for surgical therapy should be broad due to the possibility of surgically removing the infection focus, microbiological diagnosis of the intraoperative specimen, as well as the possibility of early mobilization of the patient. Complete regression of infection is essential for successful treatment. Effective infection regression could be achieved with surgical therapy through instrumentation in selected cases following the application of antibiotic therapy for a minimum of six weeks, or even better, until complete normalization of the infection parameters. The absence of concomitant infections shows a good correlation with favorable outcomes, and so we strongly recommend regular screening for all patients. Our experience has shown that screening for concomitant infections should include trans-esophageal echocardiography, oral and nasal cavity examination, urinary status and a post-contrast CT of the thorax and abdomen to identify further infection foci.
Patients with significant pain reduction, improved neurological status, or unchanged neurological status in the case of patients without deficits prior to surgery, with ability to walk, without concomitant infections, and with completely normalized CRP values who have received antibiotic therapy for a period of more than six weeks show favorable outcomes. Unfavorable outcomes were shown in patients with higher preoperative CRP values in patients with spondylodiscitis following spinal surgery and in patients with recurrent spondylodiscitis.