Pola 2017
Pola 2017
Pola 2017
DOI 10.1007/s00586-017-5043-5
ORIGINAL ARTICLE
R. Cauda3 • M. Fantoni3
Received: 12 February 2017 / Revised: 7 March 2017 / Accepted: 11 March 2017 / Published online: 21 March 2017
Springer-Verlag Berlin Heidelberg 2017
123
S480 Eur Spine J (2017) 26 (Suppl 4):S479–488
2.2–5.8 cases per 100,000 person years [5]. Aging popu- radiological features to define a simple and reproducible
lation and longer life expectancy of patients affected by treatment algorithm for spine surgeons.
chronic debilitating diseases and immunodeficiency led to
an increased number of high-risk individuals, while the
spread of invasive and minimally invasive diagnostic and Materials and methods
surgical procedures exposed more patients to iatrogenic
infections. The increase of incidence is also due to the Based on data from 250 patients treated at our University
higher diagnostic efficacy obtained with the spread of MRI. Hospital from 2008 to 2015 with a 2-year follow-up, a
Estimated mortality is highly variable depending on geo- clinical-radiological classification of pyogenic spondy-
graphical areas with reported peaks up to 11% [6–10]. lodiscitis was developed. Both spine surgeons and infec-
tious diseases specialists were involved in caring of all the
Etiology and infection routes patients establishing a multidisciplinary clinical manage-
ment. Diagnostic approach included accurate anamnesis
According to etiology, pyogenic or non-specific spondy- and physical examination, serial C-reactive protein (CRP),
lodiscitis can be differentiated into bacterial, fungal or erythrocyte sedimentation rate (ESR), complete blood
parasitic infections. Among bacterial PS, Staphylococcus count, and full spine contrast-enhanced MRI (or CT when
aureus is the most frequent causative microorganism contraindicated). Blood cultures were collected from all
accounting for half of the cases, while fungal and parasitic patients after adequate antibiotics interruption and just
forms represent less than 2% of all cases [6]. PS is in most before and after every invasive procedure. Patients with
cases a hematogenous infection due to septic dissemination negative blood cultures underwent CT-guided biopsy,
from distant infectious foci. The development of PS by while surgical transpedicular biopsy was used as third line
direct inoculation is less common than hematogenous isolation technique [13].
spread and can occur following spinal surgery, epidural All patients received intravenous antibiotic therapy for
procedures and lumbar puncture with a reported prevalence at least 4 weeks followed by oral course until normaliza-
up to 18.8% [11]. Through the osteonecrosis, the infection tion of radiological and laboratory markers of infection
can spread to paravertebral soft tissues and epidural space [17]. Patients without etiological diagnosis even after sur-
producing abscesses and leading to biomechanical insta- gical biopsy, received empiric broad-spectrum antibiotic
bility and neurological impairment in about 1/3 of all cases therapy and underwent closer blood tests monitoring [17].
[3, 6, 7]. Conservative orthopedic treatment consisted of 24/7
immobilization with rigid orthosis until complete infection
Treatment goals healing. Rigid orthosis consisted on hard cervical collar
with proper chin support, or thoraco-lumbar rigid brace
Treatment of pyogenic spondylodiscitis is a story of great molded on plaster cast to avoid kyphosis. Posterior per-
successes which led from the mortality rate of about 70% cutaneous screw-rod instrumentation bridging the infected
observed by Kulowski in 1936 to nowadays optimal clin- level was used as alternative minimally invasive approach
ical outcomes [12]. First aim of the treatment strategy to orthosis in patients with single-level thoraco-lumbar PS
should be to eradicate the infection and prevent sepsis. and high functional demand. Open surgical treatment
However, while the antibiotic therapy greatly reduced included debridement of necrotic tissues, decompression of
mortality, PS is still burdened by a high rate of orthopedic neurological structures and spine instrumentation, avoiding
and neurological complications with great impact on infected vertebral bodies, through anterior or posterior
patients’ quality of life [9, 10]. The goals of orthopedic approaches. The same orthopedic treatments were used in
treatment are to preserve or establish spinal stability, to patients without microbiological diagnosis.
relieve pain, to prevent or reverse neurological deficits and Physical examination, serial blood tests and targeted
to prevent recurrence [13–16]. MRI were performed at 1, 3, 6, 12 and 24 months from
Practical guidelines for the pharmacological manage- diagnosis. At each follow-up visit, patients were also asked
ment of PS have been proposed by the Infectious Diseases to fill in Visual Analogic Scale (VAS) and Short-Form 12
Society of America (IDSA) in 2015 [17]. On the other (SF-12) questionnaires.
hand, the lack of large clinical studies and the variability of
inclusion criteria of existing clinical series still hinder the Classification criteria
development of a standard algorithm for orthopedic
treatment. Classification criteria were selected among clinical and
Aim of this study is to propose a new classification of radiological factors with known prognostic value. Three
pyogenic spondylodiscitis based on clinical and main types (A, B and C) were defined depending on to the
123
Eur Spine J (2017) 26 (Suppl 4):S479–S488 S481
Type A No No No No Yes/no
A.1 No No No No No (simple discitis)
A.2 No No No No No
A.3 No No No No Yes
A.4.1–2 No No No No Yes (muscle abscess)
Type B Yes Yes/no No No Yes/no
B.1 Yes No No No No
B.2 Yes No No No Yes
B.3.1–2 Yes Yes No No Yes
Type C Yes/no Yes/no Yes Yes/no –
C.1 Yes/no No Yes No –
C.2 Yes Yes Yes No –
C.3 Yes No Yes Yes –
C.4 Yes Yes Yes Yes –
123
S482 Eur Spine J (2017) 26 (Suppl 4):S479–488
Fig. 1 Magnetic resonance imaging (MRI) of type A pyogenic coronal T1-weighted contrast-enhanced MRI showing type A.3. PS
spondylodiscitis (PS). a Sagittal T1-weighted and axial T2-weighted involving D7–D8 vertebral bodies with paravertebral abscess (ar-
MRI showing type A.1. post-operative L4–L5 discitis. b Sagittal T1- rows). d Coronal and axial contrast-enhanced MRI showing type
weighted and axial T2-weighted MRI of type A.2. PS with A.4.2. PS with bilateral intra-psoas abscesses (arrows)
involvement of both L4 and L5 vertebral bodies. c Sagittal and
Table 2 Treatment algorithm showing the treatments of choice according to the classification scheme
Classes Treatments of choice
Type A
A.1 Rigid orthosis immobilization
A.2 Rigid orthosis immobilization or percutaneous stabilization
A.3 Rigid orthosis immobilization or percutaneous stabilization
A.4.1–2 Rigid orthosis immobilization or percutaneous stabilization
Type B
B.1 Rigid orthosis immobilization or percutaneous stabilization
B.2 Rigid orthosis immobilization or percutaneous stabilization
B.3.1–2 Percutaneous or open stabilization
Type C
C.1 Rigid orthosis immobilization or percutaneous stabilization with closer clinical-radiological monitoring
C.2 Open debridement and stabilization
C.3 Open debridement and decompression
C.4 Open debridement, decompression and stabilization
• C.3: epidural abscess and acute neurological impair- and closely monitored to evaluate neurological anoma-
ment without segmental instability (Fig. 3c). lies (Table 2). Type C.2 spondylodiscitis were treated
• C.4: epidural abscess and acute neurological impair- with surgical stabilization and abscess debridement to
ment with segmental instability (Fig. 3d). avoid impending neurological damages (Table 2). When
neurological impairment occurred (C.3 and C.4), surgical
Patients without acute neurological symptoms and
decompression of neurological structures was always
segmental instability (C.1) were treated conservatively
performed, combined with segmental stabilization in the
123
Eur Spine J (2017) 26 (Suppl 4):S479–S488 S483
Fig. 2 MRI of type B destructive pyogenic spondylodiscitis (PS). L4 and L5 vertebral bodies with paravertebral abscess (arrows).
a Sagittal T1-weighted and axial T2-weighted MRI showing type B.1 c Sagittal and axial T2-weighted MRI showing type B.3 thoracic PS
PS with partial destruction of L3 vertebral body. b Sagittal and with 46.71 kyphosis
coronal contrast-enhanced MRI of type B.2 destructive PS involving
Fig. 3 MRI of type C pyogenic spondylodiscitis (PS). a Sagittal contrast-enhanced MRI showing type C.3 lumbar PS with extended
contrast-enhanced MRI and axial T2-weighted MRI of type C.1 epidural abscess (arrows) in a 53-year-old male patient presented with
lumbar PS with limited epidural abscess. b Sagittal and axial T2- acute cauda equina syndrome. d Sagittal and axial T2-weighted MRI
weighted MRI showing type C.2 lumbar PS with limited epidural of type C.4 thoracic PS in a 68-year-old female patient presented with
abscess (arrows) and significant bone destruction. c Sagittal and axial acute paraplegia
123
S484 Eur Spine J (2017) 26 (Suppl 4):S479–488
same procedure if biomechanical stability was jeopar- Etiological diagnosis was assessed in about of all
dized (Table 2). patients [190 patients; 76.00%; 95% CI (68.91–82.21)].
Observed sensibility of blood culture, CT-guided biopsy
Statistical analysis and surgical biopsy was 57.64% [95% CI (49.13–65.82)],
46.27% [95% CI (34.00–58.88)] and 60.00% [95% CI
Baseline demographic and clinical onset characteristics (44.33–74.30)], respectively. Staphylococcus aureus was
were assessed using independent-sample t tests for con- the most frequently isolated causative agent [70 patients;
tinuous variables and v2 tests for frequency variables. 28.00%; 95% CI (20.97–36.11)]. Other commonly isolated
Analysis of variance was used to assess differences in microorganisms were Staphylococcus epidermidis,
clinical outcomes across follow-up, and p values 0.05 or Escherichia coli, and Klebsiella pneumoniae. 12 patients
less were considered significant. Continuous variables are [4.80%; 95% CI (1.95–9.63)] were infected by Methicillin-
presented as mean ± standard error. Frequency data are resistant Staphylococcus aureus (MRSA). 19 patients
presented as counts and percentages. Epi Info statistic [7.60%; 95% CI (3.75–13.69)] had polymicrobial infec-
software, version 7 (CDC, Atlanta, GA, USA), was used tions (Table 3).
for data analysis. 62 patients developed PS after surgical procedures
[24.80%; 95% CI (18.61–31.98)]. Direct inoculation of
causative agents during spine invasive procedures occurred
Results in 45 patients [18.00%; 95% CI (12.51–24.46)].
Type A spondylodiscitis occurred in 84 cases (33.60%).
A total of 250 patients (161 men and 89 women) were Types A.1 and A.2 included 11 (13.09%) and 28 (33.33%)
treated at our University Hospital from January 2008 to patients, respectively. Paravertebral abscesses (type A.3)
January 2015. Average age was 64.98 ± 0.97, moreover, were reported in 33 patients (39.29%), whereas intramus-
age distribution showed a significant peak in the cular abscesses (type A.4) occurred in 12 patients
60–75 years of age group. Average diagnostic delay was (14.29%). Among type A cases, 74 patients (88.10%) were
49.90 ± 5.53 days from symptoms onset. Most common prescribed 24/7 rigid orthosis immobilization, whereas 10
symptoms at diagnosis were localized spinal pain [236 patients (11.90%) underwent posterior percutaneous
patients; 94.40%; 95% CI (89.68–97.21)] and fever [159 stabilization.
patients; 63.60%; 95% CI (55.80–70.97)]. Limbs radiating 46 cases (18.40%) were classified as type B destructive
pain and weight loss were referred less frequently [106 spondylodiscitis. Segmental stability was preserved (types
patients; 42.40%; 95% CI (35.04–50.43) and 84 patients; B.1 and B.2) in 17 cases (36.96%). 29 patients (63.04%)
26.30%; 95% CI (26.30–41.40)]. 56 patients presented with presented segmental instability (type B.3) and 20 of them
neurological deficits at diagnosis [22.40%; 95% CI needed open surgical fixation, whereas 9 patients under-
(16.43–29.53)] (Fig. 4). Lumbar spine was the most com- went percutaneous stabilization.
monly affected [184 patients; 73.60%; 95% CI 120 cases (48.00%) were classified as type C spondy-
(66.29–80.16)] with peaks at L3–L5 levels. Other fre- lodiscitis with epidural abscesses or neurological impair-
quently involved levels were C5–C6 for cervical spine and ment. Among type C cases, 49 patients (40.83%) had no
D8–D10 for thoracic spine. No localizations were observed neurological deficits neither segmental instability (type
at C0–C3 levels. C.1), thus they were treated conservatively. Type C.2
123
Eur Spine J (2017) 26 (Suppl 4):S479–S488 S485
Table 3 Causative agents cultured from blood and/or tissue speci- Discussion
mens in overall population
Causative agents Prevalence n (%) Despite considerably improved diagnostic efficiency, there
are no standardized orthopedic treatment guidelines for
Staphylococcus aureus 70 (28.00)
pyogenic spondylodiscitis due to heterogeneous clinical
Staphylococcus epidermidis 36 (14.40)
data available in literature, often based on small patient
Escherichia coli 17 (6.80)
populations [16]. Actually, few standardized treatments are
Klebsiella pneumoniae 14 (5.60) suggested but without prospective randomized controlled
MRSA 12 (4.80) trials the level of evidence for treatment recommendations
Polymicrobial 19 (7.60) remains low [18]. Therefore, a classification of PS based on
clinical and radiological features with a standard treatment
algorithm can be very useful to spine surgeons facing this
pathology.
included 15 patients (12.50%) that underwent surgical Clinical onset of pyogenic spondylodiscitis is typically
stabilization and abscess debridement. 30 patients nonspecific and paucisymptomatic. Thus, differential
(25.00%) with acute neurological deficits without seg- diagnosis with degenerative spine pathologies is often
mental instability (type C.3) underwent surgical decom- difficult. Different reviews reported a mean diagnostic
pression of neurological structures. Open surgical delay of 90 days [6, 7]. For this reason, early diagnosis
stabilization was combined in the same procedure (type should be the first aim of clinical approach to PS. Early
C.4) in 26 cases (21.67%). diagnosis is based on a high level of suspicion with
Average time of hospitalization was 51.94 ± 3.00 days. emphasis on patients presenting acute and localized spinal
Full healing from infection was achieved in 232 patients pain combined with fever and known risk factors for
with an overall healing rate of 92.80% [95% CI infectious diseases. About 1/3 of all patients can be
(87.17–96.49)]. 14 relapses have been reported during apyretic at clinical onset hindering the differential diag-
follow-up with an overall recurrence rate of 5.60% [95% nosis with non-infectious spine pathologies. Contrast-en-
CI (2.67–10.67)]. hanced MRI showed the highest diagnostic sensibility and
Clinical outcomes for each class are shown in Table 4. provides a baseline picture on biomechanical stability and
A total of 140 patients (56.00%) were treated conserva- neurological structures [19, 20]. When MRI is promptly
tively. Average time of rigid orthosis immobilization was performed, impending neurological lesions or structural
218.17 ± 9.89 days. Among 110 cases (44.00%) treated damages can be detected earlier allowing the choice of less
surgically, 4 patients underwent procedure-related com- invasive treatments. CT may be useful when there are
plications, however, none of them reported permanent doubts on osteonecrosis extension or biomechanical sta-
damages. bility. There are no pathognomonic laboratory markers but
Self-reported VAS scores consistently decreased across CRP, ESR and WBC anomalies should raise the level of
time points in all classes reaching an average value of suspicious.
0.65 ± 0.21 at 2 years from diagnosis (Fig. 5). Similarly, The high healing rate and low recurrence rate observed
mental and physical components of SF-12 questionnaire in this study first demonstrate that a multidisciplinary
increased significantly (Fig. 6). approach to PS is the best choice. Early administration of
Residual chronic back pain occurred in 27 patients specific antibiotics prevents further damages and diffusion
(10.80%), whereas 13 patients (5.20%) showed residual of causative agent. While waiting for the microbiological
neurological deficits. Overall mortality was 4.80% [95% CI results, an empirical therapy can be started in severe cases
(3.33–6.48)]. [17]. According to 2015 IDAS guidelines, intravenous
123
S486 Eur Spine J (2017) 26 (Suppl 4):S479–488
Fig. 6 Pre- and post-treatment short-form (SF-12) mental component all classes across follow-up demonstrating a good restoration of
(left) and physical component (right) scores are shown at 1, 3, 6, 12, patients’ quality of life
and 24 months after diagnosis. Both scores significantly increased in
therapy should be administrated for at least 4 weeks fol- 7 months. Residual chronic back pain observed in 10.80%
lowed by oral course until normalization of laboratory and of our patients is mostly attributable to non-surgically
radiological markers of infection [17]. On the other hand, treated patients with postinfection kyphosis or
surgical debridement may be necessary to eradicate the pseudoarthrosis.
infection [9, 10]. The high efficiency of microbiological Since January 2010, percutaneous posterior screw-rod
isolation techniques observed in this study (76.00%) also instrumentation bridging the infected level has been used
derives from the close collaboration with infectious dis- as safe and effective alternative approach to prolonged
eases specialists. In fact, blood culture when adequately rigid bracing for single-level thoraco-lumbar PS. A retro-
collected, especially before and after invasive procedures, spective cohort study demonstrated faster recovery and
showed higher sensibility then reported in literature data. improved quality of life associated with minimally invasive
55 patients (22.00%) needed surgical biopsy. treatment [24]. Posterior percutaneous stabilization is also
When there are no neurological deficits and no signifi- indicated in patients with biomechanical instability and
cant instability, PS can be managed without surgical mild segmental kyphosis (type B.3.1).
intervention (types A.1–4, B.1–2 and C.1). Lumbar When acute neurological impairment or severe kyphosis
epidural abscess may be approached with a conservative occur (types B.3.2, C.3–4), open surgical approach is
treatment only if there is no evidence for cauda equina or mandatory. Emergency decompression is indicated if
conus dysfunction [9, 22]. Immobilization is necessary to complete plegia develops [16]. Decompression and
maintain spinal stability until bony ankylosis occurs instrumented spinal stabilization should be performed in
[9, 10]. However, spontaneous ankylosis requires the same procedure if neurological deficit exists (type C.4).
6–24 months and may not take place at all [23]. In our On the contrary, if instability and pain are present in a
population, average time of immobilization was about patient without neurological impairment (types B.3 and
123
Eur Spine J (2017) 26 (Suppl 4):S479–S488 S487
C.2) [21], correction of deformity through instrumentation 2. Beronius M, Bergman B, Andersson R (2001) Vertebral
may be delayed until infection has been cleared [22, 25]. osteomyelitis in Göteborg, Sweden: a retrospective study of
patients during 1990–95. Scand J Infect Dis 33:527–532
Debridement and arthrodesis may be sufficient in cases 3. Carragee EJ (1997) Pyogenic vertebral osteomyelitis. J Bone Jt
without instability (type C.3), combined with bed rest and Surg Am 79:874–880
bracing [17, 26]. When the bone loss created by debride- 4. Skaf GS, Domloj NT, Fehlings MG, Bouclaous CH, Sabbagh AS,
ment leads to potential instability, surgical reconstruction Kanafani ZA, Kanj SS (2010) Pyogenic spondylodiscitis: an
overview. J Infect Public Health 3:5–16. doi:10.1016/j.jiph.2010.
through interbody fusion or posterior stabilization is nec- 01.001
essary [23]. 5. Kehrer M, Pedersen C, Jensen TG, Lassen AT (2014) Increasing
The choice of surgical techniques and appropriate incidence of pyogenic spondylodiscitis: a 14-year population-
approaches and instrumentation to treat PS is still a matter based study. J Infect 68:313–320. doi:10.1016/j.jinf.2013.11.011
6. Fantoni M, Trecarichi EM, Rossi B, Mazzotta V, Di Giacomo G,
of controversy. Pyogenic infections predominantly involve Nasto LA, Di Meco E, Pola E (2012) Epidemiological and
the vascularized vertebral body with involvement of the clinical features of pyogenic spondylodiscitis. Eur Rev Med
posterior elements in only 5% of the cases [26]. Thus, Pharmacol Sci 16(Suppl 2):2–7
anterior surgical approach is most often used when 7. Duarte RM, Vaccaro AR (2013) Spinal infection: state of the art
and management algorithm. Eur Spine J 22:2787–2799. doi:10.
aggressive debridement is indicated. The gold standard for 1007/s00586-013-2850-1
anterior column reconstruction is the use of structural bone 8. Butler JS, Shelly MJ, Timlin M, Powderly WG, O’Byrne JM
auto- or allografting [25, 27]. An effective alternative to (2006) Nontuberculous pyogenic spinal infection in adults: a
structural bone autograft is the titanium mesh or PEEK 12-year experience from a tertiary referral center. Spine (Phila Pa
1976) 31:2695–2700. doi:10.1097/01.brs.0000244662.78725.37
cage. When cage is combined with anterior and/or posterior 9. Rutges JP, Kempen DH, van Dijk M, Oner FC (2016) Outcome of
instrumentation in a single stage procedure, this technique conservative and surgical treatment of pyogenic spondylodiscitis:
ensures immediate stability [15, 27–29]. a systematic literature review. Eur Spine J 25:983–999. doi:10.
Observed surgical complication rate was very low with 1007/s00586-015-4318-y
10. Aagaard T, Roed C, Dahl B, Obel N (2016) Long-term prognosis
no permanent disability. Among 56 patients with neuro- and causes of death after spondylodiscitis: a Danish nationwide
logical deficits at diagnosis, reverse of neurological deficits cohort study. Infect Dis (Lond) 48:201–208. doi:10.3109/
was achieved in 43 cases (76.79%). 23744235.2015.1103897
Improvement in VAS and SF-12 scores across time 11. Nasto LA, Colangelo D, Rossi B, Fantoni M, Pola E (2012) Post-
operative spondylodiscitis. Eur Rev Med Pharmacol Sci 16(Suppl
points demonstrate that an adequate treatment algorithm 2):50–57
ensures effective pain relief and good quality of life. 12. Kulowski J (1936) Pyogenic osteomyelitis of the spine: an
In conclusion, standardized treatment of pyogenic analysis and discussion of 102 cases. J Bone Jt Surg Am
spondylodiscitis based on clinical-radiological classifica- 18:343–364
13. Quiñones-Hinojosa A, Jun P, Jacobs R, Rosenberg WS, Wein-
tion is highly recommended. The proposed scheme in- stein PR (2004) General principles in the medical and surgical
cludes all available orthopedic treatments and helps spine management of spinal infections: a multidisciplinary approach.
surgeons to significantly reduce complications and avoid Neurosurg Focus 17(6):E1. doi:10.3171/foc.2004.17.6.1
overtreatment. The use of a common language to treat 14. Acosta FL Jr, Chin CT, Quiñones-Hinojosa A, Ames CP,
Weinstein PR, Chou D (2004) Diagnosis and management of
pyogenic spondylodiscitis allows shorter hospitalization adult pyogenic osteomyelitis of the cervical spine. Neurosurg
with reduced costs. This simple and reproducible scheme is Focus 17(6):E2. doi:10.3171/foc.2004.17.6.2
suitable also for spine surgeons with less experience in 15. Ruf M, Stoltze D, Merk HR, Ames M, Harms J (2007) Treatment
treating PS. of vertebral osteomyelitis by radical debridement and stabiliza-
tion using titanium mesh cages. Spine (Phila Pa 1976) 32:E275–
E280. doi:10.1097/01.brs.0000261034.83395.7f
Acknowledgements The authors declare that they received no grants 16. Grados F, Lescure FX, Senneville E, Flipo RM, Schmit JL,
or funding. Fardellone P (2007) Suggestion for managing pyogenic (nontu-
berculous) discitis in adults. Jt Bone Spine 74:133–139
Compliance with ethical standards 17. Berbari EF, Kanj SS, Kowalski TJ, Darouiche RO, Widmer AF,
Schmitt SK, Hendershot EF, Holtom PD, Huddleston PM 3rd,
Conflict of interest The authors declare that they have no conflict of Petermann GW, Osmon DR (2015) Infectious Diseases Society of
interest. America. 2015 Infectious Diseases Society of America (IDSA)
Clinical Practice Guidelines for the Diagnosis and Treatment of
Native Vertebral Osteomyelitis in Adults. Clin Infect Dis 61:e26–
References e46. doi:10.1093/cid/civ482
18. Homagk L, Homagk N, Klauss JR, Roehl K, Hofmann GO,
Marmelstein D (2016) Spondylodiscitis severity code: scoring
1. Grammatico L, Baron S, Rusch E, Lepage B, Surer N, Desenclos
system for the classification and treatment of non-specific
JC, Besnier JM (2008) Epidemiology of vertebral osteomyelitis
spondylodiscitis. Eur Spine J 25:1012–1020. doi:10.1007/s00586-
(VO) in France: analysis of hospital-discharge data 2002–2003.
015-3936-8
Epidemiol Infect 136:653–660. doi:10.1017/s0950268807008850
123
S488 Eur Spine J (2017) 26 (Suppl 4):S479–488
19. Leone A, Dell’Atti C, Magarelli N, Colelli P, Balanika A, Casale pyogenic discitis and vertebral osteomyelitis. J Neurosurg
R, Bonomo L (2012) Imaging of spondylodiscitis. Eur Rev Med 94(Suppl 1):1–7
Pharmacol Sci 16(Suppl 2):8–19 26. Pola E, Logroscino CA, Gentiempo M, Colangelo D, Mazzotta V,
20. Tins BJ, Cassar-Pullicino VN (2004) MR imaging of spinal Di Meco E, Fantoni M (2014) Medical and surgical treatment of
infection. Semin Musculoskelet Radiol 8:215–229. doi:10.1055/ pyogenic spondylodiscitis. Eur Rev Med Pharmacol Sci 16(Suppl
s-2004-835362 2):35–49
21. Chen WH, Jiang LS, Dai LY (2007) Surgical treatment of pyo- 27. Strowitzki M, Vastmans J, Vogel M, Jaksche H (2011) Complex
genic vertebral osteomyelitis with spinal instrumentation. Eur 360-reconstruction and stabilization of the cervical spine due to
Spine J 16:1307–1316. doi:10.1007/s00586-006-0251-4 osteomyelitis. Eur Spine J 20(Suppl 2):S248–S252. doi:10.1007/
22. Hsieh PC, Wienecke RJ, O’Shaughnessy BA, Koski TR, Ondra s00586-010-1645-x
SL (2004) Surgical strategies for vertebral osteomyelitis and 28. Korovessis P, Petsinis G, Koureas G, Iliopoulos P, Zacharatos S
epidural abscess. Neurosurg Focus 17(6):E4 (2006) Anterior surgery with insertion of titanium mesh cage and
23. Hadjipavlou AG, Mader JT, Necessary JT, Muffoletto AJ (2000) posterior instrumented fusion performed sequentially on the same
Hematogenous pyogenic spinal infections and their surgical day under one anesthesia for septic spondylitis of thoracolumbar
management. Spine (Phila Pa 1976) 25:1668–1679 spine: is the use of titanium mesh cages safe? Spine (Phila Pa
24. Nasto LA, Colangelo D, Mazzotta V, Di Meco E, Neri V, Nasto 1976) 20:1014–1019. doi:10.1097/01.brs.0000215049.08622.9d
RA, Fantoni M, Pola E (2014) Is posterior percutaneous screw- 29. Fukuta S, Miyamoto K, Masuda T, Hosoe H, Kodama H, Nishimoto
rod instrumentation a safe and effective alternative approach to H, Sakaeda H, Shimizu K (2003) Two-stage (posterior and anterior)
TLSO rigid bracing for single-level pyogenic spondylodiscitis? surgical treatment using posterior spinal instrumentation for pyo-
Results of a retrospective cohort analysis. Spine J 14:1139–1146. genic and tuberculotic spondylitis. Spine (Phila Pa 1976) 1:E302–
doi:10.1016/j.spinee.2013.07.479 E308. doi:10.1097/01.brs.0000083318.40123.5e
25. Przybylski GJ, Sharan AD (2001) Single-stage autogenous bone
grafting and internal fixation in the surgical management of
123