Safety and efficacy of polyetheretherketone (PEEK) cages in combination with one-stage posterior debridement and instrumentation in Lumbar Brucella Spondylitis

https://doi.org/10.1016/j.clineuro.2020.106259Get rights and content

Highlights

  • AS a last management option, diagnostic or curative surgery can be performed in brucella spondylitis.

  • The use of PEEK cage in the surgical treatment of brucella spondylitis is rarely reported.

  • We analyze the largest cohort of patients with lumbar brucella spondylitis receiving PEEK cages implantation.

Abstract

Objective

The aim of this study was to explore the efficacy and safety of surgical treatment of lumbar brucella spondylitis with PEEK cages combined with one-stage posterior debridement and instrumentation.

Methods

We performed a retrospective study for adult patients with lumbar brucella spondylitis. Medical records, imaging studies and laboratory data were collected, back pain was measured by employing the visual analog scale (VAS) and the neurological status was evaluated by using the American Spinal Injury Association (ASIA) scale.

Results

A total of 61 consecutive patients (42 males and 19 females) were enrolled with the mean age at presentation of 56.33 ± 9.16 years old. L3−4 and L4−5 were the most infected levels with the ratios of 21.31 % and 19.67 % respectively. Moreover, 12 (19.67 %) patients suffered multiple-level infection and 5 (5/12, 41.67 %) of them had non-contiguous spondylitis. In addition, epidural masses were found in 26 (42.62 %) cases and psoas abscesses were found in 14 (22.95 %) cases. The number of operative segment depended on operation indications (failure of conservative measures, instability, kyphosis, intractable pain and/or neurological impairment). VAS scores were significantly improved at 6-weeks and the last follow-up. Among the 23 (37.70 %) patients with neurological deficits, 19 (19/23, 82.61 %) obtained a full recovery and 4 (4/23, 17.39 %) had been improved incompletely during the last follow-up. All patients exhibited satisfactory bone fusion during the last follow-up. Local infection of surgical site was identified in 6 (9.84 %) cases and no other surgery-related complications were found.

Conclusion

Use of PEEK cages for interbody fusion is feasible and safe in patients suffering from lumbar brucella spondylitis.

Introduction

Humans would infect brucellosis through the contact with infected animals and the consumption of unpasteurized milk or cheese. It is shown by previous studies that a total of over 500,000 new cases of brucellosis would occur every year around the world [1]. Although brucellosis has been controlled very well in developed countries with the socio-economic development and improvement of regulatory system, it is still a serious public health problem in developing countries [1]. In China, the incidence rate of human brucellosis presents progressively elevation year by year since 1990 [2]. From 2004–2018, a total of about 4,490,000 patients were diagnosed as brucellosis with an average annual incidence rate of 0.0259 per 100,000 population [3]. Brucellosis has been identified as a systemic infectious disease that presents a variety of atypical clinical manifestations including arthralgia, fever, weakness, and low back pain [4].Spine brucellosis is viewed as the most common bony infection with the incidence rate of 2−53%, and the lumbar spine is the most encountered [5].

Over the past years, as far as brucella spondylitis is concerned, conservative treatment is deemed as the main therapeutic strategy, and a considerable amount of patients have obtained satisfactory outcome through the application of antibiotics [6]. However, the conservative approach may lead to terrible long-term problems such as recurrence, residual low back pain, and late-onset paralysis [7]. Then, diagnostic or curative surgery, which is deemed as a last management option, can be performed in brucella spondylitis [8].

Because the advantages of polyetheretherketone (PEEK) cage over titanium mesh have been observed for the radioparency and biomechanical behavior, more and more studies reported the best use of PEEK cage in pyogenic spinal infection and spinal tuberculosis [9]. However, the use of PEEK cage in the surgical treatment of brucella spondylitis is rarely reported.

Herein, we analyze the clinicopathological character of the largest cohort of patients with lumbar brucella spondylitis receiving PEEK cages implantation to evaluate the safety and effectiveness of PEEK cage usage in lumbar brucella spondylitis.

Section snippets

Study participates

A total number of 61 adult consecutive patients (42 males and 19 females) with lumbar brucella spondylitis and had received surgery of one-stage posterior debridement, instrumentation, and interbody fusion with PEEK cages from January 2015 to January 2019 in our institution were recruited in this study (Fig. 1). Clinical information was obtained from medical records and imaging, which included gender, age, Magnetic Resonance Imaging (MRI), Computed Tomography (CT), etc. All the procedures

Clinical characters

Of the 61 cases (42 males and 19 females), the mean age was 56.33 ± 9.16 years old (range, 28–73 yeas). The summary of clinical symptoms is displayed in Table 1. A titer >1:160 on the brucellosis standard tube agglutination test was detected in the entire cases and blood culture positive for Brucella was found in only in 7 (11.48 %) cases. The lumbar spine infection is listed in Table 1. As shown in Table 1, L3−4 and L4−5 levels were most commonly involved with ratios of 21.31 % and 19.67 %

Discussion

Brucella spondylitis which is one of the most encountered complication of brucellosis (2−53%), was initially described by Kulowski and Vinke in 1932 [10,11]. 24(39.34) patients in this study were 50−60 years. It is noticeable that 21 (34.43 %) patients in our study were older than 60 years, of which 5 (8.20 %) patients were older than 70 years.

In current study, back pain (100 %), which was followed by high fever (88.52%) and sweating (81.97%), was deemed as the most common symptom. The

Funding

No.

Ethical approval

This retrospective study was approved by the ethics committee of Beijing Ditan Hospital, Capital Medical University. All procedures performed in studies involving human participants were in accordance with the ethical standards of the insti- tutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards

Informed consent

Informed consent was obtained from all individual participants included in the study.

CRediT authorship contribution statement

Rugang Zhao: Data curation, Writing - original draft, Software, Validation. Rui Ding: Data curation, Writing - original draft, Investigation. Qiang Zhang: Conceptualization, Methodology, Supervision, Writing - review & editing.

Declaration of Competing Interest

The authors declare no conflict of interests.

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    These authors contributed equally to this work.

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