| Literature DB >> 35962360 |
Hong-Qi Zhang1,2, Yu-Xiang Wang3,4, Chao-Feng Guo1,2, Ming-Xing Tang1,2, Shao-Hua Liu1,2, Ang Deng1,2, Qile Gao1,2.
Abstract
BACKGROUND: Pyogenic vertebral osteomyelitis (PVO), which is a potentially life-threatening condition and is associated with significant morbidity and mortality, is a cause of back pain that can lead to neurologic deficits if not diagnosed in time and effectively treated. The objective of this study is to compare the efficacy of posterior single-segment and short-segment fixation combined with one-stage posterior debridement and fusion for the treatment of mono-segmental lumbar or lumbosacral PVO.Entities:
Keywords: Lumbar; Lumbosacral; Mono-segmental; Posterior mono-segmental instrumentation; Posterior short-segmental instrumentation; Pyogenic vertebral osteomyelitis; Titanium mesh cage
Mesh:
Year: 2022 PMID: 35962360 PMCID: PMC9373455 DOI: 10.1186/s13018-022-03269-0
Source DB: PubMed Journal: J Orthop Surg Res ISSN: 1749-799X Impact factor: 2.677
Fig. 1a–f Preoperative radiographs, CT and MRI showed that L2–L3 pyogenic vertebral osteomyelitis and lesion around vertebral body of L2–L3 developed paravertebral abscess with marked bony destruction. g Posterior interbody grafts using titanium mesh cages was applied posterolaterally. h–j Postoperative radiographs showed that posterior interbody graft using titanium mesh cage, posterior single-segmental instrumentation and fusion. Postoperative CT and MRI showed completely resolution of epidural abscess. Interbody graft using titanium mesh cages were placed satisfactorily. k, l Final follow-up radiographs and CT showed good bone fusion
Fig. 2a–c Preoperative CT, and MRI showed that L4–L5 pyogenic vertebral osteomyelitis and lesion around vertebral body of L4–L5 developed paravertebral abscess with bony destruction.The abscess involved into the spinal canal with cord compromise resulted in neurologic deficit. d–g Postoperative radiographs and CT showed that interbody graft using titanium mesh cage, posterior short-segmental instrumentation and fusion. Postoperative MRI showed completely resolution of epidural abscess and decompression of neural component. h, i Final follow-up radiographs and CT showed good bone fusion
The clinical data of patients
| Group A ( | Group B ( | ||
|---|---|---|---|
| Gender (M/F) | 19/12 | 22/14 | 0.99 |
| Age (years) | 44.4 ± 6.7 | 44.8 ± 6.3 | 0.69 |
| Blood loss (ml) | 447 ± 55 | 589 ± 86 | < 0.01 |
| Operation time (min) | 177 ± 18 | 208 ± 17 | < 0.01 |
| Duration of follow-up (months) | 77.8 ± 10.5 | 80.9 ± 10.0 | 0.22 |
| Fusion time (months) | 5.4 ± 1.0 | 5.2 ± 0.9 | 0.55 |
| VAS | |||
| Pre | 7.1 ± 0.7 | 7.2 ± 0.6 | 0.27 |
| Post | 2.1 ± 0.6 | 2.0 ± 0.7 | 0.54 |
| FFU | 0.4 ± 0.5 | 0.5 ± 0.5 | 0.36 |
| ESR(mm/h) | |||
| Pre | 84.2 ± 20.7 | 83.7 ± 17.2 | 0.92 |
| TMP | 9.0 ± 1.8 | 8.9 ± 1.5 | 0.49 |
| CRP(mg/l) | |||
| Pre | 52.9 ± 14.7 | 51.4 ± 15.1 | 0.66 |
| TMP | 4.8 ± 1.2 | 5.0 ± 1.1 | 0.79 |
M male, F female, Pre pre-operative, Post post-operative, TMP three months post-operative, FFU final follow-up
Neurological status evaluated by the ASIA impairment scale
| ASIA scale | Group A ( | Group B ( | ||
|---|---|---|---|---|
| Pre | FFU | Pre | FFU | |
| A | 0 | 0 | 0 | 0 |
| B | 1 | 0 | 2 | 0 |
| C | 4 | 0 | 3 | 0 |
| D | 12 | 2 | 14 | 3 |
| E | 14 | 29 | 17 | 33 |
Pre pre-operative, FFU final follow-up
Comparison of the local lordotic angle
| Group | Local lordotic angle (°) | Correction loss (°) | |||
|---|---|---|---|---|---|
| Pre | Post | FFU | |||
| A | 31 | − 1.7 ± 7.9# | 5.8 ± 7.1* | 4.3 ± 6.9* | 1.5 ± 0.8 |
| B | 36 | − 1.6 ± 7.8# | 13.5 ± 6.2* | 12.3 ± 6.0* | 1.3 ± 0.8 |
| Statistic | |||||
Pre pre-operative, post post-operative immediately, FFU final follow-up
*Compared with pre-operative value, P < 0.05
#Compared with the value at immediately after operative, P < 0.05