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DOI 10.3233/thc-241003

Медицинская библиотека · Technology and health care : official journal of the European Society for Engineering and Medicine · 2024

Minimal-invasive pain procedures are effective in different degenerative pain generators in CLBP: A prospective cohort study.

Veihelmann A, Beck F, Huth J, Spetzger U, Schulze-Pellengahr C, Teske W

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Аннотация

BACKGROUND

It is estimated that a significant number of spinal surgeries are performed, but many patients do not often benefit.

OBJECTIVE

Our aim was to determine how effective minimally invasive pain procedures (MIP) are in chronic low back pain (CLBP) patients with proven degenerative causes (specific low back pain).

METHODS

386 eligible patients with CLBP/sciatica resistant to conservative therapy and scheduled for open surgery were screened, and 167 could be enrolled in this study. Indications for MIP in the remaining 150 individuals were made by one experienced spinal surgeon. Before and 6 months after the intervention, the numeric rating scale (NRS) and Oswestry Disability Index (ODI) were recorded. MIP was performed, such as radiofrequency of the facet and SI-joint, intradiscal electrothermal therapy in case of discogenic pain, as well as epidural neuroplasty in patients with disc herniation/epidural fibrosis.

RESULTS

There was a statistically significant decrease in NRS (p< 0.05), as well as a significant increase in ODI (p< 0.001) 6 months after the procedures. This was also true for the results of all different pain generators and subsequent performed procedures alone.

CONCLUSIONS

The indication of MIP should be routinely reviewed in patients with CLBP to avoid potentially open surgery and a burden on healthcare costs.

Для цитирования: Veihelmann A, Beck F, Huth J, Spetzger U, Schulze-Pellengahr C, Teske W. Minimal-invasive pain procedures are effective in different degenerative pain generators in CLBP: A prospective cohort study.. Technology and health care : official journal of the European Society for Engineering and Medicine. 2024. DOI: 10.3233/thc-241003.
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