Analysis of predictive factors for the efficacy of reinforced radiculoplasty in symptomatic sacral Tarlov cysts
- PMID: 40653586
- DOI: 10.1007/s10143-025-03712-w
Analysis of predictive factors for the efficacy of reinforced radiculoplasty in symptomatic sacral Tarlov cysts
Abstract
Reinforced radiculoplasty of the sacral nerve roots has been used in the treatment of symptomatic sacral Tarlov cysts (TCs). However, there is still insufficient evidence to support the effectiveness of this procedure in relieving pain, numbness, or bowel and bladder dysfunction in TC patients. In this single-center retrospective study, we reviewed data and conducted telephone follow-ups of 41 patients who underwent surgery between 2021 and 2023. Clinical characteristics-such as age, gender, follow-up duration, cyst length, number of cysts, side of cysts, number of nerves, preoperative selective nerve root block (SNRB), and pre- and postoperative symptoms-were collected and analyzed using binary logistic regression to identify potential predictors. A total of 41 patients were included in the study. Significant improvements were observed in pain and numbness across the entire patient group, the lateral side subgroup, and the no-SNRB subgroup, as well as in pain among female patients (P < 0.05). Among the 33 patients with preoperative pain, binary logistic regression analysis revealed that of age and preoperative visual analogue scale (VAS) scores were significantly associated with pain-free status (P < 0.05). However, no variables were found to be significantly associated with numbness relief (P > 0.05). In conclusion, reinforced radiculoplasty can significantly improve pain and numbness in patients with sacral TC. Older age and lower preoperative VAS scores are associated with a greater likelihood of achieving a pain-free outcome.
Not applicable.
© 2025. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Conflict of interest statement
Declarations. Ethical approval: All procedures performed in studies involving human participants were conducted in accordance with the ethical standards of Beijing Jishuitan Hospital, Capital Medical University, and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Consent to participate: Formal consent was required for this type of study, and informed consent was obtained from all individual participants included in the study. Consent for publication: All authors approved the final manuscript and its submission to this journal. Competing interests: The authors declare no competing interests.
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- PX2020018/Beijing Municipal Administration of Hospitals Incubating Program
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