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A New Strategy for Rapid Diagnosis of the Source of Low Back Pain in Patients Scheduled to Undergo Treatment with Cooled Radiofrequency Ablation.
Chou, Shih-Hsiang; Lu, Cheng-Chang; Lin, Sung-Yen; Shen, Po-Chih; Liu, Zi-Miao; Chih, Wei-Hsing; Shih, Chia-Lung.
Affiliation
  • Chou SH; Department of Orthopedics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Lu CC; Orthopaedic Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Lin SY; Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Shen PC; Regenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Liu ZM; Department of Orthopedics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Chih WH; Orthopaedic Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
  • Shih CL; Regenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Diagnostics (Basel) ; 11(10)2021 Oct 01.
Article de En | MEDLINE | ID: mdl-34679520
ABSTRACT

OBJECTIVE:

The objective of this study was to develop a new strategy for rapid diagnosis of the source of low back pain (LBP) for treatment with cooled radiofrequency ablation (RFA). MATERIALS Patients suffering from facet joint (FJ) or sacroiliac joint (SIJ) pain for more than 3 months were included. Two methods, Technetium Tc99m methylene diphosphonate single photon emission tomography/computed tomography (99mTc-MDP SPECT/CT) and a modified Fortin finger test were used to identify the source of LBP for treatment with cooled RFA. The visual analog scale (VAS) and Oswestry disability index (ODI) were used to assess the patients' pain levels and disabilities respectively. These two measures were recorded at baseline and 1-week, 1-month, 3-month, and 6-month follow-up visits.

RESULTS:

A total of 40 patients with LBP were included in this study. Our results demonstrated that the patients with LBP identified by our new strategy had significant improvements in VAS or ODI score at 1-week to 6-month follow-up visits (p < 0.001) after receiving cooled RFA. Similar results were also found in patients with FJ pain and those with FJ and SIJ pain respectively. Among all the patients, over 70% had greater than or equal to 50% reduction in VAS and ODI scores. No serious adverse events were observed after treatment.

CONCLUSIONS:

This new strategy could be successfully adopted for rapid diagnosis of the source of comprehensive LBP.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Prognostic_studies Langue: En Journal: Diagnostics (Basel) Année: 2021 Type de document: Article Pays d'affiliation: Taïwan

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Prognostic_studies Langue: En Journal: Diagnostics (Basel) Année: 2021 Type de document: Article Pays d'affiliation: Taïwan