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Randomized Sham-controlled Double-Blind Multicenter Clinical Trial to Ascertain the Effect of Percutaneous Radiofrequency Treatment for Sacroiliac Joint Pain: Three-month Results

OBJECTIVES: To investigate the effect of a percutaneous radiofrequency (RF) heat lesion compared with a sham procedure, applied to the lateral branches of L5, S1, S2, S3, and S4 nerve roots. MATERIALS AND METHODS: Sixty patients aged 18 years and above with a medical history and physical examination...

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Detalles Bibliográficos
Autores principales: van Tilburg, Cornelis W.J., Schuurmans, Fleur A., Stronks, Dirk L., Groeneweg, Johannes G., Huygen, Frank J.P.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640001/
https://www.ncbi.nlm.nih.gov/pubmed/26889616
http://dx.doi.org/10.1097/AJP.0000000000000351
Descripción
Sumario:OBJECTIVES: To investigate the effect of a percutaneous radiofrequency (RF) heat lesion compared with a sham procedure, applied to the lateral branches of L5, S1, S2, S3, and S4 nerve roots. MATERIALS AND METHODS: Sixty patients aged 18 years and above with a medical history and physical examination suggestive for sacroiliac joint pain and a reduction of 2 or more on a numerical rating scale (NRS, 0 to 10) after a sacroiliac joint test block were included in this study. Treatment group: percutaneous RF heat lesion at the lateral branches of S1, S2, S3, and S4 nerve roots and the posterior ramus dorsalis of L5; sham group: same procedure as the treatment group except for the RF heat lesion. Primary outcome measure: pain reduction (NRS). Secondary outcome measure: Global Perceived Effect. RESULTS: No statistically significant differences in pain level over time between the groups (Group×Period) (F(1,58)=0.353; P=0.56) nor within the treatment Group (F(1,58)=0.212; P=0.65) were found. The Period factor, however, yielded a significant difference (F(1,58)=61.67; P<0.001), that is, when pooled together the mean pain level of the patients was significantly reduced at T1 compared with T0. In the crossover group, 42.1% experienced a reduction in NRS of 2 or more at 1 month (P=0.65). No statistically significant difference in satisfaction over time between the groups was found (F(1,50)=2.1; P=0.15). The independent factors Group (F(1,50)=2.02; P=0.16) and Period (F(1,50)=0.95; P=0.33) also showed no statistically significant difference. The same applies to recovery: no statistically significant Group×Period effect (F(1,51)=0.09; P=0.77) was found, neither an effect of Group (F(1,51)=0.004; P=0.95) nor of Period (F(1,51)=0.27; P=0.60). DISCUSSION: The hypothesis of no difference in pain reduction or in Global Perceived Effect between the treatment and sham group cannot be rejected. LEVEL OF EVIDENCE: Level 1A.