학술논문

Qualitative Sensory Testing in Outcome Prediction of Transforaminal Epidural Steroid Injection for Chronic Painful Unilateral Lumbosacral Radiculopathy: Prospective Observational Study.
Document Type
Article
Source
Pain Practice. Jul2021, Vol. 21 Issue 6, p618-629. 12p. 1 Diagram, 7 Charts, 2 Graphs.
Subject
*CHRONIC pain
*SENSES
*STATISTICAL significance
*KRUSKAL-Wallis Test
*PAIN measurement
*LUMBOSACRAL plexus
*SCIENTIFIC observation
*ANALYSIS of variance
*STEROIDS
*TIME
*ONE-way analysis of variance
*MULTIVARIATE analysis
*HEALTH outcome assessment
*RADICULOPATHY
*PSYCHOLOGICAL tests
*TREATMENT effectiveness
*REPEATED measures design
*SCALE analysis (Psychology)
*DESCRIPTIVE statistics
*EPIDURAL injections
*ALLERGIES
*DATA analysis software
*LONGITUDINAL method
Language
ISSN
1530-7085
Abstract
Background: Transforaminal epidural steroid injection (TFESI) is widely practiced for the treatment of radicular pain. As its effectiveness is still subject to debate, a better patient selection for TFESI is necessary. We aimed to evaluate the potential of bedside‐suitable qualitative sensory testing (QualST) to determine the early effectiveness of TFESI for the treatment of chronic lumbosacral radiculopathy (LSR)‐related pain. Methods: Thirty‐six patients with chronic painful unilateral LSR were evaluated in a prospective observational study using five standardized sensory tests (10 g monofilament, 200 to 400 mN brush, Lindblom rollers with controlled 25 and 40°C temperature, and 40 g neurological pin). Quality of sensory perceptions on the painful leg was compared to the non‐painful leg and rated as normal sensitivity, hyposensitivity, or hypersensitivity. Pain and related characteristics were evaluated before TFESI, 1 week after and 4 weeks after intervention. Results: Seven sensory phenotypes were distinguished according to individual sets of sensory disturbances acquired with five sensory tests. Patients were grouped into four groups of allied phenotypes (normal sensitivity, hyposensitivity to 1 to 3 modalities, hyposensitivity to 4 to 5 modalities, and hypersensitivity). The whole study group showed significant improvement in most parameters of outcome measurements. Statistical analysis revealed some significant differences between sensory groups in patient‐reported treatment effect scales after 4 weeks. We also detected significant differences between sensory groups in repeated measures after 1 and 4 weeks in some pain intensity characteristics and patient‐reported treatment effect scales. Conclusion: QualST might be clinically applicable for detecting patient subgroups that could differ in the early treatment results of radicular pain by TFESI. [ABSTRACT FROM AUTHOR]