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Multicenter Study Clinical Trial
Efficacy, Safety, and Predictors of Intradiscal Methylene Blue Injection for Discogenic Low Back Pain: Results of a Multicenter Prospective Clinical Series.
- Jan Willem Kallewaard, José W Geurts, Alphons Kessels, Paul Willems, Henk van Santbrink, and van Kleef Maarten M Department of Anaesthesiology and Pain Medicine, Maastricht University Medical Centre, Maastricht, the Netherlands..
- Department of Anaesthesiology and Pain Management, Rijnstate Hospital, Arnhem, the Netherlands.
- Pain Pract. 2016 Apr 1; 16 (4): 405-12.
Study DesignProspective clinical study of intradiscal methylene blue injection for the treatment of lumbar discogenic pain.ObjectiveThe objective of this study was to collect information about efficacy, safety, and acceptability of the intervention, gain and burden of outcome measures, and sample size assumptions for a potential following randomized controlled trial (RCT). If the pilot study demonstrates that this treatment is potentially effective and safe, and the methods and procedures used in this study are feasible, a RCT follows.Summary Of Background DataLow back pain (LBP) is a highly common problem with a lifetime prevalence of more than 70%. A substantial part of chronic LBP is attributable to degenerative changes in the intervertebral disc. A recently published RCT assessing the treatment intradiscal injection of methylene blue for chronic discogenic LBP, showed exceptionally good results.MethodsPatients were selected on clinical criteria, magnetic resonance imaging, and a positive provocative discogram. The primary outcome measure was mean pain reduction at 6 months.ResultsFifteen consecutive patients with chronic lumbar discogenic pain enrolled in a multicenter prospective case series in two interventional pain treatment centers in the Netherlands. Six months after the intervention, 40% of the patients claimed at least 30% pain relief. In patients who responded, physical function improved and medication use diminished. We observed no procedural complications or adverse events. Predictors for success were Pfirrmann grading of 2 or less and higher quality of life mental component scores.ConclusionsOur findings of 40% positive respondents, and no complications, give reason to set up a randomized, double-blind, placebo-controlled, trial.© 2015 World Institute of Pain.
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