scholarly journals Chronic back pain cured by low-dose levodopa: is it a variant of restless legs syndrome?

2018 ◽  
Vol Volume 11 ◽  
pp. 277-279 ◽  
Author(s):  
Zhi-Fen Zeng ◽  
Yan-Ran Liang ◽  
Ying Chen ◽  
Xiuna Jing ◽  
Su-Dan Peng ◽  
...  
2007 ◽  
Vol 17 (4) ◽  
pp. 323-327 ◽  
Author(s):  
Svenja Happe ◽  
Cornelius G. Bachmann ◽  
Kathrin Helmschmied ◽  
Karin Neubert ◽  
Wolfgang Wuttke ◽  
...  

2004 ◽  
Vol 50 (1) ◽  
pp. 65-70 ◽  
Author(s):  
Karin Stiasny-Kolster ◽  
Wolfgang H. Oertel

2016 ◽  
Vol 11 (2) ◽  
pp. 172-173 ◽  
Author(s):  
Ahmet Z. Soyata ◽  
Fahri Celebi ◽  
Lutfi I. Yargc

Pain Medicine ◽  
2020 ◽  
Vol 21 (9) ◽  
pp. 1921-1928
Author(s):  
Timothy Ade ◽  
Justin Roh ◽  
Gautam Sharma ◽  
Mahesh Mohan ◽  
Sarah J DeLozier ◽  
...  

Abstract Objective Targeted intrathecal drug delivery (TIDD) is an effective interventional pain management modality often used in postlaminectomy patients with refractory chronic low back pain. A combination of intrathecal bupivacaine with an opioid is often used. However, intrathecal catheter tip granulomas have occurred with use of morphine or hydromorphone but generally not with fentanyl. The objective of this study was to compare the efficacy of TIDD using bupivacaine/fentanyl vs bupivacaine/hydromorphone in patients with chronic intractable low back pain postlaminectomy. Materials and Methods A retrospective comparative analysis of consecutive patients with lumbar postlaminectomy syndrome who were trialed and later received TIDD with a combination of bupivacaine/hydromorphone or bupivacaine/fentanyl between June 2009 and May 2016 at a single tertiary medical center. Results We identified a cohort of 58 lumbar postlaminectomy patients receiving a TIDD admixture of either hydromorphone/bupivacaine (30 patients) or low-dose fentanyl/bupivacaine (28 patients) with at least two years of follow-up. The fentanyl group had significantly lower baseline opioid consumption and a lower rate of intrathecal opioid dose escalation. Both groups had similar and significant reductions in pain scores over the two-year follow-up period. No granulomas were observed. Conclusion TIDD using a low-dose fentanyl admixture with bupivacaine in patients with postlaminectomy syndrome and refractory chronic low back pain results in similar pain relief to TIDD with hydromorphone and bupivacaine. Low-dose intrathecal fentanyl leads to a lower rate of opioid escalation and may be safer than hydromorphone.


Author(s):  
Sadiye Visal Buturak ◽  
Kemal Yazici ◽  
Aylin Ertekin Yazici ◽  
Senel Tot ◽  
Ayse Devrim Basterzi

Neurosurgery ◽  
2008 ◽  
Vol 62 (1) ◽  
pp. E263-E263 ◽  
Author(s):  
Donald A. Ross ◽  
Michael S. Narus ◽  
John G. Nutt

Abstract OBJECTIVE Restless legs syndrome is now widely recognized and is usually successfully treated with medication. Occasionally, it may be severe and refractory to medication. Intrathecal opiates have been previously described to be useful in this situation in a single report. CLINICAL PRESENTATION We report the successful use of low-dose intrathecal morphine in a severe case of restless legs syndrome refractory to medication. TECHNIQUE The surgery was complicated by extreme restlessness in the recovery room resulting in withdrawal or breakage of the catheter on multiple occasions. Relief of symptoms was lost with each catheter malfunction. We describe the possible origin of this complication and a solution to the problem resulting in the successful control of symptoms for 7 months since the last surgery. CONCLUSION Intrathecal opiates for restless legs syndrome are currently considered investigational, but we hope, with this second report of the efficacy of low-dose intrathecal narcotics in this condition, to stimulate further investigation of this treatment modality.


2020 ◽  
Vol 7 ◽  
pp. 205435812096895
Author(s):  
David Collister ◽  
Kayla Pohl ◽  
Gwen Herrington ◽  
Shun Fu Lee ◽  
Christian Rabbat ◽  
...  

Background: Restless legs syndrome (RLS) affects approximately 30% of patients with end-stage kidney disease and is associated with impaired sleep and health-related quality of life. Medications used to treat RLS in patients receiving dialysis may have an increased risk of adverse events with dose titration, and residual RLS symptoms are common despite the use of effective treatments. Randomized controlled trials of monotherapy and combination pharmacologic therapy for RLS in hemodialysis are needed. Objective: To perform a randomized, crossover, placebo-controlled blinded trial of pharmacologic therapy for RLS in hemodialysis. Design/setting: The DIalysis Symptom COntrol-Restless Legs Syndrome (DISCO-RLS) trial is a randomized, crossover, placebo-controlled blinded trial of fixed low-dose pharmacologic therapy in patients receiving hemodialysis in 10 centers across Canada. It uses patient partners in its design, conduct, and reporting. Participants: Adults receiving thrice-weekly hemodialysis for at least 3 months with RLS of at least mild symptoms defined International Restless Legs Syndrome Study Group Rating Scale (IRLS) of 10 or more will enter a double placebo run-in period to exclude nonadherent participants and those unable to tolerate double placebo. Seventy-two participants who completed the run-in period will be randomized to 1 of 8 treatment sequences based on modeling with 4 treatment periods. Methods: Each treatment period lasts 4 weeks and consists of ropinirole 0.5 mg daily and gabapentin 100 mg daily, both together or neither with a double dummy placebo control for each treatment. The primary outcome is the difference in change scores of the IRLS between study treatments. Secondary outcomes are the differences in change scores of the Restless Legs Syndrome-6 Scale, patient global impression, 5-level EQ-5D version, and safety outcomes. Results: This randomized, crossover, placebo-controlled blinded trial will evaluate the efficacy and safety of fixed low-dose combination of ropinirole and gabapentin in patients receiving hemodialysis with RLS. Limitations: Patients with chronic kidney disease not on dialysis, kidney transplant recipients and those receiving peritoneal dialysis or home hemodialysis are not included. The intervention’s long term safety and efficacy including the risk of augmentation is not captured. Conclusion: This randomized crossover placebo controlled blinded trial will evaluate the efficacy and safety of fixed low-dose combination ropinirole and gabapentin in patients receiving hemodialysis with RLS. Trial Registration: ClinicalTrials.gov (NCT03806530)


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