Bachmann’s bundle potential during atrial lead placement: a case series

Heart Rhythm ◽  
2021 ◽  
Author(s):  
Margaret Infeld ◽  
Nicole Habel ◽  
Kramer Wahlberg ◽  
Sean Meagher ◽  
Markus Meyer ◽  
...  
2014 ◽  
Vol 3;17 (3;5) ◽  
pp. E397-E403
Author(s):  
Dr. Susie S Jang

Background: Stimulation-evoked discomfort secondary to ligamentum flavum stimulation (LFS) is a technological limitation of percutaneous spinal cord stimulator (SCS) lead implants. There is a paucity of literature describing the clinical presentation and time periods at which this side effect may present following insertion of cylindrical lead(s). Objective: To describe a series of 5 patients who presented at varying time periods after SCS lead placement with LFS. Study Design: Retrospective case series. Methods: We performed a chart review of online medical records of patients with symptoms consistent with LFS at an academic interventional pain clinic identified over 7 consecutive years (2006 - 2013). Results: LFS most frequently presented within months of implantation of cylindrical leads. One patient complained of LFS during the temporary trial while another developed LFS after lead revision. All patients were successfully treated when paddle electrodes replaced percutaneous cylindrical leads. Conclusion: LFS may present as a barrier to successful SCS treatment. Clinicians placing percutaneous SCS leads should be aware of the variable time course of LFS presentation. Paddle style electrodes seem to offer an enduring solution to LFS so that patients may continue to benefit from SCS therapy. Key words: Percutaneous electrodes, cylindrical electrode, paddle electrodes, ligamentum flavum stimulation, unwanted stimulation


Neurosurgery ◽  
2019 ◽  
Vol 66 (Supplement_1) ◽  
Author(s):  
Steven M Falowski

Abstract INTRODUCTION The procedure to place leads on the spinal cord traditionally required patients to be awake for reporting of device-induced paresthesias. Conversely, neuromonitoring using electromyography (EMG) recording determines optimal lead location while the patient is under general anesthesia. These techniques have been compared with regards to safety and efficacy, favoring the use of neuromonitoring1-2We present 7 subjects, incorporating the use of Evoked Compound Action Potential (ECAP) recording from implanted electrodes, using a new SCS system, and comparing the results with EMG recording. METHODS Standard neuromonitoring protocols were employed at 2 institutions Once leads were implanted, stimulation current was increased until the following were observed: ECAP and EMG signal (late response [LR]), and EMG signal on the neuromonitoring EMG electrodes. An x-ray was obtained; postoperative paresthesia testing was performed to assess coverage obtained at different points along the implanted leads. RESULTS Data were obtained from 7 patients, across 2 sites. Onset of EMG signals on implanted electrodes and EMG electrodes correlated. Furthermore, the ratio of current amplitude between EMG onset and ECAP onset (LR: ECAP), on implanted leads, provides a potential estimate of lead laterality and objective lead placement. Whereby a ratio <1 indicates leads are too lateral. This technique was used successfully to place leads under general anesthesia (1 case), without utilizing EMG recording as a dermatomal coverage marker. CONCLUSION Intraoperative recording of ECAPs and EMG signals from implanted leads may facilitate optimized lead placement, without requiring additional equipment and setup. Analysis of ECAP morphology and its relationship with different waveforms could have diagnostic capabilities intraoperatively. This could be correlative with recent results showing the effect of different waveforms on EMG recording.


2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
N. Shaparin ◽  
K. Gritsenko ◽  
P. Agrawal ◽  
S. Kim ◽  
S. Wahezi ◽  
...  

Background. Spinal cord stimulation is an established treatment option for certain chronic pain conditions which have been previously unresponsive to conservative therapies or potentially for a subset of patients who have not improved following spine surgery. Prior to permanent lead implantation, stimulator lead trials are performed to ensure adequate patient benefit. During these trials, one of the most common complications and reasons for failure is the displacement and migration of the trial leads, resulting in lost therapeutic coverage. Other complications include infection and dislodged bulky dressings. There is a paucity of literature describing an adequate procedural method to prevent these common complications. Objective. This study utilizes a series of 19 patients to evaluate a new technique for securing percutaneous spinal cord simulator trial leads, which may minimize dislodgement and migration complications and improve the rate of trial success. Study Design. Retrospective case series. Setting. New Jersey Medical School, Department of Anesthesiology, Pain Management Division. Methods. A retrospective chart review was conducted on 19 consecutive patients undergoing placement of the percutaneous thoracic spinal cord stimulator trial leads for pain associated with lumbar spine pathology over a two-year period (2010–2012). Results. Of the 19 patients in our cohort, there was one trial lead displacement, no lead migrations, and no site infections. Thirteen patients went on to permanent lead implantation. This improved trial lead placement technique had a high success rate with a low number of complications. Limitations. Small sample size, retrospective case series, and no control group for comparison. Conclusion. This case series was able to demonstrate that our described novel spinal cord stimulator trial lead placement and dressing technique can decrease the incidence of lead displacement and migration, thus improving trial success.


Author(s):  
Jayson R. Baman ◽  
Varun Garg ◽  
Aravind G. Kalluri ◽  
Jeremiah Wasserlauf ◽  
Amar Trivedi ◽  
...  

2020 ◽  
Vol 4;23 (7;4) ◽  
pp. E369-E376
Author(s):  
Dawood Sayed

Background: Surgical options for thoracic pain are limited and carry significant risk and morbidity. Spinal cord stimulation has the potential to be used for treatment of thoracic pain, as it has been useful for treating multiple types of chronic pain. Conventional tonic stimulation is limited in the treatment of thoracic pain, as it can produce paresthesia that is difficult to localize. Conversely, high-frequency spinal cord stimulation (HF-SCS) does not activate dorsal column Aβ fibers and does not produce paresthesia, and thus may be more beneficial in treating thoracic back pain not manageable with tonic stimulation. Objectives: To evaluate (1) the efficacy of 10 kHz HF-SCS for patients with chronic thoracic pain; and (2) appropriate paresthesia-free lead placement and programming targets for 10 kHz HF-SCS for patients with chronic thoracic pain. Study Design: Retrospective case series. Setting: Multisite academic medical center or pain clinic. Methods: A retrospective chart review was performed on 19 patients with thoracic back pain who underwent HF-SCS implantation. These patients had lead placement and stimulation between the T1-T6 vertebral levels. Outcome measures collected include location of device implant, stimulation settings, and pain scores at baseline, end of trial, and 1, 6, and 12 months postimplant. Followup phone calls collected information on if the patient reported functional improvement, improved sleep, or decreased pain medication usage. A Wilcoxon signed-rank test compared differences in mean pain scores across time points. Results: Significantly decreased Visual Analog Scale scores were observed with 17/19 (89.5%) patients demonstrating response to therapy (> 50% reduction in pain scores). These results were sustained relative to baseline at 1, 6, and 12 months postimplant, depending on length of followup. Many patients also reported functional improvement (17/19), improved sleep (14/19), and reduction in use of pain medications after implantation (9/19). A total of 15/19 patients reported best relief when contacts over T1 or T2 vertebrae were used for stimulation. Limitations: This study is limited by its retrospective design. Additionally, including documentation from multiple sites may be prone to selection and abstraction bias. Data were also not available for all patients at all time points. Conclusions: HF-SCS may be a viable option for significant, long-lasting pain relief for thoracic back pain. There may also be evidence for anatomically based lead placement and programming for thoracic back pain. Randomized, controlled trials with extended follow-up are needed to further evaluate this therapy. Key words: Thoracic pain, back pain, spinal cord stimulation, high frequency, 10 kHz


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