Abstract
Objectives
The purpose of this case report is to describe an occurrence of a rare complication of lead extrusion, which was observed 10 months after spinal cord stimulator (SCS) implantation.
Methods
A patient with low back pain and failed back surgery syndrome underwent implantation of a SCS without complications. Ten months after implantation, one SCS lead extruded from her lower back leading to surgical removal of the leads.
Results
After identifying the complication of a SCS lead extruding from the patient’s back, a surgical revision was performed to remove the SCS leads but retain the implantable pulse generator (IPG) in the gluteal region. During the surgery, it was noted that the anchors were in the appropriate position, sutured and fibrosed to a deep fascial layer. There were no complications from the surgical revision and no infectious process was observed.
Conclusions
We report the occurrence and management of a rare complication of SCS lead extrusion after SCS implantation for failed back surgery syndrome. After recognition, removal of the leads with retention of the IPG was able to effectively resolve the complication. The revising procedure was well tolerated but resulted in the recurrence of the patient’s previous low back pain. We believe that knowledge of this case and its management will aid future physicians in the recognition and management of this rare complication of SCS implantation. Furthermore, as there is a paucity of literature discussing the management of lead extrusion after SCS implantation, we hope that this case report will spur additional research on the management of this complication.
Introduction
Among patients with chronic pain in the United States, 75% of them have a diagnoses of chronic back pain in the United States [1]. According to Shmagel et al. [2], 13% of United States adults 20–69 years old experience chronic low back pain. Chronic pain is one of the most disabling illnesses and is associated with depression, reduced quality of life, absenteeism from work, and a lower household income [3]. Spinal cord stimulator (SCS) therapy is one of the treatment modalities available for selected patients with intractable chronic back pain [4]. While surgical complication from SCS implantation are not common, reported complications include surgical site infection, seroma, epidural hematoma and spinal cord injury. We report on a rare case of SCS lead extrusion through the epidermis 10 months after implantation.
Case presentation
We report a rare case of lead extrusion through epidermis ten-months after SCS implantation. A 68-year-old female with a diagnosis of intractable low back pain and multiple failed back surgeries presented to the pain clinic for further management. The patient had already failed conservative management including oral medication, physical therapy rehabilitation, injections/nerve blocks, and multiple surgical procedures with minimal improvement of her symptoms. The patient was subsequently elected for SCS therapy. After a successful trial, the patient received a SCS implant through standard procedure. The patient reported ≥50% pain relief without complications on follow-up at 10 days, one month, two months, and four months after the procedure. At her six-month follow-up, patient noted two 2 mm peri-incisional sores, which were managed by her primary care physician with antibiotics and wound care. Ten months after her SCS implantation, she returned to the clinic with a SCS lead extruding in lower back (Figure 1) with serous discharge present but no signs of infection. She was managed acutely with antibiotics, pain control, and removal of the SCS leads in the operating room for revision. During surgery, it was noted that the anchors were in the appropriate position, sutured and fibrosed to deep fascial layer. The anchors were released, and the leads were removed. The implantable pulse generator (IPG), which was in the gluteal region, was preserved as there was no sign of infection. The incision was irrigated and closed in layers. There were no complications at one-month follow-up.

SCS lead extruding from patient’s lower back.
Discussion
Although SCS is generally regarded as a safe procedure, Labaran et al. [5] reported a rate of complication requiring SCS removal or reimplantation of 0.3 and 3.4% at 90 days and one year, respectively. The most common complication associated with SCS implantation is surgical site infection, but other less frequent complications include hematoma, seroma, intraspinal abscess, incidental durotomy, and spinal cord injury. Bendel et al. [6] reported an infection rate of 2.45% after SCS implantation and found the most common organism to be Staphylococcus aureus and the most common site to be the pocket for the IPG. It is notable too that 77.6% of these patients required SCS explantation.
In this rare reporting of lead extrusion after SCS implantation, all of the leads required removal due to their proximity to the extruded, contaminated leads. This decision was made in an effort to decrease the risk of infection secondary to the patient’s complication. Because the distant location of the IPG remained intact without signs of infection, the IPG was retained during the surgical revision, and the patient did not develop any complications at this site. Soliman et al. [7] reported a similar case of lead extrusion through the epidermis without infectious signs which was managed successfully with removal of both the leads and the IPG. Additionally, Radhakrishnan et al. [8] reported another case of SCS lead migration and near extrusion through the epidermis. In this instance, the complication was managed with surgical revision for deeper placement of the leads and eventual autologous fat transfer to adequately pad the leads and resolve the complication. In contrast to the management of our patient, IPG extrusion through the epidermis, as reported by Rabi et al. [9] may require removal of the IPG and leads to prevent the complication of infection.
The possible cause of lead extrusion may be hypothesized to be due to inadequate depth of lead burial or excessive loops left at the anchor site, potentially resulting in slow unwinding of loops months or even years later. To prevent this rare complication, meticulous care should be taken to ensure loops of leads are properly seated and anchored to deep fascial layers.
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Research funding: None declared.
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Author contributions: All authors have read and approved the paper. All authors were either involved in the patient care or write up of the case.
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Competing interests: There are no conflicts of interest for any of the authors.
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Informed consent: Written informed consent was obtained from the patient.
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Ethical approval: Ethics board approval was not required for case reports and was not obtained.
References
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© 2020 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Editorial Comments
- Patients with shoulder pain referred to specialist care; treatment, predictors of pain and disability, emotional distress, main symptoms and sick-leave: a cohort study with a 6-months follow-up
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- Recurrent abdominal pain among adolescents: trends and social inequality 1991–2018
- Cross-cultural adaptation and psychometric validation of the Hausa version of Örebro Musculoskeletal Pain Screening Questionnaire in patients with non-specific low back pain
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Artikel in diesem Heft
- Frontmatter
- Editorial Comments
- Patients with shoulder pain referred to specialist care; treatment, predictors of pain and disability, emotional distress, main symptoms and sick-leave: a cohort study with a 6-months follow-up
- Inferring pain from avatars
- Systematic Review
- Repetitive transcranial magnetic stimulation of the primary motor cortex in management of chronic neuropathic pain: a systematic review
- Topical Reviews
- Exploring the underlying mechanism of pain-related disability in hypermobile adolescents with chronic musculoskeletal pain
- Pain management programmes via video conferencing: a rapid review
- Clinical Pain Research
- Prevalence of temporomandibular disorder in adult patients with chronic pain
- A cost-utility analysis of multimodal pain rehabilitation in primary healthcare
- Psychosocial subgroups in high-performance athletes with low back pain: eustress-endurance is most frequent, distress-endurance most problematic!
- Trajectories in severe persistent pain after groin hernia repair: a retrospective analysis
- Involvement of relatives in chronic non-malignant pain rehabilitation at multidisciplinary pain centres: part one – the patient perspective
- Observational Studies
- Recurrent abdominal pain among adolescents: trends and social inequality 1991–2018
- Cross-cultural adaptation and psychometric validation of the Hausa version of Örebro Musculoskeletal Pain Screening Questionnaire in patients with non-specific low back pain
- A proof-of-concept study on the impact of a chronic pain and physical activity training workshop for exercise professionals
- Intravenous patient-controlled analgesia vs nurse administered oral oxycodone after total knee arthroplasty: a retrospective cohort study
- Everyday living with pain – reported by patients with multiple myeloma
- Original Experimental
- The CA1 hippocampal serotonin alterations involved in anxiety-like behavior induced by sciatic nerve injury in rats
- A single bout of coordination training does not lead to EIH in young healthy men – a RCT
- Think twice before starting a new trial; what is the impact of recommendations to stop doing new trials?
- The association between selected genetic variants and individual differences in experimental pain
- Decoding of facial expressions of pain in avatars: does sex matter?
- Differences in personality, perceived stress and physical activity in women with burning mouth syndrome compared to controls
- Educational Case Reports
- Leiomyosarcoma of the small intestine presenting as abdominal myofascial pain syndrome (AMPS): case report
- Duloxetine for the management of sensory and taste alterations, following iatrogenic damage of the lingual and chorda tympani nerve
- Lead extrusion ten months after spinal cord stimulator implantation: a case report
- Short Communication
- Postoperative opioids and risk of respiratory depression – A cross-sectional evaluation of routines for administration and monitoring in a tertiary hospital