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DOI: 10.1055/s-0045-1810050
Surgical Approach for Spasticity: A Systematic Review
Funding This study was conducted under the research grant by Indian Council of Medical Research (grant no. IIRP-2023-2116).
Abstract
Background
Stroke and traumatic brain injury are among the leading causes of death and disability worldwide, with spasticity being a common and debilitating complication. This condition often significantly impairs mobility and quality of life, necessitating additional treatment options such as medications and botulinum toxin injections. When spasticity becomes resistant to drug therapy, surgical interventions are considered. Several surgical treatments are available, including selective dorsal rhizotomy (SDR), dorsal root entry zone (DREZ) lesioning, C7 neurectomy, selective peripheral neurotomy (SPN), and intrathecal baclofen therapy (ITB).
Objective
This systematic review aims to analyze the mechanisms, indications, and efficacy of surgical interventions for spasticity. It will also examine the most widely accepted surgical treatments currently used to reduce spasticity and improve patient outcomes in individuals with spasticity.
Methods
A comprehensive search of PubMed, Scopus, and Google Scholar (1993–2024) was conducted, including randomized controlled trials (RCTs), case reports, case series, and systematic reviews, all following PRISMA guidelines. Eligible studies focused on surgical treatments for spasticity in the upper and lower extremities, with outcome measures such as the modified Ashworth scale (MAS) and improvements in the range of motion.
Result
The search retrieved 465 abstracts, and 42 articles were finally selected. The results of the reviewed studies suggest that surgery is a useful, safe, and enduring treatment for spastic patients. SDR benefited cerebral palsy patients with long-term motor function improvement, DREZotomy reduced spasticity and neuropathic pain, SPN showed promise in focal spasticity management, and ITB effectively managed severe spasticity.
Conclusion
Surgery provides a safe and effective solution for managing spastic patients, with durable functional improvements. It is a valuable option in spasticity treatment.
Keywords
craniocerebral trauma - denervation - functional neurosurgery - muscle spasticity - rhizotomy - strokeIntroduction
Spasticity is a common consequence of stroke, and brain and spinal cord trauma, causing disability and reducing the quality of life[1] It is a frequent clinical sign in people with neurological diseases, affecting mobility and leading to serious complications such as joint pain, muscular contractions, and tightness.[2] Many upper and lower motor neuron disorders, such as cerebral palsy (CP), traumatic brain injury (TBI), stroke, multiple sclerosis (MS), and spinal cord injury (SCI), are associated with spasticity. CP is the leading cause of motor dysfunction in children.[3] [4] In patients with SCI, spasticity is especially prevalent, affecting ∼65% of individuals.[5] Many studies describe neuro-orthopedic surgeries for correcting joint and limb deformities caused by spasticity.[6]
The objective of this study is to analyze the indications, limitations, and effectiveness of various surgical treatments for drug-resistant spasticity following stroke, TBI, SCI, or CP to formulate best practices and improve patient outcomes.
Methods
This systematic review follows the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines, searching the literature from 1993 to 2024, including randomized controlled trials (RCTs); case reports; case series; observational, retrospective, clinical trials; and systematic reviews. Surgical approaches for patients with drug-resistant spasticity were evaluated for their effectiveness in improving function, pain management, care, and quality of life. The interventions involve various surgical treatments, including selective dorsal rhizotomy (SDR), dorsal root entry zone lesioning (DREZotomy), selective peripheral neurotomy (SPN), and intrathecal baclofen therapy (ITB).
PICO Framework for Surgical Approach in Spasticity
Question
Which surgical approach is effective for patients with spasticity?
Patient |
Patients with spasticity due to conditions such as stroke, cerebral palsy, multiple sclerosis, traumatic brain injury, or spinal cord injury |
Intervention |
Surgical approaches, selective dorsal rhizotomy (SDR), DREZ lesioning, SPN, and ITB |
Comparator |
Nonsurgical interventions (botulinum toxin injections, physiotherapy) |
Outcomes |
Reduction in spasticity, improved functional ability, pain relief, enhanced quality of life |
Eligibility Criteria
Titles and abstracts were screened for eligibility by two independent reviewers (L.K.B. and J.B.). The inclusion criteria were as follows: observational or experimental studies, including RCTs, case reports, case series, clinical trials, and systematic reviews, that evaluated surgical treatments for post-stroke spasticity of patients of any age. Exclusion criteria included articles not meeting the eligibility criteria based on their title and abstract.
Information Sources and Search Strategy
The PubMed, Scopus, and Google Scholar databases were searched for studies published between 1993 and 2024. The studies were selected following the PRISMA guidelines and the specified eligibility criteria. Relevant keywords for searching articles on surgical approaches for spasticity included terms related to the condition, such as “spasticity,” “muscle spasticity,” “post-stroke spasticity,” “cerebral palsy,” “traumatic brain injury,” “spinal cord injury,” and “multiple sclerosis.”
Keywords describing surgical interventions included “surgery,” “neurosurgical procedures,” “orthopedic surgery,” “rhizotomy,” “dorsal rhizotomy,” “dorsal root entry zone lesioning,” “selective dorsal rhizotomy (SDR),” “selective peripheral neurotomy, “intrathecal baclofen pump (ITB),” “Radiofrequency Method” and “ITB therapy.” Outcome-related terms included “spasticity reduction,” “functional improvement,” “motor control,” “gait improvement,” “quality of life,” “pain management,” and “rehabilitation outcomes.”
To ensure the inclusion of relevant reviews, terms such as “systematic review” and “evidence synthesis” were also incorporated. These keywords were combined strategically using Boolean operators like “AND” and “OR” to retrieve comprehensive and relevant literature.
Search Strategy Equation
(upper and lower limb) AND (post-stroke spasticity, cerebral palsy, traumatic brain injury, spinal cord injury, multiple sclerosis) AND (surgical, neurotomy, rhizotomy, ITB therapy).
Result
A comprehensive literature search across three databases—PubMed, Scopus, and Google Scholar—identified 465 records. After removing 268 duplicates, 197 reports were screened by title and abstract. A total of 155 reports were excluded as irrelevant, and 42 reports were assessed for eligibility and included in the systematic review. The included studies consisted of RCTs, case reports, case series, and systematic reviews, which were used to assess and determine the quality of the research, as shown in [Fig. 1].


The four neurosurgical techniques—SDR, dorsal root entry zone (DREZ) lesioning, ITB therapy, and SPN—are specialized interventions designed to address spasticity and neuropathic pain.
SDR is a neurosurgical procedure to reduce spasticity by selectively cutting sensory nerve rootlets in the spinal cord. Performed via laminectomy with electrophysiological monitoring, it targets 50% of dorsal rootlets while preserving ventral rootlets. SDR is suited for children with spastic diplegia from CP who have adequate lower limb strength and ambulation potential. Contraindications include mixed or dystonic CP, severe weakness, cognitive impairments, and scoliosis that may hinder surgery. Intraoperative neuromonitoring is essential during this surgery. SDR has emerged as an effective intervention for managing functional impairments and reducing spasticity in the lower extremities with CP.[7] [8] This surgical procedure is primarily employed to treat conditions such as CP, where the targeted severing of sensory nerve fibers in the spinal cord results in sustained relief from spasticity and improved mobility.[9] [10] SDR is particularly effective in improving ambulatory function in patients with lower limb spasticity, especially those with causes other than multiple sclerosis.[11] [12] On evaluating the impact of SDR combined with physical and occupational therapy on motor function in children with spastic diplegia, with follow-up at 6 and 12 months, the SDR showed good improvement in gross motor function measure (GMFM) scores (12.1%) compared with the control group (4.4%). Both groups received physical therapy and occupational therapy.[13] SDR combined with physical training significantly improves motor function, balance, and walking capacity and reduces energy cost in children with spastic diplegia. A study of 42 children (5–8 years) showed superior results for SDR compared with the control group after 6-month and 1-year follow-up (p < 0.001). Both groups improved, but SDR group was more effective.[14] ITB and SDR in non-ambulatory CP (GMFCS level IV/V) children showed reduced spasticity and improved GMF. However, complication rates were higher after ITB, due to device-related complications, compared with SDR.[15] Post-SDR CP patients included 30 studies, identifying 21 types of complications. The most common were structural complications, such as scoliosis and hyperlordosis, along with neurological complications like constipation and sensory changes.[16]
DREZ lesioning (DREZotomy) is a surgical procedure that uses microsurgery or thermocoagulation to treat intractable pain and spasticity by selectively targeting sensory nerve fibers at the spinal cord DREZ. It is typically indicated for conditions such as brachial plexus avulsion or SCI. Contraindications include poor general health, difficulty localizing pain sources, or severe spinal deformities that obstruct surgical access. Intraoperative neuromonitoring is not mandatory in this surgery. Patients with spinal cord injuries benefit from DREZ lesioning, which reduces spasticity and neuropathic pain, improving daily function. DREZ lesioning is effective in treating chronic, refractory neuropathic pain by disrupting pain transmission pathways in the spinal cord, commonly used for conditions such as brachialgia after pan-brachial plexus injury, complex regional pain syndrome, and postherpetic neuralgia.[17] It involves severing the DREZ, which severs the nociceptive pain fibers. DREZotomy has been demonstrated to be a safe, effective, and long-lasting procedure for alleviating pain associated with brachial plexus avulsion.[18] [19] Cervical DREZ lesioning, traditionally used to manage severe neuropathic pain, targets pain pathways in the spinal cord. Its established role in conditions like complex regional pain syndrome contrasts with its emerging application for treating focal dystonia in the upper limb.[20] [21] Microsurgical DREZotomy is an alternative treatment for severe spastic CP in resource-constrained settings where ITB pumps are not feasible. Conducted from 2016 to 2020, in a study that included seven patients aged 6 to 21 years, postsurgery, all patients showed improvement in Ashworth grades, from 3–4 to 0–1.[22] Spinal cord injuries, intractable cancer/postradiation pain, and brachial plexus avulsion are among the chronic pain conditions that DREZotomy effectively treats after providing pain relief for patients in whom medical management fails.[23] [24]
Radiofrequency (RF) method is a medical technique where high-frequency electrical currents are used to generate heat to target and treat specific areas of nerve tissue, in both SDR and SPN, the RF method allows for precise, controlled lesions to be made on specific nerve fibers, offering more targeted and effective treatment with minimal damage to healthy tissues. RF ablation has proven effective in reducing spasticity in neurological conditions, as demonstrated in a study involving 26 children with severe CP. This procedure targeted spinal nerve roots at the L2–S1 levels. MAS score decreased from 3.0 ± 0.2 to 1.14 ± 0.15.[25] Fan et al conducted RCT on children with CP, dividing 64 participants into four groups: conventional treatment, repeated transcranial magnetic stimulation (rTMS), action observation training (AOT), and combined rTMS-AOT intervention. After 12 weeks, the combined rTMS and AOT intervention showed the greatest improvement in motor function compared with the rTMS, AOT, and conventional treatment groups. These results suggest that the combined therapy is more effective than individual treatments or conventional rehabilitation.[26] Ultrasound-guided treatments, including thermal RF and 35% ethyl alcohol neurolysis, effectively reduce elbow spasticity by targeting the musculocutaneous nerve in focal elbow flexor spasticity and hemiparetic stroke patients.[27] [28]
SPN is a technique that targets second or third of the selective motor nerve branches to lessen spasticity while maintaining motor function. When other therapies are unsuccessful, it works well for localized spasticity brought on by diseases such as multiple sclerosis, CP, stroke, or trauma. Generalized spasticity, severe muscle weakness, poor skin conditions at the surgical site, and coagulopathies are among the contraindications. Many generalized spasticity patients with local spasticity issues are also suitable candidates. Intraoperative neuromonitoring is essential during this surgery. SPN is an effective neurosurgical intervention for managing severe focal spasticity in children. It emphasizes preoperative motor blocks for precise surgical planning and delineates specific indications for both upper and lower limb spasticity. SPN's role in improving mobility, reducing deformities, and enhancing the quality of life is good when conservative treatments fail.[29] SPN is a simple and safe procedure aimed at reducing spasticity in specific muscle groups, such as those affected by stroke, TBI, and upper and lower limb spasticity,[30] [31] and corrected equinovarus spastic foot deformities,[32] while preserving overall motor function. Selective motor fasciculotomy is a modification of SPN wherein the motor fascicles in the main trunk of the nerve are separated, stimulated, and cut to relieve the spasticity.[33] Each of the above-mentioned techniques has a distinct mechanism, indication, limitations, and outcomes. Their application is determined by the specific condition, patient needs, and treatment goals, as shown in [Table 1].
Upper motor neuron diseases often experience pain and functional issues due to a paretic shoulder, where spasticity causes an upper limb flexion pattern, leading to discomfort, restricted movement, and caregiving difficulties. Treatment options include orthotics, medications, physical therapy, and pain management techniques.[34] SPN targets focal or multifocal spasticity, showing improvements in both spasticity and shoulder function. A 2013 analysis of 141 SPN procedures revealed improved caregiver comfort and enhanced shoulder function, with an average 2.6-point reduction on the modified Ashworth scale (MAS) and a 20.6-degree increase in passive range of motion. SPN effectively reduces spasticity, enhances function, and facilitates care. Key outcomes included surgical complications, spasticity level using MAS, and range of motion.[35] Spastic deformities result from an imbalance between flexor and extensor forces at the glenohumeral joint.[36] On evaluating the effect of combined selective peripheral neurotomy (cSPN) in 14 SCI patients with severe lower limb spasticity, partial neurotomy of key nerve branches significantly reduced spasticity, improved abnormal gait patterns, enhanced walking ability, and increased independence in daily activities, demonstrating the effectiveness of cSPN in spasticity management.[37] Long-term effects of tibial nerve neurotomy in 51 post-stroke patients with lower limb deformities showed reduced spasticity, improved motor control, balance, and walking, with greater gains in more impaired patients. A slight decline in benefits occurred at 2 years. Sensory disturbances were observed as side effects. Tibial neurotomy effectively improves walking and balance in these patients.[38] [39] The effects of selective neurotomy on focal lower limb spasticity were evaluated by reviewing 25 nonrandomized studies and one RCT. The findings showed improvements in muscle tone, pain, ankle range of motion, and walking speed without any negative effects.[40] ITB has been found effective in spinal cord spasticity management due to tumors and injuries.[41] Thirty-one patients with upper-limb spasticity underwent 64 SPNs on the musculocutaneous, median, and ulnar nerves. Long-term follow-up (mean: 4.5 years) showed significant improvements in motor function, spasticity, hand function, and daily activities (p < 0.01). Four patients with painful spasticity experienced complete pain relief. The mean patient satisfaction score was 61.5. Complications occurred in 15% of patients, including hematomas and temporary sensory and motor issues.[42]
ITB pump therapy involves implanting a programmable pump to deliver baclofen directly into the cerebrospinal fluid, effectively managing generalized spasticity with minimal systemic effects. It is indicated for conditions like CP, multiple sclerosis, or SCI unresponsive to oral medications. Contraindications include infections, baclofen hypersensitivity, anatomical barriers to catheter placement, or poor compliance with pump maintenance.
ITB therapy involves an implanted pump to deliver baclofen directly into the spinal fluid, offering adjustable, reversible management of severe spasticity in conditions like multiple sclerosis or SCI.[43] [44] ITB was also effective in treating multiple sclerosis-related spasticity unresponsive to oral medications. Patients experienced reduced spasm frequency and improved quality of life, with most complications being surgical rather than pharmacological. The average 1-year ITB dose (191.93 μg/day) was lower than doses for central or spinal spasticity, highlighting its effectiveness when conventional therapies fail.[45]
The ITB has a significant reduction in spasticity, with little improvement in motor function.[46] It is an effective treatment for lower limb spasticity. In ambulatory patients with spasticity[47] with conventional medical management for poststroke spasticity, ITB showed a significantly greater reduction in Ashworth scale scores (−0.99 vs. −0.43). The adverse events were more frequent in the ITB group (96 vs. 63%).[48] MS patients with leg muscular spasms participated in a randomized controlled experiment that examined the effects of baclofen and self-applied TENS over a 4-week period. Spasticity was significantly reduced in both groups; however, TENS improved MAS scores more than baclofen.[49] In 40 patients with severe spasticity treated with ITB pumps over a 4-year follow-up, the average Ashworth score improved to 1.8 ± 0.6, with 85% of patients satisfied and willing to repeat the procedure. Functional independence remained stable, while 37% experienced complications, primarily involving the catheter or pump, and 12% had severe side-effects during refills.[50]
SDR has shown significant benefits, with 85 to 90% of patients reporting reduced spasticity and improvements in motor function, although 15 to 20% experienced complications. DREZotomy was found to be highly effective in managing chronic pain and spasticity, with 73 to 87% of patients showing pain relief. RF-based methods like percutaneous thermal rhizotomy and rTMS combined with AOT are minimally invasive options that offer substantial improvements in spasticity and motor function. SPN has been effective in reducing spasticity and improving mobility in 86.5% of patients, with minimal complications. ITB therapy also has proven effective in reducing spasticity.
Each intervention for managing spasticity and neuropathic pain is suited to specific patient needs. SDR is most effective for children with spastic diplegia from CP, significantly improving lower limb function and reducing spasticity, especially when combined with physical therapy. DREZotomy is ideal for refractory neuropathic pain and spasticity in conditions like brachial plexus avulsion or SCI, offering targeted pain relief. ITB therapy benefits patients with generalized spasticity due to CP, multiple sclerosis, or SCI, providing adjustable and reversible management, though it has higher complication rates. SPN is a safe and effective option for focal spasticity, particularly in post-stroke or CP patients, improving mobility and reducing deformities. The choice of surgical techniques depends on spasticity distribution, underlying conditions, and specific treatment goals.
Each surgical approach to managing spasticity requires rigorous evaluation and well-designed studies to establish its long-term efficacy and safety. Advances in these surgical fields will enhance patient care and contribute to better clinical outcomes and functional independence. [Table 2] gives a summary of the various studies included in this review.
Surgical approaches |
References |
Level of evidence |
Types of study |
No. of cases |
Follow-up |
Performed intervention |
Result |
---|---|---|---|---|---|---|---|
SDR |
Dudley et al[8] |
Level 4 |
Case series |
102 pre-op, 97, 62, 57, 14 |
1, 5, 10, and 15 y |
SDR with/without adjunct orthopedic procedures or Botox injections |
Long-term improvements in muscle tone, gross motor function, and ADLs, better outcomes in GMFCS I–III, diplegia, lower hip adductor spasticity |
SDR |
Kakodkar et al[11] |
Level 4 |
Case series |
141 |
Short to mid term |
SDR performed on adult patients with spasticity |
Improved ambulation and reduced spasticity |
SDR |
Lu et al[12] |
Level 1 |
Systematic review |
636 patients |
Not specified |
Systemic, epidural, and intrathecal analgesia |
Variations in regimens reported; opioid-based regimens common with evolving multimodal approaches |
SDR |
Wright et al[13] |
Level 1 |
RCT |
24 (12 RG, 12 CG) |
12 mo |
SDR with PT and OT vs. PT and OT alone |
RG showed greater GMFM improvement (+12.1% vs. +4.4% in CG, p < 0.02); reduced tone, increased |
SDR |
Abd-Elmonem et al[14] |
Level 1 |
RCT |
42 (5–8 y) |
1 y (post I and II) |
SDR + PT with progressive functional strength training and SOM |
Improvement in GMF, balance, walking capacity, SMC, and ECW compared to controls (p < 0.001) |
SDR and ITB |
Davidson et al[15] |
Level 1 |
Systematic review |
27 studies |
12–36 mo |
SDR sectioning of selective sensory nerve rootlets and ITB implantation for CP |
SDR and ITB reduce spasticity (Ashworth scale) and improve GMF (GMFM); ITB has higher complication rates due to device-related risks |
SDR |
Mishra et al[16] |
Level 2 |
Systematic review |
30 studies |
Long-term (varied) |
Sectioning of selective sensory nerve rootlets to reduce spasticity |
➢Scoliosis and sensory changes |
Cervical spinal cord DREZ lesioning (radiofrequency thermocoagulation) |
Khalifeh et al[17] |
Level 5 |
Case report |
1 patient |
3 mo postoperatively |
DREZ lesioning with radiofrequency thermocoagulation targeting pain fibers |
Complete pain relief postsurgery, sustained at 3-mo follow-up |
Cervical DREZotomy for BPA pain |
Ko et al[18] |
Level 3 |
Case series |
27 patients |
62.5 mo |
Cervical DREZotomy for BPA pain relief |
Initial success rate was 73%, but it declined to 66% after a median follow-up time of 62.5 mo |
MDZ |
Doddamani et al[19] |
Level 4 |
Case series |
56 patients |
32 mo |
Microscissor DREZotomy for post-BPA brachialgia |
87% patients experienced pain relief (>25%) |
Cervical MDT |
Sindou et al[20] |
Level 4 |
Case series |
3 patients |
Not mentioned |
Deep cervical microsurgical DREZotomy for focal dystonia |
Hypertonia reduction, suppression of dystonic postures, improved residual motor function |
Right radiofrequency dentatotomy |
Villegas-López et al[21] |
Level 5 |
Case report |
1 patient |
8 mo postoperatively |
Right radiofrequency dentatotomy for spasticity with intraoperative electrophysiological monitoring |
Significant decrease in spasticity at 1 mo (Ashworth 1), further decrease to Ashworth 0 after 8 mo, but increase in spasms |
MDT |
Goyal et al[22] |
Level 4 |
Case series |
7 patient |
Last follow-up |
MDT performed at L3–S1, L3–S4, and C5–T1 levels based on patient's spasticity pattern |
Significant improvement in Ashworth grade (from 3.14 to 0.29). Improvement in care tasks (physiotherapy, hygiene, etc.) |
DREZ lesioning (DREZotomy) |
Mongardi et al[23] |
Level 2 |
Systematic review |
1,242 patients |
Medium to long term |
DREZotomy for chronic pain in conditions like brachial plexus avulsion, spinal cord injury, etc. |
Good outcomes in brachial plexus avulsion and spinal cord injury. Lower success in phantom limb pain and post-herpetic neuralgia |
DREZ lesioning (microsurgical vs. radiofrequency assisted) |
Shekouhi et al[24] |
Level 1 |
Systematic review |
917 patients |
Variable across studies |
Comparison between microsurgical DREZotomy (MDT) and radiofrequency-assisted DREZ lesioning (RF) for pain management in BPA |
MDT results in better VAS score improvements and lower rates of motor deficits compared to RF-assisted DREZ lesioning |
Percutaneous thermal radiofrequency rhizotomy |
Shapkin et al[25] |
Level 4 |
Case series |
26 pediatric patients |
Long term |
Thermal RF rhizotomy at L2–S1 levels at 70°C for 90 s |
Significant reduction in spasticity (MAS score: from 3.0 ± 0.2 to 1.14 ± 0.15 |
rTMS, AOT, combined intervention |
Fan et al[26] |
Level 1 |
RCT |
64 children with SCP |
12 wk |
Conventional, rTMS, AOT, combined rTMS + AOT |
Combined rTMS + AOT showed the highest improvement in gross motor function, compared to conventional, rTMS, and AOT |
Thermal radiofrequency for musculocutaneous nerve |
Otero-Villaverde et al[27] |
Level 4 |
Case series |
12 patients |
6 mo |
Ultrasound-guided thermal radiofrequency at 80°C for 90 s to musculocutaneous nerve |
Improvements in spasticity |
Ultrasound-guided alcohol neurolysis |
Lee et al[28] |
Level 4 |
Case series |
10 patients |
2 mo |
Ultrasound-guided alcohol neurolysis at 35% concentration to musculocutaneous nerve |
Musculocutaneous nerve to relieve elbow spasticity in hemiparetic stroke patients |
SPN |
Sindou et al[29] |
Level 4 |
Case series |
20 patients approx. |
1–3 y |
SPN on various nerves affecting spastic muscles, including obturator nerve, hamstring, tibial, and femoral nerves |
Effective in reducing spasticity and improving motor function in children with focal spasticity. Positive outcomes in most cases |
Peripheral neurotomy for spasticity |
Decq et al[30] |
Level 4 |
Case series |
277 patients 392 neurotomies |
Not mentioned |
Peripheral neurotomy on posterior tibial nerve collateral branches for spastic foo |
Improvement ankle and improved angular variations during stance |
Hyperselective peripheral neurotomy |
Bajaj et al[31] |
Level 4 |
Case series |
21 patients |
6 mo |
Selective resection of ∼70% of terminal nerve branches of spastic muscles using neuromonitoring; tendon release in cases with contractures |
MAS score reduced to ≤2 in all patients; significant pain reduction (VAS ↓); no major motor deficits; minor complications like transient neuropathic pain in some cases |
Hyperselective tibial neurotomy for SEF |
Bajaj et al[32] |
Level 5 |
Case report |
1 patient |
6 mo |
Hyperselective tibial neurotomy |
Correction of deformities, abolition of clonus, improvement in spasticity (Modified Ashworth score decreased from 4 to 1) |
Selective motor fasciculotomy (musculocutaneous, median, ulnar nerves) |
Puligopu et al[33] |
Level 4 |
Case series |
20 patients |
Not specified |
Selective motor fasciculotomy on musculocutaneous, median, and ulnar nerves for upper limb spasticity |
Significant reduction in spasticity, improvement in selective voluntary control, hand functions (grasp), and self-care (Wee FIM) without complications or recurrence of spasticity |
Surgical management of shoulder and elbow in spasticity |
Landi et al[34] |
Level 4 |
Case series |
138 (50 shoulder/elbow surgeries |
Varies |
Shoulder/elbow deformity surgery (e.g., tendon release, muscle rebalancing) |
Improvement in shoulder stability, range of motion, and reduction in hypertonus/spasticity in most patients, with a mean FIM score improvement |
SPN |
Sitthinamsuwan et al[35] |
Level 4 |
Case series |
33 patients and 141 SPN |
Short to medium term |
SPN for severe intractable focal and multifocal spastic hypertonia |
SPN reduced spasticity (MAS: 3.0 to 0.7, p < 0.001) and improved PROM (78.3° to 102.3°, p < 0.001). Ten ambulatory patients showed gait improvement, and nine bed-bound patients had better sitting and mobility |
Combined SPN (cSPN) |
Liu et al[37] |
Level 4 |
Case series |
14 patients |
Not specified |
cSPN for severe lower limb spasticity in SCI patients |
Significant reduction in spasm, improved gait, and enhanced motor function |
Tibial nerve neurotomy |
Rousseaux et al[38] |
Level 4 |
Case series |
51 patients |
3 mo to 2 y |
Partial resection of tibial nerve motor branches in patients with lower limb deformity |
Reduced spasticity, improved motor control, balance, gait; sensory disorders in some cases |
Selective tibial neurotomy for spastic equinovarus foot |
Deltombe et al[39] |
Level 4 |
Case series |
30 patients |
2 y |
Selective neurotomy at motor nerve branches of the tibial nerve for spastic equinovarus foot |
Reduced spasticity, improved gait speed, lasting effect with no muscle weakness |
Selective neurotomy for focal lower limb spasticity |
Ploegmakers et al[40] |
Level 2 |
Systematic review |
Total: 26 studies Non-RCT (25) RCT (1) |
Variable |
Selective neurotomy for lower limb spasticity |
Improved muscle tone, pain, ankle motion, and walking speed; more evidence needed through controlled trials |
ITB for spinal cord injury with neurofibromatosis |
O'Brien et al[41] |
Level 5 |
Case report |
1 |
6 wk |
Intrathecal baclofen pump implantation after trial |
Improved spasticity (MAS 1-2/4), independence in transfers and ADLs, minimal support needed post-rehabilitation |
SPN for upper limb spasticity |
Maarrawi et al[42] |
Level 4 |
Case series |
31 patients |
4.5 y |
Selective peripheral neurotomy on musculocutaneous, median, and ulnar nerves |
Improved spasticity, hand function, daily activities. 61.5% satisfaction. Low complication rate (15%) |
ITB therapy |
Schiess et al[43] |
Level 4 |
Case series |
1,743 patients |
Long-term |
Baclofen delivered intrathecally via pump |
Reduction in severe spasticity, improved quality of life |
ITB for spinal origin spasticity |
Ochs et al[44] |
Level 4 |
Case series |
Long-term |
ITB therapy for spinal cord injury, spinal cord disease, and MS-related spasticity |
Reduced spasticity, better functional outcomes |
|
ITB |
Cozzi et al[45] |
Level 1 |
Systematic review |
17 studies |
12 mo |
ITB pump implantation for MSRS |
Significant reduction in spasm frequency, improved quality of life, and few complications |
ITB |
Masrour et al[46] |
Level 1 |
Systematic review |
501 implantations |
12 mo |
ITB therapy for spasticity in cerebral palsy patients |
40.25% reduction in spasticity, minor motor function improvement (9.62%), some complications like seizures and infections |
ITB |
Lee et al[47] |
Level 1 |
Systematic review |
534 patients |
Not specified |
ITB therapy in ambulatory patients with spasticity |
No loss of ambulatory function, improvements in gait speed and spasticity |
ITB |
Creamer et al[48] |
Level 1 |
RCT |
60 patients |
6 mo |
➢ITB vs. conventional medical management |
ITB significantly reduced spasticity compared to CMM, with more adverse events in ITB group |
Baclofen vs. TENS for spasticity in MS |
Shaygannejad et al[49] |
Level 1 |
RCT |
52 patients |
4 wk |
Baclofen vs. TENS |
Both baclofen and TENS significantly reduced spasticity, with TENS showing greater efficacy (p < 0.05) and few side effects compared to baclofen |
ITB |
Plassat et al[50] |
Level 4 |
Case series |
40 patients |
4 y |
ITB pump implantation |
Effective long-term spasticity reduction, patient satisfaction (7.4/10), 37% complication rate (catheter issues, pump malfunctions), 12% severe side effects requiring ICU |
PRISMA-based modified scoping review |
Suputtitada et al[51] |
Grade A |
Systematic review |
14 studies |
2000–2023 |
Stretching exercises, TENS, extracorporeal shock wave therapy, peripheral magnetic stimulation, noninvasive brain stimulation, ITB, whole body vibration, localized muscle vibration |
Effective for improving functional recovery and quality of life in post-stroke spasticity |
SMF of MCN |
Purohit et al[52] |
Level 4 |
Case series |
52 patients |
17 mo |
SMF of MCN for spastic elbows in cerebral palsy |
62.66% elbows achieved total relief of spasticity, improved motor function, no recurrence or side effects |
Abbreviations: ADL, activity of daily living; AOT, action observation training; BPA, brachial plexus avulsion; CP, cerebral palsy; DREZ, dorsal root entry zone; ECW, energy cost of walking; GMFM, gross motor function measure; ITB, intrathecal baclofen; MAS, modified Ashworth score; MCN, musculocutaneous nerve; MDZ, microscissor DREZotomy; MDT, microsurgical DREZotomy; MSRS, multiple sclerosis-related spasticity; OT, occupational therapy; PROM, passive range of motion; PT, physiotherapy; RCT, randomized controlled trial; rTMS, repeated transcranial magnetic stimulation; SDR, selective dorsal rhizotomy; SMC, selective motor control; SMF, Selective musculocutaneous fasciculotomy; SPN, selective peripheral neurotomy; TENS, Transcutaneous Electrical Nerve Stimulation-; TMS, transcranial magnetic stimulation.
Discussion
A systematic review of surgical treatments for spasticity, including SDR, DREZotomy, SPN, and ITB, shows promising results in improving function, reducing pain, and enhancing quality of life for patients with neurological conditions such as stroke, TBI, multiple sclerosis, and CP. SPN, particularly targeting the musculocutaneous, median, ulnar, and tibial nerves, has also demonstrated benefits in reducing spasticity and improving upper and lower limb function, with long-term follow-up revealing significant improvements.[30] [38] [39] [50] A 2013 retrospective study on SPN suggested that more data on long-term outcomes are needed.[35] ITB has demonstrated significant efficacy in treating spasticity associated with multiple sclerosis and SCI.[41] Despite positive outcomes, surgical interventions are associated with risks such as infection, nerve damage, and bleeding, emphasizing the need for expert surgical skills and careful patient selection.[32] Preserving sensory and motor fascicles is crucial to avoid complications such as sensory loss and muscle weakness. Success depends on careful patient selection, precise techniques, and intraoperative monitoring. Postsurgery rehabilitation is essential, and the complexity of the operation, which may require microscope-assisted dissection, can extend its duration. Surgical interventions hold promising potential for better outcomes and quality of life with ongoing innovations.
Future surgical interventions in neurosurgery should focus on integrating advanced neuroimaging techniques and neurophysiological monitoring to ensure precise and patient-specific treatments. This approach will aid in accurately identifying surgical targets and reducing unnecessary tissue damage. Additionally, adopting minimally invasive techniques like robotic-assisted surgeries and laser-guided interventions can enhance surgical outcomes by lowering recovery times and minimizing complications. Emphasis must also be placed on multidisciplinary care by incorporating optimized postsurgical physical and occupational therapy. Longitudinal studies are essential to evaluate the long-term impact of these strategies on patient recovery and overall quality of life.
Conclusion
Surgical treatments for spasticity need to be patient-specific. Most studies show positive results in well-selected patients. More high-quality research is required to establish the efficacy of these interventions.
Conflict of Interest
None declared.
-
References
- 1 Tamburin S, Filippetti M, Mantovani E, Smania N, Picelli A. Spasticity following brain and spinal cord injury: assessment and treatment. Curr Opin Neurol 2022; 35 (06) 728-740
- 2 Sáinz-Pelayo MP, Albu S, Murillo N, Benito-Penalva J. [Spasticity in neurological pathologies. An update on the pathophysiological mechanisms, advances in diagnosis and treatment]. Rev Neurol 2020; 70 (12) 453-460
- 3 Makoshi Z, Islam M, McKinney J, Leonard J. Postoperative outcomes and stimulation responses for sectioned nerve roots during selective dorsal rhizotomy in cerebral palsy. Acta Neurochir (Wien) 2024; 166 (01) 308
- 4 Ravera EP, Rozumalski A. Selective dorsal rhizotomy and its effect on muscle force during walking: a comprehensive study. J Biomech 2024; 164: 111968
- 5 Holtz KA, Lipson R, Noonan VK, Kwon BK, Mills PB. Prevalence and effect of problematic spasticity after traumatic spinal cord injury. Arch Phys Med Rehabil 2017; 98 (06) 1132-1138
- 6 Hashemi M, Sturbois-Nachef N, Keenan MA, Winston P. Surgical approaches to upper limb spasticity in adult patients: a literature review. Front Rehabil Sci 2021; 2: 709969
- 7 Merckx L, Poncelet F, De Houwer H. et al. Upper-extremity spasticity and functionality after selective dorsal rhizotomy for cerebral palsy: a systematic review. J Neurosurg Pediatr 2023; 32 (06) 673-685
- 8 Dudley RWR, Parolin M, Gagnon B. et al. Long-term functional benefits of selective dorsal rhizotomy for spastic cerebral palsy. J Neurosurg Pediatr 2013; 12 (02) 142-150
- 9 Abbott R, Johann-Murphy M, Shiminski-Maher T. et al. Selective dorsal rhizotomy: outcome and complications in treating spastic cerebral palsy. Neurosurgery 1993; 33 (05) 851-857 , discussion 857
- 10 Aquilina K, Graham D, Wimalasundera N. Selective dorsal rhizotomy: an old treatment re-emerging. Arch Dis Child 2015; 100 (08) 798-802
- 11 Kakodkar P, Fallah A, Tu A. Systematic review on use and efficacy of selective dorsal rhizotomy (SDR) for the management of spasticity in non-pediatric patients. Childs Nerv Syst 2021; 37 (06) 1837-1847
- 12 Lu VM, Vazquez S, Niazi TN. Postoperative pain management strategies following selective dorsal rhizotomy in pediatric cerebral palsy patients: a systematic review of published regimens. Childs Nerv Syst 2024; 40 (12) 4095-4105
- 13 Wright FV, Sheil EM, Drake JM, Wedge JH, Naumann S. Evaluation of selective dorsal rhizotomy for the reduction of spasticity in cerebral palsy: a randomized controlled trial. Dev Med Child Neurol 1998; 40 (04) 239-247
- 14 Abd-Elmonem AM, Ali HA, Saad-Eldien SS, Rabiee A, Abd El-Nabie WA. Effect of physical training on motor function of ambulant children with diplegia after selective dorsal rhizotomy: a randomized controlled study. NeuroRehabilitation 2023; 53 (04) 547-556
- 15 Davidson B, Schoen N, Sedighim S. et al. Intrathecal baclofen versus selective dorsal rhizotomy for children with cerebral palsy who are nonambulant: a systematic review. J Neurosurg Pediatr 2019; 25 (01) 69-77
- 16 Mishra D, Barik S, Raj V, Kandwal P. A systematic review of complications following selective dorsal rhizotomy in cerebral palsy. Neurochirurgie 2023; 69 (03) 101425
- 17 Khalifeh JM, Lubelski D, Ochuba A, Belzberg AJ. Dorsal root entry zone lesioning for the treatment of pain after brachial plexus avulsion injury: 2-dimensional operative video and technical report. Oper Neurosurg (Hagerstown) 2022; 22 (06) e252-e258
- 18 Ko AL, Ozpinar A, Raskin JS, Magill ST, Raslan AM, Burchiel KJ. Correlation of preoperative MRI with the long-term outcomes of dorsal root entry zone lesioning for brachial plexus avulsion pain. J Neurosurg 2016; 124 (05) 1470-1478
- 19 Doddamani RS, Garg S, Agrawal D. et al. Microscissor DREZotomy for post brachial plexus avulsion neuralgia: A single center experience. Clin Neurol Neurosurg 2021; 208: 106840
- 20 Sindou M, Georgoulis G. Focal dystonia in hemiplegic upper limb: favorable effect of cervical microsurgical DREZotomy involving the ventral horn - a report of 3 patients. Stereotact Funct Neurosurg 2016; 94 (03) 140-146
- 21 Villegas-López FA, Armas-Salazar A, Beltrán JQ. et al. A case of dentatotomy for pain and spasticity and systematic review. Stereotact Funct Neurosurg 2021; 99 (06) 521-525
- 22 Goyal N, Arora S, Kulshreshtha P, Gupta P. Microsurgical DREZotomy in spastic cerebral palsy: poor man's Baclofen pump. World Neurosurg 2021; 149: e170-e177
- 23 Mongardi L, Visani J, Mantovani G. et al. Long term results of dorsal root entry zone (DREZ) lesions for the treatment of intractable pain: a systematic review of the literature on 1242 cases. Clin Neurol Neurosurg 2021; 210: 107004
- 24 Shekouhi R, Chen X, Taylor J, Marji FP, Chim H. The safety and efficacy of dorsal root entry zone lesioning for pain management in patients with brachial plexus avulsion: a systematic review and meta-analysis. Neurosurgery 2024; 95 (02) 259-274
- 25 Shapkin AG, Iakimov I, Sufianov RA, Sufianova GZ, Sufianov AA. Percutaneous thermal radiofrequency rhizotomy of L2-S1 spinal nerve roots in children with cerebral palsy. Neurosurg Focus 2024; 56 (06) E7
- 26 Fan T, Wei H, Dai J, You G, Lu Z. Repeated transcranial magnetic stimulation combined with action observation training in children with spastic cerebral palsy. J Vis Exp 2024; (210)
- 27 Otero-Villaverde S, Formigo-Couceiro J, Martin-Mourelle R, Montoto-Marques A. Safety and effectiveness of thermal radiofrequency applied to the musculocutaneous nerve for patients with spasticity. Front Neurol 2024; 15: 1369947
- 28 Lee DG, Jang SH. Ultrasound guided alcohol neurolysis of musculocutaneous nerve to relieve elbow spasticity in hemiparetic stroke patients. NeuroRehabilitation 2012; 31 (04) 373-377
- 29 Sindou MP, Simon F, Mertens P, Decq P. Selective peripheral neurotomy (SPN) for spasticity in childhood. Childs Nerv Syst 2007; 23 (09) 957-970
- 30 Decq P, Cuny E, Filipetti P, Fève A, Kéravel Y. [Peripheral neurotomy in the treatment of spasticity. Indications, techniques and results in the lower limbs]. Neurochirurgie 1998; 44 (03) 175-182
- 31 Bajaj J, Khandelwal N, Jain A. et al. Hyperselective peripheral neurotomy for spasticity: a prospective observational study. Journal of Peripheral Nerve Surgery 2024 8. 01
- 32 Bajaj J, Verma S, Chaudhary V. et al. Hyperselective tibial neurotomy for relieving spasticity and restoring motor functions. Neurol India 2023; 71 (06) 1142-1145
- 33 Puligopu AK, Purohit AK. Outcome of selective motor fasciculotomy in the treatment of upper limb spasticity. J Pediatr Neurosci 2011; 6 (Suppl. 01) S118-S125
- 34 Landi A, Cavazza S, Caserta G. et al. The upper limb in cerebral palsy: surgical management of shoulder and elbow deformities. Hand Clin 2003; 19 (04) 631-648 , vii
- 35 Sitthinamsuwan B, Chanvanitkulchai K, Phonwijit L, Nunta-Aree S, Kumthornthip W, Ploypetch T. Surgical outcomes of microsurgical selective peripheral neurotomy for intractable limb spasticity. Stereotact Funct Neurosurg 2013; 91 (04) 248-257
- 36 Israel J, Fahrenkopf M, Rhee PC. Management of the spastic elbow deformity in adult patients with upper motor neuron syndrome. J Hand Surg Am 2024; 49 (10) 1044.e1-1044.e11
- 37 Liu H, Fan L, Li J. et al. Combined selective peripheral neurotomy in the treatment of spastic lower limbs of spinal cord injury patients. Acta Neurochir (Wien) 2022; 164 (08) 2263-2269
- 38 Rousseaux M, Buisset N, Daveluy W, Kozlowski O, Blond S. Long-term effect of tibial nerve neurotomy in stroke patients with lower limb spasticity. J Neurol Sci 2009; 278 (1-2): 71-76
- 39 Deltombe T, Gustin T. Selective tibial neurotomy in the treatment of spastic equinovarus foot in hemiplegic patients: a 2-year longitudinal follow-up of 30 cases. Arch Phys Med Rehabil 2010; 91 (07) 1025-1030
- 40 Ploegmakers DJM, Van Duijnhoven HJR, Duraku LS, Kurt E, Geurts ACH, De Jong T. Efficacy of selective neurotomy for focal lower limb spasticity: a systematic review. J Rehabil Med 2024; 56: jrm39947
- 41 O'Brien C, Stowe J, O'Connor M. et al. Intrathecal baclofen for neurofibromatosis related spinal cord injury with spasticity - a case report. J Rehabil Med Clin Commun 2024; 7: 25912
- 42 Maarrawi J, Mertens P, Luaute J. et al. Long-term functional results of selective peripheral neurotomy for the treatment of spastic upper limb: prospective study in 31 patients. J Neurosurg 2006; 104 (02) 215-225
- 43 Schiess MC, Eldabe S, Konrad P. et al. Intrathecal baclofen for severe spasticity: longitudinal data from the Product Surveillance Registry. Neuromodulation 2020; 23 (07) 996-1002
- 44 Ochs G, Naumann C, Dimitrijevic M, Sindou M. Intrathecal baclofen therapy for spinal origin spasticity: spinal cord injury, spinal cord disease, and multiple sclerosis. Neuromodulation 1999; 2 (02) 108-119
- 45 Cozzi FM, Zuckerman D, Sacknovitz A. et al. Outcomes, complications, and dosing of intrathecal baclofen in the treatment of multiple sclerosis: a systematic review. Neurosurg Focus 2024; 56 (06) E14
- 46 Masrour M, Zare A, Presedo A, Nabian MH. Intrathecal baclofen efficacy for managing motor function and spasticity severity in patients with cerebral palsy: a systematic review and meta-analysis. BMC Neurol 2024; 24 (01) 143
- 47 Lee HP, Win T, Balakrishnan S. The impact of intrathecal baclofen on the ability to walk: a systematic review. Clin Rehabil 2023; 37 (04) 462-477
- 48 Creamer M, Cloud G, Kossmehl P. et al. Intrathecal baclofen therapy versus conventional medical management for severe poststroke spasticity: results from a multicentre, randomised, controlled, open-label trial (SISTERS). J Neurol Neurosurg Psychiatry 2018; 89 (06) 642-650
- 49 Shaygannejad V, Janghorbani M, Vaezi A, Haghighi S, Golabchi K, Heshmatipour M. Comparison of the effect of baclofen and transcutaneous electrical nerve stimulation for the treatment of spasticity in multiple sclerosis. Neurol Res 2013; 35 (06) 636-641
- 50 Plassat R, Perrouin Verbe B, Menei P, Menegalli D, Mathé JF, Richard I. Treatment of spasticity with intrathecal Baclofen administration: long-term follow-up, review of 40 patients. Spinal Cord 2004; 42 (12) 686-693
- 51 Suputtitada A, Chatromyen S, Chen CP, Simpson DM. Best practice guidelines for the management of patients with post-stroke spasticity: A modified scoping review. Toxins 2024; 16 (02) 98
- 52 Purohit AK, Raju BS, Kumar KS, Mallikarjun KD. Selective musculocutaneous fasciculotomy for spastic elbow in cerebral palsy: a preliminary study. Acta Neurochir (Wien) 1998; 140 (05) 473-478
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Article published online:
09 July 2025
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References
- 1 Tamburin S, Filippetti M, Mantovani E, Smania N, Picelli A. Spasticity following brain and spinal cord injury: assessment and treatment. Curr Opin Neurol 2022; 35 (06) 728-740
- 2 Sáinz-Pelayo MP, Albu S, Murillo N, Benito-Penalva J. [Spasticity in neurological pathologies. An update on the pathophysiological mechanisms, advances in diagnosis and treatment]. Rev Neurol 2020; 70 (12) 453-460
- 3 Makoshi Z, Islam M, McKinney J, Leonard J. Postoperative outcomes and stimulation responses for sectioned nerve roots during selective dorsal rhizotomy in cerebral palsy. Acta Neurochir (Wien) 2024; 166 (01) 308
- 4 Ravera EP, Rozumalski A. Selective dorsal rhizotomy and its effect on muscle force during walking: a comprehensive study. J Biomech 2024; 164: 111968
- 5 Holtz KA, Lipson R, Noonan VK, Kwon BK, Mills PB. Prevalence and effect of problematic spasticity after traumatic spinal cord injury. Arch Phys Med Rehabil 2017; 98 (06) 1132-1138
- 6 Hashemi M, Sturbois-Nachef N, Keenan MA, Winston P. Surgical approaches to upper limb spasticity in adult patients: a literature review. Front Rehabil Sci 2021; 2: 709969
- 7 Merckx L, Poncelet F, De Houwer H. et al. Upper-extremity spasticity and functionality after selective dorsal rhizotomy for cerebral palsy: a systematic review. J Neurosurg Pediatr 2023; 32 (06) 673-685
- 8 Dudley RWR, Parolin M, Gagnon B. et al. Long-term functional benefits of selective dorsal rhizotomy for spastic cerebral palsy. J Neurosurg Pediatr 2013; 12 (02) 142-150
- 9 Abbott R, Johann-Murphy M, Shiminski-Maher T. et al. Selective dorsal rhizotomy: outcome and complications in treating spastic cerebral palsy. Neurosurgery 1993; 33 (05) 851-857 , discussion 857
- 10 Aquilina K, Graham D, Wimalasundera N. Selective dorsal rhizotomy: an old treatment re-emerging. Arch Dis Child 2015; 100 (08) 798-802
- 11 Kakodkar P, Fallah A, Tu A. Systematic review on use and efficacy of selective dorsal rhizotomy (SDR) for the management of spasticity in non-pediatric patients. Childs Nerv Syst 2021; 37 (06) 1837-1847
- 12 Lu VM, Vazquez S, Niazi TN. Postoperative pain management strategies following selective dorsal rhizotomy in pediatric cerebral palsy patients: a systematic review of published regimens. Childs Nerv Syst 2024; 40 (12) 4095-4105
- 13 Wright FV, Sheil EM, Drake JM, Wedge JH, Naumann S. Evaluation of selective dorsal rhizotomy for the reduction of spasticity in cerebral palsy: a randomized controlled trial. Dev Med Child Neurol 1998; 40 (04) 239-247
- 14 Abd-Elmonem AM, Ali HA, Saad-Eldien SS, Rabiee A, Abd El-Nabie WA. Effect of physical training on motor function of ambulant children with diplegia after selective dorsal rhizotomy: a randomized controlled study. NeuroRehabilitation 2023; 53 (04) 547-556
- 15 Davidson B, Schoen N, Sedighim S. et al. Intrathecal baclofen versus selective dorsal rhizotomy for children with cerebral palsy who are nonambulant: a systematic review. J Neurosurg Pediatr 2019; 25 (01) 69-77
- 16 Mishra D, Barik S, Raj V, Kandwal P. A systematic review of complications following selective dorsal rhizotomy in cerebral palsy. Neurochirurgie 2023; 69 (03) 101425
- 17 Khalifeh JM, Lubelski D, Ochuba A, Belzberg AJ. Dorsal root entry zone lesioning for the treatment of pain after brachial plexus avulsion injury: 2-dimensional operative video and technical report. Oper Neurosurg (Hagerstown) 2022; 22 (06) e252-e258
- 18 Ko AL, Ozpinar A, Raskin JS, Magill ST, Raslan AM, Burchiel KJ. Correlation of preoperative MRI with the long-term outcomes of dorsal root entry zone lesioning for brachial plexus avulsion pain. J Neurosurg 2016; 124 (05) 1470-1478
- 19 Doddamani RS, Garg S, Agrawal D. et al. Microscissor DREZotomy for post brachial plexus avulsion neuralgia: A single center experience. Clin Neurol Neurosurg 2021; 208: 106840
- 20 Sindou M, Georgoulis G. Focal dystonia in hemiplegic upper limb: favorable effect of cervical microsurgical DREZotomy involving the ventral horn - a report of 3 patients. Stereotact Funct Neurosurg 2016; 94 (03) 140-146
- 21 Villegas-López FA, Armas-Salazar A, Beltrán JQ. et al. A case of dentatotomy for pain and spasticity and systematic review. Stereotact Funct Neurosurg 2021; 99 (06) 521-525
- 22 Goyal N, Arora S, Kulshreshtha P, Gupta P. Microsurgical DREZotomy in spastic cerebral palsy: poor man's Baclofen pump. World Neurosurg 2021; 149: e170-e177
- 23 Mongardi L, Visani J, Mantovani G. et al. Long term results of dorsal root entry zone (DREZ) lesions for the treatment of intractable pain: a systematic review of the literature on 1242 cases. Clin Neurol Neurosurg 2021; 210: 107004
- 24 Shekouhi R, Chen X, Taylor J, Marji FP, Chim H. The safety and efficacy of dorsal root entry zone lesioning for pain management in patients with brachial plexus avulsion: a systematic review and meta-analysis. Neurosurgery 2024; 95 (02) 259-274
- 25 Shapkin AG, Iakimov I, Sufianov RA, Sufianova GZ, Sufianov AA. Percutaneous thermal radiofrequency rhizotomy of L2-S1 spinal nerve roots in children with cerebral palsy. Neurosurg Focus 2024; 56 (06) E7
- 26 Fan T, Wei H, Dai J, You G, Lu Z. Repeated transcranial magnetic stimulation combined with action observation training in children with spastic cerebral palsy. J Vis Exp 2024; (210)
- 27 Otero-Villaverde S, Formigo-Couceiro J, Martin-Mourelle R, Montoto-Marques A. Safety and effectiveness of thermal radiofrequency applied to the musculocutaneous nerve for patients with spasticity. Front Neurol 2024; 15: 1369947
- 28 Lee DG, Jang SH. Ultrasound guided alcohol neurolysis of musculocutaneous nerve to relieve elbow spasticity in hemiparetic stroke patients. NeuroRehabilitation 2012; 31 (04) 373-377
- 29 Sindou MP, Simon F, Mertens P, Decq P. Selective peripheral neurotomy (SPN) for spasticity in childhood. Childs Nerv Syst 2007; 23 (09) 957-970
- 30 Decq P, Cuny E, Filipetti P, Fève A, Kéravel Y. [Peripheral neurotomy in the treatment of spasticity. Indications, techniques and results in the lower limbs]. Neurochirurgie 1998; 44 (03) 175-182
- 31 Bajaj J, Khandelwal N, Jain A. et al. Hyperselective peripheral neurotomy for spasticity: a prospective observational study. Journal of Peripheral Nerve Surgery 2024 8. 01
- 32 Bajaj J, Verma S, Chaudhary V. et al. Hyperselective tibial neurotomy for relieving spasticity and restoring motor functions. Neurol India 2023; 71 (06) 1142-1145
- 33 Puligopu AK, Purohit AK. Outcome of selective motor fasciculotomy in the treatment of upper limb spasticity. J Pediatr Neurosci 2011; 6 (Suppl. 01) S118-S125
- 34 Landi A, Cavazza S, Caserta G. et al. The upper limb in cerebral palsy: surgical management of shoulder and elbow deformities. Hand Clin 2003; 19 (04) 631-648 , vii
- 35 Sitthinamsuwan B, Chanvanitkulchai K, Phonwijit L, Nunta-Aree S, Kumthornthip W, Ploypetch T. Surgical outcomes of microsurgical selective peripheral neurotomy for intractable limb spasticity. Stereotact Funct Neurosurg 2013; 91 (04) 248-257
- 36 Israel J, Fahrenkopf M, Rhee PC. Management of the spastic elbow deformity in adult patients with upper motor neuron syndrome. J Hand Surg Am 2024; 49 (10) 1044.e1-1044.e11
- 37 Liu H, Fan L, Li J. et al. Combined selective peripheral neurotomy in the treatment of spastic lower limbs of spinal cord injury patients. Acta Neurochir (Wien) 2022; 164 (08) 2263-2269
- 38 Rousseaux M, Buisset N, Daveluy W, Kozlowski O, Blond S. Long-term effect of tibial nerve neurotomy in stroke patients with lower limb spasticity. J Neurol Sci 2009; 278 (1-2): 71-76
- 39 Deltombe T, Gustin T. Selective tibial neurotomy in the treatment of spastic equinovarus foot in hemiplegic patients: a 2-year longitudinal follow-up of 30 cases. Arch Phys Med Rehabil 2010; 91 (07) 1025-1030
- 40 Ploegmakers DJM, Van Duijnhoven HJR, Duraku LS, Kurt E, Geurts ACH, De Jong T. Efficacy of selective neurotomy for focal lower limb spasticity: a systematic review. J Rehabil Med 2024; 56: jrm39947
- 41 O'Brien C, Stowe J, O'Connor M. et al. Intrathecal baclofen for neurofibromatosis related spinal cord injury with spasticity - a case report. J Rehabil Med Clin Commun 2024; 7: 25912
- 42 Maarrawi J, Mertens P, Luaute J. et al. Long-term functional results of selective peripheral neurotomy for the treatment of spastic upper limb: prospective study in 31 patients. J Neurosurg 2006; 104 (02) 215-225
- 43 Schiess MC, Eldabe S, Konrad P. et al. Intrathecal baclofen for severe spasticity: longitudinal data from the Product Surveillance Registry. Neuromodulation 2020; 23 (07) 996-1002
- 44 Ochs G, Naumann C, Dimitrijevic M, Sindou M. Intrathecal baclofen therapy for spinal origin spasticity: spinal cord injury, spinal cord disease, and multiple sclerosis. Neuromodulation 1999; 2 (02) 108-119
- 45 Cozzi FM, Zuckerman D, Sacknovitz A. et al. Outcomes, complications, and dosing of intrathecal baclofen in the treatment of multiple sclerosis: a systematic review. Neurosurg Focus 2024; 56 (06) E14
- 46 Masrour M, Zare A, Presedo A, Nabian MH. Intrathecal baclofen efficacy for managing motor function and spasticity severity in patients with cerebral palsy: a systematic review and meta-analysis. BMC Neurol 2024; 24 (01) 143
- 47 Lee HP, Win T, Balakrishnan S. The impact of intrathecal baclofen on the ability to walk: a systematic review. Clin Rehabil 2023; 37 (04) 462-477
- 48 Creamer M, Cloud G, Kossmehl P. et al. Intrathecal baclofen therapy versus conventional medical management for severe poststroke spasticity: results from a multicentre, randomised, controlled, open-label trial (SISTERS). J Neurol Neurosurg Psychiatry 2018; 89 (06) 642-650
- 49 Shaygannejad V, Janghorbani M, Vaezi A, Haghighi S, Golabchi K, Heshmatipour M. Comparison of the effect of baclofen and transcutaneous electrical nerve stimulation for the treatment of spasticity in multiple sclerosis. Neurol Res 2013; 35 (06) 636-641
- 50 Plassat R, Perrouin Verbe B, Menei P, Menegalli D, Mathé JF, Richard I. Treatment of spasticity with intrathecal Baclofen administration: long-term follow-up, review of 40 patients. Spinal Cord 2004; 42 (12) 686-693
- 51 Suputtitada A, Chatromyen S, Chen CP, Simpson DM. Best practice guidelines for the management of patients with post-stroke spasticity: A modified scoping review. Toxins 2024; 16 (02) 98
- 52 Purohit AK, Raju BS, Kumar KS, Mallikarjun KD. Selective musculocutaneous fasciculotomy for spastic elbow in cerebral palsy: a preliminary study. Acta Neurochir (Wien) 1998; 140 (05) 473-478

