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Review  |  Open Access  |  27 Sep 2022

A review of pain outcomes following targeted muscle reinnervation in lower extremity limb pain

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Plast Aesthet Res 2022;9:55.
10.20517/2347-9264.2022.47 |  © The Author(s) 2022.
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Abstract

Approximately 75% experience phantom (PLP), residual (RLP), or general (GLP) limb pain following lower extremity amputation. Targeted muscle reinnervation (TMR) is a peripheral nerve transfer that reroutes amputated nerves to motor endplates that can prevent or treat limb pain. This systematic review summarizes pain outcomes following primary and secondary treatment of lower extremity PLP, RLP, and GLP. Primary literature review of three databases - PubMed, EMBASE, MEDLINE - were used for all articles related to TMR and lower extremity limb pain, querying the same keywords: “targeted muscle reinnervation” AND “pain”. Citations were then reviewed and eliminated if only upper extremities were studied or the study lacked pain outcomes. Citations were categorized as primary or secondary TMR. Pain outcomes, including Numerical Rating Scales (NRS) and Patient-Reported Outcome Measurement Information System (PROMIS) Pain scores, were aggregated when appropriate. Ten studies met all inclusion and exclusion criteria after formal review for a total of 431 extremities, of which 79.1% (n = 341 limbs) were lower extremities. Average primary TMR PROMIS scores for PLP and RLP were lower than amputees without primary TMR. Average NRS scores and PROMIS Pain scores in secondary TMR demonstrated improvements in PLP, RLP, and GLP. Primary and Secondary TMR does prevent and improve PLP, RLP, and GLP; however, a minority of studies report quantifiable pain outcomes. All future TMR studies should include validated pain outcomes to better quantify the expected pain and quality of life improvements after lower extremity TMR.

Keywords

Lower extremity, amputation, phantom limb pain, residual limb pain, targeted muscle reinnervation, nerve transfer

INTRODUCTION

Chronic neurogenic pain is a common sequela of lower extremity injury and a complication that can be difficult to manage despite multimodal therapy. And with over one million lower extremity amputations performed globally annually, post-amputation pain represents a significant burden to both patients and providers[1]. Post-amputation pain, which has been reported in up to 95% of amputees, typically includes both residual limb pain as well as phantom limb pain[2,3]. Residual limb pain (RLP) is defined as pain localized to the remaining limb after amputation and is felt to be mediated by neuroma formation in a typical post-surgical pathway[3]. Phantom limb pain (PLP) is characterized by painful sensations in the lost body part and can be either nociceptive or neuropathic in nature[3,4]. While these two types of pain are distinct clinical entities, there does appear to be a significant correlation between residual limb pain and phantom limb pain[5].

Although both surgical and non-surgical treatment modalities have been trialed for post-amputation pain, the surgical procedure of targeted muscle reinnervation (TMR) has gained traction as an effective and reproducible tool in relieving both types of post-amputation pain[6-8]. TMR was originally conceptualized as a technique to power myoelectric upper extremity prostheses and serendipitously found to be effective in relieving amputee pain[1,9,10]. After early, promising data using this technique, a subsequent meta-analysis of retrospective data and randomized control trials have demonstrated significant reductions in phantom limb pain and residual limb when TMR is performed either in a primary or secondary fashion[1,8].

This study is a systematic review of primary data on patient-reported outcomes following primary and secondary TMR for the treatment of residual limb pain. We specifically focus on TMR of the lower extremities for treatment of residual limb pain, as lower extremity myoelectric prosthetic use is limited, unlike indications for upper extremity TMR.

METHODS

A literature search for all studies that met inclusion criteria were evaluated for the specific outcome tools used to assess improvement in pain following TMR. Studies using the same outcome tool were summarily aggregated to quantify the degree of improvement in lower extremity PLP and RLP following TMR. For this review, a meta-analysis was not applicable due to possible heterogeneity including mechanism of limb injury, time to treatment, length of follow-up, variability in nerve transfer techniques, and type of outcome measures. Therefore, descriptive statistics have been employed to represent the data to provide a general update on the use and effectiveness of this technique. The PRISMA checklist was followed throughout this study’s design and execution[11].

Literature search

A literature review of English-language publications was performed from January 1997 to April 2022 using MEDLINE, EMBASE, and PubMed databases to identify publications related to targeted muscle reinnervation and limb pain. All three databases were queried using the same keywords: “targeted muscle reinnervation” AND “pain”. Abstracts were reviewed in each of the database queries and duplicates were eliminated. Next, abstracts and titles were reviewed using the inclusion and exclusion criteria. Finally, one reviewer conducted a formal review of the remaining full-text articles, specifically looking for demographic information, clinical information, techniques used, and pain outcome tools.

Inclusion and exclusion criteria

Inclusion criteria are included in Table 1. In summary, we identified original English language articles studying targeted muscle reinnervation as a primary or secondary treatment for lower extremity PLP, RLP and general limb pain (GLP). After initial review, several studies that met our inclusion criteria had combined analysis of upper and lower extremity TMR and the lower extremity data pool was extracted for final analysis. Studies were categorized based on the timing of surgical intervention, either primary or secondary.

Table 1

Inclusion criteria for review of the literature for targeted muscle reinnervation in the treatment of lower extremity limb pain

Literature typeOriginal article with primary data
Human subjects
English language publication
TreatmentTargeted muscle reinnervation
Primary treatment
Secondary treatment
Indication*Lower extremity pain
Phantom limb pain
Residual limb pain
General limb pain
Type of nerve injuryAmputation
Iatrogenic injury
Report of pain outcomeNumerical rating system
PROMIS
Visual analog scale
Incidence of limb pain

Articles were excluded if they reported on one of the following: (1) Focus on TMR for myoelectric prosthetic control; (2) upper extremity TMR only; (3) evaluation of outcomes in regenerative peripheral nerve interfaces for the treatment of limb pain; (4) single case reports; (5) systematic reviews, technique reviews, or anatomical studies; and (6) failure to include patient-reported outcome data. Upper extremity studies were excluded as our team was specifically interested in lower extremity outcomes, as TMR in the upper extremity is most often used for myoelectric prosthetic control. By excluding upper extremity TMR studies, we were able to isolate our study to those primarily studying pain as the indication for surgery and exclude studies that secondarily studied pain as a result of TMR for myoelectric prosthetic control.

Data extraction and statistical analysis

After a formal review of all relevant articles, one reviewer obtained data including patient demographics, clinical and procedural characteristics, and pain outcomes including Patient-Reported Outcome Measurement Information System (PROMIS) scores, numerical rating scale (NRS) scores, and incidence of limb pain. Pain outcomes data was aggregated when appropriate and summarized for analysis.

PROMIS scores for pain behavior, pain intensity and pain interference instruments were reported in the studies included in this review. PROMIS scores for each instrument can be reported in two ways - raw summary score or T-score. PROMIS raw scores are rescaled into standardized T-scores where a score of 50 is the mean of a relevant reference population and 10 is the standard deviation of that reference population[12]. T-scores facilitate comparisons between scales with different lengths and allow for standardization relevant to population norms. A higher T-score represents higher pain interference. Studies that reported PROMIS raw scores were converted to T-scores using corresponding scoring guides for the various instruments[13]. Changes in PROMIS scores, when reported, were also converted to changes in T-scores.

Statistical analyses of quantifiable measures of pain were summarized with weight averages considering the number of patients and the reported mean score (PROMIS, NRS, or VAS). Outcomes reported as medians were treated as means to simplify the aggregation across studies. Standard deviations for pain outcomes were not calculated given this assumption, as outcomes reported as medians lacked standard deviations. No adjustments were made for studies that combined upper and lower extremity outcomes in their results. When studies did report separate outcomes for upper and lower extremities, only lower extremity outcomes were included in our analysis. The analysis of indications for TMR was a summation of the number of extremities operated on rather than the number of patients. When possible, upper extremities were excluded from this analysis. Incidences of PLP, RLP and GLP were simply totaled. All statistical analyses were performed in Microsoft Excel version 16.6 (Microsoft Corporation, Redmond, WA, USA).

RESULTS

Study retrieval and characteristics

This review started with 299 citations identified across three databases. A flow diagram is included in Figure 1, demonstrating the study’s inclusion and exclusion criteria. After eliminating all duplicate citations across the databases and initial review of titles and abstracts, 16 citations were thoroughly reviewed.

A review of pain outcomes following targeted muscle reinnervation in lower extremity limb pain

Figure 1. Flowchart of database search and references retrieved and excluded from review.

The final tally included ten studies with primary data evaluating pain outcomes following TMR for a total of 414 patients. Only two studies (174 patients) evaluated outcomes in lower extremity TMR exclusively, with eight studies (240 patients) combining upper and lower extremity TMR outcomes. Nine of the studies were conducted in the United States and one in the United Kingdom. Two studies were prospective in nature, one of which was a randomized control trial, and eight were retrospective cohort studies. Four studies exclusively reported outcomes in secondary TMR for the treatment of pain, four other studies reported outcomes in primary TMR, and two studies reported outcomes in both primary and secondary TMR.

Although 80% of the studies retrieved combined upper and lower extremity TMR outcomes, we isolated outcomes for lower extremity TMR whenever possible. A total of 431 limbs were included in this review, 341 (79.1%) were lower extremity TMR and 90 (20.9%) were upper extremity TMR. Of note, one study specifically evaluated TMR in the treatment of neuroma pain in nonamputees[14]. All other studies reported TMR outcomes in the setting of extremity amputation. A summary of all studies is included in Tables 2 and 3.

Table 2

Studies and patient demographics, targeted muscle reinnervation for primary treatment of limb pain

StudyCountryTotal patientsTotal lower extremitiesAge (yr)% MaleFollow-up (mo)Primary pain outcomeTMR technique
Chang et al., 2021[20]United States1001005970%9.6Incidence of PLP, RLP, GLP after the last follow-upSPN -> EDL
TN -> deep posterior compartment
Hoyt et al., 2021[18]United States742835*81%14*Numerical rating GLPSciatic -> gluteus maximus
Proximal TN -> semimembranosus
CPN -> biceps femoris
Femoral -> quadricep
Distal TN -> soleus or lat. Gastrocnemius
SPN -> EDL or EHL
Sural -> FHL or gastrocnemius
Valerio et al., 2019[15]United States5136n/a**59%11.*Median PROMIS raw scores for RLP, PLP

NRS for RLP, PLP
Nonspecific TMR
Frantz et al., 2020[16]United States252047.560%14.1Median PROMIS raw scores for RLP, PLPTN -> gastrocnemius, soleus, or tibialis posterior
CPN -> tibialis anterior, peroneus longus/brevis, medial soleus
SPN -> peroneus brevis/longus
Saphenous -> medial gastrocnemius, medial soleus
Sural -> lateral gastrocnemius, lateral soleus, tibialis posterior
Pet et al., 2014[19]United States12134.0100%22Incidence of PLP, RLP, GLP after one yearTN -> gastrocnemius, soleus, or tibialis posterior
CPN -> tibialis anterior, peroneus longus/brevis, medial soleus
SPN -> peroneus brevis/longus
Saphenous -> medial gastrocnemius, medial soleus
Sural -> lateral gastrocnemius, lateral soleus, tibialis posterior
Alexander et al., 2019[17]United States312149.466%14.7Mean PROMIS raw scores for RLP, PLPNonspecific TMR
Table 3

Studies and patient demographics, targeted muscle reinnervation for secondary treatment of limb pain

StudyCountryTotal patientsTotal lower extremitiesAge (yr)% MaleFollow-up (mo)Primary pain outcomeTMR technique
Dumanian et al., 2019[21]United States141239.686%17.7Change in mean PROMIS T scores for RLP, PLP

Change in mean NRS scores for worst RLP, PLP
Nonspecific TMR
Mioton et al., 2020[7]United States331442.285%12Change in mean PROMIS T-scores for RLP, PLP

Change in mean NRS scores for worst RLP, PLP
Nonspecific TMR
Kang et al., 2021[22]United Kingdom36294975%19.9Change in mean NRS scores for worst RLP, PLPSciatic -> biceps femoris, semimembranosus, or semitendinosus
CPN -> lateral gastrocnemius
TN -> soleus or medial gastrocnemius
Hoyt et al., 2021[18]United States745935*81%14*Change in numerical pain rating for GLPSciatic -> gluteus maximus
Proximal TN -> semimembranosus
CPN -> biceps femoris
Femoral -> quadricep
Distal TN -> soleus or lat. Gastrocnemius
SPN -> EDL or EHL
Sural -> FHL or gastrocnemius
Chang et al., 2020[14]United States15953.1n/a**22.0Change in numerical pain rating for GLPSPN -> EDL, peroneus brevis, or tibialis anterior
DPN -> EHL
Sural -> medial gastrocnemius or peroneus brevis
Saphenous -> medial gastrocnemius
Pet et al., 2014[19]United States23154452%8.1Incidence of RLP, PLP before and after TMRTN -> semimembranosus or semitendinosus
CPN -> biceps femoris

Indications

Among the 431 upper and lower extremity limbs in this review, we were able to categorize all lower extremities based on the mechanism of injury leading to primary or secondary TMR. Due to the constraints of several studies combining data between upper and lower extremities, 46 upper extremities were included in the aggregation. Therefore, a total of 387 limbs were included in Figure 2. 2.1% of all TMR was performed for nonamputees. The most common indication for amputation was trauma (44.7%), which included military and non-military ballistic injuries as well as motor vehicle collisions. Infection was the second most common indication for amputation (25.1%), followed by oncologic amputation (12.7%).

A review of pain outcomes following targeted muscle reinnervation in lower extremity limb pain

Figure 2. Pie chart of indications for amputation and targeted muscle reinnervation, primary or secondary treatment of pain.

TMR for primary treatment of pain

A total of 206 lower extremity limbs in six studies were treated primarily with TMR to prevent lower extremity pain [Table 2]. Primary TMR was most performed during the time of amputation in the setting of lower extremity infection (42.5%). Oncologic amputation (19.8%) and lower extremity trauma (18.4%) were the next most common indications for primary TMR.

Pain outcomes were variably reported, although all studies reported a decrease in limb pain. Median PROMIS T-scores were used in two studies to quantify pain intensity, behavior and interference for both PLP and RLP at 1-year follow-up (Valerio and Frantz). The average follow-up was 12.6 months between both Valerio et al.[15] and Frantz et al.[16]. Average PLP intensity, behavior, and interference scores were 36.3, 49.6, and 44.0, respectively, and were below the average T-score on the PROMIS scale (mean T-score = 50)[15,16]. Average RLP intensity, behavior, and interference scores were 32.5, 35.8 and 44.0, respectively, and, were below average T-score on the PROMIS scale [Table 4]. Valerio et al. and Alexander et al. compared PROMIS scores between primary TMR patients and control groups of amputees without TMR at 1-year follow-up[15,17]. PLP and RLP scores for intensity, behavior and interference were less in the TMR group in all categories and demonstrated an average difference of > 10 in four categories - PLP interference, RLP intensity, behavior and interference - which equates to a difference of 1 standard deviation on the PROMIS scale [Table 5].

Table 4

Average PROMIS T-Scores for phantom and residual limb pain at the last follow-up after primary targeted muscle reinnervation

PROMIS T-scores for PLPPROMIS T-scores for RLP
StudyFollow-up (mo)PatientsIntensityBehaviorInterferenceIntensityBehaviorInterference
Valerio et al.[15115136.350.140.730.736.740.7
Frantz et al.[16]*14.12536.348.650.736.334.150.7
Average36.349.644.032.535.844.0
Table 5

Average difference in PROMIS T-Scores for phantom and residual limb pain between TMR and non-TMR patients after primary TMR

Difference in PROMIS T-scores for PLPDifference in PROMIS T-scores for RLP
StudyFollow-up (mo)PatientsIntensityBehaviorInterferenceIntensityBehaviorInterference
Valerio et al.[151151-12.1-6.5-15.1-16.1-20.6-16.6
Alexander et al.[17]*14.731-5.85-5.9-7.44-5.48-6.2-6.82
Average-9.7-6.3-12.2-12.1-15.2-12.9

Hoyt et al.[18] and Valerio et al.[15] reported general pain scores and numerical rating scales for PLP and RLP, respectively. Hoyt demonstrated a decrease of 3.2 points in general limb pain when comparing TMR patients from baseline to final follow-up[18]. Valerio reported an average difference in PLP and RLP NRS scores of -4.0 and -3.0, respectively, compared to the non-TMR group[15].

The remaining two studies reported the incidence of PLP and RLP. Pet et al. reported one primary TMR in the lower extremity and the patient reported no PLP or RLP at 1-year follow-up[19]. Chang et al. compared 100 primary TMRs in below-knee amputees to 100 non-TMR amputees and, at 1-year follow-up, reported a significant difference in PLP (19% in TMR vs. 47% in non-TMR) and RLP incidence rates (14% vs. 57%)[20] .

It is important to note that three studies (Valerio, Frantz, and Alexander) reported results that did not distinguish between upper extremity and lower extremity patients. PROMIS T-scores did not solely reflect lower extremity pain, although, between these three studies, only 28.0% (30/107 limbs) of the TMR limbs in these studies were upper extremities[15-17].

TMR for secondary treatment of pain

A total of 138 lower limbs were treated secondarily with TMR in the setting of residual, phantom, and or general limb pain, often following amputation [Table 3]. Secondary TMR for lower extremity residual limb pain, phantom limb pain, and general limb pain was most performed after amputation in the setting of prior lower extremity trauma (73.4%). Amputation for infection was the next most common indication for secondary TMR (7.4%). Another 7.4% of nonamputee patients had TMR in the setting of post-operative neuroma pain.

Five studies reported pain scores with NRS. Mioton et al, Dumanian et al, and Kang et al. comprised 67 patients and reported a mean decrease in PLP and RLP NRS scores of 2.63 and 3.23, respectively, from 1-year follow-up to baseline pain scores[7,21,22]. Hoyt et al. and Chang et al. totaled 89 patients and presented a mean decrease in general pain score of 2.8 points from the last follow-up to baseline[14,18] [Table 6].

Table 6

Average change in the numerical rating of phantom, residual and general limb pain after secondary targeted muscle reinnervation comparing baseline to follow-up pain

StudyFollow-up (mo)PatientsMean change in NRS PLPMean change in NRS RLPMean change in NRS GLP
Dumanian et al.[2117.714-3.2-2.9
Mioton et al.[71233-2.4-2.7
Kang et al.[2219.920-2.6-4.4
Hoyt et al.[18]*1474-2.6
Chang et al.[148.115-3.6
Average-2.6-3.2-2.8

Two studies for a total of 47 patients reported mean changes in PROMIS T-scores between baseline and 1-year follow-up. The average decrease in PLP intensity, behavior and interference T-scores were 8.36, 5.70 and 7.76, respectively. The average decrease in RLP intensity, behavior and interference T-scores were 9.74, 4.21 and 8.37, respectively[7,21] [Table 7].

Table 7

Average change in PROMIS T-score of phantom, residual and general limb pain after secondary targeted muscle reinnervation comparing baseline to follow-up pain

Change in PROMIS T-scores for PLPChange in PROMIS T-scores for RLP
StudyFollow-up (mo)PatientsIntensityBehaviorInterferenceIntensityBehaviorInterference
Dumanian et al.[2117.714-13.7-7.6-9.8-11.5-4.7-7.6
Mioton et al.[7]*1233-6.1-4.9-6.9-9.0-4.0-8.7
Average-8.4-5.7-7.8-9.7-4.2-8.4

In the remaining study, Pet et al, reported incidence of PLP and RLP before TMR and at the last follow-up (mean = 22 months). Incidence of PLP decreased from 26.7% (4/15 patients) to 20% (3/15 patients). Incidence of RLP decreased from 100% (15/15) to 6.67% (1/15)[19].

The studies reporting NRS, VAS, and/or PROMIS scores included some upper extremity TMR patients. Of the five studies, 19.9% (39/196 limbs) of the TMR limbs were upper extremities[7,14,21,22]. The summarized results of Pet et al. excluded all upper extremity TMR patients[19].

DISCUSSION

The incidence of chronic pain following amputation of the lower extremity is nearly universal[2]. In and of itself, this simple conclusion is rather remarkable and stands in stark contrast to the rapid advancements made in limb salvage and restoration over the past 50 years. As awareness of this deficit in our care of amputees has grown, novel solutions including TMR, RPNI, and relocation nerve grafting have emerged. As TMR techniques have developed and become more widely adopted, the body of research has matured from observational to level 1 evidence. This study aims to assess all available evidence in support of TMR for the treatment of PLP and RLP for which pain outcomes are available. Notably, all studies queried reported improvement in pain following TMR for the lower extremity.

Among the limitations of the assessment of TMR as a modality for post-amputation pain is the heterogeneity of pain assessment tools. Tools such as the NRS, Verbal Rating Scales (VRS), Visual Analog Scales (VAS), and the Faces Pain Scale-Revised (FPS-R) are the most common rating scales available; however, these represent one-dimensional, single time point assessments of a complex, multifactorial problem[23,24]. More complex pain assessments like the PROMIS pain behavior, intensity, and interference instruments provide a measurement of well-being or suffering as a result of pain[25,26]. Further, adjuncts or proxy measurements like the Amputee Mobility Predictor (AMP), Prosthetic Evaluation Questionnaire (PEQ), Patient-Specific Functional Scale (PSFS), etc. have been utilized to assess outcomes of amputations and quality of life[27].

PROMIS was created by the National Institutes of Health (NIH) as a tool for the measurement of physical, mental and social health of patients with chronic conditions. Several validated PROMIS surveys were used by the authors, including PROMIS-Pain Intensity, which includes the typical 0-10 pain numerical rating scale, PROMIS-Pain Interference, assessing the degree to which the pain inhibits activities of daily life and mental well-being, and the PROMIS-Behavior, evaluating the effect on pain as it relates to patient movement, affect, and social interactions. These scores can be transformed to T-score distributions with a mean of 50 and a standard deviation of 10, with a lower score reflective of decreased pain. Most PROMIS pain T-scores in the primary TMR studies were found to have a profound decrease of at least one standard deviation when comparing T-scores to the respective study’s control groups[15,17]. Only PROMIS-Behavior for PLP (T-score-6.3) and PROMIS - Intensity for PLP (T-score-9.7) were below the one standard deviation change. Preventive treatment seems to be very beneficial, although there is reporting bias in this comparison as the control patients are surveyed anonymously and neither study is randomized[15,17]. It would be valuable to perform a prospective randomized study comparing pain outcomes in amputees undergoing primary TMR against those who do not. When comparing PROMIS scores to the relevant reference population (mean = 50, SD = 10), Valerio and Frantz et al. demonstrated pain scores lower than the average patient in all PROMIS pain categories for PLP and RLP at final follow-up[15,16]. Thus, if there is reporting bias in the reporting of pain scores by the control groups in Valerio and Alexander et al, we can still comfortably assume primary TMR does help control limb pain after amputation[17].

Improvements in PROMIS T-scores for secondary TMR were more modest, with all score changes within one standard deviation. In fact, in all PROMIS categories for RLP and PLP, the magnitude of benefit derived after primary TMR was greater than that derived after secondary TMR. There are several possible explanations for this finding, including pain chronification. Pain chronification has been explored and is a process that theorizes a mechanism that connects chronic pain to memory. Longitudinal neuroimaging has demonstrated that brain anatomy pertaining to memory, the hippocampus and amygdala changes in patients with chronic pain. This reorganization could explain why secondary TMR benefits for pain could be blunted in comparison to primary TMR[28]. The data from Dumanian et al. and Mioton et al. both suggest that PLP and RLP can still benefit from secondary TMR, even years after amputation, especially compared to conventional neuroma excision and nerve end burying into muscle techniques[7,21]. The median time to TMR after amputation in Dumanian et al. was 5-9 years and 1-4 years in Mioton et al.[7,21].

Pain interference scores had consistently great improvements across RLP and PLP in primary and secondary TMR. In primary TMR, RLP and PLP pain interference scores decreased by more than one standard deviation, and in secondary TMR, those scores approached one standard deviation of change. Pain interference reflects the patient’s engagement with social, cognitive, emotional, physical, and recreational activities. TMR not only can reduce limb pain severity but also enable patients to engage with society with a sense of normalcy, which many patients would argue is more important than intensity improvements alone. Intensity scores, though, also saw consistent improvements across RLP and PLP after primary and secondary TMR. This improvement was also supported by NRS scores in secondary TMR. Surgeons can advise patients with this data that pain and quality of life have the potential for improvement following TMR.

The pain numeric rating scale (NRS), on which patients rate their current pain intensity from 0 (“no pain”) to 10 (“worst possible pain”), has become the most widely used instrument for pain screening. A reduction of 2 points, or 30%, represents a clinically important difference in pain[29]. By this measure, clinically significant improvements in both PLP and RLP were seen, of 2.6 and 3.2, respectively, as well as improvements in general limb pain as documented by two authors, with a reduction of 2.8[7,14,18,21,22]. Although not as precise as the PROMIS questionnaires or reflective of the quality of life effects, NRS scores provide a quantifiable change in pain. Studies should prioritize quantifiable measures of limb pain rather than the presence or absence of limb pain, as there is almost always a spectrum of the degree and experience of pain.

There are several limitations of this study. First, selection bias is introduced in multiple studies evaluating primary TMR as control patients were assessed by outreach through conferences and not withholding TMR from eligible patients, or by comparison to historical, published outcomes treatments[15,17]. Second, the data includes TMR performed for all reasons, including trauma, infection and oncological. This introduces aggregation bias wherein these populations may be inappropriately combined. Third, technical execution differs between and even within study groups. This reflects the inherent nature of TMR, wherein the pattern of nerve transfers may vary from patient to patient, depending on the anatomy and amputation level. Moreover, management of size mismatch in nerve coaptation may vary from group to group, with the continued evolution of techniques[30].

This review demonstrated that there is a growing body of evidence supporting TMR for primary and secondary treatment of amputee pain, residual limb pain, phantom limb pain and general limb pain. Patients, on average, experience improvements in pain intensity after primary and secondary TMR. PROMIS instruments offer providers and patients the opportunity to precisely quantify the level of pain intensity, behavioral changes and social effects of post-amputation limb pain, as well as the potential for improvement with TMR.

Future studies evaluating the impact of primary TMR should aim to eliminate selection bias by carefully selecting control patients. Additionally, future studies should assess not only measures of pain, but also patient-centric outcomes such as the ability to wear a prosthetic (Orthotics and Prosthetics Users Survey, return to work, and decreased need for adjunctive medical therapies including opioid use).

Additionally, while commonly used in research, PROMIS scores should be converted to plain language descriptions to help patients and providers communicate effectively and understand the clinical impact of the findings.

DECLARATIONS

Authors’ contributions

Made substantial contributions to conception and design of the study and performed data analysis, data acquisition and interpretation, as well as provided administrative, technical, and material support: Le ELH, Greyson MA, Constantine RS, Iorio ML

Availability of data and materials

Not applicable.

Financial support and sponsorship

The authors did not receive any funding for this study. None of the authors has a financial interest in any of the products, devices, or drugs mentioned in this manuscript.

Conflicts of interest

All authors declared that there are no conflicts of interest.

Ethical approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Copyright

© The Author(s) 2022.

REFERENCES

1. Mioton LM, Dumanian GA. Targeted muscle reinnervation and prosthetic rehabilitation after limb loss. J Surg Oncol 2018;118:807-14.

2. Ephraim PL, Wegener ST, MacKenzie EJ, Dillingham TR, Pezzin LE. Phantom pain, residual limb pain, and back pain in amputees: results of a national survey. Arch Phys Med Rehabil 2005;86:1910-9.

3. Hsu E, Cohen SP. Postamputation pain: epidemiology, mechanisms, and treatment. J Pain Res 2013;6:121-36.

4. Jensen TS, Krebs B, Nielsen J, Rasmussen P. Phantom limb, phantom pain and stump pain in amputees during the first 6 months following limb amputation. Pain 1983;17:243-56.

5. Montoya P, Larbig W, Grulke N, Flor H, Taub E, Birbaumer N. The relationship of phantom limb pain to other phantom limb phenomena in upper extremity amputees. Pain 1997;72:87-93.

6. Collins KL, Russell HG, Schumacher PJ, et al. A review of current theories and treatments for phantom limb pain. J Clin Invest 2018;128:2168-76.

7. Mioton LM, Dumanian GA, Shah N, et al. Targeted muscle reinnervation improves residual limb pain, phantom limb pain, and limb function: a prospective study of 33 major limb amputees. Clin Orthop Relat Res 2020;478:2161-7.

8. McNamara CT, Iorio ML. Targeted muscle reinnervation: outcomes in treating chronic pain secondary to extremity amputation and phantom limb syndrome. J Reconstr Microsurg 2020;36:235-40.

9. Kuiken TA, Dumanian GA, Lipschutz RD, Miller LA, Stubblefield KA. The use of targeted muscle reinnervation for improved myoelectric prosthesis control in a bilateral shoulder disarticulation amputee. Prosthet Orthot Int 2004;28:245-53.

10. Hijjawi JB, Kuiken TA, Lipschutz RD, Miller LA, Stubblefield KA, Dumanian GA. Improved myoelectric prosthesis control accomplished using multiple nerve transfers. Plast Reconstr Surg 2006;118:1573-8.

11. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71.

12. PROMIS. Available from: https://www.healthmeasures.net/score-and-interpret/interpret-scores/promis [Last accessed on 27 Sep 2022].

13. PROMIS Scoring Manuals. Available from: https://staging.healthmeasures.net/score-and-interpret/calculate-scores/223-promis-scoring-manuals [Last accessed on 27 Sep 2022].

14. Chang BL, Harbour P, Mondshine J, Kleiber GM. Targeted muscle reinnervation to expendable motor nerves for the treatment of refractory symptomatic neuromas in nonamputees. Plast Reconstr Surg Glob Open 2021;9:e3436.

15. Valerio IL, Dumanian GA, Jordan SW, et al. Preemptive treatment of phantom and residual limb pain with targeted muscle reinnervation at the time of major limb amputation. J Am Coll Surg 2019;228:217-26.

16. Frantz TL, Everhart JS, West JM, Ly TV, Phieffer LS, Valerio IL. Targeted muscle reinnervation at the time of major limb amputation in traumatic amputees: early experience of an effective treatment strategy to improve pain. JB JS Open Access 2020;5:e0067.

17. Alexander JH, Jordan SW, West JM, et al. Targeted muscle reinnervation in oncologic amputees: early experience of a novel institutional protocol. J Surg Oncol 2019;120:348-58.

18. Hoyt BW, Gibson JA, Potter BK, Souza JM. Practice patterns and pain outcomes for targeted muscle reinnervation: an informed approach to targeted muscle reinnervation use in the acute amputation setting. J Bone Joint Surg Am 2021;103:681-7.

19. Pet MA, Ko JH, Friedly JL, Mourad PD, Smith DG. Does targeted nerve implantation reduce neuroma pain in amputees? Clin Orthop Relat Res 2014;472:2991-3001.

20. Chang BL, Mondshine J, Attinger CE, Kleiber GM. Targeted muscle reinnervation improves pain and ambulation outcomes in highly comorbid amputees. Plast Reconstr Surg 2021;148:376-86.

21. Dumanian GA, Potter BK, Mioton LM, et al. Targeted muscle reinnervation treats neuroma and phantom pain in major limb amputees: a randomized clinical trial. Ann Surg 2019;270:238-46.

22. Kang NV, Woollard A, Michno DA, Al-Ajam Y, Tan J, Hansen E. A consecutive series of targeted muscle reinnervation (TMR) cases for relief of neuroma and phantom limb pain: UK perspective. J Plast Reconstr Aesthet Surg 2022;75:960-9.

23. Ferreira-Valente MA, Pais-Ribeiro JL, Jensen MP. Validity of four pain intensity rating scales. Pain 2011;152:2399-404.

24. Gordon DB. Acute pain assessment tools: let us move beyond simple pain ratings. Curr Opin Anaesthesiol 2015;28:565-9.

25. Revicki DA, Chen WH, Harnam N, et al. Development and psychometric analysis of the PROMIS pain behavior item bank. Pain 2009;146:158-69.

26. Amtmann D, Cook KF, Jensen MP, et al. Development of a PROMIS item bank to measure pain interference. Pain 2010;150:173-82.

27. Resnik L, Borgia M. Reliability of outcome measures for people with lower-limb amputations: distinguishing true change from statistical error. Phys Ther 2011;91:555-65.

28. McCarberg B, Peppin J. Pain pathways and nervous system plasticity: learning and memory in pain. Pain Med 2019;20:2421-37.

29. Farrar JT, Young JP, Lamoreaux L, Werth JL, Poole MR. Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain 2001;94:149-58.

30. Valerio I, Schulz SA, West J, Westenberg RF, Eberlin KR. Targeted muscle reinnervation combined with a vascularized pedicled regenerative peripheral nerve interface. Plast Reconstr Surg Glob Open 2020;8:e2689.

Cite This Article

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Open Access
A review of pain outcomes following targeted muscle reinnervation in lower extremity limb pain
Elliot L. H. Le, ... Matthew L. Iorio

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Le, E. L. H.; Greyson, M. A.; Constantine, R. S.; Iorio, M. L. A review of pain outcomes following targeted muscle reinnervation in lower extremity limb pain. Plast. Aesthet. Res. 2022, 9, 55. http://dx.doi.org/10.20517/2347-9264.2022.47

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This article belongs to the Special Issue Targeted Muscle Reinnervation and Peripheral Nerve Transfers
© The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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