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Are neuromuscular adaptations present in people with recurrent spinal pain during a period of remission? A protocol for a systematic review
  1. Valter Devecchi,
  2. Alessio Gallina,
  3. Nicola R Heneghan,
  4. Alison B Rushton,
  5. Deborah Falla
  1. Centre of Precision Rehabilitation for Spinal Pain (CPR Spine), School of Sport, Exercise and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, Birmingham, UK
  1. Correspondence to Professor Deborah Falla; d.falla{at}bham.ac.uk

Abstract

Introduction The course of spinal pain (neck or low back pain) is often described as episodic and intermittent, with more than one-third of people continuing to experience episodic symptoms 1 year after first onset. Although ongoing neuromuscular adaptations could contribute to recurrent episodes of pain, no systematic review has synthesised evidence of ongoing neuromuscular changes in people with recurrent spinal pain during a period of symptom remission.

Methods and analysis This protocol is developed and reported following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses-P, the Update of the Cochrane Back and Neck Group guidelines and the Methodological Expectations of Cochrane Intervention Reviews. PubMed, Web of Science, MEDLINE, EMBASE, CINAHL, ZETOC, Google Scholar, grey literature sources and key journals will be searched up to September 2019. Observational studies investigating neuromuscular changes in people with recurrent spinal pain during a period of remission will be included. Neuromuscular function will be considered under five outcome domains of muscle activity, spine kinematics, muscle properties, sensorimotor control and neuromuscular performance. Two independent reviewers will search, screen studies, extract data and assess risk of bias (Newcastle-Ottawa Scale). Data will be synthesised per outcome domain. Where clinical and methodological homogeneity across studies exists, a random-effects meta-analysis will be conducted. Otherwise, results will be synthesised narratively. The overall quality of evidence will be assessed using the Grading of Recommendations, Assessment, Development and Evaluation guidelines.

Ethics and dissemination Findings of this review may aid the identification of factors that could contribute to spinal pain recurrence and aid the development of interventions for secondary prevention aimed at the restoration of optimal neuromuscular function. The results will be submitted for publication in a peer-reviewed journal and presented at conferences. No ethical approval was required.

PROSPERO registration number CRD42019141527.

  • neck pain
  • low back pain
  • electromyography
  • muscle activity
  • motor control

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Strengths and limitations of this study

  • This will be the first systematic review to synthesise evidence of neuromuscular adaptations in people with recurrent spinal pain (neck or low back pain) during a period of remission.

  • This protocol is written following the recommendations reported in version 6 of the Cochrane Handbook for Systematic Reviews of Interventions that will be published in mid-2019 (second edition of the Handbook).

  • Neuromuscular changes will be evaluated considering a broad range of outcome domains, specifically muscle activity, spine kinematics, muscle properties, sensorimotor control and neuromuscular performance.

  • In accordance with the Grading of Recommendations Assessment, Development, and Evaluation approach, the inclusion of observational studies reduces the quality of evidence.

Introduction

Low back and neck pain (spinal pain) continue to be the leading cause of disability worldwide.1 The number of years lived with disability has increased by more than 50% since 1990, creating a ‘spinal pain epidemic’.1 2 In particular, people aged between 25 and 64 years are most affected by spinal pain1 and thus the economic impact is substantial due to work absences and healthcare cost.3

Spinal pain is a particularly challenging condition since the prognosis is often poor following an acute episode and many people experience recurrent pain.4–6 For instance, more than 50% and 30% of patients experience further neck or low back pain episodes, respectively, within the first year following a first episode.7 8 Indeed, the course of spinal pain is often described as repeated episodes of pain, commonly across a lifetime, with varying degrees of recovery between episodes. Summarising 10 cohort studies, Kongsted et al 9 identified different patterns of low back pain progression, distinguishing between persistent, fluctuating, recurrent and single episode trajectories. Conceptually, it is also necessary to distinguish between new painful episodes characterising recurrent patterns10 and the notion of flare, a sudden and severe increase of symptoms affecting persistent or fluctuating conditions.11 Recurrent episodes of pain were described by de Vet et al 10 as periods of pain lasting for 1 day or more and separated by at least 1 month of symptom remission. Fluctuating patterns differ from recurrent pain because the former does not include period of remission, so patients continue to experience symptoms but with different level of intensity.9 10

Several factors may contribute to recurrent episodes of pain including ongoing maladaptive motor behaviour, neuromuscular deficits, impaired sensorimotor control and fear avoidance.12–15 More specifically, in people with spinal pain a number of common neuromuscular changes have been observed which have the potential to contribute to repeated episodes of pain. These include reduced muscle strength, endurance,16–19 range of motion,20 21 increased muscle co-activation,22 23 poorer control of the deeper muscles,24 25 poorer proprioception and changes in the quality and variability of movement.26–29 Although these changes have been contextualised to be protective in nature30 31 and occur early following the onset of pain,32–34 they appear to be sustained beyond the acute phase13 35 36 and have the potential to contribute to chronicity and repeated painful episodes.12 31 37 38 Although numerous studies have confirmed the presence of altered neuromuscular function in patients with chronic neck18 39 and back pain25 40 41 and systematic reviews have been conducted to critically appraise these studies, and synthesise findings,21 42–44 no systematic review has been conducted to evaluate evidence of neuromuscular changes during a period of remission in people with recurrent spinal pain. The assessment of patients during a period of remission allows to investigate neuromuscular function without pain interference.

The aim of this systematic review is to summarise the current literature to determine the evidence supporting the existence of ongoing neuromuscular adaptations in people with recurrent spinal pain during a period of remission. It is expected that this synthesis of evidence will influence clinical practice by highlighting the need to manage and restore neuromuscular function in addition to symptom suppression and will promote the relevance of interventions for secondary prevention.

Methods

The protocol of this review has been developed following the update of the Cochrane Back and Neck Group guidelines,45 the Methodological Expectations of Cochrane Intervention Reviews (MECIR)46 and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Protocols (online supplementary file 1).47

Supplemental material

Eligibility criteria

In order to detail the main elements of the systematic review, the PICOS framework will be used where P – Population, I – Indicator, C – Comparator, O – Outcome(s) and S - Study design.47 48

Population

Adults (age ≥18 years old) with recurrent non-specific spinal pain (neck or low back pain) are the population of interest and adults without a history of spinal pain represent the control group. For the purpose of this review and in order to avoid the exclusion of relevant articles, the definition provided by de Vet et al 10 will be partially considered due to the heterogeneity identified during the scoping search. Therefore, for the recurrent spinal pain group, we will consider studies where the individuals have experienced episodes of spinal pain on at least two occasions during the previous year.10 Participants with injury that resulted in a fracture or radiating, neuropathic pain will be excluded. Pain intensity reported before the outcome assessment will not represent an element of exclusion but it will be considered for further subgroup analysis (no pain vs minimal pain) as the initial scoping search identified that some studies define a period of remission to be minimal pain rather than absence of pain.

Indicator

The indicator of interest is the use of:

  • Surface electromyography (EMG), intramuscular EMG, ultrasound and functional magnetic resonance imaging (fMRI) to measure axial muscle activity/behaviour.49–52

  • Motion analysis systems (eg, optoelectronic systems, inertial measurement unit sensors) to quantify spine kinematics.53

  • Ultrasound and MRI to investigate muscle properties.54 55

  • Dynamometry and performance testing to assess strength and endurance of axial muscles.

Therefore, all muscles (superficial and deep) that act on the spine and movements of the lumbar, thoracic and cervical regions will be considered.

Comparison

Between-group comparisons will be analysed considering people with recurrent spinal pain during a period of remission and healthy subjects without a history of spinal pain (neck or low back pain). Moreover, studies must include comparisons related to axial muscle activity, spine kinematics, sensorimotor control, muscle properties, strength and endurance during rest or tasks (static and/or dynamic).

Outcomes

The outcomes of interest are chosen based on the purpose of the review and the theoretical framework that has been suggested for people with spinal pain.31 37 38

Moreover, in accordance with the literature neuromuscular adaptations selected can influence long-term negative consequences and they could contribute to trigger future episodes of pain.31

The main concept investigated is the neuromuscular system; therefore, broad domains such as axial muscle activity, spinal kinematics, sensorimotor control, properties of the axial muscles and performance will be considered. In order to narrow the review focus, specific outcome domains are identified within the broad domains and are summarised in table 1.

Table 1

Outcome domains

Outcome domains are operationalised and different outcome measures are considered as described in the following paragraphs.

Muscle activity domain will comprise muscle timing (during predicted and non-predicted perturbations) and muscle amplitude. The outcome measures that will be extracted to report amplitude and muscle timing with EMG are the average rectified value or root mean square and the onset of activity. Moreover, EMG variability related to the timing and amplitude of muscle activity will be considered. In the measurements obtained by ultrasound, the change of muscle thickness compared to rest value represents the outcome measure that will be used to report on changes in muscle activity. For fMRI measurements, parameters related to transverse relaxation time will be considered.51

Spine kinematics will comprise specific domains; motor variability, active range of motion and quality of movement (accuracy and smoothness) during functional tasks or tests. It is not possible to specify a priori the outcome measures because they depend on the tasks and instruments used.

Sensorimotor control of the spine will include proprioception investigated through specific tests (eg, repositioning and movement detection).

Muscle properties recorded with ultrasound or MRI include features such as the extent of fat infiltration, muscle thickness and total muscle cross-sectional area.

Strength and endurance values of the axial muscles investigated with dynamometry will be considered. Moreover, endurance related data obtained with the Borg Scale or EMG features (mean frequency or median frequency) will be included.

Study design

Based on the scoping search, observational studies will be considered because they address the PICOS framework specified in the review question.

Information sources

The search will be conducted from inception to 1 September 2019. Databases will include MEDLINE (OVID interface), EMBASE (OVID interface), CINAHL (EBSCO interface), ZETOC and Google Scholar. Moreover, specific Internet sites will be searched: PubMed, Web of Science and Cochrane Back and Neck Review Group.

The search process will be conducted using medical subject headings (MESH) where appropriate and relevant text words associated with the concepts of this review. The search strategy will be done operationalising the PICOS framework and the main concepts that will be considered are related to the population and outcomes of interest. Words associated with them will be linked with the Boolean terms AND/OR:

POPULATION:

‘Recurrent’ (using OR for all possible synonyms, such as intermittent, history of, episodes)

AND

‘Spinal pain’ (using OR for all spine regions)

AND INDICATOR:

‘electromyography’ OR ‘motion analysis’ OR ‘dynamometer’ (using OR for all possible synonyms and instruments used)

AND OUTCOMES:

‘Spine kinematics’ OR ‘muscle activity’ OR ‘sensorimotor control’ OR ‘muscle properties’ OR ‘performance’ (words/synonyms related to these concepts will be used)

Hand-searching will be conducted based on the results of the scoping search and including journals relevant for this review topic, specifically the Journal of Electromyography and Kinesiology, Clinical Biomechanics, The Clinical Journal of Pain, Spine, Musculoskeletal Science and Practice, and the Journal of Orthopaedic and Sports Physical Therapy. The eligibility of manuscripts included with hand searching will be defined using the PICOS framework. Relevant authors in the field will be contacted to obtain information about unpublished or ongoing studies. In order to reduce the risk of publication bias, grey literature will be included considering the British National Bibliography for report literature, OpenGrey and dissertation abstracts. In accordance with the MECIR standards,46 reference lists of included studies and relevant systematic reviews will be checked for any further studies.

Search strategy

The search will not be restricted by date, region or language limits. The specific search strategy has been defined in accordance with a Health Sciences Librarian with review searching experience. An example of the search strategy (draft MEDLINE search – Ovid interface) is reported in online supplementary file 2. Searching on MEDLINE (OVID interface) will be conducted using MESH. Based on other database selected, relevant terms will be adapted but search strategy consistency will be ensured.

Supplemental material

Data management

EndNote V.X9 (Clarivate Analytics) will be used to manage the data, including citations, abstracts and full-text of relevant studies. A reviewer (VD) will upload studies during the searching process and duplicates will be removed. When the list of searched studies is completed, reviewers (VD and AG) will start the screening process. Full text of the papers that will be considered potentially eligible will be stored in EndNote V.X9.

Selection process

Based on the eligibility criteria, an electronic screening tool will be created and piloted. During the first stage of the screening process, two independent reviewers (VD and AG) will assess titles and abstracts against the eligibility criteria. In an event of disagreement, reviewers will first attempt to resolve through discussion. If no consensus can be reached, a third reviewer (DF) will mediate the process. After the first screening process, full-text records will be obtained for potentially eligible studies. The full text screening will be conducted by two reviewers (VD and AG). During both stages of the screening process the agreement between the two reviewers will be assessed using the kappa statistic. The PRISMA flow diagram will used to summarise the study selection process.47

Data extraction process

Data extraction will be performed independently by two reviewers (VD, AG) using a data extraction form developed and piloted a priori on a sub-group of studies. The data extraction form and table 2 will be customised based on the recommendations provided by Li et al,56 considering the eligibility criteria and aim of the review. If discrepancies between reviewers arise, they will be resolved by discussion. A third reviewer (DF) will be consulted to mediate where necessary. The authors of the primary studies will be contacted if the description of methods or data reporting is unclear. Duplicate publications will be identified in order to reduce bias that could influence quantitative results. Multiple reports of the same study will be collated, and a specific report will be chosen. The decision of the selected report will be justified.

Table 2

Characteristics of included studies

In accordance with McKenzie et al,57 data extraction and synthesis will be simplified following specific criteria:

  • When an outcome of interest is measured more than one time, the first assessment will be considered. Baseline measurements for cross-sectional comparisons with the healthy control group will be extracted in longitudinal studies or clinical trials.

  • When an outcome of interest is measured with more than one tool, data will be selected based on the properties (reliability and validity) of the instrument.

  • Multiplicity of outcomes of the same domain (eg, strength of different muscles) will be reported and specific methods will be applied during data synthesis (see data synthesis section).

  • Studies will be grouped based on the main outcome domain investigated; moreover, clinical and methodological diversity across studies will be analysed (see data synthesis section).

Data items

Study characteristics will include details of participant, outcomes, outcome measures, study design and they are reported in table 2.

In order to reduce the impact of reporting bias, study authors will be contacted to obtain unpublished data or to clarify ambiguous results. However, if any uncertainty remains or the information provided by the author modifies the eligibility of the study, the paper will be excluded and a specific explanation will be provided. Data will be extracted from the control and recurrent pain group. If more than two groups are investigated in a study, data will be collected only from the healthy control group and the one that meets the eligibility criteria.

Risk of bias

Two independent reviewers (VD, AG) will appraise the included studies using the Newcastle-Ottawa Scale (NOS).58 Discrepancies will be resolved with discussion. The risk of bias tool has been chosen based on the review question and the design of the primary studies detected during the scoping search (observational). There is not a firm consensus about the more suitable risk of bias tool for observational studies and health assessment groups have provided poorly defined recommendations.59 60 For example, in a recent review Quigley et al 60 identified 48 critical appraisal tools for non-randomised studies. Given its strengths, the NOS has been the most used tool in non-randomised studies; especially since it is quick to complete, adaptable, validated and usable in all kind of observational studies.58 61 62 Moreover, it assesses bias in the more relevant components of the studies included in this review; sample and outcomes. Considering the strengths of the NOS described previously, the case-control version will be used.58 The scale consists of three dimensions (selection, comparability, exposure) and eight items overall. The included studies will be assessed following the specific guidelines58 and a maximum of nine stars will be assigned to each paper (0–3=poor quality, 4–7=fair quality, 8–9=good quality). A table indicating the risk of bias in each study will be reported; moreover, detailed information for each dimension assessed by the NOS will be provided.

Data synthesis

Results will be synthesised following the framework developed by McKenzie et al.63 Characteristics of each included study will be reported in a specific table. Then, studies and results will be grouped based on the main outcome domain investigated (muscle activity, spine kinematics, sensorimotor control, muscle properties, axial muscle performance) in the ‘Major Findings’ table. Moreover, data available for synthesis will be collected (mean and SD). The difference between healthy and recurrent spinal pain group will be reported using the standardised mean difference and 95% CI; data will be obtained directly from the paper or calculated using the available information. Where relevant data are missing, the authors of the primary study will be contacted.

Random-effects meta-analysis (in accordance with the Cochrane Back and Neck Group)45 will be considered for a limited number of outcomes in order to reduce the risk of type I error (due to statistical multiplicity)64; therefore, the following outcomes are selected: muscle activity, muscle timing (during a postural perturbation), range of movements (including their variability) and muscle strength. These outcomes were selected considering the feasibility of their assessment in clinical practice and the theoretical framework of motor adaptation to pain.31 38 Briefly, the features considered appear to be adopted with a protective purpose but may still be present during a period of remission (potentially contributing to long-term negative consequences).31 38

A separate meta-analysis will be conducted for each selected outcome or dependent variable where possible.

In order to decide whether results can be summarised with statistical synthesis, heterogeneity across studies will be explored. First, clinical and methodological diversity across studies will be analysed by the two reviewers considering the following elements:

  • Muscle or region of the spine investigated (lumbar, thoracic or cervical).

  • Task performed.

  • Outcome measure reported (for muscle amplitude outcomes only normalised value will be considered).

Whether clinical and methodological homogeneity across studies investigating the same outcome domain will be sufficient, statistical heterogeneity will be analysed. Disagreement between reviewers will be resolved by discussion and if it will persist a third reviewer (DF) will be consulted.

Based on the scoping search, a large number of studies included a small sample size, thus in accordance to Higgins et al,65 the Cochran’s Q test will provide low power in the detection of significant heterogeneity. Therefore, the amount of inconsistency between studies will be assessed using the I2 statistic.66 If heterogeneity will be substantial (I2 >50%), the results of the considered outcome will be described using the vote-counting procedure (direction of difference or no difference) and a narrative synthesis will be provided.67 Additionally, if an adequate number of studies will be included,68 subgroup analysis will be performed in meta-analysis splitting participants with recurrent spinal pain (neck or low back pain) in two subgroups—subjects with and without minimal pain during the assessment. This method will be used in order to explore whether the presence of any pain influences motor control features. Subgroup comparison will be investigated using the fixed-effects model (between subgroups) described by Borenstein and Higgins.69

All the outcome results not included in the statistical synthesis will be described, when possible, with the vote-counting procedure or narratively67; moreover, in the group of people with recurrent spinal pain, differences in findings between asymptomatic and symptomatic subjects during the assessment will be reported. The narrative synthesis will be conducted following specific guidance and the steps provided by the Cochrane Consumers and Communication Review Group.70 71

Results will be shown based on the method of synthesis (quantitative or qualitative) and grouped considering the outcome domains. Risk of bias will not represent elements of restriction in the presentation of findings. Risk of publication bias will be analysed adopting the search strategies described in the information source section; particularly, results from references different to peer-reviewed articles will be included, as described by Page et al.72 For example, hand searching of grey literature on trial registers will be conducted and notable authors will be contacted to obtain information on unpublished data or ongoing works.

Confidence in cumulative estimate

Quality of findings (certainty) will be assessed using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach.73 74 The GRADE process is ‘outcome centric’; therefore, the quality of evidence will be analysed for each outcome domain included in the PICOS.75 In accordance with GRADE and considering that it is not possible to manipulate the independent variable (pain remission/no history of pain), the observational studies included will be considered a low-quality source of evidence.73 75 After this initial consideration, the certainty of evidence for each outcome across studies can be increased or decreased following specific criteria. Risk of bias, inconsistency, indirectness, imprecision and publication bias are reasons for lower quality of evidence.76 On the other hand, large effect size, dose–response gradient and plausible confounding biases that underestimate the effect size are reasons to upgrade the certainty of evidence for the considered outcome across studies.76 Based on these criteria, GRADE rates the level of certainty for each outcome in four categories: ‘High’, ‘Moderate’, ‘Low’ and ‘Very Low’.76 The GRADE guidelines provide detailed information on the assessment of the quality of evidence for observational studies.74 For example, study limitations to consider in observational studies during the evaluation of the strength of evidence are suggested.77

Patient and public involvement

The protocol was presented within patient and public involvement meetings in order to discuss the topic and obtain feedback for the review and future projects. Patients will not be involved in the analysis and data collection of the systematic review.

Implication of results

The natural course of spinal pain (neck or low back pain) is not straightforward and different patterns of pain progression have been described. A previous episode of pain is one of the most relevant factors for future pain recurrences. Evidence has shown the role and relation between neuromuscular changes and pain in persistent musculoskeletal disorders and recovery of neuromuscular function has become an important component in rehabilitation. However, the focus for the management of acute pain is limited to pain management and resolution rather than full functional rehabilitation. The results of this systematic review may identify relevant neuromuscular adaptations that could play a role in the recurrent nature of spinal pain with the potential to therefore influence clinical practice.

Ethics and dissemination

Ethical approval is not required for this project as it will not involve utilisation or publication of personal data. The results of this systematic review will be disseminated through publication in a peer-reviewed journal and where appropriate, be presented in national and/or international conferences.

References

Footnotes

  • Twitter @HeneghanNicola, @abrushton, @Deb_Falla

  • Contributors VD and DF are responsible for the conception of the research question, development of the protocol and initial drafting of the manuscript. DF is lead supervisor of VD and ABR and NRH are co-supervisors. All supervisors have provided guidance on methodological decisions and proposed analyses. VD and AG will be the first and second reviewer. DF will be the third reviewer. All authors will contribute to data interpretation, conclusions and dissemination. All authors have read and subsequently approved the final manuscript. DF is the guarantor of the review.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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