Sarah B Wallwork

Dr. Sarah B Wallwork


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 January 2024 in Canadian Medical Association Journal
Verified
Journal Article
Open access
PDF file
SWSarah B Wallwork
Sarah B Wallwork
FBFelicity A. Braithwaite
Felicity A. Braithwaite
MOMary O’kEeffe
Mary O’kEeffe
MTMervyn J. Travers
Mervyn J. Travers
SSSimon J. Summers
Simon J. Summers
GMG. Lorimer Moseley
G. Lorimer Moseley
Background: Understanding the clinical course of low back pain is essential to informing treatment recommendations and patient stratification. Our aim was to update our previous systematic review and meta-analysis to gain a better understanding of the clinical course of acute, subacute and persistent low back pain. Methods: To update our 2012 systematic review and meta-analysis, we searched the Embase, MEDLINE and CINAHL databases from 2011 until January 2023, using our previous search strategy. We included prospective inception cohort studies if they reported on participants with acute (< 6 wk), subacute (6 to less than 12 wk) or persistent (12 to less than 52 wk) nonspecific low back pain at study entry. Primary outcome measures included pain and disability (0–100 scale). We assessed risk of bias of included studies using a modified tool and assessed the level of confidence in pooled estimates using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) tool. We used a mixed model design to calculate pooled estimates (mean, 95% confidence interval [CI]) of pain and disability at 0, 6, 12, 26 and 52 weeks. We treated time in 2 ways: time since study entry (inception time uncorrected) and time since pain onset (inception time corrected). We transformed the latter by adding the mean inception time to the time of study entry. Results: We included 95 studies, with 60 separate cohorts in the systematic review (n = 17 974) and 47 cohorts (n = 9224) in the meta-analysis. Risk of bias of included studies was variable, with poor study attrition and follow-up, and most studies did not select participants as consecutive cases. For the acute pain cohort, the estimated mean pain score with inception time uncorrected was 56 (95% CI 49–62) at baseline, 26 (95% CI 21–31) at 6 weeks, 22 (95% CI 18–26) at 26 weeks and 21 (95% CI 17–25) at 52 weeks (moderate-certainty evidence). For the subacute pain cohort, the mean pain score was 63 (95% CI 55–71) at baseline, 29 (95% CI 22–37) at 6 weeks, 29 (95% CI 22–36) at 26 weeks and 31 (95% 23–39) at 52 weeks (moderate-certainty evidence). For the persistent pain cohort, the mean pain score was 56 (95% CI 37–74) at baseline, 48 (95% CI 32–64) at 6 weeks, 43 (95% CI 29–57) at 26 weeks and 40 (95% CI 27–54) at 52 weeks (very low–certainty evidence). The clinical course of disability was slightly more favourable than the clinical course of pain. Interpretation: Participants with acute and subacute low back pain had substantial improvements in levels of pain and disability within the first 6 weeks ( moderate-certainty evidence); however, participants with persistent low back pain had high levels of pain and disability with minimal improvements over time (very low–certainty evidence). Identifying and escalating care in individuals with subacute low back pain who are recovering slowly could be a focus of intervention to reduce the likelihood of transition into persistent low back pain. Protocol registration: PROSPERO — CRD42020207442

1 February 2019 in The Journal of Pain
Verified
Journal Article
Closed access
JBJohn Breckenridge
John Breckenridge
KGKaren A. Ginn
Karen A. Ginn
SWSarah B Wallwork
Sarah B Wallwork
JMJames H McAuley
James H McAuley

15 February 2016 in Annals of Neurology
Verified
Journal Article
Closed access
PDF file
EREmily Reid
Emily Reid
SWSarah B Wallwork
Sarah B Wallwork
DHDaniel Harvie
Daniel Harvie
JCJane Chalmers
Jane Chalmers
AGAlberto Gallace
Alberto Gallace
GMG. Lorimer Moseley
G. Lorimer Moseley

1 June 2013 in Manual Therapy
Verified
Journal Article
Closed access
SWSarah B Wallwork
Sarah B Wallwork
DBDavid S. Butler
David S. Butler
IFIan Fulton
Ian Fulton
HSHalton Stewart
Halton Stewart
IDIgusti Darmawan
Igusti Darmawan
GMG. Lorimer Moseley
G. Lorimer Moseley

18 December 2015 in British Journal of Sports Medicine
Verified
Journal Article
Closed access
PDF file
SWSarah B Wallwork
Sarah B Wallwork
VBValeria Bellan
Valeria Bellan
MCMark J Catley
Mark J Catley
GMG Lorimer Moseley
G Lorimer Moseley
Neural representations, or neurotags, refer to the idea that networks of brain cells, distributed across multiple brain areas, work in synergy to produce outputs. The brain can be considered then, a complex array of neurotags, each influencing and being influenced by each other. The output of some neurotags act on other systems, for example, movement, or on consciousness, for example, pain. This concept of neurotags has sparked a new body of research into pain and rehabilitation. We draw on this research and the concept of a cortical body matrix—a network of representations that subserves the regulation and protection of the body and the space around it—to suggest important implications for rehabilitation of sports injury and for sports performance. Protective behaviours associated with pain have been reinterpreted in light of these conceptual models. With a particular focus on rehabilitation of the injured athlete, this review presents the theoretical underpinnings of the cortical body matrix and its application within the sporting context. Therapeutic approaches based on these ideas are discussed and the efficacy of the most tested approaches is addressed. By integrating current thought in pain and cognitive neuroscience related to sports rehabilitation, recommendations for clinical practice and future research are suggested.

1 July 2018 in Cortex
Verified
Journal Article
Closed access
EREmily J. Reid
Emily J. Reid
FBFelicity A. Braithwaite
Felicity A. Braithwaite
SWSarah B Wallwork
Sarah B Wallwork
DHDaniel Harvie
Daniel Harvie
JCJane Chalmers
Jane Chalmers
GMG. Lorimer Moseley
G. Lorimer Moseley