Abstract
Study design
Secondary analysis of an observational cohort study.
Objectives
To determine if the perceived overall limitation of neuropathic pain on activities (NP limitation) covaries in 26 specific life activities in people with SCI, taking into account the severity of injury.
Setting
Community-based in Canada.
Methods
Secondary analysis of a cohort (N = 1481) was performed using questionnaires to rate NP frequency and limitation on activities as well as participation in 26 life activities. Relative risks (RR) analyses using Poisson regression were used to examine the data.
Results
Most participants (N = 1158; 78%) reported living with NP (from once a year to every day). When NP limitation was described as “not at all” or “very little” (N = 394; 34%), there was no statistically significant RR (p > 0.0019), suggesting no additional risk of not participating “as much as wanted” in any of activities compared to participants with no NP. When NP limitation was described as “to some extent” (N = 411; 35%), a significantly higher risk was observed for 5 of the 26 activities (1.34 < RR < 1.62), and for 23 activities with a large range (1.24 < RR < 3.20) when NP limitation was rated as “to a great extent or more” (N = 353; 31%).
Conclusion
The variation of RR observed across the 26 activities suggests that the NP limitation may not be general but rather related to specific activity characteristics, which should be taken into account when evaluating NP limitations with a specific focus on the life activities being affected.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
Data availability
The data that support the findings of this study are available from The Praxis Institute, but restrictions apply to the availability of these data. Please contact one of the coauthor: Vanessa Noonan (vnoonan@praxisinstitute.org).
References
van Gorp S, Kessels AG, Joosten EA, van Kleef M, Patijn J. Pain prevalence and its determinants after spinal cord injury: a systematic review. Eur J Pain. 2015;19:5–14.
Burke D, Fullen BM, Stokes D, Lennon O. Neuropathic pain prevalence following spinal cord injury: a systematic review and meta-analysis. Eur J Pain. 2017;21:29–44.
Piatt JA, Nagata S, Zahl M, Li J, Rosenbluth JP. Problematic secondary health conditions among adults with spinal cord injury and its impact on social participation and daily life. J Spinal Cord Med. 2016;39:693–8.
Widerstrom-Noga EG, Felipe-Cuervo E, Yezierski RP. Chronic pain after spinal injury: interference with sleep and daily activities. Arch Phys Med Rehabil. 2001;82:1571–7.
Donnelly C, Eng JJ. Pain following spinal cord injury: the impact on community reintegration. Spinal Cord. 2005;43:278–82.
Kratz AL, Hirsh AT, Ehde DM, Jensen MP. Acceptance of pain in neurological disorders: associations with functioning and psychosocial well-being. Rehabil Psychol. 2013;58:1–9.
World Health Organization. International classification of functioning, disability and health (ICF). Geneva: World Health Organization; 2001. http://apps.who.int/classifications/icfbrowser/.
Hammel J, Magasi S, Heinemann A, Whiteneck G, Bogner J, Rodriguez E. What does participation mean? An insider perspective from people with disabilities. Disabil Rehabil. 2008;30:1445–60.
Martin Ginis KA, Evans MB, Mortenson WB, Noreau L. Broadening the conceptualization of participation of persons with physical disabilities: a configurative review and recommendations. Arch Phys Med Rehabil. 2017;98:395–402.
Andresen SR, Biering-Sorensen F, Hagen EM, Nielsen JF, Bach FW, Finnerup NB. Pain, spasticity and quality of life in individuals with traumatic spinal cord injury in Denmark. Spinal Cord. 2016;54:973–9.
Noreau L, Noonan VK, Cobb J, Leblond J, Dumont FS. Spinal cord injury community survey: a national, comprehensive study to portray the lives of canadians with spinal cord injury. Top Spinal Cord Inj Rehabil. 2014;20:249–64.
Mulcahey MJ, Calhoun CL, Tian F, Ni P, Vogel LC, Haley SM. Evaluation of newly developed item banks for child-reported outcomes of participation following spinal cord injury. Spinal Cord. 2012;50:915–9.
Cobb J, Dumont FS, Leblond J, Park SE, Noonan VK, Noreau L. An exploratory analysis of the potential association between SCI secondary health conditions and daily activities. Top Spinal Cord Inj Rehabil. 2014;20:277–88.
Norrbrink C, Lofgren M, Hunter JP, Ellis J. Patients’ perspectives on pain. Top Spinal Cord Inj Rehabil. 2012;18:50–6.
Norrbrink C, Lofgren M. Needs and requests–patients and physicians voices about improving the management of spinal cord injury neuropathic pain. Disabil Rehabil. 2016;38:151–8.
Noreau L, Noonan VK, Cobb J, Leblond J, Dumont FS. Spinal cord injury community survey: understanding the needs of canadians with SCI. Top Spinal Cord Inj Rehabil. 2014;20:265–76.
Noonan VK, Kwon BK, Soril L, Fehlings MG, Hurlbert RJ, Townson A, et al. The rick hansen spinal cord injury registry (RHSCIR): a national patient-registry. Spinal Cord. 2012;50:22–7.
Noreau L, Cobb J, Belanger LM, Dvorak MF, Leblond J, Noonan VK. Development and assessment of a community follow-up questionnaire for the Rick Hansen spinal cord injury registry. Arch Phys Med Rehabil. 2013;94:1753–65.
Cieza A, Kirchberger I, Biering-Sorensen F, Baumberger M, Charlifue S, Post MW, et al. ICF Core Sets for individuals with spinal cord injury in the long-term context. Spinal Cord. 2010;48:305–12.
Zou G. A modified poisson regression approach to prospective studies with binary data. Am J Epidemiol. 2004;159:702–6.
Barros AJ, Hirakata VN. Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol. 2003;3:21.
Bloemen-Vrencken JH, Post MW, Hendriks JM, De Reus EC, De Witte LP. Health problems of persons with spinal cord injury living in the Netherlands. Disabil Rehabil. 2005;27:1381–9.
Guest R, Craig A, Tran Y, Middleton J. Factors predicting resilience in people with spinal cord injury during transition from inpatient rehabilitation to the community. Spinal Cord. 2015;53:682–6.
Dibb B, Ellis-Hill C, Donovan-Hall M, Burridge J, Rushton D. Exploring positive adjustment in people with spinal cord injury. J Health Psychol. 2014;19:1043–54.
Sprangers MA, Schwartz CE. Integrating response shift into health-related quality of life research: a theoretical model. Soc Sci Med. 1999;48:1507–15.
Schwartz CE. Applications of response shift theory and methods to participation measurement: a brief history of a young field. Arch Phys Med Rehabil. 2010;91 9 Suppl:S38–43.
Kratz AL, Ehde DM, Bombardier CH, Kalpakjian CZ, Hanks RA. Pain acceptance decouples the momentary associations between pain, pain interference, and physical activity in the daily lives of people with chronic pain and spinal cord injury. J Pain. 2017;18:319–31.
Vowles KE, McCracken LM, Eccleston C. Patient functioning and catastrophizing in chronic pain: the mediating effects of acceptance. Health Psychol. 2008;27:S136–43.
Furrer A, Michel G, Terrill AL, Jensen MP, Müller R. Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing. Disabil Rehabil. 2019;41:498–507.
Alperstein D, Sharpe L. The efficacy of motivational interviewing in adults with chronic pain: a meta-analysis and systematic review. J Pain. 2016;17:393–403.
Acknowledgements
We would also like to thank all participants who have taken the time to answer the survey.
Funding
We would like to acknowledge the financial support from the Rick Hansen Institute and the Ontario Neurotrauma Foundation.
Author information
Authors and Affiliations
Contributions
LN was responsible for designing and carrying out the study including analyzing data, interpreting results, and writing the manuscript. JEC and VKN collaborated for designing and carrying out the study and interpreting results and writing the manuscript. JL was responsible for the data extraction and the statistical analyses and contributed to the writing of the report. FSD coordinated the implementation of the study and contributed to the statistical analyses and the writing of the report.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
Ethics was approved by the Canadian Institutional Research Board Services and the Research Ethics Board of Université Laval (no. 93581). Informed consent was obtained from each participant included in the study. We certify that all applicable institutional and governmental regulations concerning the ethical use of human volunteers/animals were followed during the course of this research.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
About this article
Cite this article
Noreau, L., Cobb, J.E., Noonan, V.K. et al. Impact of neuropathic pain on participation: perspectives from the Canadian SCI community survey. Spinal Cord 59, 141–150 (2021). https://doi.org/10.1038/s41393-020-0512-9
Received:
Revised:
Accepted:
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1038/s41393-020-0512-9


