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Published in: BMC Musculoskeletal Disorders 1/2014

Open Access 01-12-2014 | Research article

A systematic review and meta-synthesis of the impact of low back pain on people’s lives

Authors: Robert Froud, Sue Patterson, Sandra Eldridge, Clive Seale, Tamar Pincus, Dévan Rajendran, Christian Fossum, Martin Underwood

Published in: BMC Musculoskeletal Disorders | Issue 1/2014

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Abstract

Background

Low back pain (LBP) is a common and costly problem that many interpret within a biopsychosocial model. There is renewed concern that core-sets of outcome measures do not capture what is important. To inform debate about the coverage of back pain outcome measure core-sets, and to suggest areas worthy of exploration within healthcare consultations, we have synthesised the qualitative literature on the impact of low back pain on people’s lives.

Methods

Two reviewers searched CINAHL, Embase, PsycINFO, PEDro, and Medline, identifying qualitative studies of people’s experiences of non-specific LBP. Abstracted data were thematic coded and synthesised using a meta-ethnographic, and a meta-narrative approach.

Results

We included 49 papers describing 42 studies. Patients are concerned with engagement in meaningful activities; but they also want to be believed and have their experiences and identity, as someone ‘doing battle’ with pain, validated. Patients seek diagnosis, treatment, and cure, but also reassurance of the absence of pathology. Some struggle to meet social expectations and obligations. When these are achieved, the credibility of their pain/disability claims can be jeopardised. Others withdraw, fearful of disapproval, or unable or unwilling to accommodate social demands. Patients generally seek to regain their pre-pain levels of health, and physical and emotional stability. After time, this can be perceived to become unrealistic and some adjust their expectations accordingly.

Conclusions

The social component of the biopsychosocial model is important to patients but not well represented in current core-sets of outcome measures. Clinicians should appreciate that the broader impact of low back pain includes social factors; this may be crucial to improving patients’ experiences of health care. Researchers should consider social factors to help develop a portfolio of more relevant outcome measures.
Appendix
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Metadata
Title
A systematic review and meta-synthesis of the impact of low back pain on people’s lives
Authors
Robert Froud
Sue Patterson
Sandra Eldridge
Clive Seale
Tamar Pincus
Dévan Rajendran
Christian Fossum
Martin Underwood
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Musculoskeletal Disorders / Issue 1/2014
Electronic ISSN: 1471-2474
DOI
https://doi.org/10.1186/1471-2474-15-50

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