Abstract

BackgroundSeverely disabling chronic pain in the adult population is strongly associated with a range of negative health consequences for individuals and high health care costs, yet its prevalence in young adults is less clear.MethodsAll adults aged 18–25 years old registered with three general practices in North Staffordshire were invited to complete a postal questionnaire containing questions on pain within the last 6 months, pain location and duration. Severity of chronic pain was assessed by the Chronic Pain Grade. Severely disabling chronic pain was defined as pain within the last six months that had lasted for three months or more and was highly disabling-severely limiting (Grade IV).Results858 responses from 2,389 were received (adjusted response = 37.0%). The prevalence of any pain within the previous six months was 66.9% (95%CI: 63.7%, 70.1%). Chronic pain was reported by 14.3% (95%CI: 12.0%, 16.8%) of respondents with severely disabling chronic pain affecting 3.0% (95%CI: 2.0%, 4.4%) of this population. Late responders were very similar to early responders in their prevalence of pain. Cross-checking the practice register against the electoral roll suggested register inaccuracies contributed to non-response.ConclusionPain is a common phenomenon encountered by young adults, affecting 66.9% of this study population. Previously observed age-related trends in severely disabling chronic pain in older adults extend to younger adults. Although a small minority of younger adults are affected, they are likely to represent a group with particularly high health care needs. High levels of non-response in the present study means that these estimates should be interpreted cautiously although there was no evidence of non-response bias.

Highlights

  • Disabling chronic pain in the adult population is strongly associated with a range of negative health consequences for individuals and high health care costs, yet its prevalence in young adults is less clear

  • Previous reviews have failed to identify a clear explanation for differences between studies in prevalence estimates for chronic pain in the adult population [1] and in young adults differences in case definition, specific age banding used to define young adults, sampling frame, and method of data collection do not appear to be consistently associated with variation in prevalence estimates between previous studies

  • The unique contribution of this study is to provide for the first time an estimate for the prevalence of severely disabling chronic pain in young adults

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Summary

Introduction

Disabling chronic pain in the adult population is strongly associated with a range of negative health consequences for individuals and high health care costs, yet its prevalence in young adults is less clear. Different definitions of chronic pain have been used in these epidemiological studies, differentiating chronic pain on the basis of global severity appears to identify important subgroups [2]. Compared with chronic pain of mild intensity and minimal disability, individuals with severely disabling chronic pain are more likely to have long-term limiting illness and comorbid health conditions, to report poorer self-rated health, mental well-being and social functioning, have higher levels of depression and work loss, and account for (page number not for citation purposes). Response rate Definition of chronic pain (CP) and Prevalence in disabling chronic pain (DCP) young adults.

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