Abstract

Chronic low back pain (cLBP) is the most common reason for individual suffering and health care utilization in adults. Ample evidence suggests sociodemographic variables and socioeconomic status (SES) influence pain. However, a framework informing associations on race, SES, and the utilization of pharmacologic therapies and provider type are limited—particularly in cLBP. Thus, this study examined the extent to which sociodemographic (i.e., age, race, and gender) and socioeconomic factors (i.e., national area deprivation index, NADI) influence pain treatment (i.e., NSAIDs, opioids, antidepressants, and non-NSAIDs) and provider utilization for cLBP (i.e., no provider care, primary care, or tertiary care). Eligible participants with cLBP completed a series of questionnaires. Of the 174 participants, 58% were women, 59% were non-Hispanic Black (NHB), and the mean age was 46.10 (SD 13.58). Based on NADI distributions by race, NHB participants lived in more socioeconomically disadvantaged neighborhoods (p < 0.001) than non-Hispanic White (NHW) adults. Results suggested that the use of one or more pharmacologic therapies was associated with race (p = 0.021). Specifically, NHW adults were two times more likely to take one or more pharmacologic therapies than NHBs (p = 0.009). NHWs were also more likely to use NSAIDs (p = 0.041) and antidepressants (p < 0.001) than NHBs. Furthermore, provider utilization was significantly associated with gender (p = 0.037) and age (p = 0.018); which suggests older women were more likely to use primary or tertiary care. Findings from this study expand on the existing literature as it relates to associations between disparities in access to healthcare providers and access to medications. Future research should seek to understand differences in age and utilization of primary or tertiary care providers and continue to examine the influence of sociodemographic and SES factors to cLBP and compare with other types of chronic pain.

Highlights

  • Chronic pain is a public health problem that imposes a significant social and economic burden and reduces the quality of life and well-being for adults worldwide [1,2,3,4,5,6,7]

  • Our analysis revealed 50% of women used a primary care provider for Chronic low back pain (cLBP) compared to 42% of men and 33% of women used a tertiary care provider for cLBP compared to 26% of men

  • Men were more likely to report the use of no primary care provider for cLBP than women (33% compared to 18%, respectively)

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Summary

Introduction

Chronic pain is a public health problem that imposes a significant social and economic burden and reduces the quality of life and well-being for adults worldwide [1,2,3,4,5,6,7]. The experience of pain can be influenced by several factors, including, but not limited to, race, socioeconomic status (SES) and neighborhood-level characteristics, advanced age, and gender [9, 10]. Adults with cLBP from low SES experience significant financial burden, decreased quality of life from chronic pain symptoms, and greater morbidity and mortality than individuals at higher SES levels [12,13,14]

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