Pain among veterans with spinal cord injury

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The Department of Veterans Affairs Veterans Health Administration cares for approximately 15% of persons with spinal cord injury (SCI) in the United States.
Findings from this study confirm prior reports that pain among veterans with SCI, while at clinically significant levels, may not be greater than pain found among nonveterans. Furthermore, results suggest that pain-related catastrophizing may be a particular concern in this group. Future research might examine these models with prospective and experimental designs, allowing for more careful examinations of causality.

     

The Department of Veterans Affairs Veterans Health Administration cares for approximately 15% of persons with spinal cord injury (SCI) in the United States. However, the nature and characteristics of pain among veterans with SCI are not well understood. This study used a postal survey to compare veterans with SCI and nonveterans with SCI on pain intensity; pain interference; functioning; and other pain, demographic, and medical characteristics. Veterans tended to be older than nonveterans but these groups were otherwise comparable on demographic and medical variables.

Veterans were not significantly different from nonveterans on pain intensity or pain interference. Veterans reported lower levels of functioning than nonveterans and higher levels of pain-related catastrophizing. However, differences in functioning between veterans and non-veterans were attributable to age differences between the groups. In summary, differences between veterans with SCI and nonveterans with SCI were few and small in magnitude, suggesting that veterans with SCI are not at greater risk for pain and pain-related problems. However, pain-related catastrophizing may be a particular concern among veterans with SCI.

Most persons with spinal cord injury (SCI) endure chronic pain for years after their acute injuries are healed and rehabilitation is complete. Studies estimate that the prevalence of chronic pain after SCI is more than 75 percent [13]. Persons with SCI consistently report average pain levels between 4 and 6 in studies using the 0-10 numerical rating scale (NRS) [45], pain levels that are high enough to warrant comprehensive treatment and prompt follow-up in primary-care settings [6]. Pain is severe, with a strong negative impact on daily functioning, in about one-third of persons with SCI [12]. Of significant concern is the finding that once pain conditions following SCI emerge, they tend to persist [34] or worsen [2,7] over time, despite the many efforts to treat this pain. In summary, while pain is a ubiquitous, recalcitrant problem among persons with SCI, the degree to which pain has a pronounced effect on functioning is much more variable.
Developing a better understanding of subgroups of persons with SCI that may be especially vulnerable to pain-related functional disruptions is critical.
Veterans with SCI are a necessary focus of clinical pain research for several reasons. First, approximately 15 percent of persons with SCI in the United States are veterans, making the Department of Veterans Affairs (VA) Veterans Health Administration (VHA) the largest single network of SCI care in the nation [8]. Second, veterans as a group tend to experience a greater number of socioeconomic and lifestyle risk factors for disease and pain.
Compared with the general population, veterans are more likely to be male, older, single, unemployed, and less educated and to have lower income [9]. Third, veterans are also more likely to smoke [910] and drink heavily [11]. With this constellation of risk factors, it is not surprising that veterans have more comorbid medical conditions than their counterparts in the general population [9], and thus veterans might be expected to experience greater pain and pain-related problems than nonveterans. In support of this position, prior research has shown older age [12], poorer health status [3], unemployment [5], and lower education [5] to be associated with pain following SCI. However, demographic factors are notoriously inconsistent predictors of pain following SCI [13], making replication of research in this population all the more important.
We are aware of two studies that have compared veterans with SCI and nonveterans with SCI on pain and pain-related factors. Martz and colleagues found that veterans with SCI differed from nonveterans with SCI in ethnicity, marital status, work status, age, and cause of SCI [14]. However, NRS pain intensity scores were similar for veterans and nonveterans with SCI in their sample [14]. Rintala and colleagues found that veterans with SCI were older and reported higher levels of perceived psychological stress [15], as measured by the Perceived Stress Scale [16], than nonveterans with SCI.
Life stress has been shown to be an important predictor of pain among persons with medical conditions [1719]. How veterans with SCI compare with nonveterans in terms of other important pain constructs such as pain interference (the extent to which pain interferes with daily functioning) and catastrophizing (exaggerated negative interpretations of pain, e.g., “my pain is unbearable and will never get better”) is unknown. Pain-related catastrophizing is a particularly important variable to study, given its consistent and strong association with pain-related dysfunction in persons with SCI [20] and other medical conditions [21]. Specifically, cognitive errors such as catastrophizing may explain the impact of pain on daily functioning [22]. For example, persons who think “I cannot do anything when I am in pain” may be less likely to engage in important activities of daily living when their pain is high.
The objective of this study was to compare veterans with SCI and nonveterans with SCI on a number of important pain and functioning measures.
We hypothesized that, compared with nonveterans, veterans would evidence higher pain intensity scores and lower functioning scores on most if not all measures. We advanced this hypothesis in spite of somewhat contrary findings by Martz and colleagues [14] because we suspected that the NRS as the sole pain instrument in that study may not have been adequate to detect differences between these groups that would be expected based on socioeconomic and disease burden disparities.
Furthermore, replication of the Martz et al. study [14] using an array of pain and pain-related measures would represent an important contribution to the scientific literature. We also predicted that catastrophizing would demonstrate strong associations with functioning in our veteran sample, which would replicate findings from studies conducted among nonveterans with SCI.
Most persons with SCI can expect to experience some pain for years following injury, but little is known about which persons with SCI are at greater risk for pain-related disruptions in functioning. This study found little evidence that veterans with SCI are at greater risk for pain-related problems than nonveterans with SCI.
Veterans in this sample showed pain intensity scores in the moderate range [33], comparable to scores reported by nonveterans in this sample and to veterans with SCI in other reports [34]. Lack of significant differences in pain intensity between veterans and nonveterans was inconsistent with our hypotheses but was consistent with findings from the one prior study we are aware of that compared veterans and nonveterans with SCI on pain intensity [14].
Veterans with SCI differed significantly from nonveterans on functioning, reporting lower scores on measures of social integration and productive activity. However, our follow-up analyses suggested that these differences were explained by differences in age between samples. The single difference between veterans and nonveterans that remained robust in models controlling for age was the presence of higher levels of catastrophizing among veterans with SCI than among nonveterans with SCI.
Catastrophizing was higher among veterans in this sample, was associated with reduced functioning and higher pain intensity, and appeared to mediate associations between pain intensity and functioning. These findings replicate results of numerous other studies that have demonstrated the importance of catastrophizing in pain and pain-related dysfunction [2021,35].
Catastrophizing is conceptualized as a mediating factor between pain and functioning in most biopsychosocial models of chronic pain. For example, painful stimuli may activate “pain schemas,” or memory patterns related to pain, that support cognitive biases such as catastrophizing [21]. Biases in cognitive-processing can involve enhanced memory for, or attention toward, negatively valenced self- and illness-related information [21]. In other words, the effect of catastrophizing may be to heighten the threat of pain while highlighting inadequacies in personal coping resources, with a resultant negative impact on functioning [21,35]. The present findings are consistent with prior research among persons with SCI that supports the position that catastrophizing mediates associations between pain and functional outcomes [22].
We must discuss the unexpected finding that our sample of veterans was quite similar to the nonveterans in terms of demographic variables, as well as other pain-related variables.
With the exception of age, veterans and nonveterans were similar on demographic factors, although we expected the veterans and nonveterans to differ in terms of marital status, ethnicity, employment, and education, based on findings from large-scale epidemiological studies [9]. The implication is that results of the present study may not generalize well to veterans with SCI as a group. For example, our sample was nearly 90 percent Caucasian, whereas in the general veteran population approximately 80 percent are Caucasian [36]. Ethnicity is a particularly important demographic factor to consider when one interprets results of studies of SCI pain, because non-Caucasian persons with SCI may tend to report higher pain intensity and greater levels of pain interference [37].
On the other hand, the similarities found between veterans and nonveterans in this study may not be a result of sampling problems, but instead may reflect true characteristics of these groups. Martz and colleagues also found that veterans with SCI were similar to nonveterans with SCI in terms of pain levels, and they used a sample that demographically well represented the veteran population [14]. In parallel research involving persons with amputations, veterans were similar to nonveterans in pain characteristics [38].
SCI and other physical disabilities may serve to level veteran and nonveteran groups on factors where differences are typically found. In other words, the impact of SCI may outweigh the influence of other factors that typically account for differences between veteran and nonveteran groups. Also, important differences may exist in healthcare services received between these two groups, which could account for similarities in pain characteristics where dissimilarities were expected. Specifically, veterans with SCI receive monthly disability compensation, with additional compensation available to those veterans with greater levels of disability [8].
Compared with nonveterans with SCI, veterans with SCI may have greater access to multidisciplinary care and comprehensive psychosocial and healthcare services [8]. Finally, the lack of large differences between veterans and nonveterans in this study and past research may relate to veterans tending to be older than other patient groups; age may actually represent a protective factor in risk for pain-related problems. In persons with amputation [39] and other persons with chronic pain [40], pain appears to show a weaker association with disability than among younger patients. In other words, while older adults do experience increased incidence of pain, pain-related suffering and disability may attenuate as a function of the aging experience (cf. Molton et al. [39]).
Additional limitations to the study should be noted. Conditions under which the mailed self-report surveys were completed are unknown and could have influenced responses. Additionally, survey response rates may have been affected by the fact that many persons with SCI are unable to write; this point is particularly important to this study given the low numbers of persons with high-level injuries who responded. Administration of self-report questionnaires in controlled settings might be preferable to ensure data integrity and possibly to improve response rates.
Also, as in a prior study of veterans with SCI, surveys might be administered by telephone [41]. This study was also limited by the low number of respondents with higher-level cervical injuries. Veterans were less likely to respond to the survey questionnaire, again raising questions about how well these results might generalize to the veteran population as a whole.
CONCLUSION:
Findings from this study confirm prior reports that pain among veterans with SCI, while at clinically significant levels, may not be greater than pain found among nonveterans. Furthermore, results suggest that pain-related catastrophizing may be a particular concern in this group. Future research might examine these models with prospective and experimental designs, allowing for more careful examinations of causality.
In clinical settings, researchers may find it important to assess and manage catastrophizing as a factor important to the experience of pain, especially the impact of pain on functioning. Cognitive behavioral strategies are known to be effective in the management of pain-related catastrophizing in numerous populations with chronic illness [42]. Catastrophizing may be one factor of relevance in pain-treatment-matching paradigms that have been proposed for patients with SCI [42].
We gratefully acknowledge the contributions by Rob Hendricks, PhD, Spinal Cord Injury and Disorders Service, VA, Seattle, Washington; and data collection and database management by Amy Hoffman, Lindsay Washington, Emily Phelps, Laura Nishimura, Kristin McArthur, Kevin Gertz, Noel Pereyra-Johnston, Silvia Amtmann, Joe Skala, and Kerry Madrone, University of Washington School of Medicine Department of Rehabilitation Medicine, Seattle, Washington.
This material is based on work supported in part by grant P01 HD33988 from the National Institutes of Health, National Institute of Child Health and Human Development, National Center for Rehabilitation Research; grant H133N00003 from the National Institute on Disability and Rehabilitation Research, Office of Special Education and Rehabilitative Services, U.S. Department of Education; grant SCT 01-169 from the VA, VHA, Health Services Research and Development (HSR&D) Service, SCI Quality Enhancement Research Initiative.
This article presents the views of the authors; it does not necessarily represent the views or policies of the VA or the HSR&D Service.
The authors have declared that no competing interests exist.

Philip M. Ullrich, PhD,1,2* Mark P. Jensen, PhD,2 John D. Loeser, MD,3 Diana D. Cardenas, MD, MHA,4 and Frances M. Weaver, PhD5
1Department of Veterans Affairs (VA) Spinal Cord Injury Quality Enhancement Research Initiative (SCI QUERI), VA Puget Sound Healthcare System, Seattle, WA
2Department of Rehabilitation Medicine, University of Washington, Seattle, WA
3Department of Neurological Surgery, University of Washington, Seattle, WA
4Department of Rehabilitation Medicine, University of Miami, Miller School of Medicine, Miami, FL
5VA SCI QUERI, Edward Hines Jr VA Hospital, Hines, IL
*Address all correspondence to Philip Ullrich, PhD; HSR&D, 1100 Olive Way, Suite 1400, Seattle, WA 98101; 206-277-3911; fax: 206-764-2935. Email: [email protected]

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