Montana Disability &
Health Home Page |
RTC: Rural |
Rural Institute
| University of Montana
| Publications |
Training Calendar |
Resource Directory

Rural Disability and Rehabilitation Research Progress Report #20
Pain as a Secondary Condition Experienced by Rural Medicaid Beneficiaries with Disabilities
Research and Training Center on Disability in Rural Communities, The University of Montana Rural Institute February 2004
Secondary conditions are disability-related problems that
further limit a person's ability to engage in daily activities. People
who live independently in the community and who have mobility impairments
consistently report being limited by 14 secondary conditions annually.
Background:
As many as 80% of people with primary disabilities
report pain as a secondary condition (Ehde, Jensen,
Engel, Joyce, Turner, Hoffman, & Cardenas, 2003). Although pain may be a sign of
acute physical trauma, it often lingers long after an injury. In many instances
there is no discernable etiology (such as an injury) for pain. Over time what
may have begun as a minor ache slowly develops into a chronic, limiting
secondary condition.
In our previous work on identifying and removing barriers to health promotion
and physical activity, rural people with mobility impairments identified pain as
a greater barrier than their needs for transportation, accessibility and
personal assistance.
This brief research report is the first in a two-part series which describes how
Medicaid recipients with disabilities in two rural counties experience pain as a
secondary condition.
Methods:
Working with Montana and Maine Medicaid departments, we
identified all Medicaid beneficiaries in one rural county of each state
(N=6852). We mailed each beneficiary a letter that described study eligibility
criteria (i.e. 18 to 65 years old with a permanent mobility impairment) and a
postage paid return postcard with census-type disability questions. Using the
returned post-cards, we identified 469 individuals who were eligible and agreed
to complete surveys in return for $10 stipends. We received usable returns from
286 individuals for a 60.9% response rate.
In addition to basic demographic information, the survey included items from the
Behavior Risk Factor Surveillance System, Radloff's Centers for
Epidemiological Study of Depression Scale (CES-D, 1977), the Pain
Disability Index (Tait, Chibnall, & Krause,1990) and a health-related
Quality of Life Scale (Hadorn & Ubersax, 1995). The CES-D is a 20-item
measure of depression symptoms. The Pain Disability Index has respondents
rate the degree to which pain limits them in each of seven life areas.
We submitted study variables, including demographic information, to two
different exploratory regression analyses. The first, a logistic analysis, was
used to predict whether or not respondents reported pain as a secondary
condition. We used a forward conditional method for model building in this
analysis. Then we submitted the same predictor variables to a linear regression
analysis to predict disability due to pain as measured by the Pain Disability
Index. We used a stepwise method for model building in this analysis.
Results:
Of the 286 survey respondents, 208 (75.1%) reported ongoing pain (burning,
tingling, aching). Because this cross-disability sample included numerous
diagnoses, Table 1 shows the proportion of individuals reporting pain by each
condition. While the proportion of pain varies across conditions, clearly most
primary disability categories experienced pain as a secondary condition. We
computed chi-square for each contingency (i.e. impairment by pain status), and
Table 1 notes statistically significant associations. Also, because arthritis is
both a very prevalent primary impairment and a secondary condition, we include
the number in each disability group that did not also report arthritis. Table 1
highlights that pain is a problem across most disability groups even when the
effect of having arthritis is eliminated. Note: Conditions with fewer than 5
cases represented do not meet assumptions for Chi-square significance testing.
Table 1: Pain by Primary Impairment Group.
Description of
table.
| Condition | Overall N | % with pain | N without arthritis | % with pain, but without arthritis |
| Amputation | 6 | 66.6 | 4 | 75 |
| Arthritis | 159 | 86.8* | - | - |
| Blind/Low Vision | 29 | 62.1* | 21 | 61.9 |
| Cardiovascular Disease | 53 | 67.9 | 25 | 52 |
| Cerebral Palsy | 3 | 0 | 3 | 0 |
| Deafness | 21 | 76.2 | 2 | 0 |
| Multiple Sclerosis | 6 | 66.6 | 5 | 60.0 |
| Muscular Dystrophy | 5 | 60.0 | 5 | 60.0 |
| Post-polio | 4 | 75.0 | 2 | 50.0 |
| Spinal Cord Injury | 39 | 92.3* | 12 | 100.0 |
| Hearing Impairment | 21 | 85.7 | 6 | 100.0 |
| Other | 54 | 57.4* | 54 | 57.4 |
Results of the regression
analyses identified an overlapping set of predictor variables for both the
presence of pain and for the disability outcome of pain. For the logistic
regression, 178 individuals reported having pain and 53 indicated they did not.
The first variable to enter the equation was "quality of life". For each
one-point increase on the 10-point quality of life scale, there was a 36.6%
reduction in the likelihood of reporting pain as a secondary condition. The next
variable was "nights with poor sleep". There was a 6.7% increase in the
likelihood of reported pain for each night of poor sleep. The third variable was
"number of hours worked per average week". For each hour of work reported, the
likelihood of reported pain was 3.7% lower. Finally, "age" entered the equation
with a 2.7% decrease in likelihood of reported pain for each year of age.
Overall, this model predicted 29% of the variance in the presence or absence of
pain as a secondary condition and correctly classified 81.4% of respondents'
pain status.
It is worth noting that "depression", as measured by the CES-D, did not enter
this equation and is not associated with the presence or absence of pain in this
sample. Other variables that did not enter the equation included "gender", daily
number of "hours out of bed", weekly number of "days out of the house", and
monthly number of days "individual feels energetic".
The linear regression on the Pain Disability Index demonstrated partial
overlap of the predictors observed in the logistic analysis with one notable
exception. Depression (measured by the CES-D) was the first variable to enter
the equation and accounted for 16.9% of variance in pain disability ratings. The
number of days respondents felt energetic per month accounted for an additional
6.0% of the variance in pain disability. Lastly, typical hours worked per week
accounted for an additional 2.8% of the variance. Overall, these three variables
accounted for 25.7% of the variance in pain disability ratings.
Variables that did not enter the equation included age, gender, daily number of
hours out of bed, weekly number of days out of the house, quality of life, and
number of nights of poor sleep.
Discussion:
We used survey data to identify individuals who report
pain as a secondary condition, and then constructed two regression models to
predict both the incidence of pain and the severity of limitation due to pain. A
substantial proportion of the sample reported pain as a secondary condition and
their reports were associated with a number of other study variables.
Limitations of the study include the self-reported data collection and the
modest proportion of the eligible population completing the instrument. There
was no way to investigate the data for systematic differences between responders
and non-responders. Finally, the independent variable "hours per week spent
working" is not normally distributed in this sample. Hence, this parameter
estimate may not accurately reflect the true value of this effect if work hours
for the population of Medicaid beneficiaries with mobility impairments are
normally distributed.
This study is unique because it examines pain in a sample of people with various
types of impairment. It also examines predictors of the presence or absence of
pain, as well as the predictors of limitation due to pain. The association of
work hours and pain is a particularly valuable result. Due to this sample's
skewed distribution of work hours, these results must be interpreted with
caution, but they suggest pain reduces people's ability to work. In addition,
the number of hours people work is predictive of a significant proportion of the
variability in limitation from pain. A prospective intervention study that uses
"hours worked" as an outcome in this population might demonstrate that improved
pain outcomes lead to improved work outcomes.
Perhaps this study's most valuable finding is that depression was associated
with limitation from pain, but not with the simple presence or absence of pain.
The role of depression in these analyses highlights the difference between
simply having pain and having pain that limits activities. Many researchers have
reported the positive association between pain and depression. This study
highlights that depression is not necessarily associated with the presence of
pain, but rather is linked to the level of limitation caused by the pain. This
study does not allow us to determine whether pain causes depression or
depression causes pain; it is likely that the cause and effect are cybernetic,
with recursive effects between the two. Nonetheless, when Medicaid recipients
report limitation due to pain, they are also likely to report depression. These
findings may provide guidance for assessing and treating pain based on the
degree of limitation caused by the pain itself.
Pain exacts a toll even when it isn't associated with limitation. A person's
quality of life is affected both by the presence of pain and by the severity of
limitation caused by that pain. That is, individuals in this study might have
reported pain, but with very little pain-related limitation. The logistical
regression suggests that people reporting pain also perceive their health to be
worse and quality of life lower than people not reporting pain as a secondary
condition. The implication is that it is important to intervene in all pain,
even when the pain causes minimal limitation.
Resources and References:
Ehde, D.M., Jensen, M.P., Engel, J.M., Joyce, M., Turner, J.A. Hoffman, A.J. &
Cardenas, D.D. (2003). Chronic pain secondary to disability: A review.
Clinical Journal of Pain, 19 (1), 3-17.
Hadorn, D.C. & Ubersax, J. (1995). Large-scale health outcomes evaluation: How
should quality of life be measured? Part I, Calibration of a brief questionnaire
and a search for preference subgroups. Journal of Clinical Epidemiology,
48, 607-618.
Radloff, L. S. (1977). The Centers for Epidemiological Study of Depression
Scale: A self-report depression scale for research in the general population.
Applied Psychological Measurement, 1, 385-401.
Tait, R., Chibnall, J.T., & Krause, S. (1990.) The Pain Disability Index:
Psychometric properties. Pain, 40:171.
For more information, contact:
Craig Ravesloot, Director
of Health Projects
cravesloot@comcast.net
Office: 303-774-6196
Research and Training Center on
Disability in Rural Communities
The University of Montana Rural Institute: A Center of Excellence in Disability
Education, Research and Services, 52 Corbin Hall, Missoula, MT 59812-7056
888-268-2743 Toll-free
406-243-4200 TTY
406-243-2349 Fax
http://rtc.ruralinstitute.umt.edu
This
research is supported by grant #H133B030501 from the National Institute on
Disability and Rehabilitation Research, U.S. Department of Education. The
opinions expressed reflect those of the author and are not necessarily those of
the funding agency.
This report was prepared by Craig Ravesloot, RTC: Rural, 2004. It is also
available in standard print, large print, braille and as a DOS text file.
Montana Disability &
Health Home Page |
RTC: Rural |
Rural Institute
| University of Montana
| Publications |
Training Calendar |
Resource Directory