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Elaine Thomas a Arthritis Research Campaign Epidemiology
Unit, School of Epidemiology and Health Sciences, Medical School,
University of Manchester, Manchester M13 9PT, b University of Keele, School of
Postgraduate Medicine, Industrial and Community Health Research Centre,
Hartshill, Stoke on Trent ST4 7QB, c Rheumatic Diseases Centre,
University of Manchester, Clinical Sciences Building, Hope Hospital,
Salford M6 8HD
Correspondence to: GJ Macfarlane
G.Macfarlane{at}man.ac.uk
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Abstract |
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Objectives:
To quantify the relative contribution of
premorbid and episode specific factors in determining the long term
persistence of disabling symptoms of low back pain.
Design:
Prospective cohort study.
Setting:
Two general practices in the south Manchester area.
Participants:
180 patients, who previously
participated in a cross sectional population survey, who consulted
because of low back pain during the study period. They were followed at 1 week and 3 and 12 months after consultation.
Main outcome measure:
Persistent disabling low back
pain in the 12 months after the consultation.
Results:
Disabling low back pain persisted in
one third of participants after consultation and was more common with
increasing age, among those with a history of low back pain, and in
women. Persistence of symptoms was associated with "premorbid"
factors (high levels of psychological distress (odds ratio 3.3; 95%
confidence interval 1.5 to 7.2), poor self rated health (3.6; 1.9 to
6.8), low levels of physical activity (2.8; 1.4 to 5.6), smoking (2.1; 1.0 to 4.3), dissatisfaction with employment (2.4; 1.3 to 4.5)) and
factors related to the episode of low back pain (duration of symptoms,
pain radiating to the leg (2.6; 1.3 to 5.1), widespread pain (6.4; 2.7 to 15), and restriction in spinal mobility). A multivariate model based
on six factors identified groups whose likelihood of persistent
symptoms ranged from 6% to 70%.
Conclusions:
The presence of persistent low back pain
is determined not only by clinical factors associated with pain but also by the premorbid state.
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Key messages
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Introduction |
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Each year in the United Kingdom 7% of the adult population present to their general practitioner with low back pain1 at a cost in excess of £500 million to the NHS.2 Episodes of acute back pain are perceived to resolve rapidly with only a small proportion of sufferers experiencing persistent or recurrent symptoms leading to disability. Most of the costs linked to the treatment of back pain apply to this small proportion.
Clearly, it would be advantageous with respect to clinical management to be able to identify at presentation those patients at high risk of persistent disabling symptoms. Prediction of outcome has been examined previously with two main sources of prognostic factors: clinical data directly related to the pain episode and health, lifestyle, and individual factors. In all studies to date, however, health, lifestyle, and individual factors have been recorded after the onset of symptoms and may therefore have been influenced by the pain episode.
We used a prospective design to quantify the contribution,
firstly, of health, lifestyle, and individual factors measured before
the onset of the episode of low back pain leading to consultation and,
secondly, of factors specific to the episode, in predicting the long
term persistence of symptoms. We also determined whether subjects at
high risk of persistent disabling symptoms can be identified early on
the basis of such factors.
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Participants and methods |
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Cohort recruitment
Eligible participants were those registered with two
general practices in the south Manchester area who had participated in
a previous cross sectional study3 and had consulted because of low back pain during the subsequent 18 month study period
(fig). Ethical approval was obtained from the local health authority.
The survey had included information on demographic data, lifestyle
factors including levels of physical activity, smoking status, a single
question on self rated general health,4 and the 12 item
general health questionnaire5 to measure participants' levels of "psychological distress" and current (during the past month) and past low back pain. The lower back was defined, on a
manikin, as the area bordered above by the 12th rib and below by the
gluteal folds.
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Cohort follow up
During the 18 month study period all consultations for low
back pain were identified weekly by using the general practices'
computerised records systems. Participants had a home interview and
examination carried out by a research nurse. The median time between
consultation and the nurse visit was 1 week (interquartile range 1-2 weeks).
Outcome
At each of the three interviews participants were
asked about the presence of low back pain on that day and asked to mark
the severity of any pain on a visual analogue scale from 0 to 10; a
score of 0 or 1 was defined as no pain. Disability was measured at each
of the three interviews with the Hanover back pain activity
schedule.8 This schedule was developed for use in subjects
with back pain and has been found to compare well with other similar
instruments. It inquires about the ease of carrying out 12 items of
daily activity in the previous 2 weeks, with scores for each item being
summed to a percentage value where 100% represents total ability.
Statistical analysis
The analysis examined the relation between persistent
disabling low back pain and, firstly, premorbid factors and, secondly,
episode specific factors, among those participants who had consulted
with an episode of low back pain which started after recruitment to the
study. Univariate analysis assessed the individual associations of
these putative risk factors and are presented as odds ratios with 95%
confidence intervals. When we considered premorbid and episode specific
factors together, those variables significantly associated with
persistent symptoms were used in a backwards stepwise logistic
regression procedure to determine whether a small group of factors
could accurately predict those patients who would have persistent
disabling symptoms.
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Results |
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During the 18 month study period consultations were recorded for 442 of the 4501 participants (9.8%) from the cross sectional study conducted in the study general practices. Interviews 1 week after consultation were completed for 294. We defined a new episode to be where pain that caused the consultation started after the cross sectional survey was carried out, which resulted in the exclusion of 48 participants whose episode of back pain had started before this. Hence 246 subjects were eligible for follow up, of whom 180 provided complete information at 1 week and 3 and 12 months after consultation and are the subjects used in further analyses.
Outcome of low back pain
The percentage of participants who
reported disabling low back pain was 73% at 1 week and 48% at 3 months, with only a slight subsequent decrease to 42% at 12 months
after consultation. About a third (61; 34%) of participants were
classified as having persistent disabling low back pain
that is, low
back pain with related disability at each of the three follow up
interviews (table 1).
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Sex and age predicted persistent
disabling low back pain: a doubling in odds of a poor outcome was seen
for women compared with men (odds ratio 2.1; 95% confidence interval 1.1 to 4.1) and the likelihood of a poor outcome increased with older
age. Premorbid factors (that is, measured before the onset of the
consulting episode) associated with a poor outcome were high levels of
psychological distress, below average self rated health, low levels of
physical activity, a history of low back pain, current or previous
smoking, a low alcohol intake, not being employed, and dissatisfaction
with current employment or work status. Each of the factors was
associated with a twofold to fivefold increase in odds of persistent
symptoms (table 2).
Episode specific factors
The strongest episode
specific predictor of a poor outcome was the presence of widespread
pain (axial skeletal pain in addition to pain above and below the waist
and on the right and left side of the body); it was associated with a
sixfold increase in odds of a poor outcome (6.4; 2.7 to 15.0). A long duration of symptoms before consultation, the reporting of radiating leg pain, and restriction in spinal movement were also significantly associated with a twofold to fivefold increase in odds of a poor outcome (table 3).
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All premorbid and
episode specific factors that were significantly associated with
outcome were candidate variables for a stepwise logistic regression
model. The final model consisted of six factors: two premorbid (history
of low back pain, dissatisfaction with current employment or work
status), three episode specific (widespread pain, radiating leg pain,
restriction in two or more spinal movements), and sex (table 4). When
we used the jack knife procedure the outcome of 74% of participants was correctly classified with a higher negative predictive value (77%)
than positive predictive value (60%). The likelihood of persistent
disabling low back pain increased with the number of factors reported:
only 6% of the participants who reported fewer than three factors had
a poor outcome compared with 70% of participants who reported more
than four (table 5).
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Among patients who consulted with
low back pain and who were eligible to participate in this follow up
study, 148 (33%) refused to participate in the initial interview or
were not contacted for logistical reasons. Information on
premorbid factors found to predict poor outcome is shown for these
non-participants compared with participants in table 6.
Non-participants were more likely to be women and aged under 45 years
but otherwise did not differ. Sixty six participants initially
interviewed were subsequently lost to follow up. In table 7 they are
compared with those who completed follow up with respect to premorbid
and episode specific factors. Participants lost to follow up were younger but did not differ with respect to any other predictors of
outcome.
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Discussion |
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We have previously shown in this population that chronic symptoms are common after consultation for a new episode of low back pain.10 By using a small group of factors, both premorbid and specific to the episode, we have now shown that it is possible to define groups at high risk of a poor outcome. In comparison with the population reported in our previous paper on outcome,10 the current study population includes only those who participated in the cross sectional survey, patients consulting with back pain over the subsequent 18 month period (instead of 12 months), and those whose episode of pain started after the population survey.
Comparisons with other studies
Studies examining outcome in a cross sectional fashion at 1 year have found a poor outcome in 30-50% of
subjects,11-14 which is consistent with our finding that
34% of participants have persistent disabling pain. Results from a
recent study from the Netherlands found that at 12 months after the
initial consultation only 10% still suffered from the same episode of
pain which had originally led to consultation and that 75% had
reported at least one recurrence in the 12 month period.15
It is therefore likely that the group in the current study with
"persistent" pain are a combination of subjects with continuous
pain and those who had one or multiple recurrences during the follow up period.
that is,
patients with a less mobile spine have more severe symptoms.
Alternatively, as suggested in a cross sectional study examining the
relation between behavioural and biomechanical factors, restriction may
be associated with pain tolerance that is, in turn, subject to
psychological influences.24 A further analysis in the
present study, that stratified participants according to high and low
levels of psychological distress, showed that restriction in spinal
movements predicted poor outcome in both groups, suggesting that the
former may be the more likely explanation.
Potential bias
A concern in any follow up study is the possibility of bias
occurring due to loss to follow up at various stages. These losses are
to some extent inevitable in a study from an urban population. We have
investigated the potential for such biases on our results. With the
exception of age and sex, participants who were not followed up or who
were lost to follow up did not differ from those who were recruited and
studied for the entire follow up period in terms of factors that
predicted outcome. This increased propensity for loss in the younger
participants may be due, in part, to their moving out of the area.
These differences would bias our results, however, only if their
relation with outcome was different in participants and
non-participants. Overall, our data do not suggest any important biases
that would prevent our results being extrapolated to all those eligible
to be followed up.
Conclusions
In conclusion, we have shown that a substantial proportion
of patients who present to primary care with low back pain will have
persistent symptoms over the 12 months after consultation. By uniquely
collecting data on risk factors before the onset of the pain that
resulted in the consultation, we have shown that the presence of
persistent low back pain is not only determined by clinical factors
associated with pain but also by the premorbid state. On the basis of
five variables which are easily collected at the time of consultation
and an examination of spinal movement, we were able to define a group
who had a high risk of persistent symptoms of low back pain during the
follow up year. Furthermore, patients with these adverse prognostic
factors are likely to represent those in whom potentially effective
interventions would have the greatest impact in terms of morbidity and
healthcare costs.
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Acknowledgments |
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We thank the partners, staff, and patients of Brooklands and Bowland General Practices, Manchester, for help with conducting the study. Margaret Carrington, Jane Barnett, and Hannah Chambers carried out the study interviews.
Contributors: PRC, AJS, and ACP designed the study protocol, discussed core ideas, coordinated the study, and participated in analysis and interpretation of data and writing the paper. ET and GJM discussed core ideas and participated in data analysis and interpretation and took the lead in the writing of the paper. MIVJ participated in the design and development of the study and the writing of the paper. All the authors are guarantors for the paper.
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Footnotes |
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Funding: Arthritis Research Campaign and the National Back Pain Association.
Competing interests: None declared.
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References |
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(Accepted 31 March 1999)
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