FROM:
European Spine Journal 2014 (Oct); 23 (10): 2046–2058 ~ FULL TEXT
Zoe A. Michaleff • Steven J. Kamper • Christopher G. Maher • Roni Evans • Carolyn Broderick • Nicholas Henschke
The George Institute for Global Health and Sydney Medical School,
The University of Sydney,
Kent Street, Sydney, 2000, Australia,
zmichaleff@georgeinstitute.org.au
PURPOSE: To identify and evaluate the effectiveness of conservative treatment approaches used in children and adolescents to manage and prevent low back pain (LBP).
METHODS: Five electronic databases and the reference lists of systematic reviews were searched for relevant studies. Randomised controlled trials (RCTs) were considered eligible for inclusion if they enrolled a sample of children or adolescents (<18 years old) and evaluated the effectiveness of any conservative intervention to treat or prevent LBP. Two authors independently screened search results, extracted data, assessed risk of bias using the PEDro scale, and rated the quality of evidence using the GRADE criteria.
RESULTS: Four RCTs on intervention and eleven RCTs on prevention of LBP were included. All included studies had a high risk of bias scoring ≤7 on the PEDro scale. For the treatment of LBP, a supervised exercise program compared to no treatment improved the average pain intensity over the past month by 2.9 points (95 % CI 1.6-4.1) measured by a 0–10 scale (2 studies; n = 125). For the prevention of LBP, there was moderate quality evidence to suggest back education and promotion programs are not effective in reducing LBP prevalence in children and adolescents.
CONCLUSIONS: While exercise interventions appear to be promising to treat LBP in children and adolescents, there is a dearth of research data relevant to paediatric populations. Future studies conducted in children and adolescents with LBP should incorporate what has been learnt from adult LBP research and be of rigorous methodological quality.
Keywords Low back pain , Systematic review, Children, Adolescents
From the FULL TEXT Article
Introduction
Low back pain (LBP) is a common and costly condition in
modern society. [1] While LBP has been comprehensively
researched in adults, it is only more recently that this
condition has been studied in children and adolescents. [2]
Epidemiological studies have reported the prevalence of
LBP to be low in children (1–6 %); however, it rises
sharply in adolescents (18–51 %) to approach the prevalence
in adults. [3–6] The impact of LBP on children and
adolescents is significant with up to 94 % of those with
pain experiencing some degree of disability. [7] The direct
cost to the healthcare system was estimated at a minimum
of €100 million per year in Germany alone. [8] Furthermore,
it has been suggested that LBP experienced during
childhood and adolescence increases the risk of LBP in
adulthood [9], possibly through the development of maladaptive
beliefs, behaviours, and attitudes related to the
earlier pain events. [2, 5]
Similar to LBP in adults, the pathology underlying the
pain in children and adolescents is not well understood and
symptoms are often managed using conservative treatment
approaches including exercise, massage and electrical
therapies. [10] While the effectiveness of many of these
conservative treatments has been evaluated for adult populations,
the spine of a child and adolescent is physiologically
different to the adult spine (i.e. ligamentous laxity,
bone composition, muscle mass) and, therefore, potentially
responds differently to various interventions, movements
and loading. [11, 12] Therefore, there is reason to evaluate
the efficacy of conservative interventions for LBP in this
specific patient population. Current international clinical
guidelines for the management of LBP are restricted to
evidence from studies performed on adult populations. [13]
Synthesis of the research regarding treatment for children
and adolescents with LBP is necessary to appraise the
available evidence and identify knowledge gaps. While
some reviews have already been conducted [14, 15], all
contain important methodological shortcomings. The aim
of this systematic review was to identify and evaluate the
effectiveness of conservative treatment approaches used to
manage and prevent LBP in children and adolescents.
Methods
This systematic review was performed following the
methods recommended by the Cochrane Back Review
Group. [16] From the results of a sensitive search strategy,
studies were included if they evaluated conservative
interventions for children and adolescents with LBP or
strategies to prevent LBP in children and adolescents.
Eligibility criteria
Randomised controlled trials (RCTs) were considered for
inclusion if they enrolled a sample of children or adolescents
(<18 years old). The findings were split into two
sections, appraising the evidence for conservative interventions
to treat LBP or strategies to prevent LBP. A
conservative intervention is defined as any non-invasive,
non-surgical form of treatment.
For the intervention section, outcome measures could
include pain, disability, global perceived effect or participation
in daily activities. Data on other outcomes such as
well-being or adverse effects were also considered and
reported where possible. To be included in the prevention
section, RCTs had to enrol children and adolescents with or
without LBP and evaluate strategies to prevent the onset or
development of LBP. Outcomes had to include LBP
intensity or back-related disability (either prevalence
thereof, or mean levels across the cohort). Studies that
measured cognitions or beliefs (e.g. back beliefs, knowledge
regarding risk factors), or proposed risk factors (e.g.
motor control, backpack usage, lifting behaviour) as an
outcome were included for descriptive purposes only.
Search methods for identification of studies
Electronic databases, including the Cochrane Central
Register of Controlled Trials, PubMed, EMBASE, PEDro,
and CINAHL, were searched for potentially eligible studies
from the earliest date up to 25th November 2013. Sensitive
search strategies were designed to identify all studies on
LBP related to children and adolescents (Appendix 1). In
addition, the reference lists of included RCTs and previous
systematic reviews were searched.
Data collection and analysis
Study selection
Two authors independently reviewed all titles and
abstracts identified by the electronic search to determine
their potential relevance for the intervention or prevention
parts of the review. Two authors also independently
applied all inclusion criteria to the full text of the articles
that passed the first eligibility screening. Disagreements
were resolved by consensus and where necessary, by a
third author.
Data extractionData extraction
Two authors independently extracted data from all eligible
studies using standardised forms. Extracted data included
the following: sample characteristics (participant source,
mean age, gender proportions, duration of symptoms,
baseline pain and disability measures); details regarding
the intervention setting (e.g. tertiary pain clinic, outpatient
clinic, school) and provider type; intervention characteristics
(description of index and control interventions, duration
and number of sessions, individual or group delivery);
co-interventions; and baseline and follow-up outcome data
(e.g. pain, disability/function, adverse events). Outcomes
were categorised and extracted in three groups: short term
(post-treatment and not longer than 3 months), intermediate
term (6 months), and long term (12 months or more),
according to follow-up time after randomisation.
Risk of bias assessment
The PEDro scale [17, 18] was used to evaluate the risk of
bias in all eligible RCTs. Where available scores for eligible
trials reported on the PEDro database were used.
Otherwise, two authors independently scored the trial using
the PEDro scale. All raters were previously trained and
experienced in applying the PEDro scale. Disagreements
were resolved by consensus.
Data analysis
The clinical homogeneity of RCTs was evaluated qualitatively
based on the extracted data on population characteristics,
intervention characteristics and outcomes
measured. Statistical homogeneity was assessed by
inspecting the I2 statistic. Suitability for pooling and
selection of meta-analytic model (random or fixed effects)
was determined within the comparison categories based on
acceptable clinical and statistical homogeneity. Forest plots
were generated to present the pooled estimates where there
were two or more RCTs of sufficient clinical and statistical
homogeneity.
Quality of the evidence
Grades of recommendation, assessment, development and
evaluation (GRADE) profiles were used to evaluate the
overall quality of the evidence and the strength of the
recommendations. [19] The quality of the evidence for a
specific outcome was based upon five principal factors:
(1) methodological limitations (for example due to RCT design),
(2) inconsistency of results,
(3) indirectness (affecting generalisability of the findings),
(4) imprecision (e.g. sufficient data) and
(5) other considerations, such as reporting bias.
According to GRADE, the overall quality
of evidence is considered to be high when multiple RCTs
with a low risk of bias provide consistent, generalisable,
and precise data for a particular outcome. The quality of
the evidence was downgraded by one level for each of
the factors described above that were not met. [20]
Results were considered inconsistent when effect estimates
were heterogeneous or only one RCT was available [21], and quality was marked down for imprecision
when fewer than 400 participants were included. [22]
The following definitions of quality of the evidence were
applied [23]:
High quality: further research is very unlikely to change
our confidence in the estimate of effect.
Moderate quality: further research is likely to have an
important impact on our confidence in the estimate of
effect and may change the estimate.
Low quality: further research is very likely to have an
important impact on our confidence in the estimate of
effect and is likely to change the estimate.
Very low quality: we are very uncertain about the
estimate.
Results
Figure 1
Table 1
Table 2
Table 3 A
Table 3 B
Table 4
Table 5
Figure 2
|
The electronic search retrieved 2,466 articles (Figure 1). After screening, 5 articles reporting 4 RCTs were included
in the intervention section (Tables 1, 2) and 12 articles
reporting 11 RCTs were included in the prevention section
(Tables 3, 4).
Intervention studies
Included studies
Of the four intervention RCTs (one trial by Jones et al.
reported outcomes in two articles [24, 25]) included in the
review [24–28], two were conducted in the United Kingdom [24, 25, 28], one in Sweden [27], and one in South Africa. [26] Three of the four studies recruited participants
from a school setting [24–26] with only one study
recruiting participants who were care seeking. [27]
Sample
sizes ranged from 45 to 185 participants with a mean age
range from 12 to 14.8. The duration of pain at study entry
was either unrestricted or unreported in all studies. Three
of the studies assessed the effectiveness of supervised
exercise programs: two against a no-treatment control
group [24–26] and one against a self-directed exercise
program. [27] One RCT assessed the effect of a seat wedge
versus a no-treatment control. [28] All RCTs measured
pain intensity at follow-up, while some also collected
disability, quality of life and physical measures (Table 1).
Risk of bias
The four RCTs all met between 4 and 6 criteria on the
PEDro scale (Table 5). Three [26–28] reported concealed
allocation and none reported an intention-to-treat analysis.
Due to the nature of the interventions and the self-reported
outcomes, blinding of patients, providers or assessors was
not possible in any of the studies. Based on these considerations,
risk of bias in all studies was considered
moderate.
Effectiveness of the interventions
In two RCTs (n = 125), there was a pooled mean benefit of
2.9 points on a 0–10 pain scale for average pain over the
past month (95 % CI 1.6–4.1) of a supervised exercise
program over no treatment (Figure 2). [24–26] One study [26]
also reported that this benefit was maintained at 6–month
follow-up. There was no difference between groups in
terms of current pain at either follow-up. Sufficient data
were not available to enable pooling of other outcomes.
Ahlqwist et al. [27] reported no difference in terms of
pain intensity between a supervised and a home exercise
program. Candy et al. [28] reported a statistically significant
difference in short-term pain intensity in favour of a
seat wedge group over no treatment.
Two RCTs measured function as an outcome; Jones
et al. [24, 25] reported a reduction in absences from
physical activity in favour of supervised exercise [MD
(95 % CI): -1.0 (-1.65, -0.35) p<0.01], and Ahlqwist
et al. [27] found no difference between supervised or home
exercise on the Roland–Morris Disability Questionnaire
[MD (95 % CI): -0.8 (-2.3, 0.7) p = 0.29] (Table 2).
Secondary outcomes such as physical impairment
measures (i.e. range of motion, muscle strength and
endurance, flexibility) and self-reported quality of life were
inconsistently measured across studies (Supplementary Table 1). No studies reported adverse events associated
with the interventions; however, one study [27] reported
that some participants had to temporarily stop exercising
due to pain.
Quality of the evidence—GRADE ratings
There is a moderate quality evidence (downgraded due to
imprecision) that in the short term, supervised exercise
programs are effective in reducing average back pain over
the past month in children compared to no treatment.
There is low quality evidence (imprecision, inconsistency)
that there is no effect on LBP of supervised versus
unsupervised exercise programs.
There is very low quality evidence (imprecision,
inconsistency, limitations in design) that a foam seat wedge
reduces LBP intensity compared to no intervention; that
supervised exercise programs are effective in reducing
absences from physical activities, compared to no treatment;
and that supervised exercise programs are not
effective in reducing disability compared to home exercise
programs.
Prevention studies
Included studies
Of the 11 prevention RCTs (reported in 12 articles)
included in the review [29–40], three each were conducted
in Belgium [30, 31, 34, 35], the USA [29, 32, 39], and
Spain [33, 36, 40], and one each in Sweden [37] and Brazil. [38] All included studies recruited participants from a
school setting. The sample sizes ranged from 17 to 603 and
all participants were students attending the schools chosen
for inclusion in the various studies (Table 3). The mean
participant age was 9–11 years across the studies at the
time of randomisation. The majority of the studies identified
in this section assessed outcomes such as back care
beliefs and knowledge about posture and ergonomics, and
cognitive factors such as fear avoidance and self-efficacy.
Several studies also observed postural, manual handling or
backpack wearing behaviour and recorded this as an outcome
(Supplementary Table 2). No studies reported
adverse events associated with the interventions.
Since the focus of this part of the review was on prevention
of LBP, further discussion of the results is centred
on those studies that reported LBP prevalence or intensity
at follow-up assessment. Only four [30, 31, 34, 35, 37] of
the included prevention studies reported the effectiveness
of the interventions in terms of LBP prevalence. Three
studies assessed the effect of an educational and back care
promotion program versus no intervention [30, 31, 34, 35],
and one study assessed the effect of providing ergonomically
designed school desks against conventional furniture. [37]
Table 6
|
Risk of bias
All of the four studies met 4 or 5 criteria on the PEDro
scale (Table 6). None of the studies reported concealed
allocation and none reported an intention-to-treat analysis.
Due to the nature of the interventions and the self-reported
outcomes, blinding of patients, providers or assessors was
not possible in any of the prevention studies. Based on
these considerations, risk of bias was considered to be
moderate.
Effectiveness of the prevention interventions
Studies by Geldhof et al. [34, 35], Cardon et al. [30] and
Dolphens et al. [31] all reported no short- or long-term
effect on LBP prevalence of education and back care
promotion programs when compared to no treatment.
Linton et al. [37] reported a large effect of ergonomically
designed furniture with a LBP prevalence post-intervention
of 38 % in the intervention group and 66 % in the group
that used conventional furniture. It is noted that around
50 % of the students reported back pain prior to the
intervention, a high figure for this age group.
Quality of the evidence—GRADE ratings
There is moderate quality evidence (downgraded due to
limitations in design) that back-related education and
promotion programs are not effective in reducing LBP
prevalence in children.
There is very low quality evidence (imprecision,
inconsistency, limitations in design) that ergonomically
designed furniture reduces LBP prevalence compared to
conventional furniture.
Discussion
Four RCTs were included in the treatment section and
eleven RCTs in the prevention section of this systematic
review that evaluated the effectiveness of conservative
approaches to treat or prevent LBP in children and adolescents.
There is moderate quality evidence to suggest that
a supervised exercise intervention has a large effect on
average monthly pain scores in children and adolescents
compared to no treatment. There is very low quality evidence
supporting the use of a foam seat wedge for the
treatment of LBP in children. For the prevention of LBP,
there is moderate quality evidence to suggest that back-related
education and back care promotion programs are
not effective in preventing LBP in children and adolescents.
There is also very low quality evidence supporting
the use of ergonomically designed furniture over conventional
furniture. There are conflicting results for the treatment
and prevention of LBP when considering measures
beyond pain and disability, e.g. physical measures in
intervention studies and observed behaviour, physical
measures, and knowledge tests in prevention studies.
The findings of this review are somewhat consistent
with previous systematic reviews that report on the effectiveness
of treatment and prevention interventions for LBP
in children and adolescents. [14, 15] The strengths of this
systematic review and meta-analysis are that it was conducted
in accordance with the methods recommended by
the Cochrane Back Review Group [16], focused on clinically
meaningful outcome measures of pain and disability,
and used a sensitive search strategy, which limits the
likelihood any relevant studies have been missed. Only
RCTs were eligible for inclusion in this review as this
methodology provides the most reliable form of evidence
when evaluating treatment effectiveness. The methodological
quality of included studies was assessed using the
PEDro scale, a rigorously developed [41] and evaluated
risk of bias tool that is both valid and reliable; [17, 18] and
the strength of recommendations reported in accordance
with GRADE guidelines. At last, only studies that demonstrated
sufficient clinical and statistical homogeneity
were pooled in the meta-analysis.
The limitations of this review include the small number of
primary treatment and prevention studies and large heterogeneity
between studies that prevented the pooling of results
in the meta-analysis for all but one comparison. The inability
to pool results means that the findings of this review are
based on individual studies; as such it is not possible for
robust conclusions to be made. Newly conducted, high
quality research is likely to have a large influence on our
understanding of the effectiveness of interventions to treat
and prevent LBP in children and adolescents. Future studies
need to carefully consider the methodological issues known
to influence internal and external validity. The issue of
generalisability is of particular relevance in this field given
that study participants are often recruited from schools, as
opposed to from care providers. This choice of sampling
frame has unknown implications for the estimate of treatment
effectiveness. [42] Furthermore, limitations in the
reporting of studies included in the intervention section of
this review (e.g. no study reported the duration of pain at
study entry) negatively impact on the generalisability and
applicability of the results.
Compared to adult populations, the effectiveness of
exercise treatment programs in children appears to have a
greater effect on pain; however, a similar effect on function.
Hayden et al. [43] found no difference in short-term
pain relief or function between exercise therapy and no
treatment for adults with acute LBP and insufficient evidence
for the use of exercise in the sub-acute phase. For
adults with chronic LBP, exercise therapy appears to be
minimally effective at decreasing pain (7.29 points on a
0–100 scale) and improving function (2.50 points on a
0–100). [43] Our review found a large mean benefit for a
supervised exercise program over no treatment for average
pain over the last month (2.9 points on a 0–10 pain scale
for average pain over the past month). Despite the observed
effect on average pain, there was no effect on the current
pain or function, so this discrepancy reduces our confidence
in the effect reported. As mentioned above, the
robustness of the comparison between children and adults
is compromised due to included studies not reporting the
duration of low back pain symptoms experienced by the
children enrolled. In keeping with the findings of the current
review, the use of education and back care promotion
programs has not been recommended to prevent the onset
of LBP in adult populations [13] and there is no robust
evidence to support the use of ergonomic furniture.
This review has a number of important implications for
clinical practice and future research in the area of child and
adolescent LBP. Low back pain research conducted in
children and adolescents is an emerging area when compared
to the volume of research that has been conducted in adult
populations. The four intervention RCTs included in this
review can be compared to the several hundred conducted in
adult populations. [13] This situation provides a unique
opportunity to reflect and learn from the work that has been
done in adult populations and apply this knowledge and skill
to a new population. [44] In particular, there is a need for
large, high quality RCTs to guide clinicians treating children
and adolescents with LBP and inform the development of
evidence-based health promotion programs targeting the
prevention of spinal pain.
There is a need to use psychometrically
sound, clinically meaningful and standardised
outcome measures for pain, function, health care utilisation
and physical activity, as this will increase the clinical
applicability of the research and facilitate the pooling of RCT
results. [44] The infancy of this research area provides an
opportunity to use alternative research methods (e.g. qualitative
methods) to identify outcomes that are most important
to patients and their family caregivers and highlights the
need for detailed and systematic data collection including
duration of LBP and adverse events.
At last, while the prevention
of LBP could prove to be a major advance in musculoskeletal
research there is a need to improve our
understanding of the causative mechanisms of LBP to
facilitate the development and evaluation of targeted treatment
and prevention interventions.
Conflict of interest
None of the authors involved in the preparation of this manuscript have any potential, perceived or real conflict to disclose.
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