Download as pdf or txt
Download as pdf or txt
You are on page 1of 9

Archives of Physical Medicine and Rehabilitation

journal homepage: www.archives-pmr.org


Archives of Physical Medicine and Rehabilitation 2019;-:-------

ORIGINAL RESEARCH

The Effect of Spinal Mobilization With Leg Movement


in Patients With Lumbar RadiculopathydA Double-
Blind Randomized Controlled Trial
Kiran Satpute, MPTh, COMT,a Toby Hall, PhD, MSc, FACP,b Richa Bisen, MPT,c
Pramod Lokhande, MS DNB, MNAMS, FICS, FAAMISSd
From the aDepartment of Kinesiotherapy and Physical Diagnosis, Department of Musculoskeletal Physiotherapy, Smt. Kashibai Navale College
of Physiotherapy, Pune, Maharashtra, India; bSchool of Physiotherapy and Exercise Science, Curtin University, Perth, WA, Australia;
c
Department of Electrotherapy and Electro Diagnosis, Department of Musculoskeletal Physiotherapy, Smt. Kashibai Navale College of
Physiotherapy, Pune, Maharashtra, India; and dDepartment of Orthopaedics, Smt. Kashibai Navale Medical College and General Hospital,
Pune, Maharashtra, India.

Abstract
Objectives: To evaluate the effect of spinal mobilization with leg movement (SMWLM) on low back and leg pain intensity, disability, pain
centralization, and patient satisfaction in participants with lumbar radiculopathy.
Design: A double-blind randomized controlled trial.
Setting: General hospital.
Participants: Adults (NZ60; mean age 44y) with subacute lumbar radiculopathy.
Interventions: Participants were randomly allocated to receive SMWLM, exercise and electrotherapy (nZ30), or exercise and electrotherapy
alone (nZ30). All participants received 6 sessions over 2 weeks.
Main Outcome Measures: The primary outcomes were leg pain intensity and Oswestry Disability Index score. Secondary variables were low
back pain intensity, global rating of change (GROC), straight leg raise (SLR), and lumbar range of motion (ROM). Variables were evaluated blind
at baseline, post-intervention, and at 3 and 6 months of follow-up.
Results: Significant and clinically meaningful improvement occurred in all outcome variables. At 2 weeks the SMWLM group had significantly
greater improvement than the control group in leg pain (MD 20; 95% confidence interval [95% CI], 1.4-2.6) and disability (MD 3.9; 95% CI, 5.5-
2.2). Similarly, at 6 months, the SMWLM group had significantly greater improvement than the control group in leg pain (MD 2.6; 95% CI, 1.9-
3.2) and disability (MD 4.7; 95% CI, 6.3-3.1). The SMWLM group also reported greater improvement in the GROC and in SLR ROM.
Conclusion: In patients with lumbar radiculopathy, the addition of SMWLM provided significantly improved benefits in leg and back pain,
disability, SLR ROM, and patient satisfaction in the short and long term.
Archives of Physical Medicine and Rehabilitation 2019;-:-------
ª 2018 by the American Congress of Rehabilitation Medicine

Low back pain (LBP) is a common musculoskeletal problem Leg pain may originate from compromised lumbar spine
affecting the general population1 with global prevalence up to musculoskeletal or neural structures.7 In the case of neural
10.2%2 which is a major cause of years lived with disability.3 compromise, lumbar radiculopathy is considered as a possible
Recovery is less favorable if back pain is associated with leg diagnosis,8,9 the lifetime prevalence of which ranges up to 43%.10
pain4,5 possibly due to the associated greater disability.6 The diagnostic criterion includes sensory and motor deficits of a
specific nerve root, consistent with the distribution of leg symp-
toms.11,12 Pain associated with radiculopathy may result from
Disclosures: Kiran Satpute and Toby Hall are accredited Mulligan Concept teachers and gain a
teaching fee when running these courses.
structural damage13,14 compromising nerve roots,15-17 which in
Clinical Trial Registration No.: CTRI/2015/09/006165. some cases may lead to neuropathic pain.18-20

0003-9993/19/$36 - see front matter ª 2018 by the American Congress of Rehabilitation Medicine
https://doi.org/10.1016/j.apmr.2018.11.004
2 K. Satpute et al

According to clinical practice guidelines (National Institute for and withdrawal of informed consent. The Leeds assessment of
Health and Care Excellence 2016), conservative management is neuropathic symptoms and signs scale (>12) was used to exclude
recommended first and includes support and advice, exercise, patients with positive features of neuropathic pain.34
manual therapy, psychological therapies, and medication. Other All participants were provided with an information sheet explaining
recommendations of physiotherapy have included mobilization, the study protocol. SMWLM and neural mobilization techniques were
electrotherapy, traction, taping, and exercise,21-27 with no evi- explained as routine physiotherapy procedures to ensure patient
dence clearly supporting any 1 method.28,29 A recent systemic blinding. All participants were asked not to reveal their group identity
review reported low to moderate quality evidence in favor of at any time. At each treatment session, any increase in leg pain intensity
manual therapy for the management of lumbar radiculopathy.30 or peripheralization of pain was reported as an adverse event.
Mulligan has suggested spinal mobilization with leg movement A chart indicating flow of participants through each stage of the
(SMWLM) for the management of low backerelated leg pain. A study is shown in fig 1. A total of 60 participants were enrolled and
transverse pressure to the spinous process is maintained while the provided informed consent with the right to withdraw from the study
patient actively moves their leg in the direction of the impaired at any time. Participants were randomly allocated to SWMLM group
neurodynamic movement.25 Although there are no studies that or control group (CG) immediately after baseline assessment with the
have investigated this technique in lumbar radiculopathy, studies help of a computer-generated randomization sequence placed in
have examined other Mulligan mobilization techniques for leg sequentially numbered opaque sealed envelopes by administra-
pain with encouraging results.31,32 Despite this evidence, a recent tion staff.
systematic review indicates low to moderate quality evidence for
effectiveness of Mulligan mobilization for LBP in general.33 Outcomes
The purpose of this study was to examine the additional benefit of
SMWLM in addition to traditional interventions in patients with Baseline demographic details, physical examination criteria, and
lumbar radiculopathy over a 6-month period. We hypothesized that all outcome variables were assessed by a physiotherapist blind to
compared to standard treatment; the addition of SMWLM to standard the group allocation. Reassessment occurred at the end of the sixth
treatment would induce greater pain reduction and improved function. treatment session, as well as at 3- and 6-month follow-up.
The primary outcome measures were intensity of leg pain
measured on visual analog scale (VAS) and Oswestry Disability
Methods Index (ODI) score. LBP over the previous 24 hours measured on
This double-blind randomized controlled trial design that has been VAS, global rating of change (GROC), passive SLR and active
reported according to the recommendations of the Consolidated lumbar flexion range of motion (ROM), and area of limb pain
Standards of Reporting Trials statement investigated the efficacy recorded on a body chart were secondary outcome measures.
of SMWLM on participants with lumbar radiculopathy. A single-item 10-cm horizontal VAS (anchored from 0 pain to a
Participants with leg pain for >6 weeks were recruited from maximum pain score of 10) was used to record average intensity of leg
Smt. Kashibai Navale Medical College and General Hopsital, pain and LBP during the previous 24 hours. The minimal detectable
enrolled between November 2015 and November 2017 and eval- change (MDC) for the VAS score is 20 mm.35 Active lumbar flexion
uated for the presence of lumbar radiculopathy. The inclusion ROM to pain onset was measured with a bubble inclinometer in
criteria included unilateral radiating leg pain below the knee with standing. The difference between 2 sagittal rotation angles taken at
associated LBP, with hypoesthesia and/or myotomal weakness or T12-L1 and S1-S2 was considered as total lumbar flexion ROM.
hyporeflexia indicative of L4, L5, or S1 nerve root compromise. Intraclass correlation coefficient (ICC) values for intrarater reliability
Additional criteria were reproduction of symptoms with straight for this measurement are 0.88, whereas the MDC is 9 .36
leg raise (SLR) and tenderness on palpation of sciatic, tibial, or Passive SLR ROM with plantar-grade ankle position was
common peroneal nerves. Participants were included only if there measured at the point leg symptoms occurred using a bubble
was an increase in SLR range after a single trial application of the inclinometer. Intrarater reliability for this test is excellent with
SMWLM technique. ICC of 0.95, SEM 1.2 , and MDC 3.4 .37
Participants were excluded if they were not aged 18-60 years, The self-reported 10-item ODI was used to measure low backe
and if they had associated abnormality of bowel and bladder func- related disability,38 with the total raw score used for assessment.
tion, lower extremity vascular disease, physiotherapy or surgery for The ODI has demonstrated responsiveness to change in in-
leg pain within 6 months, any contraindications for manual therapy, dividuals with low backerelated leg pain.39 The MDC is 10
points,35 and the ICC for test-retest reliability is >0.87.40
List of abbreviations: The GROC was used to assess change in status after initiation
of treatment. The participants identified their response from a 15-
95% CI 95% confidence interval
point scale starting at a very great deal worse to a very great deal
CG control group
GROC global rating of change better. The ICC is 0.90 and MDC 2 points.41
ICC intraclass correlation coefficient The area of limb pain was assessed by requesting participants to
LBP low back pain mark their pain on a body chart. The leg was subsequently divided
MD mean difference into 3 zones: thigh, leg, and ankle or foot. Improvement was judged
MDC minimal detectable change by centralization of symptoms. The kappa value for assessing the
ODI Oswestry Disability Index reliability of centralization phenomenon ranges upward from 0.51.42
ROM range of motion
SLR straight leg raise
SMWLM spinal mobilization with leg movement Procedures
TENS transcutaneous electrical nerve stimulation
Interventions were provided by a qualified physiotherapist with 8
VAS visual analog scale
years of postgraduate experience. All participants attended the

www.archives-pmr.org
Spinal mobilization for lumbar radiculopathy 3

Fig 1 Flowchart of the participants through the study.

clinic for six 50-minute treatment sessions carried out over 2 Participants were encouraged to not seek other treatment until the
consecutive weeks. Sessions comprised neural mobilization, study was completed.
structured exercise, and transcutaneous electrical nerve stimula-
tion (TENS). In addition, participants in the SMWLM group Spinal mobilization with leg movement
received SMWLM, which took approximately 5 minutes.25 After While laying on their nonaffected side participants were asked to
this, participants were encouraged to continue with a home exer- move their affected leg to the limit of pain-free range of SLR. At
cise program. If an exacerbation of symptoms occurred, a record the same time, the physiotherapist applied firm transverse
was made and no further treatment was given on that day. pressure to the superior vertebrae at the affected spinal level (eg,

www.archives-pmr.org
4 K. Satpute et al

L4 in case of L4 or L5 and L5 in case of L5 or S1) away from Results


the painful side. Participants were instructed to stop the leg
movement at the point leg pain was provoked, easing back, and Sixty participants (35 women) were recruited and disability was
then maintaining the position for 3 seconds before returning to mostly rated as severe.38 Demographic details are shown in
the starting position. The technique was progressed from a single table 1. The flow of participants, reasons for ineligibility, and loss
set of 3 repetitions on the first occasion to 2-3 sets of 6-8 to follow-up are detailed in fig 1.
repetitions with a rest interval of 30 seconds between sets on There were no participants with neuropathic pain (see table 1)
subsequent applications. Progression was also achieved by indicating the study population could be categorized as
applying pain-free overpressure to the range of SLR. Progression compressive neuropathy or peripheral nerve sensitization.7
occurred when range of SLR achieved 50% of that on the un- All participants received all 6 treatment sessions during the 2
affected side. weeks without dropout. No adverse effects were reported.
A neural slider mobilization was applied next according to a Between group analysis revealed a significant effect of
previously published method.26 With the subject in side lying, a SMWLM on the 2 primary outcome variables (table 2). Leg pain
rhythmical movement of hip and knee flexion followed by hip and intensity reduced significantly more in the SMWLM group post-
knee extension was carried out for 30 seconds and repeated intervention (MD e2.4 points; 95% CI, e2.0 to 2.7), at 3-month
5 times. follow-up (MD e3.8 points; 95% CI, e3.4 to e4.3), and at
All participants received 2 sets of 5-7 repetitions of lumbar 6-month follow-up (MD e 4.4 points; 95% CI, e 4.0 to e 4.8).
spine ROM exercises in 4-point kneeling, comprising pelvic tilting The ODI score also reduced significantly more in the SMWLM
and heel sitting (lumbar flexion). Participants also received 4 pole group post-intervention (MD e3.9 points; 95% CI, e5.5 to 2.2),
conventional low-intensity, high-frequencies (80-100 Hz) TENS at 3-month follow-up (MD e5.0 points; 95% CI, e6.5 to e3.4),
with wave durations of 50-100 ms. Two electrodes were applied and at 6-month follow-up (MD e 4.7 points; 95% CI, e6.3
on the lumbar spine and 2 more on affected lower extremity in the to e3.1).
distribution of pain for 30 minutes.43 Within-group analysis revealed that leg pain intensity
Participants performed the exercise at home once per day with was significantly reduced post-intervention (MD e3.5 points; 95%
3 sets of 10 repetitions. Progression could be made by increasing CI, e3.0 to -4.1), at 3-month follow-up (MD from previous evalu-
the repetitions when comfortable. ation e1.9 points; 95% CI, e1.2 to e2.5) and at 6-month follow-up
Approval for this study was granted by the ethical com- (MD from previous evaluation e 0.4 points; 95% CI, e 0.1 to e 0.8).
mittee of Smt. Kashibai Navale Medical College and General
Hopsital. The trial was registered with the Clinical Trial Reg-
istry of India Ref. No. CTRI/2015/09/006165. Sample size was
Table 1 Baseline characteristics of the participants
determined a priori, based on data from a similar study.44 Sixty
participants were required to ensure that this trial was powered Characteristic SMWLM Group Control Group
to detect a difference of 1624 points out of 100 in leg pain Age (y), mean  SD 45.99.1 42.39.0
severity with 80%, a 2-tailed alpha of 5%, and an expected Sex, women, n (%) 1653.3 1963.3
dropout rate of 20%. This sample size also had 80% power to BMI (kg/m2), mean  SD 25.64.6 24.73.5
detect a difference of 912 points on the 100-point ODI. Duration of leg symptoms (d), 212.266.6 197.866.5
mean  SD
LANSS score (0-24), 8.41.3 8.11.6
Statistical analysis mean  SD
Neuropathic pain, n (%) 0 0
The Statistical Package for Social Sciences (SPSS 23) softwarea Lumbar flexion, mean  SD 38.904.54 39.674.13
was used for statistical analysis. Data were normally distributed Lumbar extension, 14.802.99 15.832.64
without outliers and with homogeneity of variances (P>.05). mean  SD
Descriptive statistics are presented and continuous variables are Lumbar side flexion (right), 14.833.03 15.13 (2.61)
summarized with means and SDs. Categorical or dichotomous mean  SD
data are summarized with frequencies. Lumbar side flexion (left), 14.802.88 14.303.30
A repeated measures general linear model (independent factor mean  SD
was group: CG vs SMWLM and repeated factor was time: pre- to SLR (affected side), 48.434.51 45.874.15
post-intervention and at 3 and 6mo of follow-up) was used to mean  SD
evaluate the differences in all outcome variables. Tukey post hoc SLR (nonaffected side), 70.037.45 69.576.17
test was used to evaluate for significant differences in the main mean  SD
effect for group, time, or interaction (group  time). The results LBP VAS (0-10), mean  SD 3.51.4 3.91.4
are presented as the mean difference (MD) and 95% confidence Leg pain VAS (0-10), 7.10.8 6.60.7
interval (95% CI) for all outcomes across all time points. Because mean  SD
dropouts were very low, data were analyzed after the intention-to- ODI (0-50), mean  SD 24.55.1 23.44.8
treat principle.45 Area of limb pain, n (%)
For area of limb pain, scores at each follow-up point were 1. Thigh 0 0
compared against baseline values and coded as centralized if the 2. Leg 10 (33.3) 11 (36.7)
symptoms cleared from their most distal area recorded on the 3. Ankle/foot 20 (66.7) 19 (63.3)
body chart or peripheralized when symptoms progressed to a more
Abbreviations: BMI, body mass index; LANSS, Leeds assessment of
distal area. For all analyses, statistical tests were 2 tailed and the neuropathic symptoms and signs.
P value<.05 was considered as significant.

www.archives-pmr.org
Spinal mobilization for lumbar radiculopathy 5

There was also a significant effect of treatment on ODI score post-

(4.9-13.3)
Table 2 Mean (SD) for continuous outcomes measured at baseline and at each follow-up time for each group, within-group mean differences (MD) with 95% CI, and between-group mean

(1.9-3.2)

(6.3-3.1)

(1.3-0.3)
intervention (MD e7.1 points; 95% CI, e5.3 to 9.4), at 3 months

SMWLM
Between-Group Difference

GdCG
6 mo
(MD from previous evaluation e2.3 points; 95% CI, e1.0 to -3.7),

2.6

4.7

0.8

9.1
as well as at 6 months (MD from previous evaluation e 0.5 points;

MD (95% CI)

(6.2-14.0)
(2.2-3.4)

(6.5-3.4)

(1.3-0.2)
95% CI, e0.1 to -1.1) as presented in table 2 and figs 2 and 3.

SMWLM
GdCG
3 mo
For the secondary outcome variables, SMWLM had a signifi-

10.1
2.8

0.8
cant effect on LBP intensity post-intervention (MD e1.2 points;

(5.7-14.3)
3.6) (1.4-2.6)

0.3) (5.5-2.2)

0.6) (1.5-0.2)
95% CI, e 0.8 to -1.7), at 3 months (MD from previous evaluation
SMWLM
GdCG
Wk 2

e0.5; 95% CI, e 0.1 to e1.0) and at 6 months (MD from previous

10
2.0

3.9

0.9
evaluation e0.4; 95% CI, e 0.1 to e 0.8). These results are
presented visually in fig 4.
There was also a significant effect of SMWLM on SLR ROM

(0.3-4.9)
0.8) ( 2.3 to

1.1) ( 1.2 to

0.8) ( 0.1 to
postintervention (MD 17.3 points; 95% CI, 19.6-15.1), at 3
2.9

0.8

0.3

2.6
6 vs 3 mo

CG

months (MD from previous evaluation 2.4 points; 95% CI, 0.3-
4.4), but not at 6 months (MD from previous evaluation 1.6 points;
95% CI, 0.1 to 3.3) as presented in table 2 and fig 5.
SMWLM G

(0.1-3.3)
( 0.1 to

( 0.1 to

( 0.1 to

Similarly, the GROC improved significantly in the group


0.4

0.5

0.4

1.6

receiving SMWLM post-intervention more than the CG (MD 2.1


points; 95% CI, 1.6-2.6) at 3 months (MD from previous evalu-
1.0) ( 0.1 to 1.2)
2.5) ( 1.7 to e2.8)

ation 1.2 points; 95% CI, .7-1.7) and at 6 months (MD from
3.7) ( 2.5 to 0)
Within-Group Difference

(0.7-3.7)

previous evaluation 1.6 points; 95% CI, 1.1-2.2), as presented


3 mo vs 2 wk
MD (95% CI)

2.2

1.2

0.6

2.2

in table 3.
CG

Between-group analysis revealed there was significant


improvement in all outcome measures at all the time points, as
presented in tables 2 and 3.
SMWLM G

(0.3-4.4)
( 1.2 to

( 1.0 to

( 0.1 to

With respect to the area of limb pain, immediately after the 2-


1.9

2.3

0.5

2.4

week intervention period, 23 of 27 (85%) participants in the


( 0.8 to 1.6)

( 0.2 to 1.2)
( 0.9 to e3.4)

SMWLM group and 14 of 29 (48%) participants in the CG re-


ported centralization of leg pain. At 6 months, 25 of 25 (100%)
(4.9-15.9)

participants in the SMWLM group and 22 of 25 (88%) partici-


1.2

2.1

0.7

9.9
Wk 2 vs 0

pants in the CG reported centralization of the leg pain with


CG

reference to the first evaluation time point.


( 3.0 to 4.1)

( 5.3 to 9.4)

( 0.8 to 1.7)

(19.6-15.1)
CG nZ30 SMWLM G
3.5

17.44 21.23.8 15 (3.9) 202.1 14.53.8 19.22.1 7.1

2.31.2 3.21.1 1.81.2 2.51.1 1.41.1 2.20.8 1.2

65.86.7 55.88.4 68.16.3 588.4 69.87.1 60.68 17.3

Discussion
1.21.2 3.81.3

This is the first randomized controlled trial evaluating the efficacy


of SMWLM in the management of patients with lumbar radicul-
6 mo

opathy. Both groups showed significant improvements in all


SMWLM G

outcome measures. However, in comparison to the CG, the group


CG nZ30 nZ30

receiving SMWLM showed significantly greater improvement


immediately after the intervention which was maintained even 6
1.61.5 4.51.2

months later.
3 mo

These results are consistent with previous intervention studies


SMWLM G

for lumbar radiculopathy where treatment comprised exercise,


CG nZ30 nZ30

traction, or neural tissue mobilization. These studies showed sig-


Mean  SD
Groups

nificant improvement in leg pain as well as disability 4-6 weeks


post-intervention27,44 and improvement was maintained at 6-
3.51.1 5.51

month follow-up.27 However, when compared to Ferreira et al,44


Wk 2

the addition of SMWLM in our study resulted in more rapid


SMWLM G

and greater improvements in leg pain severity.


CG nZ30 nZ30

Previous recommendations for the conservative management


70.78 6.70.69

of radiculopathy include exercise, neural and spinal mobilization


24.55.1 23.44.8

3.51.4 3.91.4

48.44.5 45.94.1

encouraging nerve root decompression and neural tissue desen-


sitization.7,26,46 Indeed, previous studies have shown preliminary
Abbreviation: G, group.
Wk 0
differences (95% CI)

evidence for the use of neural mobilization in the management of


SMWLM G

leg pain.26,44,47-49 Moreover, a recent systematic review was in


nZ30

favor of neural mobilization50 for the management of referred


limb pain. Previously it has been proposed that neural mobiliza-
score/50

Degrees
VAS/10

VAS/10
Back pain
Outcome

SLR ROM
Leg pain

tion should consist of slider movements without tension on nerve


Measure

tissue.51,52 However, SMWLM is a graded tensioning technique,


ODI

albeit in a pain-free range. Animal experimental evidence

www.archives-pmr.org
6 K. Satpute et al

Fig 2 Changes in mean values for leg pain intensity over time for Fig 4 Changes in mean values for low back pain intensity over time
both treatment groups. for both treatment groups. Abbreviation: VASBP, visual analog scale
back pain.

supports the use of neural tensioning techniques for experimen- CG could be related to the combination of spinal mobilization
tally induced acute nerve pain in an animal model.53 However, in along with active leg moments providing a functional mobiliza-
humans, pain-free mobilization of the nerve is preferable and tion toward increasing the pain-free range of SLR. Increasing
hence SMWLM may be a useful tool in the management of range of SLR is perhaps empowering to the patient because it
radiculopathy. reduces fear of movement and extinguishes the movement or pain
It has been suggested that neural mobilization induces hypo- association.
algesia54 by activation of the descending pain inhibitory system,55 The benefits of SMWLM may also be due to the mechanical
reducing intraneural edema,56-58 and promoting nerve recovery59 manual force applied to the lumbar spine.60 It is postulated that
which then help restore the neural tissues ability to tolerate this facilitates a change in the volume of the intervertebral fora-
stresses during activities of daily living.13 The greater improve- men decompressing the nerve root. The SLR movement compo-
ment in leg and back pain in the SMWLM group compared to the nent of SMWLM may provide similar benefits to that of neural

Fig 3 Changes in mean values for disability over time for both Fig 5 Changes in mean values for SLR over time for both treatment
treatment groups. groups.

www.archives-pmr.org
Spinal mobilization for lumbar radiculopathy 7

mobilization. Moreover, SMWLM technique produces a signifi-

1.6 (1.1-2.2)
cant sympathoexcitatory response,61 which has been linked with

SMWLMdCG
(95% CI)
the hypoalgesic effect.62-64

6 mo MD
Improvements in both groups after 2 weeks of intervention,
which was maintained at 6-month follow-up might be explained
by natural resolution, but also by the simple exercises together

Between-Group Difference
with TENS. However, the efficacy of TENS application in patients

1.2 (0.7-1.7)
with lumbar radiculopathy is reported as low.43,65 It is reported

SMWLMdCG
Mean  SD for global perceived effect at each assessment point for each group and between-group mean difference (MD) (95% CI) at each assessment point

that spinal flexibility exercises66 similar to the present study may


(95% CI)
3 mo MD
be beneficial for lumbar radiculopathy, which is also the case for
people with LBP with or without leg pain.67 Lumbar flexion is
thought to increase the volume of the intervertebral foramen,
allowing nerve root swelling and edema to resolve, and may
therefore assist in spinal nerve root decompression.68
Postintervention

2.1 (1.6-2.6)
MD (95% CI)
SMWLMdCG

Study limitations
There are several limitations to the study’s findings. First, we did
not monitor whether participants adhered to the home exercise
protocol. Second, participants from the SMWLM group received a
CG nZ30

longer treatment session than the CG. Although the difference was
4.40.9

at most 5 minutes on top of a 50-minute treatment session. Third,


TENS was only administered for 30 minutes. Fourth, all in-
6 mo Mean  SD

terventions were administered by the same physiotherapist; how-


ever, this effect was limited by equal emphasis to the treatment in
both groups. Finally, we included only those participants who
SMWLMG nZ30

responded to a trial SMWLM. Despite this, only 11 of 71 patients


were found to not respond to SMWLM, providing some confi-
60.9

dence in the generalizability of these results.


Future studies are recommended to identify the mechanism of
action of SMWLM. In addition, studies should investigate the
relative efficacy of SMWLM compared to early surgery in the
short and long terms.
CG nZ30
4.20.8
3 mo Mean  SD

Conclusion
Groups

In the treatment of patients with subacute lumbar radiculopathy,


SMWLMG nZ30

the addition of SMWLM to exercise and TENS provided signifi-


cantly improved benefits in leg and back pain, disability, SLR
5.40.9

ROM, as well as patient satisfaction in the short and long terms.

Supplier
CG nZ30
1.91.0
Postintervention Mean  SD

a. SPSS, version 23; IBM.

Keywords
SMWLMG nZ30

Low back pain; Manual therapy; Radiculopathy; Rehabilitation


4.00.9
Abbreviation: G, group.

Corresponding author
GROC (-7 to 7)

Kiran Satpute, MPTh, COMT, Department of Kinesiotherapy and


Physical Diagnosis, Department of Musculoskeletal Physiotherapy,
Outcome

Smt. Kashibai Navale College of Physiotherapy, Off Westerly


Table 3

Bypass, Narhe Pune, Maharashtra 411041, India. E-mail address:


kiran_ptist@yahoo.co.in.

www.archives-pmr.org
8 K. Satpute et al

References 25. Mulligan BR. Manual therapy: “NAGS,” “SNAGS,” “MWMS” etc.
Wellington, New: Zealand: Plane View Services LTD; 2010.
26. Schafer A, Hall T, Muller G, Briffa K. Outcomes differ between
1. Hoy D, March L, Brooks P, et al. The global burden of low back pain: subgroups of patients with low back and leg pain following neural
estimates from the Global Burden of Disease 2010 study. Ann manual therapy: a prospective cohort study. Eur Spine J 2011;20:482-
Rheum Dis 2014;73:968-74. 90.
2. Meucci R, Fassa A, Faria N. Prevalence of chronic low back pain: 27. Thackeray A, Fritz JM, Childs JD, Brennan GP. The effectiveness of
systematic review. Rev Saúde Pública 2015;49:1-10. mechanical traction among subgroups of patients with low back pain
3. Global Burden of Disease Study 2013 Collaborators. Global, and leg pain: a randomized trial. J Orthop Sports Phys Ther 2016;46:
regional, and national incidence, prevalence, and years lived with 144-54.
disability for 301 acute and chronic diseases and injuries in 188 28. Luijsterburg PA, Verhagen AP, Ostelo RW, van Os TA, Peul WC,
countries, 1990-2013: a systematic analysis for the Global Burden of Koes BW. Effectiveness of conservative treatments for the lumbo-
Disease Study 2013. Lancet 2015;386:743-800. sacral radicular syndrome: a systematic review. Eur Spine J 2007;16:
4. Kongsted A, Kent P, Jensen TS, Albert H, Manniche C. Prognostic 881-99.
implications of the Quebec Task Force classification of back-related 29. Hahne AJ, Ford JJ, McMeeken JM. Conservative management of
leg pain: an analysis of longitudinal routine clinical data. BMC lumbar disc herniation with associated radiculopathy: a systematic
Musculoskelet Disord 2013;14:171. review. Spine 2010;35:E488-504.
5. Freynhagen R, Baron R, Gockel U, Tolle TR. Screening of neuro- 30. Leininger B, Bronfort G, Evans R, Reiter T. Spinal manipulation or
pathic pain components in patients with chronic back pain associated mobilization for radiculopathy: a systematic review. Phys Med
with nerve compression: a prospective observational study Rehabil Clin N Am 2011;22:105-25.
(MIPORT). Curr Med Res Opin 2006;22:529-37. 31. Hall T, Hardt S, Schafer A, Wallin L. Mulligan bent leg raise tech-
6. Goode A, Cook C, Brown C, Isaacs R, Roman M, Richardson W. nique–a preliminary randomized trial of immediate effects after a
Differences in comorbidities on low back pain and low back related single 5 intervention. Man Ther 2006;11:130-5.
leg pain. Pain Pract 2011;11:42-7. 32. Hall T, Beyerlein G, Hansson U, Teck H, Odermark M, Sainsbury D.
7. Schafer A, Hall T, Briffa K. Classification of low back related leg Mulligan traction straight leg raise: a pilot study to investigate effects
painda proposed patho-mechanism-based approach. Man Ther on range of motion in patients with low back pain. J Man Manip Ther
2009;14:222-30. 2006;14:95-100.
8. Fairbank JCT. An archaic term. BMJ 2007;335:112. 33. Pourahmadi M, Mohsenifar H, Dariush M, Aftabi A, Amiri A.
9. Braddom RL. Physical medicine and rehabilitation. 3rd ed. Phila- Effectiveness of mobilization with movement (Mulligan concept
delphia, PA: Elsevier Inc; 2007. techniques) on low back pain: a systematic review. Clin Rehabil
10. Konstantinou K, Dunn KM. Sciatica: review of epidemiological 2018;32:1289-98.
studies and prevalence estimates. Spine 2008;33:2464-72. 34. Bennett MI. The LANSS Pain Scale: the Leeds assessment of
11. Koes BW, vanTulder MW, Peul WC. Diagnosis and treatment of neuropathic symptoms and signs. Pain 2001;92:147-57.
sciatica. BMJ 2007;334:1313-7. 35. Ostelo R, de Vet H. Clinically important outcomes in low back pain.
12. Lee-Robinson A, Lee AT. Clinical and diagnostic findings in patients Best Pract Res Clin Rheumatol 2005;19:593-607.
with lumbar radiculopathy and polyneuropathy. Am J Clin Med 36. Kolber MJ, Pizzini M, Robinson A, Yanez D, Hanney WJ. The
2010;7:2. reliability and concurrent validity of measurements used to quantify
13. Nee RJ, Butler D. Management of peripheral neuropathic pain: lumbar spine mobility: an analysis of an iPhone application and
integrating neurobiology, neurodynamics, and clinical evidence. Phys gravity based inclinometry. Int J Sports Phys Ther 2013;8:129-37.
Ther Sport 2006;7:36-49. 37. Boyd BS. Measurement properties of a hand-held inclinometer dur-
14. Topp KS, Boyd BS. Structure and biomechanics of peripheral nerves: ing straight leg raise neurodynamic testing. Physiotherapy 2012;98:
nerve responses to physical stresses and implications for physical 174-9.
therapist practice. Phys Ther 2006;86:92-109. 38. Fairbank JC, Couper J, Davies JB, O’Brien JP. The Oswestry low
15. Tarulli AW, Raynor EM. Lumbosacral radiculopathy. Neurol Clin back pain disability questionnaire. Physiotherapy 1980;66:271-3.
2007;25:387-405. 39. Frost H, Lamb SE, Stewart-Brown S. Responsiveness of a patient
16. Valat J, Genevay S, Marty M, Rozenberg S, Koes B. Sciatica. Best specific outcome measure compared with the Oswestry Disability
Pract Res Clin Rheumatol 2010;24:241-52. Index v2.1 and Roland and Morris Disability Questionnaire for
17. Ropper AH, Zafonte RD. Sciatica. N Engl J Med 2015;372:1240-8. patients with subacute and chronic low back pain. Spine 2008;33:
18. Treede RD, Jensen TS, Campbell JN, et al. Neuropathic pain: 2450-7.
redefinition and a grading system for clinical and research purposes. 40. Joshi VD, Raiturker PP, Kulkarni A. Validity and reliability of En-
Neurology 2008;70:1630-5. glish and Marathi Oswestry Disability Index (version 2.1a) in Indian
19. Freynhagen R, Baron R. The evaluation of neuropathic components population. Spine 2013;38:E662-8.
in low back pain. Curr Pain Headache Rep 2009;13:185-90. 41. Jaeschke R, Singer J, Guyatt GH. Measurement of health status.
20. Kaki AM, El-Yaski AZ, Youseif E. Identifying neuropathic pain Ascertaining the minimal clinically important difference. Control
among patients with chronic low-back pain: use of the Leeds Clin Trials 1989;10:407-15.
Assessment of Neuropathic Symptoms and Signs pain scale. Reg 42. Aina A, May S, Clare H. The centralization phenomenon of spinal
Anesth Pain Med 2005;30:422-8. symptoms–a systematic review. Man Ther 2004;9:134-43.
21. Butller DS. The sensitive nervous system. Adelaide, Australia: 43. Buchmuller A, Navez M, Milletre-Bernardin M, et al; Lombotens
Noigroup Publications; 2000. Trial Group. Value of TENS for relief of chronic low back pain with
22. McConnell J. Recalcitrant chronic low back and leg pain e a new or without radicular pain. Eur J Pain 2012;16:656-65.
theory and different approach to management. Man Ther 2002;7:183- 44. Ferreira G, Stieven F, Araujo F, et al. Neurodynamic treatment did
92. not improve pain and disability at two weeks in patients with chronic
23. Hall TM, Elvey RL. Management of mechanosensitivity of the ner- nerve-related leg pain: a randomised trial. J Physiother 2016;62:197-
vous system in spinal pain syndromes. In: Boyling JD, Jull G, editors. 202.
Grieves modern manual therapy. 3rd ed. Edinburgh: Churchill Liv- 45. Armijo-Olivo S, Warren S, Magee D. Intention to treat analysis,
ingstone; 2004. compliance, drop-outs and how to deal with missing data in clinical
24. Shacklock M. Clinical neurodynamics. Sydney: Elsevier; 2005. research: a review. Phys Therapy Rev 2009;14:36-49.

www.archives-pmr.org
Spinal mobilization for lumbar radiculopathy 9

46. Petersen SM, Scott DR. Application of a classification system and dispersion of the fourth lumbar nerve root: an unembalmed cadaveric
description of a combined manual therapy intervention: a case with investigation. J Man Manip Ther 2015;23:239-45.
low back related leg pain. J Man Manip Ther 2010;18:89-96. 58. Schmid AB, Elliott JM, Strudwick MW, Little M, Coppieters MW.
47. Nagrale AV, Patil SP, Gandhi RA, Learman K. Effect of slump Effect of splinting and exercise on intraneural edema of the median
stretching versus lumbar mobilization with exercise in subjects with nerve in carpal tunnel syndromedan MRI study to reveal therapeutic
non-radicular low back pain: a randomized clinical trial. J Man mechanisms. J Orthop Res 2012;30:1343-50.
Manip Ther 2012;20:35-42. 59. da Silva JT, Santos FM, Giardini AC, et al. Neural mobilization
48. Cleland JA, Fritz JM, Whitman JM, Heath R. Predictors of short-term promotes nerve regeneration by nerve growth factor and myelin
outcome in people with a clinical diagnosis of cervical radiculopathy. protein zero increased after sciatic nerve injury. Growth Factors
Phys Ther 2007;87:1619-32. 2015;33:8-13.
49. Beltran-Alacreu H, Jiménez-Sanz L, Fernández Carnero J, La Touche R. 60. Bialosky JE, Beneciuk JM, Bishop MD, et al. Unraveling the
Comparison of hypoalgesic effects of neural stretching vs neural gliding: mechanisms of manual therapy: modeling an approach. J Orthop
a randomized controlled trial. J Manip Physiol Ther 2015;38:644-52. Sports Phys Ther 2018;48:8-18.
50. Basson A, Olivier B, Ellis R, et al. The effectiveness of neural 61. Tsirakis V, Perry J. The effects of a modified spinal mobilization with
mobilization for neuro-musculoskeletal conditions: a systematic re- leg movement (SMWLM) technique on sympathetic outflow to the
view and meta-analysis. J Orthop Sport Phys Ther 2017;47:1-76. lower limbs. Man Ther 2015;20:103-8.
51. Coppieters MW, Butler DS. Do ‘sliders’ slide and ‘tensioners’ ten- 62. Vicenzino B, Collins D, Benson H, Wright A. An investigation of
sion? An analysis of neurodynamic techniques and considerations the interrelationship between manipulative therapy induced hypo-
regarding their application. Man Ther 2008;13:213-21. algesia and sympathoexcitation. J Manip Physiol Ther 1998;21:
52. Coppieters MW, Andersen LS, Johansen R, et al. Excursion of the 448-53.
sciatic nerve during nerve mobilization exercises: an in vivo cross- 63. Sterling M, Jull G, Wright A. Cervical mobilization: concurrent ef-
sectional study using dynamic ultrasound imaging. J Orthop Sports fects on pain, sympathetic nervous system activity and motor activity.
Phys Ther 2015;45:731-7. Man Ther 2001;6:72-81.
53. Bertolini G, Silva T, Trindade D, Ciena A, Carvalho A. Neural 64. Perry J, Green A, Singh S, Watson P. A preliminary investigation into
mobilization and static stretching in an experimental sciatica model - the magnitude of effect of lumbar extension exercises and a
an experimental study. Rev Bras Fisioter 2009;13:493-8. segmental rotator manipulation on sympathetic nervous system ac-
54. Beneciuk JM, Bishop MD, George SZ. Effects of upper extremity tivity. Man Ther 2011;16:190-5.
neural mobilization on thermal pain sensitivity: a sham-controlled 65. Resende L, Merriwether E, Rampazo EP, et al. Meta-analysis of
study in asymptomatic participants. J Orthop Sports Phys Ther transcutaneous electrical nerve stimulation for relief of spinal pain.
2009;39:428-38. Eur J Pain 2018;22:663-78.
55. Santos FM, Silva JT, Giardini AC, et al. Neural mobilization reverses 66. Kennedy DJ, Noh MY. The role of core stabilization in lumbosacral
behavioral and cellular changes that characterize neuropathic pain in radiculopathy. Phys Med Rehabil Clin N Am 2011;22:91-103.
rats. Mol Pain 2012;8:57. 67. Chen HM, Wang HH, Chen CH. Effectiveness of a stretching exer-
56. Brown CL, Gilbert KK, Brismee JM, Sizer PS, James CR, Smith MP. cise program on low back pain and exercise self-efficacy among
The effects of neurodynamic mobilization on fluid dispersion within nurses in Taiwan: a randomized clinical trial. Pain Manag Nurs 2014;
the tibial nerve at the ankle: an unembalmed cadaveric study. J Man 15:283-91.
Manip Ther 2011;19:26-34. 68. Hedberg K, Alexander LA, Cooper K, Hancock E, Ross J, Smith FW.
57. Gilbert KK, Smith MP, Sobczak S, James CR, Sizer PS, Brismee JM. Low back pain: an assessment using positional MRI and MDT. Man
Effects of lower limb neurodynamic mobilization on intraneural fluid Ther 2013;18:169-71.

www.archives-pmr.org

You might also like