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An Analysis of Reasons for Failed Back Surgery Syndrome and Partial Results after Different Types of Surgical Lumbar Nerve Root Decompression

Authors:
  • Privolzhskiy Medical Research University
  • Privolzhsky Research Medical University, Nizhniy Novgorod, Russia

Abstract and Figures

Despite the evident progress in treating vertebral column degenerative diseases, the rate of a so-called "failed back surgery syndrome" associated with pain and disability remains relatively high. However, this term has an imprecise definition and includes several different morbid conditions following spinal surgery, not all of which directly illustrate the efficacy of the applied technology; furthermore, some of them could even be irrelevant. To evaluate and systematize the reasons for persistent pain syndromes following surgical nerve root decompression. Prospective, nonrandomized, cohort study of 138 consecutive patients with radicular pain syndromes, associated with nerve root compression caused by lumbar disc herniation, and resistant to conservative therapy for at least one month. The minimal period of follow-up was 18 months. Hospital outpatient department, Russian Federation Pre-operatively, patients were examined clinically, applying the visual analog scale (VAS), Oswestry Disability Index (ODI), magnetic resonance imaging (MRI), discography and computed tomography (CT). According to the disc herniation morphology and applied type of surgery, all participants were divided into the following groups: for those with disc extrusion or sequester, microdiscectomy was applied (n = 65); for those with disc protrusion, nucleoplasty was applied (n = 46); for those with disc extrusion, nucleoplasty was applied (n = 27). After surgery, participants were examined clinically and the VAS and ODI were applied. All those with permanent or temporary pain syndromes were examined applying MRI imaging, functional roentgenograms, and, to validate the cause of pain syndromes, different types of blocks were applied (facet joint blocks, paravertebral muscular blocks, transforaminal and caudal epidural blocks). Group 1 showed a considerable rate of pain syndromes related to tissue damage during the intervention; the rates of radicular pain caused by epidural scar and myofascial pain were 12.3% and 26.1% respectively. Facet joint pain was found in 23.1% of the cases. Group 2 showed a significant rate of facet joint pain (16.9%) despite the minimally invasive intervention. The specificity of Group 3 was the very high rate of unresolved or recurred nerve root compression (63.0%); in other words, in the majority of cases, the aim of the intervention was not achieved. The results of the applied intervention were considered clinically significant if 50% pain relief on the VAS and a 40% decrease in the ODI were achieved. This study is limited because of the loss of participants to follow-up and because it is nonrandomized; also it could be criticized because the dynamics of numeric scores were not provided. The results of our study show that an analysis of the reasons for failures and partial effects of applied interventions for nerve root decompression may help to understand better the efficacy of the interventions and could be helpful in improving surgical strategies, otherwise the validity of the conclusion could be limited because not all sources of residual pain illustrate the applied technology efficacy. In the majority of cases, the cause of the residual or recurrent pain can be identified, and this may open new possibilities to improve the condition of patients presenting with failed back surgery syndrome.
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Background: Despite the evident progress in treating vertebral column degenerative diseases, the rate
of a so-called “failed back surgery syndrome” associated with pain and disability remains relatively high.
However, this term has an imprecise definition and includes several different morbid conditions following
spinal surgery, not all of which directly illustrate the efficacy of the applied technology; furthermore,
some of them could even be irrelevant.
Objective: To evaluate and systematize the reasons for persistent pain syndromes following surgical
nerve root decompression.
Study Design: Prospective, nonrandomized, cohort study of 138 consecutive patients with radicular
pain syndromes, associated with nerve root compression caused by lumbar disc herniation, and resistant
to conservative therapy for at least one month. The minimal period of follow-up was 18 months.
Setting: Hospital outpatient department, Russian Federation
Methods: Pre-operatively, patients were examined clinically, applying the visual analog scale (VAS),
Oswestry Disability Index (ODI), magnetic resonance imaging (MRI), discography and computed
tomography (CT). According to the disc herniation morphology and applied type of surgery, all participants
were divided into the following groups: for those with disc extrusion or sequester, microdiscectomy was
applied (n = 65); for those with disc protrusion, nucleoplasty was applied (n = 46); for those with disc
extrusion, nucleoplasty was applied (n = 27). After surgery, participants were examined clinically and
the VAS and ODI were applied. All those with permanent or temporary pain syndromes were examined
applying MRI imaging, functional roentgenograms, and, to validate the cause of pain syndromes,
different types of blocks were applied (facet joint blocks, paravertebral muscular blocks, transforaminal
and caudal epidural blocks).
Results: Group 1 showed a considerable rate of pain syndromes related to tissue damage during the
intervention; the rates of radicular pain caused by epidural scar and myofascial pain were 12.3% and
26.1% respectively. Facet joint pain was found in 23.1% of the cases. Group 2 showed a significant rate
of facet joint pain (16.9%) despite the minimally invasive intervention. The specificity of Group 3 was the
very high rate of unresolved or recurred nerve root compression (63.0%); in other words, in the majority of
cases, the aim of the intervention was not achieved. The results of the applied intervention were considered
clinically significant if 50% pain relief on the VAS and a 40% decrease in the ODI were achieved.
Limitations: This study is limited because of the loss of participants to follow-up and because it is
nonrandomized; also it could be criticized because the dynamics of numeric scores were not provided.
Conclusion: The results of our study show that an analysis of the reasons for failures and partial effects
of applied interventions for nerve root decompression may help to understand better the efficacy of the
interventions and could be helpful in improving surgical strategies, otherwise the validity of the conclusion
could be limited because not all sources of residual pain illustrate the applied technology efficacy. In the
majority of cases, the cause of the residual or recurrent pain can be identified, and this may open new
possibilities to improve the condition of patients presenting with failed back surgery syndrome.
Key words: microdiscectomy, nucleoplasty, epidural scar, facet joint pain, recurrent herniation,
myofascial pain
Pain Physician 2011; 14:545-557
Prospective Study
An Analysis of Reasons for Failed Back
Surgery Syndrome and Partial Results after
Different Types of Surgical Lumbar Nerve Root
Decompression
From: 1Municipal Hospital 39
of Nizhniy Novorod, Russian
Federation; 2Municipal Hospital
13 of Nizhniy Novorod, Russian
Federation; and 3Scientific
Research Institute of Traumatology
and Orthopedics, Nizhny
Novgorod, Russian Federation.
Dr. Bokov is scientific officer
and neurosurgeon with
Scientific Research Institute of
Traumatology and Orthopedics,
Nizhniy Novgorod. Dr. Istrelov is
a neurosurgeon with Municipal
Hospital 13 of Nizhniy Novgorod.
Mr. Skorodumov is with
Municipal Hospital 39 of Nizhniy
Novgorod. Dr. Aleynik is scientific
officer and neurosurgeon with
Scientific Research Institute of
Traumatology and Orthopedics,
Nizhniy Novgorod. Dr. Simonov
is a neurosurgeon with Municipal
Hospital 39 of Nizhniy Novgorod.
Dr. Mlyavykh, is a neurosurgeon
with Scientific Research
Institute of Traumatology and
Orthopedics, Nizhniy Novgorod.
Address correspondence:
Dr. Andrey Bokov
Scientific Officer
Scientific Research Institute of
Traumatology and Orthopedics
2nd Neurosurgical Department
Moskovskoye Shosse-144
Nizhny Novgorod
Russian Federation
E-mail:
Andrei_Bokov@mail.ru
Disclaimer: There was no
external funding in the
preparation of this manuscript.
Conflict of interest: None.
Manuscript received: 06/19/2011
Revised manuscript received:
09/18/2011
Accepted for publication:
10/19/2011
Free full manuscript:
www.painphysicianjournal.com
Andrey Bokov, PhD1, Alexey Istrelov, PhD2 Alexander Skorodumov, PhD1, Alexander Aleynik,3
Alexander Simonov, PhD1, and Sergey Mlyavykh, PhD1
www.painphysicianjournal.com
Pain Physician 2011; 14:545-557 • ISSN 1533-3159
Pain Physician: November/December 2011; 14:545-557
546 www.painphysicianjournal.com
can be associated with the limitations or disadvantages
of the applied type of surgery. Some of them represent
mostly the naturally determined development of the
disease or even could be irrelevant to the assessment
of the technology efficacy. This analysis of the reasons
for failed back surgery syndrome may help to under-
stand better the clinical efficacy of different surgical
techniques and to elaborate rational surgical strategies
with clear guidelines for performing different surgi-
cal techniques. Therefore, theobjective of the present
study is to evaluate and to systematize the reasons for
persistent pain syndromes after different types of surgi-
cal nerve root decompression.
Methods
Study design
This is a prospective, nonrandomized cohort study
of patients presenting with radicular pain associated
with nerve root compression caused by disc herniation.
The participants underwent surgical interventions dur-
ing the period from March 2006 to October 2007; 88
patients were treated with nucleoplasty and 74 with
microdiscectomy. The results of microdiscectomy were
analyzed in 65 participants (88%) and the results of nu-
cleoplasty in 73 participants (83%). Potential benefits,
risks, advantages and disadvantages were explained,
and written informed consent was received from all
participants (concerning the applied type of surgery
and participation in the present study).
Inclusion criteria
Patients with pain syndromes caused by nerve root
compression associated with lumbar disc herniation re-
sistant to at least one month of conservative therapy
(including different types of blocks including selective
transforaminal nerve root blocks with corticosteroids)
were selected for this study. The inclusion criteria were
a pain intensity of no less than 40 on the 100-point Vi-
sual Analog Scale (VAS) and at least a 40% decrease
on the Oswestry Disability Index (ODI). Patients were
standardized by neurological deficit and only those
with a mild neurological deficit were selected. Written
informed consent was received from all participants.
Exclusion criteria
The exclusion criteria were litigation, uncontrolled
psychological disorders, severe or progressive neurolog-
ical deficit, and other serious pathological conditions
which might impact the results. Those with evidence of
Despite the evident progress in treating
vertebral column degenerative diseases, many
problems remain unresolved, and the rate
of failed back surgery syndrome after surgical nerve
root decompression remains considerable (1-9). The
term “failed back surgery syndrome” has an imprecise
definition and includes different morbid conditions
following spinal surgery that are associated with
persistent pain and disability (1-3). According to the
results of different studies, the rate of such cases varies
from 10% to 40% (10-16) and the following reasons are
likely to be the most frequent: nerve root compression
caused by recurrent disc herniation or retained disc
fragment; epidural fibrosis; lateral and foraminal
stenosis; segment instability; progressive facet joint
degeneration; and myofascial pain (1-3,17-26).
The rate of nerve root compression caused by re-
current disc herniation ranges from 5 to 26% of micro-
discectomies and the frequency is sometimes reported
to be as high as 38% (14,15,27-32).
Epidural fibrosis is a progressive disease, which is
associated with radicular pain and unfavorable out-
comes after surgery. It has been reported that the rate
of this source of pain accounts for up to 20-36% of
all cases with failed back surgery syndrome presenta-
tion (1-9,14,15,33,34). It has been determined that this
pathological process may develop as a response to tis-
sue damage during the intervention (33,34); it also has
been established that retained hematomas are likely to
develop into scar tissue (35). Additionally, some studies
have indicated that the material of the nucleus pulpo-
sus itself is capable of initiating aseptic inflammation in
the epidural space and thus contributing to a progres-
sive epidural fibrosis formation (36,37).
Some causes of persistent pain syndromes follow-
ing surgery are likely to be associated mostly with the
progression of degenerative changes; among them
are spinal stenosis, facet joint degeneration, and seg-
ment instability. According to the results of other stud-
ies, the degenerative processes in a disc leading to disc
height loss may provoke degeneration of other struc-
tures of the vertebral segment (17,42,47), finally result-
ing in different types of stenosis or segment instability
(17,44,48-50).
Given this history, it was felt that an analysis of the
reasons for failed back surgery syndrome as a supple-
ment to the earlier studies which have had the objec-
tive of evaluating the efficacy of different surgical tech-
nologies focused on nerve root decompression could be
helpful because not all of the reasons for this failure
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Reasons for Pain Syndrome After Lumbar Nerve Root Decompression
spinal stenosis, infection, tumors, or segment instability,
and those with spinal surgery in anamnesis (any type)
were excluded.
Participants’ examination.
Before the interventions, all participants were
given a neurological examination; initially all of them
presented with compressive radicular pain pattern
(prevalence of leg pain corresponding to the relevant
autonomous zone of innervation).
All participants were examined preoperatively ap-
plying the VAS (scale 0-100 was applied) and Oswestry
disability questionnaire V1 (51-53). All patients under-
went magnetic resonance imaging tomography (MRI
tomography). According to the results of MRI tomogra-
phy, disc herniations were classified as a disc protrusion if
the greatest distance between the edges of disc material
displaced from the disc space was less than the distance
between the edges of the base measured at the same
plane (contained disc herniation) and was classified as an
extrusion (uncontained disc herniation) when displaced
disc material beyond the outer annulus had the maximal
size at any plane greater then the distance between the
edges of the base at the same plane on MRI images (54).
Discography was utilized to certify if disc herniation was
contained or not.
Surgical interventions
Nucleoplasty was performed by several surgeons in
sterile conditions under the guidance of fluoroscopy; 6
channels were created within the disc using a radio-
frequency wand applying ablation and coagulation
mode. The surgical technique was standard without ac-
ceptance of any variances; the standard technique has
been described in several manuscripts (55-57).
All microdiscestomies were performed by the same
surgeon using a standard technique: transmuscular
translaminar approach was applied in order to diminish
tissue damage; there were no cases with damage of ve-
nous vessels during the intervention and no diathermy
was used in the epidural space. The reconstruction of
the lateral channel was performed in case of narrowing
by hypertrophied facet joints and osteophytes. Abso-
lute hemostasis was achieved in all cases.
Outcome measures
Participants were examined after one month, 3
months, 6 months, 12 months, and 18 months. No less
than 50% pain intensity relief on the VAS and at least
40% decrease on the ODI were considered to be clini-
cally significant; among them, cases with total pain re-
lief were registered (25). The results were considered
unsatisfactory in case of unresolved or recurred nerve
root compression on the same level after the interven-
tion. All cases with temporary, recurrent, or permanent
pain syndromes after surgical interventions were ana-
lyzed. In order to validate the source of pain in these
cases, MRI imaging, functional roentgenograms, com-
puted tomography (CT) myelograms, diagnostic facet
joint blocks, caudal epidural blocks, transforaminal se-
lective nerve root blocks, and blocks of the paraverte-
bral muscles were applied during the follow-up period
in order to evaluate the reasons for persistent pain syn-
dromes after the different types of surgery.
The recurrence of disc compression was confirmed
by the results of MR tomography. For validation of oth-
er sources of pain, different types of blocks were ap-
plied repeatedly and in cases of a combination of pain
sources, appropriate types of diagnostic blocks were
administered.
Diagnostic facet joint blocks were performed twice
in sterile conditions under the guidance of fluoroscopy
with 2 different anesthetics and different action times.
Needles were introduced using standard landmarks
for the medial branch location (junction of the upper
border of the transverse process base and the lateral
border of the upper articular process base). At least 2
of the adjacent medial branches – the nerve supply of
the supposed source of pain – were blocked on each
side. No more than 0.5 mL of anesthetic was injected
to block each medial branch. Different types of anes-
thetic were used repeatedly (novocaine, lidocaine, bu-
pivacaine). Repeated diagnostic facet joint blocks with
different types of anesthetics are known to be the only
valid diagnostic method to confirm the facet joint as
the origin of pain (21,58,59). At least 50% pain relief
on the VAS during the time of anesthetic action was
considered to be diagnostically significant for the vali-
dation of facet joint pain.
In cases when myofascial pain was suspected, para-
vertebral muscle blocks with anesthetic and corticoste-
roid were performed in order to block trigger zones,
terminate muscular spasm, diminish the inflammatory
process, and perform a hydraulic dissection of a post-
operative scar. No less than 50% pain relief on the VAS
after the procedure was the criteria for the myofascial
origin of pain.
In the case of radicular pain syndrome after sur-
gery, caudal epidural blocks, transforaminal blocks and
percutaneous adhesiolysis were administered; those
Pain Physician: November/December 2011; 14:545-557
548 www.painphysicianjournal.com
interventions are known to be positive in regards to
short-term and long-term pain relief in patients pre-
senting with failed back surgery syndrome (59,60).
The diagnosis of epidural adhesive process was mostly
based on the combination of radicular pain correspond-
ing to the relevant autonomous zone of nerve root in-
nervation and the results of the MRI imaging showing
epidural scar formation. In those cases, caudal epidural
and transforaminal nerve root blocks with corticoste-
roids and hydraulic dissection of epidural structures
with saline solution anesthetics provided partial pain
relief. No less than 50% pain relief on the VAS was con-
sidered clinically significant.
Statistical analysis
For datasets presented in dichotomized scale,
Fisher`s exact test was applied. If a statistically signifi-
cant difference was established, the logistic regression
analysis was applied (quasi-Newton algorithm). The
power analysis was performed twice: once when plan-
ning this study in order to calculate a sample size and a
posteriori by applying the Monte Carlo method.
Results
According to the disc herniation morphology and
the applied surgical intervention, all participants were
divided into the following subgroups:
For those with a nerve root compression caused by
disc extrusion or sequester: microdiscectomy was ap-
plied (n = 65) – Group 1.
For those with a nerve root compression caused
by contained disc herniation – disc protrusion. In these
cases no contrast medium leakage beyond the disc
space was evaluated during the discography, thereby
confirming the disc herniation continuity: Nucleoplasty
was applied in all cases (n = 46) – Group 2.
For those with a nerve root compression caused
by uncontained herniation - disc extrusion. These par-
ticipants insisted on having nucleoplasty instead of mi-
crodiscectomy. The morphological type was confirmed
by MRI images and discography (the contrast medium
leakage into the epidural space was evident) (n = 27) –
Group 3.
Demographic characteristics are represented in Ta-
ble 1. Table 2 shows the percentage of participants with
total pain relief without any temporary or permanent
pain syndromes presentation and those who presented
at least satisfactory results throughout all the period of
follow-up during 18 months.
Comparing Groups 2 and 3 it is possible to conclude
that in the case of a total annulus disruption, the rate
of clinically significant results and total pain relief after
nucleoplasty is lower (the statistical significance was P =
0.0049 and P = 0.0024 respectively).
Table 1. Demographic characteristics of patients’ groups.
Group 1 Group 2 Group 3
N 65 46 27
Females 33 (50.8%) 15 (32.6%) 15 (55.5%)
Males 32 (49.2%) 31 (67.4%) 12 (44.4%)
Smoking 48 (73.8%) 22 (47.8%) 18 (66.7%)
Age m=43.55±1.3001
SD=10.48
m=43.9783±1.7327
SD=11.7521
m=41.22±2.0481
SD=10.64
Table 2. The rate of stable clinically significant results (at least satisfactory) and total pain relief in different groups of patients.
Group 1 Group 2 Group 3
N 65 46 27
At least satisfactory results 61 – 93.8%
95% CI (85%-98.3%)
36 – 73.8%
95% CI (58.9%-85.7%)
12-44.4%
95% CI (25.5%-64.7%)
The rate of total pain relief 36 – 55.4%
95% CI (42.5%-67.5%)
24 - 52,2%
95% CI (37%-67.1%)
4 – 14.8%
95% CI (4.2%-33.7%)
The rate of cases with pain
syndromes presentation
44.7%
95% CI (32.3%-57.4%)
47.8%
95% CI (32.9%-63.0%)
85.2%
95% CI (66.3%-95.2%)S
Note: All cases with permamanent and temporary pain syndromes were registered.
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Reasons for Pain Syndrome After Lumbar Nerve Root Decompression
To test the observed differences logistic regres-
sion analysis was performed and statistically significant
models were estimated for the rates of total pain relief
and clinically significant results:
Parameters of the regression model for clinically
significant results rates, Group 2 versus Group 3: Β0=
–2.7850; 95% CI [–4.4065; –1.1635], P = 0.001. Odds ra-
tio = 4.50; 95% CI [1.5731; 12.8727]. Goodness-of-fit χ2
= 8.56212, P = 0.0034.
Parameters of the regression model for total pain
relief rates, Group 2 versus Group 3: Β0 = –3.6270; 95%
CI [–5.8627; –1.3932], P = 0,0018. Odds ratio = 6.2727;
95% CI [1.8328; 21.4677]. Goodness-of-fit χ2 = 10.8693,
P = 0.00098.
Statistically significant regression coefficients con-
firm the association of observed differences and disc
herniation morphology as explanatory factor.
Comparing Groups 1 and 3 it is possible to conclude
that nucleoplasty is less effective than microdiscectomy
in case of uncontained disc herniations (statistical sig-
nificance for differences of at least satisfactory results
and total pain relief rates presented in Table 2 was P <
0.0001). This conclusion is supported by the results of
logistic regression analysis.
Parameters of the regression model estimated for
the rates of clinically significant results, Group 1 versus
group 3: Β0 = –5.6723; 95% CI [–7.8636; –3.4810], P <
0.0001. Odds ratio = 19.0625; 95% CI [2.2870; 68.7301].
Goodness-of-fit χ2 = 26.564, P < 0.0001.
Parameters of the regression model for total pain
relief rates, Group 1 versus group 3: Β0= –2.1816; 95%
CI [–3.6452; –0.7181], P = 0.0039. Odds ratio = 7.1379;
95% CI [2.1820; 23.3507]. Goodness-of-fit χ2 = 13.963,
P = 0.00019. Statistically significant regression coeffi-
cients confirm that observed differences are associated
with the type of the applied surgery.
According to the datasets represented in Table 2,
the rate of patients presenting temporary, partially re-
solved, or unresolved pain syndromes throughout all the
period of follow-up achieved 44.6% in Group 1; formed
47.8% in Group 2; and came to 85.2% in Group 3.
In cases of nerve root compression caused by recur-
rent disc herniation or retained disc fragment and cases
of epidural fibrosis, pain syndromes were presented
by radicular pain in the lower limbs corresponding to
the relevant autonomous zone of innervation of the
affected nerve root. In other cases, the pain syndrome
changed to a noncompressive type profile with the
prevalence of low back pain with irradiation to the but-
tocks or lower limbs without correspondence to exact
autonomous zones of nerve root innervation.
The overall frequencies of different residual pain
causes after different types of surgery evaluated
throughout the 18 month period of follow-up are pre-
sented in Table 3. According to these results, it is possi-
ble to conclude that each group has distinctive features
in regards to the structure of residual pain syndrome
sources.
Group 1
This group can be distinguished by the significant
rate of epidural scar formation associated with radic-
ular pain (verified in 8 cases – 12.3%), the significant
rate of myofascial pain which was identified in 17 cases
(26.1%), and the high rate of facet joint pain (verified
in 15 cases – 23.1%). It should be mentioned that in 16
cases (24.6%) there was a combination of pain sources:
the combination of epidural fibrosis and segment in-
stability was verified in one case; the combination of
epidural fibrosis and myofascial pain in 7 cases; epidur-
al fibrosis and facet joint pain in one case; and a the
combination of myofascial pain and facet joint pain in
7 cases.
Group 2
In this group, the rate of myofascial pain was rela-
tively low (6.5% - 3 cases); however, the rate of facet
joint pain was significant despite the minimal surgical
aggression. This source of pain was verified in 11 cases
(16.9%).
Table 3. The rates of different causes of pain syndromes after surgical nerve root decompression directly or indirectly related to the
applied surgery.
Recurrent Disc Herniation or
Retained Fragment
Epidural Scar
Formation
Instability of
Vertebral Segment
Facet Joint
Pain
Myofascial
Pain
Group 1 n=65 3 (4.6%) 8 (12.3%) 2 (3.1%) 15 (23.1%) 17 (26.1%)
Group 2 n=46 4 (8.7%) 0 (0%) 3 (6.5%) 11 (16.9%) 3 (6.5%)
Group 3 n=27 17 (63.0%) 0 (0%) 0 (0%) 6 (22.2%) 2 (7.4%)
Note: Cases with the onset of pain syndromes irrelevant to the applied surgery were excluded from the analysis.
Pain Physician: November/December 2011; 14:545-557
550 www.painphysicianjournal.com
Group 3
The specificity of this group was the high rate of
unresolved nerve root compression or recurrent disc
herniation (verified in 17 cases – 63.0%), facet joint
pain was determined in 6 cases (22.2%), myofascial pain
in 2 cases (7.4%), the combination of facet joint pain
and myofascial pain was diagnosed in 2 cases.
Comparing these groups of patients, it is possible
to conclude that Group 1 differs from Group 2 by a sig-
nificant rate of epidural scar formation (P = 0.0199) and
by a significantly higher rate of myofascial pain presen-
tation (P = 0.0110), however no difference in the rate
of facet joint pain was found in these 2 groups (P =
0.9988).
Group 3 can be distinguished from Group 1 and
Group 2 by the high rate of recurrent or unresolved
nerve root compression (P < 0.0001 in both cases), the
prognostic value was confirmed by significant logistic
regression models.
Group 1 versus Group 3, parameters of the regres-
sion model: Β0 = –5.6723; 95% CI (–9.0678; –4.1076), P <
0.0001. Odds ratio = 35.1333; 95% CI (8.5159; 144.7458).
Goodness-of-fit χ2 = 36.432, P < 0.0001.
Group 2 versus Group 3, parameters of the regres-
sion model: Β0 = -5.2334; 95% CI (-7.46724; -2.999517),
P < 0.0001. Odds ratio = 17.85; 95% CI (4.806283;
66.2929). Goodness-of-fit χ2 = 24.833, P < 0.0001.
Analyzing the difference in the myofascial pain rate
observed in Groups 1 and 2, it is possible to conclude that
this cause of pain syndrome is associated with a more
aggressive intervention. Estimated parameters of logistic
regression model for myofascial pain difference:
Β0 = -4.287188; 95% CI (-6.719846; -1.85453), P =
0.0007. Odds ratio = 5.0764; 95% CI (1.3710; 18.8026).
Goodness-of-fit χ2 = 7.8241, P = 0.0052.
Different types of causes of the persistent pain syn-
dromes can be illustrated by the following cases.
Case 1
Before the intervention, this participant (Group 2)
presented a typical radicular pain pattern correspond-
ing to the L5 autonomous zone of innervation. MRI to-
mography diagnosed a protrusion on the level L4-5 and
also signs of spondyloarthrosis were evident (Fig.1). Af-
ter nerve nucleoplasty, there was more than a 50-point
decrease in VAS and ODI scores. The residual pain syn-
drome was mostly axial and there was no evidence of
unresolved nerve root compression. Control MRI tomo-
grams showed a decrease in disc protrusion size after
nucleoplasty (Fig. 2). Facet joint pain was confirmed by
diagnostic blocks and this residual pain syndrome in
this case does not illustrate the inability of nucleoplasty
to provide total pain relief because nerve root compres-
sion was resolved.
Fig. 1. Case 1 MRI before nucleoplasty. Fig. 2. Case 1 MRI after nucleoplasty.
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Reasons for Pain Syndrome After Lumbar Nerve Root Decompression
Case 2
This participant presented a typical compressive
radicular pain pattern at L5 and disc extrusion was di-
agnosed on the level L4-5. (Fig. 3 represents MR to-
mograms one month before the intervention). After
microdiscectomy, total pain relief was achieved. How-
ever, after 5 months passed, pain recommenced. Pain
was mostly axial with irradiation to the buttock and
posterior hip areas. Control MR tomograms showed
only a significant progression of the spondyloarthrosis
(Fig. 4 represents MR tomograms 6 months after the
intervention) and facet joint pain was confirmed by
the results of diagnostic facet joint blocks. In this case
disc extrusion formation and consequent microdiscec-
tomy resulted in a disc space narrowing, finally result-
ing in an apparent increase in load on the facet joints;
thereafter, the progression of the spondyloarthrosis is
expected.
Case 3
This participant (Group 1) presented a severe ra-
dicular pain and a large disc sequester was diagnosed
by the MR tomograms at the level L5-S1. Figs. 5 and 6
represent MR tomograms before the intervention. In
Fig. 3. Case 2 MRI before the microdiscectomy. Fig. 4. Case 2 MRI 6 months after the microdiscectomy.
Fig. 5. Case 3 MRI before the microdiscetomy. Fig. 6. Case 3 MRI before the microscectomy
Pain Physician: November/December 2011; 14:545-557
552 www.painphysicianjournal.com
this case, microdiscectomy was applied and the result
was unsatisfactory because of the epidural fibrosis for-
mation and progression of the degenerative changes
resulting in a retrospondylolisthesis. Figures. 7 and 8
represents MR tomograms 4 months after microdis-
cectomy. In this situation, microdiscectomy was insuf-
ficient to achieve total pain relief and segment fusion
was required. However, this case mostly illustrates the
biomechanical disadvantage of the intervention.
Case 4
As mentioned above, some cases with pain pre-
sentation after surgery were excluded from the analy-
sis. This case illustrates the type of pain syndrome not
related to the applied type of surgery and thereafter
excluded from the analysis. This participant presented
a typical radicular S1 pain pattern and disc extrusion
was confirmed by the results of MR tomography (Figs.
9, 10). In this case, microdiscectomy was applied. After
Fig. 7. Case 3 MRI after microdiscectomy. Fig. 8. Case 3 MRI after microdiscectomy.
Fig. 9. Case 4 MRI before microdiscectomy. Fig. 10. Case 4 MRI before microdiscectomy.
www.painphysicianjournal.com 553
Reasons for Pain Syndrome After Lumbar Nerve Root Decompression
12 months had passed, pain recommenced; however, it
was associated with disc degeneration on the adjacent
level (Fig. 11). In this case, the recurrent pain syndrome
was irrelevant in regards to the applied surgery. Those
types of cases were excluded from the presented analy-
sesin order to avoid bias.
disCussion
Nucleoplasty applying coblation technology has
been widely introduced into clinical practice since 2000;
the reported rate of clinically significant results were
scattered from 56% to 88%. In all cases the conclusions
concerning the efficacy of the applied technologies
were based on the analysis of pain-associated numeric
scores dynamics (VAS, ODI) and none of the manu-
scripts provided the explanation for the partial results
and failures. Finally, it is impossible to explain such a
wide range of reported clinically significant results (55-
57,60-62). Even if an analysis of total pain relief and
clinically significant results is performed, it is impossible
to figure out the reason for the observed differences; in
other words, whether it was a result of an unaccounted
for factor of the groups’ inequality or whether an unfa-
vorable prognostic factor was present in some studies.
In studying the efficacy of the applied technolo-
gies, first of all it is necessary to define if the applied
intervention is capable of providing stable nerve root
decompression in the particular cases studied. The
results of our study show that nucleoplasty, being ef-
fective in cases of contained disc herniation, failed to
provide stable nerve root decompression in the major-
ity of cases when nerve root compression was caused
by uncontained disc herniation (disc extrusion), while
the results of microdiscectomy in the same situation
were considerably better despite the higher invasive-
ness and biomechanical disadvantages. By analyzing
the rates of cases when unresolved or recurred nerve
root compression was present, it is possible to make a
valid conclusion that total annulus disruption is a limi-
tation for the nucleoplasty indication because of the in-
ability to provide stable nerve root decompression and
not because of any other factors. This type of analysis
is closely related to the analysis of the clinically signifi-
cant results rate and has the advantages of comparing
with analysis based on the pain related numeric scores
dynamics (ODI, VAS), especially in case when a consid-
erable number of different interventions were applied
during the follow-up period to manage the residual
pain. The analysis based on pain related scores dynam-
ics (VAS and ODI) represents the agglomerative analysis
Fig. 11. Case 4 MRI one year after microdiscectomy.
of specific and nonspecific factors influence thereafter
the statistical significance of observed effects could be
decreased. For example, when the ability of the applied
intervention to provide stable nerve root decompres-
sion was tested, the estimated regression models were
of a higher statistical significance than those estimated
analyzing the rates of clinically significant results based
on VAS and ODI scores dynamics.
The next category of reasons for pain syndromes
after surgical nerve root decompression is related to tis-
sue damage during the intervention. However, the fre-
quency of this kind of pain source illustrates mainly the
technical disadvantage of the applied type of surgery.
Despite tissue damage being minimized during micro-
discectomy and absolute hemostasis being achieved, a
considerable rate of radicular pain associated with fi-
brosis in the epidural space was detected after open
surgery. Myofascial pain is known to be caused by mul-
tiple factors 63,64) and the results of different studies
have supported the hypothesis that myofascial pain
may contribute to failed back surgery syndrome (65,66).
According to the results of our study, the higher rate of
myofascial pain was estimated in the group of patients
treated with microdiscectomy and the association with
a more aggressive type of surgery was proved by the re-
Pain Physician: November/December 2011; 14:545-557
554 www.painphysicianjournal.com
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The third category of persistent pain syndromes is
related to the naturally determined disease develop-
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segment instability. It was proved that those degen-
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surgery (20,39,44,46,48,49). Because of the minimal
number of cases with clinical presentation of stenosis
and segment instability after surgery, the rates of these
pain sources were not analyzed. In contrast, the rate of
facet joint pain was considerable; however, it has been
reported that the higher frequency of facet joint pain
has no association with previously applied lumbar sur-
gery: while the overall prevalence of facet joint pain
achieves 31% with a 95% CI of 28%-33%, the rate of
this source of pain after lumbar surgery was 16% with
a 95% CI of 9-23% (20,21,25,58). Also, it was reported
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and a number of previous surgeries (20). Even though
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sources has a limited specificity in regards to the ap-
plied surgery, detailed analysis could provide significant
information because rapid progression of degenerative
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(67,68). Finally, this analysis may point out indirectly the
biomechanical disadvantages of surgical interventions
(69,73).
Studying the efficacy of different interventions,
it is necessary to analize the reasons for failures and
partial results in order to explain the observed effects
adn finally to understand better the efficacy of applied
technology. This information could be helpful to elabo-
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may help to discover biomechanical and technical limi-
tations. and Their disadvantages could disclose other
factors which could impact the results. Finally, the abil-
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pain makes possible the application of different mini-
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This study is limited because of the groups’ dispro-
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of analyses of technology efficacy and the significance
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ConClusion
The results of our study show that the analysis
of the reasons for failed back surgery syndrome and
partial effects of interventions applied for nerve root
decompression might help to better understand the
efficacy of the interventions and could be helpful for
improving surgical strategies. However, the conclusion
could be limited because not all sources of residual pain
illustrate the efficacy of the applied technology. In the
majority of cases, the cause of the residual or recurrent
pain can be identified, and this may open new possi-
bilities to improve the condition of patients presenting
with failed back surgery syndrome.
aCknowledgMents
The authors would like to thank the editors of Pain
Physician journal for their review and constructive criti-
cism in improving the manuscript.
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... [15] Andrew Bokov et al showed that one of the reasons for pain syndromes after surgical nerve root decompression is tissue damage (including hematoma) during the intervention. [16] Although using a microscope and a good hemostat can minimize tissue damage during microdiscectomy, a considerable rate of radicular pain associated with fibrosis in the epidural space has been reported after open surgery. [16] A high amount of bleeding will increase the risk of fibrosis in the epidural space during the healing process. ...
... [16] Although using a microscope and a good hemostat can minimize tissue damage during microdiscectomy, a considerable rate of radicular pain associated with fibrosis in the epidural space has been reported after open surgery. [16] A high amount of bleeding will increase the risk of fibrosis in the epidural space during the healing process. This study suggested that the spine surgeon should opt for less invasive interventions in order to diminish the rate of pain syndromes associated with tissue damage. ...
... This study suggested that the spine surgeon should opt for less invasive interventions in order to diminish the rate of pain syndromes associated with tissue damage. [16] Andrew Bokov et al also showed that the persistent pain syndrome is related to the naturally determined disease development such as facet joint pain, stenosis, and segment instability [16] This study reports that the overall prevalence of facet joint pain was 31%, with a 95% CI of 28% to 33%; the rate of this source of pain after lumbar surgery was 16%, with a 95% CI of 9% to 23%. A higher frequency of facet joint pain was expected in the group treated with microdiscectomy due to a more significant loss of disc height, yet there was no relationship between the pain source and the type of surgery. ...
Article
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Magnetic resonance imaging (MRI) has been extensively used in the management of patients with a herniated lumbar disc. Nevertheless, immediate postoperative MRI has not become a standard procedure, with limited research suggesting that the findings are often similar to preoperative MRI in both symptomatic and asymptomatic patients. This study aimed to determine the benefits of immediate postoperative MRI in patients with or without postoperative symptoms and its correlation with these symptoms. A total of 172 patients who underwent lumbar spine microdiscectomy at our institution between 2014 and 2021 were included. Patients who had previous spinal surgery and lumbar fusion were excluded. Patient data were collected from medical records. MRI was performed 3 days after surgery and assessed by 2 neurosurgeons to minimize bias. Immediate postoperative MRI results showed dural sac compression or foraminal stenosis in 29 patients (16.86%), of which 10 had postoperative pain and 19 were pain free. Among the 143 patients (83.14%) without these findings on MR imaging, 38 had postoperative pain. Immediate postoperative MRI did not correlate with postoperative pain (P = .421/.357). Intraoperative bleeding and the Charlson comorbidity index (CCI) showed significant correlations with postoperative pain (P = .018 and .002, respectively). In a multivariate analysis, intraoperative blood loss and CCI independently correlated with postoperative pain (P = .001 and .001, respectively). Based on our findings, intraoperative blood loss and CCI appear to be the factors that may predict the persistence of postoperative pain, despite normal findings on MRI.
... Bokov et al. [12] Patients with a pain intensity of no less than 40 on the 100-point VAS and at least a 40% decrease on the Oswestry Disability Index (ODI) -VAS > 40/100 -ODI decrease < 40% ...
... The prevalence of FBSS ranges from 10 to 40% according to different researches [12,23]. Persistent pain, frequent hospitalization and the resulting heavy financial burden will not only aggravate the doctor-patient contradictions, but also lead to an excessive occupation of medical resources [24]. ...
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Background: With the growing number of traditional posterior open surgery, the incidence of failed back surgery syndrome (FBSS) increases gradually. We aimed to investigate the incidence and risk factors for FBSS following open posterior lumbar surgery for degenerative lumbar disease (DLD). Method: A multivariable regression analysis was performed for 333 consecutive patients to identify potential risk factors for FBSS. Clinical outcomes were evaluated by the validated North American Spine Society (NASS) Questionnaire and numerical rating scale (NRS) for pain. Demographics, diagnostic characteristics, surgical data, radiographic parameters for each patient were analyzed. Result: 16.8% of the included patients were classified as FBSS. Univariate analysis showed that age, hypertension, symptom location, intermittent claudication, preoperative pain NRS-leg, HIZ, Modic changes (MCs), surgical strategy and postoperative rehabilitation were related to FBSS. Multivariable logistic regression analysis demonstrated that preoperative NRS-leg (OR:0.80, 95%CI:0.71-0.91, P = 0.001), hypertension (OR: 2.22, 95%CI: 1.10-4.51, P = 0.027), intermittent claudication with waking distance > 100 m (OR: 4.07, 95%CI: 1.75-9.47, P = 0.001) and waking distance ≤ 100 m (OR: 12.43, 95%CI: 5.54-27.92, P < 0.001), HIZ (OR: 8.26, 95%CI: 4.00-17.04, P < 0.001), MCs (OR: 3.41, 95%CI: 1.73-6.71, P < 0.001), postoperative rehabilitation (OR: 2.63, 95%CI: 1.13-6.12, P = 0.024) were risk factors for FBSS. Conclusion: Open posterior lumbar surgery is an effective treatment for DLD which provides pain reduction and lumbar curve improvement with a considerable satisfaction rate. Lower preoperative NRS-leg, hypertension, intermittent claudication, HIZ, MCs and postoperative rehabilitation are risk factors for FBSS, which can serve as a tool for clinicians to identify at-risk population and provide more effective management to mitigate the doctor-patient contradictions and further occupation of medical resources.
... In addition, incorrectly performed surgical procedures which account for approximately 2.1%-2.7% of total patients receiving spinal surgery, also contribute to the development of CPSS [14]. Surgical complications such as nerve damage [16], misdiagnosis, and mistreatment may also contribute to CPSS if surgery is performed on unaffected spinal segments and does not relieve nerve compression at the causative segment. Accordingly, increasing the surgery success rate is key to limiting the aforementioned structural factors directly related to surgical intervention. ...
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Chronic pain after spine surgery (CPSS) is often characterized by intractable low back pain and/or radiating leg pain, and has been reported in 8–40% of patients that received lumbar spine surgery. We conducted a literature search of PubMed, MEDLINE/OVID with a focus on studies about the etiology and treatments of CPSS and low back pain. Our aim was to provide a narrative review that would help us better understand the pathogenesis and current treatment options for CPSS. This knowledge will aid in the development of optimal strategies for managing postoperative pain symptoms and potentially curing the underlying etiologies. Firstly, we reviewed recent advances in the mechanistic study of CPSS, illustrated both structural (e.g., fibrosis and scaring) and non-structural factors (e.g., inflammation, neuronal sensitization, glial activation, psychological factor) causing CPSS, and highlighted those having not been given sufficient attention as the etiology of CPSS. Secondly, we summarized clinical evidence and therapeutic perspectives of CPSS. We also presented new insights about the treatments and etiology of CPSS, in order to raise awareness of medical staff in the identification and management of this complex painful disease. Finally, we discussed potential new targets for clinical interventions of CPSS and future perspectives of mechanistic and translational research. CPSS patients often have a mixed etiology. By reviewing recent findings, the authors advocate that clinicians shall comprehensively evaluate each case to formulate a patient-specific and multi-modal pain treatment, and importantly, consider an early intraoperative intervention that may decrease the risk or even prevent the onset of CPSS. Translational potential statement CPSS remains difficult to treat. This review broadens our understanding of clinical therapies and underlying mechanisms of CPSS, and provides new insights which will aid in the development of novel mechanism-based therapies for not only managing the established pain symptoms but also preventing the development of CPSS.
... Periprosthetic fractures are common and carry significant morbidity and mortality [77,91]. The rate of a so-called failed back surgery syndrome associated with pain and disability is relatively high [92]. ...
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Purpose of Review Describe the potential contribution of disorganized tissue to the pathogenesis of bone abnormalities and fractures. Especially, fractures that are unexplained by bone loss (osteoporosis) or structural deterioration. Recent Findings Currently, bone fragility is primarily viewed as due to loss, or decay (osteoporosis). However, it is also acknowledged that this view is limited because it does not explain many fractures or abnormalities such as necrosis, sclerosis, or infarcts. Atypical femoral fractures (AFFs) during antiresorptive therapy are an example. Hence, it is proposed that another distinct mechanism is responsible for bone diseases. A remarkable bone property distinct from mass and decay is the organization (arrangement) of its components. Components must be perfectly assembled or well-stacked to ensure “the right amount of bone, at the right place”. Disorganization is an aberration that is conspicuous in many diseases, more so in conditions poorly associated with bone mass and decay such as osteogenesis imperfecta, hypophosphatasia, and AFFs. However, despite the likely critical role of disorganization, this feature has received limited clinical attention. Summary This review focuses on the potential contribution of disorganization to bone in health and diseases. Particularly, we propose that disorganization, by causing ineffective transfer of loads, may produce not only bone abnormalities (pain, necrosis, infarct, sclerosis, delayed healing) but also fractures, especially AFFs or stress fractures. A disorganized element is one that is where it shouldn’t be (improperly stacked elements). Hence, disorganization can be measured by quantifying the extent to which a tissue (pixel within an image) is at an incorrect location.
... Al reported that the prevalence of lumbar facet joint pain in patients with recurrent pain after various surgical interventions was 16% (95% CI 9-23%) [19]. Bokov et.al conducted an analysis to find the reasons for persistent pain syndromes following surgical intervention in LDH patients, and they found that facet joint pain was responsible for 23.1% cases that underwent microdiscectomy [20]. Although facet joint pain is estimated to be responsible for 15-45% of LBP, LFJOA has to date received far less studies than other OA and disc degeneration [10,21,22]. ...
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Introduction A post-hoc subgroup analysis of prospective collected data in a randomized controlled trial (RCT) of minimally invasive discectomy was conducted, to find out the possible underlying reasons for patients with persistent low back pain (LBP) following surgery. Materials and methods Patients who were diagnosed with lumbar disc herniation (LDH) and underwent either percutaneous transforaminal endoscopic discectomy or microendoscopic discectomy in our RCT were analyzed. Patients with persistent LBP in 2-year follow-up were compared with the non-LBP patients to determine the underlying reasons. Then, the demographic characteristics, clinical outcomes and radiological parameters of patients with preoperative lumbar facet joint osteoarthritis (LFJOA) were assessed and compared with the non-LFJOA subgroup. Results 18 patients (8.1%) were reported to have persistent LBP in 2-year follow-up. Significantly higher proportion of preoperative LFJOA were found in the persistent LBP subgroup and was considered to be a risk factor using multivariate analysis. The prevalence of LFJOA is strongly associated with older age, female, high BMI and heavy labor in the LDH population. All of the clinical outcomes including ODI, SF36-PF, SF36-BP, EQ-5D, VAS-back and VAS-leg were worse in LFJOA subgroup in 2-year follow-up. LFJOA subgroup was associated with more adjacent segment degeneration and more lateral recess stenosis. Conclusions LFJOA is a possible underlying reason for patients with persistent LBP after minimally invasive discectomy. Surgeons should carefully review the preoperative radiological images to find out whether there is LFJOA in the LDH segment, and kindly diminish the expectation of back pain relief for those patients. Trial registration: This trial was registered at ClinicalTrials.gov at November 14, 2013, registration number NCT01997086. (https://clinicaltrials.gov/ct2/show/NCT01997086).
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The discipline of spine surgery is changing dramatically thanks to innovations in surgical technology, big data analytics, improvement of AI/ML capabilities, and diagnostic standardization. It is now possible to transform classical surgical methods of treatment into minimally invasive spine surgeries (MISS). In this rapidly changing environment the community needs to consider all new evidence for and against these MISS innovations. Which MISS have been able to prove their benefits, and to whom? Are we seeing warning signs around certain procedures or for patients with certain risk factors? With computational advancements in AI/ML technologies and big data analytics it is becoming possible to provide the necessary evidence to optimize procedures and patient specific treatment paths. The pain and disability outcomes for MISS treatments vary from patient to patient and procedure to procedure. Failed back surgery syndrome is highly prevalent, and possibly preventable. Comparisons between surgical procedures and patient characteristics will help the spine surgery community improve the treatment experience for spine patients and surgeons alike. The goal of this special collection is to optimize MISS procedures for various spinal diseases by: 1. Evaluation of the types of MISS techniques for degenerative spine diseases, spine trauma and primary spinal tumors. 2. Analysis of short- and long-term results of MISS vs open treatments for degenerative spine diseases, spinal trauma and primary spinal cord tumors 3. Situational optimization of procedure selection 4. Improvement of prognostic prediction on a patient specific basis using data analytics, AL/ML This Research Topic welcomes reviews of minimally invasive spine surgical techniques with/without meta-analysis, editorials, short communications, and original studies covering topics related to: • Minimally invasive spine surgery • New procedures showing short term efficacy results • Predicting results • Surgical selection • Comparative analysis • Complications • Function restoration • Revision surgery
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Background: We aimed to investigate the incidence and risk factors for failed back surgery syndrome (FBSS) following open posterior lumbar surgery for degenerative lumbar disease (DLD). Method: A multivariate regression analysis was performed for 333 consecutive patients to identify potential risk factors for FBSS. Clinical outcomes were evaluated by the validated North American Spine Society (NASS) Questionnaire and numerical rating scale (NRS) for pain. Demographics, diagnostic characteristics, surgical data, radiographic parameters for each patient were analyzed. Result: 16.8% of the included patients were classified as FBSS. Univariate analysis showed that age, hypertension, symptom location, intermittent claudication, preoperative pain NRS-leg, HIZ, Modic changes (MCs), surgical strategy and postoperative rehabilitation were related to FBSS. Multivariate logistic regression analysis demonstrated that preoperative NRS-leg (OR:0.80, 95%CI:0.71-0.91, P=0.001), hypertension (OR: 2.22, 95%CI: 1.10-4.51, P=0.027), intermittent claudication with waking distance > 100m (OR: 4.07, 95%CI: 1.75-9.47, P=0.001) and waking distance ≤ 100m (OR: 12.43, 95%CI: 5.54-27.92, P<0.001), HIZ (OR: 8.26, 95%CI: 4.00-17.04, P<0.001), MCs (OR: 3.41, 95%CI: 1.73-6.71, P<0.001), postoperative rehabilitation (OR: 2.63, 95%CI: 1.13-6.12 , P=0.024) were risk factors for FBSS. Conclusion: Open posterior lumbar surgery is an effective treatment for DLD which provide pain reduction and lumbar curve improvement with a considerable satisfaction rate. Lower preoperative NRS-leg, hypertension, intermittent claudication, HIZ, MCs and postoperative rehabilitation are risk factors for FBSS, who can serve as a tool for clinicians to identify at-risk population and provide more effective management to mitigate the doctor-patient contradicts and further occupation of medical resources.
Chapter
Disc herniation is a common source of acute and chronic radicular pain [1]. Percutaneous decompression techniques include arthroscopic manual extraction and nuclear ablation using plasma or laser-generated heat. Interventionalists typically consider percutaneous techniques for contained disc herniation that ideally have high water content [2]. More recent navigable decompression devices now allow targeted decompression to include noncontained herniated discs [3].
Chapter
The evolution of fluoroscopically guided procedures to help diagnose and manage the spinal pain began in the late 1970s and gradually became the standard of practice in the late 1990s. Likewise, the evolution of endoscopic disc surgery started in the late 1980s and the early 1990s. However, its widespread acceptance took longer, likely paralleling the more gradual improvement in endoscopic optics [1].
Chapter
Facet (or zygapophyseal) joint-related pain is common in patients with a spinal disorder and occurs secondary to either facet joint wear and tear (degenerative change) or injury [1–4]. Pain secondary to facet joint pathology is not restricted to the facet joint; it can also spread to surrounding areas (i.e., referred pain) [5–7] (Fig. 4.1). Medial branch nerves are small nerves that feed out from the facet joints in the spine and transfer pain signals from the facet joints to the brain [8]. The medial branches of the dorsal rami innervate the facet joints, the posterior arches of the vertebrae, and certain spinal muscles (multifidus muscles) [9]. Of these, the facet joints are the only structure that can cause pain. Initially, a medial branch block was used to determine whether a patient’s source of pain was of facet joint origin; however, several previous studies found that these blocks also reduce pain. Thus, MBNB are also used to alleviate facet joint-related pain.
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Nucleoplasty is a minimally invasive intervention use to perform disc decompression in cases of nerve root compression caused by disc herniation. It is important to find rational guidelines for choosing between nucleoplasty and microsurgery. To analyze factors that may impact the results of nucleoplasty, and to validate the rational guidelines between minimally invasive treatment and open surgery. Prospective, non-randomized, cohort study with a minimal follow-up period of 18 months. Patients were given a neurological examination, visual analogue scale and Oswestry disability questionnaire, obligatory MRI, optional RCT, and discography, only before nucleoplasty. Patients have been divided into the following groups: Group 1 - patients with a disc protrusion treated with nucleoplasty (n = 46), which has been divided into Subgroup 1A, those with a disc protrusion size ≤ 5 mm (n = 24), and Subgroup 1B, those with a disc protrusion size 6 - 9 mm (n = 22); Group 2 - patients with a disc extrusion treated with nucleoplasty (n = 27); Group 3 - patients with a disc extrusion or sequester treated with microdiscectomy (n = 65). Clinically significant outcomes were a 50% relief of pain intensity and a 40% decrease of Oswestry Disability Index (ODI). A decrease of pain intensity and disability was found in all groups of patients, P < 0.0001; SP (statistical power) = 99 - 100%. Subgroups 1A and 1B showed no clinically significant differences in outcome, P = 0.99; SP = 5.3. Clinically significant results: Group 1 - 78%; 95% CI (confidence interval) [66; 90%], Group 2 - 44%; 95% CI [25; 65%], Group 3 - 93%; 95% CI [85; 98%]. Total annulus disruption increases the rate of unsatisfactory results of nucleoplasty, OR (odds ratio) = 4.5; 95% CI [1.57; 12.87] (logistic regression model, P = 0.0034). Nucleoplasty performed in cases of uncontained disc herniation (disc extrusion) have a significantly higher rate of unsatisfactory results versus microdiscectomy, OR = 19.06; 95% CI [2.29; 68.73] (logistic regression model, P < 0.0001). This study was limited by the small number of patients in each group. The size of the disc protrusion does not significantly affect the outcome of nucleoplasty. The rational guideline for choosing between the 2 types of surgery is the integrity of the annulus.
Article
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Spinal fusion at the L4-5 disc space alters the normal biomechanics of the spine, and the loss of motion at the fused level is compensated by increased motion and load at the other unfused segments. This may lead to deterioration of the adjacent segments of the lumbar spine, called adjacent-segment disease (ASD). In this study, the authors investigate the distracted disc height of the fused segment, caused by cage or bone insertion during surgery, as a novel risk factor for ASD after posterior lumbar interbody fusion (PLIF). Radiographic L3-4 ASD is defined by development of spondylolisthesis greater than 3 mm, a decrease in disc height of more than 3 mm, or intervertebral angle at flexion smaller than -5 degrees . Symptomatic ASD is defined by a decrease of 4 points or more on the Japanese Orthopaedic Association scale. Eighty-five patients with L-4 spondylolisthesis treated by L4-5 PLIF underwent follow-up for more than 2 years (mean 38.8 +/- 17.1 months). The patients were divided into 3 groups according to the final outcome. Group A comprised those patients without ASD (58), Group B patients had radiographic ASD (14), and Group C patients had symptomatic ASD (13). The L4-5 disc space distraction by cage insertion was 3.1 mm in the group without ASD, 4.4 mm in the group with radiographic ASD, and 6.2 mm in the group with symptomatic ASD, as measured using lateral spinal radiographs just after surgery. Multivariate analysis showed that distraction was the most significant risk factor. The excessive distraction of the L4-5 disc space during PLIF surgery is a significant and potentially avoidable risk factor for the development of radiographic, symptomatic ASD.
Article
Homogenized autogenous nucleus pulposus was injected into the lumbar epidural space of four dogs through an indwelling catheter. After daily injections of the material over 5 to 7 days, the dogs were killed at 5,7,14, or 21 days after the first injection. In four dogs that served as controls, normal saline was injected on an identical schedule and the dogs were killed at times identical to the experimental group. Evaluation of the dural sac, the spinal cord and its roots was performed by gross inspection and microscopic analysis. There was evidence of an inflammatory response to the nuclear material injected, but no inflammatory response occurred in the control group.
Article
Prospective cohort study. To assess the amount of scar tissue by viewing magnetic resonance images, and to evaluate the correlation between the amount of scar tissue and clinical outcome, surgical technique, and fibrinolytic factors. The influence of fibrinolytic factors on magnetic resonance images has not been investigated previously. The relation between clinical outcome and findings on magnetic resonance imaging remains uncertain. Magnetic resonance imaging at 0.5 Tesla was performed to produce sagittal and axial spin-echo T1-weighted images before and after contrast enhancement on 78 patients 7 years after traditional lumbar discectomy with partial or full laminectomy. Before surgery all patients had been tested for fibrinolytic factors. The overall clinical success rate of the surgery was 73%. No evidence of scar formation was seen in 19 patients, a small amount was seen in 36 patients, a moderate amount in 17 patients, and a large amount was observed in 6 patients. Ten patients who had undergone surgery at two disc levels and 18 who had been treated with full laminectomy exhibited more scar tissue than those patients who had undergone surgery on a single level (P = 0.033) and those who had undergone a partial laminectomy, respectively (P = 0.017). The amount of scar formation also was associated with a poor outcome (P = 0.017) and with low preoperative values of tissue plasminogen activator antigen (P = 0.003) and tissue plasminogen activity (P = 0.048) in samples collected after venous occlusion. The intensity of contrast enhancement, however, was not influenced by these or any other parameters. The amount of scar formation after lumbar discectomy seems to be related to the clinical outcome, the size of the surgical exposure, and some fibrinolytic factors.
Article
Study Design. A retrospective evaluation of 28 patients with recurrent lumbar disc herniation. Objectives. To analyze the outcome of the revisions (repeat discectomy), the risk factors of recurrent disc herniation, and the factors that influenced the outcomes of repeat discectomy. Summary of Background Data. Recurrent herniation following disc excision has been reported in 5–11% of patients. There have been many studies on recurrent disc herniation, but these studies have analyzed mixed patient populations. Methods. Recurrent lumbar disc herniation was defined as disc herniation at the same level, regardless of ipsilateral or contralateral herniation, with a pain-free interval greater than 6 months. Eight women and 20 men were studied. The levels of disc herniation were L4–L5 (19 cases) and L5–S1 (9 cases). Gadolinium-enhanced magnetic resonance imaging was performed in all patients. Revision surgery was performed in all patients by using conventional open discectomy. The pain-free interval, side and degree of herniation, operation time, duration of hospital stay, and clinical improvement rate were recorded. Results. The mean pain-free interval was 60.8 months. There were 21 cases of ipsilateral herniation and 7 cases of contralateral herniation. The degrees of herniation in revision were protrusion (14 cases), subligamentous extrusion (3 cases), transligamentous extrusion (8 cases), and sequestration (3 cases). The degrees of herniation in the previous discectomy were protrusion (17 cases), subligamentous extrusion (10 cases), and transligamentous extrusion (1 case). The length of surgery was significantly different (P = 0.003) between the revision surgery and the previous discectomy. There were no significant differences between revision and previous surgery in terms of hospital stay or clinical improvement rates. Age, gender, smoking, professions, traumatic events, level and degree of herniation, and pain-free interval did not affect the clinical outcomes. Conclusion. Conventional open discectomy as a revision surgery for recurrent lumbar disc herniation showed satisfactory results that were comparable with those of primary discectomy. Based on the results of this study, repeat discectomy can be recommended for the management of recurrent lumbar disc herniation.
Article
Patients with radiculopathy, with or without back pain, often do not respond to conservative care and may be considered for epidural steroid injection therapy or a disc decompression procedure. Plasma disc decompression (PDD) using the Coblation SpineWand device is a percutaneous, minimally invasive interventional procedure. The purpose of this study was to evaluate clinical outcomes with PDD as compared with standard care using fluoroscopy-guided transforaminal epidural steroid injection (TFESI) over the course of 2 years. This was a multicenter randomized controlled clinical study. Ninety patients (18-66 years old) who had sciatica (visual analog scale score > or = 50) associated with a single-level lumbar contained disc herniation were enrolled. In all cases, their condition was refractory to initial conservative care and 1 epidural steroid injection had failed. Participants were randomly assigned to receive either PDD (46 patients) or TFESI (44 patients, up to 2 injections). The patients in the PDD Group had significantly greater reduction in leg pain scores and significantly improved Oswestry Disability Index and 36-Item Short Form Health Survey ([SF-36], physical function, bodily pain, social function, and physical components summary) scores than those in the TFESI Group. During the 2-year follow-up, 25 (56%) of the patients in the PDD Group and 11 (28%) of those in the TFESI Group remained free from having a secondary procedure following the study procedure (log-rank p = 0.02). A significantly higher percentage of patients in the PDD Group showed minimum clinically important change in scores for leg and back pain and SF-36 scores that exceeded literature-based minimum clinically important changes. Procedure-related adverse events, including injection site pain, increased leg or back pain, weakness, and lightheadedness, were observed in 5 patients in the PDD Group (7 events) and 7 in the TFESI Group (14 events). In study patients who had radicular pain associated with a contained lumbar disc herniation, those patients treated with PDD had significantly reduced pain and better quality of life scores than those treated using repeated TFESI. In addition, significantly more PDD patients than TFESI patients avoided having to undergo a secondary procedure during the 2-year study follow-up.
Article
Osteoarthritis is a painful and debilitating disease characterized by progressive degenerative changes in the articular cartilage and other joint tissues. Biomechanical factors play a critical role in the initiation and progression of this disease, as evidenced by clinical and animal studies of alterations in the mechanical environment of the joint caused by trauma, joint instability, disuse, or obesity. The onset of these changes after joint injury generally has been termed posttraumatic arthritis and can be accelerated by factors such as a displaced articular fracture. Within this context, there is considerable evidence that interactions between biomechanical factors and proinflammatory mediators are involved in the progression of cartilage degeneration in posttraumatic arthritis. In vivo studies have shown increased concentrations of inflammatory cytokines and mediators in the joint in mechanically induced models of osteoarthritis. In vitro explant studies confirm that mechanical load is a potent regulator of matrix metabolism, cell viability, and the production of proinflammatory mediators such as nitric oxide and prostaglandin E2. Knowledge of the interaction of inflammatory and biomechanical factors in regulating cartilage metabolism would be beneficial to an understanding of the etiopathogenesis of posttraumatic osteoarthritis and in the improvement of therapies for joint injury.
Article
• Simulations are of particular advantage in research studies where large samples are necessary to achieve statistical power and the information must be collected under uniform conditions in order to aid interpretation. • In the study reported below, simulation was achieved through the use of medical photography accompanied by case studies of the same patients. All information was collected on the same day. The purpose of the study was to determine the validity of the three pressure ulcer risk assessment scales most commonly used in clinical nursing practice in the UK. • Each clinical nurse assessed the same four patients using three risk assessment scales and a visual analogue scale designed to capture their own clinical judgement. External validity was assessed by a panel of tissue viability experts who provided independent ratings. • Data were obtained from 236 clinical nurses, yielding 941 risk assessments. • Experience with this approach to data collection suggests that it requires careful planning. This should include measures to ensure that the simulated information is valid and that all data collectors have been adequately trained and are able to motivate the nurses participating in the study. Providing consideration is given to these issues, the use of simulation can help to collect data that would be difficult to obtain by more conventional means. It is also important to recognize that clinical decisions are de‐contextualized in simulations because they are reduced to verbal and visual summaries. The decision to use simulations should thus be taken only if this is acknowledged.
Article
To evaluate the prevalence of facet joint pain in patients with chronic low back pain (CLBP) after surgical intervention(s). A prospective, nonrandomized, consecutive study. An ambulatory interventional pain management setting. The prevalence of facet joint pain was evaluated in patients with CLBP after various surgical intervention(s) referred to an interventional pain management practice. The sample was derived from 282 patients with persistent CLBP after various surgical intervention(s). Of these, 242 patients consented to undergo interventional techniques. A total of 117 consecutive patients with chronic, nonspecific low back pain, after lumbar surgical intervention(s) were evaluated with controlled, comparative local anesthetic blocks. Controlled, comparative local anesthetic blocks (1% lidocaine or 1% lidocaine followed by .25% bupivacaine) under fluoroscopic visualization using 0.5mL to block each facet joint nerve. A positive response was defined as at least 80% reduction of pain with ability to perform previously painful movements. A positive response was considered to be pain relief from the lidocaine block lasting at least 1 hour or at least 2 hours or greater than duration of relief with lidocaine when bupivacaine was used. Controlled, comparative local anesthetic blocks were used to eliminate false-positive results. Valid information is only obtained by performing controlled blocks in the form of comparative local anesthetic blocks, in which, on 2 separate occasions, the same joint is anesthetized by using local anesthetics with different durations of action. If patients obtained appropriate response with both blocks, they were considered a positive. If they obtained appropriate response with lidocaine but not with bupivacaine, they were considered false-positive, whereas if the response was negative with lidocaine, they were considered negative. The prevalence of lumbar facet joint pain in patients with recurrent pain after various surgical intervention(s) was 16% (95% confidence interval, 9%-23%). The false-positive rate with a single block with lidocaine was 49%. Facet joints are clinically important pain generators in a small but significant proportion of patients with recurrent CLBP after various surgical intervention(s).
Article
Treatment of chronic low back pain with or without lower extremity pain continues to be a challenge. Epidural steroids are commonly utilized in patients after the failure of conservative treatment. The results of epidural steroid injections have been variable based on the pathophysiology, the route of administration, injected drugs, and utilization of fluoroscopy. In patients resistant to fluoroscopically directed epidural injections, percutaneous epidural adhesiolysis and percutaneous targeted delivery of injections with or without adhesiolysis has been recommended. Percutaneous adhesiolysis has been studied in chronic pain syndromes related to post laminectomy syndrome and spinal stenosis with encouraging results. There is a paucity of literature regarding the effectiveness of the targeted delivery of medications with or without epidural adhesiolysis in patients recalcitrant to epidural steroid injections without a history of surgery and spinal stenosis. A randomized, equivalence trial of percutaneous lumbar adhesiolysis and caudal epidural steroid injections in patients with low back and/or lower extremity pain without post surgery syndrome or spinal stenosis. An interventional pain management practice setting in the United States. The study is designed to evaluate the effectiveness of percutaneous epidural adhesiolysis in managing chronic low back and/or lower extremity pain in patients without post lumbar surgery syndrome or spinal stenosis and compare it with fluoroscopically directed caudal epidural steroid injections The study design includes 120 patients randomly assigned into 2 groups. Group I (60 patients), the control group, will receive caudal epidural injections with catheterization up to S3 with local anesthetic, steroids, and 0.9% sodium chloride solution; Group II (60 patients), the intervention group, will receive percutaneous adhesiolysis with target delivery of lidocaine, 10% hypertonic sodium chloride solution, and non-participate betamethasone. Randomization will be performed by computer-generated random allocation sequence by simple randomization. Multiple outcome measures will be utilized including numeric rating scale (NRS), the Oswestry Disability Index 2.0 (ODI), employment status, and opioid intake with assessment at 3, 6, 12, 18 and 24 months post treatment. Significant pain relief is considered as 50% or more, whereas significant improvement in the disability score is defined as a reduction of 40% or more. The results will be analyzed to show significant relief as well as improvement in functional status. This study is limited by potentially inadequate double blinding and the lack of a placebo group.