You are on page 1of 8

J Neurosurg Spine 14:51–58, 2011

Reduced postoperative wound pain after lumbar spinous


process–splitting laminectomy for lumbar canal stenosis:
a randomized controlled study
Clinical article

Kota Watanabe, M.D.,1 Morio Matsumoto, M.D., 2 Takeshi Ikegami, M.D., 2,4
Yuji Nishiwaki, M.D., 3 Takashi Tsuji, M.D., 2 Ken Ishii, M.D., 2 Yuto Ogawa, M.D., 2
Hironari Takaishi, M.D., 2 Masaya Nakamura, M.D., 2 Yoshiaki Toyama, M.D., 2
and Kazuhiro Chiba, M.D. 2
1
Department of Advanced Therapy for Spine and Spinal Cord Disorders, 2Department of Orthopaedic
Surgery, and 3Clinical Epidemiology & Biostatistics Unit, Department of Preventive Medicine and Public
Health, School of Medicine, Keio University, Shinjuku; and 4Department of Orthopaedic Surgery, National
Hospital Organization, Murayama Medical Center, Tokyo, Japan

Object. To reduce intraoperative damage to the posterior supporting structures of the lumbar spine during de-
compressive surgery for lumbar canal stenosis (LCS), lumbar spinous process–splitting laminectomy (LSPSL or split
laminectomy) was developed. This prospective, randomized, controlled study was conducted to clarify whether the
split laminectomy decreases acute postoperative wound pain compared with conventional laminectomy.
Methods. Forty-one patients with LCS were enrolled in this study. The patients were randomly assigned to ei-
ther the LSPSL group (22 patients) or the conventional laminectomy group (19 patients). Questionnaires regarding
wound pain (intensity, depth, and duration) and activities of daily living (ADL) were administered at postoperative
days (PODs) 3 and 7. Additionally, the authors evaluated the pre- and postoperative serum levels of C-reactive protein
and creatine phosphokinase, the amount of pain analgesics used during a 3-day postoperative period, and the muscle
atrophy rate measured on 1-month postsurgical MR images.
Results. Data obtained in patients in the LSPSL group and in 16 patients in the conventional laminectomy group
were analyzed. The mean visual analog scale for wound pain on POD 7 was significantly lower in the LSPSL group
(16 ± 17 mm vs 34 ± 31 mm, respectively; p = 0.04). The mean depth-of-pain scores on POD 7 were significantly
lower in the LSPSL group than in the conventional group (0.9 ± 0.6 vs 1.7 ± 0.8, respectively; p = 0.013). On POD
3, the mean serum creatine phosphokinase level was significantly lower in the LSPSL group (126 ± 93 U/L) than in
the other group (207 ± 150 U/L) (p = 0.02); on POD 7, the mean serum C-reactive protein level was significantly
lower in the LSPSL group (1.1 ± 0.6 mg/dl) than in the conventional laminectomy group (1.9 ± 1.5 mg/dl) (p = 0.04).
The number of pain analgesics taken during the 3-day postoperative period was lower in the LSPSL group than in
the conventional laminectomy group (1.7 ± 1.3 tablets vs 2.3 ± 2.4 tablets, respectively; p = 0.22). The mean muscle
atrophy rate was also significantly lower in the LSPSL group (24% ± 15% vs 43% ± 22%; p = 0.004).
Conclusions. Lumbar spinous process–splitting laminectomy for the treatment of LCS reduced acute postopera-
tive wound pain and prevented postoperative muscle atrophy compared with conventional laminectomy, possibly
because of minimized damage to the paraspinal muscles. (DOI: 10.3171/2010.9.SPINE09933)

Key Words • lumbar spinal canal stenosis • randomized controlled study •


spinous process–splitting laminectomy • wound pain

L
umbar spinal canal stenosis was described in de- lumbar spinal canal. His patients had been treated us-
tail in 1954 by Verbiest,24 who reported on patients ing extensive laminectomy, which has been regarded as
with symptoms induced by the narrowing of the the standard treatment for LCS. In an extensive lami-
nectomy, bilateral paraspinal muscles are dissected and
Abbreviations used in this paper: ADL = activities of daily living;
detached extensively from the spinous processes, lami-
CPK = creatine phosphokinase; CRP = C-reactive protein; JOA = nae, and facet joints; the spinous process and laminae
Japanese Orthopaedic Association; LCS = lumbar canal stenosis; are then removed to decompress the nerve tissues. Such
LSPSL = lumbar spinous process–splitting laminectomy; POD = intraoperative damage to the posterior supporting struc-
postoperative day; VAS = visual analog scale. tures of the lumbar spine result in significant muscle atro-

J Neurosurg: Spine / Volume 14 / January 2011 51


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
K. Watanabe et al.

phy,5–7,9,13,14,20 which can lead to failed–back surgery syn- Inclusion and Exclusion Criteria
drome.21 To overcome these problems, various decom- To be eligible for the study, the following criteria
pressive surgeries for LCS have been developed with the had to be met: 1) presence of neurogenic claudication; 2)
intention of preserving the posterior supporting structures symptoms persistent for more than 6 months despite con-
of the lumbar spine.16,17,19,22,26–29
servative therapy; 3) clinical symptoms and neurological
In 2002, we developed a new lumbar laminectomy
technique for the treatment of LCS.25 In this technique, signs in the lower limbs corresponding to the level of ste-
which we named LSPSL (or the “split laminectomy”), nosis on MR imaging or myelography; and 4) 1- or 2-level
the lamina is exposed by longitudinally splitting the spi- decompression necessary.
nous process into halves, with the muscular and ligamen- Radiographic instability of the lumbar spine and de-
tous attachments to the spinous process left intact (Fig. generative spondylolisthesis were not regarded as exclusion
1). According to our retrospective study, a group of pa- criteria. However, the following exclusion criteria were ad-
tients with persistent severe pain and progressive neural opted: 1) spinal canal stenosis due to congenital, spondy-
dysfunction caused by LCS benefited from LSPSL and lolytic, traumatic, and iatrogenic causes; 2) any previous
their back muscles were significantly well preserved, operation in the lumbar area; 3) presence of other specific
compared with patients who underwent conventional spinal disorders (such as ankylosing spondylitis, neoplasm,
laminectomy.10,25 Based on our clinical experience with or metabolic diseases); 4) intermittent claudication result-
LSPSL, we assumed that the split laminectomy preserves ing from peripheral arterial disease; 5) severe osteoarthro-
the back muscles, leading to a reduction in acute wound sis or arthritis in the lower limbs; 6) neurological disease
pain after surgery. causing impaired lower-limb function, including diabetic
The purpose of this prospective, randomized, con- neuropathy; 7) psychiatric disorders; and 8) multilevel spi-
trolled study was to evaluate acute postoperative wound nal canal stenosis requiring decompression at 3 or more
pain after either LSPSL or conventional laminectomy. levels.
Patient Population
Methods
Patients were recruited between December 2004 and
This prospective, randomized study was approved by December 2005. Before randomization, eligible patients
the medical ethics committee of Keio University Hospital. were informed that they would be the candidates for a study

Fig. 1. Flow chart of the study and drawings representing the 2 laminectomies.

52 J Neurosurg: Spine / Volume 14 / January 2011


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
Reduced wound pain after spinous process–splitting laminectomy

comparing 2 different procedures for the surgical treatment Scale (JOA-ADL score) was used. One year postopera-
of LCS. Then, written consent was obtained from all par- tively, standard physical and neurological examinations
ticipants. The baseline examinations consisted of plain ra- were performed, and the JOA score was calculated.
diography of the lumbar spine, myelography, CT, and MR In addition to the questionnaire, we also evaluated
imaging. Standard physical and neurological examinations the pre- and postoperative serum levels of CRP and CPK,
were performed, and the JOA score for low-back pain4 was the amount of pain medication taken during the 3-day
calculated. The JOA Scale consists of 3 main parts: subjec- postoperative period, and the muscle atrophy rate as
tive symptoms, clinical signs, and ADL restrictions. The demonstrated on 1-month postoperative axial MR im-
subjective symptoms section has 3 components: low-back ages. Pain medication usage was determined by count-
pain, leg pain, and gait, with all 3 components having a ing the number of tablets dispensed by the nurses at each
possible score range of 0–3 points depending on severity. patient’s request. A nonsteroidal antiinflammatory drug,
The clinical signs section also has 3 components: straight Loxoprofen, which is a popular analgesic in Japan, was
leg–raising test, sensory disturbance, and muscle distur- used in the present study.
bance, with all 3 components having a possible score range To evaluate the magnitude of the surgical damage
of 0–3 depending on the severity. The ADL section has 7 to the paraspinal muscles, the cross-sectional area of the
components based on the individual’s ability to: turn over paraspinal muscles (multifidus) was measured on pre-
while lying down, stand, wash one’s face, lean forward, sit operative and 1-month postoperative T2-weighted axial
for approximately 1 hour, lift or hold heavy objects, and MR images using the NIH Image software (Imaging Re-
ambulate. Each of these components is scored according search). The axial images were obtained at the decom-
to the severity of restriction (severe restriction, 0; moder- pressed intervertebral level. In cases of 2-level decom-
ate restriction, 1; no restriction, 2). After completion of the pression, the caudal level was chosen for the evaluation
baseline examinations, identification data for the eligible of muscle atrophy because the influences of the injury to
patients who agreed to participate in the study were faxed the medial branch of the posterior ramus of the spinal
to a central office, where they were randomized into either nerve would be more evident at the caudal level. The rate
the LSPSL group or the conventional laminectomy group. of muscle atrophy was calculated using the following for-
The randomization was stratified according to sex, age (≤ mula: atrophy rate (%) = (1 - total postoperative area/
64 years or > 65 years), and the number of decompression total preoperative area) × 100.
levels (1 or 2). Only the attending surgeon of the patient
was informed about which method to use for the specific Statistical Analysis
patient. Overall, 5 spine surgeons participated in this study. Data were analyzed using the SPSS 16.0 J statistical
Forty-eight patients met the inclusion criteria for the software package. A Mann-Whitney U-test was used to
study (Fig. 1), and 41 agreed to participate. These patients compare the mean scores or values between the groups.
were assigned to either the LSPSL group (22 patients) or Statistical significance was defined as p < 0.05 for a 2-sid-
the conventional laminectomy group (19 patients). Four ed hypothesis. Mean data are presented ± SD.
patients in the LSPSL group were subsequently with-
drawn from the study because a conversion to posterior Surgical Techniques
lumbar interbody fusion was necessary in 1 patient and
the number of decompression levels was increased from Split Laminectomy. For a 1-level (L4–5) decompres-
2 to 3 after randomization in 3 patients. Three patients sion, a posterior midline skin incision is made between
in the conventional laminectomy group were also with- the L-3 and L-5 spinous processes to expose the tip of
drawn from the study. In 1 of these 3 patients, a hernioto- the L-4 spinous process (Fig. 1). The cortex of the tip of
my was performed in addition to the laminectomy, and in the L-4 spinous process is removed at the midline using
the other 2 patients the number of decompression levels a high-speed drill with a fine 2-mm diamond-tipped bur,
was increased from 2 to 3 levels after randomization. and then, using an osteotome, the spinous process is di-
vided to the base and detached from the L-4 lamina, leav-
Measurements ing the bilateral paraspinal muscles attached to the lateral
aspects of the split spinous process. The supra- and inter-
Questionnaires were administered on PODs 3 and 7. spinous ligaments between L3–4 and L4–5 are also split
The questionnaire contained 3 questions regarding wound longitudinally with a scalpel. An ample working space
pain (intensity, depth, and duration) and questions regard- for the laminectomy is obtained by retracting the split
ing ADL. For the question concerning the intensity of the halves of the spinous process bilaterally, together with its
wound pain, a VAS consisting of a numerical rating scale attached paraspinal muscles. The L-4 lamina is removed
from 0 (no pain) to 10 (worst possible pain) was used. using a high-speed drill and Kerrison rongeurs, and the
For the question concerning depth of pain, a patient in nerve tissue is decompressed in the standard fashion. Af-
whom pain felt “superficial” was assigned 1 point, “deep ter the decompression of the affected nerve roots and the
to the muscle” was assigned 2 points, and “deep to the thecal sac, the halves of the split L-4 spinous process are
bone” was assigned 3 points. For the question concerning reapproximated using a strong nonabsorbable suture. The
duration of pain (that is, from the start of the pain to the 1-level posterior L4–5 decompression, thus, can be ac-
relief of the pain), “a few seconds” was assigned 1 point, complished by removing the L-4 caudal portion of the
“a few minutes” was assigned 2 points, “a few hours” was lamina, preserving the supra- and interspinous ligaments
assigned 3 points, and “all day” was assigned 4 points. of L3–4 and L4–5 and the L-4 spinous process, with
For the evaluation of ADL, the ADL domain in the JOA minimal damage to the paraspinal muscles.

J Neurosurg: Spine / Volume 14 / January 2011 53


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
K. Watanabe et al.

Conventional Laminectomy. A posterior midline skin TABLE 2: Clinical results preoperatively and 1-year
incision is made between the L-3 and L-5 spinous process- postoperatively*
es to expose the L4–5 interlaminar space (Fig. 1). Bilateral
paraspinal muscles are detached from the L-4 and L-5 spi- Laminectomy Group
nous processes, and then, using a chisel to expose the L4–5 Possible Split
interlaminar space, the L-4 and L-5 spinous processes are Parameter Range (LSPSL) Conventional
detached from the lamina. Last, the nerve tissue is decom-
pressed in the same manner as for the LSPSL. mean preop JOA score 0–29 16.4 ± 4.7 14.9 ± 4.0
subjective symptoms 0–9 3.5 ± 1.3 3.5 ± 1.3
Postoperative Care    low-back pain 0–3 1.7 ± 0.9 1.7 ± 0.8
The patients in both groups were allowed to sit up and    lower-leg pain 0–3 0.9 ± 0.2 0.8 ± 0.4
walk without lumbar support on the 1st POD.   gait ability 0–3 0.9 ± 0.9 1.0 ± 0.7
clinical symptoms 0–6 5.1 ± 1.0 5.0 ± 0.7
Results ADL restrictions 0–14 8.9 ± 2.7 7.5 ± 2.9
mean postop 1-yr JOA score 0–29 25.8 ± 3.4 25.4 ± 2.9
Data in 18 patients (10 men and 8 women) in the
LSPSL (split-laminectomy) group and 16 patients (8 men subjective symptoms 0–9 7.5 ± 1.4 7.3 ± 1.0
and 8 women) in the conventional laminectomy group    low-back pain 0–3 2.5 ± 0.5 2.3 ± 0.5
were included in the final analyses. We observed no sig-    lower-leg pain 0–3 2.4 ± 0.8 2.3 ± 0.5
nificant intergroup differences in mean age at the time of   gait ability 0–3 2.7 ± 0.5 2.7 ± 0.5
surgery, mean number of decompressed levels, mean op- clinical symptoms 0–6 5.7 ± 0.7 5.7 ± 0.6
erative time, mean intraoperative blood loss, or number of
ADL restrictions 0–14 12.8 ± 1.6 12.5 ± 1.9
surgeries performed by each surgeon (Table 1). The mean
preoperative JOA score in the LSPSL group was 16.4 ± recovery rate (%)† 75 ± 21 74 ± 17
4.7 and that in the conventional laminectomy group was * No significant intergroup difference according to the Mann-Whitney
14.9 ± 4.0 (Table 2). The subjective symptoms portion of U-test for the JOA score or recovery rate. Mean values are presented
the JOA score indicated that lower-leg pain and gait dis- ± the SD.
turbance were severe in both groups. No significant in- † Recovery rate: (postoperative points − preoperative points)/(29 – pre-
tergroup difference was recognized in 3 parts of subjec- operative points).
tive symptoms, clinical signs, and ADL restrictions. At
1 year postoperatively, the mean preoperative JOA score
group differences were not recognized in these clinical
of 16.4 ± 4.7 was increased to 25.8 ± 3.4 (mean recovery
parameters. No obvious perioperative complication was
rate 75% ± 21%) in the split-laminectomy group, whereas
recognized. One patient in the split-laminectomy group
in the conventional laminectomy group the mean preop-
underwent posterior intervertebral fusion 1 year later to
erative JOA score of 14.9 ± 4.0 was increased to 25.4 ±
treat symptoms that recurred 6 months after LSPSL. One
2.9 (mean recovery rate 74% ± 17%). Significant inter-
patient in each group did not attend the 1-year follow-up
TABLE 1: Demographics of the split-laminectomy group (LSPSL) examination because of general health problems.
and the conventional laminectomy group* The VAS Score for Wound Pain
Laminectomy Group (%) On POD 3, the mean VAS score was 43 ± 27 mm in
Parameter Split (LSPSL) Conventional the LSPSL group and 44 ± 26 mm in the conventional
laminectomy group. Although on POD 7 the mean score
no. of patients 18 16 was reduced to 16 ± 17 mm in the LSPSL group and 34 ±
mean age (yrs)† 69 ± 10 71 ± 8 31 mm in the conventional group (p = 0.002), a significant
male/female ratio† 10:8 8:8 decrease was recognized only in the former group. Addi-
mean no. of decompressed levels† 1.4 ± 0.5 1.4 ± 0.5 tionally, on POD 7 a significant intergroup difference was
recognized (p = 0.04) (Fig. 2).
mean intraoperative time (min)† 69 ± 29 82 ± 36
mean intraoperative blood loss (g)† 44 ± 75 55 ± 48 Depth of Pain
no. of ops performed by each surgeon‡ On POD 3, the mean depth-of-pain score was 1.6 ±
K.I. 4 (22) 6 (38) 0.7 in the LSPSL group and 1.6 ± 0.7 points in the conven-
Y.O. 3 (17) 1 (6) tional laminectomy group. On POD 7, although the score
H.T. 4 (22) 2 (13) was significantly reduced to 0.9 ± 0.6 in the split-lam-
M.N. 1 (6) 1 (6) inectomy group (p = 0.021), no change was recognized
in the conventional group (depth-of-pain score 1.7 ± 0.8).
M.M. 6 (33) 6 (38)
On POD 7, a significant intergroup difference was recog-
* Mean values are presented ± the SD. nized (p = 0.013) (Fig. 3).
† No significant intergroup difference according to the Mann-Whitney
Duration of Pain
U-test.
‡ No significant intergroup difference according to the chi-square test. On POD 3, the mean duration-of-pain score was 2.5 ±

54 J Neurosurg: Spine / Volume 14 / January 2011


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
Reduced wound pain after spinous process–splitting laminectomy

Fig. 2. Bar graph identifying VAS scores of acute postoperative Fig. 4. Duration-of-pain scores on PODs 3 and 7. The mean score
wound pain on PODs 3 and 7. The mean VAS score of 43 ± 27 mm in of 2.5 ± 1.4 in the split-laminectomy group on POD 3 was significantly
the split-laminectomy group on POD 3 was significantly reduced to 16 reduced to 1.5 ± 1.5 (p = 0.045). No significant differences were recog-
± 17 mm on POD 7 (p = 0.002). A significant difference was recognized nized between the groups.
between the 2 groups on POD 7 (p = 0.04).
50 U/L on POD 7 in the split-laminectomy group. In the
1.4 in the LSPSL group and 2.9 ± 1.3 in the conventional conventional laminectomy group, the value increased to
group. On POD 7, the score was significantly reduced to 1.5 207 ± 150 U/L on POD 3 and then decreased to 106 ± 86
± 1.5 in the split-laminectomy group (p = 0.045) and 2.5 ± U/L on POD 7. A significant difference was recognized
1.6 in the conventional laminectomy group. Although the between the 2 groups only on POD 3 (p = 0.02) (Fig. 6).
mean scores were lower in the LSPSL group, no significant The mean preoperative serum CRP level was 0.3 ±
differences were recognized between the 2 groups (Fig. 4). 0.3 mg/dl in the LSPSL group and 0.2 ± 0.3 mg/dl in the
conventional laminectomy group. In the LSPSL group,
The JOA-ADL Scores the value increased to 5.3 ± 3.7 mg/dl on POD 3 and then
The preoperative mean JOA-ADL score was 8.8 ± decreased to 1.1 ± 0.6 mg/dl on POD 7. In the conven-
2.7 in the LSPSL group and 7.5 ± 2.7 in the conventional tional laminectomy group, the value increased to 5.5 ±
group. The scores decreased to 6.3 ± 3.0 in the former and 3.2 mg/dl on POD 3 and then decreased to 1.9 ± 1.5 mg/dl
4.9 ± 4.5 in the latter group POD 3. The scores increased on POD 7. A significant intergroup difference was recog-
to 7.9 ± 2.6 and 7.8 ± 4.2, respectively, on POD 7. No sig- nized between the 2 groups on POD 7 (p = 0.04) (Fig. 6).
nificant intergroup differences were recognized (Fig. 5).
Analgesics Taken During the 3-Day Postoperative Period
Serum CRP and CPK Levels Although the mean number of analgesic medications
The mean preoperative serum CPK level was 99 ± 64 taken during the 3-day postoperative period was smaller
U/L in the split-laminectomy group and 115 ± 86 U/L in in the LSPSL group than the conventional group (1.7 ±
the conventional laminectomy group. The value increased 1.3 tablets vs 2.3 ± 2.4 tablets, p = 0.22), no significant
to 126 ± 93 U/L on POD 3 and then decreased to 71 ± difference was recognized.

Fig. 3. Depth-of-pain scores reflecting acute postoperative wound Fig. 5. Bar graph identifying JOA-ADL scores on PODs 3 and 7. The
pain on PODs 3 and 7. The mean score of 1.6 ± 0.7 in the split-laminec- mean JOA-ADL score of 6.3 ± 3.0 in the split-laminectomy group and
tomy group on POD 3 was significantly reduced to 0.9 ± 0.6 (p = 0.021). 4.9 ± 4.5 in the conventional laminectomy group on POD 3 increased
A significant difference was recognized between the 2 groups on POD to 7.9 ± 2.6 and 7.8 ± 4.2, respectively, on POD 7. No significant inter-
7 (p = 0.013). group differences were recognized.

J Neurosurg: Spine / Volume 14 / January 2011 55


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
K. Watanabe et al.

Fig. 6. Serum CPK and CRP levels before surgery (Pre-Op) and on PODs 3 and 7. The mean preoperative serum CPK level
of 99 ± 64 U/L in the split-laminectomy group increased to 126 ± 93 U/L on POD 3, and then decreased to 71 ± 50 U/L on POD 7.
A significant difference was recognized between the groups only on POD 3 (p = 0.02). The mean preoperative serum CRP level
of 0.3 ± 0.3 mg/dl in the split-laminectomy group increased to 5.4 ± 3.7 mg/dl on POD 3, and then decreased to 1.1 ± 0.6 mg/dl
on POD 7. A significant difference was recognized between the groups only on POD 7 (p = 0.04).

Atrophy Rate of Paraspinal Muscles at the 1-Month terior ramus emerges from the intervertebral foramen and
Postoperative Examination passes dorsolateral to the superior articular process, and it
The mean atrophy rate in the split-laminectomy group splits into their terminal medial and lateral branches. The
was significantly lower than that in the conventional group medial branch then enters the multifidus.1–3,18 Because
(24% ± 15% and 43% ± 22%, respectively; p = 0.004). the medial branch is tethered to the periosteum, lateral
to the facet joints, by fibers of the intertransverse liga-
ments,1 the dissection of the muscles lateral to the facet
Discussion joints may increase the risk of injuring the medial branch
of the posterior ramus, which will finally result in dener-
The results of the present study indicated that, after vation of the multifidus.1 Furthermore, the medial branch
posterior decompression surgery for LCS, acute postop- of the posterior ramus is at risk of being injured, even
erative wound pain was milder in the LSPSL (split-lam- by lateral retraction of the paraspinal muscles,1,15 whereas
inectomy) group than in the conventional laminectomy in the split laminectomy a wide visualization of the cen-
group. All mean scores regarding wound pain were lower tral canal and the lateral recess is achieved by retracting
in the split-laminectomy group. In particular, significant the split spinous processes bilaterally, enabling minimal
differences were observed between the groups in the VAS dissection of the paraspinal muscles and minimal de-
scores on POD 7 and the depth of pain on POD 7. The tachment of the muscles from the facet joints. Kawagu-
reduced postoperative wound pain in the LSPSL group chi et al.5–7 reported that muscle injury is closely related
may be due to the reduction of damage to the paraspi- to retraction pressure in their experimental and clinical
nal muscles. Because serum CPK and CRP levels are the trials. In a split laminectomy, the broad visualization of
indicators of muscle damage,8,11,12,23 the results (mean se- the central canal and the lateral recess may diminish the
rum CPK levels on POD 3 and CRP level at POD 7 being retraction pressure on paraspinal muscles. Additionally,
significantly lower in the split-laminectomy group) indi- interposition of the split spinous processes between the
cated that the extent of the surgical invasiveness to the paraspinal muscles and the retractors may acts as a me-
paraspinal muscles was lesser in the split-laminectomy chanical buffer to reduce the retraction pressure against
group. Additionally, the muscle atrophy rate at 1 month the paraspinal muscles. All of these factors may explain
being significantly lower in the split-laminectomy group why the paraspinal muscles in the split-laminectomy pro-
also suggested that the procedure is less invasive in terms cedure are associated with reduced invasiveness.
of the paraspinal muscles. Regarding the timing of MR imaging, based on our
Several assumptions can be made concerning the preliminary data of consecutive MR images taken for
reasons for the more minimal invasiveness to the paraspi- evaluating paraspinal muscle atrophy after decompressive
nal muscles in LSPSL. First, the reduced dissection of the surgery, muscle edema, which would cause the muscles to
paraspinal muscles from the spinous process—the result swell, was evident within 2 weeks of surgery. Sometimes,
of splitting the spinous process—might also reduce the the muscle area after conventional laminectomy was larger
invasiveness of the procedure to the paraspinal muscles. than that of preoperative areas and that of the split lami-
Second, in conventional laminectomy, because the mid- nectomy because of muscle edema. Thus, we decided that
line structures disturb one’s access to the lateral recesses, the measurement of muscle area as a parameter of invasive-
paraspinal muscle dissection would extend to the medial ness within 2 weeks would be inappropriate. Because the
side or sometimes to the lateral side of the facet joints. muscle edema would decrease to an almost normal level by
This would be associated with an increased chance of 1 month postoperatively, we chose to obtain MR images 1
damaging the medial branch of posterior ramus. The pos- month after surgery to evaluate muscle atrophy.

56 J Neurosurg: Spine / Volume 14 / January 2011


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
Reduced wound pain after spinous process–splitting laminectomy

Limitations of this study were as follows. The surgi- 4. Inoue S, Kataoka H, Tajima T, Tajima N, Nakano N, Hasue
cal technique was not identical among the patients be- M, et al: [Assessment of treatment for low back pain.] J Jpn
cause the surgeries were not performed by a single sur- Orthop Assoc 60:391–394, 1986 (Jpn)
5. Kawaguchi Y, Matsui H, Gejo R, Tsuji H: Preventive measures
geon. Overall, 5 spine surgeons participated in this study. of back muscle injury after posterior lumbar spine surgery in
However, before starting the study, the procedures were rats. Spine 23:2282–2288, 1998
standardized among the 5 surgeons to minimize the tech- 6. Kawaguchi Y, Matsui H, Tsuji H: Back muscle injury after
nical differences. Furthermore, the proportions of sur- posterior lumbar spine surgery. A histologic and enzymatic
geries performed by each surgeon were almost identical analysis. Spine 21:941–944, 1996
between the 2 treatment groups. The other limitation was 7. Kawaguchi Y, Matsui H, Tsuji H: Back muscle injury after
the withdrawal of the 7 patients (17%) from the study. The posterior lumbar spine surgery. Part 1: Histologic and histo-
reasons for the withdrawal were the extension of decom- chemical analyses in rats. Spine 19:2590–2597, 1994
8. Kawaguchi Y, Matsui H, Tsuji H: Changes in serum creatine
pression levels or the conversion of the procedure from phosphokinase MM isoenzyme after lumbar spine surgery.
decompression to fusion after randomization. However, Spine 22:1018–1023, 1997
we do not think that these withdrawals had a major im- 9. Kawaguchi Y, Yabuki S, Styf J, Olmarker K, Rydevik B, Mat-
pact on the results. Another limitation was that the mea- sui H, et al: Back muscle injury after posterior lumbar spine
surements used in this study for evaluating the wound surgery. Topographic evaluation of intramuscular pressure
pain were not well validated except for the VAS. Because and blood flow in the porcine back muscle during surgery.
we believed that evaluation of the wound pain by only the Spine 21:2683–2688, 1996
VAS was insufficient, we added our nonvalidated origi- 10. Kim K, Isu T, Sugawara A, Matsumoto R, Isobe M: Compari-
nal measurements to provide supplemental data, knowing son of the effect of 3 different approaches to the lumbar spinal
canal on postoperative paraspinal muscle damage. Surg Neu-
that the measurements were less reliable. However, de- rol 69:109–113, 2008
spite these limitations, we believe the results of the pres- 11. Kumbhare D, Parkinson W, Dunlop B: Validity of serum cre-
ent study indicated that split laminectomy was less in- atine kinase as a measure of muscle injury produced by lum-
vasive, and reduced postoperative wound pain compared bar surgery. J Spinal Disord Tech 21:49–54, 2008
with conventional laminectomy. 12. Kumbhare D, Parkinson W, Dunlop B, Ryan E, Denkers M,
Shah AA, et al: Biochemical measurement of muscle injury
created by lumbar surgery. Clin Invest Med 30:12–20, 2007
Conclusions 13. Macnab I, Cuthbert H, Godfrey C: The incidence of dener-
vation of the sacrospinalis muscles following spinal surgery.
The present prospective, randomized, controlled study Spine 2:294–298, 1977
confirmed that LSPSL for LCS reduces acute postopera- 14. Mayer TG, Vanharanta H, Gatchel RJ, Mooney V, Barnes D,
tive wound pain compared with conventional laminecto- Judge L, et al: Comparison of CT scan muscle measurements
my, possibly because of minimized damage to the paraspi- and isokinetic trunk strength in postoperative patients. Spine
nal muscles. 14:33–36, 1989
15. Nagayama R, Nakamura H, Yamano Y, Yamamoto T, Minato
Disclosure Y, Seki M, et al: An experimental study of the effects of nerve
root retraction on the posterior ramus. Spine 25:418–424, 2000
The authors report no conflict of interest concerning the mate- 16. Nakai O, Ookawa A, Yamaura I: Long-term roentgenographic
rials or methods used in this study or the findings specified in this and functional changes in patients who were treated with wide
paper. fenestration for central lumbar stenosis. J Bone Joint Surg
Author contributions to the study and manuscript prepara- Am 73:1184–1191, 1991
tion include the following. Conception and design: Matsumoto, 17. O’Leary PF, McCance SE: Distraction laminoplasty for de-
Watanabe, Toyama, Chiba. Acquisition of data: Watanabe, Ikegami, compression of lumbar spinal stenosis. Clin Orthop Relat
Tsuji, Ishii, Ogawa, Takaishi, Nakamura. Analysis and interpreta- Res (384):26–34, 2001
tion of data: Watanabe, Nishiwaki. Drafting the article: Watanabe. 18. Pedersen HE, Blunck CF, Gardner E: The anatomy of lumbo-
Critically revising the article: Watanabe. Reviewed final version of sacral posterior rami and meningeal branches of spinal nerve
the manuscript and approved it for submission: all authors. Statistical (sinu-vertebral nerves); with an experimental study of their
analysis: Ikegami, Nishiwaki. Study supervision: Matsumoto, To­­ya­ functions. J Bone Joint Surg Am 38-A:377–391, 1956
ma, Chiba. 19. Poletti CE: Central lumbar stenosis caused by ligamentum
flavum: unilateral laminotomy for bilateral ligamentectomy:
Acknowledgments preliminary report of two cases. Neurosurgery 37:343–347,
1995
The authors thank the nurses who work in the 6-3 and 10N 20. See DH, Kraft GH: Electromyography in paraspinal muscles
wards of Keio University Hospital for their assistance and coopera- following surgery for root compression. Arch Phys Med Re-
tion during this study. habil 56:80–83, 1975
21. Sihvonen T, Herno A, Paljärvi L, Airaksinen O, Partanen J,
References Tapaninaho A: Local denervation atrophy of paraspinal mus-
cles in postoperative failed back syndrome. Spine 18:575–
1. Boelderl A, Daniaux H, Kathrein A, Maurer H: Danger of 581, 1993
damaging the medial branches of the posterior rami of spi- 22. Spetzger U, Bertalanffy H, Reinges MH, Gilsbach JM: Uni-
nal nerves during a dorsomedian approach to the spine. Clin lateral laminotomy for bilateral decompression of lumbar
Anat 15:77–81, 2002 spinal stenosis. Part II: Clinical experiences. Acta Neurochir
2. Bogduk N, Wilson AS, Tynan W: The human lumbar dorsal (Wien) 139:397–403, 1997
rami. J Anat 134:383–397, 1982 23. Stahl WM: Acute phase protein response to tissue injury. Crit
3. Edgar MA, Ghadially JA: Innervation of the lumbar spine. Care Med 15:545–550, 1987
Clin Orthop Relat Res (115):35–41, 1976 24. Verbiest H: A radicular syndrome from developmental nar-

J Neurosurg: Spine / Volume 14 / January 2011 57


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC
K. Watanabe et al.

rowing of the lumbar vertebral canal. J Bone Joint Surg Br 29. Yong-Hing K, Kirkaldy-Willis WH: Osteotomy of lumbar spi-
36-B:230–237, 1954 nous process to increase surgical exposure. Clin Orthop Relat
25. Watanabe K, Hosoya T, Shiraishi T, Matsumoto M, Chiba K, Res (134):218–220, 1978
Toyama Y: Lumbar spinous process-splitting laminectomy for
lumbar canal stenosis. Technical note. J Neurosurg Spine 3:
405–408, 2005
26. Weber BR, Grob D, Dvorák J, Müntener M: Posterior surgical
approach to the lumbar spine and its effect on the multifidus Manuscript submitted November 19, 2009.
muscle. Spine 22:1765–1772, 1997 Accepted September 22, 2010.
27. Weiner BK, Fraser RD, Peterson M: Spinous process osteoto- Please include this information when citing this paper: published
mies to facilitate lumbar decompressive surgery. Spine 24: online December 10, 2010; DOI: 10.3171/2010.9.SPINE09933.
62–66, 1999 Address correspondence to: Morio Matsumoto, M.D., Depart-
28. Weiner BK, Walker M, Brower RS, McCulloch JA: Microde- ment of Orthopaedic Surgery, Keio University School of Medi-
compression for lumbar spinal canal stenosis. Spine 24:2268– cine, 35 Shinanomachi, Shinjuku, Tokyo 160-8582, Japan. email:
2272, 1999 morio@sc.itc.keio.ac.jp.

58 J Neurosurg: Spine / Volume 14 / January 2011


Unauthenticated | Downloaded 12/25/22 10:04 AM UTC

You might also like