Study rationale and context
Study rationale and context
The choice of correct surgical treatment of adult low-grade isthmic spondylolisthesis
remains a topic of debate. Many studies in the literature analyze clinical and radiological
outcome of different fusion techniques by various approaches, including posterolateral
fusion (PLF) and lumbar interbody fusion, but considerable controversies regarding
what is the „gold standard” approach still exist [1 ]
[2 ]
[3 ]
[4 ]
[5 ]
[6 ]
[7 ]
[8 ]
[9 ]
[10 ]
[11 ]
[12 ]
[13 ]
[14 ]
[15 ]
[16 ].
Clinical question
Clinical question
Do more adult patients affected by low grade isthmic spondylolisthesis have significant
clinical and radiological improvement following posterior lumbar interbody fusion
(PLIF) than those who receive posterolateral fusion (PLF)?
Methods
Methods
Study design:
Retrospective cohort study.
Inclusion criteria:
All adult patients who had undergone posterior lumbar interbody fusion (PLIF) (Figure [2 ], [3 ]) or posterolateral fusion (PLF) (Figure [4 ]) for low grade isthmic spondylolisthesis (Meyerding grade 1 or 2) between February
2003 and April 2005, and who had a minimum of 4 years of follow-up.
Exclusion criteria:
Previous spine surgery, age less than 40 years, etiology other than isthmic, high-grade
spondylolisthesis, concomitant conditions which could compromise outcomes.
Patient population and interventions compared (Figure [1 ]):
One-hundred-and-fourteen consecutive patients met the inclusion criteria, and were
divided into two groups, according to the surgical treatment they received: PLIF group
(posterior lumbar interbody fusion) and PLF group (posterolateral fusion) (Table [1 ]). Patients were evaluated preoperatively, postoperatively and at final follow-up.
At the time of surgery all patients complained of low back and leg pain.
Posterior pedicle screw instrumentation alone was used as support to fusion in the
PLF group. Carbon fiber, titanium and peek cages were added in the PLIF group. A laminectomy
was performed in all cases. All patients received allograft bone and autograft bone
obtained from decompression.
Outcome and analysis:
Demographic, preoperative, perioperative and postoperative data were collected.
Clinical outcome was assessed by means of the Oswestry disability index (ODI), Roland
Morris Disability Questionnaire (RMDQ) and visual analogue scale (VAS), for back and
leg pain respectively, filled in by patients preoperatively and at last follow-up.
Radiographic evaluation included preoperative CT (performed to assess the isthmic
nature of the lesion) and MRI of the lumbar spine, as well as standing plain and functional
films with flexion and extension views before and after surgery and during the follow-up,
when requested. Fusion was defined as radiographic evidence of bone bridging, the
absence of lucency around the implant, and no motion during functional films.
Overall complications were noted. Major complications were those that needed revision
surgery or resulted in permanent neurological deficit.
The results were analyzed using the Student t-test. Results are expressed as the mean
(range), with a P -value of < 0.5 considered as being statistically significant.
Results
Results
The two groups were similar with respect to demographic and surgical characteristics
(Table [1 ]).
At an average follow-up of 62.1 months (range 51 – 78), 71 patients (62.3%), 28 (59.6%)
of the PLIF group and 43 (64.2%) of the PLF group, were completely reviewed.
Clinical outcome. Both techniques ensured improvement of clinical outcome, without
statistically significant differences between the two groups (P >.05). Unsatisfactory clinical results were achieved in four patients (14.3%) in
the PLIF group and in eight patients in the PLF group (18.6%) (Table [2 ]).
Radiologic outcome. The x-rays performed at final follow-up showed a fusion rate of
97% in the PLIF group, 95% in the PLF group, without statistically significant differences
(P > .05).
Complications. Complications requiring revision surgery occurred in 5 of 71 patients
reviewed (7%), one in the PLIF group (3.6%) and four in the PLF group (9.3%). Pseudarthrosis
occurred in one case in the PLIF Group, in two cases in the PLF group (Table [3 ]).
More information on complications is available in the web appendix at www.aospine.org / ebsj.
Discussion
Discussion
In our series, there does not appear to be a clear advantage of posterior lumbar interbody
fusion over posterolateral fusion in terms of clinical and radiological outcome.
A higher incidence of complications requiring surgical revision (9.3% versus 3.6%)
was found in the PLF group. Pseudarthrosis occurred in one case in the PLIF group
(3.6%) and in two cases in the PLF group (4.6%).
Despite nerve root manipulation required to insert the cages into the intervertebral
space, in our series we found only one case of sciatica at last follow-up in the PLIF
group.
Limitations. The present series should be interpreted in the context of its limitations,
including the retrospective nature of the review, the fact that patients were not
randomized between posterior lumbar interbody fusion and posterolateral fusion, the
low follow-up rate and the small sample size.
CONCLUSIONS
CONCLUSIONS
In case of adult low grade isthmic spondylolisthesis, posterior lumbar interbody fusion
doesn’t seem to provide advantages in terms of mechanical stability and fusion rate
(pseudarthrosis incidence: 3.6% verses 4.6%).
In our series, both treatments ensured good clinical results, without statistically
significant differences between the two techniques.
References
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Editorial staff perspectives
This is a CoE III treatment study.
Comparing outcomes from patients treated with PLIF with those treated with PLF is
a commendable goal and important in the debate about the best treatment options for
low-grade adult spondylolisthesis. In order to improve the quality of evidence available
to settle the debate, future studies need to address a number of key factors.
Patient selection:
Methodologically, selecting patients based on the completeness of follow-up at a specific
time or studies where > 85% are lost to follow-up creates the possibility of selection
bias. By selecting patients with a minimum of 4-years follow-up, it is possible that
those with less complete follow-up may have different clinical or other characteristics
(and outcomes!) that could influence the evaluation of the study outcome and thus
bias results. For example, if those who are lost to follow-up are more likely to have
a good outcome for a one of the treatments, the analysis would not potentially include
as many patients with a good outcome for that treatment and the results may be biased
to show that it is less effective than its comparator.
Treatment allocation:
How treatment was allocated was not well described in this paper, ie, what factors
determined whether a patient received PLIF versus PLF aside from what appears to be
institutional preference (see web appendix). Ideally, patients would be randomized
to treatment groups using an appropriate method of concealed allocation. It is common
for studies to describe treatment allocation based on surgeon preference or patient
presentation. This has the potential to bias study results. For example if patients
with more severe disease are more likely to receive one treatment over the other and
also have the potential for worse outcomes, the results may not be an accurate reflection
of either treatment in patients with the same disease severity. Allocation based on
the institution's preference may also bias results as other factors may also differ
across institutions. Factors such BMI and previous surgery may influence choice of
procedure and therefore outcomes and need to be described.
Retrospective versus prospective approaches:
In this study (and most retrospective studies), it isn't clear that a consistent perioperative
protocol (for clinical care or outcomes measurement) was used in both study groups.
With prospective study design, there is the potential to decrease study bias compared
with retrospective designs. Protocols for patient selection and treatment allocation,
perioperative care, collection of data and follow-up that are specified prospectively
help assure less biased allocation of patients to treatment and similarity of care
and measurement for both groups.
Outcomes:
Definition and evaluation of fusion status is long-held area of controversy. In this
study, it is unclear how fusion was determined and if its assessment was independent.
Factors such as use of BMP or grafts which may influence fusion and functional outcomes
need to be detailed and evaluated for their potential to influence the outcomes. In
addition factors such as reduction of deformity, disc height and restoration of lordosis
should be evaluated.
Final comments:
This study's use of validated outcomes measures and length of follow-up are two primary
strengths. The authors' acknowledgement of the significant loss to followup and limitations
imposed by retrospective, nonrandomized studies is commendable.