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Original papers Med Ultrason 2013, Vol. 15, no. 1, 10-15DOI: 10.11152/mu.2013.2066.151.jo1ugc2
Abstract
Objectives:A prospective randomized clinical trial was conducted to evaluate accuracy, time-saving, radiation doses and
pain relief of ultrasound-guided (US) facet joint injections versus Computed Tomography (CT)-controlled interventions in the
cervical spine. Material and methods: Forty adult patients were consecutively enrolled and randomly assigned to the US- or
CT group. US-guided facet joint injections were performed on a standard ultrasound device using a broadband linear-array
transducer. The corresponding comparison group underwent CT-guided instillations which were performed under standard-
ized procedures using the CT-positioning laser function. Results:The accuracy of ultrasound-guided interventions was 100%.
The mean time (min:sec) to nal needle placement in the US group was 04:46 versus 11:12 (p
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12 Jochen Obernauer et al Ultrasound-guided versus Computed Tomography-controlled facet joint injections
of the area of interest. Consistent with the US procedure,
elapsing time was recorded with the start of the initial
scan. For a precise calculation of the needle pathway, a
topogram through the targeted area was obtained with a
low-dose protocol (120 kV, 120 mA) at 3 mm slice thick-
ness. The point of entry, the angle and the depth of ap-
proach were selected and calculated. The needle entry
point was marked on the patients skin using the obtained
calculations and the CT-positioning laser function. Then
a spinal needle (20 GA 3.00 IN, 0.9 x 75 mm; BD Spinal
Needle, Becton Dickinson, Madrid, Spain) was advanced
toward the facet joint of interest, according to the prelimi-
nary calculations. To control the present and nal needle
tip position, several CT scans were obtained repeatedly,
i.e. after each reposition, until the needle was estimated
to be the in correct position. At that time the elapsed time
was recorded. Exactly as in the US procedure, 1 mL
mixture of betamethasone (CELESTAN solubile 4 mg/ml; essex-pharma GmbH, Munich, Germany) and bupi-
vacainehydrochloride (Bucain 0.25%, 2.5 mg/ml, Delta
Select GmbH, Pfullingen, Germany) was injected.
Measurements and Statistics
For both groups the periods of intervention time and
the radiation doses (as dose-length products; DLPs) are
reported. Time and radiation dose were compared sepa-
rately for one- and two-leveled injections. To follow up
the clinical benet, neck pain was assessed via a visual
analog scale (VAS) before, 30 minutes after and 4 weeks
after the intervention. Feasibility of the US procedure was
dened as percentage of patients with clearly, partially, orinvisible targets (respectively inter-articular space). Accu-
racy was calculated as CT-veried exact needle tip place-
ment. The number of repositions, unexpected problems
and complications were also recorded for both groups.
Statistical analyses were done according to the intention-
to-treat principle [23]. The primary outcomes were accu-
racy and time to nal needle placement. For the evaluation
of VAS changes we used the comparison of percentage
VAS reduction from pre- to 30-minutes post-intervention-
al and from pre- to 4-weeks post-interventional interval.
The trial was designed to detect an absolute difference of
one standard deviation with a power of 80% at a two-sid-
ed signicance level of 0.05 and a maximum dropout rate
of 20%. Comparisons between groups were performed
with an unpaired t-test, or in case of nonparametric val-
ues, with a Mann-Whitney U-test.
Results
After randomization there were no signicant differ-
ences between the two groups (table I). All patients who
were randomly assigned to the US group were judged
to be feasible for the US-guided procedure. In 20 pa-
tients the inter-articular space of the targeted facet joint,
as well as the bony landmarks, were clearly depicted by
US (100%). In 19 of these patients (95%) the interven-
tion was performed as planned and the needle was posi-
tioned correctly, as also conrmed by CT (95%). In one
case (5%) the intervention was aborted because of the
patients missing compliance (the patient was unable to
deal with the pain of needle positioning). In the US group
no needle had to be repositioned (accuracy = 100%). In
the CT group a needle reposition was necessary in 13
cases (65%): in 3 cases (15%) the respective needle po-
sition was changed once, in 6 cases (30%) twice, in 2
cases (10%) three times and in another 2 cases (10%)
even four times. Regarding the necessary needle reposi-
tions the US-guided procedure statistically showed a sig-
nicantly higher accuracy (p
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13Med Ultrason 2013; 15(1): 10-15
showed a signicant DLP saving for one- (p
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14 Jochen Obernauer et al Ultrasound-guided versus Computed Tomography-controlled facet joint injections
performed to reduce the risk of unintentional injection in
such paraspinal, e.g. radicular, vessels [27].In the present
US technique, the advantage of utilizing a real-time in-
plane needle access from dorsal is striking: any relevant
vessel is so avoided, as based on normal topography
none usually crosses the needle pathway. Also, if the
target is clearly visible under US guidance, no further
radiographic control and no systemic application of con-
trast agents or other ionizing modalities are necessarily
required. In this context, the use of Duplex-mode US im-
aging as a further guidance tool is conceivable, but was
not used in the present study because of its questionable
additional benet.
In this trial, CT controls in the US group were per-
formed only for study purposes. The recordings of these
DLPs showed that the mean radiation dose in the US
group was signicantly lower than the mean dose of
patients who had undergone CT-guided-only interven-tions, which implies a benet of US guidance even if
performed with subsequent CT control (maybe due to
forensic necessities). Although the necessary radiation
dose for one single CT-guided intervention may be rather
low, our study showed that cumulative effects have to be
taken into account, as some CT-guided instillations in our
trial required up to four CT scans. For such repeated and
multilevel injections, which are quite popular, US guid-
ance would be the recommended procedure.
A further benet of US guidance is that it helps to
minimize the risk of unexpected side effects, as those are
often associated to the application of contrast agents re-quired for the positioning control under CT- or uorosco-
py-guided procedures. The fact that US-guided injections
can be performed rather easily is mostly based on the di-
rect depiction of the structures of interest, i.e. cervical
facet joints, by US. Thus, with a little exercise, a needle
can be advanced to the target structure itself in just a few
seconds under safe and real-time controlled conditions
[1,13,16].If such an intervention is performed under CT-
guidance, calculations on access angles and entry points
of the needle are based on landmarks, followed by an
actually blind needle-positioning which is then control-
led by a subsequent scan and often followed by multiple
repositions. Control scans, if necessary, are potentially
harming to the patients, as described above, but are also
laborious and costly compared to the US procedure pre-
sented here. US-guided facet joint instillations may even
be performed very efciently under bed-side condi-
tions, e.g. in outpatients. This saves time and resources,
as US is comparatively inexepensive and broadly avail-
able, and does not imply any therapeutic compromises
for the patient, as accuracy is obviously sufcient for the
purpose described here [13].
According to the analysis on increasing numbers and
costs of spinal injection therapies, published by Carrino
et al 2002 [11], the overall cost-effectiveness of cervical
instillations must be evaluated as well. This is however
beyond the scope of this study.
Limitations
Limiting factors might be that outcome was only
measured by patient satisfaction and that the long-term
follow-up was only performed four weeks after the in-
stillation.
Conclusion
The US-guided facet joint injection in the middle
and lower cervical spine is accurate, feasible, and bears
minimal risk. It results in a signicant pain reduction,not different from CT-guided instillations. Addition-
ally a reduction of time, radiation dose and resources is
highly evident. However, as with any form of instillation
therapy needing practice for good results, a specic and
mandatory learning curve to achieve good visualization
and guidance of the instillation needle has to be taken
into account with US guidance. Upcoming projects are
supposed to evaluate this and the value of the US-guided
procedure during daily routine.
Conict of interest: none
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