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* From the Department of Anesthesiology, Erasmus Hospital, Free University of Brussels, Brussels, Belgium; and
the Division of Anesthesiology, Cantonal University Hospital, Geneva, Switzerland.
Address correspondence to: Dr. Pierre C. Pandin, Department of Anesthesiology and Intensive Care, Erasmus Hospital, Lennik Drive 808, B-1070 Brussels, Belgium. Phone: +32-2-555-39-19; Fax: +32-2-555-43-63; E-mail: ppandin{at}ulb.ac.be
| Abstract |
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Clinical features: Four MnSSER derivations (Erbs point; cutaneous projection of peripheral end of brachial plexus; posterior neck at C6 level, frontal and controlateral parietal scalp) were monitored and recorded for retrospective analysis. Continuous data acquisition were started before ropivacaine injection (baseline) and maintained for 30 min thereafter. Every three minutes after ropivacaine injection, cold and pinprick tests were performed in the hand median nerve cutaneous supply zone and were assessed using a sensory visual score (varying from 010). Data were compared using analysis of variance. Although MnSSER values were stable during baseline period, after ropivacaine administration, severe progressive amplitude depressions of selected MnSSER were detected in every patient. While clinical cold and pinprick tests became positive (score > 8) only 15.8 ± 1.2 min and 20.1 ± 1.8 min respectively after ropivacaine administration, the mean time to observe the earliest MnSSER 20% amplitude decrease at Erbs point derivation was reduced to 5.6 ± 1.1 min (P < 0.01).
Conclusion: Selected MnSSER amplitude reduction indicates objectively the onset of median nerve anesthesia following infraclavicular brachial plexus block before the appearance of clinical signs.
| Introduction |
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| Material and method |
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Median nerve somatosensory evoked response recordings
Before baseline and for 30 min after the ropivacaine administration, the median nerve was stimulated at the wrist (frequency 1 Hz and duration 0.2 msec) using the electrical stimulator of an Epoch 2000TM (Axon Systems Inc, San Francisco, CA, USA). The stimulation intensity was decreased by 2 mA when the evoked muscular twitches were observed (between 12 and 17 mA). Somatosensory evoked responses were recorded from sc needle electrodes at Erbs point (cutaneous projection of the peripheral end of the brachial plexus 23 cm above the clavicle), designated as "Erb"; from the cervical spine (just above the cutaneous projection of the spinous process of the sixth cervical vertebrae) designated as "C6" - and at the scalp, at the median prefrontal level (Fpz)- designated as "Fpz" and at the contralateral parietal level (P4) - designated as "P4". A common reference electrode (positive pole) was positioned on the ipsilateral ear designated as "A". All electrode impedances were automatically checked for values less than 5 kOhms. The recording frequency bandpass was 30 to 750 Hz and the sampling window 50 msec. Artifact rejection threshold was fixed at 25 µV. The 50 Hz notch filter was active.
Median nerve somatosensory evoked responses data acquisition methodology
Monitored MnSSER were respectively: P10, a peak present 10 ± 0.5 msec after stimulation, in A-Erb derivation; P11, at 11 ± 0.5 msec in the A-C6 derivation; N20, at 20 ± 0.5 msec in the controlateral A-P4 derivation and P22, at 22 ± 0.5 msec in the A-Fpz derivation. Before acquisition of baseline measurements, three groups of 500 averaged responses were required to assess a good visual reproducibility of evoked potential recordings. Triplicate MnSSER base-line measurement acquisitions were then performed approximatively five minutes prior to the ropivacaine injection. The average of the amplitude and latency values obtained (labelled "t5") were used as reference for subsequent comparison. Immediately after the ropivacaine injection (labelled "t0) and during the next 30 min, the averaging technique was applied continuously to obtain the MnSSER responses every 100 sweeps (MnSSER every 1520 sec). The pre- and post-ropivacaine administration previously defined signals were automatically saved for retrospective analysis from each recording site. Besides manual retrospective analysis, the automatic tracker software of our monitoring system was able to detect, from baseline values, a 20% variation either in amplitude or in latency, widely accepted as the correct threshold for significant changes. The maximal electrophysiological effect, based on a non-automated analysis by a blinded observer, was defined as an evoked response amplitude of less than 0.5 µV present in three successive averaging periods.
Infraclavicular brachial plexus block
The infraclavicular block was performed following the Rajs approach.9 After local anesthesia, a 10-cm long, short bevel insulated needle (Stimuplex ATM, BBraun Inc., Melsungen, Germany) connected to the negative pole of a nerve stimulator (Stimuplex HNS11TM BBraun Inc., Melsungen, Germany - 100 µsec pulse width, 1.5 mA initial current intensity at 1 Hz), was inserted. After median nerve location (muscular twitches corresponding to wrist, second and third finger flexion and forearm pronation), with a minimal stimulation current intensity of 0.5 mA, 40 mL of ropivacaine 0.5% were injected.
Clinical assessment of sensory blockade
After ropivacaine administration, cold and pinprick tests were performed every three minutes to assess anesthesia on the palmar face of the base of the second and third fingers (median nerve cutaneous supply zone). The patient documented his/her perceptions according to a SVAS, similarly to the Benzons method.3 The scale consisted of a 10-cm line, where the 0 cm mark stated "my cutaneous zone is not numbed at all", while 10 cm corresponded to "my cutaneous zone is completely numbed"; scores less than 1 were matched as a "no block" whereas those higher than 8 as "a good and effective block". The latter score was considered adequate for quatifying the clinical effectiveness of the block. Following cold or pinprick stimulation, we obtained cold SVAS (cSVAS) or pin-prick SVAS (pSVAS), respectively.
Data analysis
Mean values of amplitude and latency of each MnSSER (P10, P11, N20 and P22) at time t5 where considered as baseline values. The MnSSER waves, registered before and immediately after each SVAS clinical assessment performed every three minutes from t0 to t30, were extracted from the raw data and averaged. The parameters produced every three minutes after ropivacaine administration therefore consisted of mean MnSSER amplitudes and latencies, cSVAS and pSVAS values.
For statistical analysis, one way and repeated measures ANOVA tests were used (Instat 3.05TM and Prism 3.03 TM softwares - Graph Pad Software Inc, San Diego, CA, USA).
The analysis permitted: 1) evaluation of individual stability and reproducibility of the baseline MnSSER by comparison of the respective amplitudes and latencies of baseline evoked potentials from the three initial averages of 500 sweeps to confirm the initial on-line visual inspection of the profiles of the different waves; 2) testing the existence or not of a possible bias induced by the physical effect of the 40 mL anesthesia solution injection, by comparing the mean amplitudes and latencies of each monitored MnSSER at baseline and t0 (just after the injection) and; 3) the time evolution of amplitude and latency of each MnSSER and the two SVAS scores. The results are presented as mean ± SD. A P value < 0.05 was considered statistically significant.
| Results |
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Electrophysiological signal variations
The mean time to install the MnSSER equipment set and electrode insertion was 5.3 ± 0.4 min.
Values and reproducibility of baseline measurements
Before ropivacaine administration, mean MnSSER amplitudes and latencies recorded in three consecutive runs were stable (one-way ANOVA; NS) and documented normal baseline numerical values (Table I
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Median nerve somatosensory evoked responses amplitude and latency evolution after ropivacaine administration
Figure 1
depicts the evolution of mean amplitude and latency of the MnSSER over the time from base-line (t5) until 30 min after local anesthetic injection. Independently from the MnSSER, mean amplitudes have decreased progressively and significantly until they became very often undetectable. A significant reduction in peripheral MnSSER (P10 and P11) was observed faster than in central ones (N20 and P22 - Table II
and Figure 1
). Table II
summarizes the time elapsed after ropivacaine administration and the standard 20% amplitude decrease observed at P10, P11, N20 and P22. N20 and P22 alteration times were different compared to the P10 delay (P = 0.021 and P = 0.026, one way ANOVA, respectively).
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8) showed mean delays of 15.8 ± 1.2 min for cold and after 20.1 ± 1.8 min for pinprick tests (Table II
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| Discussion |
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Consistent with other published data,3,7 no significant changes in the latencies were observed, but depression of MnSSER amplitude in the diverse channels appears as a good indice for detecting the onset and the progression of a chemically induced neural blockade. In the present context, (quantification with a possible anticipation of a potentially successful neural blockade), it seems evident that limited amplitude reduction (by 20%) is a good clinical indicator. Each time a 20% amplitude reduction is observed, the MnSSER will eventually disappear, indicating effective median nerve blockade. The 20% value was chosen because the default tracking method of our monitoring system permitted an automatic detection of MnSSER alterations. However, for a human observer, the depression of amplitude and its time course can be more easily noticed and detected on the peripheral MnSSER collected at Erbs point, as their initial amplitudes (35 µV) are always higher than the ones recorded more centrally (< 2.53 µV). On the Erbs point derivation, the detection occurred during the early phase (ranging between three to six minutes) of the ropivacaine induced block.
An unresolved issue is whether or not SSEP assessment of one brachial plexus nerve is sufficient to conclude that the plexus block will be complete. Based upon our experience, we think "no". Although MnSSER can detect objectively the early occurrence of an effective brachial plexus block compared to clinical assessment, the correlation between median nerve location and plexus anatomy is variable. Accordingly, a more systematic SSEP investigation of median, ulnar and radial nerves during brachial plexus block techniques (not only infraclavicular, but also axillary, inter-scalene and subclavicular) may simplify the technique and clarify its usefulness in clinical practice.
In conclusion, MnSSER monitoring in adult patients permits objective quantification of the onset of clinical median nerve blockade after 40 mL of 0.5% ropivacaine for brachial plexus blockade. The P10 amplitude decrease is always associated with a clinically successful block, and appears about ten minutes earlier than the clinical confirmation of median nerve block. This electrophysiologically-based, pain-free monitoring may be important in clinical anesthesia, and provides a method for studying more objectively the clinical action of local anesthetic solutions.
| Footnotes |
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| References |
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5 Murphy BA, Haavik Taylor H, Wilson SA, Knight JA, Mathers KM, Schug S. Changes in median nerve soamtosensory transmission and motor output following transient deafferentation of the radial nerve in humans. Clin Neurophysiol 2003; 114: 147788.[Medline]
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8 Benzon HT, Toleikis JR, Dixit P, Goodman I, Hill JA. Onset, intensity of blockade and somatosensory evoked potential changes of the lumbosacral dermatomes after epidural anesthesia with alkalinized lidocaine. Anesth Analg 1993; 76: 32832.[Medline]
9 Raj PP, Montgomery SJ, Nettles D, Jenkins MT. Infraclavicular brachial plexus block - a new approach. Anesth Analg 1973; 52: 897904.
10 Borene SC, Edwards JN, Boezaart AP. At the cords, the pinkie towards: interpreting infraclavicular motor responses to neurostimulation. Reg Anesth Pain Med 2004; 29: 1259.[Medline]
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