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From the Department of Anesthesiology, Erasmus Hospital, Free University of Brussels, Brussels, Belgium.
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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Methods: 241 ASA physical status I to III awake, supine patients were studied prospectively. Cutaneous projections of the internal tibial condyle and the internal malleolus were marked and the needle was inserted 45° cephalad in an antero-posterior plane, midway on the line between those two points, 1 cm posterior to the tibial shafts internal edge. The catheter was introduced in the peri-nervous space using nerve stimulation (< 0.5 mA) on both the Tuohy needle and catheter. Ten millilitres of 2% lidocaine were injected through the catheter. Cutaneous and dermatomal sensory blockade were assessed using cold and pinprick tests while motor block was assessed using a modified Bromage scale. Satisfaction and analgesia scores were noted after surgery for 48 hr. Adverse events were recorded.
Results: The TN was always blocked, matching the distal L5 cutaneous nerve supply. Blood reflux was present in five patients (needle or catheter). No additional adverse events were noted. During the initial postoperative 48 hr, 0.2% ropivacaine was infused through the catheter (5 mL·hr1) which always provided effective pain relief.
Conclusion: The midleg technique of TN anesthesia and catheter insertion allows patients to remain in the supine position and results in a high rate of homogeneous anesthesia, a low incidence of side effects and effective continuous analgesia.
| Introduction |
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| Material and methods |
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Each patient was premedicated with im midazolam 0.1 mg·kg1 and was further sedated, if needed, before the regional anesthetic procedure with iv sufentanil 2 µg and midazolam 2 mg. Landmarks for the TN location and catheter insertion were marked as follows: firstly, the cutaneous projections of the internal tibial condyle and the internal malleolus were identified; secondly, a line between those two-points was marked; we identified a point midway on this line, 1 cm posterior to the tibial shafts internal edge (Figure 1
). With the patient lying supine, a 50-mm long HDCTM (HDCTM Inc., Milpitas, CA, USA) Tuohy needle, connected to an HNS StimuplexTM (BBraunTM Melsungen AG, Germany) stimulator (current intensity of 0.5 mA, decreased to 0.3 mA to refine location; frequency and duration of the stimulus of 1 Hz and 100 µsec respectively), was inserted 45° cephalad in an antero-posterior plane to locate the TN behind the internal edge of the tibial shaft (Figure 2
) until we observed plantar flexions of the first toe. The midleg level was chosen to approach the TN, for two main reasons. Firstly, below the knee and above the midleg using our insertion method, the TN must be encountered prior to the posterior tibial artery (PTA) decreasing the risk of vascular puncture (Figure 2
) because the TN is more internal and anterior than the PTA. This anatomical situation is inversed below the midleg level. Secondly, the TN is the most superficial at the midleg level. After TN location, a 20-gauge HDCTM polyethylene stimulation catheter was inserted through the Tuohy needle, using the same stimulation settings. The length of inserted catheter corresponding to the best quality of muscular twitches was recorded. Finally, the catheter was fixed to the skin using a specific Epi-FixTM (Maersk MedicalTM Stonehouse, England, UK) device. After a 1-mL negative test dose (1% lidocaine with 1/200,000 epinephrine), 10 mL of 2% lidocaine were injected through the catheter. The catheter was left in place 48 hr postoperatively.
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Systemic adverse events and local complications related to the performance of the block were recorded. Depending on the patient or the surgical procedure, one sided spinal anesthesia (SA) or general anesthesia was induced to complete the TN block. Postoperative satisfaction and visual analogue scale (VAS) scores were recorded to assess postoperative analgesia. Requirements for postoperative supplemental iv, sc or oral analgesics were recorded.
The SPSS 10.0 software (SPSS Inc., Chicago, IL, USA) was used to describe the results.
| Results |
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Mean weight of the patients was 67.8 kg (range 38112) and mean height was 173 cm (range 152191 cm).The mean depth of location of the TN was 3.7 cm (range 35 cm). The mean surgical duration was 85 min (range from 65150 min).
The TN was always located but, in five patients, blood reflux was noted through the needle (n = 4) or through the catheter (n = 1) prior to local anesthetic injection. Consequently, the needle or the catheter was withdrawn and the procedure abandoned. In the remaining 236 patients, the TN was located after one attempt in 178 patients (74%), two attempts in 56 patients (23%) and three attempts in seven patients (3%). Mean time for performance of the complete procedure was 5.2 min (4.27 min). The mean length of catheter inserted was 1.7 cm (range 13 cm).
An x-ray of the leg (Figure 3
) was taken in a female patient operated for hallux valgus. It illustrates the distribution of the radio-opaque dye (4 mL of iohexol 240 mg·mL1 added to 10 mL of the anesthetic) within the perinervous adipose space. The anesthetic solution diffused approximately 6 cm cephalad and 2 cm caudad to the tip of the catheter.
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At the end of surgery, pain control was considered optimal in every patient since none requested additional analgesia after being asked specifically. A 0.2% ropivacaine infusion was programmed for 48 hr at 5 mL·hr1 using the Pain Management ProviderTM pump (Abbott DiagnosticsTM, North Chicago, IL, USA) in 163 patients (69%) or LV5 InfusorTM pump (Baxter HealthcareTM Corporation, Deerfield, IL, USA) in 73 patients (31%). Postoperative infusion lasted 42.8 hr (range 2748 hr). One hundred eighty seven patients (79%) received the complete infusion. The infusion was stopped prematurely in 17 (7.9%) patients because of technical problems (Table
) and in 32 (14%) for patient convenience (patient leaving hospital...). The mean satisfaction score (on a five-point scale) was 4.6 (range 35) and the VAS pain score (on a ten-point scale) was 2.1 (range 05).
After the postanesthesia care unit stay (mean of 86 min, range 61128), supplemental analgesics were not prescribed systematically but only when the VAS score was more than 5 on two successive assessments. Thirty eight patients (16.1%) received iv pro-paracetamol (30 mg·kg1·hr6) while 12 of them (5%) needed additional im piritramide (0.25 mg·kg1·hr6) at least once (n = 10) and twice in two other patients. Oral tramadol hydrochloride (50 mg·hr6) was given to 21 patients (8.1%) during at least 24 hr (n = 11) and always stopped at 48 hr.
Finally, no hemodynamic instability (arterial hyper-or hypotension) or systemic toxicity was noted after the injection of the anesthetic mixture. No long-term neurological complication has been reported in the series of patients.
| Discussion |
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| Conclusion |
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| Footnotes |
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Accepted for publication March 9, 2004. Revision accepted December 10, 2004.
| References |
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