Comparison Between the Two-Injection Technique and the Four-Injection Technique in Axillary Brachial Plexus Block with Articaine/Artikain Yapilan Brakial Pleksus Bloklarinda Ikili veya Dortlu Enjeksiyon Tekniklerinin Karsilastirilmasi.
Within the axillary region, the brachial plexus divides into three major nerves: the median, radial and ulnar within the same neurovascular sheath. As shown in studies with single injection and ultrasonography, the administration of a local anesthetic within the sheath can block all of these nerves. Local anaesthetic spreads partially on median, ulnar and radial nerves because of the septal structure of the neurovascular sheath (1). Blockage obtained with single injection can cause insufficient anaesthesia in forearm surgeries, because the musculocutaneous nerve leaves brachial plexus proximally and is thus insufficiently blocked. For this reason, musculocutaneous nerve blockage is recommended separately to prevent tourniquet pain. As is known, blockage with multiple injections takes much longer and causes more pain, which negatively affects the patient's comfort. There are studies indicating that the success of blockage increases with the administration of the local anaesthetics to two or more nerves in divided doses (2, 3).
Articaine (Maxicaine Fort VEM Drug, Istanbul, Turkey) can be used in all nerve blocks. Its biological half-life is about 60 minutes when in pure form (4). It is metabolized rapidly by the plasma estherases and excreted in urine. It dissolves in water at pH 5 and can be alkalanized with Na[HCO.sub.2] in order to increase the duration of its effect.
Articaine in the ten-fold clinical blood concentration is less cardio-depressant as compared to the five-fold blood concentration of bupivacaine (5, 6). Articaine and lidocaine have similar pharmacodynamic effects in axillary brachial plexus blocks, but pharmacokinetically, articaine is eliminated more rapidly (7). Its toxicity is lower than the toxicity of lidocaine and higher than the toxicity of procaine (8).
In this study, our aim was to compare the starting and ending times of the sensory and motor block, effectiveness of the blockage, complications and satisfaction of patients operated for carpal tunnel syndrome with axillary blockage using two- and four-injection techniques with ultrasonography and nerve stimulator.
As a result of power analyses, it was determined that the sample size include 60 individuals, with at least 30 individuals in each group, so that the strength of test could be 80% and confidential- safety interval could be 90%.
Our study was a prospective, randomized and single-blind study.
Following the approval from ethical committee of the Ankara University Medical School issued on May 23, 2011, number 31-667, patients who were planned to be included in the study were informed about the study, and their consent was obtained.
There were 60 adult patients with ASA I-II group who were to be operated at the Ankara Oncology Training and Research Hospital. Patients aged between 18 and 65 years were included in the study. Patients with serious hepatitis, hematologic, metabolic, respiratory, cardiac, neurologic, psychiatric or neuromuscular diseases, patients who were pregnant or lactating, and patients with local infection risk, allergic to local anaesthetics, and with body weight under 50 kg or over 100 kg were excluded from the study.
Patients were taken to the preparation room 45 minutes before the operation. Venous access was established on the dorsal side of the hand that was not to be operated with a 20 gauge intravenous cannula, and crystalloid infusion was started. Sedation was provided for the patients with midazolam 2 mg before the block. The ECG, heart rate (HR), systolic arterial pressure (SAP), diastolic arterial pressure (DAP) and peripheral oxygen saturation were monitored preoperatively and postoperatively.
During the procedure, the patient was placed into supine position, the arm to be operated was placed at an angle of 90 degrees with the body, and the forearm was flexed to make an angle of 90 degrees with the arm. After ensuring antisepsis, probe of the high-frequency linear ultrasonography (Esaote, My LabFive-Genova, Italy) was placed. First, the axillary artery and vein and nerves around the artery (musculocutaneus nerve, median nerve, ulnar nerve, radial nerve) were detected. In all the patients, 22 gauge 50 mm insulated needles conducted the current (Stimuplex D.B. Braun Medical-Freiburg, Germany). A nerve stimulator that could be adjusted at 1.5 mA current to 1 Hz frequency and 0.1 ms velocity (Stimuplex HNS11, B Braun Medical-Melsungen, Germany) was used to investigate the motor response around the nerves. After finding the strongest responses, the current was first reduced to 1 mA, and then to 0.5 mA to obtain a motor response with the lowest current. Local anaesthetic was injected around the nerve upon seeing that no blood is drawn with aspiration, and the distribution of the local anaesthetic was observed with ultrasonography (Figure 1).
Articain 2% at 5 mg [kg.sup.-1] plus Na[HCO.sub.3] 8.4% were added in a concentration of 1 mL per 10 mL, and volume was adjusted to 30 mL with physiological saline. Patients were randomly divided into two groups. In both the groups, 6 mL of local anaesthetic were initially administered to the musculocutaneous nerve localization. In the first group (G1; n=30), 24 mL of local anaesthetic were applied to the median nerve localization in the two-injection method. In the second group (G2; n=30), 8 mL of local anaesthetic were administered to radial, median and ulnar nerve localizations.
Te time period between the puncture of the skin with the needle and taking it out after the administration of the total dosage was determined and recorded as the application time. Patient's pain during the procedure was recorded using the VAS score (VAS 0=No pain, VAS 10=the most severe pain). Motor and sensorial blocks were evaluated at 3, 6, 9, 12, 15, 20, 25 and 30 minutes after the injection.
Flexion of the fingers was monitored for the median nerve; separation of fingers for ulnar nerve; extension of the forearm for radial nerve; and flexion of the forearm for the musculocutaneus nerve function. Motor block characteristics were evaluated based on a 3-point scale (0=normal strength; 1=decreased strength: paresis; 2=no function: paralysis). For sensory block, lateral side of the forearm was evaluated for the musculocutaneus nerve; the 1st, 2nd, 3rd and 4th finger and palm were evaluated for the median nerve; dorsal sides of the hand and forearm were evaluated for the radial nerve; and the 5th finger was evaluated for the ulnar nerve function. Pinprick test (with blunt-tip 27 G dental needle) was applied, and the results were evaluated on the 3-point scale (1=feels pain; 2=partial block: analgesia; 3=complete block: anesthesia). Based on the evaluation, 0 was accepted as clinically insufficient block, and 1 and 2 were accepted as clinically sufficient block, and operation was allowed. The moment when the pain started was accepted as the termination of sensory block, and the moment that the patient was able to bend his/her fingers into a fist and fully gained the arm strength back was accepted as the termination of motor block. The times when the patients felt pain for the first time and when they gained the hand and arm strength back were recorded for all the patients.
During the block application, throughout the operation and in the postoperative 120th minute, patients were observed for complications and adverse effects. They were informed about the neurologic complications (paresthesia, anesthesia and motor weakness), and they were called 24 hours after the block, when any neurologic complications and satisfaction of the patient with the procedure were questioned and recorded (0=Unsatisfied, 1=Less satisfied, 2=Satisfied, 3=Very satisfied).
Power analysis was performed. In order to obtain 80% test strength and 90% safety interval, there should be 30 patients present in each group, which totals 60 patients.
MS-Excel 2003 and Statistical Package for the Social Sciences for Windows Ver. 15.0 (SPSS Inc.; Chicago, IL, USA) were used for statistical analyses and calculations. Data obtained from the study were analysed via Mann-Whitney U Test, which is a non-parametric test, regarding the differences of sensory and motor properties of all the nerves between the two groups. Dependence between the categorical variables was analysed by means of Chi-squared test. The value of p<0.05 was considered statistically significant.
There were no differences found between the groups regarding the demographic data of the patients (gender, ASA, age, body weight) and Sp[O.sub.2] values, systolic and diastolic blood pressure values, and heart rate in all the time periods (p>0.05). It was observed that in Group 2, there were more women than men (Table 1).
It was found that there were no differences in the sensory and motor block characteristics for all the nerves included in the study between the 15th and 30th minute. For this reason, data from the first 20 minutes were taken into consideration in relation to the sensory and motor block characteristics.
When the sensory block characteristics of the musculocutaneous nerve were analysed for all the measurement times, it was found that a suficient sensory block level was obtained at the 6th minute for the G1 group, and the 3rd minute for the G2 group. When comparing the groups, the sensory block characteristic values at minutes 3 and 6 were found significantly higher in the G2 group (p<0.05). 96.7% complete and 3.3% partial sensory block was obtained in the G1 group, where-as 93.3% complete and 6.7% partial sensory block in the G2 group was obtained at the 20th minute. 100% satisfactory sensory block was obtained with both the methods (Figure 2).
Considering the sensory block characteristics of radial nerve, it was seen that suficient blockage levels were reached in the 9th minute in the G1 group and 6th minute in the G2 group. The sensory block level was found to be significantly higher in all the time periods in Group 2 (p<0.05). 23.3% partial and 73.4% complete sensory block occurred in the G1 group, whereas 3.3% partial and 96.7% complete block was found in the G2 group at the 20th minute. Radial nerve could not be blocked in 1 patient from the G1 group (3.3%), whereas this was achieved in all the patients from the G2 group. Sensory block characteristics could not be fully achieved in 7 patients from the G1 group (23.3%) (Figure 3).
When the characteristics of the median nerve sensory block were analysed, it was found that a suficient block level was obtained at the 6th minute for G1 group and 3rd minute for G2 group. When comparing the groups, the sensory block values at minutes 3 and 6 were found significantly higher in Group 2 (p<0.05). There were no significant differences in the sensory block characteristic values between the groups in other time periods (p>0.05). For median nerve, 100% complete sensory block was obtained in G1 group, while 3.3% partial and 96.7 complete sensory block in G2 group at the 20th minute. A 100% satisfactory block could be obtained with both the methods (Figure 4).
When the characteristics of the sensory block of ulnar nerve were considered, it was found that the suficient block level was reached at the 9th minute in the G1group and 3rd minute in the G2 group. When comparing the groups, the sensory block characteristic values at minutes 3, 6, 9 and 12 were significantly higher in the G2 group (p<0.05). In the other time periods however, there were no significant differences between the groups with regard to characteristics values of sensory block (p>0.05). For ulnar nerve, 10% partial and 90% complete sensory block was achieved in the G1 group, whereas 6.7% partial and 93.3% complete block was achieved in the G2 group at the 20th minute. 100% complete block was achieved with both the methods (Figure 5).
Upon examining the sensory and motor block characteristics of all the nerves at the 20th minute (Table 2), statistically significant differences were found only in the sensory and motor block characteristics of radial nerve (p<0.05). There were no statistically significant differences for the musculocutaneous nerve, median nerve and ulnar nerve. While sensory and motor block could not be achieved in 1 patient in the G1 group, complete block could not be achieved in 9 patients from the G1 group, whereas it was achieved in all the patients from the G2 group. Suficient sensory and motor blockage was detected in both the groups. In the G2 group, satisfactory sensory and motor block was observed in 100% of the cases and for all nerves. Although no significant dependency was observed between the groups in the number of patients with a complete sensory and motor block of all the four nerves (p>0.05), the number of complete sensory and motor block for all the four nerves was greater in the G2 group. In the G2 group, a complete sensory block was recorded in 25 (83.3%) patients, and complete motor block in 22 (73.3) patients. In the G1 group, a complete sensory block was achieved in 20 (66.7%) patients and complete motor block in 17 (56.7%) patients (Table 3).
When the patient satisfiaction and additional sedation needs were evaluated (Table 4), there were no statistically significant differences found between the two groups (p>0.05). Sufficient anaesthesia level was obtained in both the groups without any need for additional local anaesthetics. Axillary block application times and VAS values in the G2 group were significantly higher than those in the G1 group (p<0.05) (Table 5). Statistical difference was found between the groups in the onset times of the sensory and motor blocks (p<0.05). The onset time of the sensory and motor block in the G1 group was longer than in the G2 group (Table 5). Total period of motor blocks (min) were 232.9[+ or -]26.3 in Group 1, 235.8[+ or -]33.9 in Group 2, and p value was 0.941. This difference was not statistically significant (Table 5).
There were no adverse effects or complications including hematoma, vascular puncture, intravascular injection, convulsions, tinnitus, nausea, vomiting, paraesthesia, and hemodynamic changes observed in patients from both the groups who were monitored during the block application, during the operation, and in the postoperative period, 1 month after the procedure.
Ambulatory surgery is becoming widespread all over the world. General anaesthesia and brachial plexus blockage have been studied in ambulatory surgery, and it was found that brachial plexus blockage provided earlier discharge (9). When it comes to axillary blockage, different success rates are reported in the literature. Successful Vester-Andersen block criteria include the effective block in the areas innervated by at least two musculocutaneous nerves, median nerve, ulnar nerve and radial nerve (10). Baranowski and Pither (11), however, as a successful block define a complete block of three major nerves. In our study, success was evaluated based on the mean block characteristics of each nerve. At the same time, the rates of complete block have been reported as 66.7% and 83.3%, respectively, for the four nerves. No additional local anaesthetic application was required.
Ultrasonography is becoming an essential and indispensable tool in the local anaesthesia. USG application leads to less axillary pain and nerve injury (3, 12). In our study, USG and neurostimulator were used together to block all the nerves. Chan and colleagues evaluated the success of axillary block in 188 patients divided into 3 groups where USG, neurostimulator, and USG plus neurostimulator were additionally used. Higher success rates were observed in the two USG groups compared to the group in which only a neurostimulator was used (12).
Sensory block is required in operations planned under regional anaesthesia for a successful operational area. While some studies found that a satisfactory sensory nerve blockade could be obtained with a local anaesthetic in low concentrations, motor blockade was low or was not found at all (13). We have applied in our study as regards the sensory block characteristics in the first place. In our study, suficient sensory block was accomplished by axillary plexus block using articaine in all the patients.
In a retrospective study, Fanelli et al. (14) reported a success rate of 93% using a local anaesthetic with volumes less than 30 mL in the upper extremity they applied with multiple injections. The investigators advocated that the high pressure created by the high volume of the local anaesthetic solution would cause tears in the septa thought to present within the sheath, which would enable an easier drug distribution between the nerves (1). In other studies on this subject, volumes of 40, 50, and 60 mL have been used, and no differences were found in the sensory and motor blockage success between the groups (10). The volume of the local anaesthetic used in our study was 30 mL, and satisfactory sensory block was obtained in 96.7%-100% of cases when using the two-injection method, and in 100% of cases when using the four-injection method for the axillary block.
In their study, Coventry et al. (2) blocked the musculocutaneous and median nerves in one group, and the musculocutaneus, median and radial nerves in the other group, and determined the ratios of patients in who a complete block was obtained for all the nerves, which was 53% and 97%, respectively. Likewise, our study has shown that the percentage of cases with a complete sensory block was higher with the multiple injection method (66.7% and 83.3%) for all the four nerves. The percentage of complete motor block was also higher in the four-injection group (56.7% and 73.3%). As the success rate in our study for radial nerve blockade was lower in the two-injection group, multiple-injection technique must be preferred in the surgical procedures to be performed on the areas innerved by the radial nerve. If the smaller number of injections is preferred, the radial nerve must be blocked separately (15).
Patient satisfaction also plays an important role in regional anaesthesia. Sia et al. (16) applied axillary block in patients who were to undergo hand surgery, and blocked only 1 or 2 nerves that innervated the operation area, and blocked the musculocutaneous nerve, median nerve and radial nerve in the other group. They found similar patient satisfaction rates in both the groups, and an additional drug requirement for sedation was less in the multiple injection group. The patient satisfaction rates and the additional sedation requirements during the operation were found to be similar in both the groups in our study. During the blockage procedure, VAS values were statistically higher in the four-injection technique. These results were found to be consistent with the other studies (17-19).
Malke et al. (20) applied an axillary brachial plexus block using 1% articaine hydrochloride and 1% mepivacaine in 40 patients who were to undergo hand and forearm surgeries. The authors suggested that articaine hydrochloride is a safe and reliable agent with rapid onset and a longer sensory and motor block period than mepivacaine. Our study also showed that articaine hydrochloride is a rapid-onset agent that provides the sensory and motor block required for surgery.
NaHC[O.sub.3] is commonly used to decrease the onset time of the brachial plexus block. Various studies have explored the effect of this additional drug. Contreras-Dominguez et al. (21) applied the brachial plexus block by adding clonidine to mepivacaine sodium bicarbonate (NaHC[O.sub.3]). They reported that adding sodium bicarbonate to mepivacaine delayed the onset of blockage time. Armstrong et al. (22) found that alkalization shortened the onset time of the sensory and motor block and slowed down the fading of sensory block.
Whereas axillary block application takes longer when using the four-injection technique during the procedure, we found in our study that with this technique, a complete block was obtained for all the four nerves more rapidly and in a greater number of patients.
In this study, we have used and compared the two- and four-injection technique for the axillary block with alkalinized articaine. In our opinion, sufficient analgesia and anaesthesia levels can be obtained with both the techniques without requiring additional local anaesthetics in selected patients, including those with carpal tunnel syndrome.
Ethics Committee Approval: Ethics committee approval was received for this study from the ethics committee of Ankara University.
Informed Consent: Written informed consent was obtained from patients who participated in this study.
Peer-review: Externally peer-reviewed.
Author Contributions: Concept--G.A.; Design--G.A., A.E.; Supervision--G.A., M.A.; Resources--G.A., A.E., M.M.; Data Collection and/or Processing--G.A., A.E., M.M.; Analysis and/or Interpretation--A.E., G.A.; Literature Search--G.A., A.E., M.M.; Writing Manuscript--G.A.; Critical Review--M.A., M.Arikan.
Conflict of Interest: No conflict of interest was declared by the authors.
Financial Disclosure: The authors declared that this study has received no financial support.
Etik Komite Onayi: Bu calisma icin etik komite onayi Ankara Universitesi'nden alinmistir.
Hasta Onami: Yazili hasta onami bu calismaya katilan hastalardan alinmistir.
Hakem Degerlendirmesi: Dis bagimsiz.
Yazar Katkilari: Fikir--G.A.; Tasarim--G.A., A.E.; Denetleme--G.A., M.A.; Kaynaklar--G.A., A.E., M.M.; Veri Toplanmasi ve/veya Islemesi--G.A., A.E., M.M.; Analiz ve/veya Yorum--A.E., G.A.; Literatur Taramasi--G.A., A.E., M.M.; Yaziyi Yazan--G.A.; Elestirel Inceleme--M.A., M.Arikan.
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Finansal Destek: Yazarlar bu calisma icin finansal destek almadiklarini beyan etmislerdir.
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(7.) Simon MA, Vree TB, Gielen MJ, Booij LH, Lagerwerf AJ, et al. Similar motor block effects with different disposition kinetics between lidocaine and articaine in patients undergoing axillary brachial plexus block during day case surgery. Int J Clin Pharmacol Ther 1999; 37: 598-607.
(8.) Muschaweck R, Rippel R. Ein neues lokal anaesthetikum (carticain) aus der thiophenreiche. Parkt Anaesth 1974; 9: 135-46.
(9.) Hadzic A, Arliss J, Kerimoglu B. A comparison of infraclavicular nerve block versus general anesthesia for hand and wrist day case surgeries. Anesthesiology 2004; 101: 127-32. [CrossRef]
(10.) Vester-Andersen T, Husum B, Lindeburg T, Borrits L, Gothgen I. Perivascular axillary block IV: blockade following 40, 50, or 60 ml mepivacaine 1 % with adrenaline. Acta Anaesthesiol Scand 1984; 28: 99-105. [CrossRef]
(11.) Baranowski A P, Pither CE. A comparison of three methods of axillary brachial plexus anaesthesia. Anaesthesia 1990; 45: 362-5.
(12.) Chan VW, Perlas A, Mmlartney CJ, Brull R, Xu D, Abbas S. Ultrasound guidance improves success rates of axillary brachial plexus block. Can J Anaesth 2007; 54: 176-82. [CrossRef]
(13.) Hempel V, Baur K F. Regional Anaesthesie fur Schulter, Arm und Hand. Urban &Schwarzenberg, Munchen 1982; 1-33.
(14.) Fanelli G, Casati A, Garancini P, Torri G. Nerve stimulator and multiple injection technique for upper and lower limb blockade: failure rate, patient amleptance, and neurologic complications. Study Group on Regional Anesthesia. Anesth Analg 1999; 88: 847-52. [CrossRef]
(15.) Rodriguez J, Taboada M, Del Rio S, Barcena M, Alvarez J. A comparison of four stimulation patterns in axillary block. Reg Anesth Pain Med 2005; 30: 324-8. [CrossRef]
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(18.) Purcu O, Yavascaoglu B, Kaya FN, Gurbet A, Turkcan S, Orhan G. Pregabalinin Aksiller Blok Sonrasi Analjeziye Etkisi, Effects of Pregabalin on Postoperative Analgesia after Axillary Block. Turk J Anaesth Reanim 2013; 41: 18-23. [CrossRef]
(19.) Imasogie N1, Ganapathy S, Singh S, Armstrong K, Armstrong P. A prospective, randomized, double-blind comparison of ultrasound-guided axillary brachial plexus blocks using 2 versus 4 injections. Anesth Analg 2010; 110: 1222-6.
(20.) Malke G. A double blind comparision of carticaine and mepivacaine. Prakt Anesth 1997; 12: 335-8.
(21.) Contreras-Dominguez V, Carbonell-Bellolio P, Sanzana Salamanca E, Ojeda- Grecie A. Addition of sodium bicarbonate and/or clonidine to mepivacaine: influence on axillary brachial plexus block characteristics. Rev Esp Anesthesiol Reanim 2006; 53: 532-7.
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Aysun Ertikin (1), Guldeniz Argun (1), Mesut Misirlioglu (2), Murat Aydin (3), Murat Arikan(2), Nihal Kadiogullari (1)
(1) Department of Anesthesiology and Reanimation, Oncology Training and Research Hospital, Ankara, Turkey
(2) Department of Orthopaedics and Traumatology, Oncology Training and Research Hospital, Ankara, Turkey
(3) Department of Orthopaedics and Traumatology, Afyonkarahisar Suhut Public Hospital, Afyonkarahisar, Turkey
Cite this article as: Ertikin A, Argun G, Misirlioglu M, Aydin M, Arikan M, Kadiogullari N. Comparison Between the Two-Injection Technique and the Four-Injection Technique in Axillary Brachial Plexus Block with Articaine. Turk J Anaesthesiol Reanim 2017; 45: 289-96
Address for Correspondence/Yazisma Adresi: Guldeniz Argun E-mail: firstname.lastname@example.org
Received / Gelis Tarihi : 06.12.2016
Accepted / Kabul Tarihi : 30.05.2017
Table 1. Demographic characteristics of groups (p<0.05) Group 1 Group 2 p Gender Female 15 (50%) 19 (63.3%) 0.434 Male 15 (50%) 11 (36.7%) ASA ASA1 14 (46.7) 15 (50%) 1.000 ASA2 16 (53.3) 15 (50%) Age 50.3[+ or -]16 46.7[+ or -]14.9 0.325 Body weight 73.6[+ or -]16.4 73.7[+ or -]12 0.756 Table 2. Sensory and motor block characteristics of all nerves at the 20th minute (n, %, Mean[+ or -]SD) Block Characteristics (0-2) Group 0 1 2 n % n % n % Musculocutaneous nerve (sensory) Group 1 0 0.0 1 3.3 29 96.7 Group 2 0 0.0 2 6.7 28 93.3 Musculocutaneous nerve (motor) Group 1 0 0.0 2 6.7 28 93.3 Group 2 0 0.0 3 10.0 27 90.0 Radial nerve (sensory) Group 1 1 3.3 7 23.3 22 73.4 Group 2 0 0.0 1 3.3 29 96.7 Radial nerve (motor) Group 1 1 3.3 9 30.0 20 66.7 Group 2 0 0.0 3 10.0 27 90.0 Median nerve (sensory) Group 1 0 0.0 0 0.0 30 100.0 Group 2 0 0.0 1 3.3 29 96.7 Median nerve (motor) Group 1 0 0.0 0 0.0 30 100.0 Group 2 0 0.0 1 3.3 29 96.7 Ulnar nerve (sensory) Group 1 0 0.0 3 10.0 27 90.0 Group 2 0 0.0 2 6.7 28 93.3 Ulnar nerve (motor) Group 1 0 0.0 4 13.3 26 86.7 Group 2 0 0.0 3 10.0 27 90.0 Block Characteristics (0-2) Mean[+ or -]SD p Musculocutaneous nerve (sensory) 1.96[+ or -]0.18 0.557 1.93[+ or -]0.25 Musculocutaneous nerve (motor) 1.93[+ or -]0.25 0.643 1.9[+ or -]0.31 Radial nerve (sensory) 1.7[+ or -]0.53 0.012 (*) 1.96[+ or -]0.18 Radial nerve (motor) 1.63[+ or -]0.56 0.028 (*) 1.9[+ or -]0.31 Median nerve (sensory) 2[+ or -]0 0.317 1.96[+ or -]0.18 Median nerve (motor) 2[+ or -]0 0.317 1.96[+ or -]0.18 Ulnar nerve (sensory) 1.9[+ or -]0.31 0.643 1.93[+ or -]0.25 Ulnar nerve (motor) 1.87[+ or -]0.35 0.690 1.9[+ or -]0.31 (*) p<0.05 Table 3. Complete sensory and motor block Group 1 Group 2 n % n % p Complete sensory No 10 33.3 5 16.7 0.233 block Yes 20 66.7 25 83.3 Complete motor No 13 43.3 8 26.7 0.279 block Yes 17 56.7 22 73.3 Table 4. Additional need for sedation and satisfaction in groups Group 1 Group 2 n % n % p Additional No 21 70.0 22 73.3 0.77 sedation need Ye s 9 30.0 8 26.7 Satisfaction Not satisfied 0 0.0 1 3.3 0.053 Low satisfaction 1 3.3 4 13.3 Satisfied 24 80.0 23 76.7 Very satisfied 5 16.7 2 6.7 Table 5. Block application times, VAS values in groups, sensory and motor block times Group 1 Group 2 (n=30) (n=30) Application time (min) 6.27[+ or -]1.26 9.8[+ or -]1.32 VAS (0-10) 1.03[+ or -]0.72 1.5[+ or -]0.78 Sensory block onset time (min) 4.5[+ or -]1.5 3[+ or -]0 Total period of sensory block (min) 242.2[+ or -]29.5 249.6[+ or -]36.5 Motor block onset time (min) 4.6[+ or -]1.5 3[+ or -]0 Total period of motor block (min) 232.9[+ or -]26.3 235.8[+ or -]33.9 p Application time (min) 0.000 (*) VAS (0-10) 0.018 (*) Sensory block onset time (min) 0.000 (*) Total period of sensory block (min) 0.459 Motor block onset time (min) 0.000 (*) Total period of motor block (min) 0.941 (*) p<0.5
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|Title Annotation:||Original Article / Ozgun Arastirma|
|Author:||Ertikin, Aysun; Argun, Guldeniz; Misirlioglu, Mesut; Aydin, Murat; Arikan, Murat; Kadiogullari, Niha|
|Publication:||Turkish Journal of Anaesthesiology and Reanimation|
|Date:||Oct 1, 2017|
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