Comparison of lidocaine-dexmedetomidine and lidocaine-saline on the characteristics of the modified forearm bier block: A clinical trial

Background and Aims: Forearm Modified Bier Block (FMBB) reduces local anesthetic systemic toxicity risks compared to the traditional method. This study was designed and implemented to compare the effects of lidocaine-dexmedetomidine (LD) and lidocaine-saline (LS) on the characteristics of the MFBB i...

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Main Authors: Kamal Ghaderi (Author), Khaled Rahmani (Author), Nasser Rahmanpanah (Author), Shoaleh Shami (Author), Farhad Zahedi (Author), Karim Nasseri (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2021-01-01T00:00:00Z.
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001 doaj_8ff03f5aeee34efb86c2aea7743ce3a2
042 |a dc 
100 1 0 |a Kamal Ghaderi  |e author 
700 1 0 |a Khaled Rahmani  |e author 
700 1 0 |a Nasser Rahmanpanah  |e author 
700 1 0 |a Shoaleh Shami  |e author 
700 1 0 |a Farhad Zahedi  |e author 
700 1 0 |a Karim Nasseri  |e author 
245 0 0 |a Comparison of lidocaine-dexmedetomidine and lidocaine-saline on the characteristics of the modified forearm bier block: A clinical trial 
260 |b Wolters Kluwer Medknow Publications,   |c 2021-01-01T00:00:00Z. 
500 |a 0970-9185 
500 |a 10.4103/joacp.JOACP_54_20 
520 |a Background and Aims: Forearm Modified Bier Block (FMBB) reduces local anesthetic systemic toxicity risks compared to the traditional method. This study was designed and implemented to compare the effects of lidocaine-dexmedetomidine (LD) and lidocaine-saline (LS) on the characteristics of the MFBB in distal forearm and hand surgery. Material and Methods: In this randomized double-blind trial, which was conducted after obtaining institutional ethical committee approval, 60 patients were enrolled and randomly divided into two groups. In both groups, the analgesic base of the block was 20 mL lidocaine 0.5% that was supplemented by 1 μg/kg dexmedetomidine in the LD group or 1 mL of 0.9% saline in the LS group. Patients were evaluated for the onset and duration of sensory block, time of the first request for postoperative analgesic, and analgesic request frequency during the first 24 h after surgery. Results: Sensory block onset in the LD group (7.1 ± 1.4 min) compared to the LS group (8.4 ± 1.4) was faster (P = 0.008). Duration of the sensory block in LD group (49.7 ± 7.2 min) was longer than LS group (33.3 ± 2.6) (P < 0.001). Compared to LS group, time of the first request for postoperative analgesic in LD group was later (P = 0.6), and had lesser analgesic requests during the first 24 h after surgery (P < 0.001). Conclusion: Based on our study's finding, adding dexmedetomidine to lidocaine in the MFBB increases the duration of sensory block. 
546 |a EN 
690 |a analgesics 
690 |a anesthesia 
690 |a dexmedetomidine 
690 |a nerve block 
690 |a pain 
690 |a Anesthesiology 
690 |a RD78.3-87.3 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Journal of Anaesthesiology Clinical Pharmacology, Vol 37, Iss 4, Pp 610-615 (2021) 
787 0 |n http://www.joacp.org/article.asp?issn=0970-9185;year=2021;volume=37;issue=4;spage=610;epage=615;aulast=Ghaderi 
787 0 |n https://doaj.org/toc/0970-9185 
856 4 1 |u https://doaj.org/article/8ff03f5aeee34efb86c2aea7743ce3a2  |z Connect to this object online.