Pub Date : 2026-01-08eCollection Date: 2026-01-01DOI: 10.2147/LRA.S558076
Jiahe Liu, Tao Zhang, Zewen Wang, Ting He, Wanqi Xiong, Yan Cui, Zhenhao Li, Fan Yang, Baoyi Liu
Objective: To evaluate the efficacy of modified cocktail analgesia in relieving pain after minimally invasive chevron osteotomy for hallux valgus.
Methods: A retrospective cohort study was conducted to analyze the clinical data of 90 patients with moderate to severe hallux valgus admitted to our hospital from January 2020 to December 2023. Based on the treatment method and the number of affected limbs, the patients were divided into three groups: the modified group (Imp) treated with minimally invasive chevron and Akin (MICA) osteotomy combined with modified cocktail therapy, the traditional group (Tro) treated with MICA osteotomy combined with conventional cocktail therapy, and the control group (NC) treated with MICA osteotomy alone without cocktail therapy. The visual analog scale (VAS) scores for ankle-foot pain from 6 hours preoperatively to 14 days postoperatively, the need for postoperative rescue analgesia, adverse reactions, and complications were observed and compared among the three groups.
Results: There were no significant differences in basic conditions such as age and BMI among the three groups. It is in line with the epidemiological statistics of hallux valgus in terms of gender. The VAS scores at 6 hours and 1 day postoperatively were significantly lower in the modified group [(0.67±0.60), (0.68±0.59) respectively] compared to the traditional group [(0.82±0.50), (0.78±0.90) respectively] (P < 0.05). There were no statistically significant differences in VAS scores between groups at 6 hours preoperatively and 7 days and 14 days postoperatively (P > 0.05). Five patients (5.56%) in the modified group required postoperative rescue analgesia, which was significantly fewer than the 12 patients (13.33%) in the traditional group (P < 0.05).
Conclusion: Based on the comprehensive statistical results and clinical significance, the modified cocktail therapy has certain clinical reference value in the short-term analgesia management after MICA. It is beneficial for the early postoperative rehabilitation functional exercise of patients and has a good safety effect. It can be used as an optional option for early postoperative pain control. However, it is necessary to objectively recognize the timeliness of its therapeutic advantages. Its long-term analgesic effect shows no significant clinical difference from the traditional cocktail therapy and the simple MICA procedure.
目的:评价改良鸡尾酒镇痛对拇外翻微创截骨术后疼痛的疗效。方法:采用回顾性队列研究方法,对2020年1月至2023年12月我院收治的90例中重度拇外翻患者的临床资料进行分析。根据治疗方法及患肢数将患者分为改良组(Imp)微创chevron and Akin (MICA)截骨联合改良鸡尾酒疗法,传统组(Tro) MICA截骨联合常规鸡尾酒疗法,对照组(NC)单独MICA截骨不加鸡尾酒疗法。观察并比较三组患者术前6小时至术后14天踝足疼痛视觉模拟评分(VAS)、术后救急镇痛需求、不良反应及并发症。结果:三组患者年龄、BMI等基本情况无明显差异。在性别方面与拇外翻的流行病学统计一致。改良组术后6 h、1 d VAS评分[分别为(0.67±0.60)、(0.68±0.59)分]显著低于传统组[分别为(0.82±0.50)、(0.78±0.90)分](P < 0.05)。两组患者术前6 h、术后7 d、14 d VAS评分比较,差异均无统计学意义(P < 0.05)。改良组术后需抢救性镇痛5例(5.56%),明显少于传统组12例(13.33%),差异有统计学意义(P < 0.05)。结论:综合统计结果及临床意义,改良鸡尾酒疗法在MICA术后短期镇痛管理中具有一定的临床参考价值。有利于患者术后早期的康复功能锻炼,具有良好的安全效果。它可以作为术后早期疼痛控制的可选方案。但有必要客观认识其治疗优势的时效性。其长期镇痛效果与传统的鸡尾酒疗法和简单的MICA程序无显著临床差异。
{"title":"Therapeutic Efficacy of Modified Cocktail Analgesia After Minimally Invasive Chevron Osteotomy for Hallux Valgus: A Retrospective Case Series Study.","authors":"Jiahe Liu, Tao Zhang, Zewen Wang, Ting He, Wanqi Xiong, Yan Cui, Zhenhao Li, Fan Yang, Baoyi Liu","doi":"10.2147/LRA.S558076","DOIUrl":"10.2147/LRA.S558076","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the efficacy of modified cocktail analgesia in relieving pain after minimally invasive chevron osteotomy for hallux valgus.</p><p><strong>Methods: </strong>A retrospective cohort study was conducted to analyze the clinical data of 90 patients with moderate to severe hallux valgus admitted to our hospital from January 2020 to December 2023. Based on the treatment method and the number of affected limbs, the patients were divided into three groups: the modified group (Imp) treated with minimally invasive chevron and Akin (MICA) osteotomy combined with modified cocktail therapy, the traditional group (Tro) treated with MICA osteotomy combined with conventional cocktail therapy, and the control group (NC) treated with MICA osteotomy alone without cocktail therapy. The visual analog scale (VAS) scores for ankle-foot pain from 6 hours preoperatively to 14 days postoperatively, the need for postoperative rescue analgesia, adverse reactions, and complications were observed and compared among the three groups.</p><p><strong>Results: </strong>There were no significant differences in basic conditions such as age and BMI among the three groups. It is in line with the epidemiological statistics of hallux valgus in terms of gender. The VAS scores at 6 hours and 1 day postoperatively were significantly lower in the modified group [(0.67±0.60), (0.68±0.59) respectively] compared to the traditional group [(0.82±0.50), (0.78±0.90) respectively] (P < 0.05). There were no statistically significant differences in VAS scores between groups at 6 hours preoperatively and 7 days and 14 days postoperatively (P > 0.05). Five patients (5.56%) in the modified group required postoperative rescue analgesia, which was significantly fewer than the 12 patients (13.33%) in the traditional group (P < 0.05).</p><p><strong>Conclusion: </strong>Based on the comprehensive statistical results and clinical significance, the modified cocktail therapy has certain clinical reference value in the short-term analgesia management after MICA. It is beneficial for the early postoperative rehabilitation functional exercise of patients and has a good safety effect. It can be used as an optional option for early postoperative pain control. However, it is necessary to objectively recognize the timeliness of its therapeutic advantages. Its long-term analgesic effect shows no significant clinical difference from the traditional cocktail therapy and the simple MICA procedure.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"19 ","pages":"1-9"},"PeriodicalIF":1.9,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12794548/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-27eCollection Date: 2025-01-01DOI: 10.2147/LRA.S563087
Takeaki Aizawa, Nami Sugiura, Shinji Sugita
Purpose: Peripheral nerve block safety and pharmacology for patients with inherited antithrombin III (ATIII) deficiency remains unclear because of the rarity of the disease. Here, we report a case of unexpectedly prolonged motor and sensory inhibition following single-shot femoral and sciatic nerve blocks in a patient with inherited ATIII deficiency. We hypothesized that venous stasis, microcirculatory impairment, elevated peripheral venous pressure, and increased local tissue pressure might have contributed to prolonged nerve dysfunction and peripheral nerve injury.
Case report: The patient was a 58-year-old man (170 cm, 69 kg) with inherited ATIII deficiency. He was scheduled for 1-hour surgical debridement of recurrent venous stasis ulcers with microcirculatory impairment on his lower left leg. Nerve blocks resulted in motor and sensory deficits in the lower leg that lasted 2 and 8 days, respectively. The prolonged duration of this nerve block might have been related to his inherited ATIII deficiency. This condition can contribute to thrombosis of vessels such as the inferior vena cava, potentially leading to venous microcirculatory impairment in the lower limbs and complex coagulopathy.
Conclusion: While peripheral nerve blocks are widely used for their efficacy and safety, the risk-benefit profile of regional anesthesia may be atypical in patients with coagulation disorders. This case highlights the need for cautious nerve block administration in patients with inherited ATIII deficiency.
{"title":"Prolonged Neural Block After Lower-Limb Nerve Blocks in a Patient with Inherited Antithrombin III Deficiency: Implications for Regional Anesthesia.","authors":"Takeaki Aizawa, Nami Sugiura, Shinji Sugita","doi":"10.2147/LRA.S563087","DOIUrl":"10.2147/LRA.S563087","url":null,"abstract":"<p><strong>Purpose: </strong>Peripheral nerve block safety and pharmacology for patients with inherited antithrombin III (ATIII) deficiency remains unclear because of the rarity of the disease. Here, we report a case of unexpectedly prolonged motor and sensory inhibition following single-shot femoral and sciatic nerve blocks in a patient with inherited ATIII deficiency. We hypothesized that venous stasis, microcirculatory impairment, elevated peripheral venous pressure, and increased local tissue pressure might have contributed to prolonged nerve dysfunction and peripheral nerve injury.</p><p><strong>Case report: </strong>The patient was a 58-year-old man (170 cm, 69 kg) with inherited ATIII deficiency. He was scheduled for 1-hour surgical debridement of recurrent venous stasis ulcers with microcirculatory impairment on his lower left leg. Nerve blocks resulted in motor and sensory deficits in the lower leg that lasted 2 and 8 days, respectively. The prolonged duration of this nerve block might have been related to his inherited ATIII deficiency. This condition can contribute to thrombosis of vessels such as the inferior vena cava, potentially leading to venous microcirculatory impairment in the lower limbs and complex coagulopathy.</p><p><strong>Conclusion: </strong>While peripheral nerve blocks are widely used for their efficacy and safety, the risk-benefit profile of regional anesthesia may be atypical in patients with coagulation disorders. This case highlights the need for cautious nerve block administration in patients with inherited ATIII deficiency.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"151-156"},"PeriodicalIF":1.9,"publicationDate":"2025-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12755098/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145889290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-15eCollection Date: 2025-01-01DOI: 10.2147/LRA.S537907
Laura Girón-Arango, Kyle Robert Kirkham, Alexandra L Millman, Yonah Krakowsky, Yulia Wilk Goldsher, Olivia Drodge, Qixuan Li, Ella Huszti, Richard Brull
Background: Despite its association with severe postoperative pain, the use of regional anesthesia techniques for penile-inversion vaginoplasty surgery is understudied. This retrospective study aimed to assess the analgesic effects of a saddle block (ultra-low dose hyperbaric spinal anesthesia) with intrathecal (IT) morphine in transgender females undergoing penile inversion vaginoplasty.
Methods: We performed a single-centre, retrospective chart review of 72 patients who underwent penile-inversion vaginoplasty with or without saddle block with IT morphine at our institution over a 26-months period. All patients received standard multimodal intravenous analgesia, and the surgeon administered both a pudendal nerve block and a spermatic cord block as part of routine care. Our primary outcome was cumulative opioid consumption (oral morphine equivalent) at 24h postoperatively. Secondary outcomes included postoperative pain severity, duration of stay in the postoperative care unit and in-hospital, time to first opioid request and incidence of opioid- and block-related side effects.
Results: 30 patients received a saddle block with IT morphine and 42 patients received standard analgesia. We found no statistical difference in cumulative opioid consumption at 24h postoperatively (control group: 17.7 mg [5.6, 30.8] vs intervention group 12.5 mg [7.5, 22.5] P: 0.249). The addition of a saddle block was associated with clinically and statistically significant improvements in short-term postoperative pain-related outcomes in the recovery room, including mean and maximum pain severity scores, time to first analgesic request, and duration of stay. While no difference in pain scores was detected at the 24-hour time point, mixed-effects modelling demonstrated lower pain trajectories over time among patients in the intervention group, suggesting a time-dependent benefit. However, the significant time-by-group interaction (p = 0.024) indicates that the difference in pain scores between groups decreased over time. We found no differences in the rates of nausea and vomiting between groups. No saddle block procedure-related complications were reported.
Conclusion: This retrospective study suggests that despite no statistically significant difference in 24-hour opioid consumption, the addition of a saddle block with 100 mcg of IT morphine is associated with improved PACU pain scores, a longer time to first analgesic request, and a shorter PACU stay. These findings are hypothesis-generating and merit further investigation in a prospective double-blind randomized controlled trial.
{"title":"The Analgesic Effects of a Saddle Block with Intrathecal Morphine for Penile-Inversion Vaginoplasty: A Retrospective Study.","authors":"Laura Girón-Arango, Kyle Robert Kirkham, Alexandra L Millman, Yonah Krakowsky, Yulia Wilk Goldsher, Olivia Drodge, Qixuan Li, Ella Huszti, Richard Brull","doi":"10.2147/LRA.S537907","DOIUrl":"10.2147/LRA.S537907","url":null,"abstract":"<p><strong>Background: </strong>Despite its association with severe postoperative pain, the use of regional anesthesia techniques for penile-inversion vaginoplasty surgery is understudied. This retrospective study aimed to assess the analgesic effects of a saddle block (ultra-low dose hyperbaric spinal anesthesia) with intrathecal (IT) morphine in transgender females undergoing penile inversion vaginoplasty.</p><p><strong>Methods: </strong>We performed a single-centre, retrospective chart review of 72 patients who underwent penile-inversion vaginoplasty with or without saddle block with IT morphine at our institution over a 26-months period. All patients received standard multimodal intravenous analgesia, and the surgeon administered both a pudendal nerve block and a spermatic cord block as part of routine care. Our primary outcome was cumulative opioid consumption (oral morphine equivalent) at 24h postoperatively. Secondary outcomes included postoperative pain severity, duration of stay in the postoperative care unit and in-hospital, time to first opioid request and incidence of opioid- and block-related side effects.</p><p><strong>Results: </strong>30 patients received a saddle block with IT morphine and 42 patients received standard analgesia. We found no statistical difference in cumulative opioid consumption at 24h postoperatively (control group: 17.7 mg [5.6, 30.8] vs intervention group 12.5 mg [7.5, 22.5] P: 0.249). The addition of a saddle block was associated with clinically and statistically significant improvements in short-term postoperative pain-related outcomes in the recovery room, including mean and maximum pain severity scores, time to first analgesic request, and duration of stay. While no difference in pain scores was detected at the 24-hour time point, mixed-effects modelling demonstrated lower pain trajectories over time among patients in the intervention group, suggesting a time-dependent benefit. However, the significant time-by-group interaction (p = 0.024) indicates that the difference in pain scores between groups decreased over time. We found no differences in the rates of nausea and vomiting between groups. No saddle block procedure-related complications were reported.</p><p><strong>Conclusion: </strong>This retrospective study suggests that despite no statistically significant difference in 24-hour opioid consumption, the addition of a saddle block with 100 mcg of IT morphine is associated with improved PACU pain scores, a longer time to first analgesic request, and a shorter PACU stay. These findings are hypothesis-generating and merit further investigation in a prospective double-blind randomized controlled trial.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"143-150"},"PeriodicalIF":1.9,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12716076/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: External oblique intercostal (EOI) block has recently emerged as a promising analgesic method for the upper abdominal surgery. This study aimed to assess the effect of EOI block on postoperative analgesia and early recovery following open liver resection (OLR).
Patients and methods: In this prospective, randomized, controlled trial, 64 patients scheduled for OLR were randomly allocated into EOI group and control group. EOI group received 30 mL of 0.25% ropivacaine bilaterally 30 min before induction of general anesthesia, whereas control group did not receive any block. The primary outcomes were sufentanil consumption 24 h after surgery. The secondary outcomes mainly included: the visual analogue scale (VAS) pain scores at rest and on coughing at 2, 12, 24, 48 h postoperatively; number of analgesia pump compression 24 h postoperatively; quality of recovery-15 (QoR-15) scale score 48 h after surgery; Pittsburgh sleep quality index (PSQI) score the first night postoperatively; and plasma levels of norepinephrine (NE), cortisol (Cor), high mobility group box protein 1 (HMGB1), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) 1h before surgery and 6 h postoperatively.
Results: A total of 60 patients had completed the study (n = 30 per group). Sufentanil consumption 24 h postoperatively in EOI group was less than that in control group (mean difference: 4.45 μg, 95% CI, 1.6-7.2, P=0.003). The VAS scores at 2, 12, 24 h postoperatively; number of analgesia pump compression; and PSQI scores were significantly lower in EOI group than in control group. QoR-15 scale scores were higher in EOI group. The plasma levels of NE, Cor, HMGB1, TNF-α and IL-6 at 6 h postoperatively in EOI group were significantly lower than in control group.
Conclusion: EOI block given to patients undergoing OLR could provide effective postoperative analgesia, enhance the quality of postoperative recovery, and attenuate postoperative stress and inflammation.
{"title":"Effect of External Oblique Intercostal Block on Postoperative Analgesia and Early Recovery in Patients Undergoing Open Liver Resection for Hepatocellular Carcinoma or Intrahepatic Bile Duct Stones: A Randomized Controlled Clinical Trial.","authors":"Qilu Ying, Manhua Zhu, Song Zhang, Lingzhi Wang, Ruifen Zhou, Kaiyun Xie","doi":"10.2147/LRA.S557373","DOIUrl":"10.2147/LRA.S557373","url":null,"abstract":"<p><strong>Purpose: </strong>External oblique intercostal (EOI) block has recently emerged as a promising analgesic method for the upper abdominal surgery. This study aimed to assess the effect of EOI block on postoperative analgesia and early recovery following open liver resection (OLR).</p><p><strong>Patients and methods: </strong>In this prospective, randomized, controlled trial, 64 patients scheduled for OLR were randomly allocated into EOI group and control group. EOI group received 30 mL of 0.25% ropivacaine bilaterally 30 min before induction of general anesthesia, whereas control group did not receive any block. The primary outcomes were sufentanil consumption 24 h after surgery. The secondary outcomes mainly included: the visual analogue scale (VAS) pain scores at rest and on coughing at 2, 12, 24, 48 h postoperatively; number of analgesia pump compression 24 h postoperatively; quality of recovery-15 (QoR-15) scale score 48 h after surgery; Pittsburgh sleep quality index (PSQI) score the first night postoperatively; and plasma levels of norepinephrine (NE), cortisol (Cor), high mobility group box protein 1 (HMGB1), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) 1h before surgery and 6 h postoperatively.</p><p><strong>Results: </strong>A total of 60 patients had completed the study (n = 30 per group). Sufentanil consumption 24 h postoperatively in EOI group was less than that in control group (mean difference: 4.45 μg, 95% CI, 1.6-7.2, <i>P</i>=0.003). The VAS scores at 2, 12, 24 h postoperatively; number of analgesia pump compression; and PSQI scores were significantly lower in EOI group than in control group. QoR-15 scale scores were higher in EOI group. The plasma levels of NE, Cor, HMGB1, TNF-α and IL-6 at 6 h postoperatively in EOI group were significantly lower than in control group.</p><p><strong>Conclusion: </strong>EOI block given to patients undergoing OLR could provide effective postoperative analgesia, enhance the quality of postoperative recovery, and attenuate postoperative stress and inflammation.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"131-142"},"PeriodicalIF":1.9,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12684249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145714738","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-31eCollection Date: 2025-01-01DOI: 10.2147/LRA.S552555
Grant Heydinger, Josiane Kerbage, Catherine Roth, Sibelle Aurelie Yeleme Kitio, Giorgio Veneziano, Joseph D Tobias, V Rama Jayanthi
Introduction: Recently, concerns have been raised regarding the impact of anesthetic choice on outcomes for patients undergoing hypospadias repair. It has been suggested that caudal epidural anesthesia (CEA) may be associated with increased postoperative complications, such as urethrocutaneous fistula and glanular dehiscence. However, subsequent studies have found no association between CEA and increased complications. Spinal anesthesia (SA) is another technique that can provide surgical blockade during hypospadias repair. However, no studies have examined outcomes for pediatric patients undergoing hypospadias repair under awake SA.
Methods: We performed a single-center retrospective review on all patients who underwent single-stage primary hypospadias repair from 2016 until 2023. Data collected included patient demographics, anesthetic details, severity of hypospadias, duration of procedure, and postoperative complications.
Results: 805 patients underwent single-stage hypospadias repair during the study period. 117 (14.5%) had GA alone, 563 (70%) had GA with CEA, and 125 (15.5%) had SA. Duration of surgery was significantly longer for patients in the GA and CEA groups compared to the SA group, and more patients in the GA and CEA groups had a higher severity of hypospadias. We did not find significant differences in the odds ratio for postoperative complications between groups.
Discussion: In our retrospective analysis, we did not find a difference between anesthetic groups in the rate of postoperative complications. Patients who had SA were younger and had a shorter median surgical time. Because SA has a limited duration, patients with more complicated pathologies may not be offered SA as an option. SA is an underutilized technique for pediatric urologic procedures, but has several benefits over GA for infants and young children.
Conclusion: SA can be successfully utilized for hypospadias surgery in pediatric patients without an increase in postoperative complications. Future studies on this topic are warranted due to significant baseline differences between patient groups.
{"title":"Spinal Anesthesia and Postoperative Complications Following Pediatric Hypospadias Repair: A Retrospective Review.","authors":"Grant Heydinger, Josiane Kerbage, Catherine Roth, Sibelle Aurelie Yeleme Kitio, Giorgio Veneziano, Joseph D Tobias, V Rama Jayanthi","doi":"10.2147/LRA.S552555","DOIUrl":"10.2147/LRA.S552555","url":null,"abstract":"<p><strong>Introduction: </strong>Recently, concerns have been raised regarding the impact of anesthetic choice on outcomes for patients undergoing hypospadias repair. It has been suggested that caudal epidural anesthesia (CEA) may be associated with increased postoperative complications, such as urethrocutaneous fistula and glanular dehiscence. However, subsequent studies have found no association between CEA and increased complications. Spinal anesthesia (SA) is another technique that can provide surgical blockade during hypospadias repair. However, no studies have examined outcomes for pediatric patients undergoing hypospadias repair under awake SA.</p><p><strong>Methods: </strong>We performed a single-center retrospective review on all patients who underwent single-stage primary hypospadias repair from 2016 until 2023. Data collected included patient demographics, anesthetic details, severity of hypospadias, duration of procedure, and postoperative complications.</p><p><strong>Results: </strong>805 patients underwent single-stage hypospadias repair during the study period. 117 (14.5%) had GA alone, 563 (70%) had GA with CEA, and 125 (15.5%) had SA. Duration of surgery was significantly longer for patients in the GA and CEA groups compared to the SA group, and more patients in the GA and CEA groups had a higher severity of hypospadias. We did not find significant differences in the odds ratio for postoperative complications between groups.</p><p><strong>Discussion: </strong>In our retrospective analysis, we did not find a difference between anesthetic groups in the rate of postoperative complications. Patients who had SA were younger and had a shorter median surgical time. Because SA has a limited duration, patients with more complicated pathologies may not be offered SA as an option. SA is an underutilized technique for pediatric urologic procedures, but has several benefits over GA for infants and young children.</p><p><strong>Conclusion: </strong>SA can be successfully utilized for hypospadias surgery in pediatric patients without an increase in postoperative complications. Future studies on this topic are warranted due to significant baseline differences between patient groups.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"121-129"},"PeriodicalIF":1.9,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12584795/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145452230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-15eCollection Date: 2025-01-01DOI: 10.2147/LRA.S541354
Daniel Huettner, Yue Qiu, Bedda L Rosario, Steven Orebaugh
Purpose: This study examined whether chronic opioid use reduces the effectiveness of brachial plexus block in patients undergoing upper extremity surgery.
Patients and methods: Patients undergoing surgery with brachial plexus blocks were divided into two groups: opioid-dependent (daily opioid use for ≥1 month) and control (no opioid use for ≥3 months). Pain scores and opioid use were recorded over 72 hours postoperatively.
Results: Forty-six patients were included (23 opioid-dependent and 23 control). The median (IQR) NRS scores upon PACU arrival were 0 (0-0) in the control group and 0 (0-5) in the opioid group (p=0.0101). The duration of the nerve block was shorter in opioid-dependent patients (14 versus 22 hours; p=0.0035).
Conclusion: Chronic opioid users experienced shorter brachial plexus block duration and more postoperative pain after being discharged home.
{"title":"Prospective Evaluation of the Effectiveness of Brachial Plexus Nerve Block During the Perioperative Period in Long-Term Opioid Users Undergoing Upper Extremity Surgery - A Case Series.","authors":"Daniel Huettner, Yue Qiu, Bedda L Rosario, Steven Orebaugh","doi":"10.2147/LRA.S541354","DOIUrl":"10.2147/LRA.S541354","url":null,"abstract":"<p><strong>Purpose: </strong>This study examined whether chronic opioid use reduces the effectiveness of brachial plexus block in patients undergoing upper extremity surgery.</p><p><strong>Patients and methods: </strong>Patients undergoing surgery with brachial plexus blocks were divided into two groups: opioid-dependent (daily opioid use for ≥1 month) and control (no opioid use for ≥3 months). Pain scores and opioid use were recorded over 72 hours postoperatively.</p><p><strong>Results: </strong>Forty-six patients were included (23 opioid-dependent and 23 control). The median (IQR) NRS scores upon PACU arrival were 0 (0-0) in the control group and 0 (0-5) in the opioid group (p=0.0101). The duration of the nerve block was shorter in opioid-dependent patients (14 versus 22 hours; p=0.0035).</p><p><strong>Conclusion: </strong>Chronic opioid users experienced shorter brachial plexus block duration and more postoperative pain after being discharged home.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"111-119"},"PeriodicalIF":1.9,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12535725/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145337434","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-07eCollection Date: 2025-01-01DOI: 10.2147/LRA.S526163
Haolin Zhang, Liang Fang, Sheng Jing, Xiaohang Bao
Background: Both selective nerve root blocks and erector spinae plane blocks are common regional blocks in clinical practice, and they have both been shown to relieve acute and chronic pain from herpes zoster. Although selective nerve root block (SNRB) may be the theoretically most effective method of drug delivery to the DRG and requires only a small dose of drug with few complications associated with it, it does not provide effective analgesia for a prolonged period of time. However, continuous erector spinae plane block is considered to be one of the most promising minimally invasive means of analgesia that not only provides prolonged analgesia but is simple to perform, has fewer complications, and facilitates indwelling catheters. In this case report, we describe the possible synergistic mechanism of action of SNRB, continuous erector spinae plane block, and effective relief of postherpetic neuralgia with improved patient outcome.
Case presentation: In this case report, we present the case of an 81-year-old woman with comorbidities including diabetes mellitus, hypertension, and a history of multiple surgeries. She suffered from postherpetic herpes zoster pain in her left thoracic back. Despite trying various treatments such as antiviral medication, physical therapy, traditional Chinese medicine, and a single thoracic paraspinal nerve block, the pain persisted. In consultation with her anesthesiologist, the patient opted for a nerve root block combined with a continuous erector spinae plane block. The erector spinae plane catheter was removed after 14 consecutive days of infusion, although hemolytic Staphylococcus was found in the wound secretions sent for examination, antibiotic treatment was not required. At the 2-year follow-up, the patient remained free of pain recurrence.
Conclusion: Selective nerve root block combined with continuous erector spinae plane block relieves herpes zoster acute phase pain and herpes zoster neuralgia and improves patients' quality of life.
{"title":"Ultrasound-Guided Selective Thoracic Nerve Root Block Combined with Continuous Erector Spinae Plane Block for Postherpetic Neuralgia: A Case Report.","authors":"Haolin Zhang, Liang Fang, Sheng Jing, Xiaohang Bao","doi":"10.2147/LRA.S526163","DOIUrl":"10.2147/LRA.S526163","url":null,"abstract":"<p><strong>Background: </strong>Both selective nerve root blocks and erector spinae plane blocks are common regional blocks in clinical practice, and they have both been shown to relieve acute and chronic pain from herpes zoster. Although selective nerve root block (SNRB) may be the theoretically most effective method of drug delivery to the DRG and requires only a small dose of drug with few complications associated with it, it does not provide effective analgesia for a prolonged period of time. However, continuous erector spinae plane block is considered to be one of the most promising minimally invasive means of analgesia that not only provides prolonged analgesia but is simple to perform, has fewer complications, and facilitates indwelling catheters. In this case report, we describe the possible synergistic mechanism of action of SNRB, continuous erector spinae plane block, and effective relief of postherpetic neuralgia with improved patient outcome.</p><p><strong>Case presentation: </strong>In this case report, we present the case of an 81-year-old woman with comorbidities including diabetes mellitus, hypertension, and a history of multiple surgeries. She suffered from postherpetic herpes zoster pain in her left thoracic back. Despite trying various treatments such as antiviral medication, physical therapy, traditional Chinese medicine, and a single thoracic paraspinal nerve block, the pain persisted. In consultation with her anesthesiologist, the patient opted for a nerve root block combined with a continuous erector spinae plane block. The erector spinae plane catheter was removed after 14 consecutive days of infusion, although hemolytic Staphylococcus was found in the wound secretions sent for examination, antibiotic treatment was not required. At the 2-year follow-up, the patient remained free of pain recurrence.</p><p><strong>Conclusion: </strong>Selective nerve root block combined with continuous erector spinae plane block relieves herpes zoster acute phase pain and herpes zoster neuralgia and improves patients' quality of life.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"103-109"},"PeriodicalIF":1.9,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12514953/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145280677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-17eCollection Date: 2025-01-01DOI: 10.2147/LRA.S529154
Antonio Coviello, Giorgio Ranieri, Filomena Coppola, Rossella Damonte, Dario Cirillo, Andrea Uriel De Siena, Fabrizio Fattorini, Paolo Scimia, Gaetano Castellano, Federico Rucci, Giuseppe Servillo
Background and aim: Interscalene Brachial Plexus Block (ISBPB) is commonly used for shoulder surgery anesthesia to reduce opioid use and general anesthesia complications. However, it may cause diaphragmatic paresis due to phrenic nerve involvement. This study compares the incidence of hemidiaphragmatic paralysis and the frequency of side effects-including hemodynamic changes and postoperative complications-between the Extrafascial (ExF) and Intrafascial (InF) approaches for ISBPB using reduced anesthetic volume. The aim is to assess whether the ExF approach may be preferable in patients with reduced cardiopulmonary reserve (eg, COPD or heart failure).
Methods: A retrospective study was conducted at Federico II University in Naples, Italy, including 61 patients undergoing shoulder surgery from January 2024 to October 2024. About 33 patients received ExF while 28 received InF ISBPB, all with Ropivacaine 0.5% (10 mL), Mepivacaine 2% (5 mL), and Dexamethasone (4 mg). The primary outcome was the incidence of hemidiaphragmatic paralysis, evaluated via ultrasound pre and 30 minutes after the block by assessing diaphragm excursion, thickness, and thickening fraction. Secondary outcomes included intraoperative hemodynamic changes and postoperative complications: pain (NRS), analgesic/antiemetic requests, PONV, pruritus, shivering, anxiety, and discomfort.
Results: The TF significantly decreased after the block in both groups (p < 0.001), with no intergroup. Diaphragm paralysis occurred in 28 patients in each group (p = 0.093), without clinical respiratory effects. The InF group had more hypotension episodes (100% vs 30.3%, p = 0.002), and significantly lower mean and systolic blood pressure values at 1 and 2 hours after-block. No cases of anxiety, pruritus, shivering, or discomfort were observed. NRS was higher in the InF group at 6 hours but lower at 12 and 24 hours. Analgesic/antiemetic needs were similar; PONV was more frequent in the ExF.
Conclusion: Both approaches resulted in similar rates of hemidiaphragmatic paralysis. However, ExF was associated with fewer hemodynamic effects, suggesting potential benefit in high-risk cardiopulmonary patients.
背景与目的:斜角肌间臂丛阻滞(ISBPB)常用于肩部手术麻醉,以减少阿片类药物的使用和全身麻醉并发症。然而,由于膈神经受累,它可能引起膈神经麻痹。本研究比较了采用减少麻醉量的筋膜外(ExF)和筋膜内(InF)入路治疗ISBPB的半膈肌麻痹的发生率和副作用的频率,包括血流动力学改变和术后并发症。目的是评估ExF方法在心肺储备减少(如COPD或心力衰竭)的患者中是否更可取。方法:在意大利那不勒斯Federico II大学进行回顾性研究,包括61例于2024年1月至2024年10月接受肩部手术的患者。约33例患者接受ExF治疗,28例接受ifisbpb治疗,所有患者均使用0.5%罗哌卡因(10 mL)、2%美哌卡因(5 mL)和地塞米松(4 mg)。主要结局是半膈肌麻痹的发生率,在阻滞前和阻滞后30分钟通过超声评估膈肌偏移、厚度和增厚分数来评估。次要结局包括术中血流动力学改变和术后并发症:疼痛(NRS)、止痛/止吐要求、PONV、瘙痒、寒战、焦虑和不适。结果:两组阻断后TF均显著降低(p < 0.001),组间无差异。两组共发生膈肌麻痹28例(p = 0.093),无临床呼吸影响。干扰素组有更多的低血压发作(100% vs 30.3%, p = 0.002),阻滞后1和2小时的平均血压和收缩压值显著降低。没有观察到焦虑、瘙痒、颤抖或不适的病例。在6小时时,干扰素组的NRS较高,但在12和24小时时较低。镇痛/止吐需求相似;PONV在ExF中更为常见。结论:两种方法导致的半膈肌麻痹发生率相似。然而,ExF与较少的血流动力学影响相关,提示对高危心肺患者有潜在的益处。
{"title":"Retrospective Comparison of Extrafascial versus Intrafascial Interscalene Brachial Plexus Block with Reduced Volume: Impact on Hemidiaphragmatic Paralysis and Hemodynamic Effects in Shoulder Surgery Patients.","authors":"Antonio Coviello, Giorgio Ranieri, Filomena Coppola, Rossella Damonte, Dario Cirillo, Andrea Uriel De Siena, Fabrizio Fattorini, Paolo Scimia, Gaetano Castellano, Federico Rucci, Giuseppe Servillo","doi":"10.2147/LRA.S529154","DOIUrl":"10.2147/LRA.S529154","url":null,"abstract":"<p><strong>Background and aim: </strong>Interscalene Brachial Plexus Block (ISBPB) is commonly used for shoulder surgery anesthesia to reduce opioid use and general anesthesia complications. However, it may cause diaphragmatic paresis due to phrenic nerve involvement. This study compares the incidence of hemidiaphragmatic paralysis and the frequency of side effects-including hemodynamic changes and postoperative complications-between the Extrafascial (ExF) and Intrafascial (InF) approaches for ISBPB using reduced anesthetic volume. The aim is to assess whether the ExF approach may be preferable in patients with reduced cardiopulmonary reserve (eg, COPD or heart failure).</p><p><strong>Methods: </strong>A retrospective study was conducted at Federico II University in Naples, Italy, including 61 patients undergoing shoulder surgery from January 2024 to October 2024. About 33 patients received ExF while 28 received InF ISBPB, all with Ropivacaine 0.5% (10 mL), Mepivacaine 2% (5 mL), and Dexamethasone (4 mg). The primary outcome was the incidence of hemidiaphragmatic paralysis, evaluated via ultrasound pre and 30 minutes after the block by assessing diaphragm excursion, thickness, and thickening fraction. Secondary outcomes included intraoperative hemodynamic changes and postoperative complications: pain (NRS), analgesic/antiemetic requests, PONV, pruritus, shivering, anxiety, and discomfort.</p><p><strong>Results: </strong>The TF significantly decreased after the block in both groups (p < 0.001), with no intergroup. Diaphragm paralysis occurred in 28 patients in each group (p = 0.093), without clinical respiratory effects. The InF group had more hypotension episodes (100% vs 30.3%, p = 0.002), and significantly lower mean and systolic blood pressure values at 1 and 2 hours after-block. No cases of anxiety, pruritus, shivering, or discomfort were observed. NRS was higher in the InF group at 6 hours but lower at 12 and 24 hours. Analgesic/antiemetic needs were similar; PONV was more frequent in the ExF.</p><p><strong>Conclusion: </strong>Both approaches resulted in similar rates of hemidiaphragmatic paralysis. However, ExF was associated with fewer hemodynamic effects, suggesting potential benefit in high-risk cardiopulmonary patients.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"87-102"},"PeriodicalIF":1.9,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450379/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145125150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-27eCollection Date: 2025-01-01DOI: 10.2147/LRA.S538162
James Harvey Jones, Stuart Alan Grant
Background: The influence of nerve blocks on treatment bias, a form of implicit bias where patient characteristics lead to inequal treatment, remains unexplored.
Methods: This was a pilot study that utilized a survey to collect data from nurses at a single academic medical center. The following information was collected from the respondents: age (years); gender (male, female, other); nursing experience (years); specialization (surgery, medicine, emergency, perioperative, other); prior formal training on pain management in patients with or without nerve blocks; and how frequently they encounter patients with nerve blocks. Hypothetical clinical scenarios were presented to investigate pain medication dosing strategies that were rated with a 3-point Likert scale (more, equal, or less medication). Impacts of various patient conditions (alcohol abuse, anxiety, depression, marijuana use, nerve block, opioid abuse, and substance abuse) on pain medication and opioid dosing strategies were further investigated with a 5-point Likert scale (ranging from strongly disagree to strongly agree).
Results: Overall, the survey had a 32.59% response rate. Treatment bias towards patients with nerve blocks was evident in 21.43% (9/42) and 11/30 (36.67%) of respondents for pain medications and opioids, respectively.
Conclusion: This pilot study suggests that patients with nerve blocks may be treated differently than those without blocks, regardless of their reported pain. However, given the study's exploratory design, these findings should be interpreted as hypothesis-generating.
{"title":"Perspectives on Analgesia in Patients with Nerve Blocks: A Pilot Survey of Perioperative Nurses.","authors":"James Harvey Jones, Stuart Alan Grant","doi":"10.2147/LRA.S538162","DOIUrl":"10.2147/LRA.S538162","url":null,"abstract":"<p><strong>Background: </strong>The influence of nerve blocks on treatment bias, a form of implicit bias where patient characteristics lead to inequal treatment, remains unexplored.</p><p><strong>Methods: </strong>This was a pilot study that utilized a survey to collect data from nurses at a single academic medical center. The following information was collected from the respondents: age (years); gender (male, female, other); nursing experience (years); specialization (surgery, medicine, emergency, perioperative, other); prior formal training on pain management in patients with or without nerve blocks; and how frequently they encounter patients with nerve blocks. Hypothetical clinical scenarios were presented to investigate pain medication dosing strategies that were rated with a 3-point Likert scale (more, equal, or less medication). Impacts of various patient conditions (alcohol abuse, anxiety, depression, marijuana use, nerve block, opioid abuse, and substance abuse) on pain medication and opioid dosing strategies were further investigated with a 5-point Likert scale (ranging from strongly disagree to strongly agree).</p><p><strong>Results: </strong>Overall, the survey had a 32.59% response rate. Treatment bias towards patients with nerve blocks was evident in 21.43% (9/42) and 11/30 (36.67%) of respondents for pain medications and opioids, respectively.</p><p><strong>Conclusion: </strong>This pilot study suggests that patients with nerve blocks may be treated differently than those without blocks, regardless of their reported pain. However, given the study's exploratory design, these findings should be interpreted as hypothesis-generating.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"77-86"},"PeriodicalIF":1.9,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12399090/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144959658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-19eCollection Date: 2025-01-01DOI: 10.2147/LRA.S527808
Christian Dumps, Stefanie Nothofer, Manfred Weiss, Wolfgang Hoelz, Rainer J Litz, Robert Bocher, Felicitas Kies, Richard Funk, Axel Rüdiger Heller, Philipp Simon
Purpose: Substantial understanding of anatomic landmarks remains mandatory for regional anesthesia procedures of the lower limbs, even in times of ultrasound-guided techniques. Theoretically, applying a diagonal vector (DIVE) from the posterior superior iliac spine towards the spinous process of lumbar vertebra 3 leads to a higher error tolerance and closer nerve approximation when compared to Chayen's approach. The purpose of this study was to compare both techniques regarding clinical applicability, accuracy and risk profile.
Patients and methods: Lumbar plexus block was performed bilaterally according to Chayen's technique and the DIVE method in embalmed bodies donated to science. The posterior medial half of the psoas major muscle was predefined as the puncture target area. Essential anatomical landmarks were labelled, photographed and a computer-aided analysis of the images was conducted. Both approaches were compared regarding the puncture success rate, spatial nerve approximation and complications such as vessel or kidney punctures.
Results: Both techniques were applied bilaterally on 34 embalmed bodies (50% male, mean age ± standard deviation 82 ± 8 years, height 167 ± 10cm) and led to similar success rates of a psoas muscle hit (Chayen vs DIVE 86.3% vs 82.8%). DIVE punctures were more often localized in the medial third of the psoas (p<0.001), whereas the risk for vessel or kidney punctures was similar (p=0.473; p=0.367, respectively).
Conclusion: Punctures according to the DIVE method resulted in a higher puncture accuracy compared to Chayen's technique with comparable practicability and risk profile. When using the DIVE Block, a window for a successful puncture can be expected between a quarter and a third of the PSIS- L3SP distance.
目的:对解剖标志的充分了解仍然是下肢区域麻醉手术的必要条件,即使在超声引导技术的时代。从理论上讲,与Chayen入路相比,从髂后上棘向腰椎棘突3应用斜向矢量(DIVE)可获得更高的容错性和更接近的神经近似。本研究的目的是比较两种技术在临床适用性、准确性和风险方面的差异。患者和方法:采用Chayen技术和DIVE方法对捐赠给科学研究的防腐尸体进行双侧腰丛神经阻滞。腰大肌后内侧半部预先确定为穿刺靶区。必要的解剖标志被标记,拍摄和计算机辅助分析的图像进行。比较两种入路的穿刺成功率、空间神经逼近及血管或肾脏穿刺等并发症。结果:两种技术分别应用于34具防腐尸体(50%为男性,平均年龄±标准差82±8岁,身高167±10cm),腰肌撞击成功率相似(Chayen vs DIVE分别为86.3% vs 82.8%)。DIVE穿刺更常定位于腰肌内侧三分之一(结论:与Chayen技术相比,DIVE穿刺方法具有更高的穿刺准确性,具有相当的实用性和风险。当使用DIVE Block时,预期成功穿刺的窗口在PSIS- L3SP距离的四分之一到三分之一之间。
{"title":"The Diagonal Vector (DIVE) Approach for Lumbar Plexus Block - A Comparison with Chayen's Technique.","authors":"Christian Dumps, Stefanie Nothofer, Manfred Weiss, Wolfgang Hoelz, Rainer J Litz, Robert Bocher, Felicitas Kies, Richard Funk, Axel Rüdiger Heller, Philipp Simon","doi":"10.2147/LRA.S527808","DOIUrl":"10.2147/LRA.S527808","url":null,"abstract":"<p><strong>Purpose: </strong>Substantial understanding of anatomic landmarks remains mandatory for regional anesthesia procedures of the lower limbs, even in times of ultrasound-guided techniques. Theoretically, applying a diagonal vector (DIVE) from the posterior superior iliac spine towards the spinous process of lumbar vertebra 3 leads to a higher error tolerance and closer nerve approximation when compared to Chayen's approach. The purpose of this study was to compare both techniques regarding clinical applicability, accuracy and risk profile.</p><p><strong>Patients and methods: </strong>Lumbar plexus block was performed bilaterally according to Chayen's technique and the DIVE method in embalmed bodies donated to science. The posterior medial half of the psoas major muscle was predefined as the puncture target area. Essential anatomical landmarks were labelled, photographed and a computer-aided analysis of the images was conducted. Both approaches were compared regarding the puncture success rate, spatial nerve approximation and complications such as vessel or kidney punctures.</p><p><strong>Results: </strong>Both techniques were applied bilaterally on 34 embalmed bodies (50% male, mean age ± standard deviation 82 ± 8 years, height 167 ± 10cm) and led to similar success rates of a psoas muscle hit (Chayen vs DIVE 86.3% vs 82.8%). DIVE punctures were more often localized in the medial third of the psoas (p<0.001), whereas the risk for vessel or kidney punctures was similar (p=0.473; p=0.367, respectively).</p><p><strong>Conclusion: </strong>Punctures according to the DIVE method resulted in a higher puncture accuracy compared to Chayen's technique with comparable practicability and risk profile. When using the DIVE Block, a window for a successful puncture can be expected between a quarter and a third of the PSIS- L3SP distance.</p>","PeriodicalId":18203,"journal":{"name":"Local and Regional Anesthesia","volume":"18 ","pages":"67-76"},"PeriodicalIF":1.9,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375508/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144959620","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}