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Correction: Pathophysiology and etiology of nerve injury following peripheral nerve blockade 更正:外周神经阻滞术后神经损伤的病理生理学和病因学
Pub Date : 2024-05-01 DOI: 10.1136/aap.0000000000000125corr1
BMJ Publishing Group Ltd
Brull R, Hadzic A, Reina MA, et al. Pathophysiology and Etiology of Nerve Injury Following Peripheral Nerve Blockade. Reg Anesth Pain Med 2015;40:479-490. Under the discussion section, in the anatomical considerations paragraph the article reads: A nerve can be considered a distinct organ composed
Brull R、Hadzic A、Reina MA 等:《外周神经阻滞术后神经损伤的病理生理学和病因学》。Reg Anesth Pain Med 2015;40:479-490。在讨论部分的解剖学考虑段落中,文章写道:神经可被视为一个独特的器官,由
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引用次数: 0
Regional versus general anesthesia for total hip and knee arthroplasty: a nationwide retrospective cohort study 全髋关节和膝关节置换术的区域麻醉与全身麻醉:一项全国性回顾性队列研究
Pub Date : 2024-04-30 DOI: 10.1136/rapm-2024-105440
Tak Kyu Oh, In-Ae Song
Introduction We aimed to determine whether regional anesthesia (RA) has any advantages over general anesthesia (GA) in total joint arthroplasty (TJA) in terms of mortality and postoperative complications. Methods This population-based retrospective cohort study included data of adults who underwent total knee or hip arthroplasty under RA or GA between 2016 and 2021 from the National Health Insurance Service of South Korea. RA included spinal or epidural anesthesia or a combination of both. Endpoints were 30-day mortality, 90-day mortality, and postoperative complications. Propensity score (PS) matching was used for statistical analysis. Results We included 517 960 patients (RA, n=380 698; GA, n=137 262) who underwent TJA. After PS matching, 186 590 patients (93 295 in each group) were included in the final analysis. In the logistic regression analyses using the PS-matched cohort, the RA group compared with the GA group showed 31% (OR: 0.69; 95% CI, 0.60 to 0.80; p<0.001) and 22% (OR: 0.78; 95% CI, 0.72 to 0.85; p<0.001) lower 30-day and 90-day mortality rates, respectively. However, the total postoperative complication rate did not differ significantly between the two groups (p=0.105). Conclusion RA compared with GA was associated with improved 30-day and 90-day survival outcomes in patients who underwent TJA. However, the postoperative complication rate did not differ significantly. Therefore, our results should be interpreted with caution, and more well-designed future studies are needed to clarify the most appropriate type of anesthesia for TJA. Data are available upon reasonable request.
导言 我们旨在确定在全关节置换术(TJA)中,就死亡率和术后并发症而言,区域麻醉(RA)是否比全身麻醉(GA)更具优势。方法 这项基于人群的回顾性队列研究纳入了韩国国民健康保险服务局提供的 2016 年至 2021 年期间在 RA 或 GA 下接受全膝关节或全髋关节置换术的成人数据。RA包括脊髓或硬膜外麻醉,或两者的组合。终点为30天死亡率、90天死亡率和术后并发症。统计分析采用倾向评分(PS)匹配法。结果 我们纳入了 517 960 名接受 TJA 的患者(RA,n=380 698;GA,n=137 262)。经过 PS 匹配后,186 590 名患者(每组 93 295 人)被纳入最终分析。在使用 PS 匹配队列进行的逻辑回归分析中,RA 组与 GA 组相比,30 天和 90 天死亡率分别降低了 31% (OR: 0.69; 95% CI, 0.60 to 0.80; p<0.001)和 22% (OR: 0.78; 95% CI, 0.72 to 0.85; p<0.001)。然而,两组的术后总并发症发生率并无显著差异(P=0.105)。结论 与 GA 相比,RA 可改善 TJA 患者的 30 天和 90 天生存率。然而,术后并发症发生率并无明显差异。因此,在解释我们的结果时应谨慎,今后还需要更多精心设计的研究来明确 TJA 最合适的麻醉类型。如有合理要求,可提供相关数据。
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引用次数: 0
Postsurgical opioid prescribing among veterans using community care for orthopedic surgery at non-VA hospitals compared to a VA hospital with a transitional pain service: a retrospective cohort study 在非退伍军人医院接受骨科手术的退伍军人在手术后使用阿片类药物的情况与在退伍军人医院接受过渡性疼痛服务的退伍军人相比:一项回顾性队列研究
Pub Date : 2024-04-27 DOI: 10.1136/rapm-2023-105162
Michael Jacob Buys, Zachary Anderson, Kimberlee Bayless, Chong Zhang, Angela P Presson, Julie Hales, Benjamin Sands Brooke
Background The USA provides medical services to its military veterans through Veterans Health Administration (VHA) medical centers. Passage of recent legislation has increased the number of veterans having VHA-paid orthopedic surgery at non-VHA facilities. Methods We conducted a retrospective cohort study among veterans who underwent orthopedic joint surgery paid for by the VHA either at the Salt Lake City VHA Medical Center (VAMC) or at non-VHA hospitals between January 2018 and December 2021. 562 patients were included in the study, of which 323 used a non-VHA hospital and 239 patients the VAMC. The number of opioid tablets prescribed at discharge, the total number prescribed by postdischarge day 90, and the number of patients still filling opioid prescriptions between 90 and 120 days after surgery were compared between groups. Results Veterans who underwent orthopedic surgery at a non-VHA hospital were prescribed more opioid tablets at discharge (median (IQR)); (40 (30–60) non-VHA vs 30 (20–47.5) VAMC, p<0.001) and in the first 90 days after surgery than patients who had surgery at the Salt Lake City VAMC (60 (40–120) vs 35 (20–60), p<0.001). Patients who had surgery at Salt Lake City VAMC were also significantly less likely to fill opioid prescriptions past 90 days after hospital discharge (OR (95% CI) 0.06 (0.01 to 0.48), p=0.007). Conclusion These results suggest that veterans who have surgery at a veterans affairs hospital with a transitional pain service are at lower risk for larger opioid prescriptions both at discharge and within 90 days after surgery as well as persistent opioid use beyond 90 days after discharge than if they have surgery at a community hospital. Data are available upon reasonable request.
背景 美国通过退伍军人健康管理局(VHA)医疗中心为退伍军人提供医疗服务。最近通过的立法增加了在非退伍军人健康管理局设施接受由退伍军人健康管理局付费的骨科手术的退伍军人人数。方法 我们对 2018 年 1 月至 2021 年 12 月期间在盐湖城退伍军人健康管理局医疗中心(VAMC)或非退伍军人健康管理局医院接受由退伍军人健康管理局付费的骨科关节手术的退伍军人进行了一项回顾性队列研究。研究共纳入了 562 名患者,其中 323 名患者在非 VHA 医院就诊,239 名患者在 VAMC 就诊。研究人员比较了不同组别患者出院时开具的阿片类药物处方数量、出院后第 90 天开具的处方总数以及术后 90 天至 120 天内仍在开具阿片类药物处方的患者人数。结果 与在盐湖城退伍军人医疗中心接受手术的患者(60 (40-120) vs 35 (20-60),p<0.001)相比,在非退伍军人医疗中心医院接受骨科手术的退伍军人在出院时(中位数(IQR))和术后前 90 天内开出的阿片类药物处方更多。在盐湖城退伍军人医疗中心接受手术的患者在出院后 90 天内服用阿片类药物处方的可能性也明显较低(OR (95% CI) 0.06 (0.01 to 0.48),P=0.007)。结论 这些结果表明,与在社区医院接受手术的退伍军人相比,在设有过渡性疼痛服务的退伍军人事务医院接受手术的退伍军人在出院时和术后 90 天内服用大量阿片类药物处方以及出院后 90 天后持续服用阿片类药物的风险较低。如有合理要求,可提供相关数据。
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引用次数: 0
Anesthesia start time documentation accuracy where peripheral nerve block is the primary anesthetic 以周围神经阻滞为主要麻醉方式时,麻醉开始时间记录的准确性
Pub Date : 2024-04-19 DOI: 10.1136/rapm-2024-105292
Alexander B Stone, Andrés Zorrilla Vaca, Philipp Lirk, Philipp Gerner, Kamen Vlassakov
Introduction When used as the primary anesthetic, nerve blocks are not billed as separate procedures. In this scenario, the anesthesia start (A Start ) time should include the block procedural time. We measured how often A Start time was documented before the nerve block was placed in the preoperative area, and compared cases where a block team performed the nerve block and cases where the intraoperative anesthesia attending supervised the nerve block. We hypothesized that the involvement of a regional anesthesia team would lead to more accurate documentation of A Start . We also estimated the lost revenue due to inaccurate start time documentation. Methods The study population were patients undergoing surgery with a peripheral nerve block as the primary anesthetic. For this analysis, A Start occurring less than 10 min before the in-operating room time was defined as potentially inaccurate. Lost potential revenue was estimated by taking the difference between the documented time of local anesthetic administration and the documented A Start time. Results A total of 745 cases were analyzed. Overall, 439 cases (58%) cases were identified as having potentially inaccurate start times. There were higher rates of inaccurate A Start documentation by the block team (316/482, 65.5%) compared with blocks supervised by the in-room anesthesia attendings (123/263, 46.7%, p<0.001). Overall, the estimated loss in billable revenue during the study period was a total of $70 265. Conclusions The performance of primary regional anesthesia procedure by a block team increased the incidence of inaccurate documentation and uncaptured potential revenue. There is need for education about accurate nerve block documentation for anesthesiologists, especially when separate teams are used. No data are available.
导言:神经阻滞作为主要麻醉手段使用时,不作为单独程序计费。在这种情况下,麻醉开始(A Start)时间应包括阻滞程序时间。我们测量了在术前区域进行神经阻滞前记录 "A 开始 "时间的频率,并比较了由阻滞小组实施神经阻滞的病例和由术中麻醉主治医师监督神经阻滞的病例。我们假设,区域麻醉团队的参与将使 "开始时间 "的记录更加准确。我们还估算了因起始时间记录不准确而造成的收入损失。方法 研究对象是以周围神经阻滞作为主要麻醉方式的手术患者。在本次分析中,在手术室时间之前 10 分钟内发生的 "开始 "时间被定义为可能不准确。潜在收入损失根据记录的局麻药给药时间与记录的 A 开始时间之间的差值进行估算。结果 共分析了 745 个病例。总体而言,有 439 个病例(58%)的开始时间可能不准确。与室内麻醉主治医师监督的阻滞相比,阻滞小组记录的 A 开始时间不准确的比例更高(316/482,65.5%)(123/263,46.7%,p<0.001)。总体而言,在研究期间,估计共损失了 70 265 美元的计费收入。结论 由阻滞小组实施初级区域麻醉手术增加了不准确记录的发生率和未捕获的潜在收入。有必要对麻醉医生进行有关神经阻滞准确记录的教育,尤其是在使用独立团队的情况下。暂无数据。
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引用次数: 0
Multisite prospective study of perioperative pain management practices for anterior cruciate ligament reconstruction in adolescents: Society for Pediatric Anesthesia Improvement Network (SPAIN) Project Report 青少年前十字韧带重建术围手术期疼痛管理实践的多点前瞻性研究:儿科麻醉改进网络学会(SPAIN)项目报告
Pub Date : 2024-04-18 DOI: 10.1136/rapm-2024-105381
Kesavan Sadacharam, James S Furstein, Steven J Staffa, Galaxy Li, Rami Karroum, Jocelyn M Booth, Eugene Kim, Suzanne M McCahan, Wallis T Muhly, Vidya Chidambaran
Introduction Although 200 000 adolescents undergo anterior cruciate ligament reconstruction (ACLR) surgery annually, no benchmarks for pediatric post-ACLR pain management exist. We created a multicenter, prospective, observational registry to describe pain practices, pain, and functional recovery after pediatric ACLR. Methods Participants (n=519; 12–17.5 years) were enrolled from 15 sites over 2 years. Data on perioperative management and surgical factors were collected. Pain/opioid use and Lysholm scores were assessed preoperatively, on postoperative day 1 (POD1), POD3, week 6, and month 6. Descriptive statistics and trends for opioid use, pain, and function are presented. Results Regional analgesia was performed in 447/519 (86%) subjects; of these, adductor canal single shot was most frequent (54%), nerve catheters placed in 24%, and perineural adjuvants used in 43%. On POD1, POD3, week 6, and month 6, survey response rates were 73%, 71%, 61%, and 45%, respectively. Over these respective time points, pain score >3/10 was reported by 64% (95% CI: 59% to 69%), 46% (95% CI: 41% to 52%), 5% (95% CI: 3% to 8%), and 3% (95% CI: 1% to 6%); the number of daily oxycodone doses used was 2.8 (SD 0.19), 1.8 (SD 0.13), 0, and 0. There was considerable variability in timing and tests for postdischarge functional assessments. Numbness and weakness were reported by 11% and 4% at week 6 (n=315) and 16% and 2% at month 6 (n=233), respectively. Conclusion We found substantial variability in the use of blocks to manage post-ACLR pain in children, with a small percentage experiencing long-term pain and neurological symptoms. Studies are needed to determine best practices for regional anesthesia and functional assessments in this patient population. Data are available upon reasonable request.
引言 尽管每年有 20 万青少年接受前交叉韧带重建(ACLR)手术,但目前还没有儿科 ACLR 术后疼痛管理的基准。我们建立了一个多中心、前瞻性、观察性登记处,以描述小儿前交叉韧带重建术后的疼痛治疗方法、疼痛和功能恢复情况。方法 在 2 年时间里,15 个医疗机构招募了参与者(n=519;12-17.5 岁)。收集了围手术期管理和手术因素的数据。对术前、术后第 1 天 (POD1)、POD3、第 6 周和第 6 个月的疼痛/阿片类药物使用情况和 Lysholm 评分进行了评估。报告列出了阿片类药物使用、疼痛和功能的描述性统计数字和趋势。结果 447/519 例受试者(86%)进行了区域镇痛;其中,内收肌管单次注射最为常见(54%),24% 的受试者放置了神经导管,43% 的受试者使用了硬膜外佐剂。在 POD1、POD3、第 6 周和第 6 个月,调查回复率分别为 73%、71%、61% 和 45%。在这些时间点上,疼痛评分大于 3/10 的比例分别为 64%(95% CI:59% 至 69%)、46%(95% CI:41% 至 52%)、5%(95% CI:3% 至 8%)和 3%(95% CI:1% 至 6%);每天使用的羟考酮剂量分别为 2.8(标清 0.19)、1.8(标清 0.13)、0 和 0。在第 6 周(人数=315)和第 6 个月(人数=233)分别有 11% 和 4% 和 16% 的患者报告麻木和无力。结论 我们发现,在使用阻滞治疗来控制儿童 ACLR 术后疼痛方面存在很大差异,一小部分患儿会出现长期疼痛和神经症状。需要进行研究以确定区域麻醉和功能评估在这一患者群体中的最佳实践。如有合理要求,可提供相关数据。
{"title":"Multisite prospective study of perioperative pain management practices for anterior cruciate ligament reconstruction in adolescents: Society for Pediatric Anesthesia Improvement Network (SPAIN) Project Report","authors":"Kesavan Sadacharam, James S Furstein, Steven J Staffa, Galaxy Li, Rami Karroum, Jocelyn M Booth, Eugene Kim, Suzanne M McCahan, Wallis T Muhly, Vidya Chidambaran","doi":"10.1136/rapm-2024-105381","DOIUrl":"https://doi.org/10.1136/rapm-2024-105381","url":null,"abstract":"Introduction Although 200 000 adolescents undergo anterior cruciate ligament reconstruction (ACLR) surgery annually, no benchmarks for pediatric post-ACLR pain management exist. We created a multicenter, prospective, observational registry to describe pain practices, pain, and functional recovery after pediatric ACLR. Methods Participants (n=519; 12–17.5 years) were enrolled from 15 sites over 2 years. Data on perioperative management and surgical factors were collected. Pain/opioid use and Lysholm scores were assessed preoperatively, on postoperative day 1 (POD1), POD3, week 6, and month 6. Descriptive statistics and trends for opioid use, pain, and function are presented. Results Regional analgesia was performed in 447/519 (86%) subjects; of these, adductor canal single shot was most frequent (54%), nerve catheters placed in 24%, and perineural adjuvants used in 43%. On POD1, POD3, week 6, and month 6, survey response rates were 73%, 71%, 61%, and 45%, respectively. Over these respective time points, pain score >3/10 was reported by 64% (95% CI: 59% to 69%), 46% (95% CI: 41% to 52%), 5% (95% CI: 3% to 8%), and 3% (95% CI: 1% to 6%); the number of daily oxycodone doses used was 2.8 (SD 0.19), 1.8 (SD 0.13), 0, and 0. There was considerable variability in timing and tests for postdischarge functional assessments. Numbness and weakness were reported by 11% and 4% at week 6 (n=315) and 16% and 2% at month 6 (n=233), respectively. Conclusion We found substantial variability in the use of blocks to manage post-ACLR pain in children, with a small percentage experiencing long-term pain and neurological symptoms. Studies are needed to determine best practices for regional anesthesia and functional assessments in this patient population. Data are available upon reasonable request.","PeriodicalId":21046,"journal":{"name":"Regional Anesthesia & Pain Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140629797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Orally administered ketamine and postoperative opioid use in colorectal surgery: a retrospective cohort study 口服氯胺酮与结直肠手术术后阿片类药物的使用:一项回顾性队列研究
Pub Date : 2024-04-16 DOI: 10.1136/rapm-2023-105218
Aria Lucchesi, Eric S Schwenk, Eric R Silverman
Ketamine infusions for acute pain management have received substantial interest in recent years.[1][1] While studies have been encouraging, safety concerns have prompted some state professional licensing boards to issue memorandums, limiting patient access.[2][2] Despite poor bioavailability,[3][3
近年来,氯胺酮输注用于急性疼痛治疗受到了广泛关注。[1][1] 虽然研究结果令人鼓舞,但对安全性的担忧已促使一些州的专业执照委员会发布备忘录,限制患者使用氯胺酮。
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引用次数: 0
Age and pain: are pain management clinicians keeping up with the increasing Medicare population? 年龄与疼痛:疼痛管理临床医生是否跟上了医疗保险人口增长的步伐?
Pub Date : 2024-04-10 DOI: 10.1136/rapm-2023-104556
Aditya Khurana, Layth Mahdi, Christopher Wie, Natalie H Strand
There is an increasing need for pain management clinicians in the USA in the midst of the opioid epidemic and aging population.[1][1] The population of adults older than 65 years is estimated to make up 20% of the US population by 2030.[2][2] Some estimates indicate that the prevalence of chronic
在阿片类药物流行和人口老龄化的背景下,美国对疼痛管理临床医生的需求日益增长。
{"title":"Age and pain: are pain management clinicians keeping up with the increasing Medicare population?","authors":"Aditya Khurana, Layth Mahdi, Christopher Wie, Natalie H Strand","doi":"10.1136/rapm-2023-104556","DOIUrl":"https://doi.org/10.1136/rapm-2023-104556","url":null,"abstract":"There is an increasing need for pain management clinicians in the USA in the midst of the opioid epidemic and aging population.[1][1] The population of adults older than 65 years is estimated to make up 20% of the US population by 2030.[2][2] Some estimates indicate that the prevalence of chronic","PeriodicalId":21046,"journal":{"name":"Regional Anesthesia & Pain Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140598079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fluoroscopy-guided high-intensity focused ultrasound neurotomy of the lumbar zygapophyseal joints: a prospective, open-label study 透视引导下的腰椎颧骨关节高强度聚焦超声神经切除术:一项前瞻性开放标签研究
Pub Date : 2024-04-05 DOI: 10.1136/rapm-2024-105345
Michael Gofeld, Kevin J Smith, Anuj Bhatia, Vladimir Djuric, Suzanne Leblang, Niv Rebhun, Ron Aginsky, Eric Miller, Brian Skoglind, Arik Hananel
Objective The objective of this study is to investigate safety and effectiveness of a fluoroscopy-guided high-intensity focused ultrasound (HIFU) system for thermal ablation of the lumbar medial branch nerves. Methods This dual center prospective cohort study enrolled 30 participants with lumbar zygapophyseal joint syndrome. Each participant previously had a positive response to either a single diagnostic analgesic block or radiofrequency ablation (RFA). The primary effectiveness outcome was individual responder rate, defined as a reduction of two points or more on the pain intensity numerical rating scale without an increase in opioid intake, or a reduction in opioid intake without an increase in pain at 6 months after the intervention. The primary safety outcome was procedure-related or device-related adverse events (AEs). Secondary outcome variables included MRI evidence of tissue ablation, Oswestry Disability Index, 12-Item Short Form Health Survey, Brief Pain Inventory, and Patient Global Impression of Change. Results The individual responder rate was 89.7% at 2 days, 89.7% at 7 days, 72.4% at 14 days, 82.1% at 30 days, 59.3% at 90 days and 82.6% at 180 days. The average Numeric Rating Scale for pain severity decreased from 7.1 at baseline to 3.0 (N=29) after 2 days, 3.0 (N=29) after 7 days, 3.1 (N=29) after 14 days, 3.2 (N=28) after 30 days, 4.3 (N=27) after 90 days, and 3.3 (N=23) after 180 days. All participants tolerated the procedure well with no significant side effects or complications. Conclusions Fluoroscopy-guided HIFU neurotomy achieved clinical responses comparable with RFA, and there were no significant device-related or procedure-related AEs. Trial registration number [NCT04129034][1]. Data are available on reasonable request. [1]: /lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT04129034&atom=%2Frapm%2Fearly%2F2024%2F04%2F04%2Frapm-2024-105345.atom
目的 本研究旨在探讨透视引导下的高强度聚焦超声(HIFU)系统用于腰椎内侧支神经热消融的安全性和有效性。方法 这项双中心前瞻性队列研究共招募了 30 名腰椎颧骨关节综合征患者。每位患者之前都对单次诊断性镇痛阻滞或射频消融术(RFA)有过积极反应。主要疗效指标是个体应答率,即在干预6个月后,疼痛强度数值评定量表降低两分或更多,而阿片类药物摄入量没有增加,或阿片类药物摄入量减少而疼痛没有增加。主要安全性结果是与手术或设备相关的不良事件(AEs)。次要结果变量包括核磁共振成像组织消融证据、Oswestry 残疾指数、12 项简表健康调查、简明疼痛量表和患者总体变化印象。结果 2 天、7 天、14 天、30 天、90 天和 180 天的个体应答率分别为 89.7%、89.7%、72.4%、82.1%、59.3% 和 82.6%。疼痛严重程度的平均数字评级量表从基线时的 7.1 分降至 2 天后的 3.0 分(29 人)、7 天后的 3.0 分(29 人)、14 天后的 3.1 分(29 人)、30 天后的 3.2 分(28 人)、90 天后的 4.3 分(27 人)和 180 天后的 3.3 分(23 人)。所有参与者都能很好地耐受手术,没有出现明显的副作用或并发症。结论 透视引导下 HIFU 神经切除术取得了与 RFA 相当的临床疗效,而且没有出现明显的设备相关或手术相关的 AEs。试验注册号[NCT04129034][1]。如有合理要求,可提供相关数据。[1]:/lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT04129034&atom=%2Frapm%2Fearly%2F2024%2F04%2F04%2Frapm-2024-105345.atom
{"title":"Fluoroscopy-guided high-intensity focused ultrasound neurotomy of the lumbar zygapophyseal joints: a prospective, open-label study","authors":"Michael Gofeld, Kevin J Smith, Anuj Bhatia, Vladimir Djuric, Suzanne Leblang, Niv Rebhun, Ron Aginsky, Eric Miller, Brian Skoglind, Arik Hananel","doi":"10.1136/rapm-2024-105345","DOIUrl":"https://doi.org/10.1136/rapm-2024-105345","url":null,"abstract":"Objective The objective of this study is to investigate safety and effectiveness of a fluoroscopy-guided high-intensity focused ultrasound (HIFU) system for thermal ablation of the lumbar medial branch nerves. Methods This dual center prospective cohort study enrolled 30 participants with lumbar zygapophyseal joint syndrome. Each participant previously had a positive response to either a single diagnostic analgesic block or radiofrequency ablation (RFA). The primary effectiveness outcome was individual responder rate, defined as a reduction of two points or more on the pain intensity numerical rating scale without an increase in opioid intake, or a reduction in opioid intake without an increase in pain at 6 months after the intervention. The primary safety outcome was procedure-related or device-related adverse events (AEs). Secondary outcome variables included MRI evidence of tissue ablation, Oswestry Disability Index, 12-Item Short Form Health Survey, Brief Pain Inventory, and Patient Global Impression of Change. Results The individual responder rate was 89.7% at 2 days, 89.7% at 7 days, 72.4% at 14 days, 82.1% at 30 days, 59.3% at 90 days and 82.6% at 180 days. The average Numeric Rating Scale for pain severity decreased from 7.1 at baseline to 3.0 (N=29) after 2 days, 3.0 (N=29) after 7 days, 3.1 (N=29) after 14 days, 3.2 (N=28) after 30 days, 4.3 (N=27) after 90 days, and 3.3 (N=23) after 180 days. All participants tolerated the procedure well with no significant side effects or complications. Conclusions Fluoroscopy-guided HIFU neurotomy achieved clinical responses comparable with RFA, and there were no significant device-related or procedure-related AEs. Trial registration number [NCT04129034][1]. Data are available on reasonable request. [1]: /lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT04129034&atom=%2Frapm%2Fearly%2F2024%2F04%2F04%2Frapm-2024-105345.atom","PeriodicalId":21046,"journal":{"name":"Regional Anesthesia & Pain Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140597968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Incomplete sensorimotor paresis after upper abdominal surgery with TEA and spinal epidural lipomatosis: a case report 上腹部手术伴 TEA 和脊髓硬膜外脂肪瘤病后的不完全感觉运动麻痹:病例报告
Pub Date : 2024-04-05 DOI: 10.1136/rapm-2024-105342
Marco Richard Zugaj, Oliver Gutzeit, Victoria Louise Mayer, Basem Ishak, Christoph Gumbinger, Markus Alexander Weigand, Jens Keßler
Introduction This case report documents a postoperative, incomplete sensorimotor paraparesis from thoracic vertebral body 6 (Th6) after combined anesthesia for upper abdominal surgery in a patient who had a thoracic localization of spinal epidural lipomatosis (SEL). Case presentation The patient was treated in our clinic with a thoracic epidural catheter (TEA) for perioperative analgesia during a partial duodenopancreatectomy. Paraparetic symptoms occurred 20 hours after surgery. Initial MRI did not show bleeding, infection or spinal cord damage and the neurosurgeon consultants recommended observation. The neurological examination and the third follow-up MRI on 15th postoperative day showed ventrolateral damage of the spinal cord at level Th6. It is possible that local anesthetic compressed the spinal cord in addition to the existing lipomatosis and the thoracic kyphosis. The paraparesis improved during follow-up paraplegiologic treatment. Conclusion So far, only two uncomplicated lumbar epidural catheter anesthesias have been described in patients who had a lumbar SEL. Epidural catheter anesthesia is a safe and effective method of pain control. But it is important to carefully identify and stratify patients with risk factors during the premedication visit. In patients who had kyphosis and thoracic localization of SEL, TEA may only be used after a risk–benefit assessment.
导言:本病例报告记录了一名胸椎硬膜外脂肪瘤病(SEL)患者在上腹部手术联合麻醉后,因胸椎第 6 椎体(Th6)引起的术后不完全感觉运动麻痹。病例介绍 该患者在我院接受十二指肠部分切除术,在围手术期使用胸硬膜外导管(TEA)进行镇痛。术后 20 小时出现瘫痪症状。最初的核磁共振成像未显示出血、感染或脊髓损伤,神经外科顾问建议观察。神经系统检查和术后第 15 天的第三次核磁共振随访显示,Th6 水平的脊髓腹侧受损。可能是局部麻醉剂压迫了脊髓,再加上原有的脂肪瘤和胸椎后凸。在后续的副脊髓治疗过程中,偏瘫症状有所改善。结论 到目前为止,仅有两例腰椎 SEL 患者无并发症的腰椎硬膜外导管麻醉。硬膜外导管麻醉是一种安全有效的止痛方法。但重要的是,在用药前的访视中要仔细识别有风险因素的患者并对其进行分层。对于有脊柱后凸和胸椎定位 SEL 的患者,只有在进行风险效益评估后才能使用 TEA。
{"title":"Incomplete sensorimotor paresis after upper abdominal surgery with TEA and spinal epidural lipomatosis: a case report","authors":"Marco Richard Zugaj, Oliver Gutzeit, Victoria Louise Mayer, Basem Ishak, Christoph Gumbinger, Markus Alexander Weigand, Jens Keßler","doi":"10.1136/rapm-2024-105342","DOIUrl":"https://doi.org/10.1136/rapm-2024-105342","url":null,"abstract":"Introduction This case report documents a postoperative, incomplete sensorimotor paraparesis from thoracic vertebral body 6 (Th6) after combined anesthesia for upper abdominal surgery in a patient who had a thoracic localization of spinal epidural lipomatosis (SEL). Case presentation The patient was treated in our clinic with a thoracic epidural catheter (TEA) for perioperative analgesia during a partial duodenopancreatectomy. Paraparetic symptoms occurred 20 hours after surgery. Initial MRI did not show bleeding, infection or spinal cord damage and the neurosurgeon consultants recommended observation. The neurological examination and the third follow-up MRI on 15th postoperative day showed ventrolateral damage of the spinal cord at level Th6. It is possible that local anesthetic compressed the spinal cord in addition to the existing lipomatosis and the thoracic kyphosis. The paraparesis improved during follow-up paraplegiologic treatment. Conclusion So far, only two uncomplicated lumbar epidural catheter anesthesias have been described in patients who had a lumbar SEL. Epidural catheter anesthesia is a safe and effective method of pain control. But it is important to carefully identify and stratify patients with risk factors during the premedication visit. In patients who had kyphosis and thoracic localization of SEL, TEA may only be used after a risk–benefit assessment.","PeriodicalId":21046,"journal":{"name":"Regional Anesthesia & Pain Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140597969","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Use of natural language processing method to identify regional anesthesia from clinical notes 使用自然语言处理方法从临床笔记中识别区域麻醉
Pub Date : 2024-04-04 DOI: 10.1136/rapm-2024-105340
Laura A Graham, Samantha S Illarmo, Sherry M Wren, Michelle C Odden, Seshadri C Mudumbai
Introduction Accurate data capture is integral for research and quality improvement efforts. Unfortunately, limited guidance for defining and documenting regional anesthesia has resulted in wide variation in documentation practices, even within individual hospitals, which can lead to missing and inaccurate data. This cross-sectional study sought to evaluate the performance of a natural language processing (NLP)-based algorithm developed to identify regional anesthesia within unstructured clinical notes. Methods We obtained postoperative clinical notes for all patients undergoing elective non-cardiac surgery with general anesthesia at one of six Veterans Health Administration hospitals in California between January 1, 2017, and December 31, 2022. After developing and executing our algorithm, we compared our results to a frequently used referent, the Corporate Data Warehouse structured data, to assess the completeness and accuracy of the currently available data. Measures of agreement included sensitivity, positive predictive value, false negative rate, and accuracy. Results We identified 27,713 procedures, of which 9310 (33.6%) received regional anesthesia. 96.6% of all referent regional anesthesia cases were identified in the clinic notes with a very low false negative rate and good accuracy (false negative rate=0.8%, accuracy=82.5%). Surprisingly, the clinic notes documented more than two times the number of regional anesthesia cases that were documented in the referent (algorithm n=9154 vs referent n=4606). Discussion While our algorithm identified nearly all regional anesthesia cases from the referent, it also identified more than two times as many regional anesthesia cases as the referent, raising concerns about the accuracy and completeness of regional anesthesia documentation in administrative and clinical databases. We found that NLP was a promising alternative for identifying clinical information when existing databases lack complete documentation.
导言 准确的数据采集是研究和质量改进工作不可或缺的一部分。遗憾的是,由于区域麻醉的定义和记录指南有限,导致即使是在单个医院内,记录方法也存在很大差异,这可能会导致数据缺失和不准确。本横断面研究旨在评估一种基于自然语言处理 (NLP) 的算法的性能,该算法可在非结构化临床笔记中识别区域麻醉。方法 我们获取了 2017 年 1 月 1 日至 2022 年 12 月 31 日期间在加利福尼亚州六家退伍军人健康管理局医院之一接受选择性非心脏手术并进行全身麻醉的所有患者的术后临床笔记。在开发并执行算法后,我们将结果与常用的参考数据(企业数据仓库结构化数据)进行了比较,以评估当前可用数据的完整性和准确性。衡量一致性的指标包括灵敏度、阳性预测值、假阴性率和准确性。结果 我们确定了 27713 例手术,其中 9310 例(33.6%)接受了区域麻醉。96.6%的区域麻醉参考病例在门诊病历中得到了确认,假阴性率极低,准确率很高(假阴性率=0.8%,准确率=82.5%)。令人惊讶的是,临床笔记中记录的区域麻醉病例数是参考病例数的两倍多(算法 n=9154 vs 参考病例 n=4606)。讨论 虽然我们的算法识别出了参考文献中几乎所有的区域麻醉病例,但它识别出的区域麻醉病例数量也是参考文献的两倍多,这引起了人们对行政和临床数据库中区域麻醉记录的准确性和完整性的关注。我们发现,在现有数据库缺乏完整文档的情况下,NLP 是识别临床信息的一种很有前途的替代方法。
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Regional Anesthesia & Pain Medicine
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