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Preoperative test requests for elective surgeries of different complexity: Appropriateness and interhospital variability 不同复杂性择期手术的术前检查要求:适当性和医院间的可变性。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-16 DOI: 10.1016/j.jclinane.2025.112033
Antonio Sánchez-Hidalgo , Iratxe Urreta Barallobre , Ignasi Bolibar Ribas , Eva Bassas Parga , Miren Arrieta Bernaras , Gaizka Gutiérrez Sánchez , David Sánchez Cirera , Francisco José González Moraga , Inigo Gorostiza , Raúl de Frutos Parra , Susana Álvarez Gómez , Pablo Manuel Keenoy , Marta Roqué Figuls , Carolina Requeijo

Background

Numerous studies have questioned the usefulness of routine preoperative tests, and several guidelines have published recommendations aimed at reducing unnecessary preoperative testing.

Study objectives

To analyze the appropriateness of preoperative test requests and interhospital variability in criteria for requesting preoperative tests.

Design

Cross-sectional retrospective multicenter observational study.

Setting

Nine Spanish National Health System hospitals.

Patients

Patients over 18 years of age undergoing elective cataract surgery, inguinal hernia, laparoscopic cholecystectomy, colon surgery or primary knee replacement, in any department of the participating hospitals during 5 working days in June 2022 (n = 1522).

Exposure

Hospitals where patients underwent surgery.

Measurements

Appropriateness of requested preoperative tests according to hospital protocols and NICE guidelines analyzed with random-intercept multilevel models considering hospital-level and patient-level variables. Hospital protocol score to determine disagreement with the NICE guidelines.

Main results

Preoperative test request inappropriateness was 12.03 % according to hospital protocols and 72.99 % according to the NICE guidelines. Inappropriateness was mostly due to excessive requests and differed by hospital and surgery type. Independent factors determining inappropriateness at the hospital-level were center complexity and availability of computerized preoperative request templates; at the patient-level were age, ASA grades and surgical complexity. Protocol criteria for requesting preoperative tests varied notably between hospitals, and most protocols showed low agreement with NICE recommendations, especially in terms of over-requested preoperative tests.

Conclusions

Inappropriateness of preoperative test requests was high according to hospital protocols and especially high according to the NICE guidelines. Appropriateness was determined by patient characteristics, surgical complexity, and institutional factors. Interhospital variability in inappropriateness was explained by differing criteria for preoperative test requests.
背景:大量研究质疑常规术前检查的有效性,一些指南已发表建议,旨在减少不必要的术前检查。研究目的:分析术前检查要求的适宜性和医院间术前检查要求标准的差异。设计:横断面回顾性多中心观察研究。环境:九家西班牙国家卫生系统医院。患者:于2022年6月5个工作日在参与医院任一科室接受选择性白内障手术、腹股沟疝手术、腹腔镜胆囊切除术、结肠手术或原发性膝关节置换术的18岁以上患者(n = 1522)。暴露:病人接受手术的医院。测量:根据医院方案和NICE指南,采用随机截距多水平模型分析了考虑医院水平和患者水平变量的术前检查的适当性。医院方案评分以确定与NICE指南的不一致。主要结果:根据医院规程,术前检查要求不恰当率为12.03%,根据NICE指南,不恰当率为72.99%。不当性主要是由于过度要求,因医院和手术类型而异。决定医院层面不适宜的独立因素是中心复杂性和计算机化术前请求模板的可用性;在患者水平是年龄、ASA分级和手术复杂程度。要求术前检查的方案标准因医院而异,大多数方案与NICE建议的一致性较低,特别是在要求过多的术前检查方面。结论:根据医院协议,术前检查要求的不适当性很高,特别是根据NICE指南。适当性由患者特征、手术复杂性和机构因素决定。医院间不适宜性的差异可以通过术前检查要求的不同标准来解释。
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引用次数: 0
Trust your gut? Evaluating non-expert gastric ultrasound performance – A prospective observational cohort study 相信自己的直觉?评估非专家胃超声表现-一项前瞻性观察队列研究。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-10 DOI: 10.1016/j.jclinane.2025.112053
Sarah Baumann , Firmin Kamber MD , Thierry Girard MD , Eckhard Mauermann MD, PhD, M.Sc , Reza Kaviani MD

Background

Aspiration of gastric content is a serious complication of anesthesia, associated with high mortality and morbidity. Recent studies demonstrated that fasting status can be assessed accurately by gastric ultrasound. However, there is still a lack of evidence regarding the application of this technique by inexperienced examiners. We aimed to determine the accuracy of gastric ultrasound performed by medical students after a standardized training sequence.

Outcome

Accuracy of identifying the fasting status by gastric ultrasound performed by inexperienced examiners.

Methods

In this prospective observational cohort study, five medical students performed 80 gastric ultrasound examinations on healthy, non-obese volunteers. Standardized training consisted of blended online training, one plenary lecture, and 2 h of hands-on-training. Volunteers were randomized in a 2:1:1 ratio to "fasted", "non-fasted, fluid", and "non-fasted, solid" with the examiners being blinded to the fasting status. The examiners determined the fasting status using gastric ultrasound and recorded the gastric cross-sectional area. Beforehand, an expert examiner also conducted all examinations for comparison. Sensitivity, specificity, positive and negative predictive values were calculated from the acquired data. The cross-sectional area was pooled for the expert and non-experts and the results plotted and interrater reliability assessed by the intraclass correlation coefficient (ICC).

Results

Data from 80 individuals were analyzed. The inexperienced examiners correctly identified all non-fasted volunteers (sensitivity 1.00,95 % CI: 0.91–1.00). They wrongly classified 18 out of 40 fasted volunteers as "non-fasted" (specificity 0.55, 95 % CI: 0.40–0.69). Positive predictive value was 0.69 (95 % CI: 0.56–0.79) and negative predictive value 1.00 (95 % CI: 0.85–1.00). The overall ICC was 0.72 (95 % CI 0.57–0.82), and 0.30 (95 % CI -0.32–0.63), 0.66 (95 % CI -0.16–0.87), and 0.27 (95 % CI -0.82–0.71), for the "fasted", "non-fasted, fluid", and "non-fasted, solid" states, respectively.

Conclusions

Examiners with limited experience in ultrasound diagnostics may accurately identify a full stomach in normal-weight volunteers after a standardized training sequence. However, the detected specificity of 0.63 was low, and more focused training on the ultrasound anatomy of an empty stomach may be needed to rule out an empty stomach in a clinical scenario.
背景:胃内容物误吸是麻醉的严重并发症,死亡率和发病率高。最近的研究表明,胃超声可以准确地评估空腹状态。然而,关于没有经验的审查员应用该技术的证据仍然缺乏。我们的目的是确定医学生在标准化训练后进行胃超声检查的准确性。结果:没有经验的检查人员通过胃超声检查确定禁食状态的准确性。方法:在这项前瞻性观察队列研究中,五名医学生对健康的非肥胖志愿者进行了80次胃超声检查。标准化培训包括混合在线培训、一次全体讲座和2小时的实践培训。志愿者按2:1:1的比例随机分为“禁食”、“非禁食、流质”和“非禁食、固体”,审查员对禁食状态不知情。检查人员使用胃超声确定空腹状态并记录胃横截面积。在此之前,一名专家审查员也进行了所有的检查以进行比较。根据获得的数据计算敏感性、特异性、阳性预测值和阴性预测值。将专家和非专家的横截面积汇总,绘制结果,并通过类内相关系数(ICC)评估组间信度。结果:分析了80例个体的数据。没有经验的检查人员正确地识别出所有未禁食的志愿者(灵敏度1.00,95% CI: 0.91-1.00)。他们错误地将40名禁食志愿者中的18人归类为“非禁食”(特异性0.55,95% CI: 0.40-0.69)。阳性预测值为0.69 (95% CI: 0.56 ~ 0.79),阴性预测值为1.00 (95% CI: 0.85 ~ 1.00)。对于“禁食”、“非禁食、流质”和“非禁食、固体”状态,总体ICC分别为0.72 (95% CI 0.57-0.82)、0.30 (95% CI -0.32-0.63)、0.66 (95% CI -0.16-0.87)和0.27 (95% CI -0.82-0.71)。结论:超声诊断经验有限的检查人员可以在标准化的训练序列后准确地识别正常体重志愿者的饱胃。然而,0.63的检测特异性较低,可能需要对空腹超声解剖进行更集中的培训,以排除临床场景中的空腹。
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引用次数: 0
The expanding role of critical care anesthesiologists outside the ICU 重症监护麻醉医师在ICU外的作用日益扩大。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-02-20 DOI: 10.1016/j.jclinane.2025.111779
Siddharth Dave MD , Brigid Flynn MD, FCCM , Kunal Karamchandani MD, FCCP, FCCM
CCACritical care anesthesiologist
ICUintensive care unit
PSHperioperative surgical home
ASAAmerican Society of Anesthesiologists
RRSrapid response system
ECMOextracorporeal membrane oxygenation
QIquality improvement
EMRelectronic medical record
PCPprimary care practitioner
重症监护麻醉科重症监护病房围手术期外科医院美国麻醉医师学会快速反应系统体外膜氧合质量改善电子病历初级保健医生
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引用次数: 0
Efficacy and safety of intravenous iron supplementation for perioperative iron deficiency anemia: a systematic review and network meta-analysis of randomized controlled trials 静脉补铁治疗围手术期缺铁性贫血的疗效和安全性:随机对照试验的系统评价和网络荟萃分析。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-03 DOI: 10.1016/j.jclinane.2025.112062
Qingxia Xue , Bei Zhang , Zhicong Xing , Fudong Sun , Quan Zhao , Shengjun Mu

Objective

Anemia is common in the perioperative period, with approximately one-third of surgical patients presenting with preoperative anemia and even higher rates of anemia postoperatively due to blood loss. The comparative efficacy and safety of different intravenous iron preparations for perioperative anemia remain unclear. This study aims to evaluate their efficacy and safety by a comprehensive network meta-analysis (NMA).

Methods

A systematic search of PubMed, Embase, and the Cochrane Library was conducted from inception to December 10, 2024, to identify randomized controlled trials (RCTs) involving intravenous iron administration in the perioperative period. Two independent researchers extracted and cross-checked the data. Outcomes included transfusion rate, hemoglobin (Hb) concentrations, adverse events, quality of life (QoL), hypersensitivity reactions, and hypophosphatemia. A Bayesian NMA was performed.

Results

Thirty-four RCTs with a total of 4688 participants were included in the NMA. Ferric carboxymaltose (FCM, mean difference [MD] 0.76 g/dL, 95 % credible interval [CrI] 0.56 to 0.96) and iron isomaltoside (IIM, MD 0.65 g/dL, 95 % CrI 0.33 to 0.97) significantly increased Hb concentrations compared with placebo. However, only FCM reduced transfusion requirements (odds ratio [OR] 0.72, 95 % CrI 0.55 to 0.91). The safety analysis revealed no significant differences in adverse events between the groups. Descriptive analysis indicated improved QoL with FCM compared to placebo for fatigue and dyspnea (QLQ-C30) and physical functioning (SF-36). For NMA, no significant inconsistencies were found between direct and indirect evidence.

Conclusions

FCM improves perioperative Hb concentrations and reduces transfusion requirements. All intravenous iron preparations demonstrated acceptable safety profiles. Further research is needed to validate these findings and refine perioperative iron supplementation strategies.
目的:围手术期贫血很常见,约三分之一的手术患者术前出现贫血,术后因失血而出现贫血的比例更高。不同静脉铁制剂治疗围手术期贫血的相对疗效和安全性尚不清楚。本研究旨在通过综合网络荟萃分析(NMA)评估其有效性和安全性。方法:系统检索PubMed, Embase和Cochrane图书馆,从成立到2024年12月10日,确定围手术期静脉给铁的随机对照试验(RCTs)。两名独立研究人员提取并交叉核对了这些数据。结果包括输血率、血红蛋白(Hb)浓度、不良事件、生活质量(QoL)、过敏反应和低磷血症。进行贝叶斯神经网络分析。结果:34项随机对照试验共4688名受试者被纳入NMA。与安慰剂相比,三羧基麦芽糖铁(FCM,平均差[MD] 0.76 g/dL, 95%可信区间[CrI] 0.56 ~ 0.96)和异麦芽糖铁(IIM, MD 0.65 g/dL, 95%可信区间[CrI] 0.33 ~ 0.97)显著增加了Hb浓度。然而,只有FCM减少了输血需求(优势比[OR] 0.72, 95% CrI 0.55至0.91)。安全性分析显示两组之间的不良事件没有显著差异。描述性分析表明,与安慰剂相比,FCM改善了疲劳和呼吸困难(QLQ-C30)和身体功能(SF-36)的生活质量。对于NMA,在直接和间接证据之间没有发现显著的不一致。结论:流式细胞术提高围手术期血红蛋白浓度,减少输血需求。所有静脉注射铁制剂均表现出可接受的安全性。需要进一步的研究来验证这些发现并完善围手术期补铁策略。
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引用次数: 0
Response to: Letter to the editor regarding “Unpacking the Bundled Intervention and Interpreting the Outcomes in the Individualized Blood Pressure Strategy Trial” 回复:致编辑的关于“在个体化血压策略试验中解开捆绑干预和解释结果”的信。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-17 DOI: 10.1016/j.jclinane.2025.112068
Zheng Fang, Xin-qi Cheng
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引用次数: 0
Letter to the editor on ‘Preoperative cognitive function and surgical outcomes under general anesthesia among older patients’ 致编辑关于“老年患者全麻术前认知功能与手术结果”的信
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-25 DOI: 10.1016/j.jclinane.2025.112052
Weizhi Qiu
{"title":"Letter to the editor on ‘Preoperative cognitive function and surgical outcomes under general anesthesia among older patients’","authors":"Weizhi Qiu","doi":"10.1016/j.jclinane.2025.112052","DOIUrl":"10.1016/j.jclinane.2025.112052","url":null,"abstract":"","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"108 ","pages":"Article 112052"},"PeriodicalIF":5.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Response to “Revisiting the hypoxemia-SSI relationship” 对“重新审视低氧与ssi的关系”的回应。
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-21 DOI: 10.1016/j.jclinane.2025.112035
Eva Rivas MD , Barak Cohen MD , Jacqueline Palermo MS , Daniel I. Sessler MD
{"title":"Response to “Revisiting the hypoxemia-SSI relationship”","authors":"Eva Rivas MD ,&nbsp;Barak Cohen MD ,&nbsp;Jacqueline Palermo MS ,&nbsp;Daniel I. Sessler MD","doi":"10.1016/j.jclinane.2025.112035","DOIUrl":"10.1016/j.jclinane.2025.112035","url":null,"abstract":"","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"108 ","pages":"Article 112035"},"PeriodicalIF":5.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145345677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The laryngeal mask airway for prone procedures 俯卧手术的喉罩气道
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-01 DOI: 10.1016/j.jclinane.2025.112061
Justin Bessette, Juan Cotte Cabarcas
{"title":"The laryngeal mask airway for prone procedures","authors":"Justin Bessette,&nbsp;Juan Cotte Cabarcas","doi":"10.1016/j.jclinane.2025.112061","DOIUrl":"10.1016/j.jclinane.2025.112061","url":null,"abstract":"","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"108 ","pages":"Article 112061"},"PeriodicalIF":5.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145418669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Opioid-free versus opioid-based anaesthesia and analgesia for patients at low risk for acute postoperative pain undergoing laparoscopic surgery: A randomised controlled trial 无阿片类药物与基于阿片类药物的麻醉和镇痛在低风险的腹腔镜术后急性疼痛患者中的应用:一项随机对照试验
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-31 DOI: 10.1016/j.jclinane.2025.112058
Krister Mogianos MD , Josefine Holgersson , Johan Undén M.D PhD , Anna K.M. Persson M.D PhD

Objective

To evaluate if opioid-free anaesthesia (OFA), is non-inferior to standard of care (SOC), in patients at low risk for acute postoperative pain (APOP).
Design: Patient- and assessor-blinded, non-inferiority, randomised, controlled trial.

Setting

Single centre between March 2022 to February 2024.

Patients

154 adult patients, ASA I – II, planned for elective laparoscopic surgery and risk-classified as low risk for APOP based on perceived pain during venous cannulation (VAS < 2.0).

Intervention

Patients were randomised to receiving OFA, including sevoflurane, dexmedetomidine, esketamine and lidocaine, or standard of care (SOC), a traditional GABAA and opioid-based strategy. Patients were subjected to the intervention from time to arrival at the day of surgery until discharge from the PACU.

Measurements

Primary outcome: worst pain intensity in the PACU. Secondary outcomes: worst pain, and proportion having NRS ≥ 4, at 24 h (during rest and movement), worst pain and proportion having NRS ≥ 1, at 3- and 6-months (during rest and movement), postoperative recovery at 24 h, PONV in the PACU and at 24 h. Rescue dose opioids in the PACU was an exploratory outcome.

Results

Pain scores were 4.8 in the OFA group and 4.6 in SOC group (P = 0.67). At 24 h, worst pain at rest was 5.7 vs 5.0 (P = 0.11), and during movement 5.6 vs 5.3 (P = 0.43). Proportion of patients with NRS ≥ 4 in the PACU was 66 % vs 69 % (P = 0.65) and at 24 h 76 % vs 60 % at rest (P = 0.042) and 73 % vs 69 % during movement (P = 0.65). There was no significant difference in PPOP at 3 or 6 months, either at rest (P = 0.51, P = 0.56) or movement (P = 0.72, P = 0.48), PONV (PACU: P = 0.93), at 24 h: (P = 0.52) or postoperative recovery at 24 h (99 vs 102, P = 0.44). OFA group required less rescue opioids in the PACU (3.4 mg vs 5.1 mg, P = 0.039).

Conclusion

When individualising anaesthesia based on predicted risk for APOP, OFA is non-inferior to a traditional GABAA and opioid-based anaesthesia strategy, for patients with a low risk for APOP undergoing laparoscopic surgery. No secondary advantages, i.e. lower PONV, less PPOP, better quality of recovery, was associated with OFA.
目的评价无阿片类药物麻醉(OFA)在低风险急性术后疼痛(APOP)患者中的应用是否优于标准护理(SOC)。设计:患者和评估者双盲、非劣效性、随机对照试验。在2022年3月至2024年2月之间设置单一中心。患者:154例成人患者,ASA I - II,计划进行选择性腹腔镜手术,根据静脉插管过程中感知到的疼痛(VAS < 2.0)将APOP风险分类为低风险。干预:患者随机接受OFA治疗,包括七氟醚、右美托咪定、艾氯胺酮和利多卡因,或标准护理(SOC),传统的GABAA和阿片类药物治疗。患者从手术当天到PACU出院时一直接受干预。主要结果:PACU中疼痛强度最大。次要结局:24小时(休息和运动期间)疼痛最严重,NRS≥4的比例最大,3个月和6个月(休息和运动期间)疼痛最严重,NRS≥1的比例最大,24小时术后恢复,PACU和24小时的PONV。PACU的救援剂量阿片类药物是一个探索性结局。结果OFA组西班牙评分为4.8分,SOC组为4.6分(P = 0.67)。24 h时,静息时最痛5.7 vs 5.0 (P = 0.11),运动时最痛5.6 vs 5.3 (P = 0.43)。PACU中NRS≥4的患者比例为66%对69% (P = 0.65), 24小时时为76%对60% (P = 0.042),运动时为73%对69% (P = 0.65)。3个月或6个月的PPOP,无论是休息(P = 0.51, P = 0.56)或运动(P = 0.72, P = 0.48), 24小时的PONV (PACU: P = 0.93) (P = 0.52)或24小时的术后恢复(99 vs 102, P = 0.44)均无显著差异。OFA组在PACU中需要较少的阿片类药物(3.4 mg vs 5.1 mg, P = 0.039)。结论在预测APOP风险的基础上进行个体化麻醉时,对于腹腔镜手术低风险APOP患者,OFA的麻醉效果不逊于传统的GABAA和阿片类药物麻醉策略。与OFA无关的次要优势,即较低的PONV,较低的PPOP,较好的恢复质量。
{"title":"Opioid-free versus opioid-based anaesthesia and analgesia for patients at low risk for acute postoperative pain undergoing laparoscopic surgery: A randomised controlled trial","authors":"Krister Mogianos MD ,&nbsp;Josefine Holgersson ,&nbsp;Johan Undén M.D PhD ,&nbsp;Anna K.M. Persson M.D PhD","doi":"10.1016/j.jclinane.2025.112058","DOIUrl":"10.1016/j.jclinane.2025.112058","url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate if opioid-free anaesthesia (OFA), is non-inferior to standard of care (SOC), in patients at low risk for acute postoperative pain (APOP).</div><div><em>Design</em>: Patient- and assessor-blinded, non-inferiority, randomised, controlled trial.</div></div><div><h3>Setting</h3><div>Single centre between March 2022 to February 2024.</div></div><div><h3>Patients</h3><div>154 adult patients, ASA I – II, planned for elective laparoscopic surgery and risk-classified as low risk for APOP based on perceived pain during venous cannulation (VAS &lt; 2.0).</div></div><div><h3>Intervention</h3><div>Patients were randomised to receiving OFA, including sevoflurane, dexmedetomidine, esketamine and lidocaine, or standard of care (SOC), a traditional GABA<sub>A</sub> and opioid-based strategy. Patients were subjected to the intervention from time to arrival at the day of surgery until discharge from the PACU.</div></div><div><h3>Measurements</h3><div>Primary outcome: worst pain intensity in the PACU. Secondary outcomes: worst pain, and proportion having NRS ≥ 4, at 24 h (during rest and movement), worst pain and proportion having NRS ≥ 1, at 3- and 6-months (during rest and movement), postoperative recovery at 24 h, PONV in the PACU and at 24 h. Rescue dose opioids in the PACU was an exploratory outcome.</div></div><div><h3>Results</h3><div>Pain scores were 4.8 in the OFA group and 4.6 in SOC group (<em>P</em> = 0.67). At 24 h, worst pain at rest was 5.7 vs 5.0 (<em>P</em> = 0.11), and during movement 5.6 vs 5.3 (<em>P</em> = 0.43). Proportion of patients with NRS ≥ 4 in the PACU was 66 % vs 69 % <em>(P</em> = 0.65) and at 24 h 76 % vs 60 % at rest (<em>P</em> = 0.042) and 73 % vs 69 % during movement (<em>P</em> = 0.65). There was no significant difference in PPOP at 3 or 6 months, either at rest (<em>P</em> = 0.51, <em>P</em> = 0.56) or movement (<em>P</em> = 0.72, <em>P</em> = 0.48), PONV (PACU: <em>P</em> = 0.93), at 24 h: (<em>P</em> = 0.52) or postoperative recovery at 24 h (99 vs 102, <em>P</em> = 0.44). OFA group required less rescue opioids in the PACU (3.4 mg vs 5.1 mg, <em>P</em> = 0.039).</div></div><div><h3>Conclusion</h3><div>When individualising anaesthesia based on predicted risk for APOP, OFA is non-inferior to a traditional GABA<sub>A</sub> and opioid-based anaesthesia strategy, for patients with a low risk for APOP undergoing laparoscopic surgery. No secondary advantages, i.e. lower PONV, less PPOP, better quality of recovery, was associated with OFA.</div></div>","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"108 ","pages":"Article 112058"},"PeriodicalIF":5.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145418714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A simplified standardized ultrasound-guided plane block for the Intercostobrachial nerve: Effective volume of 0.5 % ropivacaine determined by Dixon's up-and-down method 超声引导肋间臂神经平面阻滞的简化标准化:用Dixon上下法测定0.5%罗哌卡因的有效容积
IF 5.1 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-29 DOI: 10.1016/j.jclinane.2025.112081
Wenchao Chen MD , Guojun Yu MD , Hongmin Cai MD , Cuiying Du MD , Liang Feng MD , Jing Bian MD , Zhe Yuan MD , Ning Wang MD

Objective

The success rates of the intercostobrachial nerve (ICBN) blocks varied from 51 % to 100 % by different techniques, which required rich expertise from the operators and/or high-resolution ultrasound. We proposed a simplified ultrasound-guided plane block and explored the 50 % effective volume (EV50) and the 95 % effective volume (EV95) with corresponding 95 % confidence intervals.

Methods

We recruited patients undergoing surgery of the upper limb and performed the simplified block. The needle target was positioned at 3 cm caudal to the centre of the axillary artery on the anterior surface of the conjoint tendon. The EV of 0.5 % ropivacaine was determined by Dixon's up-and-down method with an initial volume of 5 mL, and a successful or failed block could produce a 0.5 mL decrement or increment. Probit regression was fitted to determine the EV. To enhance robustness, a bootstrap analysis with 1000 resamples was performed. We recorded the block performance and adverse events.

Results

A total of 28 patients were included. The EV50 calculated by the Dixon's up-and-down method was 3.29 ± 0.60 mL. Based on Probit regression analysis, the EV50 and EV95 were 3.31 (3.09–3.53) and 3.94 (3.46–4.42) mL. The bootstrap-derived EV50 and EV95 were 3.32 (3.05–3.52) and 3.90 (3.54–4.41) mL. No adverse events occurred.

Conclusions

This simplified standardized ultrasound-guided plane block can provide a reliable anesthesia of the intercostobrachial nerve, with an EV50 of 3.31 mL and an EV95 of 3.94 mL for 0.5 % ropivacaine. This approach may enhance teaching and clinical practice by improving ergonomics, procedural efficiency, and reproducibility, while minimizing local anesthetic dosage and enhancing safety.
目的采用不同的技术进行肋间臂神经阻滞的成功率从51%到100%不等,这需要术者丰富的专业知识和/或高分辨率的超声。我们提出了一种简化的超声引导平面块,并以相应的95%置信区间探索了50%有效体积(EV50)和95%有效体积(EV95)。方法选取上肢手术患者进行简易阻滞。针靶位于关节肌腱前表面腋窝动脉中心尾侧3cm处。0.5%罗哌卡因的EV采用Dixon上下法测定,初始体积为5ml,阻断成功或失败可产生0.5 mL的减少或增加。拟合概率回归确定EV。为了增强稳健性,进行了1000个样本的自举分析。我们记录阻滞表现和不良事件。结果共纳入28例患者。采用Dixon上下法计算EV50为3.29±0.60 mL, Probit回归分析EV50和EV95分别为3.31(3.09-3.53)和3.94 (3.46-4.42)mL, bootstrap导出EV50和EV95分别为3.32(3.05-3.52)和3.90 (3.54-4.41)mL,未发生不良事件。结论该简化的标准化超声引导平面阻滞可提供可靠的肋间臂神经麻醉,0.5%罗哌卡因的EV50为3.31 mL, EV95为3.94 mL。这种方法可以通过改善人体工程学、手术效率和可重复性来提高教学和临床实践,同时减少局麻剂量并提高安全性。
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引用次数: 0
期刊
Journal of Clinical Anesthesia
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