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Point-of-Care Lung Ultrasound to Evaluate Lung Isolation During One-Lung Ventilation in Children: A Blinded Observational Feasibility Study. 护理点肺部超声评估儿童单肺通气期间的肺隔离情况:盲法观察可行性研究。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000007155
Alok Moharir,Yoshikazu Yamaguchi,Jennifer H Aldrink,Andrea Martinez,Mauricio Arce-Villalobos,Sibelle Aurelie Yemele Kitio,Julie Rice-Weimer,Joseph D Tobias
BACKGROUNDMinimally invasive thoracic surgical techniques require effective lung isolation using one-lung ventilation (OLV). Verification of lung isolation may be confirmed by auscultation, visual confirmation using fiberoptic bronchoscopy (FOB), or more recently, point-of-care ultrasound (POCUS). The aim of this study was to prospectively compare lung ultrasound with clinical auscultation to confirm OLV before thoracic surgery in pediatric patients.METHODSThis prospectively blinded feasibility study included 40 patients ranging in age from 0 to 20 years. After confirmation of lung separation by the primary anesthesia team using FOB, the sonographer and the auscultator, both blinded to the laterality of surgery and lung separation, entered the operating room. The sonographer evaluated for pleural lung sliding and the auscultator listened for breath sounds. Successful lung separation was definitively confirmed by direct visualization of lung collapse during the operation.RESULTSIn confirming effective single-lung ventilation, lung ultrasound had a diagnostic accuracy of 95% (95% confidence interval [CI], 82.7%-98.5%). In contrast, auscultation could only reliably confirm lung isolation with 68% accuracy (95% CI, 51.5%-80.4%). The McNemar test showed a statistically significant difference between the use of lung ultrasound and auscultation (P < .001). The median time to perform ultrasonography was 67 seconds (interquartile range [IQR], 46-142) and the median time to perform auscultation was 21 seconds (IQR, 10-32).CONCLUSIONSBased on the initial results of our feasibility trial, lung ultrasound proved to be a fast and reliable method to verify single-lung ventilation in pediatric patients presenting for thoracic surgery with a high degree of diagnostic accuracy.
背景微创胸外科技术要求使用单肺通气(OLV)进行有效的肺隔离。肺隔离的确认可通过听诊、纤维支气管镜(FOB)视觉确认或最新的床旁超声(POCUS)进行。本研究旨在前瞻性地比较肺部超声与临床听诊,以便在儿科患者进行胸腔手术前确认 OLV。在主麻醉团队使用 FOB 确认肺分离后,超声波技师和听诊器医师进入手术室,他们对手术侧位和肺分离情况都是盲法。超声技师评估胸膜肺滑动,听诊器听呼吸音。结果 在确认有效的单肺通气时,肺部超声的诊断准确率为 95%(95% 置信区间 [CI],82.7%-98.5%)。相比之下,听诊确认肺隔离的准确率仅为 68%(95% 置信区间 [CI],51.5%-80.4%)。McNemar 检验显示,使用肺部超声波和听诊之间存在显著的统计学差异(P < .001)。结论根据我们的可行性试验的初步结果,肺部超声被证明是一种快速可靠的方法,可用于验证前来接受胸外科手术的儿科患者的单肺通气,且诊断准确率较高。
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引用次数: 0
Preoperative Multidisciplinary Team Huddle Improves Communication and Safety for Unscheduled Cesarean Deliveries: A System Redesign Using Improvement Science. 术前多学科团队会议改善了非计划剖宫产的沟通和安全性:利用改进科学重新设计系统。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000006905
Andrea Girnius,Candice Snyder,Heather Czarny,Thomas Minges,Michael Stacey,Tamara Supinski,John Crowe,Judith Strong,Sean A Josephs,Muhammad A Zafar
BACKGROUNDOptimal communication between care teams is a critical component in providing safe, timely, and appropriate patient care. Labor and delivery (L&D) units experience rapidly changing clinical scenarios often requiring escalation in care and unplanned cesarean deliveries (CDs). The University of Cincinnati Medical Center (UCMC) is a 550-bed academic level 4 maternal care center with a 13-bed L&D unit in Cincinnati, OH. There are approximately 2500 deliveries/y with a CD rate of 33%. The L&D unit is staffed with dedicated anesthesia personnel 24 hours a day. In our L&D unit, there was widespread dissatisfaction with multidisciplinary communication surrounding unscheduled CD. Near-miss safety events in our obstetric unit were attributed to preoperative communication failures. Initial surveys identified challenges in preoperative communication among nursing, anesthesiology, and obstetric teams leading to potential risk for compromised care.METHODUsing the UC Health Performance Improvement Way, we first sought to understand the process leading up to unscheduled CD. Change ideas were developed based on observed failures in communication. Interventions were tested and refined through iterative plan-do-study-act (PDSA) cycles. One key intervention was the introduction of a bedside, multidisciplinary, patient-centered, pre-CD huddle attended by nursing, anesthesia, and obstetrics representatives using a standard checklist for critical information. Qualitative patient feedback was elicited to inform change efforts. We compared patient and procedure characteristics from the baseline and huddle implementation phases.MEASURESOur primary outcome measure was the satisfaction of care team members with communication around unscheduled CD. A secondary outcome was the general anesthesia (GA) rate for unscheduled CD. Our key process measure was adherence to the preoperative huddle. We tracked decision-to-incision interval (DTI) as a balancing measure.RESULTSHuddle adherence reached 96% for unscheduled CD within 6 months of testing and implementation. A combined survey of anesthesia, nursing, and obstetrics showed that satisfaction scores related to unscheduled CD communication improved from 3.3/5 to 4.7/5 after huddle implementation. The rate of GA use and the median DTI remained unchanged. Patients felt more engaged and reported positive experiences by being a part of the huddle discussion.CONCLUSIONSIn an academic obstetric unit, communication failures surrounding unscheduled CD were identified as a contributor to staff dissatisfaction and perception of safety risk. Implementation of a bedside multidisciplinary pre-CD huddle improved communication between teams and contributed to creating a culture of safety without causing significant delays in care.
背景:护理团队之间的最佳沟通是为患者提供安全、及时和适当护理的关键要素。分娩室(L&D)的临床情况瞬息万变,经常需要升级护理和计划外剖宫产(CD)。辛辛那提大学医疗中心(UCMC)是一家拥有 550 张床位的四级学术性孕产妇护理中心,位于俄亥俄州辛辛那提市,拥有 13 张床位的产科。每年约有 2500 例分娩,剖宫产率为 33%。该产科每天 24 小时都有专职麻醉人员值班。在我们的产科和妇产科中,人们对围绕计划外分娩的多学科沟通普遍不满。在我们的产科病房,险些发生的安全事件都归咎于术前沟通失败。初步调查发现,护理、麻醉和产科团队之间在术前沟通方面存在挑战,导致潜在的护理受损风险。方法利用加州大学健康绩效改进方法,我们首先试图了解导致计划外 CD 的流程。根据观察到的沟通失败情况,我们提出了改革意见。通过 "计划-实施-研究-行动"(PDSA)的反复循环,对干预措施进行了测试和改进。其中一项关键的干预措施是引入床旁、多学科、以患者为中心的 CD 前会议,由护理、麻醉和产科代表参加,使用标准核对表了解关键信息。我们还征求了患者的定性反馈意见,为改革工作提供参考。我们比较了基线阶段和会议实施阶段的患者和手术特征。我们的主要结果是护理团队成员对计划外 CD 沟通的满意度。次要结果是计划外 CD 的全身麻醉 (GA) 率。我们的关键流程指标是对术前讨论的遵守情况。结果在测试和实施的 6 个月内,计划外 CD 的合班率达到 96%。一项针对麻醉、护理和产科的联合调查显示,实施分组后,与计划外 CD 沟通相关的满意度评分从 3.3/5 提高到 4.7/5。GA 使用率和 DTI 中位数保持不变。在一个学术产科病房,围绕计划外 CD 的沟通失败被认为是导致员工不满和安全风险感的一个因素。实施床旁多学科 CD 前讨论改善了团队之间的沟通,有助于创建安全文化,同时不会造成护理的严重延误。
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引用次数: 0
Oxygen-Sparing Anesthesia with Electrically Controlled Ventilators: A Bench Study with Implications for Clinical Practice and Resource Management. 使用电控呼吸机进行节氧麻醉:一项对临床实践和资源管理具有重要意义的临床研究。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000007270
Vito Torrano,Francesco Zadek,Abbiati Giacomo,Chiara Deli,Roberto Fumagalli,Thomas Langer
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引用次数: 0
An Exploratory Analysis of ChatGPT Compared to Human Performance With the Anesthesiology Oral Board Examination: Initial Insights and Implications. 麻醉学口试中 ChatGPT 与人类表现的对比探索性分析:初步见解和启示。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000006875
Samuel N Blacker,Fei Chen,Daniel Winecoff,Benjamin L Antonio,Harendra Arora,Bryan J Hierlmeier,Rachel M Kacmar,Anthony N Passannante,Anthony R Plunkett,David Zvara,Benjamin Cobb,Alexander Doyal,Daniel Rosenkrans,Kenneth Bradbury Brown,Michael A Gonzalez,Courtney Hood,Tiffany T Pham,Abhijit V Lele,Lesley Hall,Ameer Ali,Robert S Isaak
BACKGROUNDChat Generative Pre-Trained Transformer (ChatGPT) has been tested and has passed various high-level examinations. However, it has not been tested on an examination such as the American Board of Anesthesiology (ABA) Standardized Oral Examination (SOE). The SOE is designed to assess higher-level competencies, such as judgment, organization, adaptability to unexpected clinical changes, and presentation of information.METHODSFour anesthesiology fellows were examined on 2 sample ABA SOEs. Their answers were compared to those produced by the same questions asked to ChatGPT. All human and ChatGPT responses were transcribed, randomized by module, and then reproduced as complete examinations, using a commercially available software-based human voice replicator. Eight ABA applied examiners listened to and scored the topic and modules from 1 of the 4 versions of each of the 2 sample examinations. The ABA did not provide any support or collaboration with any authors.RESULTSThe anesthesiology fellow's answers were found to have a better median score than ChatGPT, for the module topics scores (P = .03). However, there was no significant difference in the median overall global module scores between the human and ChatGPT responses (P = .17). The examiners were able to identify the ChatGPT-generated answers for 23 of 24 modules (95.83%), with only 1 ChatGPT response perceived as from a human. In contrast, the examiners thought the human (fellow) responses were artificial intelligence (AI)-generated in 10 of 24 modules (41.67%). Examiner comments explained that ChatGPT generated relevant content, but were lengthy answers, which at times did not focus on the specific scenario priorities. There were no comments from the examiners regarding Chat GPT fact "hallucinations."CONCLUSIONSChatGPT generated SOE answers with comparable module ratings to anesthesiology fellows, as graded by 8 ABA oral board examiners. However, the ChatGPT answers were deemed subjectively inferior due to the length of responses and lack of focus. Future curation and training of an AI database, like ChatGPT, could produce answers more in line with ideal ABA SOE answers. This could lead to higher performance and an anesthesiology-specific trained AI useful for training and examination preparation.
背景Chat Generative Pre-Trained Transformer(ChatGPT)已经过测试,并通过了各种高级考试。但是,它还没有在美国麻醉学委员会(ABA)标准化口试(SOE)等考试中接受过测试。SOE 旨在评估更高层次的能力,如判断力、组织能力、对意外临床变化的适应能力以及信息表达能力。他们的答案与 ChatGPT 的相同问题所产生的答案进行了比较。所有人类和 ChatGPT 的回答都被转录下来,按模块随机排列,然后使用市售的基于软件的人类语音复制器将其复制为完整的考试内容。八名 ABA 应用考官聆听了 2 个样本考试 4 个版本中的 1 个版本的题目和模块,并进行了评分。结果在模块题目得分方面,麻醉学研究员的答案中位数得分高于 ChatGPT(P = .03)。但是,人类和 ChatGPT 回答的模块总分中位数没有明显差异(P = .17)。在 24 个模块中,有 23 个模块(95.83%)的答案是由 ChatGPT 生成的,只有 1 个模块的 ChatGPT 答案被认为来自人类。相反,在 24 个模块中,有 10 个模块(41.67%)的人类(同伴)回答被考官认为是人工智能(AI)生成的。考官们的评论解释说,ChatGPT 生成了相关内容,但答案冗长,有时没有关注具体情景的优先事项。考官们没有对 ChatGPT 事实 "幻觉 "发表任何评论。结论根据 8 位 ABA 口试考官的评分,ChatGPT 生成的 SOE 答案与麻醉学研究员的模块评分相当。然而,由于回答冗长且缺乏重点,ChatGPT 的答案在主观上被认为较差。未来对人工智能数据库(如 ChatGPT)的整理和训练可以生成更符合理想的 ABA SOE 答案。这可能会带来更高的性能,并使麻醉学专用的训练有素的人工智能在培训和考试准备中发挥作用。
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引用次数: 0
Association Between Glycemic Variability and Persistent Acute Kidney Injury After Noncardiac Major Surgery: A Multicenter Retrospective Cohort Study. 非心脏大手术后血糖变化与持续急性肾损伤之间的关系:一项多中心回顾性队列研究。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000007131
Siyu Kong,Ke Ding,Huili Jiang,Fan Yang,Chen Zhang,Liu Han,Yali Ge,Lihai Chen,Hongwei Shi,Jifang Zhou
BACKGROUNDWhile the relationship between glycemic variability (GV) and acute kidney injury (AKI) has been a subject of interest, the specific association of GV with persistent AKI beyond 48 hours postoperative after noncardiac surgery is not well-established.METHODSThis retrospective cohort study aimed to describe the patterns of different GV metrics in the immediate 48 hours after noncardiac surgery, evaluate the association between GV indices and persistent AKI within the 7-day postoperative window, and compare the risk identification capabilities of various GV for persistent AKI. A total of 10,937 patients who underwent major noncardiac surgery across 3 medical centers in eastern China between January 2015 and September 2023 were enrolled. GV was characterized using the coefficient of variations (CV), mean amplitude of glycemic excursions (MAGE), and the blood glucose risk index (BGRI). Multivariable logistic regression was used to examine the relationship between GV and AKI. Optimal cutoff values for GV metrics were calculated through the risk identification models, and an independent cohort from the INformative Surgical Patient dataset for Innovative Research Environment (INSPIRE) database with 7714 eligible cases served to externally validate the risk identification capability.RESULTSOverall, 274 (2.5%) of the 10,937 patients undergoing major noncardiac surgery met the criteria of persistent AKI. Higher GV was associated with an increased risk of persistent AKI (CV: odds ratio [OR] = 1.26, 95% confidence interval [CI], 1.08-1.46; MAGE: OR = 1.31, 95% CI, 1.15-1.49; BGRI: OR = 1.18, 95% CI, 1.08-1.29). Compared to models that did not consider glycemic factors, MAGE and BGRI independently contributed to predicting persistent AKI (MAGE: areas under the curve [AUC] = 0.768, P = .011; BGRI: AUC = 0.764, P = .014), with cutoff points of 3.78 for MAGE, and 3.02 for BGRI. The classification of both the internal and external validation cohorts using cutoffs demonstrated good performance, achieving the best AUC values of 0.768 for MAGE in the internal cohort and 0.777 for MAGE in the external cohort.CONCLUSIONSGV measured within 48 hours postoperative period is an independent risk factor for persistent AKI in patients undergoing noncardiac surgery. Specific cutoff points can be used to stratify at-risk patients. These findings indicate that stabilizing GV may potentially mitigate adverse kidney outcomes after noncardiac surgery, highlighting the importance of glycemic control in the perioperative period.
背景虽然血糖变异性(GV)与急性肾损伤(AKI)之间的关系一直备受关注,但 GV 与非心脏手术后 48 小时后的持续性 AKI 的具体关系尚未得到充分证实。方法这项回顾性队列研究旨在描述非心脏手术后 48 小时内不同 GV 指标的模式,评估 GV 指数与术后 7 天内持续性 AKI 之间的关联,并比较各种 GV 对持续性 AKI 的风险识别能力。2015年1月至2023年9月期间,华东地区3家医疗中心共纳入了10937名接受非心脏大手术的患者。使用变异系数(CV)、血糖偏移平均幅度(MAGE)和血糖风险指数(BGRI)对血糖风险进行表征。多变量逻辑回归用于研究 GV 与 AKI 之间的关系。通过风险识别模型计算出了 GV 指标的最佳临界值,并从创新研究环境手术患者信息数据集 (INSPIRE) 数据库的 7714 个合格病例中挑选出一个独立队列,对风险识别能力进行外部验证。结果在 10937 名接受重大非心脏手术的患者中,有 274 人(2.5%)符合持续性 AKI 的标准。较高的 GV 与持续性 AKI 风险增加有关(CV:几率比 [OR] = 1.26,95% 置信区间 [CI],1.08-1.46;MAGE:OR=1.31,95% CI,1.15-1.49;BGRI:OR=1.18,95% CI,1.08-1.29)。与不考虑血糖因素的模型相比,MAGE 和 BGRI 可独立预测持续性 AKI(MAGE:曲线下面积 [AUC] = 0.768,P = .011;BGRI:AUC = 0.764,P = .014),MAGE 临界点为 3.78,BGRI 临界点为 3.02。使用截断点对内部和外部验证队列进行分类显示出良好的性能,内部队列中 MAGE 的最佳 AUC 值为 0.768,外部队列中 MAGE 的最佳 AUC 值为 0.777。特定的临界点可用于对高危患者进行分层。这些研究结果表明,稳定 GV 有可能减轻非心脏手术后肾脏的不良预后,突出了围手术期血糖控制的重要性。
{"title":"Association Between Glycemic Variability and Persistent Acute Kidney Injury After Noncardiac Major Surgery: A Multicenter Retrospective Cohort Study.","authors":"Siyu Kong,Ke Ding,Huili Jiang,Fan Yang,Chen Zhang,Liu Han,Yali Ge,Lihai Chen,Hongwei Shi,Jifang Zhou","doi":"10.1213/ane.0000000000007131","DOIUrl":"https://doi.org/10.1213/ane.0000000000007131","url":null,"abstract":"BACKGROUNDWhile the relationship between glycemic variability (GV) and acute kidney injury (AKI) has been a subject of interest, the specific association of GV with persistent AKI beyond 48 hours postoperative after noncardiac surgery is not well-established.METHODSThis retrospective cohort study aimed to describe the patterns of different GV metrics in the immediate 48 hours after noncardiac surgery, evaluate the association between GV indices and persistent AKI within the 7-day postoperative window, and compare the risk identification capabilities of various GV for persistent AKI. A total of 10,937 patients who underwent major noncardiac surgery across 3 medical centers in eastern China between January 2015 and September 2023 were enrolled. GV was characterized using the coefficient of variations (CV), mean amplitude of glycemic excursions (MAGE), and the blood glucose risk index (BGRI). Multivariable logistic regression was used to examine the relationship between GV and AKI. Optimal cutoff values for GV metrics were calculated through the risk identification models, and an independent cohort from the INformative Surgical Patient dataset for Innovative Research Environment (INSPIRE) database with 7714 eligible cases served to externally validate the risk identification capability.RESULTSOverall, 274 (2.5%) of the 10,937 patients undergoing major noncardiac surgery met the criteria of persistent AKI. Higher GV was associated with an increased risk of persistent AKI (CV: odds ratio [OR] = 1.26, 95% confidence interval [CI], 1.08-1.46; MAGE: OR = 1.31, 95% CI, 1.15-1.49; BGRI: OR = 1.18, 95% CI, 1.08-1.29). Compared to models that did not consider glycemic factors, MAGE and BGRI independently contributed to predicting persistent AKI (MAGE: areas under the curve [AUC] = 0.768, P = .011; BGRI: AUC = 0.764, P = .014), with cutoff points of 3.78 for MAGE, and 3.02 for BGRI. The classification of both the internal and external validation cohorts using cutoffs demonstrated good performance, achieving the best AUC values of 0.768 for MAGE in the internal cohort and 0.777 for MAGE in the external cohort.CONCLUSIONSGV measured within 48 hours postoperative period is an independent risk factor for persistent AKI in patients undergoing noncardiac surgery. Specific cutoff points can be used to stratify at-risk patients. These findings indicate that stabilizing GV may potentially mitigate adverse kidney outcomes after noncardiac surgery, highlighting the importance of glycemic control in the perioperative period.","PeriodicalId":7799,"journal":{"name":"Anesthesia & Analgesia","volume":"62 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142233481","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
Developments in Transfusion Medicine: Pulmonary Transfusion Reactions and Novel Blood Cell Labeling Techniques. 输血医学的发展:肺部输血反应和新型血细胞标记技术。
Pub Date : 2024-09-13 DOI: 10.1213/ane.0000000000007136
Philippa G Phelp,Stefan F van Wonderen,Alexander P J Vlaar,Rick Kapur,Robert B Klanderman
Staying updated on advancements in transfusion medicine is crucial, especially in critical care and perioperative setting, where timely and accurate transfusions can be lifesaving therapeutic interventions. This narrative review explores the landscape of transfusion-related adverse events, focusing on pulmonary transfusion reactions such as transfusion-associated circulatory overload (TACO) and transfusion-related acute lung injury (TRALI). TACO and TRALI are the leading causes of transfusion-related morbidity and mortality; however, specific treatments are lacking. Understanding the current incidence, diagnostic criteria, pathogenesis, treatment, and prevention strategies can equip clinicians to help reduce the incidence of these life-threatening complications. The review discusses emerging pathogenic mechanisms, including the possible role of inflammation in TACO and the mechanisms of reverse TRALI and therapeutic targets for TACO and TRALI, emphasizing the need for further research to uncover preventive and treatment modalities. Despite advancements, significant gaps remain in our understanding of what occurs during transfusions, highlighting the necessity for improved monitoring methods. To address this, the review also presents novel blood cell labeling techniques in transfusion medicine used for improving monitoring, quality assessment, and as a consequence, potentially reducing transfusion-related complications. This article aims to provide an update for anesthesiologists, critical care specialists, and transfusion medicine professionals regarding recent advancements and developments in the field of transfusion medicine.
了解输血医学的最新进展至关重要,尤其是在重症监护和围手术期环境中,及时准确的输血可成为挽救生命的治疗干预措施。这篇叙述性综述探讨了输血相关不良事件的现状,重点关注肺部输血反应,如输血相关循环负荷过重(TACO)和输血相关急性肺损伤(TRALI)。输血相关循环负荷过重(TACO)和输血相关急性肺损伤(TRALI)是输血相关发病率和死亡率的主要原因;然而,目前还缺乏具体的治疗方法。了解目前的发病率、诊断标准、发病机理、治疗和预防策略可帮助临床医生降低这些危及生命的并发症的发病率。综述讨论了新出现的致病机制,包括炎症在 TACO 中可能扮演的角色、逆转 TRALI 的机制以及 TACO 和 TRALI 的治疗靶点,强调了进一步研究以发现预防和治疗方法的必要性。尽管取得了进展,但我们对输血过程中发生的情况的了解仍有很大差距,这突出说明了改进监测方法的必要性。针对这一问题,本综述还介绍了输血医学中用于改善监测和质量评估的新型血细胞标记技术,从而有可能减少输血相关并发症。本文旨在为麻醉师、重症监护专家和输血医学专业人员提供有关输血医学领域最新进展和发展的最新信息。
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引用次数: 0
Bronchial Blocker Versus Endobronchial Intubation in Young Children Undergoing One-Lung Ventilation: A Multicenter Retrospective Cohort Study. 在接受单肺通气的幼儿中使用支气管阻断器与支气管内插管:一项多中心回顾性队列研究。
Pub Date : 2024-09-12 DOI: 10.1213/ane.0000000000006973
Christopher S McLaughlin,Anusha Samant,Amit K Saha,Lisa K Lee,Ruchika Gupta,Leah B Templeton,Michael R Mathis,Susan Vishneski,T Wesley Templeton,
BACKGROUNDThoracic surgery and one-lung ventilation in young children carry significant risks. Approaches to one-lung ventilation in young children include endobronchial intubation (mainstem intubation) and use of a bronchial blocker. We hypothesized that endobronchial intubation is associated with a greater prevalence of airway complications compared to use of a bronchial blocker.METHODSThe Multicenter Perioperative Outcomes Group database was queried from 2004 to 2022 for one-lung ventilation cases in children, 2 months to 3 years of age, inclusive. Airway notes and free-text comments were manually reviewed for airway complications. Documented airway complications were considered the primary outcome and were divided into "Moderate" and "Critical." Moderate airway complications were bronchial blocker or endotracheal tube movement leading to loss of isolation, hypoxemia requiring ventilatory intervention, bronchial blocker migration into the trachea, significant impairment of ventilation, and other. Critical complications included reintubation or airway replacement intraoperatively, complete endotracheal tube occlusion, cardiac arrest or airway-related bradycardia, and procedure aborted due to an airway issue. An adjusted propensity score-matched analysis was then used to assess the impact of a bronchial blocker on the outcomes of moderate and critical complications.RESULTSAfter exclusions, 704 patients were included in the primary analysis. In unadjusted analyses, no statistically significant difference was observed in moderate airway complications between endobronchial intubation and bronchial blocker cohorts: 37 of 444 (8.3%; 95% confidence interval [CI], 5.9%-11.3%) vs 28 of 260 (10.8%; 95% CI, 7.3%-15.2%) with P = .281. In the unadjusted analysis, the prevalence of critical airway complications was significantly higher in the endobronchial intubation cohort compared to the bronchial blocker cohort: 28 of 444 (6.3%; 95% CI, 4.2%-9.0%) vs 5 of 260 (1.9%; 95% CI, 0.6%-4.4%) with P = .008. In the propensity-matched cohort analysis, endobronchial intubation was associated with a slightly increased risk of critical complications compared to use of a bronchial blocker: 14 of 243 (5.8%; 95% CI, 2.8%-8.7%) vs 5 of 243 (2.1%; 95% CI, 0.3%-3.8%) with P = .035.CONCLUSIONSEndobronchial intubation might be associated with a slightly increased risk of critical airway complications compared to use of a bronchial blocker in young children undergoing thoracic surgery and one-lung ventilation. Further, prospective studies are needed before a definitive change in practice is recommended.
背景幼儿胸外科手术和单肺通气具有很大的风险。幼儿单肺通气的方法包括支气管内插管(主干插管)和使用支气管阻断器。我们假设,与使用支气管阻断剂相比,支气管内插管与气道并发症的发生率更高。方法查询了多中心围手术期结果小组数据库 2004 年至 2022 年期间 2 个月至 3 岁(含)儿童的单肺通气病例。人工审核了气道记录和自由文本注释中的气道并发症。记录的气道并发症被视为主要结果,分为 "中度 "和 "重度"。中度气道并发症包括支气管封堵器或气管导管移动导致隔离丧失、需要通气干预的低氧血症、支气管封堵器移入气管、通气严重受损及其他。严重并发症包括术中重新插管或更换气道、气管导管完全闭塞、心脏骤停或气道相关心动过缓,以及因气道问题导致手术中止。然后使用调整后的倾向评分匹配分析来评估支气管阻断剂对中度和严重并发症结果的影响。在未经调整的分析中,观察到支气管内插管和支气管阻断器两组患者在中度气道并发症方面没有显著的统计学差异:444 例中的 37 例(8.3%;95% 置信区间 [CI],5.9%-11.3%)vs 260 例中的 28 例(10.8%;95% 置信区间 [CI],7.3%-15.2%),P = .281。在未经调整的分析中,支气管内插管队列的严重气道并发症发生率明显高于支气管阻断剂队列:444 例中有 28 例(6.3%;95% CI,4.2%-9.0%)vs 260 例中有 5 例(1.9%;95% CI,0.6%-4.4%),P = .008。在倾向匹配队列分析中,与使用支气管阻断剂相比,支气管内插管导致危重并发症的风险略有增加:243 例中有 14 例(5.8%;95% CI,2.8%-8.7%)vs 243 例中有 5 例(2.1%;95% CI,0.3%-3.结论在接受胸腔手术和单肺通气的幼儿中,与使用支气管阻断剂相比,支气管内插管可能与危重气道并发症风险略有增加有关。在建议明确改变做法之前,还需要进行进一步的前瞻性研究。
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引用次数: 0
A New Scoring System to Evaluate the Position and Functioning of Supraglottic Airway Devices in Research and Clinical Audits. 在研究和临床审核中评估声门上气道装置位置和功能的新评分系统。
Pub Date : 2024-09-12 DOI: 10.1213/ane.0000000000006970
André A J van Zundert,Stephen P Gatt,Tom C R V van Zundert,Carin A Hagberg,Jaideep J Pandit
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引用次数: 0
An Evaluation of the Transfer of Skills and Knowledge from Two World Federation of Societies of Anaesthesiologists Fellowship Programs. 对两个世界麻醉医师学会联合会研究金项目技能和知识转移的评估。
Pub Date : 2024-09-11 DOI: 10.1213/ane.0000000000006923
M Dylan Bould,J Bradley Cousins,Jenny Hoang,Yuanting Zha,Lydia Yilma,V Mark Gacii,Balavenkat Subramanian,Faye M Evans
BACKGROUNDSubspecialist training is an important part of developing human resources for health and for some learners, may require taking place in another, higher-resourced country. Despite effective learning of skills and knowledge in a different, more highly resourced context, transfer of these skills and knowledge back to a more poorly resourced context can be a challenge. We aimed to evaluate the transfer of skills and knowledge in 2 World Federation of Societies of Anaesthesiologists (WFSA) fellowship programs.METHODSThis qualitative program evaluation study, guided by Guskey's evaluation framework, used in-depth interviews of both faculty and graduates of the 2 fellowship programs. Interviews were conducted remotely, transcribed verbatim, and analyzed using qualitative content and pattern analysis.RESULTSWe interviewed 2 administrators, 10 faculty members, 17 graduated fellows, and 3 graduated fellows now in the role of faculty member in that fellowship. Key themes were barriers and enablers to the transfer of skills, including workplace and staffing, resources, mentorship, the interprofessional team, and leadership. Graduated fellows were able to have an impact on returning home in the areas of practice and service development, research, and teaching.CONCLUSIONSOur study found that the 2 fellowship programs had variable success in the transfer of learned skills and knowledge back to the fellows' "home" institutions. Contextual differences between the fellowship institution and the home institution were the main source of barriers to transfer, and fellows from different countries had diverse needs. Supporting the transfer of knowledge and skills should be an explicit goal of these fellowship programs, and as such, should be considered in the recruitment of fellows, curriculum development, and in how the success of a fellowship is evaluated. Curricula should not just focus on medical knowledge and skills, but also skills in leading change and in education.
背景亚专科培训是开发卫生人力资源的重要组成部分,对一些学员来说,可能需要在另一个资源较丰富的国家进行培训。尽管在不同的、资源更丰富的环境中可以有效地学习技能和知识,但将这些技能和知识转移到资源更贫乏的环境中可能是一个挑战。我们的目的是评估世界麻醉医师协会联合会(WFSA)的两个奖学金项目中技能和知识的传授情况。访谈以远程方式进行,逐字记录,并使用定性内容和模式分析法进行分析。结果我们访谈了 2 名管理人员、10 名教员、17 名已毕业的研究员和 3 名现在担任该研究项目教员的已毕业研究员。关键主题是技能转移的障碍和促进因素,包括工作场所和人员配备、资源、导师制、跨专业团队和领导力。我们的研究发现,这两个研究金项目在将所学技能和知识传回研究员 "母校 "方面取得了不同程度的成功。来自不同国家的研究人员有着不同的需求,而研究机构与母校之间的环境差异是阻碍知识转移的主要原因。支持知识和技能的传授应该是这些研究金项目的明确目标,因此在招募研究员、制定课程以及评估研究金成功与否时都应该考虑到这一点。课程不应只注重医学知识和技能,还应注重领导变革和教育方面的技能。
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引用次数: 0
Comparison of Clinical Performance of I-gel and Fastrach Laryngeal Mask Airway as an Intubating Device in Adults: A Systematic Review and Meta-Analysis. I-gel 和 Fastrach 喉罩气道作为成人插管设备的临床性能比较:系统回顾与元分析》。
Pub Date : 2024-09-11 DOI: 10.1213/ane.0000000000007000
Maria Luisa Machado Assis,Fabricio Batistella Zasso,Matheus Pedrotti Chavez,Eduardo Cirne Toledo,Gabriel Motta,Leonardo Duarte Moraes,Eric Pasqualotto,Rafael Oliva Morgado Ferreira,Naveed Siddiqui,Kong Eric You-Ten
BACKGROUNDThe supraglottic airway device (SGD) was introduced as a breakthrough in airway management. The Fastrach emerged as the first commercially available intubating SGD, drawing extensive investigation. I-gel is a more recent device that has gained popularity, can be used as an intubating SGD, and replaced Fastrach in many institutions. However, there is uncertainty regarding the comparison between these devices in terms of efficacy for intubation and ventilation, and safety in an airway rescue situation.METHODSPubMed, EMBASE, Scopus, and Cochrane databases were searched for randomized controlled trials (RCTs) comparing I-gel and Fastrach SGD in adult patients undergoing intubation. The primary outcome was the first-pass success rate for tracheal intubation. Secondary outcomes were tracheal intubation time, SGD insertion time and success, and complications. We computed risk ratios (RRs) to assess binary end points and weighted mean differences (WMDs) for continuous outcomes, with corresponding 95% confidence intervals (CIs) for the primary outcome and its subgroup analysis (P < .05 was considered statistically significant) and 99% CI after Bonferroni correction for the secondary outcomes (P < .01 was considered statistically significant).RESULTSThis study included a total of 14 RCTs encompassing 1340 patients. The results indicated a significant difference in the first-pass success rate favoring Fastrach (RR, 0.81; 95% CI, 0.67-0.98; P = .03; I² = 91%). In the subgroup analysis, when a flexible scope was utilized through I-gel, providers achieved a better tracheal intubation first-pass success rate (RR, 1.05; 95% CI, 1.01-1.11; P = .03; I² = 0%), compared with the Fastrach. Overall intubation success rates (RR, 0.92; 99% CI, 0.82-1.04; P = .08, I² = 92%) and time (WMD - 1.03 seconds; 99% CI, -4.75 to 2.69; P = .48; I² = 84%) showed no significant difference irrespective of the device used. There was no significant difference regarding device insertion time by the providers (WMD -6.48 seconds; 99% CI, -13.23 to 0.27; P = .01; I2 = 98%). Success rates of the providers' initial SGD insertion and complications such as sore throat (RR, 1.01; 99% CI, 0.65-1.57; P = .95, I² = 33%) and blood presence post-SGD removal (RR, 0.89; 99% CI, 0.42-1.86; P = .68, I² = 0%) showed no significant difference.CONCLUSIONSBased on our findings, a higher first-pass success rate was observed with the use of Fastrach when compared to I-gel. However, the use of I-gel might result in a better intubation success rate with the flexible scope-guided intubation. There are no significant differences in performance in terms of the success rate for intubation overall, time for device insertion, or time to intubation or complications regardless of the device used.
背景声门上气道装置(SGD)作为气道管理的一项突破而问世。Fastrach 是第一款商用插管 SGD,引起了广泛的研究。I-gel 是最近才流行起来的一种设备,可用作插管式 SGD,并在许多机构中取代了 Fastrach。方法检索了 SpubMed、EMBASE、Scopus 和 Cochrane 数据库中的随机对照试验 (RCT),比较了 I-gel 和 Fastrach SGD 在成人插管患者中的应用。主要结果是气管插管的首次成功率。次要结果是气管插管时间、SGD 插入时间和成功率以及并发症。我们计算了风险比(RRs)以评估二元终点,并计算了连续结果的加权平均差(WMDs),对主要结果及其亚组分析计算了相应的 95% 置信区间(CIs)(P < .05 为有统计学意义),对次要结果计算了 Bonferroni 校正后的 99% CI(P < .01 为有统计学意义)。结果表明,法斯拉赫的首次通过成功率与其他疗法有显著差异(RR,0.81;95% CI,0.67-0.98;P = .03;I² = 91%)。在亚组分析中,与 Fastrach 相比,当通过 I-gel 使用柔性探头时,医护人员的气管插管一次成功率更高(RR,1.05;95% CI,1.01-1.11;P = .03;I² = 0%)。总体插管成功率(RR,0.92;99% CI,0.82-1.04;P = .08;I² = 92%)和时间(WMD - 1.03 秒;99% CI,-4.75 至 2.69;P = .48;I² = 84%)显示,无论使用哪种设备,均无显著差异。医疗服务提供者插入器械的时间也无明显差异(WMD -6.48 秒;99% CI,-13.23 至 0.27;P = .01;I2 = 98%)。医疗服务提供者初次插入 SGD 的成功率以及咽喉痛(RR,1.01;99% CI,0.65-1.57;P = .95,I² = 33%)和取出 SGD 后出现血迹(RR,0.89;99% CI,0.42-1.86;P = .68,I² = 0%)等并发症无显著差异。然而,使用 I-gel 可能会使柔性镜引导下的插管成功率更高。无论使用哪种器械,在总体插管成功率、器械插入时间、插管时间或并发症方面都没有明显差异。
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引用次数: 0
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Anesthesia & Analgesia
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