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Benefits in adults allowed to drink clear liquids before anaesthesia until called to the operating room: A randomised pilot study. 在被叫到手术室之前,允许成年人在麻醉前喝透明液体的益处:一项随机试点研究。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-11-18 DOI: 10.1097/EJA.0000000000002309
Tobias E Haas, Peter Kranke, Miriam N Stegemann, Philipp Helmer, Benedikt Schmid, Franziska M Diehl, Peter U Heuschmann, Viktoria Rücker, Anna K Seitz, Joachim Diessner, Timo Heintel, Thomas Saller, Anne Rüggeberg, Silvia Krönert, Jona von Keitz, Patrick Meybohm

Background: Liquid fasting durations often exceed current recommendations, resulting in patient discomfort.

Objective: To investigate the feasibility of three preoperative liquid fasting protocols in patients with low risk of aspiration in preparation for a future large-scale trial, with a particular focus on patient-centred benefits.

Design: Prospective, randomised, controlled, pilot trial.

Setting: Secondary care; single academic centre in Germany.

Patients: One hundred and seventy-four adult surgical patients with low risk of aspiration.

Intervention: Patients were randomised either to 'control group' (usual care, 2 h liquid fasting protocol), 'conservative intervention' (patients received assistance in adhering to a 2 h liquid fasting protocol) or 'liberal intervention' (patients could drink until they were called to the operating room).

Main outcome measures: Piloting process endpoints and performance endpoints were assessed. The primary outcome was patient-reported thirst before anaesthesia induction categorised as none, moderate, or severe.

Results: No patient dropped out or was lost to follow-up. Blinding was successful in 98.3%. The conservative and liberal interventions reduced the median [interquartile range or IQR] fluid fasting time from 5.38 h [3.67 to 9.53 h] in the control group to 3.00 h [2.23 to 4.25 h], P  < 0.001, and 1.97 h [1.20 to 3.02 h], P  < 0.001, respectively. Both conservative and liberal intervention significantly reduced the risk of preoperative thirst compared with the control group, presented as odds ratio (OR) and 95% confidence intervals (CI); conservative intervention OR 0.41 (CI, 0.20 to 0.82), P  = 0.013; liberal intervention: OR 0.21 (CI, 0.10 to 0.43), P  < 0.001. In the liberal intervention group, postoperative thirst, OR 0.32 (CI, 0.13 to 0.75), P  = 0.009, and preoperative headache, OR 0.24 (CI, 0.07 to 0.66), P  = 0.009, were significantly reduced compared with those in the control group. No adverse events were reported.

Conclusions: The trial design proved feasible. Liberal fluid intake reduced thirst and headache. The trial was not powered to provide definitive conclusions on safety.

Trial registration: The clinical investigation plan can be accessed at ClinicalTrials.gov identifier NCT06253052. Deidentified individual participant data, the data dictionary, and statistical code can be accessed upon reasonable request from the corresponding author.

背景:液体禁食时间经常超过目前推荐的时间,导致患者不适。目的:探讨三种术前空腹方案在低误吸风险患者中的可行性,为未来的大规模试验做准备,特别关注以患者为中心的益处。设计:前瞻性、随机、对照、先导试验。环境:二级保健;德国唯一的学术中心。患者:174例低误吸风险的成人外科患者。干预:患者被随机分为“对照组”(常规护理,2小时禁食方案),“保守干预”(患者在坚持2小时禁食方案方面得到帮助)或“自由干预”(患者在被叫到手术室之前可以喝水)。主要结果测量:评估试点过程终点和绩效终点。主要结局是麻醉诱导前患者报告的口渴,分为无、中度和重度。结果:无患者中途退出或失访。盲法成功率为98.3%。保守和自由干预使对照组的中位[四分位数间距或IQR]空腹时间从5.38 h [3.67 ~ 9.53 h]减少到3.00 h [2.23 ~ 4.25 h]。大量饮水减少口渴和头痛。该试验未能提供关于安全性的明确结论。试验注册:临床研究计划可在ClinicalTrials.gov网站上访问,识别码为NCT06253052。根据通信作者的合理要求,可以访问已识别的个人参与者数据、数据字典和统计代码。
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引用次数: 0
Generation Z versus generative artificial intelligence: a cross-sectional study assessing medical students' confidence and over-reliance on artificial intelligence in perioperative clinical scenarios. Z世代与生成式人工智能:一项评估医学生在围手术期临床场景中对人工智能的信心和过度依赖的横断面研究
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-09-17 DOI: 10.1097/EJA.0000000000002282
Sarah Saxena, Marc Nkana Tsobgnie, Roberta Südy, Mia Gisselbaek, Jerome R Lechien, Michele Carella, Pierre Luigi Ingrassia, Peter Dieckmann, Joana Berger-Estilita
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引用次数: 0
Addition of metamizole to paracetamol at home after painful ambulatory arthroscopic shoulder surgery: A double-blind randomised controlled superiority trial. 疼痛的关节镜肩关节手术后,在家中对乙酰氨基酚中加入安咪唑:一项双盲随机对照优势试验。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-11-18 DOI: 10.1097/EJA.0000000000002318
Björn Stessel, Niels Mulkers, Ina Callebaut, Jeroen Vandenbrande, Cedric Vanderstappen, Stefan Evers, Kristof Nijs, Elke De Troy, Martijn Droogmans, Anneleen Neuts, Jasperina Dubois, Marc Van de Velde
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引用次数: 0
The effect of high-flow nasal oxygen on gastric volume: A prospective MRI study in awake volunteers. 高流量鼻吸氧对胃容量的影响:一项清醒志愿者的前瞻性MRI研究。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-11-20 DOI: 10.1097/EJA.0000000000002316
Benjamin Javillier, Thomas Knapen, Guillaume Henrard, Flavien Grandjean, Romain Gillard, Paul Meunier, Vincent Bonhomme, Eric Deflandre
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引用次数: 0
In response: Delayed adoption of ultrasound guidance for resiting of failed epidurals and placement of CSE and DPE. 回应:延迟采用超声引导抵制硬膜外失败和放置CSE和DPE。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2026-02-04 DOI: 10.1097/EJA.0000000000002288
Nicolas Brogly, Emilia Guasch, Alexander Ioscovich
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引用次数: 0
Glasgow coma scale score before prehospital tracheal intubation in trauma vs. nontrauma patients: A multicentre retrospective observational study. 创伤与非创伤患者院前气管插管前格拉斯哥昏迷评分:一项多中心回顾性观察研究
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-08-22 DOI: 10.1097/EJA.0000000000002263
Urs Pietsch, Benedick Satari, Julian Klug, Pedro David Wendel-Garcia, Martin Müller, Lea Weber, Roland Albrecht, Robert Greif, Alexander Fuchs

Background: Prehospital tracheal intubation intends to provide respiratory support and protect the airway from possible pulmonary aspiration. Trauma guidelines recommend tracheal intubation in patients with a Glasgow Coma Scale (GCS) score of <9.

Objectives: We hypothesised that in clinical practice, GCS scores before prehospital tracheal intubation are lower in trauma and medical patients.

Design: Retrospective observational cohort study.

Setting: Swiss anaesthetist-staffed helicopter emergency medical system between 07 September 2020 and 11 December 2023.

Patients: Intubated trauma and nontrauma patients ≥18 years and nonintubated patients with GCS <9 admitted to three tertiary referral Swiss hospitals.

Interventions: Prehospital tracheal intubation.

Main outcome measures: GCS score before prehospital tracheal intubation. Association of GCS score before prehospital tracheal intubation with length of ventilator days, intensive care unit stay, hospitalisation, and 28-day survival.

Results: We screened 35 021 missions, of which 401 (335 intubated vs. 66 nonintubated) met inclusion criteria. The median GCS before prehospital tracheal intubation was 4 [IQR 3 to 6] for nontrauma and 6 [3 to 8] for trauma patients. Trauma patients with burns had a GCS score of 14 [13 to 15] before prehospital tracheal intubation. In the trauma cohort, women had a median GCS score of 5 [3 to 7] compared to men with 6 [3 to 8] ( P  = 0.043). The GCS before prehospital tracheal intubation was associated with length of intensive care unit stay ( P  = 0.042) and survival ( P  = 0.036) but not with length of ventilation and hospital stay.

Conclusions: Overall median GCS score before prehospital tracheal intubation was lower than 8. Our data suggests that the GCS score is not suitable as the sole indicator for prehospital tracheal intubation. Further randomised controlled trials should investigate more robust intubation criteria to be included in the guidelines for trauma and nontrauma patients. Finally, a patient-centred approach should be emphasised, especially in patients with burns.

院前气管插管旨在提供呼吸支持和保护气道免受可能的肺误吸。创伤指南推荐对格拉斯哥昏迷量表(GCS)评分为:目的:我们假设在临床实践中,创伤和内科患者院前气管插管前的GCS评分较低。设计:回顾性观察队列研究。背景:2020年9月7日至2023年12月11日期间,配备麻醉师的瑞士直升机紧急医疗系统。患者:≥18岁的创伤和非创伤患者以及非插管GCS患者。干预措施:院前气管插管。主要观察指标:院前气管插管前GCS评分。院前气管插管前GCS评分与呼吸机天数、重症监护病房住院时间、住院时间和28天生存期的关系结果:我们筛选了35 021个任务,其中401个(335个插管对66个非插管)符合纳入标准。非外伤患者院前气管插管前GCS中位数为4 [IQR 3 ~ 6],外伤患者为6[3 ~ 8]。创伤合并烧伤患者院前气管插管前GCS评分为14[13 ~ 15]。在创伤组中,女性的中位GCS评分为5[3 ~ 7],而男性为6 [3 ~ 8](P = 0.043)。院前气管插管前GCS与重症监护病房住院时间(P = 0.042)和生存时间(P = 0.036)相关,但与通气时间和住院时间无关。结论:院前气管插管前GCS评分中位数低于8分。我们的数据表明,GCS评分不适合作为院前气管插管的唯一指标。进一步的随机对照试验应该研究更可靠的插管标准,以纳入创伤和非创伤患者的指南。最后,应强调以患者为中心的方法,特别是对烧伤患者。试验注册:无。
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引用次数: 0
Reversal is not enough: fixed-dose sugammadex may fail in elderly patients without postoperative monitoring. 仅仅逆转是不够的:在没有术后监测的老年患者中,固定剂量的sugammadex可能失效。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2026-02-04 DOI: 10.1097/EJA.0000000000002287
Hua Chen, Fu-Lan Chuang, Chen-Hua Wen, Ming-Hui Hung
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引用次数: 0
Methodology series of ESAIC guidelines: standards in guidelines production. ESAIC指南方法论系列:指南制作中的标准。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-12-23 DOI: 10.1097/EJA.0000000000002341
Ignacio Neumann, Arash Afshari, Roberta Sudy, Marc Van de Velde, Sophie Debouche, Pierre Harlet, Peter Kranke, Idit Matot, Wolfgang Buhre, Carolina S Romero

Over the past decade, clinical guideline development has undergone significant advancements, with an increased focus on rigour, transparency and stakeholder engagement. In this study, the first in a series of four articles, the European Society of Anaesthesiology and Intensive Care (ESAIC) outlines key principles that guide the development of high-quality guidelines within ESAIC. Starting in 2025, ESAIC will progressively adopt the GRADE approach to enhance the quality and applicability of its guidelines. Core methodological principles include the use of systematic reviews, a multidisciplinary development process, conflict-of-interest management, a transparent link between evidence and recommendations, and ensuring that recommendations are specific and actionable. This study provides an overview of the roles and processes involved in guideline production and details the transition of ESAIC from its traditional grading systems to the updated GRADE standards. Strong recommendations indicate that one option offers a clear net benefit and should be implemented with all or nearly all patients. In contrast, conditional recommendations reflect uncertainty in the balance between benefits and harms, emphasising the need for careful consideration of clinical contexts and patient values. Although specific methodological decisions may vary, the principles outlined here provide a foundation for rigorous, evidence-based guideline development within ESAIC.

在过去的十年中,临床指南的制定经历了重大进展,更加注重严谨性、透明度和利益相关者的参与。本研究是四篇系列文章中的第一篇,欧洲麻醉与重症监护学会(ESAIC)概述了指导ESAIC内部制定高质量指南的关键原则。从2025年开始,ESAIC将逐步采用GRADE方法,以提高其指南的质量和适用性。核心方法原则包括使用系统审查、多学科开发过程、利益冲突管理、证据和建议之间的透明联系,以及确保建议是具体和可操作的。本研究概述了指南制定过程中所涉及的角色和过程,并详细介绍了ESAIC从传统分级系统向更新后的GRADE标准的过渡。强烈的建议表明,一种选择提供了明确的净收益,应在所有或几乎所有患者中实施。相反,有条件的建议反映了利弊平衡的不确定性,强调需要仔细考虑临床情况和患者价值。虽然具体的方法决定可能会有所不同,但这里概述的原则为在ESAIC内部制定严格的、基于证据的指南奠定了基础。
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引用次数: 0
Postoperative hypotension in patients recovering from noncardiac surgery. 非心脏手术恢复期患者的术后低血压。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2026-02-04 DOI: 10.1097/EJA.0000000000002310
Cheng Chu, Yu Chang
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引用次数: 0
Congenital insensitivity to pain with anhidrosis: a case report. 先天性无汗性疼痛不敏感1例。
IF 6.8 2区 医学 Q1 ANESTHESIOLOGY Pub Date : 2026-03-01 Epub Date: 2025-12-29 DOI: 10.1097/EJA.0000000000002324
Natalie Lenggenhager-Krakoski, Anne Coakley, Hassan Murtaza, Brian O'Brien

Although it is very rare, the syndrome of Congenital Insensitivity to Pain with Anhidrosis (CIPA) should be known to anaesthetic practitioners due to its perioperative implications. We report the first case of this in the British Isles, in a 5-year-old girl, whose osteomyelitis required surgical intervention. The genetics, the cellular basis and pathophysiology of the condition are outlined, and the relevance of analgesia in this challenging setting is considered in this report.

虽然它是非常罕见的,先天性无汗性疼痛不敏感综合征(CIPA)应该知道麻醉从业人员由于其围手术期的影响。我们报告的第一例这种情况下,在不列颠群岛,在一个5岁的女孩,骨髓炎需要手术干预。遗传学,细胞基础和病理生理条件概述,并在这一具有挑战性的设置镇痛的相关性考虑在本报告。
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引用次数: 0
期刊
European Journal of Anaesthesiology
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