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Journal of Anesthesia, Analgesia and Critical Care (Online)最新文献

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To B or not to B-lines. 要不要 B 线
Pub Date : 2024-09-05 DOI: 10.1186/s44158-024-00196-w
Filipe André Gonzalez, Jacobo Bacariza, Joao Leote
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引用次数: 0
Radiofrequency stimulation of the dorsal root ganglion as a diagnostic tool for radicular pain syndromes: six representative cases. 射频刺激背根神经节作为根性疼痛综合征的诊断工具:六个代表性病例。
Pub Date : 2024-09-03 DOI: 10.1186/s44158-024-00194-y
Laura Demartini, David Michael Abbott, Cesare Bonezzi, Silvia Natoli

Background: We discuss the diagnostic benefit of pulsed radiofrequency (PRF) of the dorsal root ganglion (DRG) in a case series of patients with different pathologies. We expand the diagnostic potential of DRG stimulation beyond paresthesia mapping by using DRG stimulation to help determine the role of the DRG in the patient's pain and narrow down the etiology. In some cases, DRG stimulation was also part of the treatment plan.

Methods: Six patients underwent DRG radiofrequency as a diagnostic/therapeutic step before considering implantation of a DRG neurostimulator. First, patients underwent a basic bedside neurological evaluation. Next, an electrode was placed in the epidural space through the sacral hiatus or between vertebral laminae. Then, sensory stimulation was applied at 50 Hz and gradually increased from 0.1 V until the patient reported paresthesia or until a maximum intensity of 2 V was reached. Patients were asked to describe where the stimulation was felt and outline the anatomical area the paresthesia covered. Then a motor stimulation was applied at 2 Hz until muscle twitching was reported by the patient or observed by the physician.

Results: The information obtained helped diagnose the type of lesion as principally preganglionic, ganglionic, or postganglionic. This information guided patient management.

Conclusion: PRF of the DRG can provide valuable diagnostic information and is a useful step before ganglionic electrode implantation. In all cases, PRF of the DRG provided valuable diagnostic information and guided management options.

背景:我们讨论了脉冲射频(PRF)对背根神经节(DRG)的诊断作用,并对不同病因的患者进行了病例系列分析。通过使用 DRG 刺激来帮助确定 DRG 在患者疼痛中的作用并缩小病因范围,我们将 DRG 刺激的诊断潜力扩展到了痛觉测绘之外。在某些病例中,DRG 刺激也是治疗方案的一部分:六名患者在考虑植入 DRG 神经刺激器之前接受了 DRG 射频治疗,作为诊断/治疗步骤。首先,患者接受了基本的床边神经评估。然后,通过骶骨裂孔或椎骨板之间将电极放置在硬膜外腔。然后,以 50 Hz 的频率施加感觉刺激,刺激强度从 0.1 V 开始逐渐增加,直到患者出现麻痹感或达到 2 V 的最大强度。要求患者描述感觉到刺激的部位,并概述麻痹所覆盖的解剖区域。然后以 2 Hz 的频率进行运动刺激,直到患者报告或医生观察到肌肉抽搐为止:结果:获得的信息有助于诊断病变类型,主要是节前性、节段性或节段后性。这些信息为患者管理提供了指导:结论:DRG 的 PRF 可以提供有价值的诊断信息,是神经节电极植入前的一个有用步骤。在所有病例中,DRG PRF 都能提供有价值的诊断信息并指导治疗方案。
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引用次数: 0
Airway management and ventilation techniques in resuscitation during advanced life support: an update. 高级生命支持复苏中的气道管理和通气技术:最新进展。
Pub Date : 2024-08-24 DOI: 10.1186/s44158-024-00195-x
Clemens Kill, Randi Katrin Manegold, David Fistera, Joachim Risse

For many years, ventilation has been an essential part of advanced life support (ALS) in cardiopulmonary resuscitation (CPR). Nevertheless, there is little evidence about the best method of ventilation during resuscitation for both out-of-hospital cardiac arrest (OHCA) and inhospital cardiac arrest (IHCA) patients. Effective ventilation is one of the two main keys to successful resuscitation. In this context, the question always arises as to which airway management, along with which ventilation mode, constitutes the best strategy. Conventional ventilation modes are not designed for cardiac arrest and show important limitations that must be considered when used in CPR. Manual ventilation without the use of an automated transport ventilator (ATV) could be shown to be uncontrolled in applied volumes and pressures and should be avoided. Mechanical ventilation with an ATV is therefore superior to manual ventilation, but both volume- and pressure-controlled ventilation modes are significantly influenced by chest compressions. With the newly designed chest compression synchronized ventilation (CCSV), a special ventilation mode for resuscitation is available. Further research should be conducted to obtain more evidence of the effect of ventilation during CPR on outcomes following OHCA and not only about how to secure the airway for ventilation during CPR.

多年来,通气一直是心肺复苏 (CPR) 高级生命支持 (ALS) 的重要组成部分。然而,关于院外心脏骤停 (OHCA) 和院内心脏骤停 (IHCA) 患者复苏期间最佳通气方法的证据却很少。有效通气是复苏成功的两大关键之一。在这种情况下,问题就在于哪种气道管理方式和哪种通气模式才是最佳策略。传统的通气模式并非为心脏骤停而设计,在心肺复苏中使用时必须考虑到其重要的局限性。在不使用自动转运呼吸机(ATV)的情况下进行手动通气可能会导致通气量和压力失控,因此应避免使用。因此,使用 ATV 进行机械通气优于手动通气,但容量和压力控制的通气模式都会受到胸外按压的显著影响。新设计的胸外按压同步通气(CCSV)为复苏提供了一种特殊的通气模式。应开展进一步研究,以获得更多关于心肺复苏期间通气对 OHCA 后果影响的证据,而不仅仅是如何在心肺复苏期间确保通气的气道。
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引用次数: 0
Nociception level index variations in ICU: curarized vs non-curarized patients - a pilot study. 重症监护室中的痛觉水平指数变化:接受治疗与未接受治疗的患者--一项试点研究。
Pub Date : 2024-08-20 DOI: 10.1186/s44158-024-00193-z
Emilio Bonvecchio, Davide Vailati, Federica Della Mura, Giovanni Marino

Purpose: Pain is a major physiological stressor that can worsen critical medical conditions in many ways. Currently, there is no reliable monitoring tool which is available for pain monitoring in the deeply sedated ± curarized critically ill patients. This study aims to assess the effectiveness of the multiparameter nociception index (NOL®) in the critical care setting. We compared NOL with traditionally used neurovegetative signs and examined its correlation with sedation depth measured by bispectral index (BIS®) electroencephalographic (EEG) monitoring.

Methods: This retrospective monocentric cohort study was conducted in a general intensive care unit, including patients who required moderate-to-deep levels of sedation with or without continuous neuromuscular blockade. The performance of NOL was evaluated both in the entire studied population, as well as in two subgroups: curarized and non-curarized patients.

Results: NOL demonstrated greater accuracy than all other indicators in pain detection in the overall population. In the non-curare subgroup, all indices correctly recognized painful stimulation, while in the patients subjected to neuromuscular blocking agent's infusion, only NOL properly identified nociception. In the former group, EEG's relation to nociception was on the border of statistical significance, whereas in the latter BIS showed no correlation with NOL.

Conclusion: NOL emerges as a promising device for pain assessment in the critical care setting and exhibits its best performance precisely in the clinical context where reliable pain assessment methods are most lacking. Furthermore, our research confirms the distinction between sedation and analgesia, highlighting the necessity for distinct monitoring instruments to accurately assess them.

目的:疼痛是一种主要的生理应激源,会以多种方式加重危重病人的病情。目前,还没有可靠的监测工具可用于监测深度镇静±静注的重症患者的疼痛。本研究旨在评估多参数痛觉指数(NOL®)在重症监护环境中的有效性。我们将 NOL 与传统使用的神经瘫痪体征进行了比较,并研究了其与通过双谱指数 (BIS®) 脑电图 (EEG) 监测测量的镇静深度的相关性:这项回顾性单中心队列研究是在普通重症监护病房进行的,包括需要中度至深度镇静并使用或不使用持续神经肌肉阻滞的患者。NOL 的性能在整个研究人群以及两个亚组(使用镇静剂和未使用镇静剂的患者)中进行了评估:结果显示:在整个研究人群中,NOL 在疼痛检测方面的准确性高于所有其他指标。在非卷曲亚组中,所有指标都能正确识别疼痛刺激,而在输注神经肌肉阻断剂的患者中,只有 NOL 能正确识别痛觉。在前一组患者中,脑电图与痛觉的关系接近统计学意义,而在后一组患者中,BIS 与 NOL 没有相关性:结论:NOL 是重症监护环境中一种很有前景的疼痛评估设备,在最缺乏可靠疼痛评估方法的临床环境中表现出最佳性能。此外,我们的研究还证实了镇静与镇痛之间的区别,强调有必要使用不同的监测仪器来准确评估镇静与镇痛。
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引用次数: 0
The use of angiotensin II for the management of distributive shock: expert consensus statements. 使用血管紧张素 II 治疗分布性休克:专家共识声明。
Pub Date : 2024-08-16 DOI: 10.1186/s44158-024-00186-y
Giovanni Landoni, Andrea Cortegiani, Elena Bignami, Gennaro De Pascale, Katia Donadello, Abele Donati, Giacomo Grasselli, Fabio Guarracino, Gianpaola Monti, Gianluca Paternoster, Luigi Tritapepe, Massimo Girardis

Background: Despite the growing body of evidence supporting the use of angiotensin II (ATII) in distributive shock, its integration into existing treatment algorithms requires careful consideration of factors related to patient comorbidities, hemodynamic parameters, cost-effectiveness, and risk-benefit balance. Moreover, several questions regarding its use in clinical practice warrant further investigations. To address these challenges, a group of Italian intensive care specialists (the panel) developed a consensus process using a modified Delphi technique.

Methods: The panel defined five clinical questions during an online scoping workshop and then provided a short list of statements related to each clinical question based on literature review and clinical experience. A total of 20 statements were collected. Two coordinators screened and selected the final list of statements to be included in the online survey, which consisted of 17 statements. The consensus was reached when ≥ 75% of respondents assigned a score within the 3-point range of 1-3 (disagreement) or 7-9 (agreement).

Results: Overall, a consensus on agreement was reached on 13 statements defining the existing gaps in scientific evidence, the possibility of evaluating the addition of drugs with different mechanisms of action for the treatment of refractory shock, the utility of ATII in reducing the catecholamine requirements in the treatment of vasopressor-resistant septic shock, and the effectiveness of ATII in treating patients in whom angiotensin-converting enzyme activity is reduced or pharmacologically blocked. It was widely shared that renin concentration can be used to identify patients who most likely benefit from ATII to restore vascular tone. Thus, the patients who might benefit most from using ATII were defined. Lastly, some potential barriers to the use of ATII were described.

Conclusions: ATII was recognized as a useful treatment to reduce catecholamine requirements in treating vasopressor-resistant septic shock. At the same time, the need for additional clinical trials to further elucidate the efficacy and safety of ATII, as well as investigations into potential mechanisms of action and optimization of treatment protocols in patients with refractory distributive shock, emerged.

背景:尽管越来越多的证据支持在分布性休克中使用血管紧张素 II (ATII),但将其纳入现有的治疗算法需要仔细考虑与患者合并症、血液动力学参数、成本效益和风险-效益平衡相关的因素。此外,有关其在临床实践中应用的几个问题也需要进一步研究。为了应对这些挑战,一个由意大利重症监护专家组成的小组(小组)采用改良的德尔菲技术达成了共识:方法:专家小组在一次在线范围界定研讨会上确定了五个临床问题,然后根据文献综述和临床经验提供了与每个临床问题相关的简短声明列表。共收集到 20 条陈述。两位协调人筛选并选出了将纳入在线调查的最终陈述列表,其中包括 17 项陈述。当≥75%的受访者在1-3分(不同意)或7-9分(同意)的3分范围内打分时,即达成共识:总体而言,13 项声明达成了共识,这些声明界定了现有科学证据的不足、评估添加不同作用机制的药物治疗难治性休克的可能性、ATII 在治疗血管加压耐药脓毒性休克时减少儿茶酚胺需求的效用,以及 ATII 在治疗血管紧张素转换酶活性降低或药物阻断的患者时的有效性。人们普遍认为,肾素浓度可用于确定哪些患者最有可能从 ATII 中获益,以恢复血管张力。因此,可以确定哪些患者最有可能从使用 ATII 中获益。最后,还介绍了使用 ATII 的一些潜在障碍:ATII被认为是治疗血管加压耐药脓毒性休克时减少儿茶酚胺需求的有效疗法。结论:ATⅡ被认为是治疗血管加压耐药脓毒性休克时减少儿茶酚胺需求的有效疗法,同时,需要进行更多的临床试验,以进一步阐明ATⅡ的疗效和安全性,研究其潜在的作用机制,并优化难治性分布性休克患者的治疗方案。
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引用次数: 0
VV-ECMO in critical COVID-19 obese patients: a cohort study. 危重 COVID-19 肥胖症患者的 VV-ECMO:一项队列研究。
Pub Date : 2024-08-13 DOI: 10.1186/s44158-024-00191-1
Joana Nogueira, Ricardo Freitas, José Eduardo Sousa, Luís Linhares Santos

Background: Obesity causes significant difficulties in successful extracorporeal membrane oxygenation (ECMO) support and may interfere with patient outcomes. During the COVID-19 pandemic, we experienced an increased number of obese patients supported with ECMO in our intensive care unit due to severe illness in this population.

Methods: We designed a single-center retrospective study to identify prognostic factors for 180-day survival in obese critical COVID-19 patients receiving venovenous ECMO (VV-ECMO). We included adult critical COVID-19 patients on VV-ECMO, who were obese and overweight (according to the World Health Organization) and admitted to a tertiary hospital's intensive care unit from April 1, 2020, to May 31, 2022. Univariate logistic regression analysis was performed to assess differences in 180-day mortality.

Results: Forty-one patients were included. The median age was 55 (IQR 45-60) years, and 70.7% of the patients were male. The median body mass index (BMI) was 36 (IQR 31-42.5) kg/m2; 39% of patients had a BMI ≥ 40 kg/m2. The participants had 3 (IQR 1.5-4) days of mechanical ventilation prior to ECMO, and 63.4% were weaned from VV-ECMO support after a median of 19 (IQR 10-34) days. The median ICU length of stay was 31.9 (IQR 17.5-44.5) days. The duration of mechanical ventilation was 30 (IQR 19-49.5) days. The 180-day mortality rate was 41.5%. Univariate logistic regression analysis revealed that a higher BMI was associated with greater 180-day survival (OR 1.157 [1.038-1.291], p = 0.009). Younger age, female sex, less invasive ventilation time before ECMO, and fewer complications at the time of ECMO cannulation were associated with greater 180-day survival [OR 0.858 (0.774-0.953), p 0.004; OR 0.074 (0.008-0.650), p 0.019; OR 0.612 (0.401-0.933), p 0.022; OR 0.13 (0.03-0.740), p 0.022), respectively].

Conclusion: In this retrospective cohort of critical COVID-19 obese adult patients supported by VV-ECMO, a higher BMI, younger age, and female sex were associated with greater 180-day survival. A shorter invasive ventilation time before ECMO and fewer complications at ECMO cannulation were also associated with increased survival.

背景:肥胖给成功的体外膜氧合(ECMO)支持带来了巨大困难,并可能影响患者的预后。在 COVID-19 大流行期间,由于肥胖患者病情严重,我们的重症监护病房接受 ECMO 支持的肥胖患者人数有所增加:我们设计了一项单中心回顾性研究,以确定接受静脉 ECMO(VV-ECMO)治疗的 COVID-19 重症肥胖患者 180 天存活率的预后因素。我们纳入了 2020 年 4 月 1 日至 2022 年 5 月 31 日期间在一家三级医院重症监护病房住院的肥胖和超重(根据世界卫生组织的标准)COVID-19 重症成人患者。对这些患者进行了单变量逻辑回归分析,以评估180天死亡率的差异:结果:共纳入 41 名患者。中位年龄为 55 岁(IQR 45-60 岁),70.7% 的患者为男性。体重指数(BMI)中位数为 36(IQR 31-42.5)kg/m2;39% 的患者体重指数≥ 40 kg/m2。参与者在接受 ECMO 之前接受了 3 天(IQR 1.5-4 天)的机械通气,63.4% 的患者在接受 VV-ECMO 支持中位数 19 天(IQR 10-34 天)后断奶。重症监护室的中位住院时间为 31.9 天(IQR 17.5-44.5 天)。机械通气时间为 30 天(IQR 19-49.5)。180 天的死亡率为 41.5%。单变量逻辑回归分析显示,体重指数越高,180 天存活率越高(OR 1.157 [1.038-1.291],P = 0.009)。年龄较小、性别为女性、ECMO 前侵入性通气时间较短、ECMO 插管时并发症较少与 180 天存活率较高相关[分别为 OR 0.858 (0.774-0.953),P 0.004;OR 0.074 (0.008-0.650),P 0.019;OR 0.612 (0.401-0.933),P 0.022;OR 0.13 (0.03-0.740),P 0.022]:结论:在这组由 VV-ECMO 支持的 COVID-19 重症肥胖成年患者的回顾性队列中,体重指数越高、年龄越小、性别为女性的患者 180 天存活率越高。ECMO 前侵入性通气时间较短以及 ECMO 插管时并发症较少也与存活率提高有关。
{"title":"VV-ECMO in critical COVID-19 obese patients: a cohort study.","authors":"Joana Nogueira, Ricardo Freitas, José Eduardo Sousa, Luís Linhares Santos","doi":"10.1186/s44158-024-00191-1","DOIUrl":"10.1186/s44158-024-00191-1","url":null,"abstract":"<p><strong>Background: </strong>Obesity causes significant difficulties in successful extracorporeal membrane oxygenation (ECMO) support and may interfere with patient outcomes. During the COVID-19 pandemic, we experienced an increased number of obese patients supported with ECMO in our intensive care unit due to severe illness in this population.</p><p><strong>Methods: </strong>We designed a single-center retrospective study to identify prognostic factors for 180-day survival in obese critical COVID-19 patients receiving venovenous ECMO (VV-ECMO). We included adult critical COVID-19 patients on VV-ECMO, who were obese and overweight (according to the World Health Organization) and admitted to a tertiary hospital's intensive care unit from April 1, 2020, to May 31, 2022. Univariate logistic regression analysis was performed to assess differences in 180-day mortality.</p><p><strong>Results: </strong>Forty-one patients were included. The median age was 55 (IQR 45-60) years, and 70.7% of the patients were male. The median body mass index (BMI) was 36 (IQR 31-42.5) kg/m<sup>2</sup>; 39% of patients had a BMI ≥ 40 kg/m<sup>2</sup>. The participants had 3 (IQR 1.5-4) days of mechanical ventilation prior to ECMO, and 63.4% were weaned from VV-ECMO support after a median of 19 (IQR 10-34) days. The median ICU length of stay was 31.9 (IQR 17.5-44.5) days. The duration of mechanical ventilation was 30 (IQR 19-49.5) days. The 180-day mortality rate was 41.5%. Univariate logistic regression analysis revealed that a higher BMI was associated with greater 180-day survival (OR 1.157 [1.038-1.291], p = 0.009). Younger age, female sex, less invasive ventilation time before ECMO, and fewer complications at the time of ECMO cannulation were associated with greater 180-day survival [OR 0.858 (0.774-0.953), p 0.004; OR 0.074 (0.008-0.650), p 0.019; OR 0.612 (0.401-0.933), p 0.022; OR 0.13 (0.03-0.740), p 0.022), respectively].</p><p><strong>Conclusion: </strong>In this retrospective cohort of critical COVID-19 obese adult patients supported by VV-ECMO, a higher BMI, younger age, and female sex were associated with greater 180-day survival. A shorter invasive ventilation time before ECMO and fewer complications at ECMO cannulation were also associated with increased survival.</p>","PeriodicalId":73597,"journal":{"name":"Journal of Anesthesia, Analgesia and Critical Care (Online)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11320846/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141972415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anesthesiologists ultrasound-guided regional anesthesia core curriculum: a Delphi consensus from Italian regional anesthesia experts. 麻醉医师超声引导区域麻醉核心课程:意大利区域麻醉专家达成的德尔菲共识。
Pub Date : 2024-08-10 DOI: 10.1186/s44158-024-00190-2
Alessandro De Cassai, Astrid Behr, Dario Bugada, Danilo Canzio, Gianluca Capelleri, Fabio Costa, Giorgio Danelli, Grazia De Angelis, Romualdo Del Buono, Fabrizio Fattorini, Pierfrancesco Fusco, Fabio Gori, Alberto Manassero, Ilaria Pacini, Giuseppe Pascarella, Mauro Proietti Pannunzi, Gianluca Russo, Raffaele Russo, Domenico Pietro Santonastaso, Marco Scardino, Giuseppe Sepolvere, Paolo Scimia, Alessandro Strumia, Mario Tedesco, Andrea Tognù, Vito Torrano

Introduction: The need for a standardized core curriculum in regional anesthesia has become essential, particularly with the integration of ultrasound revolutionizing and exponentially increasing clinical practice and possibilities. In fact, numerous novel techniques, often overlapping, can confuse practitioners. This study aims to establish a core curriculum for upper limb, lower limb, paraspinal and fascial plane blocks for residency training, addressing potential educational gaps caused by the multitude of techniques, through a Delphi consensus process involving recognized Italian regional anesthesia experts.

Methods: A steering committee was formed in order to select a panel of experts in regional anesthesia. A three-round Delphi consensus was planned: two rounds of electronic voting and a final round of mixed electronic voting and round table discussion. The consensus was defined as ≥ 75% agreement for inclusion and lower than ≤ 25% agreement for exclusion from the core curriculum list. Techniques reaching the 50% threshold were included with low consensus.

Results: Twenty-nine techniques were selected to be included in the ultrasound-guided regional anesthesia core curriculum. Twenty-two were included with strong consensus: Upper limb: interscalene brachial plexus block, supraclavicular brachial plexus block, infraclavicular brachial plexus block, axillary brachial plexus block, intermediate cervical plexus block Lower limb: femoral nerve block, pericapsular nerve group block, adductor canal block, sciatic nerve block (transgluteal approach, infragluteal approach, and at the popliteal fossa), ankle block Paraspinal/fascial plane blocks: erector spinae plane block, deep serratus anterior plane block, superficial pectointercostal plane block, interpectoral plane block, pectoserratus plane block, rectus sheath block, ilioinguinal iliohypogastric nerves block, transversus abdominis plane block (with subcostal and midaxillary approaches) The remaining seven techniques were included with low consensus: superficial cervical plexus block, lumbar plexus block, fascia iliaca block (suprainguinal approach), anterior quadratus lumborum block, lateral quadratus lumborum block, paravertebral block, and serratus anterior plane block.

Conclusions: This curriculum aims to standardize training and ensure that residents acquire the essential skills required for effective and safe practice regardless of the residents' subsequent specialization. By incorporating these techniques, educational programs can provide a structured and consistent approach to regional anesthesia, enhancing the quality of patient care and improving outcomes.

导言:区域麻醉需要一个标准化的核心课程,这一点已变得至关重要,特别是随着超声波的融入,临床实践和可能性发生了革命性的变化并呈指数级增长。事实上,众多新技术往往相互重叠,会使从业人员无所适从。本研究旨在通过德尔菲共识程序,由公认的意大利区域麻醉专家参与,为住院医师培训建立上肢、下肢、脊柱旁和筋膜平面阻滞的核心课程,解决因技术繁多而可能造成的教育差距:方法:成立了一个指导委员会,以挑选区域麻醉专家小组。计划达成三轮德尔菲共识:两轮电子投票,最后一轮混合电子投票和圆桌讨论。共识的定义是:≥ 75% 的一致同意可纳入核心课程列表,低于 25% 的一致同意可排除在核心课程列表之外。达到50%的技术被纳入,但共识度较低:结果:29 项技术被选入超声引导区域麻醉核心课程。结果:29 项技术被选入超声引导下区域麻醉核心课程:上肢:椎间孔臂丛阻滞、锁骨上臂丛阻滞、锁骨下臂丛阻滞、腋窝臂丛阻滞、中颈丛阻滞 下肢:股神经阻滞、包膜神经群阻滞、内收肌管阻滞、坐骨神经阻滞(经臀部入路、臀下入路和腘窝处)、踝关节阻滞 副脊柱/筋膜平面阻滞:直肌鞘阻滞、髂腹股沟髂下胃神经阻滞、腹横肌平面阻滞(采用肋下和腋中入 路):颈浅丛阻滞、腰丛阻滞、髂筋膜阻滞(腹股沟上途径)、腰前区阻滞、腰侧区阻滞、椎旁阻滞和前锯肌平面阻滞。结论:该课程旨在规范培训,确保住院医师掌握有效、安全实践所需的基本技能,无论住院医师以后的专业方向如何。通过纳入这些技术,教育计划可为区域麻醉提供结构化和一致的方法,从而提高患者护理质量并改善疗效。
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引用次数: 0
Advanced statistical approaches for predicting pain after pediatric thoracotomy: a cross-sectional study using zero-inflated and Poisson models. 预测小儿胸廓切开术后疼痛的先进统计方法:使用零膨胀和泊松模型的横断面研究。
Pub Date : 2024-08-05 DOI: 10.1186/s44158-024-00188-w
Alessandro Vittori, Marco Cascella, Piergiacomo Di Gennaro, Giuliano Marchetti, Elisa Francia, Ilaria Mascilini, Riccardo Tarquini, Massimo Antonio Innamorato, Emiliano Petrucci, Franco Marinangeli, Sergio Coluccia, Sergio Giuseppe Picardo

Background: Thoracotomy is one of the surgical procedures most burdened by chronic post-operative pain. There is poor evidence regarding the possibility that even in pediatric patients, thoracotomy can be followed by post-operative pain. The primary objective of this analysis is to identify associations with home pain therapy, pain intensity, and possible protective factors acting on chronic pain in this population.

Methods: A retrospective cross-sectional study was conducted at Ospedale Pediatrico Bambino Gesù IRCCS. The study included pediatric patients undergoing thoracotomy. For statistical analyses, a logistic model and a zero-inflated strategy were implemented to explore associations and predict factors related to home-based analgesic therapy and pain intensity.

Results: Gender and age were identified as significant factors in the assignment of home therapy, with males having over seven times the risk compared to females (OR = 7.06, 95% CI = [2.11, 29.7]). At the last measurement, pain intensity was positively associated with age and the number of pain events during the week.

Conclusions: The study highlights significant factors influencing post-thoracotomy pain management in pediatric patients. These findings underscore the importance of tailored pain management strategies that consider gender and age to improve post-operative care and outcomes in pediatric thoracotomy patients.

背景:胸廓切开术是术后慢性疼痛负担最重的外科手术之一。即使是小儿患者,胸廓切开术后也可能出现术后疼痛,但这方面的证据不足。本分析的主要目的是确定该人群与家庭疼痛治疗、疼痛强度以及可能的慢性疼痛保护因素之间的关系:一项回顾性横断面研究在 Ospedale Pediatrico Bambino Gesù IRCCS 进行。研究对象包括接受开胸手术的儿科患者。为了进行统计分析,研究人员采用了逻辑模型和零膨胀策略来探究和预测与家庭镇痛疗法和疼痛强度相关的因素:结果:性别和年龄是影响居家治疗的重要因素,男性的风险是女性的七倍多(OR = 7.06,95% CI = [2.11,29.7])。在最后一次测量中,疼痛强度与年龄和一周内疼痛事件的次数呈正相关:本研究强调了影响儿童患者胸廓切开术后疼痛治疗的重要因素。这些发现强调了考虑性别和年龄的定制疼痛管理策略对改善小儿胸廓切开术患者术后护理和预后的重要性。
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引用次数: 0
Influence of aging on opioid dosing for perioperative pain management: a focus on pharmacokinetics. 老龄化对围术期疼痛治疗中阿片类药物剂量的影响:关注药物动力学。
Pub Date : 2024-08-01 DOI: 10.1186/s44158-024-00182-2
Sebastiano Mercadante

The older population continues to grow in all countries, and surgeons are encountering older patients more frequently. The management of postoperative pain in older patients can be a difficult task. Opioids are the mainstay of perioperative pain control. This paper assesses some pharmacokinetic age-related aspects and their relationship with the use of opioids in the perioperative period. Changes in body composition and organ function, and pharmacokinetics in older patients, as well as characteristics of opioids commonly used in the perioperative period are described. Specific problems, dose titration, and patient-controlled analgesia in the elderly are also reviewed. Opioids can be safety used in perioperative period, even in the elderly. The choice of drugs and doses can be individualized according to the surgery, opioid pharmacokinetics, comorbidities, and routes of administration.

所有国家的老年人口都在持续增长,外科医生也越来越频繁地遇到老年患者。处理老年患者的术后疼痛是一项艰巨的任务。阿片类药物是围手术期疼痛控制的主要药物。本文评估了一些与年龄有关的药代动力学方面及其与围手术期阿片类药物使用的关系。本文介绍了老年患者身体成分和器官功能的变化、药代动力学以及围手术期常用阿片类药物的特点。此外,还对老年人的具体问题、剂量滴定和患者自控镇痛进行了综述。阿片类药物可以安全地用于围手术期,即使是老年人。可根据手术、阿片类药物的药代动力学、合并症和给药途径来个性化选择药物和剂量。
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引用次数: 0
Correction: Anesthetic approach to pregnant patients with malaria: a narrative review of the literature. 更正:疟疾孕妇的麻醉方法:文献综述。
Pub Date : 2024-08-01 DOI: 10.1186/s44158-024-00189-9
Itay Zahavi, Meir Fons, Michal Meir, Mark Volevich, Emilia Guasch, Mark Nunnally, Sharon Einav
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Journal of Anesthesia, Analgesia and Critical Care (Online)
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