pediatric anesthesia

小儿麻醉
  • 文章类型: Journal Article
    人工智能是一种不断发展的方式,彻底改变了医学科学领域。它利用各种计算模型和算法,并在医疗保健的不同部门提供帮助。这里,在这次范围审查中,我们正在尝试评估人工智能(AI)在小儿麻醉领域的使用,特别是在更具挑战性的领域,儿科气道。AI领域中的不同组件包括机器学习,神经网络,深度学习,机器人,计算机视觉。像谷歌学者这样的电子数据库,Cochrane数据库,并搜索了Pubmed。不同的研究具有年龄组的异质性,因此,所有18岁以下儿童的研究都被纳入和评估。术前审查了AI的使用,术中,以及小儿麻醉的术后领域。AI的适用性需要通过临床判断来补充,以便在医学的各个领域进行最终预期。
    Artificial intelligence is an ever-growing modality revolutionizing the field of medical science. It utilizes various computational models and algorithms and helps out in different sectors of healthcare. Here, in this scoping review, we are trying to evaluate the use of Artificial intelligence (AI) in the field of pediatric anesthesia, specifically in the more challenging domain, the pediatric airway. Different components within the domain of AI include machine learning, neural networks, deep learning, robotics, and computer vision. Electronic databases like Google Scholar, Cochrane databases, and Pubmed were searched. Different studies had heterogeneity of age groups, so all studies with children under 18 years of age were included and assessed. The use of AI was reviewed in the preoperative, intraoperative, and postoperative domains of pediatric anesthesia. The applicability of AI needs to be supplemented by clinical judgment for the final anticipation in various fields of medicine.
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  • 文章类型: Journal Article
    背景:儿科区域麻醉是由于阿片类药物保留策略的采用逐渐增加以及对全身麻醉药对神经发育可能的不利影响的日益关注。尽管如此,在儿科人群中进行区域麻醉研究具有挑战性,并且是缺乏证据的原因.这项研究旨在回顾尸体研究的科学基础,以评估儿童的区域麻醉技术。
    方法:我们搜索了以下数据库MEDLINE,EMBASE,和WebofScience。我们纳入了评估儿童周围神经阻滞的解剖尸体研究。从研究中收集的核心数据包含在表格中,包括块类型,块评估,结果,和结论。
    结果:搜索确定了2409项研究,其中,16是对儿科人群的解剖学研究。评估的技术是竖脊肌平面块,髂腹股沟/髂腹下神经阻滞,坐骨神经阻滞,上颌神经阻滞,椎旁阻滞,股神经阻滞,桡骨神经阻滞,枕大神经阻滞,锁骨下臂丛神经阻滞,和眶下神经阻滞.
    结论:区域麻醉技术通常在儿童中进行,但是缺乏解剖学研究可能会导致对局部麻醉药的分散和吸收有所保留。对小儿区域麻醉的进一步解剖研究可以指导实践。
    BACKGROUND: Pediatric regional anesthesia has been driven by the gradual rise in the adoption of opioid-sparing strategies and the growing concern over the possible adverse effects of general anesthetics on neurodevelopment. Nonetheless, performing regional anesthesia studies in a pediatric population is challenging and accounts for the scarce evidence. This study aimed to review the scientific foundation of studies in cadavers to assess regional anesthesia techniques in children.
    METHODS: We searched the following databases MEDLINE, EMBASE, and Web of Science. We included anatomical cadaver studies assessing peripheral nerve blocks in children. The core data collected from studies were included in tables and comprised block type, block evaluation, results, and conclusion.
    RESULTS: The search identified 2409 studies, of which, 16 were anatomical studies on the pediatric population. The techniques evaluated were the erector spinae plane block, ilioinguinal/iliohypogastric nerve block, sciatic nerve block, maxillary nerve block, paravertebral block, femoral nerve block, radial nerve block, greater occipital nerve block, infraclavicular brachial plexus block, and infraorbital nerve block.
    CONCLUSIONS: Regional anesthesia techniques are commonly performed in children, but the lack of anatomical studies may result in reservations regarding the dispersion and absorption of local anesthetics. Further anatomical research on pediatric regional anesthesia may guide the practice.
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  • 文章类型: Journal Article
    背景:腺样体扁桃体切除术是全世界最常见的外科手术之一。在进行腺样体扁桃体切除术的患者中固定气道的当前标准是气管内导管(ETT)插管。一些研究已经调查了喉罩气道(LMA)在此过程中的使用。我们进行了系统评价和荟萃分析,以比较LMA和ETT在腺扁桃体切除术中的安全性和有效性。
    方法:从开始到2022年检索数据库中的随机对照试验和比较研究。遵循系统审查和荟萃分析(PRISMA)指南的首选报告项目。主要结果是围手术期呼吸不良事件(PRAEs)的发生率。次要结果包括转换为ETT的比率,去饱和,恶心/呕吐,和手术时间。亚组分析,偏见的风险,出版偏见,和建议评估的分级,发展,还进行了评估(GRADE)。
    结果:12项研究纳入分析(4176例患者)。ETT的平均总转化率为8.36%[95%置信区间(CI)=8.17,8.54],儿科组为8.27%(95%CI=8.08,8.47)。继发于并发症的ETT的平均转化率为2.89%(95%CI=2.76,3.03),其余患者来自手术入路不良。总的来说,PRAE没有显着差异[比值比(OR)1.16,95%CI=0.60,2.22],去饱和(OR0.79,95%CI=0.38,1.64),或轻微并发症(OR0.89,95%CI=0.50,1.55)。使用LMA可显著缩短手术时间(平均差-4.38分钟,95%CI=-8.28,-0.49)和出现时间(平均差-4.15分钟,95%CI=-5.63,-2.67)。
    结论:对于腺样体扁桃体切除术,LMA是ETT的安全替代品,需要更少的手术时间。仔细的病人选择和外科医生和麻醉师的判断是必要的,特别是考虑到8%的ETT转化率。
    BACKGROUND: Adenotonsillectomy is one of the most common surgical procedures worldwide. The current standard for securing the airway in patients undergoing adenotonsillectomy is endotracheal tube (ETT) intubation. Several studies have investigated the use of the laryngeal mask airway (LMA) in this procedure. We conducted a systematic review and meta-analysis to compare the safety and efficacy of the LMA versus ETT in adenotonsillectomy.
    METHODS: Databases were searched from inception to 2022 for randomized controlled trials and comparative studies. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed. The primary outcome is the rate of perioperative respiratory adverse events (PRAEs). Secondary outcomes included the rate of conversion to ETT, desaturations, nausea/vomiting, and surgical time. A subgroup analysis, risk of bias, publication bias, and Grading of Recommendations Assessment, Development, and Evaluation (GRADE) assessments were also performed.
    RESULTS: Twelve studies were included in the analysis (4176 patients). The mean overall conversion to ETT was 8.36% [95% confidence interval (CI) = 8.17, 8.54], and for the pediatric group 8.27% (95% CI = 8.08, 8.47). The mean rate of conversion to ETT secondary to complications was 2.89% (95% CI = 2.76, 3.03) while the rest was from poor surgical access. Overall, there was no significant difference in PRAEs [odds ratio (OR) 1.16, 95% CI = 0.60, 2.22], desaturations (OR 0.79, 95% CI = 0.38, 1.64), or minor complications (OR 0.89, 95% CI = 0.50, 1.55). The use of LMA yielded significantly shorter operative time (mean difference -4.38 minutes, 95% CI = -8.28, -0.49) and emergence time (mean difference -4.15 minutes, 95% CI = -5.63, -2.67).
    CONCLUSIONS: For adenotonsillectomy surgery, LMA is a safe alternative to ETT and requires less operative time. Careful patient selection and judgment of the surgeon and anesthesiologist are necessary, especially given the 8% conversion to ETT rate.
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  • 文章类型: Journal Article
    目的:在全身麻醉期间接受气道管理的儿童可能会出现气道并发症,导致罕见但危及生命的情况,称为“无法插管,不能氧化\“。这种情况需要立即得到承认,先进的气道管理,并最终紧急进入颈部。缺乏标准化的程序,缺乏现成的设备,知识不足,训练通常会导致紧急的前颈通道失败,导致灾难性的结果。在这篇叙述性评论中,我们检查了儿童紧急进入颈部的最新证据。
    方法:对婴儿和儿童使用紧急颈前通道(eFONA)进行了全面的文献。
    结果:86篇论文被认为与摘要相关。最后,包括8项关于eFONA技术和动物模型模拟的研究.对于所有文章,他们的主要和次要结果,他们特定的动物模型,实验设计,目标参与者,并报告了设备。
    结论:根据现有证据,我们提出了eFONA技术的一般方法,以及实施本地协议和培训的指南。此外,我们介绍了创新工具的应用,如3D模型,超声,和人工智能,可以提高精度,安全,和训练这个罕见但关键的程序。
    Children undergoing airway management during general anesthesia may experience airway complications resulting in a rare but life-threatening situation known as \"Can\'t Intubate, Can\'t Oxygenate\". This situation requires immediate recognition, advanced airway management, and ultimately emergency front-of-neck access. The absence of standardized procedures, lack of readily available equipment, inadequate knowledge, and training often lead to failed emergency front-of-neck access, resulting in catastrophic outcomes. In this narrative review, we examined the latest evidence on emergency front-of-neck access in children.
    A comprehensive literature was performed the use of emergency front-of-neck access (eFONA) in infants and children.
    Eighty-six papers were deemed relevant by abstract. Finally, eight studies regarding the eFONA technique and simulations in animal models were included. For all articles, their primary and secondary outcomes, their specific animal model, the experimental design, the target participants, and the equipment were reported.
    Based on the available evidence, we propose a general approach to the eFONA technique and a guide for implementing local protocols and training. Additionally, we introduce the application of innovative tools such as 3D models, ultrasound, and artificial intelligence, which can improve the precision, safety, and training of this rare but critical procedure.
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  • 文章类型: Journal Article
    小儿麻醉下术中脑电图(EEG)监测已开始引起越来越多的兴趣,由儿科专用脑电图监测仪的可用性驱动,并且认识到基于患者运动或血液动力学反应变化的传统给药方法通常会导致不精确的给药,尤其是在可能经历不良事件的年幼婴儿中(例如,低血压)由于过度麻醉。脑电图直接测量麻醉药对大脑的影响,这是导致意识丧失的目标最终器官。在过去的十年里,麻醉和计算神经科学的研究提高了我们对术中儿科脑电图监测的理解,并扩大了脑电图在临床实践中的实用性。我们现在对儿童大脑发育中的神经发育变化有了更好的见解,功能连接,使用非专有脑电图参数来指导麻醉剂量,癫痫样脑电图在诱导过程中的变化,脊髓/区域麻醉引起的脑电图变化,脑电图不连续,以及使用EEG改善临床结果。本文总结了近年来有关小儿麻醉围手术期脑电图监测的文献。突出了上面提到的几个主题。
    Intraoperative electroencephalography (EEG) monitoring under pediatric anesthesia has begun to attract increasing interest, driven by the availability of pediatric-specific EEG monitors and the realization that traditional dosing methods based on patient movement or changes in hemodynamic response often lead to imprecise dosing, especially in younger infants who may experience adverse events (e.g., hypotension) due to excess anesthesia. EEG directly measures the effects of anesthetics on the brain, which is the target end-organ responsible for inducing loss of consciousness. Over the past ten years, research on anesthesia and computational neuroscience has improved our understanding of intraoperative pediatric EEG monitoring and expanded the utility of EEG in clinical practice. We now have better insights into neurodevelopmental changes in the developing pediatric brain, functional connectivity, the use of non-proprietary EEG parameters to guide anesthetic dosing, epileptiform EEG changes during induction, EEG changes from spinal/regional anesthesia, EEG discontinuity, and the use of EEG to improve clinical outcomes. This review article summarizes the recent literature on EEG monitoring in perioperative pediatric anesthesia, highlighting several of the topics mentioned above.
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  • 文章类型: Systematic Review
    背景:在脊柱侧凸手术期间,运动诱发电位(MEP),据报道,使用较高剂量的麻醉剂会影响体感诱发电位(SSEP)。右美托咪定,一种交感神经解毒剂,α-2受体激动剂,已被用作降低麻醉剂剂量的辅助剂。然而,关于右美托咪定对术中MEP和SSEP的神经生理学监测的影响存在相互矛盾的证据,尤其是儿科患者。
    目的:本系统综述旨在确定,在脊柱侧凸患儿的脊柱融合手术中,右美托咪定改变MEP幅度或SSEP潜伏期和幅度,如果是,不同剂量的右美托咪定是否显示不同的效果(PROSPERO注册号CRD42022300562)。
    方法:我们搜索了PubMed,Scopus,和CochraneLibrary于2022年1月1日进行,并纳入了随机对照试验,观察性队列研究和病例对照研究以及病例系列研究了目标人群中的右美托咪定,并与不含右美托咪定的标准麻醉方案进行了比较,或比较了多剂量右美托咪定.排除了动物和体外研究以及会议摘要。
    结果:我们发现纳入的文章(n=5)的偏倚风险存在显著异质性(根据Cochrane首选工具);结果在没有荟萃分析的情况下进行总结。偏倚风险最低的文章指出,右美托咪定与MEP损失相关,而较高剂量的右美托咪定会增加风险。相比之下,文章报告右美托咪定和MEP损失之间没有关联,偏倚风险较高,包括可疑或确认的混杂问题,结果测量,参与者选择,结果报告,缺乏统计透明度和权力。
    结论:鉴于文献中现有研究的局限性,建议采用更多样本量进行严格的随机对照试验,以评估右美托咪定在小儿脊柱侧凸手术中的应用效果.
    During scoliosis surgery, motor evoked potentials (MEP), and somatosensory evoked potentials (SSEP) have been reported to be affected by the use of higher doses of anesthetic agents. Dexmedetomidine, a sympatholytic agent, an alpha-2 receptor agonist, has been used as an adjunctive agent to lower anesthetic dose. However, there is conflicting evidence regarding the effects of dexmedetomidine on the intraoperative neurophysiological monitoring of MEP and SSEP during surgery, particularly among pediatric patients.
    This systematic review aimed to determine whether, during spinal fusion surgery in pediatric patients with scoliosis, dexmedetomidine alters MEP amplitude or SSEP latency and amplitude and, if so, whether different doses of dexmedetomidine display different effects (PROSPERO registration number CRD42022300562).
    We searched PubMed, Scopus, and Cochrane Library on January 1, 2022 and included randomized controlled trials, observational cohort and case-control studies and case series investigating dexmedetomidine in the population of interest and comparing against a standardized anesthesia regimen without dexmedetomidine or comparing multiple doses of dexmedetomidine. Animal and in vitro studies and conference abstracts were excluded.
    We found substantial heterogeneity in the risk of bias (per Cochrane-preferred tools) of the included articles (n = 5); results are summarized without meta-analysis. Articles with the lowest risk of bias indicated that dexmedetomidine was associated with MEP loss and that higher doses of dexmedetomidine increased risk. In contrast, articles reporting no association between dexmedetomidine and MEP loss suffered from higher risk of bias, including suspected or confirmed problems with confounding, outcome measurement, participant selection, results reporting, and lack of statistical transparency and power.
    Given the limitations of the studies available in the literature, it would be advisable to conduct rigorous randomized controlled trials with larger sample sizes to assess the effects of dexmedetomidine use of in scoliosis surgery in pediatric patients.
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  • 文章类型: Journal Article
    Postoperative nausea and vomiting (PONV) is common in pediatric patients undergoing general anesthesia, and clinicians seek prophylactic interventions to prevent its ill effects on patients as well as its ramifications on perioperative care. We sought to assess the body of evidence around prophylactic strategies, both pharmacologic and nonpharmacologic, targeting pediatric PONV.
    We searched MEDLINE, MEDLINE ePubs Ahead of Print and In-Process Citations, Embase Classic+Embase, the Cochrane Database of Systematic Reviews, Cochrane CENTRAL (via the Ovid platform), Scopus (Elsevier), Web of Science (Clarivate Analytics), ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform, and the International Standard Randomized Controlled Trial Number Registry, from their inception to 23 September 2022.
    Of 188 clinical trials, 157 (83%) investigated pharmacologic interventions, 25 (13%) investigated nonpharmacologic interventions, and six (3%) investigated mixed pharmacologic and nonpharmacologic interventions. The most common surgeries investigated for pediatric PONV were strabismus surgery (68 trials, 36%) and tonsillectomy or tympanoplasty (45 trials, 23%). Of four measurement tools used to assess PONV in the included trials, the most common was clinical judgement (170 trials, 90%).
    The majority of data in pediatric PONV prophylaxis is based on pharmacologic interventions, with a paucity of research in nonpharmacologic or mixed interventions. Assessing and documenting PONV using tools such as the Baxter Animated Retching Faces Scale or PONV numeric scoring system may help standardize pediatric PONV prophylaxis research moving forward. Furthermore, concurrently assessing pain and adverse effects associated with PONV might further inform our understanding of this complex clinical entity.
    RéSUMé: OBJECTIF: Les nausées et vomissements postopératoires (NVPO) sont fréquents chez la patientèle pédiatrique bénéficiant d’une anesthésie générale, et les équipes cliniques recherchent des interventions prophylactiques pour prévenir leurs effets néfastes sur les patient·es ainsi que leurs ramifications sur les soins périopératoires. Nous avons cherché à évaluer l’ensemble des données probantes entourant les stratégies prophylactiques pharmacologiques et non pharmacologiques ciblant les NVPO pédiatriques.
    Nous avons effectué des recherches dans les bases de données MEDLINE, MEDLINE ePubs Ahead of Print and In-Process Citations, Embase Classic+Embase, la base de données des revues systématiques Cochrane, Cochrane CENTRAL (via la plateforme Ovid), Scopus (Elsevier), Web of Science (Clarivate Analytics), ClinicalTrials.gov, le système d’enregistrement international des essais cliniques de l’OMS et le registre international normalisé des numéros d’essais contrôlés randomisés, depuis leur création jusqu’au 23 septembre 2022.
    Sur 188 études cliniques, 157 (83 %) portaient sur des interventions pharmacologiques, 25 (13 %) sur des interventions non pharmacologiques et six (3 %) sur des interventions pharmacologiques et non pharmacologiques mixtes. Les chirurgies les plus fréquemment étudiées pour les NVPO pédiatriques étaient les chirurgies de strabisme (68 études, 36 %) et les amygdalectomies ou tympanoplasties (45 études, 23 %). Parmi les quatre outils de mesure utilisés pour évaluer les NVPO dans les études incluses, le plus fréquemment utilisé était le jugement clinique (170 études, 90 %).
    La majorité des données sur les prophylaxies pédiatriques pour prévenir les NVPO sont basées sur des interventions pharmacologiques, avec peu de recherche sur les interventions non pharmacologiques ou mixtes. L’évaluation et la documentation des NVPO à l’aide d’outils tels que l’échelle Baxter Animated Retching Faces Scale ou un système de notation numérique des NVPO peuvent aider à normaliser la recherche sur la prophylaxie pédiatrique des NVPO à l’avenir. De plus, l’évaluation simultanée de la douleur et des effets indésirables associés aux NVPO pourrait éclairer davantage notre compréhension de cette entité clinique complexe.
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  • 文章类型: Meta-Analysis
    暂无摘要。
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  • 文章类型: Journal Article
    恶性高热是一种罕见但危及生命的药物遗传学障碍,由暴露于特定的麻醉剂引发。尽管这种情况在围手术期几乎可以影响任何患者,儿科人群特别脆弱,与成人相比,儿童发病率高五倍。在过去的几十年里,领先的麻醉学之间的协同努力,儿科,和神经病学协会产生了关于诊断途径的新证据,避免不必要的测试和限制错误的诊断。然而,个性化的方法和有效的预防政策,重点是明确识别高风险人群,定义围手术期无触发住院,和支持疗法的快速激活应得到改善。根据流行病学数据,许多国家科学学会制定了一致的指导方针,但是许多误解在医生和医护人员中很常见。本审查应考虑所有这些方面,并总结最近的更新。
    Malignant hyperthermia is a rare but life-threatening pharmacogenetic disorder triggered by exposure to specific anesthetic agents. Although this occurrence could affect virtually any patient during the perioperative time, the pediatric population is particularly vulnerable, and it has a five-fold higher incidence in children compared to adults. In the last few decades, synergistic efforts among leading anesthesiology, pediatrics, and neurology associations have produced new evidence concerning the diagnostic pathway, avoiding unnecessary testing and limiting false diagnoses. However, a personalized approach and an effective prevention policy focused on clearly recognizing the high-risk population, defining perioperative trigger-free hospitalization, and rapid activation of supportive therapy should be improved. Based on epidemiological data, many national scientific societies have produced consistent guidelines, but many misconceptions are common among physicians and healthcare workers. This review shall consider all these aspects and summarize the most recent updates.
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  • 文章类型: Journal Article
    小儿麻醉中最常见的关键事件是围手术期呼吸不良事件(PRAEs)。本荟萃分析旨在评估右美托咪定对儿童PRAEs的预防作用。右美托咪定是一种高选择性α2-肾上腺素受体激动剂,可提供镇静作用,抗焦虑和镇痛作用,而不会引起呼吸抑制。右美托咪定可以减少儿童拔管期间的气道和循环反应。分析原始随机对照试验数据以研究右美托咪定对PRAEs的推定作用。通过搜索Cochrane图书馆,EMBASE和PubMed,共纳入10项随机对照试验(1,056例患者).PRAE包括咳嗽,屏住呼吸,喉痉挛,支气管痉挛,去饱和(经皮氧饱和度<95%),身体运动和肺部啰音。与安慰剂相比,右美托咪定导致咳嗽的发生率显着降低,屏住呼吸,喉痉挛和出现躁动。与活性比较组相比,右美托咪定组PRAE的发生率明显降低。此外,右美托咪定使心率降低,麻醉后监护病房停留时间延长11.18min.目前的分析提示右美托咪定改善了患儿的气道功能,降低了与全身麻醉相关的风险。目前的数据表明,右美托咪定可能是预防儿童PRAEs的良好选择。
    The most common critical incidents in pediatric anesthesia are perioperative respiratory adverse events (PRAEs). The present meta-analysis aimed to assess the preventive effect of dexmedetomidine on PRAEs in children. Dexmedetomidine is a highly selective α2-adrenoceptor agonist that provides sedation, anxiolysis and analgesic effects without causing respiratory depression. Dexmedetomidine can diminish airway and circulatory responses during extubation in children. Original randomized controlled trial data were analyzed to study the putative effect of dexmedetomidine on PRAEs. By searched the Cochrane Library, EMBASE and PubMed, a total of ten randomized controlled trials (1,056 patients) was identified. PRAEs included cough, breath holding, laryngospasm, bronchospasm, desaturation (percutaneous oxygen saturation <95%), body movement and pulmonary rales. Compared with placebo, dexmedetomidine resulted in a significant reduction of incidence of cough, breath holding, laryngospasm and emergence agitation. The incidence of PRAEs was significantly reduced in dexmedetomidine compared with active comparators group. Moreover, dexmedetomidine decreased heart rate and increased post-anesthesia care unit stay duration by 11.18 min. The present analysis suggested that dexmedetomidine improved the airway function and decreased risks associated with general anesthesia in children. The present data demonstrated that dexmedetomidine may be a good choice to prevent PRAEs in children.
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