Duodenoscopes

  • 文章类型: Journal Article
    目的:十二指肠镜定期培养对及时检测污染至关重要,但他们的敏感性仍然未知。这项研究旨在确定十二指肠镜培养物的敏感性,并估计受污染的十二指肠镜使用的患病率。
    方法:我们将2015年3月至2022年6月的十二指肠镜微生物监测数据与使用数据相结合,以评估患者暴露于被肠道或口腔来源的微生物(MGO)污染的十二指肠镜。我们确定了十二指肠镜在一年内重复的物种水平污染,并使用分子分型来确认遗传相关性。单个十二指肠镜的多个十二指肠镜培养物中的遗传相关微生物表明持续污染期,并且将簇定义为不同十二指肠镜之间持续污染的重叠期。如果微生物不能用于分子分析,我们将这一时期标记为未经证实。如果样品在持续污染期间未显示靶微生物,则将其定义为假阴性。我们使用了三种情况来假设污染使用和培养敏感性。
    结果:我们纳入了556个十二指肠镜培养物,其中185个(33.3%)被MGO污染。十二指肠镜的总使用量为5226。我们发现了一个持续的污染期,六个未经证实的时期,和两个集群。根据我们的场景假设,受污染的使用百分比从12.3%到23.7%不等,培养敏感性为82.2%~98.9%。
    结论:十二指肠镜培养物的敏感性有限,导致临床使用的十二指肠镜清除不当,不断增加的疫情风险。应重新评估单一培养物结束十二指肠镜隔离的适用性。
    OBJECTIVE: Periodic duodenoscope cultures are essential to timely detect contamination, but their sensitivity remains unknown. This study aims to determine the sensitivity of duodenoscope cultures and to estimate the prevalence of contaminated duodenoscope use.
    METHODS: We combined duodenoscope microbiological surveillance data from March 2015 to June 2022 with usage data to evaluate patient exposure to duodenoscopes contaminated with microorganisms of gut or oral origin (MGO). We identified duodenoscopes with repeated species-level contamination within a year and used molecular typing to confirm genetic relatedness. Genetically related microorganisms over multiple duodenoscope cultures of a single duodenoscope indicated a period of sustained contamination and a cluster was defined as overlapping periods of sustained contamination between different duodenoscopes. If microorganisms were not available for molecular analysis, we marked the period as unconfirmed. A sample was defined as false-negative if it did not show the target microorganism(s) in a period of sustained contamination. We used three scenarios to hypothesize about contaminated use and culture sensitivity.
    RESULTS: We included 556 duodenoscope cultures with 185 (33.3%) contaminated with MGO. The total usage of duodenoscopes was 5226. We identified one period of sustained contamination, six unconfirmed periods, and two clusters. Depending on our scenario assumptions, the percentage of contaminated use varied from 12.3% to 23.7%, and culture sensitivity ranged from 82.2% to 98.9%.
    CONCLUSIONS: Limited sensitivity of duodenoscope cultures leads to improper clearance of duodenoscopes for clinical use, increasing risks of outbreaks. The applicability of a single culture to end a duodenoscope\'s quarantine should be reevaluated.
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  • 文章类型: Systematic Review
    目的:内窥镜是诊断的重要工具,筛选,和治疗胃肠道疾病。2019年,食品药品监督管理局发布了新闻稿,建议十二指肠镜制造商和医疗保健机构逐步淘汰具有固定端帽的完全可重复使用的十二指肠镜,以代替完全一次性或包含一次性端帽的十二指肠镜。通过这项研究,我们系统回顾了已发表的关于一次性使用一次性胃肠镜的文献,以描述文献的现状,并就一次性胃肠镜的作用提供总结建议.
    方法:对于我们的纳入标准,我们搜索了2015年及之后发表的研究.我们在PubMed中使用关键字进行了文献检索,“一次性的,\"\"可重复使用,\"\"胆道镜,\"\"结肠镜,\"\"十二指肠镜,\"\"食管镜,“\”胃镜,\"和\"乙状结肠镜。“经过我们的审查,我们确定了我们的最终文章集,包括与一次性示波器有关的13篇文章,2015年至2023年出版。
    结果:在这篇综述中,我们展示了13篇文章讨论感染率,功能,安全,与可重复使用的胃肠镜相比,一次性胃肠镜的可负担性。在讨论感染率的3篇文章中(福布斯及其同事,Ridtitid和他的同事们,和Ofosu及其同事),在一次性胃肠镜中,每种方法均显示感染风险降低.功能是这些文章中的另一个共同主题。六篇文章(由Muthusamy及其同事,Bang和同事们,Lisotti和他的同事们,罗斯和同事们,Kang和同事们,和福布斯及其同事)展示了一次性示波器与可重复使用示波器的可比功能。一次性示波器中报告最多的功能问题是相机分辨率降低。与可重复使用的范围相比,一次性范围也显示出可比的安全性。六篇文章(由Kalipershad及其同事,Muthusamy和他的同事们,Bang和同事们,Lisotti和他的同事们,罗和同事们,和Huynh及其同事)显示出相当的AE率,而一篇文章(由Ofosu及其同事撰写)显示一次性内窥镜的不良事件发生率增加。最后,在其中的3篇文章中进行了成本分析。两篇文章(由Larsen等人和Ross及其同事)指出,需要进一步的研究来了解一次性内窥镜的成本,而一篇文章(Kang及其同事)显示出有利的成本分析。
    结论:在回顾了自2015年食品药品监督管理局安全沟通以来发表的文献后,已证明一次性镜可有效降低感染风险,同时保持与传统可重复使用镜相似的安全特征。然而,在功能和成本效益方面,需要更多的研究来比较一次性和可重复使用的范围。
    OBJECTIVE: Endoscopes are an essential tool in the diagnosis, screening, and treatment of gastrointestinal diseases. In 2019, the Food and Drug Administration issued a news release, recommending that duodenoscope manufacturers and health care facilities phase out fully reusable duodenoscopes with fixed endcaps in lieu of duodenoscopes that are either fully disposable or those that contain disposable endcaps. With this study, we systematically reviewed the published literature on single-use disposable gastrointestinal scopes to describe the current state of the literature and provide summary recommendations on the role of disposable gastrointestinal endoscopes.
    METHODS: For our inclusion criteria, we searched for studies that were published in the year 2015 and afterward. We performed a literature search in PubMed using the keywords, \"disposable,\" \"reusable,\" \"choledochoscope,\" \"colonoscope,\" \"duodenoscope,\" \"esophagoscope,\" \"gastroscope,\" and \"sigmoidoscope.\" After our review, we identified our final article set, including 13 articles relating to disposable scopes, published from 2015 to 2023.
    RESULTS: In this review, we show 13 articles discussing the infection rate, functionality, safety, and affordability of disposable gastrointestinal scopes in comparison to reusable gastrointestinal scopes. Of the 3 articles that discussed infection rates (by Forbes and colleagues, Ridtitid and colleagues, and Ofosu and colleagues), each demonstrated a decreased risk of infection in disposable gastrointestinal scopes. Functionality was another common theme among these articles. Six articles (by Muthusamy and colleagues, Bang and colleagues, Lisotti and colleagues, Ross and colleagues, Kang and colleagues, and Forbes and colleagues) demonstrated comparable functionality of disposable scopes to reusable scopes. The most reported functionality issue in disposable scopes was decreased camera resolution. Disposable scopes also showed comparable safety profiles compared with reusable scopes. Six articles (by Kalipershad and colleagues, Muthusamy and colleagues, Bang and colleagues, Lisotti and colleagues, Luo and colleagues, and Huynh and colleagues) showed comparable rates of AEs, whereas 1 article (by Ofosu and colleagues) demonstrated increased rates of AEs with disposable scopes. Lastly, a cost analysis was looked at in 3 of the articles. Two articles (by Larsen et al and Ross and colleagues) remarked that further research is needed to understand the cost of disposable scopes, whereas 1 article (by Kang and colleagues) showed a favorable cost analysis.
    CONCLUSIONS: After a review of the literature published since the 2015 Food and Drug Administration safety communication, disposable scopes have been shown to be effective in decreasing infection risks while maintaining similar safety profiles to conventional reusable scopes. However, more research is required to compare disposable and reusable scopes in terms of functionality and cost-effectiveness.
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  • 文章类型: Journal Article
    背景:与咪达唑仑相比,瑞米唑仑具有更快的起效和抵消催眠作用,以及心肺稳定性,本研究旨在确定在内镜逆行胰胆管造影术(ERCP)过程中瑞米唑仑的90%有效剂量(ED90),以抑制对插入十二指肠镜的反应.
    方法:在2021年9月至2021年11月期间,在接受使用10µg/kg阿芬太尼的瑞马唑仑-阿芬太尼麻醉的ERCP过程中进行了剂量反应研究。瑞马唑仑的初始剂量为0.2mg/kg。然后通过根据9:1偏置硬币设计利用顺序上升和下降,基于早期患者的反应来决定剂量。一旦失败,在下一位患者中,瑞咪唑安定的剂量增加了0.025mg/kg.当插入成功时,随后的患者被随机分配给相同剂量或低0.025mg/kg的剂量.计算了在ERCP过程中抑制十二指肠镜插入反应的瑞咪唑安定的ED90。记录瑞米唑仑的不良事件和并发症。
    结果:共有55名老年患者(年龄>65岁)纳入研究。45名患者成功麻醉,10不成功瑞马唑仑的ED90为0.300mg/kg(95%CI=0.287-0.320)。ED95为0.315(95%CI=0.312-0.323),ED99为0.323(95%CI=0.323-0.325)。在患者中,9例患者出现低血压,2例患者出现心动过缓,1例患者出现心动过速,2例患者发生缺氧。
    结论:对行ERCP的老年患者使用0.300mg/kg负荷剂量的瑞米唑仑,有效地,并迅速诱导患者入睡并抑制对插入十二指肠镜的反应。
    背景:研究方案于2021年9月22日在ClinicalTrials.gov网站上注册(NCT05053763)。
    BACKGROUND: Compared to midazolam, remimazolam has a faster onset and offset of hypnotic effect, as well as cardiorespiratory stability, this study aims to determine the 90% effective dose (ED90) of remimazolam to inhibit responses to insertion of a duodenoscope during endoscopic retrograde cholangiopancreatography (ERCP).
    METHODS: A dose-response study was carried out undergoing ERCP who received remimazolam-alfentanil anesthesia using 10 µg/kg of alfentanil between September 2021 and November 2021. The initial dose of remimazolam was 0.2 mg/kg. The dose was then decided based on the responses of earlier patients by exploiting the sequential ascend and descend according to a 9: 1 biased coin design. Upon failure, the dose of remimazolam was increased by 0.025 mg/kg in the next patient. When the insertion was successful, the succeeding patient was randomized to an identical dose or a dose that was lower by 0.025 mg/kg.The ED90 of remimazolam for inhibiting responses to the insertion of a duodenoscope during ERCP was calculated. Adverse events and complications of remimazolam were recorded.
    RESULTS: A total of 55 elderly patients (age > 65) were included in the study. 45 successfully anesthetized patients, and 10 unsuccessfully. The ED90 of remimazolam was 0.300 mg/kg (95% CI = 0.287-0.320). ED95 was 0.315 (95% CI = 0.312-0.323) and ED99 was 0.323 (95% CI = 0.323-0.325). Among the patients, 9 patients developed hypotension, 2 patients developed bradycardia and 1 patient developed tachycardia, and hypoxia occurred in 2 patients.
    CONCLUSIONS: A loading dose of 0.300 mg / kg of remimazolam for elderly patients undergoing ERCP can safely, effectively, and quickly induce patients to fall asleep and inhibit responses to the insertion of a duodenoscope.
    BACKGROUND: The study protocol was registered at the website ClinicalTrials.gov on 22/09/2021(NCT05053763).
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  • 文章类型: Journal Article
    背景:在临床实践中正在使用一次性十二指肠镜和带有一次性端帽的十二指肠镜,以降低或消除传播感染的风险。该研究的目的是评估国家代表性样本中高级内窥镜研究员对这些十二指肠镜使用的看法和经验。
    方法:向74个高级内窥镜检查培训项目发送了17项电子调查。调查由50名参与者完成,他们的回答被纳入分析。
    结果:大多数参与者来自学术培训计划(82.7%),并被确定为研究生培训的第7年(92%;PGY-7)。参与者平均进行了414次ERCP。29%的人报告使用一次性十二指肠镜插管困难,而15.7%的人使用带有一次性端帽的十二指肠镜(与标准十二指肠镜)。96%的学员认为一次性十二指肠镜不划算,92%的学员表示他们在独立实践中不会使用该设备。100%的学员表示,他们将在独立实践中使用带有一次性端帽的十二指肠镜。对于他们最具挑战性的案例,90%的受训者更喜欢使用标准的可再处理十二指肠镜,而没有受训者表示他们更喜欢在这种情况下使用一次性十二指肠镜。82%的参与者表示,一次性十二指肠镜和一次性端帽应专门或优先用于高风险患者,理由是成本。功能,以及对环境影响的担忧。
    结论:高级内镜研究员认为一次性十二指肠镜影响技术可操作性。对功能的关注,成本效益和环境影响是采用的障碍。
    BACKGROUND: Disposable duodenoscopes and duodenoscopes with disposable endcaps are being used in clinical practice to reduce or eliminate the risk of transmitting infections. The study aim was to assess perceptions and experiences regarding the use of these duodenoscopes among advanced endoscopy fellows in a nationally representative sample.
    METHODS: A 17-item electronic survey was sent to 74 advanced endoscopy training programs. The survey was completed by 50 participants and their responses were included for analysis.
    RESULTS: Most participants were from academic training programs (82.7%) and identified as being in their 7th year of post graduate training (92%; PGY-7). Participants performed an average of 414 ERCPs. 29% reported difficulty with cannulation using disposable duodenoscopes versus 15.7% with duodenoscopes with disposable endcaps (vs. standard duodenoscope). 96% of trainees perceived disposable duodenoscopes as not cost effective and 92% stated they would not use this device during independent practice. 100% of trainees stated that they would use duodenoscopes with disposable endcaps during independent practice. For their most challenging cases, 90% of trainees preferred using standard reprocessable duodenoscopes while no trainee indicated they would prefer using a disposable duodenoscope in this scenario. 82% of participants stated that disposable duodenoscopes and disposable endcaps should be used exclusively or preferentially for high-risk patients citing cost, functionality, and concerns regarding environmental impact.
    CONCLUSIONS: Advanced endoscopy fellows perceive disposable duodenoscopes as impacting technical maneuverability. Concerns about functionality, cost effectiveness and environmental impact are barriers to adoption.
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  • 文章类型: Case Reports
    背景:内镜逆行胰胆管造影术(ERCP)已在儿科患者中广泛使用;然而,治疗性ERCP在婴儿中的应用仍然存在挑战.
    方法:本病例报告详细介绍了一名5.9公斤患有梗阻性黄疸和疑似溶血性贫血的婴儿,他接受了ERCP以减轻胆道梗阻。婴儿因泥色大便入院,黄疸,和肝损伤。超声和磁共振胰胆管造影(MRCP)显示胆总管(CBD)扩张并伴有结石。在全身麻醉下使用JF-260V十二指肠镜进行ERCP。成功取出结石和胆道引流。
    结论:在ERCP和小儿麻醉方面具有相当专业知识的中心,使用常规成人十二指肠镜治疗婴儿ERCP是安全可行的,如果采用仔细和严格的患者选择标准。在未来,应针对儿科ERCP的适应证和操作制定明确的指南和标准化方案.
    BACKGROUND: Endoscopic retrograde cholangiopancreatography (ERCP) has found extensive use in pediatric patients; however, challenges persist in the application of therapeutic ERCP in infants.
    METHODS: This case report details the presentation of a 5.9-kilogram infant with obstructive jaundice and suspected hemolytic anemia who underwent ERCP to alleviate biliary obstruction. The infant was admitted due to clay-colored stools, jaundice, and liver injury. Ultrasound and magnetic resonance cholangiopancreatography (MRCP) revealed dilation of the common bile duct (CBD) accompanied by the presence of stones. ERCP was conducted using a JF-260V duodenoscope under general anesthesia. Successful stone extraction and biliary drainage were achieved.
    CONCLUSIONS: In centers with considerable expertise in ERCP and pediatric anesthesia, the use of a conventional adult duodenoscope for therapeutic ERCP in infants can be considered safe and feasible, provided careful and stringent patient selection criteria are applied. In the future, clear guidelines and standardized protocols for the indications and procedures of pediatric ERCP should be established.
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  • 文章类型: Journal Article
    文献中报道的患者就绪柔性内窥镜的污染率从0.4%到49%不等。不幸的是,这些结果的比较和解释几乎是不可能的,因为包括采样和培养方法在内的几个因素,污染的目标水平或指示微生物的定义在不同的研究中差异很大。这项研究的目的是通过提取功效比较来比较六种十二指肠镜采样和培养方法的功效,同时确定提供最佳微生物回收的关键参数。使用ISO11737-1:2018中描述的重复回收方法评估每种方法的十二指肠镜样品提取功效。获得的结果表明,平均总生物负载提取效率从澳大利亚方法的1%到法国方法的39%不等。最低的内窥镜样本提取效率与没有任何中和剂有关,摩擦,或张力活性剂,并且仅将收集的一小部分采样溶液接种到培养基上。取样和培养方法的功效也根据内窥镜中存在的微生物的性质而变化。以及取样和培养之间的时间。这项研究支持对柔性内窥镜的统一和标准化采样和培养方法的需求。
    BACKGROUND: Contamination rates reported in the literature for patient-ready flexible endoscopes vary from 0.4% to 49%. Unfortunately, the comparison and interpretation of these results is almost impossible since several factors including sampling and culturing methods, target levels for contamination, or definition of indicator micro-organisms vary widely from one study to the other.
    OBJECTIVE: To compare the efficacy of six duodenoscope sampling and culturing methods by means of extraction efficacy comparison, while at the same time identifying key parameters that provide optimal microbial recovery.
    METHODS: The duodenoscope sample extraction efficacy of each method was assessed using the repetitive recovery method described in ISO 11737-1: 2018.
    RESULTS: Mean overall bioburden extraction efficacy varied from 1% for the Australian method to 39% for the French one. The lowest endoscope sample extraction efficacy was associated with the absence of any neutralizer, friction, or tensioactive agent, and when only a small portion of the sampling solution collected was inoculated on to culture media. The efficacy of the sampling and culturing methods also varied according to the nature of micro-organisms present in the endoscope, and the time between sampling and culturing.
    CONCLUSIONS: This study supports the need for a harmonized and standardized sampling and culturing method for flexible endoscopes.
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  • 文章类型: Journal Article
    目的:据报道,经十二指肠镜传播的继发性感染在3%的内镜逆行胰胆管造影术中。建议使用一次性十二指肠镜。我们调查了这些十二指肠镜在胰胆管造影术中使用的成本效益。
    方法:进行了成本效益分析,以比较使用可重复使用的十二指肠镜与一次性十二指肠镜的胰胆管造影术的性能。从国家卫生系统的角度通过计算质量调整生命年(QALY)来分析有效性。考虑了从一次性使用到可重复使用的十二指肠镜的交叉可能性。设定了25,000欧元/QALY的支付意愿,计算了增量成本效益比(ICER),并进行了确定性和概率敏感性分析。
    结果:考虑使用一次性和可重复使用的十二指肠镜进行胰胆管造影,费用分别为2900欧元和1333欧元,10%的一次性十二指肠镜使用率,ICER超过3,000,000欧元/QALY。较低的一次性十二指肠镜费用为1211欧元,导致ICER为23,583欧元/QALY。当一次性十二指肠镜的单位成本为1211欧元时,超过9.5%的交叉率使得一次性十二指肠镜的使用效率低下。
    结论:单用十二指肠镜在一定比例的胰胆管造影术中是具有成本效益的,如果其成本降低。交叉率的增加使得单次使用十二指肠镜使用不具成本效益。
    OBJECTIVE: Secondary infections due to transmission via the duodenoscope have been reported in up to 3% of endoscopic retrograde cholangiopancreatographies. The use of single-use duodenoscopes has been suggested. We investigate the cost-effectiveness of these duodenoscopes use in cholangiopancreatography.
    METHODS: A cost-effectiveness analysis was implemented to compare the performance of cholangiopancreatographies with reusable duodenoscopes versus single-use duodenoscopes. Effectiveness was analyzed by calculating quality-adjusted life years (QALY) from the perspective of the National Health System. Possibility of crossover from single-use to reusable duodenoscopes was considered. A willingness-to-pay of €25,000/QALY was set, the incremental cost-effectiveness ratio (ICER) was calculated, and deterministic and probabilistic sensitivity analyses were performed.
    RESULTS: Considering cholangiopancreatographies with single-use and reusable duodenoscopes at a cost of €2900 and €1333, respectively, and a 10% rate of single-use duodenoscopes, ICER was greater than €3,000,000/QALY. A lower single-use duodenoscope cost of €1211 resulted in an ICER of €23,583/QALY. When the unit cost of the single-use duodenoscope was €1211, a crossover rate of more than 9.5% made the use of the single-use duodenoscope inefficient.
    CONCLUSIONS: Single-use duodenoscopes are cost-effective in a proportion of cholangiopancreatographies if its cost is reduced. Increased crossover rate makes single-use duodenoscope use not cost-effective.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    目的:针对多药耐药菌的十二指肠镜相关传染病暴发,美国食品和药物管理局建议过渡到具有创新设计的十二指肠镜,包括具有一次性部件或完全一次性十二指肠镜的十二指肠镜。我们旨在表征一次性使用的一次性十二指肠镜的学习曲线(LC)。
    方法:我们对前瞻性收集的数据库进行了回顾性分析,该数据库来自31例接受ERCP的患者,经验丰富的操作员使用EXALTModelD®(波士顿科学,马尔伯勒)在单个三级转诊中心的一次性十二指肠镜。通过使用累积和(CUSUM)分析达到熟练程度所需的病例数来描述该设备的LC。尝试插入导管的次数和插入所需导管的时间被评估为单独的终点。尝试的总平均次数和插管的总平均时间用作各自CUSUM分析中的目标值。熟练程度定义为在CUSUM图中达到拐点的程序数量。该观察表明改善了操作者的表现,如通过在限定数量的程序之后的尝试数量的减少和插管时间的缩短所显示的。
    结果:总体而言,31例患者接受ERCP使用EXALT模型D一次性十二指肠镜由一位经验丰富的内镜医师。6例(19%)患者具有天然乳头,这些程序中的大多数被归类为ASGE复杂性2级或以上。仅使用一次性十二指肠镜完成了27例患者(87%)的手术,而4例患者(13%)需要可重复使用的十二指肠镜完成手术。交叉在整个业绩期间均匀分布。手术相关的不良事件包括:ERCP术后胰腺炎(3%),出血(3%)和无穿孔。在两个终点的分析中,在10例病例中实现了CUSUM曲线的拐点,表明插管尝试和插管时间的持续减少。
    结论:在经验丰富的胰胆管内镜医师中,约10个ERCP是手术相关因素(包括插管成功率和手术时间)得以改善的阈值.与手术相关的不良事件与可重复使用的十二指肠镜的预期事件一致。从一次性十二指肠镜过渡到可重复使用的十二指肠镜的需要似乎与学习曲线无关,因为它们在整个研究期间均匀分布。这些结果可用于指导将一次性十二指肠镜应用于临床实践。
    OBJECTIVE: In response to documented duodenoscope-related infectious outbreaks of multidrug-resistant organisms, the Food and Drug Administration has recommended a transition to duodenoscopes with innovative designs, including duodenoscopes with disposable components or fully disposable duodenoscopes. We aim to characterize the learning curve (LC) for a single-use disposable duodenoscope.
    METHODS: We performed a retrospective analysis of a prospectively collected database from 31 patients who underwent ERCP by a single, experienced operator using the EXALT Model D® (Boston Scientific, Marlborough) disposable duodenoscope at a single tertiary referral center. The LC for this device was described by the number of cases needed to achieve proficiency using cumulative sum (CUSUM) analysis. Number of attempts to cannulate and time to cannulate the desired duct were assessed as separate endpoints. The overall mean number of attempts and overall mean time to cannulation were used as the target values in the respective CUSUM analyses. Proficiency was defined as the number of procedures where an inflection point was reached in the CUSUM graph. This observation indicates improving operator performance as shown by a decrease in the number of attempts and shortening of cannulation time after the defined number of procedures.
    RESULTS: Overall, 31 patients underwent ERCP using the EXALT Model D disposable duodenoscope by a single experienced endoscopist. 6 (19%) patients had a native papilla and the majority of these procedures were classified as ASGE complexity level 2 or above. The procedure was completed using solely the disposable duodenoscope in 27 patients (87%), while a reusable duodenoscope was required for procedure completion in 4 patients (13%). The cross-overs were distributed evenly across the performance period. Procedure-related adverse events included: post-ERCP pancreatitis (3%), bleeding (3%) and no perforations. In the analyses of both endpoints, an inflection of the CUSUM curves is achieved at 10 cases, indicating sustained reduction of cannulation attempts and time to cannulation.
    CONCLUSIONS: Among experienced pancreaticobiliary endoscopists, approximately 10 ERCPs is the threshold whereby procedure-related factors including cannulation success and procedural time improves. Procedure-related adverse events are consistent with those expected with reusable duodenoscopes. The need to cross-over from single-use duodenoscope to reusable duodenoscope did not appear to be related to the learning curve, as they were evenly distributed across the study period. These results can be used to guide adoption of single-use duodenoscopes into clinical practice.
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  • 文章类型: Journal Article
    目的:采用一次性端盖的十二指肠镜,以最大程度地降低感染风险,但没有在儿科研究。
    方法:我们收集了18个月内一次性使用端帽与可重复使用的十二指肠镜的临床数据和内窥镜评估。
    结果:对1-18岁(平均14.2岁)的患者进行了106例ERCP。四十六个涉及一次性端盖,9需要交叉到可重复使用的十二指肠镜。涉及一次性使用端帽的ERCP导致更多的粘膜创伤(10vs0,p<0.05)和ERCP后胰腺炎(4vs1,p<0.05),并占需要先进插管技术的9个ERCP中的8个。没有发生ERCP后感染。报告的挑战包括一次性端盖的刚度和难以对齐的插管。
    结论:我们报告进展困难,更加依赖先进的插管技术,在儿科ERCP中使用带有一次性端帽的十二指肠镜时,PEP的发生率更高。这一领域值得进一步研究。
    OBJECTIVE: Duodenoscopes with single-use end caps were introduced to minimize infection risk, but they are unstudied in pediatrics.
    METHODS: We collected clinical data and endoscopists\' evaluations of duodenoscopes with single-use end caps versus reusable duodenoscopes over 18 months.
    RESULTS: A total of 106 ERCPs were performed for patients aged 1 to 18 (mean, 14.2) years. Forty-six involved single-use end caps, with 9 requiring crossover to reusable duodenoscopes. ERCPs involving single-use end caps resulted in more instances of mucosal trauma (10 vs 0; P < .05) and post-ERCP pancreatitis (4 vs 1; P < .05) and accounted for 8 of 9 ERCPs requiring advanced cannulation techniques. No post-ERCP infections occurred. Reported challenges included single-use end cap stiffness and difficulty with their alignment for cannulation.
    CONCLUSIONS: We report difficulty with advancement, greater reliance on advanced cannulation techniques, and higher rates of post-ERCP pancreatitis when using duodenoscopes with single-use end caps in pediatric ERCP. This area warrants further study.
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