Central Venous Catheters

中心静脉导管
  • 文章类型: Systematic Review
    背景:经外周插入的中央导管(PICC)和中线导管(MC)可以提供方便的静脉通路,但是支持他们在姑息治疗中地位的证据是有限的。本综述旨在评估导管适应症,利用率,并发症,停留时间,以及接受姑息治疗的癌症患者的患者体验。
    方法:在Medline进行了关于导管使用支持或症状治疗的系统研究,Embase,CINAHL,WebofScience,科克伦,和中央数据库。包括研究人群或姑息治疗癌症患者亚组的研究。使用有效公共卫生实践质量评估工具评估研究质量。
    结果:在7631个独特的标题中,详细研究了17篇文章,均在2002年至2022年之间发布。导管中值停留时间从15天到194天不等。用于家庭肠外营养的时间最长。对于疼痛和症状管理,典型的持续时间是2-4周,通常直到病人死亡。并发症发生率很低,血栓形成,感染,和闭塞范围从0到2.46事件/1000导管天。在姑息治疗服务的研究中,患者在手术过程中报告的痛苦最小,用户满意度高。术后生活质量评估有所改善,可能受同时提供专科姑息治疗的影响。所有研究均被评估为中等或较弱的质量。
    结论:PICC和MC是姑息治疗癌症患者的安全和有价值的工具,他们将受益于静脉介入治疗的症状管理。需要进一步的研究来阐明PICC或MC在姑息治疗中的适应症。
    BACKGROUND: Peripherally inserted central catheters (PICCs) and midline catheters (MCs) may offer convenient intravenous access, but evidence to support their place in palliative care is limited. This review aimed to assess catheter indications, utilization, complications, dwell time, and patient experiences in cancer patients receiving palliative care.
    METHODS: A systematic search for studies on catheter utilization for supportive or symptom treatment was conducted in Medline, Embase, CINAHL, Web of Science, Cochrane, and CENTRAL databases. Studies with a study population or a subgroup of palliative care cancer patients were included. Study quality was assessed using the Effective Public Health Practice Quality assessment tool.
    RESULTS: Of 7631 unique titles, 17 articles were examined in detail, all published between 2002 and 2022. Median catheter dwell time varied from 15 to 194 days, the longest when utilized for home parenteral nutrition. For pain and symptom management, the typical duration was 2-4 weeks, often until the patient\'s death. Complication rates were minimal, with thrombosis, infections, and occlusion ranging from 0 to 2.46 incidents per 1000 catheter days. In studies from palliative care services, patients reported minimal distress during procedures and high user satisfaction. Quality of life assessments post-procedure improved, possibly influenced by concurrent specialist palliative care provision. All studies were assessed to be of moderate or weak quality.
    CONCLUSIONS: PICC and MC are safe and valuable tools in palliative care cancer patients who would benefit from intravenous access for symptom management. Further studies are needed to clarify indications for PICC or MC in palliative care.
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  • 文章类型: Journal Article
    目的:这篇综述总结了关于这些特征的最新发现和建议,外周和中央长期静脉接入装置的适应症和使用。这些设备固有的各种并发症越来越为人所知,它们的影响因素决定了,这可以减少它们的发病率。
    结果:一些措施被整合到良好做法的建议中,例如适当选择设备,优先使用最薄的导管,以及用氯己定浸渍的氰基丙烯酸酯胶和敷料。
    结论:提高对导致感染和血栓性并发症的现象的认识,以及更好地了解静脉注射装置及其各自适应症之间的差异,应改善院内和院外护理。
    OBJECTIVE: This review summarizes the latest findings and recommendations about the characteristics, indications and use of peripheral and central long-term venous access devices.The various complications inherent in these devices are becoming better known, and their contributing factors determined, which could make it possible to reduce their incidence.
    RESULTS: Some measures are integrated into recommendations for good practice, such as appropriate selection of devices, the preferential use of the thinnest catheters, and cyanoacrylate glue and dressings impregnated with chlorhexidine.
    CONCLUSIONS: Improving understanding of the phenomena leading to infectious and thrombotic complications, as well as better knowing the differences between intravenous devices and their respective indications, should lead to improvement of in-hospital and out-of-hospital care.
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  • 文章类型: Journal Article
    目的:评估癌症患者和/或其看护者或家庭的教学计划在预防和控制与长期中心静脉接入装置相关的感染方面的有效性。
    方法:本系统综述使用CINAHL,科克伦图书馆,EMBASE,LILACS,和MEDLINE通过PubMed门户,Scopus,和WebofScience。谷歌学者被用于灰色文献检索。对纳入的研究进行了分析,并对所得数据进行定性合成。使用Cochrane工具评估偏倚风险:RoB2和ROBINS-I。使用等级对证据的确定性进行评估。审查方案在PROSPERO(CRD42021267530)中注册。
    结论:在五个和两个研究中,通过理论-实践和理论维度实施了教学计划,分别。研究中偏倚的风险很低,中度,严重,高一,三,两个,其中一个,分别。确定性非常低。针对癌症患者和/或其护理人员或家庭的中心静脉接入设备护理的教学计划可以有效地降低感染率。
    结论:本系统评价涉及预防和控制与长期中心静脉接入装置相关的感染的教学计划。我们发现,大多数计划都能有效降低感染率。结果可能会影响肿瘤科护士的临床实践,因此,教育策略和方法不仅为这些患者提供,而且为护理人员和家庭提供。
    OBJECTIVE: To evaluate the effectiveness of teaching-learning programs for cancer patients and/or their caregivers or family in preventing and controlling infections associated with long-term central venous access devices.
    METHODS: This systematic review used the CINAHL, Cochrane Library, EMBASE, LILACS, and MEDLINE via PubMed portal, Scopus, and Web of Science. Google Scholar was used for the gray literature search. The included studies were analyzed, and the obtained data were qualitatively synthesized. The risk of bias was assessed using Cochrane tools: RoB 2 and ROBINS-I. The certainty of the evidence was evaluated using the GRADE. The review protocol was registered in PROSPERO (CRD42021267530).
    CONCLUSIONS: The teaching-learning programs were implemented through theoretical-practical and theoretical dimensions in five and two studies, respectively. The risk of bias in the studies was low, moderate, severe, and high in one, three, two, and one of them, respectively. The certainty was very low. Teaching-learning programs on central venous access devices care for cancer patients and/or their caregivers or families could be effective in reducing infection rates.
    CONCLUSIONS: This systematic review addressed the teaching-learning programs for preventing and controlling infections associated with long-term central venous access devices. We identified that the most programs were effective in reducing the infection rates. The results may influence the clinical practice of oncology nurses, and consequently, the educational strategies and methods provided not only to these patients but for caregivers and families.
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  • 文章类型: Journal Article
    背景:中央导管血流感染(CRBSI)是医疗保健相关感染的主要原因。然而,很少有因素被普遍接受,一些研究对一些因素有矛盾的发现,可能是由于与个体研究相关的局限性引起的。本研究旨在确定重症监护病房CRBSI的危险因素。
    方法:我们搜索了PubMed,科克伦图书馆,Webofscience和EMBASE数据库以及4个顶级中文数据库,包括万方数据,中国国家知识基础设施(CNKI),和中国科技期刊数据库(VIP),截至2023年7月的中国生物制药圆盘(CBM)。纳入病例对照和队列研究。两位作者独立筛选了文献,并使用纽卡斯尔-渥太华量表(NOS)评估了研究质量。使用比值比(OR)估计合并效应大小,计算相应的95%置信区间(CI)。CochraneQ(χ2)和I2检验用于评估研究之间的异质性,并使用固定或随机效应模型测试每个风险因素的稳健性。
    结果:共纳入32项研究,其中确定了11个因素,它们分为两类:可改变的和不可改变的因素。可改变的因素:导管插入时间(≥5d)(OR:2.07,95CI:1.41-3.03),导管插入时间(≥7d)(OR:3.62,95CI:2.65-4.97),导管插入时间(≥14d)(OR:4.85,95CI:3.35-7.01),总肠外营养(OR:2.27,95CI:1.56-3.29),使用多腔导管(OR:3.41,95CI:2.27-5.11),管留置次数(OR:3.50,95CI:2.93-4.17),ICU住院时间(OR:4.05,95CI:2.41-6.80),留置位置(OR:2.41,95CI:2.03-2.85);不可修改因素:APACHEII评分(OR:1.84,95CI:1.54-2.20),年龄≥60岁(OR:2.19,95CI:1.76-2.73),抗生素的广泛使用(OR:3.54,95CI:1.65-7.61),糖尿病(OR:3.06,95CI:2.56-3.66),免疫抑制(OR:2.87,95CI:2.08-3.95)。
    结论:针对上述可改变因素的有效干预措施可能会降低ICU发生CRBSI的风险,并改善患者的临床预后。需要进一步的前瞻性研究来证实这些发现。
    BACKGROUND: Central catheter bloodstream infections (CRBSI) is a major cause of healthcare-associated infections. However, few factors are generally accepted and some studies have conflicting finding about some factors, possibly caused by limitation associated with an individual study. This study was to identify risk factors for CRBSI in intensive care units.
    METHODS: We searched the PubMed, Cochrane Library, Web of science and EMBASE databases and the 4 top Chinese-language databases, including WanFang data, China National Knowledge Infrastructure (CNKI), and Chinese Science and Technology Journal Database (VIP), China Biology Medicine disc (CBM) as of July 2023. Case control and cohort studies were included. Two authors independently screened the literature and evaluated the quality of the studies using the Newcastle-Ottawa scale (NOS). The pooled effect size was estimated using the odds ratio (OR), and the corresponding 95% confidence interval (CI) was calculated. The Cochrane Q (χ2) and I2 tests were used to assess heterogeneity among studies, and each risk factor was tested for its robustness using fixed- or random-effects models.
    RESULTS: A total of 32 studies enrolled, among which eleven factors were identified, they were divided into two categories: modifiable and unmodifiable factors. Modifiable factors: duration of catheterization (≥ 5d) (OR: 2.07, 95%CI: 1.41-3.03), duration of catheterization (≥ 7d) (OR: 3.62, 95%CI: 2.65-4.97), duration of catheterization (≥ 14d)(OR: 4.85, 95%CI: 3.35-7.01), total parenteral nutrition (OR: 2.27,95%CI: 1.56-3.29), use of multiple-lumen catheters(OR: 3.41, 95%CI: 2.27-5.11), times of tube indwelling (OR: 3.50, 95%CI: 2.93-4.17), length of ICU stay (OR: 4.05, 95%CI: 2.41-6.80), the position of indwelling(OR: 2.41, 95%CI: 2.03-2.85); Unmodifiable factors: APACHEII scores (OR: 1.84, 95%CI: 1.54-2.20), Age≥ 60 years old (OR: 2.19, 95%CI: 1.76-2.73), the extensive use of antibiotic (OR: 3.54, 95%CI: 1.65-7.61), Diabetes mellitus (OR: 3.06, 95%CI: 2.56-3.66), Immunosuppression (OR: 2.87, 95%CI: 2.08-3.95).
    CONCLUSIONS: Effective interventions targeting the above modifiable factors may reduce the risk of developing CRBSI in ICU and improve the clinical outcome of patients. Further prospective studies are needed to confirm these findings.
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  • 文章类型: Review
    背景:医疗保健中缺乏一致的术语和定义会损害沟通,患者安全,不良事件的优化管理,和研究进展。本范围审查的目的是了解用于描述中心静脉接入装置(CVAD)的术语,在接受癌症治疗的人中,相关的并发症和过早切除的原因。它还试图确定并发症和过早切除原因的定义来源。目的是映射所使用的语言和描述,并探索标准化的机会。
    方法:对MedLine的系统搜索,PubMed,科克伦,进行CINAHLComplete和Embase数据库。资格标准包括,但不仅限于,成人癌症患者,以及2017年至2022年之间发表的研究。在Covidence中筛选文章并提取数据。数据图表包括研究特征和CVAD的详细信息,包括并发症和过早切除原因的术语和定义来源。描述性统计,表格和条形图用于总结图表数据。
    结果:从总共2363项可能符合条件的研究中,292人被纳入审查。大多数是观察性研究(n=174/60%)。总共使用了213个独特的描述符来指代CVAD,在193项研究中仅有84项(44%)定义了过早去除CVAD的所有原因,和并发症定义在292项研究中的56(57%)。如有,定义来自作者和/或来自国家资源和/或其他已发表的研究。
    结论:发现CVAD术语存在很大差异,缺乏相关并发症和过早切除原因的标准定义。这项范围审查表明,有必要标准化CVAD命名法,以加强医疗保健专业人员之间的沟通,因为正在接受癌症治疗的患者在急性和长期护理之间过渡。为了提高患者的安全性和研究方案的严谨性,提高数据共享能力。
    BACKGROUND: Lack of agreed terminology and definitions in healthcare compromises communication, patient safety, optimal management of adverse events, and research progress. The purpose of this scoping review was to understand the terminologies used to describe central venous access devices (CVADs), associated complications and reasons for premature removal in people undergoing cancer treatment. It also sought to identify the definitional sources for complications and premature removal reasons. The objective was to map language and descriptions used and to explore opportunities for standardisation.
    METHODS: A systematic search of MedLine, PubMed, Cochrane, CINAHL Complete and Embase databases was performed. Eligibility criteria included, but were not limited to, adult patients with cancer, and studies published between 2017 and 2022. Articles were screened and data extracted in Covidence. Data charting included study characteristics and detailed information on CVADs including terminologies and definitional sources for complications and premature removal reasons. Descriptive statistics, tables and bar graphs were used to summarise charted data.
    RESULTS: From a total of 2363 potentially eligible studies, 292 were included in the review. Most were observational studies (n = 174/60%). A total of 213 unique descriptors were used to refer to CVADs, with all reasons for premature CVAD removal defined in 84 (44%) of the 193 studies only, and complications defined in 56 (57%) of the 292 studies. Where available, definitions were author-derived and/or from national resources and/or other published studies.
    CONCLUSIONS: Substantial variation in CVAD terminology and a lack of standard definitions for associated complications and premature removal reasons was identified. This scoping review demonstrates the need to standardise CVAD nomenclature to enhance communication between healthcare professionals as patients undergoing cancer treatment transition between acute and long-term care, to enhance patient safety and rigor of research protocols, and improve the capacity for data sharing.
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  • 文章类型: Journal Article
    背景:隧道式中心静脉导管(CVC)是现代肿瘤学实践的基石。建立癌症患儿导管管理的最佳实践对于优化护理至关重要,但很少有指导方针来指导安置和管理。
    目的:解决四个问题:1)导管组成是否会影响并发症的发生率;2)是否存在血小板计数,低于导管放置会增加并发症的风险;3)是否存在绝对中性粒细胞计数(ANC),低于导管放置会增加并发症的风险;以及4)是否有管理中央导管相关性血流感染的最佳实践(MedABSI文章来源:OviaB:
    PubMed,Embase,WebofScience,和Cochrane数据库。
    方法:由2名评审员独立执行,第三审稿人解决了分歧。
    方法:由4名审稿人对协商一致设计的表格执行,用等级方法评估质量。
    结果:数据来自110份手稿。骨折率无显著差异,静脉血栓形成,导管阻塞或导管成分感染。最低阈值为30,000-50,000血小板/mcl的血小板减少与主要血肿无关。有限的证据表明,血小板计数<30,000/mcL与血肿的小风险增加相关。虽然很少有研究发现在ANC<500Kcells/dl的中性粒细胞减少患者的CVC中CLABSI显著增加,荟萃分析表明,该人群略有增加。对于复杂或持续性感染,建议拔除导管。有限的证据支持抗生素,乙醇,或最终导管抢救中的盐酸锁定疗法。没有高质量的数据来回答任何提出的问题。
    结论:尽管在北美每年有超过15,000个隧道导管植入癌症患儿体内,缺乏指导实践的证据,建议多种机会来改善护理。
    方法:III.本研究注册为PROSPERO2019CRD42019124077。
    BACKGROUND: Tunneled central venous catheters (CVCs) are the cornerstone of modern oncologic practice. Establishing best practices for catheter management in children with cancer is essential to optimize care, but few guidelines exist to guide placement and management.
    OBJECTIVE: To address four questions: 1) Does catheter composition influence the incidence of complications; 2) Is there a platelet count below which catheter placement poses an increased risk of complications; 3) Is there an absolute neutrophil count (ANC) below which catheter placement poses an increased risk of complications; and 4) Are there best practices for the management of a central line associated bloodstream infection (CLABSI)?
    METHODS: Data Sources: English language articles in Ovid Medline, PubMed, Embase, Web of Science, and Cochrane Databases.
    METHODS: Independently performed by 2 reviewers, disagreements resolved by a third reviewer.
    METHODS: Performed by 4 reviewers on forms designed by consensus, quality assessed by GRADE methodology.
    RESULTS: Data were extracted from 110 manuscripts. There was no significant difference in fracture rate, venous thrombosis, catheter occlusion or infection by catheter composition. Thrombocytopenia with minimum thresholds of 30,000-50,000 platelets/mcl was not associated with major hematoma. Limited evidence suggests a platelet count <30,000/mcL was associated with small increased risk of hematoma. While few studies found a significant increase in CLABSI in CVCs placed in neutropenic patients with ANC<500Kcells/dl, meta-analysis suggests a small increase in this population. Catheter removal remains recommended in complicated or persistent infections. Limited evidence supports antibiotic, ethanol, or hydrochloric lock therapy in definitive catheter salvage. No high-quality data were available to answer any of the proposed questions.
    CONCLUSIONS: Although over 15,000 tunneled catheters are placed annually in North America into children with cancer, there is a paucity of evidence to guide practice, suggesting multiple opportunities to improve care.
    METHODS: III. This study was registered as PROSPERO 2019 CRD42019124077.
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  • 文章类型: Systematic Review
    目的:评价中心静脉导管相关性血栓形成(CRT)临床实践指南的质量和内容,为制定循证实践方案和预防CRT风险评估量表提供依据。
    方法:使用AGREEII和AGREEREX量表对指南进行评分和分析。
    方法:发布,Embase,科克伦图书馆,WebofScience,CNKI,万方,VIP,和中国生物医学文献,以及该指南的相关网站,从2017年1月1日至2022年3月26日进行了搜索。
    方法:涵盖CRT治疗的指南,预防,或管理纳入时间为2017年1月1日至2022年3月26日.
    方法:选择了三名接受过使用AGREEII和AGREEREX量表系统培训的独立评审人员来评估这些指南。
    结果:包括9个指南,质量等级结果显示,3人处于A级,6人处于B级。纳入的指南主要从三个方面建议了中心静脉CRT的预防措施:风险筛查,预防策略,和知识培训,共提出22项建议。
    结论:指南的总体质量很高,但是指南中很少涉及中心静脉CRT的预防措施。所有预防措施尚待系统整合和评估,并且没有推荐专门用于该领域的风险评估量表。因此,迫切需要制定基于证据的实践协议和风险评估量表来预防这种情况。
    OBJECTIVE: To evaluate the quality and analyse the content of clinical practice guidelines regarding central venous catheter-related thrombosis (CRT) to provide evidence for formulating an evidence-based practice protocol and a risk assessment scale to prevent it.
    METHODS: Scoring and analysis of the guidelines using the AGREE II and AGREE REX scales.
    METHODS: Pubmed, Embase, Cochrane Library, Web of Science, CNKI, Wanfang, VIP, and the Chinese Biomedical Literature, and the relevant websites of the guideline, were searched from 1 January 2017 to 26 March 2022.
    METHODS: Guidelines covering CRT treatment, prevention, or management were included from 1 January 2017 to 26 March 2022.
    METHODS: Three independent reviewers systematically trained in using the AGREE II and AGREE REX scales were selected to evaluate these guidelines.
    RESULTS: Nine guidelines were included, and the quality grade results showed that three were at A-level and six were at B-level. The included guidelines mainly recommended the prevention measure of central venous CRT from three aspects: risk screening, prevention strategies, and knowledge training, with a total of 22 suggestions being recommended.
    CONCLUSIONS: The overall quality of the guidelines is high, but there are few preventive measures for central venous CRT involved in the guidelines. All preventive measures have yet to be systematically integrated and evaluated, and no risk assessment scale dedicated to this field has been recommended. Therefore, developing an evidence-based practice protocol and a risk assessment scale to prevent it is urgent.
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  • 文章类型: Journal Article
    中心静脉导管(CVC)是常用的,但与并发症有关。量化并发症发生率对于指导CVC利用决策至关重要。
    总结当前CVC相关并发症的发生率。
    MEDLINE,Embase,CINAHL,在CENTRAL数据库中搜索了2015年至2023年间发表的观察性研究和随机临床试验.
    本研究包括英语观察性研究和成年患者的随机临床试验,这些研究报告了短期中央插入性CVC的并发症发生率和1个或多个目标结局的数据。评估长期血管内装置的研究,专注于通常不用于药物管理的透析导管,或由放射科医师放置的研究导管被排除.
    两名评审员独立提取数据并评估偏倚风险。贝叶斯随机效应荟萃分析用于总结事件发生率。估计了放置并发症(事件/1000个导管,95%可信间隔[CrI])和使用并发症(事件/1000个导管天,95%CrI)的发生率。
    与CVC放置相关的十种预设并发症(放置失败,动脉穿刺,动脉插管,气胸,出血事件需要采取行动,神经损伤,动静脉瘘,心脏填塞,心律失常,血管加压药给药延迟≥1小时)和5种与CVC使用相关的预设并发症(功能障碍,感染,深静脉血栓形成[DVT],血栓性静脉炎,和静脉狭窄)进行评估。4种严重并发症的复合(动脉插管,气胸,感染,或DVT)在CVC暴露3天后也进行了评估。
    在11722项筛选研究中,130人被纳入分析。对15种预设并发症中的7种进行了荟萃分析。放置失败发生在20.4(95%CrI,10.9-34.4)每放置1000个导管的事件。CVC置入并发症的其他发生率(每1000根导管)为动脉插管(2.8;95%CrI,0.1-10),动脉穿刺(16.2;95%CrI,11.5-22),和气胸(4.4;95%CrI,2.7-6.5)。CVC使用并发症的发生率(每1000个导管天)为故障(5.5;95%CrI,0.6-38),感染(4.8;95%CrI,3.4-6.6),和DVT(2.7;95%CrI,1.0-6.2)。据估计,30.2(95%CrI,21.8-43.0)在1000例CVC持续3天的患者中,会出现1种或更严重的并发症(动脉插管,气胸,感染,或DVT)。使用超声检查与较低的动脉穿刺率相关(风险比[RR],0.20;95%CrI,0.09-0.44;13.5事件vs68.8事件/1000导管)和气胸(RR,0.25;95%CrI,0.08-0.80;2.4事件vs9.9事件/1000导管)。
    大约3%的CVC植入与主要并发症相关。使用超声引导可以降低特定风险,包括动脉穿刺和气胸。
    UNASSIGNED: Central venous catheters (CVCs) are commonly used but are associated with complications. Quantifying complication rates is essential for guiding CVC utilization decisions.
    UNASSIGNED: To summarize current rates of CVC-associated complications.
    UNASSIGNED: MEDLINE, Embase, CINAHL, and CENTRAL databases were searched for observational studies and randomized clinical trials published between 2015 to 2023.
    UNASSIGNED: This study included English-language observational studies and randomized clinical trials of adult patients that reported complication rates of short-term centrally inserted CVCs and data for 1 or more outcomes of interest. Studies that evaluated long-term intravascular devices, focused on dialysis catheters not typically used for medication administration, or studied catheters placed by radiologists were excluded.
    UNASSIGNED: Two reviewers independently extracted data and assessed risk of bias. Bayesian random-effects meta-analysis was applied to summarize event rates. Rates of placement complications (events/1000 catheters with 95% credible interval [CrI]) and use complications (events/1000 catheter-days with 95% CrI) were estimated.
    UNASSIGNED: Ten prespecified complications associated with CVC placement (placement failure, arterial puncture, arterial cannulation, pneumothorax, bleeding events requiring action, nerve injury, arteriovenous fistula, cardiac tamponade, arrhythmia, and delay of ≥1 hour in vasopressor administration) and 5 prespecified complications associated with CVC use (malfunction, infection, deep vein thrombosis [DVT], thrombophlebitis, and venous stenosis) were assessed. The composite of 4 serious complications (arterial cannulation, pneumothorax, infection, or DVT) after CVC exposure for 3 days was also assessed.
    UNASSIGNED: Of 11 722 screened studies, 130 were included in the analyses. Seven of 15 prespecified complications were meta-analyzed. Placement failure occurred at 20.4 (95% CrI, 10.9-34.4) events per 1000 catheters placed. Other rates of CVC placement complications (per 1000 catheters) were arterial canulation (2.8; 95% CrI, 0.1-10), arterial puncture (16.2; 95% CrI, 11.5-22), and pneumothorax (4.4; 95% CrI, 2.7-6.5). Rates of CVC use complications (per 1000 catheter-days) were malfunction (5.5; 95% CrI, 0.6-38), infection (4.8; 95% CrI, 3.4-6.6), and DVT (2.7; 95% CrI, 1.0-6.2). It was estimated that 30.2 (95% CrI, 21.8-43.0) in 1000 patients with a CVC for 3 days would develop 1 or more serious complication (arterial cannulation, pneumothorax, infection, or DVT). Use of ultrasonography was associated with lower rates of arterial puncture (risk ratio [RR], 0.20; 95% CrI, 0.09-0.44; 13.5 events vs 68.8 events/1000 catheters) and pneumothorax (RR, 0.25; 95% CrI, 0.08-0.80; 2.4 events vs 9.9 events/1000 catheters).
    UNASSIGNED: Approximately 3% of CVC placements were associated with major complications. Use of ultrasonography guidance may reduce specific risks including arterial puncture and pneumothorax.
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  • DOI:
    文章类型: Case Reports
    血液透析患者中中心静脉导管(CVC)的患病率约为20-30%。在这种情况下,通常观察到与使用CVC有关的并发症,需要肾病学家的积极管理。这些包括感染性并发症以及与CVC故障相关的并发症。在后者中,与异物反应有关的导管周围纤维蛋白鞘的形成可能以多种方式导致CVC功能障碍。即使在拔掉导管后,纤维蛋白鞘可以保留在血管腔内(幽灵纤维蛋白鞘),很少发生钙化。我们描述了一个血液透析患者的临床案例,在移除故障后,卡滞CVC,上腔静脉管腔内呈现钙化的管状结构,诊断为钙化纤维蛋白鞘(CFS)。这种罕见的情况,文献中描述了另外8个案例,虽然罕见,当然是诊断不足,可能导致并发症,如CFS引起的败血症,肺栓塞,血管血栓形成.治疗方法应仅在有症状的情况下考虑,并且涉及侵入性手术方法。
    The prevalence of central venous catheters (CVC) in hemodialysis patients is around 20-30%. In this scenario, complications related to the use of the CVC are commonly observed, requiring active management by nephrologists. These include infectious complications as well as those related to CVC malfunction. Among the latter, the formation of a fibrin sheath around the catheter linked to foreign body reaction could cause CVC malfunction in various ways. Even after the removal of the catheter, the fibrin sheath can remain inside the vascular lumen (ghost fibrin sheath) and rarely undergo calcification. We describe the clinical case of a hemodialysis patient who, following the removal of a malfunctioning, stuck CVC, presented a calcified tubular structure in the lumen of the superior vena cava, diagnosed as calcified fibrin sheath (CFS). This rare occurrence, described in the literature in 8 other cases, although rare, is certainly underdiagnosed and can lead to complications such as sepsis resulting from CFS, pulmonary embolisms, and vascular thrombosis. Therapeutic approaches should be considered only in symptomatic cases and involve an invasive surgical approach.
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  • 文章类型: Systematic Review
    背景:血管内导管是医疗实践中的关键设备,会增加医疗保健相关感染(HAIs)的风险,以及相关的健康经济不良结果。本范围审查旨在全面概述已发布的用于监测导管相关血流感染(CRBSI)和中心线相关血流感染(CLABSI)的自动算法。
    方法:我们根据2000年1月1日至2021年12月31日在PubMed和EMBASE中对文献的系统搜索进行了范围审查。如果他们评估CLABSI/CRBSI检测的自动监测算法的预测性能并使用手动收集的监测数据作为参考,则包括研究。我们评估了自动化系统的设计,包括用于开发算法的定义(CLABSI与CRBSI),使用的数据集和分母,和每个研究中评估的算法。
    结果:我们根据标题和摘要筛选了586项研究,99人基于全文进行评估。九项研究被纳入范围审查。大多数研究是单中心的(n=5),他们确定CLABSI(n=7)作为结果。大多数研究使用管理和微生物数据(n=9),五项研究包括在其自动化系统中存在血管中心线。六项研究解释了他们选择的分母,其中五个选择了中线日。算法中使用的最常见的规则和步骤被归类为医院获取的规则,感染规则(感染与污染),重复数据删除,剧集分组,辅助BSI规则(辅助与主BSI),和导管相关规则。
    结论:我们确定的自动监测系统在定义方面是异构的,使用的数据集和分母,每个算法中的规则组合。需要进一步的指南和研究来开发和实施检测CLABSI/CRBSI的算法,有了标准化的定义,适当的数据源和适当的分母。
    BACKGROUND: Intravascular catheters are crucial devices in medical practice that increase the risk of healthcare-associated infections (HAIs), and related health-economic adverse outcomes. This scoping review aims to provide a comprehensive overview of published automated algorithms for surveillance of catheter-related bloodstream infections (CRBSI) and central line-associated bloodstream infections (CLABSI).
    METHODS: We performed a scoping review based on a systematic search of the literature in PubMed and EMBASE from 1 January 2000 to 31 December 2021. Studies were included if they evaluated predictive performance of automated surveillance algorithms for CLABSI/CRBSI detection and used manually collected surveillance data as reference. We assessed the design of the automated systems, including the definitions used to develop algorithms (CLABSI versus CRBSI), the datasets and denominators used, and the algorithms evaluated in each of the studies.
    RESULTS: We screened 586 studies based on title and abstract, and 99 were assessed based on full text. Nine studies were included in the scoping review. Most studies were monocentric (n = 5), and they identified CLABSI (n = 7) as an outcome. The majority of the studies used administrative and microbiological data (n = 9) and five studies included the presence of a vascular central line in their automated system. Six studies explained the denominator they selected, five of which chose central line-days. The most common rules and steps used in the algorithms were categorized as hospital-acquired rules, infection rules (infection versus contamination), deduplication, episode grouping, secondary BSI rules (secondary versus primary BSI), and catheter-associated rules.
    CONCLUSIONS: The automated surveillance systems that we identified were heterogeneous in terms of definitions, datasets and denominators used, with a combination of rules in each algorithm. Further guidelines and studies are needed to develop and implement algorithms to detect CLABSI/CRBSI, with standardized definitions, appropriate data sources and suitable denominators.
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