Schoot Reineke A, van Dalen Elvira C, van Ommen Cornelia H, van de Wetering Marianne D
Department of Paediatric Oncology, Emma Children’s Hospital / Academic Medical Center, Amsterdam, Netherlands.
Cochrane Database Syst Rev. 2013 Jun 25;2013(6):CD008975. doi: 10.1002/14651858.CD008975.pub2.
The risk of developing a tunnelled central venous catheter (CVC)-related infection ranges between 0.1 and 2.3 per 1000 catheter days for children with cancer. These infections are difficult to treat with systemic antibiotics (salvage rate 24% - 66%) due to biofilm formation in the CVC. Lock treatments can achieve 100 - 1000 times higher concentrations locally without exposure to high systemic concentrations.
Our objective was to investigate the efficacy of antibiotic and other lock treatments in the treatment of CVC-related infections in children with cancer compared to a control intervention. We also assessed adverse events of lock treatments.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, issue 3, 2011), MEDLINE/PubMed (1945 to August 2011) and EMBASE/Ovid (1980 to August 2011). In addition we searched reference lists from relevant articles and the conference proceedings of the International Society for Paediatric Oncology (SIOP) (from 2006 to 2010), American Society of Clinical Oncology (ASCO) (from 2006 to 2010), the Multinational Association of Supportive Care in Cancer (MASCC) (from 2006 to 2011), the American Society of Hematology (ASH) (from 2006 to 2010) and the International Society of Thrombosis and Haematology (ISTH) (from 2006 to 2011). We scanned the ISRCTN Register and the National Institute of Health Register for ongoing trials (www.controlled-trials.com) (August 2011).
Randomised controlled trials (RCTs) and controlled clinical trials (CCTs) comparing an antibiotic lock or other lock treatment (with or without concomitant systemic antibiotics) with a control intervention (other lock treatment with or without concomitant systemic antibiotics or systemic antibiotics alone) for the treatment of CVC-related infections in children with cancer. For the description of adverse events, cohort studies were also eligible for inclusion.
Two authors independently selected studies, extracted data and performed 'Risk of bias' assessments of included studies. Analyses were performed according to the guidelines of the Cochrane Handbook for Systematic Reviews of Interventions.
Two RCTs evaluated urokinase lock treatment with concomitant systemic antibiotics (n = 56) versus systemic antibiotics alone (n = 48), and one CCT evaluated ethanol lock treatment with concomitant systemic antibiotics (n = 15) versus systemic antibiotics alone (n = 13). No RCTs or CCTs evaluating antibiotic lock treatments were identified. All studies had methodological limitations and clinical heterogeneity between studies was present. We found no evidence of significant difference between ethanol or urokinase lock treatments with concomitant systemic antibiotics and systemic antibiotics alone regarding the number of participants cured, the number of recurrent CVC-related infections, the number of days until the first negative blood culture, the number of CVCs prematurely removed, ICU admission and sepsis. Not all studies were included in all analyses. No adverse events occurred in the five publications of cohort studies (one cohort was included in two publications) assessing this outcome; CVC malfunctioning occurred in three out of five publications of cohort studies assessing this outcome.
AUTHORS' CONCLUSIONS: No significant effect of urokinase or ethanol lock in addition to systemic antibiotics was found. However, this could be due to low power or a too-short follow-up. The cohort studies identified no adverse events; some cohort studies reported CVC malfunctioning. No RCTs or CCTs were published on antibiotic lock treatment alone. More well-designed RCTs are needed to further explore the effect of antibiotic or other lock treatments in the treatment of CVC-related infections in children with cancer.
癌症患儿发生带隧道中心静脉导管(CVC)相关感染的风险为每1000导管日0.1至2.3例。由于CVC中生物膜的形成,这些感染难以用全身抗生素治疗(挽救率为24% - 66%)。封管治疗可在局部实现高100 - 1000倍的浓度,而不会使全身暴露于高浓度药物。
我们的目的是研究与对照干预相比,抗生素封管及其他封管治疗在癌症患儿CVC相关感染治疗中的疗效。我们还评估了封管治疗的不良事件。
我们检索了Cochrane对照试验中心注册库(CENTRAL)(《Cochrane图书馆》,2011年第3期)、MEDLINE/PubMed(1945年至2011年8月)和EMBASE/Ovid(1980年至2011年8月)。此外,我们还检索了相关文章的参考文献列表以及国际小儿肿瘤学会(SIOP)(2006年至2010年)、美国临床肿瘤学会(ASCO)(2006年至2010年)、癌症支持治疗多国协会(MASCC)(2006年至2011年)、美国血液学会(ASH)(2006年至2010年)和国际血栓与止血学会(ISTH)(2006年至2011年)的会议记录。我们浏览了ISRCTN注册库和美国国立卫生研究院注册库以查找正在进行的试验(www.controlled-trials.com)(2011年8月)。
随机对照试验(RCT)和对照临床试验(CCT),比较抗生素封管或其他封管治疗(伴或不伴全身抗生素)与对照干预(其他封管治疗伴或不伴全身抗生素或仅用全身抗生素)用于治疗癌症患儿CVC相关感染。对于不良事件的描述,队列研究也符合纳入标准。
两位作者独立选择研究、提取数据并对纳入研究进行“偏倚风险”评估。分析按照Cochrane干预措施系统评价手册的指南进行。
两项RCT评估了尿激酶封管治疗联合全身抗生素(n = 56)与单纯全身抗生素(n = 48),一项CCT评估了乙醇封管治疗联合全身抗生素(n = 15)与单纯全身抗生素(n = 13)。未发现评估抗生素封管治疗的RCT或CCT。所有研究均存在方法学局限性,且研究间存在临床异质性。我们发现,在治愈的参与者数量、CVC相关感染复发的数量、首次血培养转阴前的天数、过早拔除的CVC数量、入住重症监护病房(ICU)情况和败血症方面,乙醇或尿激酶封管治疗联合全身抗生素与单纯全身抗生素之间未发现显著差异。并非所有研究都纳入了所有分析。在评估该结果的队列研究的五篇出版物中(一项队列研究包含在两篇出版物中)未发生不良事件;在评估该结果的队列研究的五篇出版物中有三篇报道了CVC功能障碍。
未发现尿激酶或乙醇封管联合全身抗生素有显著效果。然而,这可能是由于检验效能低或随访时间过短。队列研究未发现不良事件;一些队列研究报告了CVC功能障碍。未发表关于单纯抗生素封管治疗的RCT或CCT。需要更多设计良好的RCT来进一步探索抗生素或其他封管治疗在癌症患儿CVC相关感染治疗中的效果。