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Minimally invasive endoscopic staging for mediastinal lymphadenopathy in lung cancer: a systematic review protocol

机译:肺癌纵隔淋巴结肿大的微创内镜分期:系统评价方案

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Introduction Minimally invasive endoscopic biopsy techniques have been widely available as potential alternatives for mediastinal lesions staging in patients with known or suspected lung cancer. Previous efforts have been made to evaluate the diagnostic performance of specific endoscopic modality alone at the level of the mediastinum for staging lung cancer, however, few studies focus on the accuracy of comparisons between different endoscopic modalities, especially at the level of any individual lymph node station. The objective of our study is to determine the diagnostic yields of different endoscopic modalities for staging mediastinal lymphadenopathy in lung cancer, especially concerning the individual lymph node station. Methods/design A systematic electronic search of MEDLINE, EMBASE, SinoMed and ISI Web of Science were performed to identify studies evaluating endoscopic modalities accuracy with restriction of English and Chinese languages from inception to an update until May 2014. Data were extracted with the patient as the unit of analysis with regards to the abilities of different endoscopic modalities at the level of mediastinum and particular lymph node station. The methodological quality was assessed independently according to the Quality Assessment of Diagnostic Accuracy Study (QADAS) criteria. An exact binomial rendition of bivariate mixed-effects regression model was used to estimate the pooled sensitivity and specificity. Also, pre–post probability analysis, publication bias analysis and sensitivity analysis were performed for a synthesis of knowledge of this context. Dissemination The findings will advance our better available knowledge of optimal clinical decision-making when dealing with staging of mediastinal metastasis in lung cancer. Trial registration number PROSPERO—NIHR Prospective Register of Systematic Reviews (CRD42014009792).
机译:简介微创内窥镜活检技术已被广泛用作已知或疑似肺癌患者纵隔病变分期的潜在替代方法。以往曾尝试在纵隔水平上评估特定内镜方式对肺癌分期的诊断性能,但是,很少有研究侧重于不同内窥镜方式之间比较的准确性,特别是在任何单个淋巴结水平上站。我们研究的目的是确定肺癌内镜纵隔淋巴结病分期的不同内窥镜检查方法的诊断率,特别是涉及单个淋巴结站。方法/设计从开始到更新至2014年5月,进行了MEDLINE,EMBASE,SinoMed和ISI Web of Science的系统电子搜索,以鉴定评估内窥镜检查方式准确性并限制英语和汉语的研究。关于纵隔和特定淋巴结站水平的不同内窥镜检查方式的能力的分析单位。方法学质量是根据诊断准确性研究质量评估(QADAS)标准独立评估的。使用双变量混合效应回归模型的精确二项式表示法来估计合并的敏感性和特异性。此外,还进行了事前概率分析,出版物偏倚分析和敏感性分析,以综合了解这种情况。传播这些发现将有助于我们更好地掌握有关肺癌纵隔转移分期的最佳临床决策知识。试用注册号PROSPERO-NIHR系统评价预期注册(CRD42014009792)。

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