FNB

FNB
  • 文章类型: Journal Article
    目的:采用系统评价方法定量比较超声内镜引导下细针穿刺活检(EUS-FNA)和超声内镜引导下细针穿刺活检(EUS-FNB)对胰腺实性肿块病变的诊断价值。方法:在公共数据库上进行系统的文献检索,包括比较EUS-FNA和EUS-FNB在胰腺实性肿块性病变中的诊断价值的研究。综合效应大小分别用平均差(MD)和风险差(RD)估计,计算相应的95%置信区间(CI)。结果:12篇文献(7篇随机对照试验和5篇队列研究)符合本研究的纳入标准。Meta分析显示,与EUS-FNB相比,EUS-FNA具有较低的诊断准确性(RD:-0.08,95%CI:-0.15,-0.01)和标本充分性(RD:-0.08,95%CI:-0.15,-0.02),而所需的针头通过次数较高(MD:0.42,95%CI:0.12,0.73)。然而,EUS-FNB和EUS-FNA表现出相似的总体并发症(RD:0.00,95%CI:-0.01,0.02)和技术故障(RD:-0.01,95%CI:-0.02,0.00),没有统计学上的显著差异。结论:与EUS-FNA相比,EUS-FNB似乎是诊断可疑胰腺病变的更好选择。
    Objective: To quantitatively compare the diagnostic value of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) and endoscopic ultrasound-guided fine needle biopsy (EUS-FNB) in solid pancreatic mass lesions using a systematic evaluation method.Methods: A systematic literature search was conducted on public databases to include studies comparing the diagnostic value of EUS-FNA and EUS-FNB in solid pancreatic mass lesions. The combined effect size was estimated using mean difference (MD) and risk difference (RD) respectively, and the corresponding 95% confidence interval (CI) was calculated.Results: The 12 articles (7 RCTs and 5 cohort studies) met the inclusion criteria of this study. The meta-analysis showed that compared with EUS-FNB, EUS-FNA had lower diagnostic accuracy (RD: -0.08, 95% CI: -0.15, -0.01) and specimen adequacy (RD: -0.08, 95% CI: -0.15, -0.02), while higher required number of needle passes (MD: 0.42, 95% CI: 0.12, 0.73). However, EUS-FNB and EUS-FNA presented similar overall complications (RD: 0.00, 95% CI: -0.01, 0.02) and technical failures (RD: -0.01, 95% CI: -0.02, 0.00), without statistically significant differences.Conclusions: Compared with EUS-FNA, EUS-FNB seems to be a better choice for diagnosing suspected pancreatic lesions.
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  • 文章类型: Journal Article
    Medicago truncatula has been selected as a model species for legume molecular genetics and functional genomics studies. With the completion of the Medicago truncatula cv. Jemalong A17 genome sequencing, a major challenge is to determine the function of the large number of genes in the genome. Development of diverse mutant resources is crucial for gene functional studies. In the past years, M2 seeds from over 150,000 Medicago truncatula mutant lines in the Jemalong A17 background have been generated coordinately at the Noble Research Institute, USA, and the John Innes Centre, UK, using fast neutron bombardment (FNB) mutagenesis. These mutant resources have been used in screening and characterization of different categories of mutants including symbiotic nitrogen fixation, nodule development, and growth and patterning of leaf, stem, and root system architecture in the legume system. Here, we describe the detail procedure that has been used for screening of mutants derived from fast neutron bombardment mutagenesis in Medicago truncatula.
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