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Time gated fluorescence spectroscopy in Barrett’s oesophagus

机译:巴雷特食管中的时间门控荧光光谱

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摘要

>Background and aims: Specialised intestinal metaplasia and its dysplastic transformation, which precedes cancer in Barrett’s oesophagus cannot be differentiated in standard gastroscopy. The aim of this study was to investigate whether laser induced protoporphyrin IX fluorescence permits the detection of specialised intestinal metaplasia and dysplasia during endoscopy and to take biopsy specimens in a guided rather than random manner.>Methods: In 53 patients with Barrett’s oesophagus 5-aminolaevulinic acid was sprayed on the mucosa. Approximately 60 to 120 minutes later, biopsy specimens were taken based on point-like measurements of delayed fluorescence intensity ratios of protoporphyrin IX in vivo. Two independent pathologists examined the 596 biopsy specimens taken, 168 of which were selected to be investigated by a third pathologist. Among these specimens only those (n=141) with a consensus diagnosis by at least two pathologists and p53 expression as additional marker were included in the analysis.>Results: The median of normalised fluorescence intensity (ratio of delayed PpIX fluorescence intensity to immediate autofluorescence intensity) in non-dysplastic specialised intestinal metaplasia (0.51, 68% CI 0.09 to 1.92) and low grade dysplasia (1.89, 68% CI 0.55 to 3.92) differed significantly (p<0.005). Dysplasia was detected at a rate 2.8-fold higher compared with screening endoscopy despite taking fewer specimens. In addition, three early cancers were detected for the first time. Moreover, this method permitted differentiation of specialised intestinal metaplasia from junctional or gastric-fundic type epithelium (p<0.013).>Conclusions: For the first time it was possible to differentiate low grade dysplasia from non-dysplastic Barrett’s mucosa during endoscopy based on delayed laser induced fluorescence endoscopy of PpIX. Furthermore, the method helps to detect specialised intestinal metaplasia in short Barrett’s oesophagus.
机译:>背景和目标:标准的胃镜检查无法区分发生在Barrett食道癌发生之前的特殊肠化生及其异常增生性转化。这项研究的目的是调查激光诱导的原卟啉IX荧光是否可以在内窥镜检查过程中检测到特殊的肠化生和异型增生,并以指导方式而非随机方式获取活检标本。>方法:用巴雷特氏食管将5-氨基乳油酸喷在粘膜上。大约60至120分钟后,根据体内原卟啉IX的延迟荧光强度比的点状测量,获取活检标本。两名独立的病理学家检查了所采集的596个活检标本,其中的168个被选择由第三位病理学家进行检查。在这些标本中,仅包括至少由两名病理学家诊断为共识且p53表达为其他标记物的标本(n = 141)。>结果:归一化荧光强度的中位数(延迟比)在非典型增生性肠上皮化生(0.51,68%CI 0.09至1.92)和低度异型增生(1.89,68%CI 0.55至3.92)中,PpIX荧光强度与即刻自身荧光强度有显着差异(p <0.005)。尽管减少了标本的采集,但与筛查内窥镜检查相比,异型增生的发生率高出2.8倍。此外,首次发现了三种早期癌症。此外,这种方法可以区分特殊的肠上皮化生与结节型或胃底型上皮(p <0.013)。>结论:首次有可能将低度不典型增生与非典型增生性Barrett病区分开。基于延迟激光诱导的PpIX荧光内窥镜检查的内镜检查中的粘膜。此外,该方法还有助于检测短巴雷特食管中特殊的肠上皮化生。

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