Abstract

Although rapid on-site cytologic evaluation provides high efficacy of EUS-guided FNA (EUS-FNA), its availability is limited. Alternatively, macroscopic on-site quality evaluation (MOSE) may increase the efficacy of EUS-FNA. To assess the efficacy of MOSE in estimating the adequacy of histologic core specimens obtained by EUS-FNA using a standard 19-gauge needle (19GN) for solid lesions. A prospective pilot study. Tertiary-care referral center. One hundred patients with solid lesions (n= 111 lesions). EUS-FNA using 19GN MAIN OUTCOME MEASUREMENTS: The relation of a macroscopic visible core (MVC) in the FNA specimens on MOSE with histologic core and the diagnostic yields were studied. The feasibility of EUS-FNA using a 19GN was 99%. The final diagnoses were malignancy in 83 lesions and benign in 28. MOSE revealed MVC in 91.1% with the median length of 8mm. Histologic core was confirmed in 78.9%. The receiver-operating characteristic curve of the length of MVC for the presence of histologic core showed the cut-off MVC length of 4mm with area under the curve of .893. Comparisons of per-pass diagnosticyields showed significantly superior histologic, cytologic, and overall diagnostic yields in MVC≥ 4mm as compared with<4mm. The multivariate analysis for false-negative pass identified lesion in the pancreas and MVC<4mm as significant risk factors. No adverse events were seen. Single center, limited operators MVC of≥4mm on MOSE can be an indicator of specimen adequacy and can improve diagnostic yield; however, additional FNA may be recommended for pancreatic lesions. ( UMIN000010417.).

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