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      Accuracy and Quality Assessment of EUS-FNA: A Single-Center Large Cohort of Biopsies

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          Abstract

          Introduction. Thorough quality control (QC) study with systemic monitoring and evaluation is crucial to optimizing the effectiveness of EUS-FNA. Methods. Retrospective analysis was composed of investigating consecutive patient files that underwent EUS-FNA. QC specifically focused on diagnostic accuracy, impacts on preexisting diagnoses, and case management. Results. 268 patient files were evaluated. EUS-FNA cytology helped establish accurate diagnoses in 92.54% (248/268) of patients. Sensitivity, specificity, PPV, NPV, and accuracy were 83%, 100%, 100%, 91.6%, and 94%, respectively. The most common biopsy site was the pancreas (68%). The most accurate location for EUS-FNA was the esophagus, 13/13 (100%), followed by the pancreas (89.6%). EUS-FNA was least informative for abdominal lymph nodes (70.5%). After FNA and followup, eight false negatives for tumors were found (3%), while 7.5% of samples still lacked a definitive diagnosis. Discussion. QC suggests that the diagnostic accuracy of EUS-FNA might be improved further by (1) taking more FNA passes from suspected lesions, (2) optimizing needle selection (3) having an experienced echo-endoscopist available during the learning curve, and (4) having a cytologist present during the procedure. QC also identified remediable reporting errors. In conclusion, QC study is valuable in identifying weaknesses and thereby augmenting the effectiveness of EUS-FNA.

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          Most cited references21

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          Assessment of morbidity and mortality associated with EUS-guided FNA: a systematic review.

          EUS-guided FNA (EUS-FNA) permits both morphologic and cytologic analysis of lesions within or adjacent to the GI tract. Although previous studies have evaluated the accuracy of EUS-FNA, little is known about the complications of EUS-FNA. Moreover, the frequency and severity of complications may vary from center to center and may be related to differences in individual experience. To systematically review the morbidity and mortality associated with EUS-FNA. MEDLINE and EMBASE were searched to identify relevant English-language articles. EUS-FNA-specific morbidity and mortality rates. We identified 51 articles with a total of 10,941 patients who met our inclusion and exclusion criteria; the overall rate of EUS-FNA-specific morbidity was 0.98% (107/10,941). In the small proportion of patients with complications of any kind, the rates of pancreatitis (36/8246; 0.44%) and postprocedure pain (37/10,941; 0.34%) were 33.64% (36/107) and 34.58% (37/107), respectively. The mortality rate attributable to EUS-FNA-specific morbidity was 0.02% (2/10,941). Subgroup analysis showed that the morbidity rate was 2.44% in prospective studies compared with 0.35% in retrospective studies for pancreatic mass lesions (P=.000), whereas it was 2.33% versus 5.07% for pancreatic cysts (P=.036). Few articles reported well-designed, prospective studies and few focused on overall complications after EUS-FNA. EUS-FNA-related morbidity and mortality rates are relatively low, and most associated events are mild to moderate in severity. Copyright © 2011 American Society for Gastrointestinal Endoscopy. Published by Mosby, Inc. All rights reserved.
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            BIOPSY BY NEEDLE PUNCTURE AND ASPIRATION.

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              Role of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) for diagnosis of solid pancreatic masses.

              Since it was developed in 1992, endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) has been widely used and has been adapted for gastrointestinal and perigastrointestinal lesions. A medical literature review to evaluate the role of EUS-FNA for diagnosis of solid pancreatic masses showed a 78-95% sensitivity, 75-100% specificity, 98-100% positive predictive value, 46-80% negative predictive value and a 78-95% accuracy. The reported complication rates of EUS-FNA for pancreatic solid masses were 0-2%, although the criteria for complications varied among the studies. Because of its high diagnostic yield and low complication rate, EUS-FNA is cost-effective and widely applicable for the diagnosis of solid pancreatic masses, and is the best initial and the preferred secondary method compared with other biopsy techniques, such as endoscopic retrograde cholangiopancreatography-guided biopsy, computed tomography/ultrasound-FNA and surgery. Although EUS-FNA is 'a nearly perfected procedure,' controversy remains, such as the most suitable diameter of the needle, the appropriate number of needle passes and the necessity of on-site cytopathological evaluation. Recently investigators reported that using molecular analysis of EUS-FNA samples can achieve a higher diagnostic efficacy. Further research is encouraged to optimize the EUS-FNA procedure to reach its maximum diagnostic yield for solid pancreatic masses. © 2011 The Authors. Digestive Endoscopy © 2011 Japan Gastroenterological Endoscopy Society.
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                Author and article information

                Journal
                Diagn Ther Endosc
                Diagn Ther Endosc
                DTE
                Diagnostic and Therapeutic Endoscopy
                Hindawi Publishing Corporation
                1070-3608
                1029-0516
                2012
                31 October 2012
                : 2012
                : 139563
                Affiliations
                1Technion-Israel Institute of Technology, The Bruce and Ruth Rappaport Faculty of Medicine, Israel
                2Technion-Israel Institute of Technology and EUS Service, The Bruce and Ruth Rappaport Faculty of Medicine, Rambam Healthcare Campus, Haifa, Israel
                3Departments of Gastroenterology and Community Medicine, Rambam Health Care Campus, Haifa, Israel
                4Oncology Ambulatory Care, Rambam Healthcare Campus, Haifa, Israel
                Author notes
                *Benjamin Ephraim Bluen: bbluen@ 123456gmail.com

                Academic Editor: Arthur Hoffman

                Article
                10.1155/2012/139563
                3503321
                23197929
                2cb12692-bfe1-4b79-a6bf-4187f1fcbfdd
                Copyright © 2012 Benjamin Ephraim Bluen et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 May 2012
                : 28 August 2012
                Categories
                Research Article

                Radiology & Imaging
                Radiology & Imaging

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