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Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size

Background and study aims: Despite a well-established tool for diagnosis of pancreatic masses, endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) studies have shown suboptimal diagnostic performance at divergent mass sizes. Since the impact of gold standard follow-up and presence of on-si...

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Autores principales: Ramesh, Jayapal, Kim, Hwasoon, Reddy, Kartika, Eltoum, Isam-Eldin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: © Georg Thieme Verlag KG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831926/
https://www.ncbi.nlm.nih.gov/pubmed/27092323
http://dx.doi.org/10.1055/s-0035-1569969
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author Ramesh, Jayapal
Kim, Hwasoon
Reddy, Kartika
Eltoum, Isam-Eldin A.
author_facet Ramesh, Jayapal
Kim, Hwasoon
Reddy, Kartika
Eltoum, Isam-Eldin A.
author_sort Ramesh, Jayapal
collection PubMed
description Background and study aims: Despite a well-established tool for diagnosis of pancreatic masses, endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) studies have shown suboptimal diagnostic performance at divergent mass sizes. Since the impact of gold standard follow-up and presence of on-site evaluation on this observation is unknown, we aimed to study the performance characteristics of EUS-FNA under these strict conditions. Patients and methods: EUS-FNA results from pancreatic mass lesions performed between July 2000 and March 2013 were evaluated. All patients with histological follow-up were then stratified into four groups: Group A ( ≤ 10 mm), Group B (11 – 20 mm), Group C (21 – 40 mm), and Group D (> 40 mm). Sensitivity and diagnostic accuracy were calculated for each group and compared. Results: A total of 612 /3832 (16 %) patients with pancreatic masses who underwent EUS-FNA had histology confirmation. Of these, 81 were excluded due to unavailable lesion size, while the rest formed the study cohort. Mean age (SD) was 65.8 years (9.3) with 51.2 % female. The mean number of passes for the entire cohort was 2.9 (SD 1.9; range 1 – 12); patients in group D had a significantly higher number of passes for on-site diagnosis (P = 0.0124). There was no significant difference between the groups for sensitivity (P = 0.1134) or diagnostic accuracy (P = 0.2111). Proportional trend analysis revealed no significant correlation between size and sensitivity (P = 0.6192). The size of lesion measured by EUS was not associated with sensitivity or specificity after adjusting for age, sex, and pancreatic location. Conclusion: In the presence of rapid on-site cytopathology and when final histology is taken as the gold standard, pancreatic mass size does not affect the performance characteristics of EUS-FNA.
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spelling pubmed-48319262016-04-18 Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size Ramesh, Jayapal Kim, Hwasoon Reddy, Kartika Eltoum, Isam-Eldin A. Endosc Int Open Article Background and study aims: Despite a well-established tool for diagnosis of pancreatic masses, endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) studies have shown suboptimal diagnostic performance at divergent mass sizes. Since the impact of gold standard follow-up and presence of on-site evaluation on this observation is unknown, we aimed to study the performance characteristics of EUS-FNA under these strict conditions. Patients and methods: EUS-FNA results from pancreatic mass lesions performed between July 2000 and March 2013 were evaluated. All patients with histological follow-up were then stratified into four groups: Group A ( ≤ 10 mm), Group B (11 – 20 mm), Group C (21 – 40 mm), and Group D (> 40 mm). Sensitivity and diagnostic accuracy were calculated for each group and compared. Results: A total of 612 /3832 (16 %) patients with pancreatic masses who underwent EUS-FNA had histology confirmation. Of these, 81 were excluded due to unavailable lesion size, while the rest formed the study cohort. Mean age (SD) was 65.8 years (9.3) with 51.2 % female. The mean number of passes for the entire cohort was 2.9 (SD 1.9; range 1 – 12); patients in group D had a significantly higher number of passes for on-site diagnosis (P = 0.0124). There was no significant difference between the groups for sensitivity (P = 0.1134) or diagnostic accuracy (P = 0.2111). Proportional trend analysis revealed no significant correlation between size and sensitivity (P = 0.6192). The size of lesion measured by EUS was not associated with sensitivity or specificity after adjusting for age, sex, and pancreatic location. Conclusion: In the presence of rapid on-site cytopathology and when final histology is taken as the gold standard, pancreatic mass size does not affect the performance characteristics of EUS-FNA. © Georg Thieme Verlag KG 2016-04 2016-03-30 /pmc/articles/PMC4831926/ /pubmed/27092323 http://dx.doi.org/10.1055/s-0035-1569969 Text en © Thieme Medical Publishers
spellingShingle Article
Ramesh, Jayapal
Kim, Hwasoon
Reddy, Kartika
Eltoum, Isam-Eldin A.
Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title_full Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title_fullStr Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title_full_unstemmed Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title_short Performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
title_sort performance characteristic of endoscopic ultrasound-guided fine needle aspiration is unaffected by pancreatic mass size
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831926/
https://www.ncbi.nlm.nih.gov/pubmed/27092323
http://dx.doi.org/10.1055/s-0035-1569969
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