On-site stereomicroscope quality evaluations to estimate white core cutoff lengths using EUS-FNA biopsy sampling with 22-gauge needles.


Journal

Gastrointestinal endoscopy
ISSN: 1097-6779
Titre abrégé: Gastrointest Endosc
Pays: United States
ID NLM: 0010505

Informations de publication

Date de publication:
12 2019
Historique:
received: 05 04 2019
accepted: 18 08 2019
pubmed: 8 9 2019
medline: 4 6 2020
entrez: 8 9 2019
Statut: ppublish

Résumé

Although rapid on-site cytologic evaluation (ROSE) during EUS-guided FNA biopsy (EUS-FNAB) sampling may improve accuracy of pathologic analyses, cytopathologists are not widely available. We calculated the cutoff lengths required for accurate pathologic diagnoses from stereomicroscopically visible white cores (SVWCs) sampled using 22-gauge needles. Overall, 118 patients with mediastinal or upper abdominal solid masses requiring pathologic diagnoses were included. EUS-FNAB sampling was performed using 22-gauge needles. SVWCs were isolated and measured using stereomicroscopy, and the utility of calculated cutoff lengths in diagnosis was investigated. The procedure success and SVWC sampling rates were both 100%, and the median SVWC length was 10 mm. Pathologic examination identified 75, 31, and 12 patients with pancreatic neoplasms (PNs), subepithelial lesions (SELs), and other lesions, respectively. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for diagnosing malignancy using EUS-FNAB sampling were 93.1%, 100%, 100%, 69.6%, and 94%, respectively. The final diagnostic accuracy in the entire cohort, PNs, and SELs was 92.4%, 90.7%, and 93.5%, respectively. Receiver operating characteristic curves demonstrated the overall SVWC cutoff length to be 11 mm (11 mm for PNs, 3.5 mm for SELs). The overall sensitivity according to SVWC cutoff length was 91.4% (87.6% for PNs, 98.8% for SELs). Compared with cutoff length, multivariate analysis confirmed SVWC length to be a stronger independent factor for tissue diagnosis in both groups. Diagnosis improved significantly with SVWC cutoff lengths ≥11 mm. This may be a useful index for endoscopists, particularly where ROSE is unavailable. (Clinical trial registration number: UMIN000023013.).

Sections du résumé

BACKGROUND AND AIMS
Although rapid on-site cytologic evaluation (ROSE) during EUS-guided FNA biopsy (EUS-FNAB) sampling may improve accuracy of pathologic analyses, cytopathologists are not widely available. We calculated the cutoff lengths required for accurate pathologic diagnoses from stereomicroscopically visible white cores (SVWCs) sampled using 22-gauge needles.
METHODS
Overall, 118 patients with mediastinal or upper abdominal solid masses requiring pathologic diagnoses were included. EUS-FNAB sampling was performed using 22-gauge needles. SVWCs were isolated and measured using stereomicroscopy, and the utility of calculated cutoff lengths in diagnosis was investigated.
RESULTS
The procedure success and SVWC sampling rates were both 100%, and the median SVWC length was 10 mm. Pathologic examination identified 75, 31, and 12 patients with pancreatic neoplasms (PNs), subepithelial lesions (SELs), and other lesions, respectively. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for diagnosing malignancy using EUS-FNAB sampling were 93.1%, 100%, 100%, 69.6%, and 94%, respectively. The final diagnostic accuracy in the entire cohort, PNs, and SELs was 92.4%, 90.7%, and 93.5%, respectively. Receiver operating characteristic curves demonstrated the overall SVWC cutoff length to be 11 mm (11 mm for PNs, 3.5 mm for SELs). The overall sensitivity according to SVWC cutoff length was 91.4% (87.6% for PNs, 98.8% for SELs). Compared with cutoff length, multivariate analysis confirmed SVWC length to be a stronger independent factor for tissue diagnosis in both groups.
CONCLUSIONS
Diagnosis improved significantly with SVWC cutoff lengths ≥11 mm. This may be a useful index for endoscopists, particularly where ROSE is unavailable. (Clinical trial registration number: UMIN000023013.).

Identifiants

pubmed: 31493384
pii: S0016-5107(19)32203-5
doi: 10.1016/j.gie.2019.08.033
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

947-956

Informations de copyright

Copyright © 2019 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.

Auteurs

Hironori Masutani (H)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Kosuke Okuwaki (K)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Mitsuhiro Kida (M)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Tsutomu Yoshida (T)

Department of Pathology, Kitasato University School of Medicine, Kanagawa, Japan.

Hiroshi Imaizumi (H)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Hiroshi Yamauchi (H)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Tomohisa Iwai (T)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Toru Kaneko (T)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Rikiya Hasegawa (R)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Eiji Miyata (E)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

Wasaburo Koizumi (W)

Department of Gastroenterology, Kitasato University School of Medicine, Kanagawa, Japan.

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