Prospective, multicenter, observational study of tissue acquisition through EUS-guided fine-needle biopsy using a 25G Franseen needle.

EUS EUS-guided fine-needle biopsy Franseen needle tissue acquisition

Journal

Endoscopic ultrasound
ISSN: 2303-9027
Titre abrégé: Endosc Ultrasound
Pays: China
ID NLM: 101622292

Informations de publication

Date de publication:
Historique:
pubmed: 19 3 2019
medline: 19 3 2019
entrez: 19 3 2019
Statut: ppublish

Résumé

Recently, EUS-guided fine-needle biopsy (EUS-FNB) using a Franseen needle was developed for histological tissue acquisition. However, the yield of a 25G Franseen needle when acquiring histological core tissue has been unclear. We performed a prospective, multicenter, and observational cohort study that included 100 solid lesions scheduled for EUS-FNB using a 25G Franseen needle at eight centers in Hokkaido, Japan. Only EUS-FNB specimens acquired at the first pass were evaluated without a rapid on-site evaluation. The tissue acquisition rate, acquisition rate of an adequate specimen for histological assessment, the quality of tissue sample, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), diagnostic accuracy, and adverse events were evaluated. We analyzed a total of 100 solid lesions in 100 patients. The patients were 57 males and 43 females with a median age of 70 years. The technical success rate was 100%. The tissue acquisition rate was 95.0%. The acquisition rate of an adequate specimen for histological assessment was 82.0%. The sensitivity, specificity, PPV, NPV, and diagnostic accuracy were 87.0%, 100%, 100%, 40.0%, and 88.0%, respectively. The adverse event rate was 1.0%, and it was reported in only one patient who had a moderate pancreatic fistula. EUS-FNB using the 25G Franseen needle was feasible, and adequate histological core tissue samples were acquired with this method.

Sections du résumé

BACKGROUND BACKGROUND
Recently, EUS-guided fine-needle biopsy (EUS-FNB) using a Franseen needle was developed for histological tissue acquisition. However, the yield of a 25G Franseen needle when acquiring histological core tissue has been unclear.
PATIENTS AND METHODS METHODS
We performed a prospective, multicenter, and observational cohort study that included 100 solid lesions scheduled for EUS-FNB using a 25G Franseen needle at eight centers in Hokkaido, Japan. Only EUS-FNB specimens acquired at the first pass were evaluated without a rapid on-site evaluation. The tissue acquisition rate, acquisition rate of an adequate specimen for histological assessment, the quality of tissue sample, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), diagnostic accuracy, and adverse events were evaluated.
RESULTS RESULTS
We analyzed a total of 100 solid lesions in 100 patients. The patients were 57 males and 43 females with a median age of 70 years. The technical success rate was 100%. The tissue acquisition rate was 95.0%. The acquisition rate of an adequate specimen for histological assessment was 82.0%. The sensitivity, specificity, PPV, NPV, and diagnostic accuracy were 87.0%, 100%, 100%, 40.0%, and 88.0%, respectively. The adverse event rate was 1.0%, and it was reported in only one patient who had a moderate pancreatic fistula.
CONCLUSIONS CONCLUSIONS
EUS-FNB using the 25G Franseen needle was feasible, and adequate histological core tissue samples were acquired with this method.

Identifiants

pubmed: 30880724
pii: 254011
doi: 10.4103/eus.eus_66_18
pmc: PMC6791109
doi:

Types de publication

Journal Article

Langues

eng

Pagination

321-328

Déclaration de conflit d'intérêts

None

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Auteurs

Ryo Sugiura (R)

Department of Gastroenterology and Hepatology, Hokkaido University, Faculty of Medicine and Graduate School of Medicine, Sapporo, Japan.

Masaki Kuwatani (M)

Department of Gastroenterology and Hepatology, Hokkaido University, Faculty of Medicine and Graduate School of Medicine; Division of Endoscopy, Hokkaido University Hospital, Sapporo, Japan.

Kei Yane (K)

Center for Gastroenterology, Teine-Keijinkai Hospital, Sapporo, Japan.

Yoko Taya (Y)

Department of Gastroenterology, Hokkaido Medical Center, Sapporo, Japan.

Hideyuki Ihara (H)

Department of Gastroenterology, Tonan Hospital, Sapporo, Japan.

Manabu Onodera (M)

Department of Gastroenterology, NTT East Sapporo Hospital, Sapporo, Japan.

Kazunori Eto (K)

Department of Gastroenterology, Tomakomai City Hospital, Tomakomai, Japan.

Itsuki Sano (I)

Department of Internal Medicine, Kushiro Rosai Hospital, Kushiro, Japan.

Taiki Kudo (T)

Department of Gastroenterology and Hepatology, Hakodate Municipal Hospital, Hakodate, Japan.

Tomoko Mitsuhashi (T)

Department of Surgical Pathology, Hokkaido University Hospital, Sapporo, Japan.

Akio Katanuma (A)

Center for Gastroenterology, Teine-Keijinkai Hospital, Sapporo, Japan.

Naoya Sakamoto (N)

Department of Gastroenterology and Hepatology, Hokkaido University, Faculty of Medicine and Graduate School of Medicine, Sapporo, Japan.

Classifications MeSH