Utility of Elastography with Endoscopic Ultrasonography Shear-Wave Measurement for Diagnosing Chronic Pancreatitis.


Journal

Gut and liver
ISSN: 2005-1212
Titre abrégé: Gut Liver
Pays: Korea (South)
ID NLM: 101316452

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 15 05 2019
revised: 20 08 2019
accepted: 12 09 2019
pubmed: 15 11 2019
medline: 14 9 2021
entrez: 14 11 2019
Statut: ppublish

Résumé

Rosemont classification (RC) with endoscopic ultrasonography (EUS) is important for diagnosing chronic pancreatitis (CP) but is based only on subjective judgement. EUS shear wave measurement (EUS-SWM) is a precise modality based on objective judgment, but its usefulness has not been extensively studied yet. This study evaluated the utility of EUS-SWM for diagnosing CP and estimating CP severity by determining the presence of endocrine dysfunction along with diabetes mellitus (DM). Between June 2018 and December 2018, 52 patients who underwent EUS and EUS-SWM were classified into two groups according to RC: non-CP (indeterminate CP and normal) and CP (consistent and suggestive of CP). The EUSSWM value by shear wave velocity was evaluated with a median value. The EUS-SWM value was compared with RC and the number of EUS features. The diagnostic accuracy and cutoff value of EUS-SWM for CP and DM and its sensitivity and specificity were calculated. The EUS-SWM value significantly positively correlated with the RC and the number of EUS features. The EUS-SWM values that were consistent and suggestive of CP were significantly higher than that of normal. The area under the receiver operating characteristic (AUROC) curve for the diagnostic accuracy of EUS-SWM for CP was 0.97. The cutoff value of 2.19 had 100% sensitivity and 94% specificity. For endocrine dysfunction in CP, the AUROC was 0.75. The cutoff value of 2.78 had 70% sensitivity and 56% specificity. EUS-SWM provides an objective assessment and can be an alternative diagnostic tool for diagnosing CP. EUS-SWM may also be useful for predicting the presence of endocrine dysfunction.

Sections du résumé

Background/Aims
Rosemont classification (RC) with endoscopic ultrasonography (EUS) is important for diagnosing chronic pancreatitis (CP) but is based only on subjective judgement. EUS shear wave measurement (EUS-SWM) is a precise modality based on objective judgment, but its usefulness has not been extensively studied yet. This study evaluated the utility of EUS-SWM for diagnosing CP and estimating CP severity by determining the presence of endocrine dysfunction along with diabetes mellitus (DM).
Methods
Between June 2018 and December 2018, 52 patients who underwent EUS and EUS-SWM were classified into two groups according to RC: non-CP (indeterminate CP and normal) and CP (consistent and suggestive of CP). The EUSSWM value by shear wave velocity was evaluated with a median value. The EUS-SWM value was compared with RC and the number of EUS features. The diagnostic accuracy and cutoff value of EUS-SWM for CP and DM and its sensitivity and specificity were calculated.
Results
The EUS-SWM value significantly positively correlated with the RC and the number of EUS features. The EUS-SWM values that were consistent and suggestive of CP were significantly higher than that of normal. The area under the receiver operating characteristic (AUROC) curve for the diagnostic accuracy of EUS-SWM for CP was 0.97. The cutoff value of 2.19 had 100% sensitivity and 94% specificity. For endocrine dysfunction in CP, the AUROC was 0.75. The cutoff value of 2.78 had 70% sensitivity and 56% specificity.
Conclusions
EUS-SWM provides an objective assessment and can be an alternative diagnostic tool for diagnosing CP. EUS-SWM may also be useful for predicting the presence of endocrine dysfunction.

Identifiants

pubmed: 31722469
pii: gnl19170
doi: 10.5009/gnl19170
pmc: PMC7492489
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

659-664

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Auteurs

Yasunobu Yamashita (Y)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Kensuke Tanioka (K)

Clinical Study Support Center, Wakayama Medical University Hospital, Wakayama, Japan.

Yuki Kawaji (Y)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Takashi Tamura (T)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Junya Nuta (J)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Keiichi Hatamaru (K)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Masahiro Itonaga (M)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Takeichi Yoshida (T)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Yoshiyuki Ida (Y)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Takao Maekita (T)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Mikitaka Iguchi (M)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

Masayuki Kitano (M)

Second Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan.

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