Outcomes and timing of endoscopic retrograde cholangiopancreatography for acute biliary pancreatitis.


Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
09 2019
Historique:
received: 30 12 2018
revised: 20 03 2019
accepted: 21 03 2019
pubmed: 30 4 2019
medline: 9 4 2020
entrez: 30 4 2019
Statut: ppublish

Résumé

Indication of endoscopic retrograde cholangiopancreatography (ERCP) in acute biliary pancreatitis (ABP) is challenging. In this retrospective study, we analyzed real-world data to understand the ERCP practice in ABP in Hungarian centers. Clinical data on ABP patients (2013-2015) were extracted from our large multicentric database. Outcomes, quality indicators and the role of early timing of ERCP (<24 h from admission) were analyzed. There were 356 patients with ABP. ERCP was performed in 267 (75%). Performance indicators of ERCP proved to be suboptimal with a biliary cannulation rate of 84%. Successful vs unsuccessful cannulation of naïve papilla resulted in lower rates of local [22.9% vs 40.9%, (P = 0.012)] and systemic [4.9% vs 13.6%, (P = 0.042)] complications. Successful vs unsuccessful clearance resulted in lower rates of local complications [22.5% vs 40.8%, (P = 0.008)]. Successful cannulation and drainage correlated with less severe course of ABP [3.6% vs 15.9%, (P = 0.001) and 4.1% vs 12.2%, (P = 0.033)] respectively. A tendency of an increased rate of local complications was observed if ERCP was performed later [<24 h: 21.1% (35/166); between 24-48 h: 23.4% (11/47); >48h: 37.2% (16/43) (P = 0.088)]. Optimization of ERCP indication in ABP patients is critical as suboptimal ERCP practices in ABP without definitive stone detection are associated with poorer clinical outcomes.

Sections du résumé

BACKGROUND
Indication of endoscopic retrograde cholangiopancreatography (ERCP) in acute biliary pancreatitis (ABP) is challenging.
AIMS
In this retrospective study, we analyzed real-world data to understand the ERCP practice in ABP in Hungarian centers.
METHODS
Clinical data on ABP patients (2013-2015) were extracted from our large multicentric database. Outcomes, quality indicators and the role of early timing of ERCP (<24 h from admission) were analyzed.
RESULTS
There were 356 patients with ABP. ERCP was performed in 267 (75%). Performance indicators of ERCP proved to be suboptimal with a biliary cannulation rate of 84%. Successful vs unsuccessful cannulation of naïve papilla resulted in lower rates of local [22.9% vs 40.9%, (P = 0.012)] and systemic [4.9% vs 13.6%, (P = 0.042)] complications. Successful vs unsuccessful clearance resulted in lower rates of local complications [22.5% vs 40.8%, (P = 0.008)]. Successful cannulation and drainage correlated with less severe course of ABP [3.6% vs 15.9%, (P = 0.001) and 4.1% vs 12.2%, (P = 0.033)] respectively. A tendency of an increased rate of local complications was observed if ERCP was performed later [<24 h: 21.1% (35/166); between 24-48 h: 23.4% (11/47); >48h: 37.2% (16/43) (P = 0.088)].
CONCLUSION
Optimization of ERCP indication in ABP patients is critical as suboptimal ERCP practices in ABP without definitive stone detection are associated with poorer clinical outcomes.

Identifiants

pubmed: 31031177
pii: S1590-8658(19)30524-9
doi: 10.1016/j.dld.2019.03.018
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1281-1286

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Adrienn Halász (A)

Szent György Teaching Hospital of Fejér County, Székesfehérvár, Hungary. Electronic address: ahalasz@mail.fmkorhaz.hu.

Dániel Pécsi (D)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: daniel.pecsi1991@gmail.com.

Nelli Farkas (N)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary; Institute of Bioanalysis and Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: nelli.farkas@aok.pte.hu.

Ferenc Izbéki (F)

Szent György Teaching Hospital of Fejér County, Székesfehérvár, Hungary. Electronic address: fizbeki@gmail.com.

László Gajdán (L)

Szent György Teaching Hospital of Fejér County, Székesfehérvár, Hungary. Electronic address: lgajdan@yahoo.com.

Roland Fejes (R)

Szent György Teaching Hospital of Fejér County, Székesfehérvár, Hungary. Electronic address: rolldoc@vipmail.hu.

József Hamvas (J)

Bajcsy-Zsilinszky Teaching Hospital of Semmelweis University, Budapest, Hungary. Electronic address: hamvas.jozsef@bajcsy.hu.

Tamás Takács (T)

First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: takacs.tamas@med.u-szeged.hu.

Zoltán Szepes (Z)

First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: szepes.zoltan@med.u-szeged.hu.

László Czakó (L)

First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: czako.laszlo@med.u-szeged.hu.

Áron Vincze (Á)

First Department of Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: vincze.aron@pte.hu.

Szilárd Gódi (S)

First Department of Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: godi.szilard@pte.hu.

Andrea Szentesi (A)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary; First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: szentesiai@gmail.com.

Andrea Párniczky (A)

Heim Pál National Institute for Pediatrics, Budapest, Hungary. Electronic address: andrea.parniczky@gmail.com.

Dóra Illés (D)

First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: illes.dora@med.u-szeged.hu.

Balázs Kui (B)

First Department of Medicine, University of Szeged, Szeged, Hungary. Electronic address: k.kubali@gmail.com.

Péter Varjú (P)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: varjupet@gmail.com.

Katalin Márta (K)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: katalin.martak@gmail.com.

Márta Varga (M)

BMKK, Dr. Réthy Pál Hospital, Békéscsaba, Hungary. Electronic address: drvargamarta@gmail.com.

János Novák (J)

BMKK, Pándy Kálmán Hospital, Gyula, Hungary. Electronic address: drnovakjanos@gmail.com.

Attila Szepes (A)

Bács-Kiskun County University Teaching Hospital, Kecskemét, Hungary. Electronic address: szepesaz@gmail.com.

Barnabás Bod (B)

Dr. Bugyi István Hospital of Csongrád County, Szentes, Hungary. Electronic address: bancikab@freemail.hu.

Miklós Ihász (M)

Markusovszky Teaching Hospital, Szombathely, Szombathely, Hungary. Electronic address: ihasz.miklos@gmail.com.

Péter Hegyi (P)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary; First Department of Medicine, University of Pécs, Pécs, Hungary; MTA-SZTE Momentum Translational Gastroenterology Research Group, Szeged, Hungary. Electronic address: hegyi2009@gmail.com.

István Hritz (I)

First Department of Surgery, Center for Therapeutic Endoscopy, Semmelweis University, Budapest, Hungary. Electronic address: istvan.hritz@freemail.hu.

Bálint Erőss (B)

Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: eross.balint@pte.hu.

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