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Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs

OBJECTIVES: This study aimed to compare the clinical course of 5-aminosalicylic acid–derived, drug-induced acute pancreatitis (5-ASA–DIAP) to acute pancreatitis (AP) caused by other etiologies. METHODS: A cohort of patients with 5-ASA–DIAP was established through literature search. As a control AP (...

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Autores principales: Meczker, Ágnes, Mikó, Alexandra, Gede, Noémi, Szentesi, Andrea, Párniczky, Andrea, Gódi, Szilárd, Hegyi, Péter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6493669/
https://www.ncbi.nlm.nih.gov/pubmed/30946233
http://dx.doi.org/10.1097/MPA.0000000000001297
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author Meczker, Ágnes
Mikó, Alexandra
Gede, Noémi
Szentesi, Andrea
Párniczky, Andrea
Gódi, Szilárd
Hegyi, Péter
author_facet Meczker, Ágnes
Mikó, Alexandra
Gede, Noémi
Szentesi, Andrea
Párniczky, Andrea
Gódi, Szilárd
Hegyi, Péter
author_sort Meczker, Ágnes
collection PubMed
description OBJECTIVES: This study aimed to compare the clinical course of 5-aminosalicylic acid–derived, drug-induced acute pancreatitis (5-ASA–DIAP) to acute pancreatitis (AP) caused by other etiologies. METHODS: A cohort of patients with 5-ASA–DIAP was established through literature search. As a control AP (CAP) group, a cohort was generated from a registry. Data on the diagnostic procedure, symptoms, enzyme elevation, imaging, severity, and recovery parameters were collected. Causality was assessed using the Naranjo algorithm. RESULTS: Twenty-nine articles were included, which describe 36 patients with fifty-one 5-ASA–DIAP episodes (60.78% female, 39.22% male). There were 88.2% mild, 3.92% moderate, and 7.84% severe cases of AP in the 5-ASA–DIAP group, and 70.6%, 25.5%, and 3.92% such cases in the CAP population, respectively. Symptoms improved significantly faster (mean ± SE, 2.5 ± 0.34 vs 3.74 ± 0.42 days; P = 0.018); however, pancreatic enzyme levels normalized significantly more slowly (6.27 ± 1.53 vs 3.63 ± 0.61 days, P = 0.008) in the 5-ASA–DIAP cohort compared with the CAP group. This study confirms that there are no diagnostic differences between 5-ASA–DIAP and AP of other etiologies. CONCLUSIONS: Fewer moderate but more severe cases were found in the 5-ASA–DIAP group; therefore, 5-ASA–DIAP must be taken as seriously as AP of other etiologies.
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spelling pubmed-64936692019-05-29 Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs Meczker, Ágnes Mikó, Alexandra Gede, Noémi Szentesi, Andrea Párniczky, Andrea Gódi, Szilárd Hegyi, Péter Pancreas Original Articles OBJECTIVES: This study aimed to compare the clinical course of 5-aminosalicylic acid–derived, drug-induced acute pancreatitis (5-ASA–DIAP) to acute pancreatitis (AP) caused by other etiologies. METHODS: A cohort of patients with 5-ASA–DIAP was established through literature search. As a control AP (CAP) group, a cohort was generated from a registry. Data on the diagnostic procedure, symptoms, enzyme elevation, imaging, severity, and recovery parameters were collected. Causality was assessed using the Naranjo algorithm. RESULTS: Twenty-nine articles were included, which describe 36 patients with fifty-one 5-ASA–DIAP episodes (60.78% female, 39.22% male). There were 88.2% mild, 3.92% moderate, and 7.84% severe cases of AP in the 5-ASA–DIAP group, and 70.6%, 25.5%, and 3.92% such cases in the CAP population, respectively. Symptoms improved significantly faster (mean ± SE, 2.5 ± 0.34 vs 3.74 ± 0.42 days; P = 0.018); however, pancreatic enzyme levels normalized significantly more slowly (6.27 ± 1.53 vs 3.63 ± 0.61 days, P = 0.008) in the 5-ASA–DIAP cohort compared with the CAP group. This study confirms that there are no diagnostic differences between 5-ASA–DIAP and AP of other etiologies. CONCLUSIONS: Fewer moderate but more severe cases were found in the 5-ASA–DIAP group; therefore, 5-ASA–DIAP must be taken as seriously as AP of other etiologies. Lippincott Williams & Wilkins 2019-04 2019-04-10 /pmc/articles/PMC6493669/ /pubmed/30946233 http://dx.doi.org/10.1097/MPA.0000000000001297 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Articles
Meczker, Ágnes
Mikó, Alexandra
Gede, Noémi
Szentesi, Andrea
Párniczky, Andrea
Gódi, Szilárd
Hegyi, Péter
Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title_full Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title_fullStr Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title_full_unstemmed Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title_short Retrospective Matched-Cohort Analysis of Acute Pancreatitis Induced by 5-Aminosalicylic Acid–Derived Drugs
title_sort retrospective matched-cohort analysis of acute pancreatitis induced by 5-aminosalicylic acid–derived drugs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6493669/
https://www.ncbi.nlm.nih.gov/pubmed/30946233
http://dx.doi.org/10.1097/MPA.0000000000001297
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