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Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study

OBJECTIVE: A wide mucosal defect after endoscopic submucosal dissection (ESD) for esophageal cancer is associated with increased risk of stricture. This study was conducted to evaluate the feasibility of short-period, high-dose intravenous methylprednisolone administration (steroid pulse therapy) in...

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Autores principales: Nakamura, Jun, Hikichi, Takuto, Watanabe, Ko, Sato, Masaki, Obara, Katsutoshi, Ohira, Hiromasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554574/
https://www.ncbi.nlm.nih.gov/pubmed/28828004
http://dx.doi.org/10.1155/2017/9312517
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author Nakamura, Jun
Hikichi, Takuto
Watanabe, Ko
Sato, Masaki
Obara, Katsutoshi
Ohira, Hiromasa
author_facet Nakamura, Jun
Hikichi, Takuto
Watanabe, Ko
Sato, Masaki
Obara, Katsutoshi
Ohira, Hiromasa
author_sort Nakamura, Jun
collection PubMed
description OBJECTIVE: A wide mucosal defect after endoscopic submucosal dissection (ESD) for esophageal cancer is associated with increased risk of stricture. This study was conducted to evaluate the feasibility of short-period, high-dose intravenous methylprednisolone administration (steroid pulse therapy) in preventing post-ESD esophageal stricture. METHODS: This prospective study examined 13 lesions in 11 consecutive patients with esophageal squamous cell carcinoma who underwent ESD that involved three-quarters or more of the circumference of the esophagus or who had a longitudinal resected specimen diameter of ≥5 cm. Steroid pulse therapy was initiated the day after ESD and continued for 3 consecutive days. The primary endpoint was the stricture rate after ESD. Secondary endpoints were adverse events (AEs) associated with steroid pulse therapy, time until the development of stricture, and the frequency and duration of endoscopic balloon dilation (EBD). RESULTS: The stricture rate was 54.5% (6/11). The median time until stricture development was 15 days. The median number of EBD sessions required was 2.5. The median duration of EBD was 14.5 days. AEs related to steroid pulse therapy and postprocedure complications were not observed. CONCLUSION: No preventive effect of the stricture after esophageal ESD by steroid pulse therapy was found, although the therapy was administered safely.
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spelling pubmed-55545742017-08-21 Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study Nakamura, Jun Hikichi, Takuto Watanabe, Ko Sato, Masaki Obara, Katsutoshi Ohira, Hiromasa Gastroenterol Res Pract Clinical Study OBJECTIVE: A wide mucosal defect after endoscopic submucosal dissection (ESD) for esophageal cancer is associated with increased risk of stricture. This study was conducted to evaluate the feasibility of short-period, high-dose intravenous methylprednisolone administration (steroid pulse therapy) in preventing post-ESD esophageal stricture. METHODS: This prospective study examined 13 lesions in 11 consecutive patients with esophageal squamous cell carcinoma who underwent ESD that involved three-quarters or more of the circumference of the esophagus or who had a longitudinal resected specimen diameter of ≥5 cm. Steroid pulse therapy was initiated the day after ESD and continued for 3 consecutive days. The primary endpoint was the stricture rate after ESD. Secondary endpoints were adverse events (AEs) associated with steroid pulse therapy, time until the development of stricture, and the frequency and duration of endoscopic balloon dilation (EBD). RESULTS: The stricture rate was 54.5% (6/11). The median time until stricture development was 15 days. The median number of EBD sessions required was 2.5. The median duration of EBD was 14.5 days. AEs related to steroid pulse therapy and postprocedure complications were not observed. CONCLUSION: No preventive effect of the stricture after esophageal ESD by steroid pulse therapy was found, although the therapy was administered safely. Hindawi 2017 2017-07-30 /pmc/articles/PMC5554574/ /pubmed/28828004 http://dx.doi.org/10.1155/2017/9312517 Text en Copyright © 2017 Jun Nakamura et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Nakamura, Jun
Hikichi, Takuto
Watanabe, Ko
Sato, Masaki
Obara, Katsutoshi
Ohira, Hiromasa
Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title_full Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title_fullStr Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title_full_unstemmed Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title_short Feasibility of Short-Period, High-Dose Intravenous Methylprednisolone for Preventing Stricture after Endoscopic Submucosal Dissection for Esophageal Cancer: A Preliminary Study
title_sort feasibility of short-period, high-dose intravenous methylprednisolone for preventing stricture after endoscopic submucosal dissection for esophageal cancer: a preliminary study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554574/
https://www.ncbi.nlm.nih.gov/pubmed/28828004
http://dx.doi.org/10.1155/2017/9312517
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