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Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial

BACKGROUND: The efficacy of low-dose lansoprazole has not been established for the prevention of recurrent gastric or duodenal ulcers in those receiving long-term low-dose aspirin (LDA) for cardiovascular and cerebrovascular protection. This study sought to examine the efficacy of low-dose lansopraz...

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Autores principales: Sugano, Kentaro, Matsumoto, Yasushi, Itabashi, Tsukasa, Abe, Sumihisa, Sakaki, Nobuhiro, Ashida, Kiyoshi, Mizokami, Yuji, Chiba, Tsutomu, Matsui, Shigeyuki, Kanto, Tatsuya, Shimada, Kazuyuki, Uchiyama, Shinichiro, Uemura, Naomi, Hiramatsu, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117278/
https://www.ncbi.nlm.nih.gov/pubmed/21499703
http://dx.doi.org/10.1007/s00535-011-0397-7
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author Sugano, Kentaro
Matsumoto, Yasushi
Itabashi, Tsukasa
Abe, Sumihisa
Sakaki, Nobuhiro
Ashida, Kiyoshi
Mizokami, Yuji
Chiba, Tsutomu
Matsui, Shigeyuki
Kanto, Tatsuya
Shimada, Kazuyuki
Uchiyama, Shinichiro
Uemura, Naomi
Hiramatsu, Naoki
author_facet Sugano, Kentaro
Matsumoto, Yasushi
Itabashi, Tsukasa
Abe, Sumihisa
Sakaki, Nobuhiro
Ashida, Kiyoshi
Mizokami, Yuji
Chiba, Tsutomu
Matsui, Shigeyuki
Kanto, Tatsuya
Shimada, Kazuyuki
Uchiyama, Shinichiro
Uemura, Naomi
Hiramatsu, Naoki
author_sort Sugano, Kentaro
collection PubMed
description BACKGROUND: The efficacy of low-dose lansoprazole has not been established for the prevention of recurrent gastric or duodenal ulcers in those receiving long-term low-dose aspirin (LDA) for cardiovascular and cerebrovascular protection. This study sought to examine the efficacy of low-dose lansoprazole (15 mg once daily) for the secondary prevention of LDA-associated gastric or duodenal ulcers. METHODS: Patients were randomized to receive lansoprazole 15 mg daily (n = 226) or gefarnate 50 mg twice daily (n = 235) for 12 months or longer in a prospective, multicenter, double-blind, randomized active-controlled trial, followed by a 6-month follow-up study with open-label lansoprazole treatment. The study utilized 94 sites in Japan and 461 Japanese patients with a history of gastric or duodenal ulcers who required long-term LDA therapy for cardiovascular and cerebrovascular disease. RESULTS: The primary endpoint was the development of gastric or duodenal ulcers. The cumulative incidence of gastric or duodenal ulcers on days 91, 181, and 361 from the start of the study was calculated by the Kaplan–Meier method as 1.5, 2.1, and 3.7%, respectively, in the lansoprazole group versus 15.2, 24.0, and 31.7%, respectively, in the gefarnate group. The risk of ulcer development was significantly (log-rank test, P < 0.001) lower in the lansoprazole group than in the gefarnate group, with the hazard ratio being 0.099 (95% confidence interval [CI] 0.042–0.230). CONCLUSION: Lansoprazole was superior to gefarnate in reducing the risk of gastric or duodenal ulcer recurrence in patients with a definite history of gastric or duodenal ulcers who required long-term LDA therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00535-011-0397-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-31172782011-07-14 Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial Sugano, Kentaro Matsumoto, Yasushi Itabashi, Tsukasa Abe, Sumihisa Sakaki, Nobuhiro Ashida, Kiyoshi Mizokami, Yuji Chiba, Tsutomu Matsui, Shigeyuki Kanto, Tatsuya Shimada, Kazuyuki Uchiyama, Shinichiro Uemura, Naomi Hiramatsu, Naoki J Gastroenterol Original Article—Alimentary Tract BACKGROUND: The efficacy of low-dose lansoprazole has not been established for the prevention of recurrent gastric or duodenal ulcers in those receiving long-term low-dose aspirin (LDA) for cardiovascular and cerebrovascular protection. This study sought to examine the efficacy of low-dose lansoprazole (15 mg once daily) for the secondary prevention of LDA-associated gastric or duodenal ulcers. METHODS: Patients were randomized to receive lansoprazole 15 mg daily (n = 226) or gefarnate 50 mg twice daily (n = 235) for 12 months or longer in a prospective, multicenter, double-blind, randomized active-controlled trial, followed by a 6-month follow-up study with open-label lansoprazole treatment. The study utilized 94 sites in Japan and 461 Japanese patients with a history of gastric or duodenal ulcers who required long-term LDA therapy for cardiovascular and cerebrovascular disease. RESULTS: The primary endpoint was the development of gastric or duodenal ulcers. The cumulative incidence of gastric or duodenal ulcers on days 91, 181, and 361 from the start of the study was calculated by the Kaplan–Meier method as 1.5, 2.1, and 3.7%, respectively, in the lansoprazole group versus 15.2, 24.0, and 31.7%, respectively, in the gefarnate group. The risk of ulcer development was significantly (log-rank test, P < 0.001) lower in the lansoprazole group than in the gefarnate group, with the hazard ratio being 0.099 (95% confidence interval [CI] 0.042–0.230). CONCLUSION: Lansoprazole was superior to gefarnate in reducing the risk of gastric or duodenal ulcer recurrence in patients with a definite history of gastric or duodenal ulcers who required long-term LDA therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00535-011-0397-7) contains supplementary material, which is available to authorized users. Springer Japan 2011-04-16 2011 /pmc/articles/PMC3117278/ /pubmed/21499703 http://dx.doi.org/10.1007/s00535-011-0397-7 Text en © (c) Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article—Alimentary Tract
Sugano, Kentaro
Matsumoto, Yasushi
Itabashi, Tsukasa
Abe, Sumihisa
Sakaki, Nobuhiro
Ashida, Kiyoshi
Mizokami, Yuji
Chiba, Tsutomu
Matsui, Shigeyuki
Kanto, Tatsuya
Shimada, Kazuyuki
Uchiyama, Shinichiro
Uemura, Naomi
Hiramatsu, Naoki
Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title_full Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title_fullStr Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title_full_unstemmed Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title_short Lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
title_sort lansoprazole for secondary prevention of gastric or duodenal ulcers associated with long-term low-dose aspirin therapy: results of a prospective, multicenter, double-blind, randomized, double-dummy, active-controlled trial
topic Original Article—Alimentary Tract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117278/
https://www.ncbi.nlm.nih.gov/pubmed/21499703
http://dx.doi.org/10.1007/s00535-011-0397-7
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