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Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study

BACKGROUND: Middle gastrointestinal bleeding (MGIB) risk has not been fully investigated due to its extremely rare occurrence and the need for multiple endoscopies to exclude upper and lower gastrointestinal bleeding. This study investigated whether MGIB is associated with the use of non-steroidal a...

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Autores principales: Nagata, Naoyoshi, Niikura, Ryota, Yamada, Atsuo, Sakurai, Toshiyuki, Shimbo, Takuro, Kobayashi, Yuka, Okamoto, Makoto, Mitsuno, Yuzo, Ogura, Keiji, Hirata, Yoshihiro, Fujimoto, Kazuma, Akiyama, Junichi, Uemura, Naomi, Koike, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792424/
https://www.ncbi.nlm.nih.gov/pubmed/26978517
http://dx.doi.org/10.1371/journal.pone.0151332
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author Nagata, Naoyoshi
Niikura, Ryota
Yamada, Atsuo
Sakurai, Toshiyuki
Shimbo, Takuro
Kobayashi, Yuka
Okamoto, Makoto
Mitsuno, Yuzo
Ogura, Keiji
Hirata, Yoshihiro
Fujimoto, Kazuma
Akiyama, Junichi
Uemura, Naomi
Koike, Kazuhiko
author_facet Nagata, Naoyoshi
Niikura, Ryota
Yamada, Atsuo
Sakurai, Toshiyuki
Shimbo, Takuro
Kobayashi, Yuka
Okamoto, Makoto
Mitsuno, Yuzo
Ogura, Keiji
Hirata, Yoshihiro
Fujimoto, Kazuma
Akiyama, Junichi
Uemura, Naomi
Koike, Kazuhiko
author_sort Nagata, Naoyoshi
collection PubMed
description BACKGROUND: Middle gastrointestinal bleeding (MGIB) risk has not been fully investigated due to its extremely rare occurrence and the need for multiple endoscopies to exclude upper and lower gastrointestinal bleeding. This study investigated whether MGIB is associated with the use of non-steroidal anti-inflammatory drugs (NSAIDs), low-dose aspirin (LDA), thienopyridines, anticoagulants, and proton-pump inhibitors (PPIs), and whether PPI use affects the interactions between MGIB and antithrombotic drugs. METHODS: In this multicenter, hospital-based, case-control study, 400 patients underwent upper and lower endoscopy, 80 had acute overt MGIB and 320 had no bleeding and were matched for age and sex as controls (1:4). MGIB was additionally evaluated by capsule and/or double-balloon endoscopy, after excluding upper and lower GI bleeding. Adjusted odds ratios (AOR) for MGIB risk were calculated using conditional logistic regression. To estimate the propensity score, we employed a logistic regression model for PPI use. RESULTS: In patients with MGIB, mean hemoglobin level was 9.4 g/dL, and 28 patients (35%) received blood transfusions. Factors significantly associated with MGIB were chronic kidney disease (p<0.001), liver cirrhosis (p = 0.034), NSAIDs (p<0.001), thienopyridines (p<0.001), anticoagulants (p = 0.002), and PPIs (p<0.001). After adjusting for these factors, NSAIDs (AOR, 2.5; p = 0.018), thienopyridines (AOR, 3.2; p = 0.015), anticoagulants (AOR, 4.3; p = 0.028), and PPIs (AOR; 2.0; p = 0.021) were independently associated with MGIB. After adjusting for propensity score, the use of PPIs remained an independent risk factors for MGIB (AOR, 1.94; p = 0.034). No significant interactions were observed between PPIs and NSAIDs (AOR, 0.7; p = 0.637), LDA (AOR, 0.3; p = 0.112), thienopyridine (AOR, 0.7, p = 0.671), or anticoagulants (AOR, 0.5; p = 0.545). CONCLUSIONS: One-third of patients with acute small intestinal bleeding required blood transfusion. NSAIDs, thienopyridines, anticoagulants, and PPIs increased the risk of acute small intestinal bleeding. However, there were no significant interactions found between antithrombotic drugs and PPI use for bleeding risk.
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spelling pubmed-47924242016-03-23 Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study Nagata, Naoyoshi Niikura, Ryota Yamada, Atsuo Sakurai, Toshiyuki Shimbo, Takuro Kobayashi, Yuka Okamoto, Makoto Mitsuno, Yuzo Ogura, Keiji Hirata, Yoshihiro Fujimoto, Kazuma Akiyama, Junichi Uemura, Naomi Koike, Kazuhiko PLoS One Research Article BACKGROUND: Middle gastrointestinal bleeding (MGIB) risk has not been fully investigated due to its extremely rare occurrence and the need for multiple endoscopies to exclude upper and lower gastrointestinal bleeding. This study investigated whether MGIB is associated with the use of non-steroidal anti-inflammatory drugs (NSAIDs), low-dose aspirin (LDA), thienopyridines, anticoagulants, and proton-pump inhibitors (PPIs), and whether PPI use affects the interactions between MGIB and antithrombotic drugs. METHODS: In this multicenter, hospital-based, case-control study, 400 patients underwent upper and lower endoscopy, 80 had acute overt MGIB and 320 had no bleeding and were matched for age and sex as controls (1:4). MGIB was additionally evaluated by capsule and/or double-balloon endoscopy, after excluding upper and lower GI bleeding. Adjusted odds ratios (AOR) for MGIB risk were calculated using conditional logistic regression. To estimate the propensity score, we employed a logistic regression model for PPI use. RESULTS: In patients with MGIB, mean hemoglobin level was 9.4 g/dL, and 28 patients (35%) received blood transfusions. Factors significantly associated with MGIB were chronic kidney disease (p<0.001), liver cirrhosis (p = 0.034), NSAIDs (p<0.001), thienopyridines (p<0.001), anticoagulants (p = 0.002), and PPIs (p<0.001). After adjusting for these factors, NSAIDs (AOR, 2.5; p = 0.018), thienopyridines (AOR, 3.2; p = 0.015), anticoagulants (AOR, 4.3; p = 0.028), and PPIs (AOR; 2.0; p = 0.021) were independently associated with MGIB. After adjusting for propensity score, the use of PPIs remained an independent risk factors for MGIB (AOR, 1.94; p = 0.034). No significant interactions were observed between PPIs and NSAIDs (AOR, 0.7; p = 0.637), LDA (AOR, 0.3; p = 0.112), thienopyridine (AOR, 0.7, p = 0.671), or anticoagulants (AOR, 0.5; p = 0.545). CONCLUSIONS: One-third of patients with acute small intestinal bleeding required blood transfusion. NSAIDs, thienopyridines, anticoagulants, and PPIs increased the risk of acute small intestinal bleeding. However, there were no significant interactions found between antithrombotic drugs and PPI use for bleeding risk. Public Library of Science 2016-03-15 /pmc/articles/PMC4792424/ /pubmed/26978517 http://dx.doi.org/10.1371/journal.pone.0151332 Text en © 2016 Nagata et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nagata, Naoyoshi
Niikura, Ryota
Yamada, Atsuo
Sakurai, Toshiyuki
Shimbo, Takuro
Kobayashi, Yuka
Okamoto, Makoto
Mitsuno, Yuzo
Ogura, Keiji
Hirata, Yoshihiro
Fujimoto, Kazuma
Akiyama, Junichi
Uemura, Naomi
Koike, Kazuhiko
Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title_full Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title_fullStr Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title_full_unstemmed Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title_short Acute Middle Gastrointestinal Bleeding Risk Associated with NSAIDs, Antithrombotic Drugs, and PPIs: A Multicenter Case-Control Study
title_sort acute middle gastrointestinal bleeding risk associated with nsaids, antithrombotic drugs, and ppis: a multicenter case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792424/
https://www.ncbi.nlm.nih.gov/pubmed/26978517
http://dx.doi.org/10.1371/journal.pone.0151332
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