The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa

<i>Background and objectives:</i> Although treatment with novel oral non-vitamin K antagonist 3anticoagulants (NOACs) is associated with an overall decrease in hemorrhagic complications compared to warfarin, the incidence of gastrointestinal bleeding remains contradictory. <i>Mater...

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Main Authors: Lubomir Mihalkanin, Branislav Stancak
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Medicina
Subjects:
Online Access:https://www.mdpi.com/1010-660X/56/7/363
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author Lubomir Mihalkanin
Branislav Stancak
author_facet Lubomir Mihalkanin
Branislav Stancak
author_sort Lubomir Mihalkanin
collection DOAJ
description <i>Background and objectives:</i> Although treatment with novel oral non-vitamin K antagonist 3anticoagulants (NOACs) is associated with an overall decrease in hemorrhagic complications compared to warfarin, the incidence of gastrointestinal bleeding remains contradictory. <i>Materials and Methods:</i> After the exclusion of patients with pre-existing pathological lesions in the upper gastrointestinal tract (GIT) on esophageal-gastroduodenoscopy (EGD) at entry, a cohort of 80 patients (mean age of 74.8 ± 2.0 years) was randomly divided into four equivalent groups, treated with dabigatran, rivaroxaban, apixaban, or warfarin. Patients were prospectively followed up for three months of treatment, with a focus on anamnestic and endoscopic signs of bleeding. In addition, bleeding risk factors were evaluated. <i>Results:</i> In none of the patients treated with warfarin or NOACs was any serious or clinically significant bleeding recorded within the follow-up period. The incidence of clinical bleeding and endoscopically detected bleeding in the upper GT after three months of treatment was not statistically different among groups (χ<sup>2</sup> = 2.8458; <i>p</i> = 0.41608). The presence of <i>Helicobacter pylori</i> (HP) was a risk factor for upper GIT bleeding (<i>p</i> < 0.05), while the use of proton pump inhibitors (PPIs) was a protective factor (<i>p</i> = 0.206; Spearman’s correlation coefficient = 0.205). We did not record any post-biopsy continued bleeding. <i>Conclusions:</i> No significant GIT bleeding was found in any of the treatment groups, so we consider it beneficial to perform routine EGD before the initiation of any anticoagulant therapy in patients with an increased risk of upper GIT bleeding. Detection and eradication of HP as well as preventive PPI treatment may mitigate the occurrence of endoscopic bleeding. Endoscopic biopsy during the NOAC treatment is safe.
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spelling doaj.art-c67d310a11fd4f5abcf086d03b15c6b42023-09-03T03:15:17ZengMDPI AGMedicina1010-660X2020-07-015636336310.3390/medicina56070363The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract MucosaLubomir Mihalkanin0Branislav Stancak1Gastroenterology Department, Gastro-LM, 080 01 Presov, SlovakiaCardiology Department, East Slovakia Institute for Cardiovascular Diseases, 040 11 Kosice, Slovakia<i>Background and objectives:</i> Although treatment with novel oral non-vitamin K antagonist 3anticoagulants (NOACs) is associated with an overall decrease in hemorrhagic complications compared to warfarin, the incidence of gastrointestinal bleeding remains contradictory. <i>Materials and Methods:</i> After the exclusion of patients with pre-existing pathological lesions in the upper gastrointestinal tract (GIT) on esophageal-gastroduodenoscopy (EGD) at entry, a cohort of 80 patients (mean age of 74.8 ± 2.0 years) was randomly divided into four equivalent groups, treated with dabigatran, rivaroxaban, apixaban, or warfarin. Patients were prospectively followed up for three months of treatment, with a focus on anamnestic and endoscopic signs of bleeding. In addition, bleeding risk factors were evaluated. <i>Results:</i> In none of the patients treated with warfarin or NOACs was any serious or clinically significant bleeding recorded within the follow-up period. The incidence of clinical bleeding and endoscopically detected bleeding in the upper GT after three months of treatment was not statistically different among groups (χ<sup>2</sup> = 2.8458; <i>p</i> = 0.41608). The presence of <i>Helicobacter pylori</i> (HP) was a risk factor for upper GIT bleeding (<i>p</i> < 0.05), while the use of proton pump inhibitors (PPIs) was a protective factor (<i>p</i> = 0.206; Spearman’s correlation coefficient = 0.205). We did not record any post-biopsy continued bleeding. <i>Conclusions:</i> No significant GIT bleeding was found in any of the treatment groups, so we consider it beneficial to perform routine EGD before the initiation of any anticoagulant therapy in patients with an increased risk of upper GIT bleeding. Detection and eradication of HP as well as preventive PPI treatment may mitigate the occurrence of endoscopic bleeding. Endoscopic biopsy during the NOAC treatment is safe.https://www.mdpi.com/1010-660X/56/7/363novel anticoagulantsgastrointestinal bleeding<i>Helicobacter pylori</i>proton pump inhibitorsendoscopic biopsy
spellingShingle Lubomir Mihalkanin
Branislav Stancak
The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
Medicina
novel anticoagulants
gastrointestinal bleeding
<i>Helicobacter pylori</i>
proton pump inhibitors
endoscopic biopsy
title The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
title_full The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
title_fullStr The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
title_full_unstemmed The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
title_short The Impact of Novel Anticoagulants on the Upper Gastrointestinal Tract Mucosa
title_sort impact of novel anticoagulants on the upper gastrointestinal tract mucosa
topic novel anticoagulants
gastrointestinal bleeding
<i>Helicobacter pylori</i>
proton pump inhibitors
endoscopic biopsy
url https://www.mdpi.com/1010-660X/56/7/363
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