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Gallbladder hemorrhage during orally administered edoxaban therapy: a case report
BACKGROUND: Edoxaban is an orally administered anticoagulant treatment that is used in patients with cerebral infarction, venous thrombosis, or other conditions, with a reported incidence of gastrointestinal hemorrhage at approximately 1%. We encountered the rare case of a patient who developed a ga...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931242/ https://www.ncbi.nlm.nih.gov/pubmed/31875787 http://dx.doi.org/10.1186/s13256-019-2328-9 |
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author | Itagaki, Hideya Katuhiko, Suzuki |
author_facet | Itagaki, Hideya Katuhiko, Suzuki |
author_sort | Itagaki, Hideya |
collection | PubMed |
description | BACKGROUND: Edoxaban is an orally administered anticoagulant treatment that is used in patients with cerebral infarction, venous thrombosis, or other conditions, with a reported incidence of gastrointestinal hemorrhage at approximately 1%. We encountered the rare case of a patient who developed a gallbladder hemorrhage after the administration of edoxaban. CASE PRESENTATION: An 86-year-old Japanese woman visited our gastrointestinal department due to the chief complaint of melena lasting for a week. Her medical history included hypertension and embolic cerebral infarction, and she was taking orally administered carvedilol (5 mg/day) and edoxaban (30 mg/day). Her palpebral conjunctiva was pale during a physical examination, indicating the possibility of anemia. Her blood test results confirmed severe anemia with red blood cells at 1.7 × 10(6)/μL and hemoglobin at 4.7 g/dL. An upper gastrointestinal endoscopy revealed bile and fresh blood on the duodenal bulb and in more distal regions; hemobilia was suspected. A computed tomography scan on the ninth hospitalization day confirmed the hemobilia with a gallbladder fundus high-density signal. She was discharged on the 30th day of hospitalization with only fluid therapy and no progression of anemia. Moreover, she underwent a laparoscopic cholecystectomy 1 month after discharge, but the pathologist did not identify false aneurysms or neoplastic lesions. She has not been shown to develop anemia for 5 months after surgery. CONCLUSIONS: Our case suggests that gallbladder hemorrhage needs to be considered a possible complication for patients on direct oral anticoagulants. |
format | Online Article Text |
id | pubmed-6931242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69312422019-12-30 Gallbladder hemorrhage during orally administered edoxaban therapy: a case report Itagaki, Hideya Katuhiko, Suzuki J Med Case Rep Case Report BACKGROUND: Edoxaban is an orally administered anticoagulant treatment that is used in patients with cerebral infarction, venous thrombosis, or other conditions, with a reported incidence of gastrointestinal hemorrhage at approximately 1%. We encountered the rare case of a patient who developed a gallbladder hemorrhage after the administration of edoxaban. CASE PRESENTATION: An 86-year-old Japanese woman visited our gastrointestinal department due to the chief complaint of melena lasting for a week. Her medical history included hypertension and embolic cerebral infarction, and she was taking orally administered carvedilol (5 mg/day) and edoxaban (30 mg/day). Her palpebral conjunctiva was pale during a physical examination, indicating the possibility of anemia. Her blood test results confirmed severe anemia with red blood cells at 1.7 × 10(6)/μL and hemoglobin at 4.7 g/dL. An upper gastrointestinal endoscopy revealed bile and fresh blood on the duodenal bulb and in more distal regions; hemobilia was suspected. A computed tomography scan on the ninth hospitalization day confirmed the hemobilia with a gallbladder fundus high-density signal. She was discharged on the 30th day of hospitalization with only fluid therapy and no progression of anemia. Moreover, she underwent a laparoscopic cholecystectomy 1 month after discharge, but the pathologist did not identify false aneurysms or neoplastic lesions. She has not been shown to develop anemia for 5 months after surgery. CONCLUSIONS: Our case suggests that gallbladder hemorrhage needs to be considered a possible complication for patients on direct oral anticoagulants. BioMed Central 2019-12-26 /pmc/articles/PMC6931242/ /pubmed/31875787 http://dx.doi.org/10.1186/s13256-019-2328-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Itagaki, Hideya Katuhiko, Suzuki Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title | Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title_full | Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title_fullStr | Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title_full_unstemmed | Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title_short | Gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
title_sort | gallbladder hemorrhage during orally administered edoxaban therapy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931242/ https://www.ncbi.nlm.nih.gov/pubmed/31875787 http://dx.doi.org/10.1186/s13256-019-2328-9 |
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