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665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients
BACKGROUND: To prevent spontaneous bacterial peritonitis (SBP), re-bleeding, mortality, and long hospital stays in patients with acute variceal hemorrhage, the American Association for the Study of Liver Diseases recommends up to 7 days of ceftriaxone, with guidance to consider discontinuing when he...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678710/ http://dx.doi.org/10.1093/ofid/ofad500.728 |
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author | Tedeschi, Carissa M Hoff, Abigail Scherrer, Nicole Shigle, Amanda Burwell, Sheena |
author_facet | Tedeschi, Carissa M Hoff, Abigail Scherrer, Nicole Shigle, Amanda Burwell, Sheena |
author_sort | Tedeschi, Carissa M |
collection | PubMed |
description | BACKGROUND: To prevent spontaneous bacterial peritonitis (SBP), re-bleeding, mortality, and long hospital stays in patients with acute variceal hemorrhage, the American Association for the Study of Liver Diseases recommends up to 7 days of ceftriaxone, with guidance to consider discontinuing when hemorrhage resolves and vasoactive drugs are stopped. Due to the ambiguous recommendation, practices vary surrounding duration of SBP prophylaxis. To our knowledge, no study has been completed on the duration of SBP prophylaxis within our current standard of care. METHODS: This was a retrospective, non-inferiority trial of adult patients receiving an octreotide infusion with confirmed variceal hemorrhage diagnosed via esophagogastroduodenoscopy at WVU Hospitals from 1/1/2020 - 12/31/2022. Medical records were reviewed to include demographic information, antibiotic selection, and duration of therapy for SBP prophylaxis, in addition to outcome measures such as infection, re-bleeding, length of stay, and mortality. Patients who received 5 or fewer days (shorter group) of prophylactic antibiotics were compared to those who received more than 5 days (longer group). RESULTS: 84 patients were included: 39 patients in the shorter group, and 45 patients in the longer group. There was no statistically significant difference found between the shorter and longer groups in terms of demographic information. The primary outcome was development of infection. Four (10.3%) patients in the shorter group developed infection, and three (6.7%) patients in the longer group developed infection. The number of patients gathered met power for a 20% non-inferiority margin. There was no statistically significant difference found in any of the secondary outcomes. Results [Figure: see text] Primary and Secondary Outcomes CONCLUSION: We can conclude that shorter durations of SBP prophylaxis are non-inferior to longer durations for preventing infections. In general, decreasing the duration of antibiotics to only what is necessary allows for preventing the development of resistance and fewer secondary infections. Additional studies are needed to confirm the results and impact guideline recommendations. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10678710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106787102023-11-27 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients Tedeschi, Carissa M Hoff, Abigail Scherrer, Nicole Shigle, Amanda Burwell, Sheena Open Forum Infect Dis Abstract BACKGROUND: To prevent spontaneous bacterial peritonitis (SBP), re-bleeding, mortality, and long hospital stays in patients with acute variceal hemorrhage, the American Association for the Study of Liver Diseases recommends up to 7 days of ceftriaxone, with guidance to consider discontinuing when hemorrhage resolves and vasoactive drugs are stopped. Due to the ambiguous recommendation, practices vary surrounding duration of SBP prophylaxis. To our knowledge, no study has been completed on the duration of SBP prophylaxis within our current standard of care. METHODS: This was a retrospective, non-inferiority trial of adult patients receiving an octreotide infusion with confirmed variceal hemorrhage diagnosed via esophagogastroduodenoscopy at WVU Hospitals from 1/1/2020 - 12/31/2022. Medical records were reviewed to include demographic information, antibiotic selection, and duration of therapy for SBP prophylaxis, in addition to outcome measures such as infection, re-bleeding, length of stay, and mortality. Patients who received 5 or fewer days (shorter group) of prophylactic antibiotics were compared to those who received more than 5 days (longer group). RESULTS: 84 patients were included: 39 patients in the shorter group, and 45 patients in the longer group. There was no statistically significant difference found between the shorter and longer groups in terms of demographic information. The primary outcome was development of infection. Four (10.3%) patients in the shorter group developed infection, and three (6.7%) patients in the longer group developed infection. The number of patients gathered met power for a 20% non-inferiority margin. There was no statistically significant difference found in any of the secondary outcomes. Results [Figure: see text] Primary and Secondary Outcomes CONCLUSION: We can conclude that shorter durations of SBP prophylaxis are non-inferior to longer durations for preventing infections. In general, decreasing the duration of antibiotics to only what is necessary allows for preventing the development of resistance and fewer secondary infections. Additional studies are needed to confirm the results and impact guideline recommendations. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678710/ http://dx.doi.org/10.1093/ofid/ofad500.728 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Tedeschi, Carissa M Hoff, Abigail Scherrer, Nicole Shigle, Amanda Burwell, Sheena 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title | 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title_full | 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title_fullStr | 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title_full_unstemmed | 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title_short | 665. Duration of Spontaneous Bacterial Peritonitis Prophylaxis in Acute Variceal Hemorrhage Patients |
title_sort | 665. duration of spontaneous bacterial peritonitis prophylaxis in acute variceal hemorrhage patients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678710/ http://dx.doi.org/10.1093/ofid/ofad500.728 |
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