Cargando…
616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events
BACKGROUND: The gut microbiome of hematopoietic cell transplant (HCT) recipients correlates with the risk of acute graft- vs.-host disease (aGVHD). IV vancomycin is the most commonly used nonprophylactic antibiotic in HCT recipients at our center. We evaluated indications for vancomycin use and impa...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255572/ http://dx.doi.org/10.1093/ofid/ofy210.623 |
_version_ | 1783373972925054976 |
---|---|
author | Golob, Jonathan Stohs, Erica Sweet, Ania Pergam, Steven Boeckh, Michael Fredricks, David Liu, Catherine |
author_facet | Golob, Jonathan Stohs, Erica Sweet, Ania Pergam, Steven Boeckh, Michael Fredricks, David Liu, Catherine |
author_sort | Golob, Jonathan |
collection | PubMed |
description | BACKGROUND: The gut microbiome of hematopoietic cell transplant (HCT) recipients correlates with the risk of acute graft- vs.-host disease (aGVHD). IV vancomycin is the most commonly used nonprophylactic antibiotic in HCT recipients at our center. We evaluated indications for vancomycin use and impact of vancomycin exposure on the microbiome. METHODS: Antibiotic exposures and provider-documented indications for vancomycin use were assessed through chart review. We assessed adherence to guideline-based recommendations for vancomycin use for courses during neutropenic fever. Weekly stool samples collected from HCT patients before and up to 100 days post-transplant in a previously described cohort had bacterial composition determined from 16S rRNA amplicons analyzed with a phylogeny classifier and was correlated with vancomycin exposure using mixed effects modeling to correct for overlapping and repeated antibiotic exposures. RESULTS: Thirty-seven of 70 (53%) of patients received vancomycin over 61 courses with a mean duration of 8 days; 14 (23%) of these courses were with neutropenic fever. No indication was documented by the provider for 21 (34%) vancomycin courses (Figure 1). Almost half of all courses given for neutropenic fever did not meet guideline indications (Figure 2). Adverse effects occurred in 19 (31%) of vancomycin courses, including 11 (18%) associated with acute kidney injury. Vancomycin was associated with reduced relative abundance of organisms correlated with reduced risk of subsequent severe acute graft vs. host disease and Clostridium scindens, an organism protective against C. difficile infection (CDI) (Figure 3, in bold). CONCLUSION: Indications for vancomycin were poorly documented and infrequently guideline based. Adverse events occurred in 1 in 3 courses of vancomycin. Vancomycin correlated with microbiome changes which have been associated with increased risk for aGVHD and CDI. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: S. Pergam, Merck: Consultant, Consulting fee. |
format | Online Article Text |
id | pubmed-6255572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62555722018-11-28 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events Golob, Jonathan Stohs, Erica Sweet, Ania Pergam, Steven Boeckh, Michael Fredricks, David Liu, Catherine Open Forum Infect Dis Abstracts BACKGROUND: The gut microbiome of hematopoietic cell transplant (HCT) recipients correlates with the risk of acute graft- vs.-host disease (aGVHD). IV vancomycin is the most commonly used nonprophylactic antibiotic in HCT recipients at our center. We evaluated indications for vancomycin use and impact of vancomycin exposure on the microbiome. METHODS: Antibiotic exposures and provider-documented indications for vancomycin use were assessed through chart review. We assessed adherence to guideline-based recommendations for vancomycin use for courses during neutropenic fever. Weekly stool samples collected from HCT patients before and up to 100 days post-transplant in a previously described cohort had bacterial composition determined from 16S rRNA amplicons analyzed with a phylogeny classifier and was correlated with vancomycin exposure using mixed effects modeling to correct for overlapping and repeated antibiotic exposures. RESULTS: Thirty-seven of 70 (53%) of patients received vancomycin over 61 courses with a mean duration of 8 days; 14 (23%) of these courses were with neutropenic fever. No indication was documented by the provider for 21 (34%) vancomycin courses (Figure 1). Almost half of all courses given for neutropenic fever did not meet guideline indications (Figure 2). Adverse effects occurred in 19 (31%) of vancomycin courses, including 11 (18%) associated with acute kidney injury. Vancomycin was associated with reduced relative abundance of organisms correlated with reduced risk of subsequent severe acute graft vs. host disease and Clostridium scindens, an organism protective against C. difficile infection (CDI) (Figure 3, in bold). CONCLUSION: Indications for vancomycin were poorly documented and infrequently guideline based. Adverse events occurred in 1 in 3 courses of vancomycin. Vancomycin correlated with microbiome changes which have been associated with increased risk for aGVHD and CDI. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: S. Pergam, Merck: Consultant, Consulting fee. Oxford University Press 2018-11-26 /pmc/articles/PMC6255572/ http://dx.doi.org/10.1093/ofid/ofy210.623 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Golob, Jonathan Stohs, Erica Sweet, Ania Pergam, Steven Boeckh, Michael Fredricks, David Liu, Catherine 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title | 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title_full | 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title_fullStr | 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title_full_unstemmed | 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title_short | 616. Vancomycin Is Frequently Administered to Hematopoietic Cell Transplant Recipients Without a Provider Documented Indication and Correlates with Microbiome Disruption and Adverse Events |
title_sort | 616. vancomycin is frequently administered to hematopoietic cell transplant recipients without a provider documented indication and correlates with microbiome disruption and adverse events |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255572/ http://dx.doi.org/10.1093/ofid/ofy210.623 |
work_keys_str_mv | AT golobjonathan 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT stohserica 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT sweetania 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT pergamsteven 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT boeckhmichael 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT fredricksdavid 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents AT liucatherine 616vancomycinisfrequentlyadministeredtohematopoieticcelltransplantrecipientswithoutaproviderdocumentedindicationandcorrelateswithmicrobiomedisruptionandadverseevents |