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Mortality related to Verona Integron-encoded Metallo-β-lactamase-positive Pseudomonas aeruginosa : assessment by a novel clinical tool
Verona Integron-encoded Metallo-β-lactamase-positive (VIM-PA) can cause nosocomial infections and may be responsible for increased mortality. Multidrug resistance in VIM-PA complicates treatment. We aimed to assess the contribution of VIM-PA to mortality in patients in a large tertiary care hospital...
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Published in: | Antimicrobial resistance & infection control 2019-06, Vol.8 (1), p.107-107, Article 107 |
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creator | Persoon, Marjolein C Voor In 't Holt, Anne F van Meer, Maurits P A Bokhoven, Karen C Gommers, Diederik Vos, Margreet C Severin, Juliëtte A |
description | Verona Integron-encoded Metallo-β-lactamase-positive
(VIM-PA) can cause nosocomial infections and may be responsible for increased mortality. Multidrug resistance in VIM-PA complicates treatment. We aimed to assess the contribution of VIM-PA to mortality in patients in a large tertiary care hospital in the Netherlands.
A focus group of five members created a scheme to define related mortality based on clinical and diagnostic findings. Contribution to mortality was categorized as "definitely", "probably", "possibly", or "not" related to infection with VIM-PA, or as "unknown". Patients were included when infected with or carrier of VIM-PA between January 2008 and January 2016. Patient-related data and specific data on VIM-PA cultures were retrieved from the electronic laboratory information system. For patients who died in our hospital, medical records were independently reviewed and thereafter discussed by three physicians.
A total of 198 patients with any positive culture with VIM-PA were identified, of whom 95 (48.0%) died. Sixty-seven patients died in our hospital and could be included in the analysis. The death of 15 patients (22.4%) was judged by all reviewers to be definitely related to infection with VIM-PA. In 17 additional patients (25.4%), death was probably or possibly related to an infection with VIM-PA. The level of agreement was 65.7% after the first evaluation, and 98.5% after one session of discussion.
Using our assessment tool, infections with VIM-PA were shown to have an important influence on mortality in our complex and severely ill patients. The tool may be used for other (resistant) bacteria as well but this needs further exploration. |
doi_str_mv | 10.1186/s13756-019-0556-9 |
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(VIM-PA) can cause nosocomial infections and may be responsible for increased mortality. Multidrug resistance in VIM-PA complicates treatment. We aimed to assess the contribution of VIM-PA to mortality in patients in a large tertiary care hospital in the Netherlands.
A focus group of five members created a scheme to define related mortality based on clinical and diagnostic findings. Contribution to mortality was categorized as "definitely", "probably", "possibly", or "not" related to infection with VIM-PA, or as "unknown". Patients were included when infected with or carrier of VIM-PA between January 2008 and January 2016. Patient-related data and specific data on VIM-PA cultures were retrieved from the electronic laboratory information system. For patients who died in our hospital, medical records were independently reviewed and thereafter discussed by three physicians.
A total of 198 patients with any positive culture with VIM-PA were identified, of whom 95 (48.0%) died. Sixty-seven patients died in our hospital and could be included in the analysis. The death of 15 patients (22.4%) was judged by all reviewers to be definitely related to infection with VIM-PA. In 17 additional patients (25.4%), death was probably or possibly related to an infection with VIM-PA. The level of agreement was 65.7% after the first evaluation, and 98.5% after one session of discussion.
Using our assessment tool, infections with VIM-PA were shown to have an important influence on mortality in our complex and severely ill patients. The tool may be used for other (resistant) bacteria as well but this needs further exploration.</description><identifier>ISSN: 2047-2994</identifier><identifier>EISSN: 2047-2994</identifier><identifier>DOI: 10.1186/s13756-019-0556-9</identifier><identifier>PMID: 31244998</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Antibiotics ; Antimicrobial agents ; Carbapenem ; Disease control ; Drug resistance ; Hospitals ; Infection control ; Intensive care units ; Medical records ; Microbial drug resistance ; Mortality ; Nosocomial infection ; Nosocomial infections ; Pathogens ; Patients ; Pneumonia ; Pseudomonas aeruginosa ; Sepsis</subject><ispartof>Antimicrobial resistance & infection control, 2019-06, Vol.8 (1), p.107-107, Article 107</ispartof><rights>2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s). 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4089-8d308462565cc70704fa0aeb454809e0e7a3a1f7467885a6b46780e8f296cfee3</citedby><cites>FETCH-LOGICAL-c4089-8d308462565cc70704fa0aeb454809e0e7a3a1f7467885a6b46780e8f296cfee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582487/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2242955159?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31244998$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Persoon, Marjolein C</creatorcontrib><creatorcontrib>Voor In 't Holt, Anne F</creatorcontrib><creatorcontrib>van Meer, Maurits P A</creatorcontrib><creatorcontrib>Bokhoven, Karen C</creatorcontrib><creatorcontrib>Gommers, Diederik</creatorcontrib><creatorcontrib>Vos, Margreet C</creatorcontrib><creatorcontrib>Severin, Juliëtte A</creatorcontrib><title>Mortality related to Verona Integron-encoded Metallo-β-lactamase-positive Pseudomonas aeruginosa : assessment by a novel clinical tool</title><title>Antimicrobial resistance & infection control</title><addtitle>Antimicrob Resist Infect Control</addtitle><description>Verona Integron-encoded Metallo-β-lactamase-positive
(VIM-PA) can cause nosocomial infections and may be responsible for increased mortality. Multidrug resistance in VIM-PA complicates treatment. We aimed to assess the contribution of VIM-PA to mortality in patients in a large tertiary care hospital in the Netherlands.
A focus group of five members created a scheme to define related mortality based on clinical and diagnostic findings. Contribution to mortality was categorized as "definitely", "probably", "possibly", or "not" related to infection with VIM-PA, or as "unknown". Patients were included when infected with or carrier of VIM-PA between January 2008 and January 2016. Patient-related data and specific data on VIM-PA cultures were retrieved from the electronic laboratory information system. For patients who died in our hospital, medical records were independently reviewed and thereafter discussed by three physicians.
A total of 198 patients with any positive culture with VIM-PA were identified, of whom 95 (48.0%) died. Sixty-seven patients died in our hospital and could be included in the analysis. The death of 15 patients (22.4%) was judged by all reviewers to be definitely related to infection with VIM-PA. In 17 additional patients (25.4%), death was probably or possibly related to an infection with VIM-PA. The level of agreement was 65.7% after the first evaluation, and 98.5% after one session of discussion.
Using our assessment tool, infections with VIM-PA were shown to have an important influence on mortality in our complex and severely ill patients. 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(VIM-PA) can cause nosocomial infections and may be responsible for increased mortality. Multidrug resistance in VIM-PA complicates treatment. We aimed to assess the contribution of VIM-PA to mortality in patients in a large tertiary care hospital in the Netherlands.
A focus group of five members created a scheme to define related mortality based on clinical and diagnostic findings. Contribution to mortality was categorized as "definitely", "probably", "possibly", or "not" related to infection with VIM-PA, or as "unknown". Patients were included when infected with or carrier of VIM-PA between January 2008 and January 2016. Patient-related data and specific data on VIM-PA cultures were retrieved from the electronic laboratory information system. For patients who died in our hospital, medical records were independently reviewed and thereafter discussed by three physicians.
A total of 198 patients with any positive culture with VIM-PA were identified, of whom 95 (48.0%) died. Sixty-seven patients died in our hospital and could be included in the analysis. The death of 15 patients (22.4%) was judged by all reviewers to be definitely related to infection with VIM-PA. In 17 additional patients (25.4%), death was probably or possibly related to an infection with VIM-PA. The level of agreement was 65.7% after the first evaluation, and 98.5% after one session of discussion.
Using our assessment tool, infections with VIM-PA were shown to have an important influence on mortality in our complex and severely ill patients. The tool may be used for other (resistant) bacteria as well but this needs further exploration.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>31244998</pmid><doi>10.1186/s13756-019-0556-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotics Antimicrobial agents Carbapenem Disease control Drug resistance Hospitals Infection control Intensive care units Medical records Microbial drug resistance Mortality Nosocomial infection Nosocomial infections Pathogens Patients Pneumonia Pseudomonas aeruginosa Sepsis |
title | Mortality related to Verona Integron-encoded Metallo-β-lactamase-positive Pseudomonas aeruginosa : assessment by a novel clinical tool |
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