Cargando…
Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
BACKGROUND: Changing clinical impact, as virulent clones replace less virulent ones, is a feature of many pathogenic bacterial species and can be difficult to detect. Consequently, innovative techniques monitoring infection severity are of potential clinical value. METHODS AND FINDINGS: We studied 5...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409138/ https://www.ncbi.nlm.nih.gov/pubmed/22859914 http://dx.doi.org/10.1371/journal.pmed.1001279 |
_version_ | 1782239543728013312 |
---|---|
author | Schlackow, Iryna Walker, A. Sarah Dingle, Kate Griffiths, David Oakley, Sarah Finney, John Vaughan, Ali Gill, Martin J. Crook, Derrick W. Peto, Tim E. A. Wyllie, David H. |
author_facet | Schlackow, Iryna Walker, A. Sarah Dingle, Kate Griffiths, David Oakley, Sarah Finney, John Vaughan, Ali Gill, Martin J. Crook, Derrick W. Peto, Tim E. A. Wyllie, David H. |
author_sort | Schlackow, Iryna |
collection | PubMed |
description | BACKGROUND: Changing clinical impact, as virulent clones replace less virulent ones, is a feature of many pathogenic bacterial species and can be difficult to detect. Consequently, innovative techniques monitoring infection severity are of potential clinical value. METHODS AND FINDINGS: We studied 5,551 toxin-positive and 20,098 persistently toxin-negative patients tested for Clostridium difficile infection between February 1998 and July 2009 in a group of hospitals based in Oxford, UK, and investigated 28-day mortality and biomarkers of inflammation (blood neutrophil count, urea, and creatinine concentrations) collected at diagnosis using iterative sequential regression (ISR), a novel joinpoint-based regression technique suitable for serial monitoring of continuous or dichotomous outcomes. Among C. difficile toxin-positive patients in the Oxford hospitals, mean neutrophil counts on diagnosis increased from 2003, peaked in 2006–2007, and then declined; 28-day mortality increased from early 2006, peaked in late 2006–2007, and then declined. Molecular typing confirmed these changes were likely due to the ingress of the globally distributed severe C. difficile strain, ST1. We assessed the generalizability of ISR-based severity monitoring in three ways. First, we assessed and found strong (p<0.0001) associations between isolation of the ST1 severe strain and higher neutrophil counts at diagnosis in two unrelated large multi-centre studies, suggesting the technique described might be useful elsewhere. Second, we assessed and found similar trends in a second group of hospitals in Birmingham, UK, from which 5,399 cases were analysed. Third, we used simulation to assess the performance of this surveillance system given the ingress of future severe strains under a variety of assumptions. ISR-based severity monitoring allowed the detection of the severity change years earlier than mortality monitoring. CONCLUSIONS: Automated electronic systems providing early warning of the changing severity of infectious conditions can be established using routinely collected laboratory hospital data. In the settings studied here these systems have higher performance than those monitoring mortality, at least in C. difficile infection. Such systems could have wider applicability for monitoring infections presenting in hospital. |
format | Online Article Text |
id | pubmed-3409138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34091382012-08-02 Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile Schlackow, Iryna Walker, A. Sarah Dingle, Kate Griffiths, David Oakley, Sarah Finney, John Vaughan, Ali Gill, Martin J. Crook, Derrick W. Peto, Tim E. A. Wyllie, David H. PLoS Med Research Article BACKGROUND: Changing clinical impact, as virulent clones replace less virulent ones, is a feature of many pathogenic bacterial species and can be difficult to detect. Consequently, innovative techniques monitoring infection severity are of potential clinical value. METHODS AND FINDINGS: We studied 5,551 toxin-positive and 20,098 persistently toxin-negative patients tested for Clostridium difficile infection between February 1998 and July 2009 in a group of hospitals based in Oxford, UK, and investigated 28-day mortality and biomarkers of inflammation (blood neutrophil count, urea, and creatinine concentrations) collected at diagnosis using iterative sequential regression (ISR), a novel joinpoint-based regression technique suitable for serial monitoring of continuous or dichotomous outcomes. Among C. difficile toxin-positive patients in the Oxford hospitals, mean neutrophil counts on diagnosis increased from 2003, peaked in 2006–2007, and then declined; 28-day mortality increased from early 2006, peaked in late 2006–2007, and then declined. Molecular typing confirmed these changes were likely due to the ingress of the globally distributed severe C. difficile strain, ST1. We assessed the generalizability of ISR-based severity monitoring in three ways. First, we assessed and found strong (p<0.0001) associations between isolation of the ST1 severe strain and higher neutrophil counts at diagnosis in two unrelated large multi-centre studies, suggesting the technique described might be useful elsewhere. Second, we assessed and found similar trends in a second group of hospitals in Birmingham, UK, from which 5,399 cases were analysed. Third, we used simulation to assess the performance of this surveillance system given the ingress of future severe strains under a variety of assumptions. ISR-based severity monitoring allowed the detection of the severity change years earlier than mortality monitoring. CONCLUSIONS: Automated electronic systems providing early warning of the changing severity of infectious conditions can be established using routinely collected laboratory hospital data. In the settings studied here these systems have higher performance than those monitoring mortality, at least in C. difficile infection. Such systems could have wider applicability for monitoring infections presenting in hospital. Public Library of Science 2012-07-31 /pmc/articles/PMC3409138/ /pubmed/22859914 http://dx.doi.org/10.1371/journal.pmed.1001279 Text en © 2012 Schlackow et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schlackow, Iryna Walker, A. Sarah Dingle, Kate Griffiths, David Oakley, Sarah Finney, John Vaughan, Ali Gill, Martin J. Crook, Derrick W. Peto, Tim E. A. Wyllie, David H. Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile |
title | Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
|
title_full | Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
|
title_fullStr | Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
|
title_full_unstemmed | Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
|
title_short | Surveillance of Infection Severity: A Registry Study of Laboratory Diagnosed Clostridium difficile
|
title_sort | surveillance of infection severity: a registry study of laboratory diagnosed clostridium difficile |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409138/ https://www.ncbi.nlm.nih.gov/pubmed/22859914 http://dx.doi.org/10.1371/journal.pmed.1001279 |
work_keys_str_mv | AT schlackowiryna surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT walkerasarah surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT dinglekate surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT griffithsdavid surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT oakleysarah surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT finneyjohn surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT vaughanali surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT gillmartinj surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT crookderrickw surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT petotimea surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile AT wylliedavidh surveillanceofinfectionseverityaregistrystudyoflaboratorydiagnosedclostridiumdifficile |