Cargando…

Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment

BACKGROUND: Antimicrobially pre-treated children with systemic inflammation often pose a diagnostic challenge to the physician. We aimed to evaluate the additional use of SeptiFast multiplex polymerase chain reaction (PCR) to identify causative pathogens in children with suspected systemic bacterial...

Descripción completa

Detalles Bibliográficos
Autores principales: Gies, Franziska, Tschiedel, Eva, Felderhoff-Müser, Ursula, Rath, Peter-Michael, Steinmann, Joerg, Dohna-Schwake, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977629/
https://www.ncbi.nlm.nih.gov/pubmed/27503068
http://dx.doi.org/10.1186/s12879-016-1722-9
_version_ 1782447064159879168
author Gies, Franziska
Tschiedel, Eva
Felderhoff-Müser, Ursula
Rath, Peter-Michael
Steinmann, Joerg
Dohna-Schwake, Christian
author_facet Gies, Franziska
Tschiedel, Eva
Felderhoff-Müser, Ursula
Rath, Peter-Michael
Steinmann, Joerg
Dohna-Schwake, Christian
author_sort Gies, Franziska
collection PubMed
description BACKGROUND: Antimicrobially pre-treated children with systemic inflammation often pose a diagnostic challenge to the physician. We aimed to evaluate the additional use of SeptiFast multiplex polymerase chain reaction (PCR) to identify causative pathogens in children with suspected systemic bacterial or fungal infection. METHODS: Prospective observational study in 39 children with systemic inflammatory response syndrome (SIRS) under empiric antibiotic treatment. Primary outcome was the rate of positive blood cultures (BC), compared to the rate of positive SeptiFast (SF) results. RESULTS: In total, 14 SF-samples yielded positive results, compared to 4 positive BC (p < 0.05). All blood cultures and 13 of 14 positive SF-tests were considered infection. Median time for positive BC was 2 days, and time to definite result was 6 days, compared to 12 h for SF. Antimicrobial therapy was adapted in 7 of the 14 patients with positive SeptiFast, and in 3 of the 4 patients with positive BC. Best predictive power for positive SF shown by receiver-operating characteristic was demonstrated for procalcitonin PCT (Area under the curve AUC: 0.79), compared to C-reactive protein CRP (AUC: 0.51) and leukocyte count (AUC: 0.46). A procalcitonin threshold of 0.89 ng/ml yielded a sensitivity of 0.82 and a specifity of 0.7. Children with a positive SeptiFast result on day 0 had a significantly higher risk to require treatment on the Pediatric Intensive Care Unit or to be deceased on day 30 (Odds-Ratio 8.62 (CI 1.44-51.72). CONCLUSIONS: The additional testing with SeptiFast in antimicrobially pre-treated children with systemic inflammation enhances the rate of pathogen detection. The influence of multiplex PCR on clinically relevant outcome parameters has to be further evaluated. (Trial registration: DRKS00004694)
format Online
Article
Text
id pubmed-4977629
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-49776292016-08-17 Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment Gies, Franziska Tschiedel, Eva Felderhoff-Müser, Ursula Rath, Peter-Michael Steinmann, Joerg Dohna-Schwake, Christian BMC Infect Dis Research Article BACKGROUND: Antimicrobially pre-treated children with systemic inflammation often pose a diagnostic challenge to the physician. We aimed to evaluate the additional use of SeptiFast multiplex polymerase chain reaction (PCR) to identify causative pathogens in children with suspected systemic bacterial or fungal infection. METHODS: Prospective observational study in 39 children with systemic inflammatory response syndrome (SIRS) under empiric antibiotic treatment. Primary outcome was the rate of positive blood cultures (BC), compared to the rate of positive SeptiFast (SF) results. RESULTS: In total, 14 SF-samples yielded positive results, compared to 4 positive BC (p < 0.05). All blood cultures and 13 of 14 positive SF-tests were considered infection. Median time for positive BC was 2 days, and time to definite result was 6 days, compared to 12 h for SF. Antimicrobial therapy was adapted in 7 of the 14 patients with positive SeptiFast, and in 3 of the 4 patients with positive BC. Best predictive power for positive SF shown by receiver-operating characteristic was demonstrated for procalcitonin PCT (Area under the curve AUC: 0.79), compared to C-reactive protein CRP (AUC: 0.51) and leukocyte count (AUC: 0.46). A procalcitonin threshold of 0.89 ng/ml yielded a sensitivity of 0.82 and a specifity of 0.7. Children with a positive SeptiFast result on day 0 had a significantly higher risk to require treatment on the Pediatric Intensive Care Unit or to be deceased on day 30 (Odds-Ratio 8.62 (CI 1.44-51.72). CONCLUSIONS: The additional testing with SeptiFast in antimicrobially pre-treated children with systemic inflammation enhances the rate of pathogen detection. The influence of multiplex PCR on clinically relevant outcome parameters has to be further evaluated. (Trial registration: DRKS00004694) BioMed Central 2016-08-08 /pmc/articles/PMC4977629/ /pubmed/27503068 http://dx.doi.org/10.1186/s12879-016-1722-9 Text en © The Author(s). 2016 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 Research Article
Gies, Franziska
Tschiedel, Eva
Felderhoff-Müser, Ursula
Rath, Peter-Michael
Steinmann, Joerg
Dohna-Schwake, Christian
Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title_full Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title_fullStr Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title_full_unstemmed Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title_short Prospective evaluation of SeptiFast Multiplex PCR in children with systemic inflammatory response syndrome under antibiotic treatment
title_sort prospective evaluation of septifast multiplex pcr in children with systemic inflammatory response syndrome under antibiotic treatment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977629/
https://www.ncbi.nlm.nih.gov/pubmed/27503068
http://dx.doi.org/10.1186/s12879-016-1722-9
work_keys_str_mv AT giesfranziska prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment
AT tschiedeleva prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment
AT felderhoffmuserursula prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment
AT rathpetermichael prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment
AT steinmannjoerg prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment
AT dohnaschwakechristian prospectiveevaluationofseptifastmultiplexpcrinchildrenwithsystemicinflammatoryresponsesyndromeunderantibiotictreatment