Detection of toxigenic Clostridium difficile in paediatric patients
Enferm Infecc Microbiol Clin (Engl Ed). 2018 Jun-Jul;36(6):357-361.
doi: 10.1016/j.eimc.2017.05.006.
Epub 2017 Jul 8.
[Article in
English,
Spanish]
Affiliations
- 1 Servicio de Microbiología y Parasitología Clínicas, Hospital Universitario La Paz, Madrid, España.
- 2 Servicio de Microbiología y Parasitología Clínicas, Hospital Universitario La Paz, Madrid, España; ERN TRANSPLANT-CHILD: European Reference Network of Transplantation in Children (SOT & HSTC), Hospital Universitario La Paz (coordinador). Electronic address: sgbujalance@salud.madrid.org.
- 3 Servicio de Pediatría, Enfermedades Infecciosas y Tropicales, Hospital Universitario La Paz, Madrid, España; RITIP: Red Nacional de Investigación Traslacional en Infectología Pediátrica.
- 4 Servicio de Pediatría, Enfermedades Infecciosas y Tropicales, Hospital Universitario La Paz, Madrid, España; ERN TRANSPLANT-CHILD: European Reference Network of Transplantation in Children (SOT & HSTC), Hospital Universitario La Paz (coordinador); RITIP: Red Nacional de Investigación Traslacional en Infectología Pediátrica; TEDDY Network: European Network of Excellence for Pediatric Clinical Research.
- 5 Servicio de Microbiología y Parasitología Clínicas, Hospital Universitario La Paz, Madrid, España; ERN TRANSPLANT-CHILD: European Reference Network of Transplantation in Children (SOT & HSTC), Hospital Universitario La Paz (coordinador).
Abstract
Introduction:
Our main objective was a revision of clinical, microbiological and epidemiological results of Clostridium difficile-associated infection in paediatric patients (2010-2015). We compared the diagnoses performed by detection of toxins in feces and those performed by real-time PCR.
Methods:
This retrospective study included 82 paediatric patients. Detection of toxigenic C. difficile was performed sequentially, in diarrheal feces and under clinical request.
Results:
A total of 39% of the patients were attended at Haematology-oncology Unit and >50% of them had previously received cephalosporins. Fever associated with diarrhea was more frequent in the group of toxin detection, whereas not receiving specific antibiotic treatment was more frequent in the group of positive PCR, without statistically significant differences.
Conclusions:
We highlight the presence of C. difficile infection in children under 2years old. A diagnostic testing in selected paediatric patients would be advisable when there is clinical suspicion of infection.
Keywords:
A/B toxins; Clostridium difficile; PCR B toxin gene; PCR gen toxina B; Paediatric patients; Pediatría; Toxinas A/B.
Copyright © 2017 Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica. All rights reserved.
MeSH terms
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Adolescent
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Bacterial Proteins / analysis
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Bacterial Proteins / genetics
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Bacterial Toxins / analysis
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Bacterial Toxins / genetics
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Cephalosporins / adverse effects
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Cephalosporins / therapeutic use
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Child
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Child, Preschool
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Clostridioides difficile / genetics
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Clostridioides difficile / isolation & purification*
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Clostridium Infections / epidemiology
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Clostridium Infections / microbiology*
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Diarrhea, Infantile / etiology
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Enterocolitis, Pseudomembranous / epidemiology
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Enterocolitis, Pseudomembranous / etiology
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Enterocolitis, Pseudomembranous / microbiology
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Enterotoxins / genetics
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Feces / chemistry
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Female
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Fever / epidemiology
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Fever / etiology
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Genes, Bacterial
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Humans
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Infant
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Infant, Newborn
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Male
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Real-Time Polymerase Chain Reaction
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Retrospective Studies
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Tertiary Care Centers / statistics & numerical data
Substances
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Bacterial Proteins
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Bacterial Toxins
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Cephalosporins
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Enterotoxins
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tcdA protein, Clostridium difficile
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toxB protein, Clostridium difficile