Pigment Visibility on Rectal Swabs Used To Detect Enteropathogens: a Prospective Cohort Study.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
06 2019
Historique:
received: 09 02 2019
accepted: 22 03 2019
pubmed: 5 4 2019
medline: 23 6 2020
entrez: 5 4 2019
Statut: epublish

Résumé

Data are lacking regarding the impact of visible pigment on rectal swab diagnostic accuracy. We describe the test characteristics of rectal swabs with and without pigment in children with gastroenteritis. Between December 2014 and September 2017, children (age, <18 years) with ≥3 episodes of vomiting and/or diarrhea in a 24-h period and symptoms for <7 days were enrolled through two pediatric emergency departments and from a province-wide nursing telephone advice line in Alberta, Canada. Specimens were analyzed by employing nucleic acid amplification panels. The primary outcomes were the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for the rectal swabs, with stool specimen results being used as the reference standard. An enteropathogen was detected in 76.0% (1,399/1,841) of the paired specimens. A total of 54.4% (1,001/1841) of the swabs had visible pigment. The respective enteropathogen detection characteristics of swabs with and without visible pigment were as follows: 92.2% (95% confidence interval [CI], 90.0%, 94.0%) versus 83.7% (95% CI, 80.5%, 86.4%) for sensitivity, 94.3% (95% CI, 90.5%, 96.6%) versus 91.2% (95% CI, 86.3%, 94.5%) for specificity, 97.9% (95% CI, 96.4%, 98.8%) versus 96.5% (95% CI, 94.5%, 97.8%) for PPV, and 80.9% (95% CI, 76.0%, 85.1%) versus 65.8% (95% CI, 60.0%, 71.1%) for NPV. Processing of swabs without visible pigment would increase the rate of identification of positive swabs from 50.0% (682/1,365) to 88.3% (1,205/1,365). There is a modest decrease in the reliability of a negative test on swabs without evidence of pigment, but the overall yield is significantly greater when they are not excluded from testing. Hence, rectal swabs without visible feces should not be routinely rejected from testing.

Identifiants

pubmed: 30944189
pii: JCM.00213-19
doi: 10.1128/JCM.00213-19
pmc: PMC6535614
pii:
doi:

Substances chimiques

Pigments, Biological 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK052574
Pays : United States

Informations de copyright

Copyright © 2019 American Society for Microbiology.

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Auteurs

Jianling Xie (J)

Section of Pediatric Emergency Medicine, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.

Gillian A M Tarr (GAM)

Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.

Samina Ali (S)

Department of Pediatrics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Women & Children's Health Research Institute (WCHRI), Edmonton, Alberta, Canada.

Linda Chui (L)

Provincial Laboratory for Public Health, Alberta Public Laboratories, Edmonton, Alberta, Canada.
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Xiao-Li Pang (XL)

Provincial Laboratory for Public Health, Alberta Public Laboratories, Edmonton, Alberta, Canada.
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Bonita E Lee (BE)

Department of Pediatrics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Women & Children's Health Research Institute (WCHRI), Edmonton, Alberta, Canada.

Otto G Vanderkooi (OG)

Department of Pediatrics, Microbiology, Immunology and Infectious Diseases, Pathology & Laboratory Medicine and Community Health Sciences and the Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Phillip I Tarr (PI)

Department of Pediatrics, Division of Gastroenterology, & Nutrition, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.

Ran Zhuo (R)

Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Brendon Parsons (B)

Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Byron M Berenger (BM)

Provincial Laboratory for Public Health, Alberta Public Laboratories, Edmonton, Alberta, Canada.
Department of Pathology & Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada.

Kelly Kim (K)

Section of Pediatric Emergency Medicine, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.

Stephen B Freedman (SB)

Section of Pediatric Emergency Medicine, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada stephen.freedman@ahs.ca.
Section of Pediatric Gastroenterology, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

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