Evidence map›Paper›PMID 16825509›Full record

ArticleThe Journal of molecular diagnostics : JMD2006

Evaluating the near-term infant for early onset sepsis: progress and challenges to consider with 16S rDNA polymerase chain reaction testing.

Jeanne A Jordan, Mary Beth Durso, Allyson R Butchko, Judith G Jones, Beverly S Brozanski

Open access · bronzeAbstract readComparative StudyEvaluation Study
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 4 pooled it
4.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 4 syntheses or guidelines pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Molecular assays for the diagnosis of sepsis in neonates.The Cochrane database of systematic reviews · 2017
    Pooled it
  4. Pooled it
  5. Article
  6. Observational
  7. Review
  8. Review
  9. Article
  10. Article
  11. Monitoring neonates for ototoxicity.International journal of audiology · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Early-onset neonatal sepsis.Clinical microbiology reviews · 2014
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Jeanne A JordanDepartment of Pathology, Magee-Women's Research Institute, 204 Craft Ave., Pittsburgh, PA 15213, USA. rsijaj@mwri.magee.edu
Mary Beth Durso
Allyson R Butchko
Judith G Jones
Beverly S Brozanski
University of Pittsburgh · USMagee-Womens Hospital · USMagee-Womens Research Institute · US

Funding

DETECTING NEONATAL SEPSIS USING MOLECULAR TECHNIQUESR01HD038559 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI JORDAN, JEANNE ANN · 2000 to 2003
$646k
NICHD NIH HHS R01 HD038559
6 · The paper itself

Abstract

Although the rate of early onset sepsis in the near-term neonate is low (one to eight of 1,000 cases), the rate of mortality and morbidity is high. As a result, infants receive multiple, broad-spectrum antibiotic therapy, many for up to 7 days despite blood cultures showing no growth. Maternal intrapartum antibiotic prophylaxis and small blood volume collections from infants are cited as reasons for the lack of confidence in negative culture results. Incorporating an additional, more rapid test could facilitate a more timely diagnosis in these infants. To this end, a 16S rDNA polymerase chain reaction (PCR) assay was compared to blood culturing for use as a tool in evaluating early onset sepsis. Of 1,751 neonatal intensive care unit admissions that were screened, 1,233 near-term infants met inclusion criteria. Compared to culture, PCR demonstrated excellent analytical specificity (1,186 of 1,216, 97.5%) and negative predictive value (1,186 of 1,196, 99.2%); however, PCR failed to detect a significant number of culture-proven cases. These findings underscore the cautionary stance that should be taken at this time when considering the use of a molecular amplification test for diagnosing neonatal sepsis. The experience gained from this study illustrates the need for changes in sample collection and preparation techniques so as to improve analytical sensitivity of the assay.

Indexed as

Polymerase Chain ReactionBase SequenceBloodDNA, BacterialHumansInfant, NewbornInfant, Premature, DiseasesMolecular Diagnostic TechniquesMolecular Sequence DataPredictive Value of TestsRNA, Ribosomal, 16SSensitivity and SpecificitySepsisStaphylococcusDNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID16825509
PMCPMC1867603
OpenAlexW1589917601

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.