Evidence map›Paper›PMID 34731020›Full record

ArticleJournal of clinical microbiology2022

Multicenter Comparison of Nucleic Acid Amplification Tests for the Diagnosis of Rectal and Oropharyngeal Chlamydia trachomatis and Neisseria gonorrhoeae Infections.

Barbara Van Der Pol, Max Chernesky, Charlotte A Gaydos, Edward W Hook, Ajith M Joseph, Katherine Christensen, Rodney Arcenas, Alexander Boutwell, Harold C Wiesenfeld, Stephanie N Taylor and 6 more

Open access · hybridAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Journal of clinical microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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

16 authors at 11 institutions in 2 countries.

Barbara Van Der PolUniversity of Alabama School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0003-3064-8564
Max CherneskyMcMaster University, St Joseph's Healthcare, Hamilton, Ontario, Canada.
Charlotte A GaydosJohns Hopkins School of Medicine, Baltimore, Maryland, USA.
Edward W HookUniversity of Alabama School of Medicine, Birmingham, Alabama, USA.
Ajith M JosephAbbott, Medical Affairs, Lake Forest, Illinois, USA.
Katherine ChristensenBecton, Dickinson and Company, BD Life Sciences - Integrated Diagnostic Sciences Solutions, Sparks, Maryland, USA.
Rodney ArcenasRoche Diagnostic Systems, Pleasanton, California, USA.
Alexander BoutwellUniversity of Alabama School of Medicine, Birmingham, Alabama, USA.
Harold C WiesenfeldUniversity of Pittsburgh School of Medicine and Magee-Womens Research Institute, Pittsburgh, Pennsylvania, USA.
Stephanie N TaylorLouisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
Kenneth H MayerFenway Health, Boston Massachusetts, USA.
Matthew R GoldenUniversity of Washingtongrid.34477.33, Seattle, Washington, USA.
Jeanne MoncadaUniversity of California-San Francisco, San Francisco, California, USA.
Dan JangMcMaster University, St Joseph's Healthcare, Hamilton, Ontario, Canada.
Julius SchachterUniversity of California-San Francisco, San Francisco, California, USA.
ExGen Study Group Kristal Aaron University of Alabama at Birmingham, Paula Dixon University of Alabama at Birmingham, Karen Eckert Becton, Dickinson and Company, BD Life Sciences – Integrated Diagnostic Solutions, Shiaolan Y. Ho Abbott, Medical Affairs, Michael Lewinski Roche Diagnostic Solutions, Kevin Luk Roche Diagnostic Solutions, Carl McGill Abbott, Medical Affairs, Shiv Parmar Becton, Dickinson and Company, BD Life Sciences – Integrated Diagnostic Solutions, James Price Becton, Dickinson and Company, BD Life Sciences – Integrated Diagnostic Solutions, Charles Rivers University of Alabama at Birmingham
University of Alabama at Birmingham · USSt. Joseph’s Healthcare Hamilton · CAUniversity of California, San Francisco · USAbbott Fund · USBecton Dickinson (United States) · USFenway Health · USJohns Hopkins University · USLouisiana State University Health Sciences Center New Orleans · USRoche (United States) · USUniversity of Pittsburgh · USUniversity of Washington · US

Funding

LC: HIV Prevention Trials Network - Laboratory Support for the SARS-CoV-2 Seroprevalence Study (CoVPN 5002)UM1AI068613 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SUSAN H ESHLEMAN, Mark A Marzinke · 2011 to 2026
$100.2M
NIAID NIH HHS UM1 AI068613
6 · The paper itself

Abstract

Research using nucleic acid amplification tests (NAATs) have repeatedly found rectal and oropharyngeal infections with Chlamydia trachomatis and Neisseria gonorrhoeae to be common and potentially more difficult to treat than genital infections. Unfortunately, public health and patient care efforts have been hampered by the lack of FDA-cleared NAATs with claims for anorectal or oropharyngeal samples. At the time of the initiation of this study, no commercially available assays had these claims. We formed a novel partnership among academic institutions and diagnostic manufacturers to address this public health need. From May 2018 through August 2019, we recruited 1108 women, 1256 men, and 26 transgender persons each of whom provided 3 anal and 3 oropharyngeal swab specimens. The 3 anal swabs were pooled into a single transport tube as were the 3 oropharyngeal swabs. The performance of each of three study assays was estimated by comparison to the composite result and relative to one another. Percent positivity for chlamydia was 5.9 and 1.2% from anal and oropharyngeal specimens, respectively, compared to 4.2 and 4.1% for gonorrhea. Sensitivity for chlamydia detection ranged from 81.0 to 95.1% and 82.8 to 100% for anal and oropharyngeal specimens, respectively. Gonorrhea sensitivity ranged from 85.9 to 99.0% and 74.0 to 100% for anal and oropharyngeal samples, respectively. Specificity estimates were ≥ 98.9% for all assays, organisms, and sample types. Although there was heterogeneity between sensitivity estimates, these assays offer better ability to detect extragenital infections than culture and potential solutions for providing appropriate sexual health care for populations in which these infections are of concern.

Indexed as

Chlamydia InfectionsGonorrheaChlamydia trachomatisFemaleHumansMaleNeisseria gonorrhoeaeNucleic Acid Amplification TechniquesSensitivity and SpecificityChlamydia trachomatisextragenitalextragenital STImolecular diagnosticsmolecular methodsNeisseria gonorrhoeaeoropharyngeal infectionrectal infectionsexually transmitted infections

Identifiers

PMID34731020
PMCPMC8769746
OpenAlexW3210700444

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.