Literature DB >> 35400176

Utility of Broad-Range PCR Sequencing for Infectious Diseases Clinical Decision Making: a Pediatric Center Experience.

Caitlin Naureckas Li1,2,3, Mari M Nakamura1,2,4.   

Abstract

Broad-range PCR (BRPCR) sequencing is a promising tool for diagnosis of infectious conditions when traditional microbiologic strategies fail to identify a pathogen. Data on the optimal clinical scenarios in which to use this tool are limited. We assessed, via retrospective chart review, the rate of organism identification and impact on clinical management from BRPCR testing sent from our quaternary care children's hospital between February 2010 and June 2020. A total of 382 samples were sent from 269 individual patients. A total of 200 (74.3%) patients were immunocompromised. Median age at time of sample collection was 10.0 years (interquartile range, 4.2 to 15.8). A total of 254/377 (64.7%) samples were from patients known to be on ≥1 antimicrobial in the 24 h prior to sample collection. A total of 112/382 (29.3%) samples were from patients ultimately diagnosed with a bacterial or fungal infection by another testing modality. The most common sample types were bronchoalveolar lavage (BAL) fluid (45), lung tissue (41), and bone (39). An organism was identified from 83 (21.7%) samples, but results from only 19 (5.0%) samples led to a change in management. Organisms were identified from 18 (40%) BAL samples; only 2 (4.4%) were judged to be clinically significant. A total of 4/12 (33.3%) samples from cardiac hardware changed clinical management. We found that only 5% of BRPCR results influenced antimicrobial management in a diverse pediatric cohort. Our findings suggest that the impact on clinical management varied widely by sample type. Additional work is necessary to characterize the ideal clinical scenarios in which BRPCR should be used.

Entities:  

Keywords:  bacteria; broad-range PCR; diagnosis; diagnostic stewardship; diagnostics; fungus

Mesh:

Substances:

Year:  2022        PMID: 35400176      PMCID: PMC9116169          DOI: 10.1128/jcm.02437-21

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   11.677


  26 in total

Review 1.  Infective Endocarditis in Childhood: 2015 Update: A Scientific Statement From the American Heart Association.

Authors:  Robert S Baltimore; Michael Gewitz; Larry M Baddour; Lee B Beerman; Mary Anne Jackson; Peter B Lockhart; Elfriede Pahl; Gordon E Schutze; Stanford T Shulman; Rodney Willoughby
Journal:  Circulation       Date:  2015-09-15       Impact factor: 29.690

2.  Broad-range polymerase chain reaction for the diagnosis of Bartonella henselae endocarditis.

Authors:  Tony Walls; Karyn Moshal; John Trounce; John Hartley; Kathryn Harris; Graham Davies
Journal:  J Paediatr Child Health       Date:  2006 Jul-Aug       Impact factor: 1.954

3.  Complementarity between targeted real-time specific PCR and conventional broad-range 16S rDNA PCR in the syndrome-driven diagnosis of infectious diseases.

Authors:  A-S Morel; G Dubourg; E Prudent; S Edouard; F Gouriet; J-P Casalta; F Fenollar; P E Fournier; M Drancourt; D Raoult
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-10-28       Impact factor: 3.267

4.  Molecular diagnosis of bacterial endocarditis by broad-range PCR amplification and direct sequencing.

Authors:  D Goldenberger; A Künzli; P Vogt; R Zbinden; M Altwegg
Journal:  J Clin Microbiol       Date:  1997-11       Impact factor: 5.948

5.  Etiologic diagnosis of infective endocarditis by broad-range polymerase chain reaction: a 3-year experience.

Authors:  Philipp Peter Bosshard; Andreas Kronenberg; Reinhard Zbinden; Christian Ruef; Erik Christian Böttger; Martin Altwegg
Journal:  Clin Infect Dis       Date:  2003-07-09       Impact factor: 9.079

6.  Broad-range PCR and sequencing in routine diagnosis of infective endocarditis.

Authors:  Marianne Voldstedlund; Lisbeth Nørum Pedersen; Ulrik Baandrup; Kaj Erik Klaaborg; Kurt Fuursted
Journal:  APMIS       Date:  2008-03       Impact factor: 3.205

7.  Clinical Impact of Metagenomic Next-Generation Sequencing of Plasma Cell-Free DNA for the Diagnosis of Infectious Diseases: A Multicenter Retrospective Cohort Study.

Authors:  Catherine A Hogan; Shangxin Yang; Omai B Garner; Daniel A Green; Carlos A Gomez; Jennifer Dien Bard; Benjamin A Pinsky; Niaz Banaei
Journal:  Clin Infect Dis       Date:  2021-01-27       Impact factor: 9.079

8.  Assessment of the Clinical Utility of Plasma Metagenomic Next-Generation Sequencing in a Pediatric Hospital Population.

Authors:  Rose A Lee; Fatima Al Dhaheri; Nira R Pollock; Tanvi S Sharma
Journal:  J Clin Microbiol       Date:  2020-06-24       Impact factor: 5.948

Review 9.  Microbial Identification Using DNA Target Amplification and Sequencing: Clinical Utility and Impact on Patient Management.

Authors:  Tinzar Basein; Bradley J Gardiner; Gabriela M Andujar Vazquez; Andrew S Joel Chandranesan; Arthur R Rabson; Shira Doron; David R Snydman
Journal:  Open Forum Infect Dis       Date:  2018-10-10       Impact factor: 3.835

10.  Case Report: Comparison of Plasma Metagenomics to Bacterial PCR in a Case of Prosthetic Valve Endocarditis.

Authors:  Joshua A Lieberman; Caitlin Naureckas Li; Gabriella S Lamb; David A Kane; Mary K Stewart; Ruslan A Mamedov; Brad T Cookson; Stephen J Salipante
Journal:  Front Pediatr       Date:  2021-01-07       Impact factor: 3.418

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.