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Diagnostic Value of 16S Ribosomal RNA Gene Polymerase Chain Reaction/Sanger Sequencing in Clinical Practice.
Fida, Madiha; Khalil, Sarwat; Abu Saleh, Omar; Challener, Douglas W; Sohail, Muhammad Rizwan; Yang, Joshua N; Pritt, Bobbi S; Schuetz, Audrey N; Patel, Robin.
Afiliação
  • Fida M; Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Khalil S; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Abu Saleh O; Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Challener DW; Division of Infectious Disease and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
  • Sohail MR; Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Yang JN; Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Pritt BS; Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Schuetz AN; Division of Infectious Disease, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
  • Patel R; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Clin Infect Dis ; 73(6): 961-968, 2021 09 15.
Article em En | MEDLINE | ID: mdl-34407178
ABSTRACT

BACKGROUND:

Accurate microbiologic diagnosis is important for appropriate management of infectious diseases. Sequencing-based molecular diagnostics are increasingly used for precision diagnosis of infections. However, their clinical utility is unclear.

METHODS:

We conducted a retrospective analysis of specimens that underwent 16S ribosomal RNA (rRNA) gene polymerase chain reaction (PCR) followed by Sanger sequencing at our institution from April 2017 through March 2019.

RESULTS:

A total of 566 specimens obtained from 460 patients were studied. Patients were considered clinically infected or noninfected based on final diagnosis and management. In 17% of patients, 16S rRNA PCR/sequencing was positive and in 5% of patients, this test led to an impact on clinical care. In comparison, bacterial cultures were positive in 21% of patients. Specimens with a positive Gram stain had 12 times greater odds of having a positive molecular result than those with a negative Gram stain (95% confidence interval for odds ratio, 5.2-31.4). Overall, PCR positivity was higher in cardiovascular specimens (37%) obtained from clinically infected patients, with bacterial cultures being more likely to be positive for musculoskeletal specimens (P < .001). 16S rRNA PCR/sequencing identified a probable pathogen in 10% culture-negative specimens.

CONCLUSION:

16S rRNA PCR/sequencing can play a role in the diagnostic evaluation of patients with culture-negative infections, especially those with cardiovascular infections.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / RNA Ribossômico 16S Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / RNA Ribossômico 16S Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article