Comprehensive Molecular Testing for Respiratory Pathogens in Community-Acquired Pneumonia

Naomi J Gadsby, Clark D Russell, Martin P McHugh, Harriet Mark, Andrew Conway Morris, Ian F Laurenson, Adam T Hill, Kate E Templeton

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

BACKGROUND: The frequent lack of a microbiological diagnosis in community-acquired pneumonia (CAP) impairs pathogen-directed antimicrobial therapy. This study assessed the use of comprehensive multibacterial, multiviral molecular testing, including quantification, in adults hospitalized with CAP.

METHODS: Clinical and laboratory data were collected for 323 adults with radiologically-confirmed CAP admitted to 2 UK tertiary care hospitals. Sputum (96%) or endotracheal aspirate (4%) specimens were cultured as per routine practice and also tested with fast multiplex real-time polymerase-chain reaction (PCR) assays for 26 respiratory bacteria and viruses. Bacterial loads were also calculated for 8 bacterial pathogens. Appropriate pathogen-directed therapy was retrospectively assessed using national guidelines adapted for local antimicrobial susceptibility patterns.

RESULTS: Comprehensive molecular testing of single lower respiratory tract (LRT) specimens achieved pathogen detection in 87% of CAP patients compared with 39% with culture-based methods. Haemophilus influenzae and Streptococcus pneumoniae were the main agents detected, along with a wide variety of typical and atypical pathogens. Viruses were present in 30% of cases; 82% of these were codetections with bacteria. Most (85%) patients had received antimicrobials in the 72 hours before admission. Of these, 78% had a bacterial pathogen detected by PCR but only 32% were culture-positive (P < .0001). Molecular testing had the potential to enable de-escalation in number and/or spectrum of antimicrobials in 77% of patients.

CONCLUSIONS: Comprehensive molecular testing significantly improves pathogen detection in CAP, particularly in antimicrobial-exposed patients, and requires only a single LRT specimen. It also has the potential to enable early de-escalation from broad-spectrum empirical antimicrobials to pathogen-directed therapy.

Original languageEnglish
Pages (from-to)817-823
Number of pages7
JournalClinical Infectious Diseases
Volume62
Issue number7
DOIs
Publication statusPublished - 1 Apr 2016

Keywords / Materials (for Non-textual outputs)

  • Aged
  • Anti-Bacterial Agents
  • Bacterial Load
  • Community-Acquired Infections
  • Female
  • Haemophilus influenzae
  • Humans
  • Male
  • Microbial Sensitivity Tests
  • Middle Aged
  • Molecular Diagnostic Techniques
  • Pneumonia, Bacterial
  • Pneumonia, Viral
  • Polymerase Chain Reaction
  • Retrospective Studies
  • Streptococcus pneumoniae
  • Viral Load
  • Journal Article
  • Research Support, Non-U.S. Gov't

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