Persistence of detectable pathogens by culture independent systems (T2 Magnetic Resonance) in patients with bloodstream infection: prognostic role and possible clinical implications.

Blood culture Bloodstream Infection Rapid Diagnostic Tests

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
27 Oct 2023
Historique:
received: 03 08 2023
revised: 13 10 2023
accepted: 25 10 2023
medline: 27 10 2023
pubmed: 27 10 2023
entrez: 27 10 2023
Statut: aheadofprint

Résumé

Persistent S. aureus bacteraemia is associated with metastatic infection and adverse outcomes while Gram-negative bacteraemia is normally transient and shorter course therapy is increasingly advocated for affected patients. Whether the prolonged detection of pathogen DNA in blood by culture-independent systems could have prognostic value and guide management decisions is unknown. We performed a multicentre prospective observational study on 102 patients with bloodstream infection, to compare time to bloodstream clearance according to T2 magnetic resonance and blood cultures over a 4-day follow-up. We also explored the association between duration of detectable pathogens according to T2 Magnetic resonance (Magnetic Resonance-DNAemia, MR-DNAemia) and clinical outcomes. Time to bloodstream clearance according to T2 Magnetic Resonance was significantly longer compared to blood culture clearance (HR 0.54, 95%CI 0.39-0.75) and did not differ according to the causative pathogen (p=0.5). Each additional day of MR-DNAemia increased the odds of persistent infection (defined as metastatic infection or delayed source control) both in the overall population (OR 1.98, 95%CI 1.45-2.70) and in S. aureus (OR 1.92, 95%CI 1.12-3.29) and Gram-negative bacteraemia (OR 2.21, 95%CI 1.35-3.60). MR-DNAemia duration was also associated with no improvement in Sequential Organ Failure Assessment score at day 7 from infection onset (OR 1.76, 95%CI 1.21-2.56). T2 Magnetic Resonance may help to diagnose bloodstream infection in patients on antimicrobials with negative blood cultures as well as to identify patients with metastatic infection, source control failure or adverse short-term outcome. Future studies may inform its usefulness within the setting of antimicrobial stewardship programs.

Identifiants

pubmed: 37890109
pii: 7331279
doi: 10.1093/cid/ciad663
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Auteurs

Anna Maria Peri (AM)

The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, 4029, Australia.

Kevin O'Callaghan (K)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Nastaran Rafiei (N)

Infectious Diseases Unit, Caboolture Hospital, Caboolture, QLD 4510, Queensland, Australia.

Bianca Graves (B)

Herston Infectious Diseases Institute, Herston, Brisbane, QLD 4029, Australia.

Holly Sinclair (H)

Infectious Diseases Unit Royal Brisbane and Women's Hospital, Brisbane, QLD, 4029, Australia.

Anna Brischetto (A)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Karen Lim (K)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Jill Parkes-Smith (J)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Matthew Eustace (M)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Natalie Davidson (N)

Infectious Diseases Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Alexis Tabah (A)

Intensive Care Unit, Redcliffe Hospital, Redcliffe, QLD 4020, Australia.

Adam Stewart (A)

Central Microbiology, Pathology Queensland, Royal Brisbane and Women's Hospital, Brisbane QLD, 4029, Australia.

Mark D Chatfield (MD)

The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, 4029, Australia.

Patrick Na Harris (PN)

The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, 4029, Australia.
Herston Infectious Diseases Institute, Herston, Brisbane, QLD 4029, Australia.
Central Microbiology, Pathology Queensland, Royal Brisbane and Women's Hospital, Brisbane QLD, 4029, Australia.

David L Paterson (DL)

The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, 4029, Australia.
Infectious Diseases Unit Royal Brisbane and Women's Hospital, Brisbane, QLD, 4029, Australia.
ADVANCE-ID, Saw Swee Hock School of Public Health, National University of Singapore, Singapore.
Infectious Diseases Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Classifications MeSH