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Routine Metagenomics Service for ICU Patients with Respiratory Infection.
Charalampous, Themoula; Alcolea-Medina, Adela; Snell, Luke B; Alder, Christopher; Tan, Mark; Williams, Tom G S; Al-Yaakoubi, Noor; Humayun, Gul; Meadows, Christopher I S; Wyncoll, Duncan L A; Paul, Richard; Hemsley, Carolyn J; Jeyaratnam, Dakshika; Newsholme, William; Goldenberg, Simon; Patel, Amita; Tucker, Fearghal; Nebbia, Gaia; Wilks, Mark; Chand, Meera; Cliff, Penelope R; Batra, Rahul; O'Grady, Justin; Barrett, Nicholas A; Edgeworth, Jonathan D.
Affiliation
  • Charalampous T; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Alcolea-Medina A; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Snell LB; Infection Sciences, Synnovis, London, United Kingdom.
  • Alder C; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Tan M; Department of Infectious Diseases and.
  • Williams TGS; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Al-Yaakoubi N; Department of Infectious Diseases and.
  • Humayun G; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Meadows CIS; Department of Infectious Diseases and.
  • Wyncoll DLA; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Paul R; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Hemsley CJ; Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
  • Jeyaratnam D; Critical Care Directorate, Guy's and St Thomas' NHS Foundation Trust, London, England.
  • Newsholme W; Critical Care Directorate, Guy's and St Thomas' NHS Foundation Trust, London, England.
  • Goldenberg S; Critical Care Directorate, Guy's and St Thomas' NHS Foundation Trust, London, England.
  • Patel A; Department of Infectious Diseases and.
  • Tucker F; Department of Infectious Diseases and.
  • Nebbia G; Department of Infectious Diseases and.
  • Wilks M; Department of Infectious Diseases and.
  • Chand M; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, School of Immunology and Microbial Sciences and.
  • Cliff PR; Department of Infectious Diseases and.
  • Batra R; Infection Sciences, Synnovis, London, United Kingdom.
  • O'Grady J; Department of Infectious Diseases and.
  • Barrett NA; London School of Medicine and Dentistry, Queen Mary University, London, United Kingdom.
  • Edgeworth JD; UK Health Security Agency, London, United Kingdom; and.
Am J Respir Crit Care Med ; 209(2): 164-174, 2024 Jan 15.
Article in En | MEDLINE | ID: mdl-37938162
Rationale: Respiratory metagenomics (RMg) needs evaluation in a pilot service setting to determine utility and inform implementation into routine clinical practice. Objectives: Feasibility, performance, and clinical impacts on antimicrobial prescribing and infection control were recorded during a pilot RMg service. Methods: RMg was performed on 128 samples from 87 patients with suspected lower respiratory tract infection (LRTI) on two general and one specialist respiratory ICUs at Guy's and St Thomas' NHS Foundation Trust, London. Measurements and Main Results: During the first 15 weeks, RMg provided same-day results for 110 samples (86%), with a median turnaround time of 6.7 hours (interquartile range = 6.1-7.5 h). RMg was 93% sensitive and 81% specific for clinically relevant pathogens compared with routine testing. Forty-eight percent of RMg results informed antimicrobial prescribing changes (22% escalation; 26% deescalation) with escalation based on speciation in 20 out of 24 cases and detection of acquired-resistance genes in 4 out of 24 cases. Fastidious or unexpected organisms were reported in 21 samples, including anaerobes (n = 12), Mycobacterium tuberculosis, Tropheryma whipplei, cytomegalovirus, and Legionella pneumophila ST1326, which was subsequently isolated from the bedside water outlet. Application to consecutive severe community-acquired LRTI cases identified Staphylococcus aureus (two with SCCmec and three with luk F/S virulence determinants), Streptococcus pyogenes (emm1-M1uk clone), S. dysgalactiae subspecies equisimilis (STG62647A), and Aspergillus fumigatus with multiple treatments and public health impacts. Conclusions: This pilot study illustrates the potential of RMg testing to provide benefits for antimicrobial treatment, infection control, and public health when provided in a real-world critical care setting. Multicenter studies are now required to inform future translation into routine service.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Respiratory Tract Infections / Anti-Infective Agents Limits: Humans Country/Region as subject: Europa Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Respiratory Tract Infections / Anti-Infective Agents Limits: Humans Country/Region as subject: Europa Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2024 Type: Article