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Development and implementation of a customised rapid syndromic diagnostic test for severe pneumonia [version 3; peer review: 2 approved]

Authors :
Thomas P Hellyer
Vilas Navapurkar
Joana Pereira-Dias
Ellen Higginson
Petra Polgarova
Emma Heasman-Hunt
Lissamma Titti
Joanne Brown
Jonathan Scott
William PW Smith
David Sapsford
Anthony Rostron
Ronan McMullan
M. Estée Török
Vanessa Wong
David A Enoch
Martin D Curran
A John Simpson
Sally Forrest
Nicholas M Brown
Josefin Bartholdson Scott
Andrew Conway Morris
Jurgen Herre
Mailis Maes
Matthew Routledge
Surendra Parmar
Gordon Dougan
Source :
Wellcome Open Research, Vol 6 (2022)
Publication Year :
2022
Publisher :
Wellcome, 2022.

Abstract

Background: The diagnosis of pneumonia has been hampered by a reliance on bacterial cultures which take several days to return a result, and are frequently negative. In critically ill patients this leads to the use of empiric, broad-spectrum antimicrobials and compromises good antimicrobial stewardship. The objective of this study was to establish the performance of a syndromic molecular diagnostic approach, using a custom TaqMan array card (TAC) covering 52 respiratory pathogens, and assess its impact on antimicrobial prescribing. Methods: The TAC was validated against a retrospective multi-centre cohort of broncho-alveolar lavage samples. The TAC was assessed prospectively in patients undergoing investigation for suspected pneumonia, with a comparator cohort formed of patients investigated when the TAC laboratory team were unavailable. Co-primary outcomes were sensitivity compared to conventional microbiology and, for the prospective study, time to result. Metagenomic sequencing was performed to validate findings in prospective samples. Antibiotic free days (AFD) were compared between the study cohort and comparator group. Results: 128 stored samples were tested, with sensitivity of 97% (95% confidence interval (CI) 88-100%). Prospectively, 95 patients were tested by TAC, with 71 forming the comparator group. TAC returned results 51 hours (interquartile range 41-69 hours) faster than culture and with sensitivity of 92% (95% CI 83-98%) compared to conventional microbiology. 94% of organisms identified by sequencing were detected by TAC. There was a significant difference in the distribution of AFDs with more AFDs in the TAC group (p=0.02). TAC group were more likely to experience antimicrobial de-escalation (odds ratio 2.9 (95%1.5-5.5)). Conclusions: Implementation of a syndromic molecular diagnostic approach to pneumonia led to faster results, with high sensitivity and impact on antibiotic prescribing.

Details

Language :
English
ISSN :
2398502X
Volume :
6
Database :
Directory of Open Access Journals
Journal :
Wellcome Open Research
Publication Type :
Academic Journal
Accession number :
edsdoj.f065e84a244242ad92ad8327f4cb7f6e
Document Type :
article
Full Text :
https://doi.org/10.12688/wellcomeopenres.17099.3