Abstract

16S ribosomal-ribonucleic acid polymerase chain reaction (PCR) and targeted PCR aid microbiological diagnosis in culture-negative clinical samples. Despite routine clinical use, there remains a paucity of data on their effectiveness across a variety of clinical sample types, and cost-effectiveness. In this 4 year multicentre retrospective observational study, all clinical samples referred for 16S PCR and/or targeted PCR from a laboratory network serving seven London hospitals were identified. Laboratory, clinical, prescribing, and economic variables were analysed. 78/607 samples were 16S PCR positive; pus samples were most frequently positive (29/84; p < 0.0001), and CSF least (8/149; p = 0.003). 210/607 samples had targeted PCR (361 targets requested across 23 organisms) with 43/361 positive; respiratory samples (13/37; p = 0.01) had the highest detection rate. Molecular diagnostics provided a supportive microbiological diagnosis for 21 patients and a new diagnosis for 58. 14/91 patients with prescribing information available and a positive PCR result had antimicrobial de-escalation. For culture-negative samples, mean cost-per-positive 16S PCR result was £568.37 and £292.84 for targeted PCR, equating to £4041.76 and £1506.03 respectively for one prescription change. 16S PCR is more expensive than targeted PCR, with both assisting in microbiological diagnosis but uncommonly enabling antimicrobial change. Rigorous referral pathways for molecular tests may result in significant fiscal savings.

Highlights

  • Molecular diagnostics have significantly enhanced laboratory ability to detect and identify bacteria in clinical samples[1,2] Whilst bacterial culture is considered the gold standard for microbiological diagnosis, there may be a 24–48 hour delay in providing a result for typical organisms and longer for slow-growing organisms such as Mycobacteria spp[3]

  • We conducted a retrospective observational study to identify all samples referred for 16S Polymerase Chain Reaction (PCR) and subsequently targeted PCR from a large centralised NHS (National Health Service) clinical laboratory serving seven hospitals and analysed the frequency of positive results based on sample type, the appropriateness of testing, clinical utility in providing diagnoses and enablement of antimicrobial de-escalation, and the cost-per-positive result

  • Among those samples sent for 16S PCR, 210 had targeted PCR requested with clinicians looking for 367 bacterial targets corresponding to 23 different species

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Summary

Introduction

Molecular diagnostics have significantly enhanced laboratory ability to detect and identify bacteria in clinical samples[1,2] Whilst bacterial culture is considered the gold standard for microbiological diagnosis, there may be a 24–48 hour delay in providing a result for typical organisms and longer for slow-growing organisms such as Mycobacteria spp[3]. We conducted a retrospective observational study to identify all samples referred for 16S PCR and subsequently targeted PCR from a large centralised NHS (National Health Service) clinical laboratory serving seven hospitals and analysed the frequency of positive results based on sample type, the appropriateness of testing, clinical utility in providing diagnoses and enablement of antimicrobial de-escalation, and the cost-per-positive result

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