Evidence map›Paper›PMID 42649138›Full record

ArticleNature communications2026

Novel surveillance design exploiting network analysis for efficient, rapid detection of emerging Clostridioides difficile strains.

Diane Pople, Tjibbe Donker, Olisaeloka Nsonwu, Dakshika Jeyaratnam, Dimple Chudasama, Russell Hope, Susan Hopkins, Mark H Wilcox, David W Eyre, A Sarah Walker and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Diane PopleUnited Kingdom Health Security Agency, London, UK. diane.pople@ukhsa.gov.uk.ORCID http://orcid.org/0000-0002-5031-0109
Tjibbe DonkerMedical Center-University of Freiburg, Institute for Infection Prevention and Control, Freiburg, Germany.
Olisaeloka NsonwuUnited Kingdom Health Security Agency, London, UK.
Dakshika JeyaratnamUnited Kingdom Health Security Agency, London, UK.
Dimple ChudasamaUnited Kingdom Health Security Agency, London, UK.
Russell HopeUnited Kingdom Health Security Agency, London, UK.
Susan HopkinsUnited Kingdom Health Security Agency, London, UK.
Mark H WilcoxLeeds Institute of Medical Research, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-4565-2868
David W EyreNIHR Health Protection Research Unit in Antimicrobial Resistance and Healthcare Associated Infections, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-5095-6367
A Sarah WalkerNIHR Health Protection Research Unit in Antimicrobial Resistance and Healthcare Associated Infections, University of Oxford, Oxford, UK.
Julie V RobothamUnited Kingdom Health Security Agency, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole genome sequencing is being introduced in England to support national surveillance of key hospital-acquired pathogens, starting with Clostridioides difficile, to facilitate novel strain identification and enable timely interventions. However sequencing capacity is limited. Symptomatic and asymptomatic patients attending multiple hospitals can act as inter-facility transmission vectors; here we therefore identify the empirical network of shared patients from analysing national admission data and simulate spread of a hypothetical novel strain. Algorithmically optimising detection, incorporating logistical constraints, we identify sentinel sites which detect a novel strain 27% faster than random sentinel selection, whilst sequencing <15% cases. Sensitivity and scenario analyses using a range of plausible pathogen characteristics and historical networks confirm epidemiologically- and longitudinally-robust sentinel selection and performance. The new surveillance system, established from our findings, benefits from stress-tested sentinel set selection to deliver rapid, efficient identification of novel strains within real world constraints, to inform control interventions, and provides a roadmap for future hospital-acquired pathogen surveillance.

Indexed as

Clostridioides difficileClostridium InfectionsCross InfectionAlgorithmsEnglandGenome, BacterialHumansWhole Genome Sequencing

Identifiers

PMID42649138
PMCPMC13518965

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.