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Tackling Resistance And HealthCare Economics Through CPE Screening (TRACE-CPE)

2026年6月16日 更新者:Imperial College London

Multi-centre Evaluation of Carbapenemase-producing Enterobacterales (CPE) Prevalence and Transmission Dynamics, Recommendations on Screening Strategies, and Health Economics Outcomes Research Impact to Inform Policy Change

The goal of this clinical study is to learn if it is possible to reduce the spread of resistant bacteria called CPEs (Carbapenemase producing Enterobacterales) between patients admitted to hospital.

CPEs can be carried in the gut of people without making them ill. Normally when patients come into hospital, they may undergo a swab test on their bottom to see if CPEs can be grown. This test can take up to 24 hours to produce a result.

The investigators want to use a faster test which takes 2 hours to produce a result, and whether this can make a difference to CPE spread between person to person.

The main questions it aims to answer are:

  1. Why do people carry, transmit or get infected with CPE?
  2. If a faster test was used to look for CPE, would this be better at reducing patient spread in hospital?
  3. Is a faster test also more cost effective?

Participants will:

  1. Be tested by both the usual and faster test when they come into hospital by a swab on their bottom
  2. Where they test positive for CPE they will be asked to answer some questions about their health

調査の概要

詳細な説明

Carbapenemase-producing Enterobacterales (CPE) are a significant threat to healthcare through their ability to cause drug-resistant infections. These group of bacteria posses enzymes which break down and inactivate carbapenems, a broad spectrum class of antibiotics reserved for severe infections. Transmission of CPEs between patients occur through proximity / contact within their environment in hospital - and is therefore preventable.

Within the individual, initial colonisation with CPE is an important risk factor for development of multi-drug resistant infections which are associated with significant mortality and high hospital costs. The in-hospital transmission of CPE exerts a complex burden across almost all healthcare domains - for example, CPE infection or colonisation renders common surgical antibiotic prophylaxis ineffective, increases morbidity and mortality in vulnerable patient groups such as intensive care, places burdens on the use of single occupancy beds and imposes considerable cost and disruption to care pathways through outbreaks.

Existing microbiological diagnoses of CPEs vary, but commonly involve bacterial culture of a sample such as a rectal swab in laboratory settings followed by phenotypic testing and characterisation of common antibiotic resistant genes (ARGs) through molecular or immunochromatographic approaches, mostly focusing on the "big 5" mechanisms of CPE. Such testing pathways can however be time-consuming, with the median result turnaround time to be between 24-48 hours. Rapid molecular testing for CPE bypasses the bacterial culture step and may allow for robust IPC measures to be implemented in a near real-time fashion including rapid risk stratification of CPE carriage status. Where transmission is suspected, contact tracing using rapid testing early in the transmission cascade could reduce unwanted impact and be cost-effective.

The proposed study examines the utility, cost-benefit in adoption of a rapid based screening approach using rapid CPE testing coupled with an enhanced reporting workflow operating 24 hours a day, compared with existing standard practice. Given the complex interactions of AMR and CPE acquisition and transmission within hospital settings, a comprehensive approach including clinical, epidemiological and health economic costings will be utilised and modelled in order to accurately understand impact. Rapid CPE screening will be incorporated into clinical processes to minimise adverse impact and the research conducted as a pragmatic study.

The rapid test for use in this study is the Cepheid Xpert Carba-R which can detect genes in 5 most prevalent Carbapenemase gene families (including KPC, NDM, VIM, IMP and OXA classes) directly from a rectal swab sample in 50 minutes - this technology is CE-mark approved as an in vitro diagnostic and has undergone NICE technological appraisal

Research hypotheses to be addressed through the study:

  1. The implementation of rapid molecular CPE detection through the Cepheid Xpert Carba-R with an enhanced reporting workflow is associated with greater effectiveness and timeliness in IPC interventions, compared with the existing use of culture-based screening strategies alone. This will lead to reductions in in-hospital transmission of CPE and result in downstream effects for organisation and individuals.
  2. In-hospital screening strategies through rapid molecular CPE testing can be cost-effective from a health economic perspective and acceptable to patient and stakeholders, given particular clinical settings and baseline local CPE prevalence.

This is a multi-centre mixed methods research study consisting of:

  1. A pragmatic prospective interventional interrupted time series study to examine impact of rapid Carbapenemase producing Enterobacterales (CPE) diagnostics and an enhanced reporting workflow in parallel with screening on clinical practice and transmission.
  2. A clinical observational cohort study to characterise individual risk factors for CPE colonisation, epidemiology of colonisation including point-prevalence, and subsequent in-hospital transmission dynamics.
  3. A health economic modelling study utilising hospital and national data to estimate medical costs, patient experience and systems level impact of screening, CPE colonisation and acquisition

The study will take place across two hospital Trusts:

i) Imperial College Healthcare NHS Trust (ICNHT), London ii) Guy's and St Thomas NHS Foundation Trust (GSTT), London

Project 1 will implement the Cepheid Xpert Carba-R rapid test in parallel to routine culture for CPE screening at two hospital sites to understand impact on IPC practice.

Project 2 will capture transmission dynamics, healthcare cost, patient acceptability and quality of life metrics using national datasets, and de-identified healthcare data collected from Project 1. Modelling using health economics outcome research methods will be performed to evaluate CPE screening strategies for a range of scenarios and settings with a view of informing policy. Health economic costings will utilise routinely available clinical data as well as costings metrics and health related grouping code from NHS Hospital Episode Statistics.

研究の種類

介入

入学 (推定)

16000

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Research Governance and Integrity
  • 電話番号:020 7594 9832
  • メール:RGIT@imperial.ac.uk

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • All adult (18 years or older) medical patients admitted to the acute medical unit during the implementation period who undergo routine rectal CPE testing as per local Trust policy and test positive for CPE colonisation through either the rapid test or culture-based methods.

Exclusion Criteria:

  • Patient refusal for rectal screening or
  • Clinical contraindication to rectal swab collection

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:診断
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Rapid molecular screening
During the study period all eligible patients will undergo the intervention
Participants will undergo a rectal swab and undergo rapid molecular testing for CPE colonisation

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
In-hospital secondary transmission of CPE colonisation
時間枠:From enrolment to the end of the follow up period at 12 months
The primary outcome measure is the change in secondary in-hospital CPE transmission risk with the introduction of rapid rectal CPE screening. Quantification of transmission risk will be done using transmission dynamics modelling informed by collected clinical and epidemiological data.
From enrolment to the end of the follow up period at 12 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Health economic outcomes of CPE colonisation, infection and screening approaches
時間枠:From enrolment to the end of the follow up period at 12 months
Direct, indirect and opportunity costs associated with CPE colonisation and infection using health economic cost analysis
From enrolment to the end of the follow up period at 12 months
Laboratory measures of diagnostic comparison
時間枠:From enrolment to the end of the follow up period at 12 months
Concordance metrics between CPE rapid testing and culture including rate, genotype and species.
From enrolment to the end of the follow up period at 12 months
Epidemiological measures of CPE colonisation
時間枠:From enrolment to the end of the follow up period at 12 months
Patient level risk factors for CPE acquisition, colonisation, and transmission.
From enrolment to the end of the follow up period at 12 months
Qualitative measures including public, stakeholder understanding and acceptability
時間枠:24 months
Perspectives on CPE diagnostic implementation, patient and provider acceptability of CPE screening through stakeholder interviews, public engagement and workshops.
24 months
Qualitative study on CPE perspectives through stakeholder interviews, public engagement and focused workshops
時間枠:24 months
This will be an adjunctive study with separate approvals process involving interviews with stakeholders to understand views and approaches to the management of CPE and detection. These findings will feed back into the main TRACE-CPE project.
24 months
Point prevalence of CPE
時間枠:Over the point prevalence period of 1 week
Prevalence of CPE colonisation derived from the number of positive CPE cases divided by the number of individuals undergoing screening.
Over the point prevalence period of 1 week

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Jon Otter、Guy's and St Thomas NHS Trust

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2027年11月1日

研究の完了 (推定)

2028年3月31日

試験登録日

最初に提出

2026年6月9日

QC基準を満たした最初の提出物

2026年6月16日

最初の投稿 (実際)

2026年6月23日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月23日

QC基準を満たした最後の更新が送信されました

2026年6月16日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual patient data is recorded under the General Data Protection Regulation framework and will not be shared outside the research and clinical teams. Aggregated data will be presented and can be shared under such approvals.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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