neoAMRO: Neonatal Antimicrobial Resistance and Outcome

Sponsor
St George's, University of London (Other)
Overall Status
Recruiting
CT.gov ID
NCT05743816
Collaborator
Antibiotic Research UK (Other)
800
1
55
14.5

Study Details

Study Description

Brief Summary

This is a multicentre observational study involving NNUs across the UK. Study personnel (Neonatologists and research Nurses) from these NNUs will identify eligible babies in whom a positive culture has been obtained.

This study will help identify the infections leading to death in babies on UK neonatal units, define the clinical characteristics of babies dying from infections, and describe the management of babies dying from infections with a specific focus in their antimicrobial treatment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The neonIN surveillance network captures data on episodes of invasive neonatal infection on a web-based database. Over 30 UK neonatal units currently contribute to this database in real-time. An episode of neonatal infection is defined as a positive culture collected from a normally sterile site such as the blood, cerebrospinal fluid (CSF) or urine (via catheter or suprapubic aspirate) for which clinicians prescribed at least five days of appropriate antibiotics. Clinical, demographic and microbiological data (including antimicrobial susceptibilities) are collected using a standardised online questionnaire. Denominator data regarding the total number of live-births and neonatal-admissions are collected for each neonatal unit.

    Through our study we aim to understand and describe better those infections and risk factors that lead to death. The case-control study will enable us to determine if gaps in optimal management, such as the wrong antibiotic or the wrong dose, are associated with poor outcomes. We can then translate such information into practice and develop / improve clinical guidance in order to improve outcomes.

    For the purpose of this study, we will request information on the baby's status (alive/died/not known) at 28 days after the positive culture was obtained. If the baby is alive, then this baby becomes eligible as a control. If the baby has died, then further details will be sought including the date of death and whether death was attributed to the infection.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    800 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Neonatal Antimicrobial Resistance and Outcome (neoAMRO)
    Actual Study Start Date :
    Jul 30, 2019
    Anticipated Primary Completion Date :
    Sep 30, 2023
    Anticipated Study Completion Date :
    Feb 29, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Identifying infections [5 years]

      To identify the infections leading to death in babies on UK neonatal units

    2. Clinical characteristics [5 years]

      To define the clinical characteristics of babies dying from infections

    3. Management of infections [5 years]

      To describe the management of babies dying from infections with a specific focus in their antimicrobial treatment and the antimicrobial resistance profiles of the relevant organisms

    Secondary Outcome Measures

    1. Comparing bacterial infections [5 years]

      In a case-control study we will assess the hypothesis that babies who die from bacterial infections on neonatal units do so because they receive inappropriate antibiotic management. To do this we will compare babies who die from bacterial infections with babies who survive bacterial infections on a range of factors including appropriateness, dose and timeliness of antibiotic use.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    28 Days to 12 Months
    Sexes Eligible for Study:
    All
    Inclusion criteria:

    • Infants on participating NNUs who have an episode of infection with a positive culture.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 St George's University of London London United Kingdom SW17 0RE

    Sponsors and Collaborators

    • St George's, University of London
    • Antibiotic Research UK

    Investigators

    • Principal Investigator: Eva Galiza, MD, St George's, University of London

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    St George's, University of London
    ClinicalTrials.gov Identifier:
    NCT05743816
    Other Study ID Numbers:
    • 2019.0048
    First Posted:
    Feb 24, 2023
    Last Update Posted:
    Mar 1, 2023
    Last Verified:
    Feb 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by St George's, University of London
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 1, 2023