Lung Ultrasound Findings in Patients With COVID-19 in a UK ED

Sponsor
Chelsea and Westminster NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT05065827
Collaborator
(none)
43
1
2.4
17.7

Study Details

Study Description

Brief Summary

The investigators aim to carry out a retrospective observational study, analysing lung ultrasound images from patients who have presented to A&E for routine diagnostic purposes (ruling out cardiogenic pulmonary oedema, Pulmonary embolism and pericardial effusions) and systematically assessing for abnormalities typical for COVID-19 infection (Pleural irregularities, B lines, consolidations, pleural effusions). Doing this, the investigators will also develop a suggestion for a standardised technique for lung ultrasound which can be transferred to other clinical settings (Intensive Care, Acute medical Unit) and could form the basis for an international standard. Thirdly, the investigators aim to correlate our findings to clinical severity judged by oxygenation status on arrival in ED. To the investigators' knowledge, this is the first study of this kind.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    COVID-19 is a new disease significant morbidity and mortality which has reached pandemic status. Due to its highly contagious nature, is essential to characterise the disease pathology quickly and reliably. The lung changes that can be seen in patients with COVID-19 can precede clinical symptoms and are picked up on ultrasound more reliably than on conventional chest XR. In addition, ultrasound is devoid of harmful radiation, is quick to perform, and easily learned by doctors who routinely use ultrasound such as in the Emergency Department. To date, there is no data systematically analysing the ultrasound changes in COVID-19 and relating this to disease severity. The data from our study will be contribute significantly to developing strategies for safe triage with regards to cohorting, diagnosis and prognosis of COVID-19.

    In this research study, lung ultrasound scans will be retrospectively analysed that were obtained from patients who presented to the emergency department during March-May 2020 with shortness of breath, who were subsequently diagnosed with COVID-19 either by PCR test or composite diagnostic criteria of lymphopenia and positive Chest XR or CT scan report.

    The lung ultrasound images will be retrospectively scored for the presence of absence of 5 lung abnormalities (pleural irregularity, B lines, small peripheral consolidation, large consolidation, small effusion (<1cm) and large effusion (>1cm). Scoring will be performed by 2 independent observers with experience in lung ultrasound. In addition, each abnormality will be analysed for preferential location within the lung.

    The patients will be grouped into 4 groups of clinical severity (normal oxygenation, mild, moderate and severe deficit in oxygenation) based on the BERLIN criteria for ARDS, and lung abnormalities as seen on lung ultrasound will be analysed for correlation to clinical severity.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    43 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Lung Ultrasound Findings in Patients With COVID-19 in a UK Emergency Department
    Actual Study Start Date :
    Sep 29, 2020
    Actual Primary Completion Date :
    Dec 12, 2020
    Actual Study Completion Date :
    Dec 12, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Normal oxygenation

    Normal oxygenation based on the BERLIN criteria for ARDS

    Mild deficit in oxygenation

    Mild deficit in oxygenation based on the BERLIN criteria for ARDS

    Moderate deficit in oxygenation

    Moderate deficit in oxygenation based on the BERLIN criteria for ARDS

    Severe deficit in oxygenation

    Severe deficit in oxygenation based on the BERLIN criteria for ARDS

    Outcome Measures

    Primary Outcome Measures

    1. Characterisation of lung changes in COVID-19 patients as seen on ultrasound [2-3 months]

      Retrospective scoring of lung ultrasound images (12-zone ultrasound where clinical status allowed) for each of 5 lung abnormalities (pleural irregularity, B lines, small peripheral consolidation, large consolidation, small effusion (<1cm) and large effusion (>1cm). The images will be scored by 2 independent observers and the scores will be analysed based on the occurrence, location within the lung and clinical correlation

    Secondary Outcome Measures

    1. Correlation of lung changes as seen on ultrasound with clinical severity as per the Berlin ARDS criteria [2-3 months]

      Patients will be grouped into 4 groups of clinical severity (normal oxygenation, mild, moderate and severe deficit in oxygenation) based on the BERLIN criteria for ARDS. The data will be analysed by standard statistical tests comparing binomial data between unpaired and paired groups, as well as comparing more than three unmatched groups. This will include Chi-square, McNemar and paired t-tests and one-way ANOVA tests

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Presented to the ED between March-May 2020 with dyspnoea

    • COVID-19 positive either by PCR test or composite diagnostic criteria of lymphopenia and positive Chest XR report

    • Received lung ultrasound as part of investigations during ED attendance

    Exclusion Criteria:
    • < 18 years of age

    • Not diagnosed with COVID-19

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chelsea and Westminster Hospital London Greater London United Kingdom SW10 9NH

    Sponsors and Collaborators

    • Chelsea and Westminster NHS Foundation Trust

    Investigators

    • Principal Investigator: Paramjeet Deol, MBChB FRCEM, paramjeet.deol@chelwest.nhs.uk

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Chelsea and Westminster NHS Foundation Trust
    ClinicalTrials.gov Identifier:
    NCT05065827
    Other Study ID Numbers:
    • C&W20/050
    • IRAS number 286642
    First Posted:
    Oct 4, 2021
    Last Update Posted:
    Oct 22, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Chelsea and Westminster NHS Foundation Trust
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 22, 2021