An Adjunct Test Distinguishing Bacterial From Viral Etiology Improves Resource Utilization and Efficiency in the ED.

Last updated: May 14, 2024
Sponsor: The University of Texas Health Science Center, Houston
Overall Status: Active - Recruiting

Phase

N/A

Condition

Respiratory Syncytial Virus (Rsv) Infection

Treatment

MeMed BV® biomarker test

Usual care

Clinical Study ID

NCT06070688
HSC-MS-23-0692
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to evaluate overall changes in patient management and longer-term resource utilization between control and test arms, including (but not limited to) additional work-up (including other diagnostic tests and consults), antimicrobial treatments, disposition decisions and hospital length of stay (LOS)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Current disease duration ≤ 7 days

  • Temperature ≥ 37.8°C (100°F) or tactile fever, noted at least once within the last 7days

  • Clinical suspicion of bacterial or viral respiratory tract infection (RTI)

  • Blood tests are being ordered

Exclusion

Exclusion Criteria:

  • Systemic antibiotics taken up to 48 hours prior to presentation

  • Outpatient steroids taken within 48 hours prior to presentation

  • Suspicion and/or confirmed diagnosis of infectious gastroenteritis/colitis

  • Inflammatory disease

  • Congenital immune deficiency (CID)

  • A proven or suspected infection on the presentation with Mycobacterial ,parasitic orfungal (e.g., Candida, Histoplasma, Aspergillus) pathogen

  • Human immunodeficiency virus(HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection (self-declared or known from medical records)

  • Major trauma and/or burns in the last 7 days

  • Major surgery in the last 7 days

  • Pregnancy - Self reported or medically confirmed

  • Active malignancy - Cancer diagnosed within the previous six months, recurrent,regionally advanced, or metastatic cancer, cancer for which treatment had beenadministered within six months, or hematological cancer that is not in completeremission.

  • Current treatment with immune-suppressive or immune-modulating therapies, at somepoint in the past 10 days

  • Hemodynamically unstable (require life-saving interventions such as vasopressors)

  • Patients transferred from another facility who already have a differentiatedrespiratory illness (known diagnosis e.g., culture positive results)

  • Consider unsuitable for the study by the study team

Study Design

Total Participants: 100
Treatment Group(s): 2
Primary Treatment: MeMed BV® biomarker test
Phase:
Study Start date:
December 11, 2023
Estimated Completion Date:
December 30, 2024

Study Description

The trial seeks to compare the benefits of adding a diagnostic test that can distinguish the etiology of an acute respiratory illness early in the work-up and management. All adult patients shall be evaluated through the Emergency Department (ED) as an undiagnosed acute reparatory illness (URI). The included patient cohort must present with SIRS criteria and be ill enough to require immediate blood draw and management by the ED. Excluded are any URIs with a predetermined diagnosis or subjects presenting with illness not determined to be a URI as a primary diagnosis. The experimental arm of the study shall have in addition to the standard of care labs and diagnostics, a novel protein array blood test that can distinguish bacterial from viral disease. The control group will not receive these results. The trial seeks to examine the difference in clinical outcomes when a adjunct biomarker than can help the clinician guide more accurate therapy is available early in the diagnostic workup. Benefits are defined in the primary and secondary outcomes as reduced resources expended through reduced laboratory, radiological, blood bank, and pharmaceutical expenditures. Comparative resource utilization costs include changes in hospital and or ED length of stay, lower follow up visits and readmissions, less inpatient and outpatient physician consultants and services called for to manage the patients care, and overall costs. Both primary and secondary outcomes will be used to categorize the costs and resources required to manage the patient. Primary objective is to evaluate overall changes in patient management and longer-term resource utilization between control and test arms, including (but not limited to) additional work-up (including other diagnostic tests and consults), antimicrobial treatments, disposition decisions and hospital length of stay (LOS). The exploratory objective is to evaluate changes between control and test arm in ED LOS, bounce backs (patients returning within 72 hours), work-up costs and the impact of physician seniority.

Connect with a study center

  • The University of Texas Health Science Center at Houston

    Houston, Texas 77030
    United States

    Active - Recruiting

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