Frailty and Outcomes in Older Emergency Department Patients With Pneumonia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorEge University

About this trial

Pneumonia is one of the leading causes of infection-related mortality in the older population. Traditional severity scores used in emergency departments, such as the Pneumonia Severity Index (PSI) and CURB-65, primarily focus on acute physiological derangements and may not adequately capture biological reserve and frailty in older adults. Frailty is a geriatric syndrome reflecting increased vulnerability to stressors and reduced recovery capacity.

This prospective observational cohort study aims to evaluate the predictive value of the Clinical Frailty Scale (CFS) for in-hospital mortality, 30-day mortality, and morbidity in patients aged 65 years and older presenting to the emergency department with pneumonia. Additionally, the study will assess whether incorporating frailty assessment into existing pneumonia severity scores improves prognostic accuracy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥65 years

Clinical and radiological diagnosis of pneumonia in the emergency department

Ability to obtain informed consent from the patient or legal representative

Availability of a caregiver or relative able to describe baseline functional status

Disqualifiers

Presentation with cardiopulmonary arrest or ongoing cardiopulmonary resuscitation at admission

Confirmed COVID-19 pneumonia

Inability to obtain reliable baseline functional history due to absence of an informant

Refusal to provide informed consent

Trial population

Older adults aged 65 years and above presenting to a tertiary university hospital emergency department with a clinical and radiological diagnosis of pneumonia. The study population represents geriatric patients with acute infectious respiratory illness requiring emergency evaluation, including a wide range of comorbidity and functional status levels typical of real-world emergency department practice.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Clinical frailty scale

    Other intervention

    Frailty assessment performed at emergency department presentation using the 9-point Clinical Frailty Scale.

  • Clinical Frailty Scale (CFS)

    Diagnostic test

    The Clinical Frailty Scale (CFS) will be assessed on a 1-9 scale. The CFS score obtained at presentation will also be compared with the patient's baseline CFS prior to the onset of the current illness symptoms.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

In hospital mortality

All-cause mortality occurring during the same hospital admission after emergency department presentation.

Time frame
During index hospitalization (7 and 14 days)

Secondary outcomes

Other outcomes

Sponsors and contacts

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