ELderly REspiratory VIral Cohort

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

In addition to SarsCov2, the main viral respiratory risks are associated with influenza viruses, respiratory syncytial virus (RSV), human metapneumovirus (hMPV) parainfluenza virus (PIV), adenovirus, rhinovirus, coronavirus and others. HMPV is a respiratory virus discovered in 2001. Like RSV, it appears to be a threat in terms of morbidity and mortality in susceptible populations.

Overall, viral infections can cause significant functional decline in older patients, with 67% and 25% reported to be at least temporarily housebound or bedridden, respectively. Respiratory viral infections prevent older patients from functioning and performing their daily tasks. They therefore have a significant impact on the older patients and their families. In addition, respiratory viruses are key factors in the exacerbation of chronic diseases.

The aims of this study are to provide a better understanding of the role of hMPV compared to common respiratory viruses on morbimortality, risk of dependency, quality of life alteration in older inpatients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient aged 65 years or older

Positive PCR from a nasopharyngeal swab for a respiratory viral pathogen as listed: Influenza A and B, SarsCov2, RSV, hMPV, Rhinovirus/Enterovirus, Adenovirus, Coronavirus (229E, HKU1, NL63, OC43), Parainfluenza Virus 1, 2, 3, 4.

Hospitalized in an Acute Medicine/Geriatrics Unit

Written informed consent from patient or his/her representative, with trusted support person, a family member or, failing that, a close friend if the person is physically unable to give his or her written consent. Patients under legal protection (guardianship, curatorship, family authorisation or future protection mandate) may be included with the consent of the legally authorised person.

Disqualifiers

Refusal to participate

Patient deprived of liberty by a judicial or administrative decision

Trial population

Patients aged \>65 years with a diagnosis of acute respiratory infection and hospitalized in acute/geriatric wards

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Respiratory viral infection

    Other intervention

    Respiratory viral infection identified by a positive nasopharyngeal PCR test. The prognostic role of human metapneumovirus (hMPV) infection will be compared with that of other common respiratory viral infections in older hospitalized patients.

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: Older patients with respiratory viral infection1 intervention

Trial outcomes

Primary outcomes

1

Proportion of participants with death and/or organ decompensation at Day 180

Proportion of participants who died and/or experienced at least one major comorbidity decompensation (cardiac, renal, or respiratory) by Day 180.

Time frame
From baseline Day 0 to Day 180

Secondary outcomes

1

Proportion of participants who died

Proportion of participants who died from any cause during follow-up.

Time frame
From baseline Day 0 to Day 30, Day 180, Day 365
2

Proportion of participants with major organ decompensation

Proportion of participants experiencing major decompensation of pre-existing comorbidities, including cardiac, renal, or respiratory decompensation.

Time frame
From baseline Day 0 to Day 30, Day 180, Day 365
3

Proportion of participants with unplanned hospital readmission

Proportion of participants experiencing an unplanned hospital readmission during follow-up.

Time frame
From baseline Day 0 to Day 30, Day 180, Day 365
4

Proportion of participants developing a lower respiratory tract infection

Proportion of participants developing a lower respiratory tract infection (LRTI) following the respiratory viral infection.

Time frame
From baseline Day 0 to Day 30

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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