About this trial
currently, PROMs and PREMs are not routinely collected and compared among medical inpatients of Swiss university hospitals, nor is a standard set of PROMs and PREMs available for use in Swiss hospitals. The project aims to examine trends in patient-reported outcomes (PROMs), including symptoms, quality of life, and distress, in multimorbid hospitalized patients from admission to 30 days post-discharge. It will also investigate whether PROMs at discharge are linked to the risk of readmission or emergency visits and explore how these outcomes differ in patients who receive low-value care. Additionally, the project will assess the relationship between patient-reported experiences (PREMs) and the provision of low-value care during the hospital stay.
Eligibility criteria
Qualifiers
eligible for the LUCID registry (CER-VD AO_2023-00029) [Age ≥ 18 years, hospitalized in one of the five participating university hospitals (Geneva, Lausanne, Bern, Zürich, Basel), after 01.01.2014, and admitted to general internal medicine wards
Multimorbid patients (2 or more chronic diseases, defined as chronic conditions defined by international classification of diseases, 10th revision, codes with an estimated expected duration of at least 6 months or based on a clinical decision.
Acute illness
Signature of study specific informed consent
Disqualifiers
Not able to speak French, German or English
Foreseen length of stay of less than 4 days (estimated by study collaborators)
Prior inclusion in the TRADUCE study
Incapacity of discernment, i.e. cognitive impairment which could interfere with the ability to fill in PROMs tools
Trial design
Treatments tested in this trial
- Hospitalization
Treatment groups
Sponsors and collaborators
University of Lausanne Hospitals
Lead sponsor
Insel Gruppe AG, University Hospital Bern
Collaborator
University Hospital, Geneva
Collaborator
University Hospital, Zürich
Collaborator
University Hospital, Basel, Switzerland
Collaborator