MEESSIMEESSI-AHF Scale Impact on Acute Heart Failure Patient Prognosis and Decision Making
This study aims to evaluate the impact of the MEESSI-AHF Scale on the prognosis and decision-making for patients with acute heart failure, by measuring the number of days alive and out of hospital, and the rate of all-cause death within 30 days of randomization.
Risk stratification before decision-making about patient hospitalization or discharge
Emergencies+1
+ Pathologic Processes
+ Pathological Conditions, Signs and Symptoms
Supportive Care Study
Summary
Study start date: June 27, 2023
Actual date on which the first participant was enrolled.This study focuses on evaluating the impact of the MEESSI-AHF scale, a tool designed to assess the risk in patients diagnosed with Acute Heart Failure (AHF) in emergency departments. The study involves over 8,000 patients across 16 Spanish emergency departments. The main goal is to understand how using this scale can influence decision-making and the overall prognosis of AHF patients. This research is crucial as it could potentially improve the care and outcomes for patients with Acute Heart Failure. The study consists of three parts. In the first part, patients receive usual care and their risk is retrospectively stratified using the MEESSI-AHF scale. The second part involves a quasi-experimental approach where some patients receive usual care, while others have their risk assessed using the MEESSI-AHF scale before a decision is made. The third part is a randomized clinical trial where patients are either managed with usual care or with the use of the MEESSI-AHF scale. The primary outcomes measured include death from any cause and cardiovascular cause at 30 days and 1 year, combined events (revisit to the ED or hospitalization for AHF or death) at 30 days post-discharge, days alive and outside the hospital at 30 days after the initial ED visit, and the proportion of patients managed without hospitalization.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.3200 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 19 locations
Emergency Department, Hospital de Bellvitge
L'Hospitalet de Llobregat, SpainOpen Emergency Department, Hospital de Bellvitge in Google MapsEmergency department
Barcelona, SpainEmergency Department, Hospital de Getafe
Getafe, SpainEmergency Department, Hospital de Móstoles
Móstoles, Spain