Emergency departments (ED) are becoming increasingly over-crowded, with patients facing prolonged waiting times. Therefore, a safe and rapid assessment that identifies patients with low severity that could be treated as outpatients is essential for improving the workflow within the ED. The rationale of this IDEAL+ study is to safely decrease the number of hospital admissions through identification of low risk patients with the biomarker MR-proADM. This will has already been tested in the IDEAL - pilot study and results should be confirmed with this IDEAL+ study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
463
MR-proADM ≤ 0.87 nmol/L together with routine clinical evaluation identifies patients with low disease severity who do not need to be hospitalized
Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université
Paris, France
Policlinico Tor Vergata
Roma, Italy
Hospital Santa Maria della Misericordia
Udine, Italy
Hospital Universitario Central de Asturias (HUCA)
Number of out-patients re-presenting to the ED
Number of out-patients re-presenting to the ED
Time frame: 5 days
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Oviedo, Principality of Asturias, Spain
Hospital Clinic
Barcelona, Spain
Hospital Clinico San Carlos
Madrid, Spain
Hospital Virgen de la Macarena
Seville, Spain
Hampshire Hospitals NHS Foundation Trust
Basingstoke, United Kingdom
University Hospital Southampton NHS Foundation Trust
Southampton, United Kingdom