spoedeisende hulp bloedvergifiting sepsis
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - >18 years of age - Informed consent - Admitted to the emergency department
Exclusion criteria
Exclusion criteria: - Patients admitted to the trauma room - Subjects will be excluded if noninvasive blood pressure cannot be measured with the finger cuff according to the Instructions for Use of the CS/EV1000 system.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of this study is to predict deterioration in patients admitted to the ED. More specifically, we aim to predict sepsis, septic shock and cardiovascular instability based on the hemodynamic profile of the patient. Therefore, we will collect the continuous noninvasive arterial pressure waveform signals with the ClearSight (CS) finger cuff. In combination with the electronic medical record (EMR) data of the patient, we will develop a machine learning framework for the predictive tasks. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary aim of this study is to determine the optimal patient-specific therapeutic pathway and thereby aiming to determine fluid responsiveness of the patient. Furthermore, within the machine learning framework, we will investigate whether hospitalization (ICU or general ward) of ED patients can be predicted. | — |
Countries
Netherlands
Outcome results
None listed