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Machine Learning for Risk Stratification in the Emergency Department: A Pilot Clinical Trial

Recruiting
Conditions
Acute aandoeningen bij patiënten op de SEH
n.v.t.
Registration Number
NL-OMON54014
Lead Sponsor
Medisch Universitair Ziekenhuis Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
1300
Inclusion Criteria

- Adult, defined as >= 18 years of age
- Assessed and treated by an internal medicine specialist in the ED
- Willing to give written consent, either directly or after deferred consent
procedure

Exclusion Criteria

- <4 different laboratory results available (hematology or clinical chemistry)
within the first two hours of the ED visit (calculation ML prediction score
otherwise not possible)
- Unwilling to provide written consent, either directly or after deferred
consent procedure

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>- Calculated ML risk scores and observed mortality, to evaluate discriminatory<br /><br>performance of ML risk score to predict 31-day mortality.<br /><br>- Physicians self-reported policy changes to evaluate whether presentation of<br /><br>the ML risk score causes changes in clinical decision making. Policy changes<br /><br>include treatment policy, requesting ancillary investigations, treatment<br /><br>restrictions (i.e., no intubation or resuscitation).</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>- Clinical endpoints such as 31-day mortality, ICU and MC admission and<br /><br>readmission will be compared between the control an intervention group to<br /><br>evaluate differences.<br /><br>- Diagnostic performance of other clinical risk scores and physicians will be<br /><br>compared to the ML score.</p><br>
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