Machine Learning Prediction of Mortality After Prone Positioning in ARDS

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Zhongshan Hospital

About this trial

Acute respiratory distress syndrome (ARDS) is a life-threatening condition with high mortality. Prone position ventilation (PPV) is an evidence-based therapy that improves oxygenation and survival in patients with moderate to severe ARDS; however, outcomes remain heterogeneous. Early identification of patients at high risk of mortality after PPV may improve clinical decision-making and individualized management.

This retrospective observational study aims to develop and validate a machine learning model to predict intensive care unit (ICU) mortality in ARDS patients receiving prone position ventilation. Clinical, laboratory, and treatment variables collected from ICU electronic medical records will be used to construct prediction models using multiple machine learning algorithms. The performance of these models will be evaluated and compared to identify the optimal model for mortality prediction.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of ARDS according to the Berlin definition [15];

Receipt of at least one session of prone position ventilation (PPV) during hospitalization;

Requirement for mechanical ventilation.

Disqualifiers

Age <18 years;

PPV duration <6 hours;

ICU length of stay <24 hours;

Pregnancy;

Trial population

Adult patients diagnosed with acute respiratory distress syndrome (ARDS) who received prone position ventilation in the intensive care unit at Zhongshan Hospital, Fudan University. Clinical data were collected retrospectively from electronic medical records.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Prone Position Ventilation

    Other intervention

    Prone position ventilation applied as part of routine clinical care for patients with acute respiratory distress syndrome. No experimental intervention was assigned in this observational study.

Treatment groups

377 Participants
are divided into 1 treatment group
Group A: ARDS Patients Receiving Prone Position Ventilation1 intervention

Trial outcomes

Primary outcomes

1

ICU Mortality

Death from any cause during the intensive care unit (ICU) stay among patients with acute respiratory distress syndrome receiving prone position ventilation.

Time frame
Up to 90 days.

Secondary outcomes

Other outcomes

1

ARDS subphenotype classification based on machine learning model.

Number of patients classified into different ARDS subphenotypes using a machine learning model based on clinical and physiological variables collected at baseline.

Time frame
Baseline (at initiation of prone position ventilation).

Locations

This trial has no locations.

Sponsors and contacts

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