Integration of NAVOY® Sepsis in an Electronic Health Record System

AlgoDx1,000 enrolled

Overview

The study aims to evaluate the performance of NAVOY® Sepsis in predicting the sepsis risk in adult ICU patients. Data collection is performed via automatic retrieval from the electronic health record system to AlgoDx proprietary cloud service where it is analysed in a simulated environment.

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Sepsis

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * The subject is admitted to the ICU during the enrolment period. * The subject is 18 years of age or older at the time of admission to the ICU. Exclusion Criteria: * None.

Locations (1)

Southern General Hospital

Stockholm, Sweden

Outcomes

Primary Outcomes

NAVOY® Sepsis prediction performance

NAVOY® Sepsis prediction output within the simulated environment will be monitored and compared to the observed fulfilment of Sepsis-3 diagnosis criteria and sepsis specific management.

Time frame: 6 months

Secondary Outcomes

Integration validation

A technical checklist will be used in order to validate the integration between NAVOY® Sepsis and the electronic health record system.

Time frame: 6 months

NAVOY® Sepsis prediction results

The NAVOY® Sepsis predictions results indicate if the subject is at risk of developing sepsis within the coming hours. The results are not made available to ICU staff.

Time frame: 6 months

Fulfilment of Sepsis-3 criteria

The dimensions of the Sepsis-3 diagnosis criteria that the subjects meet during their ICU stay.

Time frame: 6 months

Sepsis specific management

Actions taken at the ICU specifically as part of sepsis detection, prevention, or treatment.

Time frame: 6 months

Data from ClinicalTrials.gov

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