search
Back to results

Realtime Streaming Clinical Use Engine for Medical Escalation (ReSCUE-ME)

Primary Purpose

Clinical Deterioration, Hospital Medicine, Monitoring, Physiologic

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MEWS++ Monitoring
Predictor Score
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Clinical Deterioration focused on measuring Medical Early Warning Systems, Patient Monitoring, Electronic Health Record, Big Data, Critical Care, Machine Learning

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients age 18 or greater who were admitted to a general care unit selected for each arm.

Exclusion Criteria:

  • Any admitted patient who has a "Do Not Resuscitate (DNR)" and/or a "Do Not Intubate (DNI)" order in the EHR,
  • any patient made "level of care" by RRT as documented in REDCap.

Sites / Locations

  • Mount Sinai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

MEWS++ Monitoring

Standard of Care Monitoring

Arm Description

This consists of all the patients that will be receiving MEWS++ escalation monitoring and provider alerting.

Patients in the control arm will have a score calculated but no alert will be sent.

Outcomes

Primary Outcome Measures

Overall rate of care escalation
The composite (sum) of the rate of escalation of care (from floor to Stepdown, Telemetry, ICU) and rate of RRT initiated therapy (including but not limited to blood pressure support, respiratory care support, anti-biotic augmentation, invasive monitoring).

Secondary Outcome Measures

Number of participants requiring blood pressure support
Number of participants requiring blood pressure support agents such as initiation of vasopressor medication or administration of fluid bolus.
Number of participants requiring respiratory support
Number of participants requiring respiratory support intervention such as initiation of nasal cannula to high flow or frequency of intubation
Number of cardiac arrest episode
Frequency of cardiac arrest episode
Mortality Rate
Number of Mortalities
Notification Frequency
The average notifications per day per patient
Number of calls
The average number of calls per patient
Sensitivity and Specificity of the RRT alert
The performance of the alert will be evaluated by calculating the sensitivity, specificity, positive predictive value, negative predictive value, precision, recall, and F1-score. This will be done both for the overall escalation rate and if possible for individual escalations (ICU, step-down, telemetry) and death.

Full Information

First Posted
July 16, 2019
Last Updated
June 24, 2020
Sponsor
Icahn School of Medicine at Mount Sinai
search

1. Study Identification

Unique Protocol Identification Number
NCT04026555
Brief Title
Realtime Streaming Clinical Use Engine for Medical Escalation
Acronym
ReSCUE-ME
Official Title
Realtime Streaming Clinical Use Engine for Medical Escalation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
June 18, 2019 (Actual)
Primary Completion Date
March 19, 2020 (Actual)
Study Completion Date
March 19, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The escalation of care for patients in a hospitalized setting between nurse practitioner managed services, teaching services, step-down units, and intensive care units is critical for appropriate care for any patient. Often such "triggers" for escalation are initiated based on the nursing evaluation of the patient, followed by physician history and physical exam, then augmented based on laboratory values. These "triggers" can enhance the care of patients without increasing the workload of responder teams. One of the goals in hospital medicine is the earlier identification of patients that require an escalation of care. The study team developed a model through a retrospective analysis of the historical data from the Mount Sinai Data Warehouse (MSDW), which can provide machine learning based triggers for escalation of care (Approved by: IRB-18-00581). This model is called "Medical Early Warning Score ++" (MEWS ++). This IRB seeks to prospectively validate the developed model through a pragmatic clinical trial of using these alerts to trigger an evaluation for appropriateness of escalation of care on two general inpatients wards, one medical and one surgical. These alerts will not change the standard of care. They will simply suggest to the care team that the patient should be further evaluated without specifying a subsequent specific course of action. In other words, these alerts in themselves does not designate any change to the care provider's clinical standard of care. The study team estimates that this study would require the evaluation of ~ 18380 bed movements and approximately 30 months to complete, based on the rate of escalation of care and rate of bed movements in the selected units.
Detailed Description
Objectives: Mount Sinai Hospital has developed a Rapid Response Team (RRT) system designed to give general floor care providers additional support for patients who may be requiring a higher level of care. This system enables both nurses and physicians to notify the RRT and have a critical care team evaluate the patients. During the period of 03/01/2018 to 09/17/2018, Mount Sinai Hospital floor units on 10W and 10E units made 357 rapid response team (RRT) calls with only 58 leading to an actual increase in the level of care (true positive rate ~ 16%). Similarly, the Electronic Health Record (EHR) generated 839 sepsis Best Practice Alerts (BPAs) yet only five led to escalations in care (true positive rate ~ 0.5%). The results above would imply that over 168 evaluations need to be made to identify a single case where the patient required an escalation in care. The goal of ReSCUE-ME is to evaluate prospective model performance and identify the best spot which the study team can incorporate MEWS++ into RRT and Primary providers workflow. The primary endpoint is rate of escalation of care on 10W and 10E during the study period. Background: In a prior study, the group has demonstrated that a machine learning model (MEWS++) significantly outperformed a standard, manually calculated MEWS score on a large retrospective cohort of hospitalized patients. To develop this model, the study team used a data set (Approved by: IRB-18-00581) of 96,645 patients with 157,984 hospital encounters and 244,343 bed movements. The study team found that MEWS++ was superior to the standard MEWS model with a sensitivity of 81.6% vs. 44.6%, specificity of 75.5% vs. 64.5%, and area under the receiver operating curve of 0.85 vs. 0.71. Encouraged by this prior result, the study team is seeking to evaluate the model in a prospective study. A silent pilot of the ReSCUE-ME alerts has been running on 10E and 10W since Feb 2019. The study team has continuously monitoring the alert performance via a real-time web-based dashboard. The results are summarized below: Median # of alerts to primary team, per floor, per day: 8 Median # of alerts to RRT, per floor, per day: 4 Sensitivity 0.76, Specificity 0.68, AUC 0.77 Accuracy 0.69, Precision 0.3, F1 Score 0.43 This performance compares very favorably to the performance seen in the retrospective historical cohort used to develop the MEWS++ model: Sensitivity 0.82, Specificity 0.76, AUC 0.85 Accuracy 0.76, Precision 0.12, F1 Score 0.19"

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clinical Deterioration, Hospital Medicine, Monitoring, Physiologic
Keywords
Medical Early Warning Systems, Patient Monitoring, Electronic Health Record, Big Data, Critical Care, Machine Learning

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
For each patient, real-time data from clinical and administrative systems will be used by ReSCUE-ME to produce a MEWS++ score predicting the likelihood that the patient will require escalation of care within the next 6 hours. Upon the patient being admitted to the unit, the patient will be evaluated based on any update in the EMR. If the prediction score exceeds a "high" threshold, the RRT team will be notified directly. If the score is between a "low" threshold and the high threshold , the nursing team will be notified and increased nursing monitoring will be initiated. If the patient has met criteria for increased nursing monitoring, a refractory 8-hour refractory window will be applied during which no nursing alerts will be sent. However if the score exceeds the high threshold, the RRT team will be notified. Throughout the trial, the performance of the alerts will be monitored via web-based dashboards. If the performance is poor, the "high" and "low" thresholds will be adjusted.
Masking
None (Open Label)
Masking Description
No masking is completed as the information/waiver of consent sheet for the two arms needed to be individualized.
Allocation
Non-Randomized
Enrollment
2915 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MEWS++ Monitoring
Arm Type
Active Comparator
Arm Description
This consists of all the patients that will be receiving MEWS++ escalation monitoring and provider alerting.
Arm Title
Standard of Care Monitoring
Arm Type
Placebo Comparator
Arm Description
Patients in the control arm will have a score calculated but no alert will be sent.
Intervention Type
Other
Intervention Name(s)
MEWS++ Monitoring
Intervention Description
Patient's electronic medical record data will undergo processing by a machine learning algorithm (MEWS++).
Intervention Type
Other
Intervention Name(s)
Predictor Score
Intervention Description
A score predicting the likelihood that the patient will experience a deterioration in their clinical condition within six hours will be generated. If the prediction score exceeds a predetermined threshold, an alert will be sent to the provider. The alerting protocol is tiered, with both a low and high threshold. If the score is above the low threshold, nursing will be notified. If the score is above the high threshold, RRT will be notified.
Primary Outcome Measure Information:
Title
Overall rate of care escalation
Description
The composite (sum) of the rate of escalation of care (from floor to Stepdown, Telemetry, ICU) and rate of RRT initiated therapy (including but not limited to blood pressure support, respiratory care support, anti-biotic augmentation, invasive monitoring).
Time Frame
30 month
Secondary Outcome Measure Information:
Title
Number of participants requiring blood pressure support
Description
Number of participants requiring blood pressure support agents such as initiation of vasopressor medication or administration of fluid bolus.
Time Frame
30 month
Title
Number of participants requiring respiratory support
Description
Number of participants requiring respiratory support intervention such as initiation of nasal cannula to high flow or frequency of intubation
Time Frame
30 month
Title
Number of cardiac arrest episode
Description
Frequency of cardiac arrest episode
Time Frame
30 month
Title
Mortality Rate
Description
Number of Mortalities
Time Frame
30 month
Title
Notification Frequency
Description
The average notifications per day per patient
Time Frame
30 month
Title
Number of calls
Description
The average number of calls per patient
Time Frame
30 month
Title
Sensitivity and Specificity of the RRT alert
Description
The performance of the alert will be evaluated by calculating the sensitivity, specificity, positive predictive value, negative predictive value, precision, recall, and F1-score. This will be done both for the overall escalation rate and if possible for individual escalations (ICU, step-down, telemetry) and death.
Time Frame
30 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients age 18 or greater who were admitted to a general care unit selected for each arm. Exclusion Criteria: Any admitted patient who has a "Do Not Resuscitate (DNR)" and/or a "Do Not Intubate (DNI)" order in the EHR, any patient made "level of care" by RRT as documented in REDCap.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew A Levin, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Study Director
Facility Information:
Facility Name
Mount Sinai Hospital
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices).

Learn more about this trial

Realtime Streaming Clinical Use Engine for Medical Escalation

We'll reach out to this number within 24 hrs