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Clinical Trials/NCT03271216
NCT03271216
Completed
Not Applicable

Surveillance Monitoring on General Wards

Johns Hopkins University0 sites422 target enrollmentFebruary 2014
ConditionsCardiac Arrest

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Arrest
Sponsor
Johns Hopkins University
Enrollment
422
Primary Endpoint
positive predictive value (PPV)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This is a study to determine if surveillance monitoring of general ward patients can reduce cardio-pulmonary arrest while maintaining an acceptable false alarms rate for nursing workload.

Detailed Description

The investigators placed a wired monitoring system (pulse oximetry, heart rate and respiratory rate) on every patient who arrived on a subject general post surgical ward who assented to wear the system. this was the Masimo PSNET system using the Radical 87 monitor and an acoustic respiratory sensor along with a Masimo pulse oximetry probe. Patients were monitored for a minimum of 48 hrs. Heart Rate (HR) parameters were set between 45-130, Respiratory rate was set between 6-20 and pulse oximetrry was 85-100%. Nurses documented in the Electronic Medical Record (EMR) any alarms they responded to as to whether they were false (vital sign not out of range when rechecked) or true and what the response was. Responses ranged from nurse managed to notification of primary service to Rapid Response Activation to Code team activation as well as transfer to a higher level of care (operating room or Intensive Care Unit (ICU)/IMC. Patient and Nursing satisfaction surveys were collected.

Registry
clinicaltrials.gov
Start Date
February 2014
End Date
February 2015
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • all post-surgical patients admitted to a post-operative general hospital ward

Exclusion Criteria

  • inability to understand English or provide verbal consent for data analysis

Outcomes

Primary Outcomes

positive predictive value (PPV)

Time Frame: 6 months

The PPV of the wired monitoring system (pulse oximetry, heart rate and respiratory rate) will be determined based on change in vital signs (HR\<45 or \>130, RR\<6 or \>20 and pulse oximetry \<85) indicating clinical deterioration

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