Surveillance Monitoring on General Wards

Last updated: August 31, 2017
Sponsor: Johns Hopkins University
Overall Status: Completed

Phase

N/A

Condition

Heart Attack (Myocardial Infarction)

Heart Failure

Circulation Disorders

Treatment

N/A

Clinical Study ID

NCT03271216
IRB00066847
  • Ages 18-90
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

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

Study Design

Total Participants: 422
Study Start date:
February 01, 2014
Estimated Completion Date:
February 28, 2015

Study 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.