Impact of a Communication and Team-working Intervention on Performance and Effectiveness of a Medical Emergency Team (IMPACT)

November 23, 2016 updated by: Dr Richard Chalwin, Lyell McEwin Hospital

Patients in hospital can have unexpected clinical emergencies. When this occurs the Medical Emergency Team (MET) are called with the intention of resolving the problem. Previous investigations have found that patients who have more than one call during their admission have worse outcomes than patients who only have one call. But it has not been established why.

The aim of this research will be to examine these repeated calls and why patients subject to them go on to have worse outcomes. A predictive model will be developed to identify potential sources of risk. One potential source is poor communication between health care providers. An intervention to improve communication around MET calls may provide benefit to patients and improve outcomes.

Study Overview

Detailed Description

This investigation will comprise a mixed methods, before-and-after study. The particulars are:

Format:

  1. Before intervention

    1. Analysis of retrospective MET activity and patient outcome data
    2. Surveying of staff for attitudes and perceptions of MET calls
  2. Intervention

    1. Twice-daily MET briefing meetings
    2. Formalised handover process for MET calls resulting in patients remaining in their current clinical area
  3. After intervention

    1. Analysis of prospective MET activity and patient outcome data
    2. Surveying of staff for attitudes and perceptions of MET calls

Setting:

Lyell McEwin Hospital, a 300 bed, university-affiliated, tertiary, metropolitan hospital located in Adelaide, South Australia. It has comprehensive in-patient medical and surgical services including a Level 3 Intensive Care Unit.

Subjects:

  1. Patients - adult in-patients attended by the MET during the study period. This will include patients attended more than once during an admission, as all calls will be a separate datapoint. It is also possible for patients to have more than one admission during the study period, so each admission will be considered discretely.
  2. Staff - members of the hospital MET and ward staff that may call the MET. The MET composition is an ICU doctor, ICU nurse, medical registrar, intern and hospital manager. Due to rostering demands, this team is supplied from a pool of staff within each of the representative departments (approximately 10 ICU doctors, 30 ICU nurses, 30 medicine registrars, 36 interns and 8 duty managers).

Data Collection:

  1. Characteristics and Outcomes

    1. Per-hospital admission data includes: age, gender, admission diagnosis, admission type, length of stay and mortality
    2. Per-MET call data includes: reason for call, location, duration of call, interventions performed, disposition and mortality
  2. Perceptions and Attitudes

    1. Ward staff question including around interactions with MET, involvement during MET calls, experience of repeat calling and reasons for repeat calling
    2. MET questions including around interactions with ward staff, involvement of ward staff during calls and resolution of calls.

Study Type

Interventional

Enrollment (Actual)

1500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • South Australia
      • Elizabeth Vale, South Australia, Australia, 5112
        • Lyell McEwin Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusions

- Medical Emergency Team (MET) calls

Exclusion Criteria:

  • Cancellation of the MET response prior to, or on arrival at, the location of activation
  • Calls to patients < 18 years of age

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Medical Emergency Team
A communication and team-working initiative
Medical Emergency Team (MET) briefings and formalised handover between MET staff and patient care teams

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Multiple Medical Emergency Team calls per patient admission
Time Frame: Measured at time of hospital discharge
Measured at time of hospital discharge

Secondary Outcome Measures

Outcome Measure
Time Frame
Mortality
Time Frame: At time of hospital discharge
At time of hospital discharge
Mortality
Time Frame: At completion of Medical Emergency Team call
At completion of Medical Emergency Team call
ICU admission rate
Time Frame: At completion of Medical Emergency Team call
At completion of Medical Emergency Team call
ICU interventions
Time Frame: At completion of Medical Emergency Team call
At completion of Medical Emergency Team call

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceptions of Interactions between Medical Emergency Team staff and patient care teams
Time Frame: 1 year
Both Medical Emergency Team staff and patient care teams will be surveyed separately
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Richard Chalwin, FCICM, Lyell McEwin Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2014

Primary Completion (Actual)

July 1, 2016

Study Completion (Actual)

September 1, 2016

Study Registration Dates

First Submitted

March 4, 2012

First Submitted That Met QC Criteria

March 7, 2012

First Posted (Estimate)

March 12, 2012

Study Record Updates

Last Update Posted (Estimate)

November 25, 2016

Last Update Submitted That Met QC Criteria

November 23, 2016

Last Verified

November 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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