|
The effect of MET systems on
outcome in hospitalised patients
|
The introduction of a MET system in Australian hospitals did
not improve patient outcome despite increasing the number of calls made to
the MET team. The introduction of MET is not warranted on current evidence.
Level of evidence:
1++ (RCT with a very low risk of bias)
Recommendation: Grade A |
Citation/s:
Merit Study Investigators. Introduction of the medical emergency team (MET)
system: a cluster randomised controlled trial. Lancet. 2005. 365: 2091-7.
Lead author's name and fax: K Hillman
K.Hillman@unsw.edu.au
Three-part Clinical Question:
Does the introduction of the MET system improve the composite outcome of death,
cardiac arrest and unplanned ICU admission in hospitalised patients.
Search
Terms: Medical emergency teams, Outreach critical care, Outcome, Mortality
The
Study: Single-blinded,
cluster-randomised, controlled trial with intention-to-treat.
The Study Patients: All comers admitted to 23 Australian hospitals over a
6 months period being care for in ward environment (excluding ICU, theatres, ICU
controlled HDU areas and A&E). Hospitals were excluded if a METs system was
already in place. There was baseline data collection for 6 months prior to MET
implementation.
Control group (N = 56,756; 56,756 analysed): Continuation of standard
emergency team set up, i.e. cardiac arrest team.
Experimental group (N =
68,376; 68,376 analysed): Education programme (MET related) for 4 months (with
the emphasis on recognition of the at-risk patient rather than their management)
followed by the introduction of a MET for the 6 months of the trial. MET team
consisted of a nurse and ICU or A+E doctor responding to a specific MET calling
system.
The
Evidence:
|
Outcome |
Time to Outcome |
CER |
EER |
RRR |
ARR |
NNT |
|
Composite primary outcome (death, unplanned cardiac arrest
and unplanned ICU admission) |
Hospital |
0.007 |
0.007 |
0% |
0.000 |
INF |
|
95% CI: |
ns |
ns |
ns |
|
Deaths |
Hospital |
0.002 |
0.002 |
0% |
0.000 |
INF |
|
95% CI |
ns |
ns |
ns |
|
Cardiac arrest |
Hospital |
0.003 |
0.002 |
33% |
0.001 |
1000 |
|
95% CI |
ns |
ns |
ns |
|
Non-Event Outcomes |
Time to outcome/s |
Control group |
Experimental group |
P-value |
|
Unplanned ICU admission |
Hospital |
300 |
339 |
ns |
|
Number of calls to team |
Hospital |
176 |
595 |
0.0001 |
There was a
significant reduction in adverse outcomes in the control hospitals over
the study period. This was not seen in the intervention group.
Comments:
This is a well-designed study with adequate power to determine a difference in
the power calculations primary outcome measure although the actual incidence of
the primary outcome did turn out to be lower than expected. . Thus in
retrospect, the study may have been underpowered for the primary outcome
measure. The reduction in incidence of the primary outcome measure may relate to
the Hawthorne effect. The study shows that despite an educational programme and
introduction of MET system, mortality, cardiac arrest rates and unplanned
admission to ICU were not reduced. It is only safe to assume that MET does not
improve outcome in hospitalised patients.
EBM
summary:
1) Do the
methods allow accurate testing of the hypothesis? Yes they do. A cluster
randomised trial methods is the highest method available for testing such a
hypothesis. The power calculations and statistical tests seem appropriate.
Effort has been made to randomise centres for baseline characteristics equally
between groups.
2) Do the statistical tests correctly test the results to allow differentiation
of statistically significant results? Yes they do. There is discussion
about the low incidence of the primary outcome in both groups. This means that
they powered on a far more common endpoint; this affects the power. They also
comment on the reduction in cardiac arrests in the control group after the
implementation period. Interestingly this effect was not seen in the MET group.
3) Are conclusions valid in light of the results? They concluded a number of
reasons why this trial was negative. They appropriately stated that the first
(and most likely reason) was lack of effect of the intervention. They have also
questioned (a) the power and (b) the presence of the Hawthorne effect in the
control group. It was also very interesting to note that only around 34% of ICU
admissions were seen by the team before admission and of these only 30%
triggered the MET system for longer than 15 minutes before the event. This
suggests that there may have been failure to recognise the sick patient rather
than purely a lack of effect of the MET teams intervention per se. The MET
relies on early recognition and calling.
4) Did results get omitted, and why? They did not.
5) Did they suggest areas of further research? They state “In
view of the overwhelming evidence that many seriously ill patients receive
inadequate care in hospitals worldwide, further research should be undertaken
and our results can assist the design and management of other such studies”.
This seems appropriate. They do not suggest further trials of MET.
6) Did they
make any recommendations based on the results and were they appropriate? They
suggest that improved monitoring, documentation and response to change as well
as education in critical illness is required due to the large number of missed
patients and poor documentation. They state that we require “frequent
and rigorous documentation of patients’ condition; and increased attention to
education to ensure a timely response by appropriately trained clinicians”.
They do not comment on whether
MET teams should be dismantled in the hospitals that have already implemented
this system. Perhaps any educational package should include ‘initial management
of the at-risk patient’ as well as ‘recognition of the at risk patient’.
7) Is the study relevant to my clinical practice? Yes it is. Although MET
is not identical to the Outreach system widely adopted in the UK, it is more
developed and has a medical lead. It may be reasonable to assume then that
Outreach will not improve outcome. We should re-evaluate the role of Outreach in
the management of the deteriorating hospital patient. The challenge is to
establish a robust system which both identifies the sick patient early and leads
to prompt, appropriate treatment.
8) What level of evidence does
this study represent? Level 1++
9) What grade of recommendation
can I make on this result alone? Grade A.
10) What
grade of recommendation can
I make when this study is considered along with other available evidence?- Grade
A
11) Should I change my practice because of these results? If you have an
Outreach team or early warming system (EWS), then you should re-evaluate their
role.
12) Should I audit my current practice because of these results? If you have an
Outreach team or EWS system you should at least rigorously audit their activity
and outcomes.
Appraised
by: Brian Cuthbertson Intensive Care Unit Aberdeen Royal Infirmary; 25 July 2005
Email: b.h.cuthbertson@abdn.ac.uk
Kill or Update By: July 2008
Edited by
RJP and CC
Printer Friendly Version
©SICS EBMG
2005
|