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Table 1. Annual numbers of patients admitted to the intensive care unit at Bundaberg Base Hospital, 20002005,
numbers analysed and exclusions
2000 (NovDec) 2001 2002 2003 2004 2005 Total
No. of patients admitted 39 320 252 191 211 278 1291
No. of patients analysed 26 139 126 106 111 177 685
Mortality 3.8% 10.8% 15.9% 23.6% 14.4% 11.3% 14.1%
APACHE III-j risk of death (SD) 2.1% 9.1% 11.1% 19.7% 15.2% 12.3% 12.7%
(10.9%) (17.6%) (19.5%) (26.2%) (22.2%) (22.7%) (21.3%)
Exclusions
Transfer to another ICU* 1 42 42 35 28 52 200
Age < 16 years or 5 51 30 24 30 31 171
ICU length of stay < 4 h
No APACHE III-j risk of death 7 88 54 26 42 18 235
or no hospital outcome
recorded
* Excluded because eventual outcome was unknown. Routine exclusions in keeping with the APACHE III-j algorithm.
of any individual at the hospital, nor would it be possible to observed mortality was higher than predicted by
do so with this analysis of overall ICU outcomes. APACHE III-j.
assessed by estimating the area under the receiver operator Input from staff at Bundaberg Base Hospital
curve, where an area greater than 0.8 indicated good The study was undertaken with the support of administrative
discrimination. Data were analysed using Intercooled Stata and clinical staff at the Bundaberg Base Hospital ICU, who
version 9.2 for Windows, and figures were constructed provided historical perspective and clinical context for the
using Microsoft Windows Excel 2007. analysis.
Figure 1. Annual standardised mortality ratio for Bundaberg Base Hospital intensive care unit for 20002005
(with 95% CIs)
3
2.5
Standardised mortality ratio
1.5
0.5
0
2000 2001 2002 2003 2004 2005
Figure 2. Exponentially weighted moving average (EWMA) chart for Bundaberg Base Hospital intensive care
unit for 20002005
Sequential admissions and year of admission are plotted on the horizontal axis. Observed mortality (black line) and 95% (light grey) and 99%
(dark grey) confidence limits for APACHE III-J predicted risk of death are plotted on the vertical axis. An arbitrary starting value of 16% was chosen,
as this was the overall mortality rate for five peer-group hospitals.
from Bundaberg ICU between November 2002 and Febru- tion and improved patient outcomes, or whether poor data
ary 2006. The Australian Council for Healthcare Standards quality led to an erroneous impression of poor outcomes in
has designated that data submission to ANZICS is a key earlier years could not be determined. Despite the exclu-
performance indicator for intensive care practice. Inability sions there appears to be a signal of periods when
to submit data may in itself be a signal of a problem. outcomes were worse than expected, highlighting a poten-
Smaller regional hospitals may have limited resources for tial benefit of this type of analysis.
data collection, data submission and audit of clinical out- APACHE III-j appeared to be an appropriate risk adjustment
comes. This was indeed the case at Bundaberg Base tool. However, the performance of any risk adjustment model
Hospital in the early 2000s. It is not known whether the itself may be affected by many factors, including changes in
perception or anticipation of poor performance was a observed mortality rate,10 patient casemix,11 admission lead
disincentive to data submission. time,12 discharge practices,13 data collection,14,15 rule interpre-
On several occasions during the period investigated, ICU tations and transcription errors.16 The contribution of each of
staff wished to assess whether outcomes were below these factors to the calculation of predicted risk of death for
expected, but did not have analysed data available. Had patients at the Bundaberg ICU was unknown.
there been timely submission of data, with analysis and Limitations to the introduction of EWMA charts into routine
feedback of results through an appropriate governance clinical practice throughout Australia require mention. In
structure (as now exists in Queensland), we speculate that recent years, outcomes for patients admitted to Australian
EWMA analysis could have led to an inspection of processes ICUs are consistently better than those predicted by APACHE
at the hospital, and possibly early detection of deteriorating III-j.17 Thus, deterioration in outcome may be more difficult to
outcomes. At the minimum, such an analysis would have detect. A more accurate, appropriate and contemporary
prompted review of data quality, highlighting the lack of mortality prediction model may need to be developed.
resources for data collection and submission.
When monitoring clinical outcomes, it is vital to avoid
over-interpretation of results and erroneous judgements Conclusions
about quality of care.9 There are significant caveats and
With appropriate risk adjustment and interpretation, the
limitations to our analysis. Firstly, this was an analysis of a
EWMA chart can provide meaningful and important clinical
cohort of ICU patients. EWMA charts constructed in this
results. It can detect fluctuations in outcome that are not
way are appropriate for monitoring the risk-adjusted out-
apparent with an SMR. Had this analysis been available in
comes of ICUs. No inference can be drawn as to whether
20002005, it might have prompted review of processes
the presence of any individual at the hospital directly
and outcomes among ICU patients at the Bundaberg Base
influenced the outcomes of patients in the ICU. In addition,
Hospital. As part of future reports from the ANZICS CORE,
the APACHE III-j predicted risk of death was calculated
techniques such as EWMA chart analysis may be beneficial
using data collected in the first 24 hours after ICU admis-
for routine monitoring of intensive care practice in Australia
sion. Thus, this analysis was not applicable to the assess-
and New Zealand. Hospitals and ICUs should be provided
ment of practices before ICU admission.
with adequate resources for the accurate and timely collec-
Secondly, although all data underwent extensive check-
tion of these important quality assurance data.
ing and cleaning before analysis by ANZICS, the impact
of data quality on this, and indeed any, analysis must be
emphasised. There were many exclusions, with 47% of
Acknowledgements
admissions to Bundaberg ICU not included in this analysis.
Some of these were standard exclusions that are routinely Initial analysis of these data was presented, with the permission of
administrative and clinical staff of Bundaberg Base Hospital ICU, at
applied to data when using APACHE III-j as the risk adjustor
the ANZICS Annual Scientific Meeting in Rotorua, New Zealand, in
and would have been applied to data from any ICU. 2007.
However, a considerable proportion were excluded because
of poor data quality no recorded hospital outcomes or
no APACHE III-j predicted risk of death. The effect of these
Author details
missing data on analysis and interpretation could not be
David V Pilcher, Director, ANZICS Adult Patient Database,1 and
determined. However, notably the proportion of ICU admis-
Intensivist2
sions without recorded hospital outcomes or APACHE III-j
Toni Hoffman, Nurse Unit Manager3
predicted risk of death was lowest in 2005, when outcomes Chris Thomas, Intensivist3
were best. Whether this was due to general improvement in David Ernest, Intensivist4
processes, which in turn led to both improved data collec- Graeme K Hart, Chair,1 and Intensivist5
1 Australian and New Zealand Intensive Care Society Centre for 8 Cook DA, Duke G, Hart GK, et al. Review of the application of risk-
Outcome and Resource Evaluation. adjusted charts to analyse mortality outcomes in critical care. Crit
2 Department of Intensive Care, Alfred Hospital, Melbourne, VIC. Care Resusc 2008; 10: 239-51.
3 Department of Intensive Care, Bundaberg Base Hospital, Bundaberg, 9 Lilford R, Mohammed MA, Spiegelhalter D, Thomson R. Use and
QLD. misuse of process and outcome data in managing performance of
acute medical care: avoiding institutional stigma. Lancet 2004; 363:
4 Department of Intensive Care, Box Hill Hospital, Box Hill, VIC.
1147-54.
5 Department of Intensive Care, Austin Hospital, Melbourne, VIC.
10 Zhu BP, Lemeshow S, Hosmer DW, et al. Factors affecting the
Correspondence: d.pilcher@alfred.org.au performance of the models in the Mortality Probability Model II
system and strategies of customization: a simulation study. Crit
Care Med 1996; 24: 57-63.
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