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Proceedings of the Annual Scientific Meeting of the
Continuing Education Committee Anaesthetists in New Zealand (New Zealand Society
of Anaesthetists and Australian & New Zealand College of Anaesthetists),
Wednesday 18 to Friday 20 September 2002
Transfusion strategies I. M
Harrison. University Division of Anaesthesiology, University of Auckland,
Auckland.
Background
Transfusion guidelines refer to the taking into account of comorbidities. There
are three main components to the decision-making process: the oxygen-carrying
capacity (Hb); the ability of the patient to increase their cardiac output; and
the patient’s ‘need’ for oxygen. The Hb concentration is the
only factor that has a numerical value in the clinical setting.
Aim The aim of the
study was to quantify comorbidities so that a model of transfusion strategies
could be constructed.
Methods Senior staff
(n = 29) in the Auckland Department of Anaesthesia completed a questionnaire on
their beliefs about patients’ abilities to increase their cardiac output
in the presence of various pathologies. In another questionnaire (n = 22) they
were asked, obliquely, about the patients’ need of oxygen. They were asked
what the likelihood of transfusion was, in the presence of certain pathologies,
if the patient’s Hb was 95 g/l. The answers to these questions (a mark on
a 100 mm visual analogue scale (VAS)) were used to rank the
pathologies.
Results The raw data
had a very broad dispersion but it was possible to rank the pathologies as shown
in the table below.
Conclusions It is
possible to rank comorbidities that are significant when deciding to transfuse a
patient, but their value has yet to be determined.
Transfusion strategies II.
M Harrison. University Division of Anaesthesiology, University of Auckland,
Auckland.
Aim The aim of the
study was to create a model of the decision to transfuse that takes into account
patients’ comorbidities.
Methods The three
main components of the transfusion decision-making process – the oxygen
carrying capacity (Hb); the ability of the patient to increase their cardiac
output (CO); and the patient’s ‘need’ for oxygen
(O2n) – were combined in a series of 30
clinical scenarios. These scenarios were presented to the senior staff of the
Auckland Department of Anaesthesia who were asked to make a decision about
transfusion.
The Hb concentration is the only factor that has a numerical
value in the clinical setting but using questionnaires the ranking of various
pathologies with regard to CO and O2n had been
achieved in a prior study.
The thirty scenarios were composed of three distinct
groupings of clinical states. In 10 the Hb and CO values were, on average,
constant, in another 10 the Hb and O2n values,
and in the final 10 the CO and O2n values. Once
these scenarios had been constructed the questions were then re-ordered using
random numbers.
Results The response
to these scenarios demonstrated correlation between the decision to transfuse
and the Hb and the CO response but there was only a very weak correlation with
O2n. From the data a graph was produced of Hb vs
CO and the likelihood that the senior anaesthetists at Auckland Hospital would
transfuse.
![]() The black squares represent over 50% likelihood of
transfusion, the circles less than 30%.
Conclusions A model
of the decision can be made from Hb and CO values. Further investigation of the
data may allow refinements to the borderline situations.
Troponin T and long-term
outcome following aortic surgery. K Jamieson, N MacLennan. Department of
Anaesthesia, Auckland Hospital, Auckland.
Aim Peri-operative
myocardial ischaemia and infarction (PMI) are frequent complications of major
vascular surgery. The criteria for the diagnosis of PMI have recently changed to
incorporate troponin assays. In addition, some studies suggest that minor
elevations in troponin T (TT) are associated with adverse long-term outcome. The
aim of this study was to examine the impact of peri-operative elevations in TT
levels on cardiac outcome of patients after aortic surgery.
Methods One hundred
and thirty six patients underwent open abdominal aortic aneurysm (AAA) repair
during the initial period of data collection. Troponin T was measured routinely
on post-operative days 1, 3 and 5. The patients were divided into three
groups:
During the follow-up period questionnaires
were sent to the patients’ general practitioners, and information sourced
from the hospital database to determine the incidence of adverse cardiac events
and death.
Results Follow-up
data were available on 85% of AAA patients. Long-term morbidity and mortality
were highest in the group with positive TT assays at the time of surgery (Group
3 = 25%). Morbidity and mortality were also elevated in those with intermediate
TT levels (Group 2 = 22%). Group 1 had the lowest complication rate
(6%).
Conclusions Our
study suggests an increased long-term risk associated with the diagnosis of PMI.
In addition, we have demonstrated that intermediate elevations of TT appear to
be associated with adverse cardiac outcome. The results suggest that TT may
provide a useful tool for identifying patients at higher long-term risk of
cardiovascular complications.
Can a small liver
transplant unit achieve good outcomes? The New Zealand Liver Transplant Unit
Experience. S Nicolson, Y Young, C Nixon. Department of Anaesthesia, Auckland
Hospital, Auckland.
Aims As orthotopic
liver transplantation (OLT) becomes a more widely performed procedure, questions
have been raised regarding the ability of smaller units to maintain quality
outcomes. We discuss the New Zealand Liver Transplant Unit (NZLTU) experience
and our approach to this problem. We present the outcomes achieved for liver
transplantation at Auckland Hospital in comparison with other liver
transplantation centres.
Methods A review of
the prospectively collected data from the NZLTU patient database from
commencement of OLT in New Zealand in February 1998 to June 2002.
Results A total of
125 liver transplants were performed to June 2002. These include four paediatric
transplants and 11 for fulminant hepatic failure. Over the four years our annual
transplant rate has increased from 13 to 36. Thirty-day mortality is 0.8% and
one-year survival is 92%, both of which figures are similar to those reported
from large international centres and the UNOS and ELTR databases.
Indications for OLT were hepatitis B (32 patients),
hepatitis C (20), primary sclerosing cholangitis (12), fulminant hepatic failure
(11), primary biliary cirrhosis (9), alcoholic liver disease (10), combined
heart-liver transplant (1) and other (30).
Eighty one patients are European, 16 Maori, 13 Polynesian,
and 15 other. Mean transfusion volumes were RBC 2198 ml, FFP 3035 ml, platelet
567 ml and cryoprecipitate 97 ml.
Critical events included line problems 4%, peri-operative
myocardial infarction 0.8%, pulmonary hypertension 2.4%, and arrhythmia 9%.There
is no evidence of a learning curve.
Conclusions With a
population of 3.6 million in New Zealand the anticipated requirement for liver
transplantation equates to 36 adults and six children per annum, putting the
NZLTU at the lower end of international unit size. Despite this, the NZLTU has
acceptable rates of morbidity and mortality.
Aortic aneurysm surgery at
Auckland Hospital. N MacLennan, K English. Department of Anaesthesia, Auckland
Hospital, Auckland.
Aims Aortic aneurysm
surgery is associated with significant morbidity and mortality. The aims of this
study were to examine the outcome of aortic aneurysm surgery at Auckland
Hospital and to identify any factors associated with adverse outcome. As cardiac
complications are the most common cause of death we specifically examined the
rate of peri-operative myocardial infarction (PMI) using troponin T
assay.
Methods All patients
undergoing abdominal aortic aneurysm (AAA) repair between 1 June 1999 and 30
September 2000 were prospectively enrolled. Data included demographic
information, comorbidities, pre-operative assessment and investigations. The
primary outcome measure was mortality. Additional outcome measures included PMI
and other peri-operative medical and surgical complications. PMI was diagnosed
when two of the following three criteria were present: a clinical event
suggestive of an MI, a troponin T level >0.1, or a new ECG change consistent
with an MI.
Results One hundred
and thirty six patients undergoing AAA repair were identified. Mortality for the
89 non-ruptured AAA patients was 5.6%. Risk factors for death included a
diagnosis of diabetes, intra-operative arrhythmia, increased post-operative
troponin T, post-operative congestive heart failure (CHF), the need for
re-operation and increased length of stay in intensive care.
Mortality for the 47 ruptured AAAs was 38%. Pre-operative
risk factors for death included a lower pre-operative Hb level, increased blood
transfusion requirements, diabetes mellitus, lower functional status (METS), and
intubation prior to arrival in theatre. Intra-operative and post-operative
factors associated with death included increased medical and surgical
complications. PMI was diagnosed in 24% of cases. Risk factors included
diabetes, use of dopamine, coagulopathy, increased number of operations,
post-operative CHF, and increased length of stay.
Conclusions Outcome
from AAA surgery in our institution is comparable with results from other
published series. However, the rate of PMI is significantly higher than
previously reported and reflects the increased sensitivity of the troponin assay
in diagnosing myocardial damage.
Redefining environmental
gas exposure: end tidal sampling of anaesthetists' breath. S
Burrows,1 R French,1
R Allardyce,2 M
McEwan,3 P
Wilson.3
1Christchurch Hospital;
2Christchurch School of Medicine;
3University of Canterbury,
Christchurch.
Background
Environmental standards for trace gas exposure in operating theatres measure
ambient gas concentrations by sampling the room air. This can be done by either
single-point measure or a timed-exposure measure. These methods have the
disadvantage of being difficult to translate into the implications for an
individual’s peak exposure.
Aim This study aimed
to assess the feasibility of end tidal gas sampling of anaesthetists’
breath during gaseous induction of anaesthesia at Christchurch
Hospital.
Methods The breath
samples were obtained by asking anaesthetists to blow the second half of a tidal
breath into a mylar gas collection bag. Samples were collected prior to and
after a gaseous induction by the anaesthetist under test. The samples were
analysed for sevoflurane concentration using a selective ion flow tube (SIFT)
mass spectrometer and for CO2 using infrared
spectrometry. This study is ongoing and data from the first 12 samples are
presented
Results The range of
pCO2 found was 31 to 42 mmHg. The peak
sevoflurane concentration found post-induction was 58 parts per million (OSH
limit = 2 ppm).
Discussion The
technique appeared reliable in returning samples containing a high proportion of
alveolar gas, as judged by CO2 content. The
measurement of CO2 allows the sevoflurane
concentration to be normalised to allow for variations in sampling technique.
This method of exposure testing may have advantages when trying to assess
single-point exposure of anaesthetists to trace gas concentrations.
A graphical trend display
leads to more rapid detection of changes. R
Kennedy,1 A
Merry,2 N
Mann.2
1Christchurch Hospital, Christchurch;
2Greenlane Hospital, Auckland.
Background
Anaesthesia involves the processing of large amounts of information. Typically
anaesthesia data are stable, with noise, but the underlying trend may change.
One task of the anaesthetist is to detect changes promptly and reliably. One
manner of presenting data in a way that may help detection of change is to
include the history of the parameter. This can be done in a variety of ways
including a graphical trend display. Although many ‘know’ that a
trend display helps detection of changes this has not been conclusively
demonstrated. The aim of this study was to examine the effect of the presence of
a graphical trend on the speed of detection of changes in simulated
data.
Methods Ten
anaesthetists each viewed 30 simulations with 4 parameters displayed. In a
random 50% of the simulations the current values only of the parameters were
displayed, while in the remainder the history of the parameters were graphed
against time. A computer model generated values for the parameters which, after
a period of stability, changed to a new random value that was at least 10 units
away from the initial value. The time constant for the change was a random
number with a rectangular distribution between three and ten minutes. Parameters
were updated at one-second intervals.
Subjects were asked to indicate when they thought a
‘significant change’ was occurring. A separate, clearly marked key
was used for each parameter and direction of change. The time between the onset
of the change and its detection was recorded. Pooled means and standard
deviations were calculated and compared using a paired t-test.
Results Data from
one subject were incomplete and were not included in the analysis. All subjects
detected changes faster with a trend display (mean delay 13.1 cycles, SD 1.9
cycles) than without (mean 15.3, SD 2.0), p = 0.002. Changes were detected
slightly more accurately without the trend display (47.7 (SD 3.1) vs 44.7 (SD
3.3)) but this difference was not statistically significant.
Conclusions In this
model a graphical display of the history of a parameter led to significantly
faster detection of changes but had no significant effect on the accuracy of
detection. The evaluation system was a useful tool and further studies are
planned.
This article was corrected
26 September 2003, to reflect the Erratum, NZ Med J 2003;116(1182): URL:
http://www.nzma.org.nz/journal/116-1182/619/
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