Abdominal Aortic Aneurysm Patients Under Surveillance Clinical Trial
Official title:
The Influence of Beta-blockade on Cardiopulmonary Function Measured by Cardiopulmonary Exercise Testing
A major determinant of perioperative mortality is the inability of the heart to increase its
output in response to surgical stress. This is termed perioperative cardiac failure (PCF),
and may only be apparent postoperatively when oxygen demand is increased. The risk of
perioperative cardiac complications is the summation of the individual patient's risk and
cardiac stress related to the surgical procedure1. The functional capacity of the patient
determines their ability to support the postoperative demand of increased oxygen
consumption, and therefore of cardiac output. Exercise capacity is one of the most powerful
predictors of cardiovascular and all cause mortality2. Cardiopulmonary exercise test (CPET)
is an established investigation used, among other applications, in the preoperative
assessment of patient fitness for surgery3. CPET involves monitoring the
electrocardiographic trace and the exhaled gas mixture (particularly CO2, whose production
depends on aerobic metabolism), during incremental exercise (usually on an exercise bike),
on room air. Several parameters can be measured during CPET, including maximal systemic
oxygen delivery, the anaerobic threshold (the oxygen delivery value at which anaerobic
metabolism begins), maximum workload, and ST segment depression/elevation (as in a standard
exercise tolerance test). The cardiopulmonary "performance" during CPET has been correlated
with postoperative outcome3. Pulmonary function tests will be performed in order to assess
lung function.
It is well known that therapy with beta-blockers in patients with ischaemic heart disease
and cardiac failure reduces perioperative morbidity and mortality4-7. However, beta blockers
reduce myocardial contractility and the heart rate response to adrenergic stimulation, thus
blunting the physiological response to stress/surgery/exercise. Whilst this mechanism may
protect the heart perioperatively, it may decrease the ability of some patients to withstand
other complications. This potential decrease in "performance" has never been quantified.
There is no agreement on whether preoperative CPET should be performed on or off
beta-blockers and, at Aintree in particular, it is standard procedure to take patients off
beta-blockers prior to their CPET. Some argue that, as beta-blockade should be maintained in
the perioperative period, CPET should be performed on medications, even if these could mask
the presence significant ischaemic heart disease (a significant, modifiable, risk factor for
surgery by beta blockade), and even if it is not always possible to maintain beta-blockade
throughout the whole postoperative period. For these reasons, other clinicians prefer to
perform CPET off beta-blockers, thus, potentially, overestimating the perioperative
cardiorespiratory "performance", which may be diminished once the medications are resumed.
Patients on long-term beta blockade may develop some tolerance to the medications, so the
effect of acute and chronic beta blockade on cardiorespiratory performance may also be
different.
Aim To compare cardiopulmonary performances on and off beta blockers as objectively assessed
by cardiopulmonary exercise testing.
Study design
We propose an interventional study investigating the effects of acute and chronic
beta-blockade on cardiorespiratory performance prior to elective surgery.
We aim to recruit 64 abdominal aortic aneurysm (AAA) patients under surveillance who will
undergo 2 cardiopulmonary exercise tests to investigate the effect of beta blockade on
cardiopulmonary performance. This sample size is calculated by using a 2-tailed sample
t-test, with 90% power to detect an estimated increase of 10% in oxygen delivery (VO2) at
anaerobic threshold. We also estimated a drop-out rate of about 25% which is built into our
power calculation estimates.
Interventions
Patients on long term beta blockade will be studied to investigate the effect of chronic
beta blocker use. They will undergo two CPETs, the first on beta blockers, the second after
discontinuing their beta blocker for at least 48 hours.
Patients not on beta blockers will be studied to investigate the effect of acute beta
blockade. They will undergo two CPETs, the first off medication, the second after
commencement of beta blockade (weight adjusted, started 48 hours prior to CPET).
Potential subjects will be provided with the patient information sheet in clinic, 1-2 weeks
prior to their initial CPET. They will be given at least 1 week to consider the study in
which the investigators will follow them up via a telephone call. Informed consent to
participate in the study will be obtained at their initial (standard care) CPET.
All consenting subjects will perform exercise using electro-magnetically braked equipment
during a ramped-incremental protocol in two different occasions. Prior to the tests full
lung function tests will be performed by body plethysmography. The exercise tests will be
performed with subjects wearing nose clips and breathing through a mouthpiece throughout the
test. The initial cycling workload will be zero but will progressively increase at a rate of
10-15 Watts/min. After a resting period of 30 seconds and 2 minutes warm up subjects will
stop when they can cycle no further. All gas exchange parameters will be measured and a
metabolic cart, heart rate and oxygen saturation will be monitored at pre and post testing.
Subjects will also be asked to score their perceived breathlessness and leg fatigue using
modified Borg scores every minute during exercise, and inspiratory capacity will be measured
every minute during the exercise test.
At the end of this test, they will be given a date for the 2nd CPET and a prescription for
oral bisoprolol once daily (dose adjusted to patients body weight), to be started 48 hours
prior to the test (two doses in total). Patients will be informed of potential side effects
of the medications at this visit. This will be weight adjusted with a specific dose as
follows: 1.25 mg if patent weighs 50-75 kg, 2.5 mg if 75-100 kg and 3.75 mg if >100 kg.
Patients will then attend for the 2nd CPET, following which bisoprolol will be discontinued
or continued based on clinical indication.
If patients are already chronically on a beta blocker, they will have their first CPET while
on medication, and then will be asked to stop the medication for a period of 48 hours before
the second CPET. It is standard procedure to take the patient off beta blockers prior to
their CPET at Aintree University Hospital. Patients will be informed of potential risks of
stopping their beta blocker at their first visit. The beta blocker will be restarted or
discontinued based on clinical indication after the second CPET.
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Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Diagnostic