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BMJ 2003;326:1073-1077 (17 May), doi:10.1136/bmj.326.7398.1073
Anthony W C Chow, consultant cardiologist1, Rebecca E Lane, research fellow2, Martin R Cowie, professor of cardiology3
1 Department of Cardiology, Royal Berkshire and Battle Hospital, Reading RG30 1AJ, 2 Department of Cardiology, St Mary's Hospital, London W2 1NY, 3 Cardiac Medicine, National Heart and Lung Institute, Faculty of Medicine, Imperial College, London SW3 6LY
Correspondence to: A W C Chow anthony.chow{at}rbbh-tr.nhs.uk
Heart failure is a sizeable problem in elderly populations, and although pharmacological treatment has improved, outcome generally remains poor. New pacing technologies have been developed to treat heart failure, with promising results
Recently, several promising new developments have taken place in pacing technology to treat selected patients with heart failure. These include atrio-biventricular pacing to correct abnormal patterns of left ventricular contraction and implantable cardiac defibrillators for treatment of malignant ventricular arrhythmias. As the scale of the problem becomes apparent new treatments that have been shown to improve morbidity and possibly mortality in patients with chronic heart failure will undoubtedly have a major impact on clinical practice and healthcare resources.
The heart failure population
In the developed world the underlying cardiac abnormality for most patients
with heart failure is impaired left ventricular systolic function due to
ischaemic heart disease or idiopathic dilated
cardiomyopathy.6
Despite maximal drug treatment many patients still experience symptoms on
minimal exertion or even at rest (New York Heart Association class III-IV),
and this functional limitation often has a marked impact on their quality of
life. Recurrent and prolonged hospital admissions for periods of
decompensation of the heart failure syndrome are common in these
patients.7 The
prognosis for people with heart failure remains poor. In clinical trials,
death is most commonly due to either malignant ventricular tachyarrhythmias or
progressive pump failure. Population based studies report a mortality of close
to 40% within one year of diagnosis and around 10% per year
thereafter.7 For
patients who remain symptomatic at rest despite maximal medical treatment
annual mortality may be as high as
40%.8
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Ventricular dyssynchrony
An estimated 30% of patients with chronic heart failure have evidence of
abnormal interventricular conduction on the 12 lead electrocardiogram, most
often in the form of left bundle branch block. The resultant abnormal
activation of the myocardium causes deranged ventricular contraction or
dyssynchrony, with regions of early and late contraction. Typically, the
interventricular septum contracts early relative to the delayed contraction of
the lateral free wall of the left ventricle. In its most severe form
dyssynchrony can result in contraction of the septum while the lateral wall is
relaxing and vice versa. If opposing ventricular walls fail to contract
together, a sizeable proportion of blood is simply shifted in the ventricular
cavity instead of being ejected into the circulation, thereby reducing cardiac
output. The proportion of the cardiac cycle available for left ventricular
filling and ejection is reduced by dyssynchronous contraction, which further
contributes to a decrease in the pumping ability of the heart. Even in
structurally normal hearts the presence of left bundle branch block impairs
cardiac ejection fraction. In patients with chronic heart failure and poor
systolic function ventricular dyssynchrony further compromises cardiac
performance and may exacerbate symptoms of heart failure.
Pacing for the treatment of heart failure
Permanent pacing has been used for many years to treat symptomatic
bradycardia and may alleviate heart failure when associated with heart block.
Several studies have examined the use of conventional dual chamber atrio-right
ventricular pacing for the treatment of heart failure, in the absence of
symptomatic bradycardia or heart block, in an attempt to enhance cardiac
performance, but results have been
inconsistent.9
10 In most studies,
right ventricular pacing produced no haemodynamic benefit or had detrimental
effects on left ventricular function. This probably reflects the fact that
right ventricular apical pacing (which creates a left bundle branch block
pattern) induces ventricular dyssynchrony, with detrimental effects on overall
pump function of the heart. Many centres now advocate pacing from the right
ventricular septum to provide a more physiological pattern of ventricular
activation. With a greater understanding of the consequences of deranged
ventricular conduction came the proposal of using more sophisticated pacing
configurations in an attempt to correct or normalise electrical activation and
improve cardiac performance. This has evolved to form the basis of the
concepts for cardiac resynchronisation.
Cardiac resynchronisation
Cardiac resynchronisation or biventricular pacing entails inserting pacing
leads via the cephalic or subclavian veins into the right atrium and right
ventricle, as in conventional dual chamber permanent pacing. In addition,
however, a third pacing lead is used to pace the left ventricle. In early
studies this was achieved by performing a thoracoscopic procedure with
placement of the electrode on the epicardial left ventricular free
wall.11
12 This necessitated
general anaesthesia and therefore carried appreciable risk in a high risk
group of patients. In 1998 Daubert et al published the results of a study of a
fully transvenous permanent biventricular pacing
system,13 which
revolutionised the technique (fig
1). Specially designed catheters are inserted through the
subclavian vein and passed down into the right atrium, from where the left
ventricular coronary venous circulation can be accessed. The coronary venous
system consists of a series of tributaries overlying the ventricular
myocardium. They drain into the coronary sinus that opens into the right
atrium. This network of coronary venous branches can be visualised by
performing a coronary sinus venogram (fig
2) and used to guide the placement of the left ventricular pacing
lead. The three pacing electrodes are then connected to the artificial
pacemaker to allow biventricular pacing
(fig 3).
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Effects of biventricular pacing
Biventricular pacing aims to restore synchronous cardiac contraction.
Studies have shown that when ventricular dyssynchrony is reduced the heart is
able to contract more efficiently and increase left ventricular ejection
fraction and cardiac output while working less and consuming less
oxygen.14 In
addition, reintroducing left ventricular synchrony can increase left
ventricular filling times, decrease pressure on the pulmonary capillary wedge,
and reduce mitral regurgitation (box 1). More advanced devices now enable
manipulation of both atrioventricular and interventricular pacing intervals
and the potential to further optimise individual haemodynamic and functional
improvement.
Clinical trials of biventricular pacing
Clinical trials have shown that biventricular pacing is effective in the
treatment of heart failure patients with left bundle branch block
(table). Several randomised
controlled clinical trials have compared biventricular pacing with medical
treatment on its own. Both the multisite stimulation in cardiomyopathies
(MUSTIC) and the multicentre insync randomised clinical evaluation (MIRACLE)
studies, which enrolled 68 and 524 heart failure patients, respectively, in a
randomised crossover trial of biventricular pacing showed significant
improvements in quality of life scores, exercise tolerance, New York Heart
Association functional class, peak oxygen uptake, and cardiac ejection
fraction during biventricular
pacing.15
16 What was particularly
impressive was the reduction in admissions to hospital for worsening heart
failure seen in the MIRACLE study. At six months the relative risk of
decompensated heart failure requiring admission to hospital was reduced by 50%
in the group receiving biventricular pacing, and a staggering 77% reduction of
total hospital days saved for treating heart failure was observed in the paced
group compared with the control group. As the clinical trial lasted only six
months it is still uncertain whether the benefits of biventricular pacing will
be sustained or increased with a longer period of follow up. Thus the benefits
seen with biventricular pacing not only seem to improve the quality of life
for individual patients but also indicate that important and substantial
economic savings may arise from using this technology.
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As yet no definitive published data are available on the effects of biventricular pacing on mortality, but several studies with end points of cardiac and all cause mortality remain in progress.17 18 The cardiac resynchronisation in heart failure (CARE-HF) study has recently completed recruitment of patients, whereas the preliminary findings of the comparison of medical treatment, pacing, and defibrillation in chronic heart failure (COMPANION) study, which randomised over 1600 patients to medical treatment alone, to biventricular pacing, and to biventricular implantable cardiac defibrillators have been announced. This study was halted prematurely because of a 20% reduction in all cause mortality and all cause admissions to hospital in the groups receiving biventricular pacing. The most notable benefits were seen in the arm of the study in which patients received biventricular implantable cardiac defibrillators, where a 40% reduction of all cause mortality was achieved. Publication of the full report is eagerly awaited, but these preliminary data indicate that biventricular pacing may confer important mortality benefits.
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Limitations and complications of biventricular pacing
The electrocardiogram is used as the screening tool for predicting
ventricular dyssynchrony and hence suit-ability for biventricular pacing. Up
to 20% of patients fulfil the criteria for biventricular pacing (box 2), yet
derive little or no clinical benefit from
resynchronisation.19
In the future, more sensitive and specific non-invasive screening tests will
be required to improve the selection of patients. This will probably be in the
form of echocardiography guided techniques such as tissue Doppler
echocardiography, which facilitates the quantification of
dyssynchrony20 and
thus may provide more accurate prediction of a favourable clinical response
with biventricular pacing.
Even with improvements in delivery systems and pacing lead technology the site of left ventricular pacing is often limited by the individual's coronary venous anatomy. Implantation of ventricular pace-makers can be technically challenging and is associated with small risks. Inability to deploy the left ventricular lead accounts for most of the 8% reported implant failures.16 Commonly encountered complications over and above those associated with any permanent pace-maker insertion are usually related to the insertion of the left ventricular lead. These include inability to intubate the coronary sinus or a venous tributary, dissection of the coronary sinus, displacement of the left ventricular lead, and diaphragmatic stimulation (box 3). Complications are largely minimised by the operator's experience, meticulous technique, stringent testing at implantation, and careful programming of the pacemaker at follow up.
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Implantable cardioverter defibrillators
Severe left ventricular dysfunction is now known to be an independent
predictor of cardiac mortality. Death is usually attributable to progressive
heart failure or the development of malignant ventricular arrhythmias. Several
large randomised controlled trials have found a sizeable reduction in
mortality among patients with ischaemic heart disease, impaired left
ventricular function, and failed sudden death or evidence of ventricular
arrhythmias who had an implantable cardiac defibrillator compared with
patients treated with antiarrhythmic
drugs.21
22 This compelling
evidence has formed the basis for guidance from the National Institute for
Clinical Evidence (NICE) on widespread use of these devices in individuals at
high risk.23 The
role of implantable cardiac defibrillators in patients with non-ischaemic
cardiomyopathy is less certain but should be addressed by the ongoing sudden
cardiac death in heart failure trial, which includes patients with both
ischaemic and non-ischaemic cardiomyopathy. In the most recently published
multicentre automatic defi-brillator implantation II (MADIT II)
trial,24 no formal
assessment of arrhythmic risk was required; the inclusion criteria were based
on the presence of ischaemic heart disease and poor left ventricular function
alone. The trial was stopped early because of a relative risk reduction of 31%
in all cause mortality seen in the group treated with implantable cardiac
defibrillators compared with controls over a 20 month follow up period. The
implications of this trial alone may expand the recommended indications for
implantation of these devices in the future.
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In the light of trials showing a reduction in mortality with implantable cardiac defibrillators and improvement in left ventricular function with biventricular pacing in patients with heart failure it seems logical that combined biventricular pacing and implantable cardiac defibrillators devices may be complementary in selected patients. The early indications from the COMPANION trial support this theory, with the greatest reduction in mortality observed with combined devices. Although final reports are yet to be published on prospective trials incorporating combined biventricular pacing and implantable cardiac defibrillators devices, the use of combined devices to provide both cardiac resynchronisation with defibrillation are likely to increase.
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