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Pre-excitation on the ECG – what next?
Kevin M W Leong
Specialty Registrar in Cardiology
Nicholas F Kelland
Consultant in Cardiology and Electrophysiology
Northern General Hospital
Sheffield Teaching Hospitals NHS
Herries Road S5 7AU
Introduction
Ventricular pre-excitation is a frequently encountered electrocardiogram abnormality, and is
estimated to occur in 0.1-0.2% of the population1. Many of these individuals will have no
symptoms of palpitations or documented arrhythmias. This pattern is due to the eccentric
activation of the ventricular myocardium via an atrioventricular accessory pathway (AP). The
increased risk of sudden cardiac death (SCD) is thought to be due to the rapid conduction of
atrial arrhythmias to the ventricle, via the AP, which degenerates into ventricular fibrillation
(VF)2. SCD associated with the asymptomatic ventricular pre-excitation is estimated to be
between 0.05%-0.5% a year1, and is greatest in the young due to the tendency of the AP to
conduct more slowly as we age3.
Over the years, there has been a swing in practice from invasive investigation and
prophylactic ablation to the current watchful waiting approach. Uncertainty over the absolute
risk of SCD,4,5, the poor positive predictive value of an invasive electrophysiological (EP)
study, and complications associated with catheter ablation, have made the management in
this group of patients challenging. The 2003 joint guidance from the AHA/ACC/ESC
recommended that EPS use should be restricted to individuals exhibiting ventricular preexcitation with high risk occupations (class IIA)4,5. NASPE went further giving catheter
ablation of an AP in the asymptomatic individual a class III indication6. Unsurprisingly,
current practice varies widely across European centres7.
In light of recently published guidance for young patients (aged 8-21 years) by HRS and
PACES4, we will review risk stratification through non-invasive and invasive testing
strategies, and discuss other considerations in the management of asymptomatic individuals
with pre-excitation on ECG.
Risk stratification
Non-invasive testing
The ECG or holter monitor allows one to establish if ventricular pre-excitation is persistent or
intermittent. The finding of intermittent pre-excitation indicates a long antegrade refectory
period of the AP, and therefore a low risk of SCD4. Although, very rarely rapid AP conduction
has been seen in such patients9,10. Intermittent pre-excitation does not exclude patients from
developing atrio-ventricular re-entry tachycardia (AVRT). In a long follow up study of military
aviators lasting 22 years, they found 8.3% with intermittent pre-excitation could develop
AVRT, but in contrast to 23% who had persistent pre-excitation11.
The ECG can also afford an assessment of the antegrade characteristics of the AP during
AF with pre-excitation. The shortest pre-excited RR interval (SPERRI) reflects the functional
refractory period of the AP. A SPERRI of <250 msec is more commonly seen in patients with
Wolf-Parkinson-White (WPW) syndrome (ventricular pre-excitation with symptoms) who
have experienced cardiac arrest4.
The ETT should be the next investigation for all individuals with persistent pre-excitation.
Sympathetic stimulation occurring during exercise will shorten the duration of the refractory
period of the AP. If the refractory period of the AP is reached during exercise, as manifested
by the sudden and clear loss of the delta wave, one can be reassured the AP is unable to
conduct at short RR intervals (≤250ms, equivalent to ≥ 240bpm) or when in AF. However,
one must be careful in ascertaining a true block in the AP, as delta wave appearance can
change during exercise due to the relative effects of sympathetic stimulation on AV nodal
conduction and anterograde conduction down the AP, where loss of the delta wave tends to
be gradual. Enhanced AV nodal conduction with exertion may also obscure the persistent
pre-excitation, especially via a left-sided accessory pathway4. Therefore, several leads
should be taken simultaneously and special attention should be given to the sudden
occurrence of block in the AP.
Nevertheless, ETT is a valuable non-invasive tool in identifying the individuals at low risk of
SCD. Persistence of pre-excitation during ETT in an adult prospective study showed a
sensitivity of 96% and specificity of 17% in predicting a SPERRI in AF ≤250ms, factors
associated with high risk of SCD12.
To summarise, the presence of intermittent pre-excitation on ECG or holter monitoring, or
the abrupt and clear loss of delta waves on exercise, suggest the AP cannot conduct rapidly.
These cases can be regarded as low risk, and current HRS/PACES guidance recommend
only follow up with counselling regarding symptom awareness4. In cases where there is
persistent or uncertain loss of pre-excitation with exercise, or when the patient is unable to
perform an ETT, an EP study is then considered.
Invasive testing
Invasive EP testing either involves a transesophageal atrial pacing study or an intracardiac
EP study. Either of these techniques is employed to determine:
1. anterograde accessory pathway effective refractory period (APERP) cycle length, where
the AP fails to conduct anterogradely on rapid atrial pacing
2. shortest pre-excited R-R interval (SPERRI) in spontaneous or induced atrial fibrillation.
The presence of a short functional refractory period of the AP in AF is assumed to increase
the risk of VF in these patients.
3. Inducibility of an AV reciprocating tachycardia, with and without isopreterenol
4. number of accessory connections
EP indices associated with high risk of SCD (SPERRI or APERP ≤250ms) were previously
derived from work on the WPW population4,13. In deriving similar markers of high risk in the
asymptomatic group, there have been four important studies published recently14-17.
The first was a prospective study of 212 asymptomatic adult patients with ventricular preexcitation of whom 33 became symptomatic over a 5-year period14. Those patients had a
shorter APERP at baseline (246 vs 283ms). The combination of a short APERP and
inducibility of SVT had a positive predictive value of 47% with a negative predictive value of
97% in regard to subsequent arrhythmic events (most commonly, occurrence of AVRT).
There were three initially asymptomatic patients with an APERP <200 ms and a SPERRI
<230 ms who subsequently developed VF.
In the second study, a review of clinical and invasive EP data of 184 asymptomatic children
with ventricular pre-excitation was performed over a median follow-up of 5 years15. The
study showed significantly different EP characteristics in patients who later became clinically
symptomatic (which included 3 VF arrests) when compared to those who remained
asymptomatic: APERP ≤240 msec (49% vs 17%), multiple accessory pathways (47% vs
6%), and intact retrograde conduction up the accessory pathway at baseline (84% vs 26%).
In a separate prospective clinical trial, 47 asymptomatic children with ventricular preexcitation on ECG at high risk for arrhythmias (APERP <250ms, and inducible AF or SVT)
were randomized to ablation (20 patients) or observation (27 patients)16. During the 3 years
of follow-up, 7 children in the observation group developed symptoms, 5 had SVTs and 2
had AF with rapid ventricular response. Five others in the observation group were observed
to have silent AF on ambulatory monitors and 1 died suddenly, though the rhythm was never
recorded. In the ablation group, 1 patient had a recurrence of AVRT and no deaths. Within
the control group, the authors found multiple accessory pathways conferred an increased
risk for developing these arrhythmias. Curiously, no comparison of the characteristics of the
AP was made between those with a single and multiple APs.
The fourth trial was a long term prospective follow up study of 293 asymptomatic adult
patients with ventricular pre-excitation17. All of whom had a baseline EP study, with the
primary end point being the occurrence of an arrhythmic event. During the median follow up
of 67 months, 18 adults developed AVRT, 14 developed AF and 1 had a VF arrest, though
no deaths occurred. The authors found younger age, APERP ≤250ms and inducibility of
AVRT were predictors of total arrhythmic events and potentially life-threatening arrhythmic
events, defined as arrhythmias having a SPERRI ≤250ms. Interestingly, whilst multiple APs
predicted total arrhythmic events as in the third study, it did not reach statistical significance
in predicting the occurrence of arrhythmias that had a SPERRI ≤250ms.
In terms of predicting SCD, the positive predictive value of the SPERRI to predict SCD
remains very low18, which is in part due to the very low incidence of SCD in this group. The
negative predictive value of the SPERRI >250 milliseconds is well established4,18, and the
effective refractory period of the AP may also be used for risk stratification. The inducibility of
atrioventricular re-entrant tachycardia predicts subsequent AVRTs, but not SCD, with
positive predictive values that vary widely between 0% and 70%, and a negative predictive
values >95%18.
Therefore, if the SPERRI or APERP is ≤ 250msec or if AVRT is induced, the risks/benefits
for catheter ablation should be discussed. If both these criteria were not fulfilled, deferment
of ablation, with follow up and counselling, would be considered reasonable.
Other considerations
Efficacy of catheter ablation
The efficacy of prophylactic ablation of the AP in high risk asymptomatic individuals was
studied by the Italian group of investigators in a randomised control trial19. There were no
deaths in either the ablation group (n=37) or control group (n=35), but found a larger
occurrence of arrhythmias in the control group over the ablation group (60% vs 5%; p<0.01)
at the end of the 5 year follow up period. 15 had SVTs, 4 had AF and one had a VF event in
the control group, compared to 2 patients who both had SVTs in the ablation group. No
deaths occurred at the end of the follow up period. A similar study was conducted in
children, already mentioned earlier, which similarly found that prophylactic ablation reduced
the likelihood of further arrhythmic events, and reported no deaths in contrast to the control
group which had one.
Complications of invasive EP study and catheter ablation
The low risk of SCD in adults will need to be weighed against an invasive procedure which
carries a small, but potentially serious, risk itself. These include venous thrombosis (1%),
pulmonary emboli (03-0.6%), infection (0.8%), perforation (0.5-0.7%), coronary artery injury
(0.8-1.3%), and catheter induced completer heart block (0.9%)4. These procedures may also
result in the induction of VF, even in those who are asymptomatic4.
Athletes
WPW syndrome accounted for approximately 1% of deaths in a long-term registry of sudden
death in atheletes20, although it is unknown if these were truly asymptomatic individuals.
Many cases of SCD with WPW have been associated with exercise, and therefore
assessment and risk stratification is advisable in all athletes. In the United States, consensus
from the 36th Bethesda Conference advocates risk stratification with an EP study in
asymptomatic athletes with ventricular pre-excitation only engaged in moderate to high level
competitive sports (what is considered medium to high level of sports is covered in the
conference document)21. Whilst in Europe, the European Society of Cardiology mandates
that all athletes with ventricular pre-excitation require an EP study as part of risk
stratification20.
An athlete is considered to be at high risk of SCD if there is a SPERRI <240ms in AF or
<220ms during stress or isoproterenol, multiple accessory pathways are present, or if AF is
easily inducible4,20. Ablation is generally recommended in asymptomatic athletes with preexcitation in both sets of guidelines (class IIA)20,21.
The very young and those with structural heart disease
In the first year of life, the accessory pathway loses its antegrade conduction in as many as
40% of patients, and AVRT becomes non-inducible in a similar percentage22. However,
SVTs can recur in 30% of individuals at an average age of 7-8 years23. If a WPW pattern and
tachycardia coexist in an individual beyond 5 years of age, they continue to be present more
than a decade later in more than 75% of individuals23. As such, NAPSE and PACES have
given catheter ablation in a child < 5 years of age a class III indication, and IIB for those ≥5
years22.
Children and young adults with structural heart disease are at risk for both atrial tachycardia
and AV reciprocating tachycardia, which make them prone to unfavourable haemodynamics.
Ablation may therefore be considered regardless of the antegrade characteristics of the
accessory pathway4.
Summary of HRS/PACES guidance 20124
1. Baseline ECG
a. If there is intermittent pre-excitation, patient can be followed up by Cardiology
and should be counselled for symptoms of arrhythmia
b. If there is persistent pre-excitation, patient should undergo stress testing. If
unable to perform stress testing, patient should undergo an invasive EP study
2. Exercise stress test
a. If there is abrupt and clear loss of pre-excitation, patient can be followed up
as 1a.
b. If there is persistent or unclear loss of pre-excitation, patient should undergo
invasive EP study
3. Diagnostic invasive testing
a. If SPERRI in AF is >250msec and absence of inducible SVT:
i. Patient can be followed as in 1a
ii. May consider ablation based on AP location and/or patient
characteristics
b. If SPERRI in AF is ≤250msec, discuss the risk/benefits of catheter ablation
c. If there is inducible SVT, discuss the risk/benefits of catheter ablation
Conclusion
Management of the asymptomatic child or adult currently involves the use of non-invasive
studies to identify the low risk patient. In patients not showing block in their AP during these
non-invasive tests, an EP study can determine the length of refractory period of the AP and
inducibility of SVT. If the AP has a short refractory period or arrhythmias can be induced, the
benefits and risk of an invasive catheter ablation should be based on individual
considerations such as age, gender, occupation, and athletic wishes.
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