Circulation. 2008;118:1-2
doi: 10.1161/CIRCULATIONAHA.108.189733
(Circulation. 2008;118:1-2.)
© 2008 American Heart Association, Inc.
Clinical Summaries
An extract of the first 250 words of the full text is provided, because this article has no abstract.
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Role of Conduction Velocity Restitution and Short-Term Memory in the Development of Action Potential Duration Alternans in Isolated Rabbit Hearts
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T-wave alternans often are a precursor to ventricular fibrillation
and thus sudden cardiac death. It has been suggested that spatially
discordant alternans (SDA) of action potential duration may
lead to T-wave alternans, but the underlying mechanisms of SDA
development are not clear. Previous studies have proposed preexisting
action potential duration heterogeneities and steep dependence
of conduction velocity in the myocardium on the preceding diastolic
interval as possible causes of SDA. Our experiments demonstrate
that a new mechanism associated with pacing history, ie, short-term
memory, might also underlie SDA formation in the heart. In addition,
we show that the heterogeneity of action potential duration
does not necessarily correlate with the onset of alternans.
Our findings have significant clinical relevance because they
suggest that new dynamic factors such as the rate at which the
heart muscle is paced also may play a role in the development
of SDA and subsequently ventricular fibrillation. This suggests
that cardiac memory needs to be considered an additional factor
that can contribute to arrhythmia initiation. Ultimately, our
findings can be used to define a new paradigm in the clinic
for testing arrhythmia inducibility and need to be considered
in the design of antiarrhythmic drugs. See p 17.
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Gender and Outcome in Adult Congenital Heart Disease
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Gender differences in prognosis have frequently been reported
in cardiovascular disease but less so in adult congenital heart
disease. In the CONgenital CORvitia (CONCOR) national registry
of adults with congenital heart disease (n=7414), we found that
women had a 33% higher risk of pulmonary hypertension, a 33%
lower risk
. . . [Full Text of this Article]
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