Ks. Spargias et al., QT dispersion as a predictor of long-term mortality in patients with acutemyocardial infarction and clinical evidence of heart failure, EUR HEART J, 20(16), 1999, pp. 1158-1165
Background QT interval dispersion is a marker of inhomogeneous ventricular
repolarization, and therefore has the potential to predict re-entry arrhyth
mias. Following acute myocardial infarction, increased QT dispersion has be
en associated with a higher risk of ventricular arrhythmias. However, wheth
er or not QT dispersion predicts prognosis post-acute myocardial infarction
is not clear. We addressed this issue by analysing the AIREX study registr
y.
Methods AIREX was a follow-up study of 603 post-acute myocardial infarction
patients who exhibited clinical signs of heart failure and were randomly a
llocated to ramipril or placebo. An interpretable 12-lead ECG obtained betw
een day 0 and day 9 after the index infarction (median time 2 days) was ava
ilable in 501 patients. We examined whether QT dispersion was a predictor o
f all-cause mortality in the AIREX study registry (mean follow-up 6 years).
Results QT dispersion measurements were significantly increased in patients
who subsequently died (QT dispersion: 92.0 +/- 38.5ms vs 82.7 +/- 34.3ms,
P=0.005; rate corrected QT dispersion: 105.7 +/- 427 ms vs 93.1 +/- 35.9 ms
, P<0001). Univariate analysis showed that QT dispersion was a predictor of
all-cause mortality risk (QT dispersion: hazard ratio per 10ms 1.05, [95%
CI 1.02 to 1.09], P=0.004; rate corrected QT dispersion: 1.07 [1.03 to 1.10
], P<0001); an increase of 10 ms added a 5-7% relative risk of death. QT di
spersion remained an independent predictor of all-cause mortality risk on m
ultivariate analysis (QT dispersion: 1.05 [1.01 to 1.09], P=0.027; rate cor
rected QT dispersion: 1.05 [1.01 to 1.09], P=0.022).
Conclusion QT dispersion, measured from a routine 12-lead ECG following acu
te myocardial infarction complicated by heart failure provides independent
information regarding the probability of long-term survival. However, the l
ow sensitivity of this electrocardiographic marker limits its usefulness fo
r risk stratification if used in isolation.