Objective-To assess the reproducibility of time and frequency domain v
ariables derived from the signal averaged P wave. Design-Longitudinal
within patient study. Setting-Regional cardiothoracic centre. Patients
-20 patients (10 with documented paroxysmal atrial fibrillation and 10
normal controls) were studied on three occasions to assess the reprod
ucibility of repeated signal averaged P wave recordings. Digital P wav
e recordings were made on a further 10 patients on a single occasion a
nd the recordings signal averaged twice in order to assess the reprodu
cibility of the averaging system itself in the absence of biological v
ariation. Main outcome measures-P wave duration, spatial velocity, and
energies contained in frequency bands from 20, 30, and 60-150 Hz of t
he P wave spectrum were measured after P wave specific signal averagin
g. Coefficients of reproducibility were calculated for paired signal a
veraged P waves derived by signal averaging the same digital recording
s on two separate occasions, for recordings performed in the same pati
ents immediately after each other (((back to back))) and those perform
ed one week apart. Results-System reproducibility when the same digita
l P wave recordings were signal averaged on two separate occasions was
high (< 11% for all variables). For P wave duration the coefficient o
f reproducibility was 11.4% for back to back recordings and 13.1% for
those one week apart. The reproducibility of spatial velocity and P wa
ve energy was low. Variation in P wave morphology was noted when succe
ssive P waves from the same subject were examined. If recordings with
the same P wave morphology were analysed the reproducibility of spatia
l velocity and P wave energy improved but remained significantly poore
r than that for P wave duration. Conclusions-P wave duration is reprod
ucible within subjects in the short and medium term. Frequency domain
and spatial velocity analysis are poorly reproducible, due more to spo
ntaneous variation in P wave morphology than to instability of the sig
nal averaging process. This may limit the utility of signal averaged P
wave variables other than duration for the prediction of atrial arrhy
thmia.