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LETTER TO THE EDITOR
Size of patent foramen ovale and
amount of microembolic signals in
patients with ischaemic stroke
V. K. Sharma
Division of Neurology, National University
Hospital, Singapore
Correspondence: Dr Vijay Sharma,
Division of Neurology, Department of
Medicine, National University Hospital,
119074 Singapore (tel.: +65 67722597;
fax: +65 68723566;
e-mail: [email protected]).
Keywords: acute ischaemic stroke,
patent foramen ovale, transcranial
Doppler
Received 7 October 2008
Accepted 20 October 2008
Sir,
I read with interest the article by Telman
et al. [1] regarding the relationship be-
tween size of patent foramen ovale (PFO)
and the number of microembolic signals
(MES) in ischaemic stroke patients.
Their findings are important in under-
standing aetiopathogenic role played by
PFO.
Trans-oesophageal echocardiography
(TEE) employed to diagnose and estimate
the size of PFO, is poorly tolerated and
the sedation limits patients� ability for
performing adequate valsalva maneuver.
Authors [1] should be congratulated to
overcome these limitations by comple-
menting TEE with transcranial Doppler
(TCD). There are certain important issues
related to the TCD performance and
interpretation.
First, mere detection of PFO does not
delineate its true aetiological role and
�functional-potential�. TCD is considered
as more sensitive and specific than TEE
for PFO detection [2] as well as quantify-
ing its �functional-potential [3]�. Using
power M-mode TCD enhances the sensi-
tivity, because of its overlapping and
contiguous multiple gates [4]. Secondly,
patient�s position during PFO testing sig-
nificantly affects the results. MES being
lighter have an inherent tendency to rise
up due to buoyancy, therefore, echocar-
diography traditionally performed in the
left-lateral position provides a physiolog-
ically unreasonable travel path for MES,
from the physically �higher� right-atriuminto the �lower� left-atrium-defying the
well-established principles of physics!
TCD can be performed in any anatomic
position and we have previously demon-
strated that the �functional-grading� ofPFO varies with different body positions,
with larger number of MES detected in
the sitting position [5]. Probably, these
methodological factors have contributed
to some of the discrepancies between the
size of PFO on TEE with the number of
microemboli observed on TCD [1]. De-
spite the statistical significance, this is
clearly evidenced even in this study [1] –
six of 22 patients with multiple emboli
(>48) had small and 10/22 had moderate-
sized PFO instead of the �expected� large-sized PFO. As rightly mentioned by
authors [1], this discrepancy could be
avoided by performing TEE and TCD
simultaneously.
In conclusion, relationship between the
size of PFO and its functional-potential is
not linear. While TEE may be performed
to detect the presence, location and size of
PFO, TCD should be employed to deter-
mine its functional-grade. The latter may
assume important logical proportions, if
closure of PFO is indicated.
References
1. Telman G, Yalonetsky S, Kouperberg E,
Sprecher E, Lorber A, Yarnitsky D. Size of
PFO and amount of microembolic signals in
patients with ischaemic stroke or TIA.
European Journal of Neurology 2008; 15:
969–972.
2. Jauss M, Kaps M, Keberle M, Haberbosch
W, Dorndorf W. A comparison of trans-
esophageal echocardiography and transcra-
nial Doppler sonography with contrast
medium in the detection of patent foramen
ovale. Stroke 1994; 25: 1265–1267.
3. Belvis R, Leta RG, Marti-Fabregas J, et al.
Almost perfect concordance between simul-
taneous transcranial Doppler and trans-
esophageal echocardiography in the
quantification of right-to-left shunts. Jour-
nal of Neuroimaging 2006; 16: 133–138.
4. MoehringMA, Spencer MP. PowerM-mode
Doppler (PMD) for observing cerebral
blood flow and tracking emboli. Ultrasound
in Medicine and Biology 2002; 28: 49–57.
5. Lao AY, Sharma VK, Tsivgoulis G, Malk-
off MD, Alexandrov AV, Frey JL. Effect of
body positioning during transcranial
Doppler detection of right-to-left shunts.
European Journal of Neurology 2007; 14:
1035–1039.
e12� 2008 The Author(s)
Journal compilation � 2008 EFNS
European Journal of Neurology 2009, 16: e12 doi:10.1111/j.1468-1331.2008.02403.x