How long do we need to monitor patients after an episode of
syncope? What a great question…
These authors used data that came from a large multicentre
study that developed the Canadian Syncope Risk Score (CSRS). They enrolled
consecutive adult patients who presented within 24 hours of a simple syncopal
episode.
They collected data on baseline characteristics and were eventually
able to risk stratify patients by using their newly derived syncope score into low,
intermediate and high-risk groups.
The primary outcome was serious arrhythmic
conditions (arrhythmias, interventions for arrhythmias, and unexplained
death) over 30 days.
The 30 day follow up was a tremendous undertaking.
They had structured review of all available medical records, subsequent visits,
hospitalisations, and deaths. They performed a scripted telephone follow up at
30 days and they looked at administrative records for subsequent visits.
A whopping 5581 patients were analysed. As expected, only
a small number 7.5% had serious outcomes. The syncope score seemed to work
pretty well. The low risk group had 0.4% 30-day arrhythmic outcomes.
The intermediate and high risk were 8% and 25%
respectively.
The authors state that one-half of arrhythmic events were
identified within 2 hours of ED arrival in low risk patients and
within 6 hours in the intermediate and high-risk patients.
Based on this, the authors suggest either 2 or 6 hours of cardiac monitoring is enough after syncope but outpatient cardiac monitoring for 15 days in higher
risk patients.
There were a few problems…
Only 11% of the patients were hospitalised and the median
ED length of stay was only 4 hours. It is no surprise that they found half
of the events early on when they were actually looking. It is quite possible
that many events were missed when the patients were not being monitored at
home. However, they should have at least they should have picked up on
mortality.
Remember the extraordinary work they did in assessing the 30-day
outcomes? Unfortunately, quality of data is often inversely proportional to
the effort and complexity in obtaining it. In other words, they may have
been making conclusions based on bad data. It’s hard to know.
There have been several attempts at creating a clinical
decision instrument for syncope. Unfortunately, these instruments don’t tend to
work in complex disease processes. The CSRS has not been externally
validated nor compared to clinician gestalt.
What’s the take home point?
From an evidence-based medicine standpoint, I don’t
believe this single study is enough to justifiably change practice. But in
our hearts, we all know that low risk patients probably don’t need to be watched
very long… and high-risk patients need to be monitored longer. 2 or 6 hours? Who
knows…
Covering
Thiruganasambandamooooorhylinglangadong, V, Rowe B, Sivilotti
M, et al. Duration of Electrocardiographic Monitoring in Emergency Department Patients
with Syncope. Circulation 2019;139:1396-1406. [link to article]
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