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Transient loss of consiousness (TLoC) Loss of postural tone Spontaneous, complete recovery
SYNCOPE
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First, confirm that there has been syncope;
Rapid onset
Short duration (secs-mins)
Complete loss of conciousness
Collapse, often to the ground
Usually results in being found on floor or slumped
No purposeful movements
Full return to baseline neurological function
No prolonged confusion or post-ictal state
No need for resuscitation or stimulation to recover
If not, then what?
Consider;
Epilepsy
Hypoglycaemia
Dissociative seizure/state
Intoxication
TIA, Basilar migraine
Cataplexy, narcolepsy
Menieres
Transient CSF obstruction
(not exhaustive)
Assess the ECG for any
high-risk features;
Next, take a detailed, structured, history
(from the patient AND any witnesses;
Consider any high-risk
features in the history;
Bradyarrhythmia
HR <40 (inappropriate for context)
Sinus pauses or arrest
Mobitz type 2 AVB
Complete AVB
Bifasicular / trifasicular block
Tachyarrhythmia
Pre-excitation (delta wave)
Frequent VEs
VT
Channelopathies
Brugada syndrome
Long/Short QT syndrome
ARVC (epsilon wave)
Structural
HCM pattern - LVH, deep “dagger like” Q waves
in lateral +/- inferior leads
Apical HCM pattern - “giant” precordial TWI
ST segment elevation
Acute ischaemia
Other features
QT alternans - indicates electrical instability
Very low voltage QRS - think pericardial
effusion/tamponade, infiltrative disease
Electrical alternans - think pericardial
effusion/tamponade
90% of patients with cardiogenic
syncope will have an abnormal ECG
Abrupt onset chest pain, radiating to the
back +/- focal neurology +/- a new murmur
Consider any high-risk
features in the exam;
New murmur (especially ESM)
+/- carotid radiation
Murmur increasing with standing / valsalva
Signs of heart failure
Hypotension (SBP <90mmHg) or hypoxia
CT
CT
without delay!
Syncope during exercise
Absence of any prodrome
Palpitations or chest pain immediately prior
Syncope with facial or head injury
Syncope whilst supine/ sleeping
Family history of young sudden cardiac
death
History of heart disease (structural or IHD)
Posture
Was the patient laying,
sitting or standing
Were they standing for
a short/prolonged time
before the LoC or did it
come on immediately
after standing?
Prodrome
No warning, prolonged
or brief warning
Lighthead/dizzy
Headache
Weakness/giddiness
Diaphoresis
Chest pain/palpitation
Visual disturbance
Nausa/vomitting
Predisposing factors
Crowded/warm space
During/after a meal
Related to fear/emotion
Intense pain
Lack of food/drink
Tight collar/shaving
shift work
Sight of blood
Preceding events
At rest
Walking
Change in posture
Exercise - during/post
Urination/ defecation
Cough/ swallow
Flashing lights
After a night out
Recent change to meds
Witness despription
Did they appear
unconcious/vacant?
Could they be roused?
Flaccidity?
Tonic-clonic
movements
Pallor, cyanosis?
Duration
Syncope typically <20
seconds, rarely >60
seconds
Seizure typically >60
seconds, often 1-2
minutes
Recovery of awareness
Quick, prolonged? Slow?
Syncope - rapid
recovery to full lucidity
Seizure - post ictal
period of confusion/
agitation lasting several
minutes to hours (often
not recalled by the
patient
Post-recovery
Fatigue?
Muscle ache?
Injury / trauma / RTC?
Retrograde amnesia?
Any rellieving factors
Chest pain?
Cerebral signs -
diplopia, dysarthria?
Check ED/EMAS notes
Other signs
Tongue biting (lateral
aspect) typical of
seizure
Urinary or faecal
incontinence more
common in seizure than
syncope
Once you have made your assessment,
consider which type is most compatible;
Reflex Syncope
Vasovagal
Situational
Carotid Sinus Hypersensitivty
Change in position, stressor, standing
Nausea, warmth, pallor, emotion/pain
triggers
Orthostatic Syncope
Drug-induced
Volume depletion
Autonomic failure
Change in position + volume loss
Dehydration, medications, haemorrhage
Primary, secondary autonomic failure
Cardiogenic Syncope
Arrhythmic
Structural
(including PE & aortic dissection)
Abrupt onset, no prodrome
Palpitation, chest pain
Related to exercise
Explore (with clinical curiosity) the patient’s;
Past medical history
Drug history
Family history
Social history - including occupation (think risk!)
Management is likely to be
lifestyle modification and
education / avoidance of
triggers.
In the instance of
autonomic failure,
specialist management is
likely to be indicated
Management more likely
to require some form of
intervention or at least
pharmacological therapy.
Must have a lower
threshold for further
investigation in this group.
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Low Risk
Classic vasovagal or orthostatic features
Prodrome: nasuea, warmth, lightheadedness
Trigger: standing, pain, emotion, micturition
Normal ECG, Age <65
No cardiac history, normal vital and exam
Discharge with safety netting
Educate on triggers and hydration
Consider fluid challenge if orthostatic
No further tests if diagnosis is clear
Follow-up if recurrent
Medium Risk
Unclear aetiology
Possible vasovagal but atypical features
Age >65
Borderline/unclear ECG abnormalities
Mild orthostatic hypotension but unclear
significance
No known structural heart disease
Consider observing on telemetry
Orthostatic vitals
Consider echocardiogram, outpatient ILR
Discharge if no recurrence, normal ECG and vitals
Consider outpatient cardiology or syncope clinic
High Risk
Syncope during exertion or while supine
No prodrome
Red flag ECG
Known heart disease or EF <20%
Family history of sudden cardiac death
Associated chest pain, dyspnoea, or trauma
Multiple episodes
Syncope during sleep
Admit for further workup
Echocardiogram, telemetry
Consider ILR as inpatient
May need MRI or other imaging to determine
aetiology, or referral on to tertiary center
Finally, consider risk and
determine management;
MUST HAVE:
Full physical exam
12-lead ECG
Full blood panel
Vitals + active stand BP test
CXR
EVERY PATIENT
EVERY PATIENT
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patient information.