Syncope
BASICS
Definition: Transient loss of consciousness (LOC) with unresponsiveness and loss of postural tone, followed by spontaneous, rapid, and complete recovery. Usually brief, caused by cerebral hypoperfusion.
Systems affected: Cardiovascular, nervous
EPIDEMIOLOGY
Prevalence:
20–35% of adults experience ≥1 episode
15% of children <18 years
Institutionalized elderly (>75 yrs): 23%
ETIOLOGY AND PATHOPHYSIOLOGY
Mechanism: Systemic hypotension → ↓ cardiac output and/or systemic vasodilation → ↓ cerebral perfusion
Cardiac causes:
Arrhythmias
Obstruction to outflow (PE, hypertrophic cardiomyopathy, aortic stenosis)
Non-cardiac causes:
Reflex-mediated vasovagal (neurally mediated syncope/NMS): inappropriate vasodilation (most common in adults/children); situational (micturition, defecation, cough, pain, emotion, hair combing)
Orthostatic hypotension (OHT): volume depletion, pregnancy, anemia, meds
Drug/alcohol induced
Primary autonomic failure (pure autonomic failure, Parkinson)
Secondary autonomic failure (diabetes, amyloidosis)
Carotid sinus hypersensitivity
Pediatric: Vast majority are benign, due to vasomotor tone alteration
RISK FACTORS
Heart disease (acquired/structural)
Dehydration
Medications (antihypertensives, antiarrhythmics, diuretics)
Primary autonomic degenerative disorders
DIAGNOSIS
HISTORY
Careful history, exam, ECG most important
Differentiate from vertigo, seizure, falls without LOC
Typical syncope: rapid onset, brief (<60 sec), rapid & complete recovery
Circumstances: prolonged standing, urination, coughing, postprandial, emotion (NMS); neck movement (carotid sinus); exertion (cardiac)
Prodromal symptoms: (NMS)
Elderly: often no prodrome
Palpitations/chest pain/dyspnea: (cardiac)
Position: supine (arrhythmia), erect (NMS), transition (OHT)
Delayed recovery: neurologic (postictal)
Family history: Long QT, Brugada, VT, hypertrophic cardiomyopathy, sudden cardiac death <50 yrs
High-risk: new chest pain, breathlessness, abdominal pain, headache, exertional or supine syncope, sudden palpitations with syncope
PHYSICAL EXAM
Orthostatic BP & pulse: drop in SBP ≥20 mmHg or DBP ≥10 mmHg (OHT)
Cardiac murmur or focal neuro abnormality
High-risk: unexplained SBP <90, GI bleed, bradycardia <40 bpm, new systolic murmur
DIFFERENTIAL DIAGNOSIS
Drop attacks
Vertigo
Seizure disorder; TIA/stroke
Psychiatric (conversion, somatization—no autonomic/hemodynamic changes)
DIAGNOSTIC TESTS
Initial:
ECG (arrhythmia, ischemia, block, QTc, preexcitation)
CBC, electrolytes, BUN, Cr, glucose, BNP, cardiac enzymes, D-dimer, urine pregnancy, drug screen as indicated
Imaging if PE/MI suspected
Follow-up (history/physical guided):
Exercise stress test (exertional syncope)
Echocardiogram (ischemic/valvular/congenital suspicion)
ECG monitoring (Holter, event, implantable loop recorder)
Head imaging, carotid US, EEG only if neuro cause suspected
Tilt-table test (vasovagal syncope)—limited reproducibility, high false positives
Psychiatric eval if psychogenic
TREATMENT
GENERAL MEASURES
Hydration, normal salt intake, premonitory sign education
Most pediatric cases: nonpharmacologic only
NMS: reassurance, behavior modification
Admit elderly/new heart disease/possible cardiac etiology
Young/healthy: outpatient workup
Treat documented, symptomatic arrhythmias; no need to treat asymptomatic arrhythmias
MEDICATION
First Line: (for recurrent NMS/OHT)
Fludrocortisone (mineralocorticoid)
Midodrine (α-agonist)
Droxidopa (norepinephrine precursor)
Second Line:
SSRIs (paroxetine, sertraline, fluoxetine)
Disopyramide (vagolytic)
Pyridostigmine (AChE inhibitor)
ADDITIONAL THERAPIES
Counterpressure maneuvers, exercise (improve vasovagal syncope)
Head-up tilt sleeping, abdominal binders/support stockings, increase fluid/salt for recurrent NMS
SURGERY/PROCEDURES
ICD placement: High-risk cardiac syncope (long QT, Brugada, VT, HCM)
Pacemaker: 2nd (Mobitz II) or 3rd-degree heart block, high risk for 3rd-degree block, sinus node recovery time ≥3 sec
ADMISSION/INPATIENT
Use risk prediction tools (e.g., ROSE rule)
Admit for serious comorbidities or high-risk features
ONGOING CARE
Frequent follow-up for cardiac/arrhythmic causes
Home video (smartphone) for recurrent/unknown episodes
Rare to find cause on follow-up if initial workup negative
DIET
No specific restriction unless cardiac/NMS; consider increased salt/fluid for NMS
PATIENT EDUCATION
Most cardiac causes are treatable; noncardiac generally have excellent prognosis
Teach avoidance of triggers, preventative maneuvers, and position changes
Advise about driving restrictions during evaluation per local laws
PROGNOSIS
80% have no recurrence
Prognosis worse with cardiac etiology or significant comorbidity
COMPLICATIONS
Traumatic injury from falls
REFERENCES
Shen WK, Sheldon RS, Benditt DG, et al. 2017 ACC/AHA/HRS guideline for syncope. Circulation. 2017;136(5):e60-e122.
Brignole M, Moya A, de Lange FJ, et al. 2018 ESC guidelines for syncope. Eur Heart J. 2018;39(21):1883-1948.
Albassam OT, Redelmeier RJ, Shadowitz S, et al. JAMA. 2019;321(24):2448-2457.
ICD-10
CLINICAL PEARLS
Careful history and exam are keys to diagnosis
Use ECG/event recorder for arrhythmia evaluation
Vasovagal/neurocardiogenic is most common in all ages
True neurologic syncope is rare