SUMMARYSyncope is common, with a lifetime prevalence of over 40% and annual incidence of up to 6%. 1,2 At all ages, vasovagal syncope is the most frequent cause of transient loss of consciousness. For the majority of people the condition is self-limiting and does not present to medical attention. It often occurs with an identifiable, and subsequently avoidable, provocative circumstance and is usually a single event. However, in those individuals where syncope recurs, it can become life impacting.The diagnosis of vasovagal syncope is predominantly clinical, arrived at through a detailed history of the episodes, with no further investigations required. If there is uncertainty about the diagnosis, symptoms are atypical, syncope is recurrent in the absence of heart disease, or is impacting on employment or driving eligibility, head up tilt table testing can help establish a diagnosis. 3 Surprisingly, given the high prevalence of vasovagal syncope, the evidence base for treatment regimens is sparse or contradictory. The mainstay of management is conservative. A combination of explanation of the mechanism, reassurance, information on avoiding provocative circumstances, good oral fluid intake and actions to take at the onset of prodromal symptoms to minimise the frequency and severity of symptoms are advocated. 4 Physical counterpressure manoeuvres have been demonstrated to significantly reduce syncope recurrence rates. 5 Despite these measures, a proportion of patients continue to experience disabling symptoms and recurrent syncope. A range of different pharmacological agents have been investigated such as midodrine, 6 beta blockers, 7 selective serotonin re-uptake inhibitors, 8 and fludrocortisone in children, 9 mainly in small scale studies in select populations over short timeframes. The results have been inconclusive.The multi-centre Prevention of Syncope Trial 2 (POST 2) is the first randomised placebo-controlled trial of fludrocortisone in vasovagal syncope in adults. 10 The investigators recruited patients who had experienced two or more episodes of vasovagal syncope and were symptomatic with Calgary Syncope Symptom Score >=3. Exclusion criteria included hypertension, diabetes mellitus, orthostatic hypotension and previous fludrocortisone use. Subjects were randomised in a double-blind protocol to receive fludrocortisone or placebo with titration of fludrocortisone dose to a maximum of 200 mcg daily. The primary outcome was first recurrence of syncope.The intended sample size was calculated as 310 patients in order to detect a treatment effect of fludrocortisone equivalent to a clinically relevant relative risk reduction in syncope recurrence of 40%. Despite the high prevalence of vasovagal syncope, only 210 patients were recruited, at a slower than anticipated rate. A reduction in the planned sample size was possible when the combined event rate at interim analysis was higher than anticipated at 50%. Of the sample, 70% were female, median age 30 years (range 21-47). They were a symptomatic population with a me...