Key result
Review summarizes guidelines for the diagnosis, risk stratification, and management of presumed arrhythmic syncope.
Why the study?
Syncope encompasses etiologies ranging from benign conditions to high-risk diseases carrying sudden death risk, making the identification of patients with potentially severe cardiac causes crucial.
This review summarizes current guidelines and approaches for the diagnosis, risk stratification, and management of arrhythmic syncope.
Offers clinicians a synthesized guide to arrhythmic syncope management; leaves open the need for prospective validation of recommendations.
Syncope is a concerning symptom that affects a large proportion of patients. It can be related to a heterogeneous group of pathologies ranging from trivial causes to diseases with a high risk of sudden death. However, benign causes are the most frequent, and identifying high-risk patients with potentially severe etiologies is crucial to establish an accurate diagnosis, initiate effective therapy, and alter the prognosis. The term cardiac syncope refers to those episodes where the cause of the cerebral hypoperfusion is directly related to a cardiac disorder, while arrhythmic syncope is cardiac syncope specifically due to rhythm disorders. Indeed, arrhythmias are the most common cause of cardiac syncope. Both bradyarrhythmia and tachyarrhythmia can cause a sudden decrease in cardiac output and produce syncope. In this review, we summarized the main guidelines in the management of patients with syncope of presumed arrhythmic origin. Therefore, we presented a thorough approach to syncope work-up through different tests depending on the clinical characteristics of the patients, risk stratification, and the management of syncope in different scenarios such as structural heart disease and channelopathies.
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Francisco‐Pascual et al. (2023) conducted a review in Arrhythmic syncope. Diagnostic and management guidelines was evaluated. This review summarizes the main guidelines for the diagnostic work-up, risk stratification, and management of patients with syncope of presumed arrhythmic origin.
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