Swallow Syncope: Difference between revisions

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Swallow syncope incorporates two separate conditions:  
Swallow syncope incorporates two separate conditions:  
# a pharyngeal form which is usually associated with pain (“syncopal glossopharyneal neuralgia”)
# a pharyngeal form which is usually associated with pain (“syncopal glossopharyneal neuralgia”)
# an oesophageal variety, also known as “oesophageal” or “deglutition syncope” (fig. 7)(Basker & Cooper, 2000).  
# an oesophageal variety, also known as “oesophageal” or “deglutition syncope” (fig. 7)<cite>Basker</cite>.  


The first isolated case description dates to 1906 (Mackenzie, 1906). Based on the fact that up to date there are only about sixty single cases reported (DEUCHAR & TROUNCE, 1960;Basker & Cooper, 2000), swallow syncope is probably rare.
The first isolated case description dates to 1906 (Mackenzie, 1906). Based on the fact that up to date there are only about sixty single cases reported (DEUCHAR & TROUNCE, 1960;Basker & Cooper, 2000), swallow syncope is probably rare.
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# Secondly, if feasible, modification of antihypertensive drugs should be considered.  
# Secondly, if feasible, modification of antihypertensive drugs should be considered.  
Surgical or pharmacological destruction of (the oesophageal branches of) the vagus nerve has shown not to be successful. Based on predominantly positive therapeutic response in over a dozen cases, the treatment of choice of oesophageal syncope is insertion of a cardiac demand pacemaker (Basker & Cooper, 2000). Management of persisting neuralgia is symptomatic.
Surgical or pharmacological destruction of (the oesophageal branches of) the vagus nerve has shown not to be successful. Based on predominantly positive therapeutic response in over a dozen cases, the treatment of choice of oesophageal syncope is insertion of a cardiac demand pacemaker (Basker & Cooper, 2000). Management of persisting neuralgia is symptomatic.
==References==
<biblio>
#Basker pmid=10932658
</biblio>