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10.14309/crj.2015.88 http://scihub22266oqcxt.onion/10.14309/crj.2015.88 C4612749!4612749!26504869     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       ACG+Case+Rep+J 2015 ; 3 (1): 20-2 Nephropedia Template TP {{tp|p=26504869|t=2015. Deglutition Syncope: A Case Report and Review of the Literature |pdf=|usr=}}{{26504869}} gab.com Text Deglutition Syncope: A Case Report and Review of the Literature JO: ACG Case Rep J http://www.kidney.de/pget.php?&tw=1&pmid=26504869 #FOAvip Deglutition syncope (DS) is a rare, neurally-mediated syncopal syndrome arising from an aberrant vagotonic reflex during swallow-associated esophageal dilation. Its association with gastroesophageal disorders often prompts gastroenterology consultation. An 89-year-old man with recent dysphagia and otalgia was admitted after a syncopal episode occurred while eating. Esophageal imaging and endoscopy demonstrated no causative abnormalities. Maxillofacial imaging revealed chronic sinusitis and mastoiditis. Telemetry monitoring demonstrated high-grade atrioventricular block and pause associated with swallowing. His symptoms and swallow-associated arrhythmia resolved after dual chamber pacemaker implantation. DS is highly treatable once identified and multidisciplinary coordination is helpful in optimizing outcomes and avoiding superfluous testing. Twit Text FOAVip Deglutition Syncope: A Case Report and Review of the Literature ????ACG Case Rep J http://www.kidney.de/pget.php?&tw=1&pmid=26504869 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26504869 #FOAvip English Wikipedia <ref>{{Cite pmid|26504869}}</ref> Deglutition Syncope: A Case Report and Review of the Literature #MMPMID26504869 Kahn A; Koepke LM; Umar SB ACG Case Rep J 2015[Oct]; 3 (1): 20-2 PMID26504869show ga Deglutition syncope (DS) is a rare, neurally-mediated syncopal syndrome arising from an aberrant vagotonic reflex during swallow-associated esophageal dilation. Its association with gastroesophageal disorders often prompts gastroenterology consultation. An 89-year-old man with recent dysphagia and otalgia was admitted after a syncopal episode occurred while eating. Esophageal imaging and endoscopy demonstrated no causative abnormalities. Maxillofacial imaging revealed chronic sinusitis and mastoiditis. Telemetry monitoring demonstrated high-grade atrioventricular block and pause associated with swallowing. His symptoms and swallow-associated arrhythmia resolved after dual chamber pacemaker implantation. DS is highly treatable once identified and multidisciplinary coordination is helpful in optimizing outcomes and avoiding superfluous testing. äDeglutition Syncope: A Case Report and Review of the Literature (epmc).pdf DeepDyve Pubget Overpricing