Abstract:Background
Swallow or deglutition syncope is an unusual type of neurally-mediated syncope associated with life-threatening bradyarrhythmia and hypotension. It is a difficult condition to diagnose with commonly delayed diagnosis and management. There is lack of review articles that elucidate the basic demographics, clinical characteristics and management of this rare condition. This publication systematically reviews the 101 case reports published since 1793 on swallow syncope.
Case … Show more
“…This is believed to be due to afferent impulses from the esophageal plexus which travel via the vagus nerve to the brain stem and then trigger efferent fibers to signal back through the vagus nerve to the heart. This type of syncope has been reported since 1793 by Spens, but literature review has not shown syncope to occur in achalasia without swallowing [2]. We present the case of a patient with achalasia and a nonswallowing syncopal episode.…”
Section: Introductionmentioning
confidence: 75%
“…This is all thought to be due to reflex arcs in the parasympathetic system between afferent and efferent fibers [3]. Dilatational treatment of the achalasia typically results in complete resolution of the deglutition syncope [2,4,5].…”
Achalasia is an uncommon disease that occurs due to inability of lower esophageal sphincter from relaxing, leading to dysphagia to liquids and solids. Clues to this diagnosis include: failed treatment with proton pump inhibitors, and changes on imaging studies including chest X-ray and barium esophagogram. Ultimately it is a diagnosis made on esophageal manometry. Swallow-induced syncope has been known in patients with achalasia for almost three centuries. Here we present the case of a patient with achalasia and a non-swallowing syncopal episode. To our knowledge and extensive search, there has been no report of a similar case.
“…This is believed to be due to afferent impulses from the esophageal plexus which travel via the vagus nerve to the brain stem and then trigger efferent fibers to signal back through the vagus nerve to the heart. This type of syncope has been reported since 1793 by Spens, but literature review has not shown syncope to occur in achalasia without swallowing [2]. We present the case of a patient with achalasia and a nonswallowing syncopal episode.…”
Section: Introductionmentioning
confidence: 75%
“…This is all thought to be due to reflex arcs in the parasympathetic system between afferent and efferent fibers [3]. Dilatational treatment of the achalasia typically results in complete resolution of the deglutition syncope [2,4,5].…”
Achalasia is an uncommon disease that occurs due to inability of lower esophageal sphincter from relaxing, leading to dysphagia to liquids and solids. Clues to this diagnosis include: failed treatment with proton pump inhibitors, and changes on imaging studies including chest X-ray and barium esophagogram. Ultimately it is a diagnosis made on esophageal manometry. Swallow-induced syncope has been known in patients with achalasia for almost three centuries. Here we present the case of a patient with achalasia and a non-swallowing syncopal episode. To our knowledge and extensive search, there has been no report of a similar case.
“…DS is often found in older adults, with a mean reported age of 57.5 years at the time of initial presentation [13]. The exact mechanism of DS remains unknown.…”
Section: Discussionmentioning
confidence: 99%
“…When it comes to diagnosing DS, it is essential to rule out any esophageal disorders and cardiac diseases beforehand [9]. The diagnosis of DS involves careful history taking and recognition of presyncopal events or syncope triggered by the process of swallowing (provocative test) [13].…”
Swallow or deglutition syncope is an uncommon cause of syncope associated with bradyarrhythmia and hypotension during food swallowing. Early recognition of this condition is imperative but challenging. We report a case of a 60-year-old female who presented with a complaint of intermittent lightheadedness after swallowing food. An episode of presyncope was observed and a reduced pulse rate from baseline was noted when she was instructed to eat a candy bar in the clinic. Further workup revealed normal inoffice electrocardiogram, bilateral carotid ultrasound, transthoracic echocardiogram, and videofluoroscopic swallow study. Our goal in presenting this case is to raise awareness of the condition in medical literature and provide a good understanding of its clinical manifestation to prevent life-threatening events.
“…The nature and severity of CI differs between types of reflex syncope. In swallow syncope asystole due to an AV-block has been frequently described (8), although a selection bias cannot be ruled out. This "reflex AV-block" differs in some respects from an intrinsic AV-block, and is probably due to stronger inhibition of the AV-than the SA-node.…”
Syncope usually lasts less than a minute, in which short time arterial blood pressure temporarily falls enough to decrease brain perfusion so much that loss of consciousness ensues. Blood pressure decreases quickest when the heart suddenly stops pumping, which happens in arrhythmia and in severe cardioinhibitory reflex syncope. Loss of consciousness starts about 8 s after the last heart beat and circulatory standstill occurs after 10-15 s. A much slower blood pressure decrease can occur in syncope due to orthostatic hypotension Standing blood pressure can then stabilize at low values often causing more subtle signs (i.e., inability to act) but often not low enough to cause loss of consciousness. Cerebral autoregulation attempts to keep cerebral blood flow constant when blood pressure decreases. In reflex syncope both the quick blood pressure decrease and its low absolute value mean that cerebral autoregulation cannot prevent syncope. It has more protective value in orthostatic hypotension. Neurological signs are related to the severity and timing of cerebral hypoperfusion. Several unanswered pathophysiological questions with possible clinical implications are identified.
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