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Self‐diagnosis of retrograde cricopharyngeus dysfunction (RCPD) or abelchia has been increasing over the past 5 years with patients seeking treatment for lifelong symptoms of inability to burp, neck gurgling, bloating, and flatulence. There is a distinct paucity of objective data in diagnosis and underlying pathophysiology of this disorder.ObjectiveThe purpose of this study was to prospectively evaluate patients with abelchia using standardized investigations to explore possible underlying mechanisms.MethodsPatients presenting with clinical scenario consistent with RCPD were recruited into the study after informed consent. All patients underwent standardized investigations: Self reporting questionnaires EAT‐10, VHI‐10, and RSI scores, as well as esophagogastroscopy, barium swallow, and high‐resolution esophageal manometry (HRM), were performed.ResultsRCPD patients demonstrated a minor increase in the mean EAT‐10 (5.2 ± 1.2) and normal RSI/VHI‐10 scores. Barium swallow revealed 53% (CI 38%–64%) were abnormal with reflux with hiatus hernia (37%) and dysmotility (16%) as most common findings.HRM showed that 67% (CI 54%–78%) were abnormal. Ineffective motility was found in 41%, a further 23% showed a complete absence of peristalsis, whereas 33% were normal.ConclusionsRCPD is a clinical condition of lifelong inability to belch and associated symptoms. The underlying pathophysiology is poorly understood. This study demonstrates that a significant number of RCPD patients have abnormal esophageal neural network with high proportion of abnormal or absent esophageal peristalsis.Level of Evidence3 Laryngoscope, 2024
Self‐diagnosis of retrograde cricopharyngeus dysfunction (RCPD) or abelchia has been increasing over the past 5 years with patients seeking treatment for lifelong symptoms of inability to burp, neck gurgling, bloating, and flatulence. There is a distinct paucity of objective data in diagnosis and underlying pathophysiology of this disorder.ObjectiveThe purpose of this study was to prospectively evaluate patients with abelchia using standardized investigations to explore possible underlying mechanisms.MethodsPatients presenting with clinical scenario consistent with RCPD were recruited into the study after informed consent. All patients underwent standardized investigations: Self reporting questionnaires EAT‐10, VHI‐10, and RSI scores, as well as esophagogastroscopy, barium swallow, and high‐resolution esophageal manometry (HRM), were performed.ResultsRCPD patients demonstrated a minor increase in the mean EAT‐10 (5.2 ± 1.2) and normal RSI/VHI‐10 scores. Barium swallow revealed 53% (CI 38%–64%) were abnormal with reflux with hiatus hernia (37%) and dysmotility (16%) as most common findings.HRM showed that 67% (CI 54%–78%) were abnormal. Ineffective motility was found in 41%, a further 23% showed a complete absence of peristalsis, whereas 33% were normal.ConclusionsRCPD is a clinical condition of lifelong inability to belch and associated symptoms. The underlying pathophysiology is poorly understood. This study demonstrates that a significant number of RCPD patients have abnormal esophageal neural network with high proportion of abnormal or absent esophageal peristalsis.Level of Evidence3 Laryngoscope, 2024
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