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Kozarek R. A. M.D.; Patterson, D. J. M.D.; Ball, T. J. M.D; Gelfand, M. G. M.D.; Jiranek, G. E. M.D.; Bredfeldt, J. E. M.D.; Brandabur, J. J. M.D.; Wolfsen, H. W. M.D.; Raltz, S. L. R.N., M.s.N.
Journal of Clinical Gastroenterology: April 1995
Clinical Studies: PDF Only

Maxims for safe esophageal dilation have included recommendations to use fluoroscopy in all instances and to limit dilation sessions to 2-mm increments. We reviewed a 34-month experience of all esophageal dilations undertaken at a large multispecialty clinic to define adherence to these recommendations and to delineate whether deviation was associated with significant complications. Four hundred thirty-two patients underwent 716 courses of esophageal dilation during this time, 92% of whom had benign disease. Eighty-nine percent of patients were dilated with polyvinyl dilators (Savary/American) and only 8% of these patients required fluoroscopic monitoring for the bougienage. Seventy-eight percent of the dilating sessions for patients without achalasia were undertaken using either a single large dilator (≥45 Fr) or employed incremental dilator sizes >2 mm (6 Fr) in a single session. There was a single perforation in 662 nonachalasia dilations and this was a consequence of attempted placement of an esophageal endoprosthesis. We conclude that use of guide wire technology and newer dilating techniques do away with the need for routine fluoroscopic control. Moreover, single large dilators or dilator increments >2 mm may be safely used, contingent on endoscopic stricture assessment.

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