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Impact of an institution-designed algorithm for the management of dislodged gastrostomy tubes
Institution:1. Department of Surgery, Children''s Mercy Kansas City, 2401 Gillham Road, Kansas City, MO 64108, United States;2. Kansas City University of Medicine and Biosciences, 1750 Independence Ave, Kansas City, MO 64106, United States;3. Department of Emergency Medicine, Children''s Mercy Kansas City, 2401 Gillham Road, Kansas City, MO 64108, United States;4. Department of Evidence Based Practice, Children''s Mercy Kansas City, 2401 Gillham Road, Kansas City, MO 64108, United States;5. University of Missouri-Kansas City School of Medicine, 2411 Holmes Street, Kansas City, MO 64108, United States
Abstract:BackgroundGastrostomy tube (GT) dislodgement is a common reason for emergency department (ED) visits. We aim to assess the efficacy of our institution's algorithm in reducing surgical consultation and GT contrast studies for replacement of dislodged GT and to examine the need for operation before and after algorithm implementation.MethodsA retrospective review was performed between March 2017-February 2018 (prealgorithm) and March 2018-December 2018 (postalgorithm) for patients <18 years presenting to the ED with GT dislodgement. Demographics and outcomes were analyzed.ResultsA total of 433 visits among 279 patients were included, 200 (46.2%) pre and 233 (53.8%) postalgorithm implementation. Median ED LOS was 2.1 h (IQR 1.4, 3.0). Surgery was consulted in 92 visits (21.3%) and a contrast study obtained in 287 (66.3%). The GT was replaced by ED providers in 363 visits (83.8%) and by surgery in 70 (16.2%). Surgical consultation increased postalgorithm (16.5% vs. 25.3%; p = 0.03). Six (1.4%) patients required reoperation, with 5 occurring postalgorithm, p = 0.22. For GTs placed < 8 weeks prior to the dislodgment, there were no differences in surgical consultations, contrast studies performed, or need for reoperation pre and postalgorithm.ConclusionAn algorithm for replacement of dislodged GT is usable, effective, and increased surgical team involvement without significant changes in patient outcomes.Type of StudyTreatment Study.Level of EvidenceLevel III.
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