Variability in perioperative evaluation and resource utilization in pediatric patients with suspected biliary dyskinesia: A multi-institutional retrospective cohort study.

Sarah B Cairo,Arturo Aranda,Marisa Bartz-Kurycki, Katherine J Baxter,Patrick Bonasso, Melvin Dassinger,Katherine J Deans, Danielle Dorey,Pamela Emengo, Elizabeth Fialkowski,Christopher Gayer, Brandy Gonzales, Nakada Gusman, Russell B Hawkins,Karen Herzing,Eunice Huang, Saleem Islam,Timothy Jancelewicz,Matthew P Landman,Kevin P Lally, Aaron Lesher,Peter C Minneci, Mehul V Raval,Robert Russell,Sohail Shah, Bethany Slater, Leah J Schoel,Shawn St Peter, Joseph Sujka, Jennifer Waterhouse,David H Rothstein

Journal of pediatric surgery(2019)

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摘要
INTRODUCTION:Biliary dyskinesia (BD) is a common indication for pediatric cholecystectomy. While diagnosis is primarily based on diminished gallbladder ejection fraction (GB-EF), work-up and management in pediatrics is controversial. METHODS:We conducted a multi-institutional retrospective review of children undergoing cholecystectomy for BD to compare perioperative work-up and outcomes. RESULTS:Six hundred seventy-eight patients across 16 institutions were included. There was no significant difference in gender, age, or BMI between institutions. Most patients were white (86.3%), non-Hispanic (79.9%), and had private insurance (55.2%). Gallbladder ejection fraction (EF) was reported in 84.5% of patients, and 44.8% had an EF <15%. 30.7% of patients were initially seen by pediatric surgeons, 31.3% by pediatric gastroenterologists, and 23.4% by the emergency department with significant variability between institutions (p < 0.001). Symptoms persisted in 35.3% of patients post-operatively with a median follow-up of 21 days (IQR 13, 34). On multivariate analysis, only non-white race and the presence of psychiatric comorbidities were associated with increased risk of post-operative symptoms. CONCLUSION:There is significant variability in evaluation and follow-up both before and after cholecystectomy for BD. Prospective research with standardized data collection and follow-up is needed to develop and validate optimal care pathways for pediatric patients with suspected BD. STUDY TYPE:Case Series, Retrospective Review. LEVEL OF EVIDENCE:Level IV.
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