Literature DB >> 27643455

Elective cholecystectomy reduces morbidity of cholelithiasis in pediatric sickle cell disease.

Emily F Goodwin1, Paige I Partain2, Jeffrey D Lebensburger1, Naomi S Fineberg1, Thomas H Howard1.   

Abstract

BACKGROUND: Cholelithiasis is a frequent complication in pediatric sickle cell disease (SCD). Though it is standard practice to perform a cholecystectomy in pediatric SCD patients with symptoms of cholelithiasis, the use of elective cholecystectomy for asymptomatic patients remains controversial. PROCEDURE: Records of 191 pediatric sickle cell patients with cholelithiasis who underwent cholecystectomy were retrospectively reviewed. Patients classified as follows: (i) elective-no preoperative symptoms, cholelithiasis on screening ultrasound, comprehensive preoperative plan; (ii) symptomatic-preoperative symptoms of cholelithiasis on diagnostic ultrasound, comprehensive preoperative plan; or (iii) emergent-hospitalization for acute cholecystitis symptoms, cholelithiasis on diagnostic ultrasound, limited preoperative preparation. We compared the morbidity of cholecystectomy by examining pre- and post-cholecystectomy hospital admission days, length of stay for cholecystectomy, and surgical complications.
RESULTS: Patients with SCD underwent a total of 191 cholecystectomies over a 10-year period: 51 elective, 110 symptomatic, and 30 emergent. Patients who required emergent cholecystectomy had a longer postoperative hospitalization time than elective or symptomatic cholecystectomy (7.3 vs 4.3, P < 0.001). Baseline values for total bilirubin and aspartate aminotransferase (AST) were significantly elevated (P < 0.02 and P < 0.07, respectively) in patients requiring emergent cholecystectomy.
CONCLUSIONS: This represents the largest reported retrospective review of pediatric cholelithiasis and cholecystectomy in SCD to date. These data strongly suggest that elective cholecystectomy decreases morbidity associated with emergent cholecystectomy. The overall outcomes for symptomatic and elective patients are favorable. However, our study indicates the need for prospective studies to identify clinical indicators for those emergent patients.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  pediatric hematology/oncology; sickle cell anemia; surgery

Mesh:

Year:  2016        PMID: 27643455     DOI: 10.1002/pbc.26179

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Risks and Benefits of Prophylactic Transfusion before Cholecystectomy in Sickle Cell Disease.

Authors:  Elise Rambaud; Brigitte Ranque; Sofia Tsiakyroudi; Laure Joseph; Nathalie Bouly; Richard Douard; Anne François; Jacques Pouchot; Jean-Benoît Arlet
Journal:  J Clin Med       Date:  2022-07-09       Impact factor: 4.964

2.  Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients.

Authors:  Slimane Allali; Mariane de Montalembert; Valentine Brousse; Claire Heilbronner; Melissa Taylor; Josephine Brice; Elisabetta Manzali; Nicolas Garcelon; Florence Lacaille
Journal:  J Clin Med       Date:  2019-09-18       Impact factor: 4.241

  2 in total

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