Literature DB >> 20714723

Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease.

Avnish Tripathi1, Jeanette M Jerrell, James R Stallworth.   

Abstract

In children with sickle cell disease (SCD), adenotonsillar hypertrophy or recurrent tonsillitis are frequently linked with an increased risk of obstructive sleep apnea, cerebrovascular ischemia, or frequent pain episodes and often require an adenoidectomy and/or tonsillectomy. Interventions designed to prevent these complications, control vaso-occlusive pain episodes, and avoid hospitalizations may reduce the significant personal and economic burden of SCD. This study compares episode recurrence and treatment costs for cerebrovascular ischemia, vaso-occlusive pain, acute chest syndrome (ACS), and obstructive sleep apnea in children who had an adenotonsillectomy (A/T surgery, N = 256; 11.7%) and a matched cohort of those who did not (N = 512; 23.3%) from a cohort of 2,194 children and adolescents with SCD from South Carolina's Medicaid system. A/T surgery was associated with a significantly reduced rate of visits over time for obstructive sleep apnea and cerebrovascular ischemia (e.g., stroke, transient ischemic attacks), but not with any change in the rate of visits for vaso-occlusive pain or ACS/pneumonia visits. The rate of mean acute (emergency and inpatient) service costs was significantly decreasing over time after an increase about the time the A/T surgery was performed. The cost-effectiveness of adenoidectomy and/or tonsillectomy for treating obstructive sleep apnea and preventing cerebrovascular ischemia without increasing vaso-occlusive pain episodes or long-term acute service costs in routine clinical practice settings was demonstrated. The matched control group of SCD patients without A/T surgery contained more patients with severe vaso-occlusive pain episodes, ACS visits, and higher mean total costs over time and appears to represent a different phenotype of children with SCD.

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Year:  2010        PMID: 20714723     DOI: 10.1007/s00277-010-1048-4

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  6 in total

Review 1.  Advances in Understanding Ischemic Stroke Physiology and the Impact of Vasculopathy in Children With Sickle Cell Disease.

Authors:  Kristin P Guilliams; Melanie E Fields; Michael M Dowling
Journal:  Stroke       Date:  2019-02       Impact factor: 7.914

Review 2.  Sleep problems in children and adolescents with common medical conditions.

Authors:  Amy S Lewandowski; Teresa M Ward; Tonya M Palermo
Journal:  Pediatr Clin North Am       Date:  2011-04-03       Impact factor: 3.278

3.  The burden of obstructive sleep apnea in pediatric sickle cell disease: a Kids' inpatient database study.

Authors:  Po-Yang Tsou; Christopher M Cielo; Melissa S Xanthopoulos; Yu-Hsun Wang; Pei-Lun Kuo; Ignacio E Tapia
Journal:  Sleep       Date:  2021-02-12       Impact factor: 5.849

Review 4.  Sleep-disordered breathing in paediatric setting: existing and upcoming of the genetic disorders.

Authors:  Marco Zaffanello; Franco Antoniazzi; Laura Tenero; Luana Nosetti; Michele Piazza; Giorgio Piacentini
Journal:  Ann Transl Med       Date:  2018-09

Review 5.  Wheezing in children with sickle cell disease.

Authors:  Jeffrey A Glassberg; Robert Strunk; Michael R DeBaun
Journal:  Curr Opin Pediatr       Date:  2014-02       Impact factor: 2.856

6.  Nocturnal oxyhemoglobin desaturation and arteriopathy in a pediatric sickle cell disease cohort.

Authors:  Nomazulu Dlamini; Dawn E Saunders; Michael Bynevelt; Sara Trompeter; Timothy C Cox; Romola S Bucks; Fenella J Kirkham
Journal:  Neurology       Date:  2017-11-08       Impact factor: 11.800

  6 in total

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