Literature DB >> 28177174

A case-controlled comparison of postoperative analgesic dosing between girls with Rett syndrome and girls with and without developmental disability undergoing spinal fusion surgery.

Chantel C Barney1, Alyssa M Merbler2, Kelsey Quest2, Breanne J Byiers2, George L Wilcox3, Scott Schwantes1, Samuel A Roiko1, Timothy Feyma4, Arthur Beisang4, Frank J Symons2.   

Abstract

BACKGROUND: Rett syndrome is associated with severe motor and communicative impairment making optimal postoperative pain management a challenge. There are case reports documenting reduced postoperative analgesic requirement in Rett syndrome. AIM: The goal of this preliminary investigation was to compare postoperative analgesic management among a sample of girls with Rett syndrome compared to girls with and without developmental disability undergoing spinal fusion surgery.
METHOD: The medical records of eight girls with Rett syndrome (mean age = 13.2 years, sd = 1.9), eight girls with developmental disability (cerebral palsy; mean age = 13.1 years, sd = 2.0), and eight girls without developmental disability (adolescent idiopathic scoliosis; mean age = 13.4, sd = 1.8) were reviewed. Data related to demographics, medications, and route of drug administration were recorded.
RESULTS: Girls with Rett syndrome received significantly fewer morphine equivalent opioids postoperatively (M = 0.26 mg·kg-1 ·day-1 , sd = 0.10) compared to girls with adolescent idiopathic scoliosis (M = 0.47mg·kg-1 ·day-1 , sd = 0.13; 95% CI -0.34 to -0.08; P = 0.001) and girls with CP (M = 0.40 mg·kg-1 per day, sd = 0.14; 95% CI -0.27 to -0.02; P = 0.01). Girls with Rett syndrome received significantly fewer opioid patient-controlled analgesic (PCA) bolus doses (given by proxy; M = 42.63, sd = 17.84) compared to girls with adolescent idiopathic scoliosis (M = 98.25, sd = 52.77; 95% CI -96.42 to -14.83; P = 0.01). There was also some evidence indicating girls with Rett syndrome received fewer bolus doses compared to girls with CP (M = 80.88, sd = 38.93; 95% CI -79.05 to 2.55; P = 0.06). On average, girls with Rett syndrome also received smaller total doses of acetaminophen, diazepam, and hydroxyzine.
CONCLUSION: This study highlights possible discrepancies in postoperative pain management specific to girls with Rett syndrome and suggests further investigation is warranted to determine best practice for postoperative analgesic management for this vulnerable patient population.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  adolescent; communication disorders; opioid; pain; pediatric; scoliosis

Mesh:

Substances:

Year:  2017        PMID: 28177174      PMCID: PMC5319894          DOI: 10.1111/pan.13066

Source DB:  PubMed          Journal:  Paediatr Anaesth        ISSN: 1155-5645            Impact factor:   2.556


  24 in total

Review 1.  Clinical manifestations and stages of Rett syndrome.

Authors:  Bengt Hagberg
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2002

2.  Pain management in children with and without cognitive impairment following spine fusion surgery.

Authors:  S Malviya; T Voepel-Lewis; A R Tait; S Merkel; A Lauer; H Munro; F Farley
Journal:  Paediatr Anaesth       Date:  2001-07       Impact factor: 2.556

3.  Rett syndrome and delayed recovery from anaesthesia.

Authors:  W H Konarzewski; S Misso
Journal:  Anaesthesia       Date:  1994-04       Impact factor: 6.955

4.  Linking MECP2 and pain sensitivity: the example of Rett syndrome.

Authors:  Jenny Downs; Sandrine M Géranton; Ami Bebbington; Peter Jacoby; Nadia Bahi-Buisson; David Ravine; Helen Leonard
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

5.  Health and function of patients with untreated idiopathic scoliosis: a 50-year natural history study.

Authors:  Stuart L Weinstein; Lori A Dolan; Kevin F Spratt; Kirk K Peterson; Mark J Spoonamore; Ignacio V Ponseti
Journal:  JAMA       Date:  2003-02-05       Impact factor: 56.272

6.  Clinical validation of the paediatric pain profile.

Authors:  Anne Hunt; Ann Goldman; Kate Seers; Nicola Crichton; Kiki Mastroyannopoulou; Vivien Moffat; Kate Oulton; Michael Brady
Journal:  Dev Med Child Neurol       Date:  2004-01       Impact factor: 5.449

7.  Assessment and management of nutrition and growth in Rett syndrome.

Authors:  Helen Leonard; Madhur Ravikumara; Gordon Baikie; Nusrat Naseem; Carolyn Ellaway; Alan Percy; Suzanne Abraham; Suzanne Geerts; Jane Lane; Mary Jones; Katherine Bathgate; Jenny Downs
Journal:  J Pediatr Gastroenterol Nutr       Date:  2013-10       Impact factor: 2.839

8.  Parent-reported pain in Rett syndrome.

Authors:  Frank J Symons; Breanne Byiers; Raymond C Tervo; Arthur Beisang
Journal:  Clin J Pain       Date:  2013-08       Impact factor: 3.442

9.  A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome.

Authors:  Rodney C Samaco; John D Fryer; Jun Ren; Sharyl Fyffe; Hsiao-Tuan Chao; Yaling Sun; John J Greer; Huda Y Zoghbi; Jeffrey L Neul
Journal:  Hum Mol Genet       Date:  2008-03-04       Impact factor: 6.150

10.  Epigenetic programming of mu-opioid receptor gene in mouse brain is regulated by MeCP2 and Brg1 chromatin remodelling factor.

Authors:  Cheol Kyu Hwang; Kyu Young Song; Chun Sung Kim; Hack Sun Choi; Xiao-Hong Guo; Ping-Yee Law; Li-Na Wei; Horace H Loh
Journal:  J Cell Mol Med       Date:  2008-10-13       Impact factor: 5.310

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  1 in total

1.  Intensive Postural and Motor Activity Program Reduces Scoliosis Progression in People with Rett Syndrome.

Authors:  Alberto Romano; Elena Ippolito; Camilla Risoli; Edoardo Malerba; Martina Favetta; Andrea Sancesario; Meir Lotan; Daniel Sender Moran
Journal:  J Clin Med       Date:  2022-01-22       Impact factor: 4.241

  1 in total

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