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Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes

INTRODUCTION: Selective dorsal rhizotomy (SDR) is a neurosurgical intervention intended to permanently reduce spasticity in the lower limbs and improve mobility in selected children with cerebral palsy (CP). Despite SDR having been performed worldwide for the past 30 years, there is moderate quality...

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Autores principales: Lewis, Jennifer, Bear, Natasha, Baker, Felicity, Fowler, Adam, Lee, Olivia, McLennan, Kim, Richardson, Emma, Scheinberg, Adam, Smith, Nadine, Thomason, Pam, Tidemann, Andrew, Wynter, Meredith, Paget, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502035/
https://www.ncbi.nlm.nih.gov/pubmed/31048430
http://dx.doi.org/10.1136/bmjopen-2018-025093
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author Lewis, Jennifer
Bear, Natasha
Baker, Felicity
Fowler, Adam
Lee, Olivia
McLennan, Kim
Richardson, Emma
Scheinberg, Adam
Smith, Nadine
Thomason, Pam
Tidemann, Andrew
Wynter, Meredith
Paget, Simon
author_facet Lewis, Jennifer
Bear, Natasha
Baker, Felicity
Fowler, Adam
Lee, Olivia
McLennan, Kim
Richardson, Emma
Scheinberg, Adam
Smith, Nadine
Thomason, Pam
Tidemann, Andrew
Wynter, Meredith
Paget, Simon
author_sort Lewis, Jennifer
collection PubMed
description INTRODUCTION: Selective dorsal rhizotomy (SDR) is a neurosurgical intervention intended to permanently reduce spasticity in the lower limbs and improve mobility in selected children with cerebral palsy (CP). Despite SDR having been performed worldwide for the past 30 years, there is moderate quality of evidence that SDR is effective in reducing spasticity with low to very low evidence of its effectiveness in improving gait, function and participation, using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) system. Published studies have described outcomes for groups that differ in selection, surgical technique and postoperative rehabilitation making it difficult for clinicians to use this information to advise families on best management. There is substantial community interest in SDR. A small number of children with CP undergo SDR in Australia each year and some families seek the intervention at international sites. Capturing clinical outcomes and adverse event (AE) data for Australian children undergoing SDR will provide clinicians with information to help guide families considering SDR. METHODS AND ANALYSIS: The Australian SDR Research Registry is a national registry of multidimensional outcomes for Australian children undergoing SDR in an Australian or overseas centre. Data will be collected for up to 10 years following the surgery, to include surgery and admission details, surgical and long-term AEs, and outcome measures across the body structure and functions, activity and participation domains of the International Classification of Functioning, Disability and Health. Data will be collected at baseline, during inpatient admission and at 1, 2, 5 and 10 years post. The aim of collecting these data is to improve understanding of short-, medium- and long-term outcomes and adverse effects of the intervention. ETHICS AND DISSEMINATION: This study was approved by the individual Human Research and Ethics committees at the five Australian tertiary hospitals involved. Results will be disseminated via peer-reviewed publications and conference presentations. TRIAL REGISTRATION NUMBER: ACTRN12618000985280; Pre-results.
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spelling pubmed-65020352019-05-21 Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes Lewis, Jennifer Bear, Natasha Baker, Felicity Fowler, Adam Lee, Olivia McLennan, Kim Richardson, Emma Scheinberg, Adam Smith, Nadine Thomason, Pam Tidemann, Andrew Wynter, Meredith Paget, Simon BMJ Open Paediatrics INTRODUCTION: Selective dorsal rhizotomy (SDR) is a neurosurgical intervention intended to permanently reduce spasticity in the lower limbs and improve mobility in selected children with cerebral palsy (CP). Despite SDR having been performed worldwide for the past 30 years, there is moderate quality of evidence that SDR is effective in reducing spasticity with low to very low evidence of its effectiveness in improving gait, function and participation, using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) system. Published studies have described outcomes for groups that differ in selection, surgical technique and postoperative rehabilitation making it difficult for clinicians to use this information to advise families on best management. There is substantial community interest in SDR. A small number of children with CP undergo SDR in Australia each year and some families seek the intervention at international sites. Capturing clinical outcomes and adverse event (AE) data for Australian children undergoing SDR will provide clinicians with information to help guide families considering SDR. METHODS AND ANALYSIS: The Australian SDR Research Registry is a national registry of multidimensional outcomes for Australian children undergoing SDR in an Australian or overseas centre. Data will be collected for up to 10 years following the surgery, to include surgery and admission details, surgical and long-term AEs, and outcome measures across the body structure and functions, activity and participation domains of the International Classification of Functioning, Disability and Health. Data will be collected at baseline, during inpatient admission and at 1, 2, 5 and 10 years post. The aim of collecting these data is to improve understanding of short-, medium- and long-term outcomes and adverse effects of the intervention. ETHICS AND DISSEMINATION: This study was approved by the individual Human Research and Ethics committees at the five Australian tertiary hospitals involved. Results will be disseminated via peer-reviewed publications and conference presentations. TRIAL REGISTRATION NUMBER: ACTRN12618000985280; Pre-results. BMJ Publishing Group 2019-05-01 /pmc/articles/PMC6502035/ /pubmed/31048430 http://dx.doi.org/10.1136/bmjopen-2018-025093 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Paediatrics
Lewis, Jennifer
Bear, Natasha
Baker, Felicity
Fowler, Adam
Lee, Olivia
McLennan, Kim
Richardson, Emma
Scheinberg, Adam
Smith, Nadine
Thomason, Pam
Tidemann, Andrew
Wynter, Meredith
Paget, Simon
Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title_full Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title_fullStr Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title_full_unstemmed Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title_short Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
title_sort australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional outcomes
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502035/
https://www.ncbi.nlm.nih.gov/pubmed/31048430
http://dx.doi.org/10.1136/bmjopen-2018-025093
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