Literature DB >> 25978940

Pain in adolescents with spinal muscular atrophy and Duchenne and Becker muscular dystrophy.

Christina Lager1, Anna-Karin Kroksmark2.   

Abstract

BACKGROUND/
PURPOSE: The purpose of this study was to explore the prevalence, nature and scope of pain in adolescents with spinal muscular atrophy and Duchenne and Becker muscular dystrophy and whether the pain differs between diagnostic groups or between adolescents with different ambulation status. Furthermore to study the consequences of pain and to identify pain-exacerbating and pain-relieving factors.
METHODS: In a national survey, fifty-five adolescents with spinal muscular atrophy and dystrophinopathy completed a questionnaire assessing pain frequency, duration, location using a body map, intensity and discomfort using visual analogue scales, pain interference using a modified version of Brief Pain Inventory and factors exacerbating and relieving pain.
RESULTS: Sixty-nine per cent of the adolescents reported pain during the past three months and 50% reported chronic pain. The pain prevalence did not differ significantly between diagnostic groups or between ambulators and non-ambulators. The average pain intensity was graded as mild and the worst pain as moderate. The pain typically occurred weekly, most frequently in the neck/back or legs. General activity and mood were the areas that were most affected by pain. Common pain-exacerbating factors were sitting, too much movement/activity and being lifted or transferred.
CONCLUSION: Pain is a frequent problem in adolescents with spinal muscular atrophy and dystrophinopathy. The assessments used enable an understanding both of the nature and scope of pain and of the impact of pain in everyday life. The study highlights the importance of assessing pain in a systematic manner and offering an individual approach to interventions designed to reduce pain in this population.
Copyright © 2015 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Adolescent; Becker muscular dystrophy; Duchenne muscular dystrophy; Neuromuscular disorders; Pain; Spinal muscular atrophy

Mesh:

Year:  2015        PMID: 25978940     DOI: 10.1016/j.ejpn.2015.04.005

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  10 in total

Review 1.  Emergencies in motoneuron disease.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Intern Emerg Med       Date:  2017-03-09       Impact factor: 3.397

2.  Occurrence of symptoms in different stages of Duchenne muscular dystrophy and their impact on social participation.

Authors:  Saskia L S Houwen-van Opstal; Lotte Heutinck; Merel Jansen; Yvonne D Krom; Edith H C Cup; Jos G M Hendriksen; Michel A A P Willemsen; Jan J G M Verschuuren; Erik H Niks; Imelda J M de Groot
Journal:  Muscle Nerve       Date:  2021-09-09       Impact factor: 3.852

3.  Pain characteristics among individuals with Duchenne muscular dystrophy according to their clinical stage.

Authors:  Aram Kim; Mina Park; Hyung-Ik Shin
Journal:  BMC Musculoskelet Disord       Date:  2022-06-04       Impact factor: 2.562

Review 4.  Pain Phenotypes in Rare Musculoskeletal and Neuromuscular Diseases.

Authors:  Anthony Tucker-Bartley; Jordan Lemme; Andrea Gomez-Morad; Nehal Shah; Miranda Veliu; Frank Birklein; Claudia Storz; Seward Rutkove; David Kronn; Alison M Boyce; Eduard Kraft; Jaymin Upadhyay
Journal:  Neurosci Biobehav Rev       Date:  2021-02-10       Impact factor: 9.052

5.  SMN deficiency causes pain hypersensitivity in a mild SMA mouse model through enhancing excitability of nociceptive dorsal root ganglion neurons.

Authors:  Ruobing Qu; Fuping Yao; Xiaomin Zhang; Yuan Gao; Tong Liu; Yimin Hua
Journal:  Sci Rep       Date:  2019-04-24       Impact factor: 4.379

6.  Frequency of reported pain in adult males with muscular dystrophy.

Authors:  Matthew F Jacques; Rachel C Stockley; Emma I Bostock; Jonathon Smith; Christian G DeGoede; Christopher I Morse
Journal:  PLoS One       Date:  2019-02-14       Impact factor: 3.240

7.  The Burden of Spinal Muscular Atrophy on Informal Caregivers.

Authors:  Isaac Aranda-Reneo; Luz María Peña-Longobardo; Juan Oliva-Moreno; Svenja Litzkendorf; Isabelle Durand-Zaleski; Eduardo F Tizzano; Julio López-Bastida
Journal:  Int J Environ Res Public Health       Date:  2020-12-02       Impact factor: 3.390

8.  Subacute Pain Trajectories following major musculoskeletal surgery in adolescents: A Pilot Study.

Authors:  Jennifer A Rabbitts; Cornelius B Groenewald; Chuan Zhou
Journal:  Can J Pain       Date:  2020-12-30

9.  Prevalence of Pain within Limb Girdle Muscular Dystrophy R9 and Implications for Other Degenerative Diseases.

Authors:  Mark Richardson; Anna Mayhew; Robert Muni-Lofra; Lindsay B Murphy; Volker Straub
Journal:  J Clin Med       Date:  2021-11-25       Impact factor: 4.241

Review 10.  Duchenne and Becker muscular dystrophy in adolescents: current perspectives.

Authors:  Jennifer G Andrews; Richard A Wahl
Journal:  Adolesc Health Med Ther       Date:  2018-03-15
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.