Use of the Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) in Spinal Muscular Atrophy

被引:0
|
作者
Brown, Laurey [1 ,2 ]
Hoffman, Katie [1 ,2 ]
Corbo-Galli, Chiara [3 ]
Dong, Siyuan [4 ]
Zumpf, Katelyn [4 ]
Weigel, Christa [1 ]
Blomgren, Colleen [1 ]
Munson, Hannah [2 ]
Bidwell, Jessa [2 ]
Rao, Vamshi [2 ,5 ]
Kuntz, Nancy L. [2 ,5 ]
Schwaede, Abigail [2 ]
Krosschell, Kristin J. [5 ,6 ]
机构
[1] Ann & Robert H Lurie Childrens Hosp Chicago, Dept Rehabil Serv, Chicago, IL 60611 USA
[2] Ann & Robert H Lurie Childrens Hosp Chicago, Div Neurol, Chicago, IL 60611 USA
[3] Northwestern Univ, Weinberg Coll Arts & Sci, Evanston, IL 60208 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Div Biostat, Chicago, IL 60611 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL 60611 USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Phys Therapy & Human Movement Sci, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
spinal muscular atrophy; caregiver burden; quality of life; neuromuscular; pediatric; ACEND; FUNCTIONAL MOTOR SCALE; VALIDATION;
D O I
10.3390/jcm13040921
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Spinal muscular atrophy (SMA) has a remarkable impact on function and participation. Subsequently, the caregivers of individuals with SMA are impacted as well. Providers and the SMA community should be aware of the presence of and likely expectations for the existence of caregiver burden. Methods: The Assessment of Caregiver Experience with Neuromuscular Disease (ACEND) quantifies caregivers' perceptions of function and quality of life pertaining to time, finance and emotion. Analyses were conducted among SMA types and ambulatory and ventilatory status. Participants with SMA had varying ranges of function and were on pharmaceutical treatment. Total ACEND score, longitudinal change in total ACEND score, total quality of life (QOL) score, change in total QOL score and subdomains for QOL, including time, emotion and finance, were all explored. Results: Overall, the ACEND demonstrated discriminant validity and some observed trends. Total ACEND scores improved for caregivers of those with SMA 2, remained stable longitudinally for caregivers of those with SMA 1 and 3 and were not influenced by ventilation status. The caregivers of individuals with SMA 1 had the lowest total quality of life (QOL) score, as did the caregivers of non-ambulatory individuals and those requiring assisted ventilation. Longitudinally, there were no changes in total QOL between caregivers of individuals with different SMA types or ambulatory or ventilation status. There were some differences in emotional needs, but no differences in financial impact between the caregivers of individuals with different types of SMA or ambulatory and ventilatory status. Conclusions: With this information enlightening the presence of caregiver burden and expected changes in burden with pharmaceutical treatment, providers, third party payors and the SMA community at large can better assist, equip and empower those providing the necessary assistance to enable the lives of those with SMA.
引用
收藏
页数:15
相关论文
共 50 条
  • [31] Neuromuscular Junctions as Key Contributors and Therapeutic Targets in Spinal Muscular Atrophy
    Boido, Marina
    Vercelli, Alessandro
    FRONTIERS IN NEUROANATOMY, 2016, 10
  • [32] Spinal muscular atrophy: Motoneurone or muscle disease?
    Vrbova, Gerta
    NEUROMUSCULAR DISORDERS, 2008, 18 (01) : 81 - 82
  • [33] Disease burden of spinal muscular atrophy in Germany
    Constanze Klug
    Olivia Schreiber-Katz
    Simone Thiele
    Elisabeth Schorling
    Janet Zowe
    Peter Reilich
    Maggie C. Walter
    Klaus H. Nagels
    Orphanet Journal of Rare Diseases, 11
  • [34] Gene therapy for spinal muscular atrophy: the Qatari experience
    Hossamaldein Gaber Ali
    Khalid Ibrahim
    Mahmoud Fawzi Elsaid
    Reem Babiker Mohamed
    Mahmoud I. A. Abeidah
    Azhar Othman Al Rawwas
    Khaled Elshafey
    Hajer Almulla
    Karen El-Akouri
    Mariam Almulla
    Amna Othman
    Sara Musa
    Fatma Al-Mesaifri
    Rehab Ali
    Noora Shahbeck
    Mariam Al-Mureikhi
    Reem Alsulaiman
    Saad Alkaabi
    Tawfeg Ben-Omran
    Gene Therapy, 2021, 28 : 676 - 680
  • [35] Biomarkers in Rare Disorders: The Experience with Spinal Muscular Atrophy
    Tiziano, Francesco D.
    Neri, Giovanni
    Brahe, Christina
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2011, 12 (01) : 24 - 38
  • [36] Gene therapy for spinal muscular atrophy: the Qatari experience
    Ali, Hossamaldein Gaber
    Ibrahim, Khalid
    Elsaid, Mahmoud Fawzi
    Mohamed, Reem Babiker
    Abeidah, Mahmoud I. A.
    Al Rawwas, Azhar Othman
    Elshafey, Khaled
    Almulla, Hajer
    El-Akouri, Karen
    Almulla, Mariam
    Othman, Amna
    Musa, Sara
    Al-Mesaifri, Fatma
    Ali, Rehab
    Shahbeck, Noora
    Al-Mureikhi, Mariam
    Alsulaiman, Reem
    Alkaabi, Saad
    Ben-Omran, Tawfeg
    GENE THERAPY, 2021, 28 (10-11) : 676 - 680
  • [37] In Search of Spinal Muscular Atrophy Disease Modifiers
    Chudakova, Daria
    Kuzenkova, Ludmila
    Fisenko, Andrey
    Savostyanov, Kirill
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (20)
  • [38] Disease burden of spinal muscular atrophy in Germany
    Klug, Constanze
    Schreiber-Katz, Olivia
    Thiele, Simone
    Schorling, Elisabeth
    Zowe, Janet
    Reilich, Peter
    Walter, Maggie C.
    Nagels, Klaus H.
    ORPHANET JOURNAL OF RARE DISEASES, 2016, 11
  • [39] Spinal muscular atrophy: A modifiable disease emerges
    Fitzgerald, Dominic A.
    Abel, Francois
    Jones, Kristi J.
    Farrar, Michelle A.
    PAEDIATRIC RESPIRATORY REVIEWS, 2018, 28 : 1 - 2
  • [40] Synaptic pathology at the neuromuscular junction in a mouse model of childhood motor neuron disease (spinal muscular atrophy)
    Murray, L. M.
    Thomson, D.
    Wishart, T. M.
    Gillingwater, T. H.
    JOURNAL OF ANATOMY, 2008, 212 (01) : 84 - 84