Development and Initial Validation of the Assessment of Caregiver Experience With Neuromuscular Disease
@article{Matsumoto2011DevelopmentAI, title={Development and Initial Validation of the Assessment of Caregiver Experience With Neuromuscular Disease}, author={Hiroko Matsumoto and Debra Clayton-Krasinski and Stephen A. Klinge and Jaime A. G{\'o}mez and Whitney A. Booker and Joshua E. Hyman and David P. Roye and Michael G. Vitale}, journal={Journal of Pediatric Orthopaedics}, year={2011}, volume={31}, pages={284–292} }
Background Orthopaedic intervention can have a wide range of functional and psychosocial effects on children with neuromuscular disease (NMD). In the multihandicapped child (Gross Motor Classification System IV/V), functional status, pain, psychosocial function, and health-related quality of life also have effects on the families of these child. The purpose of this study is to report the development and initial validation of an outcomes instrument specifically designed to assess the caregiver…
27 Citations
Evaluation of assessment of caregiver experience with neuromuscular disease: reliability and responsiveness of a new caregiver-reported outcome measure in patients with cerebral palsy
- 2020
Medicine, Psychology
Translational pediatrics
The reliability of ACEND is demonstrated through strong correlations of scores before and after botulinum toxin injection, while the burden of care is largely determined by ICD-10 diagnosis and the GMFCS level and changes in care burden are only related to the gender of the patient and the follow-up time interval.
A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy
- 2019
Medicine, Psychology
Neuromuscular Disorders
Health-Related Quality of Life and Care Giver Burden Following Spinal Fusion in Children With Cerebral Palsy
- 2017
Medicine, Psychology
Spine
Evaluated changes in caregivers’ perceptions of health-related quality of life (HRQOL) and caregiver burden in children with severe cerebral palsy (CP) following spinal fusion found HRQOL improves 1 year following spine fusion but regresses to baseline after 2 years.
Development of a proxy-reported scale to assess motor function in infants and young children with early-onset neuromuscular disorders.
- 2020
Medicine, Psychology
Journal of advanced nursing
A preliminary proxy-reported instrument, the PMOM, is developed to evaluate motor function in infants and young children with early-onset NMD and may complement clinic-based motor function testing.
Factors associated with caregiver experience in families with a child with cerebral palsy.
- 2016
Medicine, Psychology
Journal of pediatric rehabilitation medicine
Caregiver experience varied widely and is associated with a range of factors among families caring for a child with CP and whether interventions to minimize the areas of greatest stress could make a meaningful difference in family functioning is tested.
Condition-specific quality of life questionnaires for caregivers of children with pediatric conditions: a systematic review
- 2012
Medicine, Psychology
Quality of Life Research
Data collected by condition-specific questionnaires can assist clinicians and health economists in estimating caregiver burden and the types of healthcare services caregivers require and may be useful for healthcare administrators to evaluate interventions.
Estimation of the Quality-of-Life Impact of X-Linked Myotubular Myopathy
- 2021
Psychology, Medicine
Journal of neuromuscular diseases
A substantial impact of XLMTM on utility weights is demonstrated, especially in terms of psychological wellbeing, pain and discomfort, and communication.
Parental Caregiver Expectations and Satisfaction Following Hip Reconstruction and Spinal Fusion in Children With Cerebral Palsy
- 2023
Medicine
Orthopedic nursing
A deeper understanding surrounding caregiver expectation and satisfaction following surgical procedures is needed.
Factors predicting distress among parents/caregivers of children with neurological disease and home enteral nutrition.
- 2014
Medicine, Psychology
Child: care, health and development
A high prevalence of symptoms of anxiety-depression, perception of burden overload and psychological distress in caregivers of children with HEN is found and greater practical and emotional support is required for these families.
Impact of Non‐medical Out‐of‐pocket Expenses on Families of Children With Cerebral Palsy Following Orthopaedic Surgery
- 2017
Medicine, Psychology
Journal of pediatric nursing
42 References
Initial development and validation of the Caregiver Priorities and Child Health Index of Life with Disabilities (CPCHILD).
- 2006
Medicine, Psychology
Developmental medicine and child neurology
The CPCHILD seems to be a reliable and valid measure of caregivers' perspectives on the health status, functional limitations, and well-being of these children.
Responsiveness and Uniqueness of the Pediatric Outcomes Data Collection Instrument Compared to the Gross Motor Function Measure for Measuring Orthopaedic and Neurosurgical Outcomes in Cerebral Palsy
- 2005
Medicine
Journal of pediatric orthopedics
The goal of this study was to evaluate the responsiveness, and secondarily the uniqueness, of the PODCI compared with the GMFM for evaluating surgical outcomes in CP.
Health-related quality of life and functional outcome measures for children with cerebral palsy.
- 2001
Psychology, Medicine
Developmental medicine and child neurology
The fair relationship found between the CQ and WeeFIM suggests that the constructs measured in these two assessments overlap, and the lack of correlation between the total summary scores of the CHQ and CQ suggests the C Q may be a more specific measure of HRQL for this population that reflects the impact of the child's condition on the caregiver.
Capturing Quality of Life in Pediatric Orthopaedics: Two Recent Measures Compared
- 2001
Medicine
Journal of pediatric orthopedics
The Child Health Questionnaire and the American Academy of Orthopaedic Surgeons Pediatric Outcomes Data Collection Instrument, two new pediatric health status measures, were assessed for their ability to detect differences in health states in a pediatric orthopaedics population.
Health-Related Quality of Life Outcomes Improve After Multilevel Surgery in Ambulatory Children With Cerebral Palsy
- 2007
Medicine, Psychology
Journal of pediatric orthopedics
Investigating the impact of multilevel surgery on the function and HRQOL in a group of ambulatory children with CP found that improved functional well-being does not imply improved psychosocial well- Being, and patients and their families should be counseled accordingly.
Psychometric properties of the quality of life questionnaire for children with CP
- 2007
Psychology, Medicine
Developmental medicine and child neurology
The validity of the CP QOL is supported by the pattern of correlations between CP Q OL‐Child scales with the CHQ, KIDSCREEN, and GMFCS, and preliminary statistics suggest that the child self‐report questionnaire has acceptable psychometric properties.
The health of primary caregivers of children with cerebral palsy: how does it compare with that of other Canadian caregivers?
- 2004
Medicine, Psychology
Pediatrics
Compared with the general population of CGs, CGs of children with cerebral palsy (CP) had lower incomes and were less likely to report working for pay, and more likely to list caring for their families as their main activity.
Assessment of Health Status in Patients With Cerebral Palsy: What is the Role of Quality-of-Life Measures?
- 2005
Medicine, Psychology
Journal of pediatric orthopedics
The CHQ was more effective for the quadriplegic group, but the diplegic and hemiplegic diagnostic groups exhibited a ceiling effect on 2 of the 12 domains in that questionnaire, and dynamic assessment would help to avoid ceiling and floor effects.
The Health and Well-Being of Caregivers of Children With Cerebral Palsy
- 2005
Psychology, Medicine
Pediatrics
The primary objective of the current study was to examine, within a single theory-based multidimensional model, the determinants of physical and psychological health of adult caregivers of children with CP.
Comparison of the Gross Motor Function Measure and Paediatric Evaluation of Disability Inventory in assessing motor function in children undergoing selective dorsal rhizotomy
- 2000
Medicine, Psychology
Developmental medicine and child neurology
Assessment with the functional outcome measures Gross Motor Function Measure (GMFM) and Pediatric Evaluation of Disability Inventory (PEDI) over time, in children with cerebral palsy undergoing selective dorsal rhizotomy combined with individualised physiotherapeutic interventions are compared.