Quality of life in pediatric asthma patients and their parents: a meta-analysis on 20 years of research
@article{Silva2015QualityOL, title={Quality of life in pediatric asthma patients and their parents: a meta-analysis on 20 years of research}, author={Neuza Silva and Carlos Carona and Carla Crespo and Maria Cristina Canavarro}, journal={Expert Review of Pharmacoeconomics \& Outcomes Research}, year={2015}, volume={15}, pages={499 - 519} }
Introduction: This meta-analytic review was conducted to estimate the magnitude of quality of life (QoL) impairments in children/adolescents with asthma and their parents. Method: A systematic search in four electronic databases revealed 15 quantitative studies published between 1994–2013 that directly compared the QoL of 7- to 18-year-old asthma patients/parents to community/healthy controls. Pooled mean differences (MD) with 95% CI were estimated using the inverse-variance random-effects…
30 Citations
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Physical HRQoL is not impaired in the majority of parents seeking treatment for their child's functional abdominal pain, however, the time demands and worries due to the child’s pain deserve specific attention.
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- Medicine, PsychologyApplied research in quality of life
- 2018
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- MedicineJournal of Korean Academy of Nursing
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Strategies for promoting self-efficacy and enforcing asthma knowledge will be helpful for the improvement of health-related quality of life with school-aged asthmatic children.
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Evidence of adequate psychometrics for the KIDSCREEN-27 in young children with chronic physical illness is provided, and measurement invariance testing and discriminant and convergent validity assessments are conducted.
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- Medicine, Psychology
- 2017
The results showed that the asthma module assesses unique aspects of living with asthma and is more sensitive to asthma severity than the generic module, showing its usefulness in clinical practice.
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Broad-spectrum family-centred interventions in paediatric asthma settings can target the development of the parents’ coping tendencies characterised by greater acceptance and less denial as a way of reappraising caregiving demands as less burdensome and improving their QoL.
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