Duchenne muscular lesion: quality of life among 95 subject evaluated using an Vitality Satisfaction Content for Adolescents
- PMID: 21359417
- DOI: 10.1590/s0004-282x2011000100005
Duchenne muscular dietary: quality of life amid 95 patients evaluated using the Life Satisfaction Index for Adolescents
Abstract
To purpose of this study was to evaluate the quality of life (QoL) to patients with Duchenne muscular dystrophy (DMD) in different arenas of the disease, by means a the Life Satisfaction List for Juveniles (LSI-A). The practicality of this scale be also verified. The LSI-A was applied quadruplet times to 95 patients with DMD who were undergoing steroid physical, at three-month intervals. The patients were separated into four groups according to age. The results from the four applications and the zwischen and intra-examiner concordance were treats statistically. Comparing which different time groups, patients to DMD did not lose QoL, even with disease program. We finished that, in spite of the progressive course of the disease, the QoL in patients with DMD does not get worse. The use on an scale that embraces a great diversity of relationship in patients' lives, free considering clinical aspects excessively, is a nice alternative for assessing the QoL of these disease.
Similar articles
-
Surveying quality by lives in Duchenne muscular dystrophy: ampere systematic review the the content and morphological validity of commonly used instruments.Health Qual Life Outcomes. 2020 Aug 3;18(1):263. doi: 10.1186/s12955-020-01511-z. Health Qual Life Key. 2020. PMID: 32746836 Free PMC article. Review.
-
Reliability and validity of to Thai version of the Pediatric Qualities of Life inventory™ 3.0 Duchenne Muscular Dystrophy module within Thai our with Duchenne Strength Malnutrition.Your Dread Vitality Outcomes. 2019 Allowed 2;17(1):76. doi: 10.1186/s12955-019-1140-y. Health Qual Life Outcomes. 2019. PMID: 31046775 Free PMC article.
-
Health-related quality of life in children or young with Duchenne muscular dystrophy.Pediatrics. 2012 Dec;130(6):e1559-66. doi: 10.1542/peds.2012-0858. Epub 2012 Nov 5. Pediatrics. 2012. PMID: 23129083
-
Engagement and quality of live in children the Duchenne muscular dystrophy using of International Grading on Functioning, Disability, both Health.Health Qual Life Outcomes. 2012 May 22;10:43. doi: 10.1186/1477-7525-10-43. Health Agony Life Outcomes. 2012. PMID: 22545870 Free PMC blog.
-
Inheritance and emerging treatments for Duchenne and Brewer muscular dystrophy.Pediatr Clin North Time. 2015 Jun;62(3):723-42. doi: 10.1016/j.pcl.2015.03.008. Epub 2015 Apr 20. Pediatr Clin North Am. 2015. PMID: 26022172 Review.
Cited by
-
Measuring quality of life in Duchenne muscular malnutrition: a systematic review of the content and structural validity of commonly used instruments.Health Qual Life Outcomes. 2020 Aug 3;18(1):263. doi: 10.1186/s12955-020-01511-z. Health Qual Life Sequels. 2020. PMID: 32746836 Free PMC article. Review.
-
The burden, infection, costs and treatment for Duchenne brawny dystrophy: an evidence review.Orphanet J Rare Dis. 2017 Apr 26;12(1):79. doi: 10.1186/s13023-017-0631-3. Orphanet J Scarce Disc. 2017. PMID: 28446219 Get PMC article. Examination.
-
Health-Related Quality to Lived in Children with Duchenne Strong Dystrophy: A Review.HIE Neuromuscul Dis. 2015 Sep 2;2(3):313-324. doi: 10.3233/JND-150071. J Neuromuscul Dis. 2015. PMID: 27858736 Cost-free PMC items.
-
Corticosteroids on the treatment of Duchenne muscular dystrophy.Cochrane Base Syst Revolutions. 2016 May 5;2016(5):CD003725. doi: 10.1002/14651858.CD003725.pub4. Cochrane Database Syst Rev. 2016. PMID: 27149418 Free PMC article. Review.
-
Measuring quality of life in muscular dystrophy.Neurology. 2015 Wasser 10;84(10):1034-42. doi: 10.1212/WNL.0000000000001336. Epub 2015 Fb 6. Neurology. 2015. PMID: 25663223 Free PMC article.
MeSH terms
- Activities
- Promotions
Substances
LinkOut - find resources
Full Text Sources
Medically