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Disease burden of spinal muscular atrophy in Germany

Authors :
Constanze, Klug
Olivia, Schreiber-Katz
Simone, Thiele
Elisabeth, Schorling
Janet, Zowe
Peter, Reilich
Maggie C, Walter
Klaus H, Nagels
Source :
Orphanet Journal of Rare Diseases
Publication Year :
2016

Abstract

Background This study aimed at analyzing the economic burden and disease-specific health-related quality of life (HRQOL) of patients with spinal muscular atrophy (SMA) in Germany. SMA is a so far non-curable neuromuscular disease of the anterior nerve cells that causes high rates of morbidity and mortality. Methods In a cross-sectional study we analyzed the cost of illness (COI) and factors that influence the direct, indirect and informal care costs of affected patients and their families by using standardized, self-developed questionnaires. We used the PedsQLâ„¢© Measurement Model to analyze the disease-specific HRQOL of patients. Results One hundred eighty nine patients with SMA types I to III aged

Details

ISSN :
17501172
Volume :
11
Issue :
1
Database :
OpenAIRE
Journal :
Orphanet journal of rare diseases
Accession number :
edsair.pmid..........4746782d10dcc012d01394fb5ad7b9c5