Home-Based Care for Patients with Lysosomal Storage Disease: Experiences in Argentina
J. inborn errors metab. screen
; 7: e20180002, 2019. tab
Article
in En
|
LILACS-Express
| LILACS
| ID: biblio-1090980
Responsible library:
BR1.1
ABSTRACT
ABSTRACT Enzyme replacement therapy (ERT) is a long term treatment for patients who suffer from lysosomal storage disease. A transversal descriptive study was conducted to evaluate advantages and disadvantages of a home-based care program for patients with Gaucher, Fabry and Mucopolysaccharidosis II (MPS II) diseases. A survey among patients and nurses involved in healthcare delivery at home was utilized for this study. The adherence rate was 92.9% over the study period. Eighty six point nine percent chose to carry out the treatment at home and 88.5% felt that their quality of life had improved. Additional advantages reported were comfort (77%), treatment adjustment to daily activities (69%) and flexibility (58%). Disadvantages expressed were lack of confidence with the health care provider at home (1.6%) and a shortage of disposable materials available (1.6%). The main benefits of home-based treatment were the high treatment adherence and the improvement in quality of life.
Full text:
1
Collection:
01-internacional
Database:
LILACS
Aspects:
Patient_preference
Country/Region as subject:
America do sul
/
Argentina
Language:
En
Journal:
J. inborn errors metab. screen
Journal subject:
Medicina Cl¡nica
/
Patologia
Year:
2019
Document type:
Article
Affiliation country:
Argentina
Country of publication:
Brazil