Journal of Inborn Errors of Metabolism and Screening (Mar 2019)

Home-Based Care for Patients with Lysosomal Storage Disease: Experiences in Argentina

  • Maria Victoria Brunelli,
  • Maria Margarita Rabhansl,
  • Clara Delacre,
  • Maria Magdalena Dankert,
  • Maria Victoria Cuevillas,
  • Catalina Terán Frias

DOI
https://doi.org/10.1590/2326-4594-jiems-2018-0002
Journal volume & issue
Vol. 7

Abstract

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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.

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