| Autor: |
Juliana Passos da Silva, Janete Lane Amadei |
| Jazyk: |
English<br />Spanish; Castilian<br />Portuguese |
| Rok vydání: |
2016 |
| Předmět: |
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| Zdroj: |
Revista Brasileira de Reumatologia, Vol 56, Iss 3, Pp 198-205 (2016) |
| Druh dokumentu: |
article |
| ISSN: |
1809-4570 |
| DOI: |
10.1016/j.rbre.2015.08.017 |
| Popis: |
ABSTRACT Lupus requires careful treatment by medical specialists. This study aimed to evaluate the quality of life of patients living with Systemic Lupus Erythematosus (SLE). The method approached women with a confirmed diagnosis of SLE under medical supervision in a University hospital outpatient clinic or in a private clinic. We used an instrument containing relevant information of the patient and also the Portuguese version of the World Health Organization Quality of Life Group (WHOQOL-100) questionnaire. The study population consisted of 39 women, married in their majority (56.4%); prevalently aged 37–60 years old; prevalence of diagnosis time over five years (66.7%); and in use of less than 5 medications (69.2%). 92.3% had the disease inactive with higher means in mobility (p = 0.0463) and quality of life (p = 0.0199) facets; on the other hand, the physical safety and security facet (p = 0.0093) showed higher mean for people with active disease. Health and social care analysis showed availability and quality (p = 0.0434), even when with other associated diseases (33.3%); and the highest means were Dependence on medicinal substances and medical aids (p = 0.0143). The negative results for associated diseases were higher in sexual activity (p = 0.0431) and transportation (p = 0.0319) facets. In conclusion: if women living with SLE receive continuous medical attention, they will enjoy good quality of life, while minimizing the complications inherent in this condition. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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