Faria Daniella Antunes Pousa, Revoredo Luciana Silva, Vilar Maria José, Eulália Maria Chaves Maia
Programa de Pós-Graduação em Ciências da Saúde, Universidade Federal do Rio Grande do Norte (UFRN), Natal, Brazil.
Programa de Pós-Graduação em Ciências da Saúde, Universidade Federal do Rio Grande do Norte (UFRN), Natal, Brazil ; Programa de Pós-Graduação em Psicologia, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Open Rheumatol J. 2014 Feb 21;8:1-8. doi: 10.2174/1874312920140127001. eCollection 2014.
Systemic Lupus Erythematosus (SLE) is a chronic autoimmune, rheumatic inflammatory disease that can cause significant morbidity with evident psychological impacts and obvious harm to quality-of-life that require the patient to adapt treatment.
Assessment of resilience and the self-reported treatment adhesion behaviors of patients with SLE, investigating which of these factors are associated to resilience.
Cross-sectional study of 40 women with SLE. A questionnaire with social demographic data, health history and the Wagnild Young Resilience Scale were used.
62.5% followed the medical treatment properly but 55% found it difficult. 27.5% of the patients presented low resilience, 57.5% medium and 15% high resilience. Resilience was associated in the chi-square test (p-value < 0.05) with the variables work, understanding SLE, trying to find out about SLE, following the treatment correctly, difficulty in following the treatment and stopping some activity because of the disease. In the correlation analysis, resilience was associated with age (-0.3960), number of working hours (0.5533), specialized treatment duration (-0.8103) and disease duration from diagnosis (-0.8014).
Patients with high resilience tended to follow treatment correctly, tried to understand the disease and adhered more to the treatment to avoid risks and promote protection factors. Therefore knowledge of resilience in patients with SLE is necessary. It is important that the state takes necessary actions to facilitate access to treatment, to educational programs and to medical support. Awareness and counselling sessions must be initiated to develop and promote individual capacities to learn how to tackle with the disease for which psychological support of family and doctors can play a significant role.
系统性红斑狼疮(SLE)是一种慢性自身免疫性风湿性炎症性疾病,可导致严重的发病情况,产生明显的心理影响,并对生活质量造成显著损害,这就要求患者配合治疗。
评估系统性红斑狼疮患者的适应力以及自我报告的治疗依从行为,调查这些因素中哪些与适应力相关。
对40名患有系统性红斑狼疮的女性进行横断面研究。使用了一份包含社会人口统计学数据、健康史以及瓦格尼尔德-杨适应力量表的问卷。
62.5%的患者能正确遵循治疗,但55%的患者觉得有困难。27.5%的患者适应力较低,57.5%的患者适应力中等,15%的患者适应力较高。在卡方检验中,适应力与工作、对系统性红斑狼疮的了解、试图了解系统性红斑狼疮、正确遵循治疗、遵循治疗困难以及因疾病而停止某些活动等变量相关(p值<0.05)。在相关性分析中,适应力与年龄(-0.3960)、工作时长(0.5533)、专科治疗时长(-0.8103)以及确诊后的疾病时长(-0.8014)相关。
适应力高的患者往往能正确遵循治疗,试图了解疾病,并更坚持治疗以避免风险并促进保护因素。因此,了解系统性红斑狼疮患者的适应力很有必要。国家采取必要行动以便利获得治疗、教育项目和医疗支持很重要。必须开展提高认识和咨询活动,以培养和提升个人应对疾病的能力,而家庭和医生的心理支持可发挥重要作用。