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首页> 外文期刊>The journal of asthma >The relationship between caregivers' subjective social status and asthma symptoms and management for urban children
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The relationship between caregivers' subjective social status and asthma symptoms and management for urban children

机译:城市儿童的护理人员主观社会地位与哮喘症状与管理的关系

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Objective: Subjective social status (SSS) is a person's perception of his/her social standing among others. We explored the relationship between caregivers' SSS and asthma symptoms, visits, and medication use among children with persistent asthma. Methods: We analyzed baseline data of children (3-10 years) from the SB-TEAM trial in Rochester, NY. Using a modified MacArthur Scale of SSS, caregivers rated themselves "a lot worse off" to "a lot better off" compared to 4 groups (e.g., neighbors). "Low SSS" was defined by a response of "a lot worse off" or "somewhat worse off" for any of the referent groups. Caregivers reported their child's asthma symptoms, healthcare visits for asthma, and medication use. Bivariate and multivariate statistics were used. Results: We found that, of the 230 children enrolled (participation rate:78%, 62% Black, 72% Medicaid), 29% of caregivers had low SSS. Caregivers with low SSS had more depressive symptoms (46% vs. 28%) and lower social support (69.1 vs. 77.7). In multivariable analyses, children of caregivers with low SSS had fewer symptom-free days/2 weeks (5.8 vs. 7.9, p = .01). While they were more likely to have a routine asthma visit in the past year (35% vs. 23%, adjusted p = .03), there was no difference in their use of preventive medication. Conclusions: Many caregivers of children with persistent asthma report low SSS. While children of these caregivers had fewer symptom-free days, they were not more likely to use preventive medications. Efforts are needed to support these caregivers to ensure optimal preventive care and reduce morbidity.
机译:目的:主观的社会地位(SSS)是一个人对他/她社会站立等人的看法。我们探讨了护理人员患者和哮喘症状,访问和患有持续性哮喘的儿童之间的关系。方法:我们分析了纽约州罗切斯特的SB-Team审判中儿童(3 - 10年)的基线数据。使用SSS的改进的宏图量级,看护人与4组(例如,邻居)相比,看护人自己“更好地更好”到“更好”。 “低SSS”由任何指示小组的“较小”或“稍微差”的响应定义。护理人员报告了孩子的哮喘症状,医疗保健访问哮喘和药物使用。使用了生物化和多变量统计数据。结果:我们发现,230名儿童注册(参与率:78%,62%的黑色,72%的医疗补助),29%的护理人员有低SSS。低SSS的护理人员具有更高的抑郁症状(46%与28%)和较低的社会支持(69.1与77.7)。在多变量分析中,低SSS的护理人员的儿童无症状天数/ 2周(5.8与7.9,P = .01)。在过去的一年中,他们更有可能在常规哮喘访问(35%对23%,调整的P = .03),但它们使用预防性药物没有差异。结论:持久性哮喘报告低SSS的儿童的许多照顾者。虽然这些护理人员的儿童无症状天数较少,但它们并不可能使用预防性药物。需要努力来支持这些护理人员,以确保最佳的预防性保健和降低发病率。

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