College of Nursing, The University of Iowa, Iowa City, IA, USA.
Nurs Res. 2013 Mar-Apr;62(2):106-14. doi: 10.1097/NNR.0b013e3182843b77.
Factors contributing to patient-reported experiences of diabetes self-management support are not understood well, particularly over time.
The aim of the study was to identify the contribution of patient characteristics to patient-reported quality of SMS.
Using secondary data from a prospective clinical trial (n = 339) comparing three approaches of providing diabetes self-management support (Group Medical Visits, Automated Telephone Support, and Usual Care) in a diverse, underserved population, the influence of patient characteristics (e.g., age, gender, income, and health status) was examined on Patient Assessment of Chronic Illness Care ratings.
At baseline, older age (p = .014), being female (p = .038), and having lower income (p = .001) were associated with lower ratings. Income and interactions involving income combined explained 12% of the variance in baseline ratings. Compared with White patients, African American and Asian patients tended to have higher baseline ratings (p = .076 and p = .045, respectively). Race or ethnicity influenced perceptions throughout the trial, explaining 5% of the variance at baseline and 2% of the variance in 1-year changes in Patient Assessment of Chronic Illness Care ratings. As expected, over 1 year, ratings increased more for patients in both intervention groups compared with the control group (p < .001).
Ratings of healthcare quality are influenced by patient characteristics independent of the nature of the care provided. Understanding more precisely how these differences are associated with differences in clinical processes will be particularly important for efforts aiming to integrate patient-reported measures into assessments of healthcare quality during routine clinical care and clinical trials.
导致患者报告的糖尿病自我管理支持体验的因素尚不清楚,尤其是随着时间的推移。
本研究旨在确定患者特征对患者报告的 SMS 质量的贡献。
利用一项前瞻性临床试验(n=339)的二次数据,该试验比较了三种提供糖尿病自我管理支持的方法(团体医疗访视、自动电话支持和常规护理)在多样化、服务不足的人群中的效果,考察了患者特征(如年龄、性别、收入和健康状况)对慢性病患者评估的影响。
在基线时,年龄较大(p=0.014)、女性(p=0.038)和收入较低(p=0.001)与较低的评分相关。收入和涉及收入的交互作用共同解释了基线评分的 12%的差异。与白人患者相比,非裔美国人和亚裔患者的基线评分较高(p=0.076 和 p=0.045)。种族或族裔影响整个试验期间的看法,在基线时解释了 5%的差异,在慢性病患者评估的 1 年变化中解释了 2%的差异。正如预期的那样,与对照组相比,干预组的患者在 1 年内的评分增加更多(p<0.001)。
医疗质量的评分受到患者特征的影响,而与提供的护理性质无关。更准确地了解这些差异与临床过程差异的关联,对于将患者报告的测量结果纳入常规临床护理和临床试验中的医疗质量评估将特别重要。