Department of Sociology, University of Massachusetts Boston and Harvard Medical School, Boston, MA, 02125-3393, USA.
MLW Associates, LLC, Southborough, USA.
BMC Health Serv Res. 2020 Mar 6;20(1):175. doi: 10.1186/s12913-020-5009-x.
Cancer control programs have added patient navigation to improve effectiveness in underserved populations, but research has yielded mixed results about their impact on patient satisfaction. This study focuses on three related research questions in a U.S. state cancer screening program before and after a redesign that added patient navigators and services for chronic illness: Did patient diversity increase; Did satisfaction levels improve; Did socioeconomic characteristics or perceived barriers explain improved satisfaction.
Representative statewide patient samples were surveyed by phone both before and after the program design. Measures included satisfaction with overall health care and specific services, as well as experience of eleven barriers to accessing health care and self-reported health and sociodemographic characteristics. Multiple regression analysis is used to identify independent effects.
After the program redesign, the percentage of Hispanic and African American patients increased by more than 200% and satisfaction with overall health care quality rose significantly, but satisfaction with the program and with primary program staff declined. Sociodemographic characteristics explained the apparent program effects on overall satisfaction, but perceived barriers did not. Further analysis indicates that patients being seen for cancer risk were more satisfied if they had a patient navigator.
Health care access can be improved and patient diversity increased in public health programs by adding patient navigators and delivering more holistic care. Effects on patient satisfaction vary with patient health needs, with those being seen for chronic illness likely to be less satisfied with their health care than those being seen for cancer risk. It is important to use appropriate comparison groups when evaluating the effect of program changes on patient satisfaction and to consider establishing appropriate satisfaction benchmarks for patients being seen for chronic illness.
癌症控制项目增加了患者导航员以改善服务不足人群的效果,但研究对其对患者满意度的影响得出的结果喜忧参半。本研究关注美国癌症筛查项目在重新设计后增加患者导航员和慢性病服务之前和之后的三个相关研究问题:患者多样性是否增加;满意度是否提高;社会经济特征或感知障碍是否解释了满意度的提高。
在项目设计前后,通过电话对全州有代表性的患者样本进行调查。措施包括对整体医疗保健和特定服务的满意度,以及对 11 项获取医疗保健障碍的体验以及自我报告的健康和社会人口统计学特征。多回归分析用于确定独立影响。
在项目重新设计后,西班牙裔和非裔美国患者的比例增加了 200%以上,整体医疗保健质量满意度显著提高,但对项目和主要项目工作人员的满意度下降。社会人口统计学特征解释了总体满意度的明显项目效果,但感知障碍没有。进一步分析表明,如果患者有患者导航员,那么他们对癌症风险的就诊满意度更高。
通过增加患者导航员并提供更全面的护理,可以改善公共卫生计划的医疗保健获取并增加患者多样性。对患者满意度的影响因患者的健康需求而异,与因癌症风险就诊的患者相比,因慢性病就诊的患者可能对其医疗保健满意度较低。在评估项目变更对患者满意度的影响时,使用适当的对照组非常重要,并考虑为慢性病就诊的患者建立适当的满意度基准。