目的:了解如何通过与医疗保健提供者沟通来影响乳腺癌和宫颈癌筛查,患者激活,和健康的社会决定因素。
方法:数据来自美国国家癌症研究所的健康信息国家趋势调查,重点研究21岁以上无癌症史的女性(N=1466)进行宫颈癌筛查,40岁以上的女性(N=1114)进行乳腺癌筛查。变量包括以患者为中心的沟通,电子医疗通信,患者激活,种族/民族,教育,健康保险状况,阿巴拉契亚住宅,金融不安全。
结果:电子通信预测了两种癌症筛查,尤其是白人女性。以患者为中心的沟通仅对有保险的女性影响宫颈癌筛查。它只会影响那些没有保险的人的乳房X光检查。患者激活并不影响任何癌症筛查行为。
结论:这些数据表明,需要更多细微差别来解析提倡的医疗保健行为的潜在影响。使用来自的公开可用数据集可以提供信息,但在方法上是有限的。
结论:医疗保健提供者和系统应在所有患者的常规临床就诊之外促进患者门户和其他电子交互手段的使用。然而,需要注意他们为患者提供的不平等福利。
OBJECTIVE: To understand how breast and cervical cancer screening are influenced by communicating with a healthcare provider, patient activation, and social determinants of health.
METHODS: Data were from the National Cancer Institute\'s Health Information National Trends Survey, focusing on women with no history of cancer at least 21 years old (N = 1466) to study cervical cancer screening and those at least 40 years old (N = 1114) to study breast cancer screening. Variables included patient-centered communication, electronic healthcare communication, patient activation, race/ethnicity, education, health insurance status, Appalachian residence, and financial insecurity.
RESULTS: Electronic communication predicted both cancer screens, but especially for White women. Patient-centered communication influenced cervical cancer screening only for women with insurance. It only influenced mammography for those without insurance. Patient activation did not influence either cancer screen behavior.
CONCLUSIONS: These data demonstrate more nuance is needed to parse potential effects of advocated-for healthcare behaviors. Use of publicly available datasets from can be informative but are limited methodologically.
CONCLUSIONS: Healthcare providers and systems should promote use of patient portals and other electronic means of interaction outside regular clinical visits for all patients. However, attention needs to be paid to the unequal benefits they afford to patients.