Stein Kevin D, Alcaraz Kassandra I, Kamson Chelsey, Fallon Elizabeth A, Smith Tenbroeck G
Behavioral Research Center, American Cancer Society, Atlanta, Georgia, USA.
Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Psychooncology. 2016 Oct;25(10):1212-1221. doi: 10.1002/pon.4218. Epub 2016 Aug 12.
Research has increasingly documented sociodemographic inequalities in the assessment and management of cancer-related pain. Most studies have focused on racial/ethnic disparities, while less is known about the impact of other sociodemographic factors, including age and education. We analyzed data from a large, national, population-based study of cancer survivors to examine the influence of sociodemographic factors, and physical and mental health comorbidities on barriers to cancer pain management.
The study included data from 4707 cancer survivors in the American Cancer Society's Study of Cancer Survivors-II, who reported experiencing pain from their cancer. A multilevel, socioecological, conceptual framework was used to generate a list of 15 barriers to pain management, representing patient, provider, and system levels. Separate multivariable logistic regressions for each barrier identified sociodemographic and health-related inequalities in cancer pain management, controlling for years since diagnosis, disease stage, and cancer treatment.
Two-thirds of survivors reported at least 1 barrier to pain management. While patient-related barriers were most common, the greatest disparities were noted in provider- and system-level barriers. Specifically, inequalities by race/ethnicity, education, age, and physical and mental health comorbidities were observed.
Findings indicate survivors who were nonwhite, less educated, older, and/or burdened by comorbidities were most adversely affected. Future efforts in research, clinical practice, and policy should identify and/or implement new strategies to address sociodemographic inequalities in cancer pain management.
研究越来越多地记录了癌症相关疼痛评估与管理中的社会人口统计学不平等现象。大多数研究集中在种族/族裔差异方面,而对于包括年龄和教育程度在内的其他社会人口统计学因素的影响了解较少。我们分析了一项基于全国人口的大型癌症幸存者研究的数据,以检验社会人口统计学因素以及身心健康合并症对癌症疼痛管理障碍的影响。
该研究纳入了美国癌症协会癌症幸存者研究-II中4707名癌症幸存者的数据,这些幸存者报告称患有因癌症引起的疼痛。采用多层次社会生态概念框架生成了一份包含15项疼痛管理障碍的清单,代表患者、医护人员和系统层面。针对每项障碍分别进行多变量逻辑回归,以确定癌症疼痛管理中社会人口统计学和健康相关的不平等现象,同时控制自诊断以来的年限、疾病阶段和癌症治疗情况。
三分之二的幸存者报告至少存在1项疼痛管理障碍。虽然与患者相关的障碍最为常见,但在医护人员和系统层面的障碍中观察到的差异最大。具体而言,观察到了种族/族裔、教育程度、年龄以及身心健康合并症方面的不平等现象。
研究结果表明,非白人、受教育程度较低、年龄较大和/或患有合并症的幸存者受到的不利影响最大。未来在研究、临床实践和政策方面的努力应确定和/或实施新策略,以解决癌症疼痛管理中的社会人口统计学不平等问题。