Abstract C24: Determinants of delays in care-seeking for ovarian cancer symptoms in African American women

M. Mullins, M. Cote, Sarah E. Abbott, A. Alberg, E. Bandera, J. Barnholtz-Sloan, M. Bondy, F. Camacho, E. Funkhouser, P. Moorman, L. Peres, A. Schwartz, P. Terry, Frances F Wang, J. Schildkraut, E. Peters
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However, several studies, performed in samples predominantly comprised of White women, suggest insurance and income do not sufficiently reflect access to care. Here, we examine whether delay in care-seeking (captured through duration of symptoms prior to diagnosis) among African American women is more strongly influenced by socioeconomic status, access to care, or social access barriers (discrimination and trust in physicians). Methods: This analysis includes data from 550 African American women with ovarian cancer enrolled in the African American Cancer Epidemiology Study (AACES). AACES is a case-control study spanning 11 geographic regions in the United States: North Carolina, South Carolina, Georgia, Alabama, Tennessee, Louisiana, Texas, New Jersey, Ohio, Chicago, and Detroit. Included in the phone-administered AACES survey were questions about symptoms associated with ovarian cancer such as abdominal lumps, changes in bowel habits, and abnormal vaginal bleeding, in the year prior to ovarian cancer diagnosis. If a woman indicated she had a symptom, duration of the symptom was recorded in months. Logistic regression was used to estimate the odds ratios between predictors of accessing care and the outcome of treatment delay. The outcome was defined as having any of the 10 symptoms for at least eight months prior to diagnosis (i.e., those exceeding the seven-month mean symptom duration in this population). Models were adjusted for region, age at diagnosis, histotype, first-degree family history of breast or ovarian cancer, marital status, body mass index, Charlson comorbidity score, pelvic-inflammatory disease history, education, and income. Access to care variables included regular source of health care, insurance, regular physician relationship, and experiencing a barrier to accessing health care. Perceived discrimination was evaluated using the mean response score for questions from Williams9 Everyday Discrimination Scale. Trust in physicians was modeled using the mean response score from the Anderson Dedrick Trust in Physicians Scale. Results: 41% (n=227) of women reported having at least one symptom for eight months prior to diagnosis. After adjustment for confounders, trust in physicians was inversely associated with longer duration of symptoms. A one-unit increase in the mean trust score was associated with 0.73 times the odds of women reporting undiagnosed symptoms in the previous 8 months (OR 0.73 CI 0.55-0.96). Conversely, a one-unit increase in frequency of mean everyday discrimination score was associated with 1.56 times the odds of 8 months of undiagnosed symptoms (OR 1.56 CI 1.14-2.15), after adjustment for confounders. Access to care measures and socioeconomic variables were not associated with longer symptom length in this study population. Conclusions: Various studies have considered access to care mainly in terms of availability of health insurance. Our results suggest perceived discrimination and lack of trust in physicians are important barriers to African American women seeking treatment for their ovarian cancer symptoms, even after controlling for socioeconomic status, insurance, and source of care. Citation Format: Megan Mullins, Michele L. Cote, Sarah Abbott, Anthony J. Alberg, Elisa V. Bandera, Jill Barnholtz-Sloan, Melissa Bondy, Fabian Camacho, Ellen Funkhouser, Patricia G. Moorman, Lauren C. Peres, Ann G. Schwartz, Paul D. Terry, Frances Wang, Joellen M. Schildkraut, Edward S. Peters. Determinants of delays in care-seeking for ovarian cancer symptoms in African American women [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. 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引用次数: 0

Abstract

Introduction: Ovarian cancer is the most deadly gynecologic cancer, and the mortality burden is disproportionately higher among African American women. Women diagnosed with stage IV disease have less than a 30% 5-year survival rate, compared to 90% 5-year survival in stage I disease, which highlights the importance of early diagnosis. Lack of financial means and limited access to care may contribute to delays in symptomatic women seeking treatment, with consequent later stage at diagnosis. However, several studies, performed in samples predominantly comprised of White women, suggest insurance and income do not sufficiently reflect access to care. Here, we examine whether delay in care-seeking (captured through duration of symptoms prior to diagnosis) among African American women is more strongly influenced by socioeconomic status, access to care, or social access barriers (discrimination and trust in physicians). Methods: This analysis includes data from 550 African American women with ovarian cancer enrolled in the African American Cancer Epidemiology Study (AACES). AACES is a case-control study spanning 11 geographic regions in the United States: North Carolina, South Carolina, Georgia, Alabama, Tennessee, Louisiana, Texas, New Jersey, Ohio, Chicago, and Detroit. Included in the phone-administered AACES survey were questions about symptoms associated with ovarian cancer such as abdominal lumps, changes in bowel habits, and abnormal vaginal bleeding, in the year prior to ovarian cancer diagnosis. If a woman indicated she had a symptom, duration of the symptom was recorded in months. Logistic regression was used to estimate the odds ratios between predictors of accessing care and the outcome of treatment delay. The outcome was defined as having any of the 10 symptoms for at least eight months prior to diagnosis (i.e., those exceeding the seven-month mean symptom duration in this population). Models were adjusted for region, age at diagnosis, histotype, first-degree family history of breast or ovarian cancer, marital status, body mass index, Charlson comorbidity score, pelvic-inflammatory disease history, education, and income. Access to care variables included regular source of health care, insurance, regular physician relationship, and experiencing a barrier to accessing health care. Perceived discrimination was evaluated using the mean response score for questions from Williams9 Everyday Discrimination Scale. Trust in physicians was modeled using the mean response score from the Anderson Dedrick Trust in Physicians Scale. Results: 41% (n=227) of women reported having at least one symptom for eight months prior to diagnosis. After adjustment for confounders, trust in physicians was inversely associated with longer duration of symptoms. A one-unit increase in the mean trust score was associated with 0.73 times the odds of women reporting undiagnosed symptoms in the previous 8 months (OR 0.73 CI 0.55-0.96). Conversely, a one-unit increase in frequency of mean everyday discrimination score was associated with 1.56 times the odds of 8 months of undiagnosed symptoms (OR 1.56 CI 1.14-2.15), after adjustment for confounders. Access to care measures and socioeconomic variables were not associated with longer symptom length in this study population. Conclusions: Various studies have considered access to care mainly in terms of availability of health insurance. Our results suggest perceived discrimination and lack of trust in physicians are important barriers to African American women seeking treatment for their ovarian cancer symptoms, even after controlling for socioeconomic status, insurance, and source of care. Citation Format: Megan Mullins, Michele L. Cote, Sarah Abbott, Anthony J. Alberg, Elisa V. Bandera, Jill Barnholtz-Sloan, Melissa Bondy, Fabian Camacho, Ellen Funkhouser, Patricia G. Moorman, Lauren C. Peres, Ann G. Schwartz, Paul D. Terry, Frances Wang, Joellen M. Schildkraut, Edward S. Peters. Determinants of delays in care-seeking for ovarian cancer symptoms in African American women [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr C24.
C24:非洲裔美国妇女卵巢癌症状延迟求医的决定因素
卵巢癌是最致命的妇科癌症,非裔美国妇女的死亡率负担不成比例地高。被诊断为IV期疾病的妇女的5年生存率不到30%,而I期疾病的5年生存率为90%,这突出了早期诊断的重要性。缺乏经济手段和获得护理的机会有限,可能导致有症状的妇女延误寻求治疗,从而导致诊断阶段较晚。然而,在主要由白人妇女组成的样本中进行的几项研究表明,保险和收入并不能充分反映获得医疗服务的机会。在这里,我们研究了非裔美国妇女的求诊延迟(通过诊断前症状的持续时间来衡量)是否受到社会经济地位、获得护理的机会或社会准入障碍(歧视和对医生的信任)的更强烈影响。方法:本分析包括了参加非裔美国人癌症流行病学研究(AACES)的550名患有卵巢癌的非裔美国妇女的数据。AACES是一项横跨美国11个地理区域的病例对照研究:北卡罗来纳州、南卡罗来纳州、佐治亚州、阿拉巴马州、田纳西州、路易斯安那州、德克萨斯州、新泽西州、俄亥俄州、芝加哥和底特律。在电话管理的aace调查中,包括在卵巢癌诊断前一年与卵巢癌相关的症状,如腹部肿块、排便习惯的改变和阴道异常出血。如果一名妇女表示她有症状,症状的持续时间以月为单位记录下来。使用逻辑回归来估计获得护理的预测因子与治疗延迟结果之间的比值比。结果定义为在诊断前至少8个月出现上述10种症状中的任何一种(即,在该人群中超过7个月的平均症状持续时间)。根据地区、诊断年龄、组织型、乳腺癌或卵巢癌一级家族史、婚姻状况、体重指数、Charlson合并症评分、盆腔炎性病史、教育程度和收入对模型进行调整。获得医疗服务的变量包括定期的医疗服务来源、保险、定期的医生关系以及在获得医疗服务方面遇到的障碍。感知歧视使用威廉斯日常歧视量表问题的平均回答得分来评估。对医生的信任使用安德森·德德里克医生信任量表的平均反应得分来建模。结果:41% (n=227)的女性报告在诊断前8个月至少有一种症状。调整混杂因素后,对医生的信任与症状持续时间呈负相关。平均信任评分每增加一个单位,在过去8个月内报告未确诊症状的女性几率增加0.73倍(OR 0.73 CI 0.55-0.96)。相反,在调整混杂因素后,平均每日辨别评分频率每增加一个单位,8个月未确诊症状的几率就增加1.56倍(OR 1.56 CI 1.14-2.15)。在本研究人群中,获得护理措施和社会经济变量与较长的症状长度无关。结论:各种研究主要从健康保险的可得性角度来考虑获得保健的机会。我们的研究结果表明,即使在控制了社会经济地位、保险和护理来源之后,对医生的感知歧视和缺乏信任是非洲裔美国妇女寻求卵巢癌症状治疗的重要障碍。引文格式:Megan Mullins, Michele L. Cote, Sarah Abbott, Anthony J. Alberg, Elisa V. Bandera, Jill Barnholtz-Sloan, Melissa Bondy, Fabian Camacho, Ellen Funkhouser, Patricia G. Moorman, Lauren C. Peres, Ann G. Schwartz, Paul D. Terry, Frances Wang, Joellen M. Schildkraut, Edward S. Peters。非裔美国妇女卵巢癌症状延迟求医的决定因素[摘要]。见:第十届AACR会议论文集:种族/少数民族和医疗服务不足人群的癌症健康差异科学;2017年9月25-28日;亚特兰大,乔治亚州。费城(PA): AACR;癌症流行病学杂志,2018;27(7增刊):摘要nr C24。
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