Yang Ou, Zhang Yuting, To Yat Hang, M J IJzerman Maarten, Liu Judith, Gibbs Peter, Trapani Karen, Pearson Sallie-Anne, Franchini Fanny
Melbourne Institute: Applied Economic & Social Research, The University of Melbourne, Melbourne, Victoria, Australia
Melbourne Institute: Applied Economic & Social Research, The University of Melbourne, Melbourne, Victoria, Australia.
BMJ Open. 2024 Dec 9;14(12):e081483. doi: 10.1136/bmjopen-2023-081483.
We study how clinical and socioeconomic factors influence colorectal cancer (CRC) costs for patients and Medicare in Australia. The study seeks to extend the limited Australian literature on CRC costs by analysing comprehensive patient-level medical services and pharmaceutical cost data.
DESIGN, SETTING AND PARTICIPANTS: Using the Victorian Cancer Registry, we identified all patients in Victoria who were diagnosed with CRC from 2010 to 2019 and extracted their linked 2010-2021 Medicare data. This data includes expenses from the Pharmaceutical Benefits Scheme and Medicare Benefits Schedule services. We examined variables such as disease stage, CRC type, molecular profile, metastasis status and demographics (eg, age, birth country, socioeconomic level via the SEIFA index, and native language). We applied descriptive and log-linear multivariate regression analyses to explore patient and Medicare costs related to CRC treatment.
Costs significantly rise with advanced cancer stages, especially on medication costs. Patients' average out-of-pocket (OOP) expenses are roughly $A441 per year. Key cost influencers are gender, age and socioeconomic status. On average, males incur 13.5% higher annual costs, a significantly larger OOP expense, than females. Compared with patients aged 50 or below, there is a 7.1% cost increase for individuals aged 50-70 and an 8.8% decrease post-70, likely reflecting less intensive treatment for the elderly. Socioeconomic factors show a clear gradient. Wealthier areas experience higher costs, especially among native English speakers. Costs also vary based on cancer's anatomical location and specific genetic mutations.
The research highlights that CRC treatment expenses for patients and Medicare differ considerably due to factors such as diagnostic stage, demographics, anatomical location of the tumour and mutations. These cost variations lead to concerns about healthcare equality and decision-making autonomy. Policymakers may need to focus on early detection, increased support for advanced-stage patients, gender-sensitive healthcare, and equitable access to treatment across different socioeconomic groups.
我们研究临床和社会经济因素如何影响澳大利亚患者及医疗保险中结直肠癌(CRC)的费用。该研究旨在通过分析全面的患者层面医疗服务和药品费用数据,扩展澳大利亚关于CRC费用的有限文献。
设计、设置和参与者:利用维多利亚癌症登记处,我们确定了2010年至2019年在维多利亚被诊断为CRC的所有患者,并提取了他们2010 - 2021年的关联医疗保险数据。该数据包括药品福利计划和医疗保险福利计划服务的费用。我们研究了疾病阶段、CRC类型、分子特征、转移状态和人口统计学特征(如年龄、出生国家、通过社会经济指数反映的社会经济水平以及母语)等变量。我们应用描述性和对数线性多元回归分析来探索与CRC治疗相关的患者和医疗保险费用。
随着癌症分期的进展,费用显著增加,尤其是药物费用。患者每年的平均自付费用约为441澳元。关键的费用影响因素是性别、年龄和社会经济地位。平均而言,男性每年的费用比女性高13.5%,自付费用显著更高。与50岁及以下的患者相比,50 - 70岁的个体费用增加7.1%,70岁以后费用下降8.8%,这可能反映了老年人接受的治疗强度较低。社会经济因素呈现出明显的梯度。较富裕地区的费用更高,尤其是在以英语为母语的人群中。费用也因癌症的解剖位置和特定基因突变而有所不同。
该研究强调,由于诊断阶段、人口统计学特征、肿瘤的解剖位置和突变等因素,患者及医疗保险的CRC治疗费用存在显著差异。这些费用差异引发了对医疗保健平等和决策自主性的担忧。政策制定者可能需要关注早期检测、增加对晚期患者的支持、性别敏感的医疗保健以及不同社会经济群体公平获得治疗的机会。