在纽约州癌症登记处报告的患者中确定与随访损失相关的因素。

Q4 Medicine
Journal of registry management Pub Date : 2022-01-01
Baozhen Qiao, April A Austin, Maria J Schymura, Xiuling Zhang, Colleen G Sherman
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引用次数: 0

摘要

背景:美国各州癌症登记处是估计以人群为基础的癌症生存率的数据来源。然而,患者随访的完整性会影响生存估计的准确性。与许多登记处一样,纽约州癌症登记处(NYSCR)主要通过与其他数据源的联系来进行患者随访。即使在付出了巨大的努力之后,仍然有一小部分患者失去了随访(LTFU)。在这项研究中,我们确定了与NYSCR中LTFU可能性相关的因素。方法:选择2000-2018年期间在纽约州居民中诊断出的原发性癌症(序列号为00或01,不包括死亡证明和尸检病例)进行研究。所有患者随访至2018年12月31日。根据每位患者的生命体征和最后一次接触日期,将随访状态分为两组:LTFU患者和非LTFU患者。通过人口统计学和肿瘤特征检查患者的LTFU。进行多变量logistic回归分析以评估人口统计学/肿瘤特征与LTFU可能性之间的关系。对于LTFU患者,LTFU的时间(1年内,1至10年)进一步描述。癌症诊断后5年内的LTFU率也进行了检查。结果:在1,797,228例患者中,2018年12月31日前有74,722例LTFU,占所有患者的4.2%,占在世患者的7.6%。约60%的LTFU发生在癌症诊断后1年内。与参照组相比,logistic回归分析表明,LTFU患者更可能是女性、黑人、亚洲/太平洋岛民(API)、西班牙裔、外国出生、医疗补助保险、无保险、老年。结论:确定与患者LTFU相关的因素对癌症登记处改善随访数据很重要。我们发现LTFU不是随机的;相反,某些患者组的LTFU发生率高于其他患者组。对于通过联系开展后续工作的登记处来说,收集高质量和完整的人口数据至关重要,特别是关于女性、儿童、外国出生和少数种族/族裔群体的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identifying Factors Associated with Loss to Follow-up Among Patients Reported to the New York State Cancer Registry.

Identifying Factors Associated with Loss to Follow-up Among Patients Reported to the New York State Cancer Registry.

Background: State cancer registries in the United States are data sources for estimating population-based cancer survival. However, the completeness of patient follow-up can affect the accuracy of survival estimates. Like many registries, the New York State Cancer Registry (NYSCR) conducts patient follow-up largely through linkages with other data sources. Even after expending great effort on linkages, a small proportion of patients remain lost to follow-up (LTFU). In this study, we identified factors that are associated with the likelihood of LTFU in the NYSCR.

Methods: First primary cancers (sequence number, 00 or 01 and excluding death-certificate- and autopsy-only cases) diagnosed during 2000-2018 among New York State residents were selected for study. All patients were followed through December 31, 2018. Based on each patient's vital status and last contact date, follow-up status was categorized into 2 groups: patients LTFU and patients not LTFU. Patients LTFU were examined by demographic and tumor characteristics. Multivariate logistic regression analyses were performed to evaluate the association between demographic/tumor characteristics and likelihood of LTFU. For patients LTFU, the timing of LTFU (within 1 year, 1 to <5 years, 5 to <10 years, or >10 years) was further described. LTFU rates within 5 years after cancer diagnosis were also examined.

Results: Among 1,797,228 patients, 74,722 were LTFU prior to December 31, 2018, representing 4.2% of all patients and 7.6% of alive patients. About 60% of LTFU occurred within 1 year after cancer diagnosis. Compared to the reference group, logistic regression analyses indicated that patients LTFU were more likely to be female, Black, Asian/Pacific Islander (API), Hispanic, foreign born, insured by Medicaid, uninsured, aged <20 years, and living in New York City or metropolitan counties. Cases reported by laboratories only and physician offices also had a higher likelihood of LTFU. Similar patterns and effects were identified when evaluating 5-year LTFU.

Conclusion: Identifying factors associated with patient LTFU is important for cancer registries to improve follow-up data. We found that LTFU is not random; rather, certain patient groups have higher LTFU rates than others. For registries that conduct follow-up through linkages, it is critical to collect high-quality and complete demographic data, especially for females, children, the foreign born, and minority race/ethnicity groups.

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Journal of registry management
Journal of registry management Medicine-Medicine (all)
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