Inequities in the Time to Colon Cancer Diagnosis Among Individuals With Severe Psychiatric Illness

IF 3.1 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2025-02-17 DOI:10.1002/cam4.70623
Jonah H. Gorodensky, Laura Davis, Rebecca Griffiths, Oyedeji Ayonrinde, Colleen Webber, Timothy P. Hanna, Natalie Coburn, Alyson L. Mahar
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Abstract

Introduction

Early colon cancer detection is critical for improving outcomes. The diagnostic interval is a useful approach to conceptualizing time-to-diagnosis within the healthcare system and understanding the diagnostic journey. Adults with severe psychiatric illness (SPI) are less likely to participate in cancer screening and more likely to be diagnosed with advanced cancers. We investigated the association between having an SPI and the colon cancer diagnostic interval.

Methods

We conducted a cross-sectional study of adults diagnosed with colon cancer in Ontario, Canada between 2007 and 2019 using administrative health data. Individuals with healthcare encounters consistent with pre-existing major depression, schizophrenia, bipolar disorder, or other non-organic psychotic illnesses were considered as having SPI. Individuals with an SPI-related hospitalization were categorized as having an inpatient SPI; the rest were considered outpatient. We calculated the diagnostic interval as the number of days from first colon cancer-related healthcare encounter to cancer diagnosis. Diagnostic pathways were assessed descriptively, including whether diagnosis was made symptomatically or with no symptom recorded. Quantile regression (stratified by symptom status) was used to quantify the association between SPI status and the diagnostic interval.

Results

We identified 42,143 individuals with colon cancer: 40,884 with no history of mental illness, 835 with a history of outpatient SPI, and 424 with inpatient SPI. Adults with SPI were significantly more likely to be diagnosed symptomatically (inpatient: 89.9%, outpatient: 86.6%, no SPI: 80.9%, p < 0.001). Individuals with SPI experienced a significantly longer median symptomatic diagnostic interval and a similar median diagnostic interval when diagnosed with no symptom recorded, relative to those without a history of mental illness. After adjusting for covariates, the median symptomatic diagnostic interval was 48 days longer (95% CI 28, 68) among individuals with outpatient SPI and 55 days longer (95% CI 28, 82) among individuals with inpatient SPI compared to those with no SPI.

Conclusion

Individuals with SPI were more likely to be diagnosed symptomatically and had longer symptomatic diagnostic intervals than those without. This study represents a first step in targeting and improving cancer diagnostic processes for individuals with SPI.

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在患有严重精神疾病的个体中,结肠癌诊断时间的不公平
早期结肠癌检测对改善预后至关重要。诊断间隔是概念化医疗保健系统内的诊断时间和理解诊断过程的有用方法。患有严重精神疾病(SPI)的成年人不太可能参加癌症筛查,更有可能被诊断为晚期癌症。我们调查了SPI与结肠癌诊断间隔的关系。方法:我们对2007年至2019年加拿大安大略省诊断为结肠癌的成年人进行了一项横断面研究,使用了行政健康数据。患有先前存在的严重抑郁症、精神分裂症、双相情感障碍或其他非器质性精神病的个体被认为患有SPI。与SPI相关住院的个体被归类为住院SPI;其余的被认为是门诊病人。我们将诊断间隔计算为从第一次结肠癌相关医疗就诊到癌症诊断的天数。描述性地评估诊断途径,包括诊断是否有症状或无症状记录。分位数回归(按症状状态分层)用于量化SPI状态与诊断间隔之间的关系。结果我们确定了42,143名结肠癌患者:40,884人没有精神病史,835人有门诊SPI病史,424人有住院SPI病史。患有SPI的成年人更有可能被诊断出有症状(住院患者:89.9%,门诊患者:86.6%,无SPI: 80.9%, p < 0.001)。与没有精神病史的个体相比,SPI个体的中位症状诊断间隔时间明显更长,而在诊断时无症状记录的中位诊断间隔时间相似。调整协变量后,门诊SPI患者的中位症状诊断间隔比无SPI患者长48天(95% CI 28, 68),住院SPI患者的中位症状诊断间隔比无SPI患者长55天(95% CI 28, 82)。结论SPI患者比非SPI患者更容易出现症状,且症状诊断间隔时间更长。这项研究代表了针对和改善SPI患者癌症诊断过程的第一步。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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