Internal Medicine, Albert Schweitzer Hospital Location Dordwijk, Dordrecht, The Netherlands
Clinical Chemistry, Albert Schweitzer Hospital Location Dordwijk, Dordrecht, The Netherlands.
BMJ Open. 2019 Nov 28;9(11):e032930. doi: 10.1136/bmjopen-2019-032930.
To describe all iron deficiency anaemia (IDA)-related causes during follow-up of patients newly diagnosed with IDA and to assess whether a delayed colorectal cancer (CRC) diagnosis influences survival.
Retrospective cohort study of patients from general practices in the Dordrecht area, the Netherlands.
Men and women aged ≥50 years with a new diagnosis of IDA (ie, no anaemia 2 years previously).
From February 2007 to February 2018, all relevant data were collected from the files of the referral hospital. Early IDA-related cause was defined as established within 18 weeks after IDA diagnosis. Cox proportional-hazards regression was used to analyse survival of patients with CRC diagnosis.
587 patients with IDA were included with a median follow-up of 4.6 years. Early and late IDA-related causes could be established in 32% and 8% of patients, respectively. Early and late CRC was found in 8% and 2% of patients, respectively, and were located mainly right sided. After adjustment for age, gender and TNM classification, mortality risk was lower in patients with IDA with early CRC diagnosis, but not significantly (HR 0.30, 95% CI 0.09 to 1.02).
Even with extended follow-up, the cause of IDA remains elusive in the majority of patients with IDA in general practice. However, patients with IDA are at increased risk for in particular right-sided CRC and a late diagnosis of CRC appears to have a detrimental effect on survival in patients with IDA.
描述新诊断为缺铁性贫血(IDA)患者随访期间所有与铁缺乏性贫血相关的病因,并评估延迟诊断结直肠癌(CRC)是否会影响生存。
荷兰多德雷赫特地区普通诊所的患者回顾性队列研究。
年龄≥50 岁、新诊断为 IDA(即 2 年前无贫血)的男性和女性。
从 2007 年 2 月至 2018 年 2 月,从转诊医院的档案中收集所有相关数据。早期 IDA 相关病因定义为在 IDA 诊断后 18 周内确立。采用 Cox 比例风险回归分析 CRC 诊断患者的生存情况。
纳入 587 例 IDA 患者,中位随访时间为 4.6 年。分别有 32%和 8%的患者可以确立早期和晚期 IDA 相关病因。分别有 8%和 2%的患者早期和晚期发现 CRC,且主要位于右侧。调整年龄、性别和 TNM 分类后,IDA 患者早期 CRC 诊断的死亡率风险较低,但无统计学意义(HR 0.30,95%CI 0.09 至 1.02)。
即使进行了扩展随访,大多数普通诊所的 IDA 患者仍难以确定 IDA 的病因。然而,IDA 患者发生特别是右侧 CRC 的风险增加,CRC 的延迟诊断似乎对 IDA 患者的生存产生不利影响。