P1089 现代成人炎症性肠病诊断时的疾病特征与静脉血栓栓塞风险--2007-2021年瑞典全国队列研究

G Bröms, A Forss, J Eriksson, M Linder, C Eriksson, J Askling, J Halfvarson, J F Ludvigsson, O Olen
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The primary outcome was VTE, including pulmonary embolism and deep vein thrombosis. Incidence rates per 1,000 person-years and hazard ratios (HR) were calculated for IBD in general and according to disease subtype, sex, age and disease characteristics at diagnosis. HRs stratified by matching variables (model 1) and additionally adjusted for comorbidities and socioeconomic factors (model 2) were estimated by using Cox regression. Results The incidence rate of VTE among patients with IBD was 5.03 per 1,000 person-years compared with 2.34 per 1,000 person-years among reference individuals (Table 1). This corresponded to a doubled incidence of VTE (HR=2.18, 95% confidence interval (CI)=2.07-2.29, model 1). Adjusting further for covariates in model 2 had only minor effects on the HR. The HR was consistent across IBD subtypes and sex. The relative risk was higher for those with younger age (18-39 years) at IBD diagnosis (HR 2.52, 95% CI: 2.22-2.83) with a risk difference of 1.25 per 1,000 person-years. The IR, 10.64 per 1,000 person-years, and risk difference, 5.42 per 1,000 person-years, was the highest for those with elderly onset (≥60 years) IBD. There was a stronger association for those with extensive ulcerative colitis (E3), primary sclerosing cholangitis, extraintestinal manifestations and perianal disease. HRs for VTE were persistently elevated across follow-up time, but was higher during the first year of follow-up (Figure 1). Conclusion The risk of VTE was doubled in these modern-day data and remained elevated across follow-up time. Disease characteristics associated with higher inflammatory burden at diagnosis and older age are markers of increased risk. 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引用次数: 0

摘要

背景 研究表明,炎症性肠病(IBD)患者罹患静脉血栓栓塞症(VTE)的风险加倍。我们研究了现代 IBD 患者队列中的 VTE 风险,包括总体风险和疾病特征亚组风险。方法 我们利用瑞典医疗保健登记册,在全国范围内确定了一个基于人群的队列,该队列包含 55,252 名在 2007 年至 2021 年间发病的 IBD 患者,中位随访时间为 6.5 年。患者按年龄、性别、日历年和居住地县与多达 10 个来自普通人群的参照个体(N=536,067)进行配对。主要结果是VTE,包括肺栓塞和深静脉血栓。根据疾病亚型、性别、年龄和诊断时的疾病特征,计算了一般 IBD 患者的每千人年发病率和危险比 (HR)。采用 Cox 回归法估算了按匹配变量分层(模型 1)并根据合并症和社会经济因素进行额外调整(模型 2)后的危险比。结果 IBD 患者的 VTE 发病率为每千人年 5.03 例,而参照个体的发病率为每千人年 2.34 例(表 1)。这相当于VTE发病率翻了一番(模型1,HR=2.18,95%置信区间(CI)=2.07-2.29)。在模型2中进一步调整协变量对HR的影响很小。不同IBD亚型和性别的HR是一致的。诊断 IBD 时年龄较小(18-39 岁)的人群相对风险更高(HR 2.52,95% CI:2.22-2.83),每千人年的风险差异为 1.25。老年(≥60 岁)IBD 患者的IR(每千人年 10.64 例)和风险差异(每千人年 5.42 例)最高。与广泛性溃疡性结肠炎(E3)、原发性硬化性胆管炎、肠道外表现和肛周疾病相关的风险更高。在整个随访期间,VTE 的 HR 值持续升高,但在随访的第一年更高(图 1)。结论 在这些现代数据中,发生 VTE 的风险增加了一倍,并且在整个随访期间持续升高。与诊断时炎症负担较重和年龄较大相关的疾病特征是风险增加的标志。这强调了对 IBD 患者 VTE 风险因素持续警惕和个体评估的重要性。
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P1089 Disease characteristics at time of diagnosis of adult onset inflammatory bowel disease and the risk of venous thromboembolism in the modern era – A Swedish nationwide cohort study 2007-2021
Background Studies from mainly before the wide use of targeted therapies and guidelines for thromboprophylaxis indicate that patients with inflammatory bowel disease (IBD) are at a doubled risk of venous thromboembolism (VTE). We studied the risk of VTE in a modern-day cohort of patients with IBD, overall and in subgroups of disease characteristics. Methods Using Swedish healthcare registers, we identified a nationwide population-based cohort of 55,252 patients with incident IBD between 2007 and 2021 with a median follow-up time of 6.5 years. Patients were matched by age, sex, calendar year and county of residence with up to ten reference individuals from the general population (N=536,067). The primary outcome was VTE, including pulmonary embolism and deep vein thrombosis. Incidence rates per 1,000 person-years and hazard ratios (HR) were calculated for IBD in general and according to disease subtype, sex, age and disease characteristics at diagnosis. HRs stratified by matching variables (model 1) and additionally adjusted for comorbidities and socioeconomic factors (model 2) were estimated by using Cox regression. Results The incidence rate of VTE among patients with IBD was 5.03 per 1,000 person-years compared with 2.34 per 1,000 person-years among reference individuals (Table 1). This corresponded to a doubled incidence of VTE (HR=2.18, 95% confidence interval (CI)=2.07-2.29, model 1). Adjusting further for covariates in model 2 had only minor effects on the HR. The HR was consistent across IBD subtypes and sex. The relative risk was higher for those with younger age (18-39 years) at IBD diagnosis (HR 2.52, 95% CI: 2.22-2.83) with a risk difference of 1.25 per 1,000 person-years. The IR, 10.64 per 1,000 person-years, and risk difference, 5.42 per 1,000 person-years, was the highest for those with elderly onset (≥60 years) IBD. There was a stronger association for those with extensive ulcerative colitis (E3), primary sclerosing cholangitis, extraintestinal manifestations and perianal disease. HRs for VTE were persistently elevated across follow-up time, but was higher during the first year of follow-up (Figure 1). Conclusion The risk of VTE was doubled in these modern-day data and remained elevated across follow-up time. Disease characteristics associated with higher inflammatory burden at diagnosis and older age are markers of increased risk. This underscores the importance of continuous vigilance and individual assessment of risk factors for VTE in patients with IBD.
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