Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Epidemiology Research, Statens Serum Institute, Copenhagen, Denmark.
Lancet Child Adolesc Health. 2019 Mar;3(3):158-165. doi: 10.1016/S2352-4642(18)30401-2. Epub 2019 Jan 24.
Studies have shown an association between use of azathioprine and increased risk of acute pancreatitis in adult inflammatory bowel disease. However, whether an association exists among paediatric patients is not known. We aimed to investigate whether use of azathioprine is associated with the risk of acute pancreatitis in children with inflammatory bowel disease.
We did a nationwide register-based cohort study in Sweden (2006-16) and Denmark (2000-16). All paediatric patients (<18 years of age) with inflammatory bowel disease during the study period were identified through hospital records. Episodes of incident azathioprine use and no use of any thiopurine were matched (1:1) using propensity scores, controlling for sociodemographic characteristics, comorbidities, previous treatment, indicators of disease severity, and health care use. Incident acute pancreatitis (physician-assigned diagnosis with ICD-10 code K85) occurring in the 90 days following treatment initiation were identified through outpatient and inpatient hospital records.
We identified 3574 azathioprine episodes and 18 700 no-use episodes, which resulted in 3374 pairs after propensity score matching; baseline characteristics in the matched cohort were well balanced. Among the matched azathioprine episodes, mean age was 14·3 years (SD 3·1), 1854 (54·9%) were male, 1923 (57·0%) had Crohn's disease, and 1451 (43·0%) had ulcerative colitis or unclassified inflammatory bowel disease. Within the first 90 days following initiation of azathioprine, 40 acute pancreatitis events occurred (incidence rate 49·1 events per 1000 person-years) compared with six events in the no-use group (8·4 events per 1000 person-years). Azathioprine use was associated with an increased risk of acute pancreatitis (incidence rate ratio 5·82 [95% CI 2·47-13·72]; absolute difference 1·0 [95% CI 0·3-2·6] events per 100 patients) during the 90-day risk period.
Use of azathioprine was associated with an increased risk of acute pancreatitis in children with inflammatory bowel disease during the first 90 days following treatment initiation, suggesting the need for regular and rigorous monitoring. The risk of acute pancreatitis needs to be considered when deciding on optimal treatment strategies.
Swedish Research Council, Frimurare Barnhuset Foundation, and the Åke Wiberg Foundation.
研究表明,在成人炎症性肠病中,使用硫唑嘌呤与急性胰腺炎风险增加之间存在关联。然而,在儿科患者中是否存在这种关联尚不清楚。我们旨在研究在患有炎症性肠病的儿童中,使用硫唑嘌呤是否与急性胰腺炎的风险相关。
我们在瑞典(2006-16 年)和丹麦(2000-16 年)进行了一项全国性基于登记的队列研究。通过医院记录,确定了研究期间所有年龄在 18 岁以下的炎症性肠病患儿。使用倾向评分对新使用硫唑嘌呤和未使用任何硫嘌呤的患儿进行了(1:1)匹配,控制了社会人口统计学特征、合并症、既往治疗、疾病严重程度指标和医疗保健使用情况。通过门诊和住院病历记录确定治疗开始后 90 天内发生的新发急性胰腺炎(由 ICD-10 代码 K85 分配的医生诊断)。
我们确定了 3574 例硫唑嘌呤发作和 18700 例无使用发作,经倾向评分匹配后得到 3374 对;匹配队列中的基线特征平衡良好。在匹配的硫唑嘌呤发作中,平均年龄为 14.3 岁(SD 3.1),1854 例(54.9%)为男性,1923 例(57.0%)患有克罗恩病,1451 例(43.0%)患有溃疡性结肠炎或未分类的炎症性肠病。在开始使用硫唑嘌呤后的前 90 天内,有 40 例发生急性胰腺炎事件(发生率为 49.1 例/1000 人年),而无使用组有 6 例(8.4 例/1000 人年)。使用硫唑嘌呤与急性胰腺炎风险增加相关(发生率比 5.82 [95%CI 2.47-13.72];绝对差异 1.0 [95%CI 0.3-2.6]每 100 例患者事件)在治疗开始后 90 天的风险期内。
在开始治疗后的前 90 天内,使用硫唑嘌呤与儿童炎症性肠病患者急性胰腺炎的风险增加相关,这表明需要进行定期和严格的监测。在决定最佳治疗策略时,需要考虑急性胰腺炎的风险。
瑞典研究委员会、Frimurare Barnhuset 基金会和 Åke Wiberg 基金会。