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首页> 外文期刊>Gastroenterology research and practice >Prevalence of Anemia in Pediatric IBD Patients and Impact on Disease Severity: Results of the Pediatric IBD-Registry CEDATA-GPGE (R)
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Prevalence of Anemia in Pediatric IBD Patients and Impact on Disease Severity: Results of the Pediatric IBD-Registry CEDATA-GPGE (R)

机译:儿科IBD患者贫血患病率及对疾病严重程度的影响:儿科IBD-Registry CEDATA-GPGE(R)的结果

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摘要

Aim. To determine the prevalence of anemia and its association with disease severity in children and adolescents with IBD. Methods. CEDATA-GPGE is a registry for pediatric patients with IBD in Germany and Austria from 90 specialized centers. As markers of disease severity, analysis included patient self-assessment on a Likert scale (1-5; 1 = very good) and physicians' general assessment (0 = no activity to 4 = severe disease) and the disease indices. Anemia was defined as hemoglobin concentration below the 3rd percentile. Results. Prevalence of anemia was 65.2% in CD and 60.2% in UC. Anemic CD and UC patients showed significantly worse self-assessment than patients without anemia (average +/- standard deviation; CD: 3.0 +/- 0.9 versus 2.5 +/- 0.9, p < 0 0001; UC: 2.9 +/- 0.9 versus 2.3 +/- 0.9, p < 0 0001). Accordingly, physicians' general assessment (PGA) was significantly worse in anemic than in nonanemic patients in CD (p < 0 0001) and UC (p < 0 0001). PCDAI in anemic CD, p < 0 0001, and PUCAI in anemic UC patients, p < 0 0001, were significantly higher than in nonanemic patients. 40.0% of anemic CD and 47.8% of anemic UC patients received iron during follow-up. Conclusion. Almost 2/3 of pediatric IBD patients are anemic. Patients' self-assessment and disease severity as determined by PGA and activity indices are worse in anemic patients. Contrastingly, only a minority received iron therapy.
机译:目的。确定贫血的患病率及其与IBD儿童和青少年疾病严重程度的关系。方法。 CEDATA-GPGE是德国和奥地利的90个专门中心的IBD儿科患者的注册表。作为疾病严重程度的标志性,分析包括患者对李克特量表(1-5; 1 =非常好)和医生的一般评估(0 =无活性至4 =严重疾病)和疾病指数的患者自我评估。贫血被定义为低于3百分位数的血红蛋白浓度。结果。贫血患病率为CD为65.2%,UC的60.2%。贫血CD和UC患者的自我评估显着更差,而不是没有贫血的患者(平均+/-标准差; CD:3.0 +/- 0.9与2.5 +/- 0.9,P <0 0001; UC:2.9 +/- 0.9与2.3 +/- 0.9,p <0 0001)。因此,医生的一般评估(PGA)在贫血中缺乏在CD(P <0 0001)和UC(P <0 0001)中的嗜睡症。 PCDAI在贫血CD中,P <0 0001和贫血UC患者的PUCAI,P <0 0001,显着高于非血症患者。 40.0%的贫血CD和47.8%的贫血UC患者在随访期间接受铁。结论。近2/3的儿科IBD患者是贫血的。 PGA和活动指数确定的患者的自我评估和疾病严重程度在贫血患者中更差。比较地,只有少数群体接受了铁疗法。

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