炎症性肠病中的缺铁性贫血。

Sindhu Kaitha, Muhammad Bashir, Tauseef Ali
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引用次数: 112

摘要

贫血是炎症性肠病(IBD)常见的肠外表现,但作为一种并发症经常被忽视。IBD患者通常伴有继发于慢性失血的缺铁性贫血(IDA),以及因组织炎症导致的铁吸收受损。缺铁患者可能并不总是表现出体征和症状;因此,必须定期监测IBD患者的血红蛋白水平,以便及早发现贫血。IBD中的IDA与生活质量差有关,需要及时诊断和适当治疗。IDA通常与IBD患者的炎症有关。因此,常用的实验室参数不足以诊断IDA,需要更新的铁指标,如网织红细胞血红蛋白含量或低色红细胞百分比或原卟啉锌,以区分IDA与慢性病贫血。口服铁制剂可用于轻度疾病活动的患者。这些制剂既便宜又方便,但可能产生胃肠道副作用,如腹痛和腹泻,这限制了它们的使用和患者的依从性。这些制剂由于发炎而部分被吸收。未被吸收的铁可能有毒并使IBD疾病活动性恶化。尽管具有成本效益的静脉注射铁制剂广泛可用,并且安全性有所提高,但医生不愿使用它们。我们综述了IDA在IBD中的病理生理机制,改进的诊断和治疗策略,铁替代治疗IBD的有效性和安全性。
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Iron deficiency anemia in inflammatory bowel disease.

Anemia is a common extraintestinal manifestation of inflammatory bowel disease (IBD) and is frequently overlooked as a complication. Patients with IBD are commonly found to have iron deficiency anemia (IDA) secondary to chronic blood loss, and impaired iron absorption due to tissue inflammation. Patients with iron deficiency may not always manifest with signs and symptoms; so, hemoglobin levels in patients with IBD must be regularly monitored for earlier detection of anemia. IDA in IBD is associated with poor quality of life, necessitating prompt diagnosis and appropriate treatment. IDA is often associated with inflammation in patients with IBD. Thus, commonly used laboratory parameters are inadequate to diagnose IDA, and newer iron indices, such as reticulocyte hemoglobin content or percentage of hypochromic red cells or zinc protoporphyrin, are required to differentiate IDA from anemia of chronic disease. Oral iron preparations are available and are used in patients with mild disease activity. These preparations are inexpensive and convenient, but can produce gastrointestinal side effects, such as abdominal pain and diarrhea, that limit their use and patient compliance. These preparations are partly absorbed due to inflammation. Non-absorbed iron can be toxic and worsen IBD disease activity. Although cost-effective intravenous iron formulations are widely available and have improved safety profiles, physicians are reluctant to use them. We present a review of the pathophysiologic mechanisms of IDA in IBD, improved diagnostic and therapeutic strategies, efficacy, and safety of iron replacement in IBD.

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