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首页> 外文期刊>Journal of Asthma and Allergy >Parasitic (Helminthic) Infection While on Asthma Biologic Treatment: Not Everything Is What It Seems
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Parasitic (Helminthic) Infection While on Asthma Biologic Treatment: Not Everything Is What It Seems

机译:寄生(蠕虫)感染,同时在哮喘生物治疗中:并非一切都是它似乎的一切

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Asthma is a chronic inflammatory disorder of the airway that is characterized by bronchial hyperresponsiveness and variable airflow limitation. Approximately 235 million people are affected by asthma worldwide and 5–10% are considered to be refractory to standard asthma treatment. These patients are known to have repeated exacerbations requiring multiple courses of systemic corticosteroids and as a result, are at risk for increased adverse effects (i.e., osteoporosis, infections). Several new medications known as biologic agents have been approved for the treatment of moderate-to-severe asthmatics. These biologic agents target essential parts of the cell-mediated allergic and to a lesser degree non-allergic immune response (IgE, IL-5, and IL-4/IL-13). They are gaining more favor in the treatment of moderate-to-severe asthma due to their efficacy and excellent safety profile. Despite the most common adverse events being minor, such as injection site reactions, upper respiratory infections, or headaches, these agents carry a small risk of more severe complications such as anaphylaxis and decreased defense against parasitic infections (PI). The incidence of PI compared with other rare adverse events is not well reported, and there are no consensus guidelines for risk prevention of PI in asthmatics undergoing evaluation for, or currently using, biologic therapy. Thus, this article sets out to review the incidence of reported PI and other rare adverse events among asthmatics using current FDA-approved biologic therapies. Secondly, we discuss the clinical implications for the importance of risk prevention of PI with the use of biologic therapies in asthmatics. Lastly, we share an educational handout to assist providers in informing their patients of behaviors that could potentially increase their risk of PI while being on a biologic agent.
机译:哮喘是气道的慢性炎症障碍,其特征是支气管高反应性和可变气流限制。全球哮喘的影响约为2.35亿人,5-10%被认为是标准哮喘治疗的难治性。已知这些患者重复加剧需要多种全身皮质类固醇的疗程,因此存在增加不良反应的风险(即骨质疏松症,感染)。已批准称为生物学药物的几种新药物用于治疗中度至严重的哮喘学。这些生物学剂靶向细胞介导的过敏性的基本部位和较小程度的非过敏性免疫应答(IgE,IL-5和IL-4 / IL-13)。由于它们的功效和优异的安全性剖面,它们在治疗中度至严重的哮喘方面取得更多青睐。尽管有常见的不良事件是轻微的,例如注射部位反应,上呼吸道感染或头痛,但这些药剂具有更严重的并发症的少量风险,例如过敏反应和对寄生感染的防御减少(PI)。与其他罕见不良事件相比,PI与其他罕见不良事件相比的发病率并未得到很好的报道,并且在哮喘学中,哮喘患者的风险预防没有共识指南,正在进行评估或目前使用生物治疗。因此,本文旨在使用当前的FDA批准的生物疗法审查报告的PI和其他罕见不良事件的发病率。其次,我们讨论了在哮喘学中使用生物学疗法的PI风险预防的重要性临床意义。最后,我们分享一个教育讲义,以帮助提供者通知他们的行为患者可能在生物制剂上时可能增加其Pi的风险。

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