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评估免疫疗法在过敏性疾病中的作用时的安全性考量

Safety considerations in assessing the role of immunotherapy in allergic disorders.

作者信息

Bousquet J, Michel F B

机构信息

Clinique des Maladies Respiratoires, Hôpital Arnaud de Villeneuve, Centre Hospitalier Universitaire, Montpellier, France.

出版信息

Drug Saf. 1994 Jan;10(1):5-17. doi: 10.2165/00002018-199410010-00002.

Abstract

Specific immunotherapy (SIT) is accepted as an effective treatment of allergic diseases when high quality extracts are used. However, this form of treatment can cause untoward reactions among which systemic reactions are the most severe. Although life-threatening reactions are rare and deaths exceptionally reported, SIT should be prescribed by allergists to patients with well defined characteristics, and administered with care by (or under the close supervision of) physicians trained to deal rapidly with the reactions. Reactions with standardised extracts occur mostly during the dose increase phase but they can be prevented using adapted schedules and premedication. During maintenance injections or when vial batches are changed, standardised extracts of known shelf-life usually result in a low rate of systemic reactions. Patients with asthma are more prone to develop systemic reactions, and allergens should not be administered to patients with a forced expiratory volume in 1 second (FEV1) under 70% of predicted or in those who have unstable or symptomatic asthma. Systemic reactions may be observed with all allergens and allergenic preparations although it appears that high molecular weight extracts may be safer.

摘要

当使用高质量提取物时,特异性免疫疗法(SIT)被公认为是治疗过敏性疾病的有效方法。然而,这种治疗方式可能会引起不良反应,其中全身反应最为严重。尽管危及生命的反应很少见,死亡病例也鲜有报道,但SIT应由过敏症专科医生开给具有明确特征的患者,并由经过培训能迅速处理反应的医生(或在其密切监督下)谨慎给药。使用标准化提取物时的反应大多发生在剂量增加阶段,但可以通过调整给药方案和预先用药来预防。在维持注射期间或更换药瓶批次时,已知保质期的标准化提取物通常会导致较低的全身反应发生率。哮喘患者更容易发生全身反应,对于1秒用力呼气量(FEV1)低于预测值70%的患者或患有不稳定或有症状哮喘的患者,不应给予过敏原。所有过敏原和致敏制剂都可能观察到全身反应,尽管高分子量提取物似乎可能更安全。

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