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[奥马珠单抗治疗重度过敏性哮喘青少年——上市后监测结果]

[Omalizumab therapy in adolescents with severe allergic asthma - results of a post-marketing surveillance].

作者信息

Klyucheva M, von Berg A, Gappa M, Suerbaum C, Berdel D

机构信息

Forschungsinstitut zur Prävention von Allergien und Atemwegserkrankungen an der Klinik für Kinder- und Jugendmedizin des Marien-Hospitals Wesel, Germany.

出版信息

Pneumologie. 2013 Apr;67(4):233-7. doi: 10.1055/s-0032-1326356. Epub 2013 Apr 10.

Abstract

BACKGROUND

Omalizumab has been successfully established as add-on therapy to improve asthma control in adults and children aged 6 years and older with uncontrolled severe persistent allergic asthma (GINA 2009 step 5).

PATIENTS AND METHODS

15 patients between 12 and 20 years of age with severe allergic asthma, which was inadequately controlled despite intensive antiasthmatic therapy according to NVL step 4 /5, received treatment with omalizumab for 6 - 69 months. After 12 months of treatment the effect was evaluated by means of objective parameters.

RESULTS

Significant improvements were found for the asthma-exacerbation rate and emergency treatment as well as for most of the lung function parameters. Systemic steroids could be discontinued in 10 of 11 patients. Asthma control has improved in all patients according to the ACT. Omalizumab was well tolerated by 13 patients. Adverse effects occurred in two patients in the first two and after 5 months, respectively. Only in one of them omalizumab had to be discontinued after 6 months due to the development of serum disease.

CONCLUSIONS

Omalizumab can be considered a valuable add-on therapy in adolescent patients with severe allergic asthma that is inadequately controlled despite GINA step 5 treatment. A significant effect on clinical and functional parameters was shown over 12 months.

摘要

背景

奥马珠单抗已成功确立为附加疗法,用于改善6岁及以上成人和儿童严重持续性过敏性哮喘(GINA 2009第5步)控制不佳的哮喘症状。

患者与方法

15例年龄在12至20岁之间的严重过敏性哮喘患者,尽管按照NVL第4/5步进行了强化抗哮喘治疗,但哮喘控制仍不佳,接受了奥马珠单抗治疗6至69个月。治疗12个月后,通过客观参数评估疗效。

结果

哮喘加重率、急诊治疗以及大多数肺功能参数均有显著改善。11例患者中有10例停用了全身性激素。根据ACT,所有患者的哮喘控制均有改善。13例患者对奥马珠单抗耐受性良好。分别有2例患者在前两个月和5个月后出现不良反应。仅其中1例患者在6个月后因血清病的发生而不得不停用奥马珠单抗。

结论

对于尽管接受了GINA第5步治疗但控制不佳的青少年严重过敏性哮喘患者,奥马珠单抗可被视为一种有价值的附加疗法。在12个月内对临床和功能参数显示出显著效果。

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