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重度过敏性哮喘:述情障碍是否会影响奥马珠单抗的治疗效果?

Severe allergic asthma: Does alexithymia interfere with omalizumab treatment outcome?

作者信息

Liotta Marta, Liotta Marco, Saitta Salvatore, Ricciardi Luisa

机构信息

Allergy and Clinical Immunology Unit, University of Messina, Messina, Italy.

Specialist in Psichology, Messina, Italy.

出版信息

Asian Pac J Allergy Immunol. 2023 Mar;41(1):53-59. doi: 10.12932/AP-040121-1031.

Abstract

BACKGROUND

Alexithymia is among psychological factors reported to interfere with asthma management. Severe allergic asthma (SAA) is characterized by uncontrolled asthma despite maximal standard pharmacological treatment which can benefit from an add-on treatment with Omalizumab, an anti-IgE monoclonal antibody.

OBJECTIVE

To evaluate if alexithymia influences the efficacy of omalizumab in SAA.

METHODS

The total alexithymia score 20 (TAS 20) questionnaire allowed to detect alexithymia. SAA was monitored recording number of exacerbations, asthma control test (ACT) and asthma quality of life questionnaire (AQLQ) scores, as well as forced expiratory volumes in 1 second % (FEV1%) levels before starting omalizumab, 1 and 2 years after.

RESULTS

The study was conducted on 18 patients; Group 1, TAS 20 ≥ 61, was of 2 males and 4 females with SAA and alexithymia, while Group 2 , TAS 20 ≤ 51, was of 8 males and 4 females, without alexithymia. Group 1 had a statistically significant decrease in asthma exacerbations "p = 0.004", while ACT "p = 0.008" and AQLQ scores statistically increased. FEV1 values increased but not statistically significantly. Group 2 had a highly statistically significant decrease in the number of exacerbations and a highly statistically significant increase of ACT "p < 0.0001", FEV1 "p = 0.008" and AQLQ scores.

CONCLUSIONS

Regardless the presence or not of alexithymia, all patients with SAA obtained a marked improvement after starting treatment with omalizumab. Therefore alexithymia does not seem to influence the treatment outcome of omalizumab.

摘要

背景

述情障碍是据报道会干扰哮喘管理的心理因素之一。重度过敏性哮喘(SAA)的特征是尽管进行了最大标准的药物治疗,但哮喘仍未得到控制,而抗IgE单克隆抗体奥马珠单抗的附加治疗可能会使其受益。

目的

评估述情障碍是否会影响奥马珠单抗治疗SAA的疗效。

方法

使用多伦多述情障碍量表20(TAS 20)问卷来检测述情障碍。通过记录发作次数、哮喘控制测试(ACT)、哮喘生活质量问卷(AQLQ)得分以及在开始使用奥马珠单抗前、用药1年和2年后的1秒用力呼气量百分比(FEV1%)水平来监测SAA。

结果

该研究对18名患者进行;第1组,TAS 20≥61,包括2名男性和4名患有SAA和述情障碍的女性,而第2组,TAS 20≤51,包括8名男性和4名无述情障碍的女性。第1组哮喘发作次数有统计学显著下降“p = 0.004”,而ACT“p = 0.008”和AQLQ得分有统计学显著升高。FEV1值升高但无统计学显著性。第2组发作次数有高度统计学显著下降,ACT“p < 0.0001”、FEV1“p = 0.008”和AQLQ得分有高度统计学显著升高。

结论

无论是否存在述情障碍,所有SAA患者在开始使用奥马珠单抗治疗后均有显著改善。因此,述情障碍似乎不影响奥马珠单抗的治疗效果。

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