Herzig Markus, Vom Hove Maike, Bertsche Astrid, Lipek Tobias, Kiess Wieland, Bertsche Thilo, Prenzel Freerk, Neininger Martina Patrizia
Clinical Pharmacy, Institute of Pharmacy, Medical Faculty, Leipzig University and Drug Safety Center, Leipzig University and University Hospital, Bruederstrasse 32, D-04103, Leipzig, Germany.
Leipzig Interdisciplinary Center for Allergy (LICA), Liebigstraße 20a, 04103, Leipzig, Germany.
Allergy Asthma Clin Immunol. 2025 Apr 7;21(1):16. doi: 10.1186/s13223-025-00961-8.
Severe asthma and moderate-to-severe atopic dermatitis can significantly impact the lives of children and adolescents. However, real-world data on pediatric patients' perceptions of their medication are limited.
This non-interventional cross-sectional study at a university hospital explored patients' perceptions. We included patients aged between 6 and 17 with severe asthma and/or moderate-to-severe atopic dermatitis. For patients treated with dupilumab, a minimum dupilumab treatment duration of 16 weeks was required. We conducted one structured interview per patient, based on a questionnaire consisting of open questions and ratings on 6-point Likert scales (response scale range: "0: not at all" to "5: very strongly").
The study included 57 participants (severe asthma: n = 31; moderate-to-severe atopic dermatitis: n = 21; both: n = 5) who reported a "rather moderate" burden of asthma (median: 2; Q25/Q75: 0.3/2.8) or atopic dermatitis (3; 1.5/3.5). They experienced their current medications as "rather helpful" (asthma: 4; 3/5; atopic dermatitis: 4; 3/5). Twelve of the participants (21%) reported refusing to take their medication because of reluctance, but all resumed treatment. All participants receiving dupilumab therapy (n = 16) reported an improvement in their disease within a maximum of 2.5 months after starting treatment. The median fear of injection decreased from 3 (0/5) before the first injection to 0.5 (0/1) at the time of the survey.
In this real-world, interview-based study, we found that pediatric patients perceived treatment as highly beneficial for asthma and atopic dermatitis. Furthermore, pediatric patients seemed to respond well to dupilumab therapy in terms of both disease improvement and less fear of injection.
DRKSID DRKS00028092.
重度哮喘和中重度特应性皮炎会对儿童和青少年的生活产生重大影响。然而,关于儿科患者对其药物治疗看法的真实世界数据有限。
在一家大学医院进行的这项非干预性横断面研究探讨了患者的看法。我们纳入了年龄在6至17岁之间患有重度哮喘和/或中重度特应性皮炎的患者。对于接受度普利尤单抗治疗的患者,度普利尤单抗的最短治疗持续时间为16周。我们根据一份由开放式问题和6点李克特量表评分(回答量表范围:“0:完全不”至“5:非常强烈”)组成的问卷,对每位患者进行了一次结构化访谈。
该研究纳入了57名参与者(重度哮喘:n = 31;中重度特应性皮炎:n = 21;两者皆有:n = 5),他们报告哮喘(中位数:2;四分位数间距Q25/Q75:0.3/2.8)或特应性皮炎(3;1.5/3.5)的负担“较为中度”。他们认为目前的药物治疗“相当有帮助”(哮喘:4;3/5;特应性皮炎:4;3/5)。12名参与者(21%)报告因不情愿而拒绝服药,但均恢复了治疗。所有接受度普利尤单抗治疗的参与者(n = 16)报告在开始治疗后的最长2.5个月内病情有所改善。对注射的恐惧中位数从首次注射前的3(0/5)降至调查时的0.5(0/1)。
在这项基于访谈的真实世界研究中,我们发现儿科患者认为治疗对哮喘和特应性皮炎非常有益。此外,儿科患者在病情改善和减少对注射的恐惧方面似乎对度普利尤单抗治疗反应良好。
DRKSID DRKS00028092。