Delayed drug hypersensitivity to anti-tuberculosis drug: a new desensitization scheme.

IF 1.4 4区 医学 Q3 ALLERGY Postepy Dermatologii I Alergologii Pub Date : 2024-08-01 Epub Date: 2024-08-12 DOI:10.5114/ada.2024.142187
İsmet Bulut, Zeynep Yegin Katran, Aylin Babalık, Metin Keren, Fatma Merve Tepetam
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Abstract

Introduction: Tuberculosis is a communicable illness and one of the leading causes of death, especially in developing countries like Turkey. One of the problems that must be managed well in the treatment of tuberculosis is drug hypersensitivity. The first-line agents are very important for the success of treatment. Alternative drugs are more toxic and less successful in treatment. Therefore, it is very important to be able to include first-line drugs in the post-hypersensitivity regimen. At this point, the success of desensitization comes to the fore. There are fewer studies on rapid drug desensitization in delayed-type drug hypersensitivity to anti-tuberculosis drugs.

Aim: The primary aim of the study was to determine the prevalence of delayed-type hypersensitivity reactions in drug-sensitive cases; the secondary aim was to determine the appropriate treatment management.

Material and methods: This was a retrospective study. Demographic features, tuberculosis diagnostic indicator, clinical signs of developing a hypersensitivity reaction, reaction time, desensitization scheme and treatment were evaluated.

Results: A total of 41 tuberculosis cases were included in the study. Twenty-six of the cases were male; mean age (mean ± SD) 55.44 ±16.93 years; 70.7% of them were diagnosed bacteriologically; 70.7% of them were diagnosed with pulmonary tuberculosis. The most common skin finding was maculopapular drug eruption. The development time (mean ± SD) of the reaction in patients who developed a reaction was 34.93 ±39.62 days. The responsible agent could be identified in 15 reactions. The most common drug responsible for the reaction was rifampicin. Successful desensitization was achieved in 19 (46.3%) cases with the sensitive regimen. The duration of treatment was 8.97 ±3.44 months. When evaluated in terms of treatment results, cure and treatment completion were accepted as treatment success. In this case, 30 (73.2%) patients successfully completed the treatment.

Conclusions: Our study is one of the largest series in which delayed-type hypersensitivity develops under tuberculosis treatment and the desensitization scheme is recommended. A practical, easy desensitization scheme had been shared in this paper.

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对抗结核药物的迟发性药物过敏:一种新的脱敏方案。
导言:结核病是一种传染性疾病,也是导致死亡的主要原因之一,尤其是在土耳其这样的发展中国家。治疗结核病必须妥善处理的问题之一是药物过敏。一线药物对治疗的成功非常重要。替代药物毒性较大,治疗效果较差。因此,将一线药物纳入药物过敏后的治疗方案非常重要。此时,脱敏治疗的成功与否就显得尤为重要。关于抗结核药物迟发型超敏反应的快速药物脱敏研究较少。目的:本研究的主要目的是确定药物敏感病例中迟发型超敏反应的发生率;次要目的是确定适当的治疗方法:这是一项回顾性研究。对人口统计学特征、结核病诊断指标、发生超敏反应的临床表现、反应时间、脱敏方案和治疗进行了评估:研究共纳入 41 例肺结核病例。其中 26 例为男性;平均年龄(平均 ± SD)55.44 ±16.93 岁;70.7% 的病例经细菌学诊断;70.7% 的病例被诊断为肺结核。最常见的皮肤症状是斑丘疹药物性糜烂。出现反应的患者的反应发展时间(平均值±标准差)为 34.93±39.62 天。有 15 例反应的病原体可以确定。最常见的致敏药物是利福平。有 19 例(46.3%)患者采用敏感方案成功脱敏。治疗时间为 8.97 ± 3.44 个月。在对治疗结果进行评估时,治愈和治疗完成被视为治疗成功。本病例中有 30 例(73.2%)患者成功完成了治疗:我们的研究是结核病治疗过程中出现迟发型超敏反应的最大系列研究之一,建议采用脱敏方案。本文分享了一个实用、简便的脱敏方案。
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来源期刊
CiteScore
2.60
自引率
7.10%
发文量
107
审稿时长
6-12 weeks
期刊介绍: Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii is a bimonthly aimed at allergologists and dermatologists.
期刊最新文献
Association between single nucleotide polymorphisms of interleukin-35 genes and atopic dermatitis. Cannabidiol modulation of immune cell function: in vitro insights and therapeutic implications for atopic dermatitis. Delayed drug hypersensitivity to anti-tuberculosis drug: a new desensitization scheme. Dermatophagoides pteronyssinus proteins and their role in the diagnostics and management of house dust mite allergy: exploring allergenic components. Hidradenitis suppurativa: a new therapeutic approach for an old disease.
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