drug hypersensitivity reactions

  • 文章类型: Journal Article
    人粒细胞集落刺激因子(G-CSF)是一种用于治疗化疗后中性粒细胞减少症的粒细胞生长因子,清髓性治疗,或准备同种异体移植的健康供体。很少有过敏反应(HRs)的报道,其真正的流行率是未知的。我们旨在系统地表征G-CSF诱导的HR,同时包括全面的不良反应列表。我们通过在PubMed中搜索来审查2024年1月之前发表的文章,Embase,科克伦图书馆,和WebofScience数据库使用列出的关键字的组合,选择了需要的,并提取相关数据。搜索结果有68个条目,与我们的研究相关的17个,以及从手动搜索书目来源中发现的其他7个。总共描述了40例G-CSF诱导的HR,并分为立即(29)或延迟(11)。近期主要是由非格司亭(最少13例)引起的,在WAO过敏反应量表上至少有9人是5级。延迟反应主要是斑丘疹性皮疹,并允许G-CSF继续。首次暴露后的反应经常出现,并且在40例中的至少11例中存在。在分析的数据中,仅发现了五种脱敏方案。我们相信这项研究揭示了该主题的研究兴趣,可以从进一步的探索中受益,并建议定期更新,以包括最近发布的证据。
    Human granulocyte colony-stimulating factor (G-CSF) is a granulopoietic growth factor used in the treatment of neutropenia following chemotherapy, myeloablative treatment, or healthy donors preparing for allogeneic transplantation. Few hypersensitivity reactions (HRs) have been reported, and its true prevalence is unknown. We aimed to systematically characterize G-CSF-induced HRs while including a comprehensive list of adverse reactions. We reviewed articles published before January 2024 by searching in the PubMed, Embase, Cochrane Library, and Web of Science databases using a combination of the keywords listed, selected the ones needed, and extracted relevant data. The search resulted in 68 entries, 17 relevant to our study and 7 others found from manually searching bibliographic sources. A total of 40 cases of G-CSF-induced HR were described and classified as immediate (29) or delayed (11). Immediate ones were mostly caused by filgrastim (13 minimum), with at least 9 being grade 5 on the WAO anaphylaxis scale. Delayed reactions were mostly maculopapular exanthemas and allowed for the continuation of G-CSF. Reactions after first exposure frequently appeared and were present in at least 11 of the 40 cases. Only five desensitization protocols have been found concerning the topic at hand in the analyzed data. We believe this study brings to light the research interest in this topic that could benefit from further exploration, and propose regular updating to include the most recently published evidence.
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  • 文章类型: Meta-Analysis
    背景:药物超敏反应(DHRs)是药物不良反应(ADRs),对健康相关生活质量(HRQoL)和心理健康尤其有影响。尽管HRQoL作为重要的患者报告结果的作用已在过去几年中得到认可,对ADR患者的HRQoL和心理健康的研究仍然很少。
    目的:本系统评价的目的是评估患病率,严重程度,DHR的HRQoL和心理健康的危险因素,特别关注药物引起的过敏反应。
    方法:Medline,Scopus,搜索了美国心理学会的Psycharticles数据库,以确定所有的研究,截至2022年12月31日,包括至少一次DHR发作的受试者以及心理健康和/或生活质量的评估。结果报告为定性和定量分析,在评估偏倚和异质性风险后进行荟萃分析。
    结果:共纳入45项观察性研究。总的来说,抑郁症的患病率很高(高达51.4%,OR2.94,95CI:1.42-6.10)和焦虑(高达48%,OR3.92,95CI:1.91-8.05)报告,与健康的受试者相比。HRQoL受到显著影响,特别是在药物引起的过敏反应的情况下(平均评分5.88,95CI:0.77-10.98)。
    结论:尽管对该主题的研究很少且异质,审查显示,ADR后HRQoL和心理健康受到显着影响。更好地评估HRQoL和表征患者的精神状态可能会提高治疗策略的疗效,这也应该包括心理支持。
    Drug hypersensitivity reactions (DHRs) are adverse drug reactions (ADRs) that are particularly impactful on health-related quality of life (HRQoL) and mental health. Although the role of HRQoL as an important patient-reported outcome has been recognized in past years, HRQoL and mental health in patients with ADRs are still poorly investigated.
    To evaluate the prevalence, severity, and risk factors of HRQoL and mental health in DHRs, with a particular focus on drug-induced anaphylaxis.
    We searched the MEDLINE, Scopus, and American Psychological Association PsycArticles databases to identify all studies up to December 31, 2022 that included subjects with at least one episode of DHR and assessments of mental health and/or quality of life. Results were reported as qualitative and quantitative analyses, with meta-analyses after assessment for risk of bias and heterogeneity.
    A total of 45 observational studies were included. Overall, a high prevalence of depression (up to 51.4%; odd ratio = 2.94; 95% CI, 1.42-6.10) and anxiety (up to 48%; odd ratio = 3.92; 95% CI, 1.91-8.05) were reported compared with healthy subjects. The HRQoL was significantly affected, especially in the case of drug-induced anaphylaxis (mean score, +5.88; 95% CI, 0.77-10.98).
    Despite the scarce and heterogeneous studies on this topic, the review shows that HRQoL and mental health are markedly affected after ADRs. A better assessment of HRQoL and characterization of patients\' mental status may improve the efficacy of therapeutic strategies, which should include psychological support.
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  • 文章类型: Journal Article
    据报道,囊性纤维化(CF)是药物超敏反应的危险因素。然而,关于CF患儿药物超敏反应的真实患病率存在相互矛盾的数据.
    欧洲药物过敏网络(ENDA)问卷询问了CF患儿的可疑药物超敏反应(DHRs),皮肤试验和/或药物激发试验均按照既定指南进行.
    二百十九名儿童(男孩占48.9%;[IQR]年龄中位数,8.4年[4.8-12.4年])的囊性纤维化纳入研究,对其中22例患者和24例疑似DHRs进行了评估.大多数可疑DHR是非即时型(n=16,66.6%),有问题的药物是阿莫西林-克拉维酸(n=7),大环内酯类(n=4),甲氧苄啶-磺胺甲恶唑(TMP/SMX)(n=2),哌拉西林他唑巴坦(n=1),胰脂肪酶(n=1),和熊去氧胆酸(n=1)。八个(33.3%)的DHR被分类为直接(头孢曲松[n=2],头孢他啶[n=2],美罗培南[n=1],AmBisome[n=2],和万古霉素[n=1])。临床表现主要为斑丘疹(41.6%)和荨麻疹(37.5%),伴有血管性水肿(8.3%),冲洗(12.5%),和呕吐(8.3%)。进行了9次皮肤试验(6例患者采用β-内酰胺方案)和24次DPT,没有一项皮肤测试显示阳性结果;然而,2DPTs与TMP/SMX呈阳性。
    使用非β-内酰胺类抗生素的219例患者中有2例(0.9%)出现了实际的药物超敏反应。这些结果与以前的研究显示药物超敏反应率较高,但与最近的一些研究一致。在可疑DHR的情况下,囊性纤维化患者必须进行变态反应诊断检查。
    Cystic fibrosis (CF) is reported to be a risk factor for drug hypersensitivity. However, there are conflicting data about true prevalence of drug hypersensitivity in children with CF.
    The suspicious drug hypersensitivity reactions (DHRs) of children with CF were enquired by the European Network for Drug Allergy (ENDA) questionnaire, and skin tests and/or drug provocation tests were performed according to the established guidelines.
    Two hundred and nineteen children (48.9% boys; median [IQR] age, 8.4 years [4.8-12.4 years]) with cystic fibrosis were included in the study, among which 22 patients with 24 suspected DHRs were evaluated. Most of the suspected DHRs were of non-immediate (n = 16, 66.6%) type, and the offending drugs were amoxicillin-clavulanic acid (n = 7), macrolides (n = 4), trimethoprim-sulfamethoxazole (TMP/SMX) (n = 2), piperacillin-tazobactam (n = 1), pancrelipase (n = 1), and ursodeoxycholic acid (n = 1). Eight (33.3%) of the DHRs were classified as immediate (ceftriaxone [n = 2], ceftazidime [n = 2], meropenem [n = 1], AmBisome [n = 2], and vancomycin [n = 1]). The main clinical presentations were maculopapular eruption (41.6%) and urticaria (37.5%), accompanied by angioedema (8.3%), flushing (12.5%), and vomiting (8.3%). Nine skin tests (with beta-lactam protocol in 6 patients) and 24 DPTs were performed, and none of the skin tests revealed a positive result; however, 2 DPTs with TMP/SMX were positive.
    Actual drug hypersensitivity was demonstrated in 2 of 219 patients (0.9%) with non-beta-lactam antibiotics. These results conflict with previous researches that showed higher drug hypersensitivity rates but are consistent with some recent studies. Allergological diagnostic workup is mandatory in patients with cystic fibrosis in case of a suspicious DHR.
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