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Bibliometric analysis of the trends and evolution in β-lactam allergy research 对β-内酰胺过敏研究趋势和演变的文献计量分析
Pub Date : 2024-08-24 DOI: 10.1016/j.jacig.2024.100328
Hugo W.F. Mak MBBS , Jason A. Trubiano MBBS, PhD , Kimberly G. Blumenthal MD, MSc , Philip H. Li MD, FRCP

Background

β-Lactams remain the most reported drug allergy globally, with the volume and diversity of related drug allergy research continuing to accumulate. Recognizing evolving research trends can help inform future directions and encourage synergistic collaborations.

Objective

We conducted a comprehensive bibliometric analysis of all publications relevant to β-lactam allergy, with a focus on longitudinal publication rates, international collaborations, and key word/trend analysis.

Methods

Meta-data from all original articles, letters, and reviews relevant to β-lactam allergy on the Web of Science Core Collection up until December 31, 2023, were analyzed.

Results

From 1966 to 2023, there were 4451 records (3536 articles, 631 reviews, and 284 letters) from 78 countries. There was an exponential increase in publications, especially during the past decade, with half of all publications on β-lactam allergy published during this time (50.6% [2252 of 4452]). Overall, 18.1% of the publications (805 of 4452) involved international coauthorships, with a significant increase since the previous decade (12.7% vs 23.3% [P < .001]). The most frequent key words in the first published half of articles were skin testing (84 of 1919), IgE (57 of 1919), and anaphylaxis (49 of 1919); in contrast to the key word skin testing (137 of 3351), the key words drug provocation test (121 of 3351), antimicrobial resistance (120 of 3351), and antimicrobial stewardship (118 of 3351) were the most frequent key words in the latter half.

Conclusion

There has been a surge in publications, international collaboration, and shifting paradigms in β-lactam allergy research. The field has evolved beyond focusing on in vitro tests or desensitization toward antimicrobial stewardship. However, there still seems to be relatively fewer collaborations with non-Western countries. Further international collaborations to harmonize delabeling strategies against the threat of mislabeled β-lactam allergy should be encouraged.

背景β-内酰胺类药物仍然是全球报道最多的药物过敏,相关药物过敏研究的数量和多样性也在不断积累。我们对所有与β-内酰胺过敏相关的出版物进行了全面的文献计量分析,重点关注纵向发表率、国际合作和关键词/趋势分析。结果从 1966 年到 2023 年,共有来自 78 个国家的 4451 条记录(3536 篇文章、631 篇综述和 284 封信函)。特别是在过去十年中,发表的论文呈指数级增长,在此期间发表的有关β-内酰胺过敏的论文占所有论文的一半(50.6% [4452 篇中的 2252 篇])。总体而言,18.1% 的论文(4452 篇中的 805 篇)涉及国际合著,与前十年相比显著增加(12.7% vs 23.3% [P<.001])。在前半部分发表的文章中,最常见的关键词是皮试(1919 篇中的 84 篇)、IgE(1919 篇中的 57 篇)和过敏性休克(1919 篇中的 49 篇);与皮试(3351 篇中的 137 篇)这一关键词相反,药物激发试验(3351 篇中的 121 篇)、抗菌药物耐药性(3351 篇中的 120 篇)和抗菌药物管理(3351 篇中的 118 篇)是后半部分最常见的关键词。结论β-内酰胺类药物过敏研究的出版物、国际合作和范式转变激增。该领域已从关注体外测试或脱敏向抗菌药物管理发展。然而,与非西方国家的合作似乎仍然相对较少。应鼓励进一步开展国际合作,以协调脱标策略,应对误贴β-内酰胺过敏标签的威胁。
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引用次数: 0
Monitoring and stopping Hymenoptera venom immunotherapy: Contribution of IgE blocking activity 监控和停止膜翅目昆虫毒液免疫疗法:IgE 阻断活性的贡献
Pub Date : 2024-08-24 DOI: 10.1016/j.jacig.2024.100329
Julie Poulat MD , Elisabeth Bellet-Fraysse MD , François Touraine MD , Camille Coumes-Salomon MD , Boris Melloni MD, PhD , François Belle-Moudourou MSc , Stéphane Charret MSc , François Vincent MD, PhD , Ahmed Boumediene MD, PhD

Background

Hymenoptera venom allergy is a public health issue and has an undeniable impact on quality of life. Allergen immunotherapy (AIT) has shown long-term efficacy in this severe and potentially lethal allergy. However, no biomarker can predict the effectiveness of this treatment.

Objectives

We evaluated the contribution of IgE blocking activity, a functional biomarker carried out in our center using flow cytometry, to predict the efficacy of AIT.

Methods

This retrospective study from 1985 to 2022 describes in detail the demographic, clinical, and biological characteristics of patients who benefited from AIT with Hymenoptera venom at the University Hospital of Limoges. The outcome measure used was the presence of anaphylactic reaction (grade I to IV according to Ring and Messmer) in case of a new sting after discontinuation of AIT.

Results

Our study, mainly composed of patients allergic to Vespula wasp venom, did not emphasize the interest of IgE blocking activity in the prediction of a relapse after a new sting. However, this inhibition showed a significant correlation with the amount of IgG4 antibodies.

Conclusion

There is no biomarker that can help make the decision of stopping AIT. However, low levels of IgE blocking activity may suggest a likelihood of relapse. Serum IgG4, in correlation with IgE blocking activity, could be useful for monitoring treatment response. Additional studies are necessary to gain a thorough understanding of the composition of inhibitory antibodies.

背景膜翅目昆虫毒液过敏是一个公共卫生问题,对生活质量造成了不可否认的影响。过敏原免疫疗法(AIT)对这种严重且可能致命的过敏症具有长期疗效。我们评估了 IgE 阻断活性对预测 AIT 疗效的贡献,这是我们中心使用流式细胞术进行的一种功能性生物标志物。方法这项 1985 年至 2022 年的回顾性研究详细描述了利摩日大学医院使用膜翅目昆虫毒液进行 AIT 治疗的患者的人口统计学、临床和生物学特征。结果我们的研究主要由对蝰蛇毒过敏的患者组成,并没有强调 IgE 阻断活性在预测新的蜇伤后复发方面的作用。但是,这种抑制作用与 IgG4 抗体的数量有显著的相关性。然而,低水平的 IgE 阻断活性可能暗示着复发的可能性。血清 IgG4 与 IgE 阻断活性相关,可用于监测治疗反应。要彻底了解抑制性抗体的组成,还需要进行更多的研究。
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引用次数: 0
Assessing sterility techniques in bronchodilator responsiveness testing by practicing allergists in North America 北美过敏症执业医师评估支气管扩张剂反应性测试中的无菌技术
Pub Date : 2024-08-22 DOI: 10.1016/j.jacig.2024.100325
Kabir Chhabra MD , Dhruva Gupta BS , Neel Singh , Naba Sharif MD , Sudhir Sekhsaria MD

Background

The American Thoracic Society has published general guidelines for sterility when testing for bronchodilator responsiveness. However, the extent to which practicing allergists implement sterility measures is currently unknown.

Objective

This study aims to understand the adherence to the American Thoracic Society guidelines for sterility among practicing allergists.

Methods

In 2015, a questionnaire was approved and distributed by the American Academy of Allergy, Asthma & Immunology to all its members. The anonymous responses were recorded and tabulated after a 3-week period.

Results

Of the 6800 allergists who received surveys from the American Academy of Allergy, Asthma & Immunology members, 496 participated in the survey (response rate 7.3%). Using metered dose inhalers with a spacer and nebulizers were the most common bronchodilator administration techniques, as indicated by 59.35% and 58.52% of responses, respectively. Whereas 69.25% of the allergists considered their bronchodilator administration techniques to be sterile, 14.05% did not consider their administration technique to be sterile and 16.70% were unsure. For maintaining sterility, 38.75% of the respondents indicated using a new disposable attachment for reused inhalers, 18.71% indicated using a new inhaler for each patient, and 9.13% reported wiping inhalers with a cleaning agent.

Conclusions

When asked about the sterility of the techniques used by them, nearly one-third of the allergists either stated that the measures used by them were unsterile or stated that they were were unsure. To increase adherence to sterility measures among North American allergists, promoting guideline awareness and proposing updated guidelines focused on the most common bronchodilator administration techniques is essential.

背景美国胸科学会发布了支气管扩张剂反应性测试无菌性一般指南。方法 2015 年,美国过敏、哮喘及免疫学学会批准并向其所有会员分发了一份调查问卷。结果在6800名收到美国过敏、哮喘及免疫学学会会员调查问卷的过敏学家中,有496人参与了调查(回复率为7.3%)。59.35%和58.52%的受访者表示,最常用的支气管扩张剂给药方法是使用带间隔器的定量吸入器和雾化器。69.25%的过敏症医生认为他们的支气管扩张剂给药技术是无菌的,14.05%的过敏症医生认为他们的给药技术不是无菌的,16.70%的过敏症医生不确定。在保持无菌方面,38.75% 的受访者表示对重复使用的吸入器使用新的一次性附件,18.71% 的受访者表示对每位患者使用新的吸入器,9.13% 的受访者表示使用清洁剂擦拭吸入器。为了提高北美过敏症医生对无菌措施的遵守程度,必须提高对指南的认识,并针对最常见的支气管扩张剂给药技术提出最新指南。
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引用次数: 0
Patient-related factors impact the implementation of inpatient antibiotic allergy delabeling 患者相关因素对住院患者抗生素过敏标签实施的影响
Pub Date : 2024-08-21 DOI: 10.1016/j.jacig.2024.100326
Susan Herrmann PhD , Rishabh Kulkarni MBChB , Michelle Trevenen PhD , Hana Karuppasamy CN , Catherine Willis MBBS , Renee Berry MBBS , Britta Von Ungern-Sternberg MD , Niklesh Warrier BMedSci , Ian Li PhD , Kevin Murray PhD , Michaela Lucas MD

Background

The clinical consequences of an antibiotic allergy label are detrimental, impacting health care delivery and patient outcomes. We assessed hospital inpatients with intent to offer free antibiotic allergy labeling (AAL) assessment within a randomized controlled trial.

Objective

We sought to determine the feasibility of establishing an adult antibiotic allergy delabeling service in a Western Australian tertiary public hospital.

Methods

Inpatients (N = 1503) with AAL were identified through medical records and screened for eligibility to participate in a randomized controlled trial. Those recruited were randomized to undergo assessment by skin testing ± oral challenge, or direct oral challenge. A control group received usual care.

Results

Of the 1503 inpatients with an AAL, 429 (28.5%) were eligible for AAL assessment. The primary excluding factor (1074 [71.5%]) was contraindicated medication use (387 [36.0%]), followed by cognitive impairment (298 [27.9%]). Thirty-nine patients were randomized, of which 20 received allergy testing and 19 usual care; all patients were followed up for 5 years. Older patients were less likely to be eligible (10-year increase: odds ratio, 0.82; 95% CI, 0.77-0.88; P < .0001), whereas surgical patients were more likely to be eligible than medical patients (odds ratio, 2.49; 95% CI, 1.97-3.16; P < .0001).

Conclusions

Antibiotic allergy delabeling in the acute care context is not straightforward. Competing clinical concerns and patient acceptance are some barriers to an inpatient service. Nor is it apparent that inpatient versus outpatient testing is cost saving although select patient groups may benefit. Testing younger people and those with predicted high antibiotic usage will derive maximal individual and health system benefits.
背景抗生素过敏标签的临床后果是有害的,会影响医疗服务的提供和患者的治疗效果。我们对医院住院病人进行了评估,并打算在随机对照试验中提供免费抗生素过敏标签(AAL)评估。方法通过医疗记录确定AAL患者(N = 1503),并筛选出有资格参与随机对照试验的患者。被招募的患者被随机分配接受皮肤测试±口腔挑战或直接口腔挑战评估。结果 在 1503 名 AAL 住院患者中,429 人(28.5%)符合 AAL 评估条件。主要的排除因素(1074 例 [71.5%])是用药禁忌(387 例 [36.0%]),其次是认知障碍(298 例 [27.9%])。39 名患者接受了随机治疗,其中 20 人接受了过敏测试,19 人接受了常规治疗;所有患者均接受了为期 5 年的随访。老年患者符合条件的可能性较低(10 年增加:几率比,0.82;95% CI,0.77-0.88;P <;.0001),而外科患者符合条件的可能性高于内科患者(几率比,2.49;95% CI,1.97-3.16;P <;.0001)。相互竞争的临床问题和患者的接受程度是住院服务的一些障碍。住院病人与门诊病人检测相比,显然也不能节省成本,尽管特定的病人群体可能从中受益。对年轻人和预计抗生素使用率较高的人群进行检测将为个人和医疗系统带来最大益处。
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引用次数: 0
Peak nasal inspiratory flow assessment of polyp size and response from SYNAPSE 鼻腔吸气流量峰值评估息肉大小和 SYNAPSE 反应
Pub Date : 2024-08-20 DOI: 10.1016/j.jacig.2024.100327
Amber U. Luong MD, PhD , Joshua M. Levy MD, MPH, MSc , Ludger Klimek MD, PhD , Richard J. Harvey MD , Jared Silver MD, PhD , Steven G. Smith PhD , Abby Fuller MSc , Robert Chan MD , Peter W. Hellings MD, PhD

Background

In the phase III SYNAPSE study, mepolizumab plus standard of care reduced total endoscopic nasal polyp score (NPS) versus that with placebo in patients with chronic rhinosinusitis with nasal polyps.

Objective

Our aim was to investigate relationships between NPS and (1) peak nasal inspiratory flow (PNIF) and (2) patient-reported outcomes.

Methods

In this post hoc analysis, patients randomized 1:1 received mepolizumab, 100 mg, or placebo subcutaneously every 4 weeks (plus standard of care). Changes from baseline in PNIF (week 52), visual analog scale scores (overall symptoms, nasal obstruction, and loss of smell [weeks 49-52]), and total 22-Item Sino-Nasal Outcome Test score (week 52) were assessed in patients with or without improvements in NPS (improvement of ≥1 point) or without (improvement of <1 point or worsening).

Results

Patients with improvements in NPS had greater improvements in PNIF (a median of 50 L per minute [interquartile range (IQR) = 10.5-87.5] with mepolizumab vs a median of 40 L per minute [IQR = 0-85.0] with placebo) than did those patients without improvements in NPS (a median of 0.0 L per minute [IQR = –10.0 to 45.0] with mepolizumab vs a median of 0.0 L per minute [IQR = –30.0 to 30.0] with placebo). Similar results were seen for the following: change from baseline in overall symptoms (a median of –5.8 [IQR = –8.1 to –3.80] with mepolizumab and a median of –4.1 [IQR = –7.0 to –1.2] with placebo with improvement in NPS vs a median of –1.3 [IQR = –6.3 to 0.0] with mepolizumab and a median of –0.1 [IQR = –3.4 to 0.0] with placebo without improvement in NPS); change in nasal obstruction (a median of –5.7 [IQR = –8.2 to –3.5] with mepolizumab and a median of –4.5 [IQR = –7.3 to –1.2] with placebo with improvement in NPS vs a median of –1.3 [IQR = –6.6 to 0.0] with mepolizumab and a median of 0.0 [IQR = –3.6 to 0.0] with placebo without improvement in NPS); change in loss of smell (a median of –2.8 [IQR = –7.9 to 0.0] with mepolizumab and a median of –0.7 [IQR = –4.0 to 0.0] with placebo with improvement in NPS vs a median of 0.0 [IQR = –2.4 to 0.0] with mepolizumab and a median of 0.0 [IQR = –0.3 to 0.0]) with placebo without improvement in NPS); and change in visual analog scale score and 22-Item Sino-Nasal Outcome Test total score (a median of –37.0 [IQR = –52.0 to –24.0] with mepolizumab and a median of –29.0 [IQR = –43.0 to –9.0] with placebo with improvement in NPS vs a median of –16.0 [IQR = –42.0 to 0.0] with mepolizumab and a median of 0.0 [IQR = –27.0 to 0.0] with placebo without improvement in NPS).

Conclusion

Improvement in NPS was associated with improvements in PNIF and patient-reported outcomes irrespective of treatment. PNIF could be a useful noninvasive tool for monitoring nasal polyp size.
背景在III期SYNAPSE研究中,对于伴有鼻息肉的慢性鼻窦炎患者,美泊利珠单抗加标准治疗与安慰剂相比可降低内窥镜鼻息肉总评分(NPS)。我们的目的是研究 NPS 与 (1) 鼻吸气流量峰值 (PNIF) 和 (2) 患者报告结果之间的关系。方法在这项事后分析中,患者按 1:1 随机分配,每 4 周一次皮下注射 100 毫克的麦泊利单抗或安慰剂(加上标准护理)。在NPS改善或未改善(改善≥1分)或未改善(改善<1分或恶化)的患者中,评估PNIF(第52周)、视觉模拟量表评分(总体症状、鼻阻塞和嗅觉丧失[第49-52周])和22项中鼻结果测试总分(第52周)与基线相比的变化。结果与安慰剂相比,NPS改善的患者的PNIF改善幅度更大(使用mepolizumab的中位数为每分钟50升[四分位距(IQR)=10.5-87.5],而使用安慰剂的中位数为每分钟40升[IQR=0-85.中位数为每分钟 0.0 升[IQR = -10.0 至 45.0],而安慰剂的中位数为每分钟 0.0 升[IQR = -30.0 至 30.0])。以下方面也出现了类似的结果:总体症状与基线相比的变化(使用 mepolizumab 的中位数为 -5.8 [IQR = -8.1 至 -3.80],使用安慰剂的中位数为 -4.1 [IQR = -7.0 至 -1.2] ,NPS 有所改善;使用 mepolizumab 的中位数为 -1.3 [IQR = -6.3 至 0.0],使用安慰剂的中位数为 -0.1 [IQR = -3.4 至 0.0],NPS 没有改善。0],而安慰剂的中位数为-0.1[IQR = -3.4至0.0],NPS没有改善);鼻阻塞的变化(使用mepolizumab的中位数为-5.7[IQR = -8.2至-3.5],而使用安慰剂的中位数为-4.5[IQR = -7.3至-1.2],而安慰剂的中位数为-1.3[IQR = -6.6 to 0.0],安慰剂的中位数为0.0[IQR = -3.6 to 0.0],NPS没有改善);嗅觉丧失的变化(mepolizumab的中位数为-2.8[IQR = -7.9至0.0],安慰剂的中位数为-0.7[IQR = -4.0至0.0],NPS有所改善;与之相比,甲泼尼单抗的中位数为0.0[IQR = -2.4至0.0],安慰剂的中位数为0.0[IQR=-0.3至0.0]),安慰剂则无改善);以及视觉模拟量表评分和22项鼻结果测试总分的变化(中位数为-37.0[IQR=-52.0至-24.结论无论治疗方法如何,NPS 的改善与 PNIF 和患者报告结果的改善相关。PNIF可能是监测鼻息肉大小的一种有用的无创工具。
{"title":"Peak nasal inspiratory flow assessment of polyp size and response from SYNAPSE","authors":"Amber U. Luong MD, PhD ,&nbsp;Joshua M. Levy MD, MPH, MSc ,&nbsp;Ludger Klimek MD, PhD ,&nbsp;Richard J. Harvey MD ,&nbsp;Jared Silver MD, PhD ,&nbsp;Steven G. Smith PhD ,&nbsp;Abby Fuller MSc ,&nbsp;Robert Chan MD ,&nbsp;Peter W. Hellings MD, PhD","doi":"10.1016/j.jacig.2024.100327","DOIUrl":"10.1016/j.jacig.2024.100327","url":null,"abstract":"<div><h3>Background</h3><div>In the phase III SYNAPSE study, mepolizumab plus standard of care reduced total endoscopic nasal polyp score (NPS) versus that with placebo in patients with chronic rhinosinusitis with nasal polyps.</div></div><div><h3>Objective</h3><div>Our aim was to investigate relationships between NPS and (1) peak nasal inspiratory flow (PNIF) and (2) patient-reported outcomes.</div></div><div><h3>Methods</h3><div>In this <em>post hoc</em> analysis, patients randomized 1:1 received mepolizumab, 100 mg, or placebo subcutaneously every 4 weeks (plus standard of care). Changes from baseline in PNIF (week 52), visual analog scale scores (overall symptoms, nasal obstruction, and loss of smell [weeks 49-52]), and total 22-Item Sino-Nasal Outcome Test score (week 52) were assessed in patients with or without improvements in NPS (improvement of ≥1 point) or without (improvement of &lt;1 point or worsening).</div></div><div><h3>Results</h3><div>Patients with improvements in NPS had greater improvements in PNIF (a median of 50 L per minute [interquartile range (IQR) = 10.5-87.5] with mepolizumab vs a median of 40 L per minute [IQR = 0-85.0] with placebo) than did those patients without improvements in NPS (a median of 0.0 L per minute [IQR = –10.0 to 45.0] with mepolizumab vs a median of 0.0 L per minute [IQR = –30.0 to 30.0] with placebo). Similar results were seen for the following: change from baseline in overall symptoms (a median of –5.8 [IQR = –8.1 to –3.80] with mepolizumab and a median of –4.1 [IQR = –7.0 to –1.2] with placebo with improvement in NPS vs a median of –1.3 [IQR = –6.3 to 0.0] with mepolizumab and a median of –0.1 [IQR = –3.4 to 0.0] with placebo without improvement in NPS); change in nasal obstruction (a median of –5.7 [IQR = –8.2 to –3.5] with mepolizumab and a median of –4.5 [IQR = –7.3 to –1.2] with placebo with improvement in NPS vs a median of –1.3 [IQR = –6.6 to 0.0] with mepolizumab and a median of 0.0 [IQR = –3.6 to 0.0] with placebo without improvement in NPS); change in loss of smell (a median of –2.8 [IQR = –7.9 to 0.0] with mepolizumab and a median of –0.7 [IQR = –4.0 to 0.0] with placebo with improvement in NPS vs a median of 0.0 [IQR = –2.4 to 0.0] with mepolizumab and a median of 0.0 [IQR = –0.3 to 0.0]) with placebo without improvement in NPS); and change in visual analog scale score and 22-Item Sino-Nasal Outcome Test total score (a median of –37.0 [IQR = –52.0 to –24.0] with mepolizumab and a median of –29.0 [IQR = –43.0 to –9.0] with placebo with improvement in NPS vs a median of –16.0 [IQR = –42.0 to 0.0] with mepolizumab and a median of 0.0 [IQR = –27.0 to 0.0] with placebo without improvement in NPS).</div></div><div><h3>Conclusion</h3><div>Improvement in NPS was associated with improvements in PNIF and patient-reported outcomes irrespective of treatment. PNIF could be a useful noninvasive tool for monitoring nasal polyp size.</div></div>","PeriodicalId":75041,"journal":{"name":"The journal of allergy and clinical immunology. Global","volume":"3 4","pages":"Article 100327"},"PeriodicalIF":0.0,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772829324001231/pdfft?md5=e5262e8b6da447332de44d97623622ce&pid=1-s2.0-S2772829324001231-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142315434","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Agaricus bisporus mushroom anaphylaxis: A case report and review of the literature 双孢蘑菇过敏性休克:病例报告和文献综述
Pub Date : 2024-08-12 DOI: 10.1016/j.jacig.2024.100324
Syed B. Ali MBBS, FRACP , William Smith MBBS, FRACP, PhD

Background

Anaphylaxis in response to edible mushrooms is uncommon, and sensitization may be independent of occupational exposure. Globally, Agaricus bisporus is one the most cultivated mushroom species, comprising the button, portobello, and Swiss brown varietals.

Objective

Our aim was to describe a case of anaphylaxis in an older nonatopic patient following ingestion of A bisporus and undertake a review of the literature.

Methods

A 77-year-old female was referred to the allergy clinic with a history of grade 3 hypotensive anaphylaxis following ingestion of a mushroom omelette. Her tryptase level 4 hours following acute symptoms was elevated. She continued to consume all other omelette ingredients with the exception of mushroom. Additional investigations included specific IgE testing as well as comprehensive skin prick testing (SPT) to raw and boiled mushrooms.

Results

One month after her index reaction, the result of SPT to boiled button mushroom was positive. The patient’s baseline tryptase level was normal. The results of further SPT with other commonly available boiled mushrooms (the A bisporus mushrooms portobello and Swiss brown, as well as enoki, oyster, and shiitake mushrooms) were also positive.

A review of the literature revealed 27 other cases, with an average patient age of 28.8 years (range 8-68 years) and no gender predisposition. Cases from Europe (n = 14, 51.8%) and Asia (n = 12, 44.4%) comprised the majority of the reports. A bisporus was reported in more than one-third of the cases (n = 10, 37.1%) from Australia, India, Portugal, Spain, and the United Kingdom. Cross-sensitization among the edible mushroom species was evident for those individuals who were tested, but no clear and consistent pattern was identified. In some cases, further diagnostics identified α-mannosidase, α-trehalose, mannitol, and ribosomal protein as specific mushroom allergens.

Conclusion

Clinicians should be aware of mushroom as a cause for anaphylaxis, especially in nonatopic and de novo presentations.

背景食用菌引起的过敏性休克并不常见,过敏可能与职业接触无关。在全球范围内,双孢蘑菇是栽培最多的蘑菇品种之一,包括金针菇、波多贝罗蘑菇和瑞士褐蘑菇。我们的目的是描述一例老年非特异性患者在摄入双孢蘑菇后发生过敏性休克的病例,并对文献进行回顾。急性症状出现 4 小时后,她的胰蛋白酶水平升高。她继续食用除蘑菇外的所有其他煎蛋配料。其他检查包括特异性 IgE 检测以及对生蘑菇和水煮蘑菇的全面皮肤点刺试验(SPT)。患者的基线色氨酸酶水平正常。对其他常见水煮蘑菇(双孢蘑菇、波多贝罗蘑菇、瑞士褐蘑菇、金针菇、杏鲍菇和香菇)的进一步 SPT 结果也呈阳性。来自欧洲(14 例,占 51.8%)和亚洲(12 例,占 44.4%)的病例占报告病例的大多数。在来自澳大利亚、印度、葡萄牙、西班牙和英国的病例中,超过三分之一的病例(10 例,37.1%)患有双孢菇。在接受检测的个体中,食用菌种类之间的交叉致敏现象很明显,但没有发现明确一致的模式。在某些病例中,进一步诊断发现α-甘露糖苷酶、α-曲哈糖、甘露醇和核糖体蛋白是特异性蘑菇过敏原。
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引用次数: 0
The common cold: The need for an effective treatment amid the FDA discussion on oral phenylephrine 普通感冒:在美国食品及药物管理局讨论口服苯肾上腺素之际,需要一种有效的治疗方法
Pub Date : 2024-08-07 DOI: 10.1016/j.jacig.2024.100318
Emina Išerić BSc , Joris C. Verster PhD

An episode of the common cold can have a significant negative impact on quality of life, mood, and daily activities. In line with this fact, there is a growing demand for health care and treatments associated with the common cold. Current treatments aim to (1) inhibit symptom severity and (2) shorten the duration of an episode of the common cold. These products include analgesics, antihistamines, and decongestants. In addition, various supplements, including vitamins, minerals, and herbs, are marketed to treat the common cold. The current products marketed for treating the common cold may reduce the severity of some (but not all) common cold symptoms, but they usually do not shorten the common cold episode. The recent indication that phenylephrine is not effective means that it will ultimately need to be removed from the over-the-counter monograph. Manufacturers will consequently need to reformulate their products and withdraw oral phenylephrine-containing products. Several newly developed common cold products are currently under investigation. These clinical trials should evaluate their efficacy and safety, as there remains a clear need for common cold products that significantly reduce both the symptom severity and the duration of episodes of the common cold.

普通感冒的发作会对生活质量、情绪和日常活动产生严重的负面影响。因此,人们对普通感冒的保健和治疗需求日益增长。目前的治疗方法旨在:(1)抑制症状的严重程度;(2)缩短普通感冒发作的持续时间。这些产品包括镇痛剂、抗组胺剂和减充血剂。此外,市场上还有各种治疗普通感冒的补充剂,包括维生素、矿物质和草药。目前市场上销售的治疗普通感冒的产品可能会减轻一些(但不是全部)普通感冒症状的严重程度,但通常不会缩短普通感冒的发作时间。最近有迹象表明苯肾上腺素无效,这意味着最终需要将其从非处方药专论中删除。因此,生产商需要重新配制产品,并撤下含有苯肾上腺素的口服产品。目前正在对几种新开发的普通感冒产品进行调查。这些临床试验应评估其疗效和安全性,因为目前仍明显需要能显著降低普通感冒症状严重程度和缩短发病时间的普通感冒产品。
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引用次数: 0
Daratumumab-based treatment of monoclonal gammopathy–associated angioedema due to acquired C1-inhibitor deficiency 基于达拉单抗治疗获得性 C1 抑制剂缺乏引起的单克隆抗体病相关性血管性水肿
Pub Date : 2024-08-05 DOI: 10.1016/j.jacig.2024.100322
Remy S. Petersen MD , Lauré M. Fijen MD, PhD , Laurens E. Franssen MD, PhD , Josephine M.I. Vos MD, PhD , Danny M. Cohn MD, PhD

Daratumumab-based treatment could control severe, treatment-refractory, life-threatening angioedema due to acquired C1-inhibitor deficiency associated with monoclonal gammopathy.

基于达拉土单抗的治疗可以控制严重的、治疗难治的、危及生命的血管性水肿,这种水肿是由于后天C1抑制剂缺乏并伴有单克隆抗体病引起的。
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引用次数: 0
Running into trouble with soy: A case report and review of our shopping carts 大豆带来的麻烦病例报告和购物车回顾
Pub Date : 2024-08-05 DOI: 10.1016/j.jacig.2024.100321
Fionnuala Cox BA Hons, MB, BCh, BAO, MRCPI, FRCPath, PhD, Khairin Khalib MBBCh, MRCPI, FRCPath, Mary Keogan MD, FRCPI, FRCPath

Soy-dependent exercise-induced anaphylaxis is likely underdiagnosed and potentially on the rise. As soy gains popularity in Western diets, we highlight it as a hidden allergen in a variety of processed foods, including those marketed toward exercise enthusiasts.

大豆依赖性运动诱发过敏性休克很可能诊断不足,而且有可能呈上升趋势。随着大豆在西方饮食中的普及,我们强调它是各种加工食品(包括面向运动爱好者销售的食品)中隐藏的过敏原。
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引用次数: 0
Successful treatment of the dupilumab-induced psoriatic dermatitis/arthritis and atopic dermatitis with a JAK inhibitor: A case report and literature review 用 JAK 抑制剂成功治疗杜必鲁单抗诱发的银屑病皮炎/关节炎和特应性皮炎:病例报告和文献综述
Pub Date : 2024-08-05 DOI: 10.1016/j.jacig.2024.100323
Misuzu Tsunoda MD , Takeya Adachi MD, PhD , Yuuri Nakajima MD , Yoshihiro Yatomi MD , Tomoko Shimizu MD, PhD , Katsuki Nakasute MD

Dupilumab-induced psoriatic dermatitis and arthritis in a patient with atopic dermatitis were effectively managed with upadacitinib, highlighting the use of Janus kinase inhibitors as a possible treatment for biologic therapy side effects.

一位特应性皮炎患者因使用杜匹单抗引发的银屑病皮炎和关节炎,在使用达帕替尼后得到了有效控制,这凸显了使用Janus激酶抑制剂治疗生物疗法副作用的可能性。
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引用次数: 0
期刊
The journal of allergy and clinical immunology. Global
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