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1.
Laryngorhinootologie ; 103(7): 529-541, 2024 Jul.
Article de Allemand | MEDLINE | ID: mdl-38955155

RÉSUMÉ

Allergies play a pivotal role in the daily practice of ENT specialists. Allergic symptoms induced by inhalant allergens are widespread in the population and can manifest through a wide range of symptoms, including rhinorrhea, sneezing, conjunctival redness, cough and dyspnea. Inconsistent diagnosis and treatment of allergic conditions can lead to reduced quality of life, decreased work performance, and socioeconomically significant secondary diseases. In addition to the medical history, the skin prick test and serological IgE diagnostics are the most important diagnostic procedure for detecting type-I allergies. To clarify clinical relevance, molecular diagnostics and nasal provocation testing may be employed. The key to effective treatment lies in a comprehensive allergological diagnosis coupled with a detailed patient history. General treatment recommendations such as allergen avoidance and nasal irrigation should complement pharmacological therapy. In the treatment of allergic rhinitis topical steroids are first line treatment options. The primary goal of treatment is symptom control, and if control is insufficient, causal therapy through specific allergen immunotherapy is recommended. Challenges in the ENT clinic involve selecting the necessary diagnostics and appropriate, effective treatments. Hence, using diagnostic and treatment algorithms, as well as standardized patient history questionnaires, can serve as invaluable tools in daily patient interactions, especially considering limited time availability.


Sujet(s)
Immunoglobuline E , Humains , Immunoglobuline E/sang , Tests cutanés , Désensibilisation immunologique/méthodes , Orientation vers un spécialiste , Hypersensibilité/diagnostic , Hypersensibilité/thérapie , Hypersensibilité/immunologie
2.
Zhonghua Yu Fang Yi Xue Za Zhi ; 58(6): 806-814, 2024 Jun 06.
Article de Chinois | MEDLINE | ID: mdl-38955727

RÉSUMÉ

Objective: To investigate the distribution rules of artemisia pollen and the clinical sensitization characteristics of allergic rhinitis (AR) induced by artemisia pollen in three urban and rural areas of Inner Mongolia. Methods: From March to October 2019, in 3 central cities (Chifeng, Hohhot, Ordos) and rural areas of Inner Mongolia, an epidemiological investigation method combining multi-stage stratified random sampling and face-to-face questionnaire survey was adopted to screen suspected AR patients, and skin prick test (SPT) was applied for diagnosis. At the same time, pollen monitoring was carried out in 3 areas to analyze the distribution and clinical sensitization characteristics of artemisia pollen.SPSS26.0 statistical software was used to process all the data. Chi-square test was used to compare rates among different age, sex, region and nationality, Spearman test was used to describe correlation analysis, and pairwise comparison of positive rates among multiple samples was used Bonferroni method. Results: Among the 6 393 subjects, 1 093 cases were diagnosed with AR, and the prevalence of AR was 17.10% (1 093/6 393). Among them, pollen-induced allergic rhinitis, the prevalence of PiAR was 10.97% (701/6 393), accounting for 64.14%(701/1 093).The highest incidence was in the youth group (20-39 years old), accounting for 46.94% (329/701).The diagnosed prevalence was higher in females than in males (11.35% vs. 10.64%, χ2 value 12.304, P<0.001).The prevalence rate of ethnic minority was higher than that of Han nationality (13.01% vs. 10.65%, χ2 value 6.296, P=0.008).The prevalence in urban areas was also significantly higher than that in rural areas (18.40% vs. 5.50%, χ2 value 10.497, P<0.001).There was significant difference in prevalence rate among the three regions in Inner Mongolia (6.06% in Chifeng, 13.46% in Hohhot, 16.39% in Ordos, χ2 value 70.054, P<0.001).The main clinical symptoms of artemisia PiAR were sneezing (95.58%), nasal congestion (91.73%) and nasal itching (89.30%).Allergic conjunctivitis accounted for 79.60% (558/701), chronic sinusitis for 55.63% (390/701), asthma for 23.25% (163/701).The pattern of artemisia pollen sensitization was mainly multiple sensitization, and the frequency of clinical symptoms and clinical diseases induced by hypersensitization with other allergens accounted for more than that caused by single artemisia pollen. The spread period of Artemisia pollen in the three regions was from June to October, and the peak state was in August in summer. The peak time of clinical symptoms in artemisia PiAR patients was about 2 weeks earlier than the peak time of pollen concentration, and the two were significantly positively correlated (R=0.7671, P<0.001). Conclusion: Artemisia pollens are the dominant pollens in late summer and early autumn in Inner Mongolia, and the prevalence of artemisia PiAR is high. Controlling the spread of Artemisia pollens is of great significance for the prevention and treatment of AR.


Sujet(s)
Artemisia , Pollen , Rhinite allergique , Population rurale , Tests cutanés , Population urbaine , Humains , Pollen/immunologie , Chine/épidémiologie , Prévalence , Rhinite allergique/épidémiologie , Enquêtes et questionnaires , Allergènes , Rhinite allergique saisonnière/épidémiologie , Mâle , Femelle , Adulte , Jeune adulte
3.
Int J Mol Sci ; 25(13)2024 Jul 06.
Article de Anglais | MEDLINE | ID: mdl-39000522

RÉSUMÉ

(1) Peanut allergy is associated with high risk of anaphylaxis which could be prevented by oral immunotherapy. Patients eligible for immunotherapy are selected on the basis of a food challenge, although currently the assessment of antibodies against main peanut molecules (Ara h 1, 2, 3 and 6) is thought to be another option. (2) The current study assessed the relationship between the mentioned antibodies, challenge outcomes, skin tests and some other parameters in peanut-sensitized children. It involved 74 children, divided into two groups, based on their response to a food challenge. (3) Both groups differed in results of skin tests, levels of component-specific antibodies and peanut exposure history. The antibody levels were then used to calculate thresholds for prediction of challenge results or symptom severity. While the antibody-based challenge prediction revealed statistical significance, it failed in cases of severe symptoms. Furthermore, no significant correlation was observed between antibody levels, symptom-eliciting doses and the risk of severe anaphylaxis. Although in some patients it could result from interference with IgG4, the latter would not be a universal explanation of this phenomenon. (4) Despite some limitations, antibody-based screening may be an alternative to the food challenge, although its clinical relevance still requires further studies.


Sujet(s)
Arachis , Hypersensibilité aux arachides , Humains , Hypersensibilité aux arachides/diagnostic , Hypersensibilité aux arachides/immunologie , Enfant , Femelle , Mâle , Enfant d'âge préscolaire , Arachis/immunologie , Arachis/effets indésirables , Tests cutanés/méthodes , Anaphylaxie/diagnostic , Anaphylaxie/immunologie , Allergènes/immunologie , Immunoglobuline E/immunologie , Immunoglobuline E/sang , Étude de validation de principe , Adolescent , Immunoglobuline G/sang , Immunoglobuline G/immunologie , Antigènes végétaux/immunologie
4.
Allergy Asthma Proc ; 45(4): e31-e37, 2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38982605

RÉSUMÉ

Background: Fruit allergy usually presents with mild-to-moderate symptoms but serious systemic reactions, e.g., anaphylaxis, may also occur. Objective: This study aimed to examine the clinical and laboratory characteristics of patients with fruit allergy and fruit-induced anaphylaxis. Methods: Patients diagnosed with fruit allergy at Diskapi Hematology and Oncology Hospital and Bilkent City Hospital between January 2017 and January 2023 were included in the study. The diagnosis of anaphylaxis was made according to the European Allergy and Clinical Immunology Anaphylaxis Guideline. Results: During the study period, skin-prick tests with food allergens were performed on 9432 patients in our clinic, and fruit allergy was detected in 78 patients (0.82%). Five patients with inaccessible medical records were excluded from the study. 40 (54.8%) were boys. The median (interquartile range) age at the onset of symptoms was 72 months (12.5-144 months). Sixty-eight of the patients (93.2%) had a concomitant allergic disease, the most common of which was allergic rhinitis (n = 48 [65.8%]). The 73 patients had a history of reaction to 126 fruits. Twenty-five patients (19.8%) were allergic to multiple fruits. The most common fruit allergen was banana (22/126 [17.4%]), followed by peach (18/126 [14.2%]) and kiwi (17/126 [13.5%]). Mucocutaneous findings were observed most frequently after fruit consumption (120/126 [95.2%]). Anaphylaxis occurred in 17 patients (23.2%) with 21 fruits.The fruits most commonly associated with anaphylaxis were banana (6/21 [28.6%]) and kiwi (6/21 [28.6%]). Conclusion: Fruit allergy generally presents with mild symptoms, e.g., oral allergy syndrome, but severe systemic symptoms, e.g., anaphylaxis, can also be observed. Kiwi and banana are the fruits that most commonly cause anaphylaxis. Although more comprehensive studies are needed to comment on the development of tolerance, especially in patients with anaphylaxis, responsible fruit avoidance is still the most important strategy.


Sujet(s)
Allergènes , Anaphylaxie , Hypersensibilité alimentaire , Fruit , Tests cutanés , Humains , Anaphylaxie/diagnostic , Anaphylaxie/étiologie , Anaphylaxie/épidémiologie , Mâle , Femelle , Enfant , Hypersensibilité alimentaire/diagnostic , Hypersensibilité alimentaire/complications , Hypersensibilité alimentaire/épidémiologie , Fruit/effets indésirables , Fruit/immunologie , Enfant d'âge préscolaire , Allergènes/immunologie , Nourrisson , Adolescent
5.
Allergy Asthma Proc ; 45(4): e23-e30, 2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38982610

RÉSUMÉ

Background: ß-Lactams are the most widely used antibiotic family in the world. Nevertheless, they also stand out as the primary culprits for inducing drug hypersensitivity reactions (HSR). Methods: Between May 2018 and March 2023, patients with suspected HSRs to ß-lactams, who underwent skin tests (ST), were retrospectively screened. The determinants of allergenic penicillin (DAP) tests, which include penicillin minor and major determinants, clavulanic acid, and amoxicillin, along with ampicillin, sulbactam, the identified culprit drugs, and alternative cephalosporins, which include cefuroxime, ceftriaxone prick and/or intradermal tests, were administered. The analysis focused on identifying positive ST results and determining the true HSRs rates in this patient cohort. Results: Of the 147 patients, 78.9% (n = 116) were women and the median (minimum-maximum) age was 41 years (18-71 years). Mild HSRs (grades 1-2) were observed in 72.78% (n = 107), whereas 24.4% (n = 36) had severe reactions (grades 3-4) and 2.7% (n = 4) had an unknown grade. Of the patients, 64% (n = 94) experienced HSRs within the first hour after the last dose of the identified culprit drug. The overall positivity rate for all STs was 26.5% (n = 39). ST positivity rates were notably higher in individuals who had experienced HSRs within the past 6 months (p = 0.02) and those with severe anaphylaxis (p < 0.001). Conclusion: ß-Lactam ST positivity is higher, especially in those with grades 3-4 reactions and consulted a physician within the first 6 months after their HSRs.


Sujet(s)
Antibactériens , Hypersensibilité médicamenteuse , Tests cutanés , bêta-Lactames , Humains , Femelle , Mâle , Adulte , Adulte d'âge moyen , Hypersensibilité médicamenteuse/diagnostic , bêta-Lactames/effets indésirables , bêta-Lactames/immunologie , Adolescent , Sujet âgé , Jeune adulte , Études rétrospectives , Antibactériens/effets indésirables , Indice de gravité de la maladie , Allergènes/immunologie
6.
Medicine (Baltimore) ; 103(27): e38628, 2024 Jul 05.
Article de Anglais | MEDLINE | ID: mdl-38968527

RÉSUMÉ

BACKGROUND: The skin prick test (SPT) is a standard procedure in allergy/immunology clinics, crucial for evaluating conditions like allergic rhinitis and food allergies. As a cornerstone in investigating immunoglobulin E-mediated allergy, it plays a vital role in diagnosing allergies, including those triggered by common dust mites like Dermatophagoides pteronyssinus, Dermatophagoides farinae, Euroglyphus maynei, and Blomia tropicalis. Despite its widespread use, adverse reactions to SPT are uncommon (15 per 100,000 patients), though the procedure is not entirely risk-free. This article presents a clinical case involving a 17-year-old female who experienced a moderately delayed allergic reaction 120 minutes post-SPT, managed effectively with subsequent symptom resolution. METHODS: The patient, with a history of persistent rhinorrhea, itchy nose, eyes, and postnasal drip, sought consultation due to worsening symptoms. Diagnostic measures, including patient-reported outcomes and SPT with a standard aeroallergen panel, revealed sensitization to various allergens. RESULTS: Post-test, the patient reported ocular pruritus, left eyelid swelling, and moderate rhinorrhea, persisting for about 24 hours. On the subsequent medical visit, the patient received rupatadine and deflazacort, leading to symptom resolution within 3 hours. CONCLUSION: This article delves into a systemic allergic reaction post-SPT, emphasizing the 2 main stages of type I hypersensitivity reactions. While the acute phase involves mast cell-driven mediators within 15 minutes, the delayed phase (4-8 hours) includes de novo cytokine release. Vigilance regarding symptom onset and differentiation between mild and severe reactions is crucial. Notably, the absence of specific waiting time guidelines post-SPT underscores the need for reporting to enhance understanding and subsequent management. Performing these procedures in specialized centers with qualified professionals is essential for effectively managing potential anaphylactic reactions. Addressing these knowledge gaps will contribute to enhanced patient safety during diagnostic procedures.


Sujet(s)
Tests cutanés , Humains , Femelle , Adolescent , Tests cutanés/méthodes , Établissements de soins ambulatoires , Hypersensibilité/diagnostic
7.
Allergol Immunopathol (Madr) ; 52(4): 1-8, 2024.
Article de Anglais | MEDLINE | ID: mdl-38970258

RÉSUMÉ

BACKGROUND: Dermatophagoides pteronyssinus and Dermatophagoides farinae belong to the family Pyroglyphidae (subfamily: "Dermatophagoidinae") and have the respective allergenic proteins of Der p1, Der p2, and Der p23 and Der f1 and Der f2. Euroglyphus maynei, belongs to the family Pyroglyphidae (subfamily: "Pyroglyphinae") and its main allergenic protein is Eur m1, a source of sensitization. Sensitization to D. pteronyssinus and D. farinae is assessed through skin tests, while sensitization to E. maynei is assessed less frequently. OBJECTIVE: This experimental work aims to analyze the prevalence of sensitization to E. maynei in patients with respiratory allergies treated at M. Albanesi Allergy and Immunology Unit in Bari, Italy, and the sequence homology of major allergenic proteins of E. maynei with D. farinae and D. pteronyssinus was analyzed. METHODS: In this real-life study, 65 patients were enrolled. In particular, patients with respiratory allergy were subjected to skin prick tests for common respiratory allergens, including Euroglyphus maynei. The sequence homology analysis was performed between the major allergenic proteins of E. maynei and those of D. pteronyssinus and D. farinae. RESULTS: Sensitization to E. maynei accounts for 41.5% of patients. All patients with E. maynei sensitization had concomitant sensitization to D. farinae and D. pteronyssinus. The analysis of sequence homology of Der p1 and Der f1 proteins with the sequence of Eur m1 protein demonstrated an identity of 84.4% and 86%, respectively. CONCLUSIONS: Nearly 50% of house dust mites-sensitized patients have a concomitant sensitization to E. maynei. The cross-sensitization could be due to Der f1, Der p1, and Eur m1 similarity.


Sujet(s)
Allergènes , Antigènes de Dermatophagoides , Biologie informatique , Hypersensibilité respiratoire , Tests cutanés , Humains , Animaux , Mâle , Antigènes de Dermatophagoides/immunologie , Femelle , Adulte , Adulte d'âge moyen , Prévalence , Hypersensibilité respiratoire/épidémiologie , Hypersensibilité respiratoire/immunologie , Hypersensibilité respiratoire/diagnostic , Italie/épidémiologie , Allergènes/immunologie , Pyroglyphidae/immunologie , Protéines d'arthropode/immunologie , Jeune adulte , Adolescent , Sujet âgé
8.
Allergol Immunopathol (Madr) ; 52(4): 9-14, 2024.
Article de Anglais | MEDLINE | ID: mdl-38970259

RÉSUMÉ

BACKGROUND: Allergy to lipid transfer proteins (LPT) is common in Mediterranean Europe, and it causes severe reactions in patients and affects multiple foods, impairing the quality of life. OBJECTIVE: This study aimed to describe the clinical and sensitization profile of patients with LTP syndrome and to determine a clinical pattern of severity. Molecular diagnosis is shown in a broad population through microarrays. MATERIAL AND METHODS: This study was performed at the LTP Allergy Consultation of the Reina Sofia Hospital in Murcia, Spain. We analyzed the patients' characteristics, reactions, cofactors, food implicated, quality of life, skin prick test to food and aeroallergens, and serologic parameters, such as total immunoglobulin E, peach LTP (Pru p 3 IgE) and immunoglobulin G4, and microarray Immuno Solid-phase Allergen Chip (ISAC). We related the severity of the reactions with other variables. RESULTS: We presented a series of 236 patients diagnosed with LTP allergy, 54.66% suffering from anaphylaxis, 36.02% from urticaria angioedema, and 9.32% from oral allergy syndrome. The most frequently implicated food was peach, producing symptoms in 70% of patients, followed by walnut in 55%, peanut in 45%, hazelnut in 44%, and apple in 38% patients. Regarding the food that provoked anaphylaxis, walnut was the most frequent instigator, along with peach, peanut, hazelnut, almond, sunflower seed, and apple. According to the severity of LPT reaction, we did not discover significant differences in gender, age, food group involved, and serologic parameters. We found differences in the presence of cofactors, with 48.84% of cofactors in patients with anaphylaxis, compared to 27.1% in patients without anaphylaxis and in family allergy background (P < 0.0001). CONCLUSION: In our series of patients, 54% presented anaphylaxis, and the foods that most frequently produced symptoms were peaches, apples, and nuts. Cofactors and family allergy backgrounds were associated with the severity of LPT reaction.


Sujet(s)
Allergènes , Antigènes végétaux , Hypersensibilité alimentaire , Immunoglobuline E , Tests cutanés , Humains , Mâle , Femelle , Hypersensibilité alimentaire/immunologie , Hypersensibilité alimentaire/diagnostic , Hypersensibilité alimentaire/épidémiologie , Immunoglobuline E/sang , Immunoglobuline E/immunologie , Adulte , Adulte d'âge moyen , Antigènes végétaux/immunologie , Allergènes/immunologie , Espagne/épidémiologie , Adolescent , Protéines végétales/immunologie , Jeune adulte , Protéines de transport/immunologie , Enfant , Immunoglobuline G/sang , Immunoglobuline G/immunologie , Sujet âgé , Qualité de vie , Anaphylaxie/immunologie , Anaphylaxie/diagnostic , Anaphylaxie/étiologie , Enfant d'âge préscolaire
9.
Allergol Immunopathol (Madr) ; 52(4): 21-29, 2024.
Article de Anglais | MEDLINE | ID: mdl-38970261

RÉSUMÉ

BACKGROUND: Molecular diagnosis in allergology helps to identify multiple allergenic molecules simultaneously. The use of purified and/or recombinant allergens increases the accuracy of individual sensitization profiles in allergic patients. OBJECTIVE: To assess the impact of molecular diagnosis through the ImmunoCAPTM ISAC 112 microarray on etiological diagnosis and specific immunotherapy (SIT) prescription. This was compared to the use of conventional diagnoses in pediatric, adolescent, and young adult patients with rhinitis or rhinoconjunctivitis and/or allergic asthma, sensitized to three or more pollen allergens of different botanical species. METHODS: A multicenter, prospective, observational study was conducted in patients aged 3-25 years who received care at the Allergology service of 14 hospitals in Catalonia from 2017 to 2020. Allergology diagnosis was established based on the patient's clinical assessment and the results of the skin prick test and specific immunoglobulin E assays. Subsequently, molecular diagnosis was conducted using ImmunoCAPTM ISAC® 112 to recombinant and/or purified allergen components. RESULTS: A total of 109 patients were included; 35 (32.1%) were pediatric patients and 74 (67.9%) were adolescents or young adults (mean age: 18 years), with 58.0% being females. A change of 51.0% was observed in SIT prescription following molecular etiological diagnosis by means of a multi-parameter microarray. CONCLUSIONS: Molecular diagnosis by means of multi-parameter tests increases the accuracy of etiological diagnosis and helps to define an accurate composition of SIT.


Sujet(s)
Allergènes , Désensibilisation immunologique , Pollen , Rhinite allergique saisonnière , Humains , Femelle , Espagne , Adolescent , Mâle , Enfant , Études prospectives , Pollen/immunologie , Jeune adulte , Adulte , Enfant d'âge préscolaire , Allergènes/immunologie , Allergènes/administration et posologie , Désensibilisation immunologique/méthodes , Rhinite allergique saisonnière/diagnostic , Rhinite allergique saisonnière/immunologie , Rhinite allergique saisonnière/thérapie , Immunoglobuline E/immunologie , Immunoglobuline E/sang , Tests cutanés , Techniques de diagnostic moléculaire
11.
Pediatr Allergy Immunol ; 35(7): e14204, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-39016336

RÉSUMÉ

BACKGROUND: Allergy to peanuts and tree nuts is a common cause of food allergy in Spain, with lipid transfer proteins (LTP) being the most frequently recognized panallergen. LTP sensitization often leads to multiple food group sensitivities, resulting in overly restrictive diets that hinder patient's quality of life. This study aimed to assess the tolerance of peanuts and tree nuts (hazelnuts and walnuts) in children sensitized to LTP, potentially mitigating the need for such diets. METHODS: This prospective study enrolled individuals diagnosed with allergy to peanuts, hazelnuts, or walnuts. Data were collected from medical records, including demographics and clinical history. Allergological assessment comprised skin prick tests using commercial extracts and the nuts in question, alongside measurements of total and specific IgE to nuts and their primary molecular components. Participants showing positive LTP sensitization without sensitization to seed storage proteins underwent open oral nut challenges. RESULTS: A total of 75 individuals labeled as allergic to peanuts, 44 to hazelnuts, and 51 to walnuts were included. All of them underwent an open oral provocation test with the incriminated nut, showing a high tolerance rate. Peanut was tolerated by 98.6% of patients, 97.72% tolerated hazelnut, and 84.3% tolerated walnut. CONCLUSION: The findings suggest that the majority of patients allergic to peanuts, hazelnuts, or walnuts, due to LTP sensitization and lacking IgE reactivity to seed storage proteins, can tolerate these nuts. This supports the need for personalized nut tolerance assessments to avoid unnecessary dietary restrictions.


Sujet(s)
Arachis , Protéines de transport , Tolérance immunitaire , Immunoglobuline E , Hypersensibilité aux noix , Tests cutanés , Humains , Mâle , Femelle , Protéines de transport/immunologie , Enfant , Espagne , Études prospectives , Enfant d'âge préscolaire , Immunoglobuline E/sang , Immunoglobuline E/immunologie , Hypersensibilité aux noix/immunologie , Hypersensibilité aux noix/diagnostic , Arachis/immunologie , Hypersensibilité aux arachides/immunologie , Hypersensibilité aux arachides/diagnostic , Allergènes/immunologie , Juglans/immunologie , Noix/immunologie , Adolescent , Corylus/immunologie , Hypersensibilité aux noix et aux arachides/immunologie , Antigènes végétaux/immunologie
12.
J Allergy Clin Immunol Pract ; 12(3): 705-713.e6, 2024 Mar.
Article de Anglais | MEDLINE | ID: mdl-39056227

RÉSUMÉ

BACKGROUND: Two-dimensional (2D) classifications of iodinated contrast media (ICM) are insufficient to explain the observed skin test (ST) reactivity patterns in patients with drug hypersensitivity reactions (DHRs) to ICM. OBJECTIVE: To refine the current view on allergic DHRs to ICM by analyzing ST reactivity patterns in patients with previous reactions to ICM. METHODS: Patients with a history of DHR to ICM and positive STs, who presented at the University Hospital of Montpellier between 2004 and 2022, were included in the study. The relative difference between every two ICM products was measured by Manhattan distance and odds ratios were computed for all pairs of products in the immediate reaction (IR) and non-immediate reaction (NIR) ST groups. RESULTS: A total of 181 patients were included in the study. Odds ratio analysis identified significant associations between classical cross-reactive ICM, such as iohexol-ioversol, iohexol-iomeprol, iomeprol-ioversol, and iohexol-iodixanol in the IR ST group and iohexol-ioversol, iopromide-iohexol, and iomeprol-ioversol in the NIR ST group. We also identified uncommon associations, such as ioxitalamate-amidotrizoate in the IR ST group and amidotrizoate-iopamidol and amidotrizoate-ioxitalamate in the NIR ST group. The results were reflected by the Manhattan distance, which suggested the existence of clusters containing the same classically associated ICM as well as uncommon associations, which we hypothesize to be related to similarities in the 3D structure of the respective ICM. CONCLUSIONS: Current chemical (2D) classifications cannot explain all observed ST reactivity patterns. Whether the 3D structure can be integrated into the current classifications to interpret the observed ST reactivity patterns and predict tolerance to alternative ICM requires further research.


Sujet(s)
Produits de contraste , Hypersensibilité médicamenteuse , Iohexol , Iopamidol , Tests cutanés , Acides triiodo-benzoïques , Humains , Produits de contraste/effets indésirables , Hypersensibilité médicamenteuse/diagnostic , Hypersensibilité médicamenteuse/épidémiologie , Femelle , Mâle , Adulte d'âge moyen , Iopamidol/effets indésirables , Iopamidol/analogues et dérivés , Acides triiodo-benzoïques/effets indésirables , Adulte , Iohexol/effets indésirables , Iohexol/analogues et dérivés , Sujet âgé , Composés de l'iode/effets indésirables
13.
Pediatr Allergy Immunol ; 35(7): e14195, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38989807

RÉSUMÉ

BACKGROUND: Complete avoidance of milk is the usual management for IgE-mediated cow's milk protein allergy (CMPA). A baked milk ladder is a method of dietary advancement therapy in IgE-mediated CMPA in Ireland, while in Spain, avoidance of milk awaiting natural tolerance acquisition through an oral food challenge (OFC) is employed. The aim of this study was to evaluate the use of dietary advancement therapy using a milk ladder compared with complete avoidance of milk for managing IgE-mediated CMPA. METHODS: This is a retrospective chart review of 371 pediatric patients from the population who have been treated for IgE-mediated CMPA between 2011 and 2020, with the milk ladder (Ireland) or complete avoidance followed by an OFC (Spain). The main outcome was the introduction of cow's milk. RESULTS: Milk ladder patients were 3.67 times more likely to succeed in comparison with milk avoidance (p < .001). Anaphylaxis during the treatment period occurred in 34 patients in the milk avoidance groups, while three patients in the milk ladder group experienced anaphylaxis due to accidental exposure to milk (p < .001). Failure to complete treatment was associated with a higher skin prick test in the milk avoidance group and a raised specific IgE in the milk ladder group. CONCLUSION: This is the first study that compares outcomes of dietary advancement therapy to complete avoidance for CMPA management, demonstrating that cow's milk can be successfully and safely reintroduced using dietary advancement therapy using a milk ladder.


Sujet(s)
Immunoglobuline E , Hypersensibilité au lait , Protéines de lait , Humains , Hypersensibilité au lait/immunologie , Hypersensibilité au lait/thérapie , Études rétrospectives , Immunoglobuline E/sang , Immunoglobuline E/immunologie , Femelle , Mâle , Enfant d'âge préscolaire , Animaux , Protéines de lait/immunologie , Enfant , Nourrisson , Espagne , Lait/immunologie , Irlande , Anaphylaxie/prévention et contrôle , Anaphylaxie/immunologie , Anaphylaxie/étiologie , Tests cutanés , Tolérance immunitaire , Bovins , Allergènes/immunologie , Allergènes/administration et posologie , Résultat thérapeutique
14.
Front Immunol ; 15: 1324987, 2024.
Article de Anglais | MEDLINE | ID: mdl-38827735

RÉSUMÉ

Introduction: The COVID vaccination program with new types of vaccinations and early reports of allergic reactions to vaccines led to vaccination hesitancy in patients with allergies. In this study, we aimed to characterize patients who present at an allergy center with specific questions regarding risk assessment to COVID vaccines in comparison to regular allergy center patients. Methods: A total of 50 patient charts of patients with risk assessment for COVID vaccination (COV group) and 50 regular allergy center patients (ALL group) were assessed for documented allergies, comorbidities, total IgE, and tryptase levels and hospital anxiety and depression score (HADS). Skin prick testing (SPT) with additives of COVID vaccines [polyethylene glycol (PEG), polysorbate] were performed if indicated based on medical history. Results: Patients who presented for examination prior to a possible COVID vaccination were mostly female (86%) and had more frequently reported allergic reactions to drugs in the past, but only in a minor group (28%) were the reactions qualified as anaphylaxis. The group COV patients scored significantly higher in the HADS for anxiety and depression than the regular group ALL patients. The same trend was observed when data were corrected for gender. It is worth noting that patients without any prior contact to COVID vaccines scored comparable regarding anxiety to patients with prior reaction to COVID vaccinations, but significantly higher in the depression score. In 19 patients (38%) who met the indications for SPT for the suspicious contents PEG and Polysorbate 80, the tests did not show a positive result. Furthermore, 84% of patients underwent the prick test, but only 15% of patients who received consultation alone agreed to vaccination at our center. No vaccination-related event was documented in these patients. Discussion: In conclusion, vaccination hesitancy was frequently elicited by negative experiences with drugs and putative drug allergies. Female patients predominate in this patient group, and the anxiety and depression scores were significantly elevated. Allergological workup, including SPT, led to a high rate of subsequent vaccinations, whereas a discussion with the patients about risks and individualized advice for vaccination without testing only rarely resulted in documented vaccinations.


Sujet(s)
Vaccins contre la COVID-19 , COVID-19 , Réticence à l'égard de la vaccination , Vaccination , Adulte , Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Anxiété/psychologie , COVID-19/prévention et contrôle , COVID-19/psychologie , Vaccins contre la COVID-19/effets indésirables , Dépression , Hypersensibilité/psychologie , Santé mentale , Tests cutanés , Vaccination/psychologie , Réticence à l'égard de la vaccination/psychologie
16.
Arerugi ; 73(4): 347-352, 2024.
Article de Japonais | MEDLINE | ID: mdl-38880634

RÉSUMÉ

Gibberellin-regulated protein (GRP) is a newly discovered allergen in systemic fruit allergies. The kind of fruits which cause allergy is extensive as GRP is universally included in plants. Two children with GRP allergy were reported. Case 1: A 6-year-old boy experienced anaphylaxis while running after school lunch, which included canned peaches. A skin prick test (SPT) and blood examination suggested that he had peach GRP allergy. Six months and three years later, he experienced a similar episode after eating apple and citrus flesh, respectively. Case 2: An 11-year-old boy experienced anaphylaxis while running after consuming canned peaches during school lunch. A SPT implied that he had peach GRP allergy. However, a similar episode occurred after eating strawberry flesh 18 months later.Patients with GRP allergy often have one or more allergies to fruits other than peaches, as in these cases, and relevant fruits differ depending on the case. Particularly, clinicians should recognize that apple and citrus fruits are frequently included in school lunches as fruit flesh and as flavoring or seasoning in ready-made sauces or dressings. Therefore, an appropriate removal strategy should be considered in school lunches depending on each case of GRP allergy.


Sujet(s)
Hypersensibilité alimentaire , Fruit , Enfant , Mâle , Humains , Hypersensibilité alimentaire/immunologie , Fruit/immunologie , Établissements scolaires , Protéines végétales/immunologie , Déjeuner , Allergènes/immunologie , Tests cutanés
17.
BMJ Open ; 14(6): e085212, 2024 Jun 08.
Article de Anglais | MEDLINE | ID: mdl-38851228

RÉSUMÉ

INTRODUCTION: Perioperative anaphylaxis (POA) can lead to significant complications. Therefore, accurate identification of allergens for POA patients is critical to ensure the safety of future surgical and anaesthetic procedures. Existing perioperative allergen detection methods face challenges in sensitivity and specificity. The passive mast cell activation test (pMAT) has recently emerged as a potential diagnostic tool. Our study aims to evaluate the diagnostic efficacy of pMAT for identifying perioperative allergens, with a focus on non-depolarising neuromuscular blocking agents, the most common culprits of POA. METHODS AND ANALYSIS: This prospective diagnostic accuracy study will measure the diagnostic accuracy of pMAT in POA patients. Participants will undergo skin testing (ST), basophil activation testing (BAT) and pMAT. The diagnostic validity of pMAT will be assessed based on the results of ST and BAT. The assessment of diagnostic accuracy will include sensitivity, specificity, likelihood ratios, and false-positive and false-negative rates while measurement of the consistency rate will assess reliability. ETHICS AND DISSEMINATION: This study has been approved by the Institutional Review Board of China-Japan Friendship Hospital (2023-KY-247). Results will be disseminated through academic presentations and peer-reviewed journal publications and will provide valuable scientific data and some new insights into the diagnostic accuracy of pMAT.


Sujet(s)
Allergènes , Anaphylaxie , Humains , Anaphylaxie/diagnostic , Études prospectives , Allergènes/immunologie , Reproductibilité des résultats , Mastocytes/immunologie , Tests cutanés/méthodes , Curarisants/effets indésirables , Sensibilité et spécificité , Test de dégranulation des basophiles/méthodes , Période périopératoire
18.
BMC Anesthesiol ; 24(1): 204, 2024 Jun 08.
Article de Anglais | MEDLINE | ID: mdl-38851690

RÉSUMÉ

BACKGROUND: Remimazolam is a recently developed, ultrashort-acting benzodiazepine that is used as a general anesthetic. Some cases of remimazolam anaphylaxis have been reported, but its characteristics are not fully understood. We present an interesting case report and review of the literature to better understand remimazolam anaphylaxis. CASE PRESENTATION: A 75-year-old man scheduled for robot-assisted gastrectomy was administered remimazolam for the induction of general anesthesia. After intubation, low end-expiratory CO2, high airway pressure and concurrent circulatory collapse were observed. Bronchoscopy revealed marked tracheal and bronchial edema, which we diagnosed as anaphylaxis. The patient suffered cardiac arrest after bronchoscopy but recovered immediately with intravenous adrenaline administration and chest compressions. We performed skin prick tests for the drugs used during induction except for remimazolam, considering the high risk of systemic adverse reactions to remimazolam. We diagnosed remimazolam anaphylaxis because the skin prick test results for the other drugs used during anesthesia were negative, and these drugs could have been used without allergic reactions during the subsequent surgery. Furthermore, this patient had experienced severe anaphylactic-like reactions when he underwent cardiac surgery a year earlier, in which midazolam had been used, but it was not thought to be the allergen at that time. Based on these findings, cross-reactivity to remimazolam and midazolam was suspected. However, the patient had previously received another benzodiazepine, brotizolam, to which he was not allergic, suggesting that cross-reactivity of remimazolam may vary among benzodiazepines. In this article, we reviewed the 11 cases of remimazolam anaphylaxis that have been described in the literature. CONCLUSIONS: Remimazolam is an ultrashort-acting sedative; however, it can cause life-threatening anaphylaxis. In addition, its cross-reactivity with other benzodiazepines is not fully understood. To increase the safety of this drug, further research and more experience in its use are needed.


Sujet(s)
Anaphylaxie , Benzodiazépines , Hypnotiques et sédatifs , Humains , Mâle , Sujet âgé , Anaphylaxie/induit chimiquement , Benzodiazépines/effets indésirables , Hypnotiques et sédatifs/effets indésirables , Hypersensibilité médicamenteuse/diagnostic , Tests cutanés/méthodes , Anesthésie générale/effets indésirables
19.
Int J Tuberc Lung Dis ; 28(6): 287-294, 2024 Jun 01.
Article de Anglais | MEDLINE | ID: mdl-38822484

RÉSUMÉ

BACKGROUNDGiven the high prevalence of asthma-chronic obstructive pulmonary disease overlap (ACO) in Vietnam, there is an urgent need to establish a simplified strategy for categorising patients as either having asthma or chronic obstructive pulmonary disease (COPD). This classification would streamline the application of treatment recommendations outlined by the Global Initiative for Asthma (GINA) and the Global Initiative for Chronic Obstructive Lung Disease (GOLD).METHODSPatients with obstructive lung function were classified as having COPD, asthma, or ACO based on GINA/GOLD guidelines. We hypothesised that ACO-like asthma (ACO-A) would present with positive skin prick tests (SPTs) or early onset of symptoms without a history of tuberculosis (TB), while those with ACO-like COPD (ACO-B) would exhibit negative SPTs and late onset of symptoms and/or a history of TB.RESULTSAmong 235 patients, the prevalence of asthma, ACO-A, ACO-B, and COPD was respectively 21%, 22%, 17%, and 40%. Allergic history, rhinitis, and childhood asthma were associated with ACO-A, while high cumulative smoking was correlated with ACO-B. Socio-economic and demographic parameters, medical history, clinical features, smoking habits, lung function, and para-clinical investigations significantly differed between "all asthma" (i.e., individuals with asthma combined with ACO-A) and "all COPD" (i.e., individuals with COPD combined with ACO-B).CONCLUSIONBased on SPTs, history of TB, and onset age, ACO patients may be defined as people with asthma or COPD..


Sujet(s)
Asthme , Phénotype , Broncho-pneumopathie chronique obstructive , Humains , Adulte d'âge moyen , Mâle , Femelle , Prévalence , Broncho-pneumopathie chronique obstructive/épidémiologie , Broncho-pneumopathie chronique obstructive/diagnostic , Adulte , Asthme/épidémiologie , Asthme/diagnostic , Vietnam/épidémiologie , Sujet âgé , Tests cutanés , Syndrome de chevauchement asthme-BPCO/épidémiologie , Syndrome de chevauchement asthme-BPCO/diagnostic
20.
Nutrients ; 16(9)2024 Apr 26.
Article de Anglais | MEDLINE | ID: mdl-38732550

RÉSUMÉ

BACKGROUND: Early-life vitamin D is a potentially modifiable risk factor for the development of eczema, but there is a lack of data on longitudinal associations. METHOD: We measured 25(OH)D3 levels from neonatal dried blood spots in 223 high-allergy-risk children. Latent class analysis was used to define longitudinal eczema phenotype up to 25 years (4 subclasses). Skin prick tests (SPTs) to 6 allergens and eczema outcomes at 6 time points were used to define eczema/sensitization phenotypes. Associations between 25(OH)D3 and prevalent eczema and eczema phenotypes were assessed using logistic regression models. RESULTS: Median 25(OH)D3 level was 32.5 nmol/L (P25-P75 = 23.1 nmol/L). Each 10 nmol/L increase in neonatal 25(OH)D3 was associated with a 26% reduced odds of early-onset persistent eczema (adjusted multinomial odds ratio (aMOR) = 0.74, 95% CI = 0.56-0.98) and 30% increased odds of early-onset-resolving eczema (aMOR = 1.30, 95% CI = 1.05-1.62) when compared to minimal/no eczema up to 12 years. Similar associations were seen for eczema phenotype up to 25 years. We did not see any strong evidence for the association between neonatal 25(OH)D3 and prevalent eczema or eczema/sensitization phenotype. CONCLUSIONS: Higher neonatal 25(OH)D3 levels, a reflection of maternal vitamin D levels in pregnancy, may reduce the risk of early-onset persistent eczema.


Sujet(s)
Eczéma , Vitamine D , Humains , Eczéma/épidémiologie , Eczéma/sang , Nouveau-né , Femelle , Mâle , Nourrisson , Études longitudinales , Enfant d'âge préscolaire , Vitamine D/sang , Enfant , Adolescent , Adulte , Facteurs de risque , Jeune adulte , Tests cutanés , Prévalence , Carence en vitamine D/épidémiologie , Carence en vitamine D/sang , Carence en vitamine D/complications , Calcifédiol/sang , Phénotype
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